| geneid | 8745 |
|---|---|
| ensemblid | ENSG00000114948.13 |
| hgncid | 202 |
| symbol | ADAM23 |
| name | ADAM metallopeptidase domain 23 |
| refseq_nuc | NM_003812.4 |
| refseq_prot | NP_003803.1 |
| ensembl_nuc | ENST00000264377.8 |
| ensembl_prot | ENSP00000264377.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 206443532 |
| end | 206621127 |
| strand | + |
| ver | v1.2 |
| region | chr2:206443532-206621127 |
| region5000 | chr2:206438532-206626127 |
| regionname0 | ADAM23_chr2_206443532_206621127 |
| regionname5000 | ADAM23_chr2_206438532_206626127 |
| 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 | 1/1 | 832 | 354 | 87 | 68 | 153 | 14 | 30 | 126 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0002 | 0/0 | 832 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0003 | 0/0 | 832 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0004 | 0/0 | 832 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0005 | 0/0 | 832 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| 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 | 1/1 | 2499 | 275 | 60 | 55 | 123 | 12 | 23 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| c0002 | 0/0 | 2499 | 77 | 26 | 13 | 30 | 2 | 6 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| c0003 | 0/0 | 2499 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| c0004 | 0/0 | 2499 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| c0005 | 0/0 | 2499 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| c0006 | 0/0 | 2499 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| c0007 | 0/0 | 2499 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| c0008 | 0/0 | 2499 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| 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 | 0/1 | 3835 | 171 | 40 | 35 | 74 | 10 | 11 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| t0002 | 0/0 | 3836 | 79 | 19 | 7 | 42 | 0 | 11 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| t0003 | 0/0 | 3836 | 16 | 0 | 12 | 0 | 2 | 2 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| t0004 | 0/0 | 3836 | 11 | 0 | 3 | 8 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| t0005 | 0/0 | 3836 | 10 | 0 | 0 | 9 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| t0006 | 0/0 | 3836 | 6 | 0 | 2 | 0 | 0 | 4 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| t0007 | 1/0 | 3836 | 6 | 4 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| t0008 | 0/0 | 3835 | 4 | 3 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| t0009 | 0/0 | 3835 | 4 | 0 | 0 | 4 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| t0010 | 0/0 | 3836 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| t0011 | 0/0 | 3836 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| t0012 | 0/0 | 3835 | 3 | 0 | 3 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| t0013 | 0/0 | 3835 | 3 | 2 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| t0014 | 0/0 | 3836 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| t0015 | 0/0 | 3836 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| t0016 | 0/0 | 3836 | 2 | 0 | 1 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| t0017 | 0/0 | 3835 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| t0018 | 0/0 | 3835 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| t0019 | 0/0 | 3836 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| t0020 | 0/0 | 3835 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| t0021 | 0/0 | 3835 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| t0022 | 0/0 | 3836 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| t0023 | 0/0 | 3835 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| t0024 | 0/0 | 3835 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| t0025 | 0/0 | 3836 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| t0026 | 0/0 | 3836 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| t0027 | 0/0 | 3836 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| t0028 | 0/0 | 3836 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| t0029 | 0/0 | 3836 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| t0030 | 0/0 | 3835 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| t0031 | 0/0 | 3836 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| t0032 | 0/0 | 3836 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| t0033 | 0/0 | 3836 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| t0034 | 0/0 | 3836 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| t0035 | 0/0 | 3836 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| t0036 | 0/0 | 3836 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| t0037 | 0/0 | 3836 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| t0038 | 0/0 | 3836 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| t0039 | 0/0 | 3835 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| t0040 | 0/0 | 3835 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| t0041 | 0/0 | 3835 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| t0042 | 0/0 | 3835 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| t0043 | 0/0 | 3835 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| 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 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0171 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0343 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| 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 | 1/1 | 2499 | 275 | 60 | 55 | 123 | 12 | 23 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0002 | 0/0 | 2499 | 77 | 26 | 13 | 30 | 2 | 6 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0005 | 0/0 | 2499 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0007 | 0/0 | 2499 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0002c0003 | 0/0 | 2499 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0003c0004 | 0/0 | 2499 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0004c0006 | 0/0 | 2499 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0005c0008 | 0/0 | 2499 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 6333 | 163 | 36 | 35 | 73 | 10 | 8 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0001t0002 | 0/0 | 6334 | 39 | 7 | 7 | 18 | 0 | 7 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0001t0004 | 0/0 | 6334 | 11 | 0 | 3 | 8 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0001t0005 | 0/0 | 6334 | 9 | 0 | 0 | 8 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0001t0006 | 0/0 | 6334 | 6 | 0 | 2 | 0 | 0 | 4 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0001t0007 | 1/0 | 6334 | 6 | 4 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0001t0008 | 0/0 | 6333 | 4 | 3 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0001t0009 | 0/0 | 6333 | 4 | 0 | 0 | 4 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0001t0012 | 0/0 | 6333 | 3 | 0 | 3 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0001t0013 | 0/0 | 6333 | 2 | 1 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0001t0016 | 0/0 | 6334 | 2 | 0 | 1 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0001t0017 | 0/0 | 6333 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0001t0018 | 0/0 | 6333 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0001t0020 | 0/0 | 6333 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0001t0021 | 0/0 | 6333 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0001t0023 | 0/0 | 6333 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0001t0024 | 0/0 | 6333 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0001t0026 | 0/0 | 6334 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0001t0028 | 0/0 | 6334 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0001t0030 | 0/0 | 6333 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0001t0031 | 0/0 | 6334 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0001t0032 | 0/0 | 6334 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0001t0033 | 0/0 | 6334 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0001t0034 | 0/0 | 6334 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0001t0035 | 0/0 | 6334 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0001t0036 | 0/0 | 6334 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0001t0037 | 0/0 | 6334 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0001t0038 | 0/0 | 6334 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0001t0039 | 0/0 | 6333 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0001t0040 | 0/0 | 6333 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0001t0041 | 0/0 | 6333 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0001t0042 | 0/0 | 6333 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0001t0043 | 0/0 | 6333 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0002t0001 | 0/0 | 6333 | 5 | 4 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0002t0002 | 0/0 | 6334 | 40 | 12 | 0 | 24 | 0 | 4 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0002t0003 | 0/0 | 6334 | 16 | 0 | 12 | 0 | 2 | 2 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0002t0010 | 0/0 | 6334 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0002t0011 | 0/0 | 6334 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0002t0014 | 0/0 | 6334 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0002t0015 | 0/0 | 6334 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0002t0019 | 0/0 | 6334 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0002t0022 | 0/0 | 6334 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0002t0025 | 0/0 | 6334 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0002t0029 | 0/0 | 6334 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0005t0027 | 0/0 | 6334 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0001c0007t0001 | 0/0 | 6333 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0002c0003t0001 | 0/0 | 6333 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0003c0004t0013 | 0/0 | 6333 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0004c0006t0001 | 0/0 | 6333 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| a0005c0008t0005 | 0/0 | 6334 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | copy fasta | chr2 | 206438532 | 206626127 |
| 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 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0171 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0004g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0004g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0004g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0005g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0005g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0005g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0005g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0005g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0005g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0005g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0005g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0005g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0006g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0006g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0006g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0006g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0006g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0006g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0007g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0007g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0007g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0007g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0007g0343 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0007g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0008g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0008g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0008g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0008g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0009g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0009g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0009g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0009g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0012g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0012g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0012g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0013g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0013g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0016g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0016g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0017g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0017g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0018g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0018g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0020g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0020g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0021g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0021g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0023g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0024g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0026g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0028g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0030g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0031g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0032g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0033g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0034g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0035g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0036g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0037g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0038g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0039g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0040g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0041g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0042g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0001t0043g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0010g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0010g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0010g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0011g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0011g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0011g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0014g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0014g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0015g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0015g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0019g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0019g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0022g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0022g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0025g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0002t0029g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0005t0027g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0001c0007t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0002c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0003c0004t0013g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0004c0006t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| a0005c0008t0005g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0133 | EUR | GBR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0324 | EUR | GBR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG00140 | hp1 | a0001 | c0001 | t0016 | g0234 | EUR | GBR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | GBR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG00280 | hp1 | a0001 | c0002 | t0003 | g0174 | EUR | FIN | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0061 | EUR | FIN | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0290 | EUR | FIN | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0129 | EUR | FIN | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | CHS | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | CHS | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG00544 | hp2 | a0001 | c0001 | t0009 | g0018 | EAS | CHS | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG00558 | hp1 | a0001 | c0001 | t0005 | g0145 | EAS | CHS | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG00609 | hp1 | a0001 | c0001 | t0031 | g0243 | EAS | CHS | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG00609 | hp2 | a0001 | c0001 | t0023 | g0281 | EAS | CHS | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG00673 | hp1 | a0001 | c0001 | t0009 | g0067 | EAS | CHS | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG00673 | hp2 | a0001 | c0002 | t0002 | g0262 | EAS | CHS | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG00733 | hp2 | a0001 | c0001 | t0008 | g0347 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0333 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG00738 | hp2 | a0001 | c0002 | t0003 | g0161 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01069 | hp2 | a0001 | c0001 | t0007 | g0340 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01081 | hp1 | a0001 | c0001 | t0006 | g0349 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01099 | hp1 | a0001 | c0002 | t0003 | g0126 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01106 | hp2 | a0001 | c0001 | t0036 | g0270 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0245 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01192 | hp2 | a0001 | c0001 | t0016 | g0235 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01243 | hp1 | a0001 | c0001 | t0013 | g0030 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0244 | AMR | CLM | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01256 | hp1 | a0001 | c0002 | t0003 | g0137 | AMR | CLM | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01257 | hp2 | a0001 | c0002 | t0003 | g0178 | AMR | CLM | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01261 | hp1 | a0001 | c0002 | t0003 | g0165 | AMR | CLM | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0193 | AMR | CLM | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0238 | AMR | CLM | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01361 | hp1 | a0001 | c0002 | t0003 | g0158 | AMR | CLM | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01361 | hp2 | a0001 | c0001 | t0012 | g0304 | AMR | CLM | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01433 | hp1 | a0001 | c0001 | t0012 | g0306 | AMR | CLM | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01496 | hp1 | a0001 | c0001 | t0012 | g0305 | AMR | CLM | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01496 | hp2 | a0001 | c0001 | t0006 | g0348 | AMR | CLM | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0156 | EUR | IBS | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01515 | hp2 | a0001 | c0001 | t0041 | g0028 | EUR | IBS | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01517 | hp1 | a0001 | c0002 | t0003 | g0162 | EUR | IBS | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01884 | hp1 | a0001 | c0005 | t0027 | g0188 | AFR | ACB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0230 | AMR | PEL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01952 | hp1 | a0001 | c0002 | t0003 | g0167 | AMR | PEL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01975 | hp1 | a0001 | c0002 | t0003 | g0157 | AMR | PEL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0139 | AMR | PEL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02004 | hp1 | a0001 | c0002 | t0003 | g0160 | AMR | PEL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02055 | hp1 | a0001 | c0002 | t0019 | g0189 | AFR | ACB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | KHV | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02056 | hp2 | a0001 | c0002 | t0022 | g0076 | EAS | KHV | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02071 | hp1 | a0001 | c0001 | t0004 | g0223 | EAS | KHV | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | KHV | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | KHV | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02132 | hp1 | a0005 | c0008 | t0005 | g0242 | EAS | KHV | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02145 | hp1 | a0001 | c0002 | t0002 | g0009 | AFR | ACB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02148 | hp2 | a0001 | c0002 | t0003 | g0166 | AMR | PEL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0144 | EAS | CDX | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | CDX | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | CDX | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0219 | EAS | CDX | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0307 | AFR | ACB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | ACB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02273 | hp2 | a0001 | c0002 | t0003 | g0163 | AMR | PEL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | ACB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02280 | hp2 | a0001 | c0001 | t0007 | g0344 | AFR | ACB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02300 | hp1 | a0001 | c0002 | t0025 | g0159 | AMR | PEL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02300 | hp2 | a0001 | c0001 | t0004 | g0292 | AMR | PEL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0011 | AFR | ACB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | ACB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | KHV | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02523 | hp2 | a0001 | c0002 | t0010 | g0206 | EAS | KHV | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0241 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02602 | hp1 | a0001 | c0001 | t0006 | g0345 | SAS | PJL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02615 | hp1 | a0001 | c0001 | t0034 | g0079 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0320 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0259 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02698 | hp1 | a0001 | c0001 | t0040 | g0040 | SAS | PJL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0240 | SAS | PJL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0147 | SAS | PJL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02738 | hp1 | a0001 | c0001 | t0024 | g0273 | SAS | PJL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0327 | SAS | PJL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02809 | hp1 | a0001 | c0001 | t0008 | g0330 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02809 | hp2 | a0001 | c0001 | t0020 | g0329 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0092 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02886 | hp2 | a0001 | c0001 | t0007 | g0339 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02895 | hp1 | a0001 | c0002 | t0015 | g0182 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02896 | hp1 | a0001 | c0002 | t0011 | g0187 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0123 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02897 | hp1 | a0001 | c0002 | t0011 | g0186 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02897 | hp2 | a0001 | c0002 | t0015 | g0183 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | ESN | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02922 | hp2 | a0001 | c0001 | t0007 | g0342 | AFR | ESN | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | ESN | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | ESN | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG03017 | hp1 | a0001 | c0001 | t0006 | g0350 | SAS | PJL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG03041 | hp1 | a0001 | c0002 | t0002 | g0024 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | MSL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG03098 | hp2 | a0001 | c0002 | t0002 | g0008 | AFR | MSL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | ESN | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG03139 | hp2 | a0001 | c0001 | t0042 | g0295 | AFR | ESN | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG03195 | hp1 | a0001 | c0001 | t0026 | g0299 | AFR | ESN | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0336 | AFR | ESN | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG03209 | hp1 | a0001 | c0002 | t0002 | g0007 | AFR | MSL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG03209 | hp2 | a0001 | c0002 | t0011 | g0298 | AFR | MSL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | MSL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0257 | AFR | MSL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG03453 | hp1 | a0001 | c0001 | t0028 | g0297 | AFR | MSL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG03453 | hp2 | a0003 | c0004 | t0013 | g0031 | AFR | MSL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0301 | AFR | MSL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG03486 | hp2 | a0001 | c0002 | t0014 | g0020 | AFR | MSL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | ESN | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0258 | AFR | ESN | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG03540 | hp1 | a0001 | c0002 | t0002 | g0033 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG03579 | hp1 | a0001 | c0002 | t0014 | g0037 | AFR | MSL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG03579 | hp2 | a0001 | c0002 | t0002 | g0302 | AFR | MSL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG03669 | hp1 | a0001 | c0001 | t0005 | g0221 | SAS | PJL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG03669 | hp2 | a0001 | c0001 | t0033 | g0294 | SAS | PJL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0254 | SAS | PJL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG03704 | hp2 | a0001 | c0007 | t0001 | g0072 | SAS | PJL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG03710 | hp1 | a0001 | c0002 | t0003 | g0164 | SAS | PJL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0146 | SAS | BEB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0239 | SAS | BEB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0138 | SAS | BEB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG03834 | hp2 | a0001 | c0002 | t0003 | g0093 | SAS | BEB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG03927 | hp1 | a0001 | c0001 | t0006 | g0352 | SAS | BEB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0255 | SAS | BEB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG03942 | hp1 | a0001 | c0001 | t0006 | g0351 | SAS | BEB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | BEB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | BEB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0022 | SAS | BEB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG04204 | hp1 | a0002 | c0003 | t0001 | g0062 | SAS | STU | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0246 | SAS | STU | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG04228 | hp1 | a0004 | c0006 | t0001 | g0044 | SAS | STU | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG04228 | hp2 | a0001 | c0002 | t0002 | g0140 | SAS | STU | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18522 | hp1 | a0001 | c0001 | t0013 | g0034 | AFR | YRI | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0194 | AFR | YRI | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0202 | EAS | CHB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | CHB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | YRI | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | YRI | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18939 | hp1 | a0001 | c0001 | t0004 | g0224 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18943 | hp1 | a0001 | c0001 | t0018 | g0276 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18943 | hp2 | a0001 | c0001 | t0017 | g0038 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18946 | hp1 | a0001 | c0001 | t0004 | g0253 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18951 | hp1 | a0001 | c0002 | t0010 | g0207 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18951 | hp2 | a0001 | c0001 | t0005 | g0229 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18952 | hp1 | a0001 | c0001 | t0004 | g0252 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18956 | hp1 | a0001 | c0002 | t0002 | g0198 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18957 | hp1 | a0001 | c0001 | t0009 | g0057 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18957 | hp2 | a0001 | c0001 | t0005 | g0215 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0149 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0177 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18962 | hp2 | a0001 | c0001 | t0004 | g0249 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18963 | hp2 | a0001 | c0002 | t0002 | g0066 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18964 | hp1 | a0001 | c0002 | t0002 | g0323 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18965 | hp1 | a0001 | c0002 | t0002 | g0141 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18965 | hp2 | a0001 | c0001 | t0005 | g0214 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18969 | hp2 | a0001 | c0002 | t0010 | g0210 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18973 | hp2 | a0001 | c0002 | t0002 | g0142 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18974 | hp2 | a0001 | c0002 | t0002 | g0148 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18975 | hp1 | a0001 | c0002 | t0002 | g0205 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18975 | hp2 | a0001 | c0001 | t0032 | g0056 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18982 | hp1 | a0001 | c0001 | t0038 | g0218 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18984 | hp1 | a0001 | c0001 | t0004 | g0250 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18987 | hp1 | a0001 | c0002 | t0002 | g0204 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18988 | hp1 | a0001 | c0001 | t0039 | g0134 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18989 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18993 | hp2 | a0001 | c0002 | t0002 | g0199 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19000 | hp1 | a0001 | c0002 | t0022 | g0075 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19004 | hp1 | a0001 | c0001 | t0018 | g0274 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0143 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19009 | hp2 | a0001 | c0001 | t0004 | g0251 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | LWK | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19030 | hp2 | a0001 | c0001 | t0030 | g0179 | AFR | LWK | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19043 | hp1 | a0001 | c0001 | t0008 | g0023 | AFR | LWK | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19043 | hp2 | a0001 | c0002 | t0029 | g0296 | AFR | LWK | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19056 | hp1 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19058 | hp1 | a0001 | c0001 | t0021 | g0196 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19058 | hp2 | a0001 | c0001 | t0009 | g0049 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19072 | hp2 | a0001 | c0002 | t0002 | g0054 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19074 | hp2 | a0001 | c0002 | t0002 | g0053 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19077 | hp1 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19077 | hp2 | a0001 | c0001 | t0005 | g0328 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19079 | hp2 | a0001 | c0001 | t0021 | g0332 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19081 | hp1 | a0001 | c0001 | t0005 | g0213 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19082 | hp1 | a0001 | c0001 | t0017 | g0039 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19083 | hp1 | a0001 | c0001 | t0005 | g0236 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19086 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19087 | hp1 | a0001 | c0001 | t0037 | g0228 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19088 | hp2 | a0001 | c0002 | t0002 | g0200 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19090 | hp1 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19091 | hp1 | a0001 | c0002 | t0002 | g0201 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0337 | AFR | YRI | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA19240 | hp2 | a0001 | c0001 | t0007 | g0341 | AFR | YRI | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0032 | AFR | ASW | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | ASW | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0192 | EUR | TSI | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0190 | EUR | TSI | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | CLM | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG01123 | hp2 | a0001 | c0002 | t0003 | g0109 | AMR | CLM | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02109 | hp1 | a0001 | c0002 | t0002 | g0172 | AFR | ACB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02109 | hp2 | a0001 | c0001 | t0035 | g0078 | AFR | ACB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02486 | hp1 | a0001 | c0001 | t0020 | g0151 | AFR | ACB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | ACB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02559 | hp1 | a0001 | c0002 | t0019 | g0325 | AFR | ACB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | ACB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | MSL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | USA | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| HG06807 | hp2 | a0001 | c0001 | t0043 | g0019 | AFR | USA | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA18955 | hp2 | a0001 | c0001 | t0005 | g0222 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA21309 | hp1 | a0001 | c0001 | t0008 | g0346 | AFR | LWK | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | LWK | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0171 | REF | REF | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0007 | g0343 | REF | REF | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:206445520
|
A | G | 1 | a0005 | 1 | HG02132.hp1 | missense_variant | MODERATE | c.428A>G | p.Asn143Ser | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/26 | 763/6334 | 428/2499 | 143/832 | chr2 | 206445520 | ||
| chr2:206530907
|
G | A | 1 | a0002 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.532G>A | p.Val178Met | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/26 | 867/6334 | 532/2499 | 178/832 | chr2 | 206530907 | ||
| chr2:206559969
|
G | C | 1 | a0003 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.1020G>C | p.Gln340His | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 11/26 | 1355/6334 | 1020/2499 | 340/832 | chr2 | 206559969 | ||
| chr2:206596141
|
C | G | 1 | a0004 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.2338C>G | p.Pro780Ala | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/26 | 2673/6334 | 2338/2499 | 780/832 | chr2 | 206596141 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:206573171
|
A | G | 1 | a0001c0007 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.1713A>G | p.Glu571Glu | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/26 | 2048/6334 | 1713/2499 | 571/832 | chr2 | 206573171 | ||
| chr2:206594737
|
T | C | 1 | a0001c0005 | 1 | HG01884.hp1 | splice_region_variant&synonymous_variant | LOW | c.2079T>C | p.Ser693Ser | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 23/26 | 2414/6334 | 2079/2499 | 693/832 | chr2 | 206594737 | ||
| chr2:206594743
|
C | T | 2 | a0001c0002a0001c0005 | 78 | HG00280.hp1 HG00673.hp2 HG00738.hp2 others(75): Show |
synonymous_variant | LOW | c.2085C>T | p.Ala695Ala | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 23/26 | 2420/6334 | 2085/2499 | 695/832 | chr2 | 206594743 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:206443534
|
C | T | 1 | a0001c0001t0004 | 11 | HG01175.hp1 HG01943.hp1 HG02071.hp1 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-333C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 1/26 | 333 | chr2 | 206443534 | |||||
| chr2:206443584
|
G | A | 1 | a0001c0001t0023 | 1 | HG00609.hp2 | 5_prime_UTR_variant | MODIFIER | c.-283G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 1/26 | 283 | chr2 | 206443584 | |||||
| chr2:206443619
|
G | C | 1 | a0001c0002t0014 | 2 | HG03486.hp2 HG03579.hp1 |
5_prime_UTR_variant | MODIFIER | c.-248G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 1/26 | 248 | chr2 | 206443619 | |||||
| chr2:206443741
|
G | C | 1 | a0001c0001t0024 | 1 | HG02738.hp1 | 5_prime_UTR_variant | MODIFIER | c.-126G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 1/26 | 126 | chr2 | 206443741 | |||||
| chr2:206443744
|
G | C | 1 | a0001c0002t0015 | 2 | HG02895.hp1 HG02897.hp2 |
5_prime_UTR_variant | MODIFIER | c.-123G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 1/26 | 123 | chr2 | 206443744 | |||||
| chr2:206443754
|
C | A | 1 | a0001c0002t0025 | 1 | HG02300.hp1 | 5_prime_UTR_variant | MODIFIER | c.-113C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 1/26 | 113 | chr2 | 206443754 | |||||
| chr2:206617686
|
G | A | 1 | a0001c0001t0026 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*59G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 59 | chr2 | 206617686 | |||||
| chr2:206617856
|
G | A | 1 | a0001c0005t0027 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*229G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 229 | chr2 | 206617856 | |||||
| chr2:206618052
|
A | T | 1 | a0001c0001t0043 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*425A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 425 | chr2 | 206618052 | |||||
| chr2:206618074
|
A | T | 1 | a0001c0001t0009 | 4 | HG00544.hp2 HG00673.hp1 NA18957.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*447A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 447 | chr2 | 206618074 | |||||
| chr2:206618088
|
T | G | 1 | a0001c0002t0010 | 3 | HG02523.hp2 NA18951.hp1 NA18969.hp2 |
3_prime_UTR_variant | MODIFIER | c.*461T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 461 | chr2 | 206618088 | |||||
| chr2:206618116
|
G | A | 2 | a0001c0001t0028a0001c0002t0029 | 2 | HG03453.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*489G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 489 | chr2 | 206618116 | |||||
| chr2:206618368
|
G | A | 1 | a0001c0001t0016 | 2 | HG00140.hp1 HG01192.hp2 |
3_prime_UTR_variant | MODIFIER | c.*741G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 741 | chr2 | 206618368 | |||||
| chr2:206618549
|
G | T | 1 | a0001c0002t0022 | 2 | HG02056.hp2 NA19000.hp1 |
3_prime_UTR_variant | MODIFIER | c.*922G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 922 | chr2 | 206618549 | |||||
| chr2:206618693
|
G | A | 1 | a0001c0001t0030 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1066G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 1066 | chr2 | 206618693 | |||||
| chr2:206618787
|
G | A | 1 | a0001c0001t0031 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1160G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 1160 | chr2 | 206618787 | |||||
| chr2:206618802
|
T | A | 1 | a0001c0001t0032 | 1 | NA18975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1175T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 1175 | chr2 | 206618802 | |||||
| chr2:206618882
|
G | T | 2 | a0001c0001t0013a0003c0004t0013 | 3 | HG01243.hp1 HG03453.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1255G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 1255 | chr2 | 206618882 | |||||
| chr2:206618890
|
G | A | 1 | a0001c0002t0011 | 3 | HG02896.hp1 HG02897.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1263G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 1263 | chr2 | 206618890 | |||||
| chr2:206618922
|
T | C | 1 | a0001c0001t0017 | 2 | NA18943.hp2 NA19082.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1295T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 1295 | chr2 | 206618922 | |||||
| chr2:206619003
|
T | C | 1 | a0001c0001t0018 | 2 | NA18943.hp1 NA19004.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1376T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 1376 | chr2 | 206619003 | |||||
| chr2:206619189
|
T | C | 1 | a0001c0001t0033 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1562T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 1562 | chr2 | 206619189 | |||||
| chr2:206619237
|
A | G | 1 | a0001c0001t0042 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1610A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 1610 | chr2 | 206619237 | |||||
| chr2:206619405
|
G | A | 3 | a0001c0001t0012a0001c0001t0034a0001c0001t0035 | 5 | HG01361.hp2 HG01433.hp1 HG01496.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1778G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 1778 | chr2 | 206619405 | |||||
| chr2:206619432
|
T | C | 49 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(46): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
3_prime_UTR_variant | MODIFIER | c.*1805T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 1805 | chr2 | 206619432 | |||||
| chr2:206619485
|
C | T | 2 | a0001c0001t0034a0001c0001t0035 | 2 | HG02109.hp2 HG02615.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1858C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 1858 | chr2 | 206619485 | |||||
| chr2:206619509
|
GC | G | 22 | a0001c0001t0001a0001c0001t0008a0001c0001t0009others(19): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
3_prime_UTR_variant | MODIFIER | c.*1891delC | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 1891 | INFO_REALIGN_3_PRIME | chr2 | 206619509 | ||||
| chr2:206619511
|
C | T | 1 | a0001c0001t0043 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1884C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 1884 | chr2 | 206619511 | |||||
| chr2:206619648
|
G | A | 4 | a0001c0002t0003a0001c0002t0015a0001c0002t0019others(1): Show | 21 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2021G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 2021 | chr2 | 206619648 | |||||
| chr2:206619732
|
A | G | 1 | a0001c0001t0035 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2105A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 2105 | chr2 | 206619732 | |||||
| chr2:206619736
|
T | C | 1 | a0001c0001t0039 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2109T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 2109 | chr2 | 206619736 | |||||
| chr2:206619951
|
A | G | 1 | a0001c0001t0038 | 1 | NA18982.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2324A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 2324 | chr2 | 206619951 | |||||
| chr2:206619988
|
C | G | 1 | a0001c0001t0026 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2361C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 2361 | chr2 | 206619988 | |||||
| chr2:206620050
|
A | G | 2 | a0001c0001t0006a0001c0001t0008 | 10 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2423A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 2423 | chr2 | 206620050 | |||||
| chr2:206620062
|
A | T | 1 | a0001c0001t0041 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2435A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 2435 | chr2 | 206620062 | |||||
| chr2:206620163
|
T | G | 1 | a0001c0001t0020 | 2 | HG02486.hp1 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2536T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 2536 | chr2 | 206620163 | |||||
| chr2:206620327
|
C | A | 1 | a0001c0001t0040 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2700C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 2700 | chr2 | 206620327 | |||||
| chr2:206620542
|
A | T | 1 | a0001c0005t0027 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2915A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 2915 | chr2 | 206620542 | |||||
| chr2:206620606
|
G | T | 1 | a0001c0001t0037 | 1 | NA19087.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2979G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 2979 | chr2 | 206620606 | |||||
| chr2:206620734
|
C | G | 1 | a0001c0001t0021 | 2 | NA19058.hp1 NA19079.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3107C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 3107 | chr2 | 206620734 | |||||
| chr2:206620849
|
G | A | 1 | a0001c0001t0028 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3222G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 3222 | chr2 | 206620849 | |||||
| chr2:206620850
|
G | A | 5 | a0001c0001t0005a0001c0001t0031a0001c0001t0037others(2): Show | 13 | HG00558.hp1 HG00609.hp1 HG02132.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3223G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 3223 | chr2 | 206620850 | |||||
| chr2:206620910
|
C | T | 2 | a0001c0001t0042a0001c0002t0019 | 3 | HG02055.hp1 HG02559.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3283C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 3283 | chr2 | 206620910 | |||||
| chr2:206620931
|
T | C | 1 | a0001c0001t0021 | 2 | NA19058.hp1 NA19079.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3304T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 3304 | chr2 | 206620931 | |||||
| chr2:206621003
|
C | T | 1 | a0001c0001t0036 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3376C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 3376 | chr2 | 206621003 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:206444237
|
A | G | 8 | a0001c0001t0006g0345a0001c0001t0006g0348a0001c0001t0006g0349others(5): Show | 8 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+157A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 1/25 | chr2 | 206444237 | ||||||
| chr2:206444373
|
C | A | 346 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(343): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.214+293C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 1/25 | chr2 | 206444373 | ||||||
| chr2:206444659
|
G | A | 5 | a0001c0002t0002g0007a0001c0002t0002g0008a0001c0002t0002g0009others(2): Show | 5 | HG02145.hp1 HG02451.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.214+579G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 1/25 | chr2 | 206444659 | ||||||
| chr2:206444786
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.215-521G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 1/25 | chr2 | 206444786 | ||||||
| chr2:206444998
|
A | AC | 15 | a0001c0001t0001g0324a0001c0001t0001g0331a0001c0001t0001g0334others(12): Show | 15 | HG00099.hp2 HG00738.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.215-299dupC | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr2 | 206444998 | |||||
| chr2:206444998
|
AC | A | 92 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(89): Show | 95 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.215-299delC | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr2 | 206444998 | |||||
| chr2:206444998
|
ACC | A | 91 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(88): Show | 94 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.215-300_215-299del others(2): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr2 | 206444998 | |||||
| chr2:206445557
|
A | G | 1 | a0001c0002t0002g0323 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.432+33A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206445557 | ||||||
| chr2:206445582
|
G | T | 9 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0085others(6): Show | 10 | HG01952.hp2 HG02040.hp2 NA18946.hp2 others(7): Show |
intron_variant | MODIFIER | c.432+58G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206445582 | ||||||
| chr2:206445592
|
C | A | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.432+68C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206445592 | ||||||
| chr2:206445886
|
A | G | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083 | 3 | HG00733.hp1 HG00741.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.432+362A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206445886 | ||||||
| chr2:206445888
|
G | A | 1 | a0001c0001t0001g0084 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.432+364G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206445888 | ||||||
| chr2:206446093
|
A | G | 1 | a0001c0001t0002g0322 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.432+569A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206446093 | ||||||
| chr2:206446182
|
T | C | 1 | a0001c0001t0001g0181 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.432+658T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206446182 | ||||||
| chr2:206446500
|
A | G | 1 | a0001c0001t0001g0080 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.432+976A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206446500 | ||||||
| chr2:206446556
|
G | A | 1 | a0001c0002t0003g0093 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.432+1032G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206446556 | ||||||
| chr2:206446625
|
T | A | 8 | a0001c0001t0006g0345a0001c0001t0006g0348a0001c0001t0006g0349others(5): Show | 8 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.432+1101T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206446625 | ||||||
| chr2:206446740
|
C | T | 1 | a0001c0001t0001g0321 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.432+1216C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206446740 | ||||||
| chr2:206446768
|
T | G | 1 | a0001c0001t0001g0321 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.432+1244T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206446768 | ||||||
| chr2:206446915
|
G | A | 1 | a0001c0001t0001g0013 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.432+1391G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206446915 | ||||||
| chr2:206446935
|
T | C | 29 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0095others(26): Show | 30 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.432+1411T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206446935 | ||||||
| chr2:206446971
|
A | G | 23 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0308others(20): Show | 23 | HG01361.hp2 HG01433.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.432+1447A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206446971 | ||||||
| chr2:206447174
|
G | A | 2 | a0001c0002t0015g0182a0001c0002t0015g0183 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.432+1650G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206447174 | ||||||
| chr2:206447177
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.432+1653G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206447177 | ||||||
| chr2:206447191
|
T | C | 94 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(91): Show | 97 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.432+1667T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206447191 | ||||||
| chr2:206447465
|
A | T | 1 | a0001c0001t0001g0303 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.432+1941A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206447465 | ||||||
| chr2:206447723
|
G | T | 81 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(78): Show | 84 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.432+2199G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206447723 | ||||||
| chr2:206447750
|
T | A | 2 | a0001c0002t0011g0186a0001c0002t0011g0187 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.432+2226T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206447750 | ||||||
| chr2:206447937
|
T | C | 1 | a0001c0001t0002g0014 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.432+2413T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206447937 | ||||||
| chr2:206448048
|
C | G | 103 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(100): Show | 106 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.432+2524C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206448048 | ||||||
| chr2:206448130
|
C | A | 1 | a0001c0002t0003g0126 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.432+2606C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206448130 | ||||||
| chr2:206448290
|
C | G | 1 | a0001c0002t0003g0178 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.432+2766C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206448290 | ||||||
| chr2:206448479
|
G | C | 216 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(213): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.432+2955G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206448479 | ||||||
| chr2:206448497
|
ATGAG | A | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(86): Show | 92 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.432+2976_432+2979d others(6): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206448497 | |||||
| chr2:206448543
|
C | T | 8 | a0001c0001t0001g0300a0001c0001t0002g0301a0001c0001t0026g0299others(5): Show | 8 | HG02572.hp2 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.432+3019C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206448543 | ||||||
| chr2:206448679
|
C | T | 1 | a0001c0001t0033g0294 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.432+3155C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206448679 | ||||||
| chr2:206448713
|
A | G | 23 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0308others(20): Show | 23 | HG01361.hp2 HG01433.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.432+3189A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206448713 | ||||||
| chr2:206448955
|
C | A | 1 | a0001c0001t0001g0127 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.432+3431C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206448955 | ||||||
| chr2:206449051
|
A | G | 96 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(93): Show | 99 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.432+3527A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206449051 | ||||||
| chr2:206449155
|
A | G | 1 | a0001c0002t0003g0174 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.432+3631A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206449155 | ||||||
| chr2:206449264
|
C | T | 2 | a0001c0002t0015g0182a0001c0002t0015g0183 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.432+3740C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206449264 | ||||||
| chr2:206449431
|
TC | T | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083 | 3 | HG00733.hp1 HG00741.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.432+3909delC | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206449431 | |||||
| chr2:206449493
|
C | T | 4 | a0001c0002t0002g0074a0001c0002t0002g0077a0001c0002t0022g0075others(1): Show | 4 | HG02056.hp2 NA19000.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.432+3969C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206449493 | ||||||
| chr2:206449515
|
C | T | 1 | a0001c0001t0001g0293 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.432+3991C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206449515 | ||||||
| chr2:206449595
|
C | G | 1 | a0001c0001t0004g0292 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.432+4071C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206449595 | ||||||
| chr2:206449640
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.432+4116C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206449640 | ||||||
| chr2:206449718
|
G | A | 2 | a0001c0002t0019g0189a0001c0002t0019g0325 | 2 | HG02055.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.432+4194G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206449718 | ||||||
| chr2:206449843
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.432+4319G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206449843 | ||||||
| chr2:206449874
|
G | A | 1 | a0001c0001t0030g0179 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.432+4350G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206449874 | ||||||
| chr2:206450077
|
A | G | 1 | a0001c0001t0001g0321 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.432+4553A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206450077 | ||||||
| chr2:206450095
|
C | G | 1 | a0001c0002t0019g0189 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.432+4571C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206450095 | ||||||
| chr2:206450227
|
A | G | 1 | a0001c0002t0002g0320 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.432+4703A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206450227 | ||||||
| chr2:206450376
|
T | C | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017 | 3 | NA18961.hp1 NA19011.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.432+4852T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206450376 | ||||||
| chr2:206450590
|
G | A | 1 | a0001c0001t0009g0018 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.432+5066G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206450590 | ||||||
| chr2:206450695
|
C | T | 1 | a0001c0002t0002g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.432+5171C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206450695 | ||||||
| chr2:206450808
|
C | T | 1 | a0001c0001t0001g0017 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.432+5284C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206450808 | ||||||
| chr2:206450809
|
A | G | 84 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(81): Show | 87 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.432+5285A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206450809 | ||||||
| chr2:206450810
|
T | C | 2 | a0001c0002t0011g0186a0001c0002t0011g0187 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.432+5286T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206450810 | ||||||
| chr2:206450853
|
A | G | 1 | a0001c0001t0001g0171 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.432+5329A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206450853 | ||||||
| chr2:206450920
|
T | G | 3 | a0001c0001t0028g0297a0001c0001t0042g0295a0001c0002t0029g0296 | 3 | HG03139.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.432+5396T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206450920 | ||||||
| chr2:206450953
|
G | T | 1 | a0001c0001t0002g0333 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.432+5429G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206450953 | ||||||
| chr2:206451380
|
C | T | 91 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(88): Show | 94 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.432+5856C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206451380 | ||||||
| chr2:206451457
|
C | G | 1 | a0001c0001t0001g0121 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.432+5933C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206451457 | ||||||
| chr2:206451732
|
A | T | 1 | a0001c0001t0001g0319 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.432+6208A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206451732 | ||||||
| chr2:206451816
|
A | G | 31 | a0001c0001t0001g0190a0001c0001t0001g0267a0001c0001t0001g0268others(28): Show | 31 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.432+6292A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206451816 | ||||||
| chr2:206451824
|
C | T | 22 | a0001c0001t0001g0181a0001c0001t0001g0300a0001c0001t0001g0309others(19): Show | 22 | HG02258.hp1 HG02559.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.432+6300C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206451824 | ||||||
| chr2:206451901
|
G | A | 4 | a0001c0001t0001g0309a0001c0001t0001g0319a0001c0001t0001g0336others(1): Show | 4 | HG02258.hp1 HG03195.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.432+6377G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206451901 | ||||||
| chr2:206451987
|
G | A | 2 | a0001c0001t0001g0192a0001c0001t0002g0191 | 2 | NA19090.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.432+6463G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206451987 | ||||||
| chr2:206452029
|
T | C | 2 | a0001c0002t0015g0182a0001c0002t0015g0183 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.432+6505T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206452029 | ||||||
| chr2:206452072
|
C | T | 5 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0073others(2): Show | 5 | HG00733.hp1 HG01255.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.432+6548C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206452072 | ||||||
| chr2:206452132
|
C | T | 1 | a0001c0001t0002g0266 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.432+6608C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206452132 | ||||||
| chr2:206452199
|
T | C | 2 | a0001c0001t0001g0173a0001c0001t0030g0179 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.432+6675T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206452199 | ||||||
| chr2:206452286
|
A | G | 1 | a0001c0001t0021g0332 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.432+6762A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206452286 | ||||||
| chr2:206452372
|
G | A | 39 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0095others(36): Show | 40 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.432+6848G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206452372 | ||||||
| chr2:206452399
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.432+6875C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206452399 | ||||||
| chr2:206452448
|
T | G | 1 | a0001c0001t0001g0121 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.432+6924T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206452448 | ||||||
| chr2:206452694
|
A | G | 2 | a0001c0001t0001g0264a0001c0001t0001g0265 | 2 | HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.432+7170A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206452694 | ||||||
| chr2:206452850
|
C | T | 31 | a0001c0001t0001g0173a0001c0001t0001g0190a0001c0001t0001g0267others(28): Show | 31 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.432+7326C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206452850 | ||||||
| chr2:206452989
|
T | C | 1 | a0001c0001t0001g0021 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.432+7465T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206452989 | ||||||
| chr2:206453081
|
G | A | 2 | a0001c0002t0003g0137a0001c0002t0003g0174 | 2 | HG00280.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.432+7557G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206453081 | ||||||
| chr2:206453149
|
C | T | 88 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(85): Show | 91 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.432+7625C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206453149 | ||||||
| chr2:206453210
|
A | G | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(86): Show | 92 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.432+7686A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206453210 | ||||||
| chr2:206453306
|
G | C | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.432+7782G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206453306 | ||||||
| chr2:206453338
|
A | T | 26 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0154others(23): Show | 28 | HG00099.hp2 HG00280.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.432+7814A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206453338 | ||||||
| chr2:206453397
|
C | A | 1 | a0001c0001t0001g0128 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.432+7873C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206453397 | ||||||
| chr2:206453467
|
G | A | 1 | a0001c0001t0001g0127 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.432+7943G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206453467 | ||||||
| chr2:206453507
|
C | A | 5 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269others(2): Show | 5 | HG01081.hp2 HG01106.hp2 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.432+7983C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206453507 | ||||||
| chr2:206453579
|
A | G | 1 | a0001c0002t0002g0077 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.432+8055A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206453579 | ||||||
| chr2:206453765
|
A | G | 4 | a0001c0001t0006g0349a0001c0001t0006g0350a0001c0001t0006g0351others(1): Show | 4 | HG01081.hp1 HG03017.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.432+8241A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206453765 | ||||||
| chr2:206454282
|
G | T | 2 | a0001c0002t0015g0182a0001c0002t0015g0183 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.432+8758G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206454282 | ||||||
| chr2:206454575
|
G | C | 87 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(84): Show | 90 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.432+9051G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206454575 | ||||||
| chr2:206454627
|
G | A | 87 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(84): Show | 90 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.432+9103G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206454627 | ||||||
| chr2:206454844
|
C | T | 1 | a0001c0001t0001g0263 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.432+9320C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206454844 | ||||||
| chr2:206454861
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.432+9337A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206454861 | ||||||
| chr2:206454904
|
C | T | 6 | a0001c0001t0001g0300a0001c0001t0002g0301a0001c0001t0026g0299others(3): Show | 6 | HG02572.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.432+9380C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206454904 | ||||||
| chr2:206454926
|
G | T | 6 | a0001c0001t0001g0300a0001c0001t0002g0301a0001c0001t0026g0299others(3): Show | 6 | HG02572.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.432+9402G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206454926 | ||||||
| chr2:206454929
|
C | T | 10 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0006g0345others(7): Show | 10 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.432+9405C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206454929 | ||||||
| chr2:206455417
|
A | G | 1 | a0001c0001t0001g0290 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.432+9893A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206455417 | ||||||
| chr2:206455423
|
G | A | 1 | a0001c0001t0035g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.432+9899G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206455423 | ||||||
| chr2:206455554
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.432+10030C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206455554 | ||||||
| chr2:206455694
|
C | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(82): Show | 88 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.432+10170C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206455694 | ||||||
| chr2:206455808
|
A | G | 1 | a0001c0002t0002g0320 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.432+10284A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206455808 | ||||||
| chr2:206455902
|
G | C | 87 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(84): Show | 90 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.432+10378G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206455902 | ||||||
| chr2:206455911
|
A | G | 78 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(75): Show | 81 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.432+10387A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206455911 | ||||||
| chr2:206456014
|
C | A | 2 | a0001c0001t0001g0184a0001c0001t0043g0019 | 2 | HG02622.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.432+10490C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206456014 | ||||||
| chr2:206456030
|
A | G | 2 | a0001c0002t0002g0010a0001c0002t0002g0011 | 2 | HG02451.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.432+10506A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206456030 | ||||||
| chr2:206456258
|
G | A | 5 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0073others(2): Show | 5 | HG00733.hp1 HG01255.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.432+10734G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206456258 | ||||||
| chr2:206456324
|
A | G | 1 | a0001c0002t0002g0262 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.432+10800A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206456324 | ||||||
| chr2:206456342
|
C | G | 7 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0184others(4): Show | 7 | HG02055.hp2 HG02486.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.432+10818C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206456342 | ||||||
| chr2:206456524
|
T | C | 2 | a0001c0001t0002g0139a0001c0002t0002g0138 | 2 | HG01975.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.432+11000T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206456524 | ||||||
| chr2:206456654
|
T | C | 3 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125 | 3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.432+11130T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206456654 | ||||||
| chr2:206456729
|
C | T | 1 | a0001c0001t0001g0289 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.432+11205C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206456729 | ||||||
| chr2:206456943
|
A | G | 346 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(343): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.432+11419A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206456943 | ||||||
| chr2:206456954
|
C | T | 2 | a0001c0001t0001g0006a0001c0001t0001g0170 | 3 | HG02257.hp2 HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.432+11430C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206456954 | ||||||
| chr2:206457056
|
A | T | 2 | a0001c0002t0015g0182a0001c0002t0015g0183 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.432+11532A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206457056 | ||||||
| chr2:206457427
|
A | C | 7 | a0001c0001t0001g0300a0001c0001t0002g0301a0001c0001t0026g0299others(4): Show | 7 | HG02572.hp2 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.432+11903A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206457427 | ||||||
| chr2:206457567
|
C | T | 29 | a0001c0001t0001g0190a0001c0001t0001g0267a0001c0001t0001g0268others(26): Show | 29 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.432+12043C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206457567 | ||||||
| chr2:206457641
|
A | C | 1 | a0001c0001t0001g0069 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.432+12117A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206457641 | ||||||
| chr2:206458077
|
A | G | 1 | a0001c0001t0001g0288 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.432+12553A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206458077 | ||||||
| chr2:206458157
|
TC | T | 31 | a0001c0001t0001g0173a0001c0001t0001g0190a0001c0001t0001g0267others(28): Show | 31 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.432+12634delC | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206458157 | ||||||
| chr2:206458174
|
T | G | 3 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0041g0028 | 3 | HG00642.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.432+12650T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206458174 | ||||||
| chr2:206458227
|
C | CACATGGA others(67): Show |
86 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(83): Show | 89 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.432+12703_432+1270 others(78): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206458227 | ||||||
| chr2:206458239
|
G | A | 2 | a0001c0001t0001g0184a0001c0001t0043g0019 | 2 | HG02622.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.432+12715G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206458239 | ||||||
| chr2:206458273
|
T | C | 2 | a0001c0001t0042g0295a0001c0002t0029g0296 | 2 | HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.432+12749T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206458273 | ||||||
| chr2:206458370
|
A | C | 5 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0185others(2): Show | 5 | HG02055.hp2 HG02486.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.432+12846A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206458370 | ||||||
| chr2:206458426
|
G | A | 10 | a0001c0001t0001g0036a0001c0001t0001g0069a0001c0001t0002g0035others(7): Show | 10 | HG01243.hp1 HG02895.hp2 HG03098.hp1 others(7): Show |
intron_variant | MODIFIER | c.432+12902G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206458426 | ||||||
| chr2:206458471
|
A | G | 2 | a0001c0001t0001g0068a0001c0001t0001g0080 | 2 | HG02717.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.432+12947A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206458471 | ||||||
| chr2:206458575
|
A | G | 86 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(83): Show | 89 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.432+13051A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206458575 | ||||||
| chr2:206458715
|
G | A | 2 | a0001c0001t0002g0193a0001c0001t0002g0194 | 2 | HG01261.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.432+13191G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206458715 | ||||||
| chr2:206458956
|
T | G | 29 | a0001c0001t0001g0094a0001c0001t0001g0197a0001c0001t0001g0203others(26): Show | 29 | HG00673.hp2 HG02083.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.432+13432T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206458956 | ||||||
| chr2:206459077
|
A | G | 23 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0308others(20): Show | 23 | HG01361.hp2 HG01433.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.432+13553A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206459077 | ||||||
| chr2:206459080
|
G | T | 1 | a0001c0001t0009g0067 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.432+13556G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206459080 | ||||||
| chr2:206459193
|
G | A | 1 | a0001c0001t0002g0212 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.432+13669G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206459193 | ||||||
| chr2:206459236
|
T | C | 1 | a0001c0002t0002g0302 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.432+13712T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206459236 | ||||||
| chr2:206459440
|
A | G | 1 | a0001c0001t0001g0308 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.432+13916A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206459440 | ||||||
| chr2:206459558
|
A | G | 216 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(213): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.432+14034A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206459558 | ||||||
| chr2:206459578
|
C | T | 1 | a0001c0002t0002g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.432+14054C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206459578 | ||||||
| chr2:206459586
|
A | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | NA19011.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.432+14062A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206459586 | ||||||
| chr2:206459656
|
C | T | 39 | a0001c0001t0001g0004a0001c0001t0001g0095a0001c0001t0001g0096others(36): Show | 40 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.432+14132C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206459656 | ||||||
| chr2:206459728
|
A | G | 25 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0308others(22): Show | 25 | HG01361.hp2 HG01433.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.432+14204A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206459728 | ||||||
| chr2:206459936
|
C | T | 1 | a0001c0002t0001g0150 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.432+14412C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206459936 | ||||||
| chr2:206459997
|
G | A | 1 | a0001c0001t0013g0030 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.432+14473G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206459997 | ||||||
| chr2:206460040
|
A | G | 1 | a0001c0002t0002g0320 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.432+14516A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206460040 | ||||||
| chr2:206460105
|
C | CT | 26 | a0001c0001t0001g0197a0001c0001t0001g0203a0001c0001t0001g0208others(23): Show | 26 | HG00673.hp2 HG01496.hp2 HG02083.hp1 others(23): Show |
intron_variant | MODIFIER | c.432+14596dupT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206460105 | |||||
| chr2:206460105
|
CT | C | 30 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0154others(27): Show | 32 | HG00099.hp2 HG00280.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.432+14596delT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206460105 | |||||
| chr2:206460105
|
CTT | C | 75 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(72): Show | 78 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.432+14595_432+1459 others(6): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206460105 | |||||
| chr2:206460541
|
T | A | 7 | a0001c0001t0001g0300a0001c0001t0002g0301a0001c0001t0026g0299others(4): Show | 7 | HG02572.hp2 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.432+15017T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206460541 | ||||||
| chr2:206460764
|
T | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0170 | 3 | HG02257.hp2 HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.432+15240T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206460764 | ||||||
| chr2:206460968
|
T | C | 1 | a0001c0002t0003g0126 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.432+15444T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206460968 | ||||||
| chr2:206460996
|
A | C | 1 | a0001c0001t0001g0012 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.432+15472A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206460996 | ||||||
| chr2:206461063
|
C | CT | 11 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0260others(8): Show | 11 | HG00438.hp2 HG02486.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.432+15556dupT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206461063 | |||||
| chr2:206461063
|
CT | C | 9 | a0001c0001t0001g0015a0001c0001t0002g0195a0001c0001t0005g0213others(6): Show | 9 | HG01243.hp1 HG02886.hp1 HG03453.hp2 others(6): Show |
intron_variant | MODIFIER | c.432+15556delT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206461063 | |||||
| chr2:206461131
|
T | C | 281 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(278): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.432+15607T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206461131 | ||||||
| chr2:206461135
|
T | C | 1 | a0001c0001t0001g0027 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.432+15611T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206461135 | ||||||
| chr2:206461505
|
T | C | 1 | a0001c0002t0002g0007 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.432+15981T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206461505 | ||||||
| chr2:206461532
|
G | A | 250 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(247): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.432+16008G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206461532 | ||||||
| chr2:206461641
|
A | G | 4 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(1): Show | 4 | HG02280.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.432+16117A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206461641 | ||||||
| chr2:206461687
|
C | T | 1 | a0001c0001t0002g0014 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.432+16163C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206461687 | ||||||
| chr2:206461982
|
A | T | 1 | a0001c0001t0001g0169 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.432+16458A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206461982 | ||||||
| chr2:206462055
|
C | T | 2 | a0001c0001t0002g0193a0001c0001t0002g0194 | 2 | HG01261.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.432+16531C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206462055 | ||||||
| chr2:206462162
|
G | A | 4 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(1): Show | 4 | HG02280.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.432+16638G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206462162 | ||||||
| chr2:206462178
|
C | G | 1 | a0001c0001t0001g0026 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.432+16654C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206462178 | ||||||
| chr2:206462213
|
G | A | 175 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(172): Show | 180 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.432+16689G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206462213 | ||||||
| chr2:206462428
|
T | G | 2 | a0001c0001t0042g0295a0001c0002t0029g0296 | 2 | HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.432+16904T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206462428 | ||||||
| chr2:206462513
|
A | C | 20 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0308others(17): Show | 20 | HG01884.hp1 HG02257.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.432+16989A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206462513 | ||||||
| chr2:206462566
|
C | T | 4 | a0001c0001t0008g0023a0001c0001t0008g0330a0001c0002t0019g0189others(1): Show | 4 | HG02055.hp1 HG02559.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.432+17042C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206462566 | ||||||
| chr2:206462581
|
G | C | 2 | a0001c0001t0001g0180a0001c0002t0002g0307 | 2 | HG02257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.432+17057G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206462581 | ||||||
| chr2:206463007
|
G | A | 1 | a0001c0001t0043g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.432+17483G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206463007 | ||||||
| chr2:206463171
|
G | A | 250 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(247): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.432+17647G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206463171 | ||||||
| chr2:206463294
|
A | G | 2 | a0001c0001t0001g0180a0001c0002t0002g0307 | 2 | HG02257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.432+17770A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206463294 | ||||||
| chr2:206463300
|
T | C | 4 | a0001c0001t0001g0197a0001c0002t0002g0198a0001c0002t0002g0199others(1): Show | 4 | NA18956.hp1 NA18964.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.432+17776T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206463300 | ||||||
| chr2:206463385
|
G | A | 1 | a0001c0001t0001g0293 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.433-17847G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206463385 | ||||||
| chr2:206463502
|
G | A | 1 | a0001c0002t0002g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.433-17730G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206463502 | ||||||
| chr2:206463545
|
A | G | 2 | a0001c0002t0014g0020a0001c0002t0014g0037 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.433-17687A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206463545 | ||||||
| chr2:206463625
|
C | T | 3 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125 | 3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.433-17607C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206463625 | ||||||
| chr2:206463644
|
G | C | 4 | a0001c0002t0002g0074a0001c0002t0002g0077a0001c0002t0022g0075others(1): Show | 4 | HG02056.hp2 NA19000.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.433-17588G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206463644 | ||||||
| chr2:206463683
|
G | C | 1 | a0001c0002t0002g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.433-17549G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206463683 | ||||||
| chr2:206463725
|
G | A | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG00558.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.433-17507G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206463725 | ||||||
| chr2:206463871
|
A | G | 30 | a0001c0001t0001g0190a0001c0001t0001g0267a0001c0001t0001g0268others(27): Show | 30 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.433-17361A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206463871 | ||||||
| chr2:206464038
|
C | G | 1 | a0001c0001t0001g0065 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.433-17194C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206464038 | ||||||
| chr2:206464050
|
T | C | 1 | a0001c0001t0001g0190 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.433-17182T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206464050 | ||||||
| chr2:206464193
|
G | A | 5 | a0001c0001t0026g0299a0001c0002t0002g0302a0001c0002t0011g0186others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.433-17039G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206464193 | ||||||
| chr2:206464276
|
A | G | 1 | a0001c0001t0001g0256 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.433-16956A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206464276 | ||||||
| chr2:206464283
|
GT | G | 76 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(73): Show | 79 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.433-16947delT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206464283 | |||||
| chr2:206464436
|
G | A | 1 | a0001c0001t0033g0294 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.433-16796G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206464436 | ||||||
| chr2:206464483
|
G | A | 5 | a0001c0001t0026g0299a0001c0002t0002g0302a0001c0002t0011g0186others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.433-16749G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206464483 | ||||||
| chr2:206464530
|
G | A | 4 | a0001c0001t0012g0304a0001c0001t0012g0305a0001c0001t0012g0306others(1): Show | 4 | HG01361.hp2 HG01433.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.433-16702G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206464530 | ||||||
| chr2:206464560
|
G | T | 36 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0095others(33): Show | 37 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.433-16672G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206464560 | ||||||
| chr2:206464572
|
C | CA | 7 | a0001c0001t0001g0070a0001c0002t0001g0092a0001c0002t0002g0007others(4): Show | 7 | HG02145.hp1 HG02451.hp1 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.433-16649dupA | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206464572 | |||||
| chr2:206464581
|
A | T | 1 | a0001c0001t0002g0255 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.433-16651A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206464581 | ||||||
| chr2:206464584
|
T | A | 16 | a0001c0001t0001g0004a0001c0001t0001g0097a0001c0001t0006g0345others(13): Show | 17 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.433-16648T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206464584 | ||||||
| chr2:206464588
|
A | G | 1 | a0001c0002t0001g0150 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.433-16644A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206464588 | ||||||
| chr2:206464591
|
A | C | 24 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0308others(21): Show | 24 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.433-16641A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206464591 | ||||||
| chr2:206464653
|
CA | C | 18 | a0001c0001t0001g0006a0001c0001t0001g0170a0001c0002t0003g0093others(15): Show | 19 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.433-16578delA | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206464653 | ||||||
| chr2:206464695
|
T | A | 2 | a0001c0002t0002g0032a0001c0002t0002g0033 | 2 | HG03540.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.433-16537T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206464695 | ||||||
| chr2:206464754
|
G | A | 41 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0095others(38): Show | 42 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.433-16478G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206464754 | ||||||
| chr2:206464771
|
G | A | 1 | a0001c0001t0001g0098 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.433-16461G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206464771 | ||||||
| chr2:206464779
|
C | T | 1 | a0001c0001t0002g0254 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.433-16453C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206464779 | ||||||
| chr2:206464900
|
C | A | 1 | a0001c0001t0021g0196 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.433-16332C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206464900 | ||||||
| chr2:206464949
|
A | G | 2 | a0001c0002t0002g0148a0001c0002t0002g0149 | 2 | NA18959.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.433-16283A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206464949 | ||||||
| chr2:206465031
|
G | A | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.433-16201G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206465031 | ||||||
| chr2:206465123
|
G | A | 1 | a0001c0001t0006g0345 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.433-16109G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206465123 | ||||||
| chr2:206465165
|
C | T | 5 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284others(2): Show | 5 | NA18945.hp1 NA18966.hp2 NA19057.hp1 others(2): Show |
intron_variant | MODIFIER | c.433-16067C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206465165 | ||||||
| chr2:206465202
|
C | T | 1 | a0001c0001t0001g0015 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.433-16030C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206465202 | ||||||
| chr2:206465305
|
A | T | 1 | a0001c0001t0001g0192 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.433-15927A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206465305 | ||||||
| chr2:206465353
|
A | C | 4 | a0001c0001t0001g0184a0001c0001t0043g0019a0001c0002t0029g0296others(1): Show | 4 | HG01884.hp1 HG02622.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.433-15879A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206465353 | ||||||
| chr2:206465545
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.433-15687A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206465545 | ||||||
| chr2:206465569
|
A | G | 5 | a0001c0001t0004g0249a0001c0001t0004g0250a0001c0001t0004g0251others(2): Show | 5 | NA18946.hp1 NA18952.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.433-15663A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206465569 | ||||||
| chr2:206465619
|
T | C | 2 | a0001c0002t0002g0010a0001c0002t0002g0011 | 2 | HG02451.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.433-15613T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206465619 | ||||||
| chr2:206465858
|
T | C | 5 | a0001c0001t0026g0299a0001c0002t0002g0302a0001c0002t0011g0186others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.433-15374T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206465858 | ||||||
| chr2:206466099
|
A | G | 25 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0015others(22): Show | 26 | HG00140.hp2 HG00280.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.433-15133A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206466099 | ||||||
| chr2:206466342
|
T | G | 1 | a0001c0001t0040g0040 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.433-14890T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206466342 | ||||||
| chr2:206466420
|
G | A | 3 | a0001c0002t0002g0200a0001c0002t0002g0201a0001c0002t0002g0202 | 3 | NA18747.hp1 NA19088.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.433-14812G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206466420 | ||||||
| chr2:206466434
|
T | G | 4 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0185others(1): Show | 4 | HG02055.hp2 HG02486.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.433-14798T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206466434 | ||||||
| chr2:206466587
|
T | C | 1 | a0001c0001t0006g0348 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.433-14645T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206466587 | ||||||
| chr2:206466664
|
T | C | 1 | a0001c0001t0039g0134 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.433-14568T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206466664 | ||||||
| chr2:206466769
|
A | G | 2 | a0001c0001t0002g0193a0001c0001t0002g0194 | 2 | HG01261.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.433-14463A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206466769 | ||||||
| chr2:206466807
|
G | T | 8 | a0001c0001t0006g0345a0001c0001t0006g0348a0001c0001t0006g0349others(5): Show | 8 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.433-14425G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206466807 | ||||||
| chr2:206466926
|
G | A | 1 | a0001c0001t0001g0015 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.433-14306G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206466926 | ||||||
| chr2:206466941
|
G | T | 44 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0095others(41): Show | 45 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.433-14291G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206466941 | ||||||
| chr2:206467002
|
TAAC | T | 76 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(73): Show | 79 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.433-14223_433-1422 others(7): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206467002 | |||||
| chr2:206467060
|
TCACCTCC others(10): Show |
T | 3 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125 | 3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.433-14164_433-1414 others(21): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206467060 | |||||
| chr2:206467069
|
A | G | 1 | a0001c0001t0020g0151 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.433-14163A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206467069 | ||||||
| chr2:206467334
|
A | G | 10 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0112others(7): Show | 10 | HG00438.hp1 NA18939.hp2 NA18952.hp2 others(7): Show |
intron_variant | MODIFIER | c.433-13898A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206467334 | ||||||
| chr2:206467394
|
G | A | 32 | a0001c0001t0001g0173a0001c0001t0001g0190a0001c0001t0001g0267others(29): Show | 32 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.433-13838G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206467394 | ||||||
| chr2:206467496
|
C | G | 1 | a0001c0001t0007g0344 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.433-13736C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206467496 | ||||||
| chr2:206467674
|
C | A | 1 | a0001c0002t0029g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.433-13558C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206467674 | ||||||
| chr2:206468220
|
A | T | 1 | a0001c0001t0002g0261 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.433-13012A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206468220 | ||||||
| chr2:206468257
|
C | G | 1 | a0001c0002t0002g0323 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.433-12975C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206468257 | ||||||
| chr2:206468317
|
A | G | 3 | a0001c0001t0002g0139a0001c0001t0024g0273a0001c0002t0002g0138 | 3 | HG01975.hp2 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.433-12915A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206468317 | ||||||
| chr2:206468333
|
A | G | 1 | a0001c0001t0001g0248 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.433-12899A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206468333 | ||||||
| chr2:206468507
|
G | T | 2 | a0001c0002t0014g0020a0001c0002t0014g0037 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.433-12725G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206468507 | ||||||
| chr2:206468548
|
C | G | 1 | a0001c0001t0020g0329 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.433-12684C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206468548 | ||||||
| chr2:206468559
|
A | T | 1 | a0001c0001t0002g0261 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.433-12673A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206468559 | ||||||
| chr2:206468601
|
A | C | 1 | a0001c0001t0002g0247 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.433-12631A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206468601 | ||||||
| chr2:206468820
|
C | T | 76 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(73): Show | 79 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.433-12412C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206468820 | ||||||
| chr2:206468863
|
C | G | 3 | a0001c0002t0001g0257a0001c0002t0001g0258a0001c0002t0001g0259 | 3 | HG02647.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.433-12369C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206468863 | ||||||
| chr2:206468952
|
G | A | 1 | a0001c0001t0021g0196 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.433-12280G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206468952 | ||||||
| chr2:206469055
|
T | C | 1 | a0001c0001t0030g0179 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.433-12177T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206469055 | ||||||
| chr2:206469101
|
A | G | 9 | a0001c0001t0006g0345a0001c0001t0006g0348a0001c0001t0006g0349others(6): Show | 9 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.433-12131A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206469101 | ||||||
| chr2:206469137
|
G | A | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.433-12095G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206469137 | ||||||
| chr2:206469171
|
T | G | 32 | a0001c0001t0001g0173a0001c0001t0001g0190a0001c0001t0001g0267others(29): Show | 32 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.433-12061T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206469171 | ||||||
| chr2:206469205
|
C | T | 1 | a0001c0002t0002g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.433-12027C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206469205 | ||||||
| chr2:206469467
|
A | C | 3 | a0001c0002t0001g0257a0001c0002t0001g0258a0001c0002t0001g0259 | 3 | HG02647.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.433-11765A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206469467 | ||||||
| chr2:206469697
|
T | G | 5 | a0001c0001t0026g0299a0001c0002t0002g0302a0001c0002t0011g0186others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.433-11535T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206469697 | ||||||
| chr2:206469707
|
A | G | 19 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0308others(16): Show | 19 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.433-11525A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206469707 | ||||||
| chr2:206469765
|
C | G | 32 | a0001c0001t0001g0173a0001c0001t0001g0190a0001c0001t0001g0267others(29): Show | 32 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.433-11467C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206469765 | ||||||
| chr2:206469959
|
C | T | 1 | a0001c0002t0003g0093 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.433-11273C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206469959 | ||||||
| chr2:206470167
|
A | G | 1 | a0001c0001t0002g0246 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.433-11065A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206470167 | ||||||
| chr2:206470256
|
A | G | 2 | a0001c0001t0004g0245a0001c0001t0040g0040 | 2 | HG01175.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.433-10976A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206470256 | ||||||
| chr2:206470310
|
A | G | 1 | a0001c0001t0001g0110 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.433-10922A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206470310 | ||||||
| chr2:206470375
|
C | T | 3 | a0001c0001t0002g0193a0001c0001t0002g0194a0001c0001t0043g0019 | 3 | HG01261.hp2 HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.433-10857C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206470375 | ||||||
| chr2:206470397
|
C | T | 1 | a0001c0002t0014g0037 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.433-10835C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206470397 | ||||||
| chr2:206470446
|
G | C | 1 | a0001c0002t0029g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.433-10786G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206470446 | ||||||
| chr2:206470472
|
C | G | 1 | a0001c0001t0008g0330 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.433-10760C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206470472 | ||||||
| chr2:206470612
|
T | C | 249 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(246): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.433-10620T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206470612 | ||||||
| chr2:206470659
|
G | C | 1 | a0001c0001t0001g0129 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.433-10573G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206470659 | ||||||
| chr2:206470731
|
G | A | 1 | a0001c0002t0002g0142 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.433-10501G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206470731 | ||||||
| chr2:206470763
|
G | C | 1 | a0001c0002t0002g0262 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.433-10469G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206470763 | ||||||
| chr2:206470818
|
A | C | 1 | a0001c0001t0001g0170 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.433-10414A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206470818 | ||||||
| chr2:206471118
|
G | C | 1 | a0001c0001t0001g0324 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.433-10114G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206471118 | ||||||
| chr2:206471129
|
G | A | 76 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(73): Show | 79 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.433-10103G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206471129 | ||||||
| chr2:206471153
|
A | G | 1 | a0001c0001t0001g0173 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.433-10079A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206471153 | ||||||
| chr2:206471536
|
C | T | 2 | a0001c0001t0001g0184a0001c0001t0043g0019 | 2 | HG02622.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.433-9696C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206471536 | ||||||
| chr2:206471841
|
A | G | 1 | a0001c0002t0003g0167 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.433-9391A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206471841 | ||||||
| chr2:206472041
|
A | G | 1 | a0001c0001t0001g0063 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.433-9191A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206472041 | ||||||
| chr2:206472049
|
C | T | 1 | a0001c0001t0002g0193 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.433-9183C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206472049 | ||||||
| chr2:206472316
|
T | C | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.433-8916T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206472316 | ||||||
| chr2:206472327
|
C | T | 1 | a0001c0001t0002g0255 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.433-8905C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206472327 | ||||||
| chr2:206472350
|
C | T | 14 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0026others(11): Show | 15 | HG00099.hp2 HG01070.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.433-8882C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206472350 | ||||||
| chr2:206472376
|
G | A | 2 | a0001c0002t0015g0182a0001c0002t0015g0183 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.433-8856G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206472376 | ||||||
| chr2:206472520
|
C | T | 2 | a0001c0002t0015g0182a0001c0002t0015g0183 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.433-8712C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206472520 | ||||||
| chr2:206472521
|
G | A | 67 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0095others(64): Show | 68 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.433-8711G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206472521 | ||||||
| chr2:206472598
|
G | A | 6 | a0001c0001t0001g0005a0001c0001t0001g0154a0001c0001t0001g0155others(3): Show | 7 | HG01070.hp1 HG01074.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.433-8634G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206472598 | ||||||
| chr2:206472615
|
G | A | 1 | a0001c0001t0001g0310 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.433-8617G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206472615 | ||||||
| chr2:206472615
|
G | GA | 247 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(244): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.433-8604dupA | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206472615 | |||||
| chr2:206472843
|
C | T | 20 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0308others(17): Show | 20 | HG00609.hp2 HG02257.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.433-8389C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206472843 | ||||||
| chr2:206472927
|
T | C | 4 | a0001c0001t0012g0304a0001c0001t0012g0305a0001c0001t0012g0306others(1): Show | 4 | HG01361.hp2 HG01433.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.433-8305T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206472927 | ||||||
| chr2:206473056
|
G | A | 44 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0095others(41): Show | 45 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.433-8176G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206473056 | ||||||
| chr2:206473212
|
T | C | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG00558.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.433-8020T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206473212 | ||||||
| chr2:206473418
|
A | G | 2 | a0001c0002t0015g0182a0001c0002t0015g0183 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.433-7814A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206473418 | ||||||
| chr2:206473452
|
T | C | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.433-7780T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206473452 | ||||||
| chr2:206473494
|
G | A | 2 | a0001c0001t0001g0184a0001c0001t0043g0019 | 2 | HG02622.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.433-7738G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206473494 | ||||||
| chr2:206473560
|
G | T | 1 | a0001c0001t0002g0244 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.433-7672G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206473560 | ||||||
| chr2:206473572
|
A | AAAT | 5 | a0001c0001t0001g0059a0001c0001t0001g0180a0001c0002t0002g0307others(2): Show | 5 | HG02257.hp1 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.433-7633_433-7631d others(5): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206473572 | |||||
| chr2:206473572
|
A | AAATAAT | 21 | a0001c0001t0001g0015a0001c0001t0001g0099a0001c0001t0001g0291others(18): Show | 21 | HG02258.hp1 HG02451.hp2 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.433-7636_433-7631d others(8): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206473572 | |||||
| chr2:206473572
|
A | AAATAATA others(2): Show |
3 | a0001c0001t0001g0005a0001c0001t0001g0317a0001c0001t0042g0295 | 4 | HG01074.hp2 HG01106.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.433-7639_433-7631d others(11): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206473572 | |||||
| chr2:206473572
|
A | AAATAATA others(5): Show |
9 | a0001c0001t0001g0094a0001c0001t0001g0100a0001c0001t0001g0155others(6): Show | 9 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.433-7642_433-7631d others(14): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206473572 | |||||
| chr2:206473572
|
A | AAATAATA others(8): Show |
10 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0101others(7): Show | 10 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(7): Show |
intron_variant | MODIFIER | c.433-7645_433-7631d others(17): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206473572 | |||||
| chr2:206473572
|
A | AAATAATA others(11): Show |
27 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0102others(24): Show | 27 | HG00642.hp2 HG01074.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.433-7648_433-7631d others(20): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206473572 | |||||
| chr2:206473572
|
A | AAATAATA others(14): Show |
5 | a0001c0001t0001g0004a0001c0001t0001g0110a0001c0001t0001g0133others(2): Show | 6 | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.433-7651_433-7631d others(23): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206473572 | |||||
| chr2:206473579
|
A | AATATAAT others(9): Show |
1 | a0001c0001t0001g0127 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.433-7650_433-7649i others(18): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206473579 | |||||
| chr2:206473599
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.433-7633T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206473599 | ||||||
| chr2:206473599
|
T | TAATAATA others(5): Show |
1 | a0001c0001t0001g0154 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.433-7631_433-7630i others(14): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206473599 | |||||
| chr2:206473614
|
C | T | 1 | a0001c0001t0020g0151 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.433-7618C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206473614 | ||||||
| chr2:206473642
|
ATAT | A | 12 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0026others(9): Show | 13 | HG00099.hp2 HG01070.hp1 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.433-7586_433-7584d others(5): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206473642 | |||||
| chr2:206473725
|
G | A | 1 | a0001c0001t0043g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.433-7507G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206473725 | ||||||
| chr2:206474011
|
C | CA | 7 | a0001c0001t0001g0181a0001c0001t0001g0309a0001c0001t0001g0316others(4): Show | 7 | HG02258.hp1 HG03195.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.433-7208dupA | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206474011 | |||||
| chr2:206474024
|
A | AAC | 10 | a0001c0001t0001g0308a0001c0001t0001g0310a0001c0001t0001g0311others(7): Show | 10 | HG02451.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.433-7208_433-7207i others(4): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206474024 | ||||||
| chr2:206474025
|
C | A | 10 | a0001c0001t0001g0308a0001c0001t0001g0310a0001c0001t0001g0311others(7): Show | 10 | HG02451.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.433-7207C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206474025 | ||||||
| chr2:206474025
|
C | CA | 17 | a0001c0001t0001g0036a0001c0001t0001g0069a0001c0001t0001g0085others(14): Show | 17 | HG01243.hp1 HG01952.hp2 HG02895.hp2 others(14): Show |
intron_variant | MODIFIER | c.433-7195dupA | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206474025 | |||||
| chr2:206474032
|
A | C | 2 | a0001c0001t0001g0184a0001c0001t0043g0019 | 2 | HG02622.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.433-7200A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206474032 | ||||||
| chr2:206474443
|
A | G | 1 | a0001c0001t0040g0040 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.433-6789A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206474443 | ||||||
| chr2:206474581
|
T | A | 1 | a0001c0001t0005g0215 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.433-6651T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206474581 | ||||||
| chr2:206474864
|
T | G | 5 | a0001c0002t0002g0141a0001c0002t0002g0142a0001c0002t0002g0143others(2): Show | 5 | NA18959.hp1 NA18965.hp1 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.433-6368T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206474864 | ||||||
| chr2:206474866
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.433-6366C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206474866 | ||||||
| chr2:206474904
|
T | A | 1 | a0001c0001t0002g0216 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.433-6328T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206474904 | ||||||
| chr2:206474951
|
C | T | 4 | a0001c0001t0012g0304a0001c0001t0012g0305a0001c0001t0012g0306others(1): Show | 4 | HG01361.hp2 HG01433.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.433-6281C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206474951 | ||||||
| chr2:206475031
|
C | T | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.433-6201C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206475031 | ||||||
| chr2:206475083
|
C | G | 12 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0026others(9): Show | 13 | HG00099.hp2 HG01070.hp1 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.433-6149C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206475083 | ||||||
| chr2:206475169
|
A | G | 1 | a0001c0001t0043g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.433-6063A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206475169 | ||||||
| chr2:206475233
|
A | G | 1 | a0001c0001t0031g0243 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.433-5999A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206475233 | ||||||
| chr2:206475362
|
G | T | 5 | a0001c0001t0026g0299a0001c0002t0002g0302a0001c0002t0011g0186others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.433-5870G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206475362 | ||||||
| chr2:206475415
|
T | C | 214 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.433-5817T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206475415 | ||||||
| chr2:206475637
|
T | A | 67 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0095others(64): Show | 68 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.433-5595T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206475637 | ||||||
| chr2:206476002
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.433-5230A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206476002 | ||||||
| chr2:206476008
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.433-5224A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206476008 | ||||||
| chr2:206476077
|
C | T | 10 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0026others(7): Show | 11 | HG00099.hp2 HG01070.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.433-5155C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206476077 | ||||||
| chr2:206476086
|
A | G | 5 | a0001c0001t0026g0299a0001c0002t0002g0302a0001c0002t0011g0186others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.433-5146A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206476086 | ||||||
| chr2:206476096
|
T | C | 1 | a0001c0001t0002g0266 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.433-5136T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206476096 | ||||||
| chr2:206476183
|
T | C | 3 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103 | 3 | HG01358.hp1 HG01943.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.433-5049T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206476183 | ||||||
| chr2:206476232
|
T | C | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.433-5000T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206476232 | ||||||
| chr2:206476272
|
T | C | 8 | a0001c0001t0006g0345a0001c0001t0006g0348a0001c0001t0006g0349others(5): Show | 8 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.433-4960T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206476272 | ||||||
| chr2:206476432
|
T | G | 1 | a0001c0002t0002g0001 | 2 | NA18989.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.433-4800T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206476432 | ||||||
| chr2:206476438
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.433-4794G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206476438 | ||||||
| chr2:206476538
|
C | T | 1 | a0001c0002t0002g0199 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.433-4694C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206476538 | ||||||
| chr2:206476773
|
T | G | 2 | a0001c0001t0001g0217a0001c0001t0002g0022 | 2 | HG01433.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.433-4459T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206476773 | ||||||
| chr2:206476872
|
A | G | 1 | a0001c0001t0005g0214 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.433-4360A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206476872 | ||||||
| chr2:206477082
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.433-4150T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477082 | ||||||
| chr2:206477235
|
C | T | 1 | a0001c0002t0002g0202 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.433-3997C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477235 | ||||||
| chr2:206477322
|
T | C | 2 | a0001c0001t0017g0038a0001c0001t0017g0039 | 2 | NA18943.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.433-3910T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477322 | ||||||
| chr2:206477569
|
G | A | 4 | a0001c0002t0002g0074a0001c0002t0002g0077a0001c0002t0022g0075others(1): Show | 4 | HG02056.hp2 NA19000.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.433-3663G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477569 | ||||||
| chr2:206477804
|
A | G | 1 | a0001c0001t0002g0022 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.433-3428A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477804 | ||||||
| chr2:206477880
|
T | TA | 6 | a0001c0001t0001g0217a0001c0001t0001g0232a0001c0001t0002g0233others(3): Show | 6 | HG01257.hp2 HG01433.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.433-3334dupA | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477880 | |||||
| chr2:206477880
|
TA | T | 21 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269others(18): Show | 21 | HG00280.hp1 HG00673.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.433-3334delA | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477880 | |||||
| chr2:206477880
|
TAA | T | 12 | a0001c0001t0001g0190a0001c0001t0001g0264a0001c0001t0001g0265others(9): Show | 12 | HG00323.hp1 HG00544.hp1 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.433-3335_433-3334d others(4): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477880 | |||||
| chr2:206477887
|
A | AATATATA others(15): Show |
1 | a0001c0002t0002g0142 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.433-3344_433-3343i others(24): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477887 | |||||
| chr2:206477887
|
A | AATATATA others(21): Show |
1 | a0001c0002t0002g0140 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.433-3344_433-3343i others(30): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477887 | |||||
| chr2:206477887
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0034g0079 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.433-3345_433-3344i others(15): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477887 | ||||||
| chr2:206477889
|
A | AATATATA others(15): Show |
3 | a0001c0001t0002g0301a0001c0002t0002g0143a0001c0002t0002g0147 | 3 | HG02735.hp1 HG03486.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.433-3342_433-3341i others(24): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477889 | |||||
| chr2:206477889
|
A | AATATATA others(17): Show |
1 | a0001c0002t0002g0141 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.433-3342_433-3341i others(26): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477889 | |||||
| chr2:206477889
|
A | ATATATAT others(4): Show |
17 | a0001c0001t0001g0013a0001c0001t0001g0048a0001c0001t0001g0050others(14): Show | 17 | HG00673.hp1 HG01192.hp1 HG01981.hp2 others(14): Show |
intron_variant | MODIFIER | c.433-3343_433-3342i others(13): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477889 | ||||||
| chr2:206477889
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0009g0018 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.433-3343_433-3342i others(15): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477889 | ||||||
| chr2:206477889
|
A | T | 9 | a0001c0001t0001g0029a0001c0001t0006g0349a0001c0001t0006g0350others(6): Show | 9 | HG01081.hp1 HG01515.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.433-3343A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477889 | ||||||
| chr2:206477891
|
A | AATATATA others(7): Show |
1 | a0001c0001t0001g0319 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.433-3340_433-3339i others(16): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477891 | |||||
| chr2:206477891
|
A | AATATATA others(11): Show |
1 | a0001c0001t0035g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.433-3340_433-3339i others(20): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477891 | |||||
| chr2:206477891
|
A | AATATATA others(13): Show |
1 | a0001c0001t0001g0156 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.433-3340_433-3339i others(22): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477891 | |||||
| chr2:206477891
|
A | AATATATA others(15): Show |
1 | a0001c0001t0001g0314 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.433-3340_433-3339i others(24): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477891 | |||||
| chr2:206477891
|
A | AATATATA others(17): Show |
1 | a0001c0001t0001g0315 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.433-3340_433-3339i others(26): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477891 | |||||
| chr2:206477891
|
A | ATATATAT others(6): Show |
1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.433-3341_433-3340i others(15): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477891 | ||||||
| chr2:206477891
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0324 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.433-3341_433-3340i others(17): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477891 | ||||||
| chr2:206477891
|
A | T | 84 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(81): Show | 87 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.433-3341A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477891 | ||||||
| chr2:206477893
|
A | AATATATA others(3): Show |
1 | a0001c0001t0012g0306 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.433-3338_433-3337i others(12): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477893 | |||||
| chr2:206477893
|
A | AATATATA others(11): Show |
1 | a0001c0002t0002g0146 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.433-3338_433-3337i others(20): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477893 | |||||
| chr2:206477893
|
A | AATATATA others(15): Show |
1 | a0001c0001t0002g0153 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.433-3338_433-3337i others(24): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477893 | |||||
| chr2:206477893
|
A | AATATATA others(17): Show |
1 | a0001c0001t0001g0313 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.433-3338_433-3337i others(26): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477893 | |||||
| chr2:206477893
|
A | AATATATA others(19): Show |
2 | a0001c0001t0001g0318a0001c0001t0001g0337 | 2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.433-3338_433-3337i others(28): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477893 | |||||
| chr2:206477893
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0155 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.433-3339_433-3338i others(13): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477893 | ||||||
| chr2:206477893
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0005 | 2 | HG01074.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.433-3339_433-3338i others(15): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477893 | ||||||
| chr2:206477893
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0171 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.433-3339_433-3338i others(17): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477893 | ||||||
| chr2:206477893
|
A | ATATATAT others(10): Show |
2 | a0001c0001t0001g0300a0001c0002t0001g0150 | 2 | HG02572.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.433-3339_433-3338i others(19): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477893 | ||||||
| chr2:206477893
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0309 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.433-3339_433-3338i others(25): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477893 | ||||||
| chr2:206477893
|
A | T | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(95): Show | 101 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.433-3339A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477893 | ||||||
| chr2:206477893
|
AAAAAATA others(7): Show |
A | 4 | a0001c0001t0026g0299a0001c0002t0011g0186a0001c0002t0011g0187others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.433-3337_433-3324d others(16): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477893 | |||||
| chr2:206477894
|
AAAAATAT others(8): Show |
A | 1 | a0001c0002t0002g0302 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.433-3336_433-3322d others(17): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477894 | |||||
| chr2:206477895
|
A | AATATATA others(11): Show |
1 | a0001c0001t0001g0335 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.433-3336_433-3335i others(20): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477895 | |||||
| chr2:206477895
|
A | AATATATA others(13): Show |
2 | a0001c0001t0001g0308a0001c0001t0001g0310 | 2 | HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.433-3336_433-3335i others(22): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477895 | |||||
| chr2:206477895
|
A | AATATATA others(15): Show |
1 | a0001c0001t0002g0152 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.433-3336_433-3335i others(24): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477895 | |||||
| chr2:206477895
|
A | AATATATA others(17): Show |
2 | a0001c0001t0001g0312a0001c0001t0002g0123 | 2 | HG02896.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.433-3336_433-3335i others(26): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477895 | |||||
| chr2:206477895
|
A | AATATATA others(19): Show |
1 | a0001c0001t0002g0124 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.433-3336_433-3335i others(28): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477895 | |||||
| chr2:206477895
|
A | AATATATA others(21): Show |
1 | a0001c0001t0001g0338 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.433-3336_433-3335i others(30): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477895 | |||||
| chr2:206477895
|
A | AATATATA others(31): Show |
1 | a0001c0001t0001g0317 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.433-3336_433-3335i others(40): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477895 | |||||
| chr2:206477895
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0154 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.433-3337_433-3336i others(15): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477895 | ||||||
| chr2:206477895
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0042g0295 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.433-3337_433-3336i others(17): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477895 | ||||||
| chr2:206477895
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0169 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.433-3337_433-3336i others(19): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477895 | ||||||
| chr2:206477895
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0336 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.433-3337_433-3336i others(21): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477895 | ||||||
| chr2:206477895
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0316 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.433-3337_433-3336i others(25): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477895 | ||||||
| chr2:206477895
|
A | T | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(113): Show | 120 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.433-3337A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477895 | ||||||
| chr2:206477897
|
A | AAAAAAAA others(29): Show |
1 | a0001c0002t0015g0182 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.433-3334_433-3333i others(38): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | |||||
| chr2:206477897
|
A | AAAAAAAA others(28): Show |
1 | a0001c0002t0015g0183 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.433-3334_433-3333i others(37): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | |||||
| chr2:206477897
|
A | AAAAAAAT others(10): Show |
1 | a0001c0001t0001g0095 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.433-3334_433-3333i others(19): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | |||||
| chr2:206477897
|
A | AAAAAAAT others(12): Show |
1 | a0001c0001t0001g0121 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.433-3334_433-3333i others(21): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | |||||
| chr2:206477897
|
A | AAAAAATA others(11): Show |
1 | a0001c0001t0001g0180 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.433-3334_433-3333i others(20): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | |||||
| chr2:206477897
|
A | AAAAAATA others(11): Show |
1 | a0001c0001t0001g0094 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.433-3334_433-3333i others(20): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | |||||
| chr2:206477897
|
A | AAAAAATA others(19): Show |
1 | a0001c0002t0002g0307 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.433-3334_433-3333i others(28): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | |||||
| chr2:206477897
|
A | AAAAATAT others(6): Show |
1 | a0001c0001t0001g0136 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.433-3334_433-3333i others(15): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | |||||
| chr2:206477897
|
A | AAAAATAT others(8): Show |
2 | a0001c0001t0001g0099a0001c0001t0001g0104 | 2 | NA18990.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.433-3334_433-3333i others(17): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | |||||
| chr2:206477897
|
A | AAAAATAT others(10): Show |
1 | a0001c0001t0001g0100 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.433-3334_433-3333i others(19): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | |||||
| chr2:206477897
|
A | AAAATATA others(3): Show |
5 | a0001c0001t0001g0098a0001c0001t0001g0105a0001c0001t0001g0112others(2): Show | 5 | HG02004.hp2 NA18939.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.433-3334_433-3333i others(12): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | |||||
| chr2:206477897
|
A | AAAATATA others(5): Show |
3 | a0001c0001t0001g0106a0001c0001t0001g0115a0001c0001t0001g0118 | 3 | HG01346.hp2 NA18989.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.433-3334_433-3333i others(14): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | |||||
| chr2:206477897
|
A | AAAATATA others(7): Show |
2 | a0001c0001t0001g0111a0001c0001t0001g0168 | 2 | HG00438.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.433-3334_433-3333i others(16): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | |||||
| chr2:206477897
|
A | AAAATATA others(9): Show |
2 | a0001c0001t0001g0096a0001c0002t0003g0109 | 2 | HG01123.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.433-3334_433-3333i others(18): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | |||||
| chr2:206477897
|
A | AAAATATA others(13): Show |
1 | a0001c0001t0001g0026 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.433-3334_433-3333i others(22): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | |||||
| chr2:206477897
|
A | AAATATAT others(6): Show |
1 | a0001c0001t0001g0135 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.433-3334_433-3333i others(15): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | |||||
| chr2:206477897
|
A | AAATATAT others(8): Show |
3 | a0001c0001t0001g0116a0001c0001t0001g0127a0001c0001t0001g0128 | 3 | NA18940.hp2 NA18962.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.433-3334_433-3333i others(17): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | |||||
| chr2:206477897
|
A | AAATATAT others(10): Show |
3 | a0001c0001t0001g0122a0001c0001t0001g0181a0001c0001t0039g0134 | 3 | NA18988.hp1 NA19011.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.433-3334_433-3333i others(19): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | |||||
| chr2:206477897
|
A | AAATATAT others(16): Show |
2 | a0001c0001t0001g0025a0001c0001t0001g0130 | 2 | HG01169.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.433-3334_433-3333i others(25): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | |||||
| chr2:206477897
|
A | AATATATA others(5): Show |
1 | a0001c0001t0001g0120 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.433-3321_433-3310d others(14): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | |||||
| chr2:206477897
|
A | AATATATA others(7): Show |
3 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0108 | 3 | HG01943.hp2 HG02148.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.433-3323_433-3310d others(16): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | |||||
| chr2:206477897
|
A | AATATATA others(9): Show |
1 | a0001c0001t0001g0101 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.433-3325_433-3310d others(18): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | |||||
| chr2:206477897
|
A | AATATATA others(13): Show |
2 | a0001c0001t0001g0004a0001c0001t0001g0097 | 3 | HG01069.hp1 HG01071.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.433-3329_433-3310d others(22): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | |||||
| chr2:206477897
|
A | AATATATA others(15): Show |
2 | a0001c0001t0001g0131a0001c0001t0001g0311 | 2 | HG01167.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.433-3331_433-3310d others(24): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | |||||
| chr2:206477897
|
A | AT | 10 | a0001c0001t0001g0286a0001c0001t0020g0329a0001c0002t0003g0093others(7): Show | 10 | HG00738.hp2 HG01361.hp1 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.433-3335_433-3334i others(3): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477897 | ||||||
| chr2:206477897
|
A | ATAT | 3 | a0001c0001t0001g0173a0001c0002t0003g0164a0001c0002t0003g0165 | 3 | HG01261.hp1 HG01884.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.433-3335_433-3334i others(5): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477897 | ||||||
| chr2:206477897
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0129 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.433-3335_433-3334i others(17): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477897 | ||||||
| chr2:206477897
|
A | ATATATAT others(10): Show |
4 | a0001c0001t0001g0110a0001c0001t0001g0132a0001c0001t0001g0133others(1): Show | 4 | HG00099.hp1 HG02055.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.433-3335_433-3334i others(19): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477897 | ||||||
| chr2:206477897
|
A | T | 149 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(146): Show | 154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.433-3335A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477897 | ||||||
| chr2:206477898
|
AT | A | 12 | a0001c0001t0001g0211a0001c0001t0001g0331a0001c0001t0002g0139others(9): Show | 12 | HG01943.hp1 HG01975.hp2 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.433-3333delT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477898 | ||||||
| chr2:206477899
|
T | A | 62 | a0001c0001t0001g0197a0001c0001t0001g0203a0001c0001t0001g0226others(59): Show | 62 | HG00438.hp2 HG00609.hp1 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.433-3333T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477899 | ||||||
| chr2:206477899
|
T | TATATATA others(5): Show |
2 | a0001c0001t0001g0027a0001c0001t0002g0014 | 2 | HG00642.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.433-3322_433-3321i others(14): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477899 | |||||
| chr2:206477899
|
T | TATATATA others(7): Show |
2 | a0001c0001t0001g0029a0001c0001t0041g0028 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.433-3320_433-3319i others(16): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477899 | |||||
| chr2:206477901
|
T | A | 10 | a0001c0001t0001g0263a0001c0001t0002g0246a0001c0001t0002g0327others(7): Show | 10 | HG02145.hp1 HG02451.hp1 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.433-3331T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477901 | ||||||
| chr2:206477901
|
T | C | 18 | a0001c0001t0001g0013a0001c0001t0001g0048a0001c0001t0001g0050others(15): Show | 18 | HG00544.hp2 HG00673.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.433-3331T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477901 | ||||||
| chr2:206477901
|
T | TATATATA others(3): Show |
2 | a0001c0001t0001g0043a0001c0001t0001g0065 | 2 | HG02145.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.433-3324_433-3323i others(12): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477901 | |||||
| chr2:206477901
|
T | TATATATA others(3): Show |
47 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(44): Show | 50 | HG00140.hp2 HG00280.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.433-3322_433-3321i others(12): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477901 | |||||
| chr2:206477903
|
T | TATATATA others(1): Show |
5 | a0001c0001t0013g0030a0001c0001t0013g0034a0001c0002t0002g0032others(2): Show | 5 | HG01243.hp1 HG03453.hp2 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.433-3322_433-3321i others(10): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477903 | |||||
| chr2:206477923
|
A | T | 13 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0026others(10): Show | 14 | HG00099.hp2 HG01070.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.433-3309A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477923 | ||||||
| chr2:206478143
|
G | A | 19 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0308others(16): Show | 19 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.433-3089G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206478143 | ||||||
| chr2:206478258
|
A | G | 2 | a0001c0001t0001g0184a0001c0001t0043g0019 | 2 | HG02622.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.433-2974A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206478258 | ||||||
| chr2:206478332
|
T | C | 4 | a0001c0001t0001g0309a0001c0001t0001g0319a0001c0001t0001g0336others(1): Show | 4 | HG02258.hp1 HG03195.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.433-2900T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206478332 | ||||||
| chr2:206478437
|
T | C | 1 | a0001c0001t0043g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.433-2795T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206478437 | ||||||
| chr2:206478507
|
T | TATG | 64 | a0001c0001t0001g0004a0001c0001t0001g0045a0001c0001t0001g0094others(61): Show | 65 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.433-2691_433-2689d others(5): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206478507 | |||||
| chr2:206478507
|
T | TATGATG | 24 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0026others(21): Show | 25 | HG00099.hp2 HG01070.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.433-2694_433-2689d others(8): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206478507 | |||||
| chr2:206478623
|
T | C | 1 | a0001c0001t0020g0329 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.433-2609T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206478623 | ||||||
| chr2:206478755
|
A | G | 17 | a0001c0001t0002g0139a0001c0001t0002g0152a0001c0001t0002g0153others(14): Show | 17 | HG00558.hp1 HG01975.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.433-2477A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206478755 | ||||||
| chr2:206478899
|
G | A | 1 | a0001c0001t0001g0316 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.433-2333G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206478899 | ||||||
| chr2:206479001
|
C | T | 19 | a0001c0001t0002g0139a0001c0001t0002g0152a0001c0001t0002g0153others(16): Show | 19 | HG00558.hp1 HG01975.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.433-2231C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206479001 | ||||||
| chr2:206479297
|
C | T | 84 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0025others(81): Show | 86 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.433-1935C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206479297 | ||||||
| chr2:206479386
|
C | T | 10 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0026others(7): Show | 11 | HG00099.hp2 HG01070.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.433-1846C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206479386 | ||||||
| chr2:206479550
|
A | C | 3 | a0001c0001t0002g0139a0001c0001t0024g0273a0001c0002t0002g0138 | 3 | HG01975.hp2 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.433-1682A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206479550 | ||||||
| chr2:206479605
|
G | A | 1 | a0001c0001t0006g0345 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.433-1627G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206479605 | ||||||
| chr2:206479622
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.433-1610A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206479622 | ||||||
| chr2:206479664
|
A | G | 4 | a0001c0001t0008g0023a0001c0001t0008g0330a0001c0002t0019g0189others(1): Show | 4 | HG02055.hp1 HG02559.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.433-1568A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206479664 | ||||||
| chr2:206479682
|
C | T | 4 | a0001c0001t0012g0304a0001c0001t0012g0305a0001c0001t0012g0306others(1): Show | 4 | HG01361.hp2 HG01433.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.433-1550C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206479682 | ||||||
| chr2:206480150
|
C | T | 4 | a0001c0001t0008g0023a0001c0001t0008g0330a0001c0002t0019g0189others(1): Show | 4 | HG02055.hp1 HG02559.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.433-1082C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206480150 | ||||||
| chr2:206480323
|
A | G | 17 | a0001c0001t0001g0181a0001c0001t0001g0308a0001c0001t0001g0309others(14): Show | 17 | HG02258.hp1 HG02451.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.433-909A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206480323 | ||||||
| chr2:206480422
|
T | C | 48 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0095others(45): Show | 49 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.433-810T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206480422 | ||||||
| chr2:206480429
|
A | G | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.433-803A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206480429 | ||||||
| chr2:206480438
|
T | C | 4 | a0001c0001t0008g0023a0001c0001t0008g0330a0001c0002t0019g0189others(1): Show | 4 | HG02055.hp1 HG02559.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.433-794T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206480438 | ||||||
| chr2:206480461
|
CT | C | 9 | a0001c0001t0001g0132a0001c0001t0001g0156a0001c0001t0038g0218others(6): Show | 9 | HG01361.hp1 HG01515.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.433-756delT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206480461 | |||||
| chr2:206480719
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.433-513A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206480719 | ||||||
| chr2:206480946
|
G | A | 1 | a0001c0002t0002g0141 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.433-286G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206480946 | ||||||
| chr2:206481102
|
G | A | 76 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(73): Show | 79 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.433-130G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206481102 | ||||||
| chr2:206481484
|
A | G | 1 | a0001c0001t0002g0209 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.509+176A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206481484 | ||||||
| chr2:206481514
|
C | A | 247 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(244): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.509+206C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206481514 | ||||||
| chr2:206481571
|
T | TTAAATGT others(6): Show |
1 | a0001c0001t0042g0295 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.509+272_509+273ins others(13): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206481571 | |||||
| chr2:206481681
|
A | G | 2 | a0001c0001t0001g0184a0001c0001t0043g0019 | 2 | HG02622.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.509+373A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206481681 | ||||||
| chr2:206481695
|
C | G | 3 | a0001c0001t0001g0300a0001c0001t0002g0301a0001c0001t0042g0295 | 3 | HG02572.hp2 HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.509+387C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206481695 | ||||||
| chr2:206481937
|
C | T | 5 | a0001c0001t0001g0310a0001c0001t0001g0314a0001c0001t0001g0315others(2): Show | 5 | HG02559.hp2 HG02615.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.509+629C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206481937 | ||||||
| chr2:206482218
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.509+910G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206482218 | ||||||
| chr2:206482542
|
C | T | 76 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(73): Show | 79 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.509+1234C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206482542 | ||||||
| chr2:206483029
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.509+1721G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206483029 | ||||||
| chr2:206483193
|
A | G | 67 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0095others(64): Show | 68 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.509+1885A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206483193 | ||||||
| chr2:206483242
|
G | A | 6 | a0001c0001t0006g0345a0001c0001t0006g0348a0001c0001t0006g0349others(3): Show | 6 | HG01081.hp1 HG01496.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.509+1934G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206483242 | ||||||
| chr2:206483433
|
G | A | 2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 2 | HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.509+2125G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206483433 | ||||||
| chr2:206483500
|
G | C | 76 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(73): Show | 79 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.509+2192G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206483500 | ||||||
| chr2:206483624
|
G | T | 2 | a0001c0001t0034g0079a0001c0001t0035g0078 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.509+2316G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206483624 | ||||||
| chr2:206483971
|
G | A | 74 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0095others(71): Show | 75 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.509+2663G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206483971 | ||||||
| chr2:206484028
|
G | A | 1 | a0001c0001t0041g0028 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.509+2720G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206484028 | ||||||
| chr2:206484084
|
G | A | 1 | a0001c0002t0001g0150 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.509+2776G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206484084 | ||||||
| chr2:206484121
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.509+2813A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206484121 | ||||||
| chr2:206484186
|
A | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 2 | HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.509+2878A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206484186 | ||||||
| chr2:206484362
|
A | G | 5 | a0001c0001t0026g0299a0001c0002t0002g0302a0001c0002t0011g0186others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+3054A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206484362 | ||||||
| chr2:206484385
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.509+3077A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206484385 | ||||||
| chr2:206484602
|
A | G | 1 | a0001c0002t0029g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.509+3294A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206484602 | ||||||
| chr2:206484701
|
G | T | 1 | a0001c0001t0001g0303 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.509+3393G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206484701 | ||||||
| chr2:206484885
|
C | T | 1 | a0001c0001t0001g0256 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.509+3577C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206484885 | ||||||
| chr2:206484944
|
A | G | 1 | a0001c0001t0002g0333 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.509+3636A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206484944 | ||||||
| chr2:206484973
|
C | T | 4 | a0001c0001t0012g0304a0001c0001t0012g0305a0001c0001t0012g0306others(1): Show | 4 | HG01361.hp2 HG01433.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.509+3665C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206484973 | ||||||
| chr2:206485114
|
T | A | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.509+3806T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206485114 | ||||||
| chr2:206485266
|
G | C | 1 | a0001c0001t0001g0173 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.509+3958G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206485266 | ||||||
| chr2:206485562
|
A | C | 1 | a0001c0001t0001g0271 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.509+4254A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206485562 | ||||||
| chr2:206485580
|
A | T | 2 | a0001c0002t0015g0182a0001c0002t0015g0183 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.509+4272A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206485580 | ||||||
| chr2:206485581
|
G | T | 2 | a0001c0002t0015g0182a0001c0002t0015g0183 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.509+4273G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206485581 | ||||||
| chr2:206485827
|
A | G | 5 | a0001c0001t0026g0299a0001c0002t0002g0302a0001c0002t0011g0186others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+4519A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206485827 | ||||||
| chr2:206485913
|
A | C | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.509+4605A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206485913 | ||||||
| chr2:206486021
|
G | A | 1 | a0001c0001t0018g0274 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.509+4713G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206486021 | ||||||
| chr2:206486129
|
T | C | 18 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0308others(15): Show | 18 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.509+4821T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206486129 | ||||||
| chr2:206486174
|
T | G | 2 | a0001c0001t0002g0209a0001c0001t0002g0326 | 2 | NA19057.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.509+4866T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206486174 | ||||||
| chr2:206486256
|
G | C | 10 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0026others(7): Show | 11 | HG00099.hp2 HG01070.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.509+4948G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206486256 | ||||||
| chr2:206486269
|
T | C | 18 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0308others(15): Show | 18 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.509+4961T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206486269 | ||||||
| chr2:206486278
|
G | A | 1 | a0001c0002t0002g0307 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.509+4970G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206486278 | ||||||
| chr2:206486281
|
G | A | 1 | a0001c0001t0001g0260 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.509+4973G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206486281 | ||||||
| chr2:206486319
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.509+5011G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206486319 | ||||||
| chr2:206486324
|
A | G | 1 | a0001c0001t0002g0216 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.509+5016A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206486324 | ||||||
| chr2:206486340
|
C | CT | 7 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0026g0299others(4): Show | 7 | HG02630.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.509+5044dupT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206486340 | |||||
| chr2:206486341
|
T | C | 2 | a0001c0001t0002g0175a0001c0001t0002g0322 | 2 | NA19056.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.509+5033T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206486341 | ||||||
| chr2:206486471
|
A | T | 8 | a0001c0001t0006g0345a0001c0001t0006g0348a0001c0001t0006g0349others(5): Show | 8 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.509+5163A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206486471 | ||||||
| chr2:206486616
|
G | A | 14 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0005g0145others(11): Show | 14 | HG00558.hp1 HG02109.hp1 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.509+5308G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206486616 | ||||||
| chr2:206486816
|
T | C | 1 | a0001c0001t0001g0099 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.509+5508T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206486816 | ||||||
| chr2:206486838
|
C | A | 1 | a0001c0001t0002g0176 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.509+5530C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206486838 | ||||||
| chr2:206486838
|
C | T | 4 | a0001c0001t0001g0314a0001c0001t0001g0315a0001c0001t0001g0318others(1): Show | 4 | HG02559.hp2 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.509+5530C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206486838 | ||||||
| chr2:206486897
|
T | G | 119 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(116): Show | 122 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.509+5589T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206486897 | ||||||
| chr2:206486916
|
C | T | 17 | a0001c0001t0001g0181a0001c0001t0001g0308a0001c0001t0001g0309others(14): Show | 17 | HG02258.hp1 HG02451.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.509+5608C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206486916 | ||||||
| chr2:206486934
|
C | T | 76 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(73): Show | 79 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.509+5626C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206486934 | ||||||
| chr2:206486950
|
C | T | 237 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(234): Show | 242 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.509+5642C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206486950 | ||||||
| chr2:206487093
|
G | A | 3 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125 | 3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.509+5785G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206487093 | ||||||
| chr2:206487141
|
G | C | 2 | a0001c0002t0015g0182a0001c0002t0015g0183 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.509+5833G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206487141 | ||||||
| chr2:206487184
|
A | G | 2 | a0001c0001t0018g0274a0001c0001t0018g0276 | 2 | NA18943.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.509+5876A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206487184 | ||||||
| chr2:206487382
|
G | A | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.509+6074G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206487382 | ||||||
| chr2:206487545
|
C | G | 6 | a0001c0001t0001g0055a0001c0001t0001g0058a0001c0001t0009g0018others(3): Show | 6 | HG00544.hp2 HG00673.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.509+6237C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206487545 | ||||||
| chr2:206487555
|
A | C | 19 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0308others(16): Show | 19 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.509+6247A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206487555 | ||||||
| chr2:206487623
|
G | A | 5 | a0001c0001t0001g0184a0001c0001t0002g0123a0001c0001t0002g0124others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.509+6315G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206487623 | ||||||
| chr2:206487701
|
C | T | 3 | a0001c0001t0021g0196a0001c0002t0010g0207a0001c0002t0010g0210 | 3 | NA18951.hp1 NA18969.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.509+6393C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206487701 | ||||||
| chr2:206487704
|
T | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0170 | 3 | HG02257.hp2 HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.509+6396T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206487704 | ||||||
| chr2:206487865
|
C | T | 1 | a0001c0002t0003g0165 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.509+6557C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206487865 | ||||||
| chr2:206487877
|
G | T | 1 | a0001c0001t0002g0195 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.509+6569G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206487877 | ||||||
| chr2:206487967
|
C | A | 76 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0095others(73): Show | 77 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.509+6659C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206487967 | ||||||
| chr2:206488037
|
T | C | 1 | a0001c0001t0034g0079 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.509+6729T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206488037 | ||||||
| chr2:206488050
|
G | A | 1 | a0001c0002t0001g0150 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.509+6742G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206488050 | ||||||
| chr2:206488252
|
G | A | 19 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0308others(16): Show | 19 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.509+6944G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206488252 | ||||||
| chr2:206488311
|
A | G | 2 | a0001c0001t0001g0173a0001c0001t0030g0179 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.509+7003A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206488311 | ||||||
| chr2:206488828
|
C | T | 2 | a0001c0002t0002g0140a0001c0002t0002g0147 | 2 | HG02735.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.509+7520C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206488828 | ||||||
| chr2:206488870
|
A | C | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.509+7562A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206488870 | ||||||
| chr2:206488874
|
G | T | 19 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0308others(16): Show | 19 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.509+7566G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206488874 | ||||||
| chr2:206488957
|
A | T | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.509+7649A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206488957 | ||||||
| chr2:206488968
|
G | A | 2 | a0001c0001t0016g0234a0001c0001t0016g0235 | 2 | HG00140.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.509+7660G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206488968 | ||||||
| chr2:206489070
|
G | C | 18 | a0001c0001t0001g0006a0001c0001t0001g0170a0001c0002t0003g0093others(15): Show | 19 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.509+7762G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206489070 | ||||||
| chr2:206489147
|
C | T | 5 | a0001c0002t0002g0007a0001c0002t0002g0008a0001c0002t0002g0009others(2): Show | 5 | HG02145.hp1 HG02451.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.509+7839C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206489147 | ||||||
| chr2:206489213
|
C | G | 1 | a0001c0002t0003g0163 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.509+7905C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206489213 | ||||||
| chr2:206489214
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.509+7906G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206489214 | ||||||
| chr2:206489334
|
C | T | 1 | a0004c0006t0001g0044 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.509+8026C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206489334 | ||||||
| chr2:206489335
|
A | G | 1 | a0001c0001t0002g0014 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.509+8027A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206489335 | ||||||
| chr2:206489557
|
A | C | 19 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0308others(16): Show | 19 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.509+8249A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206489557 | ||||||
| chr2:206489593
|
G | A | 4 | a0001c0001t0012g0304a0001c0001t0012g0305a0001c0001t0012g0306others(1): Show | 4 | HG01361.hp2 HG01433.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.509+8285G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206489593 | ||||||
| chr2:206489901
|
A | G | 5 | a0001c0001t0026g0299a0001c0002t0002g0302a0001c0002t0011g0186others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+8593A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206489901 | ||||||
| chr2:206489940
|
T | C | 1 | a0001c0001t0001g0208 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.509+8632T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206489940 | ||||||
| chr2:206490058
|
G | A | 19 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0308others(16): Show | 19 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.509+8750G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206490058 | ||||||
| chr2:206490101
|
A | G | 1 | a0001c0001t0001g0096 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.509+8793A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206490101 | ||||||
| chr2:206490120
|
G | A | 1 | a0001c0002t0002g0024 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.509+8812G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206490120 | ||||||
| chr2:206490343
|
C | T | 41 | a0001c0001t0001g0036a0001c0001t0001g0069a0001c0001t0001g0173others(38): Show | 41 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.509+9035C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206490343 | ||||||
| chr2:206490385
|
C | G | 19 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0308others(16): Show | 19 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.509+9077C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206490385 | ||||||
| chr2:206490487
|
C | T | 1 | a0001c0001t0001g0303 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.509+9179C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206490487 | ||||||
| chr2:206490630
|
G | T | 252 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(249): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.509+9322G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206490630 | ||||||
| chr2:206490649
|
G | T | 5 | a0001c0002t0002g0007a0001c0002t0002g0008a0001c0002t0002g0009others(2): Show | 5 | HG02145.hp1 HG02451.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.509+9341G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206490649 | ||||||
| chr2:206490973
|
C | T | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.509+9665C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206490973 | ||||||
| chr2:206490975
|
A | T | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.509+9667A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206490975 | ||||||
| chr2:206491191
|
T | C | 2 | a0001c0001t0001g0291a0001c0001t0001g0334 | 2 | NA18995.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.509+9883T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206491191 | ||||||
| chr2:206491373
|
G | A | 5 | a0001c0001t0026g0299a0001c0002t0002g0302a0001c0002t0011g0186others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+10065G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206491373 | ||||||
| chr2:206491574
|
T | C | 2 | a0001c0001t0001g0180a0001c0002t0002g0307 | 2 | HG02257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.509+10266T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206491574 | ||||||
| chr2:206491609
|
T | C | 38 | a0001c0001t0001g0006a0001c0001t0001g0170a0001c0001t0001g0185others(35): Show | 39 | HG00280.hp1 HG00558.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.509+10301T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206491609 | ||||||
| chr2:206491750
|
C | T | 48 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0095others(45): Show | 49 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.509+10442C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206491750 | ||||||
| chr2:206491819
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.509+10511G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206491819 | ||||||
| chr2:206491866
|
T | G | 241 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(238): Show | 246 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.509+10558T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206491866 | ||||||
| chr2:206491918
|
A | T | 3 | a0001c0001t0012g0304a0001c0001t0012g0305a0001c0001t0012g0306 | 3 | HG01361.hp2 HG01433.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.509+10610A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206491918 | ||||||
| chr2:206491976
|
G | T | 4 | a0001c0001t0012g0304a0001c0001t0012g0305a0001c0001t0012g0306others(1): Show | 4 | HG01361.hp2 HG01433.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.509+10668G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206491976 | ||||||
| chr2:206491981
|
C | T | 163 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(160): Show | 167 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.509+10673C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206491981 | ||||||
| chr2:206492034
|
T | A | 41 | a0001c0001t0001g0036a0001c0001t0001g0069a0001c0001t0001g0173others(38): Show | 41 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.509+10726T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206492034 | ||||||
| chr2:206492170
|
A | G | 7 | a0001c0001t0006g0345a0001c0001t0006g0348a0001c0001t0006g0349others(4): Show | 7 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.509+10862A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206492170 | ||||||
| chr2:206492213
|
C | T | 1 | a0001c0002t0003g0165 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.509+10905C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206492213 | ||||||
| chr2:206492261
|
T | A | 1 | a0001c0001t0001g0334 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.509+10953T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206492261 | ||||||
| chr2:206492342
|
G | A | 1 | a0001c0001t0039g0134 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.509+11034G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206492342 | ||||||
| chr2:206492494
|
T | A | 2 | a0001c0001t0001g0180a0001c0002t0002g0307 | 2 | HG02257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.509+11186T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206492494 | ||||||
| chr2:206492570
|
A | C | 1 | a0001c0001t0002g0014 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.509+11262A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206492570 | ||||||
| chr2:206492632
|
G | A | 125 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(122): Show | 128 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.509+11324G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206492632 | ||||||
| chr2:206492692
|
A | G | 5 | a0001c0002t0002g0007a0001c0002t0002g0008a0001c0002t0002g0009others(2): Show | 5 | HG02145.hp1 HG02451.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.509+11384A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206492692 | ||||||
| chr2:206492765
|
C | T | 1 | a0001c0001t0002g0240 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.509+11457C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206492765 | ||||||
| chr2:206493292
|
G | T | 237 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(234): Show | 242 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.509+11984G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206493292 | ||||||
| chr2:206493394
|
C | CG | 3 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0041g0028 | 3 | HG00642.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.509+12088dupG | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206493394 | |||||
| chr2:206493395
|
G | A | 3 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125 | 3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.509+12087G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206493395 | ||||||
| chr2:206493435
|
C | T | 4 | a0001c0001t0001g0036a0001c0001t0001g0069a0001c0001t0001g0173others(1): Show | 4 | HG01884.hp2 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.509+12127C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206493435 | ||||||
| chr2:206493624
|
C | T | 1 | a0001c0001t0020g0151 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.509+12316C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206493624 | ||||||
| chr2:206493652
|
G | A | 1 | a0001c0001t0024g0273 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.509+12344G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206493652 | ||||||
| chr2:206493703
|
CAA | C | 3 | a0001c0001t0001g0300a0001c0001t0002g0301a0001c0001t0042g0295 | 3 | HG02572.hp2 HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.509+12399_509+1240 others(6): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206493703 | |||||
| chr2:206493803
|
G | C | 5 | a0001c0001t0026g0299a0001c0002t0002g0302a0001c0002t0011g0186others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+12495G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206493803 | ||||||
| chr2:206493856
|
C | T | 1 | a0001c0001t0002g0244 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.509+12548C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206493856 | ||||||
| chr2:206493953
|
G | A | 74 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0095others(71): Show | 75 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.509+12645G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206493953 | ||||||
| chr2:206494049
|
G | A | 44 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0095others(41): Show | 45 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.509+12741G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206494049 | ||||||
| chr2:206494087
|
ATCACC | A | 4 | a0001c0001t0008g0023a0001c0001t0008g0330a0001c0002t0019g0189others(1): Show | 4 | HG02055.hp1 HG02559.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.509+12783_509+1278 others(9): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206494087 | |||||
| chr2:206494158
|
A | G | 1 | a0001c0001t0042g0295 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.509+12850A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206494158 | ||||||
| chr2:206494163
|
A | G | 1 | a0001c0001t0033g0294 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.509+12855A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206494163 | ||||||
| chr2:206494165
|
A | C | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.509+12857A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206494165 | ||||||
| chr2:206494302
|
A | G | 2 | a0001c0001t0001g0291a0001c0001t0001g0334 | 2 | NA18995.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.509+12994A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206494302 | ||||||
| chr2:206494429
|
A | G | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.509+13121A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206494429 | ||||||
| chr2:206494524
|
G | T | 3 | a0001c0001t0012g0304a0001c0001t0012g0305a0001c0001t0012g0306 | 3 | HG01361.hp2 HG01433.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.509+13216G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206494524 | ||||||
| chr2:206494595
|
A | C | 4 | a0001c0001t0012g0304a0001c0001t0012g0305a0001c0001t0012g0306others(1): Show | 4 | HG01361.hp2 HG01433.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.509+13287A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206494595 | ||||||
| chr2:206494832
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.509+13524C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206494832 | ||||||
| chr2:206494839
|
T | A | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.509+13531T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206494839 | ||||||
| chr2:206495167
|
C | T | 1 | a0001c0001t0037g0228 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.509+13859C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206495167 | ||||||
| chr2:206495234
|
T | A | 1 | a0001c0002t0002g0219 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.509+13926T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206495234 | ||||||
| chr2:206495304
|
G | A | 74 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0095others(71): Show | 75 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.509+13996G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206495304 | ||||||
| chr2:206495424
|
A | C | 5 | a0001c0001t0026g0299a0001c0002t0002g0302a0001c0002t0011g0186others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+14116A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206495424 | ||||||
| chr2:206495441
|
A | G | 1 | a0001c0002t0029g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.509+14133A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206495441 | ||||||
| chr2:206495483
|
A | G | 38 | a0001c0001t0001g0006a0001c0001t0001g0170a0001c0001t0001g0185others(35): Show | 39 | HG00280.hp1 HG00558.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.509+14175A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206495483 | ||||||
| chr2:206495524
|
C | T | 2 | a0001c0001t0001g0184a0001c0001t0043g0019 | 2 | HG02622.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.509+14216C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206495524 | ||||||
| chr2:206495525
|
G | A | 2 | a0001c0001t0001g0101a0001c0001t0002g0220 | 2 | HG01099.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.509+14217G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206495525 | ||||||
| chr2:206495596
|
T | C | 1 | a0001c0002t0002g0262 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.509+14288T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206495596 | ||||||
| chr2:206495656
|
A | G | 1 | a0001c0002t0002g0009 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.509+14348A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206495656 | ||||||
| chr2:206495810
|
A | G | 1 | a0001c0002t0002g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.509+14502A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206495810 | ||||||
| chr2:206495859
|
G | T | 5 | a0001c0001t0026g0299a0001c0002t0002g0302a0001c0002t0011g0186others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+14551G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206495859 | ||||||
| chr2:206495863
|
T | G | 5 | a0001c0001t0026g0299a0001c0002t0002g0302a0001c0002t0011g0186others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+14555T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206495863 | ||||||
| chr2:206495875
|
A | C | 1 | a0001c0002t0029g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.509+14567A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206495875 | ||||||
| chr2:206496127
|
A | C | 2 | a0001c0001t0001g0309a0001c0001t0001g0319 | 2 | HG02258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.509+14819A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206496127 | ||||||
| chr2:206496136
|
C | G | 76 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(73): Show | 79 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.509+14828C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206496136 | ||||||
| chr2:206496185
|
C | G | 3 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125 | 3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.509+14877C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206496185 | ||||||
| chr2:206496368
|
C | T | 74 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0095others(71): Show | 75 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.509+15060C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206496368 | ||||||
| chr2:206496414
|
C | T | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.509+15106C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206496414 | ||||||
| chr2:206496415
|
G | A | 19 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0308others(16): Show | 19 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.509+15107G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206496415 | ||||||
| chr2:206496501
|
A | G | 2 | a0001c0002t0015g0182a0001c0002t0015g0183 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.509+15193A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206496501 | ||||||
| chr2:206496527
|
T | C | 1 | a0001c0001t0007g0339 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.509+15219T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206496527 | ||||||
| chr2:206496658
|
C | G | 1 | a0001c0001t0001g0331 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.509+15350C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206496658 | ||||||
| chr2:206496669
|
A | C | 8 | a0001c0001t0006g0345a0001c0001t0006g0348a0001c0001t0006g0349others(5): Show | 8 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.509+15361A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206496669 | ||||||
| chr2:206496698
|
T | C | 3 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125 | 3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.509+15390T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206496698 | ||||||
| chr2:206496922
|
G | C | 5 | a0001c0001t0026g0299a0001c0002t0002g0302a0001c0002t0011g0186others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+15614G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206496922 | ||||||
| chr2:206497101
|
G | C | 1 | a0001c0001t0001g0317 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.509+15793G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206497101 | ||||||
| chr2:206497147
|
T | C | 1 | a0001c0002t0002g0074 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.509+15839T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206497147 | ||||||
| chr2:206497199
|
A | G | 1 | a0001c0001t0002g0014 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.509+15891A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206497199 | ||||||
| chr2:206497281
|
A | G | 3 | a0001c0001t0001g0105a0001c0002t0015g0182a0001c0002t0015g0183 | 3 | HG02004.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.509+15973A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206497281 | ||||||
| chr2:206497338
|
C | T | 19 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0308others(16): Show | 19 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.509+16030C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206497338 | ||||||
| chr2:206497417
|
A | G | 5 | a0001c0001t0026g0299a0001c0002t0002g0302a0001c0002t0011g0186others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+16109A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206497417 | ||||||
| chr2:206497516
|
G | A | 48 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0095others(45): Show | 49 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.509+16208G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206497516 | ||||||
| chr2:206497571
|
C | T | 15 | a0001c0001t0001g0185a0001c0001t0002g0152a0001c0001t0002g0153others(12): Show | 15 | HG00558.hp1 HG02055.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.509+16263C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206497571 | ||||||
| chr2:206497587
|
T | C | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.509+16279T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206497587 | ||||||
| chr2:206497676
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.509+16368T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206497676 | ||||||
| chr2:206497766
|
C | T | 1 | a0001c0002t0002g0047 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.509+16458C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206497766 | ||||||
| chr2:206498283
|
T | G | 85 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0025others(82): Show | 87 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.509+16975T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206498283 | ||||||
| chr2:206498567
|
A | G | 1 | a0001c0002t0003g0162 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.509+17259A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206498567 | ||||||
| chr2:206498615
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.509+17307C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206498615 | ||||||
| chr2:206498743
|
A | T | 1 | a0001c0001t0002g0194 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.509+17435A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206498743 | ||||||
| chr2:206498866
|
A | G | 10 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0026others(7): Show | 11 | HG00099.hp2 HG01070.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.509+17558A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206498866 | ||||||
| chr2:206498873
|
T | C | 1 | a0001c0002t0025g0159 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.509+17565T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206498873 | ||||||
| chr2:206498937
|
C | T | 17 | a0001c0001t0001g0181a0001c0001t0001g0308a0001c0001t0001g0309others(14): Show | 17 | HG02258.hp1 HG02451.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.509+17629C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206498937 | ||||||
| chr2:206499035
|
T | G | 2 | a0001c0001t0001g0154a0001c0001t0001g0169 | 2 | HG01070.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.509+17727T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499035 | ||||||
| chr2:206499150
|
G | A | 281 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(278): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.509+17842G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499150 | ||||||
| chr2:206499209
|
T | C | 2 | a0001c0002t0015g0182a0001c0002t0015g0183 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.509+17901T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499209 | ||||||
| chr2:206499269
|
G | A | 1 | a0001c0001t0001g0278 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.509+17961G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499269 | ||||||
| chr2:206499270
|
G | C | 30 | a0001c0001t0001g0190a0001c0001t0001g0267a0001c0001t0001g0268others(27): Show | 30 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.509+17962G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499270 | ||||||
| chr2:206499289
|
G | A | 1 | a0001c0001t0001g0108 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.509+17981G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499289 | ||||||
| chr2:206499299
|
T | TGGA | 3 | a0001c0001t0001g0106a0001c0001t0001g0108a0001c0001t0001g0120 | 3 | HG00642.hp2 HG01346.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.509+17991_509+1799 others(7): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499299 | ||||||
| chr2:206499301
|
T | C | 2 | a0001c0001t0001g0106a0001c0001t0001g0120 | 2 | HG00642.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.509+17993T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499301 | ||||||
| chr2:206499302
|
A | G | 1 | a0001c0001t0001g0108 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.509+17994A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499302 | ||||||
| chr2:206499321
|
G | T | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 244 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.509+18013G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499321 | ||||||
| chr2:206499334
|
T | A | 1 | a0001c0001t0001g0108 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.509+18026T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499334 | ||||||
| chr2:206499453
|
T | C | 3 | a0001c0002t0001g0257a0001c0002t0001g0258a0001c0002t0001g0259 | 3 | HG02647.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.509+18145T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499453 | ||||||
| chr2:206499505
|
A | G | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017 | 3 | NA18961.hp1 NA19011.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.509+18197A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499505 | ||||||
| chr2:206499508
|
G | A | 4 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(1): Show | 4 | HG01496.hp2 NA18961.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.509+18200G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499508 | ||||||
| chr2:206499508
|
G | GAGGA | 38 | a0001c0001t0001g0006a0001c0001t0001g0170a0001c0001t0001g0185others(35): Show | 39 | HG00280.hp1 HG00558.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.509+18200_509+1820 others(8): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499508 | ||||||
| chr2:206499511
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017 | 3 | NA18961.hp1 NA19011.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.509+18203G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499511 | ||||||
| chr2:206499552
|
A | G | 1 | a0001c0001t0001g0045 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.509+18244A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499552 | ||||||
| chr2:206499564
|
A | C | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(87): Show | 93 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.509+18256A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499564 | ||||||
| chr2:206499569
|
A | G | 5 | a0001c0001t0001g0036a0001c0001t0001g0069a0001c0001t0001g0173others(2): Show | 5 | HG01884.hp2 HG02622.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+18261A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499569 | ||||||
| chr2:206499598
|
C | T | 2 | a0001c0002t0015g0182a0001c0002t0015g0183 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.509+18290C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499598 | ||||||
| chr2:206499623
|
A | G | 1 | a0001c0001t0002g0233 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.509+18315A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499623 | ||||||
| chr2:206499676
|
A | G | 1 | a0001c0001t0043g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.509+18368A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499676 | ||||||
| chr2:206500243
|
T | G | 5 | a0001c0001t0026g0299a0001c0002t0002g0302a0001c0002t0011g0186others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+18935T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206500243 | ||||||
| chr2:206500275
|
C | T | 1 | a0001c0001t0001g0336 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.509+18967C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206500275 | ||||||
| chr2:206500304
|
A | G | 79 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(76): Show | 82 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.509+18996A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206500304 | ||||||
| chr2:206500318
|
A | G | 1 | a0001c0001t0001g0324 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.509+19010A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206500318 | ||||||
| chr2:206500711
|
T | G | 1 | a0005c0008t0005g0242 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.509+19403T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206500711 | ||||||
| chr2:206500784
|
G | A | 7 | a0001c0001t0005g0215a0001c0001t0005g0221a0001c0001t0005g0222others(4): Show | 7 | HG00609.hp1 HG03669.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.509+19476G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206500784 | ||||||
| chr2:206500993
|
C | CT | 23 | a0001c0001t0001g0006a0001c0001t0001g0170a0001c0001t0001g0185others(20): Show | 24 | HG00558.hp1 HG01975.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.509+19699dupT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206500993 | |||||
| chr2:206500995
|
T | A | 5 | a0001c0001t0026g0299a0001c0002t0002g0302a0001c0002t0011g0186others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+19687T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206500995 | ||||||
| chr2:206501511
|
G | A | 1 | a0001c0001t0043g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.509+20203G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206501511 | ||||||
| chr2:206501611
|
A | G | 1 | a0001c0002t0002g0320 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.509+20303A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206501611 | ||||||
| chr2:206501614
|
T | C | 19 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0308others(16): Show | 19 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.509+20306T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206501614 | ||||||
| chr2:206501616
|
A | AAGGCATG others(6): Show |
19 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0308others(16): Show | 19 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.509+20310_509+2031 others(17): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206501616 | |||||
| chr2:206501629
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.509+20321G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206501629 | ||||||
| chr2:206501735
|
A | G | 8 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284others(5): Show | 8 | NA18940.hp1 NA18945.hp1 NA18966.hp2 others(5): Show |
intron_variant | MODIFIER | c.509+20427A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206501735 | ||||||
| chr2:206502133
|
C | T | 1 | a0001c0001t0002g0194 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.509+20825C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206502133 | ||||||
| chr2:206502148
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.509+20840G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206502148 | ||||||
| chr2:206502206
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.509+20898A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206502206 | ||||||
| chr2:206502241
|
A | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0170 | 3 | HG02257.hp2 HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.509+20933A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206502241 | ||||||
| chr2:206502258
|
G | A | 2 | a0001c0001t0001g0312a0001c0001t0001g0313 | 2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.509+20950G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206502258 | ||||||
| chr2:206502342
|
A | G | 1 | a0001c0001t0002g0333 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.509+21034A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206502342 | ||||||
| chr2:206502501
|
A | G | 4 | a0001c0001t0008g0023a0001c0001t0008g0330a0001c0002t0019g0189others(1): Show | 4 | HG02055.hp1 HG02559.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.509+21193A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206502501 | ||||||
| chr2:206502514
|
C | G | 1 | a0001c0002t0029g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.509+21206C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206502514 | ||||||
| chr2:206502723
|
C | T | 1 | a0001c0001t0030g0179 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.509+21415C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206502723 | ||||||
| chr2:206502797
|
C | A | 206 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(203): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.509+21489C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206502797 | ||||||
| chr2:206502929
|
G | T | 1 | a0001c0001t0001g0203 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.509+21621G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206502929 | ||||||
| chr2:206502936
|
C | A | 206 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(203): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.509+21628C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206502936 | ||||||
| chr2:206503084
|
C | T | 11 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0026others(8): Show | 12 | HG00099.hp2 HG01070.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.509+21776C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206503084 | ||||||
| chr2:206503113
|
T | C | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG01255.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.509+21805T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206503113 | ||||||
| chr2:206503146
|
G | A | 1 | a0001c0001t0043g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.509+21838G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206503146 | ||||||
| chr2:206503334
|
A | G | 1 | a0001c0002t0003g0158 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.509+22026A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206503334 | ||||||
| chr2:206503403
|
C | T | 1 | a0001c0001t0001g0208 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.509+22095C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206503403 | ||||||
| chr2:206503412
|
T | C | 2 | a0001c0001t0001g0291a0001c0001t0001g0334 | 2 | NA18995.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.509+22104T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206503412 | ||||||
| chr2:206503661
|
C | T | 35 | a0001c0001t0001g0036a0001c0001t0001g0069a0001c0001t0001g0173others(32): Show | 35 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.509+22353C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206503661 | ||||||
| chr2:206504084
|
T | C | 1 | a0001c0001t0001g0317 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.509+22776T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206504084 | ||||||
| chr2:206504246
|
A | G | 1 | a0001c0001t0001g0063 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.509+22938A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206504246 | ||||||
| chr2:206504251
|
A | G | 1 | a0001c0001t0001g0317 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.509+22943A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206504251 | ||||||
| chr2:206504337
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.509+23029T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206504337 | ||||||
| chr2:206504381
|
T | C | 1 | a0001c0002t0029g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.509+23073T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206504381 | ||||||
| chr2:206504397
|
A | G | 1 | a0001c0001t0001g0285 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.509+23089A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206504397 | ||||||
| chr2:206504486
|
T | C | 9 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284others(6): Show | 9 | NA18940.hp1 NA18945.hp1 NA18966.hp2 others(6): Show |
intron_variant | MODIFIER | c.509+23178T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206504486 | ||||||
| chr2:206504578
|
T | G | 1 | a0001c0001t0006g0349 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.509+23270T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206504578 | ||||||
| chr2:206504581
|
A | G | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.509+23273A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206504581 | ||||||
| chr2:206504670
|
G | T | 1 | a0001c0001t0002g0239 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.509+23362G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206504670 | ||||||
| chr2:206504726
|
G | A | 77 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(74): Show | 80 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.509+23418G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206504726 | ||||||
| chr2:206504745
|
A | G | 1 | a0001c0001t0002g0227 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.509+23437A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206504745 | ||||||
| chr2:206504862
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.509+23554G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206504862 | ||||||
| chr2:206504933
|
T | C | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.509+23625T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206504933 | ||||||
| chr2:206504940
|
G | T | 1 | a0001c0001t0001g0154 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.509+23632G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206504940 | ||||||
| chr2:206505093
|
G | T | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.509+23785G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206505093 | ||||||
| chr2:206505112
|
A | G | 38 | a0001c0001t0001g0006a0001c0001t0001g0170a0001c0001t0002g0139others(35): Show | 39 | HG00280.hp1 HG00558.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.509+23804A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206505112 | ||||||
| chr2:206505165
|
T | A | 10 | a0001c0001t0006g0345a0001c0001t0006g0348a0001c0001t0006g0349others(7): Show | 10 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.509+23857T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206505165 | ||||||
| chr2:206505201
|
A | G | 2 | a0001c0002t0002g0053a0001c0002t0002g0054 | 2 | NA19072.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.509+23893A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206505201 | ||||||
| chr2:206505384
|
G | T | 2 | a0001c0002t0015g0182a0001c0002t0015g0183 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.509+24076G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206505384 | ||||||
| chr2:206505492
|
G | A | 1 | a0001c0001t0002g0247 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.509+24184G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206505492 | ||||||
| chr2:206505492
|
G | T | 2 | a0001c0002t0015g0182a0001c0002t0015g0183 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.509+24184G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206505492 | ||||||
| chr2:206505645
|
C | T | 2 | a0001c0002t0015g0182a0001c0002t0015g0183 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.509+24337C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206505645 | ||||||
| chr2:206505665
|
T | C | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.509+24357T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206505665 | ||||||
| chr2:206505720
|
A | C | 1 | a0001c0002t0002g0320 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.509+24412A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206505720 | ||||||
| chr2:206505772
|
G | A | 2 | a0001c0002t0015g0182a0001c0002t0015g0183 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.509+24464G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206505772 | ||||||
| chr2:206506238
|
G | T | 48 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0095others(45): Show | 49 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.510-24647G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206506238 | ||||||
| chr2:206506459
|
G | A | 2 | a0001c0001t0001g0073a0001c0007t0001g0072 | 2 | HG01257.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.510-24426G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206506459 | ||||||
| chr2:206506974
|
A | G | 11 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0026others(8): Show | 12 | HG00099.hp2 HG01070.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.510-23911A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206506974 | ||||||
| chr2:206507154
|
A | G | 1 | a0001c0001t0021g0332 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.510-23731A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206507154 | ||||||
| chr2:206507233
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.510-23652C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206507233 | ||||||
| chr2:206507274
|
G | A | 10 | a0001c0001t0001g0308a0001c0001t0001g0310a0001c0001t0001g0311others(7): Show | 10 | HG02451.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.510-23611G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206507274 | ||||||
| chr2:206507302
|
G | C | 76 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(73): Show | 79 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.510-23583G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206507302 | ||||||
| chr2:206507474
|
C | G | 1 | a0001c0002t0003g0137 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.510-23411C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206507474 | ||||||
| chr2:206507635
|
A | C | 1 | a0001c0002t0002g0146 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.510-23250A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206507635 | ||||||
| chr2:206507650
|
A | G | 2 | a0001c0001t0002g0176a0001c0001t0002g0212 | 2 | NA19003.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.510-23235A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206507650 | ||||||
| chr2:206507711
|
T | C | 3 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125 | 3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.510-23174T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206507711 | ||||||
| chr2:206507736
|
C | T | 1 | a0001c0001t0026g0299 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.510-23149C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206507736 | ||||||
| chr2:206507745
|
A | C | 1 | a0001c0001t0001g0045 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.510-23140A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206507745 | ||||||
| chr2:206507770
|
T | C | 20 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0308others(17): Show | 20 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.510-23115T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206507770 | ||||||
| chr2:206507782
|
C | T | 1 | a0001c0001t0002g0139 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.510-23103C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206507782 | ||||||
| chr2:206507806
|
C | G | 1 | a0001c0001t0035g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.510-23079C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206507806 | ||||||
| chr2:206507933
|
G | A | 1 | a0001c0001t0002g0239 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.510-22952G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206507933 | ||||||
| chr2:206508061
|
G | A | 5 | a0001c0001t0004g0249a0001c0001t0004g0250a0001c0001t0004g0251others(2): Show | 5 | NA18946.hp1 NA18952.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.510-22824G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206508061 | ||||||
| chr2:206508068
|
T | C | 5 | a0001c0001t0004g0249a0001c0001t0004g0250a0001c0001t0004g0251others(2): Show | 5 | NA18946.hp1 NA18952.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.510-22817T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206508068 | ||||||
| chr2:206508069
|
T | G | 5 | a0001c0001t0004g0249a0001c0001t0004g0250a0001c0001t0004g0251others(2): Show | 5 | NA18946.hp1 NA18952.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.510-22816T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206508069 | ||||||
| chr2:206508113
|
C | T | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG00099.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.510-22772C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206508113 | ||||||
| chr2:206508176
|
T | C | 1 | a0001c0002t0002g0219 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.510-22709T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206508176 | ||||||
| chr2:206508231
|
G | A | 2 | a0001c0001t0001g0122a0001c0001t0039g0134 | 2 | NA18988.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.510-22654G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206508231 | ||||||
| chr2:206508250
|
T | C | 2 | a0001c0001t0001g0108a0001c0001t0040g0040 | 2 | HG02698.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.510-22635T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206508250 | ||||||
| chr2:206508251
|
G | A | 1 | a0001c0001t0021g0332 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.510-22634G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206508251 | ||||||
| chr2:206508273
|
A | G | 1 | a0001c0001t0001g0100 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.510-22612A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206508273 | ||||||
| chr2:206508285
|
T | C | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.510-22600T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206508285 | ||||||
| chr2:206508305
|
C | G | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.510-22580C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206508305 | ||||||
| chr2:206508306
|
G | A | 1 | a0001c0002t0002g0077 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.510-22579G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206508306 | ||||||
| chr2:206508340
|
T | C | 1 | a0001c0001t0001g0260 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.510-22545T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206508340 | ||||||
| chr2:206508382
|
G | A | 2 | a0001c0001t0001g0180a0001c0002t0002g0307 | 2 | HG02257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.510-22503G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206508382 | ||||||
| chr2:206508511
|
C | T | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.510-22374C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206508511 | ||||||
| chr2:206508554
|
G | T | 2 | a0001c0001t0001g0180a0001c0002t0002g0307 | 2 | HG02257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.510-22331G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206508554 | ||||||
| chr2:206508592
|
G | A | 1 | a0001c0001t0002g0333 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.510-22293G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206508592 | ||||||
| chr2:206508655
|
C | CA | 42 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0248others(39): Show | 42 | HG00609.hp1 HG00642.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.510-22213dupA | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206508655 | |||||
| chr2:206508655
|
CA | C | 146 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(143): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.510-22213delA | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206508655 | |||||
| chr2:206508655
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0073 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.510-22225_510-2221 others(17): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206508655 | |||||
| chr2:206508669
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.510-22216A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206508669 | ||||||
| chr2:206509104
|
A | G | 189 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(186): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.510-21781A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206509104 | ||||||
| chr2:206509172
|
T | C | 1 | a0001c0001t0001g0324 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.510-21713T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206509172 | ||||||
| chr2:206509212
|
C | T | 2 | a0001c0001t0017g0038a0001c0001t0017g0039 | 2 | NA18943.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.510-21673C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206509212 | ||||||
| chr2:206509389
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.510-21496A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206509389 | ||||||
| chr2:206509549
|
A | G | 1 | a0001c0001t0001g0331 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.510-21336A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206509549 | ||||||
| chr2:206509573
|
C | T | 1 | a0001c0001t0021g0332 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.510-21312C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206509573 | ||||||
| chr2:206509614
|
A | G | 5 | a0001c0001t0026g0299a0001c0002t0002g0302a0001c0002t0011g0186others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.510-21271A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206509614 | ||||||
| chr2:206509664
|
G | A | 1 | a0001c0001t0001g0289 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.510-21221G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206509664 | ||||||
| chr2:206509691
|
C | T | 23 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0308others(20): Show | 23 | HG02055.hp1 HG02257.hp1 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.510-21194C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206509691 | ||||||
| chr2:206509856
|
G | A | 52 | a0001c0001t0001g0006a0001c0001t0001g0170a0001c0001t0005g0145others(49): Show | 54 | HG00280.hp1 HG00558.hp1 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.510-21029G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206509856 | ||||||
| chr2:206510213
|
G | A | 5 | a0001c0002t0002g0007a0001c0002t0002g0008a0001c0002t0002g0009others(2): Show | 5 | HG02145.hp1 HG02451.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.510-20672G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206510213 | ||||||
| chr2:206510239
|
G | A | 1 | a0001c0002t0001g0150 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.510-20646G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206510239 | ||||||
| chr2:206510720
|
A | G | 1 | a0001c0001t0001g0192 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.510-20165A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206510720 | ||||||
| chr2:206510823
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.510-20062A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206510823 | ||||||
| chr2:206510848
|
C | A | 1 | a0001c0001t0030g0179 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.510-20037C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206510848 | ||||||
| chr2:206510948
|
C | A | 1 | a0001c0001t0002g0124 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.510-19937C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206510948 | ||||||
| chr2:206511328
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.510-19557G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206511328 | ||||||
| chr2:206511424
|
A | G | 1 | a0001c0001t0002g0195 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.510-19461A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206511424 | ||||||
| chr2:206512306
|
A | T | 1 | a0001c0001t0002g0327 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.510-18579A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206512306 | ||||||
| chr2:206512351
|
C | G | 1 | a0001c0001t0001g0334 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.510-18534C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206512351 | ||||||
| chr2:206512468
|
G | A | 1 | a0001c0001t0001g0300 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.510-18417G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206512468 | ||||||
| chr2:206512473
|
A | G | 1 | a0001c0001t0008g0330 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.510-18412A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206512473 | ||||||
| chr2:206512699
|
T | A | 1 | a0001c0001t0002g0261 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.510-18186T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206512699 | ||||||
| chr2:206512723
|
A | G | 1 | a0001c0001t0001g0013 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.510-18162A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206512723 | ||||||
| chr2:206512778
|
G | A | 64 | a0001c0001t0001g0036a0001c0001t0001g0069a0001c0001t0001g0173others(61): Show | 64 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.510-18107G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206512778 | ||||||
| chr2:206512795
|
G | A | 64 | a0001c0001t0001g0036a0001c0001t0001g0069a0001c0001t0001g0173others(61): Show | 64 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.510-18090G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206512795 | ||||||
| chr2:206512812
|
A | G | 3 | a0001c0001t0013g0030a0001c0001t0013g0034a0003c0004t0013g0031 | 3 | HG01243.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.510-18073A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206512812 | ||||||
| chr2:206512830
|
A | G | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.510-18055A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206512830 | ||||||
| chr2:206513126
|
C | T | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.510-17759C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206513126 | ||||||
| chr2:206513289
|
T | C | 1 | a0001c0001t0006g0350 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.510-17596T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206513289 | ||||||
| chr2:206513378
|
AT | A | 64 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(61): Show | 66 | HG00280.hp2 HG00544.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.510-17506delT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206513378 | ||||||
| chr2:206513430
|
G | A | 4 | a0001c0001t0006g0349a0001c0001t0006g0350a0001c0001t0006g0351others(1): Show | 4 | HG01081.hp1 HG03017.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.510-17455G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206513430 | ||||||
| chr2:206513557
|
A | G | 11 | a0001c0001t0005g0213a0001c0001t0005g0214a0001c0001t0005g0215others(8): Show | 11 | HG00609.hp1 HG03669.hp1 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.510-17328A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206513557 | ||||||
| chr2:206513706
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.510-17179T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206513706 | ||||||
| chr2:206513822
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.510-17063T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206513822 | ||||||
| chr2:206513920
|
C | T | 66 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(63): Show | 68 | HG00280.hp2 HG00544.hp2 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.510-16965C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206513920 | ||||||
| chr2:206514024
|
A | G | 2 | a0001c0001t0020g0151a0001c0002t0001g0092 | 2 | HG02486.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.510-16861A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206514024 | ||||||
| chr2:206514185
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0041g0028 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.510-16700G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206514185 | ||||||
| chr2:206514210
|
A | T | 1 | a0001c0001t0001g0129 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.510-16675A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206514210 | ||||||
| chr2:206514215
|
A | G | 1 | a0001c0001t0001g0104 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.510-16670A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206514215 | ||||||
| chr2:206514353
|
G | A | 2 | a0001c0001t0016g0234a0001c0001t0016g0235 | 2 | HG00140.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.510-16532G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206514353 | ||||||
| chr2:206514353
|
G | C | 203 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(200): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.510-16532G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206514353 | ||||||
| chr2:206514481
|
G | C | 1 | a0001c0001t0001g0248 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.510-16404G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206514481 | ||||||
| chr2:206514488
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.510-16397C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206514488 | ||||||
| chr2:206514558
|
C | T | 41 | a0001c0001t0001g0036a0001c0001t0001g0069a0001c0001t0001g0173others(38): Show | 41 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.510-16327C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206514558 | ||||||
| chr2:206514574
|
G | T | 1 | a0001c0001t0001g0317 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.510-16311G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206514574 | ||||||
| chr2:206514575
|
C | T | 1 | a0001c0001t0001g0317 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.510-16310C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206514575 | ||||||
| chr2:206514707
|
A | G | 1 | a0001c0001t0001g0300 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.510-16178A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206514707 | ||||||
| chr2:206514711
|
T | C | 3 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125 | 3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.510-16174T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206514711 | ||||||
| chr2:206514718
|
A | G | 1 | a0001c0001t0038g0218 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.510-16167A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206514718 | ||||||
| chr2:206514880
|
T | G | 1 | a0001c0001t0002g0195 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.510-16005T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206514880 | ||||||
| chr2:206515213
|
T | C | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.510-15672T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206515213 | ||||||
| chr2:206515233
|
T | C | 2 | a0001c0001t0020g0151a0001c0002t0001g0092 | 2 | HG02486.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.510-15652T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206515233 | ||||||
| chr2:206515413
|
CGCTCCAT others(7): Show |
C | 1 | a0001c0002t0002g0147 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.510-15449_510-1543 others(18): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206515413 | |||||
| chr2:206515461
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.510-15424A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206515461 | ||||||
| chr2:206515489
|
G | A | 2 | a0001c0001t0002g0139a0001c0002t0002g0138 | 2 | HG01975.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.510-15396G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206515489 | ||||||
| chr2:206515497
|
C | A | 2 | a0001c0001t0002g0139a0001c0002t0002g0138 | 2 | HG01975.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.510-15388C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206515497 | ||||||
| chr2:206515533
|
A | C | 2 | a0001c0001t0020g0151a0001c0002t0001g0092 | 2 | HG02486.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.510-15352A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206515533 | ||||||
| chr2:206515666
|
A | G | 1 | a0001c0001t0043g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.510-15219A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206515666 | ||||||
| chr2:206515761
|
A | G | 1 | a0001c0001t0001g0026 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.510-15124A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206515761 | ||||||
| chr2:206515777
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.510-15108A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206515777 | ||||||
| chr2:206515829
|
G | GT | 19 | a0001c0001t0001g0181a0001c0001t0001g0308a0001c0001t0001g0309others(16): Show | 19 | HG02258.hp1 HG02451.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.510-15048dupT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206515829 | |||||
| chr2:206516051
|
C | T | 4 | a0001c0002t0015g0182a0001c0002t0015g0183a0001c0002t0019g0189others(1): Show | 4 | HG02055.hp1 HG02559.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.510-14834C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206516051 | ||||||
| chr2:206516159
|
G | A | 3 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125 | 3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.510-14726G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206516159 | ||||||
| chr2:206516166
|
C | G | 1 | a0001c0001t0001g0026 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.510-14719C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206516166 | ||||||
| chr2:206516171
|
C | T | 8 | a0001c0001t0006g0345a0001c0001t0006g0348a0001c0001t0006g0349others(5): Show | 8 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.510-14714C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206516171 | ||||||
| chr2:206516233
|
TA | T | 11 | a0001c0001t0001g0036a0001c0001t0001g0069a0001c0001t0001g0169others(8): Show | 11 | HG01069.hp2 HG01070.hp1 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.510-14638delA | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206516233 | |||||
| chr2:206516319
|
A | G | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG01255.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.510-14566A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206516319 | ||||||
| chr2:206516324
|
G | A | 1 | a0001c0002t0029g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.510-14561G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206516324 | ||||||
| chr2:206516324
|
G | GT | 5 | a0001c0001t0001g0287a0001c0001t0001g0310a0001c0001t0002g0246others(2): Show | 5 | HG01884.hp1 HG02647.hp1 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.510-14553dupT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206516324 | |||||
| chr2:206516419
|
T | G | 19 | a0001c0001t0001g0181a0001c0001t0001g0308a0001c0001t0001g0309others(16): Show | 19 | HG02258.hp1 HG02451.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.510-14466T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206516419 | ||||||
| chr2:206516571
|
G | C | 7 | a0001c0001t0001g0185a0001c0001t0001g0264a0001c0001t0001g0265others(4): Show | 7 | HG01243.hp1 HG02055.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.510-14314G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206516571 | ||||||
| chr2:206516844
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.510-14041C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206516844 | ||||||
| chr2:206516982
|
A | G | 3 | a0001c0002t0001g0257a0001c0002t0001g0258a0001c0002t0001g0259 | 3 | HG02647.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.510-13903A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206516982 | ||||||
| chr2:206516984
|
A | G | 8 | a0001c0001t0006g0345a0001c0001t0006g0348a0001c0001t0006g0349others(5): Show | 8 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.510-13901A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206516984 | ||||||
| chr2:206517093
|
G | A | 3 | a0001c0002t0002g0200a0001c0002t0002g0201a0001c0002t0002g0202 | 3 | NA18747.hp1 NA19088.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.510-13792G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206517093 | ||||||
| chr2:206517287
|
C | T | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017 | 3 | NA18961.hp1 NA19011.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.510-13598C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206517287 | ||||||
| chr2:206517320
|
G | A | 11 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0025others(8): Show | 12 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.510-13565G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206517320 | ||||||
| chr2:206517344
|
T | C | 1 | a0001c0002t0002g0302 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.510-13541T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206517344 | ||||||
| chr2:206517416
|
A | T | 47 | a0001c0001t0001g0004a0001c0001t0001g0088a0001c0001t0001g0094others(44): Show | 48 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.510-13469A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206517416 | ||||||
| chr2:206517596
|
C | T | 1 | a0001c0001t0001g0003 | 2 | NA18990.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.510-13289C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206517596 | ||||||
| chr2:206517638
|
T | G | 1 | a0001c0001t0004g0292 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.510-13247T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206517638 | ||||||
| chr2:206517676
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.510-13209G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206517676 | ||||||
| chr2:206517763
|
A | C | 16 | a0001c0001t0001g0197a0001c0001t0002g0209a0001c0001t0002g0326others(13): Show | 16 | HG00673.hp2 HG02523.hp2 NA18747.hp1 others(13): Show |
intron_variant | MODIFIER | c.510-13122A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206517763 | ||||||
| chr2:206517944
|
C | G | 3 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125 | 3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.510-12941C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206517944 | ||||||
| chr2:206517977
|
G | A | 3 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0041g0028 | 3 | HG00642.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.510-12908G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206517977 | ||||||
| chr2:206518103
|
T | C | 1 | a0001c0002t0002g0320 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.510-12782T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206518103 | ||||||
| chr2:206518255
|
T | C | 1 | a0001c0001t0002g0261 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.510-12630T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206518255 | ||||||
| chr2:206518352
|
A | C | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.510-12533A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206518352 | ||||||
| chr2:206518693
|
A | T | 2 | a0001c0002t0002g0009a0001c0002t0002g0024 | 2 | HG02145.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.510-12192A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206518693 | ||||||
| chr2:206518787
|
T | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0155a0001c0001t0001g0171 | 4 | HG01074.hp2 HG01106.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.510-12098T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206518787 | ||||||
| chr2:206518933
|
C | T | 1 | a0001c0002t0010g0206 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.510-11952C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206518933 | ||||||
| chr2:206519203
|
G | A | 1 | a0001c0002t0002g0143 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.510-11682G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206519203 | ||||||
| chr2:206519304
|
T | A | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.510-11581T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206519304 | ||||||
| chr2:206519327
|
C | T | 1 | a0001c0001t0030g0179 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.510-11558C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206519327 | ||||||
| chr2:206519341
|
A | G | 1 | a0001c0002t0002g0141 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.510-11544A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206519341 | ||||||
| chr2:206519413
|
G | A | 253 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(250): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.510-11472G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206519413 | ||||||
| chr2:206519603
|
G | A | 1 | a0001c0002t0002g0032 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.510-11282G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206519603 | ||||||
| chr2:206519648
|
G | A | 2 | a0001c0001t0001g0068a0001c0001t0001g0080 | 2 | HG02717.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.510-11237G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206519648 | ||||||
| chr2:206519694
|
C | A | 1 | a0001c0001t0035g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.510-11191C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206519694 | ||||||
| chr2:206519740
|
G | A | 1 | a0001c0001t0001g0192 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.510-11145G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206519740 | ||||||
| chr2:206519981
|
T | C | 2 | a0001c0001t0002g0176a0001c0001t0002g0212 | 2 | NA19003.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.510-10904T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206519981 | ||||||
| chr2:206520053
|
C | T | 20 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0308others(17): Show | 20 | HG02258.hp1 HG02451.hp2 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.510-10832C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206520053 | ||||||
| chr2:206520619
|
T | C | 2 | a0001c0002t0002g0053a0001c0002t0002g0054 | 2 | NA19072.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.510-10266T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206520619 | ||||||
| chr2:206520877
|
A | G | 2 | a0001c0001t0034g0079a0001c0001t0035g0078 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.510-10008A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206520877 | ||||||
| chr2:206520886
|
A | G | 1 | a0001c0001t0001g0136 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.510-9999A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206520886 | ||||||
| chr2:206520890
|
T | G | 1 | a0001c0001t0002g0261 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.510-9995T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206520890 | ||||||
| chr2:206520946
|
T | TAGGC | 4 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(1): Show | 4 | HG02280.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.510-9938_510-9935d others(6): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206520946 | |||||
| chr2:206521140
|
G | T | 1 | a0001c0002t0002g0007 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.510-9745G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206521140 | ||||||
| chr2:206521665
|
G | A | 21 | a0001c0001t0001g0006a0001c0001t0001g0170a0001c0001t0034g0079others(18): Show | 22 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.510-9220G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206521665 | ||||||
| chr2:206521899
|
A | C | 9 | a0001c0001t0006g0345a0001c0001t0006g0348a0001c0001t0006g0349others(6): Show | 9 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.510-8986A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206521899 | ||||||
| chr2:206521974
|
G | A | 4 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(1): Show | 4 | HG02280.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.510-8911G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206521974 | ||||||
| chr2:206522097
|
TTTA | T | 4 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(1): Show | 4 | HG02280.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.510-8785_510-8783d others(5): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206522097 | |||||
| chr2:206522106
|
A | G | 6 | a0001c0001t0006g0345a0001c0001t0006g0348a0001c0001t0006g0349others(3): Show | 6 | HG01081.hp1 HG01496.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.510-8779A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206522106 | ||||||
| chr2:206522157
|
A | C | 1 | a0001c0001t0002g0193 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.510-8728A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206522157 | ||||||
| chr2:206522159
|
C | A | 4 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(1): Show | 4 | HG02280.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.510-8726C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206522159 | ||||||
| chr2:206522284
|
A | C | 1 | a0001c0002t0029g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.510-8601A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206522284 | ||||||
| chr2:206522381
|
C | A | 1 | a0001c0001t0018g0276 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.510-8504C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206522381 | ||||||
| chr2:206522492
|
GAA | G | 4 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(1): Show | 4 | HG00099.hp1 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.510-8390_510-8389d others(4): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206522492 | |||||
| chr2:206522553
|
G | A | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.510-8332G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206522553 | ||||||
| chr2:206522804
|
A | AT | 134 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(131): Show | 138 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.510-8068dupT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206522804 | |||||
| chr2:206522804
|
AT | A | 7 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(4): Show | 7 | HG01099.hp2 HG02280.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.510-8068delT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206522804 | |||||
| chr2:206522979
|
C | T | 256 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(253): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.510-7906C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206522979 | ||||||
| chr2:206523082
|
G | C | 17 | a0001c0001t0001g0181a0001c0001t0001g0308a0001c0001t0001g0309others(14): Show | 17 | HG02258.hp1 HG02451.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.510-7803G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206523082 | ||||||
| chr2:206523304
|
AC | A | 280 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(277): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.510-7576delC | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206523304 | |||||
| chr2:206523332
|
T | C | 1 | a0001c0001t0002g0139 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.510-7553T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206523332 | ||||||
| chr2:206523436
|
C | T | 1 | a0001c0002t0002g0047 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.510-7449C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206523436 | ||||||
| chr2:206523516
|
G | A | 46 | a0001c0001t0001g0004a0001c0001t0001g0088a0001c0001t0001g0094others(43): Show | 47 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.510-7369G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206523516 | ||||||
| chr2:206523812
|
A | G | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 115 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.510-7073A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206523812 | ||||||
| chr2:206523934
|
G | A | 1 | a0001c0001t0002g0035 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.510-6951G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206523934 | ||||||
| chr2:206523959
|
C | T | 1 | a0001c0002t0002g0138 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.510-6926C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206523959 | ||||||
| chr2:206524047
|
G | A | 1 | a0001c0001t0004g0249 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.510-6838G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206524047 | ||||||
| chr2:206524074
|
A | G | 4 | a0001c0002t0015g0182a0001c0002t0015g0183a0001c0002t0019g0189others(1): Show | 4 | HG02055.hp1 HG02559.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.510-6811A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206524074 | ||||||
| chr2:206524224
|
A | T | 3 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0041g0028 | 3 | HG00642.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.510-6661A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206524224 | ||||||
| chr2:206524583
|
A | G | 282 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(279): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.510-6302A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206524583 | ||||||
| chr2:206524782
|
C | T | 1 | a0001c0001t0002g0327 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.510-6103C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206524782 | ||||||
| chr2:206525065
|
G | C | 3 | a0001c0001t0001g0300a0001c0001t0002g0301a0001c0001t0042g0295 | 3 | HG02572.hp2 HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.510-5820G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206525065 | ||||||
| chr2:206525117
|
A | C | 1 | a0001c0002t0002g0142 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.510-5768A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206525117 | ||||||
| chr2:206525215
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0041g0028 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.510-5670G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206525215 | ||||||
| chr2:206525286
|
A | G | 2 | a0001c0001t0002g0333a0001c0001t0020g0329 | 2 | HG00738.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.510-5599A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206525286 | ||||||
| chr2:206525354
|
TC | T | 15 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0025others(12): Show | 16 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.510-5529delC | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206525354 | |||||
| chr2:206525751
|
C | A | 1 | a0001c0001t0001g0335 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.510-5134C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206525751 | ||||||
| chr2:206525829
|
A | T | 1 | a0001c0001t0001g0107 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.510-5056A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206525829 | ||||||
| chr2:206525882
|
G | C | 1 | a0001c0001t0002g0327 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.510-5003G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206525882 | ||||||
| chr2:206525932
|
A | T | 2 | a0001c0001t0013g0030a0003c0004t0013g0031 | 2 | HG01243.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.510-4953A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206525932 | ||||||
| chr2:206526141
|
T | TAC | 24 | a0001c0001t0001g0055a0001c0001t0002g0022a0001c0001t0002g0123others(21): Show | 24 | HG00140.hp1 HG00609.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.510-4706_510-4705d others(4): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206526141 | |||||
| chr2:206526141
|
T | TACACACA others(3): Show |
1 | a0001c0001t0002g0333 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.510-4714_510-4705d others(12): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206526141 | |||||
| chr2:206526141
|
TAC | T | 68 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0015others(65): Show | 70 | HG00642.hp1 HG00741.hp1 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.510-4706_510-4705d others(4): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206526141 | |||||
| chr2:206526141
|
TACAC | T | 81 | a0001c0001t0001g0004a0001c0001t0001g0036a0001c0001t0001g0088others(78): Show | 82 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.510-4708_510-4705d others(6): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206526141 | |||||
| chr2:206526141
|
TACACAC | T | 58 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(55): Show | 61 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.510-4710_510-4705d others(8): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206526141 | |||||
| chr2:206526141
|
TACACACA others(1): Show |
T | 12 | a0001c0001t0001g0277a0001c0001t0001g0280a0001c0001t0001g0285others(9): Show | 12 | HG00733.hp2 HG01081.hp1 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.510-4712_510-4705d others(10): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206526141 | |||||
| chr2:206526141
|
TACACACA others(3): Show |
T | 6 | a0001c0002t0001g0150a0001c0002t0002g0142a0001c0002t0002g0147others(3): Show | 6 | HG02735.hp1 HG04228.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.510-4714_510-4705d others(12): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206526141 | |||||
| chr2:206526154
|
A | ACG | 4 | a0001c0001t0005g0222a0001c0001t0005g0229a0001c0001t0005g0236others(1): Show | 4 | NA18951.hp2 NA18955.hp2 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.510-4730_510-4729i others(4): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206526154 | |||||
| chr2:206526157
|
C | G | 11 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0025others(8): Show | 12 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.510-4728C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206526157 | ||||||
| chr2:206526169
|
CACACACA others(15): Show |
C | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.510-4709_510-4688d others(24): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206526169 | |||||
| chr2:206526177
|
CACAG | C | 3 | a0001c0001t0001g0190a0001c0001t0001g0290a0001c0001t0028g0297 | 3 | HG00323.hp1 HG03453.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.510-4704_510-4701d others(6): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206526177 | |||||
| chr2:206526438
|
C | T | 40 | a0001c0001t0001g0036a0001c0001t0001g0069a0001c0001t0001g0173others(37): Show | 40 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.510-4447C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206526438 | ||||||
| chr2:206526546
|
T | G | 1 | a0001c0001t0002g0022 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.510-4339T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206526546 | ||||||
| chr2:206526949
|
A | G | 20 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0308others(17): Show | 20 | HG02258.hp1 HG02451.hp2 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.510-3936A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206526949 | ||||||
| chr2:206527032
|
A | G | 4 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(1): Show | 4 | HG02280.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.510-3853A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206527032 | ||||||
| chr2:206527132
|
A | G | 3 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0041g0028 | 3 | HG00642.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.510-3753A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206527132 | ||||||
| chr2:206527290
|
A | G | 1 | a0001c0001t0043g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.510-3595A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206527290 | ||||||
| chr2:206527504
|
C | T | 1 | a0001c0002t0002g0201 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.510-3381C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206527504 | ||||||
| chr2:206527526
|
T | G | 1 | a0001c0002t0029g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.510-3359T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206527526 | ||||||
| chr2:206527646
|
G | A | 1 | a0001c0001t0002g0327 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.510-3239G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206527646 | ||||||
| chr2:206527666
|
G | T | 20 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0308others(17): Show | 20 | HG02258.hp1 HG02451.hp2 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.510-3219G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206527666 | ||||||
| chr2:206527897
|
C | A | 1 | a0001c0001t0033g0294 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.510-2988C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206527897 | ||||||
| chr2:206527951
|
T | C | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.510-2934T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206527951 | ||||||
| chr2:206528201
|
T | C | 1 | a0001c0001t0020g0151 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.510-2684T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206528201 | ||||||
| chr2:206528596
|
C | T | 68 | a0001c0001t0001g0036a0001c0001t0001g0069a0001c0001t0001g0173others(65): Show | 68 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.510-2289C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206528596 | ||||||
| chr2:206528700
|
G | A | 11 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0025others(8): Show | 12 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.510-2185G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206528700 | ||||||
| chr2:206528710
|
C | T | 2 | a0001c0001t0001g0043a0001c0001t0001g0065 | 2 | HG02145.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.510-2175C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206528710 | ||||||
| chr2:206528839
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.510-2046C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206528839 | ||||||
| chr2:206528885
|
G | A | 5 | a0001c0001t0004g0249a0001c0001t0004g0250a0001c0001t0004g0251others(2): Show | 5 | NA18946.hp1 NA18952.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.510-2000G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206528885 | ||||||
| chr2:206528955
|
C | T | 1 | a0001c0001t0001g0336 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.510-1930C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206528955 | ||||||
| chr2:206529054
|
C | T | 8 | a0001c0001t0006g0345a0001c0001t0006g0348a0001c0001t0006g0349others(5): Show | 8 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.510-1831C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206529054 | ||||||
| chr2:206529105
|
T | C | 69 | a0001c0001t0001g0036a0001c0001t0001g0069a0001c0001t0001g0173others(66): Show | 69 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.510-1780T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206529105 | ||||||
| chr2:206529146
|
A | G | 41 | a0001c0001t0001g0036a0001c0001t0001g0069a0001c0001t0001g0173others(38): Show | 41 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.510-1739A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206529146 | ||||||
| chr2:206529173
|
A | T | 2 | a0001c0001t0020g0151a0001c0002t0001g0092 | 2 | HG02486.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.510-1712A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206529173 | ||||||
| chr2:206529224
|
A | G | 11 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0025others(8): Show | 12 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.510-1661A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206529224 | ||||||
| chr2:206529334
|
G | A | 20 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0308others(17): Show | 20 | HG02258.hp1 HG02451.hp2 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.510-1551G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206529334 | ||||||
| chr2:206529629
|
C | T | 23 | a0001c0001t0002g0209a0001c0001t0002g0326a0001c0001t0021g0196others(20): Show | 23 | HG00673.hp2 HG02145.hp1 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.510-1256C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206529629 | ||||||
| chr2:206529795
|
ATG | A | 2 | a0001c0001t0001g0006a0001c0001t0001g0170 | 3 | HG02257.hp2 HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.510-1076_510-1075d others(4): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206529795 | |||||
| chr2:206529819
|
A | AT | 65 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(62): Show | 67 | HG00280.hp2 HG00544.hp2 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.510-1056dupT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206529819 | |||||
| chr2:206529892
|
A | G | 45 | a0001c0001t0001g0004a0001c0001t0001g0088a0001c0001t0001g0094others(42): Show | 46 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.510-993A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206529892 | ||||||
| chr2:206529960
|
T | G | 3 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125 | 3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.510-925T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206529960 | ||||||
| chr2:206529972
|
C | T | 65 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(62): Show | 67 | HG00280.hp2 HG00544.hp2 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.510-913C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206529972 | ||||||
| chr2:206530042
|
C | T | 3 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125 | 3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.510-843C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206530042 | ||||||
| chr2:206530074
|
G | A | 1 | a0001c0002t0003g0158 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.510-811G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206530074 | ||||||
| chr2:206530104
|
C | T | 2 | a0001c0001t0002g0035a0001c0002t0002g0307 | 2 | HG02257.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.510-781C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206530104 | ||||||
| chr2:206530166
|
A | G | 47 | a0001c0001t0001g0004a0001c0001t0001g0088a0001c0001t0001g0094others(44): Show | 48 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.510-719A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206530166 | ||||||
| chr2:206530325
|
A | G | 2 | a0001c0001t0034g0079a0001c0001t0035g0078 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.510-560A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206530325 | ||||||
| chr2:206530389
|
A | G | 1 | a0001c0001t0002g0266 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.510-496A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206530389 | ||||||
| chr2:206530395
|
T | C | 1 | a0001c0001t0001g0055 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.510-490T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206530395 | ||||||
| chr2:206530416
|
T | C | 2 | a0001c0001t0020g0151a0001c0002t0001g0092 | 2 | HG02486.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.510-469T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206530416 | ||||||
| chr2:206530436
|
T | C | 1 | a0001c0001t0001g0226 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.510-449T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206530436 | ||||||
| chr2:206530516
|
T | C | 4 | a0001c0001t0001g0197a0001c0002t0002g0198a0001c0002t0002g0199others(1): Show | 4 | NA18956.hp1 NA18964.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.510-369T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206530516 | ||||||
| chr2:206530536
|
C | T | 1 | a0001c0002t0003g0164 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.510-349C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206530536 | ||||||
| chr2:206530541
|
G | A | 1 | a0001c0002t0002g0320 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.510-344G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206530541 | ||||||
| chr2:206530616
|
A | G | 2 | a0001c0001t0002g0209a0001c0001t0002g0326 | 2 | NA19057.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.510-269A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206530616 | ||||||
| chr2:206530621
|
GA | G | 195 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(192): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.510-247delA | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206530621 | |||||
| chr2:206530669
|
C | CT | 77 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0045others(74): Show | 79 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.510-194dupT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206530669 | |||||
| chr2:206530669
|
C | CTT | 6 | a0001c0001t0006g0345a0001c0001t0006g0348a0001c0001t0006g0349others(3): Show | 6 | HG01081.hp1 HG01496.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.510-195_510-194dup others(2): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206530669 | |||||
| chr2:206530669
|
CT | C | 17 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0025others(14): Show | 18 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.510-194delT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206530669 | |||||
| chr2:206530694
|
G | C | 1 | a0001c0001t0001g0310 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.510-191G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206530694 | ||||||
| chr2:206530695
|
C | T | 1 | a0001c0001t0001g0310 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.510-190C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206530695 | ||||||
| chr2:206530768
|
C | G | 1 | a0001c0001t0001g0226 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.510-117C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206530768 | ||||||
| chr2:206530806
|
G | A | 1 | a0001c0001t0037g0228 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.510-79G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206530806 | ||||||
| chr2:206530978
|
A | G | 20 | a0001c0001t0002g0139a0001c0001t0005g0145a0001c0002t0001g0150others(17): Show | 21 | HG00558.hp1 HG01975.hp2 HG02056.hp2 others(18): Show |
intron_variant | MODIFIER | c.573+30A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206530978 | ||||||
| chr2:206531105
|
A | G | 68 | a0001c0001t0001g0036a0001c0001t0001g0069a0001c0001t0001g0173others(65): Show | 68 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.573+157A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206531105 | ||||||
| chr2:206531168
|
G | T | 8 | a0001c0001t0006g0345a0001c0001t0006g0348a0001c0001t0006g0349others(5): Show | 8 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.573+220G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206531168 | ||||||
| chr2:206531177
|
T | C | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.573+229T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206531177 | ||||||
| chr2:206531207
|
C | T | 1 | a0001c0001t0043g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.573+259C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206531207 | ||||||
| chr2:206531256
|
A | G | 1 | a0004c0006t0001g0044 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.573+308A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206531256 | ||||||
| chr2:206531376
|
T | C | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.573+428T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206531376 | ||||||
| chr2:206531504
|
G | A | 201 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(198): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.573+556G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206531504 | ||||||
| chr2:206532133
|
G | A | 2 | a0001c0001t0001g0173a0001c0001t0001g0331 | 2 | HG01884.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.573+1185G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206532133 | ||||||
| chr2:206532300
|
G | A | 1 | a0001c0002t0029g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.573+1352G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206532300 | ||||||
| chr2:206532325
|
CT | C | 8 | a0001c0001t0001g0100a0001c0001t0001g0130a0001c0001t0001g0314others(5): Show | 8 | HG00544.hp2 HG01169.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.573+1392delT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206532325 | |||||
| chr2:206532566
|
C | T | 5 | a0001c0001t0026g0299a0001c0002t0002g0302a0001c0002t0011g0186others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.573+1618C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206532566 | ||||||
| chr2:206532703
|
G | A | 65 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(62): Show | 67 | HG00280.hp2 HG00544.hp2 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.573+1755G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206532703 | ||||||
| chr2:206532760
|
C | G | 1 | a0001c0001t0002g0233 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.573+1812C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206532760 | ||||||
| chr2:206533033
|
T | C | 3 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125 | 3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.573+2085T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206533033 | ||||||
| chr2:206533055
|
A | G | 3 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125 | 3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.573+2107A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206533055 | ||||||
| chr2:206533078
|
A | G | 1 | a0001c0002t0029g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.573+2130A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206533078 | ||||||
| chr2:206533239
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.573+2291C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206533239 | ||||||
| chr2:206533399
|
T | C | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.573+2451T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206533399 | ||||||
| chr2:206533514
|
A | G | 20 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0308others(17): Show | 20 | HG02258.hp1 HG02451.hp2 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.573+2566A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206533514 | ||||||
| chr2:206533579
|
G | A | 1 | a0001c0002t0002g0066 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.573+2631G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206533579 | ||||||
| chr2:206533610
|
G | T | 16 | a0001c0001t0001g0088a0001c0001t0001g0098a0001c0001t0001g0105others(13): Show | 16 | HG00438.hp1 HG00642.hp2 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.573+2662G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206533610 | ||||||
| chr2:206533833
|
C | A | 189 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(186): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.573+2885C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206533833 | ||||||
| chr2:206534161
|
A | C | 6 | a0001c0001t0001g0122a0001c0001t0001g0127a0001c0001t0001g0128others(3): Show | 6 | NA18940.hp2 NA18988.hp1 NA19003.hp1 others(3): Show |
intron_variant | MODIFIER | c.573+3213A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206534161 | ||||||
| chr2:206534166
|
C | T | 1 | a0001c0002t0003g0174 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.573+3218C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206534166 | ||||||
| chr2:206534170
|
C | T | 31 | a0001c0001t0001g0004a0001c0001t0001g0088a0001c0001t0001g0094others(28): Show | 32 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.573+3222C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206534170 | ||||||
| chr2:206534191
|
A | G | 60 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0048others(57): Show | 61 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.573+3243A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206534191 | ||||||
| chr2:206534199
|
C | T | 1 | a0001c0001t0016g0234 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.573+3251C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206534199 | ||||||
| chr2:206534344
|
T | C | 60 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0048others(57): Show | 61 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.573+3396T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206534344 | ||||||
| chr2:206534481
|
C | CT | 7 | a0001c0002t0001g0257a0001c0002t0001g0258a0001c0002t0001g0259others(4): Show | 7 | HG02055.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.573+3545dupT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206534481 | |||||
| chr2:206534519
|
C | G | 1 | a0001c0002t0002g0143 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.573+3571C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206534519 | ||||||
| chr2:206534643
|
G | A | 3 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125 | 3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.573+3695G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206534643 | ||||||
| chr2:206534798
|
A | G | 5 | a0001c0002t0002g0141a0001c0002t0002g0142a0001c0002t0002g0143others(2): Show | 5 | NA18959.hp1 NA18965.hp1 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.573+3850A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206534798 | ||||||
| chr2:206534964
|
C | CT | 22 | a0001c0001t0001g0006a0001c0001t0001g0170a0001c0001t0034g0079others(19): Show | 23 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.573+4026dupT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206534964 | |||||
| chr2:206535019
|
T | C | 1 | a0001c0001t0001g0045 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.573+4071T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206535019 | ||||||
| chr2:206535152
|
T | C | 2 | a0001c0001t0020g0151a0001c0002t0001g0092 | 2 | HG02486.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.573+4204T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206535152 | ||||||
| chr2:206535183
|
T | C | 69 | a0001c0001t0001g0036a0001c0001t0001g0069a0001c0001t0001g0173others(66): Show | 69 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.573+4235T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206535183 | ||||||
| chr2:206535191
|
G | T | 2 | a0001c0001t0002g0139a0001c0002t0002g0138 | 2 | HG01975.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.573+4243G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206535191 | ||||||
| chr2:206535315
|
C | T | 1 | a0001c0001t0002g0254 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.573+4367C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206535315 | ||||||
| chr2:206535451
|
C | T | 202 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(199): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.573+4503C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206535451 | ||||||
| chr2:206535566
|
A | G | 1 | a0001c0001t0002g0233 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.573+4618A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206535566 | ||||||
| chr2:206535569
|
G | A | 1 | a0001c0001t0024g0273 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.573+4621G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206535569 | ||||||
| chr2:206535706
|
G | A | 3 | a0001c0002t0002g0032a0001c0002t0002g0033a0001c0002t0002g0172 | 3 | HG02109.hp1 HG03540.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.573+4758G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206535706 | ||||||
| chr2:206535720
|
G | A | 1 | a0001c0001t0001g0055 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.573+4772G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206535720 | ||||||
| chr2:206535728
|
T | A | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.573+4780T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206535728 | ||||||
| chr2:206535758
|
A | G | 1 | a0001c0002t0029g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.573+4810A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206535758 | ||||||
| chr2:206535903
|
T | C | 1 | a0001c0001t0002g0333 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.573+4955T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206535903 | ||||||
| chr2:206535951
|
A | G | 8 | a0001c0001t0006g0345a0001c0001t0006g0348a0001c0001t0006g0349others(5): Show | 8 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.573+5003A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206535951 | ||||||
| chr2:206536124
|
T | C | 17 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0025others(14): Show | 18 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.573+5176T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206536124 | ||||||
| chr2:206536225
|
T | TTG | 12 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0025others(9): Show | 13 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.573+5293_573+5294d others(4): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206536225 | |||||
| chr2:206536226
|
T | C | 1 | a0001c0002t0029g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.573+5278T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206536226 | ||||||
| chr2:206536282
|
C | T | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.573+5334C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206536282 | ||||||
| chr2:206536299
|
T | A | 1 | a0001c0001t0002g0123 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.573+5351T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206536299 | ||||||
| chr2:206536331
|
G | A | 1 | a0001c0001t0001g0300 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.573+5383G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206536331 | ||||||
| chr2:206536383
|
A | G | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.573+5435A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206536383 | ||||||
| chr2:206536399
|
T | A | 54 | a0001c0001t0001g0006a0001c0001t0001g0170a0001c0001t0005g0145others(51): Show | 56 | HG00280.hp1 HG00558.hp1 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.573+5451T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206536399 | ||||||
| chr2:206536476
|
G | T | 2 | a0001c0001t0016g0234a0001c0001t0016g0235 | 2 | HG00140.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.573+5528G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206536476 | ||||||
| chr2:206536643
|
T | A | 1 | a0001c0001t0004g0177 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.574-5409T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206536643 | ||||||
| chr2:206536756
|
A | G | 1 | a0001c0001t0002g0191 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.574-5296A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206536756 | ||||||
| chr2:206536814
|
T | C | 3 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0024 | 3 | HG02145.hp1 HG03041.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.574-5238T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206536814 | ||||||
| chr2:206536862
|
C | T | 1 | a0001c0001t0002g0014 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.574-5190C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206536862 | ||||||
| chr2:206536894
|
C | T | 1 | a0001c0001t0004g0177 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.574-5158C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206536894 | ||||||
| chr2:206537543
|
C | T | 2 | a0001c0001t0034g0079a0001c0001t0035g0078 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.574-4509C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206537543 | ||||||
| chr2:206537710
|
A | G | 37 | a0001c0001t0001g0190a0001c0001t0001g0203a0001c0001t0001g0208others(34): Show | 37 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.574-4342A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206537710 | ||||||
| chr2:206537760
|
T | C | 1 | a0001c0001t0001g0084 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.574-4292T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206537760 | ||||||
| chr2:206537813
|
T | A | 1 | a0001c0001t0002g0244 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.574-4239T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206537813 | ||||||
| chr2:206537848
|
A | G | 1 | a0001c0002t0003g0174 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.574-4204A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206537848 | ||||||
| chr2:206537880
|
C | G | 23 | a0001c0001t0002g0209a0001c0001t0002g0326a0001c0001t0021g0196others(20): Show | 23 | HG00673.hp2 HG02145.hp1 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.574-4172C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206537880 | ||||||
| chr2:206538037
|
A | C | 1 | a0001c0001t0002g0333 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.574-4015A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206538037 | ||||||
| chr2:206538056
|
A | G | 1 | a0001c0002t0002g0302 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.574-3996A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206538056 | ||||||
| chr2:206538326
|
A | G | 4 | a0001c0001t0004g0177a0001c0001t0004g0223a0001c0001t0004g0224others(1): Show | 4 | HG02071.hp1 HG02165.hp2 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-3726A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206538326 | ||||||
| chr2:206538470
|
G | A | 188 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(185): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.574-3582G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206538470 | ||||||
| chr2:206538570
|
T | C | 20 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0308others(17): Show | 20 | HG02258.hp1 HG02451.hp2 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.574-3482T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206538570 | ||||||
| chr2:206538619
|
G | A | 2 | a0001c0002t0019g0189a0001c0002t0019g0325 | 2 | HG02055.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.574-3433G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206538619 | ||||||
| chr2:206538633
|
G | A | 3 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125 | 3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.574-3419G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206538633 | ||||||
| chr2:206538853
|
A | G | 11 | a0001c0001t0005g0213a0001c0001t0005g0214a0001c0001t0005g0215others(8): Show | 11 | HG00609.hp1 HG03669.hp1 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.574-3199A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206538853 | ||||||
| chr2:206539006
|
C | A | 11 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0025others(8): Show | 12 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.574-3046C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206539006 | ||||||
| chr2:206539108
|
A | G | 1 | a0001c0001t0033g0294 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.574-2944A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206539108 | ||||||
| chr2:206539123
|
G | C | 6 | a0001c0001t0001g0122a0001c0001t0001g0127a0001c0001t0001g0128others(3): Show | 6 | NA18940.hp2 NA18988.hp1 NA19003.hp1 others(3): Show |
intron_variant | MODIFIER | c.574-2929G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206539123 | ||||||
| chr2:206539262
|
G | T | 1 | a0001c0001t0001g0043 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.574-2790G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206539262 | ||||||
| chr2:206539293
|
C | T | 2 | a0001c0001t0001g0101a0001c0001t0001g0103 | 2 | HG01358.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.574-2759C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206539293 | ||||||
| chr2:206539321
|
C | T | 65 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(62): Show | 67 | HG00280.hp2 HG00544.hp2 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.574-2731C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206539321 | ||||||
| chr2:206539626
|
C | T | 47 | a0001c0001t0001g0004a0001c0001t0001g0088a0001c0001t0001g0094others(44): Show | 48 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.574-2426C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206539626 | ||||||
| chr2:206540064
|
C | A | 69 | a0001c0001t0001g0036a0001c0001t0001g0069a0001c0001t0001g0173others(66): Show | 69 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.574-1988C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206540064 | ||||||
| chr2:206540076
|
G | A | 54 | a0001c0001t0001g0006a0001c0001t0001g0170a0001c0001t0005g0145others(51): Show | 56 | HG00280.hp1 HG00558.hp1 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.574-1976G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206540076 | ||||||
| chr2:206540160
|
C | T | 3 | a0001c0001t0001g0288a0001c0001t0001g0291a0001c0001t0001g0334 | 3 | NA18995.hp1 NA19005.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.574-1892C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206540160 | ||||||
| chr2:206540187
|
G | T | 1 | a0001c0001t0002g0216 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.574-1865G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206540187 | ||||||
| chr2:206540216
|
T | TAC | 27 | a0001c0001t0001g0087a0001c0001t0001g0197a0001c0001t0001g0237others(24): Show | 27 | HG00438.hp2 HG01099.hp2 HG01358.hp2 others(24): Show |
intron_variant | MODIFIER | c.574-1784_574-1783d others(4): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206540216 | |||||
| chr2:206540216
|
T | TACAC | 16 | a0001c0001t0001g0089a0001c0001t0001g0232a0001c0001t0001g0312others(13): Show | 16 | HG00673.hp2 HG00733.hp2 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.574-1786_574-1783d others(6): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206540216 | |||||
| chr2:206540216
|
T | TACACAC | 11 | a0001c0001t0001g0192a0001c0001t0001g0308a0001c0001t0001g0319others(8): Show | 11 | HG02258.hp1 HG02451.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.574-1788_574-1783d others(8): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206540216 | |||||
| chr2:206540216
|
T | TACACACA others(1): Show |
7 | a0001c0001t0001g0335a0001c0001t0001g0337a0001c0001t0002g0193others(4): Show | 7 | HG01261.hp2 HG01884.hp1 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.574-1790_574-1783d others(10): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206540216 | |||||
| chr2:206540216
|
T | TACACACA others(3): Show |
6 | a0001c0001t0001g0180a0001c0001t0002g0139a0001c0001t0035g0078others(3): Show | 6 | HG01975.hp2 HG02109.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.574-1792_574-1783d others(12): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206540216 | |||||
| chr2:206540216
|
T | TACACACA others(5): Show |
3 | a0001c0001t0036g0270a0001c0001t0043g0019a0001c0002t0010g0207 | 3 | HG01106.hp2 HG06807.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.574-1794_574-1783d others(14): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206540216 | |||||
| chr2:206540216
|
T | TACACACA others(11): Show |
1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.574-1800_574-1783d others(20): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206540216 | |||||
| chr2:206540216
|
TAC | T | 69 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0015others(66): Show | 71 | HG00280.hp1 HG00609.hp1 HG00738.hp2 others(68): Show |
intron_variant | MODIFIER | c.574-1784_574-1783d others(4): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206540216 | |||||
| chr2:206540216
|
TACAC | T | 36 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0027others(33): Show | 36 | HG00140.hp2 HG00280.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.574-1786_574-1783d others(6): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206540216 | |||||
| chr2:206540216
|
TACACAC | T | 23 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0081others(20): Show | 24 | HG00099.hp2 HG00609.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.574-1788_574-1783d others(8): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206540216 | |||||
| chr2:206540216
|
TACACACA others(1): Show |
T | 38 | a0001c0001t0001g0063a0001c0001t0001g0122a0001c0001t0001g0127others(35): Show | 38 | HG00544.hp1 HG01069.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.574-1790_574-1783d others(10): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206540216 | |||||
| chr2:206540216
|
TACACACA others(3): Show |
T | 6 | a0001c0001t0001g0110a0001c0001t0001g0190a0001c0001t0001g0290others(3): Show | 6 | HG00323.hp1 HG00738.hp1 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.574-1792_574-1783d others(12): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206540216 | |||||
| chr2:206540216
|
TACACACA others(5): Show |
T | 42 | a0001c0001t0001g0004a0001c0001t0001g0036a0001c0001t0001g0069others(39): Show | 43 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.574-1794_574-1783d others(14): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206540216 | |||||
| chr2:206540216
|
TACACACA others(7): Show |
T | 2 | a0001c0001t0001g0103a0001c0001t0001g0184 | 2 | HG02148.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.574-1796_574-1783d others(16): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206540216 | |||||
| chr2:206540216
|
TACACACA others(11): Show |
T | 1 | a0001c0001t0033g0294 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.574-1800_574-1783d others(20): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206540216 | |||||
| chr2:206540216
|
TACACACA others(13): Show |
T | 4 | a0001c0001t0012g0304a0001c0001t0012g0305a0001c0001t0012g0306others(1): Show | 4 | HG01361.hp2 HG01433.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-1802_574-1783d others(22): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206540216 | |||||
| chr2:206540216
|
TACACACA others(15): Show |
T | 2 | a0001c0001t0001g0155a0001c0001t0020g0151 | 2 | HG02486.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.574-1804_574-1783d others(24): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206540216 | |||||
| chr2:206540373
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.574-1679T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206540373 | ||||||
| chr2:206540471
|
A | G | 2 | a0001c0001t0001g0263a0001c0001t0001g0275 | 2 | NA18956.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.574-1581A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206540471 | ||||||
| chr2:206540497
|
A | C | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.574-1555A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206540497 | ||||||
| chr2:206540633
|
C | T | 1 | a0001c0002t0002g0077 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.574-1419C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206540633 | ||||||
| chr2:206540688
|
A | G | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.574-1364A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206540688 | ||||||
| chr2:206540739
|
A | G | 20 | a0001c0001t0001g0006a0001c0001t0001g0170a0001c0001t0034g0079others(17): Show | 21 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.574-1313A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206540739 | ||||||
| chr2:206540759
|
T | C | 1 | a0001c0002t0002g0307 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.574-1293T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206540759 | ||||||
| chr2:206540923
|
TTTA | T | 18 | a0001c0001t0001g0006a0001c0001t0001g0170a0001c0002t0003g0093others(15): Show | 19 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.574-1121_574-1119d others(5): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206540923 | |||||
| chr2:206540963
|
T | C | 1 | a0001c0002t0001g0150 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.574-1089T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206540963 | ||||||
| chr2:206541870
|
G | A | 12 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0025others(9): Show | 13 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.574-182G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206541870 | ||||||
| chr2:206541903
|
T | C | 1 | a0001c0001t0042g0295 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.574-149T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206541903 | ||||||
| chr2:206541970
|
ATTTCTTT others(5): Show |
A | 1 | a0001c0001t0020g0151 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.574-79_574-68delTC others(10): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206541970 | |||||
| chr2:206542023
|
A | G | 1 | a0005c0008t0005g0242 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.574-29A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206542023 | ||||||
| chr2:206542150
|
A | T | 1 | a0001c0002t0002g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.656+16A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 5/25 | chr2 | 206542150 | ||||||
| chr2:206542258
|
A | T | 1 | a0001c0001t0002g0035 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.656+124A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 5/25 | chr2 | 206542258 | ||||||
| chr2:206542572
|
G | A | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.656+438G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 5/25 | chr2 | 206542572 | ||||||
| chr2:206542583
|
G | A | 3 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125 | 3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.656+449G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 5/25 | chr2 | 206542583 | ||||||
| chr2:206542656
|
C | T | 2 | a0001c0001t0002g0139a0001c0002t0002g0138 | 2 | HG01975.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.656+522C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 5/25 | chr2 | 206542656 | ||||||
| chr2:206542785
|
G | A | 2 | a0001c0001t0034g0079a0001c0001t0035g0078 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.657-468G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 5/25 | chr2 | 206542785 | ||||||
| chr2:206543081
|
G | C | 3 | a0001c0001t0001g0005a0001c0001t0001g0155a0001c0001t0001g0171 | 4 | HG01074.hp2 HG01106.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.657-172G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 5/25 | chr2 | 206543081 | ||||||
| chr2:206543441
|
A | G | 2 | a0001c0001t0008g0023a0001c0001t0008g0330 | 2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.720+125A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206543441 | ||||||
| chr2:206543523
|
A | T | 1 | a0001c0001t0002g0225 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.720+207A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206543523 | ||||||
| chr2:206543617
|
C | G | 1 | a0001c0001t0001g0061 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.720+301C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206543617 | ||||||
| chr2:206543684
|
G | A | 1 | a0001c0001t0004g0177 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.720+368G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206543684 | ||||||
| chr2:206543750
|
T | TAC | 21 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0025others(18): Show | 22 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.720+453_720+454dup others(2): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr2 | 206543750 | |||||
| chr2:206543975
|
C | T | 2 | a0001c0001t0002g0261a0001c0001t0006g0345 | 2 | HG00438.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.720+659C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206543975 | ||||||
| chr2:206543976
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.720+660G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206543976 | ||||||
| chr2:206544269
|
C | T | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.720+953C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206544269 | ||||||
| chr2:206544439
|
T | C | 1 | a0001c0001t0002g0216 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.720+1123T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206544439 | ||||||
| chr2:206544551
|
G | A | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.720+1235G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206544551 | ||||||
| chr2:206544613
|
AT | A | 264 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(261): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.720+1316delT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr2 | 206544613 | |||||
| chr2:206544613
|
ATT | A | 33 | a0001c0001t0001g0271a0001c0001t0001g0308a0001c0001t0001g0309others(30): Show | 33 | HG00673.hp2 HG01169.hp2 HG02258.hp1 others(30): Show |
intron_variant | MODIFIER | c.720+1315_720+1316d others(4): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr2 | 206544613 | |||||
| chr2:206544713
|
C | T | 15 | a0001c0001t0002g0209a0001c0001t0002g0326a0001c0001t0021g0196others(12): Show | 15 | HG00673.hp2 HG02523.hp2 NA18747.hp1 others(12): Show |
intron_variant | MODIFIER | c.720+1397C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206544713 | ||||||
| chr2:206544718
|
T | G | 2 | a0001c0001t0028g0297a0001c0002t0029g0296 | 2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.720+1402T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206544718 | ||||||
| chr2:206544762
|
G | A | 5 | a0001c0001t0026g0299a0001c0002t0002g0302a0001c0002t0011g0186others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.720+1446G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206544762 | ||||||
| chr2:206544771
|
C | T | 1 | a0001c0001t0001g0303 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.720+1455C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206544771 | ||||||
| chr2:206544772
|
C | G | 1 | a0001c0001t0020g0329 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.720+1456C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206544772 | ||||||
| chr2:206545270
|
G | A | 1 | a0001c0001t0001g0317 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.720+1954G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206545270 | ||||||
| chr2:206545331
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.720+2015C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206545331 | ||||||
| chr2:206545475
|
G | A | 66 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(63): Show | 68 | HG00280.hp2 HG00544.hp2 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.721-1954G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206545475 | ||||||
| chr2:206545493
|
A | T | 3 | a0001c0001t0001g0005a0001c0001t0001g0155a0001c0001t0001g0184 | 4 | HG01074.hp2 HG01106.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.721-1936A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206545493 | ||||||
| chr2:206545496
|
T | C | 5 | a0001c0001t0026g0299a0001c0002t0002g0302a0001c0002t0011g0186others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.721-1933T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206545496 | ||||||
| chr2:206545497
|
T | A | 70 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(67): Show | 72 | HG00280.hp2 HG00544.hp2 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.721-1932T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206545497 | ||||||
| chr2:206545783
|
C | G | 1 | a0001c0001t0001g0168 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.721-1646C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206545783 | ||||||
| chr2:206545907
|
A | C | 1 | a0001c0001t0001g0285 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.721-1522A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206545907 | ||||||
| chr2:206546070
|
A | C | 2 | a0001c0002t0002g0200a0001c0002t0002g0201 | 2 | NA19088.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.721-1359A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206546070 | ||||||
| chr2:206546181
|
A | G | 21 | a0001c0001t0001g0006a0001c0001t0001g0170a0001c0001t0034g0079others(18): Show | 22 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.721-1248A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206546181 | ||||||
| chr2:206546234
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.721-1195C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206546234 | ||||||
| chr2:206546480
|
A | G | 1 | a0001c0001t0002g0191 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.721-949A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206546480 | ||||||
| chr2:206546588
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.721-841C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206546588 | ||||||
| chr2:206546591
|
C | G | 7 | a0001c0002t0001g0257a0001c0002t0001g0258a0001c0002t0001g0259others(4): Show | 7 | HG02055.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.721-838C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206546591 | ||||||
| chr2:206546778
|
G | T | 3 | a0001c0002t0002g0200a0001c0002t0002g0201a0001c0002t0002g0202 | 3 | NA18747.hp1 NA19088.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.721-651G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206546778 | ||||||
| chr2:206546935
|
T | C | 8 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0085others(5): Show | 9 | HG01952.hp2 HG02040.hp2 NA18946.hp2 others(6): Show |
intron_variant | MODIFIER | c.721-494T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206546935 | ||||||
| chr2:206547118
|
A | G | 1 | a0001c0001t0017g0038 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.721-311A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206547118 | ||||||
| chr2:206547516
|
A | C | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.793+15A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 7/25 | chr2 | 206547516 | ||||||
| chr2:206547598
|
G | A | 3 | a0001c0001t0001g0180a0001c0001t0008g0023a0001c0001t0008g0330 | 3 | HG02717.hp1 HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.793+97G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 7/25 | chr2 | 206547598 | ||||||
| chr2:206547726
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.793+225A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 7/25 | chr2 | 206547726 | ||||||
| chr2:206547955
|
G | T | 1 | a0001c0001t0001g0127 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.794-326G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 7/25 | chr2 | 206547955 | ||||||
| chr2:206547997
|
ATAG | A | 52 | a0001c0001t0001g0006a0001c0001t0001g0170a0001c0001t0005g0145others(49): Show | 54 | HG00280.hp1 HG00558.hp1 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.794-280_794-278del others(3): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr2 | 206547997 | |||||
| chr2:206548050
|
A | G | 1 | a0001c0001t0002g0022 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.794-231A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 7/25 | chr2 | 206548050 | ||||||
| chr2:206548153
|
T | A | 2 | a0001c0001t0001g0043a0001c0001t0001g0065 | 2 | HG02145.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.794-128T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 7/25 | chr2 | 206548153 | ||||||
| chr2:206548233
|
C | G | 1 | a0001c0001t0001g0154 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.794-48C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 7/25 | chr2 | 206548233 | ||||||
| chr2:206548372
|
C | T | 1 | a0001c0002t0002g0320 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.867+18C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 8/25 | chr2 | 206548372 | ||||||
| chr2:206548425
|
A | G | 1 | a0001c0001t0009g0018 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.867+71A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 8/25 | chr2 | 206548425 | ||||||
| chr2:206548446
|
T | G | 12 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0025others(9): Show | 13 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.867+92T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 8/25 | chr2 | 206548446 | ||||||
| chr2:206548649
|
G | A | 4 | a0001c0002t0002g0032a0001c0002t0002g0033a0001c0002t0014g0020others(1): Show | 4 | HG03486.hp2 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.867+295G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 8/25 | chr2 | 206548649 | ||||||
| chr2:206548678
|
C | T | 3 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0041g0028 | 3 | HG00642.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.867+324C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 8/25 | chr2 | 206548678 | ||||||
| chr2:206548689
|
A | G | 1 | a0001c0001t0002g0191 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.867+335A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 8/25 | chr2 | 206548689 | ||||||
| chr2:206548874
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.867+520A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 8/25 | chr2 | 206548874 | ||||||
| chr2:206548901
|
G | A | 66 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(63): Show | 69 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.867+547G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 8/25 | chr2 | 206548901 | ||||||
| chr2:206548986
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.867+632C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 8/25 | chr2 | 206548986 | ||||||
| chr2:206549080
|
A | G | 1 | a0001c0002t0002g0147 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.867+726A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 8/25 | chr2 | 206549080 | ||||||
| chr2:206549131
|
T | C | 1 | a0001c0002t0002g0320 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.867+777T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 8/25 | chr2 | 206549131 | ||||||
| chr2:206549219
|
T | A | 6 | a0001c0001t0006g0345a0001c0001t0006g0348a0001c0001t0006g0349others(3): Show | 6 | HG01081.hp1 HG01496.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.867+865T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 8/25 | chr2 | 206549219 | ||||||
| chr2:206549402
|
G | A | 1 | a0001c0001t0002g0239 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.868-693G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 8/25 | chr2 | 206549402 | ||||||
| chr2:206549643
|
T | A | 1 | a0001c0001t0016g0235 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.868-452T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 8/25 | chr2 | 206549643 | ||||||
| chr2:206549687
|
A | G | 2 | a0001c0001t0008g0023a0001c0001t0008g0330 | 2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.868-408A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 8/25 | chr2 | 206549687 | ||||||
| chr2:206549720
|
A | G | 1 | a0001c0001t0001g0025 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.868-375A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 8/25 | chr2 | 206549720 | ||||||
| chr2:206549877
|
G | A | 196 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(193): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.868-218G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 8/25 | chr2 | 206549877 | ||||||
| chr2:206550298
|
C | T | 1 | a0001c0001t0024g0273 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.933+138C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206550298 | ||||||
| chr2:206550299
|
G | A | 1 | a0001c0001t0004g0223 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.933+139G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206550299 | ||||||
| chr2:206550345
|
T | C | 2 | a0001c0002t0010g0207a0001c0002t0010g0210 | 2 | NA18951.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.933+185T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206550345 | ||||||
| chr2:206550599
|
C | CT | 22 | a0001c0001t0001g0060a0001c0001t0001g0103a0001c0001t0001g0232others(19): Show | 22 | HG02056.hp2 HG02109.hp2 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.933+457dupT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr2 | 206550599 | |||||
| chr2:206550680
|
C | T | 1 | a0001c0001t0001g0286 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.933+520C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206550680 | ||||||
| chr2:206550763
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.933+603G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206550763 | ||||||
| chr2:206550938
|
C | G | 2 | a0001c0001t0002g0035a0001c0002t0002g0307 | 2 | HG02257.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.933+778C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206550938 | ||||||
| chr2:206551180
|
T | C | 1 | a0002c0003t0001g0062 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.933+1020T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206551180 | ||||||
| chr2:206551296
|
G | A | 1 | a0001c0001t0004g0250 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.933+1136G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206551296 | ||||||
| chr2:206551305
|
C | T | 4 | a0001c0001t0004g0177a0001c0001t0004g0223a0001c0001t0004g0224others(1): Show | 4 | HG02071.hp1 HG02165.hp2 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.933+1145C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206551305 | ||||||
| chr2:206551402
|
A | G | 1 | a0001c0002t0002g0204 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.933+1242A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206551402 | ||||||
| chr2:206551450
|
G | A | 3 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125 | 3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.933+1290G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206551450 | ||||||
| chr2:206551598
|
C | T | 8 | a0001c0001t0006g0345a0001c0001t0006g0348a0001c0001t0006g0349others(5): Show | 8 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.933+1438C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206551598 | ||||||
| chr2:206551604
|
T | C | 1 | a0001c0001t0001g0127 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.933+1444T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206551604 | ||||||
| chr2:206551967
|
C | A | 12 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0025others(9): Show | 13 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.933+1807C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206551967 | ||||||
| chr2:206552008
|
G | C | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.933+1848G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206552008 | ||||||
| chr2:206552272
|
T | C | 1 | a0001c0001t0001g0113 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.933+2112T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206552272 | ||||||
| chr2:206552739
|
G | A | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.933+2579G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206552739 | ||||||
| chr2:206552800
|
T | C | 17 | a0001c0001t0001g0181a0001c0001t0001g0308a0001c0001t0001g0309others(14): Show | 17 | HG02258.hp1 HG02451.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.933+2640T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206552800 | ||||||
| chr2:206552836
|
AT | A | 231 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(228): Show | 236 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.933+2688delT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr2 | 206552836 | |||||
| chr2:206552860
|
G | A | 4 | a0001c0002t0002g0074a0001c0002t0002g0077a0001c0002t0022g0075others(1): Show | 4 | HG02056.hp2 NA19000.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.933+2700G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206552860 | ||||||
| chr2:206552907
|
A | T | 1 | a0001c0001t0001g0129 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.933+2747A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206552907 | ||||||
| chr2:206552948
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017 | 3 | NA18961.hp1 NA19011.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.933+2788G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206552948 | ||||||
| chr2:206553051
|
G | A | 3 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125 | 3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.933+2891G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553051 | ||||||
| chr2:206553068
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.933+2908G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553068 | ||||||
| chr2:206553069
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.933+2909G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553069 | ||||||
| chr2:206553070
|
G | T | 1 | a0001c0001t0001g0099 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.933+2910G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553070 | ||||||
| chr2:206553102
|
G | A | 12 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0025others(9): Show | 13 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.933+2942G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553102 | ||||||
| chr2:206553125
|
C | T | 2 | a0001c0001t0002g0333a0001c0001t0020g0329 | 2 | HG00738.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.933+2965C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553125 | ||||||
| chr2:206553196
|
G | A | 1 | a0001c0001t0001g0015 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.933+3036G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553196 | ||||||
| chr2:206553197
|
G | A | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 115 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.933+3037G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553197 | ||||||
| chr2:206553268
|
T | A | 1 | a0001c0001t0001g0331 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.933+3108T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553268 | ||||||
| chr2:206553279
|
T | A | 1 | a0001c0001t0001g0280 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.933+3119T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553279 | ||||||
| chr2:206553293
|
G | A | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.933+3133G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553293 | ||||||
| chr2:206553302
|
G | A | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.933+3142G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553302 | ||||||
| chr2:206553353
|
T | G | 1 | a0001c0001t0001g0088 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.933+3193T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553353 | ||||||
| chr2:206553404
|
C | T | 65 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(62): Show | 67 | HG00280.hp2 HG00544.hp2 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.933+3244C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553404 | ||||||
| chr2:206553525
|
C | G | 43 | a0001c0001t0001g0004a0001c0001t0001g0088a0001c0001t0001g0094others(40): Show | 44 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.933+3365C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553525 | ||||||
| chr2:206553606
|
A | T | 254 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(251): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.933+3446A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553606 | ||||||
| chr2:206553732
|
G | A | 1 | a0001c0001t0001g0256 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.933+3572G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553732 | ||||||
| chr2:206553755
|
G | C | 20 | a0001c0001t0005g0145a0001c0002t0001g0150a0001c0002t0002g0001others(17): Show | 21 | HG00558.hp1 HG02056.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.933+3595G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553755 | ||||||
| chr2:206553811
|
G | T | 11 | a0001c0001t0005g0213a0001c0001t0005g0214a0001c0001t0005g0215others(8): Show | 11 | HG00609.hp1 HG03669.hp1 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.934-3616G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553811 | ||||||
| chr2:206553840
|
G | A | 3 | a0001c0001t0009g0018a0001c0001t0009g0057a0001c0001t0032g0056 | 3 | HG00544.hp2 NA18957.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.934-3587G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553840 | ||||||
| chr2:206553865
|
C | G | 1 | a0001c0001t0024g0273 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.934-3562C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553865 | ||||||
| chr2:206553870
|
C | T | 52 | a0001c0001t0001g0006a0001c0001t0001g0170a0001c0001t0005g0145others(49): Show | 54 | HG00280.hp1 HG00558.hp1 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.934-3557C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553870 | ||||||
| chr2:206553871
|
G | T | 12 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0025others(9): Show | 13 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.934-3556G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553871 | ||||||
| chr2:206553926
|
A | C | 8 | a0001c0001t0006g0345a0001c0001t0006g0348a0001c0001t0006g0349others(5): Show | 8 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.934-3501A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553926 | ||||||
| chr2:206553962
|
A | G | 1 | a0002c0003t0001g0062 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.934-3465A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553962 | ||||||
| chr2:206554175
|
C | T | 37 | a0001c0001t0001g0190a0001c0001t0001g0203a0001c0001t0001g0208others(34): Show | 37 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.934-3252C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206554175 | ||||||
| chr2:206554365
|
A | T | 2 | a0001c0001t0002g0176a0001c0001t0002g0212 | 2 | NA19003.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.934-3062A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206554365 | ||||||
| chr2:206554734
|
A | T | 1 | a0001c0001t0001g0100 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.934-2693A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206554734 | ||||||
| chr2:206554788
|
A | C | 1 | a0001c0001t0020g0329 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.934-2639A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206554788 | ||||||
| chr2:206554878
|
C | T | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.934-2549C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206554878 | ||||||
| chr2:206555183
|
A | G | 1 | a0001c0001t0002g0233 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.934-2244A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206555183 | ||||||
| chr2:206555383
|
C | T | 1 | a0001c0001t0033g0294 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.934-2044C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206555383 | ||||||
| chr2:206555592
|
A | G | 12 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0025others(9): Show | 13 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.934-1835A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206555592 | ||||||
| chr2:206555811
|
G | C | 2 | a0001c0001t0034g0079a0001c0001t0035g0078 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.934-1616G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206555811 | ||||||
| chr2:206555827
|
C | T | 2 | a0001c0002t0022g0075a0001c0002t0022g0076 | 2 | HG02056.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.934-1600C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206555827 | ||||||
| chr2:206555830
|
A | C | 1 | a0001c0001t0002g0216 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.934-1597A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206555830 | ||||||
| chr2:206555965
|
A | G | 1 | a0001c0001t0006g0352 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.934-1462A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206555965 | ||||||
| chr2:206556203
|
AATTT | A | 3 | a0001c0001t0001g0185a0001c0001t0001g0264a0001c0001t0001g0265 | 3 | HG02055.hp2 HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.934-1218_934-1215d others(6): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr2 | 206556203 | |||||
| chr2:206556254
|
A | G | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.934-1173A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206556254 | ||||||
| chr2:206556682
|
T | C | 1 | a0001c0001t0002g0233 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.934-745T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206556682 | ||||||
| chr2:206557076
|
C | T | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.934-351C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206557076 | ||||||
| chr2:206557137
|
T | C | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.934-290T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206557137 | ||||||
| chr2:206557156
|
C | G | 1 | a0001c0001t0001g0017 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.934-271C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206557156 | ||||||
| chr2:206557601
|
A | G | 8 | a0001c0001t0006g0345a0001c0001t0006g0348a0001c0001t0006g0349others(5): Show | 8 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1005+103A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 10/25 | chr2 | 206557601 | ||||||
| chr2:206557880
|
G | A | 61 | a0001c0001t0001g0036a0001c0001t0001g0069a0001c0001t0001g0173others(58): Show | 61 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.1005+382G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 10/25 | chr2 | 206557880 | ||||||
| chr2:206557957
|
G | C | 1 | a0001c0001t0001g0331 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1005+459G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 10/25 | chr2 | 206557957 | ||||||
| chr2:206558040
|
A | C | 1 | a0001c0001t0006g0345 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1005+542A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 10/25 | chr2 | 206558040 | ||||||
| chr2:206558183
|
T | A | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1005+685T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 10/25 | chr2 | 206558183 | ||||||
| chr2:206558243
|
G | T | 2 | a0001c0002t0010g0207a0001c0002t0010g0210 | 2 | NA18951.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.1005+745G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 10/25 | chr2 | 206558243 | ||||||
| chr2:206558349
|
A | G | 1 | a0001c0001t0004g0253 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1005+851A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 10/25 | chr2 | 206558349 | ||||||
| chr2:206558382
|
A | T | 2 | a0001c0001t0008g0023a0001c0001t0008g0330 | 2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1005+884A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 10/25 | chr2 | 206558382 | ||||||
| chr2:206558919
|
GTTTT | G | 35 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0043others(32): Show | 35 | HG00280.hp2 HG01255.hp1 HG01361.hp2 others(32): Show |
intron_variant | MODIFIER | c.1006-1034_1006-103 others(8): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr2 | 206558919 | |||||
| chr2:206558921
|
T | G | 52 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(49): Show | 54 | HG00544.hp2 HG00642.hp1 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.1006-1034T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 10/25 | chr2 | 206558921 | ||||||
| chr2:206558921
|
TTTTG | T | 13 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0154others(10): Show | 14 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.1006-1002_1006-999 others(7): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr2 | 206558921 | |||||
| chr2:206558921
|
TTTTGTTT others(1): Show |
T | 55 | a0001c0001t0001g0004a0001c0001t0001g0088a0001c0001t0001g0094others(52): Show | 56 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.1006-1006_1006-999 others(11): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr2 | 206558921 | |||||
| chr2:206558923
|
T | G | 3 | a0001c0001t0026g0299a0001c0002t0002g0302a0001c0002t0011g0298 | 3 | HG03195.hp1 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1006-1032T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 10/25 | chr2 | 206558923 | ||||||
| chr2:206558931
|
T | G | 2 | a0001c0002t0011g0186a0001c0002t0011g0187 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1006-1024T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 10/25 | chr2 | 206558931 | ||||||
| chr2:206559071
|
A | C | 12 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0025others(9): Show | 13 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.1006-884A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 10/25 | chr2 | 206559071 | ||||||
| chr2:206559196
|
G | T | 1 | a0001c0001t0001g0129 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1006-759G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 10/25 | chr2 | 206559196 | ||||||
| chr2:206559463
|
A | G | 1 | a0001c0001t0018g0274 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1006-492A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 10/25 | chr2 | 206559463 | ||||||
| chr2:206559549
|
T | C | 1 | a0001c0002t0029g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1006-406T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 10/25 | chr2 | 206559549 | ||||||
| chr2:206559660
|
T | C | 1 | a0001c0002t0002g0144 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1006-295T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 10/25 | chr2 | 206559660 | ||||||
| chr2:206560140
|
T | C | 4 | a0001c0001t0001g0036a0001c0001t0001g0069a0001c0001t0001g0173others(1): Show | 4 | HG01884.hp2 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1169+22T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 11/25 | chr2 | 206560140 | ||||||
| chr2:206560188
|
G | T | 2 | a0001c0001t0001g0154a0001c0001t0001g0169 | 2 | HG01070.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.1169+70G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 11/25 | chr2 | 206560188 | ||||||
| chr2:206560370
|
T | C | 65 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(62): Show | 67 | HG00280.hp2 HG00544.hp2 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.1169+252T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 11/25 | chr2 | 206560370 | ||||||
| chr2:206560377
|
C | T | 2 | a0001c0001t0002g0035a0001c0002t0002g0307 | 2 | HG02257.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1169+259C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 11/25 | chr2 | 206560377 | ||||||
| chr2:206560447
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0041g0028 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1169+329G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 11/25 | chr2 | 206560447 | ||||||
| chr2:206560514
|
C | G | 1 | a0001c0001t0001g0058 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1169+396C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 11/25 | chr2 | 206560514 | ||||||
| chr2:206561085
|
G | A | 1 | a0001c0001t0001g0335 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1170-43G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 11/25 | chr2 | 206561085 | ||||||
| chr2:206561452
|
A | T | 1 | a0001c0001t0008g0023 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1254+240A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 12/25 | chr2 | 206561452 | ||||||
| chr2:206561579
|
A | G | 3 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125 | 3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1254+367A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 12/25 | chr2 | 206561579 | ||||||
| chr2:206561593
|
T | A | 5 | a0001c0001t0001g0308a0001c0001t0001g0311a0001c0001t0001g0312others(2): Show | 5 | HG02451.hp2 HG02976.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1254+381T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 12/25 | chr2 | 206561593 | ||||||
| chr2:206561683
|
CATT | C | 3 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125 | 3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1254+472_1254+474d others(5): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 12/25 | chr2 | 206561683 | ||||||
| chr2:206561703
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1254+491T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 12/25 | chr2 | 206561703 | ||||||
| chr2:206561869
|
G | T | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017 | 3 | NA18961.hp1 NA19011.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1255-334G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 12/25 | chr2 | 206561869 | ||||||
| chr2:206561880
|
A | G | 54 | a0001c0001t0001g0006a0001c0001t0001g0170a0001c0001t0002g0301others(51): Show | 56 | HG00280.hp1 HG00558.hp1 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.1255-323A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 12/25 | chr2 | 206561880 | ||||||
| chr2:206562377
|
A | T | 12 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0025others(9): Show | 13 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.1345+84A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206562377 | ||||||
| chr2:206562607
|
C | T | 1 | a0001c0001t0002g0194 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1345+314C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206562607 | ||||||
| chr2:206562698
|
C | T | 1 | a0001c0001t0002g0333 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1345+405C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206562698 | ||||||
| chr2:206562709
|
T | C | 2 | a0001c0001t0001g0300a0001c0001t0042g0295 | 2 | HG02572.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1345+416T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206562709 | ||||||
| chr2:206562713
|
A | G | 21 | a0001c0001t0001g0006a0001c0001t0001g0170a0001c0001t0034g0079others(18): Show | 22 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.1345+420A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206562713 | ||||||
| chr2:206562894
|
A | G | 5 | a0001c0001t0026g0299a0001c0002t0002g0302a0001c0002t0011g0186others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1345+601A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206562894 | ||||||
| chr2:206562913
|
C | T | 3 | a0001c0001t0001g0036a0001c0001t0001g0069a0001c0001t0001g0173 | 3 | HG01884.hp2 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1345+620C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206562913 | ||||||
| chr2:206562949
|
G | A | 284 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(281): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.1345+656G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206562949 | ||||||
| chr2:206562961
|
G | A | 254 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(251): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.1345+668G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206562961 | ||||||
| chr2:206563011
|
A | G | 18 | a0001c0001t0001g0006a0001c0001t0001g0170a0001c0002t0003g0093others(15): Show | 19 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.1345+718A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206563011 | ||||||
| chr2:206563060
|
T | A | 1 | a0004c0006t0001g0044 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1345+767T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206563060 | ||||||
| chr2:206563266
|
A | G | 33 | a0001c0001t0001g0006a0001c0001t0001g0170a0001c0001t0002g0301others(30): Show | 34 | HG00280.hp1 HG00733.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1345+973A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206563266 | ||||||
| chr2:206563323
|
C | A | 9 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0154others(6): Show | 10 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.1345+1030C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206563323 | ||||||
| chr2:206563388
|
A | G | 1 | a0001c0001t0001g0087 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1345+1095A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206563388 | ||||||
| chr2:206563727
|
CTTTTTT | C | 12 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(9): Show | 12 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1346-1278_1346-127 others(10): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 206563727 | |||||
| chr2:206563727
|
CTTTTTTT | C | 242 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(239): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.1346-1279_1346-127 others(11): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 206563727 | |||||
| chr2:206563890
|
C | T | 1 | a0001c0001t0043g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1346-1130C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206563890 | ||||||
| chr2:206563904
|
G | A | 1 | a0001c0001t0001g0293 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1346-1116G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206563904 | ||||||
| chr2:206563993
|
G | A | 1 | a0001c0001t0002g0240 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1346-1027G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206563993 | ||||||
| chr2:206564116
|
G | A | 1 | a0001c0001t0004g0292 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1346-904G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206564116 | ||||||
| chr2:206564144
|
C | A | 135 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(132): Show | 137 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.1346-876C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206564144 | ||||||
| chr2:206564216
|
C | T | 69 | a0001c0001t0001g0036a0001c0001t0001g0069a0001c0001t0001g0173others(66): Show | 69 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.1346-804C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206564216 | ||||||
| chr2:206564217
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1346-803G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206564217 | ||||||
| chr2:206564224
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1346-796C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206564224 | ||||||
| chr2:206564498
|
T | C | 1 | a0001c0001t0001g0104 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1346-522T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206564498 | ||||||
| chr2:206564547
|
C | T | 52 | a0001c0001t0001g0006a0001c0001t0001g0170a0001c0001t0002g0301others(49): Show | 53 | HG00280.hp1 HG00558.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.1346-473C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206564547 | ||||||
| chr2:206564548
|
G | A | 4 | a0001c0002t0003g0137a0001c0002t0003g0164a0001c0002t0003g0165others(1): Show | 4 | HG00280.hp1 HG01256.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.1346-472G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206564548 | ||||||
| chr2:206564660
|
C | G | 47 | a0001c0001t0001g0004a0001c0001t0001g0088a0001c0001t0001g0094others(44): Show | 48 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.1346-360C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206564660 | ||||||
| chr2:206564789
|
A | G | 1 | a0001c0001t0001g0277 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1346-231A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206564789 | ||||||
| chr2:206564909
|
T | C | 1 | a0001c0001t0002g0244 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1346-111T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206564909 | ||||||
| chr2:206564913
|
A | G | 2 | a0001c0002t0002g0148a0001c0002t0002g0149 | 2 | NA18959.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.1346-107A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206564913 | ||||||
| chr2:206565487
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1394+419A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 14/25 | chr2 | 206565487 | ||||||
| chr2:206565523
|
A | C | 1 | a0001c0001t0001g0288 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1394+455A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 14/25 | chr2 | 206565523 | ||||||
| chr2:206565629
|
T | C | 1 | a0001c0001t0002g0191 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1394+561T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 14/25 | chr2 | 206565629 | ||||||
| chr2:206566005
|
A | T | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1394+937A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 14/25 | chr2 | 206566005 | ||||||
| chr2:206566069
|
T | C | 1 | a0001c0001t0007g0340 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1394+1001T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 14/25 | chr2 | 206566069 | ||||||
| chr2:206566219
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1395-1004A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 14/25 | chr2 | 206566219 | ||||||
| chr2:206566316
|
A | G | 1 | a0001c0001t0043g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1395-907A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 14/25 | chr2 | 206566316 | ||||||
| chr2:206566322
|
A | G | 2 | a0001c0001t0005g0215a0001c0001t0031g0243 | 2 | HG00609.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.1395-901A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 14/25 | chr2 | 206566322 | ||||||
| chr2:206566463
|
G | A | 1 | a0001c0002t0003g0093 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1395-760G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 14/25 | chr2 | 206566463 | ||||||
| chr2:206566479
|
TTAAC | T | 72 | a0001c0001t0001g0006a0001c0001t0001g0170a0001c0001t0001g0180others(69): Show | 73 | HG00280.hp1 HG00558.hp1 HG00733.hp2 others(70): Show |
intron_variant | MODIFIER | c.1395-739_1395-736d others(6): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr2 | 206566479 | |||||
| chr2:206566521
|
G | C | 1 | a0001c0001t0001g0271 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1395-702G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 14/25 | chr2 | 206566521 | ||||||
| chr2:206566571
|
C | T | 8 | a0001c0001t0006g0345a0001c0001t0006g0348a0001c0001t0006g0349others(5): Show | 8 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1395-652C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 14/25 | chr2 | 206566571 | ||||||
| chr2:206566582
|
T | C | 2 | a0001c0001t0001g0300a0001c0001t0042g0295 | 2 | HG02572.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1395-641T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 14/25 | chr2 | 206566582 | ||||||
| chr2:206566666
|
T | C | 2 | a0001c0001t0001g0029a0001c0001t0041g0028 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1395-557T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 14/25 | chr2 | 206566666 | ||||||
| chr2:206566685
|
C | T | 5 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0002g0225others(2): Show | 6 | HG00741.hp2 NA18943.hp2 NA19062.hp2 others(3): Show |
intron_variant | MODIFIER | c.1395-538C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 14/25 | chr2 | 206566685 | ||||||
| chr2:206566751
|
G | C | 16 | a0001c0002t0003g0093a0001c0002t0003g0126a0001c0002t0003g0137others(13): Show | 16 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.1395-472G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 14/25 | chr2 | 206566751 | ||||||
| chr2:206566852
|
CA | C | 206 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(203): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.1395-359delA | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr2 | 206566852 | |||||
| chr2:206567386
|
G | A | 1 | a0001c0001t0002g0139 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1494+64G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206567386 | ||||||
| chr2:206567438
|
T | G | 5 | a0001c0001t0001g0272a0001c0001t0001g0279a0001c0001t0001g0288others(2): Show | 5 | HG00544.hp1 NA18967.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.1494+116T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206567438 | ||||||
| chr2:206567792
|
A | G | 1 | a0001c0001t0001g0026 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1494+470A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206567792 | ||||||
| chr2:206568178
|
G | A | 1 | a0001c0001t0002g0333 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1494+856G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206568178 | ||||||
| chr2:206568227
|
G | A | 1 | a0001c0001t0002g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1494+905G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206568227 | ||||||
| chr2:206568276
|
T | C | 4 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(1): Show | 4 | HG02280.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1494+954T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206568276 | ||||||
| chr2:206568316
|
C | T | 1 | a0001c0002t0002g0302 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1494+994C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206568316 | ||||||
| chr2:206568776
|
T | A | 1 | a0001c0001t0001g0088 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1494+1454T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206568776 | ||||||
| chr2:206568777
|
T | C | 1 | a0001c0001t0001g0088 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1494+1455T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206568777 | ||||||
| chr2:206568782
|
A | G | 1 | a0001c0001t0001g0088 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1494+1460A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206568782 | ||||||
| chr2:206568784
|
C | T | 1 | a0001c0001t0001g0088 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1494+1462C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206568784 | ||||||
| chr2:206568785
|
T | C | 1 | a0001c0001t0001g0088 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1494+1463T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206568785 | ||||||
| chr2:206568787
|
A | C | 1 | a0001c0001t0001g0088 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1494+1465A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206568787 | ||||||
| chr2:206568789
|
A | T | 1 | a0001c0001t0001g0088 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1494+1467A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206568789 | ||||||
| chr2:206568791
|
A | T | 1 | a0001c0001t0001g0088 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1494+1469A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206568791 | ||||||
| chr2:206568887
|
C | T | 1 | a0001c0001t0002g0326 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1494+1565C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206568887 | ||||||
| chr2:206568981
|
G | A | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1494+1659G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206568981 | ||||||
| chr2:206569013
|
G | A | 1 | a0001c0001t0001g0021 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1494+1691G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206569013 | ||||||
| chr2:206569226
|
T | C | 4 | a0001c0001t0002g0209a0001c0001t0002g0326a0001c0002t0002g0204others(1): Show | 4 | NA18975.hp1 NA18987.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.1495-1514T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206569226 | ||||||
| chr2:206569388
|
A | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1495-1352A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206569388 | ||||||
| chr2:206569393
|
T | C | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1495-1347T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206569393 | ||||||
| chr2:206569415
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1495-1325T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206569415 | ||||||
| chr2:206569534
|
A | G | 23 | a0001c0001t0034g0079a0001c0001t0035g0078a0001c0002t0003g0093others(20): Show | 23 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.1495-1206A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206569534 | ||||||
| chr2:206569562
|
T | G | 5 | a0001c0002t0001g0092a0001c0002t0002g0302a0001c0002t0011g0186others(2): Show | 5 | HG02886.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1495-1178T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206569562 | ||||||
| chr2:206569700
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1495-1040A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206569700 | ||||||
| chr2:206569780
|
T | C | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(35): Show | 40 | HG00544.hp2 HG00673.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.1495-960T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206569780 | ||||||
| chr2:206569784
|
C | T | 2 | a0001c0001t0008g0023a0001c0001t0008g0330 | 2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1495-956C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206569784 | ||||||
| chr2:206569884
|
A | G | 5 | a0001c0002t0001g0092a0001c0002t0002g0302a0001c0002t0011g0186others(2): Show | 5 | HG02886.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1495-856A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206569884 | ||||||
| chr2:206569894
|
A | T | 1 | a0001c0001t0001g0105 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1495-846A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206569894 | ||||||
| chr2:206570003
|
C | G | 4 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269others(1): Show | 4 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1495-737C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206570003 | ||||||
| chr2:206570097
|
C | G | 14 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(11): Show | 16 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.1495-643C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206570097 | ||||||
| chr2:206570098
|
ATGGCACC others(17): Show |
A | 5 | a0001c0001t0001g0203a0001c0001t0001g0208a0001c0001t0001g0211others(2): Show | 5 | HG02083.hp1 HG02155.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.1495-640_1495-617d others(26): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr2 | 206570098 | |||||
| chr2:206570128
|
A | C | 5 | a0001c0001t0001g0203a0001c0001t0001g0208a0001c0001t0001g0211others(2): Show | 5 | HG02083.hp1 HG02155.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.1495-612A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206570128 | ||||||
| chr2:206570131
|
A | T | 40 | a0001c0001t0002g0209a0001c0001t0002g0233a0001c0001t0002g0326others(37): Show | 40 | HG00673.hp2 HG02056.hp2 HG02109.hp1 others(37): Show |
intron_variant | MODIFIER | c.1495-609A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206570131 | ||||||
| chr2:206570252
|
A | G | 7 | a0001c0001t0001g0122a0001c0001t0001g0127a0001c0001t0001g0128others(4): Show | 7 | HG02040.hp1 NA18940.hp2 NA18988.hp1 others(4): Show |
intron_variant | MODIFIER | c.1495-488A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206570252 | ||||||
| chr2:206570262
|
C | A | 1 | a0001c0001t0001g0155 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1495-478C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206570262 | ||||||
| chr2:206570340
|
T | C | 3 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125 | 3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1495-400T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206570340 | ||||||
| chr2:206570638
|
A | G | 1 | a0001c0001t0036g0270 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1495-102A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206570638 | ||||||
| chr2:206570680
|
AT | A | 21 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0308others(18): Show | 21 | HG02258.hp1 HG02451.hp2 HG02559.hp2 others(18): Show |
intron_variant | MODIFIER | c.1495-59delT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206570680 | ||||||
| chr2:206571043
|
G | A | 258 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(255): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.1566+232G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 16/25 | chr2 | 206571043 | ||||||
| chr2:206571108
|
A | G | 2 | a0001c0001t0001g0154a0001c0001t0001g0169 | 2 | HG01070.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.1566+297A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 16/25 | chr2 | 206571108 | ||||||
| chr2:206571198
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1566+387G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 16/25 | chr2 | 206571198 | ||||||
| chr2:206571211
|
G | C | 1 | a0001c0001t0043g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1566+400G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 16/25 | chr2 | 206571211 | ||||||
| chr2:206571242
|
G | A | 1 | a0001c0001t0043g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1566+431G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 16/25 | chr2 | 206571242 | ||||||
| chr2:206571324
|
A | G | 1 | a0001c0001t0001g0316 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1567-403A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 16/25 | chr2 | 206571324 | ||||||
| chr2:206571368
|
G | A | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1567-359G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 16/25 | chr2 | 206571368 | ||||||
| chr2:206571445
|
G | A | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(112): Show | 117 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.1567-282G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 16/25 | chr2 | 206571445 | ||||||
| chr2:206571534
|
A | G | 1 | a0001c0001t0043g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1567-193A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 16/25 | chr2 | 206571534 | ||||||
| chr2:206571562
|
G | A | 1 | a0001c0001t0002g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1567-165G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 16/25 | chr2 | 206571562 | ||||||
| chr2:206571631
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1567-96A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 16/25 | chr2 | 206571631 | ||||||
| chr2:206571709
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1567-18G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 16/25 | chr2 | 206571709 | ||||||
| chr2:206571967
|
A | G | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1656+151A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 17/25 | chr2 | 206571967 | ||||||
| chr2:206572272
|
A | G | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1656+456A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 17/25 | chr2 | 206572272 | ||||||
| chr2:206572280
|
G | A | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1656+464G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 17/25 | chr2 | 206572280 | ||||||
| chr2:206572401
|
T | G | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(142): Show | 147 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.1656+585T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 17/25 | chr2 | 206572401 | ||||||
| chr2:206572483
|
C | T | 284 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(281): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.1657-632C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 17/25 | chr2 | 206572483 | ||||||
| chr2:206572581
|
C | G | 3 | a0001c0001t0012g0304a0001c0001t0012g0305a0001c0001t0012g0306 | 3 | HG01361.hp2 HG01433.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.1657-534C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 17/25 | chr2 | 206572581 | ||||||
| chr2:206572641
|
A | G | 8 | a0001c0001t0006g0345a0001c0001t0006g0348a0001c0001t0006g0349others(5): Show | 8 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1657-474A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 17/25 | chr2 | 206572641 | ||||||
| chr2:206572743
|
GTA | G | 4 | a0001c0002t0002g0032a0001c0002t0002g0033a0001c0002t0014g0020others(1): Show | 4 | HG03486.hp2 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1657-366_1657-365d others(4): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr2 | 206572743 | |||||
| chr2:206572938
|
G | A | 1 | a0001c0002t0002g0141 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1657-177G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 17/25 | chr2 | 206572938 | ||||||
| chr2:206572967
|
C | T | 2 | a0001c0001t0001g0043a0001c0001t0001g0065 | 2 | HG02145.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1657-148C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 17/25 | chr2 | 206572967 | ||||||
| chr2:206573318
|
A | T | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1737+123A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206573318 | ||||||
| chr2:206573408
|
G | T | 1 | a0001c0001t0002g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1737+213G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206573408 | ||||||
| chr2:206573454
|
T | G | 1 | a0001c0001t0001g0267 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1737+259T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206573454 | ||||||
| chr2:206573568
|
A | G | 1 | a0001c0001t0001g0197 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1737+373A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206573568 | ||||||
| chr2:206573577
|
A | G | 1 | a0001c0001t0005g0221 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1737+382A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206573577 | ||||||
| chr2:206573624
|
T | TA | 6 | a0001c0001t0001g0006a0001c0001t0001g0170a0001c0001t0001g0203others(3): Show | 7 | HG01261.hp1 HG02155.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1737+442dupA | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr2 | 206573624 | |||||
| chr2:206573744
|
G | A | 1 | a0001c0001t0043g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1737+549G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206573744 | ||||||
| chr2:206573772
|
C | T | 50 | a0001c0001t0001g0004a0001c0001t0001g0088a0001c0001t0001g0094others(47): Show | 51 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.1737+577C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206573772 | ||||||
| chr2:206573874
|
C | T | 2 | a0001c0001t0002g0035a0001c0001t0026g0299 | 2 | HG02895.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1737+679C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206573874 | ||||||
| chr2:206574052
|
C | A | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(125): Show | 130 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.1737+857C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206574052 | ||||||
| chr2:206574189
|
G | A | 1 | a0001c0001t0002g0247 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1737+994G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206574189 | ||||||
| chr2:206574261
|
C | T | 46 | a0001c0001t0001g0004a0001c0001t0001g0088a0001c0001t0001g0094others(43): Show | 47 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.1737+1066C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206574261 | ||||||
| chr2:206574402
|
C | CT | 42 | a0001c0001t0001g0064a0001c0001t0002g0233a0001c0002t0001g0150others(39): Show | 43 | HG00673.hp2 HG02056.hp2 HG02071.hp2 others(40): Show |
intron_variant | MODIFIER | c.1737+1221dupT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr2 | 206574402 | |||||
| chr2:206574553
|
C | T | 4 | a0001c0002t0002g0302a0001c0002t0011g0186a0001c0002t0011g0187others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1737+1358C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206574553 | ||||||
| chr2:206574564
|
T | C | 14 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(11): Show | 16 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.1737+1369T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206574564 | ||||||
| chr2:206574588
|
G | A | 1 | a0001c0002t0003g0158 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1737+1393G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206574588 | ||||||
| chr2:206575047
|
G | A | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(112): Show | 117 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.1737+1852G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206575047 | ||||||
| chr2:206575101
|
C | G | 4 | a0001c0002t0002g0302a0001c0002t0011g0186a0001c0002t0011g0187others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1737+1906C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206575101 | ||||||
| chr2:206575432
|
G | A | 3 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125 | 3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1737+2237G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206575432 | ||||||
| chr2:206575591
|
T | A | 1 | a0001c0001t0001g0104 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1737+2396T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206575591 | ||||||
| chr2:206575694
|
T | C | 1 | a0001c0001t0002g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1737+2499T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206575694 | ||||||
| chr2:206575822
|
G | A | 3 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125 | 3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1737+2627G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206575822 | ||||||
| chr2:206575953
|
A | G | 5 | a0001c0002t0001g0092a0001c0002t0002g0302a0001c0002t0011g0186others(2): Show | 5 | HG02886.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1737+2758A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206575953 | ||||||
| chr2:206576024
|
C | T | 1 | a0001c0001t0043g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1737+2829C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206576024 | ||||||
| chr2:206576025
|
C | G | 1 | a0001c0001t0006g0348 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1737+2830C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206576025 | ||||||
| chr2:206576125
|
G | A | 2 | a0001c0001t0001g0309a0001c0001t0001g0319 | 2 | HG02258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1737+2930G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206576125 | ||||||
| chr2:206576128
|
A | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0170 | 3 | HG02257.hp2 HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1737+2933A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206576128 | ||||||
| chr2:206576271
|
TAAAA | T | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(205): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.1737+3078_1737+308 others(8): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr2 | 206576271 | |||||
| chr2:206576277
|
C | G | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(205): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.1737+3082C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206576277 | ||||||
| chr2:206576364
|
AT | A | 4 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0227others(1): Show | 4 | HG04204.hp2 NA18945.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.1737+3174delT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr2 | 206576364 | |||||
| chr2:206576386
|
G | A | 1 | a0001c0001t0002g0139 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1737+3191G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206576386 | ||||||
| chr2:206576532
|
G | A | 2 | a0001c0001t0001g0309a0001c0001t0001g0319 | 2 | HG02258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1737+3337G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206576532 | ||||||
| chr2:206576760
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1737+3565T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206576760 | ||||||
| chr2:206576781
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1737+3586A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206576781 | ||||||
| chr2:206576840
|
G | A | 3 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125 | 3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1737+3645G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206576840 | ||||||
| chr2:206576864
|
C | G | 281 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(278): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.1737+3669C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206576864 | ||||||
| chr2:206576915
|
T | C | 1 | a0001c0001t0001g0237 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1737+3720T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206576915 | ||||||
| chr2:206577002
|
A | G | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1737+3807A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206577002 | ||||||
| chr2:206577041
|
G | A | 1 | a0001c0001t0001g0293 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1737+3846G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206577041 | ||||||
| chr2:206577043
|
C | G | 46 | a0001c0001t0002g0233a0001c0002t0001g0150a0001c0002t0002g0007others(43): Show | 46 | HG00673.hp2 HG02056.hp2 HG02109.hp1 others(43): Show |
intron_variant | MODIFIER | c.1737+3848C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206577043 | ||||||
| chr2:206577046
|
A | G | 1 | a0001c0001t0001g0335 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1737+3851A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206577046 | ||||||
| chr2:206577137
|
A | G | 3 | a0001c0002t0001g0257a0001c0002t0001g0258a0001c0002t0001g0259 | 3 | HG02647.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1737+3942A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206577137 | ||||||
| chr2:206577411
|
C | T | 1 | a0001c0002t0003g0157 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1737+4216C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206577411 | ||||||
| chr2:206577478
|
G | A | 1 | a0001c0001t0001g0110 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1737+4283G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206577478 | ||||||
| chr2:206577531
|
C | T | 1 | a0001c0001t0002g0247 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1737+4336C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206577531 | ||||||
| chr2:206577541
|
C | T | 3 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0041g0028 | 3 | HG00642.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1737+4346C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206577541 | ||||||
| chr2:206577560
|
G | A | 280 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(277): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.1737+4365G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206577560 | ||||||
| chr2:206577586
|
A | G | 4 | a0001c0002t0002g0302a0001c0002t0011g0186a0001c0002t0011g0187others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1737+4391A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206577586 | ||||||
| chr2:206577592
|
T | C | 1 | a0001c0002t0002g0198 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1737+4397T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206577592 | ||||||
| chr2:206577594
|
A | G | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1737+4399A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206577594 | ||||||
| chr2:206577694
|
G | A | 3 | a0001c0001t0001g0085a0001c0001t0001g0090a0001c0001t0001g0091 | 3 | HG01952.hp2 NA18946.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.1737+4499G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206577694 | ||||||
| chr2:206577842
|
A | G | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(140): Show | 145 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.1737+4647A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206577842 | ||||||
| chr2:206577884
|
G | C | 1 | a0001c0002t0029g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1737+4689G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206577884 | ||||||
| chr2:206577886
|
A | C | 1 | a0001c0001t0001g0100 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1737+4691A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206577886 | ||||||
| chr2:206577898
|
A | G | 1 | a0001c0001t0002g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1737+4703A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206577898 | ||||||
| chr2:206577910
|
C | T | 25 | a0001c0001t0034g0079a0001c0001t0035g0078a0001c0002t0003g0093others(22): Show | 25 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.1737+4715C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206577910 | ||||||
| chr2:206578173
|
TTTTA | T | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(140): Show | 145 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.1737+4986_1737+498 others(8): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr2 | 206578173 | |||||
| chr2:206578289
|
G | T | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1737+5094G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206578289 | ||||||
| chr2:206578321
|
C | G | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1737+5126C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206578321 | ||||||
| chr2:206578322
|
C | T | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1737+5127C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206578322 | ||||||
| chr2:206578424
|
A | T | 4 | a0001c0002t0002g0302a0001c0002t0011g0186a0001c0002t0011g0187others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1737+5229A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206578424 | ||||||
| chr2:206578433
|
C | T | 216 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(213): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.1737+5238C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206578433 | ||||||
| chr2:206578481
|
A | G | 5 | a0001c0002t0001g0092a0001c0002t0002g0302a0001c0002t0011g0186others(2): Show | 5 | HG02886.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1737+5286A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206578481 | ||||||
| chr2:206578559
|
CAT | C | 282 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(279): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.1737+5377_1737+537 others(6): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr2 | 206578559 | |||||
| chr2:206578676
|
C | A | 2 | a0001c0001t0001g0336a0001c0001t0001g0337 | 2 | HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1737+5481C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206578676 | ||||||
| chr2:206578815
|
C | T | 1 | a0001c0001t0002g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1737+5620C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206578815 | ||||||
| chr2:206578921
|
A | G | 47 | a0001c0001t0001g0004a0001c0001t0001g0088a0001c0001t0001g0094others(44): Show | 49 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.1737+5726A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206578921 | ||||||
| chr2:206579019
|
G | T | 46 | a0001c0001t0001g0004a0001c0001t0001g0088a0001c0001t0001g0094others(43): Show | 47 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.1737+5824G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206579019 | ||||||
| chr2:206579067
|
C | T | 1 | a0002c0003t0001g0062 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1737+5872C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206579067 | ||||||
| chr2:206579093
|
T | C | 1 | a0001c0001t0002g0209 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1737+5898T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206579093 | ||||||
| chr2:206579119
|
A | G | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(140): Show | 145 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.1737+5924A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206579119 | ||||||
| chr2:206579255
|
T | C | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1737+6060T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206579255 | ||||||
| chr2:206579316
|
A | G | 3 | a0001c0002t0001g0257a0001c0002t0001g0258a0001c0002t0001g0259 | 3 | HG02647.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1737+6121A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206579316 | ||||||
| chr2:206579565
|
G | C | 2 | a0001c0001t0002g0035a0001c0001t0026g0299 | 2 | HG02895.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1737+6370G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206579565 | ||||||
| chr2:206579855
|
G | A | 1 | a0001c0002t0029g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1737+6660G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206579855 | ||||||
| chr2:206579876
|
A | G | 1 | a0001c0002t0002g0001 | 2 | NA18989.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1737+6681A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206579876 | ||||||
| chr2:206579961
|
T | G | 47 | a0001c0001t0001g0004a0001c0001t0001g0088a0001c0001t0001g0094others(44): Show | 48 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.1737+6766T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206579961 | ||||||
| chr2:206580069
|
A | G | 1 | a0001c0001t0002g0022 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1737+6874A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206580069 | ||||||
| chr2:206580160
|
A | C | 1 | a0001c0002t0002g0302 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1737+6965A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206580160 | ||||||
| chr2:206580189
|
T | C | 291 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(288): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.1737+6994T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206580189 | ||||||
| chr2:206580254
|
T | C | 1 | a0001c0001t0001g0267 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1737+7059T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206580254 | ||||||
| chr2:206580474
|
T | C | 3 | a0001c0001t0001g0154a0001c0001t0001g0169a0001c0001t0001g0217 | 3 | HG01070.hp1 HG01256.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1738-6851T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206580474 | ||||||
| chr2:206580476
|
A | G | 1 | a0001c0001t0001g0013 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1738-6849A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206580476 | ||||||
| chr2:206580783
|
T | A | 5 | a0001c0002t0001g0092a0001c0002t0002g0302a0001c0002t0011g0186others(2): Show | 5 | HG02886.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1738-6542T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206580783 | ||||||
| chr2:206580861
|
G | A | 1 | a0001c0001t0002g0327 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1738-6464G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206580861 | ||||||
| chr2:206580862
|
T | G | 1 | a0001c0001t0002g0327 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1738-6463T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206580862 | ||||||
| chr2:206580866
|
T | TTTCCACT others(90): Show |
1 | a0001c0001t0002g0327 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1738-6457_1738-645 others(101): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr2 | 206580866 | |||||
| chr2:206580987
|
C | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0170 | 3 | HG02257.hp2 HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1738-6338C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206580987 | ||||||
| chr2:206581221
|
T | A | 23 | a0001c0001t0034g0079a0001c0001t0035g0078a0001c0002t0003g0093others(20): Show | 23 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.1738-6104T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206581221 | ||||||
| chr2:206581258
|
C | T | 10 | a0001c0001t0001g0197a0001c0001t0001g0282a0001c0001t0001g0283others(7): Show | 10 | NA18940.hp1 NA18945.hp1 NA18966.hp2 others(7): Show |
intron_variant | MODIFIER | c.1738-6067C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206581258 | ||||||
| chr2:206581268
|
A | T | 1 | a0001c0001t0001g0267 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1738-6057A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206581268 | ||||||
| chr2:206581404
|
A | G | 2 | a0001c0001t0001g0309a0001c0001t0001g0319 | 2 | HG02258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1738-5921A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206581404 | ||||||
| chr2:206581650
|
A | G | 1 | a0001c0001t0020g0329 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1738-5675A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206581650 | ||||||
| chr2:206581747
|
A | C | 3 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125 | 3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1738-5578A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206581747 | ||||||
| chr2:206581765
|
T | C | 3 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0192 | 3 | HG01167.hp1 HG01169.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1738-5560T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206581765 | ||||||
| chr2:206581907
|
C | T | 1 | a0001c0001t0002g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1738-5418C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206581907 | ||||||
| chr2:206581914
|
G | C | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1738-5411G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206581914 | ||||||
| chr2:206581925
|
T | A | 48 | a0001c0001t0002g0209a0001c0001t0002g0233a0001c0001t0002g0326others(45): Show | 49 | HG00673.hp2 HG02056.hp2 HG02109.hp1 others(46): Show |
intron_variant | MODIFIER | c.1738-5400T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206581925 | ||||||
| chr2:206581970
|
C | G | 1 | a0001c0001t0020g0329 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1738-5355C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206581970 | ||||||
| chr2:206581991
|
C | T | 1 | a0001c0001t0002g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1738-5334C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206581991 | ||||||
| chr2:206582012
|
G | A | 2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 2 | HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1738-5313G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206582012 | ||||||
| chr2:206582030
|
A | C | 1 | a0001c0001t0001g0025 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1738-5295A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206582030 | ||||||
| chr2:206582121
|
G | A | 14 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(11): Show | 16 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.1738-5204G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206582121 | ||||||
| chr2:206582158
|
G | A | 96 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(93): Show | 98 | HG00280.hp2 HG00544.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.1738-5167G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206582158 | ||||||
| chr2:206582169
|
C | T | 3 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0020g0151 | 3 | HG02486.hp1 HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1738-5156C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206582169 | ||||||
| chr2:206582291
|
A | G | 1 | a0001c0001t0002g0327 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1738-5034A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206582291 | ||||||
| chr2:206582413
|
CTTTAAG | C | 3 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125 | 3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1738-4907_1738-490 others(10): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr2 | 206582413 | |||||
| chr2:206582580
|
C | T | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1738-4745C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206582580 | ||||||
| chr2:206582790
|
C | T | 1 | a0001c0001t0002g0254 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1738-4535C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206582790 | ||||||
| chr2:206582826
|
G | T | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.1738-4499G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206582826 | ||||||
| chr2:206582878
|
T | C | 1 | a0001c0001t0002g0239 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1738-4447T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206582878 | ||||||
| chr2:206582975
|
G | T | 3 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125 | 3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1738-4350G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206582975 | ||||||
| chr2:206583084
|
T | G | 5 | a0001c0002t0001g0092a0001c0002t0002g0302a0001c0002t0011g0186others(2): Show | 5 | HG02886.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1738-4241T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206583084 | ||||||
| chr2:206583169
|
C | T | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1738-4156C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206583169 | ||||||
| chr2:206583229
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1738-4096C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206583229 | ||||||
| chr2:206583370
|
C | T | 2 | a0001c0001t0034g0079a0001c0001t0035g0078 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1738-3955C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206583370 | ||||||
| chr2:206583386
|
G | A | 66 | a0001c0001t0034g0079a0001c0001t0035g0078a0001c0002t0001g0150others(63): Show | 67 | HG00280.hp1 HG00673.hp2 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.1738-3939G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206583386 | ||||||
| chr2:206583402
|
C | T | 1 | a0001c0001t0001g0316 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1738-3923C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206583402 | ||||||
| chr2:206583414
|
A | T | 5 | a0001c0001t0004g0249a0001c0001t0004g0250a0001c0001t0004g0251others(2): Show | 5 | NA18946.hp1 NA18952.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.1738-3911A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206583414 | ||||||
| chr2:206583522
|
C | T | 1 | a0001c0001t0002g0333 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1738-3803C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206583522 | ||||||
| chr2:206583594
|
A | C | 1 | a0001c0001t0001g0288 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1738-3731A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206583594 | ||||||
| chr2:206583678
|
A | AT | 5 | a0001c0002t0001g0092a0001c0002t0002g0302a0001c0002t0011g0186others(2): Show | 5 | HG02886.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1738-3645dupT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr2 | 206583678 | |||||
| chr2:206583684
|
A | C | 3 | a0001c0002t0001g0257a0001c0002t0001g0258a0001c0002t0001g0259 | 3 | HG02647.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1738-3641A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206583684 | ||||||
| chr2:206583713
|
G | T | 1 | a0001c0001t0002g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1738-3612G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206583713 | ||||||
| chr2:206584156
|
A | C | 2 | a0001c0001t0008g0023a0001c0001t0008g0330 | 2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1738-3169A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206584156 | ||||||
| chr2:206584244
|
C | T | 3 | a0001c0001t0017g0038a0001c0001t0018g0274a0001c0001t0018g0276 | 3 | NA18943.hp1 NA18943.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.1738-3081C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206584244 | ||||||
| chr2:206584563
|
G | A | 26 | a0001c0001t0034g0079a0001c0001t0035g0078a0001c0002t0001g0257others(23): Show | 26 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.1738-2762G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206584563 | ||||||
| chr2:206584574
|
G | A | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1738-2751G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206584574 | ||||||
| chr2:206584747
|
T | C | 6 | a0001c0001t0034g0079a0001c0001t0035g0078a0001c0002t0015g0182others(3): Show | 6 | HG02055.hp1 HG02109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1738-2578T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206584747 | ||||||
| chr2:206584774
|
A | T | 1 | a0001c0002t0002g0008 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1738-2551A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206584774 | ||||||
| chr2:206584780
|
T | C | 5 | a0001c0002t0001g0092a0001c0002t0002g0302a0001c0002t0011g0186others(2): Show | 5 | HG02886.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1738-2545T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206584780 | ||||||
| chr2:206584848
|
C | T | 1 | a0001c0001t0002g0246 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1738-2477C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206584848 | ||||||
| chr2:206585022
|
G | A | 1 | a0001c0001t0001g0260 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1738-2303G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206585022 | ||||||
| chr2:206585045
|
T | C | 1 | a0001c0002t0029g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1738-2280T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206585045 | ||||||
| chr2:206585096
|
G | C | 2 | a0001c0001t0001g0309a0001c0001t0001g0319 | 2 | HG02258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1738-2229G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206585096 | ||||||
| chr2:206585121
|
C | G | 1 | a0001c0002t0014g0037 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1738-2204C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206585121 | ||||||
| chr2:206585172
|
A | G | 3 | a0001c0001t0017g0038a0001c0001t0018g0274a0001c0001t0018g0276 | 3 | NA18943.hp1 NA18943.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.1738-2153A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206585172 | ||||||
| chr2:206585200
|
C | T | 5 | a0001c0001t0004g0249a0001c0001t0004g0250a0001c0001t0004g0251others(2): Show | 5 | NA18946.hp1 NA18952.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.1738-2125C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206585200 | ||||||
| chr2:206585237
|
A | G | 14 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(11): Show | 16 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.1738-2088A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206585237 | ||||||
| chr2:206585418
|
G | A | 1 | a0001c0001t0033g0294 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1738-1907G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206585418 | ||||||
| chr2:206585554
|
T | A | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1738-1771T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206585554 | ||||||
| chr2:206585558
|
G | A | 9 | a0001c0001t0001g0197a0001c0001t0001g0282a0001c0001t0001g0283others(6): Show | 9 | NA18940.hp1 NA18945.hp1 NA18966.hp2 others(6): Show |
intron_variant | MODIFIER | c.1738-1767G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206585558 | ||||||
| chr2:206585681
|
T | G | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1738-1644T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206585681 | ||||||
| chr2:206585707
|
A | G | 3 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103 | 3 | HG01358.hp1 HG01943.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1738-1618A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206585707 | ||||||
| chr2:206585827
|
A | C | 3 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0286 | 3 | NA18966.hp2 NA19057.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.1738-1498A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206585827 | ||||||
| chr2:206585923
|
G | A | 1 | a0001c0002t0002g0320 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1738-1402G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206585923 | ||||||
| chr2:206586035
|
G | A | 46 | a0001c0001t0001g0004a0001c0001t0001g0088a0001c0001t0001g0094others(43): Show | 47 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.1738-1290G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206586035 | ||||||
| chr2:206586098
|
T | C | 13 | a0001c0001t0001g0013a0001c0001t0001g0048a0001c0001t0001g0050others(10): Show | 13 | HG00544.hp2 HG00673.hp1 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.1738-1227T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206586098 | ||||||
| chr2:206586193
|
A | G | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1738-1132A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206586193 | ||||||
| chr2:206586254
|
G | A | 3 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125 | 3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1738-1071G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206586254 | ||||||
| chr2:206586346
|
G | A | 1 | a0001c0001t0001g0321 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1738-979G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206586346 | ||||||
| chr2:206586480
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1738-845G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206586480 | ||||||
| chr2:206586510
|
T | C | 2 | a0001c0002t0015g0182a0001c0002t0015g0183 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1738-815T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206586510 | ||||||
| chr2:206586870
|
A | C | 45 | a0001c0001t0001g0004a0001c0001t0001g0088a0001c0001t0001g0094others(42): Show | 47 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.1738-455A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206586870 | ||||||
| chr2:206586920
|
T | C | 1 | a0001c0001t0002g0176 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1738-405T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206586920 | ||||||
| chr2:206587158
|
A | C | 20 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0184others(17): Show | 20 | HG02451.hp2 HG02559.hp2 HG02615.hp2 others(17): Show |
intron_variant | MODIFIER | c.1738-167A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206587158 | ||||||
| chr2:206587241
|
C | A | 8 | a0001c0001t0006g0345a0001c0001t0006g0348a0001c0001t0006g0349others(5): Show | 8 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1738-84C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206587241 | ||||||
| chr2:206587427
|
GT | G | 288 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(285): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.1788+61delT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr2 | 206587427 | |||||
| chr2:206587580
|
G | GA | 124 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(121): Show | 126 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.1788+216dupA | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr2 | 206587580 | |||||
| chr2:206587580
|
G | GAA | 39 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(36): Show | 41 | HG00544.hp2 HG00673.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.1788+215_1788+216d others(4): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr2 | 206587580 | |||||
| chr2:206587811
|
G | A | 1 | a0001c0001t0002g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1789-280G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 19/25 | chr2 | 206587811 | ||||||
| chr2:206587993
|
A | G | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1789-98A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 19/25 | chr2 | 206587993 | ||||||
| chr2:206588163
|
C | T | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1852+9C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 20/25 | chr2 | 206588163 | ||||||
| chr2:206588178
|
C | T | 3 | a0001c0001t0002g0022a0001c0001t0002g0220a0001c0001t0002g0225 | 3 | HG00741.hp2 HG01099.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1852+24C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 20/25 | chr2 | 206588178 | ||||||
| chr2:206588187
|
A | G | 1 | a0001c0002t0001g0258 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1852+33A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 20/25 | chr2 | 206588187 | ||||||
| chr2:206588321
|
GA | G | 5 | a0001c0001t0006g0348a0001c0001t0006g0349a0001c0001t0006g0350others(2): Show | 5 | HG01081.hp1 HG01496.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.1852+171delA | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 20/25 | INFO_REALIGN_3_PRIME | chr2 | 206588321 | |||||
| chr2:206588325
|
A | G | 1 | a0001c0001t0012g0306 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1852+171A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 20/25 | chr2 | 206588325 | ||||||
| chr2:206588352
|
G | A | 9 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0154others(6): Show | 10 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.1852+198G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 20/25 | chr2 | 206588352 | ||||||
| chr2:206588530
|
G | T | 110 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(107): Show | 112 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1852+376G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 20/25 | chr2 | 206588530 | ||||||
| chr2:206588548
|
T | C | 5 | a0001c0002t0001g0092a0001c0002t0002g0302a0001c0002t0011g0186others(2): Show | 5 | HG02886.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1852+394T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 20/25 | chr2 | 206588548 | ||||||
| chr2:206588586
|
C | T | 75 | a0001c0002t0001g0092a0001c0002t0001g0150a0001c0002t0001g0257others(72): Show | 75 | HG00280.hp1 HG00673.hp2 HG00738.hp2 others(72): Show |
intron_variant | MODIFIER | c.1852+432C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 20/25 | chr2 | 206588586 | ||||||
| chr2:206588587
|
A | G | 4 | a0001c0002t0003g0137a0001c0002t0003g0164a0001c0002t0003g0165others(1): Show | 4 | HG00280.hp1 HG01256.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.1852+433A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 20/25 | chr2 | 206588587 | ||||||
| chr2:206588826
|
C | G | 2 | a0001c0001t0035g0078a0001c0005t0027g0188 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1853-583C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 20/25 | chr2 | 206588826 | ||||||
| chr2:206588983
|
C | T | 27 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0308others(24): Show | 27 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.1853-426C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 20/25 | chr2 | 206588983 | ||||||
| chr2:206589135
|
A | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0045 | 2 | NA18961.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1853-274A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 20/25 | chr2 | 206589135 | ||||||
| chr2:206589261
|
T | A | 1 | a0001c0001t0001g0319 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1853-148T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 20/25 | chr2 | 206589261 | ||||||
| chr2:206589344
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1853-65C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 20/25 | chr2 | 206589344 | ||||||
| chr2:206589791
|
C | A | 3 | a0001c0001t0017g0038a0001c0001t0017g0039a0001c0001t0018g0276 | 3 | NA18943.hp1 NA18943.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1958+277C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206589791 | ||||||
| chr2:206589792
|
A | G | 3 | a0001c0001t0017g0038a0001c0001t0017g0039a0001c0001t0018g0276 | 3 | NA18943.hp1 NA18943.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1958+278A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206589792 | ||||||
| chr2:206589810
|
A | G | 1 | a0001c0001t0001g0080 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1958+296A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206589810 | ||||||
| chr2:206589836
|
T | A | 1 | a0001c0001t0001g0102 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1958+322T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206589836 | ||||||
| chr2:206589918
|
C | T | 44 | a0001c0002t0001g0150a0001c0002t0002g0007a0001c0002t0002g0008others(41): Show | 44 | HG00673.hp2 HG02056.hp2 HG02109.hp1 others(41): Show |
intron_variant | MODIFIER | c.1958+404C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206589918 | ||||||
| chr2:206589923
|
A | G | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1958+409A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206589923 | ||||||
| chr2:206590208
|
G | A | 22 | a0001c0001t0036g0270a0001c0002t0003g0093a0001c0002t0003g0109others(19): Show | 22 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.1958+694G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206590208 | ||||||
| chr2:206590491
|
G | A | 1 | a0001c0001t0043g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1958+977G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206590491 | ||||||
| chr2:206590523
|
A | G | 1 | a0001c0002t0029g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1958+1009A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206590523 | ||||||
| chr2:206590564
|
T | C | 1 | a0001c0002t0002g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1958+1050T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206590564 | ||||||
| chr2:206590821
|
C | A | 1 | a0001c0001t0002g0014 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1958+1307C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206590821 | ||||||
| chr2:206591023
|
G | T | 1 | a0001c0001t0002g0035 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1958+1509G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206591023 | ||||||
| chr2:206591051
|
A | C | 1 | a0004c0006t0001g0044 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1958+1537A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206591051 | ||||||
| chr2:206591347
|
T | C | 2 | a0001c0002t0019g0189a0001c0002t0019g0325 | 2 | HG02055.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1959-1270T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206591347 | ||||||
| chr2:206591467
|
T | A | 1 | a0001c0001t0007g0341 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1959-1150T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206591467 | ||||||
| chr2:206591543
|
A | G | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1959-1074A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206591543 | ||||||
| chr2:206591680
|
G | T | 4 | a0001c0001t0001g0272a0001c0001t0001g0279a0001c0001t0001g0288others(1): Show | 4 | HG00544.hp1 NA18967.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.1959-937G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206591680 | ||||||
| chr2:206591681
|
C | T | 4 | a0001c0001t0001g0272a0001c0001t0001g0279a0001c0001t0001g0288others(1): Show | 4 | HG00544.hp1 NA18967.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.1959-936C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206591681 | ||||||
| chr2:206591815
|
A | G | 4 | a0001c0002t0002g0302a0001c0002t0011g0186a0001c0002t0011g0187others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1959-802A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206591815 | ||||||
| chr2:206591981
|
A | G | 1 | a0001c0001t0002g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1959-636A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206591981 | ||||||
| chr2:206592306
|
T | C | 4 | a0001c0001t0001g0036a0001c0001t0001g0069a0001c0001t0001g0173others(1): Show | 4 | HG01884.hp2 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1959-311T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206592306 | ||||||
| chr2:206592541
|
T | C | 21 | a0001c0002t0003g0093a0001c0002t0003g0109a0001c0002t0003g0126others(18): Show | 21 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.1959-76T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206592541 | ||||||
| chr2:206592561
|
T | G | 1 | a0001c0001t0001g0272 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1959-56T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206592561 | ||||||
| chr2:206592746
|
T | G | 2 | a0001c0001t0001g0099a0001c0001t0001g0104 | 2 | NA18990.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.2078+10T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 22/25 | chr2 | 206592746 | ||||||
| chr2:206592768
|
G | A | 30 | a0001c0001t0001g0004a0001c0001t0001g0088a0001c0001t0001g0094others(27): Show | 31 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.2078+32G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 22/25 | chr2 | 206592768 | ||||||
| chr2:206592971
|
C | A | 1 | a0001c0001t0002g0227 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2078+235C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 22/25 | chr2 | 206592971 | ||||||
| chr2:206592994
|
T | C | 1 | a0001c0001t0001g0285 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2078+258T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 22/25 | chr2 | 206592994 | ||||||
| chr2:206593155
|
A | G | 212 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.2078+419A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 22/25 | chr2 | 206593155 | ||||||
| chr2:206593202
|
G | A | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2078+466G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 22/25 | chr2 | 206593202 | ||||||
| chr2:206593638
|
A | G | 4 | a0001c0002t0002g0302a0001c0002t0011g0186a0001c0002t0011g0187others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2078+902A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 22/25 | chr2 | 206593638 | ||||||
| chr2:206593639
|
G | A | 1 | a0001c0001t0001g0324 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2078+903G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 22/25 | chr2 | 206593639 | ||||||
| chr2:206593856
|
A | G | 3 | a0001c0001t0012g0304a0001c0001t0012g0305a0001c0001t0012g0306 | 3 | HG01361.hp2 HG01433.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.2079-881A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 22/25 | chr2 | 206593856 | ||||||
| chr2:206593879
|
T | G | 49 | a0001c0001t0002g0209a0001c0001t0002g0233a0001c0001t0002g0326others(46): Show | 50 | HG00673.hp2 HG02056.hp2 HG02109.hp1 others(47): Show |
intron_variant | MODIFIER | c.2079-858T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 22/25 | chr2 | 206593879 | ||||||
| chr2:206593964
|
G | A | 159 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(156): Show | 162 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.2079-773G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 22/25 | chr2 | 206593964 | ||||||
| chr2:206594185
|
T | C | 1 | a0001c0001t0001g0107 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2079-552T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 22/25 | chr2 | 206594185 | ||||||
| chr2:206594202
|
G | T | 2 | a0001c0001t0008g0023a0001c0001t0008g0330 | 2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2079-535G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 22/25 | chr2 | 206594202 | ||||||
| chr2:206594353
|
G | A | 230 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(227): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.2079-384G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 22/25 | chr2 | 206594353 | ||||||
| chr2:206594428
|
T | C | 1 | a0001c0002t0003g0164 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2079-309T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 22/25 | chr2 | 206594428 | ||||||
| chr2:206594473
|
G | A | 44 | a0001c0001t0001g0004a0001c0001t0001g0088a0001c0001t0001g0094others(41): Show | 45 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.2079-264G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 22/25 | chr2 | 206594473 | ||||||
| chr2:206595052
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2247+147G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 23/25 | chr2 | 206595052 | ||||||
| chr2:206595138
|
G | A | 16 | a0001c0002t0003g0093a0001c0002t0003g0109a0001c0002t0003g0126others(13): Show | 16 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.2247+233G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 23/25 | chr2 | 206595138 | ||||||
| chr2:206595158
|
C | T | 1 | a0001c0001t0001g0110 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2247+253C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 23/25 | chr2 | 206595158 | ||||||
| chr2:206595201
|
G | A | 2 | a0001c0002t0015g0182a0001c0002t0015g0183 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2247+296G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 23/25 | chr2 | 206595201 | ||||||
| chr2:206595336
|
C | T | 2 | a0001c0001t0001g0087a0001c0001t0001g0089 | 2 | HG02040.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.2247+431C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 23/25 | chr2 | 206595336 | ||||||
| chr2:206595408
|
G | A | 8 | a0001c0001t0006g0345a0001c0001t0006g0348a0001c0001t0006g0349others(5): Show | 8 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.2247+503G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 23/25 | chr2 | 206595408 | ||||||
| chr2:206595462
|
A | G | 3 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125 | 3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2247+557A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 23/25 | chr2 | 206595462 | ||||||
| chr2:206595631
|
T | C | 18 | a0001c0001t0001g0088a0001c0001t0001g0098a0001c0001t0001g0099others(15): Show | 18 | HG00438.hp1 HG00642.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.2248-420T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 23/25 | chr2 | 206595631 | ||||||
| chr2:206595800
|
AAAT | A | 15 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(12): Show | 17 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.2248-245_2248-243d others(5): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr2 | 206595800 | |||||
| chr2:206595823
|
G | T | 1 | a0001c0001t0009g0049 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2248-228G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 23/25 | chr2 | 206595823 | ||||||
| chr2:206595829
|
C | A | 2 | a0001c0001t0001g0116a0001c0001t0001g0118 | 2 | NA18962.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.2248-222C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 23/25 | chr2 | 206595829 | ||||||
| chr2:206596219
|
A | G | 4 | a0001c0002t0002g0302a0001c0002t0011g0186a0001c0002t0011g0187others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2359+57A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206596219 | ||||||
| chr2:206596256
|
A | G | 2 | a0001c0001t0005g0229a0005c0008t0005g0242 | 2 | HG02132.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.2359+94A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206596256 | ||||||
| chr2:206596394
|
T | C | 1 | a0001c0001t0002g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2359+232T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206596394 | ||||||
| chr2:206596435
|
C | A | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(106): Show | 111 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.2359+273C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206596435 | ||||||
| chr2:206596518
|
G | A | 2 | a0001c0001t0034g0079a0001c0001t0035g0078 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.2359+356G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206596518 | ||||||
| chr2:206596559
|
G | A | 46 | a0001c0001t0001g0004a0001c0001t0001g0088a0001c0001t0001g0094others(43): Show | 47 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.2359+397G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206596559 | ||||||
| chr2:206596694
|
G | A | 2 | a0001c0001t0001g0068a0001c0001t0001g0080 | 2 | HG02717.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2359+532G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206596694 | ||||||
| chr2:206596780
|
C | A | 14 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(11): Show | 16 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.2359+618C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206596780 | ||||||
| chr2:206596899
|
C | CT | 10 | a0001c0001t0002g0227a0001c0001t0002g0233a0001c0001t0002g0254others(7): Show | 10 | HG01175.hp1 HG02109.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.2359+763dupT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr2 | 206596899 | |||||
| chr2:206596899
|
CT | C | 52 | a0001c0001t0001g0237a0001c0001t0002g0193a0001c0001t0002g0194others(49): Show | 53 | HG00558.hp1 HG00673.hp2 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.2359+763delT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr2 | 206596899 | |||||
| chr2:206596899
|
CTT | C | 52 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0059others(49): Show | 53 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.2359+762_2359+763d others(4): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr2 | 206596899 | |||||
| chr2:206596899
|
CTTT | C | 103 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(100): Show | 105 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.2359+761_2359+763d others(5): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr2 | 206596899 | |||||
| chr2:206596899
|
CTTTT | C | 52 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(49): Show | 54 | HG00099.hp2 HG00140.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.2359+760_2359+763d others(6): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr2 | 206596899 | |||||
| chr2:206597032
|
A | G | 28 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0184others(25): Show | 28 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.2359+870A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206597032 | ||||||
| chr2:206597113
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2359+951G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206597113 | ||||||
| chr2:206597178
|
C | CT | 17 | a0001c0001t0001g0115a0001c0001t0001g0120a0001c0001t0001g0128others(14): Show | 17 | HG00642.hp2 HG00733.hp2 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.2359+1035dupT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr2 | 206597178 | |||||
| chr2:206597178
|
C | T | 1 | a0001c0002t0002g0054 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2359+1016C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206597178 | ||||||
| chr2:206597178
|
CT | C | 7 | a0001c0001t0001g0026a0001c0001t0001g0043a0001c0001t0001g0268others(4): Show | 7 | HG01167.hp2 HG01943.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.2359+1035delT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr2 | 206597178 | |||||
| chr2:206597209
|
C | T | 211 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(208): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.2359+1047C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206597209 | ||||||
| chr2:206597238
|
G | A | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2359+1076G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206597238 | ||||||
| chr2:206597264
|
C | G | 14 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(11): Show | 16 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.2359+1102C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206597264 | ||||||
| chr2:206597595
|
A | G | 1 | a0001c0001t0002g0238 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2359+1433A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206597595 | ||||||
| chr2:206597722
|
G | A | 1 | a0001c0001t0042g0295 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2359+1560G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206597722 | ||||||
| chr2:206597745
|
A | C | 2 | a0001c0001t0002g0193a0001c0001t0002g0194 | 2 | HG01261.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2359+1583A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206597745 | ||||||
| chr2:206597746
|
A | G | 2 | a0001c0001t0034g0079a0001c0001t0035g0078 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.2359+1584A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206597746 | ||||||
| chr2:206597918
|
G | T | 44 | a0001c0002t0001g0150a0001c0002t0002g0007a0001c0002t0002g0008others(41): Show | 44 | HG00673.hp2 HG02056.hp2 HG02109.hp1 others(41): Show |
intron_variant | MODIFIER | c.2359+1756G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206597918 | ||||||
| chr2:206597937
|
G | A | 1 | a0001c0001t0001g0084 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2359+1775G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206597937 | ||||||
| chr2:206598236
|
A | G | 1 | a0001c0002t0003g0158 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2359+2074A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206598236 | ||||||
| chr2:206598269
|
G | A | 1 | a0001c0001t0002g0322 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2359+2107G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206598269 | ||||||
| chr2:206598571
|
T | A | 2 | a0001c0002t0003g0137a0001c0002t0003g0174 | 2 | HG00280.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.2359+2409T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206598571 | ||||||
| chr2:206598656
|
T | C | 1 | a0001c0001t0001g0171 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2359+2494T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206598656 | ||||||
| chr2:206598668
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2359+2506G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206598668 | ||||||
| chr2:206598715
|
C | T | 2 | a0001c0002t0015g0182a0001c0002t0015g0183 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2359+2553C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206598715 | ||||||
| chr2:206598881
|
T | C | 14 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(11): Show | 16 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.2359+2719T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206598881 | ||||||
| chr2:206598991
|
G | A | 1 | a0001c0002t0029g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2359+2829G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206598991 | ||||||
| chr2:206599030
|
A | C | 282 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(279): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.2359+2868A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206599030 | ||||||
| chr2:206599057
|
T | C | 1 | a0001c0001t0001g0099 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2359+2895T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206599057 | ||||||
| chr2:206599058
|
A | G | 1 | a0001c0001t0001g0051 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2359+2896A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206599058 | ||||||
| chr2:206599165
|
A | G | 3 | a0001c0001t0013g0030a0001c0001t0013g0034a0003c0004t0013g0031 | 3 | HG01243.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2359+3003A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206599165 | ||||||
| chr2:206599204
|
C | CA | 13 | a0001c0001t0001g0068a0001c0001t0001g0080a0001c0001t0001g0211others(10): Show | 13 | HG02055.hp1 HG02155.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.2359+3059dupA | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr2 | 206599204 | |||||
| chr2:206599229
|
G | A | 13 | a0001c0001t0005g0145a0001c0001t0005g0213a0001c0001t0005g0214others(10): Show | 13 | HG00558.hp1 HG00609.hp1 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.2359+3067G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206599229 | ||||||
| chr2:206599287
|
A | G | 2 | a0001c0001t0034g0079a0001c0001t0035g0078 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.2359+3125A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206599287 | ||||||
| chr2:206599313
|
G | C | 1 | a0001c0001t0001g0319 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2359+3151G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206599313 | ||||||
| chr2:206599554
|
C | T | 281 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(278): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.2359+3392C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206599554 | ||||||
| chr2:206599706
|
A | G | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2359+3544A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206599706 | ||||||
| chr2:206599785
|
A | G | 2 | a0001c0001t0002g0239a0001c0001t0002g0254 | 2 | HG03704.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.2359+3623A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206599785 | ||||||
| chr2:206599928
|
A | G | 17 | a0001c0001t0001g0013a0001c0001t0001g0048a0001c0001t0001g0050others(14): Show | 17 | HG00544.hp2 HG00673.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.2359+3766A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206599928 | ||||||
| chr2:206599968
|
A | G | 18 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0184others(15): Show | 18 | HG02451.hp2 HG02559.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.2359+3806A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206599968 | ||||||
| chr2:206600018
|
A | G | 2 | a0001c0001t0001g0087a0001c0001t0001g0089 | 2 | HG02040.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.2359+3856A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206600018 | ||||||
| chr2:206600024
|
G | A | 2 | a0001c0001t0001g0087a0001c0001t0001g0089 | 2 | HG02040.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.2359+3862G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206600024 | ||||||
| chr2:206600027
|
T | C | 2 | a0001c0001t0001g0087a0001c0001t0001g0089 | 2 | HG02040.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.2359+3865T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206600027 | ||||||
| chr2:206600046
|
A | T | 1 | a0001c0001t0001g0334 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2359+3884A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206600046 | ||||||
| chr2:206600066
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2359+3904G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206600066 | ||||||
| chr2:206600071
|
A | G | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(16): Show | 21 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.2359+3909A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206600071 | ||||||
| chr2:206600099
|
G | A | 1 | a0001c0001t0002g0153 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2359+3937G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206600099 | ||||||
| chr2:206600240
|
C | G | 56 | a0001c0001t0002g0022a0001c0001t0002g0139a0001c0001t0002g0152others(53): Show | 56 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.2359+4078C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206600240 | ||||||
| chr2:206600520
|
T | A | 1 | a0001c0001t0001g0319 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2359+4358T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206600520 | ||||||
| chr2:206600657
|
T | A | 1 | a0001c0002t0002g0008 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2359+4495T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206600657 | ||||||
| chr2:206600806
|
T | C | 44 | a0001c0001t0001g0004a0001c0001t0001g0088a0001c0001t0001g0094others(41): Show | 46 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.2359+4644T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206600806 | ||||||
| chr2:206601106
|
A | G | 163 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(160): Show | 167 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2359+4944A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206601106 | ||||||
| chr2:206601203
|
A | G | 12 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0025others(9): Show | 13 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.2359+5041A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206601203 | ||||||
| chr2:206601524
|
A | G | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2359+5362A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206601524 | ||||||
| chr2:206601601
|
C | T | 2 | a0001c0001t0008g0023a0001c0001t0008g0330 | 2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2359+5439C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206601601 | ||||||
| chr2:206601602
|
G | A | 2 | a0001c0001t0002g0176a0001c0001t0002g0212 | 2 | NA19003.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.2359+5440G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206601602 | ||||||
| chr2:206601745
|
G | C | 1 | a0001c0001t0002g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2359+5583G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206601745 | ||||||
| chr2:206601772
|
C | CA | 12 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0025others(9): Show | 13 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.2359+5627dupA | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr2 | 206601772 | |||||
| chr2:206601772
|
CA | C | 49 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(46): Show | 49 | HG01975.hp1 HG02056.hp2 HG02109.hp1 others(46): Show |
intron_variant | MODIFIER | c.2359+5627delA | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr2 | 206601772 | |||||
| chr2:206601836
|
C | T | 73 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(70): Show | 73 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(70): Show |
intron_variant | MODIFIER | c.2359+5674C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206601836 | ||||||
| chr2:206601932
|
T | TTA | 5 | a0001c0002t0001g0092a0001c0002t0002g0302a0001c0002t0011g0186others(2): Show | 5 | HG02886.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.2359+5774_2359+577 others(6): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr2 | 206601932 | |||||
| chr2:206602004
|
G | A | 2 | a0001c0001t0002g0176a0001c0001t0002g0212 | 2 | NA19003.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.2359+5842G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206602004 | ||||||
| chr2:206602527
|
C | G | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2359+6365C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206602527 | ||||||
| chr2:206602698
|
T | G | 1 | a0001c0001t0008g0347 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2359+6536T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206602698 | ||||||
| chr2:206603037
|
C | G | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2360-6873C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206603037 | ||||||
| chr2:206603038
|
G | A | 1 | a0001c0001t0001g0282 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2360-6872G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206603038 | ||||||
| chr2:206603190
|
AT | A | 14 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(11): Show | 16 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.2360-6713delT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr2 | 206603190 | |||||
| chr2:206603283
|
C | T | 4 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269others(1): Show | 4 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.2360-6627C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206603283 | ||||||
| chr2:206603827
|
A | T | 1 | a0001c0001t0002g0216 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2360-6083A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206603827 | ||||||
| chr2:206603961
|
C | CA | 7 | a0001c0001t0001g0136a0001c0001t0017g0039a0001c0001t0037g0228others(4): Show | 7 | HG02886.hp1 NA18973.hp2 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.2360-5932dupA | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr2 | 206603961 | |||||
| chr2:206603980
|
T | A | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2360-5930T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206603980 | ||||||
| chr2:206603987
|
C | T | 8 | a0001c0001t0006g0345a0001c0001t0006g0348a0001c0001t0006g0349others(5): Show | 8 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.2360-5923C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206603987 | ||||||
| chr2:206604123
|
G | T | 1 | a0001c0001t0002g0240 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2360-5787G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206604123 | ||||||
| chr2:206604191
|
G | A | 1 | a0001c0001t0002g0327 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2360-5719G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206604191 | ||||||
| chr2:206604220
|
C | A | 1 | a0001c0001t0004g0230 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2360-5690C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206604220 | ||||||
| chr2:206604580
|
A | G | 4 | a0001c0002t0002g0302a0001c0002t0011g0186a0001c0002t0011g0187others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2360-5330A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206604580 | ||||||
| chr2:206604605
|
A | G | 1 | a0001c0001t0002g0333 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2360-5305A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206604605 | ||||||
| chr2:206604681
|
A | G | 2 | a0001c0001t0005g0213a0001c0001t0005g0214 | 2 | NA18965.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.2360-5229A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206604681 | ||||||
| chr2:206604766
|
T | C | 1 | a0001c0001t0030g0179 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2360-5144T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206604766 | ||||||
| chr2:206604925
|
C | T | 17 | a0001c0002t0003g0093a0001c0002t0003g0109a0001c0002t0003g0126others(14): Show | 17 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.2360-4985C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206604925 | ||||||
| chr2:206605246
|
A | G | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2360-4664A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206605246 | ||||||
| chr2:206605258
|
C | T | 1 | a0001c0001t0002g0240 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2360-4652C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206605258 | ||||||
| chr2:206605527
|
CAAATT | C | 12 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0025others(9): Show | 13 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.2360-4382_2360-437 others(9): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206605527 | ||||||
| chr2:206605558
|
G | A | 1 | a0002c0003t0001g0062 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2360-4352G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206605558 | ||||||
| chr2:206605644
|
T | C | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2360-4266T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206605644 | ||||||
| chr2:206605742
|
A | G | 1 | a0001c0001t0001g0290 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2360-4168A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206605742 | ||||||
| chr2:206605947
|
C | T | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2360-3963C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206605947 | ||||||
| chr2:206605974
|
G | A | 1 | a0001c0001t0004g0223 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2360-3936G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206605974 | ||||||
| chr2:206606105
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2360-3805G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206606105 | ||||||
| chr2:206606160
|
T | C | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(108): Show | 113 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.2360-3750T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206606160 | ||||||
| chr2:206606437
|
T | C | 2 | a0001c0001t0002g0035a0001c0001t0026g0299 | 2 | HG02895.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2360-3473T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206606437 | ||||||
| chr2:206606553
|
A | G | 2 | a0001c0001t0002g0014a0001c0001t0007g0342 | 2 | HG02056.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2360-3357A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206606553 | ||||||
| chr2:206606602
|
A | G | 1 | a0001c0001t0001g0190 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2360-3308A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206606602 | ||||||
| chr2:206606913
|
A | G | 1 | a0001c0001t0002g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2360-2997A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206606913 | ||||||
| chr2:206606982
|
A | G | 1 | a0001c0002t0002g0138 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2360-2928A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206606982 | ||||||
| chr2:206607443
|
T | TA | 4 | a0001c0002t0002g0302a0001c0002t0011g0186a0001c0002t0011g0187others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2360-2466dupA | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr2 | 206607443 | |||||
| chr2:206607593
|
A | G | 1 | a0001c0001t0001g0319 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2360-2317A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206607593 | ||||||
| chr2:206607762
|
A | G | 1 | a0001c0002t0002g0144 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2360-2148A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206607762 | ||||||
| chr2:206607832
|
G | T | 18 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0184others(15): Show | 18 | HG02451.hp2 HG02559.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.2360-2078G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206607832 | ||||||
| chr2:206607849
|
A | G | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(108): Show | 113 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.2360-2061A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206607849 | ||||||
| chr2:206607882
|
G | GT | 196 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(193): Show | 200 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.2360-2018dupT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr2 | 206607882 | |||||
| chr2:206607914
|
T | C | 2 | a0001c0001t0021g0196a0001c0001t0021g0332 | 2 | NA19058.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.2360-1996T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206607914 | ||||||
| chr2:206607959
|
C | CTA | 291 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(288): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.2360-1950_2360-194 others(6): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr2 | 206607959 | |||||
| chr2:206608140
|
A | G | 1 | a0001c0002t0029g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2360-1770A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206608140 | ||||||
| chr2:206608259
|
G | A | 28 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0308others(25): Show | 28 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.2360-1651G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206608259 | ||||||
| chr2:206608314
|
A | G | 2 | a0001c0001t0002g0139a0001c0001t0002g0238 | 2 | HG01358.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.2360-1596A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206608314 | ||||||
| chr2:206608504
|
G | A | 2 | a0001c0001t0002g0035a0001c0001t0026g0299 | 2 | HG02895.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2360-1406G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206608504 | ||||||
| chr2:206608569
|
T | C | 3 | a0001c0001t0002g0231a0001c0001t0002g0233a0001c0001t0002g0266 | 3 | HG02523.hp1 NA19004.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.2360-1341T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206608569 | ||||||
| chr2:206608635
|
A | G | 1 | a0001c0001t0001g0300 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2360-1275A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206608635 | ||||||
| chr2:206608702
|
G | A | 1 | a0001c0001t0001g0017 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2360-1208G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206608702 | ||||||
| chr2:206608749
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0097 | 3 | HG01069.hp1 HG01071.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.2360-1161C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206608749 | ||||||
| chr2:206608939
|
T | C | 1 | a0001c0002t0002g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2360-971T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206608939 | ||||||
| chr2:206609022
|
G | A | 161 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(158): Show | 165 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.2360-888G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206609022 | ||||||
| chr2:206609029
|
A | G | 1 | a0001c0001t0002g0022 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2360-881A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206609029 | ||||||
| chr2:206609553
|
G | C | 1 | a0001c0001t0002g0022 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2360-357G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206609553 | ||||||
| chr2:206610404
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0097 | 3 | HG01069.hp1 HG01071.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.2450+404A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206610404 | ||||||
| chr2:206610624
|
T | C | 1 | a0001c0001t0002g0231 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2450+624T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206610624 | ||||||
| chr2:206610732
|
G | T | 1 | a0001c0001t0002g0246 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2450+732G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206610732 | ||||||
| chr2:206610737
|
C | A | 4 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0001t0002g0227others(1): Show | 4 | HG04204.hp2 NA18945.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.2450+737C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206610737 | ||||||
| chr2:206611193
|
T | G | 2 | a0001c0002t0002g0066a0001c0002t0002g0146 | 2 | HG03831.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.2450+1193T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206611193 | ||||||
| chr2:206611222
|
C | A | 2 | a0001c0001t0001g0099a0001c0001t0001g0104 | 2 | NA18990.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.2450+1222C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206611222 | ||||||
| chr2:206611228
|
T | G | 1 | a0001c0001t0001g0282 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2450+1228T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206611228 | ||||||
| chr2:206611435
|
TTTTC | T | 15 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(12): Show | 17 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.2450+1438_2450+144 others(8): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr2 | 206611435 | |||||
| chr2:206611440
|
T | G | 15 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(12): Show | 17 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.2450+1440T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206611440 | ||||||
| chr2:206611441
|
T | A | 15 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(12): Show | 17 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.2450+1441T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206611441 | ||||||
| chr2:206611519
|
A | T | 4 | a0001c0002t0002g0302a0001c0002t0011g0186a0001c0002t0011g0187others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2450+1519A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206611519 | ||||||
| chr2:206611537
|
C | A | 1 | a0001c0001t0001g0248 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2450+1537C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206611537 | ||||||
| chr2:206611598
|
C | T | 2 | a0001c0001t0002g0231a0001c0001t0002g0266 | 2 | HG02523.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.2450+1598C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206611598 | ||||||
| chr2:206611641
|
G | A | 1 | a0001c0002t0003g0167 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2450+1641G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206611641 | ||||||
| chr2:206611681
|
T | G | 2 | a0001c0001t0034g0079a0001c0001t0035g0078 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.2450+1681T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206611681 | ||||||
| chr2:206611846
|
A | G | 2 | a0001c0002t0002g0204a0001c0002t0002g0205 | 2 | NA18975.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.2450+1846A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206611846 | ||||||
| chr2:206611961
|
T | C | 1 | a0001c0001t0002g0233 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2450+1961T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206611961 | ||||||
| chr2:206612064
|
G | A | 1 | a0001c0002t0003g0160 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2450+2064G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206612064 | ||||||
| chr2:206612244
|
G | T | 1 | a0001c0001t0002g0231 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2450+2244G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206612244 | ||||||
| chr2:206612591
|
A | G | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2450+2591A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206612591 | ||||||
| chr2:206612595
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2450+2595T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206612595 | ||||||
| chr2:206612599
|
C | T | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(108): Show | 113 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.2450+2599C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206612599 | ||||||
| chr2:206612782
|
G | A | 1 | a0001c0001t0036g0270 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2450+2782G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206612782 | ||||||
| chr2:206613436
|
G | A | 159 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(156): Show | 162 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.2450+3436G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206613436 | ||||||
| chr2:206613676
|
C | A | 1 | a0001c0001t0001g0070 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2450+3676C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206613676 | ||||||
| chr2:206613719
|
G | T | 2 | a0001c0001t0021g0196a0001c0001t0021g0332 | 2 | NA19058.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.2450+3719G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206613719 | ||||||
| chr2:206613896
|
G | A | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2451-3683G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206613896 | ||||||
| chr2:206613925
|
T | C | 51 | a0001c0001t0002g0035a0001c0001t0002g0123a0001c0001t0002g0124others(48): Show | 52 | HG02056.hp2 HG02109.hp1 HG02145.hp1 others(49): Show |
intron_variant | MODIFIER | c.2451-3654T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206613925 | ||||||
| chr2:206614032
|
G | A | 1 | a0001c0001t0002g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2451-3547G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206614032 | ||||||
| chr2:206614052
|
A | G | 1 | a0001c0001t0001g0045 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2451-3527A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206614052 | ||||||
| chr2:206614415
|
C | CAGCACTT others(4): Show |
283 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(280): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.2451-3162_2451-316 others(15): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr2 | 206614415 | |||||
| chr2:206614528
|
G | A | 1 | a0001c0001t0001g0300 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2451-3051G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206614528 | ||||||
| chr2:206614577
|
G | A | 1 | a0001c0002t0003g0162 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.2451-3002G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206614577 | ||||||
| chr2:206614766
|
A | T | 3 | a0001c0002t0002g0198a0001c0002t0002g0199a0001c0002t0002g0323 | 3 | NA18956.hp1 NA18964.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.2451-2813A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206614766 | ||||||
| chr2:206614785
|
A | G | 5 | a0001c0002t0001g0092a0001c0002t0002g0302a0001c0002t0011g0186others(2): Show | 5 | HG02886.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.2451-2794A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206614785 | ||||||
| chr2:206614911
|
T | C | 5 | a0001c0002t0001g0092a0001c0002t0002g0302a0001c0002t0011g0186others(2): Show | 5 | HG02886.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.2451-2668T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206614911 | ||||||
| chr2:206614953
|
C | T | 1 | a0001c0001t0006g0345 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2451-2626C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206614953 | ||||||
| chr2:206614967
|
G | A | 12 | a0001c0001t0001g0013a0001c0001t0001g0048a0001c0001t0001g0050others(9): Show | 12 | HG00544.hp2 HG00673.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.2451-2612G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206614967 | ||||||
| chr2:206614978
|
C | T | 74 | a0001c0001t0002g0035a0001c0001t0002g0123a0001c0001t0002g0124others(71): Show | 75 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(72): Show |
intron_variant | MODIFIER | c.2451-2601C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206614978 | ||||||
| chr2:206615034
|
C | T | 1 | a0001c0001t0002g0191 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2451-2545C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206615034 | ||||||
| chr2:206615121
|
G | A | 4 | a0001c0002t0002g0074a0001c0002t0002g0077a0001c0002t0022g0075others(1): Show | 4 | HG02056.hp2 NA19000.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.2451-2458G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206615121 | ||||||
| chr2:206615168
|
T | C | 1 | a0001c0001t0001g0278 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2451-2411T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206615168 | ||||||
| chr2:206615230
|
A | C | 1 | a0001c0001t0002g0194 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2451-2349A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206615230 | ||||||
| chr2:206615347
|
G | A | 1 | a0001c0002t0010g0206 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2451-2232G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206615347 | ||||||
| chr2:206615354
|
A | G | 3 | a0001c0001t0013g0030a0001c0001t0013g0034a0003c0004t0013g0031 | 3 | HG01243.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2451-2225A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206615354 | ||||||
| chr2:206615357
|
C | T | 4 | a0001c0002t0002g0302a0001c0002t0011g0186a0001c0002t0011g0187others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2451-2222C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206615357 | ||||||
| chr2:206615397
|
C | T | 1 | a0001c0001t0001g0203 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2451-2182C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206615397 | ||||||
| chr2:206615403
|
A | G | 1 | a0001c0001t0002g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2451-2176A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206615403 | ||||||
| chr2:206615464
|
C | G | 1 | a0001c0001t0001g0336 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2451-2115C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206615464 | ||||||
| chr2:206615644
|
T | C | 1 | a0001c0001t0001g0156 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2451-1935T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206615644 | ||||||
| chr2:206615690
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2451-1889G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206615690 | ||||||
| chr2:206615884
|
C | T | 266 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(263): Show | 270 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.2451-1695C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206615884 | ||||||
| chr2:206615965
|
CTTGGT | C | 3 | a0001c0002t0001g0257a0001c0002t0001g0258a0001c0002t0001g0259 | 3 | HG02647.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2451-1610_2451-160 others(9): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr2 | 206615965 | |||||
| chr2:206616071
|
T | G | 1 | a0001c0001t0001g0319 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2451-1508T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206616071 | ||||||
| chr2:206616238
|
C | T | 1 | a0001c0002t0003g0178 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2451-1341C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206616238 | ||||||
| chr2:206616548
|
A | G | 1 | a0001c0001t0002g0233 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2451-1031A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206616548 | ||||||
| chr2:206616600
|
A | C | 1 | a0001c0001t0001g0293 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2451-979A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206616600 | ||||||
| chr2:206616718
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2451-861C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206616718 | ||||||
| chr2:206616730
|
C | T | 1 | a0001c0001t0002g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2451-849C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206616730 | ||||||
| chr2:206616901
|
T | A | 4 | a0001c0002t0015g0182a0001c0002t0015g0183a0001c0002t0019g0189others(1): Show | 4 | HG02055.hp1 HG02559.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2451-678T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206616901 | ||||||
| chr2:206617219
|
T | C | 159 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(156): Show | 162 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.2451-360T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206617219 | ||||||
| chr2:206617291
|
C | T | 8 | a0001c0001t0006g0345a0001c0001t0006g0348a0001c0001t0006g0349others(5): Show | 8 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.2451-288C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206617291 | ||||||
| chr2:206617301
|
C | T | 1 | a0001c0001t0006g0350 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2451-278C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206617301 | ||||||
| chr2:206617313
|
C | T | 45 | a0001c0001t0001g0004a0001c0001t0001g0088a0001c0001t0001g0094others(42): Show | 46 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.2451-266C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206617313 | ||||||
| chr2:206617464
|
C | T | 4 | a0001c0002t0002g0302a0001c0002t0011g0186a0001c0002t0011g0187others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2451-115C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206617464 |