Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 283383 |
|---|---|
| ensemblid | ENSG00000111452.13 |
| hgncid | 19893 |
| symbol | ADGRD1 |
| name | adhesion G protein-coupled receptor D1 |
| refseq_nuc | NM_198827.5 |
| refseq_prot | NP_942122.2 |
| ensembl_nuc | ENST00000261654.10 |
| ensembl_prot | ENSP00000261654.5 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 130953907 |
| end | 131141469 |
| strand | + |
| ver | v1.2 |
| region | chr12:130953907-131141469 |
| region5000 | chr12:130948907-131146469 |
| regionname0 | ADGRD1_chr12_130953907_131141469 |
| regionname5000 | ADGRD1_chr12_130948907_131146469 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 874 | 214 | 56 | 53 | 62 | 12 | 30 | 42 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0002 | 0/0 | 874 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0003 | 0/0 | 874 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0004 | 0/0 | 874 | 4 | 0 | 4 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0005 | 0/0 | 874 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0006 | 0/0 | 874 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0007 | 0/0 | 874 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0008 | 0/0 | 874 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0009 | 0/0 | 874 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0010 | 0/0 | 874 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0011 | 0/0 | 874 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0012 | 0/1 | 874 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 2625 | 52 | 10 | 14 | 19 | 3 | 6 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0002 | 0/0 | 2625 | 50 | 4 | 13 | 23 | 2 | 8 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0003 | 0/0 | 2625 | 43 | 14 | 13 | 7 | 3 | 6 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0004 | 0/0 | 2625 | 19 | 1 | 5 | 6 | 3 | 4 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0005 | 0/0 | 2625 | 10 | 7 | 1 | 2 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0006 | 1/0 | 2625 | 7 | 6 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0007 | 0/0 | 2625 | 5 | 4 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0008 | 0/0 | 2625 | 4 | 0 | 0 | 2 | 0 | 2 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0009 | 0/0 | 2625 | 4 | 1 | 0 | 2 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0010 | 0/0 | 2625 | 4 | 1 | 1 | 1 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0011 | 0/0 | 2625 | 2 | 0 | 1 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0012 | 0/0 | 2625 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0013 | 0/0 | 2625 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0014 | 0/0 | 2625 | 2 | 0 | 1 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0015 | 0/0 | 2625 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0016 | 0/0 | 2625 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0017 | 0/0 | 2625 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0018 | 0/0 | 2625 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0019 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0020 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0021 | 0/0 | 2625 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0022 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0023 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0024 | 0/1 | 2625 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0025 | 0/0 | 2625 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0026 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0027 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0028 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0029 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0030 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0031 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0032 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0033 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0034 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0035 | 0/0 | 2625 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0036 | 0/0 | 2625 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0037 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0038 | 0/0 | 2625 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0039 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0040 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0041 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0042 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0043 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0044 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0045 | 0/0 | 2625 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| c0046 | 0/0 | 2625 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 2766 | 43 | 18 | 10 | 7 | 1 | 6 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0002 | 0/1 | 2766 | 37 | 5 | 11 | 8 | 6 | 6 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0003 | 0/0 | 2766 | 28 | 4 | 7 | 11 | 0 | 6 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0004 | 0/0 | 2767 | 23 | 10 | 9 | 0 | 1 | 3 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0005 | 0/0 | 2766 | 12 | 0 | 5 | 6 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0006 | 0/0 | 2767 | 9 | 2 | 4 | 1 | 1 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0007 | 0/0 | 2766 | 7 | 5 | 1 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0008 | 0/0 | 2766 | 7 | 4 | 2 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0009 | 0/0 | 2766 | 6 | 0 | 1 | 4 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0010 | 0/0 | 2766 | 6 | 0 | 1 | 5 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0011 | 0/0 | 2766 | 5 | 0 | 0 | 5 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0012 | 0/0 | 2767 | 5 | 1 | 1 | 1 | 1 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0013 | 0/0 | 2767 | 4 | 4 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0014 | 0/0 | 2767 | 4 | 0 | 0 | 3 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0015 | 0/0 | 2766 | 4 | 0 | 2 | 0 | 2 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0016 | 0/0 | 2766 | 3 | 3 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0017 | 0/0 | 2766 | 3 | 2 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0018 | 0/0 | 2767 | 3 | 3 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0019 | 0/0 | 2767 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0020 | 0/0 | 2766 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0021 | 0/0 | 2767 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0022 | 0/0 | 2766 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0023 | 0/0 | 2766 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0024 | 0/0 | 2766 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0025 | 0/0 | 2766 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0026 | 0/0 | 2766 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0027 | 0/0 | 2766 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0028 | 0/0 | 2766 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0029 | 0/0 | 2766 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0030 | 0/0 | 2767 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0031 | 0/0 | 2767 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0032 | 0/0 | 2767 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0033 | 0/0 | 2767 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0034 | 0/0 | 2767 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0035 | 0/0 | 2767 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0036 | 0/0 | 2767 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0037 | 0/0 | 2766 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0038 | 0/0 | 2766 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0039 | 0/0 | 2766 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0040 | 0/0 | 2766 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0041 | 0/0 | 2766 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0042 | 0/0 | 2766 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0043 | 0/0 | 2767 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0044 | 0/0 | 2767 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0045 | 0/0 | 2767 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0046 | 0/0 | 2766 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0047 | 0/0 | 2767 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| t0048 | 0/0 | 2767 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0196 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0241 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2625 | 52 | 10 | 14 | 19 | 3 | 6 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0002 | 0/0 | 2625 | 50 | 4 | 13 | 23 | 2 | 8 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0003 | 0/0 | 2625 | 43 | 14 | 13 | 7 | 3 | 6 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0004 | 0/0 | 2625 | 19 | 1 | 5 | 6 | 3 | 4 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0005 | 0/0 | 2625 | 10 | 7 | 1 | 2 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0006 | 1/0 | 2625 | 7 | 6 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0007 | 0/0 | 2625 | 5 | 4 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0008 | 0/0 | 2625 | 4 | 0 | 0 | 2 | 0 | 2 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0009 | 0/0 | 2625 | 4 | 1 | 0 | 2 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0010 | 0/0 | 2625 | 4 | 1 | 1 | 1 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0013 | 0/0 | 2625 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0014 | 0/0 | 2625 | 2 | 0 | 1 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0017 | 0/0 | 2625 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0019 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0020 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0022 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0023 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0025 | 0/0 | 2625 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0036 | 0/0 | 2625 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0042 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0043 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0045 | 0/0 | 2625 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0046 | 0/0 | 2625 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0002c0018 | 0/0 | 2625 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0002c0027 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0002c0028 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0002c0029 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0002c0030 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0002c0044 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0003c0012 | 0/0 | 2625 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0003c0031 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0003c0032 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0003c0033 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0003c0040 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0003c0041 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0004c0015 | 0/0 | 2625 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0004c0016 | 0/0 | 2625 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0005c0011 | 0/0 | 2625 | 2 | 0 | 1 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0005c0021 | 0/0 | 2625 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0006c0037 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0007c0039 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0008c0034 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0009c0035 | 0/0 | 2625 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0010c0026 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0011c0038 | 0/0 | 2625 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0012c0024 | 0/1 | 2625 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5390 | 11 | 2 | 5 | 0 | 1 | 3 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0001t0002 | 0/0 | 5390 | 18 | 3 | 5 | 7 | 1 | 2 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0001t0003 | 0/0 | 5390 | 2 | 1 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0001t0005 | 0/0 | 5390 | 4 | 0 | 2 | 2 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0001t0009 | 0/0 | 5390 | 5 | 0 | 0 | 4 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0001t0011 | 0/0 | 5390 | 5 | 0 | 0 | 5 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0001t0015 | 0/0 | 5390 | 2 | 0 | 1 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0001t0016 | 0/0 | 5390 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0001t0023 | 0/0 | 5390 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0001t0027 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0001t0028 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0002t0001 | 0/0 | 5390 | 14 | 2 | 4 | 5 | 0 | 3 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0002t0002 | 0/0 | 5390 | 4 | 0 | 3 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0002t0003 | 0/0 | 5390 | 19 | 1 | 4 | 11 | 0 | 3 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0002t0005 | 0/0 | 5390 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0002t0008 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0002t0010 | 0/0 | 5390 | 6 | 0 | 1 | 5 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0002t0025 | 0/0 | 5390 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0002t0037 | 0/0 | 5390 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0002t0040 | 0/0 | 5390 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0002t0046 | 0/0 | 5390 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0002t0048 | 0/0 | 5391 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0003t0001 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0003t0002 | 0/0 | 5390 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0003t0004 | 0/0 | 5391 | 15 | 4 | 7 | 0 | 1 | 3 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0003t0006 | 0/0 | 5391 | 8 | 1 | 4 | 1 | 1 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0003t0012 | 0/0 | 5391 | 4 | 1 | 1 | 1 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0003t0013 | 0/0 | 5391 | 3 | 3 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0003t0018 | 0/0 | 5391 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0003t0019 | 0/0 | 5391 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0003t0029 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0003t0033 | 0/0 | 5391 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0003t0034 | 0/0 | 5391 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0003t0035 | 0/0 | 5391 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0003t0036 | 0/0 | 5391 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0003t0041 | 0/0 | 5390 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0003t0044 | 0/0 | 5391 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0003t0045 | 0/0 | 5391 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0004t0002 | 0/0 | 5390 | 8 | 1 | 1 | 1 | 2 | 3 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0004t0005 | 0/0 | 5390 | 6 | 0 | 1 | 4 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0004t0009 | 0/0 | 5390 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0004t0015 | 0/0 | 5390 | 2 | 0 | 1 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0004t0024 | 0/0 | 5390 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0004t0043 | 0/0 | 5391 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0005t0001 | 0/0 | 5390 | 6 | 5 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0005t0003 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0005t0008 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0005t0014 | 0/0 | 5391 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0006t0001 | 1/0 | 5390 | 6 | 5 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0006t0008 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0007t0004 | 0/0 | 5391 | 3 | 2 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0007t0006 | 0/0 | 5391 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0007t0018 | 0/0 | 5391 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0008t0001 | 0/0 | 5390 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0008t0003 | 0/0 | 5390 | 2 | 0 | 0 | 0 | 0 | 2 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0009t0004 | 0/0 | 5391 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0009t0014 | 0/0 | 5391 | 2 | 0 | 0 | 1 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0009t0019 | 0/0 | 5391 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0010t0007 | 0/0 | 5390 | 3 | 1 | 1 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0010t0039 | 0/0 | 5390 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0013t0007 | 0/0 | 5390 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0014t0004 | 0/0 | 5391 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0014t0012 | 0/0 | 5391 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0017t0008 | 0/0 | 5390 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0019t0004 | 0/0 | 5391 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0020t0002 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0022t0016 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0023t0004 | 0/0 | 5391 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0025t0021 | 0/0 | 5391 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0036t0003 | 0/0 | 5390 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0042t0007 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0043t0008 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0045t0002 | 0/0 | 5390 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0001c0046t0017 | 0/0 | 5390 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0002c0018t0020 | 0/0 | 5390 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0002c0027t0001 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0002c0028t0001 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0002c0029t0031 | 0/0 | 5391 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0002c0030t0032 | 0/0 | 5391 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0002c0044t0007 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0003c0012t0017 | 0/0 | 5390 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0003c0031t0003 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0003c0032t0038 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0003c0033t0030 | 0/0 | 5391 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0003c0040t0022 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0003c0041t0004 | 0/0 | 5391 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0004c0015t0003 | 0/0 | 5390 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0004c0015t0005 | 0/0 | 5390 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0004c0016t0002 | 0/0 | 5390 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0004c0016t0003 | 0/0 | 5390 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0005c0011t0002 | 0/0 | 5390 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0005c0011t0008 | 0/0 | 5390 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0005c0021t0021 | 0/0 | 5391 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0006c0037t0042 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0007c0039t0001 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0008c0034t0026 | 0/0 | 5390 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0009c0035t0047 | 0/0 | 5391 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0010c0026t0013 | 0/0 | 5391 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0011c0038t0002 | 0/0 | 5390 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| a0012c0024t0002 | 0/1 | 5390 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | copy fasta | chr12 | 130948907 | 131146469 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0005g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0005g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0005g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0005g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0009g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0009g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0009g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0009g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0009g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0011g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0011g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0011g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0011g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0011g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0015g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0015g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0016g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0016g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0023g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0027g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0001t0028g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0002g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0002g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0003g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0005g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0008g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0010g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0010g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0010g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0010g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0010g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0010g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0025g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0037g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0040g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0046g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0002t0048g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0004g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0004g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0004g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0004g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0004g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0004g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0004g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0004g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0004g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0004g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0004g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0006g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0006g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0006g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0006g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0006g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0006g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0006g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0006g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0012g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0012g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0012g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0012g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0013g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0013g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0013g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0018g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0018g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0019g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0029g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0033g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0034g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0035g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0036g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0041g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0044g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0003t0045g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0004t0002g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0004t0002g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0004t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0004t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0004t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0004t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0004t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0004t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0004t0005g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0004t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0004t0005g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0004t0005g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0004t0005g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0004t0005g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0004t0009g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0004t0015g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0004t0015g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0004t0024g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0004t0043g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0005t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0005t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0005t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0005t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0005t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0005t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0005t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0005t0008g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0005t0014g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0005t0014g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0006t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0006t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0006t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0006t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0006t0001g0241 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0006t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0006t0008g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0007t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0007t0004g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0007t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0007t0006g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0007t0018g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0008t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0008t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0008t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0008t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0009t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0009t0014g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0009t0014g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0009t0019g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0010t0007g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0010t0007g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0010t0007g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0010t0039g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0013t0007g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0013t0007g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0014t0004g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0014t0012g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0017t0008g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0017t0008g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0019t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0020t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0022t0016g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0023t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0025t0021g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0036t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0042t0007g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0043t0008g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0045t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0001c0046t0017g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0002c0018t0020g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0002c0018t0020g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0002c0027t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0002c0028t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0002c0029t0031g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0002c0030t0032g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0002c0044t0007g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0003c0012t0017g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0003c0012t0017g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0003c0031t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0003c0032t0038g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0003c0033t0030g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0003c0040t0022g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0003c0041t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0004c0015t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0004c0015t0005g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0004c0016t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0004c0016t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0005c0011t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0005c0011t0008g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0005c0021t0021g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0006c0037t0042g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0007c0039t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0008c0034t0026g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0009c0035t0047g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0010c0026t0013g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0011c0038t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| a0012c0024t0002g0196 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0004 | t0002 | g0193 | EUR | GBR | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG00140 | hp2 | a0001 | c0001 | t0015 | g0060 | EUR | GBR | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG00280 | hp1 | a0005 | c0011 | t0008 | g0047 | EUR | FIN | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG00280 | hp2 | a0001 | c0002 | t0040 | g0035 | EUR | FIN | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG00323 | hp1 | a0001 | c0014 | t0012 | g0069 | EUR | FIN | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0106 | EUR | FIN | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG00609 | hp1 | a0001 | c0002 | t0003 | g0076 | EAS | CHS | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG00609 | hp2 | a0001 | c0002 | t0037 | g0194 | EAS | CHS | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG00621 | hp1 | a0001 | c0003 | t0006 | g0216 | EAS | CHS | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG00621 | hp2 | a0001 | c0002 | t0003 | g0083 | EAS | CHS | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG00639 | hp2 | a0004 | c0015 | t0005 | g0086 | AMR | PUR | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG00735 | hp1 | a0001 | c0003 | t0006 | g0092 | AMR | PUR | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG00735 | hp2 | a0001 | c0004 | t0002 | g0155 | AMR | PUR | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0203 | AMR | PUR | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG00738 | hp2 | a0009 | c0035 | t0047 | g0219 | AMR | PUR | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG00741 | hp1 | a0001 | c0004 | t0043 | g0024 | AMR | PUR | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0107 | AMR | PUR | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01069 | hp1 | a0001 | c0003 | t0004 | g0101 | AMR | PUR | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0204 | AMR | PUR | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01071 | hp1 | a0001 | c0014 | t0004 | g0105 | AMR | PUR | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01071 | hp2 | a0001 | c0003 | t0004 | g0108 | AMR | PUR | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0023 | AMR | PUR | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01074 | hp2 | a0004 | c0016 | t0002 | g0065 | AMR | PUR | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01099 | hp1 | a0001 | c0004 | t0015 | g0099 | AMR | PUR | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01099 | hp2 | a0001 | c0003 | t0006 | g0215 | AMR | PUR | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01106 | hp1 | a0005 | c0011 | t0002 | g0110 | AMR | PUR | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01109 | hp1 | a0001 | c0007 | t0004 | g0102 | AMR | PUR | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01109 | hp2 | a0001 | c0003 | t0006 | g0058 | AMR | PUR | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01167 | hp1 | a0001 | c0005 | t0001 | g0127 | AMR | PUR | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0146 | AMR | PUR | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01168 | hp1 | a0001 | c0003 | t0004 | g0104 | AMR | PUR | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01168 | hp2 | a0001 | c0017 | t0008 | g0029 | AMR | PUR | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01169 | hp1 | a0001 | c0017 | t0008 | g0030 | AMR | PUR | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0145 | AMR | PUR | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01175 | hp1 | a0001 | c0003 | t0006 | g0211 | AMR | PUR | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01175 | hp2 | a0001 | c0003 | t0004 | g0237 | AMR | PUR | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01243 | hp1 | a0001 | c0010 | t0007 | g0213 | AMR | PUR | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01243 | hp2 | a0004 | c0015 | t0003 | g0052 | AMR | PUR | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01257 | hp1 | a0001 | c0003 | t0004 | g0189 | AMR | CLM | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01258 | hp1 | a0001 | c0001 | t0015 | g0097 | AMR | CLM | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01258 | hp2 | a0001 | c0003 | t0004 | g0190 | AMR | CLM | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01261 | hp1 | a0001 | c0003 | t0033 | g0181 | AMR | CLM | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01261 | hp2 | a0001 | c0001 | t0005 | g0045 | AMR | CLM | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01346 | hp1 | a0001 | c0002 | t0010 | g0167 | AMR | CLM | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01346 | hp2 | a0001 | c0004 | t0005 | g0082 | AMR | CLM | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0149 | AMR | CLM | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01361 | hp2 | a0001 | c0003 | t0004 | g0188 | AMR | CLM | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01433 | hp1 | a0001 | c0002 | t0005 | g0040 | AMR | CLM | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01496 | hp1 | a0001 | c0003 | t0012 | g0025 | AMR | CLM | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01496 | hp2 | a0001 | c0002 | t0003 | g0061 | AMR | CLM | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0163 | EUR | IBS | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01515 | hp2 | a0001 | c0003 | t0006 | g0185 | EUR | IBS | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01516 | hp1 | a0001 | c0004 | t0015 | g0093 | EUR | IBS | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01516 | hp2 | a0001 | c0003 | t0004 | g0192 | EUR | IBS | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0228 | AFR | ACB | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01928 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | PEL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01928 | hp2 | a0001 | c0004 | t0009 | g0168 | AMR | PEL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01934 | hp1 | a0001 | c0046 | t0017 | g0221 | AMR | PEL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01934 | hp2 | a0001 | c0025 | t0021 | g0119 | AMR | PEL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01943 | hp1 | a0001 | c0001 | t0005 | g0028 | AMR | PEL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0098 | AMR | PEL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01978 | hp1 | a0001 | c0002 | t0003 | g0038 | AMR | PEL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01981 | hp1 | a0001 | c0002 | t0003 | g0039 | AMR | PEL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG01981 | hp2 | a0005 | c0021 | t0021 | g0048 | AMR | PEL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02040 | hp1 | a0001 | c0005 | t0014 | g0049 | EAS | KHV | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02040 | hp2 | a0001 | c0001 | t0009 | g0137 | EAS | KHV | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02055 | hp1 | a0001 | c0007 | t0004 | g0236 | AFR | ACB | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02055 | hp2 | a0001 | c0007 | t0006 | g0021 | AFR | ACB | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02056 | hp1 | a0001 | c0001 | t0005 | g0087 | EAS | KHV | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0169 | EAS | KHV | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02071 | hp1 | a0001 | c0002 | t0003 | g0081 | EAS | KHV | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02071 | hp2 | a0001 | c0002 | t0003 | g0064 | EAS | KHV | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02083 | hp1 | a0001 | c0004 | t0005 | g0072 | EAS | KHV | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | KHV | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02132 | hp1 | a0001 | c0005 | t0014 | g0054 | EAS | KHV | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02132 | hp2 | a0001 | c0001 | t0011 | g0066 | EAS | KHV | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02135 | hp1 | a0001 | c0003 | t0012 | g0063 | EAS | KHV | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02135 | hp2 | a0001 | c0002 | t0003 | g0068 | EAS | KHV | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02155 | hp1 | a0001 | c0009 | t0014 | g0037 | EAS | CDX | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02155 | hp2 | a0001 | c0002 | t0003 | g0057 | EAS | CDX | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02257 | hp1 | a0001 | c0003 | t0036 | g0209 | AFR | ACB | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02257 | hp2 | a0002 | c0044 | t0007 | g0126 | AFR | ACB | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02258 | hp1 | a0003 | c0041 | t0004 | g0178 | AFR | ACB | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02258 | hp2 | a0001 | c0005 | t0001 | g0206 | AFR | ACB | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | PEL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02273 | hp2 | a0004 | c0016 | t0003 | g0051 | AMR | PEL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02280 | hp1 | a0001 | c0001 | t0016 | g0147 | AFR | ACB | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02280 | hp2 | a0001 | c0003 | t0029 | g0214 | AFR | ACB | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02293 | hp2 | a0001 | c0002 | t0002 | g0009 | AMR | PEL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0202 | AMR | PEL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02300 | hp2 | a0001 | c0002 | t0003 | g0053 | AMR | PEL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02451 | hp1 | a0001 | c0001 | t0027 | g0118 | AFR | ACB | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02451 | hp2 | a0001 | c0006 | t0001 | g0148 | AFR | ACB | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02572 | hp1 | a0001 | c0007 | t0004 | g0018 | AFR | GWD | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02572 | hp2 | a0001 | c0007 | t0018 | g0132 | AFR | GWD | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02602 | hp1 | a0001 | c0002 | t0003 | g0077 | SAS | PJL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02602 | hp2 | a0001 | c0003 | t0006 | g0015 | SAS | PJL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02630 | hp1 | a0001 | c0003 | t0013 | g0129 | AFR | GWD | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02630 | hp2 | a0003 | c0031 | t0003 | g0089 | AFR | GWD | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02647 | hp1 | a0001 | c0003 | t0004 | g0207 | AFR | GWD | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02647 | hp2 | a0001 | c0001 | t0028 | g0205 | AFR | GWD | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0100 | SAS | PJL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02683 | hp2 | a0001 | c0003 | t0004 | g0013 | SAS | PJL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02698 | hp2 | a0001 | c0002 | t0003 | g0050 | SAS | PJL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02717 | hp1 | a0001 | c0010 | t0007 | g0160 | AFR | GWD | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02717 | hp2 | a0001 | c0003 | t0018 | g0232 | AFR | GWD | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02723 | hp1 | a0001 | c0003 | t0001 | g0152 | AFR | GWD | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02723 | hp2 | a0010 | c0026 | t0013 | g0238 | AFR | GWD | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02735 | hp1 | a0001 | c0003 | t0034 | g0014 | SAS | PJL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02735 | hp2 | a0001 | c0009 | t0014 | g0078 | SAS | PJL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02809 | hp1 | a0001 | c0005 | t0001 | g0044 | AFR | GWD | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02809 | hp2 | a0001 | c0042 | t0007 | g0176 | AFR | GWD | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02818 | hp1 | a0001 | c0003 | t0006 | g0019 | AFR | GWD | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02818 | hp2 | a0001 | c0013 | t0007 | g0153 | AFR | GWD | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02895 | hp1 | a0001 | c0005 | t0001 | g0112 | AFR | GWD | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02895 | hp2 | a0001 | c0003 | t0004 | g0122 | AFR | GWD | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02896 | hp1 | a0001 | c0003 | t0013 | g0224 | AFR | GWD | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02896 | hp2 | a0001 | c0002 | t0008 | g0016 | AFR | GWD | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02897 | hp1 | a0001 | c0003 | t0004 | g0121 | AFR | GWD | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02897 | hp2 | a0001 | c0003 | t0013 | g0225 | AFR | GWD | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02922 | hp1 | a0001 | c0043 | t0008 | g0227 | AFR | ESN | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02922 | hp2 | a0003 | c0012 | t0017 | g0158 | AFR | ESN | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02965 | hp1 | a0002 | c0018 | t0020 | g0123 | AFR | ESN | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02965 | hp2 | a0002 | c0027 | t0001 | g0179 | AFR | ESN | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG03041 | hp1 | a0001 | c0006 | t0001 | g0120 | AFR | GWD | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG03041 | hp2 | a0001 | c0005 | t0003 | g0056 | AFR | GWD | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG03098 | hp1 | a0001 | c0006 | t0001 | g0233 | AFR | MSL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0125 | AFR | MSL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG03139 | hp1 | a0002 | c0018 | t0020 | g0124 | AFR | ESN | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | ESN | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG03195 | hp1 | a0001 | c0006 | t0008 | g0177 | AFR | ESN | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG03195 | hp2 | a0001 | c0003 | t0012 | g0027 | AFR | ESN | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG03209 | hp1 | a0001 | c0006 | t0001 | g0242 | AFR | MSL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG03209 | hp2 | a0003 | c0033 | t0030 | g0231 | AFR | MSL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG03225 | hp1 | a0007 | c0039 | t0001 | g0229 | AFR | MSL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG03225 | hp2 | a0002 | c0028 | t0001 | g0022 | AFR | MSL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG03239 | hp1 | a0001 | c0004 | t0002 | g0007 | SAS | PJL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG03239 | hp2 | a0001 | c0008 | t0003 | g0059 | SAS | PJL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0235 | AFR | MSL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG03453 | hp2 | a0001 | c0020 | t0002 | g0180 | AFR | MSL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG03486 | hp1 | a0002 | c0030 | t0032 | g0159 | AFR | MSL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG03486 | hp2 | a0008 | c0034 | t0026 | g0043 | AFR | MSL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG03540 | hp1 | a0001 | c0005 | t0001 | g0239 | AFR | GWD | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG03540 | hp2 | a0001 | c0004 | t0002 | g0114 | AFR | GWD | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG03579 | hp1 | a0001 | c0005 | t0001 | g0128 | AFR | MSL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG03579 | hp2 | a0001 | c0003 | t0018 | g0117 | AFR | MSL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0184 | SAS | PJL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG03669 | hp2 | a0001 | c0036 | t0003 | g0075 | SAS | PJL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG03688 | hp1 | a0001 | c0003 | t0004 | g0012 | SAS | STU | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | STU | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG03704 | hp1 | a0001 | c0002 | t0003 | g0071 | SAS | PJL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG03704 | hp2 | a0001 | c0002 | t0046 | g0084 | SAS | PJL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG03710 | hp1 | a0001 | c0004 | t0002 | g0164 | SAS | PJL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG03710 | hp2 | a0001 | c0003 | t0012 | g0088 | SAS | PJL | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0195 | SAS | BEB | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG03831 | hp2 | a0001 | c0001 | t0009 | g0136 | SAS | BEB | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0157 | SAS | BEB | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG03834 | hp2 | a0001 | c0010 | t0039 | g0031 | SAS | BEB | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG03942 | hp1 | a0001 | c0002 | t0048 | g0151 | SAS | BEB | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG03942 | hp2 | a0001 | c0008 | t0003 | g0067 | SAS | BEB | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG04115 | hp1 | a0001 | c0004 | t0005 | g0095 | SAS | STU | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG04115 | hp2 | a0001 | c0045 | t0002 | g0091 | SAS | STU | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG04199 | hp1 | a0001 | c0004 | t0002 | g0011 | SAS | STU | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG04199 | hp2 | a0001 | c0003 | t0004 | g0198 | SAS | STU | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0217 | SAS | STU | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | STU | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA18612 | hp1 | a0001 | c0002 | t0010 | g0142 | EAS | CHB | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA18612 | hp2 | a0001 | c0003 | t0041 | g0080 | EAS | CHB | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA18906 | hp1 | a0001 | c0023 | t0004 | g0165 | AFR | YRI | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA18906 | hp2 | a0001 | c0003 | t0004 | g0234 | AFR | YRI | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA18957 | hp1 | a0001 | c0001 | t0011 | g0074 | EAS | JPT | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA18957 | hp2 | a0001 | c0002 | t0003 | g0073 | EAS | JPT | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA18959 | hp2 | a0001 | c0002 | t0010 | g0134 | EAS | JPT | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA18961 | hp2 | a0001 | c0001 | t0009 | g0140 | EAS | JPT | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA18970 | hp1 | a0001 | c0008 | t0001 | g0170 | EAS | JPT | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA18970 | hp2 | a0001 | c0001 | t0009 | g0144 | EAS | JPT | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA18973 | hp1 | a0001 | c0002 | t0003 | g0085 | EAS | JPT | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA18973 | hp2 | a0001 | c0003 | t0035 | g0200 | EAS | JPT | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA18974 | hp1 | a0001 | c0004 | t0005 | g0094 | EAS | JPT | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA18974 | hp2 | a0001 | c0002 | t0003 | g0020 | EAS | JPT | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA18982 | hp1 | a0001 | c0001 | t0005 | g0055 | EAS | JPT | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA18982 | hp2 | a0001 | c0002 | t0010 | g0138 | EAS | JPT | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA18983 | hp1 | a0001 | c0001 | t0009 | g0166 | EAS | JPT | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA18983 | hp2 | a0001 | c0001 | t0023 | g0143 | EAS | JPT | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA18986 | hp1 | a0001 | c0010 | t0007 | g0150 | EAS | JPT | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA18986 | hp2 | a0001 | c0008 | t0001 | g0183 | EAS | JPT | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA18992 | hp1 | a0001 | c0002 | t0025 | g0141 | EAS | JPT | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA18992 | hp2 | a0001 | c0004 | t0002 | g0131 | EAS | JPT | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA19002 | hp1 | a0001 | c0001 | t0011 | g0220 | EAS | JPT | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA19002 | hp2 | a0001 | c0003 | t0044 | g0079 | EAS | JPT | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA19009 | hp1 | a0001 | c0001 | t0011 | g0062 | EAS | JPT | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA19009 | hp2 | a0001 | c0002 | t0010 | g0201 | EAS | JPT | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA19010 | hp1 | a0001 | c0003 | t0019 | g0218 | EAS | JPT | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA19030 | hp1 | a0003 | c0040 | t0022 | g0096 | AFR | LWK | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | LWK | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA19043 | hp1 | a0001 | c0006 | t0001 | g0240 | AFR | LWK | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA19043 | hp2 | a0001 | c0022 | t0016 | g0109 | AFR | LWK | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA19080 | hp1 | a0001 | c0001 | t0011 | g0033 | EAS | JPT | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA19080 | hp2 | a0001 | c0004 | t0005 | g0070 | EAS | JPT | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0199 | EAS | JPT | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA19084 | hp1 | a0001 | c0003 | t0045 | g0042 | EAS | JPT | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA19084 | hp2 | a0001 | c0009 | t0019 | g0135 | EAS | JPT | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA19088 | hp2 | a0001 | c0002 | t0003 | g0034 | EAS | JPT | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA19089 | hp1 | a0001 | c0002 | t0010 | g0139 | EAS | JPT | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA19090 | hp1 | a0001 | c0002 | t0003 | g0041 | EAS | JPT | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA19090 | hp2 | a0001 | c0004 | t0024 | g0133 | EAS | JPT | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA19091 | hp1 | a0001 | c0004 | t0005 | g0036 | EAS | JPT | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA20129 | hp1 | a0001 | c0005 | t0008 | g0226 | AFR | ASW | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA20129 | hp2 | a0001 | c0009 | t0004 | g0103 | AFR | ASW | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA20752 | hp1 | a0001 | c0004 | t0002 | g0004 | EUR | TSI | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA20752 | hp2 | a0001 | c0003 | t0002 | g0186 | EUR | TSI | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0171 | EUR | TSI | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA20805 | hp2 | a0011 | c0038 | t0002 | g0162 | EUR | TSI | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02109 | hp1 | a0001 | c0019 | t0004 | g0230 | AFR | ACB | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02109 | hp2 | a0003 | c0012 | t0017 | g0017 | AFR | ACB | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02486 | hp1 | a0006 | c0037 | t0042 | g0046 | AFR | ACB | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02486 | hp2 | a0001 | c0001 | t0016 | g0182 | AFR | ACB | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02559 | hp1 | a0003 | c0032 | t0038 | g0090 | AFR | ACB | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0223 | AFR | ACB | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG06807 | hp1 | a0001 | c0002 | t0003 | g0032 | AFR | USA | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| HG06807 | hp2 | a0001 | c0013 | t0007 | g0154 | AFR | USA | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA21309 | hp1 | a0002 | c0029 | t0031 | g0222 | AFR | LWK | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | LWK | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| homoSapiens_chm13v2 | hp1 | a0012 | c0024 | t0002 | g0196 | REF | REF | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| homoSapiens_grch38 | hp1 | a0001 | c0006 | t0001 | g0241 | REF | REF | ADGRD1_chr12_130948907_131146469 | ADGRD1 | chr12 | 130948907 | 131146469 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:130987154
|
G | A | 1 | a0005 | 3 | HG00280.hp1 HG01106.hp1 HG01981.hp2 |
missense_variant | MODERATE | c.550G>A | p.Val184Ile | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/25 | 1109/5390 | 550/2625 | 184/874 | chr12 | 130987154 | ||
| chr12:130991062
|
C | A | 1 | a0012 | 1 | homoSapiens_chm13v2.hp1 | missense_variant | MODERATE | c.794C>A | p.Ser265Tyr | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 7/25 | 1353/5390 | 794/2625 | 265/874 | chr12 | 130991062 | ||
| chr12:131003249
|
A | G | 1 | a0011 | 1 | NA20805.hp2 | missense_variant | MODERATE | c.1091A>G | p.Asn364Ser | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 10/25 | 1650/5390 | 1091/2625 | 364/874 | chr12 | 131003249 | ||
| chr12:131006044
|
C | T | 1 | a0006 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.1328C>T | p.Thr443Ile | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/25 | 1887/5390 | 1328/2625 | 443/874 | chr12 | 131006044 | ||
| chr12:131014239
|
G | A | 1 | a0010 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1372G>A | p.Ala458Thr | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/25 | 1931/5390 | 1372/2625 | 458/874 | chr12 | 131014239 | ||
| chr12:131014257
|
T | G | 1 | a0002 | 7 | HG02257.hp2 HG02965.hp1 HG02965.hp2 others(4): Show |
missense_variant | MODERATE | c.1390T>G | p.Ser464Ala | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/25 | 1949/5390 | 1390/2625 | 464/874 | chr12 | 131014257 | ||
| chr12:131076849
|
G | A | 3 | a0003a0006a0007 | 9 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(6): Show |
missense_variant | MODERATE | c.1522G>A | p.Val508Met | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/25 | 2081/5390 | 1522/2625 | 508/874 | chr12 | 131076849 | ||
| chr12:131084560
|
C | T | 1 | a0004 | 4 | HG00639.hp2 HG01074.hp2 HG01243.hp2 others(1): Show |
missense_variant | MODERATE | c.1568C>T | p.Ser523Leu | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/25 | 2127/5390 | 1568/2625 | 523/874 | chr12 | 131084560 | ||
| chr12:131105848
|
C | T | 1 | a0008 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.1870C>T | p.Arg624Cys | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 17/25 | 2429/5390 | 1870/2625 | 624/874 | chr12 | 131105848 | ||
| chr12:131136098
|
G | A | 1 | a0009 | 1 | HG00738.hp2 | missense_variant | MODERATE | c.2329G>A | p.Val777Met | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 22/25 | 2888/5390 | 2329/2625 | 777/874 | chr12 | 131136098 | ||
| chr12:131139241
|
G | A | 1 | a0007 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.2603G>A | p.Arg868His | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 25/25 | 3162/5390 | 2603/2625 | 868/874 | chr12 | 131139241 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:130981897
|
T | C | 2 | a0001c0019a0001c0020 | 2 | HG02109.hp1 HG03453.hp2 |
synonymous_variant | LOW | c.324T>C | p.Ser108Ser | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/25 | 883/5390 | 324/2625 | 108/874 | chr12 | 130981897 | ||
| chr12:130982017
|
T | C | 40 | a0001c0001a0001c0002a0001c0003others(37): Show | 225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
synonymous_variant | LOW | c.444T>C | p.Tyr148Tyr | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/25 | 1003/5390 | 444/2625 | 148/874 | chr12 | 130982017 | ||
| chr12:130991021
|
T | C | 4 | a0001c0019a0001c0020a0001c0022others(1): Show | 4 | HG02109.hp1 HG03453.hp2 NA18906.hp1 others(1): Show |
synonymous_variant | LOW | c.753T>C | p.His251His | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 7/25 | 1312/5390 | 753/2625 | 251/874 | chr12 | 130991021 | ||
| chr12:130991045
|
A | G | 4 | a0001c0019a0001c0020a0001c0022others(1): Show | 4 | HG02109.hp1 HG03453.hp2 NA18906.hp1 others(1): Show |
synonymous_variant | LOW | c.777A>G | p.Pro259Pro | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 7/25 | 1336/5390 | 777/2625 | 259/874 | chr12 | 130991045 | ||
| chr12:130992359
|
C | T | 5 | a0001c0042a0001c0043a0003c0040others(2): Show | 5 | HG02258.hp1 HG02809.hp2 HG02922.hp1 others(2): Show |
synonymous_variant | LOW | c.933C>T | p.Ser311Ser | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/25 | 1492/5390 | 933/2625 | 311/874 | chr12 | 130992359 | ||
| chr12:131000397
|
C | T | 1 | a0001c0017 | 2 | HG01168.hp2 HG01169.hp1 |
synonymous_variant | LOW | c.981C>T | p.Ala327Ala | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 9/25 | 1540/5390 | 981/2625 | 327/874 | chr12 | 131000397 | ||
| chr12:131004244
|
G | A | 1 | a0001c0025 | 1 | HG01934.hp2 | synonymous_variant | LOW | c.1203G>A | p.Pro401Pro | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 11/25 | 1762/5390 | 1203/2625 | 401/874 | chr12 | 131004244 | ||
| chr12:131105757
|
C | T | 2 | a0002c0030a0010c0026 | 2 | HG02723.hp2 HG03486.hp1 |
synonymous_variant | LOW | c.1779C>T | p.Ser593Ser | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 17/25 | 2338/5390 | 1779/2625 | 593/874 | chr12 | 131105757 | ||
| chr12:131105763
|
C | T | 1 | a0001c0036 | 1 | HG03669.hp2 | synonymous_variant | LOW | c.1785C>T | p.Ser595Ser | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 17/25 | 2344/5390 | 1785/2625 | 595/874 | chr12 | 131105763 | ||
| chr12:131105826
|
G | A | 1 | a0008c0034 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.1848G>A | p.Gln616Gln | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 17/25 | 2407/5390 | 1848/2625 | 616/874 | chr12 | 131105826 | ||
| chr12:131105859
|
G | A | 5 | a0001c0004a0001c0008a0001c0009others(2): Show | 29 | HG00140.hp1 HG00735.hp2 HG00741.hp1 others(26): Show |
synonymous_variant | LOW | c.1881G>A | p.Pro627Pro | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 17/25 | 2440/5390 | 1881/2625 | 627/874 | chr12 | 131105859 | ||
| chr12:131120898
|
C | T | 1 | a0001c0014 | 2 | HG00323.hp1 HG01071.hp1 |
synonymous_variant | LOW | c.2160C>T | p.Ala720Ala | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/25 | 2719/5390 | 2160/2625 | 720/874 | chr12 | 131120898 | ||
| chr12:131120910
|
C | T | 1 | a0001c0020 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.2172C>T | p.Ile724Ile | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/25 | 2731/5390 | 2172/2625 | 724/874 | chr12 | 131120910 | ||
| chr12:131131814
|
C | T | 1 | a0002c0044 | 1 | HG02257.hp2 | splice_region_variant&synonymous_variant | LOW | c.2265C>T | p.Phe755Phe | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/25 | 2824/5390 | 2265/2625 | 755/874 | chr12 | 131131814 | ||
| chr12:131136043
|
A | G | 35 | a0001c0001a0001c0003a0001c0004others(32): Show | 162 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
synonymous_variant | LOW | c.2274A>G | p.Thr758Thr | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 22/25 | 2833/5390 | 2274/2625 | 758/874 | chr12 | 131136043 | ||
| chr12:131138190
|
T | C | 28 | a0001c0001a0001c0002a0001c0004others(25): Show | 159 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
synonymous_variant | LOW | c.2490T>C | p.Ser830Ser | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 24/25 | 3049/5390 | 2490/2625 | 830/874 | chr12 | 131138190 | ||
| chr12:131139185
|
A | C | 8 | a0001c0010a0001c0013a0001c0042others(5): Show | 13 | HG01243.hp1 HG02257.hp2 HG02559.hp1 others(10): Show |
synonymous_variant | LOW | c.2547A>C | p.Pro849Pro | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 25/25 | 3106/5390 | 2547/2625 | 849/874 | chr12 | 131139185 | ||
| chr12:131139242
|
C | T | 3 | a0001c0046a0003c0012a0006c0037 | 4 | HG01934.hp1 HG02109.hp2 HG02486.hp1 others(1): Show |
synonymous_variant | LOW | c.2604C>T | p.Arg868Arg | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 25/25 | 3163/5390 | 2604/2625 | 868/874 | chr12 | 131139242 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:130953978
|
C | T | 1 | a0001c0002t0048 | 1 | HG03942.hp1 | 5_prime_UTR_variant | MODIFIER | c.-488C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 1/25 | 488 | chr12 | 130953978 | |||||
| chr12:130954136
|
G | A | 1 | a0003c0040t0022 | 1 | NA19030.hp1 | 5_prime_UTR_variant | MODIFIER | c.-330G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 1/25 | 330 | chr12 | 130954136 | |||||
| chr12:130954148
|
C | T | 11 | a0001c0001t0015a0001c0002t0008a0001c0004t0015others(8): Show | 14 | HG00140.hp2 HG00280.hp1 HG00738.hp2 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-318C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 1/25 | 318 | chr12 | 130954148 | |||||
| chr12:130954282
|
G | A | 8 | a0001c0001t0009a0001c0001t0023a0001c0002t0010others(5): Show | 17 | HG01346.hp1 HG01928.hp2 HG02040.hp2 others(14): Show |
5_prime_UTR_variant | MODIFIER | c.-184G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 1/25 | 184 | chr12 | 130954282 | |||||
| chr12:130954426
|
G | T | 26 | a0001c0001t0003a0001c0001t0005a0001c0001t0011others(23): Show | 63 | HG00280.hp2 HG00323.hp1 HG00609.hp1 others(60): Show |
5_prime_UTR_variant | MODIFIER | c.-40G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 1/25 | 40 | chr12 | 130954426 | |||||
| chr12:131139305
|
A | AC | 33 | a0001c0002t0048a0001c0003t0004a0001c0003t0006others(30): Show | 64 | HG00323.hp1 HG00621.hp1 HG00735.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*49dupC | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 25/25 | 50 | INFO_REALIGN_3_PRIME | chr12 | 131139305 | ||||
| chr12:131139311
|
C | G | 2 | a0001c0002t0037a0001c0002t0046 | 2 | HG00609.hp2 HG03704.hp2 |
3_prime_UTR_variant | MODIFIER | c.*48C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 25/25 | 48 | chr12 | 131139311 | |||||
| chr12:131139363
|
G | C | 1 | a0003c0033t0030 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*100G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 25/25 | 100 | chr12 | 131139363 | |||||
| chr12:131139491
|
G | A | 2 | a0001c0001t0011a0001c0001t0023 | 6 | HG02132.hp2 NA18957.hp1 NA18983.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*228G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 25/25 | 228 | chr12 | 131139491 | |||||
| chr12:131139511
|
G | C | 2 | a0002c0029t0031a0003c0033t0030 | 2 | HG03209.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*248G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 25/25 | 248 | chr12 | 131139511 | |||||
| chr12:131139589
|
G | A | 1 | a0003c0032t0038 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*326G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 25/25 | 326 | chr12 | 131139589 | |||||
| chr12:131139615
|
C | T | 3 | a0001c0046t0017a0003c0012t0017a0006c0037t0042 | 4 | HG01934.hp1 HG02109.hp2 HG02486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*352C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 25/25 | 352 | chr12 | 131139615 | |||||
| chr12:131139616
|
G | A | 3 | a0001c0046t0017a0003c0012t0017a0006c0037t0042 | 4 | HG01934.hp1 HG02109.hp2 HG02486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*353G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 25/25 | 353 | chr12 | 131139616 | |||||
| chr12:131139729
|
G | T | 1 | a0001c0002t0025 | 1 | NA18992.hp1 | 3_prime_UTR_variant | MODIFIER | c.*466G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 25/25 | 466 | chr12 | 131139729 | |||||
| chr12:131139901
|
G | A | 10 | a0001c0010t0007a0001c0010t0039a0001c0013t0007others(7): Show | 14 | HG01243.hp1 HG02257.hp2 HG02559.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*638G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 25/25 | 638 | chr12 | 131139901 | |||||
| chr12:131139950
|
G | C | 36 | a0001c0001t0002a0001c0001t0005a0001c0001t0009others(33): Show | 86 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*687G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 25/25 | 687 | chr12 | 131139950 | |||||
| chr12:131139969
|
C | T | 16 | a0001c0003t0006a0001c0003t0019a0001c0003t0035others(13): Show | 26 | HG00621.hp1 HG00735.hp1 HG00738.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*706C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 25/25 | 706 | chr12 | 131139969 | |||||
| chr12:131140030
|
C | T | 1 | a0001c0004t0024 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*767C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 25/25 | 767 | chr12 | 131140030 | |||||
| chr12:131140059
|
G | A | 1 | a0001c0002t0040 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*796G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 25/25 | 796 | chr12 | 131140059 | |||||
| chr12:131140135
|
G | C | 32 | a0001c0001t0027a0001c0003t0004a0001c0003t0006others(29): Show | 63 | HG00323.hp1 HG00621.hp1 HG00735.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*872G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 25/25 | 872 | chr12 | 131140135 | |||||
| chr12:131140147
|
G | A | 13 | a0001c0003t0006a0001c0003t0019a0001c0003t0035others(10): Show | 22 | HG00621.hp1 HG00735.hp1 HG00738.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*884G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 25/25 | 884 | chr12 | 131140147 | |||||
| chr12:131140261
|
C | T | 1 | a0008c0034t0026 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*998C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 25/25 | 998 | chr12 | 131140261 | |||||
| chr12:131140352
|
C | T | 1 | a0001c0003t0044 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1089C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 25/25 | 1089 | chr12 | 131140352 | |||||
| chr12:131140389
|
T | C | 66 | a0001c0001t0002a0001c0001t0005a0001c0001t0009others(63): Show | 147 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(144): Show |
3_prime_UTR_variant | MODIFIER | c.*1126T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 25/25 | 1126 | chr12 | 131140389 | |||||
| chr12:131140428
|
T | C | 14 | a0001c0001t0027a0001c0010t0007a0001c0010t0039others(11): Show | 19 | HG01243.hp1 HG01934.hp1 HG02109.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1165T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 25/25 | 1165 | chr12 | 131140428 | |||||
| chr12:131140490
|
G | A | 2 | a0001c0003t0035a0001c0003t0045 | 2 | NA18973.hp2 NA19084.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1227G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 25/25 | 1227 | chr12 | 131140490 | |||||
| chr12:131140496
|
C | T | 2 | a0001c0003t0018a0001c0007t0018 | 3 | HG02572.hp2 HG02717.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1233C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 25/25 | 1233 | chr12 | 131140496 | |||||
| chr12:131140515
|
T | C | 30 | a0001c0003t0004a0001c0003t0006a0001c0003t0012others(27): Show | 61 | HG00323.hp1 HG00621.hp1 HG00735.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*1252T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 25/25 | 1252 | chr12 | 131140515 | |||||
| chr12:131140742
|
C | A | 2 | a0002c0018t0020a0002c0030t0032 | 3 | HG02965.hp1 HG03139.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1479C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 25/25 | 1479 | chr12 | 131140742 | |||||
| chr12:131140883
|
G | A | 10 | a0001c0010t0007a0001c0010t0039a0001c0013t0007others(7): Show | 14 | HG01243.hp1 HG02257.hp2 HG02559.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1620G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 25/25 | 1620 | chr12 | 131140883 | |||||
| chr12:131141004
|
G | T | 10 | a0001c0003t0006a0001c0003t0019a0001c0003t0035others(7): Show | 19 | HG00621.hp1 HG00735.hp1 HG00738.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1741G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 25/25 | 1741 | chr12 | 131141004 | |||||
| chr12:131141032
|
A | G | 7 | a0001c0001t0016a0001c0003t0013a0001c0003t0018others(4): Show | 11 | HG02280.hp1 HG02486.hp2 HG02559.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1769A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 25/25 | 1769 | chr12 | 131141032 | |||||
| chr12:131141075
|
G | A | 1 | a0001c0001t0028 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1812G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 25/25 | 1812 | chr12 | 131141075 | |||||
| chr12:131141242
|
C | T | 1 | a0001c0003t0033 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1979C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 25/25 | 1979 | chr12 | 131141242 | |||||
| chr12:131141305
|
A | G | 1 | a0001c0003t0029 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2042A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 25/25 | 2042 | chr12 | 131141305 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:130954692
|
G | A | 14 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0002g0005others(11): Show | 14 | HG01257.hp2 HG01433.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.103+32G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130954692 | ||||||
| chr12:130954694
|
T | C | 115 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0115others(112): Show | 115 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.103+34T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130954694 | ||||||
| chr12:130954899
|
T | C | 95 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0191others(92): Show | 95 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.103+239T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130954899 | ||||||
| chr12:130954919
|
T | TCTC | 217 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0115others(214): Show | 217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.103+261_103+262ins others(3): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 130954919 | |||||
| chr12:130954979
|
C | CTTTT | 5 | a0001c0001t0027g0118a0001c0003t0018g0117a0001c0006t0001g0120others(2): Show | 5 | HG01934.hp2 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.103+323_103+326dup others(4): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 130954979 | |||||
| chr12:130954979
|
C | CTTTTT | 12 | a0001c0001t0002g0228a0001c0002t0001g0125a0001c0003t0004g0121others(9): Show | 12 | HG01167.hp1 HG01884.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.103+322_103+326dup others(5): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 130954979 | |||||
| chr12:130955011
|
G | A | 5 | a0001c0001t0027g0118a0001c0003t0018g0117a0001c0006t0001g0120others(2): Show | 5 | HG01934.hp2 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.103+351G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130955011 | ||||||
| chr12:130955123
|
C | CTTTT | 73 | a0001c0001t0003g0023a0001c0001t0003g0026a0001c0001t0005g0028others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.103+473_103+476dup others(4): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 130955123 | |||||
| chr12:130955123
|
C | CTTTTT | 5 | a0001c0003t0006g0092a0001c0004t0005g0094a0001c0004t0005g0095others(2): Show | 5 | HG00735.hp1 HG01516.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.103+472_103+476dup others(5): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 130955123 | |||||
| chr12:130955123
|
C | CTTTTTTT others(5): Show |
5 | a0001c0001t0002g0130a0001c0003t0004g0121a0001c0003t0004g0122others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.103+465_103+476dup others(12): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 130955123 | |||||
| chr12:130955123
|
C | CTTTTTTT others(6): Show |
80 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0191others(77): Show | 80 | HG00140.hp1 HG00609.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.103+464_103+476dup others(13): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 130955123 | |||||
| chr12:130955123
|
C | CTTTTTTT others(7): Show |
18 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0002g0217others(15): Show | 18 | HG00621.hp1 HG00738.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.103+476_103+477ins others(14): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 130955123 | |||||
| chr12:130955123
|
C | CTTTTTTT others(8): Show |
10 | a0001c0001t0027g0118a0001c0002t0001g0223a0001c0003t0013g0224others(7): Show | 10 | HG01934.hp1 HG01934.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.103+476_103+477ins others(15): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 130955123 | |||||
| chr12:130955123
|
C | CTTTTTTT others(9): Show |
9 | a0001c0001t0002g0098a0001c0001t0015g0097a0001c0002t0001g0100others(6): Show | 9 | HG01069.hp1 HG01099.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.103+476_103+477ins others(16): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 130955123 | |||||
| chr12:130955123
|
C | CTTTTTTT others(10): Show |
7 | a0001c0001t0002g0107a0001c0002t0002g0106a0001c0003t0004g0104others(4): Show | 7 | HG00323.hp2 HG00741.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.103+476_103+477ins others(17): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 130955123 | |||||
| chr12:130955123
|
C | CTTTTTTT others(11): Show |
5 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0004t0002g0114others(2): Show | 5 | HG01106.hp1 HG01978.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.103+476_103+477ins others(18): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 130955123 | |||||
| chr12:130955123
|
C | CTTTTTTT others(12): Show |
2 | a0001c0001t0001g0115a0001c0001t0002g0116 | 2 | HG03139.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.103+476_103+477ins others(19): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 130955123 | |||||
| chr12:130955167
|
G | T | 5 | a0001c0002t0001g0125a0001c0003t0004g0121a0001c0003t0004g0122others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.103+507G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130955167 | ||||||
| chr12:130955215
|
T | G | 30 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0115others(27): Show | 30 | HG00323.hp2 HG00741.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.103+555T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130955215 | ||||||
| chr12:130955268
|
G | A | 23 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0115others(20): Show | 23 | HG00323.hp2 HG00741.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.103+608G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130955268 | ||||||
| chr12:130955465
|
C | T | 1 | a0001c0045t0002g0091 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.103+805C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130955465 | ||||||
| chr12:130955504
|
C | T | 78 | a0001c0001t0003g0023a0001c0001t0003g0026a0001c0001t0005g0028others(75): Show | 78 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.103+844C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130955504 | ||||||
| chr12:130955646
|
C | T | 102 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0191others(99): Show | 102 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.103+986C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130955646 | ||||||
| chr12:130955716
|
C | T | 102 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0191others(99): Show | 102 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.103+1056C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130955716 | ||||||
| chr12:130955773
|
A | T | 217 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0115others(214): Show | 217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.103+1113A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130955773 | ||||||
| chr12:130955782
|
A | AT | 83 | a0001c0001t0003g0023a0001c0001t0003g0026a0001c0001t0005g0028others(80): Show | 83 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.103+1127dupT | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 130955782 | |||||
| chr12:130955788
|
G | T | 84 | a0001c0001t0003g0023a0001c0001t0003g0026a0001c0001t0005g0028others(81): Show | 84 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.103+1128G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130955788 | ||||||
| chr12:130955876
|
C | G | 1 | a0001c0001t0002g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.103+1216C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130955876 | ||||||
| chr12:130955911
|
T | C | 217 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0115others(214): Show | 217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.103+1251T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130955911 | ||||||
| chr12:130955946
|
G | A | 7 | a0001c0002t0001g0223a0001c0003t0013g0224a0001c0003t0013g0225others(4): Show | 7 | HG01934.hp1 HG02559.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.103+1286G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130955946 | ||||||
| chr12:130955959
|
T | C | 84 | a0001c0001t0003g0023a0001c0001t0003g0026a0001c0001t0005g0028others(81): Show | 84 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.103+1299T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130955959 | ||||||
| chr12:130956045
|
T | C | 2 | a0001c0001t0002g0228a0007c0039t0001g0229 | 2 | HG01884.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.103+1385T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130956045 | ||||||
| chr12:130956046
|
C | T | 2 | a0001c0001t0002g0228a0007c0039t0001g0229 | 2 | HG01884.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.103+1386C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130956046 | ||||||
| chr12:130956111
|
A | G | 2 | a0001c0001t0002g0228a0007c0039t0001g0229 | 2 | HG01884.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.103+1451A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130956111 | ||||||
| chr12:130956248
|
C | G | 2 | a0001c0001t0028g0205a0001c0005t0001g0206 | 2 | HG02258.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.103+1588C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130956248 | ||||||
| chr12:130956303
|
C | T | 1 | a0001c0001t0002g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.103+1643C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130956303 | ||||||
| chr12:130956390
|
T | C | 93 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0191others(90): Show | 93 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.103+1730T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130956390 | ||||||
| chr12:130956436
|
C | T | 4 | a0001c0003t0013g0129a0001c0005t0001g0127a0001c0005t0001g0128others(1): Show | 4 | HG01167.hp1 HG02257.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.103+1776C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130956436 | ||||||
| chr12:130956437
|
G | A | 2 | a0001c0001t0002g0130a0001c0004t0002g0131 | 2 | NA18992.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.103+1777G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130956437 | ||||||
| chr12:130956472
|
G | A | 8 | a0001c0002t0001g0125a0001c0003t0004g0121a0001c0003t0004g0122others(5): Show | 8 | HG02055.hp2 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.103+1812G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130956472 | ||||||
| chr12:130956507
|
C | T | 6 | a0001c0002t0001g0125a0001c0003t0004g0121a0001c0003t0004g0122others(3): Show | 6 | HG02895.hp2 HG02897.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.103+1847C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130956507 | ||||||
| chr12:130956763
|
G | A | 8 | a0001c0002t0001g0125a0001c0003t0004g0121a0001c0003t0004g0122others(5): Show | 8 | HG02055.hp2 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.103+2103G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130956763 | ||||||
| chr12:130956793
|
GC | G | 115 | a0001c0001t0001g0111a0001c0001t0001g0115a0001c0001t0002g0098others(112): Show | 115 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.103+2140delC | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 130956793 | |||||
| chr12:130956835
|
C | A | 76 | a0001c0001t0003g0023a0001c0001t0003g0026a0001c0001t0005g0028others(73): Show | 76 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.103+2175C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130956835 | ||||||
| chr12:130956884
|
T | C | 2 | a0001c0001t0002g0228a0007c0039t0001g0229 | 2 | HG01884.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.103+2224T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130956884 | ||||||
| chr12:130956884
|
TAC | T | 3 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0002t0008g0016 | 3 | HG00738.hp1 HG01069.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.103+2235_103+2236d others(4): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 130956884 | |||||
| chr12:130956968
|
C | G | 1 | a0001c0001t0002g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.103+2308C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130956968 | ||||||
| chr12:130956993
|
A | G | 90 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0191others(87): Show | 90 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.103+2333A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130956993 | ||||||
| chr12:130956997
|
G | A | 2 | a0001c0001t0002g0228a0007c0039t0001g0229 | 2 | HG01884.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.103+2337G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130956997 | ||||||
| chr12:130957033
|
A | G | 8 | a0001c0001t0002g0098a0001c0001t0002g0107a0001c0001t0015g0097others(5): Show | 8 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.103+2373A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130957033 | ||||||
| chr12:130957070
|
CAT | C | 23 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0115others(20): Show | 23 | HG00323.hp2 HG01071.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.103+2411_103+2412d others(4): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130957070 | ||||||
| chr12:130957111
|
T | C | 217 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0115others(214): Show | 217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.103+2451T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130957111 | ||||||
| chr12:130957113
|
T | C | 2 | a0001c0001t0002g0228a0007c0039t0001g0229 | 2 | HG01884.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.103+2453T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130957113 | ||||||
| chr12:130957172
|
A | G | 85 | a0001c0001t0003g0023a0001c0001t0003g0026a0001c0001t0005g0028others(82): Show | 85 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.103+2512A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130957172 | ||||||
| chr12:130957230
|
A | G | 1 | a0001c0005t0001g0206 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.103+2570A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130957230 | ||||||
| chr12:130957247
|
G | A | 2 | a0001c0003t0004g0207a0001c0007t0018g0132 | 2 | HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.103+2587G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130957247 | ||||||
| chr12:130957295
|
A | G | 1 | a0001c0043t0008g0227 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.103+2635A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130957295 | ||||||
| chr12:130957309
|
A | G | 217 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0115others(214): Show | 217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.103+2649A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130957309 | ||||||
| chr12:130957356
|
C | T | 1 | a0009c0035t0047g0219 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.103+2696C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130957356 | ||||||
| chr12:130957416
|
ACG | A | 8 | a0001c0001t0002g0098a0001c0001t0002g0107a0001c0001t0015g0097others(5): Show | 8 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.103+2757_103+2758d others(4): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130957416 | ||||||
| chr12:130957418
|
G | A | 130 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0115others(127): Show | 130 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(127): Show |
intron_variant | MODIFIER | c.103+2758G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130957418 | ||||||
| chr12:130957420
|
CCA | C | 10 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0115others(7): Show | 10 | HG00323.hp2 HG01071.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.103+2768_103+2769d others(4): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 130957420 | |||||
| chr12:130957597
|
T | C | 231 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(228): Show | 231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.103+2937T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130957597 | ||||||
| chr12:130957909
|
G | A | 5 | a0001c0003t0004g0121a0001c0003t0004g0122a0001c0003t0018g0117others(2): Show | 5 | HG02055.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.103+3249G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130957909 | ||||||
| chr12:130958022
|
C | T | 55 | a0001c0001t0002g0098a0001c0001t0002g0107a0001c0001t0005g0087others(52): Show | 55 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.103+3362C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130958022 | ||||||
| chr12:130958036
|
C | A | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(134): Show | 137 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.103+3376C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130958036 | ||||||
| chr12:130958129
|
G | A | 5 | a0001c0002t0001g0125a0001c0003t0004g0121a0001c0003t0004g0122others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.103+3469G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130958129 | ||||||
| chr12:130958179
|
C | T | 8 | a0001c0001t0002g0098a0001c0001t0002g0107a0001c0001t0015g0097others(5): Show | 8 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.103+3519C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130958179 | ||||||
| chr12:130958207
|
C | CT | 183 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0191others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.103+3557dupT | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 130958207 | |||||
| chr12:130958261
|
G | A | 115 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0191others(112): Show | 115 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(112): Show |
intron_variant | MODIFIER | c.103+3601G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130958261 | ||||||
| chr12:130958289
|
C | T | 26 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0001g0208others(23): Show | 26 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.103+3629C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130958289 | ||||||
| chr12:130958290
|
C | G | 91 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0191others(88): Show | 91 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.103+3630C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130958290 | ||||||
| chr12:130958294
|
G | A | 73 | a0001c0001t0005g0028a0001c0001t0005g0045a0001c0001t0005g0055others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.103+3634G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130958294 | ||||||
| chr12:130958305
|
C | T | 89 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0115others(86): Show | 89 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.103+3645C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130958305 | ||||||
| chr12:130958324
|
C | T | 17 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0115others(14): Show | 17 | HG00323.hp2 HG01071.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.103+3664C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130958324 | ||||||
| chr12:130958430
|
C | T | 1 | a0001c0002t0003g0057 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.103+3770C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130958430 | ||||||
| chr12:130958527
|
C | T | 1 | a0001c0003t0019g0218 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.103+3867C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130958527 | ||||||
| chr12:130958538
|
G | A | 213 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(210): Show | 213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.103+3878G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130958538 | ||||||
| chr12:130958570
|
G | A | 1 | a0001c0019t0004g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.103+3910G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130958570 | ||||||
| chr12:130958780
|
G | A | 1 | a0001c0001t0005g0028 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.103+4120G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130958780 | ||||||
| chr12:130958908
|
G | A | 3 | a0001c0001t0002g0098a0001c0001t0015g0097a0001c0004t0015g0099 | 3 | HG01099.hp1 HG01258.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.103+4248G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130958908 | ||||||
| chr12:130958920
|
G | A | 1 | a0001c0001t0027g0118 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.103+4260G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130958920 | ||||||
| chr12:130958991
|
A | G | 107 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0115others(104): Show | 107 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.103+4331A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130958991 | ||||||
| chr12:130959034
|
A | G | 1 | a0001c0002t0003g0057 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.103+4374A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130959034 | ||||||
| chr12:130959065
|
G | A | 2 | a0003c0031t0003g0089a0003c0032t0038g0090 | 2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.103+4405G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130959065 | ||||||
| chr12:130959129
|
G | A | 1 | a0001c0003t0018g0232 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.103+4469G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130959129 | ||||||
| chr12:130959396
|
A | T | 7 | a0001c0001t0002g0130a0001c0002t0001g0145a0001c0002t0001g0146others(4): Show | 7 | HG00738.hp2 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.103+4736A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130959396 | ||||||
| chr12:130959514
|
T | C | 2 | a0001c0001t0028g0205a0001c0005t0001g0206 | 2 | HG02258.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.103+4854T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130959514 | ||||||
| chr12:130959678
|
T | G | 1 | a0001c0002t0008g0016 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.103+5018T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130959678 | ||||||
| chr12:130959883
|
C | T | 20 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0115others(17): Show | 20 | HG00323.hp2 HG00741.hp2 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.103+5223C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130959883 | ||||||
| chr12:130959904
|
A | T | 1 | a0001c0003t0004g0012 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.103+5244A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130959904 | ||||||
| chr12:130959980
|
C | T | 1 | a0001c0003t0006g0015 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.103+5320C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130959980 | ||||||
| chr12:130960015
|
C | A | 94 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0191others(91): Show | 94 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.103+5355C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130960015 | ||||||
| chr12:130960184
|
G | A | 2 | a0001c0001t0011g0062a0001c0003t0012g0063 | 2 | HG02135.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.103+5524G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130960184 | ||||||
| chr12:130960273
|
GT | G | 3 | a0001c0004t0002g0114a0001c0007t0004g0102a0001c0022t0016g0109 | 3 | HG01109.hp1 HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.103+5616delT | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 130960273 | |||||
| chr12:130960431
|
A | G | 217 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(214): Show | 217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.103+5771A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130960431 | ||||||
| chr12:130960501
|
A | G | 1 | a0001c0006t0001g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.103+5841A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130960501 | ||||||
| chr12:130960540
|
T | C | 2 | a0001c0007t0006g0021a0002c0028t0001g0022 | 2 | HG02055.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.103+5880T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130960540 | ||||||
| chr12:130960553
|
G | T | 1 | a0001c0004t0002g0011 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.103+5893G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130960553 | ||||||
| chr12:130960557
|
T | G | 3 | a0001c0003t0004g0207a0001c0008t0001g0183a0003c0033t0030g0231 | 3 | HG02647.hp1 HG03209.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.103+5897T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130960557 | ||||||
| chr12:130960566
|
A | AT | 94 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0191others(91): Show | 94 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.104-5892dupT | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 130960566 | |||||
| chr12:130960572
|
G | T | 94 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0191others(91): Show | 94 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.104-5891G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130960572 | ||||||
| chr12:130960661
|
T | A | 1 | a0001c0002t0001g0100 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.104-5802T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130960661 | ||||||
| chr12:130960661
|
TCA | T | 217 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(214): Show | 217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.104-5787_104-5786d others(4): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 130960661 | |||||
| chr12:130960665
|
A | T | 160 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0191others(157): Show | 160 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.104-5798A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130960665 | ||||||
| chr12:130960861
|
C | T | 2 | a0001c0003t0029g0214a0001c0003t0033g0181 | 2 | HG01261.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.104-5602C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130960861 | ||||||
| chr12:130960932
|
T | C | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(236): Show | 239 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.104-5531T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130960932 | ||||||
| chr12:130961069
|
A | G | 230 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(227): Show | 230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.104-5394A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130961069 | ||||||
| chr12:130961150
|
A | G | 126 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0156others(123): Show | 126 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(123): Show |
intron_variant | MODIFIER | c.104-5313A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130961150 | ||||||
| chr12:130961176
|
G | A | 2 | a0001c0001t0002g0107a0001c0003t0006g0019 | 2 | HG00741.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.104-5287G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130961176 | ||||||
| chr12:130961299
|
C | T | 1 | a0001c0025t0021g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.104-5164C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130961299 | ||||||
| chr12:130961300
|
G | A | 2 | a0001c0003t0004g0207a0003c0033t0030g0231 | 2 | HG02647.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.104-5163G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130961300 | ||||||
| chr12:130961369
|
G | C | 2 | a0001c0003t0004g0121a0001c0003t0004g0122 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.104-5094G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130961369 | ||||||
| chr12:130961402
|
C | CCT | 7 | a0001c0006t0008g0177a0001c0010t0007g0213a0001c0020t0002g0180others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.104-5047_104-5046d others(4): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 130961402 | |||||
| chr12:130961442
|
T | A | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0115others(113): Show | 116 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.104-5021T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130961442 | ||||||
| chr12:130961568
|
A | G | 4 | a0001c0001t0002g0107a0001c0003t0006g0019a0005c0011t0008g0047others(1): Show | 4 | HG00280.hp1 HG00741.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.104-4895A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130961568 | ||||||
| chr12:130961679
|
T | A | 8 | a0001c0001t0028g0205a0001c0003t0001g0152a0001c0003t0004g0234others(5): Show | 8 | HG02258.hp2 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.104-4784T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130961679 | ||||||
| chr12:130961681
|
C | T | 3 | a0003c0031t0003g0089a0003c0032t0038g0090a0003c0040t0022g0096 | 3 | HG02559.hp1 HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.104-4782C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130961681 | ||||||
| chr12:130961711
|
T | A | 5 | a0001c0001t0002g0098a0001c0001t0015g0097a0001c0004t0015g0099others(2): Show | 5 | HG00280.hp1 HG01099.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.104-4752T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130961711 | ||||||
| chr12:130961919
|
C | T | 1 | a0001c0001t0009g0144 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.104-4544C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130961919 | ||||||
| chr12:130961964
|
A | G | 225 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(222): Show | 225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.104-4499A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130961964 | ||||||
| chr12:130962003
|
G | A | 5 | a0001c0001t0002g0098a0001c0001t0015g0097a0001c0004t0015g0099others(2): Show | 5 | HG00280.hp1 HG01099.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.104-4460G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130962003 | ||||||
| chr12:130962343
|
G | A | 2 | a0001c0001t0027g0118a0001c0006t0001g0120 | 2 | HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.104-4120G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130962343 | ||||||
| chr12:130962403
|
C | T | 1 | a0001c0003t0004g0198 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.104-4060C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130962403 | ||||||
| chr12:130962568
|
A | G | 1 | a0002c0044t0007g0126 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.104-3895A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130962568 | ||||||
| chr12:130962618
|
T | C | 5 | a0001c0001t0002g0098a0001c0001t0015g0097a0001c0004t0015g0099others(2): Show | 5 | HG00280.hp1 HG01099.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.104-3845T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130962618 | ||||||
| chr12:130962624
|
A | G | 20 | a0001c0001t0002g0130a0001c0002t0001g0010a0001c0002t0001g0202others(17): Show | 20 | HG00639.hp2 HG00735.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.104-3839A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130962624 | ||||||
| chr12:130962679
|
T | C | 2 | a0001c0003t0004g0121a0001c0003t0004g0122 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.104-3784T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130962679 | ||||||
| chr12:130962691
|
G | A | 2 | a0001c0002t0003g0064a0001c0004t0005g0094 | 2 | HG02071.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.104-3772G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130962691 | ||||||
| chr12:130962978
|
A | G | 2 | a0001c0001t0002g0175a0001c0002t0001g0174 | 2 | NA19088.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.104-3485A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130962978 | ||||||
| chr12:130963046
|
C | T | 15 | a0001c0001t0002g0116a0001c0001t0016g0182a0001c0001t0028g0205others(12): Show | 15 | HG01243.hp1 HG01934.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.104-3417C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130963046 | ||||||
| chr12:130963047
|
G | T | 1 | a0006c0037t0042g0046 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.104-3416G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130963047 | ||||||
| chr12:130963048
|
C | T | 1 | a0001c0003t0045g0042 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.104-3415C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130963048 | ||||||
| chr12:130963091
|
C | A | 2 | a0005c0011t0008g0047a0005c0021t0021g0048 | 2 | HG00280.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.104-3372C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130963091 | ||||||
| chr12:130963091
|
C | T | 1 | a0001c0002t0003g0085 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.104-3372C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130963091 | ||||||
| chr12:130963092
|
G | A | 4 | a0001c0003t0004g0012a0001c0003t0006g0092a0001c0003t0018g0117others(1): Show | 4 | HG00735.hp1 HG01261.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.104-3371G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130963092 | ||||||
| chr12:130963096
|
G | A | 1 | a0001c0003t0018g0117 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.104-3367G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130963096 | ||||||
| chr12:130963103
|
G | A | 1 | a0001c0003t0018g0117 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.104-3360G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130963103 | ||||||
| chr12:130963105
|
A | G | 10 | a0001c0002t0003g0085a0001c0003t0004g0012a0001c0003t0006g0092others(7): Show | 10 | HG00735.hp1 HG01261.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.104-3358A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130963105 | ||||||
| chr12:130963106
|
G | A | 1 | a0001c0003t0018g0117 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.104-3357G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130963106 | ||||||
| chr12:130963116
|
C | G | 1 | a0001c0003t0033g0181 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.104-3347C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130963116 | ||||||
| chr12:130963116
|
C | T | 1 | a0001c0003t0018g0117 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.104-3347C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130963116 | ||||||
| chr12:130963119
|
A | G | 10 | a0001c0003t0004g0012a0001c0003t0006g0092a0001c0003t0018g0117others(7): Show | 10 | HG00735.hp1 HG01261.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.104-3344A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130963119 | ||||||
| chr12:130963125
|
G | C | 17 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0028g0205others(14): Show | 17 | HG00735.hp1 HG01261.hp1 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.104-3338G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130963125 | ||||||
| chr12:130963132
|
A | G | 5 | a0001c0002t0001g0010a0001c0003t0034g0014a0001c0020t0002g0180others(2): Show | 5 | HG02735.hp1 HG02809.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.104-3331A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130963132 | ||||||
| chr12:130963148
|
A | G | 1 | a0001c0007t0004g0018 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.104-3315A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130963148 | ||||||
| chr12:130963176
|
C | T | 1 | a0001c0004t0002g0114 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.104-3287C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130963176 | ||||||
| chr12:130963177
|
A | G | 1 | a0001c0004t0002g0114 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.104-3286A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130963177 | ||||||
| chr12:130963188
|
C | T | 1 | a0001c0003t0012g0027 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.104-3275C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130963188 | ||||||
| chr12:130963228
|
G | C | 3 | a0001c0001t0028g0205a0001c0003t0001g0152a0001c0003t0029g0214 | 3 | HG02280.hp2 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.104-3235G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130963228 | ||||||
| chr12:130963285
|
A | G | 1 | a0001c0003t0004g0207 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.104-3178A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130963285 | ||||||
| chr12:130963319
|
CA | C | 21 | a0001c0001t0001g0163a0001c0001t0001g0208a0001c0001t0002g0184others(18): Show | 21 | HG00735.hp2 HG01099.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.104-3121delA | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 130963319 | |||||
| chr12:130963319
|
CAA | C | 161 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(158): Show | 161 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.104-3122_104-3121d others(4): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 130963319 | |||||
| chr12:130963339
|
AAAAG | A | 26 | a0001c0001t0002g0098a0001c0001t0002g0130a0001c0001t0015g0097others(23): Show | 26 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.104-3116_104-3113d others(6): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 130963339 | |||||
| chr12:130963340
|
AAAG | A | 9 | a0001c0002t0001g0010a0001c0003t0004g0122a0001c0003t0012g0025others(6): Show | 9 | HG01496.hp1 HG01934.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.104-3120_104-3118d others(5): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 130963340 | |||||
| chr12:130963341
|
AAG | A | 5 | a0001c0001t0002g0116a0001c0003t0004g0121a0001c0003t0018g0117others(2): Show | 5 | HG01106.hp1 HG02897.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.104-3120_104-3119d others(4): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 130963341 | |||||
| chr12:130963342
|
AG | A | 3 | a0001c0001t0028g0205a0001c0003t0001g0152a0001c0003t0029g0214 | 3 | HG02280.hp2 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.104-3120delG | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130963342 | ||||||
| chr12:130963347
|
G | T | 5 | a0001c0001t0002g0098a0001c0001t0015g0097a0001c0004t0015g0099others(2): Show | 5 | HG00280.hp1 HG01099.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.104-3116G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130963347 | ||||||
| chr12:130963348
|
A | T | 5 | a0001c0001t0002g0098a0001c0001t0015g0097a0001c0004t0015g0099others(2): Show | 5 | HG00280.hp1 HG01099.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.104-3115A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130963348 | ||||||
| chr12:130963349
|
A | C | 5 | a0001c0001t0002g0098a0001c0001t0015g0097a0001c0004t0015g0099others(2): Show | 5 | HG00280.hp1 HG01099.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.104-3114A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130963349 | ||||||
| chr12:130963442
|
C | A | 3 | a0001c0001t0028g0205a0001c0003t0001g0152a0001c0003t0029g0214 | 3 | HG02280.hp2 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.104-3021C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130963442 | ||||||
| chr12:130963809
|
A | G | 5 | a0001c0001t0002g0098a0001c0001t0015g0097a0001c0004t0015g0099others(2): Show | 5 | HG00280.hp1 HG01099.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.104-2654A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130963809 | ||||||
| chr12:130963812
|
G | T | 1 | a0001c0001t0002g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.104-2651G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130963812 | ||||||
| chr12:130963842
|
A | G | 5 | a0001c0001t0002g0098a0001c0001t0015g0097a0001c0004t0015g0099others(2): Show | 5 | HG00280.hp1 HG01099.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.104-2621A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130963842 | ||||||
| chr12:130964201
|
A | AAACAACA others(37): Show |
1 | a0001c0001t0002g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.104-2261_104-2260i others(46): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 130964201 | |||||
| chr12:130964203
|
T | C | 1 | a0001c0001t0002g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.104-2260T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130964203 | ||||||
| chr12:130964205
|
C | G | 1 | a0001c0001t0002g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.104-2258C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130964205 | ||||||
| chr12:130964207
|
T | A | 1 | a0001c0001t0002g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.104-2256T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130964207 | ||||||
| chr12:130964211
|
A | T | 1 | a0001c0001t0002g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.104-2252A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130964211 | ||||||
| chr12:130964214
|
T | A | 1 | a0001c0001t0002g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.104-2249T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130964214 | ||||||
| chr12:130964223
|
C | A | 1 | a0001c0001t0002g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.104-2240C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130964223 | ||||||
| chr12:130964226
|
A | T | 1 | a0001c0001t0002g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.104-2237A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130964226 | ||||||
| chr12:130964228
|
A | T | 1 | a0001c0001t0002g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.104-2235A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130964228 | ||||||
| chr12:130964230
|
C | G | 1 | a0001c0001t0002g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.104-2233C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130964230 | ||||||
| chr12:130964231
|
T | C | 1 | a0001c0001t0002g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.104-2232T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130964231 | ||||||
| chr12:130964232
|
T | C | 1 | a0001c0001t0002g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.104-2231T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130964232 | ||||||
| chr12:130964242
|
A | T | 1 | a0001c0001t0002g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.104-2221A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130964242 | ||||||
| chr12:130964397
|
G | C | 2 | a0001c0001t0028g0205a0001c0003t0001g0152 | 2 | HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.104-2066G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130964397 | ||||||
| chr12:130964489
|
T | C | 221 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(218): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.104-1974T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130964489 | ||||||
| chr12:130964546
|
A | G | 1 | a0002c0028t0001g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.104-1917A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130964546 | ||||||
| chr12:130964673
|
G | A | 7 | a0001c0002t0001g0223a0001c0003t0012g0025a0001c0003t0012g0027others(4): Show | 7 | HG01106.hp1 HG01496.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.104-1790G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130964673 | ||||||
| chr12:130964745
|
TATGTACT others(15): Show |
T | 1 | a0001c0001t0005g0055 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.104-1715_104-1694d others(24): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr12 | 130964745 | |||||
| chr12:130964779
|
G | A | 1 | a0001c0003t0018g0117 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.104-1684G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130964779 | ||||||
| chr12:130964795
|
G | A | 1 | a0001c0005t0014g0049 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.104-1668G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130964795 | ||||||
| chr12:130964797
|
G | A | 1 | a0001c0019t0004g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.104-1666G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130964797 | ||||||
| chr12:130964845
|
T | C | 1 | a0001c0025t0021g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.104-1618T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130964845 | ||||||
| chr12:130964910
|
A | G | 7 | a0001c0002t0001g0010a0001c0003t0004g0012a0001c0003t0004g0121others(4): Show | 7 | HG00735.hp1 HG02735.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.104-1553A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130964910 | ||||||
| chr12:130964955
|
C | T | 5 | a0001c0001t0002g0098a0001c0001t0015g0097a0001c0004t0015g0099others(2): Show | 5 | HG00280.hp1 HG01099.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.104-1508C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130964955 | ||||||
| chr12:130965004
|
G | A | 1 | a0001c0003t0018g0117 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.104-1459G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130965004 | ||||||
| chr12:130965093
|
T | C | 7 | a0001c0002t0001g0010a0001c0003t0004g0012a0001c0003t0004g0121others(4): Show | 7 | HG00735.hp1 HG02735.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.104-1370T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130965093 | ||||||
| chr12:130965284
|
T | G | 1 | a0001c0003t0019g0218 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.104-1179T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130965284 | ||||||
| chr12:130965312
|
G | A | 1 | a0001c0001t0011g0062 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.104-1151G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130965312 | ||||||
| chr12:130965533
|
A | G | 1 | a0001c0025t0021g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.104-930A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130965533 | ||||||
| chr12:130965571
|
G | A | 1 | a0001c0025t0021g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.104-892G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130965571 | ||||||
| chr12:130965861
|
A | C | 4 | a0001c0003t0013g0129a0001c0005t0001g0127a0001c0005t0001g0128others(1): Show | 4 | HG01167.hp1 HG02630.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.104-602A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130965861 | ||||||
| chr12:130966091
|
T | C | 2 | a0005c0011t0008g0047a0005c0021t0021g0048 | 2 | HG00280.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.104-372T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130966091 | ||||||
| chr12:130966223
|
G | T | 1 | a0005c0011t0002g0110 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.104-240G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 2/24 | chr12 | 130966223 | ||||||
| chr12:130966700
|
C | T | 2 | a0001c0001t0001g0002a0001c0001t0001g0003 | 2 | HG01433.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.187+154C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130966700 | ||||||
| chr12:130966792
|
C | CT | 186 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(183): Show | 186 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.187+256dupT | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr12 | 130966792 | |||||
| chr12:130967007
|
A | C | 6 | a0001c0006t0008g0177a0001c0020t0002g0180a0001c0042t0007g0176others(3): Show | 6 | HG02258.hp1 HG02809.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.187+461A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130967007 | ||||||
| chr12:130967494
|
G | A | 1 | a0001c0001t0002g0149 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.187+948G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130967494 | ||||||
| chr12:130967494
|
G | T | 35 | a0001c0001t0001g0113a0001c0001t0001g0163a0001c0001t0001g0212others(32): Show | 35 | HG01069.hp1 HG01071.hp2 HG01175.hp1 others(32): Show |
intron_variant | MODIFIER | c.187+948G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130967494 | ||||||
| chr12:130967564
|
A | G | 3 | a0001c0003t0013g0129a0001c0005t0001g0127a0001c0005t0001g0128 | 3 | HG01167.hp1 HG02630.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.187+1018A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130967564 | ||||||
| chr12:130967685
|
A | G | 1 | a0001c0003t0004g0207 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.187+1139A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130967685 | ||||||
| chr12:130967719
|
TCA | T | 5 | a0001c0002t0001g0223a0001c0019t0004g0230a0001c0046t0017g0221others(2): Show | 5 | HG01934.hp1 HG02109.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.187+1174_187+1175d others(4): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130967719 | ||||||
| chr12:130967780
|
C | T | 1 | a0001c0007t0004g0018 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.187+1234C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130967780 | ||||||
| chr12:130967879
|
C | T | 3 | a0001c0003t0004g0234a0001c0005t0001g0206a0001c0006t0001g0242 | 3 | HG02258.hp2 HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.187+1333C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130967879 | ||||||
| chr12:130967880
|
G | A | 1 | a0001c0006t0008g0177 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.187+1334G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130967880 | ||||||
| chr12:130968036
|
T | G | 1 | a0001c0003t0002g0186 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.187+1490T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130968036 | ||||||
| chr12:130968060
|
G | A | 175 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(172): Show | 175 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.187+1514G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130968060 | ||||||
| chr12:130968151
|
A | T | 5 | a0001c0002t0001g0010a0001c0003t0004g0012a0001c0003t0006g0092others(2): Show | 5 | HG00735.hp1 HG02735.hp1 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.187+1605A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130968151 | ||||||
| chr12:130968269
|
C | T | 1 | a0001c0019t0004g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.187+1723C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130968269 | ||||||
| chr12:130968280
|
T | C | 1 | a0001c0001t0002g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.187+1734T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130968280 | ||||||
| chr12:130968326
|
T | C | 5 | a0001c0002t0001g0010a0001c0003t0004g0012a0001c0003t0006g0092others(2): Show | 5 | HG00735.hp1 HG02735.hp1 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.187+1780T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130968326 | ||||||
| chr12:130968509
|
G | A | 5 | a0001c0006t0008g0177a0001c0020t0002g0180a0001c0042t0007g0176others(2): Show | 5 | HG02258.hp1 HG02809.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.187+1963G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130968509 | ||||||
| chr12:130968537
|
G | A | 1 | a0001c0004t0002g0011 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.187+1991G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130968537 | ||||||
| chr12:130968565
|
C | T | 5 | a0001c0001t0005g0045a0001c0002t0003g0038a0001c0002t0003g0039others(2): Show | 5 | HG01261.hp2 HG01433.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.187+2019C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130968565 | ||||||
| chr12:130968694
|
T | C | 3 | a0001c0003t0013g0129a0001c0005t0001g0127a0001c0005t0001g0128 | 3 | HG01167.hp1 HG02630.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.187+2148T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130968694 | ||||||
| chr12:130968833
|
T | C | 202 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(199): Show | 202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.187+2287T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130968833 | ||||||
| chr12:130968916
|
G | T | 25 | a0001c0001t0001g0113a0001c0001t0001g0163a0001c0001t0001g0212others(22): Show | 25 | HG01069.hp1 HG01071.hp2 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.187+2370G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130968916 | ||||||
| chr12:130968995
|
T | C | 1 | a0002c0044t0007g0126 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.187+2449T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130968995 | ||||||
| chr12:130969069
|
G | A | 1 | a0001c0003t0001g0152 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.188-2389G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130969069 | ||||||
| chr12:130969154
|
A | G | 17 | a0001c0001t0028g0205a0001c0002t0001g0223a0001c0003t0001g0152others(14): Show | 17 | HG00280.hp1 HG01106.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.188-2304A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130969154 | ||||||
| chr12:130969248
|
C | T | 3 | a0001c0003t0013g0129a0001c0005t0001g0127a0001c0005t0001g0128 | 3 | HG01167.hp1 HG02630.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.188-2210C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130969248 | ||||||
| chr12:130969315
|
C | T | 5 | a0001c0003t0004g0121a0001c0003t0004g0122a0001c0003t0012g0025others(2): Show | 5 | HG01106.hp1 HG01496.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.188-2143C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130969315 | ||||||
| chr12:130969341
|
C | T | 9 | a0001c0001t0028g0205a0001c0002t0001g0223a0001c0003t0001g0152others(6): Show | 9 | HG01934.hp1 HG02109.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.188-2117C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130969341 | ||||||
| chr12:130969352
|
G | C | 1 | a0001c0019t0004g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.188-2106G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130969352 | ||||||
| chr12:130969409
|
A | G | 2 | a0005c0011t0008g0047a0005c0021t0021g0048 | 2 | HG00280.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.188-2049A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130969409 | ||||||
| chr12:130969417
|
G | A | 174 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(171): Show | 174 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.188-2041G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130969417 | ||||||
| chr12:130969420
|
C | G | 1 | a0002c0044t0007g0126 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.188-2038C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130969420 | ||||||
| chr12:130969421
|
G | A | 2 | a0005c0011t0008g0047a0005c0021t0021g0048 | 2 | HG00280.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.188-2037G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130969421 | ||||||
| chr12:130969447
|
G | A | 14 | a0001c0001t0028g0205a0001c0002t0001g0223a0001c0003t0001g0152others(11): Show | 14 | HG01106.hp1 HG01496.hp1 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.188-2011G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130969447 | ||||||
| chr12:130969614
|
C | T | 8 | a0001c0002t0001g0223a0001c0003t0036g0209a0001c0013t0007g0153others(5): Show | 8 | HG01934.hp1 HG01934.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-1844C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130969614 | ||||||
| chr12:130969736
|
C | T | 2 | a0005c0011t0008g0047a0005c0021t0021g0048 | 2 | HG00280.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.188-1722C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130969736 | ||||||
| chr12:130969767
|
C | T | 3 | a0001c0001t0027g0118a0001c0003t0004g0237a0001c0006t0001g0120 | 3 | HG01175.hp2 HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.188-1691C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130969767 | ||||||
| chr12:130969770
|
T | C | 1 | a0001c0003t0004g0198 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.188-1688T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130969770 | ||||||
| chr12:130969839
|
T | C | 2 | a0005c0011t0008g0047a0005c0021t0021g0048 | 2 | HG00280.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.188-1619T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130969839 | ||||||
| chr12:130969929
|
T | C | 1 | a0001c0005t0008g0226 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.188-1529T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130969929 | ||||||
| chr12:130970064
|
A | G | 225 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(222): Show | 225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.188-1394A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130970064 | ||||||
| chr12:130970104
|
A | G | 2 | a0005c0011t0008g0047a0005c0021t0021g0048 | 2 | HG00280.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.188-1354A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130970104 | ||||||
| chr12:130970207
|
A | G | 179 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(176): Show | 179 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.188-1251A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130970207 | ||||||
| chr12:130970217
|
G | A | 1 | a0001c0002t0001g0010 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.188-1241G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130970217 | ||||||
| chr12:130970260
|
A | G | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(175): Show | 178 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.188-1198A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130970260 | ||||||
| chr12:130970403
|
C | G | 8 | a0001c0001t0002g0116a0001c0001t0002g0130a0001c0002t0001g0202others(5): Show | 8 | HG00639.hp2 HG01257.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.188-1055C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130970403 | ||||||
| chr12:130970410
|
C | CA | 17 | a0001c0001t0028g0205a0001c0002t0001g0223a0001c0003t0001g0152others(14): Show | 17 | HG01106.hp1 HG01167.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.188-1043dupA | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr12 | 130970410 | |||||
| chr12:130970494
|
A | G | 179 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(176): Show | 179 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.188-964A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130970494 | ||||||
| chr12:130970495
|
T | C | 179 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(176): Show | 179 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.188-963T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130970495 | ||||||
| chr12:130970574
|
G | A | 2 | a0005c0011t0008g0047a0005c0021t0021g0048 | 2 | HG00280.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.188-884G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130970574 | ||||||
| chr12:130970676
|
T | G | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(170): Show | 173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.188-782T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130970676 | ||||||
| chr12:130970694
|
T | C | 1 | a0003c0012t0017g0158 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.188-764T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130970694 | ||||||
| chr12:130970695
|
T | C | 228 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(225): Show | 228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.188-763T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130970695 | ||||||
| chr12:130970708
|
G | A | 7 | a0001c0001t0002g0130a0001c0002t0001g0202a0001c0002t0002g0001others(4): Show | 7 | HG00639.hp2 HG01257.hp2 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.188-750G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130970708 | ||||||
| chr12:130970708
|
G | C | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(170): Show | 173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.188-750G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130970708 | ||||||
| chr12:130970848
|
G | A | 193 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(190): Show | 193 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.188-610G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130970848 | ||||||
| chr12:130970897
|
G | A | 164 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(161): Show | 164 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.188-561G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130970897 | ||||||
| chr12:130970988
|
C | T | 9 | a0001c0002t0001g0010a0001c0003t0004g0012a0001c0003t0006g0092others(6): Show | 9 | HG00735.hp1 HG01934.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.188-470C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130970988 | ||||||
| chr12:130971046
|
C | T | 1 | a0001c0002t0002g0009 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.188-412C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130971046 | ||||||
| chr12:130971220
|
T | C | 1 | a0003c0032t0038g0090 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.188-238T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130971220 | ||||||
| chr12:130971228
|
A | C | 13 | a0001c0003t0004g0121a0001c0003t0004g0122a0001c0003t0012g0025others(10): Show | 13 | HG00738.hp2 HG01106.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.188-230A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130971228 | ||||||
| chr12:130971246
|
G | GAC | 33 | a0001c0001t0002g0116a0001c0001t0002g0130a0001c0001t0027g0118others(30): Show | 33 | HG00639.hp2 HG00735.hp1 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.188-210_188-209dup others(2): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr12 | 130971246 | |||||
| chr12:130971282
|
T | TAATTA | 33 | a0001c0001t0002g0116a0001c0001t0002g0130a0001c0001t0027g0118others(30): Show | 33 | HG00639.hp2 HG00735.hp1 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.188-173_188-172ins others(5): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr12 | 130971282 | |||||
| chr12:130971290
|
C | A | 33 | a0001c0001t0002g0116a0001c0001t0002g0130a0001c0001t0027g0118others(30): Show | 33 | HG00639.hp2 HG00735.hp1 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.188-168C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130971290 | ||||||
| chr12:130971306
|
T | TAAC | 33 | a0001c0001t0002g0116a0001c0001t0002g0130a0001c0001t0027g0118others(30): Show | 33 | HG00639.hp2 HG00735.hp1 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.188-151_188-150ins others(3): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr12 | 130971306 | |||||
| chr12:130971359
|
C | T | 1 | a0001c0003t0006g0019 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.188-99C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130971359 | ||||||
| chr12:130971369
|
C | G | 1 | a0001c0003t0006g0019 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.188-89C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 3/24 | chr12 | 130971369 | ||||||
| chr12:130971693
|
G | A | 170 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(167): Show | 170 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.310+113G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130971693 | ||||||
| chr12:130971707
|
G | A | 168 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(165): Show | 168 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.310+127G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130971707 | ||||||
| chr12:130971887
|
C | T | 31 | a0001c0001t0002g0116a0001c0001t0002g0130a0001c0001t0027g0118others(28): Show | 31 | HG00639.hp2 HG00735.hp1 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.310+307C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130971887 | ||||||
| chr12:130971904
|
G | A | 27 | a0001c0001t0002g0116a0001c0001t0002g0130a0001c0001t0027g0118others(24): Show | 27 | HG00639.hp2 HG01175.hp2 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.310+324G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130971904 | ||||||
| chr12:130972061
|
C | T | 2 | a0001c0005t0001g0044a0008c0034t0026g0043 | 2 | HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.310+481C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130972061 | ||||||
| chr12:130972111
|
A | T | 1 | a0001c0001t0001g0197 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.310+531A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130972111 | ||||||
| chr12:130972131
|
C | G | 31 | a0001c0001t0002g0116a0001c0001t0002g0130a0001c0001t0027g0118others(28): Show | 31 | HG00639.hp2 HG00735.hp1 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.310+551C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130972131 | ||||||
| chr12:130972346
|
G | T | 224 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(221): Show | 224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.310+766G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130972346 | ||||||
| chr12:130972469
|
G | A | 1 | a0001c0001t0009g0166 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.310+889G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130972469 | ||||||
| chr12:130972537
|
C | T | 3 | a0001c0001t0028g0205a0001c0003t0001g0152a0001c0003t0029g0214 | 3 | HG02280.hp2 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.310+957C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130972537 | ||||||
| chr12:130972568
|
G | A | 5 | a0001c0002t0001g0223a0001c0005t0001g0112a0001c0005t0008g0226others(2): Show | 5 | HG02559.hp2 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.310+988G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130972568 | ||||||
| chr12:130972608
|
T | C | 1 | a0001c0003t0034g0014 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.310+1028T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130972608 | ||||||
| chr12:130972649
|
A | G | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(170): Show | 173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.310+1069A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130972649 | ||||||
| chr12:130972712
|
G | A | 1 | a0001c0001t0002g0187 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.310+1132G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130972712 | ||||||
| chr12:130972720
|
C | G | 1 | a0001c0003t0012g0027 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.310+1140C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130972720 | ||||||
| chr12:130972720
|
CG | C | 12 | a0001c0001t0027g0118a0001c0001t0028g0205a0001c0003t0001g0152others(9): Show | 12 | HG01175.hp2 HG02258.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.310+1145delG | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr12 | 130972720 | |||||
| chr12:130972875
|
C | T | 1 | a0001c0003t0002g0186 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.310+1295C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130972875 | ||||||
| chr12:130972941
|
G | A | 7 | a0001c0001t0002g0130a0001c0002t0001g0169a0001c0002t0001g0202others(4): Show | 7 | HG00639.hp2 HG02056.hp2 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.310+1361G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130972941 | ||||||
| chr12:130972956
|
C | T | 12 | a0001c0001t0027g0118a0001c0001t0028g0205a0001c0003t0001g0152others(9): Show | 12 | HG01175.hp2 HG02258.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.310+1376C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130972956 | ||||||
| chr12:130972995
|
T | C | 2 | a0001c0005t0001g0112a0001c0005t0008g0226 | 2 | HG02895.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.310+1415T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130972995 | ||||||
| chr12:130973016
|
G | A | 221 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(218): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.310+1436G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130973016 | ||||||
| chr12:130973153
|
C | T | 13 | a0001c0001t0027g0118a0001c0001t0028g0205a0001c0003t0001g0152others(10): Show | 13 | HG01175.hp2 HG02258.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.310+1573C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130973153 | ||||||
| chr12:130973175
|
C | T | 3 | a0001c0002t0001g0223a0002c0029t0031g0222a0010c0026t0013g0238 | 3 | HG02559.hp2 HG02723.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.310+1595C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130973175 | ||||||
| chr12:130973211
|
C | T | 1 | a0001c0003t0018g0117 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.310+1631C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130973211 | ||||||
| chr12:130973441
|
G | C | 1 | a0001c0043t0008g0227 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.310+1861G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130973441 | ||||||
| chr12:130973453
|
T | C | 1 | a0001c0019t0004g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.310+1873T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130973453 | ||||||
| chr12:130973481
|
A | G | 179 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(176): Show | 179 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.310+1901A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130973481 | ||||||
| chr12:130973543
|
C | G | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(194): Show | 197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.310+1963C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130973543 | ||||||
| chr12:130973622
|
C | T | 7 | a0001c0001t0002g0116a0001c0005t0001g0044a0001c0005t0001g0127others(4): Show | 7 | HG01167.hp1 HG02572.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.310+2042C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130973622 | ||||||
| chr12:130973705
|
T | C | 171 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(168): Show | 171 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.310+2125T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130973705 | ||||||
| chr12:130973805
|
A | AACAAAG | 224 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(221): Show | 224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.310+2225_310+2226i others(8): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130973805 | ||||||
| chr12:130973808
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0002g0149others(1): Show | 4 | HG01361.hp1 HG01433.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.310+2228G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130973808 | ||||||
| chr12:130973809
|
G | A | 2 | a0005c0011t0008g0047a0005c0021t0021g0048 | 2 | HG00280.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.310+2229G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130973809 | ||||||
| chr12:130973827
|
C | T | 1 | a0003c0012t0017g0158 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.310+2247C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130973827 | ||||||
| chr12:130974009
|
T | C | 2 | a0003c0031t0003g0089a0003c0040t0022g0096 | 2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.310+2429T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130974009 | ||||||
| chr12:130974119
|
C | T | 5 | a0001c0001t0002g0116a0001c0005t0001g0044a0001c0005t0001g0127others(2): Show | 5 | HG01167.hp1 HG02809.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.310+2539C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130974119 | ||||||
| chr12:130974250
|
G | A | 1 | a0001c0002t0003g0050 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.310+2670G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130974250 | ||||||
| chr12:130974263
|
G | A | 9 | a0001c0003t0004g0121a0001c0003t0004g0122a0001c0003t0012g0025others(6): Show | 9 | HG00738.hp2 HG01106.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.310+2683G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130974263 | ||||||
| chr12:130974282
|
C | T | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(170): Show | 173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.310+2702C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130974282 | ||||||
| chr12:130974591
|
A | G | 16 | a0001c0001t0027g0118a0001c0001t0028g0205a0001c0002t0001g0010others(13): Show | 16 | HG00735.hp1 HG01168.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.310+3011A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130974591 | ||||||
| chr12:130974660
|
ATT | A | 17 | a0001c0001t0002g0116a0001c0002t0001g0223a0001c0003t0004g0121others(14): Show | 17 | HG00738.hp2 HG01106.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.310+3082_310+3083d others(4): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr12 | 130974660 | |||||
| chr12:130974688
|
C | T | 1 | a0001c0002t0003g0083 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.310+3108C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130974688 | ||||||
| chr12:130974793
|
TCCCTGCT others(4): Show |
T | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(194): Show | 197 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.310+3221_310+3231d others(13): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr12 | 130974793 | |||||
| chr12:130974802
|
T | C | 2 | a0005c0011t0008g0047a0005c0021t0021g0048 | 2 | HG00280.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.310+3222T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130974802 | ||||||
| chr12:130974825
|
C | T | 6 | a0001c0006t0008g0177a0001c0042t0007g0176a0001c0043t0008g0227others(3): Show | 6 | HG02258.hp1 HG02559.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.310+3245C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130974825 | ||||||
| chr12:130974905
|
G | A | 1 | a0001c0003t0004g0198 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.310+3325G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130974905 | ||||||
| chr12:130975002
|
G | T | 8 | a0001c0003t0004g0121a0001c0003t0004g0122a0001c0003t0012g0025others(5): Show | 8 | HG00738.hp2 HG01106.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.310+3422G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130975002 | ||||||
| chr12:130975243
|
T | C | 1 | a0001c0004t0002g0164 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.310+3663T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130975243 | ||||||
| chr12:130975282
|
C | G | 13 | a0001c0001t0002g0130a0001c0001t0027g0118a0001c0001t0028g0205others(10): Show | 13 | HG00639.hp2 HG01175.hp2 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.310+3702C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130975282 | ||||||
| chr12:130975292
|
G | C | 223 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(220): Show | 223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.310+3712G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130975292 | ||||||
| chr12:130975349
|
C | T | 6 | a0001c0003t0004g0121a0001c0003t0004g0122a0001c0003t0012g0025others(3): Show | 6 | HG00738.hp2 HG01106.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.310+3769C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130975349 | ||||||
| chr12:130975365
|
C | G | 1 | a0003c0032t0038g0090 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.310+3785C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130975365 | ||||||
| chr12:130975378
|
G | A | 1 | a0001c0004t0005g0094 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.310+3798G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130975378 | ||||||
| chr12:130975722
|
G | A | 15 | a0001c0002t0001g0010a0001c0003t0004g0012a0001c0003t0004g0121others(12): Show | 15 | HG00735.hp1 HG00738.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.310+4142G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130975722 | ||||||
| chr12:130975744
|
A | G | 6 | a0001c0001t0027g0118a0001c0001t0028g0205a0001c0003t0001g0152others(3): Show | 6 | HG01175.hp2 HG02280.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.310+4164A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130975744 | ||||||
| chr12:130975752
|
A | G | 216 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(213): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.310+4172A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130975752 | ||||||
| chr12:130975802
|
T | C | 2 | a0005c0011t0008g0047a0005c0021t0021g0048 | 2 | HG00280.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.310+4222T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130975802 | ||||||
| chr12:130975885
|
T | A | 2 | a0001c0005t0001g0127a0001c0005t0001g0128 | 2 | HG01167.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.310+4305T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130975885 | ||||||
| chr12:130975885
|
T | C | 13 | a0001c0001t0027g0118a0001c0002t0001g0010a0001c0003t0004g0012others(10): Show | 13 | HG00735.hp1 HG01175.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.310+4305T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130975885 | ||||||
| chr12:130976092
|
T | A | 1 | a0001c0002t0002g0001 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.310+4512T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130976092 | ||||||
| chr12:130976101
|
C | T | 31 | a0001c0002t0001g0010a0001c0002t0001g0223a0001c0003t0004g0012others(28): Show | 31 | HG00280.hp1 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.310+4521C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130976101 | ||||||
| chr12:130976224
|
ACT | A | 171 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(168): Show | 171 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.310+4649_310+4650d others(4): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr12 | 130976224 | |||||
| chr12:130976380
|
C | T | 30 | a0001c0002t0001g0010a0001c0002t0001g0223a0001c0003t0004g0012others(27): Show | 30 | HG00280.hp1 HG00735.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.310+4800C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130976380 | ||||||
| chr12:130976397
|
T | C | 16 | a0001c0002t0001g0010a0001c0003t0004g0012a0001c0003t0006g0092others(13): Show | 16 | HG00735.hp1 HG02257.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.310+4817T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130976397 | ||||||
| chr12:130976464
|
T | C | 31 | a0001c0002t0001g0010a0001c0002t0001g0223a0001c0003t0004g0012others(28): Show | 31 | HG00280.hp1 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.310+4884T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130976464 | ||||||
| chr12:130976588
|
C | T | 5 | a0001c0002t0001g0223a0001c0005t0001g0112a0001c0005t0008g0226others(2): Show | 5 | HG02559.hp2 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.310+5008C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130976588 | ||||||
| chr12:130976597
|
G | A | 10 | a0001c0002t0001g0010a0001c0003t0004g0012a0001c0003t0006g0092others(7): Show | 10 | HG00735.hp1 HG02257.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.310+5017G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130976597 | ||||||
| chr12:130976788
|
G | A | 2 | a0005c0011t0008g0047a0005c0021t0021g0048 | 2 | HG00280.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.311-5096G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130976788 | ||||||
| chr12:130976813
|
A | G | 161 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(158): Show | 161 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.311-5071A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130976813 | ||||||
| chr12:130976859
|
GA | G | 25 | a0001c0002t0001g0010a0001c0002t0001g0223a0001c0003t0004g0012others(22): Show | 25 | HG00735.hp1 HG01169.hp1 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.311-5009delA | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr12 | 130976859 | |||||
| chr12:130976870
|
A | G | 1 | a0001c0004t0005g0082 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.311-5014A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130976870 | ||||||
| chr12:130976897
|
G | A | 1 | a0001c0003t0004g0104 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.311-4987G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130976897 | ||||||
| chr12:130977004
|
C | T | 9 | a0001c0006t0001g0120a0001c0006t0008g0177a0001c0042t0007g0176others(6): Show | 9 | HG00280.hp1 HG01981.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.311-4880C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130977004 | ||||||
| chr12:130977073
|
C | T | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(197): Show | 200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.311-4811C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130977073 | ||||||
| chr12:130977114
|
A | G | 6 | a0001c0002t0001g0223a0001c0005t0001g0112a0001c0005t0008g0226others(3): Show | 6 | HG02559.hp2 HG02630.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.311-4770A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130977114 | ||||||
| chr12:130977152
|
T | C | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(197): Show | 200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.311-4732T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130977152 | ||||||
| chr12:130977185
|
T | G | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(197): Show | 200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.311-4699T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130977185 | ||||||
| chr12:130977199
|
G | A | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(197): Show | 200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.311-4685G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130977199 | ||||||
| chr12:130977245
|
C | T | 2 | a0001c0005t0001g0127a0001c0005t0001g0128 | 2 | HG01167.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.311-4639C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130977245 | ||||||
| chr12:130977326
|
G | A | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(197): Show | 200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.311-4558G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130977326 | ||||||
| chr12:130977362
|
A | G | 9 | a0001c0006t0001g0120a0001c0006t0008g0177a0001c0042t0007g0176others(6): Show | 9 | HG00280.hp1 HG01981.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.311-4522A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130977362 | ||||||
| chr12:130977369
|
G | A | 1 | a0003c0031t0003g0089 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.311-4515G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130977369 | ||||||
| chr12:130977420
|
C | T | 1 | a0001c0043t0008g0227 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.311-4464C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130977420 | ||||||
| chr12:130977468
|
G | A | 12 | a0001c0002t0001g0010a0001c0003t0004g0012a0001c0003t0006g0092others(9): Show | 12 | HG00735.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.311-4416G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130977468 | ||||||
| chr12:130977536
|
T | C | 202 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(199): Show | 202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.311-4348T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130977536 | ||||||
| chr12:130977537
|
G | A | 3 | a0001c0003t0013g0129a0001c0013t0007g0153a0001c0013t0007g0154 | 3 | HG02630.hp1 HG02818.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.311-4347G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130977537 | ||||||
| chr12:130977663
|
G | A | 2 | a0005c0011t0008g0047a0005c0021t0021g0048 | 2 | HG00280.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.311-4221G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130977663 | ||||||
| chr12:130977694
|
G | A | 1 | a0001c0003t0006g0019 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.311-4190G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130977694 | ||||||
| chr12:130977766
|
T | G | 190 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(187): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.311-4118T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130977766 | ||||||
| chr12:130977799
|
T | C | 1 | a0001c0003t0004g0234 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.311-4085T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130977799 | ||||||
| chr12:130977801
|
T | C | 202 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(199): Show | 202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.311-4083T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130977801 | ||||||
| chr12:130977830
|
T | C | 202 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(199): Show | 202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.311-4054T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130977830 | ||||||
| chr12:130978057
|
A | T | 2 | a0001c0005t0001g0044a0001c0007t0018g0132 | 2 | HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.311-3827A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130978057 | ||||||
| chr12:130978272
|
C | T | 1 | a0001c0002t0003g0083 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.311-3612C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130978272 | ||||||
| chr12:130978320
|
T | C | 9 | a0001c0006t0001g0120a0001c0006t0008g0177a0001c0042t0007g0176others(6): Show | 9 | HG00280.hp1 HG01981.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.311-3564T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130978320 | ||||||
| chr12:130978373
|
C | T | 1 | a0004c0016t0002g0065 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.311-3511C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130978373 | ||||||
| chr12:130978428
|
T | C | 2 | a0005c0011t0008g0047a0005c0021t0021g0048 | 2 | HG00280.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.311-3456T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130978428 | ||||||
| chr12:130978566
|
T | G | 2 | a0001c0003t0013g0224a0001c0003t0013g0225 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.311-3318T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130978566 | ||||||
| chr12:130978572
|
C | T | 22 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(19): Show | 22 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.311-3312C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130978572 | ||||||
| chr12:130978659
|
C | T | 6 | a0001c0001t0027g0118a0001c0001t0028g0205a0001c0003t0001g0152others(3): Show | 6 | HG01175.hp2 HG02280.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.311-3225C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130978659 | ||||||
| chr12:130978666
|
A | G | 6 | a0001c0002t0001g0223a0001c0005t0001g0112a0001c0005t0008g0226others(3): Show | 6 | HG02559.hp2 HG02630.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.311-3218A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130978666 | ||||||
| chr12:130978707
|
A | G | 169 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(166): Show | 169 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.311-3177A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130978707 | ||||||
| chr12:130978820
|
A | G | 1 | a0003c0031t0003g0089 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.311-3064A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130978820 | ||||||
| chr12:130978914
|
C | T | 5 | a0001c0002t0001g0010a0001c0003t0004g0012a0001c0003t0006g0092others(2): Show | 5 | HG00735.hp1 HG02735.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.311-2970C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130978914 | ||||||
| chr12:130978966
|
C | T | 2 | a0001c0001t0002g0217a0001c0003t0006g0015 | 2 | HG02602.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.311-2918C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130978966 | ||||||
| chr12:130979054
|
C | T | 1 | a0003c0031t0003g0089 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.311-2830C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130979054 | ||||||
| chr12:130979104
|
G | A | 3 | a0001c0002t0001g0145a0001c0002t0001g0146a0001c0004t0043g0024 | 3 | HG00741.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.311-2780G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130979104 | ||||||
| chr12:130979156
|
A | G | 225 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(222): Show | 225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.311-2728A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130979156 | ||||||
| chr12:130979177
|
G | A | 1 | a0001c0003t0006g0019 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.311-2707G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130979177 | ||||||
| chr12:130979181
|
A | G | 202 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(199): Show | 202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.311-2703A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130979181 | ||||||
| chr12:130979218
|
C | A | 3 | a0001c0003t0013g0129a0001c0013t0007g0153a0001c0013t0007g0154 | 3 | HG02630.hp1 HG02818.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.311-2666C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130979218 | ||||||
| chr12:130979241
|
C | T | 32 | a0001c0002t0001g0010a0001c0002t0001g0223a0001c0003t0004g0012others(29): Show | 32 | HG00280.hp1 HG00735.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.311-2643C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130979241 | ||||||
| chr12:130979374
|
C | T | 4 | a0001c0005t0001g0112a0001c0005t0008g0226a0002c0029t0031g0222others(1): Show | 4 | HG02723.hp2 HG02895.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.311-2510C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130979374 | ||||||
| chr12:130979479
|
T | C | 199 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(196): Show | 199 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.311-2405T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130979479 | ||||||
| chr12:130979580
|
T | C | 24 | a0001c0002t0001g0010a0001c0003t0004g0012a0001c0003t0006g0092others(21): Show | 24 | HG00735.hp1 HG02257.hp1 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.311-2304T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130979580 | ||||||
| chr12:130979752
|
G | A | 2 | a0001c0005t0001g0044a0007c0039t0001g0229 | 2 | HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.311-2132G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130979752 | ||||||
| chr12:130979814
|
GTC | G | 8 | a0001c0001t0001g0113a0001c0001t0002g0005a0001c0001t0002g0107others(5): Show | 8 | HG00741.hp2 HG01168.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.311-2067_311-2066d others(4): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr12 | 130979814 | |||||
| chr12:130979815
|
T | TCA | 4 | a0001c0005t0001g0112a0001c0005t0008g0226a0001c0013t0007g0153others(1): Show | 4 | HG02818.hp2 HG02895.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.311-2068_311-2067i others(4): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr12 | 130979815 | |||||
| chr12:130979815
|
T | TCACACA | 3 | a0001c0002t0001g0010a0001c0003t0006g0092a0001c0003t0034g0014 | 3 | HG00735.hp1 HG02735.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.311-2068_311-2067i others(8): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr12 | 130979815 | |||||
| chr12:130979815
|
T | TCACACAC others(5): Show |
1 | a0001c0002t0001g0169 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.311-2068_311-2067i others(14): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr12 | 130979815 | |||||
| chr12:130979815
|
T | TCACACAC others(7): Show |
1 | a0010c0026t0013g0238 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.311-2068_311-2067i others(16): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr12 | 130979815 | |||||
| chr12:130979815
|
T | TCACACAC others(9): Show |
1 | a0002c0029t0031g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.311-2068_311-2067i others(18): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr12 | 130979815 | |||||
| chr12:130979815
|
T | TCACACAC others(13): Show |
1 | a0003c0032t0038g0090 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.311-2068_311-2067i others(22): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr12 | 130979815 | |||||
| chr12:130979815
|
TCTCA | T | 23 | a0001c0001t0001g0115a0001c0001t0001g0208a0001c0001t0001g0212others(20): Show | 23 | HG00140.hp1 HG01071.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.311-2067_311-2064d others(6): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr12 | 130979815 | |||||
| chr12:130979815
|
TCTCACA | T | 126 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(123): Show | 126 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.311-2067_311-2062d others(8): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr12 | 130979815 | |||||
| chr12:130979815
|
TCTCACAC others(1): Show |
T | 11 | a0001c0001t0009g0137a0001c0001t0009g0166a0001c0001t0023g0143others(8): Show | 11 | HG01099.hp1 HG01167.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.311-2067_311-2060d others(10): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr12 | 130979815 | |||||
| chr12:130979815
|
TCTCACAC others(5): Show |
T | 2 | a0005c0011t0008g0047a0005c0021t0021g0048 | 2 | HG00280.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.311-2067_311-2056d others(14): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr12 | 130979815 | |||||
| chr12:130979815
|
TCTCACAC others(7): Show |
T | 1 | a0001c0005t0001g0044 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.311-2067_311-2054d others(16): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr12 | 130979815 | |||||
| chr12:130979815
|
TCTCACAC others(11): Show |
T | 1 | a0001c0023t0004g0165 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.311-2067_311-2050d others(20): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr12 | 130979815 | |||||
| chr12:130979817
|
T | A | 19 | a0001c0002t0001g0010a0001c0002t0001g0169a0001c0003t0004g0012others(16): Show | 19 | HG00735.hp1 HG02056.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.311-2067T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130979817 | ||||||
| chr12:130979817
|
T | TCA | 10 | a0001c0005t0001g0206a0001c0005t0001g0239a0001c0006t0001g0242others(7): Show | 10 | HG01109.hp1 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.311-2023_311-2022d others(4): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr12 | 130979817 | |||||
| chr12:130979817
|
T | TCACACAC others(1): Show |
6 | a0001c0003t0001g0152a0001c0003t0004g0013a0001c0003t0004g0189others(3): Show | 6 | HG01168.hp2 HG01169.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.311-2029_311-2022d others(10): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr12 | 130979817 | |||||
| chr12:130979817
|
T | TCACACAC others(3): Show |
5 | a0001c0002t0003g0064a0001c0003t0004g0188a0001c0004t0002g0131others(2): Show | 5 | HG00639.hp2 HG01361.hp2 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.311-2031_311-2022d others(12): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr12 | 130979817 | |||||
| chr12:130979817
|
T | TCACACAC others(5): Show |
2 | a0001c0001t0001g0197a0001c0004t0005g0094 | 2 | HG00639.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.311-2033_311-2022d others(14): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr12 | 130979817 | |||||
| chr12:130979817
|
T | TCACACAC others(9): Show |
3 | a0001c0001t0002g0130a0001c0001t0003g0023a0001c0019t0004g0230 | 3 | HG01074.hp1 HG02109.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.311-2037_311-2022d others(18): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr12 | 130979817 | |||||
| chr12:130979817
|
T | TCACACAC others(11): Show |
1 | a0001c0002t0001g0202 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.311-2039_311-2022d others(20): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr12 | 130979817 | |||||
| chr12:130979817
|
TCA | T | 3 | a0001c0003t0013g0129a0001c0005t0001g0128a0001c0025t0021g0119 | 3 | HG01934.hp2 HG02630.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.311-2023_311-2022d others(4): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr12 | 130979817 | |||||
| chr12:130979817
|
TCACA | T | 3 | a0001c0001t0028g0205a0001c0003t0029g0214a0003c0040t0022g0096 | 3 | HG02280.hp2 HG02647.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.311-2025_311-2022d others(6): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr12 | 130979817 | |||||
| chr12:130979817
|
TCACACAC others(3): Show |
T | 1 | a0002c0030t0032g0159 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.311-2031_311-2022d others(12): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr12 | 130979817 | |||||
| chr12:130979817
|
TCACACAC others(9): Show |
T | 1 | a0002c0044t0007g0126 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.311-2037_311-2022d others(18): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr12 | 130979817 | |||||
| chr12:130979817
|
TCACACAC others(11): Show |
T | 1 | a0001c0002t0001g0223 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.311-2039_311-2022d others(20): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr12 | 130979817 | |||||
| chr12:130979826
|
C | T | 1 | a0001c0001t0005g0028 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.311-2058C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130979826 | ||||||
| chr12:130979883
|
G | A | 30 | a0001c0002t0001g0010a0001c0003t0001g0152a0001c0003t0004g0012others(27): Show | 30 | HG00280.hp1 HG00735.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.311-2001G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130979883 | ||||||
| chr12:130979920
|
G | A | 2 | a0001c0002t0046g0084a0001c0002t0048g0151 | 2 | HG03704.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.311-1964G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130979920 | ||||||
| chr12:130979973
|
A | G | 33 | a0001c0002t0001g0010a0001c0003t0004g0012a0001c0003t0004g0121others(30): Show | 33 | HG00280.hp1 HG00735.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.311-1911A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130979973 | ||||||
| chr12:130980083
|
T | TCAGGAGC others(316): Show |
1 | a0005c0011t0008g0047 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.311-1785_311-1784i others(325): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr12 | 130980083 | |||||
| chr12:130980083
|
T | TCAGGAGC others(317): Show |
1 | a0005c0021t0021g0048 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.311-1785_311-1784i others(326): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr12 | 130980083 | |||||
| chr12:130980239
|
G | A | 52 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0156others(49): Show | 52 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.311-1645G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130980239 | ||||||
| chr12:130980326
|
G | A | 2 | a0001c0019t0004g0230a0001c0020t0002g0180 | 2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.311-1558G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130980326 | ||||||
| chr12:130980340
|
A | G | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(194): Show | 197 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.311-1544A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130980340 | ||||||
| chr12:130980364
|
T | A | 1 | a0003c0012t0017g0158 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.311-1520T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130980364 | ||||||
| chr12:130980371
|
T | C | 2 | a0001c0006t0001g0120a0001c0006t0008g0177 | 2 | HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.311-1513T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130980371 | ||||||
| chr12:130980383
|
C | T | 1 | a0001c0001t0011g0066 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.311-1501C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130980383 | ||||||
| chr12:130980384
|
G | A | 2 | a0005c0011t0008g0047a0005c0021t0021g0048 | 2 | HG00280.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.311-1500G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130980384 | ||||||
| chr12:130980554
|
C | T | 1 | a0001c0004t0043g0024 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.311-1330C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130980554 | ||||||
| chr12:130980649
|
C | T | 1 | a0001c0001t0011g0066 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.311-1235C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130980649 | ||||||
| chr12:130980693
|
C | T | 1 | a0001c0002t0001g0199 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.311-1191C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130980693 | ||||||
| chr12:130980758
|
T | C | 2 | a0001c0005t0001g0127a0001c0005t0001g0128 | 2 | HG01167.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.311-1126T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130980758 | ||||||
| chr12:130980789
|
G | C | 3 | a0001c0005t0001g0044a0001c0007t0018g0132a0001c0043t0008g0227 | 3 | HG02572.hp2 HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.311-1095G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130980789 | ||||||
| chr12:130980861
|
A | G | 21 | a0001c0002t0001g0010a0001c0003t0004g0012a0001c0003t0004g0121others(18): Show | 21 | HG00735.hp1 HG00738.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.311-1023A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130980861 | ||||||
| chr12:130980864
|
T | G | 4 | a0001c0005t0001g0044a0001c0007t0018g0132a0001c0043t0008g0227others(1): Show | 4 | HG02572.hp2 HG02630.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.311-1020T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130980864 | ||||||
| chr12:130980929
|
A | G | 1 | a0001c0022t0016g0109 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.311-955A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130980929 | ||||||
| chr12:130980935
|
C | T | 3 | a0001c0005t0001g0044a0001c0043t0008g0227a0003c0031t0003g0089 | 3 | HG02630.hp2 HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.311-949C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130980935 | ||||||
| chr12:130980936
|
G | A | 1 | a0002c0044t0007g0126 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.311-948G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130980936 | ||||||
| chr12:130980974
|
C | T | 1 | a0003c0012t0017g0158 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.311-910C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130980974 | ||||||
| chr12:130981021
|
A | G | 26 | a0001c0002t0001g0010a0001c0003t0004g0012a0001c0003t0004g0121others(23): Show | 26 | HG00280.hp1 HG00735.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.311-863A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130981021 | ||||||
| chr12:130981066
|
C | T | 26 | a0001c0002t0001g0010a0001c0003t0004g0012a0001c0003t0004g0121others(23): Show | 26 | HG00280.hp1 HG00735.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.311-818C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130981066 | ||||||
| chr12:130981408
|
T | C | 2 | a0001c0001t0027g0118a0001c0003t0004g0237 | 2 | HG01175.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.311-476T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130981408 | ||||||
| chr12:130981411
|
G | C | 21 | a0001c0001t0002g0107a0001c0001t0002g0203a0001c0001t0002g0204others(18): Show | 21 | HG00735.hp1 HG00738.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.311-473G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130981411 | ||||||
| chr12:130981536
|
G | A | 4 | a0001c0001t0011g0074a0001c0001t0011g0220a0001c0002t0003g0073others(1): Show | 4 | HG02083.hp1 NA18957.hp1 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.311-348G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130981536 | ||||||
| chr12:130981596
|
T | C | 228 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(225): Show | 228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.311-288T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130981596 | ||||||
| chr12:130981597
|
G | T | 19 | a0001c0003t0004g0121a0001c0003t0004g0122a0001c0003t0012g0027others(16): Show | 19 | HG00280.hp1 HG00738.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.311-287G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130981597 | ||||||
| chr12:130981648
|
T | A | 4 | a0001c0005t0001g0044a0003c0031t0003g0089a0005c0011t0008g0047others(1): Show | 4 | HG00280.hp1 HG01981.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.311-236T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130981648 | ||||||
| chr12:130981660
|
G | A | 1 | a0001c0002t0037g0194 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.311-224G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130981660 | ||||||
| chr12:130981874
|
C | T | 2 | a0005c0011t0008g0047a0005c0021t0021g0048 | 2 | HG00280.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.311-10C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 4/24 | chr12 | 130981874 | ||||||
| chr12:130982078
|
C | T | 1 | a0001c0001t0002g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.490+15C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130982078 | ||||||
| chr12:130982099
|
GGAGGAGT others(11): Show |
G | 3 | a0001c0005t0001g0044a0001c0043t0008g0227a0003c0031t0003g0089 | 3 | HG02630.hp2 HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.490+37_490+54delGA others(16): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130982099 | ||||||
| chr12:130982119
|
G | C | 3 | a0001c0005t0001g0044a0001c0043t0008g0227a0003c0031t0003g0089 | 3 | HG02630.hp2 HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.490+56G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130982119 | ||||||
| chr12:130982254
|
C | T | 1 | a0001c0005t0001g0044 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.490+191C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130982254 | ||||||
| chr12:130982277
|
G | A | 2 | a0001c0001t0015g0060a0001c0004t0015g0093 | 2 | HG00140.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.490+214G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130982277 | ||||||
| chr12:130982367
|
T | C | 9 | a0001c0001t0027g0118a0001c0001t0028g0205a0001c0003t0001g0152others(6): Show | 9 | HG01175.hp2 HG02257.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.490+304T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130982367 | ||||||
| chr12:130982385
|
G | A | 4 | a0001c0002t0001g0010a0001c0003t0004g0012a0001c0003t0006g0092others(1): Show | 4 | HG00735.hp1 HG02735.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.490+322G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130982385 | ||||||
| chr12:130982445
|
T | G | 2 | a0001c0019t0004g0230a0001c0020t0002g0180 | 2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.490+382T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130982445 | ||||||
| chr12:130982646
|
A | G | 184 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(181): Show | 184 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.490+583A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130982646 | ||||||
| chr12:130982647
|
G | A | 5 | a0001c0005t0001g0112a0001c0005t0008g0226a0002c0029t0031g0222others(2): Show | 5 | HG02559.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.490+584G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130982647 | ||||||
| chr12:130982694
|
A | G | 2 | a0001c0043t0008g0227a0003c0031t0003g0089 | 2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.490+631A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130982694 | ||||||
| chr12:130982834
|
G | A | 2 | a0001c0019t0004g0230a0001c0020t0002g0180 | 2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.490+771G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130982834 | ||||||
| chr12:130982892
|
G | C | 1 | a0001c0003t0018g0117 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.490+829G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130982892 | ||||||
| chr12:130982900
|
A | G | 1 | a0003c0031t0003g0089 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.490+837A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130982900 | ||||||
| chr12:130982926
|
G | A | 2 | a0001c0005t0001g0044a0003c0031t0003g0089 | 2 | HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.490+863G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130982926 | ||||||
| chr12:130982955
|
C | T | 5 | a0001c0001t0002g0107a0001c0001t0002g0203a0001c0001t0002g0204others(2): Show | 5 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.490+892C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130982955 | ||||||
| chr12:130983059
|
A | T | 1 | a0003c0040t0022g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.490+996A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130983059 | ||||||
| chr12:130983078
|
C | T | 2 | a0005c0011t0008g0047a0005c0021t0021g0048 | 2 | HG00280.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.490+1015C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130983078 | ||||||
| chr12:130983089
|
G | A | 184 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(181): Show | 184 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.490+1026G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130983089 | ||||||
| chr12:130983224
|
G | A | 186 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(183): Show | 186 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.490+1161G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130983224 | ||||||
| chr12:130983424
|
C | T | 10 | a0001c0001t0011g0066a0001c0001t0011g0074a0001c0001t0011g0220others(7): Show | 10 | HG00621.hp2 HG02071.hp1 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.490+1361C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130983424 | ||||||
| chr12:130983644
|
G | A | 184 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(181): Show | 184 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.490+1581G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130983644 | ||||||
| chr12:130983712
|
C | T | 1 | a0001c0005t0014g0054 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.490+1649C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130983712 | ||||||
| chr12:130983903
|
G | C | 2 | a0001c0019t0004g0230a0001c0020t0002g0180 | 2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.490+1840G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130983903 | ||||||
| chr12:130983924
|
C | G | 2 | a0001c0001t0002g0175a0001c0010t0007g0150 | 2 | NA18986.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.490+1861C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130983924 | ||||||
| chr12:130983948
|
C | T | 3 | a0005c0011t0002g0110a0005c0011t0008g0047a0005c0021t0021g0048 | 3 | HG00280.hp1 HG01106.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.490+1885C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130983948 | ||||||
| chr12:130984071
|
C | T | 3 | a0005c0011t0002g0110a0005c0011t0008g0047a0005c0021t0021g0048 | 3 | HG00280.hp1 HG01106.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.490+2008C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130984071 | ||||||
| chr12:130984142
|
T | C | 5 | a0001c0001t0028g0205a0001c0003t0001g0152a0001c0003t0029g0214others(2): Show | 5 | HG02280.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.490+2079T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130984142 | ||||||
| chr12:130984193
|
C | T | 1 | a0001c0003t0006g0058 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.490+2130C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130984193 | ||||||
| chr12:130984762
|
C | T | 1 | a0001c0007t0004g0236 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.491-2333C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130984762 | ||||||
| chr12:130984766
|
T | C | 21 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(18): Show | 21 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.491-2329T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130984766 | ||||||
| chr12:130984805
|
C | T | 3 | a0001c0042t0007g0176a0003c0041t0004g0178a0007c0039t0001g0229 | 3 | HG02258.hp1 HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.491-2290C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130984805 | ||||||
| chr12:130984823
|
T | C | 158 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(155): Show | 158 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.491-2272T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130984823 | ||||||
| chr12:130984932
|
T | C | 1 | a0002c0030t0032g0159 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.491-2163T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130984932 | ||||||
| chr12:130985003
|
C | T | 190 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(187): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.491-2092C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130985003 | ||||||
| chr12:130985101
|
G | GT | 9 | a0001c0001t0027g0118a0001c0001t0028g0205a0001c0003t0001g0152others(6): Show | 9 | HG01175.hp2 HG02257.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.491-1979dupT | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr12 | 130985101 | |||||
| chr12:130985101
|
GT | G | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(174): Show | 177 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.491-1979delT | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr12 | 130985101 | |||||
| chr12:130985188
|
C | T | 1 | a0001c0002t0003g0071 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.491-1907C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130985188 | ||||||
| chr12:130985189
|
A | G | 51 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0156others(48): Show | 51 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.491-1906A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130985189 | ||||||
| chr12:130985208
|
C | T | 2 | a0001c0019t0004g0230a0001c0020t0002g0180 | 2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.491-1887C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130985208 | ||||||
| chr12:130985248
|
G | A | 13 | a0001c0001t0016g0182a0001c0003t0004g0104a0001c0003t0004g0207others(10): Show | 13 | HG01168.hp1 HG01243.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.491-1847G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130985248 | ||||||
| chr12:130985333
|
T | G | 6 | a0001c0002t0001g0010a0001c0003t0004g0012a0001c0003t0004g0198others(3): Show | 6 | HG00735.hp1 HG02735.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.491-1762T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130985333 | ||||||
| chr12:130985334
|
C | G | 1 | a0001c0003t0006g0216 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.491-1761C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130985334 | ||||||
| chr12:130985469
|
T | A | 3 | a0005c0011t0002g0110a0005c0011t0008g0047a0005c0021t0021g0048 | 3 | HG00280.hp1 HG01106.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.491-1626T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130985469 | ||||||
| chr12:130985558
|
T | TTG | 10 | a0001c0003t0004g0121a0001c0003t0004g0122a0001c0003t0012g0025others(7): Show | 10 | HG00738.hp2 HG01496.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.491-1537_491-1536i others(4): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130985558 | ||||||
| chr12:130985559
|
G | GT | 162 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(159): Show | 162 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.491-1528dupT | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr12 | 130985559 | |||||
| chr12:130985559
|
G | T | 10 | a0001c0003t0004g0121a0001c0003t0004g0122a0001c0003t0012g0025others(7): Show | 10 | HG00738.hp2 HG01496.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.491-1536G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130985559 | ||||||
| chr12:130985563
|
T | TC | 6 | a0001c0002t0001g0010a0001c0003t0004g0012a0001c0003t0004g0198others(3): Show | 6 | HG00735.hp1 HG02735.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.491-1532_491-1531i others(3): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130985563 | ||||||
| chr12:130985574
|
G | A | 1 | a0001c0002t0002g0009 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.491-1521G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130985574 | ||||||
| chr12:130985637
|
A | G | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(197): Show | 200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.491-1458A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130985637 | ||||||
| chr12:130985708
|
C | T | 10 | a0001c0003t0004g0121a0001c0003t0004g0122a0001c0003t0012g0025others(7): Show | 10 | HG00738.hp2 HG01496.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.491-1387C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130985708 | ||||||
| chr12:130985885
|
C | T | 22 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(19): Show | 22 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.491-1210C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130985885 | ||||||
| chr12:130985896
|
G | A | 1 | a0001c0005t0014g0049 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.491-1199G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130985896 | ||||||
| chr12:130985917
|
G | A | 3 | a0001c0001t0027g0118a0001c0003t0004g0237a0001c0003t0036g0209 | 3 | HG01175.hp2 HG02257.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.491-1178G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130985917 | ||||||
| chr12:130985941
|
CT | C | 156 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(153): Show | 156 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.491-1150delT | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr12 | 130985941 | |||||
| chr12:130985948
|
C | T | 22 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(19): Show | 22 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.491-1147C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130985948 | ||||||
| chr12:130985993
|
G | T | 22 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(19): Show | 22 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.491-1102G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130985993 | ||||||
| chr12:130986018
|
CT | C | 50 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0156others(47): Show | 50 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.491-1076delT | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130986018 | ||||||
| chr12:130986028
|
GT | G | 22 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(19): Show | 22 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.491-1060delT | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr12 | 130986028 | |||||
| chr12:130986053
|
T | G | 1 | a0010c0026t0013g0238 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.491-1042T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130986053 | ||||||
| chr12:130986161
|
C | T | 3 | a0005c0011t0002g0110a0005c0011t0008g0047a0005c0021t0021g0048 | 3 | HG00280.hp1 HG01106.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.491-934C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130986161 | ||||||
| chr12:130986329
|
CAG | C | 9 | a0001c0001t0027g0118a0001c0001t0028g0205a0001c0003t0001g0152others(6): Show | 9 | HG01175.hp2 HG02257.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.491-763_491-762del others(2): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr12 | 130986329 | |||||
| chr12:130986402
|
T | C | 5 | a0001c0001t0028g0205a0001c0003t0001g0152a0001c0003t0029g0214others(2): Show | 5 | HG02280.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.491-693T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130986402 | ||||||
| chr12:130986455
|
G | A | 1 | a0001c0005t0001g0044 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.491-640G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130986455 | ||||||
| chr12:130986504
|
G | A | 22 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(19): Show | 22 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.491-591G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130986504 | ||||||
| chr12:130986525
|
A | G | 22 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(19): Show | 22 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.491-570A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130986525 | ||||||
| chr12:130986549
|
T | A | 6 | a0001c0005t0001g0112a0001c0005t0008g0226a0002c0029t0031g0222others(3): Show | 6 | HG02559.hp1 HG02723.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.491-546T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130986549 | ||||||
| chr12:130986622
|
T | G | 22 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(19): Show | 22 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.491-473T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130986622 | ||||||
| chr12:130986626
|
ATTC | A | 17 | a0001c0001t0027g0118a0001c0001t0028g0205a0001c0003t0001g0152others(14): Show | 17 | HG01175.hp2 HG02109.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.491-466_491-464del others(3): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr12 | 130986626 | |||||
| chr12:130986637
|
C | CT | 4 | a0001c0001t0002g0161a0001c0001t0009g0144a0001c0003t0006g0211others(1): Show | 4 | HG01175.hp1 NA18970.hp2 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.491-450dupT | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr12 | 130986637 | |||||
| chr12:130986722
|
C | G | 3 | a0005c0011t0002g0110a0005c0011t0008g0047a0005c0021t0021g0048 | 3 | HG00280.hp1 HG01106.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.491-373C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130986722 | ||||||
| chr12:130986735
|
A | AT | 22 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(19): Show | 22 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.491-354dupT | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr12 | 130986735 | |||||
| chr12:130986756
|
T | C | 10 | a0001c0003t0004g0121a0001c0003t0004g0122a0001c0003t0012g0025others(7): Show | 10 | HG00738.hp2 HG01496.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.491-339T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130986756 | ||||||
| chr12:130986913
|
C | T | 22 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(19): Show | 22 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.491-182C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130986913 | ||||||
| chr12:130987063
|
T | C | 225 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(222): Show | 225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.491-32T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130987063 | ||||||
| chr12:130987076
|
G | A | 1 | a0001c0002t0046g0084 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.491-19G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 5/24 | chr12 | 130987076 | ||||||
| chr12:130987411
|
G | A | 225 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(222): Show | 225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.745+62G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130987411 | ||||||
| chr12:130987414
|
C | T | 6 | a0001c0005t0001g0112a0001c0005t0008g0226a0002c0029t0031g0222others(3): Show | 6 | HG02559.hp1 HG02723.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.745+65C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130987414 | ||||||
| chr12:130987461
|
G | C | 22 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(19): Show | 22 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.745+112G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130987461 | ||||||
| chr12:130987466
|
G | A | 1 | a0001c0002t0003g0034 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.745+117G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130987466 | ||||||
| chr12:130987534
|
T | C | 22 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(19): Show | 22 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.745+185T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130987534 | ||||||
| chr12:130987608
|
C | G | 22 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(19): Show | 22 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.745+259C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130987608 | ||||||
| chr12:130987630
|
G | A | 22 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(19): Show | 22 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.745+281G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130987630 | ||||||
| chr12:130987634
|
G | A | 22 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(19): Show | 22 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.745+285G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130987634 | ||||||
| chr12:130987669
|
T | C | 30 | a0001c0001t0016g0182a0001c0001t0027g0118a0001c0001t0028g0205others(27): Show | 30 | HG00735.hp1 HG01168.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.745+320T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130987669 | ||||||
| chr12:130987671
|
T | A | 22 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(19): Show | 22 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.745+322T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130987671 | ||||||
| chr12:130987715
|
A | T | 22 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(19): Show | 22 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.745+366A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130987715 | ||||||
| chr12:130987734
|
G | T | 4 | a0001c0001t0002g0107a0001c0001t0002g0203a0001c0001t0002g0204others(1): Show | 4 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(1): Show |
intron_variant | MODIFIER | c.745+385G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130987734 | ||||||
| chr12:130987751
|
G | A | 1 | a0001c0046t0017g0221 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.745+402G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130987751 | ||||||
| chr12:130987779
|
G | A | 22 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(19): Show | 22 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.745+430G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130987779 | ||||||
| chr12:130987804
|
A | C | 22 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(19): Show | 22 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.745+455A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130987804 | ||||||
| chr12:130987860
|
T | A | 22 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(19): Show | 22 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.745+511T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130987860 | ||||||
| chr12:130987875
|
T | C | 22 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(19): Show | 22 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.745+526T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130987875 | ||||||
| chr12:130987896
|
A | AG | 22 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(19): Show | 22 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.745+547_745+548ins others(1): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130987896 | ||||||
| chr12:130987958
|
TC | T | 22 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(19): Show | 22 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.745+615delC | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr12 | 130987958 | |||||
| chr12:130987977
|
C | T | 1 | a0001c0001t0009g0166 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.745+628C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130987977 | ||||||
| chr12:130987980
|
A | T | 22 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(19): Show | 22 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.745+631A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130987980 | ||||||
| chr12:130987990
|
T | C | 22 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(19): Show | 22 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.745+641T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130987990 | ||||||
| chr12:130987993
|
A | G | 22 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(19): Show | 22 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.745+644A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130987993 | ||||||
| chr12:130987994
|
G | A | 1 | a0001c0002t0010g0134 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.745+645G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130987994 | ||||||
| chr12:130988068
|
T | G | 22 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(19): Show | 22 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.745+719T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130988068 | ||||||
| chr12:130988115
|
T | G | 10 | a0001c0003t0001g0152a0001c0003t0004g0207a0001c0003t0013g0224others(7): Show | 10 | HG02647.hp1 HG02717.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.745+766T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130988115 | ||||||
| chr12:130988121
|
AT | A | 22 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(19): Show | 22 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.745+782delT | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr12 | 130988121 | |||||
| chr12:130988152
|
A | ATACTAC | 22 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(19): Show | 22 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.745+807_745+808ins others(6): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr12 | 130988152 | |||||
| chr12:130988183
|
A | AAAATGAG others(11): Show |
22 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(19): Show | 22 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.745+836_745+837ins others(18): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr12 | 130988183 | |||||
| chr12:130988321
|
GTTTC | G | 21 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(18): Show | 21 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.745+976_745+979del others(4): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr12 | 130988321 | |||||
| chr12:130988385
|
A | C | 2 | a0001c0003t0004g0234a0001c0003t0018g0232 | 2 | HG02717.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.745+1036A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130988385 | ||||||
| chr12:130988404
|
T | C | 21 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(18): Show | 21 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.745+1055T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130988404 | ||||||
| chr12:130988478
|
G | A | 21 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(18): Show | 21 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.745+1129G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130988478 | ||||||
| chr12:130988517
|
G | A | 3 | a0005c0011t0002g0110a0005c0011t0008g0047a0005c0021t0021g0048 | 3 | HG00280.hp1 HG01106.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.745+1168G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130988517 | ||||||
| chr12:130988522
|
C | T | 21 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(18): Show | 21 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.745+1173C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130988522 | ||||||
| chr12:130988545
|
A | G | 21 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(18): Show | 21 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.745+1196A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130988545 | ||||||
| chr12:130988564
|
C | G | 21 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(18): Show | 21 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.745+1215C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130988564 | ||||||
| chr12:130988670
|
G | C | 21 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(18): Show | 21 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.745+1321G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130988670 | ||||||
| chr12:130988772
|
CTTCT | C | 180 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(177): Show | 180 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.745+1428_745+1431d others(6): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr12 | 130988772 | |||||
| chr12:130988892
|
T | G | 1 | a0001c0002t0001g0195 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.745+1543T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130988892 | ||||||
| chr12:130988900
|
C | G | 21 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(18): Show | 21 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.745+1551C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130988900 | ||||||
| chr12:130988901
|
T | G | 21 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(18): Show | 21 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.745+1552T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130988901 | ||||||
| chr12:130988928
|
C | G | 21 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(18): Show | 21 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.745+1579C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130988928 | ||||||
| chr12:130988985
|
G | A | 1 | a0001c0010t0007g0160 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.745+1636G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130988985 | ||||||
| chr12:130988998
|
T | G | 227 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(224): Show | 227 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.745+1649T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130988998 | ||||||
| chr12:130989096
|
C | T | 2 | a0001c0001t0023g0143a0001c0002t0010g0142 | 2 | NA18612.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.745+1747C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130989096 | ||||||
| chr12:130989149
|
A | C | 7 | a0001c0001t0002g0172a0001c0001t0002g0173a0001c0002t0001g0174others(4): Show | 7 | NA18612.hp2 NA18959.hp1 NA18982.hp2 others(4): Show |
intron_variant | MODIFIER | c.745+1800A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130989149 | ||||||
| chr12:130989163
|
G | T | 21 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(18): Show | 21 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.745+1814G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130989163 | ||||||
| chr12:130989169
|
T | C | 21 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(18): Show | 21 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.745+1820T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130989169 | ||||||
| chr12:130989388
|
A | G | 1 | a0001c0022t0016g0109 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.746-1626A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130989388 | ||||||
| chr12:130989429
|
C | T | 21 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(18): Show | 21 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.746-1585C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130989429 | ||||||
| chr12:130989490
|
C | T | 2 | a0001c0005t0001g0044a0002c0030t0032g0159 | 2 | HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.746-1524C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130989490 | ||||||
| chr12:130989569
|
T | C | 21 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(18): Show | 21 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.746-1445T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130989569 | ||||||
| chr12:130989576
|
C | T | 2 | a0001c0005t0001g0112a0001c0005t0008g0226 | 2 | HG02895.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.746-1438C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130989576 | ||||||
| chr12:130989581
|
C | A | 2 | a0001c0002t0002g0106a0001c0014t0004g0105 | 2 | HG00323.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.746-1433C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130989581 | ||||||
| chr12:130989586
|
C | T | 19 | a0001c0001t0027g0118a0001c0003t0001g0152a0001c0003t0004g0207others(16): Show | 19 | HG01175.hp2 HG01934.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.746-1428C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130989586 | ||||||
| chr12:130989772
|
C | T | 21 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(18): Show | 21 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.746-1242C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130989772 | ||||||
| chr12:130989773
|
G | A | 1 | a0001c0006t0001g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.746-1241G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130989773 | ||||||
| chr12:130989818
|
C | T | 4 | a0001c0005t0001g0044a0002c0029t0031g0222a0002c0030t0032g0159others(1): Show | 4 | HG02723.hp2 HG02809.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.746-1196C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130989818 | ||||||
| chr12:130989833
|
C | T | 21 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(18): Show | 21 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.746-1181C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130989833 | ||||||
| chr12:130989837
|
G | T | 1 | a0003c0031t0003g0089 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.746-1177G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130989837 | ||||||
| chr12:130989851
|
T | C | 21 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(18): Show | 21 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.746-1163T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130989851 | ||||||
| chr12:130989873
|
C | T | 21 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(18): Show | 21 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.746-1141C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130989873 | ||||||
| chr12:130989876
|
T | C | 21 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(18): Show | 21 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.746-1138T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130989876 | ||||||
| chr12:130989911
|
C | T | 21 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(18): Show | 21 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.746-1103C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130989911 | ||||||
| chr12:130989920
|
G | A | 19 | a0001c0001t0027g0118a0001c0003t0001g0152a0001c0003t0004g0207others(16): Show | 19 | HG01175.hp2 HG01934.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.746-1094G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130989920 | ||||||
| chr12:130989960
|
C | G | 183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.746-1054C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130989960 | ||||||
| chr12:130990188
|
G | A | 1 | a0001c0003t0019g0218 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.746-826G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130990188 | ||||||
| chr12:130990523
|
T | C | 1 | a0001c0003t0001g0152 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.746-491T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130990523 | ||||||
| chr12:130990606
|
C | T | 1 | a0001c0001t0009g0144 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.746-408C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130990606 | ||||||
| chr12:130990680
|
G | A | 1 | a0001c0003t0004g0104 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.746-334G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 6/24 | chr12 | 130990680 | ||||||
| chr12:130991105
|
C | T | 3 | a0001c0001t0027g0118a0001c0003t0004g0237a0001c0003t0036g0209 | 3 | HG01175.hp2 HG02257.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.810+27C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 7/24 | chr12 | 130991105 | ||||||
| chr12:130991228
|
A | G | 2 | a0001c0003t0044g0079a0001c0004t0005g0036 | 2 | NA19002.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.810+150A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 7/24 | chr12 | 130991228 | ||||||
| chr12:130991343
|
G | A | 2 | a0001c0001t0015g0060a0001c0004t0015g0093 | 2 | HG00140.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.810+265G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 7/24 | chr12 | 130991343 | ||||||
| chr12:130991422
|
A | T | 21 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(18): Show | 21 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.810+344A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 7/24 | chr12 | 130991422 | ||||||
| chr12:130991683
|
A | T | 48 | a0001c0001t0001g0113a0001c0001t0001g0163a0001c0001t0001g0212others(45): Show | 48 | HG00323.hp2 HG01069.hp1 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.811-554A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 7/24 | chr12 | 130991683 | ||||||
| chr12:130991730
|
G | A | 1 | a0003c0031t0003g0089 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.811-507G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 7/24 | chr12 | 130991730 | ||||||
| chr12:130991762
|
A | G | 108 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0163others(105): Show | 108 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.811-475A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 7/24 | chr12 | 130991762 | ||||||
| chr12:130991783
|
C | T | 105 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0115others(102): Show | 105 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.811-454C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 7/24 | chr12 | 130991783 | ||||||
| chr12:130992028
|
A | C | 1 | a0003c0032t0038g0090 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.811-209A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 7/24 | chr12 | 130992028 | ||||||
| chr12:130992045
|
C | T | 3 | a0001c0001t0009g0140a0001c0004t0002g0011a0001c0008t0001g0183 | 3 | HG04199.hp1 NA18961.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.811-192C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 7/24 | chr12 | 130992045 | ||||||
| chr12:130992109
|
A | C | 2 | a0001c0042t0007g0176a0003c0041t0004g0178 | 2 | HG02258.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.811-128A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 7/24 | chr12 | 130992109 | ||||||
| chr12:130992120
|
CA | C | 7 | a0001c0019t0004g0230a0001c0020t0002g0180a0001c0022t0016g0109others(4): Show | 7 | HG01934.hp2 HG02109.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.811-100delA | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr12 | 130992120 | |||||
| chr12:130992120
|
CAA | C | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0115others(108): Show | 111 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.811-101_811-100del others(2): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr12 | 130992120 | |||||
| chr12:130992120
|
CAAA | C | 106 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0163others(103): Show | 106 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.811-102_811-100del others(3): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr12 | 130992120 | |||||
| chr12:130992429
|
C | T | 1 | a0001c0002t0001g0223 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.966+37C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130992429 | ||||||
| chr12:130992530
|
T | C | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0115others(97): Show | 100 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.966+138T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130992530 | ||||||
| chr12:130992535
|
A | G | 224 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(221): Show | 224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.966+143A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130992535 | ||||||
| chr12:130992544
|
G | A | 5 | a0001c0003t0013g0224a0001c0003t0013g0225a0001c0005t0003g0056others(2): Show | 5 | HG02717.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.966+152G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130992544 | ||||||
| chr12:130992632
|
C | T | 21 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(18): Show | 21 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.966+240C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130992632 | ||||||
| chr12:130992643
|
C | T | 1 | a0001c0001t0003g0026 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.966+251C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130992643 | ||||||
| chr12:130992669
|
G | T | 18 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(15): Show | 18 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.966+277G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130992669 | ||||||
| chr12:130992767
|
C | T | 1 | a0003c0033t0030g0231 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.966+375C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130992767 | ||||||
| chr12:130992940
|
T | C | 221 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(218): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.966+548T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130992940 | ||||||
| chr12:130993011
|
G | C | 6 | a0001c0002t0001g0010a0001c0003t0004g0012a0001c0003t0004g0198others(3): Show | 6 | HG00735.hp1 HG02735.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.966+619G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130993011 | ||||||
| chr12:130993122
|
C | G | 1 | a0001c0025t0021g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.966+730C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130993122 | ||||||
| chr12:130993153
|
C | T | 1 | a0001c0003t0013g0129 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.966+761C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130993153 | ||||||
| chr12:130993277
|
G | A | 5 | a0001c0002t0001g0010a0001c0003t0004g0012a0001c0003t0004g0198others(2): Show | 5 | HG00735.hp1 HG02735.hp1 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.966+885G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130993277 | ||||||
| chr12:130993280
|
G | A | 1 | a0003c0032t0038g0090 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.966+888G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130993280 | ||||||
| chr12:130993332
|
C | A | 1 | a0001c0045t0002g0091 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.966+940C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130993332 | ||||||
| chr12:130993372
|
T | TTTCA | 39 | a0001c0001t0001g0003a0001c0001t0001g0113a0001c0001t0001g0191others(36): Show | 39 | HG00639.hp1 HG00639.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.966+1014_966+1017d others(6): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr12 | 130993372 | |||||
| chr12:130993372
|
T | TTTCATTC others(1): Show |
56 | a0001c0001t0001g0111a0001c0001t0001g0163a0001c0001t0001g0212others(53): Show | 56 | HG00280.hp1 HG00323.hp2 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.966+1010_966+1017d others(10): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr12 | 130993372 | |||||
| chr12:130993372
|
T | TTTCATTC others(5): Show |
15 | a0001c0001t0002g0175a0001c0001t0009g0140a0001c0002t0003g0041others(12): Show | 15 | HG02735.hp2 HG02809.hp2 HG02896.hp2 others(12): Show |
intron_variant | MODIFIER | c.966+1006_966+1017d others(14): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr12 | 130993372 | |||||
| chr12:130993372
|
TTTCA | T | 14 | a0001c0001t0011g0062a0001c0002t0001g0010a0001c0002t0003g0076others(11): Show | 14 | HG00609.hp1 HG00735.hp1 HG02735.hp1 others(11): Show |
intron_variant | MODIFIER | c.966+1014_966+1017d others(6): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr12 | 130993372 | |||||
| chr12:130993426
|
T | C | 16 | a0001c0001t0027g0118a0001c0003t0004g0121a0001c0003t0004g0122others(13): Show | 16 | HG00738.hp2 HG01175.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.966+1034T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130993426 | ||||||
| chr12:130993559
|
T | C | 2 | a0001c0004t0002g0004a0001c0004t0002g0007 | 2 | HG03239.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.966+1167T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130993559 | ||||||
| chr12:130993653
|
C | T | 1 | a0001c0001t0002g0149 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.966+1261C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130993653 | ||||||
| chr12:130993694
|
A | G | 114 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0163others(111): Show | 114 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(111): Show |
intron_variant | MODIFIER | c.966+1302A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130993694 | ||||||
| chr12:130993764
|
C | G | 1 | a0001c0004t0005g0094 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.966+1372C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130993764 | ||||||
| chr12:130993853
|
T | G | 1 | a0001c0001t0002g0149 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.966+1461T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130993853 | ||||||
| chr12:130993861
|
C | T | 1 | a0001c0004t0005g0094 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.966+1469C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130993861 | ||||||
| chr12:130993911
|
G | A | 12 | a0001c0003t0004g0207a0001c0013t0007g0153a0001c0013t0007g0154others(9): Show | 12 | HG00280.hp1 HG01106.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.966+1519G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130993911 | ||||||
| chr12:130994164
|
C | T | 1 | a0001c0002t0001g0157 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.966+1772C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130994164 | ||||||
| chr12:130994640
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.966+2248C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130994640 | ||||||
| chr12:130994691
|
A | G | 6 | a0001c0002t0001g0010a0001c0003t0004g0012a0001c0003t0004g0198others(3): Show | 6 | HG00735.hp1 HG02735.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.966+2299A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130994691 | ||||||
| chr12:130994826
|
C | T | 5 | a0001c0003t0004g0234a0001c0005t0001g0127a0001c0005t0001g0128others(2): Show | 5 | HG01167.hp1 HG02258.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.966+2434C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130994826 | ||||||
| chr12:130994872
|
C | T | 1 | a0001c0043t0008g0227 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.966+2480C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130994872 | ||||||
| chr12:130994898
|
A | G | 110 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0191others(107): Show | 110 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.966+2506A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130994898 | ||||||
| chr12:130994938
|
T | G | 2 | a0001c0005t0001g0044a0002c0030t0032g0159 | 2 | HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.966+2546T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130994938 | ||||||
| chr12:130994962
|
C | G | 1 | a0001c0003t0012g0088 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.966+2570C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130994962 | ||||||
| chr12:130994964
|
G | A | 1 | a0001c0003t0012g0088 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.966+2572G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130994964 | ||||||
| chr12:130995063
|
G | A | 1 | a0001c0002t0008g0016 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.966+2671G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130995063 | ||||||
| chr12:130995117
|
G | A | 3 | a0005c0011t0002g0110a0005c0011t0008g0047a0005c0021t0021g0048 | 3 | HG00280.hp1 HG01106.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.966+2725G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130995117 | ||||||
| chr12:130995247
|
G | T | 1 | a0001c0045t0002g0091 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.966+2855G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130995247 | ||||||
| chr12:130995295
|
G | A | 18 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(15): Show | 18 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.966+2903G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130995295 | ||||||
| chr12:130995319
|
G | A | 1 | a0001c0043t0008g0227 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.966+2927G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130995319 | ||||||
| chr12:130995343
|
TCCTTATT others(113): Show |
T | 1 | a0001c0001t0002g0130 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.966+2952_966+3071d others(2): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130995343 | ||||||
| chr12:130995561
|
G | A | 16 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0003g0023others(13): Show | 16 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.966+3169G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130995561 | ||||||
| chr12:130995614
|
T | C | 2 | a0002c0029t0031g0222a0010c0026t0013g0238 | 2 | HG02723.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.966+3222T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130995614 | ||||||
| chr12:130995622
|
A | G | 1 | a0003c0032t0038g0090 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.966+3230A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130995622 | ||||||
| chr12:130995718
|
G | A | 7 | a0001c0003t0004g0207a0001c0013t0007g0153a0001c0013t0007g0154others(4): Show | 7 | HG02109.hp1 HG02647.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.966+3326G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130995718 | ||||||
| chr12:130995735
|
CT | C | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0115others(103): Show | 106 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.966+3355delT | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr12 | 130995735 | |||||
| chr12:130995747
|
T | C | 2 | a0001c0003t0004g0198a0001c0003t0034g0014 | 2 | HG02735.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.966+3355T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130995747 | ||||||
| chr12:130995764
|
A | AT | 7 | a0001c0003t0004g0207a0001c0013t0007g0153a0001c0013t0007g0154others(4): Show | 7 | HG02109.hp1 HG02647.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.966+3380dupT | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr12 | 130995764 | |||||
| chr12:130995772
|
T | A | 2 | a0001c0025t0021g0119a0003c0031t0003g0089 | 2 | HG01934.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.966+3380T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130995772 | ||||||
| chr12:130995782
|
T | G | 1 | a0008c0034t0026g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.966+3390T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130995782 | ||||||
| chr12:130995830
|
A | G | 12 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0003t0004g0121others(9): Show | 12 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.966+3438A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130995830 | ||||||
| chr12:130995859
|
TAAACAAG others(7): Show |
T | 2 | a0001c0001t0028g0205a0001c0003t0029g0214 | 2 | HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.966+3469_966+3482d others(16): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr12 | 130995859 | |||||
| chr12:130995929
|
C | T | 12 | a0001c0003t0004g0207a0001c0013t0007g0153a0001c0013t0007g0154others(9): Show | 12 | HG00280.hp1 HG01106.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.966+3537C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130995929 | ||||||
| chr12:130995931
|
G | T | 1 | a0001c0043t0008g0227 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.966+3539G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130995931 | ||||||
| chr12:130995949
|
A | G | 12 | a0001c0003t0004g0207a0001c0013t0007g0153a0001c0013t0007g0154others(9): Show | 12 | HG00280.hp1 HG01106.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.966+3557A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130995949 | ||||||
| chr12:130995950
|
T | G | 12 | a0001c0003t0004g0207a0001c0013t0007g0153a0001c0013t0007g0154others(9): Show | 12 | HG00280.hp1 HG01106.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.966+3558T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130995950 | ||||||
| chr12:130995984
|
C | T | 2 | a0001c0005t0001g0112a0001c0005t0008g0226 | 2 | HG02895.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.966+3592C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130995984 | ||||||
| chr12:130996170
|
TC | T | 6 | a0001c0002t0001g0010a0001c0003t0004g0012a0001c0003t0004g0198others(3): Show | 6 | HG00735.hp1 HG02735.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.966+3779delC | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996170 | ||||||
| chr12:130996188
|
G | A | 6 | a0001c0002t0001g0010a0001c0003t0004g0012a0001c0003t0004g0198others(3): Show | 6 | HG00735.hp1 HG02735.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.966+3796G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996188 | ||||||
| chr12:130996195
|
C | A | 6 | a0001c0002t0001g0010a0001c0003t0004g0012a0001c0003t0004g0198others(3): Show | 6 | HG00735.hp1 HG02735.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.966+3803C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996195 | ||||||
| chr12:130996203
|
T | C | 109 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0191others(106): Show | 109 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(106): Show |
intron_variant | MODIFIER | c.966+3811T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996203 | ||||||
| chr12:130996229
|
T | TC | 107 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0191others(104): Show | 107 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(104): Show |
intron_variant | MODIFIER | c.966+3842dupC | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr12 | 130996229 | |||||
| chr12:130996290
|
G | A | 12 | a0001c0003t0004g0207a0001c0013t0007g0153a0001c0013t0007g0154others(9): Show | 12 | HG00280.hp1 HG01106.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.966+3898G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996290 | ||||||
| chr12:130996299
|
C | T | 2 | a0001c0001t0023g0143a0001c0002t0010g0142 | 2 | NA18612.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.966+3907C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996299 | ||||||
| chr12:130996312
|
GTGGCCGG others(119): Show |
G | 2 | a0001c0005t0001g0112a0001c0005t0008g0226 | 2 | HG02895.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.966+3929_967-3937d others(2): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr12 | 130996312 | |||||
| chr12:130996317
|
C | T | 17 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(14): Show | 17 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.966+3925C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996317 | ||||||
| chr12:130996321
|
C | T | 53 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0212others(50): Show | 53 | HG00323.hp2 HG00738.hp1 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.966+3929C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996321 | ||||||
| chr12:130996321
|
CAGAGGGG others(119): Show |
C | 17 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(14): Show | 17 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.967-3970_967-3845d others(2): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr12 | 130996321 | |||||
| chr12:130996329
|
C | T | 1 | a0003c0041t0004g0178 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.966+3937C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996329 | ||||||
| chr12:130996351
|
G | A | 1 | a0003c0032t0038g0090 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.966+3959G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996351 | ||||||
| chr12:130996378
|
T | C | 25 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0016g0182others(22): Show | 25 | HG00735.hp1 HG00738.hp2 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.966+3986T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996378 | ||||||
| chr12:130996387
|
C | T | 53 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0212others(50): Show | 53 | HG00323.hp2 HG00738.hp1 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.966+3995C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996387 | ||||||
| chr12:130996413
|
C | T | 53 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0212others(50): Show | 53 | HG00323.hp2 HG00738.hp1 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.967-3970C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996413 | ||||||
| chr12:130996435
|
CGGCTGGC others(295): Show |
C | 53 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0212others(50): Show | 53 | HG00323.hp2 HG00738.hp1 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.967-3936_967-3635d others(2): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr12 | 130996435 | |||||
| chr12:130996474
|
G | A | 1 | a0003c0032t0038g0090 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.967-3909G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996474 | ||||||
| chr12:130996504
|
T | C | 3 | a0005c0011t0002g0110a0005c0011t0008g0047a0005c0021t0021g0048 | 3 | HG00280.hp1 HG01106.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.967-3879T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996504 | ||||||
| chr12:130996513
|
C | T | 27 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0016g0182others(24): Show | 27 | HG00735.hp1 HG00738.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.967-3870C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996513 | ||||||
| chr12:130996552
|
C | T | 12 | a0001c0003t0004g0207a0001c0013t0007g0153a0001c0013t0007g0154others(9): Show | 12 | HG00280.hp1 HG01106.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.967-3831C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996552 | ||||||
| chr12:130996556
|
C | T | 17 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(14): Show | 17 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.967-3827C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996556 | ||||||
| chr12:130996561
|
C | T | 1 | a0001c0020t0002g0180 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.967-3822C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996561 | ||||||
| chr12:130996562
|
G | A | 2 | a0001c0017t0008g0029a0001c0017t0008g0030 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.967-3821G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996562 | ||||||
| chr12:130996569
|
C | T | 1 | a0001c0043t0008g0227 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.967-3814C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996569 | ||||||
| chr12:130996583
|
C | T | 4 | a0001c0001t0001g0163a0001c0001t0002g0171a0001c0003t0004g0101others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.967-3800C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996583 | ||||||
| chr12:130996602
|
C | T | 1 | a0001c0002t0001g0202 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.967-3781C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996602 | ||||||
| chr12:130996605
|
C | T | 3 | a0001c0001t0027g0118a0001c0003t0004g0237a0001c0003t0036g0209 | 3 | HG01175.hp2 HG02257.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.967-3778C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996605 | ||||||
| chr12:130996636
|
A | G | 5 | a0001c0003t0004g0121a0001c0003t0004g0122a0001c0003t0012g0025others(2): Show | 5 | HG00738.hp2 HG01496.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.967-3747A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996636 | ||||||
| chr12:130996639
|
C | T | 1 | a0001c0025t0021g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.967-3744C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996639 | ||||||
| chr12:130996651
|
CG | C | 7 | a0001c0001t0016g0182a0001c0003t0018g0232a0001c0010t0007g0160others(4): Show | 7 | HG02258.hp1 HG02486.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.967-3726delG | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr12 | 130996651 | |||||
| chr12:130996672
|
TCCCTCCC others(42): Show |
T | 1 | a0003c0031t0003g0089 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.967-3703_967-3655d others(51): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr12 | 130996672 | |||||
| chr12:130996680
|
A | G | 55 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(52): Show | 55 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.967-3703A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996680 | ||||||
| chr12:130996688
|
C | T | 17 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(14): Show | 17 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.967-3695C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996688 | ||||||
| chr12:130996697
|
G | GGGTAGAG others(120): Show |
1 | a0001c0004t0005g0070 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.967-3684_967-3683i others(129): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr12 | 130996697 | |||||
| chr12:130996721
|
A | T | 1 | a0001c0004t0005g0070 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.967-3662A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996721 | ||||||
| chr12:130996733
|
G | A | 1 | a0003c0031t0003g0089 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.967-3650G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996733 | ||||||
| chr12:130996737
|
T | C | 2 | a0001c0004t0005g0070a0003c0031t0003g0089 | 2 | HG02630.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.967-3646T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996737 | ||||||
| chr12:130996746
|
G | A | 1 | a0001c0004t0005g0070 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.967-3637G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996746 | ||||||
| chr12:130996778
|
T | C | 55 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0212others(52): Show | 55 | HG00323.hp2 HG00738.hp1 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.967-3605T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996778 | ||||||
| chr12:130996792
|
C | A | 2 | a0001c0005t0001g0112a0001c0005t0008g0226 | 2 | HG02895.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.967-3591C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996792 | ||||||
| chr12:130996806
|
C | T | 1 | a0003c0031t0003g0089 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.967-3577C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996806 | ||||||
| chr12:130996815
|
C | T | 2 | a0001c0005t0001g0112a0001c0005t0008g0226 | 2 | HG02895.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.967-3568C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996815 | ||||||
| chr12:130996824
|
GGGCGGGG others(169): Show |
G | 2 | a0001c0005t0001g0112a0001c0005t0008g0226 | 2 | HG02895.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.967-3519_967-3344d others(2): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr12 | 130996824 | |||||
| chr12:130996855
|
C | T | 53 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0212others(50): Show | 53 | HG00323.hp2 HG00738.hp1 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.967-3528C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996855 | ||||||
| chr12:130996860
|
G | A | 12 | a0001c0003t0004g0207a0001c0013t0007g0153a0001c0013t0007g0154others(9): Show | 12 | HG00280.hp1 HG01106.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.967-3523G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996860 | ||||||
| chr12:130996864
|
T | C | 12 | a0001c0003t0004g0207a0001c0013t0007g0153a0001c0013t0007g0154others(9): Show | 12 | HG00280.hp1 HG01106.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.967-3519T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996864 | ||||||
| chr12:130996872
|
C | T | 17 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(14): Show | 17 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.967-3511C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996872 | ||||||
| chr12:130996934
|
G | A | 1 | a0001c0025t0021g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.967-3449G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996934 | ||||||
| chr12:130996954
|
T | C | 107 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0191others(104): Show | 107 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(104): Show |
intron_variant | MODIFIER | c.967-3429T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996954 | ||||||
| chr12:130996982
|
C | T | 3 | a0001c0001t0027g0118a0001c0003t0004g0237a0001c0003t0036g0209 | 3 | HG01175.hp2 HG02257.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.967-3401C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130996982 | ||||||
| chr12:130997003
|
C | T | 78 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0212others(75): Show | 78 | HG00323.hp2 HG00735.hp1 HG00738.hp1 others(75): Show |
intron_variant | MODIFIER | c.967-3380C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130997003 | ||||||
| chr12:130997006
|
G | A | 6 | a0001c0002t0001g0010a0001c0003t0004g0012a0001c0003t0004g0198others(3): Show | 6 | HG00735.hp1 HG02735.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.967-3377G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130997006 | ||||||
| chr12:130997035
|
C | T | 2 | a0001c0005t0001g0112a0001c0005t0008g0226 | 2 | HG02895.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.967-3348C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130997035 | ||||||
| chr12:130997082
|
G | A | 5 | a0001c0003t0004g0121a0001c0003t0004g0122a0005c0011t0002g0110others(2): Show | 5 | HG00280.hp1 HG01106.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.967-3301G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130997082 | ||||||
| chr12:130997086
|
G | T | 1 | a0001c0002t0048g0151 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.967-3297G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130997086 | ||||||
| chr12:130997096
|
A | G | 219 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(216): Show | 219 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.967-3287A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130997096 | ||||||
| chr12:130997102
|
C | T | 80 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0212others(77): Show | 80 | HG00323.hp2 HG00735.hp1 HG00738.hp1 others(77): Show |
intron_variant | MODIFIER | c.967-3281C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130997102 | ||||||
| chr12:130997124
|
GCCGGGCG others(24): Show |
G | 5 | a0001c0002t0001g0010a0001c0003t0004g0012a0001c0003t0004g0198others(2): Show | 5 | HG00735.hp1 HG02735.hp1 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.967-3254_967-3224d others(33): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr12 | 130997124 | |||||
| chr12:130997126
|
C | T | 12 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0003t0004g0121others(9): Show | 12 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.967-3257C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130997126 | ||||||
| chr12:130997178
|
CG | C | 7 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0003t0004g0121others(4): Show | 7 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.967-3199delG | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr12 | 130997178 | |||||
| chr12:130997188
|
A | AC | 53 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0107others(50): Show | 53 | HG00280.hp1 HG00621.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.967-3184dupC | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr12 | 130997188 | |||||
| chr12:130997188
|
A | ACC | 47 | a0001c0001t0001g0111a0001c0001t0001g0212a0001c0001t0002g0161others(44): Show | 47 | HG00323.hp2 HG00735.hp1 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.967-3185_967-3184d others(4): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr12 | 130997188 | |||||
| chr12:130997188
|
A | ACCC | 25 | a0001c0001t0001g0113a0001c0001t0002g0172a0001c0001t0016g0147others(22): Show | 25 | HG01109.hp2 HG01175.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.967-3186_967-3184d others(5): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr12 | 130997188 | |||||
| chr12:130997268
|
G | A | 3 | a0005c0011t0002g0110a0005c0011t0008g0047a0005c0021t0021g0048 | 3 | HG00280.hp1 HG01106.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.967-3115G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130997268 | ||||||
| chr12:130997278
|
G | A | 1 | a0001c0007t0004g0018 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.967-3105G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130997278 | ||||||
| chr12:130997324
|
G | A | 7 | a0001c0001t0001g0208a0001c0001t0002g0184a0001c0001t0002g0217others(4): Show | 7 | HG00140.hp1 HG01099.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.967-3059G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130997324 | ||||||
| chr12:130997372
|
TGGCTGCC others(33): Show |
T | 80 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0212others(77): Show | 80 | HG00323.hp2 HG00735.hp1 HG00738.hp1 others(77): Show |
intron_variant | MODIFIER | c.967-2968_967-2929d others(42): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr12 | 130997372 | |||||
| chr12:130997419
|
C | G | 1 | a0001c0003t0033g0181 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.967-2964C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130997419 | ||||||
| chr12:130997448
|
G | A | 4 | a0001c0002t0001g0195a0001c0002t0003g0064a0001c0004t0005g0094others(1): Show | 4 | HG02071.hp2 HG03831.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.967-2935G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130997448 | ||||||
| chr12:130997452
|
CG | C | 3 | a0005c0011t0002g0110a0005c0011t0008g0047a0005c0021t0021g0048 | 3 | HG00280.hp1 HG01106.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.967-2929delG | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr12 | 130997452 | |||||
| chr12:130997460
|
A | G | 92 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0212others(89): Show | 92 | HG00280.hp1 HG00323.hp2 HG00735.hp1 others(89): Show |
intron_variant | MODIFIER | c.967-2923A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130997460 | ||||||
| chr12:130997479
|
T | C | 1 | a0001c0003t0006g0216 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.967-2904T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130997479 | ||||||
| chr12:130997506
|
C | T | 17 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(14): Show | 17 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.967-2877C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130997506 | ||||||
| chr12:130997569
|
C | A | 2 | a0001c0010t0007g0213a0003c0012t0017g0017 | 2 | HG01243.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.967-2814C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130997569 | ||||||
| chr12:130997608
|
C | T | 80 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0212others(77): Show | 80 | HG00323.hp2 HG00735.hp1 HG00738.hp1 others(77): Show |
intron_variant | MODIFIER | c.967-2775C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130997608 | ||||||
| chr12:130997609
|
G | A | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0115others(106): Show | 109 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.967-2774G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130997609 | ||||||
| chr12:130997692
|
C | T | 55 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0212others(52): Show | 55 | HG00323.hp2 HG00738.hp1 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.967-2691C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130997692 | ||||||
| chr12:130997740
|
G | T | 7 | a0001c0003t0004g0207a0001c0013t0007g0153a0001c0013t0007g0154others(4): Show | 7 | HG02109.hp1 HG02647.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.967-2643G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130997740 | ||||||
| chr12:130997796
|
C | T | 1 | a0001c0025t0021g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.967-2587C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130997796 | ||||||
| chr12:130997804
|
C | T | 1 | a0001c0001t0003g0026 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.967-2579C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130997804 | ||||||
| chr12:130997853
|
G | A | 1 | a0003c0032t0038g0090 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.967-2530G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130997853 | ||||||
| chr12:130998039
|
C | CA | 16 | a0001c0001t0001g0156a0001c0001t0002g0161a0001c0001t0003g0023others(13): Show | 16 | HG00280.hp2 HG00735.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.967-2335dupA | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr12 | 130998039 | |||||
| chr12:130998050
|
G | A | 1 | a0001c0007t0004g0018 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.967-2333G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130998050 | ||||||
| chr12:130998110
|
C | T | 1 | a0001c0025t0021g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.967-2273C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130998110 | ||||||
| chr12:130998139
|
G | A | 16 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0003g0023others(13): Show | 16 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.967-2244G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130998139 | ||||||
| chr12:130998185
|
C | T | 1 | a0001c0003t0041g0080 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.967-2198C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130998185 | ||||||
| chr12:130998278
|
C | T | 1 | a0001c0001t0009g0144 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.967-2105C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130998278 | ||||||
| chr12:130998299
|
C | A | 1 | a0001c0004t0005g0094 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.967-2084C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130998299 | ||||||
| chr12:130998395
|
G | A | 1 | a0001c0001t0002g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.967-1988G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130998395 | ||||||
| chr12:130998632
|
T | A | 1 | a0008c0034t0026g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.967-1751T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130998632 | ||||||
| chr12:130998723
|
C | T | 1 | a0006c0037t0042g0046 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.967-1660C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130998723 | ||||||
| chr12:130998800
|
A | G | 1 | a0001c0001t0003g0026 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.967-1583A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130998800 | ||||||
| chr12:130998822
|
G | A | 1 | a0001c0001t0003g0023 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.967-1561G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130998822 | ||||||
| chr12:130998923
|
A | C | 4 | a0001c0003t0013g0224a0001c0003t0013g0225a0001c0005t0003g0056others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.967-1460A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130998923 | ||||||
| chr12:130998965
|
A | G | 1 | a0001c0001t0002g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.967-1418A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130998965 | ||||||
| chr12:130999040
|
T | G | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0115others(106): Show | 109 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.967-1343T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130999040 | ||||||
| chr12:130999050
|
T | A | 1 | a0003c0033t0030g0231 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.967-1333T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130999050 | ||||||
| chr12:130999105
|
T | C | 16 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0003g0023others(13): Show | 16 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.967-1278T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130999105 | ||||||
| chr12:130999170
|
A | G | 4 | a0001c0003t0013g0224a0001c0003t0013g0225a0001c0005t0003g0056others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.967-1213A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130999170 | ||||||
| chr12:130999182
|
T | C | 221 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(218): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.967-1201T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130999182 | ||||||
| chr12:130999248
|
A | G | 3 | a0005c0011t0002g0110a0005c0011t0008g0047a0005c0021t0021g0048 | 3 | HG00280.hp1 HG01106.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.967-1135A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130999248 | ||||||
| chr12:130999381
|
G | A | 221 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(218): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.967-1002G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130999381 | ||||||
| chr12:130999435
|
G | A | 6 | a0001c0001t0002g0107a0001c0001t0002g0203a0001c0001t0002g0204others(3): Show | 6 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.967-948G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130999435 | ||||||
| chr12:130999445
|
G | A | 109 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0191others(106): Show | 109 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(106): Show |
intron_variant | MODIFIER | c.967-938G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130999445 | ||||||
| chr12:130999564
|
A | G | 1 | a0001c0007t0004g0018 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.967-819A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130999564 | ||||||
| chr12:130999729
|
C | T | 3 | a0005c0011t0002g0110a0005c0011t0008g0047a0005c0021t0021g0048 | 3 | HG00280.hp1 HG01106.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.967-654C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130999729 | ||||||
| chr12:130999730
|
G | A | 105 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0115others(102): Show | 105 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.967-653G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130999730 | ||||||
| chr12:130999821
|
T | C | 109 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0191others(106): Show | 109 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(106): Show |
intron_variant | MODIFIER | c.967-562T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130999821 | ||||||
| chr12:130999888
|
A | G | 81 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0212others(78): Show | 81 | HG00323.hp2 HG00735.hp1 HG00738.hp1 others(78): Show |
intron_variant | MODIFIER | c.967-495A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130999888 | ||||||
| chr12:130999955
|
A | G | 1 | a0003c0033t0030g0231 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.967-428A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 130999955 | ||||||
| chr12:131000095
|
C | T | 1 | a0001c0020t0002g0180 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.967-288C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 131000095 | ||||||
| chr12:131000100
|
G | A | 1 | a0001c0025t0021g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.967-283G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 131000100 | ||||||
| chr12:131000115
|
C | G | 3 | a0005c0011t0002g0110a0005c0011t0008g0047a0005c0021t0021g0048 | 3 | HG00280.hp1 HG01106.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.967-268C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 8/24 | chr12 | 131000115 | ||||||
| chr12:131000469
|
T | C | 84 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0212others(81): Show | 84 | HG00280.hp1 HG00323.hp2 HG00735.hp1 others(81): Show |
intron_variant | MODIFIER | c.1026+27T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 9/24 | chr12 | 131000469 | ||||||
| chr12:131000480
|
A | G | 109 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0191others(106): Show | 109 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(106): Show |
intron_variant | MODIFIER | c.1026+38A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 9/24 | chr12 | 131000480 | ||||||
| chr12:131000656
|
G | A | 1 | a0011c0038t0002g0162 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1026+214G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 9/24 | chr12 | 131000656 | ||||||
| chr12:131000746
|
A | C | 7 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0003t0004g0121others(4): Show | 7 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.1026+304A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 9/24 | chr12 | 131000746 | ||||||
| chr12:131000747
|
C | CA | 97 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0191others(94): Show | 97 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(94): Show |
intron_variant | MODIFIER | c.1026+323dupA | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr12 | 131000747 | |||||
| chr12:131000747
|
C | CAA | 10 | a0001c0001t0023g0143a0001c0002t0010g0142a0001c0003t0004g0207others(7): Show | 10 | HG01261.hp1 HG01934.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1026+322_1026+323d others(4): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr12 | 131000747 | |||||
| chr12:131000871
|
GAAT | G | 4 | a0001c0003t0018g0232a0001c0042t0007g0176a0003c0041t0004g0178others(1): Show | 4 | HG02258.hp1 HG02717.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026+430_1026+432d others(5): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 9/24 | chr12 | 131000871 | ||||||
| chr12:131001061
|
C | T | 9 | a0001c0003t0004g0207a0001c0013t0007g0153a0001c0013t0007g0154others(6): Show | 9 | HG01934.hp2 HG02109.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1026+619C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 9/24 | chr12 | 131001061 | ||||||
| chr12:131001453
|
T | C | 9 | a0001c0003t0004g0207a0001c0013t0007g0153a0001c0013t0007g0154others(6): Show | 9 | HG01934.hp2 HG02109.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1026+1011T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 9/24 | chr12 | 131001453 | ||||||
| chr12:131001575
|
G | A | 7 | a0001c0001t0016g0182a0001c0003t0018g0232a0001c0010t0007g0160others(4): Show | 7 | HG02258.hp1 HG02486.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1026+1133G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 9/24 | chr12 | 131001575 | ||||||
| chr12:131001614
|
C | T | 2 | a0001c0002t0002g0106a0001c0014t0004g0105 | 2 | HG00323.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1026+1172C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 9/24 | chr12 | 131001614 | ||||||
| chr12:131001700
|
T | C | 93 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0212others(90): Show | 93 | HG00280.hp1 HG00323.hp2 HG00735.hp1 others(90): Show |
intron_variant | MODIFIER | c.1026+1258T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 9/24 | chr12 | 131001700 | ||||||
| chr12:131001702
|
G | C | 1 | a0001c0020t0002g0180 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1026+1260G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 9/24 | chr12 | 131001702 | ||||||
| chr12:131001741
|
T | C | 1 | a0001c0005t0001g0239 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1026+1299T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 9/24 | chr12 | 131001741 | ||||||
| chr12:131001747
|
A | G | 1 | a0001c0002t0010g0134 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1026+1305A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 9/24 | chr12 | 131001747 | ||||||
| chr12:131001759
|
A | G | 1 | a0001c0010t0007g0160 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1026+1317A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 9/24 | chr12 | 131001759 | ||||||
| chr12:131001823
|
C | A | 1 | a0003c0031t0003g0089 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1027-1362C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 9/24 | chr12 | 131001823 | ||||||
| chr12:131001888
|
G | A | 2 | a0001c0005t0001g0044a0002c0030t0032g0159 | 2 | HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1027-1297G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 9/24 | chr12 | 131001888 | ||||||
| chr12:131001944
|
T | C | 7 | a0001c0003t0004g0207a0001c0013t0007g0153a0001c0013t0007g0154others(4): Show | 7 | HG02109.hp1 HG02647.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1027-1241T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 9/24 | chr12 | 131001944 | ||||||
| chr12:131002082
|
C | T | 1 | a0001c0001t0016g0182 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1027-1103C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 9/24 | chr12 | 131002082 | ||||||
| chr12:131002122
|
G | C | 16 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0116others(13): Show | 16 | HG00639.hp1 HG01074.hp1 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.1027-1063G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 9/24 | chr12 | 131002122 | ||||||
| chr12:131002185
|
T | TA | 110 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0191others(107): Show | 110 | HG00280.hp1 HG00323.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.1027-998dupA | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr12 | 131002185 | |||||
| chr12:131002336
|
C | T | 1 | a0001c0001t0002g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1027-849C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 9/24 | chr12 | 131002336 | ||||||
| chr12:131002378
|
T | C | 65 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0212others(62): Show | 65 | HG00323.hp2 HG00609.hp2 HG00738.hp1 others(62): Show |
intron_variant | MODIFIER | c.1027-807T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 9/24 | chr12 | 131002378 | ||||||
| chr12:131002440
|
T | C | 65 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0212others(62): Show | 65 | HG00323.hp2 HG00609.hp2 HG00738.hp1 others(62): Show |
intron_variant | MODIFIER | c.1027-745T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 9/24 | chr12 | 131002440 | ||||||
| chr12:131002444
|
A | G | 65 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0212others(62): Show | 65 | HG00323.hp2 HG00609.hp2 HG00738.hp1 others(62): Show |
intron_variant | MODIFIER | c.1027-741A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 9/24 | chr12 | 131002444 | ||||||
| chr12:131002636
|
C | G | 1 | a0001c0003t0012g0088 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1027-549C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 9/24 | chr12 | 131002636 | ||||||
| chr12:131002822
|
C | T | 1 | a0001c0004t0002g0131 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1027-363C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 9/24 | chr12 | 131002822 | ||||||
| chr12:131002853
|
G | T | 3 | a0005c0011t0002g0110a0005c0011t0008g0047a0005c0021t0021g0048 | 3 | HG00280.hp1 HG01106.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.1027-332G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 9/24 | chr12 | 131002853 | ||||||
| chr12:131003329
|
A | G | 5 | a0001c0003t0004g0121a0001c0003t0004g0122a0001c0003t0012g0025others(2): Show | 5 | HG00738.hp2 HG01496.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1144+27A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 10/24 | chr12 | 131003329 | ||||||
| chr12:131003428
|
A | G | 110 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0191others(107): Show | 110 | HG00280.hp1 HG00323.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.1144+126A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 10/24 | chr12 | 131003428 | ||||||
| chr12:131003496
|
T | C | 94 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0212others(91): Show | 94 | HG00280.hp1 HG00323.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.1144+194T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 10/24 | chr12 | 131003496 | ||||||
| chr12:131003523
|
T | C | 1 | a0001c0025t0021g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1144+221T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 10/24 | chr12 | 131003523 | ||||||
| chr12:131003625
|
G | C | 1 | a0001c0025t0021g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1144+323G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 10/24 | chr12 | 131003625 | ||||||
| chr12:131003634
|
C | A | 110 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0191others(107): Show | 110 | HG00280.hp1 HG00323.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.1144+332C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 10/24 | chr12 | 131003634 | ||||||
| chr12:131003650
|
G | A | 218 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(215): Show | 218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.1144+348G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 10/24 | chr12 | 131003650 | ||||||
| chr12:131003663
|
G | A | 110 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0191others(107): Show | 110 | HG00280.hp1 HG00323.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.1144+361G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 10/24 | chr12 | 131003663 | ||||||
| chr12:131003676
|
T | A | 1 | a0001c0004t0005g0070 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1144+374T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 10/24 | chr12 | 131003676 | ||||||
| chr12:131003680
|
C | A | 3 | a0001c0001t0011g0220a0001c0002t0003g0073a0001c0004t0005g0072 | 3 | HG02083.hp1 NA18957.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1144+378C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 10/24 | chr12 | 131003680 | ||||||
| chr12:131003768
|
C | T | 3 | a0005c0011t0002g0110a0005c0011t0008g0047a0005c0021t0021g0048 | 3 | HG00280.hp1 HG01106.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.1145-418C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 10/24 | chr12 | 131003768 | ||||||
| chr12:131003769
|
G | C | 16 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0003g0023others(13): Show | 16 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.1145-417G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 10/24 | chr12 | 131003769 | ||||||
| chr12:131003826
|
G | A | 26 | a0001c0001t0002g0116a0001c0001t0002g0228a0001c0001t0002g0235others(23): Show | 26 | HG00735.hp1 HG00738.hp2 HG01496.hp1 others(23): Show |
intron_variant | MODIFIER | c.1145-360G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 10/24 | chr12 | 131003826 | ||||||
| chr12:131003845
|
C | T | 1 | a0001c0004t0002g0193 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1145-341C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 10/24 | chr12 | 131003845 | ||||||
| chr12:131003957
|
C | T | 1 | a0001c0025t0021g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1145-229C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 10/24 | chr12 | 131003957 | ||||||
| chr12:131004021
|
C | T | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0115others(150): Show | 153 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.1145-165C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 10/24 | chr12 | 131004021 | ||||||
| chr12:131004023
|
C | CT | 55 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0212others(52): Show | 55 | HG00323.hp2 HG00609.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.1145-146dupT | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr12 | 131004023 | |||||
| chr12:131004023
|
C | CTT | 9 | a0001c0001t0002g0161a0001c0003t0004g0207a0001c0013t0007g0153others(6): Show | 9 | HG02109.hp1 HG02630.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1145-147_1145-146d others(4): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr12 | 131004023 | |||||
| chr12:131004023
|
C | T | 2 | a0001c0003t0012g0088a0003c0032t0038g0090 | 2 | HG02559.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1145-163C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 10/24 | chr12 | 131004023 | ||||||
| chr12:131004023
|
CT | C | 8 | a0001c0002t0001g0195a0001c0002t0001g0199a0001c0003t0004g0122others(5): Show | 8 | HG01516.hp1 HG01934.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1145-146delT | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr12 | 131004023 | |||||
| chr12:131004056
|
A | C | 2 | a0001c0010t0007g0213a0003c0012t0017g0017 | 2 | HG01243.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1145-130A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 10/24 | chr12 | 131004056 | ||||||
| chr12:131004178
|
C | T | 1 | a0010c0026t0013g0238 | 1 | HG02723.hp2 | splice_region_variant&intron_variant | LOW | c.1145-8C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 10/24 | chr12 | 131004178 | ||||||
| chr12:131004313
|
T | C | 63 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0212others(60): Show | 63 | HG00323.hp2 HG00609.hp2 HG00738.hp1 others(60): Show |
intron_variant | MODIFIER | c.1255+17T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 11/24 | chr12 | 131004313 | ||||||
| chr12:131004383
|
C | T | 3 | a0005c0011t0002g0110a0005c0011t0008g0047a0005c0021t0021g0048 | 3 | HG00280.hp1 HG01106.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.1255+87C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 11/24 | chr12 | 131004383 | ||||||
| chr12:131004392
|
G | GCTGCGGT others(15): Show |
59 | a0001c0001t0001g0113a0001c0001t0001g0191a0001c0001t0001g0197others(56): Show | 59 | HG00323.hp2 HG00609.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.1255+114_1255+135d others(24): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr12 | 131004392 | |||||
| chr12:131004392
|
G | GCTGCGGT others(15): Show |
1 | a0001c0001t0001g0111 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1255+115_1255+116i others(24): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr12 | 131004392 | |||||
| chr12:131004417
|
G | A | 1 | a0001c0007t0004g0018 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1255+121G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 11/24 | chr12 | 131004417 | ||||||
| chr12:131004419
|
G | A | 1 | a0001c0002t0025g0141 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1255+123G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 11/24 | chr12 | 131004419 | ||||||
| chr12:131004587
|
G | GAGC | 63 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0212others(60): Show | 63 | HG00323.hp2 HG00609.hp2 HG00738.hp1 others(60): Show |
intron_variant | MODIFIER | c.1255+293_1255+295d others(5): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr12 | 131004587 | |||||
| chr12:131004634
|
A | T | 7 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0003t0004g0121others(4): Show | 7 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.1255+338A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 11/24 | chr12 | 131004634 | ||||||
| chr12:131004665
|
A | G | 63 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0212others(60): Show | 63 | HG00323.hp2 HG00609.hp2 HG00738.hp1 others(60): Show |
intron_variant | MODIFIER | c.1255+369A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 11/24 | chr12 | 131004665 | ||||||
| chr12:131004782
|
C | G | 92 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0212others(89): Show | 92 | HG00280.hp1 HG00323.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.1255+486C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 11/24 | chr12 | 131004782 | ||||||
| chr12:131004858
|
A | C | 1 | a0001c0009t0014g0078 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1255+562A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 11/24 | chr12 | 131004858 | ||||||
| chr12:131004914
|
A | G | 2 | a0003c0012t0017g0158a0003c0031t0003g0089 | 2 | HG02630.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1255+618A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 11/24 | chr12 | 131004914 | ||||||
| chr12:131005025
|
C | T | 1 | a0001c0003t0001g0152 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1255+729C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 11/24 | chr12 | 131005025 | ||||||
| chr12:131005087
|
T | C | 65 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0212others(62): Show | 65 | HG00323.hp2 HG00609.hp2 HG00738.hp1 others(62): Show |
intron_variant | MODIFIER | c.1255+791T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 11/24 | chr12 | 131005087 | ||||||
| chr12:131005152
|
C | T | 3 | a0001c0001t0027g0118a0001c0003t0004g0237a0001c0003t0036g0209 | 3 | HG01175.hp2 HG02257.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1256-820C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 11/24 | chr12 | 131005152 | ||||||
| chr12:131005179
|
T | C | 16 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0003g0023others(13): Show | 16 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.1256-793T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 11/24 | chr12 | 131005179 | ||||||
| chr12:131005223
|
A | G | 1 | a0001c0025t0021g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1256-749A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 11/24 | chr12 | 131005223 | ||||||
| chr12:131005226
|
T | C | 1 | a0001c0003t0033g0181 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1256-746T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 11/24 | chr12 | 131005226 | ||||||
| chr12:131005229
|
C | T | 1 | a0003c0031t0003g0089 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1256-743C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 11/24 | chr12 | 131005229 | ||||||
| chr12:131005452
|
A | G | 218 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(215): Show | 218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.1256-520A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 11/24 | chr12 | 131005452 | ||||||
| chr12:131005478
|
A | G | 1 | a0001c0001t0005g0028 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1256-494A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 11/24 | chr12 | 131005478 | ||||||
| chr12:131005557
|
G | A | 2 | a0001c0005t0001g0112a0001c0005t0008g0226 | 2 | HG02895.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1256-415G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 11/24 | chr12 | 131005557 | ||||||
| chr12:131005600
|
T | C | 64 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0212others(61): Show | 64 | HG00323.hp2 HG00609.hp2 HG00738.hp1 others(61): Show |
intron_variant | MODIFIER | c.1256-372T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 11/24 | chr12 | 131005600 | ||||||
| chr12:131005650
|
G | GCCCTGGG others(90): Show |
74 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0212others(71): Show | 74 | HG00280.hp1 HG00323.hp2 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.1256-305_1256-304i others(99): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr12 | 131005650 | |||||
| chr12:131005650
|
G | GCCCTGGG others(138): Show |
7 | a0001c0001t0016g0182a0001c0003t0018g0232a0001c0010t0007g0160others(4): Show | 7 | HG02258.hp1 HG02486.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1256-305_1256-304i others(147): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr12 | 131005650 | |||||
| chr12:131005650
|
G | GCCCTGGG others(90): Show |
12 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0003t0004g0121others(9): Show | 12 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1256-305_1256-304i others(99): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr12 | 131005650 | |||||
| chr12:131005706
|
G | A | 1 | a0001c0025t0021g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1256-266G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 11/24 | chr12 | 131005706 | ||||||
| chr12:131005759
|
CAG | C | 16 | a0001c0001t0002g0116a0001c0001t0016g0182a0001c0002t0001g0010others(13): Show | 16 | HG00280.hp1 HG00735.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.1256-212_1256-211d others(4): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 11/24 | chr12 | 131005759 | ||||||
| chr12:131005787
|
C | T | 1 | a0001c0043t0008g0227 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1256-185C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 11/24 | chr12 | 131005787 | ||||||
| chr12:131005868
|
A | G | 70 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0212others(67): Show | 70 | HG00323.hp2 HG00609.hp2 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.1256-104A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 11/24 | chr12 | 131005868 | ||||||
| chr12:131005938
|
G | A | 16 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0003g0023others(13): Show | 16 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.1256-34G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 11/24 | chr12 | 131005938 | ||||||
| chr12:131006087
|
C | T | 3 | a0005c0011t0002g0110a0005c0011t0008g0047a0005c0021t0021g0048 | 3 | HG00280.hp1 HG01106.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.1331+40C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131006087 | ||||||
| chr12:131006088
|
G | C | 1 | a0003c0012t0017g0158 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1331+41G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131006088 | ||||||
| chr12:131006167
|
C | T | 23 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0016g0182others(20): Show | 23 | HG00280.hp1 HG00738.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.1331+120C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131006167 | ||||||
| chr12:131006175
|
T | C | 162 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(159): Show | 162 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.1331+128T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131006175 | ||||||
| chr12:131006176
|
G | A | 1 | a0001c0009t0004g0103 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1331+129G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131006176 | ||||||
| chr12:131006497
|
A | T | 1 | a0001c0003t0018g0117 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1331+450A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131006497 | ||||||
| chr12:131006527
|
G | A | 5 | a0001c0001t0001g0163a0001c0001t0002g0171a0001c0003t0004g0101others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.1331+480G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131006527 | ||||||
| chr12:131006551
|
C | T | 1 | a0001c0019t0004g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1331+504C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131006551 | ||||||
| chr12:131006611
|
C | T | 1 | a0008c0034t0026g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1331+564C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131006611 | ||||||
| chr12:131006687
|
C | G | 214 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(211): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.1331+640C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131006687 | ||||||
| chr12:131006725
|
A | G | 194 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(191): Show | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.1331+678A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131006725 | ||||||
| chr12:131006778
|
C | T | 1 | a0001c0001t0009g0136 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1331+731C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131006778 | ||||||
| chr12:131006913
|
A | C | 1 | a0005c0011t0002g0110 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1331+866A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131006913 | ||||||
| chr12:131006982
|
G | T | 225 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(222): Show | 225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1331+935G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131006982 | ||||||
| chr12:131007044
|
A | G | 161 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0115others(158): Show | 161 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.1331+997A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131007044 | ||||||
| chr12:131007070
|
C | T | 1 | a0002c0028t0001g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1331+1023C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131007070 | ||||||
| chr12:131007138
|
G | T | 189 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(186): Show | 189 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.1331+1091G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131007138 | ||||||
| chr12:131007295
|
A | G | 76 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0001g0212others(73): Show | 76 | HG00609.hp2 HG00639.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.1331+1248A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131007295 | ||||||
| chr12:131007326
|
G | C | 1 | a0003c0031t0003g0089 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1331+1279G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131007326 | ||||||
| chr12:131007332
|
T | C | 77 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0156others(74): Show | 77 | HG00323.hp1 HG00609.hp2 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.1331+1285T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131007332 | ||||||
| chr12:131007346
|
C | T | 1 | a0001c0001t0005g0028 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1331+1299C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131007346 | ||||||
| chr12:131007462
|
C | T | 133 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0208others(130): Show | 133 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1331+1415C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131007462 | ||||||
| chr12:131007466
|
G | A | 1 | a0003c0012t0017g0017 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1331+1419G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131007466 | ||||||
| chr12:131007491
|
C | T | 1 | a0001c0007t0006g0021 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1331+1444C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131007491 | ||||||
| chr12:131007520
|
C | T | 3 | a0001c0001t0002g0161a0001c0001t0009g0144a0001c0003t0045g0042 | 3 | NA18970.hp2 NA19082.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1331+1473C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131007520 | ||||||
| chr12:131007572
|
G | C | 12 | a0001c0001t0002g0116a0001c0002t0001g0010a0001c0003t0004g0012others(9): Show | 12 | HG00735.hp1 HG02451.hp2 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.1331+1525G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131007572 | ||||||
| chr12:131007689
|
A | G | 20 | a0001c0003t0004g0207a0001c0003t0013g0224a0001c0003t0013g0225others(17): Show | 20 | HG01934.hp1 HG01934.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.1331+1642A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131007689 | ||||||
| chr12:131007713
|
C | G | 4 | a0001c0002t0002g0006a0001c0002t0002g0009a0001c0002t0005g0040others(1): Show | 4 | HG01346.hp1 HG01433.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.1331+1666C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131007713 | ||||||
| chr12:131007727
|
T | A | 226 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(223): Show | 226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1331+1680T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131007727 | ||||||
| chr12:131007743
|
C | T | 50 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0156others(47): Show | 50 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.1331+1696C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131007743 | ||||||
| chr12:131007891
|
AATC | A | 123 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0208others(120): Show | 123 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.1331+1847_1331+184 others(7): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr12 | 131007891 | |||||
| chr12:131007935
|
A | G | 3 | a0001c0001t0028g0205a0001c0003t0029g0214a0003c0032t0038g0090 | 3 | HG02280.hp2 HG02559.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1331+1888A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131007935 | ||||||
| chr12:131008216
|
T | C | 62 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0130others(59): Show | 62 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.1331+2169T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131008216 | ||||||
| chr12:131008217
|
G | A | 1 | a0005c0011t0002g0110 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1331+2170G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131008217 | ||||||
| chr12:131008350
|
G | A | 1 | a0001c0022t0016g0109 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1331+2303G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131008350 | ||||||
| chr12:131008428
|
G | A | 6 | a0001c0002t0001g0010a0001c0003t0004g0012a0001c0003t0006g0092others(3): Show | 6 | HG00735.hp1 HG02572.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1331+2381G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131008428 | ||||||
| chr12:131008431
|
G | C | 1 | a0001c0001t0023g0143 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1331+2384G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131008431 | ||||||
| chr12:131008521
|
G | A | 23 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0003t0004g0121others(20): Show | 23 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1331+2474G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131008521 | ||||||
| chr12:131008585
|
G | T | 2 | a0001c0001t0028g0205a0001c0003t0029g0214 | 2 | HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1331+2538G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131008585 | ||||||
| chr12:131008633
|
C | T | 1 | a0003c0032t0038g0090 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1331+2586C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131008633 | ||||||
| chr12:131008681
|
G | A | 102 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0208others(99): Show | 102 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.1331+2634G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131008681 | ||||||
| chr12:131008684
|
C | G | 2 | a0001c0001t0028g0205a0001c0003t0029g0214 | 2 | HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1331+2637C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131008684 | ||||||
| chr12:131008748
|
A | G | 27 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0003t0004g0121others(24): Show | 27 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.1331+2701A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131008748 | ||||||
| chr12:131008793
|
G | C | 26 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0003t0004g0121others(23): Show | 26 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.1331+2746G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131008793 | ||||||
| chr12:131008796
|
C | T | 3 | a0001c0003t0013g0224a0001c0003t0013g0225a0001c0005t0003g0056 | 3 | HG02896.hp1 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1331+2749C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131008796 | ||||||
| chr12:131009010
|
T | A | 1 | a0003c0040t0022g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1331+2963T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131009010 | ||||||
| chr12:131009045
|
C | T | 1 | a0008c0034t0026g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1331+2998C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131009045 | ||||||
| chr12:131009118
|
G | A | 3 | a0001c0003t0013g0224a0001c0003t0013g0225a0001c0005t0003g0056 | 3 | HG02896.hp1 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1331+3071G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131009118 | ||||||
| chr12:131009164
|
C | A | 23 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0130others(20): Show | 23 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.1331+3117C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131009164 | ||||||
| chr12:131009296
|
T | G | 3 | a0001c0001t0009g0136a0001c0002t0001g0199a0001c0002t0001g0210 | 3 | HG03831.hp2 NA19066.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1331+3249T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131009296 | ||||||
| chr12:131009315
|
C | T | 5 | a0001c0003t0012g0063a0001c0003t0013g0224a0001c0003t0013g0225others(2): Show | 5 | HG02135.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1331+3268C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131009315 | ||||||
| chr12:131009372
|
G | A | 1 | a0003c0032t0038g0090 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1331+3325G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131009372 | ||||||
| chr12:131009484
|
A | G | 152 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0191others(149): Show | 152 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.1331+3437A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131009484 | ||||||
| chr12:131009492
|
C | T | 2 | a0001c0001t0002g0228a0001c0001t0002g0235 | 2 | HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1331+3445C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131009492 | ||||||
| chr12:131009529
|
T | C | 1 | a0001c0036t0003g0075 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1331+3482T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131009529 | ||||||
| chr12:131009676
|
T | C | 3 | a0001c0003t0013g0224a0001c0003t0013g0225a0001c0005t0003g0056 | 3 | HG02896.hp1 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1331+3629T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131009676 | ||||||
| chr12:131009683
|
TTG | T | 10 | a0001c0001t0016g0182a0001c0001t0027g0118a0001c0001t0028g0205others(7): Show | 10 | HG02257.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1331+3641_1331+364 others(6): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr12 | 131009683 | |||||
| chr12:131009757
|
G | A | 22 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0003t0004g0121others(19): Show | 22 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1331+3710G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131009757 | ||||||
| chr12:131009758
|
C | T | 4 | a0001c0005t0001g0112a0001c0005t0008g0226a0001c0020t0002g0180others(1): Show | 4 | HG02895.hp1 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1331+3711C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131009758 | ||||||
| chr12:131009759
|
G | A | 2 | a0002c0029t0031g0222a0010c0026t0013g0238 | 2 | HG02723.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1331+3712G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131009759 | ||||||
| chr12:131009896
|
G | A | 2 | a0001c0001t0028g0205a0001c0003t0029g0214 | 2 | HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1331+3849G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131009896 | ||||||
| chr12:131010186
|
T | C | 22 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0003t0004g0121others(19): Show | 22 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1332-4013T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131010186 | ||||||
| chr12:131010197
|
A | G | 3 | a0001c0003t0013g0129a0001c0022t0016g0109a0001c0025t0021g0119 | 3 | HG01934.hp2 HG02630.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1332-4002A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131010197 | ||||||
| chr12:131010447
|
G | A | 2 | a0001c0003t0004g0121a0001c0003t0004g0122 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1332-3752G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131010447 | ||||||
| chr12:131010546
|
A | G | 20 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0003t0004g0121others(17): Show | 20 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1332-3653A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131010546 | ||||||
| chr12:131010640
|
T | C | 1 | a0003c0031t0003g0089 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1332-3559T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131010640 | ||||||
| chr12:131010682
|
G | C | 1 | a0001c0008t0003g0067 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1332-3517G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131010682 | ||||||
| chr12:131010726
|
C | A | 28 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0003t0004g0121others(25): Show | 28 | HG00738.hp2 HG01106.hp1 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.1332-3473C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131010726 | ||||||
| chr12:131010770
|
A | G | 147 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0191others(144): Show | 147 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1332-3429A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131010770 | ||||||
| chr12:131010771
|
G | T | 1 | a0003c0040t0022g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1332-3428G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131010771 | ||||||
| chr12:131011037
|
G | A | 24 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0002t0001g0223others(21): Show | 24 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.1332-3162G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131011037 | ||||||
| chr12:131011089
|
C | G | 3 | a0001c0003t0013g0129a0001c0022t0016g0109a0001c0025t0021g0119 | 3 | HG01934.hp2 HG02630.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1332-3110C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131011089 | ||||||
| chr12:131011103
|
G | T | 3 | a0001c0001t0011g0220a0001c0003t0044g0079a0001c0004t0005g0036 | 3 | NA19002.hp1 NA19002.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1332-3096G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131011103 | ||||||
| chr12:131011103
|
GCCCCACC others(19): Show |
G | 3 | a0001c0003t0013g0129a0001c0022t0016g0109a0001c0025t0021g0119 | 3 | HG01934.hp2 HG02630.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1332-3044_1332-301 others(30): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr12 | 131011103 | |||||
| chr12:131011103
|
GCCCCACC others(45): Show |
G | 2 | a0001c0002t0003g0034a0001c0010t0007g0150 | 2 | NA18986.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1332-3070_1332-301 others(56): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr12 | 131011103 | |||||
| chr12:131011129
|
T | G | 2 | a0001c0001t0001g0002a0001c0001t0001g0003 | 2 | HG01433.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1332-3070T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131011129 | ||||||
| chr12:131011165
|
GCCCCACC others(19): Show |
G | 1 | a0003c0012t0017g0017 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1332-3021_1332-299 others(30): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr12 | 131011165 | |||||
| chr12:131011168
|
C | G | 2 | a0001c0005t0001g0112a0001c0005t0008g0226 | 2 | HG02895.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1332-3031C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131011168 | ||||||
| chr12:131011208
|
T | C | 2 | a0002c0028t0001g0022a0002c0030t0032g0159 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1332-2991T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131011208 | ||||||
| chr12:131011221
|
T | C | 173 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0191others(170): Show | 173 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.1332-2978T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131011221 | ||||||
| chr12:131011521
|
G | A | 3 | a0001c0001t0028g0205a0001c0003t0029g0214a0003c0031t0003g0089 | 3 | HG02280.hp2 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1332-2678G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131011521 | ||||||
| chr12:131011554
|
C | T | 2 | a0001c0004t0002g0164a0005c0011t0002g0110 | 2 | HG01106.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1332-2645C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131011554 | ||||||
| chr12:131011566
|
C | T | 25 | a0001c0002t0001g0223a0001c0003t0004g0121a0001c0003t0004g0122others(22): Show | 25 | HG00738.hp2 HG01496.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.1332-2633C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131011566 | ||||||
| chr12:131011602
|
G | C | 27 | a0001c0002t0001g0223a0001c0003t0004g0121a0001c0003t0004g0122others(24): Show | 27 | HG00738.hp2 HG01106.hp1 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.1332-2597G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131011602 | ||||||
| chr12:131011611
|
C | T | 1 | a0001c0004t0002g0164 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1332-2588C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131011611 | ||||||
| chr12:131011636
|
C | T | 2 | a0001c0003t0004g0121a0001c0003t0004g0122 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1332-2563C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131011636 | ||||||
| chr12:131011643
|
A | G | 2 | a0001c0004t0002g0164a0005c0011t0002g0110 | 2 | HG01106.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1332-2556A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131011643 | ||||||
| chr12:131011654
|
A | G | 228 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(225): Show | 228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.1332-2545A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131011654 | ||||||
| chr12:131011788
|
C | T | 3 | a0001c0003t0013g0129a0001c0022t0016g0109a0001c0025t0021g0119 | 3 | HG01934.hp2 HG02630.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1332-2411C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131011788 | ||||||
| chr12:131011813
|
G | A | 3 | a0001c0003t0013g0129a0001c0022t0016g0109a0001c0025t0021g0119 | 3 | HG01934.hp2 HG02630.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1332-2386G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131011813 | ||||||
| chr12:131011954
|
T | C | 153 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0191others(150): Show | 153 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1332-2245T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131011954 | ||||||
| chr12:131011980
|
C | T | 10 | a0001c0001t0016g0182a0001c0001t0027g0118a0001c0003t0013g0224others(7): Show | 10 | HG02257.hp1 HG02258.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1332-2219C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131011980 | ||||||
| chr12:131012273
|
T | A | 158 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0191others(155): Show | 158 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.1332-1926T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131012273 | ||||||
| chr12:131012277
|
A | AT | 153 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0191others(150): Show | 153 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1332-1907dupT | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr12 | 131012277 | |||||
| chr12:131012374
|
C | T | 2 | a0001c0001t0028g0205a0001c0003t0029g0214 | 2 | HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1332-1825C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131012374 | ||||||
| chr12:131012384
|
C | T | 1 | a0012c0024t0002g0196 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1332-1815C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131012384 | ||||||
| chr12:131012617
|
G | T | 1 | a0001c0002t0010g0139 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1332-1582G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131012617 | ||||||
| chr12:131012676
|
T | C | 1 | a0001c0003t0013g0129 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1332-1523T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131012676 | ||||||
| chr12:131012797
|
G | A | 2 | a0001c0003t0044g0079a0001c0004t0005g0036 | 2 | NA19002.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1332-1402G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131012797 | ||||||
| chr12:131012840
|
C | T | 1 | a0001c0007t0004g0018 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1332-1359C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131012840 | ||||||
| chr12:131012885
|
C | T | 1 | a0007c0039t0001g0229 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1332-1314C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131012885 | ||||||
| chr12:131012897
|
C | T | 1 | a0001c0003t0006g0211 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1332-1302C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131012897 | ||||||
| chr12:131012899
|
C | T | 2 | a0001c0001t0002g0228a0001c0001t0002g0235 | 2 | HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1332-1300C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131012899 | ||||||
| chr12:131012908
|
C | T | 5 | a0001c0001t0016g0182a0001c0003t0013g0224a0001c0003t0013g0225others(2): Show | 5 | HG02055.hp2 HG02486.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1332-1291C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131012908 | ||||||
| chr12:131012916
|
G | A | 1 | a0001c0001t0001g0113 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1332-1283G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131012916 | ||||||
| chr12:131012920
|
G | A | 1 | a0001c0001t0011g0074 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1332-1279G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131012920 | ||||||
| chr12:131012992
|
C | A | 21 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0130others(18): Show | 21 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1332-1207C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131012992 | ||||||
| chr12:131013165
|
C | T | 1 | a0001c0003t0044g0079 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1332-1034C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131013165 | ||||||
| chr12:131013357
|
A | G | 16 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0028g0205others(13): Show | 16 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1332-842A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131013357 | ||||||
| chr12:131013557
|
G | A | 106 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0208others(103): Show | 106 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.1332-642G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131013557 | ||||||
| chr12:131013906
|
G | A | 56 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0130others(53): Show | 56 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.1332-293G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131013906 | ||||||
| chr12:131013909
|
G | A | 1 | a0007c0039t0001g0229 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1332-290G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131013909 | ||||||
| chr12:131013936
|
G | A | 23 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0028g0205others(20): Show | 23 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1332-263G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131013936 | ||||||
| chr12:131013940
|
C | G | 56 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0130others(53): Show | 56 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.1332-259C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131013940 | ||||||
| chr12:131014050
|
G | A | 1 | a0010c0026t0013g0238 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1332-149G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131014050 | ||||||
| chr12:131014109
|
T | C | 23 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0028g0205others(20): Show | 23 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1332-90T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131014109 | ||||||
| chr12:131014147
|
G | A | 4 | a0001c0001t0011g0066a0001c0001t0011g0074a0001c0001t0023g0143others(1): Show | 4 | HG00621.hp2 HG02132.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.1332-52G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 12/24 | chr12 | 131014147 | ||||||
| chr12:131014369
|
C | T | 1 | a0001c0003t0006g0185 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1473+29C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131014369 | ||||||
| chr12:131014401
|
C | T | 171 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0191others(168): Show | 171 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.1473+61C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131014401 | ||||||
| chr12:131014450
|
G | A | 110 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0208others(107): Show | 110 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.1473+110G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131014450 | ||||||
| chr12:131014522
|
C | A | 1 | a0010c0026t0013g0238 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1473+182C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131014522 | ||||||
| chr12:131014554
|
T | C | 21 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0130others(18): Show | 21 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1473+214T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131014554 | ||||||
| chr12:131014595
|
C | T | 1 | a0005c0011t0002g0110 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1473+255C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131014595 | ||||||
| chr12:131014604
|
C | T | 1 | a0003c0012t0017g0017 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1473+264C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131014604 | ||||||
| chr12:131014622
|
A | G | 16 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0028g0205others(13): Show | 16 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1473+282A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131014622 | ||||||
| chr12:131014666
|
A | G | 1 | a0001c0002t0001g0223 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1473+326A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131014666 | ||||||
| chr12:131014765
|
G | A | 22 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0028g0205others(19): Show | 22 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1473+425G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131014765 | ||||||
| chr12:131014812
|
G | A | 9 | a0001c0002t0001g0223a0001c0003t0004g0121a0001c0003t0004g0122others(6): Show | 9 | HG00738.hp2 HG01496.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1473+472G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131014812 | ||||||
| chr12:131014980
|
C | T | 3 | a0001c0001t0028g0205a0001c0003t0029g0214a0003c0031t0003g0089 | 3 | HG02280.hp2 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1473+640C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131014980 | ||||||
| chr12:131014982
|
C | T | 6 | a0002c0018t0020g0123a0002c0018t0020g0124a0002c0027t0001g0179others(3): Show | 6 | HG02257.hp2 HG02965.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1473+642C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131014982 | ||||||
| chr12:131015028
|
G | C | 110 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0208others(107): Show | 110 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.1473+688G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131015028 | ||||||
| chr12:131015132
|
C | T | 1 | a0001c0002t0001g0157 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1473+792C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131015132 | ||||||
| chr12:131015209
|
C | A | 2 | a0001c0001t0028g0205a0001c0003t0029g0214 | 2 | HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1473+869C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131015209 | ||||||
| chr12:131015229
|
C | G | 1 | a0001c0001t0001g0113 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1473+889C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131015229 | ||||||
| chr12:131015275
|
A | G | 15 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0028g0205others(12): Show | 15 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1473+935A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131015275 | ||||||
| chr12:131015279
|
G | C | 21 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0130others(18): Show | 21 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1473+939G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131015279 | ||||||
| chr12:131015395
|
C | G | 59 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0130others(56): Show | 59 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.1473+1055C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131015395 | ||||||
| chr12:131015421
|
C | T | 109 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0208others(106): Show | 109 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.1473+1081C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131015421 | ||||||
| chr12:131015465
|
T | A | 22 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0028g0205others(19): Show | 22 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1473+1125T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131015465 | ||||||
| chr12:131015600
|
C | CTGGAGTT others(11): Show |
115 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0156others(112): Show | 115 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1473+1282_1473+129 others(22): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131015600 | |||||
| chr12:131015600
|
CTGGAGTT others(11): Show |
C | 9 | a0001c0002t0001g0223a0001c0003t0004g0121a0001c0003t0004g0122others(6): Show | 9 | HG00738.hp2 HG01496.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1473+1282_1473+129 others(22): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131015600 | |||||
| chr12:131015613
|
TGGAGATG others(8): Show |
T | 2 | a0001c0001t0028g0205a0001c0003t0029g0214 | 2 | HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1473+1275_1473+128 others(19): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131015613 | |||||
| chr12:131015758
|
C | T | 1 | a0001c0003t0034g0014 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1473+1418C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131015758 | ||||||
| chr12:131015837
|
C | G | 1 | a0001c0003t0013g0129 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1473+1497C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131015837 | ||||||
| chr12:131015954
|
C | T | 1 | a0001c0007t0004g0018 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1473+1614C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131015954 | ||||||
| chr12:131016026
|
C | T | 9 | a0001c0002t0001g0223a0001c0003t0004g0121a0001c0003t0004g0122others(6): Show | 9 | HG00738.hp2 HG01496.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1473+1686C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131016026 | ||||||
| chr12:131016138
|
G | A | 25 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0130others(22): Show | 25 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.1473+1798G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131016138 | ||||||
| chr12:131016178
|
G | A | 33 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0130others(30): Show | 33 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.1473+1838G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131016178 | ||||||
| chr12:131016186
|
A | G | 1 | a0001c0025t0021g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1473+1846A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131016186 | ||||||
| chr12:131016328
|
G | A | 1 | a0003c0012t0017g0158 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1473+1988G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131016328 | ||||||
| chr12:131016428
|
G | A | 1 | a0001c0002t0003g0077 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1473+2088G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131016428 | ||||||
| chr12:131016470
|
T | C | 176 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0156others(173): Show | 176 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.1473+2130T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131016470 | ||||||
| chr12:131016482
|
T | A | 2 | a0001c0002t0003g0020a0001c0002t0003g0057 | 2 | HG02155.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.1473+2142T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131016482 | ||||||
| chr12:131016492
|
A | G | 16 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0028g0205others(13): Show | 16 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1473+2152A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131016492 | ||||||
| chr12:131016503
|
A | G | 1 | a0004c0016t0002g0065 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1473+2163A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131016503 | ||||||
| chr12:131016567
|
G | A | 2 | a0001c0001t0001g0111a0001c0004t0002g0004 | 2 | HG01978.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1473+2227G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131016567 | ||||||
| chr12:131016668
|
G | A | 6 | a0002c0018t0020g0123a0002c0018t0020g0124a0002c0027t0001g0179others(3): Show | 6 | HG02257.hp2 HG02965.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1473+2328G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131016668 | ||||||
| chr12:131016754
|
A | T | 3 | a0001c0003t0013g0129a0001c0022t0016g0109a0001c0025t0021g0119 | 3 | HG01934.hp2 HG02630.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1473+2414A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131016754 | ||||||
| chr12:131016767
|
C | T | 20 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0130others(17): Show | 20 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1473+2427C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131016767 | ||||||
| chr12:131016892
|
C | CA | 205 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(202): Show | 205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1473+2565dupA | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131016892 | |||||
| chr12:131016892
|
C | CAA | 31 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0003g0023others(28): Show | 31 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.1473+2564_1473+256 others(6): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131016892 | |||||
| chr12:131017095
|
C | T | 1 | a0001c0020t0002g0180 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1473+2755C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131017095 | ||||||
| chr12:131017193
|
G | A | 7 | a0001c0002t0010g0142a0002c0018t0020g0123a0002c0018t0020g0124others(4): Show | 7 | HG02257.hp2 HG02965.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1473+2853G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131017193 | ||||||
| chr12:131017289
|
C | T | 111 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0156others(108): Show | 111 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.1473+2949C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131017289 | ||||||
| chr12:131017315
|
C | CACACACC others(32): Show |
6 | a0002c0018t0020g0123a0002c0018t0020g0124a0002c0027t0001g0179others(3): Show | 6 | HG02257.hp2 HG02965.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1473+3013_1473+301 others(43): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131017315 | |||||
| chr12:131017315
|
C | T | 46 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0130others(43): Show | 46 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.1473+2975C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131017315 | ||||||
| chr12:131017340
|
A | C | 2 | a0001c0001t0028g0205a0001c0003t0029g0214 | 2 | HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1473+3000A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131017340 | ||||||
| chr12:131017343
|
C | T | 1 | a0001c0020t0002g0180 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1473+3003C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131017343 | ||||||
| chr12:131017346
|
C | A | 2 | a0001c0001t0028g0205a0001c0003t0029g0214 | 2 | HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1473+3006C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131017346 | ||||||
| chr12:131017377
|
A | G | 48 | a0001c0001t0001g0115a0001c0001t0002g0005a0001c0001t0002g0098others(45): Show | 48 | HG00140.hp2 HG00280.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.1473+3037A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131017377 | ||||||
| chr12:131017380
|
C | T | 2 | a0001c0001t0028g0205a0001c0003t0029g0214 | 2 | HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1473+3040C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131017380 | ||||||
| chr12:131017385
|
C | T | 2 | a0001c0001t0028g0205a0001c0003t0029g0214 | 2 | HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1473+3045C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131017385 | ||||||
| chr12:131017411
|
A | ACTCAGTC others(6): Show |
53 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0130others(50): Show | 53 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.1473+3072_1473+307 others(17): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131017411 | |||||
| chr12:131017411
|
A | C | 2 | a0001c0001t0028g0205a0001c0003t0029g0214 | 2 | HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1473+3071A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131017411 | ||||||
| chr12:131017429
|
C | A | 175 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0156others(172): Show | 175 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.1473+3089C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131017429 | ||||||
| chr12:131017487
|
A | G | 6 | a0002c0018t0020g0123a0002c0018t0020g0124a0002c0027t0001g0179others(3): Show | 6 | HG02257.hp2 HG02965.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1473+3147A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131017487 | ||||||
| chr12:131017516
|
A | C | 10 | a0001c0001t0016g0182a0001c0001t0027g0118a0001c0003t0013g0224others(7): Show | 10 | HG02257.hp1 HG02258.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1473+3176A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131017516 | ||||||
| chr12:131017652
|
C | T | 1 | a0004c0016t0003g0051 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1473+3312C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131017652 | ||||||
| chr12:131017801
|
C | T | 1 | a0010c0026t0013g0238 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1473+3461C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131017801 | ||||||
| chr12:131017812
|
T | C | 52 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0130others(49): Show | 52 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.1473+3472T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131017812 | ||||||
| chr12:131018057
|
C | G | 1 | a0001c0020t0002g0180 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1473+3717C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131018057 | ||||||
| chr12:131018328
|
C | T | 6 | a0002c0018t0020g0123a0002c0018t0020g0124a0002c0027t0001g0179others(3): Show | 6 | HG02257.hp2 HG02965.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1473+3988C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131018328 | ||||||
| chr12:131018464
|
C | A | 117 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0156others(114): Show | 117 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.1473+4124C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131018464 | ||||||
| chr12:131018508
|
C | T | 1 | a0001c0001t0003g0026 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1473+4168C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131018508 | ||||||
| chr12:131018564
|
G | A | 145 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0156others(142): Show | 145 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1473+4224G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131018564 | ||||||
| chr12:131018574
|
C | A | 122 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0156others(119): Show | 122 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.1473+4234C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131018574 | ||||||
| chr12:131018650
|
C | T | 1 | a0001c0001t0016g0147 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1473+4310C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131018650 | ||||||
| chr12:131018699
|
C | A | 118 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0156others(115): Show | 118 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.1473+4359C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131018699 | ||||||
| chr12:131018717
|
G | A | 1 | a0004c0015t0005g0086 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1473+4377G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131018717 | ||||||
| chr12:131018737
|
G | C | 142 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0156others(139): Show | 142 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1473+4397G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131018737 | ||||||
| chr12:131018741
|
G | A | 175 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0156others(172): Show | 175 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.1473+4401G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131018741 | ||||||
| chr12:131018765
|
A | G | 1 | a0001c0023t0004g0165 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1473+4425A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131018765 | ||||||
| chr12:131018793
|
C | T | 115 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0156others(112): Show | 115 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1473+4453C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131018793 | ||||||
| chr12:131018796
|
C | T | 1 | a0001c0002t0010g0139 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1473+4456C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131018796 | ||||||
| chr12:131018956
|
C | T | 1 | a0001c0006t0001g0240 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1473+4616C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131018956 | ||||||
| chr12:131018964
|
G | A | 1 | a0001c0020t0002g0180 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1473+4624G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131018964 | ||||||
| chr12:131018980
|
G | A | 34 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0130others(31): Show | 34 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1473+4640G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131018980 | ||||||
| chr12:131019060
|
C | T | 1 | a0007c0039t0001g0229 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1473+4720C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131019060 | ||||||
| chr12:131019070
|
T | G | 122 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0156others(119): Show | 122 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.1473+4730T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131019070 | ||||||
| chr12:131019215
|
C | T | 1 | a0001c0004t0002g0004 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1473+4875C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131019215 | ||||||
| chr12:131019319
|
G | A | 42 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0130others(39): Show | 42 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.1473+4979G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131019319 | ||||||
| chr12:131019387
|
C | G | 4 | a0001c0003t0013g0129a0001c0022t0016g0109a0001c0025t0021g0119others(1): Show | 4 | HG01934.hp2 HG02630.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1473+5047C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131019387 | ||||||
| chr12:131019412
|
C | T | 2 | a0001c0004t0005g0095a0001c0045t0002g0091 | 2 | HG04115.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1473+5072C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131019412 | ||||||
| chr12:131019509
|
G | A | 1 | a0003c0032t0038g0090 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1473+5169G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131019509 | ||||||
| chr12:131019597
|
C | T | 1 | a0001c0036t0003g0075 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1473+5257C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131019597 | ||||||
| chr12:131019616
|
GA | G | 6 | a0002c0018t0020g0123a0002c0018t0020g0124a0002c0027t0001g0179others(3): Show | 6 | HG02257.hp2 HG02965.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1473+5277delA | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131019616 | ||||||
| chr12:131019737
|
G | A | 37 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0130others(34): Show | 37 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.1473+5397G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131019737 | ||||||
| chr12:131019822
|
GGAGATAT others(48): Show |
G | 127 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0156others(124): Show | 127 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.1473+5506_1473+556 others(59): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131019822 | |||||
| chr12:131019822
|
GGAGATAT others(157): Show |
G | 1 | a0001c0001t0016g0147 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1473+5506_1473+566 others(4): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131019822 | |||||
| chr12:131019912
|
A | C | 127 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0156others(124): Show | 127 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.1473+5572A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131019912 | ||||||
| chr12:131019976
|
G | A | 127 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0156others(124): Show | 127 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.1473+5636G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131019976 | ||||||
| chr12:131020005
|
G | A | 117 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0156others(114): Show | 117 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.1473+5665G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131020005 | ||||||
| chr12:131020018
|
A | G | 127 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0156others(124): Show | 127 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.1473+5678A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131020018 | ||||||
| chr12:131020021
|
CAGGGCAG others(78): Show |
C | 127 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0156others(124): Show | 127 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.1473+5682_1473+576 others(89): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131020021 | ||||||
| chr12:131020085
|
G | A | 1 | a0001c0001t0016g0147 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1473+5745G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131020085 | ||||||
| chr12:131020127
|
G | GTCCAGGG others(48): Show |
2 | a0001c0001t0002g0228a0001c0001t0002g0235 | 2 | HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1473+5794_1473+579 others(59): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131020127 | |||||
| chr12:131020127
|
G | GTCCAGGG others(48): Show |
88 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(85): Show | 88 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.1473+5832_1473+583 others(59): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131020127 | |||||
| chr12:131020127
|
G | GTCCAGGG others(48): Show |
10 | a0001c0001t0016g0182a0001c0001t0027g0118a0001c0003t0013g0224others(7): Show | 10 | HG02257.hp1 HG02258.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1473+5805_1473+580 others(59): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131020127 | |||||
| chr12:131020130
|
CAGGGCAG others(24): Show |
C | 1 | a0001c0001t0016g0147 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1473+5791_1473+582 others(35): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131020130 | ||||||
| chr12:131020173
|
G | C | 128 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0156others(125): Show | 128 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1473+5833G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131020173 | ||||||
| chr12:131020174
|
C | T | 1 | a0001c0001t0016g0147 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1473+5834C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131020174 | ||||||
| chr12:131020175
|
G | A | 127 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0156others(124): Show | 127 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.1473+5835G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131020175 | ||||||
| chr12:131020182
|
A | G | 1 | a0001c0001t0016g0147 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1473+5842A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131020182 | ||||||
| chr12:131020230
|
G | A | 1 | a0001c0001t0016g0147 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1473+5890G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131020230 | ||||||
| chr12:131020256
|
T | C | 128 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0156others(125): Show | 128 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1473+5916T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131020256 | ||||||
| chr12:131020285
|
A | G | 128 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0156others(125): Show | 128 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1473+5945A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131020285 | ||||||
| chr12:131020361
|
G | A | 2 | a0001c0001t0001g0111a0001c0004t0002g0004 | 2 | HG01978.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1473+6021G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131020361 | ||||||
| chr12:131020362
|
T | G | 10 | a0001c0001t0016g0182a0001c0001t0027g0118a0001c0003t0013g0224others(7): Show | 10 | HG02257.hp1 HG02258.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1473+6022T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131020362 | ||||||
| chr12:131020366
|
T | C | 128 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0156others(125): Show | 128 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1473+6026T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131020366 | ||||||
| chr12:131020368
|
A | G | 128 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0156others(125): Show | 128 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1473+6028A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131020368 | ||||||
| chr12:131020409
|
C | A | 2 | a0001c0001t0027g0118a0001c0003t0036g0209 | 2 | HG02257.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1473+6069C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131020409 | ||||||
| chr12:131020521
|
C | T | 134 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0156others(131): Show | 134 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.1473+6181C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131020521 | ||||||
| chr12:131020736
|
C | T | 21 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0130others(18): Show | 21 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1473+6396C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131020736 | ||||||
| chr12:131020770
|
G | C | 2 | a0003c0012t0017g0158a0007c0039t0001g0229 | 2 | HG02922.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1473+6430G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131020770 | ||||||
| chr12:131021048
|
A | G | 1 | a0001c0001t0009g0137 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1473+6708A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131021048 | ||||||
| chr12:131021089
|
GA | G | 134 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0156others(131): Show | 134 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.1473+6757delA | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131021089 | |||||
| chr12:131021104
|
G | T | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(104): Show | 107 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.1473+6764G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131021104 | ||||||
| chr12:131021289
|
C | T | 1 | a0001c0003t0029g0214 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1473+6949C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131021289 | ||||||
| chr12:131021305
|
C | T | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(104): Show | 107 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.1473+6965C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131021305 | ||||||
| chr12:131021384
|
C | T | 2 | a0001c0001t0002g0228a0001c0001t0002g0235 | 2 | HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1473+7044C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131021384 | ||||||
| chr12:131021386
|
C | T | 2 | a0001c0004t0002g0164a0005c0011t0002g0110 | 2 | HG01106.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1473+7046C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131021386 | ||||||
| chr12:131021397
|
C | T | 134 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0156others(131): Show | 134 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.1473+7057C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131021397 | ||||||
| chr12:131021429
|
C | T | 2 | a0001c0001t0002g0228a0001c0001t0002g0235 | 2 | HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1473+7089C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131021429 | ||||||
| chr12:131021451
|
C | T | 1 | a0001c0001t0001g0113 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1473+7111C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131021451 | ||||||
| chr12:131021461
|
C | T | 17 | a0001c0001t0016g0147a0001c0002t0001g0223a0001c0003t0004g0121others(14): Show | 17 | HG00738.hp2 HG01496.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1473+7121C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131021461 | ||||||
| chr12:131021547
|
C | T | 1 | a0001c0020t0002g0180 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1473+7207C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131021547 | ||||||
| chr12:131021548
|
G | A | 134 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0156others(131): Show | 134 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.1473+7208G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131021548 | ||||||
| chr12:131021566
|
T | C | 173 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0156others(170): Show | 173 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.1473+7226T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131021566 | ||||||
| chr12:131021569
|
T | C | 174 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0156others(171): Show | 174 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.1473+7229T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131021569 | ||||||
| chr12:131021570
|
G | A | 2 | a0001c0001t0002g0228a0001c0001t0002g0235 | 2 | HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1473+7230G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131021570 | ||||||
| chr12:131021604
|
G | A | 132 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0156others(129): Show | 132 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.1473+7264G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131021604 | ||||||
| chr12:131021637
|
C | T | 134 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0156others(131): Show | 134 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.1473+7297C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131021637 | ||||||
| chr12:131021683
|
C | G | 1 | a0001c0004t0005g0095 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1473+7343C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131021683 | ||||||
| chr12:131021685
|
C | T | 134 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0001g0156others(131): Show | 134 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.1473+7345C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131021685 | ||||||
| chr12:131021755
|
T | G | 39 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0130others(36): Show | 39 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.1473+7415T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131021755 | ||||||
| chr12:131021777
|
G | A | 1 | a0001c0003t0002g0186 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1473+7437G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131021777 | ||||||
| chr12:131021993
|
C | T | 3 | a0001c0004t0002g0164a0003c0031t0003g0089a0005c0011t0002g0110 | 3 | HG01106.hp1 HG02630.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1473+7653C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131021993 | ||||||
| chr12:131021996
|
G | A | 7 | a0002c0018t0020g0123a0002c0018t0020g0124a0002c0027t0001g0179others(4): Show | 7 | HG02257.hp2 HG02922.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1473+7656G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131021996 | ||||||
| chr12:131022033
|
C | T | 2 | a0001c0001t0002g0228a0001c0001t0002g0235 | 2 | HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1473+7693C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131022033 | ||||||
| chr12:131022041
|
T | C | 2 | a0001c0001t0002g0228a0001c0001t0002g0235 | 2 | HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1473+7701T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131022041 | ||||||
| chr12:131022058
|
A | G | 37 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0130others(34): Show | 37 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.1473+7718A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131022058 | ||||||
| chr12:131022072
|
T | A | 2 | a0001c0005t0001g0112a0001c0005t0008g0226 | 2 | HG02895.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1473+7732T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131022072 | ||||||
| chr12:131022162
|
C | T | 131 | a0001c0001t0001g0115a0001c0001t0001g0156a0001c0001t0001g0163others(128): Show | 131 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.1473+7822C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131022162 | ||||||
| chr12:131022292
|
C | T | 21 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0130others(18): Show | 21 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1473+7952C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131022292 | ||||||
| chr12:131022361
|
T | C | 35 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0130others(32): Show | 35 | HG00639.hp1 HG01074.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.1473+8021T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131022361 | ||||||
| chr12:131022443
|
C | G | 6 | a0001c0003t0001g0152a0001c0003t0004g0237a0001c0003t0013g0129others(3): Show | 6 | HG01175.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1473+8103C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131022443 | ||||||
| chr12:131022475
|
G | A | 60 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0130others(57): Show | 60 | HG00639.hp1 HG00639.hp2 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.1473+8135G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131022475 | ||||||
| chr12:131022513
|
G | A | 1 | a0001c0003t0013g0129 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1473+8173G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131022513 | ||||||
| chr12:131022603
|
C | T | 1 | a0001c0002t0003g0073 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1473+8263C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131022603 | ||||||
| chr12:131022760
|
G | A | 1 | a0002c0029t0031g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1473+8420G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131022760 | ||||||
| chr12:131022799
|
G | T | 11 | a0001c0001t0016g0182a0001c0001t0027g0118a0001c0003t0013g0224others(8): Show | 11 | HG02257.hp1 HG02258.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1473+8459G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131022799 | ||||||
| chr12:131022842
|
C | T | 1 | a0001c0001t0002g0161 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1473+8502C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131022842 | ||||||
| chr12:131022863
|
C | T | 122 | a0001c0001t0001g0115a0001c0001t0001g0156a0001c0001t0001g0163others(119): Show | 122 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.1473+8523C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131022863 | ||||||
| chr12:131022880
|
A | G | 157 | a0001c0001t0001g0115a0001c0001t0001g0156a0001c0001t0001g0163others(154): Show | 157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1473+8540A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131022880 | ||||||
| chr12:131022885
|
C | T | 1 | a0001c0025t0021g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1473+8545C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131022885 | ||||||
| chr12:131023181
|
TGTA | T | 3 | a0001c0001t0001g0113a0001c0001t0001g0212a0001c0003t0006g0211 | 3 | HG01175.hp1 HG03688.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1473+8844_1473+884 others(7): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131023181 | |||||
| chr12:131023359
|
G | C | 27 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0130others(24): Show | 27 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.1473+9019G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131023359 | ||||||
| chr12:131023395
|
C | T | 1 | a0001c0003t0012g0025 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1473+9055C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131023395 | ||||||
| chr12:131023420
|
T | C | 212 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(209): Show | 212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.1473+9080T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131023420 | ||||||
| chr12:131023468
|
C | CGT | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(206): Show | 209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1473+9141_1473+914 others(6): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131023468 | |||||
| chr12:131023644
|
G | A | 28 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0130others(25): Show | 28 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.1473+9304G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131023644 | ||||||
| chr12:131023677
|
C | T | 1 | a0001c0001t0023g0143 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1473+9337C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131023677 | ||||||
| chr12:131023695
|
A | G | 221 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(218): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1473+9355A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131023695 | ||||||
| chr12:131023801
|
C | T | 1 | a0001c0003t0029g0214 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1473+9461C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131023801 | ||||||
| chr12:131023874
|
G | A | 2 | a0001c0001t0011g0220a0001c0002t0003g0034 | 2 | NA19002.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1473+9534G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131023874 | ||||||
| chr12:131023990
|
G | A | 1 | a0004c0015t0005g0086 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1473+9650G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131023990 | ||||||
| chr12:131023991
|
T | C | 2 | a0001c0001t0028g0205a0001c0003t0029g0214 | 2 | HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1473+9651T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131023991 | ||||||
| chr12:131024238
|
G | T | 1 | a0001c0004t0002g0164 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1473+9898G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131024238 | ||||||
| chr12:131024250
|
C | T | 2 | a0001c0001t0002g0228a0001c0001t0002g0235 | 2 | HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1473+9910C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131024250 | ||||||
| chr12:131024273
|
T | C | 69 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(66): Show | 69 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.1473+9933T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131024273 | ||||||
| chr12:131024407
|
A | G | 1 | a0010c0026t0013g0238 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1473+10067A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131024407 | ||||||
| chr12:131024618
|
T | C | 1 | a0001c0020t0002g0180 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1473+10278T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131024618 | ||||||
| chr12:131024638
|
A | C | 1 | a0001c0004t0002g0164 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1473+10298A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131024638 | ||||||
| chr12:131024712
|
C | T | 1 | a0010c0026t0013g0238 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1473+10372C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131024712 | ||||||
| chr12:131024828
|
A | G | 7 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0003t0013g0129others(4): Show | 7 | HG01884.hp2 HG01934.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1473+10488A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131024828 | ||||||
| chr12:131024885
|
C | T | 2 | a0001c0004t0005g0082a0001c0009t0014g0078 | 2 | HG01346.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1473+10545C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131024885 | ||||||
| chr12:131024921
|
T | C | 224 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(221): Show | 224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.1473+10581T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131024921 | ||||||
| chr12:131024922
|
G | A | 65 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(62): Show | 65 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.1473+10582G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131024922 | ||||||
| chr12:131024971
|
A | C | 1 | a0001c0004t0002g0164 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1473+10631A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131024971 | ||||||
| chr12:131025165
|
A | T | 1 | a0003c0031t0003g0089 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1473+10825A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131025165 | ||||||
| chr12:131025399
|
C | T | 1 | a0001c0001t0011g0220 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1473+11059C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131025399 | ||||||
| chr12:131025454
|
C | T | 1 | a0001c0004t0002g0011 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1473+11114C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131025454 | ||||||
| chr12:131025545
|
C | CT | 36 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0130others(33): Show | 36 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.1473+11220dupT | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131025545 | |||||
| chr12:131025586
|
G | A | 226 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(223): Show | 226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1473+11246G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131025586 | ||||||
| chr12:131025628
|
T | C | 1 | a0001c0004t0002g0164 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1473+11288T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131025628 | ||||||
| chr12:131025724
|
A | G | 3 | a0001c0003t0013g0129a0001c0007t0004g0018a0003c0033t0030g0231 | 3 | HG02572.hp1 HG02630.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1473+11384A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131025724 | ||||||
| chr12:131026032
|
C | T | 70 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(67): Show | 70 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.1473+11692C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131026032 | ||||||
| chr12:131026041
|
T | C | 1 | a0003c0012t0017g0017 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1473+11701T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131026041 | ||||||
| chr12:131026115
|
T | C | 1 | a0001c0004t0002g0164 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1473+11775T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131026115 | ||||||
| chr12:131026253
|
C | T | 1 | a0001c0003t0045g0042 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1473+11913C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131026253 | ||||||
| chr12:131026310
|
TTATTCTC | T | 8 | a0001c0001t0016g0147a0001c0002t0001g0223a0001c0003t0004g0121others(5): Show | 8 | HG00738.hp2 HG01496.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1473+11971_1473+11 others(13): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131026310 | ||||||
| chr12:131026344
|
G | C | 2 | a0001c0001t0028g0205a0001c0003t0029g0214 | 2 | HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1473+12004G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131026344 | ||||||
| chr12:131026356
|
T | TCCTTTGC others(13): Show |
1 | a0003c0031t0003g0089 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1473+12037_1473+12 others(26): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131026356 | |||||
| chr12:131026370
|
C | T | 1 | a0001c0004t0002g0164 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1473+12030C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131026370 | ||||||
| chr12:131026390
|
C | T | 10 | a0001c0001t0016g0182a0001c0001t0027g0118a0001c0003t0013g0224others(7): Show | 10 | HG02257.hp1 HG02258.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1473+12050C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131026390 | ||||||
| chr12:131026405
|
G | A | 1 | a0001c0020t0002g0180 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1473+12065G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131026405 | ||||||
| chr12:131026484
|
T | C | 1 | a0001c0004t0002g0164 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1473+12144T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131026484 | ||||||
| chr12:131026491
|
G | A | 2 | a0001c0001t0002g0005a0003c0031t0003g0089 | 2 | HG02630.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1473+12151G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131026491 | ||||||
| chr12:131026722
|
T | G | 2 | a0001c0002t0001g0195a0001c0002t0048g0151 | 2 | HG03831.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1473+12382T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131026722 | ||||||
| chr12:131026731
|
C | G | 1 | a0001c0002t0001g0195 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1473+12391C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131026731 | ||||||
| chr12:131026759
|
G | A | 19 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0130others(16): Show | 19 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.1473+12419G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131026759 | ||||||
| chr12:131026783
|
C | T | 5 | a0001c0003t0013g0129a0001c0007t0004g0018a0001c0022t0016g0109others(2): Show | 5 | HG01934.hp2 HG02572.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1473+12443C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131026783 | ||||||
| chr12:131026846
|
G | A | 2 | a0001c0001t0005g0087a0001c0002t0001g0010 | 2 | HG02056.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.1473+12506G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131026846 | ||||||
| chr12:131026883
|
G | A | 2 | a0001c0003t0013g0129a0001c0007t0004g0018 | 2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1473+12543G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131026883 | ||||||
| chr12:131027096
|
T | C | 1 | a0003c0031t0003g0089 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1473+12756T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131027096 | ||||||
| chr12:131027104
|
G | T | 1 | a0001c0004t0002g0164 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1473+12764G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131027104 | ||||||
| chr12:131027206
|
A | C | 1 | a0010c0026t0013g0238 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1473+12866A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131027206 | ||||||
| chr12:131027250
|
T | C | 1 | a0001c0004t0002g0164 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1473+12910T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131027250 | ||||||
| chr12:131027278
|
T | C | 1 | a0001c0004t0002g0164 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1473+12938T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131027278 | ||||||
| chr12:131027315
|
T | C | 1 | a0001c0004t0002g0164 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1473+12975T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131027315 | ||||||
| chr12:131027369
|
A | G | 8 | a0001c0001t0016g0147a0001c0002t0001g0223a0001c0003t0004g0121others(5): Show | 8 | HG00738.hp2 HG01496.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1473+13029A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131027369 | ||||||
| chr12:131027521
|
G | A | 1 | a0001c0004t0002g0164 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1473+13181G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131027521 | ||||||
| chr12:131027806
|
G | A | 5 | a0001c0003t0013g0129a0001c0007t0004g0018a0001c0022t0016g0109others(2): Show | 5 | HG01934.hp2 HG02572.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1473+13466G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131027806 | ||||||
| chr12:131027828
|
A | G | 1 | a0002c0018t0020g0123 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1473+13488A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131027828 | ||||||
| chr12:131028041
|
C | T | 1 | a0001c0001t0002g0173 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1473+13701C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131028041 | ||||||
| chr12:131028051
|
C | T | 1 | a0001c0004t0002g0164 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1473+13711C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131028051 | ||||||
| chr12:131028052
|
C | T | 3 | a0001c0001t0011g0062a0001c0002t0003g0076a0001c0009t0019g0135 | 3 | HG00609.hp1 NA19009.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1473+13712C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131028052 | ||||||
| chr12:131028208
|
T | C | 11 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0016g0147others(8): Show | 11 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1473+13868T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131028208 | ||||||
| chr12:131028268
|
A | T | 11 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0016g0147others(8): Show | 11 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1473+13928A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131028268 | ||||||
| chr12:131028300
|
T | G | 10 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0016g0147others(7): Show | 10 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1473+13960T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131028300 | ||||||
| chr12:131028449
|
T | C | 30 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0130others(27): Show | 30 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.1473+14109T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131028449 | ||||||
| chr12:131028527
|
T | C | 67 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(64): Show | 67 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.1473+14187T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131028527 | ||||||
| chr12:131028619
|
G | C | 1 | a0001c0004t0002g0164 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1473+14279G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131028619 | ||||||
| chr12:131028662
|
G | A | 3 | a0001c0004t0002g0155a0001c0004t0015g0099a0011c0038t0002g0162 | 3 | HG00735.hp2 HG01099.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1473+14322G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131028662 | ||||||
| chr12:131028923
|
G | A | 12 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0016g0147others(9): Show | 12 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1473+14583G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131028923 | ||||||
| chr12:131028997
|
C | T | 106 | a0001c0001t0001g0115a0001c0001t0001g0156a0001c0001t0001g0163others(103): Show | 106 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.1473+14657C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131028997 | ||||||
| chr12:131029018
|
A | G | 120 | a0001c0001t0001g0115a0001c0001t0001g0156a0001c0001t0001g0163others(117): Show | 120 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.1473+14678A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029018 | ||||||
| chr12:131029053
|
G | A | 2 | a0001c0005t0001g0127a0001c0005t0001g0128 | 2 | HG01167.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1473+14713G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029053 | ||||||
| chr12:131029119
|
C | G | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(175): Show | 178 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.1473+14779C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029119 | ||||||
| chr12:131029168
|
T | C | 1 | a0001c0004t0002g0164 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1473+14828T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029168 | ||||||
| chr12:131029181
|
C | T | 1 | a0003c0031t0003g0089 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1473+14841C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029181 | ||||||
| chr12:131029218
|
T | C | 12 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0016g0147others(9): Show | 12 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1473+14878T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029218 | ||||||
| chr12:131029326
|
C | T | 2 | a0001c0001t0028g0205a0001c0003t0029g0214 | 2 | HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1473+14986C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029326 | ||||||
| chr12:131029531
|
G | A | 1 | a0003c0031t0003g0089 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1473+15191G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029531 | ||||||
| chr12:131029578
|
A | G | 2 | a0001c0001t0028g0205a0001c0003t0029g0214 | 2 | HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1473+15238A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029578 | ||||||
| chr12:131029581
|
C | G | 9 | a0001c0001t0016g0182a0001c0001t0027g0118a0001c0003t0013g0224others(6): Show | 9 | HG02257.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1473+15241C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029581 | ||||||
| chr12:131029626
|
C | CGTCGTAG others(350): Show |
3 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0004t0002g0164 | 3 | HG01884.hp2 HG03453.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1473+15322_1473+15 others(363): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131029626 | |||||
| chr12:131029663
|
A | G | 12 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0016g0147others(9): Show | 12 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1473+15323A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029663 | ||||||
| chr12:131029670
|
C | T | 9 | a0001c0001t0016g0147a0001c0002t0001g0223a0001c0003t0004g0121others(6): Show | 9 | HG00738.hp2 HG01496.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1473+15330C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029670 | ||||||
| chr12:131029671
|
C | G | 9 | a0001c0001t0016g0147a0001c0002t0001g0223a0001c0003t0004g0121others(6): Show | 9 | HG00738.hp2 HG01496.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1473+15331C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029671 | ||||||
| chr12:131029675
|
T | TAGGTGAC others(172): Show |
9 | a0001c0001t0016g0147a0001c0002t0001g0223a0001c0003t0004g0121others(6): Show | 9 | HG00738.hp2 HG01496.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1473+15336_1473+15 others(185): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131029675 | |||||
| chr12:131029676
|
A | T | 3 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0004t0002g0164 | 3 | HG01884.hp2 HG03453.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1473+15336A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029676 | ||||||
| chr12:131029677
|
T | C | 12 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0016g0147others(9): Show | 12 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1473+15337T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029677 | ||||||
| chr12:131029700
|
A | G | 12 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0016g0147others(9): Show | 12 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1473+15360A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029700 | ||||||
| chr12:131029708
|
G | A | 3 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0004t0002g0164 | 3 | HG01884.hp2 HG03453.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1473+15368G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029708 | ||||||
| chr12:131029721
|
T | A | 3 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0004t0002g0164 | 3 | HG01884.hp2 HG03453.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1473+15381T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029721 | ||||||
| chr12:131029722
|
C | T | 3 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0004t0002g0164 | 3 | HG01884.hp2 HG03453.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1473+15382C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029722 | ||||||
| chr12:131029761
|
C | G | 9 | a0001c0001t0016g0147a0001c0002t0001g0223a0001c0003t0004g0121others(6): Show | 9 | HG00738.hp2 HG01496.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1473+15421C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029761 | ||||||
| chr12:131029763
|
T | C | 12 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0016g0147others(9): Show | 12 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1473+15423T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029763 | ||||||
| chr12:131029764
|
GT | G | 9 | a0001c0001t0016g0147a0001c0002t0001g0223a0001c0003t0004g0121others(6): Show | 9 | HG00738.hp2 HG01496.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1473+15426delT | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131029764 | |||||
| chr12:131029767
|
C | A | 9 | a0001c0001t0016g0147a0001c0002t0001g0223a0001c0003t0004g0121others(6): Show | 9 | HG00738.hp2 HG01496.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1473+15427C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029767 | ||||||
| chr12:131029805
|
C | T | 9 | a0001c0001t0016g0147a0001c0002t0001g0223a0001c0003t0004g0121others(6): Show | 9 | HG00738.hp2 HG01496.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1473+15465C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029805 | ||||||
| chr12:131029806
|
C | G | 9 | a0001c0001t0016g0147a0001c0002t0001g0223a0001c0003t0004g0121others(6): Show | 9 | HG00738.hp2 HG01496.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1473+15466C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029806 | ||||||
| chr12:131029809
|
T | G | 9 | a0001c0001t0016g0147a0001c0002t0001g0223a0001c0003t0004g0121others(6): Show | 9 | HG00738.hp2 HG01496.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1473+15469T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029809 | ||||||
| chr12:131029811
|
AAC | A | 9 | a0001c0001t0016g0147a0001c0002t0001g0223a0001c0003t0004g0121others(6): Show | 9 | HG00738.hp2 HG01496.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1473+15472_1473+15 others(8): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029811 | ||||||
| chr12:131029812
|
ACGGTGAC others(38): Show |
A | 3 | a0001c0001t0028g0205a0001c0020t0002g0180a0001c0025t0021g0119 | 3 | HG01934.hp2 HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1473+15505_1473+15 others(51): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131029812 | |||||
| chr12:131029836
|
A | G | 14 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0016g0147others(11): Show | 14 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1473+15496A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029836 | ||||||
| chr12:131029845
|
C | T | 223 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(220): Show | 223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1473+15505C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029845 | ||||||
| chr12:131029857
|
T | A | 3 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0004t0002g0164 | 3 | HG01884.hp2 HG03453.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1473+15517T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029857 | ||||||
| chr12:131029857
|
T | TCGGTGAC others(84): Show |
1 | a0001c0003t0004g0237 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1473+15540_1473+15 others(97): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131029857 | |||||
| chr12:131029857
|
T | TCGGTGAC others(84): Show |
207 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(204): Show | 207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1473+15540_1473+15 others(97): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131029857 | |||||
| chr12:131029858
|
C | T | 3 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0004t0002g0164 | 3 | HG01884.hp2 HG03453.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1473+15518C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029858 | ||||||
| chr12:131029881
|
A | G | 15 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0016g0147others(12): Show | 15 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1473+15541A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029881 | ||||||
| chr12:131029889
|
G | A | 9 | a0001c0001t0016g0147a0001c0002t0001g0223a0001c0003t0004g0121others(6): Show | 9 | HG00738.hp2 HG01496.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1473+15549G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029889 | ||||||
| chr12:131029900
|
G | T | 3 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0004t0002g0164 | 3 | HG01884.hp2 HG03453.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1473+15560G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029900 | ||||||
| chr12:131029901
|
T | TA | 3 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0004t0002g0164 | 3 | HG01884.hp2 HG03453.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1473+15561_1473+15 others(7): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029901 | ||||||
| chr12:131029902
|
T | A | 12 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0016g0147others(9): Show | 12 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1473+15562T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029902 | ||||||
| chr12:131029903
|
C | CGGTGACA others(84): Show |
1 | a0001c0001t0016g0182 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1473+15604_1473+15 others(97): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131029903 | |||||
| chr12:131029903
|
C | T | 17 | a0001c0001t0016g0147a0001c0001t0027g0118a0001c0002t0001g0223others(14): Show | 17 | HG00738.hp2 HG01496.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1473+15563C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029903 | ||||||
| chr12:131029904
|
G | A | 3 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0004t0002g0164 | 3 | HG01884.hp2 HG03453.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1473+15564G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029904 | ||||||
| chr12:131029926
|
G | A | 3 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0004t0002g0164 | 3 | HG01884.hp2 HG03453.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1473+15586G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029926 | ||||||
| chr12:131029926
|
G | GTTAGGTT others(39): Show |
1 | a0001c0045t0002g0091 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1473+15604_1473+15 others(52): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131029926 | |||||
| chr12:131029945
|
G | A | 3 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0004t0002g0164 | 3 | HG01884.hp2 HG03453.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1473+15605G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029945 | ||||||
| chr12:131029945
|
G | T | 1 | a0001c0003t0029g0214 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1473+15605G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029945 | ||||||
| chr12:131029947
|
T | A | 1 | a0001c0003t0029g0214 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1473+15607T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029947 | ||||||
| chr12:131029949
|
A | G | 16 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0016g0147others(13): Show | 16 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1473+15609A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029949 | ||||||
| chr12:131029971
|
G | A | 4 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0003t0029g0214others(1): Show | 4 | HG01884.hp2 HG02280.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1473+15631G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029971 | ||||||
| chr12:131029990
|
T | G | 5 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0003t0029g0214others(2): Show | 5 | HG01884.hp2 HG02280.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1473+15650T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029990 | ||||||
| chr12:131029991
|
T | TA | 11 | a0001c0001t0016g0147a0001c0001t0028g0205a0001c0002t0001g0223others(8): Show | 11 | HG00738.hp2 HG01496.hp1 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.1473+15652dupA | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131029991 | |||||
| chr12:131029991
|
TATGGTAA others(82): Show |
T | 1 | a0001c0003t0029g0214 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1473+15652_1473+15 others(95): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029991 | ||||||
| chr12:131029992
|
A | T | 4 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0004t0002g0164others(1): Show | 4 | HG01884.hp2 HG03453.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1473+15652A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029992 | ||||||
| chr12:131029993
|
T | C | 15 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0016g0147others(12): Show | 15 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1473+15653T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029993 | ||||||
| chr12:131029994
|
G | A | 1 | a0001c0045t0002g0091 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1473+15654G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029994 | ||||||
| chr12:131029997
|
A | G | 15 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0016g0147others(12): Show | 15 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1473+15657A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131029997 | ||||||
| chr12:131030003
|
C | T | 1 | a0001c0020t0002g0180 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1473+15663C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030003 | ||||||
| chr12:131030016
|
G | A | 2 | a0001c0001t0028g0205a0001c0025t0021g0119 | 2 | HG01934.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1473+15676G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030016 | ||||||
| chr12:131030022
|
A | T | 15 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0016g0147others(12): Show | 15 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1473+15682A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030022 | ||||||
| chr12:131030035
|
T | G | 11 | a0001c0001t0016g0147a0001c0001t0028g0205a0001c0002t0001g0223others(8): Show | 11 | HG00738.hp2 HG01496.hp1 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.1473+15695T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030035 | ||||||
| chr12:131030037
|
A | T | 2 | a0001c0001t0028g0205a0001c0025t0021g0119 | 2 | HG01934.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1473+15697A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030037 | ||||||
| chr12:131030038
|
T | C | 2 | a0001c0001t0028g0205a0001c0025t0021g0119 | 2 | HG01934.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1473+15698T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030038 | ||||||
| chr12:131030042
|
G | A | 3 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0004t0002g0164 | 3 | HG01884.hp2 HG03453.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1473+15702G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030042 | ||||||
| chr12:131030048
|
T | C | 14 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0016g0147others(11): Show | 14 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1473+15708T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030048 | ||||||
| chr12:131030054
|
C | G | 3 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0004t0002g0164 | 3 | HG01884.hp2 HG03453.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1473+15714C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030054 | ||||||
| chr12:131030067
|
T | A | 3 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0004t0002g0164 | 3 | HG01884.hp2 HG03453.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1473+15727T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030067 | ||||||
| chr12:131030077
|
G | C | 14 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0016g0147others(11): Show | 14 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1473+15737G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030077 | ||||||
| chr12:131030080
|
G | T | 9 | a0001c0001t0016g0147a0001c0002t0001g0223a0001c0003t0004g0121others(6): Show | 9 | HG00738.hp2 HG01496.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1473+15740G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030080 | ||||||
| chr12:131030082
|
A | AACAGTGA others(175): Show |
1 | a0003c0031t0003g0089 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1473+15742_1473+15 others(188): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030082 | ||||||
| chr12:131030082
|
A | AACAGTGA others(175): Show |
8 | a0001c0001t0016g0147a0001c0002t0001g0223a0001c0003t0004g0121others(5): Show | 8 | HG00738.hp2 HG01496.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1473+15742_1473+15 others(188): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030082 | ||||||
| chr12:131030082
|
A | AC | 3 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0004t0002g0164 | 3 | HG01884.hp2 HG03453.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1473+15742_1473+15 others(7): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030082 | ||||||
| chr12:131030082
|
A | C | 3 | a0001c0001t0028g0205a0001c0003t0029g0214a0001c0025t0021g0119 | 3 | HG01934.hp2 HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1473+15742A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030082 | ||||||
| chr12:131030083
|
G | A | 3 | a0001c0001t0028g0205a0001c0003t0029g0214a0001c0025t0021g0119 | 3 | HG01934.hp2 HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1473+15743G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030083 | ||||||
| chr12:131030092
|
C | T | 12 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0016g0147others(9): Show | 12 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1473+15752C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030092 | ||||||
| chr12:131030121
|
T | C | 3 | a0001c0001t0028g0205a0001c0003t0029g0214a0001c0025t0021g0119 | 3 | HG01934.hp2 HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1473+15781T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030121 | ||||||
| chr12:131030121
|
T | G | 12 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0016g0147others(9): Show | 12 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1473+15781T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030121 | ||||||
| chr12:131030124
|
A | G | 12 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0016g0147others(9): Show | 12 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1473+15784A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030124 | ||||||
| chr12:131030124
|
A | T | 3 | a0001c0001t0028g0205a0001c0003t0029g0214a0001c0025t0021g0119 | 3 | HG01934.hp2 HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1473+15784A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030124 | ||||||
| chr12:131030127
|
C | T | 3 | a0001c0001t0028g0205a0001c0003t0029g0214a0001c0025t0021g0119 | 3 | HG01934.hp2 HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1473+15787C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030127 | ||||||
| chr12:131030128
|
G | A | 108 | a0001c0001t0001g0115a0001c0001t0001g0156a0001c0001t0001g0163others(105): Show | 108 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1473+15788G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030128 | ||||||
| chr12:131030131
|
G | A | 3 | a0001c0001t0028g0205a0001c0003t0029g0214a0001c0025t0021g0119 | 3 | HG01934.hp2 HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1473+15791G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030131 | ||||||
| chr12:131030137
|
C | T | 12 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0016g0147others(9): Show | 12 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1473+15797C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030137 | ||||||
| chr12:131030150
|
G | A | 12 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0016g0147others(9): Show | 12 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1473+15810G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030150 | ||||||
| chr12:131030156
|
T | A | 3 | a0001c0001t0028g0205a0001c0003t0029g0214a0001c0025t0021g0119 | 3 | HG01934.hp2 HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1473+15816T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030156 | ||||||
| chr12:131030166
|
G | C | 3 | a0001c0001t0028g0205a0001c0003t0029g0214a0001c0025t0021g0119 | 3 | HG01934.hp2 HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1473+15826G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030166 | ||||||
| chr12:131030169
|
G | T | 3 | a0001c0001t0028g0205a0001c0003t0029g0214a0001c0025t0021g0119 | 3 | HG01934.hp2 HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1473+15829G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030169 | ||||||
| chr12:131030171
|
AT | A | 12 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0016g0147others(9): Show | 12 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1473+15832delT | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030171 | ||||||
| chr12:131030182
|
C | T | 3 | a0001c0001t0028g0205a0001c0003t0029g0214a0001c0025t0021g0119 | 3 | HG01934.hp2 HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1473+15842C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030182 | ||||||
| chr12:131030211
|
G | T | 12 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0016g0147others(9): Show | 12 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1473+15871G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030211 | ||||||
| chr12:131030214
|
G | A | 12 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0016g0147others(9): Show | 12 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1473+15874G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030214 | ||||||
| chr12:131030216
|
A | AC | 12 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0016g0147others(9): Show | 12 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1473+15876_1473+15 others(7): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030216 | ||||||
| chr12:131030218
|
G | A | 12 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0016g0147others(9): Show | 12 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1473+15878G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030218 | ||||||
| chr12:131030330
|
A | C | 12 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0016g0147others(9): Show | 12 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1473+15990A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030330 | ||||||
| chr12:131030333
|
T | C | 12 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0016g0147others(9): Show | 12 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1473+15993T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030333 | ||||||
| chr12:131030383
|
T | G | 10 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0016g0147others(7): Show | 10 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1473+16043T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030383 | ||||||
| chr12:131030390
|
G | C | 12 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0016g0147others(9): Show | 12 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1473+16050G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030390 | ||||||
| chr12:131030405
|
C | G | 12 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0016g0147others(9): Show | 12 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1473+16065C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030405 | ||||||
| chr12:131030406
|
T | G | 12 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0016g0147others(9): Show | 12 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1473+16066T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030406 | ||||||
| chr12:131030446
|
A | G | 2 | a0001c0001t0002g0228a0001c0001t0002g0235 | 2 | HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1473+16106A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030446 | ||||||
| chr12:131030448
|
G | A | 1 | a0001c0005t0001g0044 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1473+16108G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030448 | ||||||
| chr12:131030468
|
T | G | 29 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0130others(26): Show | 29 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.1473+16128T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030468 | ||||||
| chr12:131030487
|
C | T | 5 | a0001c0003t0013g0129a0001c0007t0004g0018a0001c0022t0016g0109others(2): Show | 5 | HG01934.hp2 HG02572.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1473+16147C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030487 | ||||||
| chr12:131030541
|
A | G | 10 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0016g0147others(7): Show | 10 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1473+16201A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030541 | ||||||
| chr12:131030740
|
G | A | 12 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0016g0147others(9): Show | 12 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1473+16400G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030740 | ||||||
| chr12:131030996
|
G | T | 19 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0130others(16): Show | 19 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.1473+16656G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131030996 | ||||||
| chr12:131031058
|
C | T | 10 | a0001c0003t0018g0232a0001c0007t0018g0132a0001c0042t0007g0176others(7): Show | 10 | HG02257.hp2 HG02258.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1473+16718C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131031058 | ||||||
| chr12:131031168
|
G | C | 108 | a0001c0001t0001g0115a0001c0001t0001g0156a0001c0001t0001g0163others(105): Show | 108 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1473+16828G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131031168 | ||||||
| chr12:131031198
|
C | T | 5 | a0001c0003t0013g0129a0001c0007t0004g0018a0001c0022t0016g0109others(2): Show | 5 | HG01934.hp2 HG02572.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1473+16858C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131031198 | ||||||
| chr12:131031419
|
C | A | 108 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(105): Show | 108 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.1473+17079C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131031419 | ||||||
| chr12:131031500
|
T | C | 218 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(215): Show | 218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.1473+17160T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131031500 | ||||||
| chr12:131031521
|
T | G | 1 | a0001c0001t0015g0060 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1473+17181T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131031521 | ||||||
| chr12:131031535
|
G | C | 8 | a0001c0001t0005g0055a0001c0001t0009g0140a0001c0001t0011g0066others(5): Show | 8 | HG00621.hp1 HG00621.hp2 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.1473+17195G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131031535 | ||||||
| chr12:131031549
|
C | T | 1 | a0003c0012t0017g0017 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1473+17209C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131031549 | ||||||
| chr12:131031593
|
G | C | 4 | a0001c0001t0027g0118a0001c0003t0036g0209a0001c0007t0004g0102others(1): Show | 4 | HG01109.hp1 HG02109.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1473+17253G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131031593 | ||||||
| chr12:131031651
|
C | A | 100 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0156others(97): Show | 100 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.1473+17311C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131031651 | ||||||
| chr12:131031695
|
T | C | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(236): Show | 239 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1473+17355T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131031695 | ||||||
| chr12:131031696
|
G | A | 1 | a0001c0020t0002g0180 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1473+17356G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131031696 | ||||||
| chr12:131031723
|
C | T | 1 | a0001c0004t0002g0164 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1473+17383C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131031723 | ||||||
| chr12:131031825
|
C | T | 40 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0016g0182others(37): Show | 40 | HG00738.hp2 HG01109.hp1 HG01167.hp1 others(37): Show |
intron_variant | MODIFIER | c.1473+17485C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131031825 | ||||||
| chr12:131031874
|
C | T | 9 | a0001c0003t0001g0152a0001c0003t0013g0129a0001c0003t0018g0232others(6): Show | 9 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1473+17534C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131031874 | ||||||
| chr12:131032029
|
C | T | 12 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0208others(9): Show | 12 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.1473+17689C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131032029 | ||||||
| chr12:131032045
|
T | C | 2 | a0001c0002t0001g0145a0001c0002t0001g0146 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1473+17705T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131032045 | ||||||
| chr12:131032109
|
T | C | 12 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0208others(9): Show | 12 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.1473+17769T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131032109 | ||||||
| chr12:131032167
|
C | T | 1 | a0001c0025t0021g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1473+17827C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131032167 | ||||||
| chr12:131032168
|
CCCAGGCT others(3): Show |
C | 12 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0208others(9): Show | 12 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.1473+17830_1473+17 others(16): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131032168 | |||||
| chr12:131032188
|
T | C | 12 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0208others(9): Show | 12 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.1473+17848T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131032188 | ||||||
| chr12:131032217
|
C | T | 1 | a0001c0003t0013g0129 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1473+17877C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131032217 | ||||||
| chr12:131032225
|
G | C | 12 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0208others(9): Show | 12 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.1473+17885G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131032225 | ||||||
| chr12:131032238
|
C | T | 1 | a0002c0030t0032g0159 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1473+17898C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131032238 | ||||||
| chr12:131032299
|
A | G | 1 | a0001c0007t0006g0021 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1473+17959A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131032299 | ||||||
| chr12:131032315
|
C | T | 1 | a0001c0003t0013g0129 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1473+17975C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131032315 | ||||||
| chr12:131032327
|
T | C | 1 | a0003c0033t0030g0231 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1473+17987T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131032327 | ||||||
| chr12:131032338
|
C | T | 12 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0208others(9): Show | 12 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.1473+17998C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131032338 | ||||||
| chr12:131032356
|
CGG | C | 12 | a0001c0003t0001g0152a0001c0003t0013g0129a0001c0003t0018g0117others(9): Show | 12 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1473+18018_1473+18 others(8): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131032356 | |||||
| chr12:131032446
|
G | A | 1 | a0009c0035t0047g0219 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1473+18106G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131032446 | ||||||
| chr12:131032460
|
C | T | 12 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0208others(9): Show | 12 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.1473+18120C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131032460 | ||||||
| chr12:131032475
|
T | C | 7 | a0001c0002t0001g0125a0001c0002t0008g0016a0001c0003t0004g0207others(4): Show | 7 | HG02647.hp1 HG02896.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1473+18135T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131032475 | ||||||
| chr12:131032475
|
TC | T | 24 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0208others(21): Show | 24 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.1473+18139delC | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131032475 | |||||
| chr12:131032521
|
G | A | 12 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0208others(9): Show | 12 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.1473+18181G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131032521 | ||||||
| chr12:131032598
|
C | T | 1 | a0001c0002t0003g0077 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1473+18258C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131032598 | ||||||
| chr12:131032605
|
G | A | 22 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0208others(19): Show | 22 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.1473+18265G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131032605 | ||||||
| chr12:131032672
|
GTCACAGA others(31): Show |
G | 10 | a0001c0003t0004g0234a0001c0005t0001g0112a0001c0005t0001g0127others(7): Show | 10 | HG01167.hp1 HG01243.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1473+18346_1473+18 others(44): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131032672 | |||||
| chr12:131032681
|
A | ATGACGCT others(31): Show |
1 | a0001c0042t0007g0176 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1473+18345_1473+18 others(44): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131032681 | |||||
| chr12:131032686
|
A | G | 1 | a0001c0042t0007g0176 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1473+18346A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131032686 | ||||||
| chr12:131032687
|
T | C | 1 | a0001c0042t0007g0176 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1473+18347T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131032687 | ||||||
| chr12:131032687
|
T | TTTATTAG others(69): Show |
1 | a0003c0040t0022g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1473+18369_1473+18 others(82): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131032687 | |||||
| chr12:131032687
|
TTTATTAG others(69): Show |
T | 3 | a0001c0001t0028g0205a0001c0003t0029g0214a0001c0007t0004g0018 | 3 | HG02280.hp2 HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1473+18370_1473+18 others(82): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131032687 | |||||
| chr12:131032710
|
A | G | 17 | a0001c0001t0016g0147a0001c0001t0027g0118a0001c0002t0001g0223others(14): Show | 17 | HG00738.hp2 HG01496.hp1 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.1473+18370A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131032710 | ||||||
| chr12:131032710
|
ATCACAGA others(31): Show |
A | 9 | a0001c0003t0001g0152a0001c0003t0013g0129a0001c0003t0018g0117others(6): Show | 9 | HG02257.hp2 HG02258.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1473+18379_1473+18 others(44): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131032710 | |||||
| chr12:131032710
|
ATCACAGA others(69): Show |
A | 6 | a0001c0001t0016g0182a0001c0003t0013g0224a0001c0003t0013g0225others(3): Show | 6 | HG02486.hp2 HG02559.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1473+18379_1473+18 others(82): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131032710 | |||||
| chr12:131032719
|
A | ATGACGCT others(108): Show |
1 | a0001c0008t0001g0183 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1473+18384_1473+18 others(121): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131032719 | |||||
| chr12:131032719
|
A | ATGACGCT others(108): Show |
2 | a0001c0002t0003g0077a0001c0005t0001g0044 | 2 | HG02602.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1473+18384_1473+18 others(121): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131032719 | |||||
| chr12:131032719
|
A | ATGACGCT others(107): Show |
42 | a0001c0001t0001g0003a0001c0001t0001g0111a0001c0001t0001g0212others(39): Show | 42 | HG00140.hp1 HG00323.hp1 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.1473+18384_1473+18 others(120): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131032719 | |||||
| chr12:131032719
|
A | ATGACGCT others(145): Show |
2 | a0001c0002t0003g0034a0001c0005t0014g0049 | 2 | HG02040.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1473+18384_1473+18 others(158): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131032719 | |||||
| chr12:131032719
|
A | G | 20 | a0001c0001t0016g0147a0001c0001t0027g0118a0001c0002t0001g0223others(17): Show | 20 | HG00738.hp2 HG01109.hp1 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.1473+18379A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131032719 | ||||||
| chr12:131032719
|
ATGACGTT others(31): Show |
A | 2 | a0001c0002t0003g0064a0001c0004t0005g0094 | 2 | HG02071.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.1473+18385_1473+18 others(44): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131032719 | |||||
| chr12:131032719
|
ATGACGTT others(259): Show |
A | 21 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0130others(18): Show | 21 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.1473+18385_1473+18 others(6): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131032719 | |||||
| chr12:131032725
|
T | C | 86 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(83): Show | 86 | HG00140.hp1 HG00323.hp1 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.1473+18385T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131032725 | ||||||
| chr12:131032725
|
T | TTTATTAG others(31): Show |
2 | a0001c0023t0004g0165a0001c0036t0003g0075 | 2 | HG03669.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1473+18645_1473+18 others(44): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131032725 | |||||
| chr12:131032725
|
TTTATTAG others(31): Show |
T | 14 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0208others(11): Show | 14 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.1473+18645_1473+18 others(44): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131032725 | |||||
| chr12:131032725
|
TTTATTAG others(69): Show |
T | 11 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0002t0001g0125others(8): Show | 11 | HG01884.hp2 HG01934.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.1473+18607_1473+18 others(82): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131032725 | |||||
| chr12:131032725
|
TTTATTAG others(107): Show |
T | 1 | a0001c0002t0046g0084 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1473+18569_1473+18 others(6): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131032725 | |||||
| chr12:131032743
|
A | ACCCCGTC others(32): Show |
1 | a0001c0004t0043g0024 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1473+18407_1473+18 others(45): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131032743 | |||||
| chr12:131032743
|
A | ACCCCGTC others(108): Show |
1 | a0001c0004t0009g0168 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1473+18407_1473+18 others(121): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131032743 | |||||
| chr12:131032763
|
C | T | 9 | a0001c0003t0001g0152a0001c0003t0013g0129a0001c0003t0018g0117others(6): Show | 9 | HG02257.hp2 HG02258.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1473+18423C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131032763 | ||||||
| chr12:131032777
|
C | T | 1 | a0001c0002t0001g0174 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1473+18437C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131032777 | ||||||
| chr12:131032781
|
A | ACCCCCGT others(109): Show |
1 | a0001c0001t0002g0217 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1473+18445_1473+18 others(122): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131032781 | |||||
| chr12:131032781
|
A | ACCCCGTC others(108): Show |
2 | a0001c0003t0006g0015a0001c0003t0006g0211 | 2 | HG01175.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1473+18445_1473+18 others(121): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131032781 | |||||
| chr12:131032792
|
G | GAGGTGAC others(29): Show |
3 | a0001c0005t0008g0226a0003c0012t0017g0017a0006c0037t0042g0046 | 3 | HG02109.hp2 HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1473+18455_1473+18 others(42): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131032792 | |||||
| chr12:131032819
|
A | AC | 6 | a0001c0003t0006g0058a0001c0003t0006g0092a0001c0003t0006g0215others(3): Show | 6 | HG00735.hp1 HG01099.hp2 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1473+18483dupC | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131032819 | |||||
| chr12:131032819
|
A | ACCCCGTC others(108): Show |
1 | a0001c0004t0015g0099 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1473+18483_1473+18 others(121): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131032819 | |||||
| chr12:131032820
|
CCCCGTCA others(68): Show |
C | 1 | a0001c0003t0004g0207 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1473+18484_1473+18 others(81): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131032820 | |||||
| chr12:131032853
|
C | T | 5 | a0001c0001t0016g0182a0001c0003t0013g0224a0001c0003t0013g0225others(2): Show | 5 | HG02486.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1473+18513C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131032853 | ||||||
| chr12:131032857
|
A | ACCCCGTC others(70): Show |
1 | a0001c0004t0043g0024 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1473+18521_1473+18 others(83): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131032857 | |||||
| chr12:131032895
|
A | AC | 5 | a0001c0001t0005g0045a0001c0001t0015g0060a0001c0003t0004g0237others(2): Show | 5 | HG00140.hp2 HG01175.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.1473+18559dupC | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131032895 | |||||
| chr12:131032895
|
A | ACCCCGTC others(108): Show |
3 | a0001c0001t0001g0002a0001c0001t0002g0149a0001c0003t0012g0088 | 3 | HG01361.hp1 HG01884.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1473+18559_1473+18 others(121): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131032895 | |||||
| chr12:131032933
|
A | ACCCCGTC others(108): Show |
1 | a0001c0002t0002g0006 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1473+18682_1473+18 others(121): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131032933 | |||||
| chr12:131032938
|
G | A | 1 | a0001c0003t0013g0129 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1473+18598G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131032938 | ||||||
| chr12:131032940
|
C | T | 1 | a0003c0033t0030g0231 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1473+18600C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131032940 | ||||||
| chr12:131033005
|
C | T | 2 | a0003c0033t0030g0231a0008c0034t0026g0043 | 2 | HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1473+18665C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131033005 | ||||||
| chr12:131033009
|
A | ACCCCCGT others(109): Show |
1 | a0001c0004t0024g0133 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1473+18673_1473+18 others(122): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131033009 | |||||
| chr12:131033013
|
C | CGTCACAG others(31): Show |
2 | a0001c0007t0018g0132a0003c0031t0003g0089 | 2 | HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1473+18682_1473+18 others(44): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131033013 | |||||
| chr12:131033051
|
C | G | 5 | a0001c0002t0002g0001a0001c0002t0002g0006a0001c0002t0002g0009others(2): Show | 5 | HG01257.hp2 HG01433.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.1473+18711C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131033051 | ||||||
| chr12:131033069
|
G | A | 1 | a0001c0022t0016g0109 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1473+18729G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131033069 | ||||||
| chr12:131033079
|
G | A | 93 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(90): Show | 93 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.1473+18739G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131033079 | ||||||
| chr12:131033106
|
C | T | 40 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0208others(37): Show | 40 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.1473+18766C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131033106 | ||||||
| chr12:131033163
|
T | C | 28 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0016g0182others(25): Show | 28 | HG01884.hp2 HG01934.hp2 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.1473+18823T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131033163 | ||||||
| chr12:131033175
|
A | G | 25 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0016g0182others(22): Show | 25 | HG01884.hp2 HG01934.hp2 HG02280.hp2 others(22): Show |
intron_variant | MODIFIER | c.1473+18835A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131033175 | ||||||
| chr12:131033185
|
T | G | 103 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(100): Show | 103 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.1473+18845T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131033185 | ||||||
| chr12:131033190
|
C | T | 1 | a0001c0002t0040g0035 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1473+18850C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131033190 | ||||||
| chr12:131033210
|
G | A | 1 | a0003c0033t0030g0231 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1473+18870G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131033210 | ||||||
| chr12:131033211
|
T | C | 33 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0208others(30): Show | 33 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.1473+18871T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131033211 | ||||||
| chr12:131033221
|
C | T | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(110): Show | 113 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.1473+18881C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131033221 | ||||||
| chr12:131033222
|
T | C | 129 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(126): Show | 129 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.1473+18882T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131033222 | ||||||
| chr12:131033223
|
G | A | 3 | a0001c0005t0008g0226a0003c0012t0017g0017a0006c0037t0042g0046 | 3 | HG02109.hp2 HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1473+18883G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131033223 | ||||||
| chr12:131033248
|
T | G | 30 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0208others(27): Show | 30 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.1473+18908T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131033248 | ||||||
| chr12:131033274
|
G | A | 1 | a0001c0003t0004g0234 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1473+18934G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131033274 | ||||||
| chr12:131033410
|
A | G | 10 | a0001c0001t0016g0182a0001c0003t0013g0224a0001c0003t0013g0225others(7): Show | 10 | HG01934.hp2 HG02109.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1473+19070A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131033410 | ||||||
| chr12:131033542
|
C | T | 1 | a0001c0006t0001g0233 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1473+19202C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131033542 | ||||||
| chr12:131033590
|
G | A | 1 | a0011c0038t0002g0162 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1473+19250G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131033590 | ||||||
| chr12:131033634
|
G | A | 1 | a0007c0039t0001g0229 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1473+19294G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131033634 | ||||||
| chr12:131033812
|
A | G | 1 | a0001c0002t0001g0202 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1473+19472A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131033812 | ||||||
| chr12:131033828
|
C | A | 5 | a0001c0001t0016g0182a0001c0003t0013g0224a0001c0003t0013g0225others(2): Show | 5 | HG02486.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1473+19488C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131033828 | ||||||
| chr12:131033828
|
C | G | 108 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(105): Show | 108 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.1473+19488C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131033828 | ||||||
| chr12:131033896
|
G | A | 11 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0002t0001g0125others(8): Show | 11 | HG01884.hp2 HG02647.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.1473+19556G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131033896 | ||||||
| chr12:131033908
|
A | G | 20 | a0001c0001t0016g0182a0001c0001t0028g0205a0001c0003t0001g0152others(17): Show | 20 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.1473+19568A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131033908 | ||||||
| chr12:131033965
|
C | A | 1 | a0001c0002t0003g0034 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1473+19625C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131033965 | ||||||
| chr12:131033988
|
C | G | 1 | a0001c0001t0015g0097 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1473+19648C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131033988 | ||||||
| chr12:131033994
|
G | A | 1 | a0001c0022t0016g0109 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1473+19654G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131033994 | ||||||
| chr12:131034077
|
A | G | 79 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(76): Show | 79 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.1473+19737A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131034077 | ||||||
| chr12:131034150
|
T | C | 3 | a0001c0001t0002g0217a0001c0003t0004g0012a0001c0003t0004g0198 | 3 | HG03688.hp1 HG04199.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1473+19810T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131034150 | ||||||
| chr12:131034172
|
C | T | 1 | a0001c0046t0017g0221 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1473+19832C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131034172 | ||||||
| chr12:131034202
|
C | T | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(109): Show | 112 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.1473+19862C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131034202 | ||||||
| chr12:131034209
|
C | T | 2 | a0001c0022t0016g0109a0001c0025t0021g0119 | 2 | HG01934.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1473+19869C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131034209 | ||||||
| chr12:131034211
|
A | G | 1 | a0001c0001t0009g0144 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1473+19871A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131034211 | ||||||
| chr12:131034278
|
C | A | 3 | a0001c0001t0002g0217a0001c0003t0004g0012a0001c0003t0004g0198 | 3 | HG03688.hp1 HG04199.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1473+19938C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131034278 | ||||||
| chr12:131034330
|
C | T | 73 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(70): Show | 73 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.1473+19990C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131034330 | ||||||
| chr12:131034436
|
T | A | 86 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(83): Show | 86 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.1473+20096T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131034436 | ||||||
| chr12:131034540
|
G | C | 1 | a0001c0002t0003g0073 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1473+20200G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131034540 | ||||||
| chr12:131034706
|
G | A | 12 | a0001c0003t0001g0152a0001c0003t0013g0129a0001c0003t0018g0232others(9): Show | 12 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1473+20366G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131034706 | ||||||
| chr12:131034720
|
G | T | 78 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(75): Show | 78 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.1473+20380G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131034720 | ||||||
| chr12:131034811
|
C | T | 6 | a0001c0002t0001g0223a0001c0003t0018g0117a0001c0007t0018g0132others(3): Show | 6 | HG01934.hp1 HG02258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1473+20471C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131034811 | ||||||
| chr12:131034819
|
T | C | 11 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0002t0001g0125others(8): Show | 11 | HG01884.hp2 HG02647.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.1473+20479T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131034819 | ||||||
| chr12:131034843
|
T | C | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(109): Show | 112 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.1473+20503T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131034843 | ||||||
| chr12:131034953
|
A | G | 8 | a0001c0001t0028g0205a0001c0003t0029g0214a0001c0005t0008g0226others(5): Show | 8 | HG01934.hp2 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1473+20613A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131034953 | ||||||
| chr12:131034977
|
A | C | 1 | a0001c0001t0011g0033 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1473+20637A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131034977 | ||||||
| chr12:131035034
|
A | G | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(97): Show | 100 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.1473+20694A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131035034 | ||||||
| chr12:131035052
|
C | T | 5 | a0001c0001t0016g0182a0001c0003t0013g0224a0001c0003t0013g0225others(2): Show | 5 | HG02486.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1473+20712C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131035052 | ||||||
| chr12:131035067
|
C | T | 12 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0208others(9): Show | 12 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.1473+20727C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131035067 | ||||||
| chr12:131035116
|
G | A | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(87): Show | 90 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1473+20776G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131035116 | ||||||
| chr12:131035118
|
G | T | 5 | a0001c0005t0008g0226a0001c0022t0016g0109a0001c0025t0021g0119others(2): Show | 5 | HG01934.hp2 HG02109.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1473+20778G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131035118 | ||||||
| chr12:131035119
|
C | A | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(87): Show | 90 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1473+20779C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131035119 | ||||||
| chr12:131035130
|
G | A | 5 | a0001c0003t0001g0152a0001c0003t0013g0129a0002c0018t0020g0123others(2): Show | 5 | HG02257.hp2 HG02630.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1473+20790G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131035130 | ||||||
| chr12:131035139
|
T | C | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(87): Show | 90 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1473+20799T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131035139 | ||||||
| chr12:131035158
|
C | G | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(87): Show | 90 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1473+20818C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131035158 | ||||||
| chr12:131035173
|
C | T | 6 | a0001c0002t0002g0001a0001c0002t0002g0006a0001c0002t0002g0009others(3): Show | 6 | HG00323.hp1 HG01257.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1473+20833C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131035173 | ||||||
| chr12:131035174
|
C | T | 1 | a0001c0003t0004g0013 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1473+20834C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131035174 | ||||||
| chr12:131035245
|
C | T | 3 | a0001c0003t0013g0224a0001c0003t0013g0225a0001c0005t0003g0056 | 3 | HG02896.hp1 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1473+20905C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131035245 | ||||||
| chr12:131035431
|
G | A | 18 | a0001c0001t0005g0055a0001c0001t0009g0137a0001c0001t0009g0140others(15): Show | 18 | HG00738.hp2 HG01496.hp1 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.1473+21091G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131035431 | ||||||
| chr12:131035451
|
C | G | 1 | a0001c0036t0003g0075 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1473+21111C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131035451 | ||||||
| chr12:131035499
|
C | T | 1 | a0001c0007t0006g0021 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1473+21159C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131035499 | ||||||
| chr12:131035512
|
C | T | 3 | a0001c0001t0028g0205a0001c0003t0029g0214a0001c0007t0004g0018 | 3 | HG02280.hp2 HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1473+21172C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131035512 | ||||||
| chr12:131035621
|
G | C | 2 | a0001c0003t0004g0101a0001c0003t0004g0108 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1473+21281G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131035621 | ||||||
| chr12:131035625
|
G | T | 73 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(70): Show | 73 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.1473+21285G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131035625 | ||||||
| chr12:131035626
|
GGT | G | 73 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(70): Show | 73 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.1473+21289_1473+21 others(8): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131035626 | |||||
| chr12:131035663
|
T | C | 123 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(120): Show | 123 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.1473+21323T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131035663 | ||||||
| chr12:131035704
|
A | G | 35 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0208others(32): Show | 35 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.1473+21364A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131035704 | ||||||
| chr12:131036130
|
T | C | 35 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0208others(32): Show | 35 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.1473+21790T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131036130 | ||||||
| chr12:131036149
|
TTACTCAC others(12): Show |
T | 8 | a0001c0001t0028g0205a0001c0003t0029g0214a0001c0005t0008g0226others(5): Show | 8 | HG01934.hp2 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1473+21827_1473+21 others(25): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131036149 | |||||
| chr12:131036194
|
C | T | 1 | a0003c0031t0003g0089 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1473+21854C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131036194 | ||||||
| chr12:131036195
|
G | T | 1 | a0001c0002t0001g0174 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1473+21855G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131036195 | ||||||
| chr12:131036201
|
C | T | 4 | a0001c0001t0016g0182a0001c0003t0013g0224a0001c0003t0013g0225others(1): Show | 4 | HG02486.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1473+21861C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131036201 | ||||||
| chr12:131036218
|
C | T | 1 | a0001c0002t0010g0134 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1473+21878C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131036218 | ||||||
| chr12:131036234
|
A | T | 8 | a0001c0001t0028g0205a0001c0003t0029g0214a0001c0005t0008g0226others(5): Show | 8 | HG01934.hp2 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1473+21894A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131036234 | ||||||
| chr12:131036293
|
T | C | 99 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(96): Show | 99 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1473+21953T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131036293 | ||||||
| chr12:131036436
|
G | GGTCTCAC others(99): Show |
33 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0208others(30): Show | 33 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.1473+22146_1473+22 others(112): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131036436 | |||||
| chr12:131036446
|
A | T | 2 | a0001c0042t0007g0176a0003c0040t0022g0096 | 2 | HG02809.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1473+22106A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131036446 | ||||||
| chr12:131036488
|
C | T | 1 | a0001c0004t0002g0164 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1473+22148C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131036488 | ||||||
| chr12:131036620
|
G | A | 1 | a0001c0001t0003g0026 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1473+22280G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131036620 | ||||||
| chr12:131036625
|
AGGCCTCA others(12): Show |
A | 13 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0002t0001g0125others(10): Show | 13 | HG01884.hp2 HG01934.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.1473+22316_1473+22 others(25): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131036625 | |||||
| chr12:131036642
|
CGGGGCCT others(88): Show |
C | 3 | a0001c0002t0001g0199a0001c0002t0003g0020a0001c0002t0003g0057 | 3 | HG02155.hp2 NA18974.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1473+22322_1473+22 others(101): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131036642 | |||||
| chr12:131036656
|
C | G | 1 | a0001c0001t0015g0097 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1473+22316C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131036656 | ||||||
| chr12:131036662
|
GGGGCCTC others(12): Show |
G | 1 | a0001c0001t0011g0033 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1473+22335_1473+22 others(25): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131036662 | |||||
| chr12:131036675
|
G | C | 47 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(44): Show | 47 | HG00140.hp1 HG00323.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.1473+22335G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131036675 | ||||||
| chr12:131036677
|
A | G | 47 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(44): Show | 47 | HG00140.hp1 HG00323.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.1473+22337A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131036677 | ||||||
| chr12:131036681
|
C | G | 47 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(44): Show | 47 | HG00140.hp1 HG00323.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.1473+22341C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131036681 | ||||||
| chr12:131036694
|
C | G | 47 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(44): Show | 47 | HG00140.hp1 HG00323.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.1473+22354C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131036694 | ||||||
| chr12:131036695
|
T | C | 1 | a0001c0001t0002g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1473+22355T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131036695 | ||||||
| chr12:131036696
|
G | A | 47 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(44): Show | 47 | HG00140.hp1 HG00323.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.1473+22356G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131036696 | ||||||
| chr12:131036700
|
C | G | 1 | a0001c0001t0011g0033 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1473+22360C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131036700 | ||||||
| chr12:131036714
|
CGCACCGG others(31): Show |
C | 1 | a0001c0001t0002g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1473+22397_1473+22 others(44): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131036714 | |||||
| chr12:131036719
|
CGGGCCTC others(12): Show |
C | 50 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(47): Show | 50 | HG00140.hp1 HG00323.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.1473+22397_1473+22 others(25): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131036719 | |||||
| chr12:131036733
|
T | C | 1 | a0001c0001t0011g0033 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1473+22393T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131036733 | ||||||
| chr12:131036737
|
T | C | 33 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0002g0098others(30): Show | 33 | HG00741.hp2 HG01106.hp1 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.1473+22397T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131036737 | ||||||
| chr12:131036738
|
G | C | 1 | a0001c0001t0011g0033 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1473+22398G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131036738 | ||||||
| chr12:131036738
|
GGGGCCTC others(12): Show |
G | 1 | a0001c0001t0016g0147 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1473+22431_1473+22 others(25): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131036738 | |||||
| chr12:131036752
|
T | C | 48 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(45): Show | 48 | HG00140.hp1 HG00323.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.1473+22412T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131036752 | ||||||
| chr12:131036776
|
C | T | 3 | a0001c0003t0004g0121a0001c0003t0004g0122a0001c0003t0012g0027 | 3 | HG02895.hp2 HG02897.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1473+22436C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131036776 | ||||||
| chr12:131036851
|
GC | G | 8 | a0001c0001t0028g0205a0001c0003t0029g0214a0001c0005t0008g0226others(5): Show | 8 | HG01934.hp2 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1473+22513delC | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131036851 | |||||
| chr12:131036883
|
C | A | 1 | a0001c0003t0004g0234 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1473+22543C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131036883 | ||||||
| chr12:131036965
|
A | AATCTTAC others(47): Show |
2 | a0001c0042t0007g0176a0003c0040t0022g0096 | 2 | HG02809.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1473+22633_1473+22 others(60): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131036965 | |||||
| chr12:131036970
|
TACTC | T | 73 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(70): Show | 73 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.1473+22634_1473+22 others(10): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131036970 | |||||
| chr12:131036984
|
A | G | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(142): Show | 145 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.1473+22644A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131036984 | ||||||
| chr12:131037108
|
C | G | 1 | a0001c0005t0001g0044 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1473+22768C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131037108 | ||||||
| chr12:131037110
|
C | T | 3 | a0001c0005t0008g0226a0003c0012t0017g0017a0006c0037t0042g0046 | 3 | HG02109.hp2 HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1473+22770C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131037110 | ||||||
| chr12:131037130
|
T | TGCACCGG others(12): Show |
5 | a0001c0001t0016g0182a0001c0003t0013g0224a0001c0003t0013g0225others(2): Show | 5 | HG02486.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1473+22808_1473+22 others(25): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131037130 | |||||
| chr12:131037136
|
G | A | 12 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0208others(9): Show | 12 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.1473+22796G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131037136 | ||||||
| chr12:131037149
|
G | A | 17 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0208others(14): Show | 17 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.1473+22809G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131037149 | ||||||
| chr12:131037208
|
AGGTCTCA others(12): Show |
A | 35 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0208others(32): Show | 35 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.1473+22888_1473+22 others(25): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131037208 | |||||
| chr12:131037234
|
A | ACTCACTG others(12): Show |
2 | a0002c0029t0031g0222a0010c0026t0013g0238 | 2 | HG02723.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1473+22906_1473+22 others(25): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131037234 | |||||
| chr12:131037273
|
G | C | 1 | a0001c0003t0004g0012 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1473+22933G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131037273 | ||||||
| chr12:131037345
|
CCTCACTC others(312): Show |
C | 4 | a0001c0001t0028g0205a0001c0003t0029g0214a0001c0004t0015g0093others(1): Show | 4 | HG01516.hp1 HG02280.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1473+23033_1473+23 others(6): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131037345 | |||||
| chr12:131037348
|
C | CACTCACT others(12): Show |
37 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0130others(34): Show | 37 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.1473+23024_1473+23 others(25): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131037348 | |||||
| chr12:131037359
|
CTGGGTCT others(86): Show |
C | 2 | a0001c0022t0016g0109a0001c0025t0021g0119 | 2 | HG01934.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1473+23020_1473+23 others(99): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131037359 | ||||||
| chr12:131037367
|
TACTCACT others(105): Show |
T | 56 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(53): Show | 56 | HG00140.hp1 HG00323.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.1473+23043_1473+23 others(6): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131037367 | |||||
| chr12:131037453
|
G | C | 2 | a0001c0022t0016g0109a0001c0025t0021g0119 | 2 | HG01934.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1473+23113G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131037453 | ||||||
| chr12:131037472
|
C | T | 3 | a0001c0004t0005g0070a0001c0022t0016g0109a0001c0025t0021g0119 | 3 | HG01934.hp2 NA19043.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1473+23132C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131037472 | ||||||
| chr12:131037476
|
C | T | 2 | a0001c0022t0016g0109a0001c0025t0021g0119 | 2 | HG01934.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1473+23136C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131037476 | ||||||
| chr12:131037476
|
CCTCACTC others(181): Show |
C | 35 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0005g0055others(32): Show | 35 | HG00738.hp2 HG01496.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.1473+23339_1473+23 others(6): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131037476 | |||||
| chr12:131037479
|
C | T | 2 | a0001c0022t0016g0109a0001c0025t0021g0119 | 2 | HG01934.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1473+23139C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131037479 | ||||||
| chr12:131037504
|
T | C | 58 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(55): Show | 58 | HG00140.hp1 HG00323.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.1473+23164T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131037504 | ||||||
| chr12:131037510
|
T | TG | 58 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(55): Show | 58 | HG00140.hp1 HG00323.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.1473+23173dupG | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131037510 | |||||
| chr12:131037552
|
TCTCACTC others(51): Show |
T | 58 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(55): Show | 58 | HG00140.hp1 HG00323.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.1473+23219_1473+23 others(64): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131037552 | |||||
| chr12:131037596
|
C | A | 1 | a0001c0002t0003g0085 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1473+23256C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131037596 | ||||||
| chr12:131037605
|
GTCTCACT others(201): Show |
G | 22 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0130others(19): Show | 22 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.1473+23269_1473+23 others(6): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131037605 | |||||
| chr12:131037641
|
GGGGCCTC others(180): Show |
G | 27 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0208others(24): Show | 27 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.1473+23305_1473+23 others(6): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131037641 | |||||
| chr12:131037664
|
T | C | 58 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(55): Show | 58 | HG00140.hp1 HG00323.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.1473+23324T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131037664 | ||||||
| chr12:131037669
|
C | T | 1 | a0001c0002t0046g0084 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1473+23329C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131037669 | ||||||
| chr12:131037722
|
C | T | 1 | a0001c0043t0008g0227 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1473+23382C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131037722 | ||||||
| chr12:131037790
|
C | T | 11 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0002t0001g0125others(8): Show | 11 | HG01884.hp2 HG02647.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.1473+23450C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131037790 | ||||||
| chr12:131037793
|
GTCTCACT others(13): Show |
G | 51 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(48): Show | 51 | HG00140.hp1 HG00323.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.1473+23457_1473+23 others(26): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131037793 | |||||
| chr12:131037828
|
T | TG | 10 | a0001c0001t0028g0205a0001c0003t0029g0214a0001c0005t0008g0226others(7): Show | 10 | HG01934.hp2 HG02109.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1473+23492dupG | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131037828 | |||||
| chr12:131037901
|
C | T | 5 | a0001c0001t0016g0182a0001c0003t0013g0224a0001c0003t0013g0225others(2): Show | 5 | HG02486.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1473+23561C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131037901 | ||||||
| chr12:131037906
|
C | T | 12 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0208others(9): Show | 12 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.1473+23566C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131037906 | ||||||
| chr12:131037909
|
G | A | 4 | a0001c0004t0002g0114a0001c0004t0002g0155a0001c0004t0015g0099others(1): Show | 4 | HG00735.hp2 HG01099.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1473+23569G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131037909 | ||||||
| chr12:131037961
|
G | A | 1 | a0001c0003t0004g0237 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1473+23621G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131037961 | ||||||
| chr12:131038218
|
A | G | 1 | a0001c0004t0005g0082 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1473+23878A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131038218 | ||||||
| chr12:131038234
|
G | A | 1 | a0001c0005t0014g0049 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1473+23894G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131038234 | ||||||
| chr12:131038282
|
C | T | 6 | a0001c0001t0027g0118a0001c0003t0036g0209a0001c0022t0016g0109others(3): Show | 6 | HG02257.hp1 HG02451.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1473+23942C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131038282 | ||||||
| chr12:131038283
|
G | A | 5 | a0001c0001t0016g0182a0001c0003t0013g0224a0001c0003t0013g0225others(2): Show | 5 | HG02486.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1473+23943G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131038283 | ||||||
| chr12:131038297
|
G | A | 2 | a0001c0022t0016g0109a0001c0025t0021g0119 | 2 | HG01934.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1473+23957G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131038297 | ||||||
| chr12:131038385
|
A | G | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(99): Show | 102 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1473+24045A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131038385 | ||||||
| chr12:131038390
|
C | T | 1 | a0001c0006t0001g0120 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1473+24050C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131038390 | ||||||
| chr12:131038412
|
G | A | 1 | a0008c0034t0026g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1473+24072G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131038412 | ||||||
| chr12:131038422
|
C | T | 3 | a0001c0001t0002g0217a0001c0003t0004g0012a0001c0003t0004g0198 | 3 | HG03688.hp1 HG04199.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1473+24082C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131038422 | ||||||
| chr12:131038534
|
C | T | 4 | a0001c0001t0016g0182a0001c0003t0013g0224a0001c0003t0013g0225others(1): Show | 4 | HG02486.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1473+24194C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131038534 | ||||||
| chr12:131038558
|
A | G | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(104): Show | 107 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.1473+24218A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131038558 | ||||||
| chr12:131038634
|
C | T | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(104): Show | 107 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.1473+24294C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131038634 | ||||||
| chr12:131038710
|
C | T | 1 | a0002c0030t0032g0159 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1473+24370C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131038710 | ||||||
| chr12:131038716
|
G | A | 80 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(77): Show | 80 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.1473+24376G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131038716 | ||||||
| chr12:131038896
|
T | C | 1 | a0001c0005t0001g0044 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1473+24556T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131038896 | ||||||
| chr12:131038906
|
G | C | 11 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0002t0001g0125others(8): Show | 11 | HG01884.hp2 HG02647.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.1473+24566G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131038906 | ||||||
| chr12:131039038
|
T | C | 108 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(105): Show | 108 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.1473+24698T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131039038 | ||||||
| chr12:131039171
|
TCCTGTGC others(42): Show |
T | 22 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0208others(19): Show | 22 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.1473+24856_1473+24 others(55): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131039171 | |||||
| chr12:131039185
|
A | AG | 7 | a0001c0001t0016g0182a0001c0003t0013g0224a0001c0003t0013g0225others(4): Show | 7 | HG02486.hp2 HG02723.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1473+24846dupG | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131039185 | |||||
| chr12:131039196
|
A | G | 7 | a0001c0001t0016g0182a0001c0003t0013g0224a0001c0003t0013g0225others(4): Show | 7 | HG02486.hp2 HG02723.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1473+24856A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131039196 | ||||||
| chr12:131039220
|
C | T | 7 | a0001c0001t0016g0182a0001c0003t0013g0224a0001c0003t0013g0225others(4): Show | 7 | HG02486.hp2 HG02723.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1473+24880C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131039220 | ||||||
| chr12:131039287
|
T | C | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(118): Show | 121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1473+24947T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131039287 | ||||||
| chr12:131039506
|
C | G | 1 | a0001c0005t0008g0226 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1473+25166C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131039506 | ||||||
| chr12:131039518
|
G | T | 2 | a0001c0042t0007g0176a0003c0040t0022g0096 | 2 | HG02809.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1473+25178G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131039518 | ||||||
| chr12:131039603
|
T | A | 1 | a0001c0005t0008g0226 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1473+25263T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131039603 | ||||||
| chr12:131039662
|
C | T | 1 | a0001c0009t0004g0103 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1473+25322C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131039662 | ||||||
| chr12:131039737
|
A | C | 234 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(231): Show | 234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.1473+25397A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131039737 | ||||||
| chr12:131039908
|
C | T | 2 | a0001c0001t0002g0228a0001c0001t0002g0235 | 2 | HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1473+25568C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131039908 | ||||||
| chr12:131039952
|
G | C | 19 | a0001c0001t0005g0055a0001c0001t0009g0137a0001c0001t0009g0140others(16): Show | 19 | HG00738.hp2 HG01496.hp1 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.1473+25612G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131039952 | ||||||
| chr12:131040085
|
G | T | 1 | a0003c0031t0003g0089 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1473+25745G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131040085 | ||||||
| chr12:131040202
|
G | A | 19 | a0001c0001t0005g0055a0001c0001t0009g0137a0001c0001t0009g0140others(16): Show | 19 | HG00738.hp2 HG01496.hp1 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.1473+25862G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131040202 | ||||||
| chr12:131040219
|
T | C | 12 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0208others(9): Show | 12 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.1473+25879T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131040219 | ||||||
| chr12:131040263
|
C | A | 3 | a0001c0003t0018g0117a0001c0007t0018g0132a0003c0041t0004g0178 | 3 | HG02258.hp1 HG02572.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1473+25923C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131040263 | ||||||
| chr12:131040383
|
A | G | 1 | a0004c0015t0003g0052 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1473+26043A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131040383 | ||||||
| chr12:131040508
|
C | T | 80 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(77): Show | 80 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.1473+26168C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131040508 | ||||||
| chr12:131040609
|
G | C | 1 | a0001c0002t0010g0138 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1473+26269G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131040609 | ||||||
| chr12:131040610
|
C | T | 1 | a0001c0002t0010g0138 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1473+26270C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131040610 | ||||||
| chr12:131040675
|
T | C | 1 | a0001c0010t0039g0031 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1473+26335T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131040675 | ||||||
| chr12:131040765
|
C | T | 72 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(69): Show | 72 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.1473+26425C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131040765 | ||||||
| chr12:131040888
|
T | C | 1 | a0001c0014t0012g0069 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1473+26548T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131040888 | ||||||
| chr12:131040989
|
T | G | 81 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(78): Show | 81 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.1473+26649T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131040989 | ||||||
| chr12:131041011
|
C | CT | 3 | a0001c0001t0002g0116a0001c0042t0007g0176a0003c0040t0022g0096 | 3 | HG02809.hp2 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1473+26671_1473+26 others(7): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131041011 | ||||||
| chr12:131041011
|
C | T | 123 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(120): Show | 123 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.1473+26671C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131041011 | ||||||
| chr12:131041030
|
C | T | 7 | a0001c0001t0016g0182a0001c0003t0013g0224a0001c0003t0013g0225others(4): Show | 7 | HG02486.hp2 HG02723.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1473+26690C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131041030 | ||||||
| chr12:131041092
|
T | C | 3 | a0001c0001t0028g0205a0001c0003t0029g0214a0001c0007t0004g0018 | 3 | HG02280.hp2 HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1473+26752T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131041092 | ||||||
| chr12:131041201
|
G | A | 2 | a0003c0033t0030g0231a0008c0034t0026g0043 | 2 | HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1473+26861G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131041201 | ||||||
| chr12:131041274
|
G | A | 3 | a0001c0001t0002g0217a0001c0003t0004g0012a0001c0003t0004g0198 | 3 | HG03688.hp1 HG04199.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1473+26934G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131041274 | ||||||
| chr12:131041296
|
C | T | 1 | a0002c0030t0032g0159 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1473+26956C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131041296 | ||||||
| chr12:131041407
|
C | T | 1 | a0003c0012t0017g0017 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1473+27067C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131041407 | ||||||
| chr12:131041409
|
A | C | 49 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0191others(46): Show | 49 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.1473+27069A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131041409 | ||||||
| chr12:131041610
|
A | C | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(106): Show | 109 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.1473+27270A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131041610 | ||||||
| chr12:131041706
|
A | G | 6 | a0001c0001t0016g0182a0001c0003t0013g0224a0001c0003t0013g0225others(3): Show | 6 | HG02486.hp2 HG02723.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1473+27366A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131041706 | ||||||
| chr12:131041752
|
C | G | 1 | a0001c0002t0001g0223 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1473+27412C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131041752 | ||||||
| chr12:131041758
|
G | T | 6 | a0001c0001t0016g0182a0001c0003t0013g0224a0001c0003t0013g0225others(3): Show | 6 | HG02486.hp2 HG02723.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1473+27418G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131041758 | ||||||
| chr12:131041776
|
C | T | 2 | a0001c0004t0005g0082a0001c0009t0014g0078 | 2 | HG01346.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1473+27436C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131041776 | ||||||
| chr12:131041777
|
A | G | 86 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(83): Show | 86 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.1473+27437A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131041777 | ||||||
| chr12:131041819
|
C | T | 6 | a0001c0001t0016g0182a0001c0003t0013g0224a0001c0003t0013g0225others(3): Show | 6 | HG02486.hp2 HG02723.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1473+27479C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131041819 | ||||||
| chr12:131041841
|
G | A | 1 | a0001c0042t0007g0176 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1473+27501G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131041841 | ||||||
| chr12:131041868
|
A | G | 1 | a0002c0030t0032g0159 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1473+27528A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131041868 | ||||||
| chr12:131042299
|
G | A | 12 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0208others(9): Show | 12 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.1473+27959G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131042299 | ||||||
| chr12:131042327
|
C | T | 1 | a0005c0021t0021g0048 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1473+27987C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131042327 | ||||||
| chr12:131042349
|
G | A | 12 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0208others(9): Show | 12 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.1473+28009G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131042349 | ||||||
| chr12:131042483
|
A | G | 2 | a0001c0003t0029g0214a0001c0007t0004g0018 | 2 | HG02280.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1473+28143A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131042483 | ||||||
| chr12:131042650
|
C | G | 4 | a0001c0001t0002g0161a0001c0001t0009g0144a0001c0003t0035g0200others(1): Show | 4 | NA18970.hp2 NA18973.hp2 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.1473+28310C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131042650 | ||||||
| chr12:131042677
|
G | A | 1 | a0001c0001t0009g0140 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1473+28337G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131042677 | ||||||
| chr12:131042741
|
G | A | 10 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0002t0001g0125others(7): Show | 10 | HG01884.hp2 HG02647.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.1473+28401G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131042741 | ||||||
| chr12:131042756
|
G | T | 75 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(72): Show | 75 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.1473+28416G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131042756 | ||||||
| chr12:131042979
|
C | G | 1 | a0001c0002t0001g0223 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1473+28639C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131042979 | ||||||
| chr12:131042987
|
G | A | 4 | a0001c0001t0002g0149a0001c0001t0002g0217a0001c0003t0004g0012others(1): Show | 4 | HG01361.hp1 HG03688.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1473+28647G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131042987 | ||||||
| chr12:131043004
|
C | A | 1 | a0008c0034t0026g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1473+28664C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131043004 | ||||||
| chr12:131043095
|
A | T | 1 | a0003c0031t0003g0089 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1473+28755A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131043095 | ||||||
| chr12:131043096
|
C | G | 8 | a0001c0002t0001g0125a0001c0002t0008g0016a0001c0003t0004g0207others(5): Show | 8 | HG02647.hp1 HG02896.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.1473+28756C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131043096 | ||||||
| chr12:131043161
|
C | T | 3 | a0001c0001t0002g0217a0001c0003t0004g0012a0001c0003t0004g0198 | 3 | HG03688.hp1 HG04199.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1473+28821C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131043161 | ||||||
| chr12:131043182
|
G | A | 3 | a0003c0033t0030g0231a0007c0039t0001g0229a0008c0034t0026g0043 | 3 | HG03209.hp2 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1473+28842G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131043182 | ||||||
| chr12:131043182
|
G | C | 1 | a0001c0001t0002g0187 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1473+28842G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131043182 | ||||||
| chr12:131043484
|
G | A | 1 | a0001c0005t0001g0044 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1473+29144G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131043484 | ||||||
| chr12:131043642
|
C | T | 1 | a0003c0031t0003g0089 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1473+29302C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131043642 | ||||||
| chr12:131043652
|
C | T | 1 | a0002c0030t0032g0159 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1473+29312C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131043652 | ||||||
| chr12:131043676
|
C | T | 1 | a0001c0004t0005g0036 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1473+29336C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131043676 | ||||||
| chr12:131043677
|
G | A | 3 | a0001c0001t0002g0217a0001c0003t0004g0012a0001c0003t0004g0198 | 3 | HG03688.hp1 HG04199.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1473+29337G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131043677 | ||||||
| chr12:131043696
|
C | T | 1 | a0001c0001t0016g0147 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1473+29356C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131043696 | ||||||
| chr12:131043946
|
G | A | 12 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0208others(9): Show | 12 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.1473+29606G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131043946 | ||||||
| chr12:131044052
|
C | T | 1 | a0003c0032t0038g0090 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1473+29712C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131044052 | ||||||
| chr12:131044162
|
C | T | 2 | a0001c0001t0001g0197a0001c0001t0003g0023 | 2 | HG00639.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1473+29822C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131044162 | ||||||
| chr12:131044306
|
G | A | 5 | a0001c0001t0001g0111a0001c0001t0001g0191a0001c0001t0001g0197others(2): Show | 5 | HG00280.hp1 HG00639.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.1473+29966G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131044306 | ||||||
| chr12:131044358
|
C | T | 12 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0208others(9): Show | 12 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.1473+30018C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131044358 | ||||||
| chr12:131044359
|
G | C | 1 | a0001c0004t0005g0095 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1473+30019G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131044359 | ||||||
| chr12:131044460
|
C | T | 1 | a0001c0001t0002g0149 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1473+30120C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131044460 | ||||||
| chr12:131044549
|
T | C | 1 | a0003c0032t0038g0090 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1473+30209T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131044549 | ||||||
| chr12:131044647
|
A | C | 118 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0191others(115): Show | 118 | HG00280.hp1 HG00280.hp2 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.1473+30307A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131044647 | ||||||
| chr12:131044656
|
C | T | 3 | a0002c0030t0032g0159a0003c0031t0003g0089a0003c0040t0022g0096 | 3 | HG02630.hp2 HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1473+30316C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131044656 | ||||||
| chr12:131044712
|
T | C | 23 | a0001c0001t0001g0111a0001c0001t0001g0191a0001c0001t0001g0197others(20): Show | 23 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.1473+30372T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131044712 | ||||||
| chr12:131044719
|
G | C | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0115others(86): Show | 89 | HG00140.hp1 HG00323.hp1 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.1473+30379G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131044719 | ||||||
| chr12:131044786
|
C | T | 1 | a0001c0001t0011g0066 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1473+30446C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131044786 | ||||||
| chr12:131044859
|
C | G | 12 | a0001c0003t0004g0207a0001c0005t0001g0044a0001c0005t0001g0112others(9): Show | 12 | HG01167.hp1 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1473+30519C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131044859 | ||||||
| chr12:131044905
|
G | A | 1 | a0001c0002t0003g0050 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1473+30565G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131044905 | ||||||
| chr12:131045505
|
AC | A | 171 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0191others(168): Show | 171 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.1473+31174delC | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131045505 | |||||
| chr12:131045632
|
G | A | 2 | a0001c0001t0016g0182a0008c0034t0026g0043 | 2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1474-31169G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131045632 | ||||||
| chr12:131045762
|
C | G | 26 | a0001c0001t0002g0005a0001c0001t0002g0161a0001c0001t0002g0175others(23): Show | 26 | HG00735.hp1 HG01099.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1474-31039C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131045762 | ||||||
| chr12:131045779
|
C | T | 1 | a0005c0011t0008g0047 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1474-31022C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131045779 | ||||||
| chr12:131045883
|
T | C | 67 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0115others(64): Show | 67 | HG00140.hp1 HG00323.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.1474-30918T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131045883 | ||||||
| chr12:131045946
|
G | A | 12 | a0001c0001t0001g0208a0001c0001t0002g0098a0001c0001t0002g0107others(9): Show | 12 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.1474-30855G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131045946 | ||||||
| chr12:131046031
|
G | T | 3 | a0001c0002t0001g0169a0001c0004t0002g0131a0001c0045t0002g0091 | 3 | HG02056.hp2 HG04115.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.1474-30770G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046031 | ||||||
| chr12:131046040
|
C | T | 14 | a0001c0001t0001g0111a0001c0001t0001g0191a0001c0001t0001g0197others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.1474-30761C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046040 | ||||||
| chr12:131046171
|
T | TCCTGGTC others(395): Show |
1 | a0001c0004t0005g0095 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1474-30601_1474-30 others(408): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131046171 | |||||
| chr12:131046200
|
G | GTC | 164 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0113others(161): Show | 164 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.1474-30601_1474-30 others(8): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046200 | ||||||
| chr12:131046200
|
GCT | G | 20 | a0001c0001t0002g0107a0001c0001t0002g0173a0001c0002t0001g0223others(17): Show | 20 | HG00741.hp2 HG01109.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1474-30599_1474-30 others(8): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131046200 | |||||
| chr12:131046203
|
C | CCCTCCCT others(26): Show |
11 | a0001c0003t0004g0013a0001c0003t0004g0104a0001c0003t0004g0121others(8): Show | 11 | HG00738.hp2 HG01168.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1474-30576_1474-30 others(39): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131046203 | |||||
| chr12:131046203
|
C | CCCTGATC others(409): Show |
1 | a0001c0025t0021g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1474-30595_1474-30 others(422): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131046203 | |||||
| chr12:131046203
|
C | CCCTGGTC others(445): Show |
9 | a0001c0001t0001g0208a0001c0001t0002g0098a0001c0001t0002g0171others(6): Show | 9 | HG00738.hp1 HG01106.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1474-30595_1474-30 others(458): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131046203 | |||||
| chr12:131046203
|
C | CCCTGGTC others(461): Show |
1 | a0001c0001t0002g0204 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1474-30595_1474-30 others(474): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131046203 | |||||
| chr12:131046203
|
C | CCCTGGTC others(427): Show |
9 | a0001c0001t0016g0182a0001c0003t0018g0117a0001c0007t0018g0132others(6): Show | 9 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1474-30595_1474-30 others(440): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131046203 | |||||
| chr12:131046203
|
C | CCCTGGTC others(409): Show |
1 | a0001c0010t0007g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1474-30595_1474-30 others(422): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131046203 | |||||
| chr12:131046203
|
C | CCCTGGTC others(409): Show |
139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0113others(136): Show | 139 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.1474-30595_1474-30 others(422): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131046203 | |||||
| chr12:131046203
|
C | CCCTGGTC others(427): Show |
2 | a0001c0002t0010g0142a0001c0002t0037g0194 | 2 | HG00609.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1474-30595_1474-30 others(440): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131046203 | |||||
| chr12:131046203
|
C | CCCTGGTC others(394): Show |
2 | a0001c0020t0002g0180a0002c0029t0031g0222 | 2 | HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1474-30595_1474-30 others(407): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131046203 | |||||
| chr12:131046203
|
C | T | 20 | a0001c0001t0002g0107a0001c0001t0002g0173a0001c0002t0001g0223others(17): Show | 20 | HG00741.hp2 HG01109.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1474-30598C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046203 | ||||||
| chr12:131046211
|
G | GGTCAGTG others(9): Show |
1 | a0001c0004t0005g0095 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1474-30575_1474-30 others(22): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131046211 | |||||
| chr12:131046211
|
G | T | 163 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0113others(160): Show | 163 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.1474-30590G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046211 | ||||||
| chr12:131046232
|
G | A | 20 | a0001c0001t0002g0107a0001c0001t0002g0173a0001c0002t0001g0223others(17): Show | 20 | HG00741.hp2 HG01109.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1474-30569G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046232 | ||||||
| chr12:131046252
|
TCCTCCTG others(46): Show |
T | 3 | a0001c0003t0013g0224a0001c0003t0013g0225a0008c0034t0026g0043 | 3 | HG02896.hp1 HG02897.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1474-30543_1474-30 others(59): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131046252 | |||||
| chr12:131046266
|
G | A | 17 | a0001c0001t0002g0107a0001c0001t0002g0173a0001c0002t0001g0223others(14): Show | 17 | HG00741.hp2 HG01109.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1474-30535G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046266 | ||||||
| chr12:131046282
|
A | ATGCTCCC others(395): Show |
1 | a0001c0003t0045g0042 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1474-30472_1474-30 others(408): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131046282 | |||||
| chr12:131046287
|
CCCTCCCT others(456): Show |
C | 1 | a0003c0040t0022g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1474-30464_1474-30 others(6): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131046287 | |||||
| chr12:131046300
|
G | GTGCTCCC others(431): Show |
1 | a0001c0001t0002g0107 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1474-30472_1474-30 others(444): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131046300 | |||||
| chr12:131046319
|
T | G | 3 | a0001c0003t0013g0224a0001c0003t0013g0225a0008c0034t0026g0043 | 3 | HG02896.hp1 HG02897.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1474-30482T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046319 | ||||||
| chr12:131046321
|
T | TCCTCCCT others(11): Show |
3 | a0001c0005t0014g0054a0002c0030t0032g0159a0003c0031t0003g0089 | 3 | HG02132.hp1 HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1474-30472_1474-30 others(24): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131046321 | |||||
| chr12:131046321
|
T | TCCTCCCT others(379): Show |
2 | a0001c0001t0002g0173a0001c0003t0019g0218 | 2 | NA18959.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1474-30472_1474-30 others(392): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131046321 | |||||
| chr12:131046330
|
G | T | 13 | a0001c0002t0001g0223a0001c0003t0001g0152a0001c0003t0004g0207others(10): Show | 13 | HG01109.hp1 HG02109.hp1 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.1474-30471G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046330 | ||||||
| chr12:131046335
|
T | C | 3 | a0001c0003t0013g0224a0001c0003t0013g0225a0008c0034t0026g0043 | 3 | HG02896.hp1 HG02897.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1474-30466T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046335 | ||||||
| chr12:131046342
|
T | TCCCTGTT others(11): Show |
10 | a0001c0002t0001g0223a0001c0003t0001g0152a0001c0003t0004g0207others(7): Show | 10 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1474-30454_1474-30 others(24): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131046342 | |||||
| chr12:131046355
|
T | TCCTCCCT others(11): Show |
2 | a0001c0001t0002g0173a0001c0003t0019g0218 | 2 | NA18959.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1474-30444_1474-30 others(24): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131046355 | |||||
| chr12:131046359
|
CCCTGGTC others(6): Show |
C | 2 | a0001c0003t0013g0224a0001c0003t0013g0225 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1474-30438_1474-30 others(19): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131046359 | |||||
| chr12:131046359
|
CCCTGGTC others(22): Show |
C | 1 | a0008c0034t0026g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1474-30438_1474-30 others(35): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131046359 | |||||
| chr12:131046364
|
G | C | 1 | a0001c0003t0001g0152 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1474-30437G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046364 | ||||||
| chr12:131046373
|
C | T | 2 | a0001c0003t0013g0224a0001c0003t0013g0225 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1474-30428C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046373 | ||||||
| chr12:131046389
|
C | T | 1 | a0008c0034t0026g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1474-30412C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046389 | ||||||
| chr12:131046391
|
TC | T | 13 | a0001c0002t0001g0223a0001c0003t0001g0152a0001c0003t0004g0207others(10): Show | 13 | HG01109.hp1 HG02109.hp1 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.1474-30407delC | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131046391 | |||||
| chr12:131046402
|
G | C | 2 | a0001c0003t0013g0224a0001c0003t0013g0225 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1474-30399G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046402 | ||||||
| chr12:131046402
|
G | T | 14 | a0001c0002t0001g0223a0001c0003t0001g0152a0001c0003t0004g0207others(11): Show | 14 | HG01109.hp1 HG02109.hp1 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.1474-30399G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046402 | ||||||
| chr12:131046403
|
G | T | 1 | a0001c0004t0002g0164 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1474-30398G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046403 | ||||||
| chr12:131046403
|
GTCCTCCC others(29): Show |
G | 2 | a0001c0003t0013g0224a0001c0003t0013g0225 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1474-30397_1474-30 others(42): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046403 | ||||||
| chr12:131046418
|
C | T | 13 | a0001c0002t0001g0223a0001c0003t0001g0152a0001c0003t0004g0207others(10): Show | 13 | HG01109.hp1 HG02109.hp1 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.1474-30383C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046418 | ||||||
| chr12:131046423
|
CCTCCCTG others(13): Show |
C | 1 | a0008c0034t0026g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1474-30358_1474-30 others(26): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131046423 | |||||
| chr12:131046437
|
GTC | G | 12 | a0001c0002t0001g0223a0001c0003t0001g0152a0001c0003t0004g0207others(9): Show | 12 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1474-30363_1474-30 others(8): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046437 | ||||||
| chr12:131046439
|
C | A | 1 | a0001c0004t0002g0007 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1474-30362C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046439 | ||||||
| chr12:131046439
|
C | CTTCTCTC others(27): Show |
1 | a0001c0042t0007g0176 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1474-30362_1474-30 others(40): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046439 | ||||||
| chr12:131046442
|
C | CCCTTGTC others(157): Show |
1 | a0001c0005t0014g0054 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1474-30359_1474-30 others(170): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046442 | ||||||
| chr12:131046443
|
T | C | 16 | a0001c0002t0001g0223a0001c0003t0001g0152a0001c0003t0004g0207others(13): Show | 16 | HG01109.hp1 HG02109.hp1 HG02132.hp1 others(13): Show |
intron_variant | MODIFIER | c.1474-30358T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046443 | ||||||
| chr12:131046443
|
T | TCTCCCTG others(27): Show |
45 | a0001c0001t0001g0208a0001c0001t0002g0098a0001c0001t0002g0107others(42): Show | 45 | HG00735.hp1 HG00738.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.1474-30329_1474-30 others(40): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131046443 | |||||
| chr12:131046450
|
G | GGTCAGTG others(311): Show |
10 | a0001c0002t0001g0223a0001c0003t0001g0152a0001c0003t0013g0129others(7): Show | 10 | HG02109.hp1 HG02257.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1474-30336_1474-30 others(324): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131046450 | |||||
| chr12:131046450
|
G | GGTCAGTG others(293): Show |
2 | a0001c0003t0004g0207a0001c0007t0004g0102 | 2 | HG01109.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1474-30336_1474-30 others(306): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131046450 | |||||
| chr12:131046450
|
G | T | 1 | a0001c0005t0014g0054 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1474-30351G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046450 | ||||||
| chr12:131046458
|
TCCTCCCT others(115): Show |
T | 1 | a0001c0013t0007g0154 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1474-30329_1474-30 others(6): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131046458 | |||||
| chr12:131046472
|
C | T | 13 | a0001c0002t0001g0223a0001c0003t0001g0152a0001c0003t0004g0207others(10): Show | 13 | HG01109.hp1 HG02109.hp1 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.1474-30329C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046472 | ||||||
| chr12:131046475
|
TC | T | 13 | a0001c0002t0001g0223a0001c0003t0001g0152a0001c0003t0004g0207others(10): Show | 13 | HG01109.hp1 HG02109.hp1 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.1474-30323delC | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131046475 | |||||
| chr12:131046495
|
TC | T | 13 | a0001c0002t0001g0223a0001c0003t0001g0152a0001c0003t0004g0207others(10): Show | 13 | HG01109.hp1 HG02109.hp1 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.1474-30303delC | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131046495 | |||||
| chr12:131046506
|
T | C | 5 | a0003c0012t0017g0017a0003c0012t0017g0158a0003c0041t0004g0178others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1474-30295T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046506 | ||||||
| chr12:131046509
|
C | T | 18 | a0001c0002t0001g0223a0001c0003t0001g0152a0001c0003t0004g0207others(15): Show | 18 | HG01109.hp1 HG02109.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1474-30292C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046509 | ||||||
| chr12:131046523
|
A | G | 5 | a0003c0012t0017g0017a0003c0012t0017g0158a0003c0041t0004g0178others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1474-30278A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046523 | ||||||
| chr12:131046525
|
GCT | G | 5 | a0003c0012t0017g0017a0003c0012t0017g0158a0003c0041t0004g0178others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1474-30274_1474-30 others(8): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131046525 | |||||
| chr12:131046528
|
C | T | 5 | a0003c0012t0017g0017a0003c0012t0017g0158a0003c0041t0004g0178others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1474-30273C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046528 | ||||||
| chr12:131046537
|
A | G | 185 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0113others(182): Show | 185 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1474-30264A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046537 | ||||||
| chr12:131046545
|
C | T | 13 | a0001c0002t0001g0223a0001c0003t0001g0152a0001c0003t0004g0207others(10): Show | 13 | HG01109.hp1 HG02109.hp1 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.1474-30256C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046545 | ||||||
| chr12:131046556
|
C | T | 18 | a0001c0002t0001g0223a0001c0003t0001g0152a0001c0003t0004g0207others(15): Show | 18 | HG01109.hp1 HG02109.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1474-30245C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046556 | ||||||
| chr12:131046559
|
G | A | 5 | a0003c0012t0017g0017a0003c0012t0017g0158a0003c0041t0004g0178others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1474-30242G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046559 | ||||||
| chr12:131046561
|
G | GCT | 5 | a0003c0012t0017g0017a0003c0012t0017g0158a0003c0041t0004g0178others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1474-30240_1474-30 others(8): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046561 | ||||||
| chr12:131046562
|
T | C | 5 | a0003c0012t0017g0017a0003c0012t0017g0158a0003c0041t0004g0178others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1474-30239T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046562 | ||||||
| chr12:131046573
|
G | C | 18 | a0001c0002t0001g0223a0001c0003t0001g0152a0001c0003t0004g0207others(15): Show | 18 | HG01109.hp1 HG02109.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1474-30228G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046573 | ||||||
| chr12:131046579
|
T | C | 5 | a0003c0012t0017g0017a0003c0012t0017g0158a0003c0041t0004g0178others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1474-30222T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046579 | ||||||
| chr12:131046590
|
T | C | 5 | a0003c0012t0017g0017a0003c0012t0017g0158a0003c0041t0004g0178others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1474-30211T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046590 | ||||||
| chr12:131046596
|
T | TCCTCCCT others(200): Show |
12 | a0001c0002t0001g0223a0001c0003t0001g0152a0001c0003t0004g0207others(9): Show | 12 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1474-30189_1474-30 others(213): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131046596 | |||||
| chr12:131046607
|
C | G | 5 | a0003c0012t0017g0017a0003c0012t0017g0158a0003c0041t0004g0178others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1474-30194C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046607 | ||||||
| chr12:131046610
|
T | TGCTCCTC others(96): Show |
1 | a0001c0005t0014g0054 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1474-30189_1474-30 others(109): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131046610 | |||||
| chr12:131046613
|
C | T | 6 | a0001c0005t0014g0054a0003c0012t0017g0017a0003c0012t0017g0158others(3): Show | 6 | HG02109.hp2 HG02132.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1474-30188C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046613 | ||||||
| chr12:131046624
|
G | T | 10 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0003t0033g0181others(7): Show | 10 | HG01106.hp2 HG01261.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.1474-30177G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046624 | ||||||
| chr12:131046647
|
T | C | 6 | a0001c0005t0014g0054a0003c0012t0017g0017a0003c0012t0017g0158others(3): Show | 6 | HG02109.hp2 HG02132.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1474-30154T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046647 | ||||||
| chr12:131046658
|
T | G | 5 | a0003c0012t0017g0017a0003c0012t0017g0158a0003c0041t0004g0178others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1474-30143T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046658 | ||||||
| chr12:131046661
|
G | A | 1 | a0001c0005t0014g0054 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1474-30140G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046661 | ||||||
| chr12:131046664
|
T | C | 1 | a0001c0005t0014g0054 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1474-30137T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046664 | ||||||
| chr12:131046692
|
G | C | 1 | a0001c0005t0014g0054 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1474-30109G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046692 | ||||||
| chr12:131046709
|
G | C | 1 | a0001c0001t0002g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1474-30092G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046709 | ||||||
| chr12:131046716
|
C | CCCTCCCT others(792): Show |
1 | a0001c0001t0002g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1474-30073_1474-30 others(805): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131046716 | |||||
| chr12:131046716
|
C | CCCTCCCT others(9): Show |
1 | a0001c0005t0014g0054 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1474-30070_1474-30 others(22): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131046716 | |||||
| chr12:131046733
|
CCCCTCCC others(27): Show |
C | 1 | a0001c0005t0001g0239 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1474-30057_1474-30 others(40): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131046733 | |||||
| chr12:131046760
|
T | A | 1 | a0003c0033t0030g0231 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1474-30041T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046760 | ||||||
| chr12:131046761
|
C | G | 1 | a0003c0031t0003g0089 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1474-30040C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046761 | ||||||
| chr12:131046784
|
T | TCCTCCCT others(97): Show |
1 | a0001c0001t0002g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1474-30002_1474-30 others(110): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131046784 | |||||
| chr12:131046794
|
T | G | 120 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0113others(117): Show | 120 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.1474-30007T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046794 | ||||||
| chr12:131046794
|
TCAGTGTC others(9): Show |
T | 2 | a0001c0001t0016g0182a0001c0042t0007g0176 | 2 | HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1474-29991_1474-29 others(22): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131046794 | |||||
| chr12:131046810
|
G | T | 1 | a0001c0001t0002g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1474-29991G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046810 | ||||||
| chr12:131046859
|
G | A | 3 | a0001c0001t0002g0116a0001c0001t0016g0182a0001c0042t0007g0176 | 3 | HG02486.hp2 HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1474-29942G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046859 | ||||||
| chr12:131046866
|
TCCTCCCT others(11): Show |
T | 4 | a0001c0002t0003g0050a0001c0004t0005g0036a0001c0004t0005g0072others(1): Show | 4 | HG02040.hp1 HG02083.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.1474-29922_1474-29 others(24): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131046866 | |||||
| chr12:131046871
|
C | T | 4 | a0001c0004t0002g0114a0001c0004t0002g0155a0001c0004t0015g0099others(1): Show | 4 | HG00735.hp2 HG01099.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1474-29930C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131046871 | ||||||
| chr12:131047062
|
C | T | 1 | a0001c0001t0009g0144 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1474-29739C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131047062 | ||||||
| chr12:131047081
|
T | C | 1 | a0008c0034t0026g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1474-29720T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131047081 | ||||||
| chr12:131047222
|
A | T | 2 | a0001c0003t0013g0224a0001c0003t0013g0225 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1474-29579A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131047222 | ||||||
| chr12:131047324
|
A | G | 230 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(227): Show | 230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.1474-29477A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131047324 | ||||||
| chr12:131047375
|
T | C | 1 | a0001c0005t0001g0112 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1474-29426T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131047375 | ||||||
| chr12:131047380
|
G | C | 1 | a0001c0002t0010g0142 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1474-29421G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131047380 | ||||||
| chr12:131047412
|
T | C | 4 | a0001c0001t0002g0116a0001c0001t0016g0182a0001c0007t0004g0018others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1474-29389T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131047412 | ||||||
| chr12:131047597
|
C | T | 1 | a0001c0003t0004g0104 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1474-29204C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131047597 | ||||||
| chr12:131047693
|
G | A | 1 | a0001c0022t0016g0109 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1474-29108G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131047693 | ||||||
| chr12:131047967
|
T | A | 3 | a0001c0001t0011g0066a0001c0001t0011g0074a0001c0001t0023g0143 | 3 | HG02132.hp2 NA18957.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1474-28834T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131047967 | ||||||
| chr12:131047989
|
G | A | 1 | a0001c0001t0002g0149 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1474-28812G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131047989 | ||||||
| chr12:131048040
|
G | A | 1 | a0001c0023t0004g0165 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1474-28761G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131048040 | ||||||
| chr12:131048207
|
G | A | 1 | a0002c0030t0032g0159 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1474-28594G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131048207 | ||||||
| chr12:131048302
|
C | T | 1 | a0001c0003t0044g0079 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1474-28499C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131048302 | ||||||
| chr12:131048362
|
A | G | 1 | a0001c0002t0003g0068 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1474-28439A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131048362 | ||||||
| chr12:131048391
|
G | A | 1 | a0001c0025t0021g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1474-28410G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131048391 | ||||||
| chr12:131048440
|
G | A | 7 | a0001c0003t0013g0224a0001c0003t0013g0225a0001c0003t0036g0209others(4): Show | 7 | HG02257.hp1 HG02559.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1474-28361G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131048440 | ||||||
| chr12:131048582
|
C | T | 1 | a0001c0003t0036g0209 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1474-28219C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131048582 | ||||||
| chr12:131048792
|
A | T | 1 | a0001c0003t0044g0079 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1474-28009A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131048792 | ||||||
| chr12:131048841
|
C | T | 10 | a0001c0001t0001g0208a0001c0001t0002g0098a0001c0001t0002g0107others(7): Show | 10 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.1474-27960C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131048841 | ||||||
| chr12:131048904
|
T | A | 1 | a0001c0004t0002g0164 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1474-27897T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131048904 | ||||||
| chr12:131048921
|
G | A | 1 | a0001c0003t0018g0117 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1474-27880G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131048921 | ||||||
| chr12:131049021
|
G | C | 1 | a0001c0001t0001g0111 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1474-27780G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131049021 | ||||||
| chr12:131049066
|
G | A | 10 | a0001c0001t0001g0208a0001c0001t0002g0098a0001c0001t0002g0107others(7): Show | 10 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.1474-27735G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131049066 | ||||||
| chr12:131049163
|
C | T | 2 | a0001c0001t0016g0182a0001c0042t0007g0176 | 2 | HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1474-27638C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131049163 | ||||||
| chr12:131049304
|
G | A | 10 | a0001c0001t0001g0208a0001c0001t0002g0098a0001c0001t0002g0107others(7): Show | 10 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.1474-27497G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131049304 | ||||||
| chr12:131049432
|
T | C | 214 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(211): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.1474-27369T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131049432 | ||||||
| chr12:131049449
|
C | T | 1 | a0001c0002t0003g0034 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1474-27352C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131049449 | ||||||
| chr12:131049646
|
C | A | 80 | a0001c0001t0002g0116a0001c0001t0002g0161a0001c0001t0002g0173others(77): Show | 80 | HG00735.hp1 HG00738.hp2 HG01099.hp2 others(77): Show |
intron_variant | MODIFIER | c.1474-27155C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131049646 | ||||||
| chr12:131049698
|
C | T | 3 | a0001c0001t0002g0116a0001c0001t0016g0182a0001c0042t0007g0176 | 3 | HG02486.hp2 HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1474-27103C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131049698 | ||||||
| chr12:131050123
|
G | C | 5 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0003g0023others(2): Show | 5 | HG00639.hp1 HG01074.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.1474-26678G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131050123 | ||||||
| chr12:131050218
|
G | GTCA | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(121): Show | 124 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.1474-26564_1474-26 others(9): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131050218 | |||||
| chr12:131050537
|
G | A | 1 | a0001c0022t0016g0109 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1474-26264G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131050537 | ||||||
| chr12:131050646
|
C | A | 2 | a0001c0001t0002g0116a0001c0042t0007g0176 | 2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1474-26155C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131050646 | ||||||
| chr12:131050655
|
G | A | 4 | a0001c0001t0011g0062a0001c0002t0010g0142a0001c0002t0037g0194others(1): Show | 4 | HG00609.hp2 NA18612.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.1474-26146G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131050655 | ||||||
| chr12:131050686
|
G | C | 4 | a0001c0001t0002g0116a0001c0001t0016g0147a0001c0001t0016g0182others(1): Show | 4 | HG02280.hp1 HG02486.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1474-26115G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131050686 | ||||||
| chr12:131050726
|
C | T | 5 | a0001c0001t0002g0130a0001c0002t0003g0050a0001c0004t0005g0036others(2): Show | 5 | HG02040.hp1 HG02083.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.1474-26075C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131050726 | ||||||
| chr12:131050951
|
G | A | 1 | a0001c0007t0004g0236 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1474-25850G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131050951 | ||||||
| chr12:131050996
|
C | A | 1 | a0001c0002t0001g0169 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1474-25805C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131050996 | ||||||
| chr12:131050998
|
C | T | 1 | a0001c0010t0007g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1474-25803C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131050998 | ||||||
| chr12:131051013
|
C | T | 23 | a0001c0001t0002g0161a0001c0001t0002g0173a0001c0001t0002g0175others(20): Show | 23 | HG00735.hp1 HG01099.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1474-25788C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131051013 | ||||||
| chr12:131051047
|
A | G | 1 | a0001c0014t0012g0069 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1474-25754A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131051047 | ||||||
| chr12:131051241
|
G | A | 2 | a0001c0002t0003g0041a0001c0002t0025g0141 | 2 | NA18992.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1474-25560G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131051241 | ||||||
| chr12:131051255
|
G | T | 1 | a0001c0002t0003g0071 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1474-25546G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131051255 | ||||||
| chr12:131051286
|
A | G | 1 | a0001c0022t0016g0109 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1474-25515A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131051286 | ||||||
| chr12:131051486
|
C | CTTTG | 207 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(204): Show | 207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1474-25312_1474-25 others(10): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131051486 | |||||
| chr12:131051486
|
C | CTTTGT | 19 | a0001c0001t0002g0173a0001c0001t0002g0175a0001c0001t0002g0228others(16): Show | 19 | HG01109.hp2 HG01884.hp2 HG01934.hp2 others(16): Show |
intron_variant | MODIFIER | c.1474-25312_1474-25 others(11): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131051486 | |||||
| chr12:131051486
|
C | CTTTGTT | 9 | a0001c0001t0002g0161a0001c0001t0009g0144a0001c0003t0006g0092others(6): Show | 9 | HG00735.hp1 HG01099.hp2 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.1474-25312_1474-25 others(12): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131051486 | |||||
| chr12:131051544
|
C | T | 16 | a0001c0002t0001g0223a0001c0003t0001g0152a0001c0003t0004g0207others(13): Show | 16 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1474-25257C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131051544 | ||||||
| chr12:131051754
|
G | C | 1 | a0003c0040t0022g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1474-25047G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131051754 | ||||||
| chr12:131052156
|
C | T | 1 | a0001c0003t0044g0079 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1474-24645C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131052156 | ||||||
| chr12:131052260
|
A | C | 1 | a0001c0010t0007g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1474-24541A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131052260 | ||||||
| chr12:131052272
|
A | G | 122 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(119): Show | 122 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.1474-24529A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131052272 | ||||||
| chr12:131052308
|
C | T | 5 | a0001c0001t0002g0116a0001c0001t0016g0147a0001c0001t0016g0182others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1474-24493C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131052308 | ||||||
| chr12:131052309
|
G | A | 3 | a0001c0002t0003g0032a0001c0002t0003g0076a0001c0002t0040g0035 | 3 | HG00280.hp2 HG00609.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1474-24492G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131052309 | ||||||
| chr12:131052524
|
G | A | 1 | a0005c0011t0008g0047 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1474-24277G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131052524 | ||||||
| chr12:131052586
|
G | A | 1 | a0001c0003t0002g0186 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1474-24215G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131052586 | ||||||
| chr12:131052605
|
G | C | 1 | a0001c0010t0007g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1474-24196G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131052605 | ||||||
| chr12:131052643
|
T | TG | 210 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(207): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.1474-24153dupG | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131052643 | |||||
| chr12:131052695
|
A | G | 1 | a0008c0034t0026g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1474-24106A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131052695 | ||||||
| chr12:131052924
|
C | T | 3 | a0001c0001t0002g0116a0001c0001t0016g0147a0001c0001t0016g0182 | 3 | HG02280.hp1 HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1474-23877C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131052924 | ||||||
| chr12:131053276
|
G | A | 1 | a0001c0002t0010g0201 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1474-23525G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131053276 | ||||||
| chr12:131053532
|
C | T | 7 | a0003c0012t0017g0017a0003c0012t0017g0158a0003c0032t0038g0090others(4): Show | 7 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1474-23269C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131053532 | ||||||
| chr12:131053615
|
A | G | 1 | a0002c0029t0031g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1474-23186A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131053615 | ||||||
| chr12:131053753
|
C | T | 19 | a0001c0001t0002g0161a0001c0001t0002g0173a0001c0001t0002g0175others(16): Show | 19 | HG00735.hp1 HG01099.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1474-23048C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131053753 | ||||||
| chr12:131053859
|
A | G | 1 | a0001c0009t0014g0037 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1474-22942A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131053859 | ||||||
| chr12:131054085
|
C | T | 11 | a0001c0003t0004g0013a0001c0003t0004g0104a0001c0003t0004g0121others(8): Show | 11 | HG00738.hp2 HG01168.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1474-22716C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131054085 | ||||||
| chr12:131054224
|
G | A | 2 | a0001c0001t0002g0161a0001c0001t0009g0144 | 2 | NA18970.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1474-22577G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131054224 | ||||||
| chr12:131054577
|
T | C | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(205): Show | 208 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.1474-22224T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131054577 | ||||||
| chr12:131054634
|
C | T | 24 | a0001c0001t0002g0161a0001c0001t0002g0173a0001c0001t0002g0175others(21): Show | 24 | HG00735.hp1 HG01099.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1474-22167C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131054634 | ||||||
| chr12:131054666
|
C | T | 2 | a0001c0002t0003g0061a0001c0006t0008g0177 | 2 | HG01496.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1474-22135C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131054666 | ||||||
| chr12:131054703
|
C | G | 1 | a0003c0031t0003g0089 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1474-22098C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131054703 | ||||||
| chr12:131054842
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1474-21959G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131054842 | ||||||
| chr12:131054966
|
C | T | 1 | a0001c0042t0007g0176 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1474-21835C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131054966 | ||||||
| chr12:131054973
|
C | T | 1 | a0001c0009t0014g0037 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1474-21828C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131054973 | ||||||
| chr12:131055026
|
G | C | 122 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(119): Show | 122 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.1474-21775G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131055026 | ||||||
| chr12:131055115
|
T | C | 122 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(119): Show | 122 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.1474-21686T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131055115 | ||||||
| chr12:131055286
|
C | T | 1 | a0001c0003t0036g0209 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1474-21515C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131055286 | ||||||
| chr12:131055374
|
C | T | 1 | a0001c0004t0005g0072 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1474-21427C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131055374 | ||||||
| chr12:131055829
|
T | C | 1 | a0001c0025t0021g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1474-20972T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131055829 | ||||||
| chr12:131055927
|
C | T | 11 | a0001c0001t0001g0208a0001c0001t0002g0098a0001c0001t0002g0107others(8): Show | 11 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.1474-20874C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131055927 | ||||||
| chr12:131055976
|
T | C | 11 | a0001c0001t0001g0208a0001c0001t0002g0098a0001c0001t0002g0107others(8): Show | 11 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.1474-20825T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131055976 | ||||||
| chr12:131056284
|
C | T | 1 | a0001c0022t0016g0109 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1474-20517C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131056284 | ||||||
| chr12:131056426
|
C | T | 7 | a0003c0012t0017g0017a0003c0012t0017g0158a0003c0032t0038g0090others(4): Show | 7 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1474-20375C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131056426 | ||||||
| chr12:131056774
|
C | T | 174 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(171): Show | 174 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.1474-20027C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131056774 | ||||||
| chr12:131056884
|
C | T | 1 | a0001c0004t0002g0193 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1474-19917C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131056884 | ||||||
| chr12:131056894
|
C | A | 1 | a0001c0010t0007g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1474-19907C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131056894 | ||||||
| chr12:131056895
|
A | T | 1 | a0001c0010t0007g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1474-19906A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131056895 | ||||||
| chr12:131056978
|
G | A | 1 | a0001c0003t0036g0209 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1474-19823G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131056978 | ||||||
| chr12:131057118
|
G | A | 3 | a0001c0003t0013g0224a0001c0003t0013g0225a0008c0034t0026g0043 | 3 | HG02896.hp1 HG02897.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1474-19683G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131057118 | ||||||
| chr12:131057435
|
C | T | 11 | a0001c0001t0001g0208a0001c0001t0002g0098a0001c0001t0002g0107others(8): Show | 11 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.1474-19366C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131057435 | ||||||
| chr12:131057489
|
G | A | 7 | a0001c0001t0005g0045a0001c0002t0001g0202a0001c0002t0002g0006others(4): Show | 7 | HG00323.hp1 HG01261.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.1474-19312G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131057489 | ||||||
| chr12:131057642
|
G | A | 1 | a0001c0003t0036g0209 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1474-19159G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131057642 | ||||||
| chr12:131057770
|
T | C | 3 | a0001c0002t0003g0032a0001c0002t0003g0076a0001c0002t0040g0035 | 3 | HG00280.hp2 HG00609.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1474-19031T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131057770 | ||||||
| chr12:131057879
|
C | A | 1 | a0002c0029t0031g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1474-18922C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131057879 | ||||||
| chr12:131058141
|
C | G | 1 | a0002c0028t0001g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1474-18660C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131058141 | ||||||
| chr12:131058346
|
T | C | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(206): Show | 209 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1474-18455T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131058346 | ||||||
| chr12:131058378
|
G | A | 3 | a0001c0001t0016g0147a0001c0001t0016g0182a0001c0042t0007g0176 | 3 | HG02280.hp1 HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1474-18423G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131058378 | ||||||
| chr12:131058386
|
T | G | 1 | a0001c0003t0041g0080 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1474-18415T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131058386 | ||||||
| chr12:131058507
|
A | G | 46 | a0001c0002t0001g0169a0001c0002t0001g0223a0001c0003t0001g0152others(43): Show | 46 | HG00738.hp2 HG01109.hp1 HG01168.hp1 others(43): Show |
intron_variant | MODIFIER | c.1474-18294A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131058507 | ||||||
| chr12:131058687
|
C | T | 1 | a0001c0025t0021g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1474-18114C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131058687 | ||||||
| chr12:131058724
|
C | A | 2 | a0001c0002t0010g0142a0001c0002t0037g0194 | 2 | HG00609.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1474-18077C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131058724 | ||||||
| chr12:131058990
|
G | A | 1 | a0002c0029t0031g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1474-17811G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131058990 | ||||||
| chr12:131059283
|
C | T | 1 | a0001c0003t0012g0088 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1474-17518C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131059283 | ||||||
| chr12:131059340
|
A | G | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(205): Show | 208 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.1474-17461A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131059340 | ||||||
| chr12:131059372
|
G | A | 1 | a0001c0001t0011g0220 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1474-17429G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131059372 | ||||||
| chr12:131059747
|
A | T | 1 | a0001c0001t0002g0173 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1474-17054A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131059747 | ||||||
| chr12:131059753
|
A | G | 11 | a0001c0001t0001g0208a0001c0001t0002g0098a0001c0001t0002g0107others(8): Show | 11 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.1474-17048A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131059753 | ||||||
| chr12:131059886
|
T | G | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(206): Show | 209 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1474-16915T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131059886 | ||||||
| chr12:131059925
|
C | T | 1 | a0001c0001t0015g0060 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1474-16876C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131059925 | ||||||
| chr12:131060040
|
A | C | 1 | a0001c0009t0014g0037 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1474-16761A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131060040 | ||||||
| chr12:131060041
|
G | T | 1 | a0002c0029t0031g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1474-16760G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131060041 | ||||||
| chr12:131060066
|
G | A | 5 | a0003c0012t0017g0017a0003c0012t0017g0158a0003c0041t0004g0178others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1474-16735G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131060066 | ||||||
| chr12:131060081
|
C | T | 1 | a0001c0020t0002g0180 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1474-16720C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131060081 | ||||||
| chr12:131060089
|
T | C | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(205): Show | 208 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.1474-16712T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131060089 | ||||||
| chr12:131060287
|
G | A | 1 | a0001c0003t0044g0079 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1474-16514G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131060287 | ||||||
| chr12:131060352
|
C | G | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(206): Show | 209 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1474-16449C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131060352 | ||||||
| chr12:131060361
|
T | G | 1 | a0001c0003t0006g0015 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1474-16440T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131060361 | ||||||
| chr12:131060837
|
T | A | 1 | a0001c0003t0004g0234 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1474-15964T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131060837 | ||||||
| chr12:131061090
|
A | G | 17 | a0001c0002t0001g0223a0001c0003t0001g0152a0001c0003t0004g0207others(14): Show | 17 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.1474-15711A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131061090 | ||||||
| chr12:131061226
|
G | A | 1 | a0001c0023t0004g0165 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1474-15575G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131061226 | ||||||
| chr12:131061341
|
C | T | 1 | a0001c0002t0003g0057 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1474-15460C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131061341 | ||||||
| chr12:131061403
|
G | A | 1 | a0001c0010t0007g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1474-15398G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131061403 | ||||||
| chr12:131061449
|
T | C | 1 | a0001c0002t0003g0064 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1474-15352T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131061449 | ||||||
| chr12:131061501
|
T | A | 1 | a0001c0002t0046g0084 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1474-15300T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131061501 | ||||||
| chr12:131062032
|
G | T | 1 | a0003c0031t0003g0089 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1474-14769G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131062032 | ||||||
| chr12:131062039
|
T | G | 241 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(238): Show | 241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.1474-14762T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131062039 | ||||||
| chr12:131062098
|
C | T | 1 | a0001c0010t0007g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1474-14703C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131062098 | ||||||
| chr12:131062325
|
A | G | 99 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(96): Show | 99 | HG00140.hp1 HG00621.hp2 HG00735.hp1 others(96): Show |
intron_variant | MODIFIER | c.1474-14476A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131062325 | ||||||
| chr12:131062390
|
C | T | 7 | a0001c0002t0001g0223a0001c0003t0001g0152a0001c0003t0013g0129others(4): Show | 7 | HG02257.hp2 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1474-14411C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131062390 | ||||||
| chr12:131062519
|
G | C | 1 | a0001c0003t0006g0019 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1474-14282G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131062519 | ||||||
| chr12:131062693
|
A | G | 11 | a0001c0001t0001g0208a0001c0001t0002g0098a0001c0001t0002g0107others(8): Show | 11 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.1474-14108A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131062693 | ||||||
| chr12:131062750
|
G | A | 2 | a0001c0002t0010g0138a0001c0002t0010g0201 | 2 | NA18982.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1474-14051G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131062750 | ||||||
| chr12:131062881
|
T | C | 99 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(96): Show | 99 | HG00140.hp1 HG00621.hp2 HG00735.hp1 others(96): Show |
intron_variant | MODIFIER | c.1474-13920T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131062881 | ||||||
| chr12:131062950
|
C | T | 1 | a0001c0001t0002g0171 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1474-13851C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131062950 | ||||||
| chr12:131062951
|
A | C | 31 | a0001c0001t0016g0147a0001c0001t0016g0182a0001c0002t0001g0169others(28): Show | 31 | HG00738.hp2 HG01168.hp1 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.1474-13850A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131062951 | ||||||
| chr12:131063068
|
C | G | 1 | a0002c0029t0031g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1474-13733C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131063068 | ||||||
| chr12:131063283
|
C | T | 11 | a0001c0001t0001g0208a0001c0001t0002g0098a0001c0001t0002g0107others(8): Show | 11 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.1474-13518C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131063283 | ||||||
| chr12:131063414
|
A | G | 1 | a0001c0002t0003g0081 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1474-13387A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131063414 | ||||||
| chr12:131063508
|
T | C | 1 | a0001c0002t0010g0167 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1474-13293T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131063508 | ||||||
| chr12:131063784
|
A | C | 68 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(65): Show | 68 | HG00140.hp1 HG00621.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.1474-13017A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131063784 | ||||||
| chr12:131064024
|
A | G | 1 | a0001c0002t0003g0041 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1474-12777A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131064024 | ||||||
| chr12:131064080
|
C | G | 11 | a0001c0001t0001g0208a0001c0001t0002g0098a0001c0001t0002g0107others(8): Show | 11 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.1474-12721C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131064080 | ||||||
| chr12:131064274
|
G | T | 1 | a0001c0002t0048g0151 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1474-12527G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131064274 | ||||||
| chr12:131064290
|
C | T | 41 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(38): Show | 41 | HG00140.hp1 HG00621.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.1474-12511C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131064290 | ||||||
| chr12:131064310
|
C | T | 1 | a0001c0002t0003g0085 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1474-12491C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131064310 | ||||||
| chr12:131064494
|
A | G | 2 | a0004c0015t0005g0086a0004c0016t0002g0065 | 2 | HG00639.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.1474-12307A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131064494 | ||||||
| chr12:131064525
|
A | G | 11 | a0001c0001t0001g0208a0001c0001t0002g0098a0001c0001t0002g0107others(8): Show | 11 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.1474-12276A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131064525 | ||||||
| chr12:131064573
|
T | G | 1 | a0003c0040t0022g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1474-12228T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131064573 | ||||||
| chr12:131064633
|
A | T | 1 | a0001c0004t0024g0133 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1474-12168A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131064633 | ||||||
| chr12:131064803
|
A | C | 2 | a0001c0001t0001g0197a0001c0001t0003g0023 | 2 | HG00639.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1474-11998A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131064803 | ||||||
| chr12:131065023
|
C | A | 1 | a0002c0029t0031g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1474-11778C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131065023 | ||||||
| chr12:131065095
|
C | T | 80 | a0001c0001t0001g0113a0001c0001t0001g0156a0001c0001t0001g0163others(77): Show | 80 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.1474-11706C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131065095 | ||||||
| chr12:131065245
|
C | G | 2 | a0001c0001t0002g0116a0001c0010t0007g0213 | 2 | HG01243.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1474-11556C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131065245 | ||||||
| chr12:131065271
|
G | T | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(35): Show | 38 | HG00140.hp1 HG00621.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.1474-11530G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131065271 | ||||||
| chr12:131065273
|
T | C | 1 | a0003c0033t0030g0231 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1474-11528T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131065273 | ||||||
| chr12:131065421
|
C | T | 11 | a0001c0001t0001g0208a0001c0001t0002g0098a0001c0001t0002g0107others(8): Show | 11 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.1474-11380C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131065421 | ||||||
| chr12:131065493
|
C | T | 3 | a0001c0002t0003g0020a0001c0002t0003g0057a0001c0004t0005g0072 | 3 | HG02083.hp1 HG02155.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.1474-11308C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131065493 | ||||||
| chr12:131065584
|
C | T | 1 | a0001c0003t0012g0025 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1474-11217C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131065584 | ||||||
| chr12:131065782
|
CCT | C | 67 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(64): Show | 67 | HG00140.hp1 HG00621.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.1474-11012_1474-11 others(8): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131065782 | |||||
| chr12:131065927
|
G | A | 1 | a0001c0003t0036g0209 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1474-10874G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131065927 | ||||||
| chr12:131066208
|
A | G | 1 | a0001c0002t0001g0202 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1474-10593A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131066208 | ||||||
| chr12:131066467
|
C | T | 2 | a0001c0020t0002g0180a0003c0031t0003g0089 | 2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1474-10334C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131066467 | ||||||
| chr12:131066481
|
C | T | 1 | a0001c0010t0007g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1474-10320C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131066481 | ||||||
| chr12:131066489
|
C | T | 11 | a0001c0001t0001g0208a0001c0001t0002g0098a0001c0001t0002g0107others(8): Show | 11 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.1474-10312C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131066489 | ||||||
| chr12:131066520
|
G | A | 1 | a0002c0029t0031g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1474-10281G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131066520 | ||||||
| chr12:131066833
|
G | A | 1 | a0001c0002t0010g0167 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1474-9968G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131066833 | ||||||
| chr12:131066839
|
G | C | 1 | a0001c0001t0009g0166 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1474-9962G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131066839 | ||||||
| chr12:131066924
|
C | T | 1 | a0011c0038t0002g0162 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1474-9877C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131066924 | ||||||
| chr12:131066930
|
G | A | 3 | a0001c0001t0002g0175a0001c0001t0005g0055a0001c0001t0009g0140 | 3 | NA18961.hp2 NA18982.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1474-9871G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131066930 | ||||||
| chr12:131067007
|
C | T | 1 | a0001c0002t0001g0202 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1474-9794C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131067007 | ||||||
| chr12:131067026
|
G | A | 1 | a0001c0009t0014g0078 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1474-9775G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131067026 | ||||||
| chr12:131067037
|
A | G | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(206): Show | 209 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1474-9764A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131067037 | ||||||
| chr12:131067049
|
G | C | 1 | a0001c0005t0001g0239 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1474-9752G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131067049 | ||||||
| chr12:131067236
|
C | T | 1 | a0001c0007t0006g0021 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1474-9565C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131067236 | ||||||
| chr12:131067280
|
A | G | 235 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(232): Show | 235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.1474-9521A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131067280 | ||||||
| chr12:131067292
|
G | A | 66 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(63): Show | 66 | HG00140.hp1 HG00621.hp2 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.1474-9509G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131067292 | ||||||
| chr12:131067327
|
G | A | 1 | a0003c0033t0030g0231 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1474-9474G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131067327 | ||||||
| chr12:131067338
|
G | A | 1 | a0001c0042t0007g0176 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1474-9463G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131067338 | ||||||
| chr12:131067412
|
A | T | 1 | a0003c0033t0030g0231 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1474-9389A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131067412 | ||||||
| chr12:131067502
|
ATATGTCT others(395): Show |
A | 1 | a0001c0007t0018g0132 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1474-9239_1474-883 others(4): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131067502 | |||||
| chr12:131067604
|
ATATGTCT others(173): Show |
A | 1 | a0001c0004t0002g0004 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1474-9137_1474-895 others(4): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131067604 | |||||
| chr12:131067664
|
ATATGTCT others(113): Show |
A | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(104): Show | 107 | HG00140.hp1 HG00621.hp2 HG00735.hp1 others(104): Show |
intron_variant | MODIFIER | c.1474-9073_1474-895 others(4): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131067664 | |||||
| chr12:131067696
|
T | A | 1 | a0001c0002t0003g0077 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1474-9105T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131067696 | ||||||
| chr12:131067706
|
G | A | 1 | a0001c0002t0040g0035 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1474-9095G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131067706 | ||||||
| chr12:131067728
|
T | G | 19 | a0001c0001t0005g0087a0001c0001t0016g0147a0001c0001t0016g0182others(16): Show | 19 | HG01109.hp1 HG02056.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1474-9073T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131067728 | ||||||
| chr12:131067777
|
A | G | 31 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0003g0023others(28): Show | 31 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.1474-9024A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131067777 | ||||||
| chr12:131067781
|
T | C | 19 | a0001c0001t0016g0147a0001c0001t0016g0182a0001c0002t0001g0223others(16): Show | 19 | HG00609.hp2 HG01109.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1474-9020T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131067781 | ||||||
| chr12:131067781
|
T | TCTGTATG others(53): Show |
8 | a0001c0001t0002g0184a0001c0005t0001g0044a0001c0005t0001g0127others(5): Show | 8 | HG01167.hp1 HG02258.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1474-8805_1474-874 others(64): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131067781 | |||||
| chr12:131067781
|
TCTGTATG others(53): Show |
T | 1 | a0001c0003t0036g0209 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1474-8805_1474-874 others(64): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131067781 | |||||
| chr12:131067904
|
G | A | 27 | a0001c0002t0001g0169a0001c0003t0004g0013a0001c0003t0004g0104others(24): Show | 27 | HG00738.hp2 HG01168.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.1474-8897G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131067904 | ||||||
| chr12:131067930
|
C | T | 7 | a0003c0012t0017g0017a0003c0012t0017g0158a0003c0032t0038g0090others(4): Show | 7 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1474-8871C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131067930 | ||||||
| chr12:131068036
|
G | C | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(106): Show | 109 | HG00140.hp1 HG00621.hp2 HG00735.hp1 others(106): Show |
intron_variant | MODIFIER | c.1474-8765G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131068036 | ||||||
| chr12:131068179
|
C | T | 3 | a0001c0003t0004g0237a0001c0010t0007g0160a0001c0046t0017g0221 | 3 | HG01175.hp2 HG01934.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1474-8622C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131068179 | ||||||
| chr12:131068381
|
T | C | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(106): Show | 109 | HG00140.hp1 HG00621.hp2 HG00735.hp1 others(106): Show |
intron_variant | MODIFIER | c.1474-8420T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131068381 | ||||||
| chr12:131068546
|
T | A | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(206): Show | 209 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1474-8255T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131068546 | ||||||
| chr12:131068605
|
T | C | 30 | a0001c0002t0001g0169a0001c0003t0004g0013a0001c0003t0004g0104others(27): Show | 30 | HG00738.hp2 HG01168.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.1474-8196T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131068605 | ||||||
| chr12:131068893
|
G | T | 20 | a0001c0002t0001g0169a0001c0003t0004g0013a0001c0003t0004g0104others(17): Show | 20 | HG00738.hp2 HG01168.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.1474-7908G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131068893 | ||||||
| chr12:131069021
|
G | A | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(98): Show | 101 | HG00140.hp1 HG00621.hp2 HG00735.hp1 others(98): Show |
intron_variant | MODIFIER | c.1474-7780G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131069021 | ||||||
| chr12:131069163
|
G | A | 1 | a0001c0009t0014g0078 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1474-7638G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131069163 | ||||||
| chr12:131069174
|
C | T | 10 | a0001c0001t0001g0208a0001c0001t0002g0098a0001c0001t0002g0107others(7): Show | 10 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.1474-7627C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131069174 | ||||||
| chr12:131069216
|
C | A | 2 | a0001c0001t0002g0116a0001c0010t0007g0213 | 2 | HG01243.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1474-7585C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131069216 | ||||||
| chr12:131069217
|
G | C | 2 | a0001c0001t0002g0116a0001c0010t0007g0213 | 2 | HG01243.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1474-7584G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131069217 | ||||||
| chr12:131069514
|
G | A | 79 | a0001c0001t0001g0113a0001c0001t0001g0156a0001c0001t0001g0163others(76): Show | 79 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.1474-7287G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131069514 | ||||||
| chr12:131069789
|
G | A | 2 | a0001c0001t0002g0116a0001c0010t0007g0213 | 2 | HG01243.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1474-7012G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131069789 | ||||||
| chr12:131069794
|
C | T | 11 | a0001c0003t0004g0013a0001c0003t0004g0104a0001c0003t0004g0121others(8): Show | 11 | HG00738.hp2 HG01168.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1474-7007C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131069794 | ||||||
| chr12:131069924
|
G | A | 1 | a0001c0025t0021g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1474-6877G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131069924 | ||||||
| chr12:131069934
|
G | A | 60 | a0001c0001t0001g0113a0001c0001t0002g0005a0001c0001t0002g0172others(57): Show | 60 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.1474-6867G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131069934 | ||||||
| chr12:131070058
|
C | T | 1 | a0001c0007t0004g0102 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1474-6743C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131070058 | ||||||
| chr12:131070074
|
C | T | 19 | a0001c0001t0016g0147a0001c0001t0016g0182a0001c0002t0001g0223others(16): Show | 19 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1474-6727C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131070074 | ||||||
| chr12:131070084
|
C | T | 1 | a0001c0025t0021g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1474-6717C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131070084 | ||||||
| chr12:131070102
|
G | C | 1 | a0001c0002t0003g0076 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1474-6699G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131070102 | ||||||
| chr12:131070421
|
G | C | 2 | a0001c0003t0001g0152a0001c0003t0013g0129 | 2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1474-6380G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131070421 | ||||||
| chr12:131070443
|
C | T | 30 | a0001c0002t0001g0169a0001c0003t0004g0013a0001c0003t0004g0104others(27): Show | 30 | HG00738.hp2 HG01168.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.1474-6358C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131070443 | ||||||
| chr12:131070504
|
T | C | 3 | a0003c0012t0017g0017a0003c0012t0017g0158a0006c0037t0042g0046 | 3 | HG02109.hp2 HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1474-6297T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131070504 | ||||||
| chr12:131070571
|
T | C | 1 | a0001c0003t0041g0080 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1474-6230T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131070571 | ||||||
| chr12:131070587
|
C | T | 2 | a0001c0001t0002g0228a0001c0001t0002g0235 | 2 | HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1474-6214C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131070587 | ||||||
| chr12:131070624
|
G | A | 1 | a0001c0003t0041g0080 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1474-6177G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131070624 | ||||||
| chr12:131070743
|
C | T | 3 | a0003c0012t0017g0017a0003c0012t0017g0158a0006c0037t0042g0046 | 3 | HG02109.hp2 HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1474-6058C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131070743 | ||||||
| chr12:131070784
|
C | A | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(205): Show | 208 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.1474-6017C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131070784 | ||||||
| chr12:131070870
|
C | T | 2 | a0001c0008t0003g0059a0002c0029t0031g0222 | 2 | HG03239.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1474-5931C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131070870 | ||||||
| chr12:131071012
|
GGCCATGT others(73): Show |
G | 79 | a0001c0001t0001g0113a0001c0001t0001g0156a0001c0001t0001g0163others(76): Show | 79 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.1474-5711_1474-563 others(84): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr12 | 131071012 | |||||
| chr12:131071240
|
C | T | 221 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(218): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1474-5561C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131071240 | ||||||
| chr12:131071254
|
G | A | 2 | a0001c0001t0002g0116a0001c0010t0007g0213 | 2 | HG01243.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1474-5547G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131071254 | ||||||
| chr12:131071411
|
G | A | 79 | a0001c0001t0001g0113a0001c0001t0001g0156a0001c0001t0001g0163others(76): Show | 79 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.1474-5390G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131071411 | ||||||
| chr12:131071498
|
C | T | 2 | a0001c0001t0016g0147a0001c0001t0016g0182 | 2 | HG02280.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1474-5303C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131071498 | ||||||
| chr12:131071591
|
T | G | 3 | a0001c0006t0001g0120a0001c0006t0001g0242a0001c0006t0008g0177 | 3 | HG03041.hp1 HG03195.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1474-5210T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131071591 | ||||||
| chr12:131071595
|
C | G | 1 | a0002c0029t0031g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1474-5206C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131071595 | ||||||
| chr12:131071600
|
A | G | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(106): Show | 109 | HG00140.hp1 HG00621.hp2 HG00735.hp1 others(106): Show |
intron_variant | MODIFIER | c.1474-5201A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131071600 | ||||||
| chr12:131071661
|
C | T | 2 | a0003c0041t0004g0178a0007c0039t0001g0229 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1474-5140C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131071661 | ||||||
| chr12:131071946
|
C | T | 2 | a0001c0001t0002g0116a0001c0010t0007g0213 | 2 | HG01243.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1474-4855C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131071946 | ||||||
| chr12:131071992
|
G | A | 10 | a0001c0001t0001g0208a0001c0001t0002g0098a0001c0001t0002g0107others(7): Show | 10 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.1474-4809G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131071992 | ||||||
| chr12:131072115
|
A | G | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(109): Show | 112 | HG00140.hp1 HG00621.hp2 HG00735.hp1 others(109): Show |
intron_variant | MODIFIER | c.1474-4686A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131072115 | ||||||
| chr12:131072177
|
C | T | 79 | a0001c0001t0001g0113a0001c0001t0001g0156a0001c0001t0001g0163others(76): Show | 79 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.1474-4624C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131072177 | ||||||
| chr12:131072305
|
C | A | 3 | a0003c0032t0038g0090a0003c0041t0004g0178a0007c0039t0001g0229 | 3 | HG02258.hp1 HG02559.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1474-4496C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131072305 | ||||||
| chr12:131072306
|
A | G | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(206): Show | 209 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1474-4495A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131072306 | ||||||
| chr12:131072449
|
G | A | 3 | a0001c0003t0006g0092a0001c0003t0006g0185a0001c0003t0006g0215 | 3 | HG00735.hp1 HG01099.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.1474-4352G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131072449 | ||||||
| chr12:131072462
|
T | G | 1 | a0001c0003t0029g0214 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1474-4339T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131072462 | ||||||
| chr12:131072560
|
C | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0115 | 3 | HG01433.hp2 HG01884.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1474-4241C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131072560 | ||||||
| chr12:131072565
|
C | T | 41 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(38): Show | 41 | HG00140.hp1 HG00621.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.1474-4236C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131072565 | ||||||
| chr12:131072655
|
A | G | 1 | a0001c0004t0002g0011 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1474-4146A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131072655 | ||||||
| chr12:131072684
|
T | C | 108 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(105): Show | 108 | HG00140.hp1 HG00621.hp2 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.1474-4117T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131072684 | ||||||
| chr12:131072791
|
C | G | 1 | a0001c0020t0002g0180 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1474-4010C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131072791 | ||||||
| chr12:131072883
|
C | T | 3 | a0003c0012t0017g0017a0003c0012t0017g0158a0006c0037t0042g0046 | 3 | HG02109.hp2 HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1474-3918C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131072883 | ||||||
| chr12:131073213
|
G | T | 1 | a0001c0005t0008g0226 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1474-3588G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131073213 | ||||||
| chr12:131073292
|
C | T | 2 | a0001c0001t0027g0118a0001c0005t0008g0226 | 2 | HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1474-3509C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131073292 | ||||||
| chr12:131073342
|
A | G | 18 | a0001c0001t0016g0147a0001c0001t0016g0182a0001c0002t0001g0223others(15): Show | 18 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1474-3459A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131073342 | ||||||
| chr12:131073423
|
T | A | 1 | a0003c0031t0003g0089 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1474-3378T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131073423 | ||||||
| chr12:131073557
|
G | A | 1 | a0011c0038t0002g0162 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1474-3244G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131073557 | ||||||
| chr12:131073614
|
A | G | 2 | a0001c0001t0002g0161a0001c0001t0009g0144 | 2 | NA18970.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1474-3187A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131073614 | ||||||
| chr12:131073700
|
G | A | 5 | a0001c0001t0016g0147a0001c0001t0016g0182a0001c0003t0013g0224others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1474-3101G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131073700 | ||||||
| chr12:131073817
|
A | G | 13 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0003g0023others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.1474-2984A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131073817 | ||||||
| chr12:131074020
|
A | G | 69 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(66): Show | 69 | HG00140.hp1 HG00621.hp2 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.1474-2781A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131074020 | ||||||
| chr12:131074073
|
A | T | 1 | a0001c0022t0016g0109 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1474-2728A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131074073 | ||||||
| chr12:131074170
|
G | A | 1 | a0001c0003t0004g0198 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1474-2631G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131074170 | ||||||
| chr12:131074206
|
G | A | 1 | a0001c0003t0012g0063 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1474-2595G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131074206 | ||||||
| chr12:131074393
|
C | T | 3 | a0001c0001t0002g0173a0001c0003t0012g0025a0001c0003t0019g0218 | 3 | HG01496.hp1 NA18959.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1474-2408C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131074393 | ||||||
| chr12:131074452
|
C | T | 19 | a0001c0001t0016g0147a0001c0001t0016g0182a0001c0002t0001g0223others(16): Show | 19 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1474-2349C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131074452 | ||||||
| chr12:131074685
|
G | C | 10 | a0001c0001t0001g0208a0001c0001t0002g0098a0001c0001t0002g0107others(7): Show | 10 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.1474-2116G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131074685 | ||||||
| chr12:131075208
|
C | T | 1 | a0001c0025t0021g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1474-1593C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131075208 | ||||||
| chr12:131075265
|
C | T | 1 | a0001c0010t0007g0150 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1474-1536C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131075265 | ||||||
| chr12:131075367
|
T | G | 39 | a0001c0001t0016g0147a0001c0001t0016g0182a0001c0002t0001g0169others(36): Show | 39 | HG00738.hp2 HG01109.hp1 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.1474-1434T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131075367 | ||||||
| chr12:131075512
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1474-1289C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131075512 | ||||||
| chr12:131075513
|
G | A | 2 | a0001c0004t0005g0036a0001c0005t0014g0049 | 2 | HG02040.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1474-1288G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131075513 | ||||||
| chr12:131075610
|
G | T | 1 | a0001c0001t0011g0074 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1474-1191G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131075610 | ||||||
| chr12:131075628
|
C | T | 78 | a0001c0001t0001g0113a0001c0001t0001g0156a0001c0001t0001g0163others(75): Show | 78 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.1474-1173C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131075628 | ||||||
| chr12:131075751
|
G | T | 9 | a0001c0001t0002g0098a0001c0001t0002g0107a0001c0001t0002g0203others(6): Show | 9 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.1474-1050G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131075751 | ||||||
| chr12:131075896
|
T | C | 79 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(76): Show | 79 | HG00140.hp1 HG00621.hp2 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.1474-905T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131075896 | ||||||
| chr12:131076109
|
C | T | 2 | a0003c0041t0004g0178a0007c0039t0001g0229 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1474-692C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131076109 | ||||||
| chr12:131076535
|
C | T | 2 | a0001c0017t0008g0029a0001c0017t0008g0030 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1474-266C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131076535 | ||||||
| chr12:131076570
|
C | T | 1 | a0001c0042t0007g0176 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1474-231C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131076570 | ||||||
| chr12:131076589
|
T | C | 127 | a0001c0001t0001g0113a0001c0001t0001g0156a0001c0001t0001g0163others(124): Show | 127 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.1474-212T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 13/24 | chr12 | 131076589 | ||||||
| chr12:131077082
|
C | G | 8 | a0003c0012t0017g0017a0003c0012t0017g0158a0003c0032t0038g0090others(5): Show | 8 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1547+208C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131077082 | ||||||
| chr12:131077237
|
GA | G | 32 | a0001c0002t0001g0169a0001c0002t0001g0223a0001c0003t0001g0152others(29): Show | 32 | HG00738.hp2 HG01109.hp1 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.1547+365delA | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr12 | 131077237 | |||||
| chr12:131077357
|
T | C | 83 | a0001c0001t0001g0113a0001c0001t0001g0156a0001c0001t0001g0163others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.1547+483T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131077357 | ||||||
| chr12:131077378
|
G | A | 2 | a0001c0001t0001g0113a0001c0001t0003g0026 | 2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1547+504G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131077378 | ||||||
| chr12:131077549
|
G | A | 83 | a0001c0001t0001g0113a0001c0001t0001g0156a0001c0001t0001g0163others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.1547+675G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131077549 | ||||||
| chr12:131077572
|
C | T | 1 | a0001c0003t0012g0088 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1547+698C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131077572 | ||||||
| chr12:131077582
|
A | G | 1 | a0010c0026t0013g0238 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1547+708A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131077582 | ||||||
| chr12:131077595
|
G | A | 1 | a0001c0010t0007g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1547+721G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131077595 | ||||||
| chr12:131077627
|
C | T | 221 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(218): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1547+753C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131077627 | ||||||
| chr12:131077628
|
T | C | 221 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(218): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1547+754T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131077628 | ||||||
| chr12:131077813
|
A | C | 38 | a0001c0001t0016g0147a0001c0001t0016g0182a0001c0002t0001g0169others(35): Show | 38 | HG00738.hp2 HG01109.hp1 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.1547+939A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131077813 | ||||||
| chr12:131078136
|
T | C | 207 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(204): Show | 207 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.1547+1262T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131078136 | ||||||
| chr12:131078137
|
G | C | 1 | a0001c0002t0003g0050 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1547+1263G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131078137 | ||||||
| chr12:131078210
|
G | T | 1 | a0001c0022t0016g0109 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1547+1336G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131078210 | ||||||
| chr12:131078220
|
A | G | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(206): Show | 209 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1547+1346A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131078220 | ||||||
| chr12:131078388
|
T | C | 123 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(120): Show | 123 | HG00140.hp1 HG00621.hp2 HG00735.hp1 others(120): Show |
intron_variant | MODIFIER | c.1547+1514T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131078388 | ||||||
| chr12:131078440
|
G | A | 1 | a0001c0002t0002g0006 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1547+1566G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131078440 | ||||||
| chr12:131078539
|
A | C | 2 | a0001c0001t0002g0116a0001c0010t0007g0213 | 2 | HG01243.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1547+1665A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131078539 | ||||||
| chr12:131078593
|
A | G | 207 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(204): Show | 207 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.1547+1719A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131078593 | ||||||
| chr12:131078622
|
A | G | 1 | a0001c0045t0002g0091 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1547+1748A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131078622 | ||||||
| chr12:131078734
|
A | G | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(205): Show | 208 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.1547+1860A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131078734 | ||||||
| chr12:131078783
|
T | C | 80 | a0001c0001t0001g0113a0001c0001t0001g0156a0001c0001t0001g0163others(77): Show | 80 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.1547+1909T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131078783 | ||||||
| chr12:131078988
|
C | T | 25 | a0001c0001t0002g0161a0001c0001t0002g0173a0001c0001t0002g0175others(22): Show | 25 | HG00735.hp1 HG01099.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1547+2114C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131078988 | ||||||
| chr12:131079007
|
C | T | 7 | a0003c0012t0017g0017a0003c0012t0017g0158a0003c0032t0038g0090others(4): Show | 7 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1547+2133C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131079007 | ||||||
| chr12:131079040
|
G | C | 1 | a0009c0035t0047g0219 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1547+2166G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131079040 | ||||||
| chr12:131079086
|
A | C | 2 | a0001c0001t0001g0113a0001c0001t0003g0026 | 2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1547+2212A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131079086 | ||||||
| chr12:131079103
|
G | A | 1 | a0001c0001t0027g0118 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1547+2229G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131079103 | ||||||
| chr12:131079123
|
T | G | 1 | a0001c0003t0001g0152 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1547+2249T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131079123 | ||||||
| chr12:131079154
|
C | T | 1 | a0001c0002t0002g0001 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1547+2280C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131079154 | ||||||
| chr12:131079267
|
A | C | 2 | a0001c0001t0002g0203a0001c0001t0002g0204 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1547+2393A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131079267 | ||||||
| chr12:131079278
|
G | C | 2 | a0001c0003t0033g0181a0001c0003t0034g0014 | 2 | HG01261.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1547+2404G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131079278 | ||||||
| chr12:131079505
|
T | C | 221 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(218): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1547+2631T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131079505 | ||||||
| chr12:131079638
|
A | C | 38 | a0001c0001t0016g0147a0001c0001t0016g0182a0001c0002t0001g0169others(35): Show | 38 | HG00738.hp2 HG01109.hp1 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.1547+2764A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131079638 | ||||||
| chr12:131079711
|
T | C | 64 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(61): Show | 64 | HG00140.hp1 HG00621.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.1547+2837T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131079711 | ||||||
| chr12:131079983
|
C | T | 1 | a0009c0035t0047g0219 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1547+3109C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131079983 | ||||||
| chr12:131080236
|
G | A | 3 | a0001c0001t0002g0130a0001c0004t0005g0036a0001c0005t0014g0049 | 3 | HG02040.hp1 NA19089.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1547+3362G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131080236 | ||||||
| chr12:131080431
|
GA | G | 5 | a0001c0001t0016g0147a0001c0001t0016g0182a0001c0003t0013g0224others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1547+3564delA | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr12 | 131080431 | |||||
| chr12:131080441
|
A | G | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(206): Show | 209 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1547+3567A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131080441 | ||||||
| chr12:131080466
|
A | C | 1 | a0001c0001t0002g0187 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1547+3592A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131080466 | ||||||
| chr12:131080489
|
G | A | 22 | a0001c0001t0002g0161a0001c0001t0002g0173a0001c0001t0002g0175others(19): Show | 22 | HG00735.hp1 HG01099.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1547+3615G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131080489 | ||||||
| chr12:131080530
|
T | C | 1 | a0001c0001t0002g0005 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1547+3656T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131080530 | ||||||
| chr12:131080634
|
T | G | 1 | a0003c0031t0003g0089 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1547+3760T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131080634 | ||||||
| chr12:131080663
|
C | T | 1 | a0001c0002t0003g0083 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1547+3789C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131080663 | ||||||
| chr12:131080856
|
G | A | 5 | a0001c0001t0002g0116a0001c0010t0007g0213a0001c0025t0021g0119others(2): Show | 5 | HG01243.hp1 HG01934.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1548-3684G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131080856 | ||||||
| chr12:131080867
|
G | A | 1 | a0001c0007t0006g0021 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1548-3673G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131080867 | ||||||
| chr12:131080917
|
G | A | 8 | a0001c0001t0002g0098a0001c0001t0002g0107a0001c0001t0002g0203others(5): Show | 8 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.1548-3623G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131080917 | ||||||
| chr12:131080940
|
T | C | 3 | a0001c0025t0021g0119a0001c0042t0007g0176a0002c0029t0031g0222 | 3 | HG01934.hp2 HG02809.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1548-3600T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131080940 | ||||||
| chr12:131081230
|
A | C | 2 | a0001c0002t0001g0125a0001c0002t0008g0016 | 2 | HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1548-3310A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131081230 | ||||||
| chr12:131081354
|
A | G | 63 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(60): Show | 63 | HG00140.hp1 HG00621.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.1548-3186A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131081354 | ||||||
| chr12:131081482
|
A | G | 2 | a0001c0001t0011g0062a0001c0009t0019g0135 | 2 | NA19009.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1548-3058A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131081482 | ||||||
| chr12:131082178
|
G | A | 1 | a0001c0020t0002g0180 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1548-2362G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131082178 | ||||||
| chr12:131082436
|
T | C | 196 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(193): Show | 196 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.1548-2104T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131082436 | ||||||
| chr12:131082452
|
C | T | 1 | a0001c0002t0001g0157 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1548-2088C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131082452 | ||||||
| chr12:131082540
|
C | T | 82 | a0001c0001t0001g0113a0001c0001t0001g0156a0001c0001t0001g0163others(79): Show | 82 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1548-2000C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131082540 | ||||||
| chr12:131082549
|
G | A | 84 | a0001c0001t0001g0113a0001c0001t0001g0156a0001c0001t0001g0163others(81): Show | 84 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.1548-1991G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131082549 | ||||||
| chr12:131082588
|
C | G | 1 | a0003c0033t0030g0231 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1548-1952C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131082588 | ||||||
| chr12:131082640
|
T | C | 1 | a0001c0001t0011g0062 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1548-1900T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131082640 | ||||||
| chr12:131082660
|
T | G | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(206): Show | 209 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1548-1880T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131082660 | ||||||
| chr12:131082693
|
T | C | 1 | a0003c0033t0030g0231 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1548-1847T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131082693 | ||||||
| chr12:131082797
|
G | A | 2 | a0001c0001t0002g0116a0001c0010t0007g0213 | 2 | HG01243.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1548-1743G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131082797 | ||||||
| chr12:131082971
|
G | A | 78 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(75): Show | 78 | HG00140.hp1 HG00621.hp2 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.1548-1569G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131082971 | ||||||
| chr12:131083004
|
C | T | 2 | a0001c0003t0004g0121a0001c0003t0004g0122 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1548-1536C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131083004 | ||||||
| chr12:131083069
|
G | A | 1 | a0003c0012t0017g0158 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1548-1471G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131083069 | ||||||
| chr12:131083085
|
C | G | 6 | a0001c0001t0016g0147a0001c0001t0016g0182a0001c0003t0013g0224others(3): Show | 6 | HG02280.hp1 HG02486.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1548-1455C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131083085 | ||||||
| chr12:131083088
|
T | C | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(206): Show | 209 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1548-1452T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131083088 | ||||||
| chr12:131083138
|
A | G | 1 | a0001c0002t0001g0157 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1548-1402A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131083138 | ||||||
| chr12:131083289
|
CT | C | 8 | a0001c0001t0016g0147a0001c0001t0016g0182a0001c0003t0013g0224others(5): Show | 8 | HG00738.hp2 HG02280.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1548-1238delT | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr12 | 131083289 | |||||
| chr12:131083522
|
A | G | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(205): Show | 208 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.1548-1018A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131083522 | ||||||
| chr12:131083530
|
G | A | 1 | a0002c0029t0031g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1548-1010G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131083530 | ||||||
| chr12:131083583
|
C | T | 9 | a0001c0001t0002g0098a0001c0001t0002g0107a0001c0001t0002g0171others(6): Show | 9 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.1548-957C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131083583 | ||||||
| chr12:131083684
|
C | T | 9 | a0001c0001t0002g0098a0001c0001t0002g0107a0001c0001t0002g0171others(6): Show | 9 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.1548-856C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131083684 | ||||||
| chr12:131083849
|
CG | C | 20 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0003g0023others(17): Show | 20 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.1548-690delG | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131083849 | ||||||
| chr12:131084029
|
A | G | 1 | a0003c0033t0030g0231 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1548-511A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131084029 | ||||||
| chr12:131084114
|
T | C | 1 | a0008c0034t0026g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1548-426T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131084114 | ||||||
| chr12:131084130
|
C | T | 43 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(40): Show | 43 | HG00140.hp1 HG00621.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.1548-410C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131084130 | ||||||
| chr12:131084181
|
G | A | 23 | a0001c0001t0002g0149a0001c0001t0015g0060a0001c0002t0001g0169others(20): Show | 23 | HG00140.hp2 HG00738.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.1548-359G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 14/24 | chr12 | 131084181 | ||||||
| chr12:131084689
|
G | A | 67 | a0001c0001t0002g0098a0001c0001t0002g0107a0001c0001t0002g0116others(64): Show | 67 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.1671+26G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131084689 | ||||||
| chr12:131084772
|
T | C | 1 | a0001c0025t0021g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1671+109T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131084772 | ||||||
| chr12:131084826
|
C | T | 1 | a0001c0004t0005g0036 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1671+163C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131084826 | ||||||
| chr12:131084831
|
G | T | 1 | a0001c0002t0003g0050 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1671+168G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131084831 | ||||||
| chr12:131084996
|
G | A | 81 | a0001c0001t0001g0113a0001c0001t0001g0156a0001c0001t0001g0163others(78): Show | 81 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.1671+333G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131084996 | ||||||
| chr12:131085012
|
G | T | 1 | a0001c0007t0004g0102 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1671+349G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131085012 | ||||||
| chr12:131085217
|
C | T | 1 | a0001c0010t0007g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1671+554C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131085217 | ||||||
| chr12:131085225
|
G | A | 13 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0003g0023others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.1671+562G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131085225 | ||||||
| chr12:131085226
|
G | T | 13 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0003g0023others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.1671+563G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131085226 | ||||||
| chr12:131085238
|
G | A | 1 | a0001c0008t0003g0067 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1671+575G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131085238 | ||||||
| chr12:131085420
|
C | T | 12 | a0001c0002t0001g0223a0001c0003t0001g0152a0001c0003t0004g0207others(9): Show | 12 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1671+757C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131085420 | ||||||
| chr12:131085423
|
GA | G | 27 | a0001c0001t0002g0149a0001c0001t0015g0060a0001c0002t0001g0169others(24): Show | 27 | HG00140.hp2 HG00738.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.1671+761delA | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131085423 | ||||||
| chr12:131085444
|
G | A | 88 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(85): Show | 88 | HG00140.hp1 HG00140.hp2 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.1671+781G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131085444 | ||||||
| chr12:131085497
|
C | G | 171 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(168): Show | 171 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.1671+834C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131085497 | ||||||
| chr12:131085656
|
C | T | 1 | a0001c0002t0001g0157 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1671+993C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131085656 | ||||||
| chr12:131085736
|
G | A | 13 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0003g0023others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.1671+1073G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131085736 | ||||||
| chr12:131085889
|
G | A | 1 | a0001c0007t0006g0021 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1671+1226G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131085889 | ||||||
| chr12:131085890
|
G | A | 13 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0003g0023others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.1671+1227G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131085890 | ||||||
| chr12:131085948
|
G | A | 1 | a0001c0007t0004g0236 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1671+1285G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131085948 | ||||||
| chr12:131086116
|
A | G | 172 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(169): Show | 172 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.1671+1453A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131086116 | ||||||
| chr12:131086416
|
C | T | 2 | a0001c0001t0011g0066a0001c0001t0011g0074 | 2 | HG02132.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.1671+1753C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131086416 | ||||||
| chr12:131086417
|
G | A | 7 | a0003c0012t0017g0017a0003c0012t0017g0158a0003c0032t0038g0090others(4): Show | 7 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1671+1754G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131086417 | ||||||
| chr12:131086417
|
G | C | 2 | a0001c0001t0002g0228a0001c0001t0002g0235 | 2 | HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1671+1754G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131086417 | ||||||
| chr12:131086454
|
C | G | 2 | a0001c0022t0016g0109a0003c0031t0003g0089 | 2 | HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1671+1791C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131086454 | ||||||
| chr12:131086512
|
C | G | 1 | a0001c0002t0001g0169 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1671+1849C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131086512 | ||||||
| chr12:131086553
|
G | A | 1 | a0003c0031t0003g0089 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1671+1890G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131086553 | ||||||
| chr12:131086670
|
G | A | 1 | a0001c0003t0012g0025 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1671+2007G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131086670 | ||||||
| chr12:131086720
|
G | A | 2 | a0001c0001t0011g0062a0001c0009t0019g0135 | 2 | NA19009.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1671+2057G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131086720 | ||||||
| chr12:131087257
|
C | T | 25 | a0001c0001t0002g0149a0001c0001t0015g0060a0001c0002t0001g0169others(22): Show | 25 | HG00140.hp2 HG00738.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.1671+2594C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131087257 | ||||||
| chr12:131087350
|
C | T | 1 | a0001c0002t0048g0151 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1671+2687C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131087350 | ||||||
| chr12:131087445
|
C | T | 25 | a0001c0001t0002g0149a0001c0001t0015g0060a0001c0002t0001g0169others(22): Show | 25 | HG00140.hp2 HG00738.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.1671+2782C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131087445 | ||||||
| chr12:131087468
|
G | C | 27 | a0001c0001t0002g0149a0001c0001t0015g0060a0001c0002t0001g0169others(24): Show | 27 | HG00140.hp2 HG00738.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.1671+2805G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131087468 | ||||||
| chr12:131087516
|
C | T | 2 | a0001c0001t0027g0118a0001c0005t0008g0226 | 2 | HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1671+2853C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131087516 | ||||||
| chr12:131087653
|
G | T | 1 | a0001c0008t0001g0183 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1671+2990G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131087653 | ||||||
| chr12:131087654
|
A | G | 1 | a0001c0008t0001g0183 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1671+2991A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131087654 | ||||||
| chr12:131087655
|
G | A | 1 | a0001c0008t0001g0183 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1671+2992G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131087655 | ||||||
| chr12:131087680
|
C | T | 1 | a0001c0003t0034g0014 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1671+3017C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131087680 | ||||||
| chr12:131087727
|
GC | G | 169 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(166): Show | 169 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.1671+3072delC | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131087727 | |||||
| chr12:131087779
|
C | G | 172 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(169): Show | 172 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.1671+3116C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131087779 | ||||||
| chr12:131087794
|
G | C | 81 | a0001c0001t0001g0113a0001c0001t0001g0156a0001c0001t0001g0163others(78): Show | 81 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.1671+3131G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131087794 | ||||||
| chr12:131087857
|
T | C | 1 | a0002c0029t0031g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1671+3194T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131087857 | ||||||
| chr12:131088195
|
CTG | C | 12 | a0001c0002t0001g0223a0001c0003t0001g0152a0001c0003t0004g0207others(9): Show | 12 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1671+3533_1671+353 others(6): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131088195 | ||||||
| chr12:131088212
|
G | T | 1 | a0001c0001t0002g0149 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1671+3549G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131088212 | ||||||
| chr12:131088276
|
G | A | 1 | a0001c0002t0001g0100 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1671+3613G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131088276 | ||||||
| chr12:131088359
|
G | A | 2 | a0001c0001t0001g0156a0001c0001t0001g0163 | 2 | HG01106.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1671+3696G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131088359 | ||||||
| chr12:131088443
|
A | G | 2 | a0002c0018t0020g0123a0002c0018t0020g0124 | 2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1671+3780A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131088443 | ||||||
| chr12:131088497
|
C | T | 1 | a0001c0001t0015g0060 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1671+3834C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131088497 | ||||||
| chr12:131088506
|
T | C | 142 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(139): Show | 142 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.1671+3843T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131088506 | ||||||
| chr12:131088677
|
G | A | 168 | a0001c0001t0001g0003a0001c0001t0001g0111a0001c0001t0001g0113others(165): Show | 168 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.1671+4014G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131088677 | ||||||
| chr12:131088727
|
G | C | 183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1671+4064G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131088727 | ||||||
| chr12:131088765
|
A | C | 170 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(167): Show | 170 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.1671+4102A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131088765 | ||||||
| chr12:131088771
|
G | T | 13 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0003g0023others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.1671+4108G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131088771 | ||||||
| chr12:131088933
|
C | T | 2 | a0004c0015t0005g0086a0004c0016t0002g0065 | 2 | HG00639.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.1671+4270C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131088933 | ||||||
| chr12:131088977
|
C | T | 1 | a0001c0002t0010g0142 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1671+4314C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131088977 | ||||||
| chr12:131089003
|
C | T | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(170): Show | 173 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.1671+4340C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131089003 | ||||||
| chr12:131089068
|
C | T | 2 | a0001c0003t0013g0224a0001c0003t0013g0225 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1671+4405C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131089068 | ||||||
| chr12:131089230
|
G | A | 9 | a0001c0001t0002g0098a0001c0001t0002g0107a0001c0001t0002g0171others(6): Show | 9 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.1671+4567G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131089230 | ||||||
| chr12:131089265
|
A | C | 13 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0002g0187others(10): Show | 13 | HG01106.hp2 HG01261.hp1 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.1671+4602A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131089265 | ||||||
| chr12:131089307
|
T | C | 1 | a0001c0020t0002g0180 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1671+4644T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131089307 | ||||||
| chr12:131089346
|
C | A | 26 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0002g0098others(23): Show | 26 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.1671+4683C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131089346 | ||||||
| chr12:131089461
|
C | T | 1 | a0003c0032t0038g0090 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1671+4798C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131089461 | ||||||
| chr12:131089502
|
G | A | 2 | a0002c0030t0032g0159a0010c0026t0013g0238 | 2 | HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1671+4839G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131089502 | ||||||
| chr12:131089538
|
C | T | 140 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(137): Show | 140 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.1671+4875C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131089538 | ||||||
| chr12:131089548
|
C | T | 9 | a0001c0001t0002g0098a0001c0001t0002g0107a0001c0001t0002g0171others(6): Show | 9 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.1671+4885C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131089548 | ||||||
| chr12:131089550
|
A | C | 1 | a0001c0001t0002g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1671+4887A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131089550 | ||||||
| chr12:131089553
|
G | C | 1 | a0001c0003t0006g0211 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1671+4890G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131089553 | ||||||
| chr12:131089601
|
A | AGTGCTCC others(11): Show |
39 | a0001c0001t0002g0149a0001c0001t0015g0060a0001c0002t0001g0169others(36): Show | 39 | HG00140.hp2 HG00738.hp2 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1671+4947_1671+496 others(22): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131089601 | |||||
| chr12:131089816
|
G | T | 22 | a0001c0001t0002g0149a0001c0001t0015g0060a0001c0002t0001g0169others(19): Show | 22 | HG00140.hp2 HG00738.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.1671+5153G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131089816 | ||||||
| chr12:131089858
|
T | G | 1 | a0001c0001t0011g0074 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1671+5195T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131089858 | ||||||
| chr12:131089940
|
A | C | 16 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0002g0116others(13): Show | 16 | HG01106.hp2 HG01243.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.1671+5277A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131089940 | ||||||
| chr12:131089945
|
G | A | 13 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0003g0023others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.1671+5282G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131089945 | ||||||
| chr12:131090058
|
C | T | 3 | a0001c0002t0001g0169a0001c0004t0002g0131a0001c0007t0006g0021 | 3 | HG02055.hp2 HG02056.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.1671+5395C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131090058 | ||||||
| chr12:131090089
|
C | T | 7 | a0003c0012t0017g0017a0003c0012t0017g0158a0003c0032t0038g0090others(4): Show | 7 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1671+5426C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131090089 | ||||||
| chr12:131090096
|
G | C | 144 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(141): Show | 144 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.1671+5433G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131090096 | ||||||
| chr12:131090271
|
T | G | 1 | a0001c0003t0002g0186 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1671+5608T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131090271 | ||||||
| chr12:131090386
|
TC | T | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(136): Show | 139 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.1671+5724delC | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131090386 | ||||||
| chr12:131090415
|
T | C | 13 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0003g0023others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.1671+5752T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131090415 | ||||||
| chr12:131090436
|
G | A | 2 | a0002c0030t0032g0159a0010c0026t0013g0238 | 2 | HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1671+5773G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131090436 | ||||||
| chr12:131090673
|
A | G | 2 | a0001c0001t0002g0116a0001c0010t0007g0213 | 2 | HG01243.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1671+6010A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131090673 | ||||||
| chr12:131090746
|
A | G | 219 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(216): Show | 219 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.1671+6083A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131090746 | ||||||
| chr12:131090768
|
C | T | 69 | a0001c0001t0001g0113a0001c0001t0001g0208a0001c0001t0002g0005others(66): Show | 69 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.1671+6105C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131090768 | ||||||
| chr12:131090845
|
T | G | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(112): Show | 115 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.1671+6182T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131090845 | ||||||
| chr12:131090952
|
C | G | 5 | a0001c0001t0002g0116a0001c0010t0007g0213a0003c0033t0030g0231others(2): Show | 5 | HG01243.hp1 HG02258.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1671+6289C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131090952 | ||||||
| chr12:131090958
|
C | T | 1 | a0001c0003t0006g0185 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1671+6295C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131090958 | ||||||
| chr12:131091094
|
G | A | 46 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(43): Show | 46 | HG00140.hp1 HG00621.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.1671+6431G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131091094 | ||||||
| chr12:131091326
|
C | T | 7 | a0003c0012t0017g0017a0003c0012t0017g0158a0003c0032t0038g0090others(4): Show | 7 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1671+6663C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131091326 | ||||||
| chr12:131091391
|
A | T | 1 | a0001c0025t0021g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1671+6728A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131091391 | ||||||
| chr12:131091457
|
C | T | 45 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(42): Show | 45 | HG00140.hp1 HG00621.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.1671+6794C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131091457 | ||||||
| chr12:131091549
|
C | T | 1 | a0008c0034t0026g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1671+6886C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131091549 | ||||||
| chr12:131091599
|
G | A | 1 | a0001c0002t0001g0195 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1671+6936G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131091599 | ||||||
| chr12:131091646
|
C | A | 12 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0002g0187others(9): Show | 12 | HG01106.hp2 HG01261.hp1 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.1671+6983C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131091646 | ||||||
| chr12:131091702
|
C | A | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(175): Show | 178 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.1671+7039C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131091702 | ||||||
| chr12:131091702
|
C | T | 19 | a0001c0001t0002g0161a0001c0001t0002g0173a0001c0001t0002g0175others(16): Show | 19 | HG00735.hp1 HG01099.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1671+7039C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131091702 | ||||||
| chr12:131091712
|
AG | A | 25 | a0001c0001t0002g0149a0001c0001t0015g0060a0001c0002t0001g0169others(22): Show | 25 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.1671+7054delG | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131091712 | |||||
| chr12:131091717
|
G | A | 1 | a0003c0033t0030g0231 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1671+7054G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131091717 | ||||||
| chr12:131091774
|
C | T | 1 | a0001c0002t0002g0009 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1671+7111C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131091774 | ||||||
| chr12:131091900
|
C | T | 16 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0002g0187others(13): Show | 16 | HG01106.hp2 HG01261.hp1 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.1671+7237C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131091900 | ||||||
| chr12:131091932
|
C | G | 2 | a0001c0001t0002g0203a0001c0001t0002g0204 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1671+7269C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131091932 | ||||||
| chr12:131091973
|
G | C | 1 | a0003c0031t0003g0089 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1671+7310G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131091973 | ||||||
| chr12:131091989
|
A | G | 223 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(220): Show | 223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1671+7326A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131091989 | ||||||
| chr12:131092048
|
G | A | 93 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(90): Show | 93 | HG00621.hp2 HG00735.hp1 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.1671+7385G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131092048 | ||||||
| chr12:131092085
|
A | G | 9 | a0001c0001t0002g0098a0001c0001t0002g0107a0001c0001t0002g0171others(6): Show | 9 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.1671+7422A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131092085 | ||||||
| chr12:131092111
|
G | A | 9 | a0001c0001t0002g0098a0001c0001t0002g0107a0001c0001t0002g0171others(6): Show | 9 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.1671+7448G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131092111 | ||||||
| chr12:131092202
|
G | C | 1 | a0001c0025t0021g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1671+7539G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131092202 | ||||||
| chr12:131092243
|
C | G | 223 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(220): Show | 223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1671+7580C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131092243 | ||||||
| chr12:131092254
|
G | A | 137 | a0001c0001t0001g0113a0001c0001t0001g0208a0001c0001t0002g0005others(134): Show | 137 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.1671+7591G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131092254 | ||||||
| chr12:131092279
|
A | G | 1 | a0001c0004t0005g0036 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1671+7616A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131092279 | ||||||
| chr12:131092401
|
G | A | 168 | a0001c0001t0001g0113a0001c0001t0001g0156a0001c0001t0001g0163others(165): Show | 168 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.1671+7738G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131092401 | ||||||
| chr12:131092406
|
C | T | 2 | a0002c0030t0032g0159a0010c0026t0013g0238 | 2 | HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1671+7743C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131092406 | ||||||
| chr12:131092493
|
G | C | 105 | a0001c0001t0001g0113a0001c0001t0001g0208a0001c0001t0002g0005others(102): Show | 105 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1671+7830G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131092493 | ||||||
| chr12:131092525
|
C | A | 1 | a0001c0004t0005g0082 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1671+7862C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131092525 | ||||||
| chr12:131092555
|
C | T | 105 | a0001c0001t0001g0113a0001c0001t0001g0208a0001c0001t0002g0005others(102): Show | 105 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1671+7892C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131092555 | ||||||
| chr12:131092882
|
C | CT | 35 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0002g0149others(32): Show | 35 | HG00140.hp2 HG00738.hp2 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.1671+8234dupT | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131092882 | |||||
| chr12:131092882
|
C | CTT | 7 | a0003c0012t0017g0017a0003c0012t0017g0158a0003c0032t0038g0090others(4): Show | 7 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1671+8233_1671+823 others(6): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131092882 | |||||
| chr12:131092882
|
CT | C | 5 | a0001c0001t0005g0028a0001c0002t0001g0157a0001c0002t0010g0139others(2): Show | 5 | HG01167.hp1 HG01943.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1671+8234delT | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131092882 | |||||
| chr12:131092901
|
TAAAAC | T | 13 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0003g0023others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.1671+8241_1671+824 others(9): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131092901 | |||||
| chr12:131092906
|
C | T | 1 | a0001c0017t0008g0029 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1671+8243C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131092906 | ||||||
| chr12:131093031
|
C | T | 2 | a0002c0030t0032g0159a0010c0026t0013g0238 | 2 | HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1671+8368C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131093031 | ||||||
| chr12:131093066
|
C | T | 9 | a0001c0001t0002g0098a0001c0001t0002g0107a0001c0001t0002g0171others(6): Show | 9 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.1671+8403C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131093066 | ||||||
| chr12:131093081
|
C | T | 24 | a0001c0001t0002g0161a0001c0001t0002g0173a0001c0001t0002g0175others(21): Show | 24 | HG00735.hp1 HG01099.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1671+8418C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131093081 | ||||||
| chr12:131093127
|
A | G | 45 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(42): Show | 45 | HG00140.hp1 HG00621.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.1671+8464A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131093127 | ||||||
| chr12:131093171
|
G | A | 2 | a0001c0001t0001g0156a0001c0001t0001g0163 | 2 | HG01106.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1671+8508G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131093171 | ||||||
| chr12:131093278
|
A | G | 168 | a0001c0001t0001g0113a0001c0001t0001g0156a0001c0001t0001g0163others(165): Show | 168 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.1671+8615A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131093278 | ||||||
| chr12:131093350
|
T | C | 213 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(210): Show | 213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.1671+8687T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131093350 | ||||||
| chr12:131093376
|
G | A | 3 | a0001c0001t0002g0116a0001c0010t0007g0213a0001c0025t0021g0119 | 3 | HG01243.hp1 HG01934.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1671+8713G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131093376 | ||||||
| chr12:131093438
|
T | C | 23 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0003g0023others(20): Show | 23 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.1671+8775T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131093438 | ||||||
| chr12:131093446
|
G | A | 1 | a0001c0003t0004g0234 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1671+8783G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131093446 | ||||||
| chr12:131093510
|
A | G | 45 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(42): Show | 45 | HG00140.hp1 HG00621.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.1671+8847A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131093510 | ||||||
| chr12:131093549
|
G | T | 3 | a0001c0001t0002g0130a0001c0004t0005g0036a0001c0005t0014g0049 | 3 | HG02040.hp1 NA19089.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1671+8886G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131093549 | ||||||
| chr12:131093615
|
G | A | 1 | a0001c0008t0001g0183 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1671+8952G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131093615 | ||||||
| chr12:131093638
|
G | A | 1 | a0001c0004t0002g0164 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1671+8975G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131093638 | ||||||
| chr12:131093853
|
G | A | 104 | a0001c0001t0001g0113a0001c0001t0001g0208a0001c0001t0002g0005others(101): Show | 104 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.1671+9190G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131093853 | ||||||
| chr12:131093853
|
G | T | 1 | a0003c0031t0003g0089 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1671+9190G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131093853 | ||||||
| chr12:131093943
|
TCAG | T | 162 | a0001c0001t0001g0113a0001c0001t0001g0156a0001c0001t0001g0163others(159): Show | 162 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.1671+9286_1671+928 others(7): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131093943 | |||||
| chr12:131093947
|
CAGCACCC others(20): Show |
C | 3 | a0001c0007t0004g0236a0002c0030t0032g0159a0010c0026t0013g0238 | 3 | HG02055.hp1 HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1671+9335_1671+936 others(31): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131093947 | |||||
| chr12:131093956
|
G | GC | 24 | a0001c0001t0002g0161a0001c0001t0002g0173a0001c0001t0002g0175others(21): Show | 24 | HG00735.hp1 HG01099.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1671+9295dupC | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131093956 | |||||
| chr12:131093960
|
C | G | 24 | a0001c0001t0002g0161a0001c0001t0002g0173a0001c0001t0002g0175others(21): Show | 24 | HG00735.hp1 HG01099.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1671+9297C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131093960 | ||||||
| chr12:131093969
|
GC | G | 24 | a0001c0001t0002g0161a0001c0001t0002g0173a0001c0001t0002g0175others(21): Show | 24 | HG00735.hp1 HG01099.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1671+9309delC | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131093969 | |||||
| chr12:131093974
|
G | C | 24 | a0001c0001t0002g0161a0001c0001t0002g0173a0001c0001t0002g0175others(21): Show | 24 | HG00735.hp1 HG01099.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1671+9311G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131093974 | ||||||
| chr12:131093974
|
G | GAGCACCC others(6): Show |
99 | a0001c0001t0001g0113a0001c0001t0001g0191a0001c0001t0001g0197others(96): Show | 99 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.1671+9323_1671+933 others(17): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131093974 | |||||
| chr12:131094056
|
C | T | 1 | a0001c0006t0001g0233 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1671+9393C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131094056 | ||||||
| chr12:131094071
|
C | T | 1 | a0001c0025t0021g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1671+9408C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131094071 | ||||||
| chr12:131094102
|
G | T | 2 | a0001c0001t0002g0173a0001c0003t0019g0218 | 2 | NA18959.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1671+9439G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131094102 | ||||||
| chr12:131094208
|
A | G | 213 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(210): Show | 213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.1671+9545A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131094208 | ||||||
| chr12:131094423
|
C | T | 12 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0003g0023others(9): Show | 12 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.1671+9760C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131094423 | ||||||
| chr12:131094442
|
T | TG | 5 | a0001c0001t0005g0045a0001c0002t0002g0001a0001c0002t0002g0006others(2): Show | 5 | HG01257.hp2 HG01261.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.1671+9784dupG | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131094442 | |||||
| chr12:131094582
|
G | GC | 102 | a0001c0001t0001g0113a0001c0001t0001g0208a0001c0001t0002g0005others(99): Show | 102 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.1671+9926dupC | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131094582 | |||||
| chr12:131094826
|
C | T | 1 | a0001c0020t0002g0180 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1672-10005C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131094826 | ||||||
| chr12:131094830
|
C | T | 12 | a0001c0001t0015g0060a0001c0003t0004g0013a0001c0003t0004g0104others(9): Show | 12 | HG00140.hp2 HG00738.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.1672-10001C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131094830 | ||||||
| chr12:131094839
|
A | G | 222 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(219): Show | 222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.1672-9992A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131094839 | ||||||
| chr12:131094869
|
T | C | 5 | a0001c0001t0002g0116a0001c0010t0007g0213a0001c0025t0021g0119others(2): Show | 5 | HG01243.hp1 HG01934.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1672-9962T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131094869 | ||||||
| chr12:131095290
|
G | A | 4 | a0001c0003t0004g0237a0001c0005t0003g0056a0001c0010t0007g0160others(1): Show | 4 | HG01175.hp2 HG01934.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1672-9541G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131095290 | ||||||
| chr12:131095309
|
G | A | 2 | a0002c0030t0032g0159a0010c0026t0013g0238 | 2 | HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1672-9522G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131095309 | ||||||
| chr12:131095345
|
C | T | 1 | a0003c0033t0030g0231 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1672-9486C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131095345 | ||||||
| chr12:131095433
|
G | A | 9 | a0001c0001t0002g0098a0001c0001t0002g0107a0001c0001t0002g0171others(6): Show | 9 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.1672-9398G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131095433 | ||||||
| chr12:131095529
|
A | G | 36 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0002g0149others(33): Show | 36 | HG00140.hp2 HG00738.hp2 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.1672-9302A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131095529 | ||||||
| chr12:131095633
|
C | T | 22 | a0001c0001t0002g0161a0001c0001t0002g0173a0001c0001t0002g0175others(19): Show | 22 | HG00735.hp1 HG01099.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1672-9198C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131095633 | ||||||
| chr12:131095666
|
C | G | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(206): Show | 209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1672-9165C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131095666 | ||||||
| chr12:131095738
|
G | A | 1 | a0001c0025t0021g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1672-9093G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131095738 | ||||||
| chr12:131095751
|
T | C | 1 | a0001c0025t0021g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1672-9080T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131095751 | ||||||
| chr12:131095865
|
G | C | 1 | a0001c0025t0021g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1672-8966G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131095865 | ||||||
| chr12:131095927
|
C | T | 36 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0002g0161others(33): Show | 36 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.1672-8904C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131095927 | ||||||
| chr12:131095975
|
C | A | 1 | a0001c0020t0002g0180 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1672-8856C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131095975 | ||||||
| chr12:131095976
|
G | A | 45 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(42): Show | 45 | HG00140.hp1 HG00621.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.1672-8855G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131095976 | ||||||
| chr12:131095989
|
G | A | 2 | a0001c0001t0001g0113a0001c0001t0003g0026 | 2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1672-8842G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131095989 | ||||||
| chr12:131095994
|
C | T | 22 | a0001c0001t0002g0149a0001c0001t0015g0060a0001c0002t0001g0169others(19): Show | 22 | HG00140.hp2 HG00738.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.1672-8837C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131095994 | ||||||
| chr12:131095994
|
CGCCTCCC others(44): Show |
C | 1 | a0001c0002t0001g0195 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1672-8829_1672-877 others(55): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131095994 | |||||
| chr12:131096002
|
AGCCCTGC others(44): Show |
A | 96 | a0001c0001t0001g0113a0001c0001t0001g0208a0001c0001t0002g0005others(93): Show | 96 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.1672-8808_1672-875 others(55): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131096002 | |||||
| chr12:131096033
|
G | A | 2 | a0001c0001t0002g0116a0001c0010t0007g0213 | 2 | HG01243.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1672-8798G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131096033 | ||||||
| chr12:131096071
|
G | A | 1 | a0001c0022t0016g0109 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1672-8760G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131096071 | ||||||
| chr12:131096082
|
G | A | 81 | a0001c0001t0001g0113a0001c0001t0001g0208a0001c0001t0002g0005others(78): Show | 81 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.1672-8749G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131096082 | ||||||
| chr12:131096441
|
G | A | 21 | a0001c0001t0002g0149a0001c0002t0001g0169a0001c0003t0004g0013others(18): Show | 21 | HG00738.hp2 HG01168.hp1 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.1672-8390G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131096441 | ||||||
| chr12:131096488
|
C | T | 5 | a0001c0001t0002g0130a0001c0004t0005g0036a0001c0005t0014g0049others(2): Show | 5 | HG01934.hp2 HG02040.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1672-8343C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131096488 | ||||||
| chr12:131096489
|
G | A | 21 | a0001c0001t0002g0161a0001c0001t0002g0173a0001c0001t0002g0175others(18): Show | 21 | HG00735.hp1 HG01099.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1672-8342G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131096489 | ||||||
| chr12:131096639
|
C | T | 2 | a0001c0003t0004g0012a0001c0003t0006g0211 | 2 | HG01175.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1672-8192C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131096639 | ||||||
| chr12:131096657
|
T | C | 1 | a0001c0020t0002g0180 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1672-8174T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131096657 | ||||||
| chr12:131096741
|
A | G | 1 | a0002c0029t0031g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1672-8090A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131096741 | ||||||
| chr12:131096751
|
C | T | 2 | a0001c0001t0002g0116a0001c0010t0007g0213 | 2 | HG01243.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1672-8080C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131096751 | ||||||
| chr12:131096777
|
G | A | 1 | a0008c0034t0026g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1672-8054G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131096777 | ||||||
| chr12:131096866
|
G | A | 47 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(44): Show | 47 | HG00140.hp1 HG00621.hp2 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.1672-7965G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131096866 | ||||||
| chr12:131096880
|
C | T | 2 | a0001c0001t0002g0116a0001c0010t0007g0213 | 2 | HG01243.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1672-7951C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131096880 | ||||||
| chr12:131096881
|
G | C | 10 | a0001c0002t0001g0223a0001c0003t0001g0152a0001c0003t0004g0207others(7): Show | 10 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1672-7950G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131096881 | ||||||
| chr12:131096884
|
C | T | 13 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0002g0187others(10): Show | 13 | HG01106.hp2 HG01261.hp1 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.1672-7947C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131096884 | ||||||
| chr12:131097030
|
T | C | 2 | a0001c0001t0005g0087a0001c0002t0001g0010 | 2 | HG02056.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.1672-7801T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131097030 | ||||||
| chr12:131097277
|
G | T | 11 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0003g0023others(8): Show | 11 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.1672-7554G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131097277 | ||||||
| chr12:131097343
|
C | G | 10 | a0001c0002t0001g0223a0001c0003t0001g0152a0001c0003t0004g0207others(7): Show | 10 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1672-7488C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131097343 | ||||||
| chr12:131097380
|
TCTC | T | 10 | a0001c0002t0001g0223a0001c0003t0001g0152a0001c0003t0004g0207others(7): Show | 10 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1672-7448_1672-744 others(7): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131097380 | |||||
| chr12:131097446
|
T | C | 10 | a0001c0002t0001g0223a0001c0003t0001g0152a0001c0003t0004g0207others(7): Show | 10 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1672-7385T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131097446 | ||||||
| chr12:131097522
|
G | A | 70 | a0001c0001t0001g0113a0001c0001t0001g0208a0001c0001t0002g0172others(67): Show | 70 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.1672-7309G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131097522 | ||||||
| chr12:131097607
|
C | T | 1 | a0008c0034t0026g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1672-7224C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131097607 | ||||||
| chr12:131097608
|
G | T | 192 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(189): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.1672-7223G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131097608 | ||||||
| chr12:131097813
|
G | T | 1 | a0001c0003t0004g0012 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1672-7018G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131097813 | ||||||
| chr12:131097893
|
C | T | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(206): Show | 209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1672-6938C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131097893 | ||||||
| chr12:131097912
|
C | T | 1 | a0001c0002t0001g0008 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1672-6919C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131097912 | ||||||
| chr12:131097977
|
C | T | 47 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(44): Show | 47 | HG00140.hp1 HG00621.hp2 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.1672-6854C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131097977 | ||||||
| chr12:131098028
|
C | T | 164 | a0001c0001t0001g0113a0001c0001t0001g0156a0001c0001t0001g0163others(161): Show | 164 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.1672-6803C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131098028 | ||||||
| chr12:131098040
|
C | T | 49 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(46): Show | 49 | HG00140.hp1 HG00621.hp2 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.1672-6791C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131098040 | ||||||
| chr12:131098093
|
C | T | 47 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(44): Show | 47 | HG00140.hp1 HG00621.hp2 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.1672-6738C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131098093 | ||||||
| chr12:131098094
|
G | A | 2 | a0001c0001t0027g0118a0001c0005t0008g0226 | 2 | HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1672-6737G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131098094 | ||||||
| chr12:131098110
|
T | C | 50 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(47): Show | 50 | HG00140.hp1 HG00621.hp2 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.1672-6721T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131098110 | ||||||
| chr12:131098128
|
C | CCTCCCAC others(32): Show |
23 | a0001c0001t0002g0161a0001c0001t0002g0173a0001c0001t0002g0175others(20): Show | 23 | HG00735.hp1 HG01099.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1672-6698_1672-669 others(43): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131098128 | |||||
| chr12:131098128
|
C | CCTCCCAC others(140): Show |
1 | a0001c0002t0040g0035 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1672-6698_1672-669 others(151): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131098128 | |||||
| chr12:131098128
|
C | CCTCCCAC others(140): Show |
2 | a0001c0002t0003g0032a0001c0002t0003g0076 | 2 | HG00609.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1672-6698_1672-669 others(151): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131098128 | |||||
| chr12:131098128
|
C | CCTCCCAC others(212): Show |
9 | a0001c0001t0002g0098a0001c0001t0002g0107a0001c0001t0002g0171others(6): Show | 9 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.1672-6698_1672-669 others(223): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131098128 | |||||
| chr12:131098134
|
G | A | 35 | a0001c0001t0002g0098a0001c0001t0002g0107a0001c0001t0002g0161others(32): Show | 35 | HG00280.hp2 HG00609.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.1672-6697G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131098134 | ||||||
| chr12:131098134
|
G | GCGGTGGC others(29): Show |
1 | a0001c0020t0002g0180 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1672-6673_1672-667 others(40): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131098134 | |||||
| chr12:131098134
|
G | GCGGTGGC others(140): Show |
65 | a0001c0001t0001g0113a0001c0001t0001g0208a0001c0001t0002g0005others(62): Show | 65 | HG00323.hp1 HG00323.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.1672-6678_1672-667 others(151): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131098134 | |||||
| chr12:131098134
|
G | GCGGTGGC others(104): Show |
1 | a0003c0033t0030g0231 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1672-6678_1672-667 others(115): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131098134 | |||||
| chr12:131098134
|
G | GCGGTGGC others(68): Show |
1 | a0001c0002t0001g0195 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1672-6678_1672-667 others(79): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131098134 | |||||
| chr12:131098142
|
CGCTGTCT others(29): Show |
C | 1 | a0001c0046t0017g0221 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1672-6677_1672-664 others(40): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131098142 | |||||
| chr12:131098146
|
G | GTCTGGGC others(68): Show |
12 | a0001c0002t0001g0223a0001c0003t0001g0152a0001c0003t0004g0207others(9): Show | 12 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1672-6678_1672-667 others(79): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131098146 | |||||
| chr12:131098146
|
G | GTCTGGGC others(176): Show |
3 | a0001c0022t0016g0109a0001c0042t0007g0176a0002c0029t0031g0222 | 3 | HG02809.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1672-6678_1672-667 others(187): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131098146 | |||||
| chr12:131098146
|
G | GTCTGGGC others(104): Show |
2 | a0001c0001t0002g0116a0001c0010t0007g0213 | 2 | HG01243.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1672-6678_1672-667 others(115): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131098146 | |||||
| chr12:131098151
|
G | GGCT | 91 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(88): Show | 91 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.1672-6678_1672-667 others(7): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131098151 | |||||
| chr12:131098159
|
T | C | 94 | a0001c0001t0001g0113a0001c0001t0001g0208a0001c0001t0002g0005others(91): Show | 94 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.1672-6672T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131098159 | ||||||
| chr12:131098160
|
T | G | 185 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(182): Show | 185 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.1672-6671T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131098160 | ||||||
| chr12:131098160
|
T | TCCTTCTC others(104): Show |
1 | a0001c0025t0021g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1672-6634_1672-663 others(115): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131098160 | |||||
| chr12:131098169
|
C | CACGGTGG others(65): Show |
45 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(42): Show | 45 | HG00140.hp1 HG00621.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.1672-6662_1672-666 others(76): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131098169 | ||||||
| chr12:131098169
|
C | CACGGTGG others(29): Show |
1 | a0001c0004t0005g0082 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1672-6662_1672-666 others(40): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131098169 | ||||||
| chr12:131098169
|
C | T | 1 | a0001c0002t0001g0195 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1672-6662C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131098169 | ||||||
| chr12:131098170
|
G | A | 75 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0191others(72): Show | 75 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1672-6661G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131098170 | ||||||
| chr12:131098171
|
C | T | 47 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(44): Show | 47 | HG00140.hp1 HG00621.hp2 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.1672-6660C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131098171 | ||||||
| chr12:131098172
|
A | G | 122 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(119): Show | 122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.1672-6659A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131098172 | ||||||
| chr12:131098174
|
T | C | 9 | a0001c0001t0002g0098a0001c0001t0002g0107a0001c0001t0002g0171others(6): Show | 9 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.1672-6657T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131098174 | ||||||
| chr12:131098178
|
T | C | 70 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0191others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.1672-6653T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131098178 | ||||||
| chr12:131098198
|
T | C | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(86): Show | 89 | HG00140.hp1 HG00621.hp2 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.1672-6633T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131098198 | ||||||
| chr12:131098324
|
C | T | 1 | a0001c0001t0002g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1672-6507C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131098324 | ||||||
| chr12:131098365
|
G | C | 47 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(44): Show | 47 | HG00140.hp1 HG00621.hp2 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.1672-6466G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131098365 | ||||||
| chr12:131098397
|
C | A | 7 | a0003c0012t0017g0017a0003c0012t0017g0158a0003c0032t0038g0090others(4): Show | 7 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1672-6434C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131098397 | ||||||
| chr12:131098407
|
G | C | 47 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(44): Show | 47 | HG00140.hp1 HG00621.hp2 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.1672-6424G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131098407 | ||||||
| chr12:131098663
|
G | A | 1 | a0001c0003t0018g0232 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1672-6168G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131098663 | ||||||
| chr12:131098709
|
C | T | 2 | a0001c0001t0002g0098a0001c0001t0015g0097 | 2 | HG01258.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.1672-6122C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131098709 | ||||||
| chr12:131099040
|
G | A | 4 | a0001c0003t0004g0237a0001c0005t0003g0056a0001c0010t0007g0160others(1): Show | 4 | HG01175.hp2 HG01934.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1672-5791G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131099040 | ||||||
| chr12:131099059
|
A | G | 9 | a0001c0001t0002g0098a0001c0001t0002g0107a0001c0001t0002g0171others(6): Show | 9 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.1672-5772A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131099059 | ||||||
| chr12:131099143
|
A | T | 2 | a0001c0001t0002g0116a0001c0010t0007g0213 | 2 | HG01243.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1672-5688A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131099143 | ||||||
| chr12:131099147
|
G | T | 1 | a0008c0034t0026g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1672-5684G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131099147 | ||||||
| chr12:131099234
|
T | C | 10 | a0001c0002t0001g0223a0001c0003t0001g0152a0001c0003t0004g0207others(7): Show | 10 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1672-5597T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131099234 | ||||||
| chr12:131099266
|
C | T | 3 | a0001c0001t0003g0026a0002c0030t0032g0159a0010c0026t0013g0238 | 3 | HG02723.hp2 HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1672-5565C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131099266 | ||||||
| chr12:131099351
|
G | A | 2 | a0001c0001t0002g0116a0001c0010t0007g0213 | 2 | HG01243.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1672-5480G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131099351 | ||||||
| chr12:131099357
|
A | G | 3 | a0001c0001t0002g0116a0001c0010t0007g0213a0003c0033t0030g0231 | 3 | HG01243.hp1 HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1672-5474A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131099357 | ||||||
| chr12:131099402
|
G | T | 2 | a0001c0001t0002g0116a0001c0010t0007g0213 | 2 | HG01243.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1672-5429G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131099402 | ||||||
| chr12:131099551
|
G | A | 9 | a0001c0001t0002g0098a0001c0001t0002g0107a0001c0001t0002g0171others(6): Show | 9 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.1672-5280G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131099551 | ||||||
| chr12:131099594
|
A | G | 1 | a0001c0045t0002g0091 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1672-5237A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131099594 | ||||||
| chr12:131099826
|
A | T | 50 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(47): Show | 50 | HG00140.hp1 HG00621.hp2 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.1672-5005A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131099826 | ||||||
| chr12:131099843
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1672-4988A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131099843 | ||||||
| chr12:131099862
|
A | G | 144 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(141): Show | 144 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1672-4969A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131099862 | ||||||
| chr12:131100122
|
A | T | 2 | a0001c0020t0002g0180a0001c0025t0021g0119 | 2 | HG01934.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1672-4709A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131100122 | ||||||
| chr12:131100171
|
GGGTT | G | 11 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0003g0023others(8): Show | 11 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.1672-4654_1672-465 others(8): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131100171 | |||||
| chr12:131100768
|
A | G | 86 | a0001c0001t0001g0113a0001c0001t0001g0191a0001c0001t0001g0197others(83): Show | 86 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.1672-4063A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131100768 | ||||||
| chr12:131100940
|
A | G | 1 | a0003c0040t0022g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1672-3891A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131100940 | ||||||
| chr12:131100993
|
G | A | 84 | a0001c0001t0001g0113a0001c0001t0001g0191a0001c0001t0001g0197others(81): Show | 84 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.1672-3838G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131100993 | ||||||
| chr12:131101005
|
C | G | 2 | a0001c0002t0003g0020a0001c0002t0003g0057 | 2 | HG02155.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.1672-3826C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131101005 | ||||||
| chr12:131101018
|
A | C | 1 | a0001c0020t0002g0180 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1672-3813A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131101018 | ||||||
| chr12:131101161
|
C | T | 1 | a0001c0002t0001g0174 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1672-3670C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131101161 | ||||||
| chr12:131101354
|
A | AT | 23 | a0001c0001t0002g0161a0001c0001t0002g0173a0001c0001t0002g0175others(20): Show | 23 | HG00735.hp1 HG01099.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1672-3469dupT | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131101354 | |||||
| chr12:131101365
|
TTTTC | T | 7 | a0001c0001t0001g0113a0001c0001t0001g0208a0001c0001t0002g0184others(4): Show | 7 | HG02293.hp1 HG02293.hp2 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.1672-3454_1672-345 others(8): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131101365 | |||||
| chr12:131101373
|
CTTTCT | C | 64 | a0001c0001t0002g0005a0001c0001t0002g0130a0001c0001t0002g0172others(61): Show | 64 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.1672-3454_1672-345 others(9): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131101373 | |||||
| chr12:131101373
|
CTTTCTT | C | 44 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(41): Show | 44 | HG00140.hp1 HG00735.hp2 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.1672-3454_1672-344 others(10): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131101373 | |||||
| chr12:131101377
|
C | CT | 43 | a0001c0001t0002g0173a0001c0001t0002g0175a0001c0001t0005g0055others(40): Show | 43 | HG00140.hp2 HG00738.hp2 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.1672-3427dupT | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131101377 | |||||
| chr12:131101377
|
C | CTT | 17 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0002g0149others(14): Show | 17 | HG00735.hp1 HG01106.hp2 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.1672-3428_1672-342 others(6): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131101377 | |||||
| chr12:131101377
|
C | CTTTCTTT others(5): Show |
1 | a0003c0032t0038g0090 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1672-3451_1672-345 others(16): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131101377 | |||||
| chr12:131101377
|
C | CTTTCTTT others(8): Show |
1 | a0003c0040t0022g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1672-3451_1672-345 others(19): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131101377 | |||||
| chr12:131101377
|
C | CTTTTTTT others(4): Show |
1 | a0008c0034t0026g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1672-3437_1672-342 others(15): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131101377 | |||||
| chr12:131101377
|
CT | C | 9 | a0001c0001t0001g0191a0001c0001t0003g0023a0001c0017t0008g0029others(6): Show | 9 | HG00280.hp1 HG00639.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.1672-3427delT | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131101377 | |||||
| chr12:131101377
|
CTT | C | 12 | a0001c0001t0001g0197a0001c0002t0001g0100a0001c0002t0001g0223others(9): Show | 12 | HG00639.hp1 HG01109.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1672-3428_1672-342 others(6): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131101377 | |||||
| chr12:131101377
|
CTTTT | C | 5 | a0001c0020t0002g0180a0001c0025t0021g0119a0003c0012t0017g0017others(2): Show | 5 | HG01934.hp2 HG02109.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1672-3430_1672-342 others(8): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131101377 | |||||
| chr12:131101382
|
T | C | 7 | a0001c0001t0001g0113a0001c0001t0001g0208a0001c0001t0002g0184others(4): Show | 7 | HG02293.hp1 HG02293.hp2 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.1672-3449T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131101382 | ||||||
| chr12:131101383
|
T | C | 60 | a0001c0001t0002g0005a0001c0001t0002g0172a0001c0001t0003g0026others(57): Show | 60 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.1672-3448T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131101383 | ||||||
| chr12:131101385
|
T | C | 3 | a0003c0012t0017g0017a0003c0012t0017g0158a0006c0037t0042g0046 | 3 | HG02109.hp2 HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1672-3446T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131101385 | ||||||
| chr12:131101456
|
C | T | 1 | a0001c0001t0002g0149 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1672-3375C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131101456 | ||||||
| chr12:131101536
|
G | A | 2 | a0001c0003t0018g0117a0001c0007t0018g0132 | 2 | HG02572.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1672-3295G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131101536 | ||||||
| chr12:131101649
|
G | A | 150 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(147): Show | 150 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.1672-3182G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131101649 | ||||||
| chr12:131101662
|
C | T | 1 | a0001c0001t0002g0235 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1672-3169C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131101662 | ||||||
| chr12:131101737
|
G | A | 47 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(44): Show | 47 | HG00140.hp1 HG00621.hp2 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.1672-3094G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131101737 | ||||||
| chr12:131101874
|
G | A | 1 | a0001c0007t0004g0018 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1672-2957G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131101874 | ||||||
| chr12:131102074
|
T | C | 2 | a0001c0001t0016g0147a0001c0001t0016g0182 | 2 | HG02280.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1672-2757T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131102074 | ||||||
| chr12:131102304
|
T | C | 96 | a0001c0001t0001g0113a0001c0001t0001g0191a0001c0001t0001g0197others(93): Show | 96 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.1672-2527T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131102304 | ||||||
| chr12:131102310
|
T | C | 3 | a0001c0003t0013g0224a0001c0003t0013g0225a0001c0003t0029g0214 | 3 | HG02280.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1672-2521T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131102310 | ||||||
| chr12:131102341
|
G | A | 74 | a0001c0001t0001g0113a0001c0001t0001g0208a0001c0001t0002g0005others(71): Show | 74 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.1672-2490G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131102341 | ||||||
| chr12:131102902
|
C | T | 2 | a0001c0001t0002g0228a0001c0001t0002g0235 | 2 | HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1672-1929C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131102902 | ||||||
| chr12:131102924
|
C | T | 1 | a0001c0003t0034g0014 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1672-1907C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131102924 | ||||||
| chr12:131102928
|
G | A | 7 | a0003c0012t0017g0017a0003c0012t0017g0158a0003c0032t0038g0090others(4): Show | 7 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1672-1903G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131102928 | ||||||
| chr12:131103124
|
T | C | 59 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(56): Show | 59 | HG00140.hp1 HG00621.hp2 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.1672-1707T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131103124 | ||||||
| chr12:131103139
|
A | G | 2 | a0002c0030t0032g0159a0010c0026t0013g0238 | 2 | HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1672-1692A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131103139 | ||||||
| chr12:131103165
|
C | T | 1 | a0001c0009t0014g0078 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1672-1666C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131103165 | ||||||
| chr12:131103223
|
C | T | 2 | a0001c0003t0004g0121a0001c0003t0004g0122 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1672-1608C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131103223 | ||||||
| chr12:131103332
|
T | A | 84 | a0001c0001t0001g0113a0001c0001t0001g0191a0001c0001t0001g0197others(81): Show | 84 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.1672-1499T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131103332 | ||||||
| chr12:131103402
|
G | A | 10 | a0001c0002t0001g0223a0001c0003t0001g0152a0001c0003t0004g0207others(7): Show | 10 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1672-1429G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131103402 | ||||||
| chr12:131103468
|
C | T | 1 | a0001c0025t0021g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1672-1363C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131103468 | ||||||
| chr12:131103569
|
G | GCACT | 104 | a0001c0001t0001g0113a0001c0001t0001g0156a0001c0001t0001g0163others(101): Show | 104 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.1672-1261_1672-125 others(8): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131103569 | |||||
| chr12:131103776
|
G | A | 1 | a0001c0008t0003g0059 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1672-1055G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131103776 | ||||||
| chr12:131103979
|
G | T | 1 | a0001c0002t0001g0199 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1672-852G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131103979 | ||||||
| chr12:131104006
|
C | T | 1 | a0001c0009t0004g0103 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1672-825C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131104006 | ||||||
| chr12:131104039
|
C | T | 2 | a0001c0001t0002g0228a0001c0001t0002g0235 | 2 | HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1672-792C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131104039 | ||||||
| chr12:131104235
|
C | CG | 11 | a0001c0001t0002g0005a0001c0002t0002g0006a0001c0002t0003g0068others(8): Show | 11 | HG00621.hp2 HG00735.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.1672-591dupG | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131104235 | |||||
| chr12:131104242
|
G | A | 2 | a0001c0017t0008g0029a0001c0017t0008g0030 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1672-589G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131104242 | ||||||
| chr12:131104272
|
T | C | 25 | a0001c0001t0002g0005a0001c0001t0002g0161a0001c0001t0002g0172others(22): Show | 25 | HG00735.hp1 HG01099.hp2 HG01515.hp2 others(22): Show |
intron_variant | MODIFIER | c.1672-559T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131104272 | ||||||
| chr12:131104450
|
G | A | 2 | a0001c0002t0003g0083a0001c0002t0010g0142 | 2 | HG00621.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1672-381G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131104450 | ||||||
| chr12:131104581
|
TGGCTGAG others(21): Show |
T | 1 | a0001c0004t0005g0072 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1672-248_1672-221d others(30): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131104581 | |||||
| chr12:131104607
|
AGGGCACC others(3): Show |
A | 2 | a0001c0002t0001g0202a0001c0002t0003g0053 | 2 | HG02300.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1672-216_1672-207d others(12): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | 131104607 | |||||
| chr12:131104613
|
C | T | 1 | a0001c0004t0005g0072 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1672-218C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131104613 | ||||||
| chr12:131104614
|
C | G | 1 | a0001c0004t0005g0072 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1672-217C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131104614 | ||||||
| chr12:131104778
|
C | T | 2 | a0001c0002t0003g0038a0001c0002t0003g0061 | 2 | HG01496.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1672-53C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | chr12 | 131104778 | ||||||
| chr12:131105107
|
G | A | 7 | a0001c0003t0004g0207a0001c0003t0013g0129a0001c0007t0004g0102others(4): Show | 7 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1775+173G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 16/24 | chr12 | 131105107 | ||||||
| chr12:131105145
|
C | T | 5 | a0001c0001t0016g0147a0001c0001t0016g0182a0001c0022t0016g0109others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1775+211C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 16/24 | chr12 | 131105145 | ||||||
| chr12:131105199
|
G | T | 5 | a0001c0001t0016g0147a0001c0001t0016g0182a0001c0022t0016g0109others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1775+265G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 16/24 | chr12 | 131105199 | ||||||
| chr12:131105223
|
C | T | 14 | a0001c0003t0004g0207a0001c0003t0013g0129a0001c0007t0004g0102others(11): Show | 14 | HG01109.hp1 HG01934.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1775+289C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 16/24 | chr12 | 131105223 | ||||||
| chr12:131106260
|
C | T | 1 | a0001c0025t0021g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1887+395C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 17/24 | chr12 | 131106260 | ||||||
| chr12:131106630
|
C | T | 1 | a0003c0031t0003g0089 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1887+765C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 17/24 | chr12 | 131106630 | ||||||
| chr12:131106668
|
C | T | 2 | a0002c0030t0032g0159a0010c0026t0013g0238 | 2 | HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1887+803C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 17/24 | chr12 | 131106668 | ||||||
| chr12:131107014
|
A | G | 7 | a0001c0001t0016g0147a0001c0001t0016g0182a0001c0022t0016g0109others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1887+1149A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 17/24 | chr12 | 131107014 | ||||||
| chr12:131107081
|
C | A | 17 | a0001c0001t0002g0116a0001c0003t0004g0207a0001c0003t0013g0129others(14): Show | 17 | HG01109.hp1 HG01243.hp1 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.1887+1216C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 17/24 | chr12 | 131107081 | ||||||
| chr12:131107181
|
C | T | 69 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(66): Show | 69 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.1887+1316C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 17/24 | chr12 | 131107181 | ||||||
| chr12:131107204
|
G | A | 24 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(21): Show | 24 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.1887+1339G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 17/24 | chr12 | 131107204 | ||||||
| chr12:131107240
|
T | C | 3 | a0001c0003t0006g0092a0001c0003t0006g0185a0001c0003t0006g0215 | 3 | HG00735.hp1 HG01099.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.1887+1375T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 17/24 | chr12 | 131107240 | ||||||
| chr12:131107270
|
T | C | 1 | a0001c0008t0003g0059 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1887+1405T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 17/24 | chr12 | 131107270 | ||||||
| chr12:131107274
|
T | C | 14 | a0001c0003t0004g0207a0001c0003t0013g0129a0001c0003t0018g0232others(11): Show | 14 | HG01109.hp1 HG01934.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1887+1409T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 17/24 | chr12 | 131107274 | ||||||
| chr12:131107302
|
C | CGAAGGGC others(45): Show |
93 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(90): Show | 93 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.1888-1383_1888-138 others(56): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr12 | 131107302 | |||||
| chr12:131107338
|
T | TGTGTCTG others(45): Show |
5 | a0001c0001t0016g0147a0001c0001t0016g0182a0001c0022t0016g0109others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1888-1383_1888-138 others(56): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr12 | 131107338 | |||||
| chr12:131107342
|
G | T | 2 | a0003c0041t0004g0178a0007c0039t0001g0229 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1888-1382G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 17/24 | chr12 | 131107342 | ||||||
| chr12:131107345
|
A | G | 2 | a0003c0041t0004g0178a0007c0039t0001g0229 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1888-1379A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 17/24 | chr12 | 131107345 | ||||||
| chr12:131107357
|
A | G | 1 | a0001c0042t0007g0176 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1888-1367A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 17/24 | chr12 | 131107357 | ||||||
| chr12:131107390
|
C | T | 2 | a0003c0041t0004g0178a0007c0039t0001g0229 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1888-1334C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 17/24 | chr12 | 131107390 | ||||||
| chr12:131107394
|
T | G | 2 | a0003c0041t0004g0178a0007c0039t0001g0229 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1888-1330T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 17/24 | chr12 | 131107394 | ||||||
| chr12:131107402
|
G | C | 2 | a0003c0041t0004g0178a0007c0039t0001g0229 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1888-1322G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 17/24 | chr12 | 131107402 | ||||||
| chr12:131107426
|
T | C | 9 | a0001c0001t0016g0147a0001c0001t0016g0182a0001c0008t0003g0067others(6): Show | 9 | HG00738.hp2 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1888-1298T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 17/24 | chr12 | 131107426 | ||||||
| chr12:131107426
|
TGCTCTCC others(45): Show |
T | 1 | a0001c0043t0008g0227 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1888-1275_1888-122 others(56): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr12 | 131107426 | |||||
| chr12:131107449
|
A | AAATCCCA others(45): Show |
1 | a0001c0008t0003g0067 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1888-1230_1888-117 others(56): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr12 | 131107449 | |||||
| chr12:131107454
|
C | G | 2 | a0003c0041t0004g0178a0007c0039t0001g0229 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1888-1270C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 17/24 | chr12 | 131107454 | ||||||
| chr12:131107478
|
C | T | 2 | a0003c0041t0004g0178a0007c0039t0001g0229 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1888-1246C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 17/24 | chr12 | 131107478 | ||||||
| chr12:131107501
|
G | A | 41 | a0001c0001t0002g0116a0001c0001t0002g0149a0001c0001t0015g0060others(38): Show | 41 | HG00140.hp2 HG00323.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.1888-1223G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 17/24 | chr12 | 131107501 | ||||||
| chr12:131107546
|
T | C | 2 | a0003c0041t0004g0178a0007c0039t0001g0229 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1888-1178T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 17/24 | chr12 | 131107546 | ||||||
| chr12:131107548
|
G | T | 2 | a0003c0041t0004g0178a0007c0039t0001g0229 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1888-1176G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 17/24 | chr12 | 131107548 | ||||||
| chr12:131107552
|
A | T | 195 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(192): Show | 195 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.1888-1172A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 17/24 | chr12 | 131107552 | ||||||
| chr12:131107903
|
G | A | 3 | a0001c0022t0016g0109a0002c0029t0031g0222a0008c0034t0026g0043 | 3 | HG03486.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1888-821G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 17/24 | chr12 | 131107903 | ||||||
| chr12:131108044
|
G | A | 33 | a0001c0001t0016g0147a0001c0001t0016g0182a0001c0004t0002g0004others(30): Show | 33 | HG00140.hp1 HG00735.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1888-680G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 17/24 | chr12 | 131108044 | ||||||
| chr12:131108435
|
C | T | 1 | a0001c0002t0037g0194 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1888-289C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 17/24 | chr12 | 131108435 | ||||||
| chr12:131108498
|
A | G | 1 | a0001c0009t0004g0103 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1888-226A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 17/24 | chr12 | 131108498 | ||||||
| chr12:131108961
|
G | A | 29 | a0001c0004t0002g0004a0001c0004t0002g0007a0001c0004t0002g0011others(26): Show | 29 | HG00140.hp1 HG00735.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.2041+84G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131108961 | ||||||
| chr12:131109164
|
T | C | 1 | a0001c0002t0010g0201 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2041+287T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131109164 | ||||||
| chr12:131109192
|
A | T | 1 | a0001c0002t0001g0223 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2041+315A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131109192 | ||||||
| chr12:131109599
|
T | G | 1 | a0012c0024t0002g0196 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2041+722T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131109599 | ||||||
| chr12:131109668
|
A | G | 1 | a0001c0020t0002g0180 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2041+791A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131109668 | ||||||
| chr12:131109784
|
G | A | 2 | a0002c0030t0032g0159a0010c0026t0013g0238 | 2 | HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2041+907G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131109784 | ||||||
| chr12:131109815
|
A | G | 24 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(21): Show | 24 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.2041+938A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131109815 | ||||||
| chr12:131109970
|
T | A | 5 | a0001c0001t0016g0147a0001c0001t0016g0182a0001c0022t0016g0109others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2041+1093T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131109970 | ||||||
| chr12:131110018
|
C | T | 71 | a0001c0001t0001g0113a0001c0001t0001g0208a0001c0001t0001g0212others(68): Show | 71 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.2041+1141C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131110018 | ||||||
| chr12:131110136
|
TA | T | 154 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(151): Show | 154 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.2041+1265delA | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr12 | 131110136 | |||||
| chr12:131110356
|
CTT | C | 152 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(149): Show | 152 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.2041+1489_2041+149 others(6): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr12 | 131110356 | |||||
| chr12:131110704
|
G | T | 1 | a0001c0036t0003g0075 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2041+1827G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131110704 | ||||||
| chr12:131110725
|
T | C | 1 | a0001c0002t0003g0034 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2041+1848T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131110725 | ||||||
| chr12:131110773
|
C | T | 7 | a0001c0003t0004g0207a0001c0003t0013g0129a0001c0007t0004g0102others(4): Show | 7 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2041+1896C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131110773 | ||||||
| chr12:131110832
|
T | C | 1 | a0001c0002t0003g0077 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2041+1955T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131110832 | ||||||
| chr12:131110912
|
C | T | 16 | a0001c0001t0002g0116a0001c0003t0004g0207a0001c0003t0013g0129others(13): Show | 16 | HG01109.hp1 HG01243.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.2041+2035C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131110912 | ||||||
| chr12:131110929
|
A | C | 24 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(21): Show | 24 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.2041+2052A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131110929 | ||||||
| chr12:131110975
|
T | C | 24 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(21): Show | 24 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.2041+2098T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131110975 | ||||||
| chr12:131111045
|
T | A | 22 | a0001c0001t0002g0149a0001c0001t0015g0060a0001c0003t0004g0013others(19): Show | 22 | HG00140.hp2 HG00323.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.2041+2168T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131111045 | ||||||
| chr12:131111097
|
C | CTT | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(20): Show | 23 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.2041+2230_2041+223 others(6): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr12 | 131111097 | |||||
| chr12:131111109
|
C | T | 1 | a0001c0001t0002g0098 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2041+2232C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131111109 | ||||||
| chr12:131111362
|
G | A | 5 | a0001c0001t0016g0147a0001c0001t0016g0182a0001c0022t0016g0109others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2041+2485G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131111362 | ||||||
| chr12:131111379
|
A | G | 24 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(21): Show | 24 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.2041+2502A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131111379 | ||||||
| chr12:131111400
|
G | C | 21 | a0001c0001t0002g0149a0001c0001t0015g0060a0001c0003t0004g0013others(18): Show | 21 | HG00140.hp2 HG00323.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.2041+2523G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131111400 | ||||||
| chr12:131111451
|
G | T | 1 | a0001c0002t0010g0138 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2041+2574G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131111451 | ||||||
| chr12:131111612
|
TTG | T | 29 | a0001c0004t0002g0004a0001c0004t0002g0007a0001c0004t0002g0011others(26): Show | 29 | HG00140.hp1 HG00735.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.2041+2737_2041+273 others(6): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr12 | 131111612 | |||||
| chr12:131111708
|
C | T | 26 | a0001c0001t0002g0161a0001c0001t0002g0172a0001c0001t0002g0175others(23): Show | 26 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.2041+2831C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131111708 | ||||||
| chr12:131111888
|
G | A | 192 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(189): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.2041+3011G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131111888 | ||||||
| chr12:131111894
|
G | A | 2 | a0001c0004t0002g0131a0001c0008t0001g0170 | 2 | NA18970.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.2041+3017G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131111894 | ||||||
| chr12:131111908
|
T | G | 1 | a0001c0001t0002g0184 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2041+3031T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131111908 | ||||||
| chr12:131111954
|
C | T | 29 | a0001c0004t0002g0004a0001c0004t0002g0007a0001c0004t0002g0011others(26): Show | 29 | HG00140.hp1 HG00735.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.2041+3077C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131111954 | ||||||
| chr12:131112132
|
ACTATTTA others(1): Show |
A | 72 | a0001c0001t0001g0113a0001c0001t0001g0208a0001c0001t0001g0212others(69): Show | 72 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.2041+3257_2041+326 others(12): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr12 | 131112132 | |||||
| chr12:131112262
|
T | C | 1 | a0001c0007t0006g0021 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2041+3385T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131112262 | ||||||
| chr12:131112317
|
C | G | 1 | a0007c0039t0001g0229 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2041+3440C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131112317 | ||||||
| chr12:131112331
|
C | G | 2 | a0001c0001t0002g0228a0001c0001t0002g0235 | 2 | HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2041+3454C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131112331 | ||||||
| chr12:131112532
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2041+3655C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131112532 | ||||||
| chr12:131112534
|
C | T | 1 | a0001c0025t0021g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2041+3657C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131112534 | ||||||
| chr12:131112818
|
C | T | 9 | a0001c0001t0001g0111a0001c0001t0001g0156a0001c0001t0001g0163others(6): Show | 9 | HG00280.hp1 HG00639.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.2041+3941C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131112818 | ||||||
| chr12:131112930
|
A | G | 1 | a0001c0007t0006g0021 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2041+4053A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131112930 | ||||||
| chr12:131112981
|
G | C | 1 | a0001c0002t0010g0134 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2041+4104G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131112981 | ||||||
| chr12:131113035
|
G | A | 17 | a0001c0001t0002g0116a0001c0003t0004g0207a0001c0003t0013g0129others(14): Show | 17 | HG01109.hp1 HG01243.hp1 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.2041+4158G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131113035 | ||||||
| chr12:131113044
|
G | A | 1 | a0001c0003t0019g0218 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2041+4167G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131113044 | ||||||
| chr12:131113064
|
G | A | 1 | a0001c0003t0013g0129 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2041+4187G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131113064 | ||||||
| chr12:131113267
|
C | CT | 71 | a0001c0001t0001g0113a0001c0001t0001g0208a0001c0001t0001g0212others(68): Show | 71 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.2041+4400dupT | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr12 | 131113267 | |||||
| chr12:131113770
|
C | T | 1 | a0008c0034t0026g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2042-4615C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131113770 | ||||||
| chr12:131113843
|
C | T | 1 | a0001c0007t0006g0021 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2042-4542C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131113843 | ||||||
| chr12:131113911
|
T | C | 1 | a0001c0020t0002g0180 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2042-4474T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131113911 | ||||||
| chr12:131114039
|
G | A | 41 | a0001c0001t0002g0116a0001c0001t0002g0149a0001c0001t0015g0060others(38): Show | 41 | HG00140.hp2 HG00323.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.2042-4346G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131114039 | ||||||
| chr12:131114370
|
A | G | 1 | a0001c0003t0029g0214 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2042-4015A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131114370 | ||||||
| chr12:131114566
|
G | A | 1 | a0001c0002t0048g0151 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2042-3819G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131114566 | ||||||
| chr12:131114638
|
G | C | 1 | a0001c0036t0003g0075 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2042-3747G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131114638 | ||||||
| chr12:131114734
|
TG | T | 15 | a0001c0001t0002g0187a0001c0001t0002g0217a0001c0001t0011g0033others(12): Show | 15 | HG01261.hp1 HG02083.hp2 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.2042-3644delG | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr12 | 131114734 | |||||
| chr12:131115031
|
C | G | 1 | a0001c0007t0006g0021 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2042-3354C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131115031 | ||||||
| chr12:131115048
|
C | T | 5 | a0001c0001t0016g0147a0001c0001t0016g0182a0001c0022t0016g0109others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2042-3337C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131115048 | ||||||
| chr12:131115073
|
A | G | 1 | a0001c0001t0005g0045 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2042-3312A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131115073 | ||||||
| chr12:131115189
|
C | G | 1 | a0001c0003t0036g0209 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2042-3196C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131115189 | ||||||
| chr12:131115241
|
G | A | 1 | a0003c0040t0022g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2042-3144G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131115241 | ||||||
| chr12:131115260
|
A | G | 31 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0004t0002g0004others(28): Show | 31 | HG00140.hp1 HG00735.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.2042-3125A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131115260 | ||||||
| chr12:131115270
|
A | G | 88 | a0001c0001t0001g0113a0001c0001t0002g0005a0001c0001t0002g0130others(85): Show | 88 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.2042-3115A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131115270 | ||||||
| chr12:131115381
|
G | A | 1 | a0001c0001t0009g0166 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2042-3004G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131115381 | ||||||
| chr12:131115492
|
G | A | 8 | a0001c0003t0004g0207a0001c0003t0013g0129a0001c0007t0004g0102others(5): Show | 8 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2042-2893G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131115492 | ||||||
| chr12:131115509
|
C | T | 29 | a0001c0004t0002g0004a0001c0004t0002g0007a0001c0004t0002g0011others(26): Show | 29 | HG00140.hp1 HG00735.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.2042-2876C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131115509 | ||||||
| chr12:131115552
|
TC | T | 29 | a0001c0004t0002g0004a0001c0004t0002g0007a0001c0004t0002g0011others(26): Show | 29 | HG00140.hp1 HG00735.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.2042-2832delC | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131115552 | ||||||
| chr12:131115677
|
T | G | 2 | a0001c0025t0021g0119a0003c0031t0003g0089 | 2 | HG01934.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2042-2708T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131115677 | ||||||
| chr12:131115697
|
C | T | 1 | a0001c0020t0002g0180 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2042-2688C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131115697 | ||||||
| chr12:131115706
|
C | T | 1 | a0010c0026t0013g0238 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2042-2679C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131115706 | ||||||
| chr12:131115778
|
G | A | 1 | a0001c0003t0033g0181 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2042-2607G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131115778 | ||||||
| chr12:131115801
|
T | C | 24 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(21): Show | 24 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.2042-2584T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131115801 | ||||||
| chr12:131115819
|
C | T | 3 | a0001c0001t0002g0116a0001c0010t0007g0213a0003c0032t0038g0090 | 3 | HG01243.hp1 HG02559.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2042-2566C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131115819 | ||||||
| chr12:131116100
|
T | C | 1 | a0001c0002t0003g0076 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2042-2285T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131116100 | ||||||
| chr12:131116109
|
C | T | 4 | a0001c0002t0001g0125a0001c0002t0008g0016a0001c0003t0013g0224others(1): Show | 4 | HG02896.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2042-2276C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131116109 | ||||||
| chr12:131116210
|
A | T | 93 | a0001c0001t0001g0113a0001c0001t0001g0208a0001c0001t0001g0212others(90): Show | 93 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.2042-2175A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131116210 | ||||||
| chr12:131116348
|
C | T | 24 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(21): Show | 24 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.2042-2037C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131116348 | ||||||
| chr12:131116482
|
A | AAGGGCAG others(41): Show |
8 | a0001c0003t0004g0207a0001c0003t0013g0129a0001c0007t0004g0102others(5): Show | 8 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2042-1857_2042-185 others(52): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr12 | 131116482 | |||||
| chr12:131116580
|
C | G | 1 | a0001c0004t0002g0164 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2042-1805C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131116580 | ||||||
| chr12:131116710
|
G | C | 72 | a0001c0001t0001g0113a0001c0001t0001g0208a0001c0001t0001g0212others(69): Show | 72 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.2042-1675G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131116710 | ||||||
| chr12:131116955
|
G | A | 171 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(168): Show | 171 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.2042-1430G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131116955 | ||||||
| chr12:131117226
|
A | G | 2 | a0003c0012t0017g0158a0007c0039t0001g0229 | 2 | HG02922.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2042-1159A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131117226 | ||||||
| chr12:131117526
|
G | A | 25 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(22): Show | 25 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.2042-859G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131117526 | ||||||
| chr12:131117535
|
A | G | 1 | a0001c0020t0002g0180 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2042-850A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131117535 | ||||||
| chr12:131117679
|
G | C | 29 | a0001c0004t0002g0004a0001c0004t0002g0007a0001c0004t0002g0011others(26): Show | 29 | HG00140.hp1 HG00735.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.2042-706G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131117679 | ||||||
| chr12:131117682
|
A | C | 72 | a0001c0001t0001g0113a0001c0001t0001g0208a0001c0001t0001g0212others(69): Show | 72 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.2042-703A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131117682 | ||||||
| chr12:131117998
|
C | T | 1 | a0001c0002t0002g0006 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2042-387C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131117998 | ||||||
| chr12:131118138
|
A | G | 1 | a0001c0003t0006g0092 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2042-247A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131118138 | ||||||
| chr12:131118222
|
G | A | 3 | a0001c0004t0002g0193a0001c0004t0009g0168a0001c0004t0043g0024 | 3 | HG00140.hp1 HG00741.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.2042-163G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131118222 | ||||||
| chr12:131118266
|
C | T | 95 | a0001c0001t0001g0113a0001c0001t0001g0208a0001c0001t0001g0212others(92): Show | 95 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.2042-119C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 18/24 | chr12 | 131118266 | ||||||
| chr12:131118486
|
G | A | 20 | a0001c0001t0002g0149a0001c0001t0015g0060a0001c0003t0004g0013others(17): Show | 20 | HG00140.hp2 HG00323.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.2108+35G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 19/24 | chr12 | 131118486 | ||||||
| chr12:131118588
|
G | A | 30 | a0001c0004t0002g0004a0001c0004t0002g0007a0001c0004t0002g0011others(27): Show | 30 | HG00140.hp1 HG00735.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.2108+137G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 19/24 | chr12 | 131118588 | ||||||
| chr12:131118750
|
C | G | 144 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(141): Show | 144 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.2108+299C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 19/24 | chr12 | 131118750 | ||||||
| chr12:131118822
|
G | A | 1 | a0001c0001t0005g0055 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2108+371G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 19/24 | chr12 | 131118822 | ||||||
| chr12:131119058
|
G | A | 25 | a0001c0001t0002g0116a0001c0001t0016g0147a0001c0001t0016g0182others(22): Show | 25 | HG01109.hp1 HG01243.hp1 HG01934.hp1 others(22): Show |
intron_variant | MODIFIER | c.2108+607G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 19/24 | chr12 | 131119058 | ||||||
| chr12:131119134
|
C | T | 170 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(167): Show | 170 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.2108+683C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 19/24 | chr12 | 131119134 | ||||||
| chr12:131119156
|
T | C | 1 | a0003c0031t0003g0089 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2108+705T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 19/24 | chr12 | 131119156 | ||||||
| chr12:131119351
|
A | G | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(142): Show | 145 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.2108+900A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 19/24 | chr12 | 131119351 | ||||||
| chr12:131119355
|
A | G | 4 | a0001c0003t0018g0232a0001c0007t0018g0132a0002c0030t0032g0159others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2108+904A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 19/24 | chr12 | 131119355 | ||||||
| chr12:131119362
|
C | T | 2 | a0001c0002t0008g0016a0001c0007t0006g0021 | 2 | HG02055.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.2108+911C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 19/24 | chr12 | 131119362 | ||||||
| chr12:131119482
|
C | G | 1 | a0001c0007t0006g0021 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2108+1031C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 19/24 | chr12 | 131119482 | ||||||
| chr12:131119644
|
C | T | 1 | a0001c0003t0004g0234 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2108+1193C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 19/24 | chr12 | 131119644 | ||||||
| chr12:131119954
|
C | T | 1 | a0001c0001t0002g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2109-893C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 19/24 | chr12 | 131119954 | ||||||
| chr12:131120094
|
A | C | 28 | a0001c0004t0002g0004a0001c0004t0002g0007a0001c0004t0002g0011others(25): Show | 28 | HG00140.hp1 HG00735.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.2109-753A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 19/24 | chr12 | 131120094 | ||||||
| chr12:131120132
|
C | T | 4 | a0001c0002t0001g0125a0001c0002t0008g0016a0001c0003t0013g0224others(1): Show | 4 | HG02896.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2109-715C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 19/24 | chr12 | 131120132 | ||||||
| chr12:131120135
|
T | A | 1 | a0001c0007t0006g0021 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2109-712T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 19/24 | chr12 | 131120135 | ||||||
| chr12:131120245
|
C | T | 1 | a0001c0007t0006g0021 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2109-602C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 19/24 | chr12 | 131120245 | ||||||
| chr12:131120308
|
C | T | 4 | a0001c0046t0017g0221a0003c0012t0017g0017a0003c0012t0017g0158others(1): Show | 4 | HG01934.hp1 HG02109.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2109-539C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 19/24 | chr12 | 131120308 | ||||||
| chr12:131120478
|
C | T | 15 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(12): Show | 15 | HG00280.hp1 HG00639.hp1 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.2109-369C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 19/24 | chr12 | 131120478 | ||||||
| chr12:131120484
|
C | T | 1 | a0001c0004t0005g0072 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2109-363C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 19/24 | chr12 | 131120484 | ||||||
| chr12:131120485
|
G | A | 1 | a0008c0034t0026g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2109-362G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 19/24 | chr12 | 131120485 | ||||||
| chr12:131120540
|
T | C | 1 | a0001c0003t0019g0218 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2109-307T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 19/24 | chr12 | 131120540 | ||||||
| chr12:131121014
|
C | T | 1 | a0001c0025t0021g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2175+101C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131121014 | ||||||
| chr12:131121025
|
G | A | 1 | a0003c0031t0003g0089 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2175+112G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131121025 | ||||||
| chr12:131121068
|
G | A | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(20): Show | 23 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.2175+155G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131121068 | ||||||
| chr12:131121077
|
G | T | 1 | a0002c0044t0007g0126 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2175+164G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131121077 | ||||||
| chr12:131121130
|
C | T | 1 | a0001c0003t0001g0152 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2175+217C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131121130 | ||||||
| chr12:131121418
|
C | G | 1 | a0001c0007t0006g0021 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2175+505C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131121418 | ||||||
| chr12:131121579
|
C | T | 1 | a0001c0002t0003g0068 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2175+666C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131121579 | ||||||
| chr12:131121689
|
T | A | 46 | a0001c0001t0002g0116a0001c0001t0002g0149a0001c0001t0015g0060others(43): Show | 46 | HG00140.hp2 HG00323.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.2175+776T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131121689 | ||||||
| chr12:131121716
|
G | C | 1 | a0001c0002t0046g0084 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2175+803G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131121716 | ||||||
| chr12:131121735
|
C | T | 2 | a0001c0001t0002g0228a0001c0001t0002g0235 | 2 | HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2175+822C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131121735 | ||||||
| chr12:131121762
|
T | C | 22 | a0001c0001t0002g0149a0001c0001t0015g0060a0001c0003t0004g0013others(19): Show | 22 | HG00140.hp2 HG00323.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.2175+849T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131121762 | ||||||
| chr12:131121809
|
C | T | 1 | a0001c0009t0004g0103 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2175+896C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131121809 | ||||||
| chr12:131121812
|
A | G | 2 | a0001c0003t0004g0101a0001c0003t0004g0108 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2175+899A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131121812 | ||||||
| chr12:131121876
|
G | A | 1 | a0003c0033t0030g0231 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2175+963G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131121876 | ||||||
| chr12:131121978
|
G | A | 1 | a0001c0045t0002g0091 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2175+1065G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131121978 | ||||||
| chr12:131121985
|
A | G | 8 | a0001c0001t0005g0028a0001c0002t0001g0008a0001c0002t0001g0202others(5): Show | 8 | HG01243.hp2 HG01496.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.2175+1072A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131121985 | ||||||
| chr12:131122113
|
G | C | 1 | a0010c0026t0013g0238 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2175+1200G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131122113 | ||||||
| chr12:131122139
|
G | T | 1 | a0004c0015t0005g0086 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2175+1226G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131122139 | ||||||
| chr12:131122207
|
C | G | 134 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(131): Show | 134 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.2175+1294C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131122207 | ||||||
| chr12:131122229
|
G | A | 4 | a0001c0046t0017g0221a0003c0012t0017g0017a0003c0012t0017g0158others(1): Show | 4 | HG01934.hp1 HG02109.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2175+1316G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131122229 | ||||||
| chr12:131122234
|
G | A | 2 | a0001c0007t0006g0021a0003c0033t0030g0231 | 2 | HG02055.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2175+1321G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131122234 | ||||||
| chr12:131122259
|
G | A | 17 | a0001c0001t0005g0087a0001c0001t0009g0137a0001c0001t0011g0062others(14): Show | 17 | HG01167.hp2 HG01169.hp2 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.2175+1346G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131122259 | ||||||
| chr12:131122303
|
A | G | 92 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0115others(89): Show | 92 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.2175+1390A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131122303 | ||||||
| chr12:131122313
|
G | T | 1 | a0001c0002t0001g0199 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2175+1400G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131122313 | ||||||
| chr12:131122381
|
C | G | 133 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(130): Show | 133 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.2175+1468C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131122381 | ||||||
| chr12:131122391
|
T | TA | 3 | a0001c0001t0002g0116a0001c0007t0006g0021a0001c0010t0007g0213 | 3 | HG01243.hp1 HG02055.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2175+1479dupA | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr12 | 131122391 | |||||
| chr12:131122445
|
C | T | 1 | a0001c0003t0036g0209 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2175+1532C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131122445 | ||||||
| chr12:131122488
|
G | T | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(148): Show | 151 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.2175+1575G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131122488 | ||||||
| chr12:131122498
|
C | T | 2 | a0001c0007t0006g0021a0003c0033t0030g0231 | 2 | HG02055.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2175+1585C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131122498 | ||||||
| chr12:131122502
|
G | A | 2 | a0001c0007t0006g0021a0003c0033t0030g0231 | 2 | HG02055.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2175+1589G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131122502 | ||||||
| chr12:131122504
|
T | G | 3 | a0001c0001t0002g0116a0001c0003t0029g0214a0001c0010t0007g0213 | 3 | HG01243.hp1 HG02280.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2175+1591T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131122504 | ||||||
| chr12:131122506
|
T | C | 2 | a0001c0007t0006g0021a0003c0033t0030g0231 | 2 | HG02055.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2175+1593T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131122506 | ||||||
| chr12:131122509
|
G | T | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(150): Show | 153 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.2175+1596G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131122509 | ||||||
| chr12:131122511
|
G | A | 2 | a0001c0007t0006g0021a0003c0033t0030g0231 | 2 | HG02055.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2175+1598G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131122511 | ||||||
| chr12:131122512
|
G | A | 2 | a0001c0001t0001g0002a0001c0001t0001g0003 | 2 | HG01433.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.2175+1599G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131122512 | ||||||
| chr12:131122530
|
A | G | 15 | a0001c0001t0016g0147a0001c0001t0016g0182a0001c0010t0007g0160others(12): Show | 15 | HG01934.hp1 HG02109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.2175+1617A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131122530 | ||||||
| chr12:131122532
|
T | C | 71 | a0001c0001t0002g0149a0001c0001t0002g0161a0001c0001t0002g0172others(68): Show | 71 | HG00140.hp2 HG00323.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.2175+1619T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131122532 | ||||||
| chr12:131122536
|
C | T | 126 | a0001c0001t0002g0107a0001c0001t0002g0149a0001c0001t0002g0161others(123): Show | 126 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.2175+1623C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131122536 | ||||||
| chr12:131122589
|
G | A | 1 | a0001c0004t0002g0164 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2175+1676G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131122589 | ||||||
| chr12:131122591
|
C | T | 50 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(47): Show | 50 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.2175+1678C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131122591 | ||||||
| chr12:131122615
|
C | G | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(33): Show | 36 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.2175+1702C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131122615 | ||||||
| chr12:131122639
|
G | C | 51 | a0001c0001t0002g0107a0001c0001t0002g0116a0001c0001t0002g0217others(48): Show | 51 | HG00140.hp1 HG00735.hp2 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.2175+1726G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131122639 | ||||||
| chr12:131122688
|
CTT | C | 4 | a0001c0001t0002g0130a0001c0001t0002g0173a0001c0001t0002g0217others(1): Show | 4 | HG03831.hp2 HG04204.hp1 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.2175+1777_2175+177 others(6): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr12 | 131122688 | |||||
| chr12:131122711
|
C | G | 1 | a0001c0002t0001g0210 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2175+1798C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131122711 | ||||||
| chr12:131122765
|
G | A | 9 | a0001c0001t0001g0111a0001c0001t0001g0156a0001c0001t0001g0163others(6): Show | 9 | HG00280.hp1 HG00639.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.2175+1852G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131122765 | ||||||
| chr12:131122793
|
T | C | 1 | a0001c0002t0001g0169 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2175+1880T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131122793 | ||||||
| chr12:131122822
|
C | T | 1 | a0001c0007t0006g0021 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2175+1909C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131122822 | ||||||
| chr12:131122867
|
G | A | 1 | a0001c0003t0004g0012 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2175+1954G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131122867 | ||||||
| chr12:131123039
|
G | GT | 26 | a0001c0001t0001g0002a0001c0001t0001g0197a0001c0001t0001g0208others(23): Show | 26 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.2175+2160dupT | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr12 | 131123039 | |||||
| chr12:131123039
|
G | GTT | 12 | a0001c0001t0001g0003a0001c0001t0001g0111a0001c0001t0001g0113others(9): Show | 12 | HG01074.hp1 HG01106.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.2175+2159_2175+216 others(6): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr12 | 131123039 | |||||
| chr12:131123039
|
GT | G | 47 | a0001c0001t0002g0005a0001c0001t0002g0107a0001c0001t0002g0130others(44): Show | 47 | HG00140.hp1 HG00609.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.2175+2160delT | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr12 | 131123039 | |||||
| chr12:131123039
|
GTT | G | 53 | a0001c0001t0002g0149a0001c0001t0002g0187a0001c0001t0005g0028others(50): Show | 53 | HG00323.hp2 HG00639.hp2 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.2175+2159_2175+216 others(6): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr12 | 131123039 | |||||
| chr12:131123039
|
GTTT | G | 25 | a0001c0001t0016g0182a0001c0002t0001g0146a0001c0002t0001g0174others(22): Show | 25 | HG00609.hp2 HG01167.hp2 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.2175+2158_2175+216 others(7): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr12 | 131123039 | |||||
| chr12:131123039
|
GTTTT | G | 23 | a0001c0001t0009g0144a0001c0001t0015g0060a0001c0001t0016g0147others(20): Show | 23 | HG00140.hp2 HG00323.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.2175+2157_2175+216 others(8): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr12 | 131123039 | |||||
| chr12:131123039
|
GTTTTT | G | 9 | a0001c0003t0004g0122a0001c0003t0006g0019a0001c0003t0006g0058others(6): Show | 9 | HG00621.hp1 HG01109.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.2175+2156_2175+216 others(9): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr12 | 131123039 | |||||
| chr12:131123039
|
GTTTTTT | G | 14 | a0001c0001t0002g0161a0001c0001t0002g0228a0001c0001t0002g0235others(11): Show | 14 | HG00735.hp1 HG01099.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.2175+2155_2175+216 others(10): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr12 | 131123039 | |||||
| chr12:131123039
|
GTTTTTTT others(3): Show |
G | 1 | a0001c0010t0007g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2175+2151_2175+216 others(14): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr12 | 131123039 | |||||
| chr12:131123039
|
GTTTTTTT others(4): Show |
G | 1 | a0001c0001t0002g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2175+2150_2175+216 others(15): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr12 | 131123039 | |||||
| chr12:131123039
|
GTTTTTTT others(6): Show |
G | 1 | a0001c0003t0029g0214 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2175+2148_2175+216 others(17): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr12 | 131123039 | |||||
| chr12:131123048
|
T | G | 1 | a0001c0001t0002g0149 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2175+2135T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131123048 | ||||||
| chr12:131123051
|
T | G | 1 | a0001c0025t0021g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2175+2138T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131123051 | ||||||
| chr12:131123052
|
T | G | 2 | a0001c0003t0012g0063a0001c0003t0034g0014 | 2 | HG02135.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.2175+2139T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131123052 | ||||||
| chr12:131123053
|
T | G | 2 | a0001c0003t0033g0181a0001c0003t0044g0079 | 2 | HG01261.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.2175+2140T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131123053 | ||||||
| chr12:131123054
|
T | G | 1 | a0006c0037t0042g0046 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2175+2141T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131123054 | ||||||
| chr12:131123055
|
T | G | 4 | a0001c0046t0017g0221a0003c0012t0017g0017a0003c0012t0017g0158others(1): Show | 4 | HG01934.hp1 HG02109.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.2175+2142T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131123055 | ||||||
| chr12:131123056
|
T | G | 7 | a0001c0001t0023g0143a0001c0003t0012g0088a0001c0010t0007g0160others(4): Show | 7 | HG02257.hp2 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2175+2143T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131123056 | ||||||
| chr12:131123057
|
T | G | 11 | a0001c0001t0002g0187a0001c0001t0011g0033a0001c0001t0011g0062others(8): Show | 11 | HG01261.hp1 HG02083.hp2 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.2175+2144T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131123057 | ||||||
| chr12:131123061
|
T | G | 1 | a0001c0001t0011g0062 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2175+2148T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131123061 | ||||||
| chr12:131123062
|
T | G | 1 | a0001c0001t0011g0220 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2175+2149T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131123062 | ||||||
| chr12:131123065
|
T | G | 1 | a0001c0003t0004g0198 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2175+2152T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131123065 | ||||||
| chr12:131123092
|
T | G | 1 | a0008c0034t0026g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2175+2179T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131123092 | ||||||
| chr12:131123272
|
T | C | 88 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(85): Show | 88 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.2175+2359T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131123272 | ||||||
| chr12:131123368
|
T | C | 6 | a0001c0003t0004g0013a0001c0003t0004g0188a0001c0003t0004g0189others(3): Show | 6 | HG01257.hp1 HG01258.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.2175+2455T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131123368 | ||||||
| chr12:131123694
|
T | C | 1 | a0004c0016t0002g0065 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2175+2781T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131123694 | ||||||
| chr12:131123715
|
G | C | 1 | a0001c0003t0012g0063 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2175+2802G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131123715 | ||||||
| chr12:131123719
|
G | C | 4 | a0001c0003t0018g0117a0001c0003t0018g0232a0001c0007t0018g0132others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2175+2806G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131123719 | ||||||
| chr12:131123739
|
G | A | 41 | a0001c0001t0002g0005a0001c0001t0002g0107a0001c0001t0002g0130others(38): Show | 41 | HG00140.hp1 HG00735.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.2175+2826G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131123739 | ||||||
| chr12:131123770
|
C | T | 4 | a0001c0003t0018g0117a0001c0003t0018g0232a0001c0007t0018g0132others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2175+2857C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131123770 | ||||||
| chr12:131123778
|
C | T | 1 | a0001c0003t0012g0063 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2175+2865C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131123778 | ||||||
| chr12:131123779
|
G | A | 1 | a0001c0001t0009g0166 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2175+2866G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131123779 | ||||||
| chr12:131123825
|
C | CA | 29 | a0001c0001t0002g0116a0001c0001t0002g0161a0001c0001t0002g0187others(26): Show | 29 | HG00280.hp2 HG00609.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.2175+2928dupA | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr12 | 131123825 | |||||
| chr12:131123860
|
A | G | 1 | a0001c0002t0010g0134 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2175+2947A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131123860 | ||||||
| chr12:131123882
|
T | C | 4 | a0001c0003t0018g0117a0001c0003t0018g0232a0001c0007t0018g0132others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2175+2969T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131123882 | ||||||
| chr12:131123915
|
T | G | 1 | a0001c0008t0003g0067 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2175+3002T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131123915 | ||||||
| chr12:131123931
|
A | G | 29 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(26): Show | 29 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.2175+3018A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131123931 | ||||||
| chr12:131123986
|
C | T | 1 | a0001c0009t0014g0037 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2175+3073C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131123986 | ||||||
| chr12:131124008
|
C | T | 1 | a0001c0004t0002g0193 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2175+3095C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131124008 | ||||||
| chr12:131124301
|
A | G | 1 | a0001c0003t0034g0014 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2175+3388A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131124301 | ||||||
| chr12:131124595
|
A | G | 1 | a0001c0001t0002g0005 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2175+3682A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131124595 | ||||||
| chr12:131124641
|
C | T | 1 | a0001c0025t0021g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2175+3728C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131124641 | ||||||
| chr12:131124652
|
AAACACAC others(39): Show |
A | 29 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(26): Show | 29 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.2175+3784_2175+382 others(50): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr12 | 131124652 | |||||
| chr12:131124683
|
A | C | 2 | a0001c0002t0001g0125a0001c0002t0008g0016 | 2 | HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2175+3770A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131124683 | ||||||
| chr12:131124733
|
G | A | 2 | a0001c0002t0001g0125a0001c0002t0008g0016 | 2 | HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2175+3820G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131124733 | ||||||
| chr12:131124828
|
G | A | 31 | a0001c0001t0002g0149a0001c0001t0015g0060a0001c0001t0016g0147others(28): Show | 31 | HG00140.hp2 HG00323.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.2175+3915G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131124828 | ||||||
| chr12:131124841
|
C | T | 40 | a0001c0001t0002g0005a0001c0001t0002g0107a0001c0001t0002g0130others(37): Show | 40 | HG00140.hp1 HG00735.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.2175+3928C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131124841 | ||||||
| chr12:131124981
|
A | G | 29 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(26): Show | 29 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.2175+4068A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131124981 | ||||||
| chr12:131125179
|
C | G | 3 | a0001c0004t0005g0036a0001c0010t0007g0150a0001c0010t0039g0031 | 3 | HG03834.hp2 NA18986.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.2175+4266C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131125179 | ||||||
| chr12:131125184
|
T | A | 40 | a0001c0001t0002g0005a0001c0001t0002g0107a0001c0001t0002g0130others(37): Show | 40 | HG00140.hp1 HG00735.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.2175+4271T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131125184 | ||||||
| chr12:131125239
|
C | T | 2 | a0001c0001t0016g0147a0001c0001t0016g0182 | 2 | HG02280.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2175+4326C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131125239 | ||||||
| chr12:131125360
|
T | C | 1 | a0011c0038t0002g0162 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2175+4447T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131125360 | ||||||
| chr12:131125450
|
G | T | 1 | a0001c0003t0013g0224 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2175+4537G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131125450 | ||||||
| chr12:131125454
|
A | T | 1 | a0001c0002t0010g0167 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2175+4541A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131125454 | ||||||
| chr12:131125507
|
T | C | 2 | a0001c0003t0035g0200a0001c0003t0045g0042 | 2 | NA18973.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.2175+4594T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131125507 | ||||||
| chr12:131125520
|
A | G | 40 | a0001c0001t0002g0005a0001c0001t0002g0107a0001c0001t0002g0130others(37): Show | 40 | HG00140.hp1 HG00735.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.2175+4607A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131125520 | ||||||
| chr12:131125597
|
G | C | 1 | a0001c0002t0010g0167 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2175+4684G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131125597 | ||||||
| chr12:131125680
|
A | G | 2 | a0001c0001t0002g0116a0001c0010t0007g0213 | 2 | HG01243.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2175+4767A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131125680 | ||||||
| chr12:131125799
|
C | T | 1 | a0001c0025t0021g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2175+4886C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131125799 | ||||||
| chr12:131126110
|
C | T | 4 | a0001c0046t0017g0221a0003c0012t0017g0017a0003c0012t0017g0158others(1): Show | 4 | HG01934.hp1 HG02109.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2175+5197C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131126110 | ||||||
| chr12:131126244
|
G | A | 2 | a0001c0003t0006g0015a0001c0003t0006g0211 | 2 | HG01175.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.2175+5331G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131126244 | ||||||
| chr12:131126371
|
G | A | 29 | a0001c0001t0002g0149a0001c0001t0015g0060a0001c0003t0004g0013others(26): Show | 29 | HG00140.hp2 HG00323.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.2176-5354G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131126371 | ||||||
| chr12:131126377
|
C | T | 23 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0027g0118others(20): Show | 23 | HG00621.hp1 HG00735.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.2176-5348C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131126377 | ||||||
| chr12:131126714
|
T | C | 1 | a0005c0011t0002g0110 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2176-5011T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131126714 | ||||||
| chr12:131126993
|
G | A | 4 | a0001c0002t0003g0032a0001c0002t0003g0076a0001c0002t0003g0083others(1): Show | 4 | HG00280.hp2 HG00609.hp1 HG00621.hp2 others(1): Show |
intron_variant | MODIFIER | c.2176-4732G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131126993 | ||||||
| chr12:131127026
|
GCTC | G | 23 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0027g0118others(20): Show | 23 | HG00621.hp1 HG00735.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.2176-4692_2176-469 others(7): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr12 | 131127026 | |||||
| chr12:131127035
|
C | G | 1 | a0001c0002t0003g0068 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2176-4690C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131127035 | ||||||
| chr12:131127112
|
G | A | 16 | a0001c0001t0027g0118a0001c0003t0006g0015a0001c0003t0006g0019others(13): Show | 16 | HG00621.hp1 HG00735.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.2176-4613G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131127112 | ||||||
| chr12:131127120
|
G | GA | 20 | a0001c0001t0002g0187a0001c0001t0011g0033a0001c0001t0011g0062others(17): Show | 20 | HG01261.hp1 HG02055.hp2 HG02083.hp2 others(17): Show |
intron_variant | MODIFIER | c.2176-4596dupA | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr12 | 131127120 | |||||
| chr12:131127198
|
A | G | 4 | a0001c0001t0016g0147a0001c0001t0016g0182a0001c0022t0016g0109others(1): Show | 4 | HG02280.hp1 HG02486.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.2176-4527A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131127198 | ||||||
| chr12:131127363
|
C | T | 40 | a0001c0001t0002g0005a0001c0001t0002g0107a0001c0001t0002g0130others(37): Show | 40 | HG00140.hp1 HG00735.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.2176-4362C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131127363 | ||||||
| chr12:131127400
|
G | A | 1 | a0001c0002t0003g0061 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2176-4325G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131127400 | ||||||
| chr12:131127561
|
G | A | 31 | a0001c0001t0002g0149a0001c0001t0015g0060a0001c0001t0016g0147others(28): Show | 31 | HG00140.hp2 HG00323.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.2176-4164G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131127561 | ||||||
| chr12:131127657
|
T | G | 1 | a0001c0002t0001g0100 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2176-4068T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131127657 | ||||||
| chr12:131127658
|
T | G | 38 | a0001c0001t0002g0149a0001c0001t0015g0060a0001c0001t0016g0147others(35): Show | 38 | HG00140.hp2 HG00323.hp1 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.2176-4067T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131127658 | ||||||
| chr12:131127667
|
C | T | 29 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(26): Show | 29 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.2176-4058C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131127667 | ||||||
| chr12:131127680
|
A | G | 74 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(71): Show | 74 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.2176-4045A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131127680 | ||||||
| chr12:131127726
|
G | A | 11 | a0001c0003t0029g0214a0001c0010t0007g0160a0001c0046t0017g0221others(8): Show | 11 | HG01934.hp1 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.2176-3999G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131127726 | ||||||
| chr12:131127747
|
G | A | 164 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(161): Show | 164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.2176-3978G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131127747 | ||||||
| chr12:131127780
|
T | TGTTGGTT others(81): Show |
1 | a0001c0001t0028g0205 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2176-3913_2176-382 others(92): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr12 | 131127780 | |||||
| chr12:131127824
|
TGTTGGTT others(169): Show |
T | 21 | a0001c0001t0027g0118a0001c0002t0001g0125a0001c0002t0008g0016others(18): Show | 21 | HG00621.hp1 HG01069.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.2176-3884_2176-370 others(4): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr12 | 131127824 | |||||
| chr12:131127841
|
T | C | 13 | a0001c0001t0002g0116a0001c0003t0029g0214a0001c0010t0007g0160others(10): Show | 13 | HG01243.hp1 HG01934.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2176-3884T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131127841 | ||||||
| chr12:131127841
|
TTCTGAGC others(169): Show |
T | 6 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0003t0006g0092others(3): Show | 6 | HG00735.hp1 HG01884.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.2176-3839_2176-366 others(4): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr12 | 131127841 | |||||
| chr12:131127842
|
TCTGAGCT others(37): Show |
T | 40 | a0001c0001t0002g0005a0001c0001t0002g0107a0001c0001t0002g0130others(37): Show | 40 | HG00140.hp1 HG00735.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.2176-3751_2176-370 others(48): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr12 | 131127842 | |||||
| chr12:131127886
|
CCTGAGCT others(169): Show |
C | 13 | a0001c0001t0002g0116a0001c0003t0029g0214a0001c0010t0007g0160others(10): Show | 13 | HG01243.hp1 HG01934.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2176-3813_2176-363 others(4): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr12 | 131127886 | |||||
| chr12:131127897
|
G | C | 7 | a0001c0002t0001g0008a0001c0002t0001g0202a0001c0002t0003g0038others(4): Show | 7 | HG01243.hp2 HG01496.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.2176-3828G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131127897 | ||||||
| chr12:131127912
|
G | C | 1 | a0001c0002t0001g0223 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2176-3813G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131127912 | ||||||
| chr12:131127962
|
T | G | 1 | a0001c0003t0012g0063 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2176-3763T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131127962 | ||||||
| chr12:131128062
|
T | C | 31 | a0001c0001t0002g0149a0001c0001t0015g0060a0001c0001t0016g0147others(28): Show | 31 | HG00140.hp2 HG00323.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.2176-3663T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131128062 | ||||||
| chr12:131128173
|
A | G | 15 | a0001c0001t0002g0116a0001c0002t0001g0125a0001c0002t0008g0016others(12): Show | 15 | HG01243.hp1 HG01934.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.2176-3552A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131128173 | ||||||
| chr12:131128176
|
G | A | 29 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(26): Show | 29 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.2176-3549G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131128176 | ||||||
| chr12:131128216
|
G | C | 1 | a0001c0004t0005g0082 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2176-3509G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131128216 | ||||||
| chr12:131128232
|
A | C | 1 | a0004c0015t0005g0086 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2176-3493A>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131128232 | ||||||
| chr12:131128338
|
C | T | 38 | a0001c0001t0002g0116a0001c0001t0002g0228a0001c0001t0002g0235others(35): Show | 38 | HG00621.hp1 HG00735.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.2176-3387C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131128338 | ||||||
| chr12:131128384
|
G | C | 4 | a0001c0003t0018g0117a0001c0003t0018g0232a0001c0007t0018g0132others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2176-3341G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131128384 | ||||||
| chr12:131128390
|
C | T | 4 | a0001c0003t0018g0117a0001c0003t0018g0232a0001c0007t0018g0132others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2176-3335C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131128390 | ||||||
| chr12:131128442
|
C | A | 24 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0027g0118others(21): Show | 24 | HG00621.hp1 HG00735.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.2176-3283C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131128442 | ||||||
| chr12:131128541
|
C | A | 2 | a0001c0001t0002g0116a0001c0010t0007g0213 | 2 | HG01243.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2176-3184C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131128541 | ||||||
| chr12:131128543
|
G | A | 9 | a0001c0001t0001g0111a0001c0001t0001g0156a0001c0001t0001g0163others(6): Show | 9 | HG00280.hp1 HG00639.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.2176-3182G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131128543 | ||||||
| chr12:131128548
|
A | T | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(125): Show | 128 | HG00140.hp1 HG00280.hp1 HG00621.hp1 others(125): Show |
intron_variant | MODIFIER | c.2176-3177A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131128548 | ||||||
| chr12:131128553
|
A | T | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(125): Show | 128 | HG00140.hp1 HG00280.hp1 HG00621.hp1 others(125): Show |
intron_variant | MODIFIER | c.2176-3172A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131128553 | ||||||
| chr12:131128561
|
A | G | 2 | a0001c0002t0001g0125a0001c0002t0008g0016 | 2 | HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2176-3164A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131128561 | ||||||
| chr12:131128687
|
T | C | 40 | a0001c0001t0002g0116a0001c0001t0002g0228a0001c0001t0002g0235others(37): Show | 40 | HG00621.hp1 HG00735.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.2176-3038T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131128687 | ||||||
| chr12:131128752
|
T | C | 25 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0027g0118others(22): Show | 25 | HG00621.hp1 HG00735.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.2176-2973T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131128752 | ||||||
| chr12:131128831
|
G | A | 165 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(162): Show | 165 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.2176-2894G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131128831 | ||||||
| chr12:131128841
|
T | C | 40 | a0001c0001t0002g0116a0001c0001t0002g0228a0001c0001t0002g0235others(37): Show | 40 | HG00621.hp1 HG00735.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.2176-2884T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131128841 | ||||||
| chr12:131128885
|
GGGTGTGA others(146): Show |
G | 18 | a0001c0001t0002g0187a0001c0001t0011g0033a0001c0001t0011g0062others(15): Show | 18 | HG01261.hp1 HG02055.hp2 HG02083.hp2 others(15): Show |
intron_variant | MODIFIER | c.2176-2754_2176-260 others(4): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr12 | 131128885 | |||||
| chr12:131128902
|
C | G | 1 | a0001c0004t0005g0094 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2176-2823C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131128902 | ||||||
| chr12:131128904
|
G | C | 1 | a0001c0004t0005g0094 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2176-2821G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131128904 | ||||||
| chr12:131128965
|
G | GGCCCTGC others(395): Show |
1 | a0003c0032t0038g0090 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2176-2755_2176-275 others(406): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr12 | 131128965 | |||||
| chr12:131128971
|
CCTGTCTG others(84): Show |
C | 31 | a0001c0001t0002g0149a0001c0001t0015g0060a0001c0001t0016g0147others(28): Show | 31 | HG00140.hp2 HG00323.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.2176-2736_2176-264 others(95): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr12 | 131128971 | |||||
| chr12:131128993
|
C | CCCCGCCC others(23): Show |
2 | a0001c0001t0001g0156a0001c0001t0001g0163 | 2 | HG01106.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.2176-2699_2176-267 others(34): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr12 | 131128993 | |||||
| chr12:131129118
|
G | A | 25 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0027g0118others(22): Show | 25 | HG00621.hp1 HG00735.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.2176-2607G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131129118 | ||||||
| chr12:131129150
|
G | A | 41 | a0001c0001t0002g0116a0001c0001t0002g0228a0001c0001t0002g0235others(38): Show | 41 | HG00621.hp1 HG00735.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.2176-2575G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131129150 | ||||||
| chr12:131129163
|
A | G | 31 | a0001c0001t0002g0149a0001c0001t0015g0060a0001c0001t0016g0147others(28): Show | 31 | HG00140.hp2 HG00323.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.2176-2562A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131129163 | ||||||
| chr12:131129210
|
C | T | 41 | a0001c0001t0002g0116a0001c0001t0002g0228a0001c0001t0002g0235others(38): Show | 41 | HG00621.hp1 HG00735.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.2176-2515C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131129210 | ||||||
| chr12:131129211
|
G | A | 6 | a0001c0001t0005g0045a0001c0002t0002g0001a0001c0002t0002g0006others(3): Show | 6 | HG00639.hp2 HG01257.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.2176-2514G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131129211 | ||||||
| chr12:131129242
|
G | A | 6 | a0001c0003t0006g0058a0001c0003t0006g0216a0001c0003t0019g0218others(3): Show | 6 | HG00621.hp1 HG01109.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.2176-2483G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131129242 | ||||||
| chr12:131129271
|
C | T | 41 | a0001c0001t0002g0116a0001c0001t0002g0228a0001c0001t0002g0235others(38): Show | 41 | HG00621.hp1 HG00735.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.2176-2454C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131129271 | ||||||
| chr12:131129334
|
T | C | 41 | a0001c0001t0002g0116a0001c0001t0002g0228a0001c0001t0002g0235others(38): Show | 41 | HG00621.hp1 HG00735.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.2176-2391T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131129334 | ||||||
| chr12:131129334
|
TGCCCTCC others(24): Show |
T | 4 | a0001c0003t0018g0117a0001c0003t0018g0232a0001c0007t0018g0132others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2176-2361_2176-233 others(35): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr12 | 131129334 | |||||
| chr12:131129364
|
T | C | 129 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(126): Show | 129 | HG00140.hp1 HG00280.hp1 HG00621.hp1 others(126): Show |
intron_variant | MODIFIER | c.2176-2361T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131129364 | ||||||
| chr12:131129365
|
G | C | 2 | a0001c0001t0002g0228a0001c0001t0002g0235 | 2 | HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2176-2360G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131129365 | ||||||
| chr12:131129365
|
G | T | 39 | a0001c0001t0002g0116a0001c0001t0027g0118a0001c0002t0001g0125others(36): Show | 39 | HG00621.hp1 HG00735.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.2176-2360G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131129365 | ||||||
| chr12:131129371
|
C | G | 41 | a0001c0001t0002g0116a0001c0001t0002g0228a0001c0001t0002g0235others(38): Show | 41 | HG00621.hp1 HG00735.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.2176-2354C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131129371 | ||||||
| chr12:131129381
|
T | C | 1 | a0001c0036t0003g0075 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2176-2344T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131129381 | ||||||
| chr12:131129396
|
C | T | 1 | a0001c0002t0003g0077 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2176-2329C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131129396 | ||||||
| chr12:131129402
|
G | C | 1 | a0001c0002t0003g0077 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2176-2323G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131129402 | ||||||
| chr12:131129416
|
AGTGACAG others(20): Show |
A | 19 | a0001c0001t0002g0187a0001c0001t0011g0033a0001c0001t0011g0062others(16): Show | 19 | HG01261.hp1 HG02055.hp2 HG02083.hp2 others(16): Show |
intron_variant | MODIFIER | c.2176-2277_2176-225 others(31): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr12 | 131129416 | |||||
| chr12:131129441
|
G | A | 18 | a0001c0001t0027g0118a0001c0003t0004g0101a0001c0003t0004g0108others(15): Show | 18 | HG00621.hp1 HG00735.hp1 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.2176-2284G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131129441 | ||||||
| chr12:131129442
|
G | A | 1 | a0001c0001t0002g0184 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2176-2283G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131129442 | ||||||
| chr12:131129443
|
T | TGTGAGTG others(212): Show |
2 | a0001c0001t0002g0228a0001c0001t0002g0235 | 2 | HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2176-2278_2176-227 others(223): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr12 | 131129443 | |||||
| chr12:131129443
|
T | TGTGAGTG others(181): Show |
18 | a0001c0001t0027g0118a0001c0003t0004g0101a0001c0003t0004g0108others(15): Show | 18 | HG00621.hp1 HG00735.hp1 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.2176-2278_2176-227 others(192): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr12 | 131129443 | |||||
| chr12:131129451
|
G | C | 38 | a0001c0001t0002g0187a0001c0001t0002g0228a0001c0001t0002g0235others(35): Show | 38 | HG00621.hp1 HG00735.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.2176-2274G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131129451 | ||||||
| chr12:131129451
|
G | GCCCGCCC others(208): Show |
5 | a0001c0003t0036g0209a0001c0025t0021g0119a0002c0030t0032g0159others(2): Show | 5 | HG01934.hp2 HG02257.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2176-2258_2176-225 others(219): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr12 | 131129451 | |||||
| chr12:131129451
|
G | GCCCGCCC others(208): Show |
13 | a0001c0001t0002g0116a0001c0003t0029g0214a0001c0010t0007g0160others(10): Show | 13 | HG01243.hp1 HG01934.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2176-2258_2176-225 others(219): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr12 | 131129451 | |||||
| chr12:131129451
|
G | GCCCGCCC others(208): Show |
1 | a0003c0040t0022g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2176-2258_2176-225 others(219): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr12 | 131129451 | |||||
| chr12:131129453
|
C | T | 1 | a0001c0002t0003g0077 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2176-2272C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131129453 | ||||||
| chr12:131129454
|
C | G | 1 | a0001c0002t0003g0077 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2176-2271C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131129454 | ||||||
| chr12:131129455
|
G | A | 6 | a0001c0003t0004g0101a0001c0003t0004g0108a0001c0003t0006g0015others(3): Show | 6 | HG01069.hp1 HG01071.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.2176-2270G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131129455 | ||||||
| chr12:131129460
|
G | C | 1 | a0001c0002t0003g0077 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2176-2265G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131129460 | ||||||
| chr12:131129468
|
G | A | 2 | a0001c0002t0001g0125a0001c0002t0008g0016 | 2 | HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2176-2257G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131129468 | ||||||
| chr12:131129471
|
G | A | 1 | a0001c0002t0001g0223 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2176-2254G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131129471 | ||||||
| chr12:131129482
|
C | G | 2 | a0001c0002t0001g0125a0001c0002t0008g0016 | 2 | HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2176-2243C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131129482 | ||||||
| chr12:131129482
|
C | T | 12 | a0001c0003t0029g0214a0001c0010t0007g0160a0001c0046t0017g0221others(9): Show | 12 | HG01934.hp1 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2176-2243C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131129482 | ||||||
| chr12:131129486
|
G | A | 1 | a0001c0003t0036g0209 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2176-2239G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131129486 | ||||||
| chr12:131129494
|
G | GTCTGGGT others(146): Show |
2 | a0001c0002t0001g0125a0001c0002t0008g0016 | 2 | HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2176-2204_2176-220 others(157): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr12 | 131129494 | |||||
| chr12:131129529
|
C | T | 1 | a0001c0002t0001g0169 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2176-2196C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131129529 | ||||||
| chr12:131129534
|
T | C | 1 | a0001c0003t0004g0198 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2176-2191T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131129534 | ||||||
| chr12:131129595
|
A | G | 2 | a0001c0001t0002g0203a0001c0001t0002g0204 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.2176-2130A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131129595 | ||||||
| chr12:131129698
|
G | A | 1 | a0001c0004t0002g0011 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2176-2027G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131129698 | ||||||
| chr12:131129921
|
C | T | 29 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(26): Show | 29 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.2176-1804C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131129921 | ||||||
| chr12:131130054
|
C | T | 27 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0027g0118others(24): Show | 27 | HG00621.hp1 HG00735.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.2176-1671C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131130054 | ||||||
| chr12:131130085
|
G | T | 27 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0027g0118others(24): Show | 27 | HG00621.hp1 HG00735.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.2176-1640G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131130085 | ||||||
| chr12:131130138
|
T | G | 1 | a0002c0029t0031g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2176-1587T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131130138 | ||||||
| chr12:131130241
|
T | A | 41 | a0001c0001t0002g0116a0001c0001t0002g0228a0001c0001t0002g0235others(38): Show | 41 | HG00621.hp1 HG00735.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.2176-1484T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131130241 | ||||||
| chr12:131130273
|
G | A | 41 | a0001c0001t0002g0116a0001c0001t0002g0228a0001c0001t0002g0235others(38): Show | 41 | HG00621.hp1 HG00735.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.2176-1452G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131130273 | ||||||
| chr12:131130344
|
T | C | 3 | a0001c0001t0016g0147a0001c0001t0016g0182a0002c0029t0031g0222 | 3 | HG02280.hp1 HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2176-1381T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131130344 | ||||||
| chr12:131130357
|
C | T | 1 | a0001c0004t0005g0082 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2176-1368C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131130357 | ||||||
| chr12:131130434
|
G | A | 24 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0027g0118others(21): Show | 24 | HG00621.hp1 HG00735.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.2176-1291G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131130434 | ||||||
| chr12:131130494
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2176-1231C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131130494 | ||||||
| chr12:131130505
|
T | C | 2 | a0001c0002t0001g0125a0001c0002t0008g0016 | 2 | HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2176-1220T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131130505 | ||||||
| chr12:131130508
|
G | C | 1 | a0001c0020t0002g0180 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2176-1217G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131130508 | ||||||
| chr12:131130555
|
G | A | 6 | a0001c0001t0002g0116a0001c0010t0007g0213a0001c0046t0017g0221others(3): Show | 6 | HG01243.hp1 HG01934.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.2176-1170G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131130555 | ||||||
| chr12:131130631
|
G | A | 2 | a0001c0001t0002g0116a0001c0010t0007g0213 | 2 | HG01243.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2176-1094G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131130631 | ||||||
| chr12:131130647
|
G | A | 2 | a0001c0002t0001g0125a0001c0002t0008g0016 | 2 | HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2176-1078G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131130647 | ||||||
| chr12:131130719
|
C | T | 2 | a0001c0002t0001g0125a0001c0002t0008g0016 | 2 | HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2176-1006C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131130719 | ||||||
| chr12:131130723
|
C | T | 1 | a0001c0001t0028g0205 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2176-1002C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131130723 | ||||||
| chr12:131130743
|
CCCATCCC others(23): Show |
C | 1 | a0003c0040t0022g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2176-966_2176-937d others(32): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr12 | 131130743 | |||||
| chr12:131130768
|
A | G | 88 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0002g0005others(85): Show | 88 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.2176-957A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131130768 | ||||||
| chr12:131130780
|
C | T | 1 | a0001c0001t0002g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2176-945C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131130780 | ||||||
| chr12:131130843
|
C | T | 9 | a0001c0001t0002g0116a0001c0003t0029g0214a0001c0010t0007g0160others(6): Show | 9 | HG01243.hp1 HG02257.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.2176-882C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131130843 | ||||||
| chr12:131131131
|
T | C | 164 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(161): Show | 164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.2176-594T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131131131 | ||||||
| chr12:131131141
|
G | T | 1 | a0001c0020t0002g0180 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2176-584G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131131141 | ||||||
| chr12:131131162
|
G | A | 1 | a0001c0002t0010g0201 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2176-563G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131131162 | ||||||
| chr12:131131172
|
A | G | 1 | a0008c0034t0026g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2176-553A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131131172 | ||||||
| chr12:131131245
|
C | T | 27 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0027g0118others(24): Show | 27 | HG00621.hp1 HG00735.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.2176-480C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131131245 | ||||||
| chr12:131131287
|
C | T | 15 | a0001c0001t0002g0116a0001c0003t0029g0214a0001c0010t0007g0160others(12): Show | 15 | HG01243.hp1 HG01934.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.2176-438C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131131287 | ||||||
| chr12:131131306
|
C | G | 14 | a0001c0001t0002g0116a0001c0003t0029g0214a0001c0010t0007g0160others(11): Show | 14 | HG01243.hp1 HG01934.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2176-419C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131131306 | ||||||
| chr12:131131319
|
C | T | 2 | a0001c0002t0001g0125a0001c0002t0008g0016 | 2 | HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2176-406C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131131319 | ||||||
| chr12:131131337
|
G | A | 13 | a0001c0001t0002g0116a0001c0003t0029g0214a0001c0010t0007g0160others(10): Show | 13 | HG01243.hp1 HG01934.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2176-388G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131131337 | ||||||
| chr12:131131596
|
T | C | 219 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(216): Show | 219 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.2176-129T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 20/24 | chr12 | 131131596 | ||||||
| chr12:131132046
|
C | T | 1 | a0001c0020t0002g0180 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2267+230C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131132046 | ||||||
| chr12:131132165
|
C | T | 13 | a0001c0001t0002g0116a0001c0010t0007g0160a0001c0010t0007g0213others(10): Show | 13 | HG01243.hp1 HG01934.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2267+349C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131132165 | ||||||
| chr12:131132322
|
C | T | 2 | a0001c0001t0002g0161a0001c0001t0009g0144 | 2 | NA18970.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.2267+506C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131132322 | ||||||
| chr12:131132459
|
G | A | 1 | a0001c0001t0027g0118 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2267+643G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131132459 | ||||||
| chr12:131132529
|
C | CG | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(118): Show | 121 | HG00140.hp1 HG00280.hp1 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.2267+713_2267+714i others(3): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131132529 | ||||||
| chr12:131132530
|
C | G | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(118): Show | 121 | HG00140.hp1 HG00280.hp1 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.2267+714C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131132530 | ||||||
| chr12:131132667
|
G | A | 4 | a0001c0003t0004g0207a0001c0007t0004g0102a0001c0007t0004g0236others(1): Show | 4 | HG01109.hp1 HG02055.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.2267+851G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131132667 | ||||||
| chr12:131132764
|
T | C | 101 | a0001c0001t0002g0005a0001c0001t0002g0107a0001c0001t0002g0116others(98): Show | 101 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(98): Show |
intron_variant | MODIFIER | c.2267+948T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131132764 | ||||||
| chr12:131132872
|
C | A | 133 | a0001c0001t0002g0005a0001c0001t0002g0107a0001c0001t0002g0116others(130): Show | 133 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.2267+1056C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131132872 | ||||||
| chr12:131132888
|
C | T | 1 | a0001c0003t0044g0079 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2267+1072C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131132888 | ||||||
| chr12:131133051
|
C | T | 19 | a0001c0001t0002g0187a0001c0001t0011g0033a0001c0001t0011g0062others(16): Show | 19 | HG01261.hp1 HG01981.hp2 HG02083.hp2 others(16): Show |
intron_variant | MODIFIER | c.2267+1235C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131133051 | ||||||
| chr12:131133090
|
C | A | 80 | a0001c0001t0002g0005a0001c0001t0002g0107a0001c0001t0002g0116others(77): Show | 80 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.2267+1274C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131133090 | ||||||
| chr12:131133205
|
C | T | 25 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0003t0004g0101others(22): Show | 25 | HG00621.hp1 HG00735.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.2267+1389C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131133205 | ||||||
| chr12:131133359
|
C | T | 29 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(26): Show | 29 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.2267+1543C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131133359 | ||||||
| chr12:131133467
|
C | G | 1 | a0001c0003t0036g0209 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2267+1651C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131133467 | ||||||
| chr12:131133519
|
A | T | 1 | a0001c0004t0005g0094 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2267+1703A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131133519 | ||||||
| chr12:131133557
|
C | A | 98 | a0001c0001t0002g0005a0001c0001t0002g0107a0001c0001t0002g0116others(95): Show | 98 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(95): Show |
intron_variant | MODIFIER | c.2267+1741C>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131133557 | ||||||
| chr12:131133584
|
G | A | 1 | a0001c0005t0001g0206 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2267+1768G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131133584 | ||||||
| chr12:131133590
|
T | C | 79 | a0001c0001t0002g0005a0001c0001t0002g0107a0001c0001t0002g0116others(76): Show | 79 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.2267+1774T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131133590 | ||||||
| chr12:131133621
|
A | T | 2 | a0001c0001t0002g0116a0001c0010t0007g0213 | 2 | HG01243.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2267+1805A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131133621 | ||||||
| chr12:131133765
|
C | G | 1 | a0001c0001t0011g0062 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2267+1949C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131133765 | ||||||
| chr12:131133826
|
G | A | 1 | a0008c0034t0026g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2267+2010G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131133826 | ||||||
| chr12:131134069
|
T | G | 10 | a0001c0010t0007g0160a0001c0046t0017g0221a0002c0018t0020g0123others(7): Show | 10 | HG01934.hp1 HG02109.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.2268-1968T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131134069 | ||||||
| chr12:131134200
|
C | G | 79 | a0001c0001t0002g0005a0001c0001t0002g0107a0001c0001t0002g0116others(76): Show | 79 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.2268-1837C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131134200 | ||||||
| chr12:131134221
|
C | T | 1 | a0001c0002t0048g0151 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2268-1816C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131134221 | ||||||
| chr12:131134253
|
G | A | 4 | a0001c0002t0003g0032a0001c0002t0003g0076a0001c0002t0003g0083others(1): Show | 4 | HG00280.hp2 HG00609.hp1 HG00621.hp2 others(1): Show |
intron_variant | MODIFIER | c.2268-1784G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131134253 | ||||||
| chr12:131134588
|
A | G | 1 | a0001c0020t0002g0180 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2268-1449A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131134588 | ||||||
| chr12:131134688
|
G | A | 1 | a0001c0007t0018g0132 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2268-1349G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131134688 | ||||||
| chr12:131134724
|
C | T | 79 | a0001c0001t0002g0005a0001c0001t0002g0107a0001c0001t0002g0116others(76): Show | 79 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.2268-1313C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131134724 | ||||||
| chr12:131134812
|
A | G | 4 | a0001c0002t0003g0038a0001c0002t0003g0039a0001c0002t0003g0053others(1): Show | 4 | HG01496.hp2 HG01978.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.2268-1225A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131134812 | ||||||
| chr12:131135202
|
C | T | 1 | a0008c0034t0026g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2268-835C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131135202 | ||||||
| chr12:131135291
|
T | C | 20 | a0001c0001t0002g0187a0001c0001t0011g0033a0001c0001t0011g0062others(17): Show | 20 | HG01261.hp1 HG01981.hp2 HG02083.hp2 others(17): Show |
intron_variant | MODIFIER | c.2268-746T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131135291 | ||||||
| chr12:131135342
|
G | A | 2 | a0002c0030t0032g0159a0010c0026t0013g0238 | 2 | HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2268-695G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131135342 | ||||||
| chr12:131135362
|
G | A | 3 | a0001c0001t0005g0028a0001c0004t0009g0168a0001c0004t0043g0024 | 3 | HG00741.hp1 HG01928.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.2268-675G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131135362 | ||||||
| chr12:131135387
|
A | G | 110 | a0001c0001t0002g0005a0001c0001t0002g0107a0001c0001t0002g0116others(107): Show | 110 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(107): Show |
intron_variant | MODIFIER | c.2268-650A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131135387 | ||||||
| chr12:131135416
|
A | G | 1 | a0003c0040t0022g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2268-621A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131135416 | ||||||
| chr12:131135420
|
C | G | 1 | a0001c0001t0002g0149 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2268-617C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131135420 | ||||||
| chr12:131135525
|
G | A | 11 | a0001c0010t0007g0160a0001c0046t0017g0221a0002c0018t0020g0123others(8): Show | 11 | HG01934.hp1 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.2268-512G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131135525 | ||||||
| chr12:131135527
|
G | A | 1 | a0001c0001t0011g0066 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2268-510G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131135527 | ||||||
| chr12:131135659
|
T | C | 29 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0003t0004g0101others(26): Show | 29 | HG00621.hp1 HG00735.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.2268-378T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131135659 | ||||||
| chr12:131135668
|
T | C | 237 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0111others(234): Show | 237 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.2268-369T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131135668 | ||||||
| chr12:131135711
|
GTTC | G | 41 | a0001c0001t0002g0005a0001c0001t0002g0107a0001c0001t0002g0130others(38): Show | 41 | HG00140.hp1 HG00735.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.2268-325_2268-323d others(5): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131135711 | ||||||
| chr12:131135712
|
T | C | 58 | a0001c0001t0002g0116a0001c0001t0002g0187a0001c0001t0002g0228others(55): Show | 58 | HG00621.hp1 HG00735.hp1 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.2268-325T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131135712 | ||||||
| chr12:131135730
|
A | G | 35 | a0001c0001t0002g0116a0001c0001t0002g0187a0001c0001t0011g0033others(32): Show | 35 | HG01243.hp1 HG01261.hp1 HG01934.hp1 others(32): Show |
intron_variant | MODIFIER | c.2268-307A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131135730 | ||||||
| chr12:131136033
|
C | T | 39 | a0001c0001t0002g0005a0001c0001t0002g0107a0001c0001t0002g0130others(36): Show | 39 | HG00140.hp1 HG00735.hp2 HG00741.hp1 others(36): Show |
splice_region_variant&intron_variant | LOW | c.2268-4C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 21/24 | chr12 | 131136033 | ||||||
| chr12:131136172
|
C | T | 1 | a0001c0002t0003g0034 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2394+9C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 22/24 | chr12 | 131136172 | ||||||
| chr12:131136192
|
C | T | 2 | a0001c0001t0016g0147a0001c0001t0016g0182 | 2 | HG02280.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2394+29C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 22/24 | chr12 | 131136192 | ||||||
| chr12:131136193
|
A | G | 133 | a0001c0001t0002g0005a0001c0001t0002g0107a0001c0001t0002g0116others(130): Show | 133 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.2394+30A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 22/24 | chr12 | 131136193 | ||||||
| chr12:131136221
|
G | T | 1 | a0001c0002t0001g0223 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2394+58G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 22/24 | chr12 | 131136221 | ||||||
| chr12:131136264
|
C | T | 8 | a0001c0010t0007g0160a0001c0010t0007g0213a0002c0018t0020g0123others(5): Show | 8 | HG01243.hp1 HG02257.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.2394+101C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 22/24 | chr12 | 131136264 | ||||||
| chr12:131136303
|
G | A | 1 | a0001c0004t0005g0095 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2394+140G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 22/24 | chr12 | 131136303 | ||||||
| chr12:131136318
|
T | A | 4 | a0001c0003t0018g0117a0001c0003t0018g0232a0001c0007t0018g0132others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2394+155T>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 22/24 | chr12 | 131136318 | ||||||
| chr12:131136334
|
GCAGGATC others(6): Show |
G | 1 | a0001c0020t0002g0180 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2394+173_2394+185d others(15): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr12 | 131136334 | |||||
| chr12:131136371
|
C | T | 24 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0003t0004g0101others(21): Show | 24 | HG00621.hp1 HG00735.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.2394+208C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 22/24 | chr12 | 131136371 | ||||||
| chr12:131136528
|
A | G | 1 | a0001c0002t0010g0167 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2394+365A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 22/24 | chr12 | 131136528 | ||||||
| chr12:131136650
|
C | T | 1 | a0001c0025t0021g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2395-323C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 22/24 | chr12 | 131136650 | ||||||
| chr12:131136651
|
G | A | 2 | a0001c0001t0027g0118a0008c0034t0026g0043 | 2 | HG02451.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2395-322G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 22/24 | chr12 | 131136651 | ||||||
| chr12:131136686
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2395-287A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 22/24 | chr12 | 131136686 | ||||||
| chr12:131136699
|
G | C | 135 | a0001c0001t0001g0113a0001c0001t0002g0005a0001c0001t0002g0107others(132): Show | 135 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.2395-274G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 22/24 | chr12 | 131136699 | ||||||
| chr12:131136711
|
C | G | 2 | a0001c0003t0013g0224a0001c0003t0013g0225 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2395-262C>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 22/24 | chr12 | 131136711 | ||||||
| chr12:131136717
|
T | C | 1 | a0001c0004t0002g0114 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2395-256T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 22/24 | chr12 | 131136717 | ||||||
| chr12:131136735
|
C | T | 26 | a0001c0001t0002g0235a0001c0001t0027g0118a0001c0003t0004g0101others(23): Show | 26 | HG00621.hp1 HG00735.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.2395-238C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 22/24 | chr12 | 131136735 | ||||||
| chr12:131136742
|
A | T | 133 | a0001c0001t0002g0005a0001c0001t0002g0107a0001c0001t0002g0116others(130): Show | 133 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.2395-231A>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 22/24 | chr12 | 131136742 | ||||||
| chr12:131136829
|
C | T | 1 | a0001c0002t0003g0032 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2395-144C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 22/24 | chr12 | 131136829 | ||||||
| chr12:131137213
|
C | T | 1 | a0001c0002t0001g0169 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2436+199C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 23/24 | chr12 | 131137213 | ||||||
| chr12:131137217
|
A | G | 133 | a0001c0001t0002g0005a0001c0001t0002g0107a0001c0001t0002g0116others(130): Show | 133 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.2436+203A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 23/24 | chr12 | 131137217 | ||||||
| chr12:131137244
|
T | G | 133 | a0001c0001t0002g0005a0001c0001t0002g0107a0001c0001t0002g0116others(130): Show | 133 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.2436+230T>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 23/24 | chr12 | 131137244 | ||||||
| chr12:131137300
|
C | T | 1 | a0001c0001t0003g0023 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2436+286C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 23/24 | chr12 | 131137300 | ||||||
| chr12:131137338
|
G | A | 2 | a0001c0010t0007g0150a0001c0010t0039g0031 | 2 | HG03834.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.2436+324G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 23/24 | chr12 | 131137338 | ||||||
| chr12:131137452
|
A | G | 142 | a0001c0001t0002g0005a0001c0001t0002g0107a0001c0001t0002g0116others(139): Show | 142 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.2436+438A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 23/24 | chr12 | 131137452 | ||||||
| chr12:131137465
|
G | T | 1 | a0001c0001t0002g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2436+451G>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 23/24 | chr12 | 131137465 | ||||||
| chr12:131137622
|
C | T | 2 | a0001c0013t0007g0154a0001c0020t0002g0180 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2437-515C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 23/24 | chr12 | 131137622 | ||||||
| chr12:131137623
|
G | A | 6 | a0001c0002t0002g0106a0001c0003t0004g0013a0001c0003t0004g0189others(3): Show | 6 | HG00323.hp1 HG00323.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.2437-514G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 23/24 | chr12 | 131137623 | ||||||
| chr12:131137692
|
G | A | 1 | a0001c0007t0006g0021 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2437-445G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 23/24 | chr12 | 131137692 | ||||||
| chr12:131137694
|
C | T | 3 | a0001c0001t0003g0023a0001c0003t0012g0025a0001c0003t0012g0027 | 3 | HG01074.hp1 HG01496.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2437-443C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 23/24 | chr12 | 131137694 | ||||||
| chr12:131137695
|
G | A | 1 | a0001c0003t0006g0015 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2437-442G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 23/24 | chr12 | 131137695 | ||||||
| chr12:131137870
|
A | G | 1 | a0001c0005t0001g0239 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2437-267A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 23/24 | chr12 | 131137870 | ||||||
| chr12:131137961
|
T | C | 143 | a0001c0001t0001g0197a0001c0001t0002g0005a0001c0001t0002g0107others(140): Show | 143 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.2437-176T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 23/24 | chr12 | 131137961 | ||||||
| chr12:131138039
|
C | T | 1 | a0008c0034t0026g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2437-98C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 23/24 | chr12 | 131138039 | ||||||
| chr12:131138090
|
G | C | 1 | a0008c0034t0026g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2437-47G>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 23/24 | chr12 | 131138090 | ||||||
| chr12:131138108
|
G | A | 1 | a0002c0029t0031g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2437-29G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 23/24 | chr12 | 131138108 | ||||||
| chr12:131138246
|
T | TA | 4 | a0001c0046t0017g0221a0003c0012t0017g0017a0003c0012t0017g0158others(1): Show | 4 | HG01934.hp1 HG02109.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2529+20dupA | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr12 | 131138246 | |||||
| chr12:131138288
|
T | C | 75 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0191others(72): Show | 75 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.2529+59T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 24/24 | chr12 | 131138288 | ||||||
| chr12:131138327
|
C | T | 1 | a0001c0002t0001g0174 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2529+98C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 24/24 | chr12 | 131138327 | ||||||
| chr12:131138421
|
G | A | 1 | a0002c0028t0001g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2529+192G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 24/24 | chr12 | 131138421 | ||||||
| chr12:131138444
|
C | T | 2 | a0001c0003t0013g0224a0001c0003t0013g0225 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2529+215C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 24/24 | chr12 | 131138444 | ||||||
| chr12:131138448
|
G | A | 1 | a0007c0039t0001g0229 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2529+219G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 24/24 | chr12 | 131138448 | ||||||
| chr12:131138556
|
G | A | 13 | a0001c0010t0007g0150a0001c0010t0007g0160a0001c0010t0007g0213others(10): Show | 13 | HG01243.hp1 HG02257.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.2529+327G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 24/24 | chr12 | 131138556 | ||||||
| chr12:131138591
|
T | C | 63 | a0001c0003t0004g0012a0001c0003t0004g0013a0001c0003t0004g0101others(60): Show | 63 | HG00323.hp1 HG00621.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.2529+362T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 24/24 | chr12 | 131138591 | ||||||
| chr12:131138600
|
T | C | 63 | a0001c0003t0004g0012a0001c0003t0004g0013a0001c0003t0004g0101others(60): Show | 63 | HG00323.hp1 HG00621.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.2529+371T>C | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 24/24 | chr12 | 131138600 | ||||||
| chr12:131138653
|
C | T | 13 | a0001c0010t0007g0150a0001c0010t0007g0160a0001c0010t0007g0213others(10): Show | 13 | HG01243.hp1 HG02257.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.2529+424C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 24/24 | chr12 | 131138653 | ||||||
| chr12:131138691
|
C | T | 1 | a0001c0001t0002g0116 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2529+462C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 24/24 | chr12 | 131138691 | ||||||
| chr12:131138702
|
C | T | 64 | a0001c0003t0004g0012a0001c0003t0004g0013a0001c0003t0004g0101others(61): Show | 64 | HG00323.hp1 HG00621.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.2530-466C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 24/24 | chr12 | 131138702 | ||||||
| chr12:131138811
|
G | A | 1 | a0008c0034t0026g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2530-357G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 24/24 | chr12 | 131138811 | ||||||
| chr12:131138822
|
A | G | 10 | a0001c0010t0007g0160a0001c0010t0007g0213a0001c0046t0017g0221others(7): Show | 10 | HG01243.hp1 HG01934.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2530-346A>G | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 24/24 | chr12 | 131138822 | ||||||
| chr12:131138838
|
C | T | 1 | a0001c0003t0004g0237 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2530-330C>T | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 24/24 | chr12 | 131138838 | ||||||
| chr12:131138839
|
G | A | 1 | a0001c0007t0004g0236 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2530-329G>A | ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 24/24 | chr12 | 131138839 |