Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 283461 |
|---|---|
| ensemblid | ENSG00000180116.15 |
| hgncid | 26846 |
| symbol | C12orf40 |
| name | chromosome 12 open reading frame 40 |
| refseq_nuc | NM_001031748.4 |
| refseq_prot | NP_001026918.2 |
| ensembl_nuc | ENST00000324616.9 |
| ensembl_prot | ENSP00000317671.5 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 39626183 |
| end | 39721914 |
| strand | + |
| ver | v1.2 |
| region | chr12:39626183-39721914 |
| region5000 | chr12:39621183-39726914 |
| regionname0 | C12orf40_chr12_39626183_39721914 |
| regionname5000 | C12orf40_chr12_39621183_39726914 |
| 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 | 652 | 300 | 72 | 51 | 131 | 9 | 35 | 101 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| a0002 | 0/0 | 652 | 47 | 5 | 10 | 27 | 0 | 5 | 17 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| a0003 | 0/0 | 652 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| a0004 | 0/0 | 652 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| a0005 | 0/0 | 652 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| a0006 | 0/0 | 652 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| a0007 | 0/0 | 652 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| a0008 | 0/0 | 652 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| a0009 | 0/0 | 652 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| a0010 | 0/0 | 652 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| a0011 | 0/0 | 652 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| 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 | 1959 | 299 | 71 | 51 | 131 | 9 | 35 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| c0002 | 0/0 | 1959 | 47 | 5 | 10 | 27 | 0 | 5 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| c0003 | 0/0 | 1959 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| c0004 | 0/0 | 1959 | 2 | 0 | 0 | 2 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| c0005 | 0/0 | 1959 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| c0006 | 0/0 | 1959 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| c0007 | 0/0 | 1959 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| c0008 | 0/0 | 1959 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| c0009 | 0/0 | 1959 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| c0010 | 0/0 | 1959 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| c0011 | 0/0 | 1959 | 1 | 0 | 0 | 0 | 1 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| c0012 | 0/0 | 1959 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 818 | 344 | 72 | 62 | 159 | 9 | 40 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| t0002 | 0/0 | 818 | 7 | 7 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| t0003 | 0/0 | 814 | 4 | 4 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| t0004 | 0/0 | 818 | 3 | 1 | 1 | 0 | 1 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| t0005 | 0/0 | 818 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| t0006 | 0/0 | 818 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| 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 | 4 | 0 | 0 | 4 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0019 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0143 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| 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 | 1959 | 299 | 71 | 51 | 131 | 9 | 35 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| a0001c0007 | 0/0 | 1959 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| a0002c0002 | 0/0 | 1959 | 47 | 5 | 10 | 27 | 0 | 5 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| a0003c0005 | 0/0 | 1959 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| a0004c0004 | 0/0 | 1959 | 2 | 0 | 0 | 2 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| a0005c0003 | 0/0 | 1959 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| a0006c0006 | 0/0 | 1959 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| a0007c0012 | 0/0 | 1959 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| a0008c0009 | 0/0 | 1959 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| a0009c0008 | 0/0 | 1959 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| a0010c0010 | 0/0 | 1959 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| a0011c0011 | 0/0 | 1959 | 1 | 0 | 0 | 0 | 1 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2776 | 284 | 59 | 49 | 131 | 8 | 35 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| a0001c0001t0002 | 0/0 | 2776 | 7 | 7 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| a0001c0001t0003 | 0/0 | 2772 | 4 | 4 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| a0001c0001t0004 | 0/0 | 2776 | 3 | 1 | 1 | 0 | 1 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| a0001c0001t0006 | 0/0 | 2776 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| a0001c0007t0001 | 0/0 | 2776 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| a0002c0002t0001 | 0/0 | 2776 | 47 | 5 | 10 | 27 | 0 | 5 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| a0003c0005t0001 | 0/0 | 2776 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| a0004c0004t0001 | 0/0 | 2776 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| a0004c0004t0005 | 0/0 | 2776 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| a0005c0003t0001 | 0/0 | 2776 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| a0006c0006t0001 | 0/0 | 2776 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| a0007c0012t0001 | 0/0 | 2776 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| a0008c0009t0001 | 0/0 | 2776 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| a0009c0008t0001 | 0/0 | 2776 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| a0010c0010t0001 | 0/0 | 2776 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| a0011c0011t0001 | 0/0 | 2776 | 1 | 0 | 0 | 0 | 1 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | copy fasta | chr12 | 39621183 | 39726914 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0019 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0143 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0002g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0002g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0001t0006g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0001c0007t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0002c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0003c0005t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0003c0005t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0004c0004t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0004c0004t0005g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0005c0003t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0005c0003t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0006c0006t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0006c0006t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0007c0012t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0008c0009t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0009c0008t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0010c0010t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| a0011c0011t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0055 | EUR | GBR | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0167 | EUR | GBR | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0211 | EUR | GBR | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0175 | EUR | GBR | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0177 | EUR | FIN | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0208 | EUR | FIN | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0122 | EAS | CHS | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | CHS | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | CHS | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | CHS | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | CHS | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | CHS | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | CHS | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | CHS | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | CHS | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | CHS | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG00642 | hp1 | a0007 | c0012 | t0001 | g0171 | AMR | PUR | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0127 | AMR | PUR | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | CHS | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG00733 | hp1 | a0001 | c0001 | t0006 | g0033 | AMR | PUR | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0105 | AMR | PUR | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0138 | AMR | PUR | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0059 | AMR | PUR | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0095 | AMR | PUR | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01175 | hp1 | a0009 | c0008 | t0001 | g0068 | AMR | PUR | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01175 | hp2 | a0010 | c0010 | t0001 | g0096 | AMR | PUR | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0137 | AMR | PUR | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0101 | AMR | CLM | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0102 | AMR | CLM | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | CLM | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0109 | AMR | CLM | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0334 | AMR | CLM | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0108 | AMR | CLM | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0219 | EUR | IBS | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0197 | EUR | IBS | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | ACB | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0107 | AMR | PEL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PEL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PEL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | PEL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0123 | EAS | KHV | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0313 | EAS | KHV | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0321 | AFR | ACB | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0112 | EAS | KHV | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | KHV | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0128 | EAS | KHV | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0132 | EAS | KHV | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | KHV | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0126 | EAS | KHV | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0134 | EAS | KHV | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | KHV | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0099 | AFR | ACB | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0331 | AFR | ACB | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0103 | EAS | CDX | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | CDX | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | ACB | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0332 | AFR | GWD | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0090 | SAS | PJL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0093 | SAS | PJL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0315 | SAS | PJL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0314 | SAS | PJL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0094 | AFR | GWD | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0326 | AFR | GWD | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0081 | AFR | GWD | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0078 | AFR | GWD | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0116 | AFR | GWD | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | GWD | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | GWD | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0328 | AFR | ESN | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | ESN | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | ESN | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0079 | AFR | GWD | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0098 | AFR | GWD | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | ESN | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03139 | hp2 | a0005 | c0003 | t0001 | g0035 | AFR | ESN | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03195 | hp1 | a0006 | c0006 | t0001 | g0106 | AFR | ESN | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | MSL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0327 | AFR | MSL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0329 | AFR | MSL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0080 | AFR | MSL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0129 | SAS | PJL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03453 | hp1 | a0008 | c0009 | t0001 | g0226 | AFR | MSL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | MSL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ESN | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ESN | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0100 | AFR | MSL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | MSL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0339 | SAS | PJL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | BEB | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | BEB | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | BEB | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | BEB | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | BEB | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | STU | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | STU | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0119 | SAS | BEB | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | STU | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | STU | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | STU | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | STU | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0325 | AFR | YRI | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18522 | hp2 | a0003 | c0005 | t0001 | g0336 | AFR | YRI | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0083 | EAS | CHB | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | CHB | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | YRI | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0320 | AFR | YRI | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0139 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18989 | hp2 | a0004 | c0004 | t0001 | g0130 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18991 | hp2 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19005 | hp1 | a0004 | c0004 | t0005 | g0135 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19006 | hp1 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | LWK | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | LWK | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0330 | AFR | LWK | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19058 | hp2 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0118 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19075 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0117 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19078 | hp2 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0124 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19240 | hp1 | a0006 | c0006 | t0001 | g0333 | AFR | YRI | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | YRI | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0319 | AFR | ASW | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA20129 | hp2 | a0003 | c0005 | t0001 | g0335 | AFR | ASW | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0206 | EUR | TSI | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA20752 | hp2 | a0011 | c0011 | t0001 | g0073 | EUR | TSI | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0104 | SAS | GIH | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | GIH | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02486 | hp2 | a0001 | c0007 | t0001 | g0024 | AFR | ACB | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | USA | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | USA | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | USA | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA20300 | hp2 | a0005 | c0003 | t0001 | g0034 | AFR | USA | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | LWK | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0060 | AFR | LWK | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0143 | REF | REF | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0019 | REF | REF | C12orf40_chr12_39621183_39726914 | C12orf40 | chr12 | 39621183 | 39726914 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:39640968
|
A | C | 1 | a0006 | 2 | HG03195.hp1 NA19240.hp1 |
missense_variant | MODERATE | c.37A>C | p.Ile13Leu | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 2/13 | 191/2776 | 37/1959 | 13/652 | chr12 | 39640968 | ||
| chr12:39643781
|
A | C | 1 | a0007 | 1 | HG00642.hp1 | missense_variant&splice_region_variant | MODERATE | c.66A>C | p.Glu22Asp | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 3/13 | 220/2776 | 66/1959 | 22/652 | chr12 | 39643781 | ||
| chr12:39650294
|
A | T | 1 | a0011 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.626A>T | p.Asp209Val | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/13 | 780/2776 | 626/1959 | 209/652 | chr12 | 39650294 | ||
| chr12:39682958
|
G | A | 1 | a0005 | 2 | HG03139.hp2 NA20300.hp2 |
missense_variant | MODERATE | c.1034G>A | p.Cys345Tyr | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 8/13 | 1188/2776 | 1034/1959 | 345/652 | chr12 | 39682958 | ||
| chr12:39683129
|
C | G | 1 | a0003 | 2 | NA18522.hp2 NA20129.hp2 |
missense_variant | MODERATE | c.1205C>G | p.Ser402Cys | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 8/13 | 1359/2776 | 1205/1959 | 402/652 | chr12 | 39683129 | ||
| chr12:39692104
|
A | T | 4 | a0002a0004a0006others(1): Show | 52 | HG00408.hp1 HG00642.hp2 HG00738.hp2 others(49): Show |
missense_variant | MODERATE | c.1403A>T | p.Lys468Met | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/13 | 1557/2776 | 1403/1959 | 468/652 | chr12 | 39692104 | ||
| chr12:39720826
|
G | T | 1 | a0004 | 2 | NA18989.hp2 NA19005.hp1 |
missense_variant | MODERATE | c.1534G>T | p.Asp512Tyr | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 13/13 | 1688/2776 | 1534/1959 | 512/652 | chr12 | 39720826 | ||
| chr12:39720875
|
A | T | 1 | a0008 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.1583A>T | p.Tyr528Phe | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 13/13 | 1737/2776 | 1583/1959 | 528/652 | chr12 | 39720875 | ||
| chr12:39720979
|
A | G | 1 | a0010 | 1 | HG01175.hp2 | missense_variant | MODERATE | c.1687A>G | p.Thr563Ala | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 13/13 | 1841/2776 | 1687/1959 | 563/652 | chr12 | 39720979 | ||
| chr12:39721048
|
G | A | 1 | a0009 | 1 | HG01175.hp1 | missense_variant | MODERATE | c.1756G>A | p.Val586Ile | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 13/13 | 1910/2776 | 1756/1959 | 586/652 | chr12 | 39721048 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:39720942
|
G | A | 1 | a0001c0007 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.1650G>A | p.Gln550Gln | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 13/13 | 1804/2776 | 1650/1959 | 550/652 | chr12 | 39720942 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:39626313
|
C | G | 1 | a0001c0001t0002 | 7 | HG02055.hp1 HG02559.hp1 HG02965.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-24C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/13 | 24 | chr12 | 39626313 | |||||
| chr12:39721362
|
T | G | 1 | a0004c0004t0005 | 1 | NA19005.hp1 | 3_prime_UTR_variant | MODIFIER | c.*111T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 13/13 | 111 | chr12 | 39721362 | |||||
| chr12:39721516
|
G | A | 1 | a0001c0001t0006 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*265G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 13/13 | 265 | chr12 | 39721516 | |||||
| chr12:39721552
|
G | A | 1 | a0001c0001t0006 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*301G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 13/13 | 301 | chr12 | 39721552 | |||||
| chr12:39721727
|
C | G | 1 | a0001c0001t0004 | 3 | HG00099.hp1 HG01070.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*476C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 13/13 | 476 | chr12 | 39721727 | |||||
| chr12:39721819
|
TATTA | T | 1 | a0001c0001t0003 | 4 | HG02809.hp1 HG02818.hp1 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*572_*575delAATT | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 13/13 | 572 | INFO_REALIGN_3_PRIME | chr12 | 39721819 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:39626616
|
C | G | 1 | a0001c0001t0001g0339 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.23+257C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39626616 | ||||||
| chr12:39626628
|
T | C | 1 | a0001c0001t0001g0339 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.23+269T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39626628 | ||||||
| chr12:39626668
|
A | G | 2 | a0001c0001t0001g0337a0001c0001t0001g0338 | 2 | NA18946.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.23+309A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39626668 | ||||||
| chr12:39626954
|
G | T | 337 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(334): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.23+595G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39626954 | ||||||
| chr12:39626966
|
A | G | 2 | a0003c0005t0001g0335a0003c0005t0001g0336 | 2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.23+607A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39626966 | ||||||
| chr12:39627042
|
G | A | 1 | a0001c0001t0001g0021 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.23+683G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39627042 | ||||||
| chr12:39627154
|
A | G | 1 | a0001c0001t0001g0334 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.23+795A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39627154 | ||||||
| chr12:39627286
|
G | A | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.23+927G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39627286 | ||||||
| chr12:39627450
|
T | C | 1 | a0001c0007t0001g0024 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.23+1091T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39627450 | ||||||
| chr12:39627484
|
A | G | 18 | a0001c0001t0001g0003a0001c0001t0001g0318a0001c0001t0001g0322others(15): Show | 19 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.23+1125A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39627484 | ||||||
| chr12:39628227
|
C | A | 255 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.23+1868C>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39628227 | ||||||
| chr12:39628257
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.23+1898G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39628257 | ||||||
| chr12:39628439
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.23+2080G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39628439 | ||||||
| chr12:39628471
|
G | C | 60 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0022others(57): Show | 62 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.23+2112G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39628471 | ||||||
| chr12:39628491
|
C | T | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG00558.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.23+2132C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39628491 | ||||||
| chr12:39628838
|
C | T | 1 | a0001c0001t0001g0334 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.23+2479C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39628838 | ||||||
| chr12:39628840
|
A | G | 1 | a0001c0001t0001g0243 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.23+2481A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39628840 | ||||||
| chr12:39628903
|
T | C | 17 | a0001c0001t0001g0003a0001c0001t0001g0318a0001c0001t0001g0322others(14): Show | 18 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.23+2544T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39628903 | ||||||
| chr12:39629085
|
G | T | 1 | a0001c0001t0001g0242 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.23+2726G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39629085 | ||||||
| chr12:39629140
|
A | C | 3 | a0001c0001t0001g0005a0001c0001t0001g0076a0001c0001t0001g0077 | 4 | HG00639.hp1 HG01074.hp2 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.23+2781A>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39629140 | ||||||
| chr12:39629200
|
G | C | 258 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(255): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.23+2841G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39629200 | ||||||
| chr12:39629413
|
A | G | 10 | a0001c0001t0001g0013a0001c0001t0001g0232a0001c0001t0001g0233others(7): Show | 11 | HG00597.hp2 HG03831.hp2 NA18941.hp2 others(8): Show |
intron_variant | MODIFIER | c.23+3054A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39629413 | ||||||
| chr12:39629500
|
G | T | 1 | a0001c0001t0001g0231 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.23+3141G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39629500 | ||||||
| chr12:39629550
|
C | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.23+3191C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39629550 | ||||||
| chr12:39629596
|
G | A | 1 | a0001c0001t0001g0250 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.23+3237G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39629596 | ||||||
| chr12:39629616
|
G | A | 2 | a0001c0001t0001g0251a0001c0001t0001g0252 | 2 | HG04228.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.23+3257G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39629616 | ||||||
| chr12:39629672
|
T | C | 4 | a0001c0001t0003g0078a0001c0001t0003g0079a0001c0001t0003g0080others(1): Show | 4 | HG02809.hp1 HG02818.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.23+3313T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39629672 | ||||||
| chr12:39629845
|
T | A | 1 | a0001c0001t0001g0244 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.23+3486T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39629845 | ||||||
| chr12:39630113
|
A | G | 1 | a0001c0001t0001g0230 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.23+3754A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39630113 | ||||||
| chr12:39630178
|
T | C | 12 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(9): Show | 13 | HG00733.hp1 HG01169.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.23+3819T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39630178 | ||||||
| chr12:39630281
|
C | T | 3 | a0001c0001t0001g0229a0001c0001t0001g0314a0001c0001t0001g0315 | 3 | HG02683.hp2 HG02698.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.23+3922C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39630281 | ||||||
| chr12:39630527
|
T | C | 2 | a0002c0002t0001g0082a0002c0002t0001g0083 | 2 | NA18747.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.23+4168T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39630527 | ||||||
| chr12:39630528
|
A | G | 1 | a0001c0001t0001g0005 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.23+4169A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39630528 | ||||||
| chr12:39630624
|
A | C | 1 | a0001c0001t0001g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.23+4265A>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39630624 | ||||||
| chr12:39630892
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.23+4533C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39630892 | ||||||
| chr12:39630928
|
G | A | 44 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(41): Show | 45 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.23+4569G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39630928 | ||||||
| chr12:39631023
|
C | T | 21 | a0001c0001t0001g0003a0001c0001t0001g0075a0001c0001t0001g0227others(18): Show | 22 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.23+4664C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39631023 | ||||||
| chr12:39631030
|
A | T | 3 | a0001c0001t0001g0330a0001c0001t0001g0331a0001c0001t0001g0332 | 3 | HG02145.hp2 HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.23+4671A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39631030 | ||||||
| chr12:39631086
|
T | C | 6 | a0001c0001t0001g0006a0001c0001t0001g0084a0001c0001t0001g0085others(3): Show | 7 | NA18945.hp2 NA18961.hp1 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.23+4727T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39631086 | ||||||
| chr12:39631102
|
C | T | 44 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(41): Show | 45 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.23+4743C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39631102 | ||||||
| chr12:39631232
|
A | G | 180 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(177): Show | 191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.23+4873A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39631232 | ||||||
| chr12:39631325
|
A | G | 25 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0204others(22): Show | 25 | HG00140.hp1 HG00280.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.23+4966A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39631325 | ||||||
| chr12:39631382
|
A | G | 2 | a0001c0001t0001g0311a0001c0001t0001g0312 | 2 | NA18945.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.23+5023A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39631382 | ||||||
| chr12:39631607
|
A | G | 3 | a0001c0007t0001g0024a0005c0003t0001g0034a0005c0003t0001g0035 | 3 | HG02486.hp2 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.23+5248A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39631607 | ||||||
| chr12:39631886
|
A | T | 82 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(79): Show | 92 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.23+5527A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39631886 | ||||||
| chr12:39631942
|
T | C | 3 | a0001c0001t0001g0330a0001c0001t0001g0331a0001c0001t0001g0332 | 3 | HG02145.hp2 HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.23+5583T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39631942 | ||||||
| chr12:39632039
|
A | G | 1 | a0001c0001t0001g0310 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.23+5680A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39632039 | ||||||
| chr12:39632051
|
G | GTA | 176 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(173): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.23+5707_23+5708dup others(2): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 39632051 | |||||
| chr12:39632051
|
G | GTATA | 3 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201 | 3 | HG00544.hp2 HG03834.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.23+5705_23+5708dup others(4): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 39632051 | |||||
| chr12:39632206
|
C | T | 1 | a0001c0001t0001g0309 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.23+5847C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39632206 | ||||||
| chr12:39632221
|
C | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.23+5862C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39632221 | ||||||
| chr12:39632448
|
T | C | 1 | a0001c0001t0001g0253 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.23+6089T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39632448 | ||||||
| chr12:39632449
|
T | A | 1 | a0001c0001t0001g0145 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.23+6090T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39632449 | ||||||
| chr12:39632658
|
A | C | 11 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(8): Show | 11 | HG00738.hp1 HG01106.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.23+6299A>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39632658 | ||||||
| chr12:39632658
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.23+6299A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39632658 | ||||||
| chr12:39632708
|
G | A | 1 | a0008c0009t0001g0226 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.23+6349G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39632708 | ||||||
| chr12:39632823
|
T | A | 1 | a0001c0001t0001g0089 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.23+6464T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39632823 | ||||||
| chr12:39632990
|
T | G | 1 | a0002c0002t0001g0090 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.23+6631T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39632990 | ||||||
| chr12:39633031
|
A | G | 1 | a0001c0001t0006g0033 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.23+6672A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39633031 | ||||||
| chr12:39633462
|
C | T | 2 | a0005c0003t0001g0034a0005c0003t0001g0035 | 2 | HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.23+7103C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39633462 | ||||||
| chr12:39633549
|
A | G | 2 | a0001c0001t0001g0227a0001c0001t0001g0230 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.23+7190A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39633549 | ||||||
| chr12:39633787
|
C | G | 1 | a0001c0001t0001g0225 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.24-7168C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39633787 | ||||||
| chr12:39633792
|
C | T | 1 | a0008c0009t0001g0226 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.24-7163C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39633792 | ||||||
| chr12:39633827
|
C | T | 1 | a0001c0001t0001g0308 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.24-7128C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39633827 | ||||||
| chr12:39633973
|
C | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.24-6982C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39633973 | ||||||
| chr12:39633990
|
G | A | 21 | a0001c0001t0001g0003a0001c0001t0001g0227a0001c0001t0001g0230others(18): Show | 22 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.24-6965G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39633990 | ||||||
| chr12:39634090
|
G | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(5): Show | 9 | HG01169.hp1 HG01192.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.24-6865G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39634090 | ||||||
| chr12:39634105
|
G | A | 58 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0022others(55): Show | 60 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.24-6850G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39634105 | ||||||
| chr12:39634286
|
C | T | 30 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(27): Show | 30 | HG00140.hp1 HG00280.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.24-6669C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39634286 | ||||||
| chr12:39634338
|
C | T | 1 | a0001c0001t0006g0033 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.24-6617C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39634338 | ||||||
| chr12:39634698
|
G | T | 1 | a0001c0001t0001g0241 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.24-6257G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39634698 | ||||||
| chr12:39634777
|
A | T | 1 | a0001c0001t0003g0081 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.24-6178A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39634777 | ||||||
| chr12:39634795
|
T | C | 2 | a0005c0003t0001g0034a0005c0003t0001g0035 | 2 | HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.24-6160T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39634795 | ||||||
| chr12:39634886
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.24-6069G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39634886 | ||||||
| chr12:39635048
|
A | G | 1 | a0002c0002t0001g0083 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.24-5907A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39635048 | ||||||
| chr12:39635123
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.24-5832C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39635123 | ||||||
| chr12:39635207
|
A | C | 1 | a0001c0001t0001g0032 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.24-5748A>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39635207 | ||||||
| chr12:39635214
|
C | A | 1 | a0001c0007t0001g0024 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.24-5741C>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39635214 | ||||||
| chr12:39635227
|
C | T | 1 | a0001c0001t0001g0016 | 2 | HG02083.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.24-5728C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39635227 | ||||||
| chr12:39635236
|
G | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(5): Show | 9 | HG01169.hp1 HG01192.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.24-5719G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39635236 | ||||||
| chr12:39635237
|
A | G | 1 | a0001c0001t0003g0081 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.24-5718A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39635237 | ||||||
| chr12:39635438
|
A | G | 31 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0247others(28): Show | 31 | HG00408.hp1 HG00642.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.24-5517A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39635438 | ||||||
| chr12:39635648
|
C | T | 4 | a0001c0001t0006g0033a0001c0007t0001g0024a0005c0003t0001g0034others(1): Show | 4 | HG00733.hp1 HG02486.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.24-5307C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39635648 | ||||||
| chr12:39635665
|
G | A | 13 | a0001c0001t0001g0003a0001c0001t0001g0318a0001c0001t0001g0322others(10): Show | 14 | HG01884.hp1 HG02055.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.24-5290G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39635665 | ||||||
| chr12:39635808
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.24-5147T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39635808 | ||||||
| chr12:39635924
|
C | G | 234 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(231): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.24-5031C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39635924 | ||||||
| chr12:39636137
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.24-4818C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39636137 | ||||||
| chr12:39636153
|
A | T | 3 | a0001c0001t0001g0330a0001c0001t0001g0331a0001c0001t0001g0332 | 3 | HG02145.hp2 HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.24-4802A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39636153 | ||||||
| chr12:39636164
|
C | T | 5 | a0001c0001t0003g0078a0001c0001t0003g0079a0001c0001t0003g0080others(2): Show | 5 | HG02809.hp1 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.24-4791C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39636164 | ||||||
| chr12:39636199
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.24-4756T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39636199 | ||||||
| chr12:39636231
|
G | A | 1 | a0001c0001t0001g0241 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.24-4724G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39636231 | ||||||
| chr12:39636302
|
C | T | 1 | a0001c0001t0006g0033 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.24-4653C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39636302 | ||||||
| chr12:39637066
|
T | C | 2 | a0005c0003t0001g0034a0005c0003t0001g0035 | 2 | HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.24-3889T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39637066 | ||||||
| chr12:39637126
|
C | T | 22 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0244others(19): Show | 24 | HG00408.hp2 HG00621.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.24-3829C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39637126 | ||||||
| chr12:39637364
|
C | A | 1 | a0001c0001t0001g0147 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.24-3591C>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39637364 | ||||||
| chr12:39637372
|
C | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.24-3583C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39637372 | ||||||
| chr12:39637390
|
A | G | 36 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0043others(33): Show | 37 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.24-3565A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39637390 | ||||||
| chr12:39637408
|
C | G | 1 | a0001c0001t0001g0012 | 2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.24-3547C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39637408 | ||||||
| chr12:39637433
|
C | T | 1 | a0001c0001t0001g0063 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.24-3522C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39637433 | ||||||
| chr12:39637548
|
A | G | 1 | a0001c0001t0001g0197 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.24-3407A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39637548 | ||||||
| chr12:39637682
|
A | G | 1 | a0001c0001t0006g0033 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.24-3273A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39637682 | ||||||
| chr12:39637757
|
T | C | 1 | a0001c0001t0001g0254 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.24-3198T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39637757 | ||||||
| chr12:39637780
|
A | G | 1 | a0001c0001t0006g0033 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.24-3175A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39637780 | ||||||
| chr12:39637953
|
T | C | 2 | a0001c0001t0001g0075a0008c0009t0001g0226 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.24-3002T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39637953 | ||||||
| chr12:39638084
|
C | T | 25 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0043others(22): Show | 26 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.24-2871C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39638084 | ||||||
| chr12:39638241
|
C | T | 255 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.24-2714C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39638241 | ||||||
| chr12:39638400
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.24-2555A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39638400 | ||||||
| chr12:39638466
|
A | G | 1 | a0001c0001t0001g0241 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.24-2489A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39638466 | ||||||
| chr12:39638758
|
C | T | 255 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.24-2197C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39638758 | ||||||
| chr12:39638759
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.24-2196G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39638759 | ||||||
| chr12:39638786
|
C | T | 2 | a0001c0001t0001g0196a0001c0001t0001g0201 | 2 | HG00544.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.24-2169C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39638786 | ||||||
| chr12:39639004
|
A | C | 2 | a0003c0005t0001g0335a0003c0005t0001g0336 | 2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.24-1951A>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39639004 | ||||||
| chr12:39639014
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.24-1941G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39639014 | ||||||
| chr12:39639108
|
T | C | 1 | a0001c0001t0001g0204 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.24-1847T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39639108 | ||||||
| chr12:39639252
|
T | C | 2 | a0001c0001t0001g0065a0001c0001t0001g0066 | 2 | HG02129.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.24-1703T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39639252 | ||||||
| chr12:39639312
|
T | C | 1 | a0001c0001t0006g0033 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.24-1643T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39639312 | ||||||
| chr12:39639335
|
G | C | 38 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(35): Show | 39 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.24-1620G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39639335 | ||||||
| chr12:39639670
|
A | G | 1 | a0001c0001t0001g0005 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.24-1285A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39639670 | ||||||
| chr12:39639841
|
T | G | 145 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(142): Show | 156 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.24-1114T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39639841 | ||||||
| chr12:39639877
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.24-1078T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39639877 | ||||||
| chr12:39639948
|
T | C | 1 | a0001c0007t0001g0024 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.24-1007T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39639948 | ||||||
| chr12:39640102
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.24-853G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39640102 | ||||||
| chr12:39640193
|
G | A | 1 | a0001c0001t0001g0241 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.24-762G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39640193 | ||||||
| chr12:39640570
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.24-385G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39640570 | ||||||
| chr12:39640662
|
C | A | 3 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0208 | 3 | HG00280.hp2 HG03239.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.24-293C>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39640662 | ||||||
| chr12:39640897
|
G | A | 58 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0022others(55): Show | 60 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.24-58G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 1/12 | chr12 | 39640897 | ||||||
| chr12:39641138
|
C | G | 2 | a0002c0002t0001g0139a0002c0002t0001g0140 | 2 | NA18971.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.63+144C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 2/12 | chr12 | 39641138 | ||||||
| chr12:39641442
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.63+448A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 2/12 | chr12 | 39641442 | ||||||
| chr12:39641490
|
A | T | 1 | a0001c0001t0001g0074 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.63+496A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 2/12 | chr12 | 39641490 | ||||||
| chr12:39641499
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.63+505A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 2/12 | chr12 | 39641499 | ||||||
| chr12:39641850
|
G | C | 1 | a0001c0001t0001g0075 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.63+856G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 2/12 | chr12 | 39641850 | ||||||
| chr12:39641965
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.63+971G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 2/12 | chr12 | 39641965 | ||||||
| chr12:39642131
|
T | C | 1 | a0001c0001t0006g0033 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.63+1137T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 2/12 | chr12 | 39642131 | ||||||
| chr12:39642237
|
T | C | 1 | a0001c0001t0001g0205 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.63+1243T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 2/12 | chr12 | 39642237 | ||||||
| chr12:39642242
|
A | G | 6 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0001g0286others(3): Show | 6 | HG00438.hp1 HG00544.hp1 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+1248A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 2/12 | chr12 | 39642242 | ||||||
| chr12:39642298
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.63+1304G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 2/12 | chr12 | 39642298 | ||||||
| chr12:39642385
|
A | G | 2 | a0001c0001t0001g0195a0001c0001t0001g0231 | 2 | HG01123.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.63+1391A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 2/12 | chr12 | 39642385 | ||||||
| chr12:39642402
|
C | T | 1 | a0001c0007t0001g0024 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.64-1377C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 2/12 | chr12 | 39642402 | ||||||
| chr12:39642536
|
C | T | 58 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0022others(55): Show | 60 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.64-1243C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 2/12 | chr12 | 39642536 | ||||||
| chr12:39642549
|
T | C | 1 | a0001c0001t0001g0318 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.64-1230T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 2/12 | chr12 | 39642549 | ||||||
| chr12:39642637
|
A | G | 1 | a0001c0001t0001g0249 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.64-1142A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 2/12 | chr12 | 39642637 | ||||||
| chr12:39642811
|
C | G | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG03017.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.64-968C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 2/12 | chr12 | 39642811 | ||||||
| chr12:39643038
|
T | A | 261 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(258): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.64-741T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 2/12 | chr12 | 39643038 | ||||||
| chr12:39643329
|
T | TGATTTG | 2 | a0001c0001t0001g0004a0001c0001t0001g0031 | 3 | HG02109.hp1 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.64-450_64-449insGA others(4): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 2/12 | chr12 | 39643329 | ||||||
| chr12:39643330
|
A | AATTTGC | 5 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0030others(2): Show | 5 | HG01192.hp2 HG02451.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-447_64-442dupTT others(4): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 39643330 | |||||
| chr12:39643330
|
A | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0031 | 3 | HG02109.hp1 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.64-449A>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 2/12 | chr12 | 39643330 | ||||||
| chr12:39643393
|
A | G | 1 | a0001c0001t0001g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.64-386A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 2/12 | chr12 | 39643393 | ||||||
| chr12:39643502
|
T | C | 1 | a0001c0001t0001g0244 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.64-277T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 2/12 | chr12 | 39643502 | ||||||
| chr12:39643925
|
A | G | 240 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(237): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
splice_region_variant&intron_variant | LOW | c.202+8A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 3/12 | chr12 | 39643925 | ||||||
| chr12:39643958
|
A | T | 1 | a0001c0001t0001g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.202+41A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 3/12 | chr12 | 39643958 | ||||||
| chr12:39644096
|
C | T | 1 | a0001c0001t0001g0075 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.202+179C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 3/12 | chr12 | 39644096 | ||||||
| chr12:39644418
|
A | G | 1 | a0001c0001t0006g0033 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.202+501A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 3/12 | chr12 | 39644418 | ||||||
| chr12:39644492
|
A | C | 56 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0247others(53): Show | 57 | HG00408.hp1 HG00642.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.202+575A>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 3/12 | chr12 | 39644492 | ||||||
| chr12:39644699
|
A | C | 238 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(235): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.202+782A>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 3/12 | chr12 | 39644699 | ||||||
| chr12:39644790
|
G | A | 1 | a0001c0001t0001g0329 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.202+873G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 3/12 | chr12 | 39644790 | ||||||
| chr12:39645103
|
G | A | 181 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(178): Show | 192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.202+1186G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 3/12 | chr12 | 39645103 | ||||||
| chr12:39645376
|
A | G | 44 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(41): Show | 45 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.203-953A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 3/12 | chr12 | 39645376 | ||||||
| chr12:39645691
|
G | A | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.203-638G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 3/12 | chr12 | 39645691 | ||||||
| chr12:39645871
|
G | T | 1 | a0001c0001t0002g0328 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.203-458G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 3/12 | chr12 | 39645871 | ||||||
| chr12:39646236
|
A | G | 3 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115 | 3 | HG02717.hp1 HG02809.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.203-93A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 3/12 | chr12 | 39646236 | ||||||
| chr12:39646257
|
G | GA | 58 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0022others(55): Show | 60 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.203-71dupA | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 39646257 | |||||
| chr12:39646527
|
C | T | 1 | a0001c0001t0003g0080 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.335+66C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 4/12 | chr12 | 39646527 | ||||||
| chr12:39646529
|
C | T | 54 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0022others(51): Show | 56 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.335+68C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 4/12 | chr12 | 39646529 | ||||||
| chr12:39646530
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.335+69G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 4/12 | chr12 | 39646530 | ||||||
| chr12:39646696
|
A | G | 6 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(3): Show | 6 | HG01884.hp2 HG02055.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.336-144A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 4/12 | chr12 | 39646696 | ||||||
| chr12:39646723
|
G | A | 58 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0022others(55): Show | 60 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.336-117G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 4/12 | chr12 | 39646723 | ||||||
| chr12:39647654
|
G | C | 1 | a0001c0001t0001g0240 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.385-138G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 5/12 | chr12 | 39647654 | ||||||
| chr12:39648196
|
C | A | 1 | a0002c0002t0001g0093 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.570+219C>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 6/12 | chr12 | 39648196 | ||||||
| chr12:39648223
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.570+246C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 6/12 | chr12 | 39648223 | ||||||
| chr12:39648375
|
CGTA | C | 7 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0029others(4): Show | 8 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.570+404_570+406del others(3): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 39648375 | |||||
| chr12:39648418
|
T | G | 180 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(177): Show | 191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.570+441T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 6/12 | chr12 | 39648418 | ||||||
| chr12:39648517
|
A | G | 1 | a0001c0001t0001g0209 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.570+540A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 6/12 | chr12 | 39648517 | ||||||
| chr12:39648831
|
T | C | 11 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(8): Show | 11 | HG00738.hp1 HG01106.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.570+854T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 6/12 | chr12 | 39648831 | ||||||
| chr12:39649090
|
T | A | 1 | a0001c0001t0001g0150 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.570+1113T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 6/12 | chr12 | 39649090 | ||||||
| chr12:39649138
|
C | T | 2 | a0001c0001t0001g0282a0001c0001t0001g0283 | 2 | HG01358.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.571-1101C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 6/12 | chr12 | 39649138 | ||||||
| chr12:39649203
|
T | G | 239 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(236): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.571-1036T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 6/12 | chr12 | 39649203 | ||||||
| chr12:39649226
|
T | C | 1 | a0001c0001t0001g0228 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.571-1013T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 6/12 | chr12 | 39649226 | ||||||
| chr12:39649307
|
G | T | 11 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(8): Show | 11 | HG00738.hp1 HG01106.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.571-932G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 6/12 | chr12 | 39649307 | ||||||
| chr12:39649419
|
C | A | 1 | a0002c0002t0001g0117 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.571-820C>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 6/12 | chr12 | 39649419 | ||||||
| chr12:39649421
|
C | A | 1 | a0002c0002t0001g0117 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.571-818C>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 6/12 | chr12 | 39649421 | ||||||
| chr12:39649427
|
TTTTGA | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(5): Show | 9 | HG01169.hp1 HG01192.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.571-807_571-803del others(5): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 39649427 | |||||
| chr12:39649479
|
C | T | 144 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(141): Show | 155 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.571-760C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 6/12 | chr12 | 39649479 | ||||||
| chr12:39649536
|
AT | A | 53 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(50): Show | 57 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.571-695delT | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 39649536 | |||||
| chr12:39649864
|
G | A | 1 | a0001c0001t0006g0033 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.571-375G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 6/12 | chr12 | 39649864 | ||||||
| chr12:39649959
|
T | C | 1 | a0002c0002t0001g0094 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.571-280T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 6/12 | chr12 | 39649959 | ||||||
| chr12:39650096
|
A | G | 1 | a0001c0001t0001g0061 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.571-143A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 6/12 | chr12 | 39650096 | ||||||
| chr12:39650224
|
A | G | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.571-15A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 6/12 | chr12 | 39650224 | ||||||
| chr12:39651380
|
T | TAAAATCT others(339): Show |
1 | a0001c0001t0006g0033 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.686+1043_686+1044i others(348): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39651380 | |||||
| chr12:39651419
|
C | A | 1 | a0001c0001t0001g0228 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.686+1065C>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39651419 | ||||||
| chr12:39651731
|
C | A | 231 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(228): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.686+1377C>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39651731 | ||||||
| chr12:39652069
|
C | T | 43 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0025others(40): Show | 44 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.686+1715C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39652069 | ||||||
| chr12:39652100
|
G | A | 2 | a0003c0005t0001g0335a0003c0005t0001g0336 | 2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.686+1746G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39652100 | ||||||
| chr12:39652109
|
T | G | 1 | a0002c0002t0001g0095 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.686+1755T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39652109 | ||||||
| chr12:39652237
|
T | C | 1 | a0001c0001t0001g0188 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.686+1883T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39652237 | ||||||
| chr12:39652323
|
C | G | 226 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(223): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.686+1969C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39652323 | ||||||
| chr12:39652377
|
C | T | 4 | a0002c0002t0001g0007a0002c0002t0001g0110a0002c0002t0001g0111others(1): Show | 5 | HG02056.hp1 NA18946.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.686+2023C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39652377 | ||||||
| chr12:39652397
|
G | A | 1 | a0001c0001t0001g0241 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.686+2043G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39652397 | ||||||
| chr12:39652562
|
G | A | 3 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0208 | 3 | HG00280.hp2 HG03239.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.686+2208G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39652562 | ||||||
| chr12:39652606
|
A | G | 56 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0247others(53): Show | 57 | HG00408.hp1 HG00642.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.686+2252A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39652606 | ||||||
| chr12:39652719
|
A | G | 181 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(178): Show | 192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.686+2365A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39652719 | ||||||
| chr12:39652947
|
G | A | 255 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.686+2593G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39652947 | ||||||
| chr12:39653327
|
C | T | 25 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0204others(22): Show | 25 | HG00140.hp1 HG00280.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.686+2973C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39653327 | ||||||
| chr12:39653346
|
G | A | 58 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0022others(55): Show | 60 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.686+2992G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39653346 | ||||||
| chr12:39653479
|
T | C | 1 | a0001c0001t0001g0243 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.686+3125T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39653479 | ||||||
| chr12:39653492
|
G | GTCT | 10 | a0001c0001t0001g0003a0001c0001t0001g0256a0001c0001t0001g0257others(7): Show | 11 | HG00558.hp2 HG01496.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.686+3182_686+3184d others(5): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653492 | |||||
| chr12:39653492
|
G | GTCTTCT | 4 | a0001c0001t0001g0017a0001c0001t0001g0322a0001c0001t0001g0329others(1): Show | 5 | HG02055.hp1 HG03225.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.686+3179_686+3184d others(8): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653492 | |||||
| chr12:39653492
|
G | GTCTTCTT others(5): Show |
2 | a0001c0001t0002g0319a0001c0001t0002g0320 | 2 | NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.686+3173_686+3184d others(14): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653492 | |||||
| chr12:39653492
|
GTCT | G | 53 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(50): Show | 58 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.686+3182_686+3184d others(5): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653492 | |||||
| chr12:39653492
|
GTCTTCT | G | 9 | a0001c0001t0001g0240a0001c0001t0001g0265a0001c0001t0001g0275others(6): Show | 9 | HG02004.hp2 HG02572.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.686+3179_686+3184d others(8): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653492 | |||||
| chr12:39653492
|
GTCTTCTT others(2): Show |
G | 6 | a0001c0001t0001g0026a0001c0001t0001g0227a0001c0001t0001g0230others(3): Show | 6 | HG01255.hp2 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.686+3176_686+3184d others(11): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653492 | |||||
| chr12:39653492
|
GTCTTCTT others(5): Show |
G | 3 | a0001c0001t0001g0075a0001c0001t0001g0244a0008c0009t0001g0226 | 3 | HG00673.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.686+3173_686+3184d others(14): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653492 | |||||
| chr12:39653494
|
C | CTTCTTCT others(51): Show |
1 | a0001c0001t0006g0033 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.686+3181_686+3182i others(60): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653494 | |||||
| chr12:39653495
|
T | G | 2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | HG02723.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.686+3141T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39653495 | ||||||
| chr12:39653515
|
CTTCTTCT others(17): Show |
C | 2 | a0001c0001t0001g0331a0001c0001t0001g0332 | 2 | HG02145.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.686+3182_686+3205d others(26): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653515 | |||||
| chr12:39653518
|
CTTCTTCT others(14): Show |
C | 1 | a0001c0001t0001g0330 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.686+3186_686+3206d others(23): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653518 | |||||
| chr12:39653521
|
C | CTTCTTCT others(24): Show |
1 | a0001c0001t0001g0062 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.686+3181_686+3182i others(33): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653521 | |||||
| chr12:39653521
|
C | CTTCTTCT others(21): Show |
1 | a0001c0001t0001g0057 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.686+3178_686+3179i others(30): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653521 | |||||
| chr12:39653524
|
C | CTTCTTCT others(21): Show |
2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG00597.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.686+3181_686+3182i others(30): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653524 | |||||
| chr12:39653524
|
C | CTTCTTCT others(18): Show |
1 | a0001c0001t0001g0058 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.686+3178_686+3179i others(27): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653524 | |||||
| chr12:39653527
|
C | CTTCTTCT others(18): Show |
3 | a0001c0001t0004g0055a0002c0002t0001g0109a0002c0002t0001g0137 | 3 | HG00099.hp1 HG01243.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.686+3181_686+3182i others(27): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653527 | |||||
| chr12:39653527
|
C | CTTCTTTT others(15): Show |
7 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0076others(4): Show | 8 | HG00639.hp1 HG00741.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.686+3178_686+3179i others(24): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653527 | |||||
| chr12:39653530
|
C | T | 1 | a0001c0007t0001g0024 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.686+3176C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39653530 | ||||||
| chr12:39653536
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.686+3182C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39653536 | ||||||
| chr12:39653538
|
T | TCTTCTTC others(6): Show |
1 | a0001c0001t0001g0056 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.686+3184_686+3185i others(15): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39653538 | ||||||
| chr12:39653539
|
T | C | 235 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(232): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.686+3185T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39653539 | ||||||
| chr12:39653542
|
C | T | 6 | a0001c0001t0001g0012a0001c0001t0001g0043a0001c0001t0001g0044others(3): Show | 7 | HG01099.hp1 HG02056.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.686+3188C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39653542 | ||||||
| chr12:39653545
|
C | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0031a0001c0001t0001g0032 | 4 | HG02109.hp1 HG02451.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.686+3191C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39653545 | ||||||
| chr12:39653548
|
C | T | 11 | a0001c0001t0001g0042a0001c0001t0001g0087a0001c0001t0001g0185others(8): Show | 11 | HG01952.hp1 HG02698.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.686+3194C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39653548 | ||||||
| chr12:39653551
|
C | T | 21 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0067others(18): Show | 23 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.686+3197C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39653551 | ||||||
| chr12:39653554
|
C | T | 33 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0021others(30): Show | 37 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.686+3200C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39653554 | ||||||
| chr12:39653557
|
C | T | 56 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(53): Show | 59 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.686+3203C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39653557 | ||||||
| chr12:39653558
|
T | C | 8 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0049others(5): Show | 8 | HG00621.hp1 HG02027.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.686+3204T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39653558 | ||||||
| chr12:39653558
|
T | TCTTCTTC others(43): Show |
1 | a0001c0001t0001g0242 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.686+3204_686+3205i others(52): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39653558 | ||||||
| chr12:39653558
|
T | TTCTTCTT others(52): Show |
1 | a0001c0007t0001g0024 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.686+3205_686+3206i others(61): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653558 | |||||
| chr12:39653558
|
T | TTCTTCTT others(22): Show |
2 | a0001c0001t0001g0029a0001c0001t0001g0030 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.686+3205_686+3206i others(31): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653558 | |||||
| chr12:39653558
|
T | TTCTTCTT others(44): Show |
1 | a0001c0001t0001g0205 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.686+3205_686+3206i others(53): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653558 | |||||
| chr12:39653558
|
T | TTCTTCTT others(47): Show |
1 | a0001c0001t0001g0164 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.686+3205_686+3206i others(56): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653558 | |||||
| chr12:39653558
|
T | TTCTTCTT others(44): Show |
38 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(35): Show | 41 | HG00099.hp2 HG00642.hp1 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.686+3205_686+3206i others(53): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653558 | |||||
| chr12:39653558
|
T | TTCTTCTT others(41): Show |
6 | a0001c0001t0001g0064a0001c0001t0001g0071a0001c0001t0001g0146others(3): Show | 6 | HG00280.hp2 HG00738.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.686+3205_686+3206i others(50): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653558 | |||||
| chr12:39653558
|
T | TTCTTCTT others(38): Show |
1 | a0001c0001t0001g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.686+3205_686+3206i others(47): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653558 | |||||
| chr12:39653558
|
T | TTCTTCTT others(44): Show |
5 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0144others(2): Show | 6 | HG00738.hp2 HG03017.hp1 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.686+3205_686+3206i others(53): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653558 | |||||
| chr12:39653558
|
T | TTCTTCTT others(41): Show |
23 | a0001c0001t0001g0001a0001c0001t0001g0041a0001c0001t0001g0066others(20): Show | 26 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.686+3205_686+3206i others(50): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653558 | |||||
| chr12:39653558
|
T | TTCTTCTT others(74): Show |
1 | a0001c0001t0003g0078 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.686+3205_686+3206i others(83): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653558 | |||||
| chr12:39653558
|
T | TTCTTCTT others(38): Show |
3 | a0001c0001t0001g0028a0001c0001t0001g0179a0001c0001t0001g0180 | 3 | HG00639.hp2 HG01169.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.686+3205_686+3206i others(47): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653558 | |||||
| chr12:39653558
|
T | TTCTTCTT others(35): Show |
1 | a0001c0001t0001g0195 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.686+3205_686+3206i others(44): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653558 | |||||
| chr12:39653558
|
T | TTCTTCTT others(44): Show |
1 | a0001c0001t0001g0188 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.686+3205_686+3206i others(53): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653558 | |||||
| chr12:39653558
|
T | TTCTTCTT others(41): Show |
1 | a0001c0001t0001g0181 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.686+3205_686+3206i others(50): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653558 | |||||
| chr12:39653558
|
T | TTCTTCTT others(38): Show |
14 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0085others(11): Show | 16 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.686+3205_686+3206i others(47): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653558 | |||||
| chr12:39653558
|
T | TTCTTCTT others(35): Show |
4 | a0001c0001t0001g0067a0001c0001t0001g0072a0001c0001t0001g0228others(1): Show | 4 | HG02109.hp2 HG03579.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.686+3205_686+3206i others(44): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653558 | |||||
| chr12:39653558
|
T | TTCTTCTT others(59): Show |
2 | a0002c0002t0001g0110a0010c0010t0001g0096 | 2 | HG01175.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.686+3205_686+3206i others(68): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653558 | |||||
| chr12:39653558
|
T | TTCTTCTT others(56): Show |
2 | a0002c0002t0001g0111a0002c0002t0001g0118 | 2 | NA19058.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.686+3205_686+3206i others(65): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653558 | |||||
| chr12:39653558
|
T | TTCTTCTT others(53): Show |
1 | a0001c0001t0001g0151 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.686+3205_686+3206i others(62): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653558 | |||||
| chr12:39653558
|
T | TTCTTCTT others(44): Show |
1 | a0005c0003t0001g0035 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.686+3205_686+3206i others(53): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653558 | |||||
| chr12:39653558
|
T | TTCTTCTT others(38): Show |
2 | a0001c0001t0001g0185a0001c0001t0001g0186 | 2 | HG02698.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.686+3205_686+3206i others(47): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653558 | |||||
| chr12:39653558
|
T | TTCTTCTT others(35): Show |
7 | a0001c0001t0001g0042a0001c0001t0001g0087a0001c0001t0001g0187others(4): Show | 7 | HG01952.hp1 HG02965.hp1 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.686+3205_686+3206i others(44): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653558 | |||||
| chr12:39653558
|
T | TTCTTCTT others(68): Show |
2 | a0001c0001t0003g0079a0001c0001t0003g0081 | 2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.686+3205_686+3206i others(77): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653558 | |||||
| chr12:39653558
|
T | TTCTTCTT others(56): Show |
3 | a0002c0002t0001g0007a0002c0002t0001g0082a0002c0002t0001g0083 | 4 | NA18747.hp1 NA18969.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.686+3205_686+3206i others(65): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653558 | |||||
| chr12:39653558
|
T | TTCTTCTT others(53): Show |
13 | a0001c0001t0001g0065a0001c0001t0001g0152a0001c0001t0001g0153others(10): Show | 13 | HG00140.hp1 HG00408.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.686+3205_686+3206i others(62): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653558 | |||||
| chr12:39653558
|
T | TTCTTCTT others(50): Show |
1 | a0006c0006t0001g0333 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.686+3205_686+3206i others(59): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653558 | |||||
| chr12:39653558
|
T | TTCTTCTT others(47): Show |
1 | a0001c0001t0001g0027 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.686+3205_686+3206i others(56): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653558 | |||||
| chr12:39653558
|
T | TTCTTCTT others(44): Show |
1 | a0003c0005t0001g0335 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.686+3205_686+3206i others(53): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653558 | |||||
| chr12:39653558
|
T | TTCTTTCT others(26): Show |
3 | a0001c0001t0001g0004a0001c0001t0001g0031a0001c0001t0001g0032 | 4 | HG02109.hp1 HG02451.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.686+3205_686+3206i others(35): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653558 | |||||
| chr12:39653558
|
T | TTCTTTTT others(53): Show |
1 | a0001c0001t0001g0215 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.686+3205_686+3206i others(62): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653558 | |||||
| chr12:39653558
|
T | TTCTTTTT others(56): Show |
1 | a0001c0001t0001g0198 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.686+3205_686+3206i others(65): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653558 | |||||
| chr12:39653558
|
T | TTCTTTTT others(53): Show |
3 | a0001c0001t0001g0189a0002c0002t0001g0112a0002c0002t0001g0313 | 3 | HG01943.hp2 HG02040.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.686+3205_686+3206i others(62): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653558 | |||||
| chr12:39653558
|
T | TTCTTTTT others(50): Show |
14 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(11): Show | 14 | HG01099.hp2 HG01123.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.686+3205_686+3206i others(59): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653558 | |||||
| chr12:39653558
|
T | TTCTTTTT others(47): Show |
2 | a0001c0001t0001g0220a0009c0008t0001g0068 | 2 | HG01175.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.686+3205_686+3206i others(56): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653558 | |||||
| chr12:39653558
|
T | TTTTTC | 16 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0053others(13): Show | 17 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.686+3206_686+3207i others(7): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653558 | |||||
| chr12:39653558
|
T | TTTTTCTT others(50): Show |
1 | a0005c0003t0001g0034 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.686+3206_686+3207i others(59): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653558 | |||||
| chr12:39653558
|
T | TTTTTCTT others(47): Show |
22 | a0001c0001t0001g0022a0001c0001t0001g0037a0001c0001t0001g0038others(19): Show | 22 | HG00642.hp2 HG01243.hp1 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.686+3206_686+3207i others(56): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653558 | |||||
| chr12:39653558
|
T | TTTTTCTT others(44): Show |
6 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0089others(3): Show | 6 | HG00741.hp2 HG01069.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.686+3206_686+3207i others(53): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653558 | |||||
| chr12:39653558
|
T | TTTTTCTT others(38): Show |
1 | a0003c0005t0001g0336 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.686+3206_686+3207i others(47): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653558 | |||||
| chr12:39653573
|
T | C | 16 | a0001c0001t0001g0012a0001c0001t0001g0043a0001c0001t0001g0044others(13): Show | 17 | HG00621.hp1 HG01099.hp1 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.686+3219T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39653573 | ||||||
| chr12:39653573
|
T | TC | 211 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(208): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.686+3219_686+3220i others(3): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39653573 | ||||||
| chr12:39653580
|
C | T | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.686+3226C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39653580 | ||||||
| chr12:39653585
|
C | CTTCTTCT others(45): Show |
1 | a0001c0001t0001g0221 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.686+3237_686+3238i others(54): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653585 | |||||
| chr12:39653585
|
C | CTTCTTCT others(36): Show |
3 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0063 | 3 | NA18940.hp1 NA18975.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.686+3237_686+3238i others(45): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653585 | |||||
| chr12:39653585
|
C | CTTCTTCT others(33): Show |
6 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(3): Show | 6 | HG01099.hp1 HG02056.hp2 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.686+3237_686+3238i others(42): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653585 | |||||
| chr12:39653585
|
C | CTTCTTTC others(43): Show |
1 | a0001c0001t0001g0209 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.686+3236_686+3237i others(52): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653585 | |||||
| chr12:39653585
|
C | CTTCTTTC others(61): Show |
3 | a0002c0002t0001g0123a0002c0002t0001g0124a0002c0002t0001g0125 | 3 | HG02027.hp1 NA18977.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.686+3236_686+3237i others(70): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653585 | |||||
| chr12:39653585
|
C | CTTCTTTT others(30): Show |
6 | a0001c0001t0001g0012a0001c0001t0001g0049a0001c0001t0001g0050others(3): Show | 7 | HG00621.hp1 HG02027.hp2 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.686+3236_686+3237i others(39): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653585 | |||||
| chr12:39653585
|
C | CTTTTTCT others(27): Show |
1 | a0001c0001t0001g0069 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.686+3233_686+3234i others(36): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39653585 | |||||
| chr12:39653585
|
C | T | 211 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(208): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.686+3231C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39653585 | ||||||
| chr12:39653648
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.686+3294G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39653648 | ||||||
| chr12:39653736
|
C | T | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.686+3382C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39653736 | ||||||
| chr12:39653828
|
G | A | 2 | a0001c0001t0001g0065a0001c0001t0001g0066 | 2 | HG02129.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.686+3474G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39653828 | ||||||
| chr12:39653959
|
T | A | 1 | a0001c0001t0001g0089 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.686+3605T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39653959 | ||||||
| chr12:39654273
|
C | T | 1 | a0001c0001t0001g0300 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.686+3919C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39654273 | ||||||
| chr12:39654754
|
CAT | C | 233 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(230): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.686+4402_686+4403d others(4): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39654754 | |||||
| chr12:39654860
|
T | C | 1 | a0001c0001t0001g0047 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.686+4506T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39654860 | ||||||
| chr12:39654896
|
A | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(218): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.686+4542A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39654896 | ||||||
| chr12:39654916
|
T | G | 1 | a0001c0001t0001g0158 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.686+4562T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39654916 | ||||||
| chr12:39655075
|
T | C | 1 | a0001c0001t0001g0056 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.686+4721T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39655075 | ||||||
| chr12:39655602
|
G | C | 1 | a0001c0001t0001g0245 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.686+5248G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39655602 | ||||||
| chr12:39655672
|
T | C | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG00558.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.686+5318T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39655672 | ||||||
| chr12:39655936
|
A | G | 2 | a0001c0001t0001g0311a0001c0001t0001g0312 | 2 | NA18945.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.686+5582A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39655936 | ||||||
| chr12:39656224
|
T | C | 6 | a0001c0001t0001g0152a0001c0001t0001g0159a0001c0001t0001g0164others(3): Show | 6 | HG01109.hp2 HG01934.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.686+5870T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39656224 | ||||||
| chr12:39656503
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.686+6149T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39656503 | ||||||
| chr12:39656670
|
C | T | 50 | a0002c0002t0001g0007a0002c0002t0001g0082a0002c0002t0001g0083others(47): Show | 51 | HG00408.hp1 HG00642.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.686+6316C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39656670 | ||||||
| chr12:39656694
|
C | T | 1 | a0001c0001t0001g0005 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.686+6340C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39656694 | ||||||
| chr12:39656711
|
T | C | 1 | a0001c0001t0001g0222 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.686+6357T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39656711 | ||||||
| chr12:39656741
|
T | A | 1 | a0001c0001t0001g0113 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.686+6387T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39656741 | ||||||
| chr12:39656801
|
G | T | 1 | a0001c0001t0001g0243 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.686+6447G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39656801 | ||||||
| chr12:39656819
|
A | G | 1 | a0001c0001t0001g0188 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.686+6465A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39656819 | ||||||
| chr12:39656874
|
A | T | 1 | a0001c0001t0001g0267 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.686+6520A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39656874 | ||||||
| chr12:39657118
|
T | G | 12 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(9): Show | 13 | HG00733.hp1 HG01169.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.686+6764T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39657118 | ||||||
| chr12:39657447
|
A | T | 1 | a0001c0001t0001g0329 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.686+7093A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39657447 | ||||||
| chr12:39657864
|
T | A | 55 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0247others(52): Show | 56 | HG00408.hp1 HG00642.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.686+7510T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39657864 | ||||||
| chr12:39658087
|
C | CT | 236 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(233): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.686+7744dupT | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39658087 | |||||
| chr12:39658174
|
G | C | 225 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(222): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.686+7820G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39658174 | ||||||
| chr12:39658451
|
C | T | 218 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(215): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.686+8097C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39658451 | ||||||
| chr12:39658799
|
T | C | 3 | a0001c0001t0001g0011a0001c0001t0001g0167a0001c0001t0001g0175 | 4 | HG00099.hp2 HG00140.hp2 HG01070.hp2 others(1): Show |
intron_variant | MODIFIER | c.686+8445T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39658799 | ||||||
| chr12:39659231
|
TTC | T | 3 | a0001c0001t0004g0055a0001c0001t0004g0059a0001c0001t0004g0060 | 3 | HG00099.hp1 HG01070.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.686+8879_686+8880d others(4): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39659231 | |||||
| chr12:39659262
|
A | C | 237 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(234): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.686+8908A>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39659262 | ||||||
| chr12:39659356
|
T | G | 237 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(234): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.686+9002T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39659356 | ||||||
| chr12:39659398
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.686+9044C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39659398 | ||||||
| chr12:39659484
|
G | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0168a0001c0001t0001g0179 | 4 | HG02071.hp2 NA18956.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.686+9130G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39659484 | ||||||
| chr12:39659605
|
T | G | 1 | a0004c0004t0001g0130 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.686+9251T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39659605 | ||||||
| chr12:39659621
|
C | T | 237 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(234): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.686+9267C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39659621 | ||||||
| chr12:39659690
|
C | CTG | 260 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(257): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.686+9337_686+9338i others(4): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39659690 | |||||
| chr12:39659702
|
T | A | 1 | a0001c0001t0001g0241 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.686+9348T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39659702 | ||||||
| chr12:39659821
|
T | A | 3 | a0001c0007t0001g0024a0005c0003t0001g0034a0005c0003t0001g0035 | 3 | HG02486.hp2 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.686+9467T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39659821 | ||||||
| chr12:39659905
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.686+9551A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39659905 | ||||||
| chr12:39659940
|
TG | T | 3 | a0001c0001t0001g0330a0001c0001t0001g0331a0001c0001t0001g0332 | 3 | HG02145.hp2 HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.686+9587delG | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39659940 | ||||||
| chr12:39660039
|
C | T | 2 | a0003c0005t0001g0335a0003c0005t0001g0336 | 2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.686+9685C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39660039 | ||||||
| chr12:39660059
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.686+9705C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39660059 | ||||||
| chr12:39660070
|
G | T | 5 | a0001c0001t0001g0004a0001c0001t0001g0029a0001c0001t0001g0030others(2): Show | 6 | HG02109.hp1 HG02451.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.686+9716G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39660070 | ||||||
| chr12:39660086
|
T | C | 3 | a0001c0007t0001g0024a0005c0003t0001g0034a0005c0003t0001g0035 | 3 | HG02486.hp2 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.686+9732T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39660086 | ||||||
| chr12:39660144
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.686+9790A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39660144 | ||||||
| chr12:39660153
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.686+9799G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39660153 | ||||||
| chr12:39660228
|
T | C | 1 | a0001c0001t0001g0292 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.686+9874T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39660228 | ||||||
| chr12:39660303
|
G | C | 260 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(257): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.686+9949G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39660303 | ||||||
| chr12:39660508
|
T | A | 225 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(222): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.686+10154T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39660508 | ||||||
| chr12:39660509
|
T | A | 237 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(234): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.686+10155T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39660509 | ||||||
| chr12:39660521
|
T | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0181a0001c0001t0001g0185 | 4 | NA18939.hp2 NA18991.hp1 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.686+10167T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39660521 | ||||||
| chr12:39660745
|
G | A | 1 | a0001c0001t0006g0033 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.686+10391G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39660745 | ||||||
| chr12:39660872
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.686+10518G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39660872 | ||||||
| chr12:39661145
|
G | A | 21 | a0001c0001t0001g0003a0001c0001t0001g0075a0001c0001t0001g0227others(18): Show | 22 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.686+10791G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39661145 | ||||||
| chr12:39661334
|
A | G | 4 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0222others(1): Show | 4 | HG01106.hp1 HG01433.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.686+10980A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39661334 | ||||||
| chr12:39661409
|
G | A | 50 | a0002c0002t0001g0007a0002c0002t0001g0082a0002c0002t0001g0083others(47): Show | 51 | HG00408.hp1 HG00642.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.686+11055G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39661409 | ||||||
| chr12:39661771
|
G | T | 1 | a0001c0001t0001g0327 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.686+11417G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39661771 | ||||||
| chr12:39662246
|
A | G | 1 | a0002c0002t0001g0129 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.686+11892A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39662246 | ||||||
| chr12:39662297
|
C | CAATGGAT others(3): Show |
21 | a0001c0001t0001g0003a0001c0001t0001g0075a0001c0001t0001g0227others(18): Show | 22 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.686+11944_686+1194 others(14): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39662297 | |||||
| chr12:39662346
|
C | T | 3 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214 | 3 | HG02071.hp1 NA18981.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.686+11992C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39662346 | ||||||
| chr12:39662477
|
A | G | 12 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(9): Show | 13 | HG00733.hp1 HG01169.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.686+12123A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39662477 | ||||||
| chr12:39662520
|
CT | C | 255 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.686+12176delT | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39662520 | |||||
| chr12:39662686
|
A | G | 1 | a0001c0001t0006g0033 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.686+12332A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39662686 | ||||||
| chr12:39662752
|
A | G | 220 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(217): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.686+12398A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39662752 | ||||||
| chr12:39663419
|
C | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0076a0001c0001t0001g0077 | 4 | HG00639.hp1 HG01074.hp2 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.686+13065C>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39663419 | ||||||
| chr12:39663470
|
C | G | 1 | a0001c0001t0002g0321 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.686+13116C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39663470 | ||||||
| chr12:39663675
|
T | A | 1 | a0001c0001t0001g0255 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.686+13321T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39663675 | ||||||
| chr12:39663773
|
G | A | 1 | a0001c0001t0001g0304 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.686+13419G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39663773 | ||||||
| chr12:39663860
|
G | A | 2 | a0003c0005t0001g0335a0003c0005t0001g0336 | 2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.686+13506G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39663860 | ||||||
| chr12:39663989
|
G | C | 1 | a0001c0001t0001g0289 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.686+13635G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39663989 | ||||||
| chr12:39664090
|
T | A | 79 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(76): Show | 82 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.686+13736T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39664090 | ||||||
| chr12:39664265
|
C | T | 7 | a0002c0002t0001g0090a0002c0002t0001g0101a0002c0002t0001g0102others(4): Show | 7 | HG01175.hp2 HG01257.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.686+13911C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39664265 | ||||||
| chr12:39664296
|
A | G | 3 | a0001c0007t0001g0024a0005c0003t0001g0034a0005c0003t0001g0035 | 3 | HG02486.hp2 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.686+13942A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39664296 | ||||||
| chr12:39664500
|
C | A | 2 | a0005c0003t0001g0034a0005c0003t0001g0035 | 2 | HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.686+14146C>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39664500 | ||||||
| chr12:39664918
|
C | T | 3 | a0001c0001t0001g0146a0001c0001t0001g0227a0001c0001t0001g0230 | 3 | HG01358.hp1 HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.686+14564C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39664918 | ||||||
| chr12:39665044
|
T | C | 29 | a0001c0001t0001g0011a0001c0001t0001g0145a0001c0001t0001g0146others(26): Show | 30 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(27): Show |
intron_variant | MODIFIER | c.686+14690T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39665044 | ||||||
| chr12:39665094
|
A | G | 8 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(5): Show | 9 | HG01169.hp1 HG01192.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.686+14740A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39665094 | ||||||
| chr12:39665132
|
C | T | 1 | a0001c0001t0001g0245 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.686+14778C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39665132 | ||||||
| chr12:39665189
|
G | A | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.686+14835G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39665189 | ||||||
| chr12:39665308
|
C | T | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.686+14954C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39665308 | ||||||
| chr12:39665330
|
A | G | 1 | a0001c0001t0001g0234 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.686+14976A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39665330 | ||||||
| chr12:39665333
|
G | C | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.686+14979G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39665333 | ||||||
| chr12:39665466
|
T | G | 233 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(230): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.686+15112T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39665466 | ||||||
| chr12:39665504
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.686+15150C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39665504 | ||||||
| chr12:39665554
|
G | C | 220 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(217): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.686+15200G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39665554 | ||||||
| chr12:39665555
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.686+15201G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39665555 | ||||||
| chr12:39665648
|
A | G | 3 | a0001c0001t0001g0066a0001c0001t0001g0195a0001c0001t0001g0231 | 3 | HG01123.hp2 HG01346.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.686+15294A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39665648 | ||||||
| chr12:39665789
|
A | G | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.686+15435A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39665789 | ||||||
| chr12:39665797
|
T | G | 2 | a0001c0001t0001g0227a0001c0001t0001g0230 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.686+15443T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39665797 | ||||||
| chr12:39665834
|
A | C | 1 | a0001c0007t0001g0024 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.686+15480A>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39665834 | ||||||
| chr12:39665915
|
T | C | 227 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(224): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.686+15561T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39665915 | ||||||
| chr12:39666030
|
C | G | 1 | a0001c0001t0001g0182 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.686+15676C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39666030 | ||||||
| chr12:39666251
|
A | G | 2 | a0001c0001t0001g0251a0001c0001t0001g0252 | 2 | HG04228.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.686+15897A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39666251 | ||||||
| chr12:39666401
|
C | T | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.686+16047C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39666401 | ||||||
| chr12:39666496
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.687-16115A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39666496 | ||||||
| chr12:39666549
|
C | T | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.687-16062C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39666549 | ||||||
| chr12:39666564
|
G | C | 3 | a0001c0001t0001g0330a0001c0001t0001g0331a0001c0001t0001g0332 | 3 | HG02145.hp2 HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.687-16047G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39666564 | ||||||
| chr12:39666649
|
T | A | 22 | a0001c0001t0001g0003a0001c0001t0001g0075a0001c0001t0001g0227others(19): Show | 23 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.687-15962T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39666649 | ||||||
| chr12:39666675
|
G | A | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.687-15936G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39666675 | ||||||
| chr12:39666703
|
G | C | 6 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(3): Show | 6 | HG01884.hp2 HG02055.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.687-15908G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39666703 | ||||||
| chr12:39666703
|
G | T | 226 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(223): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.687-15908G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39666703 | ||||||
| chr12:39666708
|
G | T | 1 | a0002c0002t0001g0118 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.687-15903G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39666708 | ||||||
| chr12:39666840
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.687-15771T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39666840 | ||||||
| chr12:39666864
|
A | T | 1 | a0001c0001t0001g0308 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.687-15747A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39666864 | ||||||
| chr12:39666874
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.687-15737C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39666874 | ||||||
| chr12:39666996
|
G | C | 1 | a0001c0001t0001g0076 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.687-15615G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39666996 | ||||||
| chr12:39667045
|
GT | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(171): Show | 185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.687-15560delT | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39667045 | |||||
| chr12:39667198
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.687-15413G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39667198 | ||||||
| chr12:39667221
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.687-15390T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39667221 | ||||||
| chr12:39667225
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.687-15386T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39667225 | ||||||
| chr12:39667469
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.687-15142G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39667469 | ||||||
| chr12:39667518
|
T | A | 1 | a0001c0001t0001g0241 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.687-15093T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39667518 | ||||||
| chr12:39667552
|
G | T | 220 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(217): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.687-15059G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39667552 | ||||||
| chr12:39667554
|
G | T | 1 | a0001c0001t0001g0223 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.687-15057G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39667554 | ||||||
| chr12:39667626
|
A | T | 1 | a0001c0001t0001g0040 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.687-14985A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39667626 | ||||||
| chr12:39667745
|
C | T | 18 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0247others(15): Show | 18 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(15): Show |
intron_variant | MODIFIER | c.687-14866C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39667745 | ||||||
| chr12:39667826
|
T | C | 1 | a0001c0001t0001g0265 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.687-14785T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39667826 | ||||||
| chr12:39667960
|
C | G | 1 | a0001c0001t0001g0241 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.687-14651C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39667960 | ||||||
| chr12:39667966
|
G | A | 1 | a0001c0001t0001g0308 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.687-14645G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39667966 | ||||||
| chr12:39668013
|
T | G | 1 | a0002c0002t0001g0118 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.687-14598T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39668013 | ||||||
| chr12:39668045
|
T | C | 1 | a0006c0006t0001g0106 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.687-14566T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39668045 | ||||||
| chr12:39668049
|
G | T | 1 | a0001c0001t0001g0237 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.687-14562G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39668049 | ||||||
| chr12:39668062
|
T | C | 4 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0247others(1): Show | 4 | NA18997.hp1 NA19001.hp2 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.687-14549T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39668062 | ||||||
| chr12:39668285
|
T | A | 2 | a0001c0001t0001g0196a0001c0001t0001g0201 | 2 | HG00544.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.687-14326T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39668285 | ||||||
| chr12:39668291
|
G | C | 38 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(35): Show | 39 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.687-14320G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39668291 | ||||||
| chr12:39668400
|
T | C | 2 | a0001c0001t0001g0089a0001c0001t0001g0228 | 2 | HG00741.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.687-14211T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39668400 | ||||||
| chr12:39668482
|
C | A | 1 | a0001c0001t0001g0075 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.687-14129C>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39668482 | ||||||
| chr12:39668549
|
A | T | 14 | a0001c0001t0001g0003a0001c0001t0001g0318a0001c0001t0001g0322others(11): Show | 15 | HG01884.hp1 HG02055.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.687-14062A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39668549 | ||||||
| chr12:39668561
|
C | T | 1 | a0001c0001t0001g0075 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.687-14050C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39668561 | ||||||
| chr12:39668598
|
G | T | 1 | a0001c0001t0001g0205 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.687-14013G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39668598 | ||||||
| chr12:39668666
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.687-13945G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39668666 | ||||||
| chr12:39668824
|
C | T | 1 | a0004c0004t0005g0135 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.687-13787C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39668824 | ||||||
| chr12:39668831
|
TC | T | 4 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(1): Show | 4 | HG02970.hp1 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.687-13778delC | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39668831 | |||||
| chr12:39668842
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.687-13769G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39668842 | ||||||
| chr12:39668888
|
T | C | 1 | a0001c0001t0001g0143 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.687-13723T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39668888 | ||||||
| chr12:39668952
|
C | T | 218 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(215): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.687-13659C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39668952 | ||||||
| chr12:39668958
|
A | AT | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.687-13646dupT | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39668958 | |||||
| chr12:39669011
|
G | T | 4 | a0001c0001t0001g0070a0001c0001t0001g0074a0009c0008t0001g0068others(1): Show | 4 | HG01175.hp1 HG02622.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.687-13600G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39669011 | ||||||
| chr12:39669054
|
A | G | 230 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(227): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.687-13557A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39669054 | ||||||
| chr12:39669126
|
G | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0029others(4): Show | 8 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.687-13485G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39669126 | ||||||
| chr12:39669312
|
G | A | 6 | a0001c0001t0001g0204a0001c0001t0001g0216a0001c0001t0001g0218others(3): Show | 6 | HG01106.hp1 HG01433.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.687-13299G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39669312 | ||||||
| chr12:39669435
|
C | T | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.687-13176C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39669435 | ||||||
| chr12:39669486
|
G | T | 2 | a0005c0003t0001g0034a0005c0003t0001g0035 | 2 | HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.687-13125G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39669486 | ||||||
| chr12:39669496
|
C | T | 2 | a0001c0001t0001g0075a0008c0009t0001g0226 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.687-13115C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39669496 | ||||||
| chr12:39669497
|
G | A | 17 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0247others(14): Show | 17 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(14): Show |
intron_variant | MODIFIER | c.687-13114G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39669497 | ||||||
| chr12:39669549
|
G | A | 4 | a0001c0001t0001g0196a0001c0001t0001g0201a0005c0003t0001g0034others(1): Show | 4 | HG00544.hp2 HG03139.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.687-13062G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39669549 | ||||||
| chr12:39669649
|
A | T | 2 | a0001c0001t0001g0065a0001c0001t0001g0066 | 2 | HG02129.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.687-12962A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39669649 | ||||||
| chr12:39669684
|
G | T | 1 | a0001c0001t0001g0315 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.687-12927G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39669684 | ||||||
| chr12:39669740
|
G | T | 1 | a0001c0007t0001g0024 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.687-12871G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39669740 | ||||||
| chr12:39669757
|
C | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(5): Show | 9 | HG01169.hp1 HG01192.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.687-12854C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39669757 | ||||||
| chr12:39669853
|
G | T | 1 | a0002c0002t0001g0118 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.687-12758G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39669853 | ||||||
| chr12:39669895
|
TG | T | 11 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(8): Show | 11 | HG00738.hp1 HG01106.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.687-12714delG | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39669895 | |||||
| chr12:39669943
|
G | A | 9 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(6): Show | 10 | HG00673.hp2 HG01169.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.687-12668G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39669943 | ||||||
| chr12:39669992
|
C | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0030 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.687-12619C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39669992 | ||||||
| chr12:39670095
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.687-12516G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39670095 | ||||||
| chr12:39670205
|
T | A | 22 | a0001c0001t0001g0003a0001c0001t0001g0075a0001c0001t0001g0227others(19): Show | 23 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.687-12406T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39670205 | ||||||
| chr12:39670206
|
T | C | 2 | a0003c0005t0001g0335a0003c0005t0001g0336 | 2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.687-12405T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39670206 | ||||||
| chr12:39670287
|
A | T | 255 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.687-12324A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39670287 | ||||||
| chr12:39670377
|
G | A | 1 | a0010c0010t0001g0096 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.687-12234G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39670377 | ||||||
| chr12:39670401
|
C | T | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.687-12210C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39670401 | ||||||
| chr12:39670402
|
A | G | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.687-12209A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39670402 | ||||||
| chr12:39670456
|
A | G | 7 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0029others(4): Show | 8 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.687-12155A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39670456 | ||||||
| chr12:39670517
|
A | C | 1 | a0001c0007t0001g0024 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.687-12094A>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39670517 | ||||||
| chr12:39670639
|
T | A | 1 | a0001c0001t0001g0240 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.687-11972T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39670639 | ||||||
| chr12:39670743
|
CT | C | 230 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(227): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.687-11854delT | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39670743 | |||||
| chr12:39670791
|
A | G | 1 | a0002c0002t0001g0094 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.687-11820A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39670791 | ||||||
| chr12:39670938
|
G | T | 255 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.687-11673G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39670938 | ||||||
| chr12:39671011
|
G | A | 1 | a0001c0001t0001g0143 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.687-11600G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39671011 | ||||||
| chr12:39671083
|
T | C | 2 | a0005c0003t0001g0034a0005c0003t0001g0035 | 2 | HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.687-11528T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39671083 | ||||||
| chr12:39671224
|
T | C | 1 | a0001c0001t0001g0207 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.687-11387T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39671224 | ||||||
| chr12:39671306
|
C | T | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.687-11305C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39671306 | ||||||
| chr12:39671691
|
A | G | 2 | a0003c0005t0001g0335a0003c0005t0001g0336 | 2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.687-10920A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39671691 | ||||||
| chr12:39671885
|
T | G | 1 | a0001c0001t0001g0215 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.687-10726T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39671885 | ||||||
| chr12:39671894
|
G | A | 3 | a0001c0007t0001g0024a0005c0003t0001g0034a0005c0003t0001g0035 | 3 | HG02486.hp2 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.687-10717G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39671894 | ||||||
| chr12:39671936
|
C | T | 1 | a0006c0006t0001g0333 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.687-10675C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39671936 | ||||||
| chr12:39672501
|
G | A | 1 | a0001c0001t0006g0033 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.687-10110G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39672501 | ||||||
| chr12:39672530
|
G | A | 1 | a0001c0001t0001g0339 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.687-10081G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39672530 | ||||||
| chr12:39672886
|
C | T | 2 | a0003c0005t0001g0335a0003c0005t0001g0336 | 2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.687-9725C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39672886 | ||||||
| chr12:39673010
|
T | C | 1 | a0001c0001t0001g0240 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.687-9601T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39673010 | ||||||
| chr12:39673228
|
A | G | 1 | a0001c0001t0001g0046 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.687-9383A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39673228 | ||||||
| chr12:39673839
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.687-8772T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39673839 | ||||||
| chr12:39674108
|
A | C | 1 | a0001c0001t0001g0237 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.687-8503A>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39674108 | ||||||
| chr12:39674122
|
A | G | 1 | a0002c0002t0001g0137 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.687-8489A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39674122 | ||||||
| chr12:39674529
|
T | C | 1 | a0001c0001t0001g0329 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.687-8082T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39674529 | ||||||
| chr12:39674579
|
A | AG | 10 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(7): Show | 10 | HG00738.hp1 HG01106.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.687-8025dupG | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39674579 | |||||
| chr12:39674630
|
T | G | 1 | a0001c0001t0001g0241 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.687-7981T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39674630 | ||||||
| chr12:39674648
|
G | T | 1 | a0001c0001t0001g0025 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.687-7963G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39674648 | ||||||
| chr12:39674776
|
C | A | 14 | a0001c0001t0001g0003a0001c0001t0001g0318a0001c0001t0001g0322others(11): Show | 15 | HG01884.hp1 HG02055.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.687-7835C>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39674776 | ||||||
| chr12:39674907
|
G | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.687-7704G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39674907 | ||||||
| chr12:39674910
|
G | A | 13 | a0001c0001t0001g0003a0001c0001t0001g0318a0001c0001t0001g0322others(10): Show | 14 | HG01884.hp1 HG02055.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.687-7701G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39674910 | ||||||
| chr12:39674964
|
G | A | 17 | a0001c0001t0001g0003a0001c0001t0001g0318a0001c0001t0001g0322others(14): Show | 18 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.687-7647G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39674964 | ||||||
| chr12:39675018
|
G | T | 3 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0208 | 3 | HG00280.hp2 HG03239.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.687-7593G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39675018 | ||||||
| chr12:39675094
|
A | G | 255 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.687-7517A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39675094 | ||||||
| chr12:39675122
|
T | C | 255 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.687-7489T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39675122 | ||||||
| chr12:39675148
|
C | T | 2 | a0001c0001t0001g0288a0001c0001t0001g0329 | 2 | HG03225.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.687-7463C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39675148 | ||||||
| chr12:39675156
|
T | G | 5 | a0001c0001t0001g0146a0001c0001t0001g0151a0001c0001t0001g0163others(2): Show | 5 | HG00639.hp2 HG01069.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.687-7455T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39675156 | ||||||
| chr12:39675318
|
A | T | 1 | a0001c0001t0001g0014 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.687-7293A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39675318 | ||||||
| chr12:39675328
|
T | C | 7 | a0001c0001t0001g0152a0001c0001t0001g0159a0001c0001t0001g0164others(4): Show | 7 | HG01109.hp2 HG01934.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.687-7283T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39675328 | ||||||
| chr12:39675489
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.687-7122G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39675489 | ||||||
| chr12:39675531
|
C | A | 218 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(215): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.687-7080C>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39675531 | ||||||
| chr12:39675531
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.687-7080C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39675531 | ||||||
| chr12:39675803
|
A | G | 7 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0029others(4): Show | 8 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.687-6808A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39675803 | ||||||
| chr12:39675900
|
A | G | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.687-6711A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39675900 | ||||||
| chr12:39676152
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.687-6459C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39676152 | ||||||
| chr12:39676206
|
C | A | 1 | a0001c0001t0006g0033 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.687-6405C>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39676206 | ||||||
| chr12:39676282
|
A | G | 1 | a0002c0002t0001g0118 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.687-6329A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39676282 | ||||||
| chr12:39676417
|
A | G | 1 | a0001c0001t0001g0244 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.687-6194A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39676417 | ||||||
| chr12:39676475
|
A | G | 1 | a0001c0001t0001g0281 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.687-6136A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39676475 | ||||||
| chr12:39676585
|
A | G | 1 | a0002c0002t0001g0128 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.687-6026A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39676585 | ||||||
| chr12:39676709
|
G | A | 2 | a0001c0001t0001g0149a0001c0001t0001g0177 | 2 | HG00280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.687-5902G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39676709 | ||||||
| chr12:39676776
|
G | A | 2 | a0002c0002t0001g0101a0002c0002t0001g0102 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.687-5835G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39676776 | ||||||
| chr12:39676830
|
C | G | 1 | a0001c0001t0006g0033 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.687-5781C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39676830 | ||||||
| chr12:39677027
|
G | GA | 10 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(7): Show | 11 | HG01168.hp2 HG01169.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.687-5571dupA | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39677027 | |||||
| chr12:39677027
|
GA | G | 219 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(216): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.687-5571delA | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39677027 | |||||
| chr12:39677183
|
A | G | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.687-5428A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39677183 | ||||||
| chr12:39677300
|
T | C | 1 | a0001c0001t0001g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.687-5311T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39677300 | ||||||
| chr12:39677303
|
C | G | 1 | a0001c0001t0001g0063 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.687-5308C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39677303 | ||||||
| chr12:39677371
|
G | A | 22 | a0001c0001t0001g0003a0001c0001t0001g0075a0001c0001t0001g0227others(19): Show | 23 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.687-5240G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39677371 | ||||||
| chr12:39677383
|
C | T | 50 | a0002c0002t0001g0007a0002c0002t0001g0082a0002c0002t0001g0083others(47): Show | 51 | HG00408.hp1 HG00642.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.687-5228C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39677383 | ||||||
| chr12:39677423
|
C | G | 2 | a0003c0005t0001g0335a0003c0005t0001g0336 | 2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.687-5188C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39677423 | ||||||
| chr12:39677599
|
A | G | 1 | a0001c0001t0001g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.687-5012A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39677599 | ||||||
| chr12:39677828
|
G | C | 1 | a0002c0002t0001g0116 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.687-4783G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39677828 | ||||||
| chr12:39677900
|
T | C | 38 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(35): Show | 39 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.687-4711T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39677900 | ||||||
| chr12:39678014
|
A | G | 1 | a0002c0002t0001g0097 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.687-4597A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39678014 | ||||||
| chr12:39678173
|
G | T | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.687-4438G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39678173 | ||||||
| chr12:39678213
|
G | C | 1 | a0001c0001t0001g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.687-4398G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39678213 | ||||||
| chr12:39678301
|
G | A | 196 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(193): Show | 208 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.687-4310G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39678301 | ||||||
| chr12:39678489
|
C | T | 1 | a0001c0007t0001g0024 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.687-4122C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39678489 | ||||||
| chr12:39678498
|
T | G | 2 | a0005c0003t0001g0034a0005c0003t0001g0035 | 2 | HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.687-4113T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39678498 | ||||||
| chr12:39678629
|
CA | C | 21 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(18): Show | 22 | HG00733.hp1 HG01074.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.687-3962delA | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39678629 | |||||
| chr12:39678629
|
CAA | C | 217 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(214): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.687-3963_687-3962d others(4): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39678629 | |||||
| chr12:39678629
|
CAAA | C | 22 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0143others(19): Show | 23 | HG00140.hp1 HG01175.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.687-3964_687-3962d others(5): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39678629 | |||||
| chr12:39678963
|
C | T | 1 | a0001c0001t0006g0033 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.687-3648C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39678963 | ||||||
| chr12:39679021
|
C | T | 1 | a0001c0007t0001g0024 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.687-3590C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39679021 | ||||||
| chr12:39679133
|
C | T | 38 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(35): Show | 39 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.687-3478C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39679133 | ||||||
| chr12:39679135
|
T | C | 8 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(5): Show | 9 | HG01169.hp1 HG01192.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.687-3476T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39679135 | ||||||
| chr12:39679327
|
A | G | 175 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(172): Show | 186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.687-3284A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39679327 | ||||||
| chr12:39679333
|
A | G | 2 | a0001c0001t0001g0314a0001c0001t0001g0315 | 2 | HG02683.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.687-3278A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39679333 | ||||||
| chr12:39679454
|
C | A | 1 | a0001c0001t0006g0033 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.687-3157C>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39679454 | ||||||
| chr12:39679521
|
T | C | 3 | a0001c0007t0001g0024a0005c0003t0001g0034a0005c0003t0001g0035 | 3 | HG02486.hp2 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.687-3090T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39679521 | ||||||
| chr12:39679845
|
A | G | 1 | a0001c0001t0001g0303 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.687-2766A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39679845 | ||||||
| chr12:39679972
|
T | TTA | 3 | a0001c0001t0001g0026a0001c0001t0001g0251a0001c0001t0001g0252 | 3 | HG01255.hp2 HG04228.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.687-2634_687-2633d others(4): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39679972 | |||||
| chr12:39680007
|
T | G | 1 | a0001c0001t0001g0154 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.687-2604T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39680007 | ||||||
| chr12:39680087
|
G | T | 220 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(217): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.687-2524G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39680087 | ||||||
| chr12:39680152
|
A | C | 1 | a0001c0001t0001g0189 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.687-2459A>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39680152 | ||||||
| chr12:39680185
|
A | G | 1 | a0001c0001t0001g0142 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.687-2426A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39680185 | ||||||
| chr12:39680188
|
C | T | 2 | a0001c0001t0001g0227a0001c0001t0001g0230 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.687-2423C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39680188 | ||||||
| chr12:39680336
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.687-2275C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39680336 | ||||||
| chr12:39680418
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.687-2193A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39680418 | ||||||
| chr12:39680488
|
C | T | 3 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0001g0278 | 3 | HG03130.hp1 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.687-2123C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39680488 | ||||||
| chr12:39680523
|
C | T | 2 | a0003c0005t0001g0335a0003c0005t0001g0336 | 2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.687-2088C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39680523 | ||||||
| chr12:39680621
|
G | A | 255 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.687-1990G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39680621 | ||||||
| chr12:39680748
|
T | G | 3 | a0001c0007t0001g0024a0005c0003t0001g0034a0005c0003t0001g0035 | 3 | HG02486.hp2 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.687-1863T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39680748 | ||||||
| chr12:39680767
|
C | T | 7 | a0001c0001t0001g0240a0001c0001t0001g0284a0001c0001t0001g0285others(4): Show | 7 | HG00438.hp1 HG00544.hp1 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.687-1844C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39680767 | ||||||
| chr12:39680768
|
G | GCA | 233 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(230): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.687-1825_687-1824d others(4): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39680768 | |||||
| chr12:39680768
|
G | GCACA | 4 | a0001c0001t0001g0184a0001c0001t0006g0033a0005c0003t0001g0034others(1): Show | 4 | HG00733.hp1 HG03139.hp2 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.687-1827_687-1824d others(6): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39680768 | |||||
| chr12:39680812
|
G | A | 1 | a0001c0001t0001g0246 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.687-1799G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39680812 | ||||||
| chr12:39680880
|
T | C | 3 | a0001c0001t0001g0250a0001c0001t0001g0259a0001c0001t0001g0266 | 3 | NA18966.hp2 NA18984.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.687-1731T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39680880 | ||||||
| chr12:39680997
|
T | C | 255 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.687-1614T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39680997 | ||||||
| chr12:39681019
|
C | T | 218 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(215): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.687-1592C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39681019 | ||||||
| chr12:39681058
|
A | G | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.687-1553A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39681058 | ||||||
| chr12:39681128
|
C | T | 2 | a0003c0005t0001g0335a0003c0005t0001g0336 | 2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.687-1483C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39681128 | ||||||
| chr12:39681129
|
G | A | 1 | a0004c0004t0005g0135 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.687-1482G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39681129 | ||||||
| chr12:39681274
|
C | G | 1 | a0001c0001t0006g0033 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.687-1337C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39681274 | ||||||
| chr12:39681479
|
A | T | 7 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0029others(4): Show | 8 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.687-1132A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39681479 | ||||||
| chr12:39681515
|
T | C | 1 | a0002c0002t0001g0095 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.687-1096T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39681515 | ||||||
| chr12:39681589
|
C | G | 1 | a0002c0002t0001g0100 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.687-1022C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39681589 | ||||||
| chr12:39681667
|
C | T | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(104): Show | 114 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.687-944C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39681667 | ||||||
| chr12:39681720
|
A | T | 1 | a0001c0001t0001g0229 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.687-891A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39681720 | ||||||
| chr12:39681845
|
T | C | 1 | a0001c0001t0001g0075 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.687-766T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39681845 | ||||||
| chr12:39681847
|
G | T | 221 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(218): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.687-764G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39681847 | ||||||
| chr12:39682002
|
A | AATT | 255 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.687-605_687-603dup others(3): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 39682002 | |||||
| chr12:39682116
|
T | C | 1 | a0002c0002t0001g0119 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.687-495T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39682116 | ||||||
| chr12:39682279
|
A | G | 30 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(27): Show | 30 | HG00140.hp1 HG00280.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.687-332A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39682279 | ||||||
| chr12:39682423
|
A | G | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.687-188A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 7/12 | chr12 | 39682423 | ||||||
| chr12:39683161
|
A | C | 1 | a0001c0001t0001g0191 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1216+21A>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 8/12 | chr12 | 39683161 | ||||||
| chr12:39683226
|
A | G | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1216+86A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 8/12 | chr12 | 39683226 | ||||||
| chr12:39683280
|
A | AGAATGGC others(20): Show |
1 | a0001c0001t0001g0301 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1217-133_1217-107d others(29): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 39683280 | |||||
| chr12:39683606
|
C | A | 1 | a0001c0001t0001g0273 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1286+122C>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 9/12 | chr12 | 39683606 | ||||||
| chr12:39683776
|
A | G | 2 | a0001c0001t0001g0113a0001c0001t0001g0262 | 2 | HG03471.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.1286+292A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 9/12 | chr12 | 39683776 | ||||||
| chr12:39683813
|
G | A | 1 | a0001c0007t0001g0024 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1286+329G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 9/12 | chr12 | 39683813 | ||||||
| chr12:39683918
|
A | G | 3 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0208 | 3 | HG00280.hp2 HG03239.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1286+434A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 9/12 | chr12 | 39683918 | ||||||
| chr12:39684198
|
A | T | 2 | a0005c0003t0001g0034a0005c0003t0001g0035 | 2 | HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1287-669A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 9/12 | chr12 | 39684198 | ||||||
| chr12:39684449
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1287-418G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 9/12 | chr12 | 39684449 | ||||||
| chr12:39684457
|
A | C | 1 | a0002c0002t0001g0108 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1287-410A>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 9/12 | chr12 | 39684457 | ||||||
| chr12:39684641
|
G | C | 1 | a0001c0001t0001g0240 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1287-226G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 9/12 | chr12 | 39684641 | ||||||
| chr12:39684649
|
G | C | 11 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(8): Show | 11 | HG00738.hp1 HG01106.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.1287-218G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 9/12 | chr12 | 39684649 | ||||||
| chr12:39685150
|
A | T | 2 | a0001c0001t0001g0305a0001c0001t0001g0306 | 2 | HG02132.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1347+223A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39685150 | ||||||
| chr12:39685327
|
C | T | 1 | a0001c0001t0001g0280 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1347+400C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39685327 | ||||||
| chr12:39685389
|
A | G | 7 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0029others(4): Show | 8 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1347+462A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39685389 | ||||||
| chr12:39685709
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1347+782C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39685709 | ||||||
| chr12:39685751
|
C | T | 2 | a0005c0003t0001g0034a0005c0003t0001g0035 | 2 | HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1347+824C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39685751 | ||||||
| chr12:39685773
|
C | A | 1 | a0001c0001t0001g0240 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1347+846C>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39685773 | ||||||
| chr12:39685793
|
C | A | 1 | a0001c0001t0001g0307 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1347+866C>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39685793 | ||||||
| chr12:39685817
|
G | T | 1 | a0002c0002t0001g0094 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1347+890G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39685817 | ||||||
| chr12:39685845
|
A | T | 3 | a0001c0001t0001g0330a0001c0001t0001g0331a0001c0001t0001g0332 | 3 | HG02145.hp2 HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1347+918A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39685845 | ||||||
| chr12:39685953
|
T | C | 12 | a0001c0001t0001g0011a0001c0001t0001g0145a0001c0001t0001g0149others(9): Show | 13 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1347+1026T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39685953 | ||||||
| chr12:39685964
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1347+1037T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39685964 | ||||||
| chr12:39686072
|
A | G | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1347+1145A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39686072 | ||||||
| chr12:39686286
|
G | T | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1347+1359G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39686286 | ||||||
| chr12:39686560
|
C | T | 2 | a0001c0001t0001g0076a0001c0001t0001g0077 | 2 | HG00639.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.1347+1633C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39686560 | ||||||
| chr12:39686935
|
C | T | 3 | a0002c0002t0001g0093a0002c0002t0001g0104a0002c0002t0001g0107 | 3 | HG01934.hp2 HG02683.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1347+2008C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39686935 | ||||||
| chr12:39687005
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1347+2078C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39687005 | ||||||
| chr12:39687038
|
A | G | 1 | a0001c0001t0001g0229 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1347+2111A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39687038 | ||||||
| chr12:39687133
|
A | G | 233 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(230): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.1347+2206A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39687133 | ||||||
| chr12:39687140
|
C | T | 2 | a0003c0005t0001g0335a0003c0005t0001g0336 | 2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1347+2213C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39687140 | ||||||
| chr12:39687169
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1347+2242C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39687169 | ||||||
| chr12:39687317
|
A | G | 1 | a0001c0001t0001g0075 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1347+2390A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39687317 | ||||||
| chr12:39687395
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1347+2468G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39687395 | ||||||
| chr12:39687463
|
A | G | 255 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1347+2536A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39687463 | ||||||
| chr12:39687489
|
A | AG | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1347+2563dupG | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 39687489 | |||||
| chr12:39687795
|
T | C | 1 | a0001c0001t0001g0210 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1347+2868T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39687795 | ||||||
| chr12:39687817
|
A | G | 220 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(217): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.1347+2890A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39687817 | ||||||
| chr12:39687871
|
C | T | 21 | a0001c0001t0001g0003a0001c0001t0001g0075a0001c0001t0001g0227others(18): Show | 22 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.1347+2944C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39687871 | ||||||
| chr12:39687935
|
G | T | 1 | a0001c0001t0001g0283 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1347+3008G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39687935 | ||||||
| chr12:39688146
|
C | T | 3 | a0001c0007t0001g0024a0005c0003t0001g0034a0005c0003t0001g0035 | 3 | HG02486.hp2 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1347+3219C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39688146 | ||||||
| chr12:39688217
|
AAG | A | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1347+3294_1347+329 others(6): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 39688217 | |||||
| chr12:39688413
|
G | C | 1 | a0001c0001t0001g0240 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1347+3486G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39688413 | ||||||
| chr12:39688506
|
G | T | 3 | a0001c0001t0001g0047a0001c0001t0001g0061a0001c0001t0001g0063 | 3 | NA18940.hp1 NA18987.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1348-3543G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39688506 | ||||||
| chr12:39688507
|
T | C | 1 | a0001c0001t0003g0078 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1348-3542T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39688507 | ||||||
| chr12:39688805
|
A | T | 1 | a0010c0010t0001g0096 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1348-3244A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39688805 | ||||||
| chr12:39689409
|
G | C | 1 | a0001c0007t0001g0024 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1348-2640G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39689409 | ||||||
| chr12:39689410
|
G | A | 1 | a0001c0001t0001g0241 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1348-2639G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39689410 | ||||||
| chr12:39689486
|
T | C | 3 | a0002c0002t0001g0120a0002c0002t0001g0121a0002c0002t0001g0126 | 3 | HG02083.hp2 NA18941.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1348-2563T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39689486 | ||||||
| chr12:39689513
|
G | C | 1 | a0001c0001t0001g0248 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1348-2536G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39689513 | ||||||
| chr12:39689632
|
G | A | 1 | a0001c0001t0001g0241 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1348-2417G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39689632 | ||||||
| chr12:39689714
|
G | A | 1 | a0001c0001t0006g0033 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1348-2335G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39689714 | ||||||
| chr12:39689827
|
A | G | 1 | a0001c0001t0001g0265 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1348-2222A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39689827 | ||||||
| chr12:39690019
|
A | T | 2 | a0005c0003t0001g0034a0005c0003t0001g0035 | 2 | HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1348-2030A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39690019 | ||||||
| chr12:39690140
|
T | A | 3 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324 | 3 | HG02895.hp2 HG02897.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1348-1909T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39690140 | ||||||
| chr12:39690156
|
G | C | 1 | a0001c0001t0001g0255 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1348-1893G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39690156 | ||||||
| chr12:39690181
|
T | C | 1 | a0001c0001t0001g0039 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1348-1868T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39690181 | ||||||
| chr12:39690324
|
A | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(171): Show | 185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.1348-1725A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39690324 | ||||||
| chr12:39690373
|
A | G | 8 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(5): Show | 9 | HG01169.hp1 HG01192.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1348-1676A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39690373 | ||||||
| chr12:39690457
|
C | T | 2 | a0001c0001t0001g0089a0001c0001t0001g0228 | 2 | HG00741.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1348-1592C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39690457 | ||||||
| chr12:39690458
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1348-1591G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39690458 | ||||||
| chr12:39690620
|
T | G | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1348-1429T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39690620 | ||||||
| chr12:39690627
|
AAATC | A | 22 | a0001c0001t0001g0003a0001c0001t0001g0075a0001c0001t0001g0227others(19): Show | 23 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.1348-1418_1348-141 others(8): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 39690627 | |||||
| chr12:39690693
|
AATAC | A | 6 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(3): Show | 6 | HG01884.hp2 HG02055.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1348-1349_1348-134 others(8): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 39690693 | |||||
| chr12:39690720
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1348-1329C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39690720 | ||||||
| chr12:39690945
|
T | C | 1 | a0001c0001t0001g0039 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1348-1104T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39690945 | ||||||
| chr12:39691002
|
A | G | 1 | a0001c0001t0001g0173 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1348-1047A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39691002 | ||||||
| chr12:39691205
|
C | T | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1348-844C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39691205 | ||||||
| chr12:39691338
|
C | G | 3 | a0001c0007t0001g0024a0005c0003t0001g0034a0005c0003t0001g0035 | 3 | HG02486.hp2 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1348-711C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39691338 | ||||||
| chr12:39691365
|
A | T | 1 | a0001c0001t0001g0243 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1348-684A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39691365 | ||||||
| chr12:39691385
|
T | C | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1348-664T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39691385 | ||||||
| chr12:39691918
|
A | T | 1 | a0001c0001t0001g0262 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1348-131A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 10/12 | chr12 | 39691918 | ||||||
| chr12:39692333
|
A | G | 3 | a0001c0001t0001g0330a0001c0001t0001g0331a0001c0001t0001g0332 | 3 | HG02145.hp2 HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1411+221A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39692333 | ||||||
| chr12:39692404
|
T | G | 1 | a0001c0001t0001g0040 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1411+292T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39692404 | ||||||
| chr12:39692537
|
CT | C | 241 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(238): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.1411+435delT | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39692537 | |||||
| chr12:39692537
|
CTT | C | 9 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(6): Show | 10 | HG00544.hp2 HG01169.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.1411+434_1411+435d others(4): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39692537 | |||||
| chr12:39692601
|
C | T | 1 | a0008c0009t0001g0226 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1411+489C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39692601 | ||||||
| chr12:39692749
|
T | A | 2 | a0001c0001t0001g0070a0009c0008t0001g0068 | 2 | HG01175.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1411+637T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39692749 | ||||||
| chr12:39692827
|
A | G | 1 | a0001c0001t0001g0300 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1411+715A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39692827 | ||||||
| chr12:39692864
|
T | A | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1411+752T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39692864 | ||||||
| chr12:39692917
|
A | G | 7 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0029others(4): Show | 8 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1411+805A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39692917 | ||||||
| chr12:39693137
|
G | A | 255 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1411+1025G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39693137 | ||||||
| chr12:39693375
|
A | G | 6 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0295others(3): Show | 6 | NA18939.hp1 NA18950.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.1411+1263A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39693375 | ||||||
| chr12:39693413
|
A | G | 2 | a0001c0001t0001g0217a0001c0001t0001g0223 | 2 | NA18955.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1411+1301A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39693413 | ||||||
| chr12:39693416
|
A | AT | 21 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0043others(18): Show | 21 | HG00597.hp1 HG00621.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.1411+1317dupT | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39693416 | |||||
| chr12:39693502
|
C | T | 20 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(17): Show | 20 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.1411+1390C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39693502 | ||||||
| chr12:39693844
|
G | T | 2 | a0002c0002t0001g0101a0002c0002t0001g0102 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1411+1732G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39693844 | ||||||
| chr12:39693928
|
T | C | 7 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0029others(4): Show | 8 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1411+1816T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39693928 | ||||||
| chr12:39694028
|
C | T | 1 | a0001c0001t0001g0316 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1411+1916C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39694028 | ||||||
| chr12:39694184
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1411+2072G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39694184 | ||||||
| chr12:39694232
|
G | A | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1411+2120G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39694232 | ||||||
| chr12:39694400
|
C | G | 3 | a0001c0001t0001g0188a0001c0001t0001g0190a0001c0001t0001g0212 | 3 | NA18940.hp2 NA18995.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1411+2288C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39694400 | ||||||
| chr12:39694425
|
TGTA | T | 81 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(78): Show | 91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.1411+2314_1411+231 others(7): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39694425 | ||||||
| chr12:39694493
|
C | T | 36 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0043others(33): Show | 37 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.1411+2381C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39694493 | ||||||
| chr12:39694567
|
G | A | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1411+2455G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39694567 | ||||||
| chr12:39694677
|
A | G | 255 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1411+2565A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39694677 | ||||||
| chr12:39694725
|
G | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(218): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.1411+2613G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39694725 | ||||||
| chr12:39694752
|
TGAGA | T | 220 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(217): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.1411+2641_1411+264 others(8): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39694752 | ||||||
| chr12:39694799
|
C | T | 1 | a0001c0001t0001g0307 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1411+2687C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39694799 | ||||||
| chr12:39695056
|
C | T | 1 | a0001c0001t0001g0330 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1411+2944C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39695056 | ||||||
| chr12:39695154
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1411+3042G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39695154 | ||||||
| chr12:39695169
|
A | T | 1 | a0001c0001t0001g0288 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1411+3057A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39695169 | ||||||
| chr12:39695329
|
A | G | 1 | a0001c0001t0001g0240 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1411+3217A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39695329 | ||||||
| chr12:39695371
|
G | A | 8 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0243others(5): Show | 8 | HG02809.hp1 HG02818.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1411+3259G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39695371 | ||||||
| chr12:39695422
|
A | G | 1 | a0001c0001t0003g0081 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1411+3310A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39695422 | ||||||
| chr12:39695457
|
G | T | 255 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1411+3345G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39695457 | ||||||
| chr12:39695505
|
G | T | 2 | a0002c0002t0001g0101a0002c0002t0001g0102 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1411+3393G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39695505 | ||||||
| chr12:39695530
|
G | T | 22 | a0001c0001t0001g0003a0001c0001t0001g0075a0001c0001t0001g0227others(19): Show | 23 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.1411+3418G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39695530 | ||||||
| chr12:39695583
|
A | AGAAT | 3 | a0001c0001t0001g0064a0001c0001t0001g0067a0001c0001t0001g0069 | 3 | HG00738.hp1 HG01106.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1411+3472_1411+347 others(8): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39695583 | |||||
| chr12:39695663
|
G | C | 2 | a0005c0003t0001g0034a0005c0003t0001g0035 | 2 | HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1411+3551G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39695663 | ||||||
| chr12:39695811
|
T | C | 2 | a0001c0001t0001g0253a0001c0001t0001g0279 | 2 | NA18959.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1411+3699T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39695811 | ||||||
| chr12:39695844
|
T | C | 2 | a0001c0001t0001g0089a0001c0001t0001g0228 | 2 | HG00741.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1411+3732T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39695844 | ||||||
| chr12:39695984
|
G | A | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1411+3872G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39695984 | ||||||
| chr12:39696101
|
T | A | 255 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1411+3989T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39696101 | ||||||
| chr12:39696118
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1411+4006C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39696118 | ||||||
| chr12:39696246
|
T | G | 1 | a0001c0001t0001g0194 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1411+4134T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39696246 | ||||||
| chr12:39696254
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1411+4142G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39696254 | ||||||
| chr12:39696266
|
G | A | 80 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(77): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.1411+4154G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39696266 | ||||||
| chr12:39696326
|
G | A | 3 | a0001c0007t0001g0024a0005c0003t0001g0034a0005c0003t0001g0035 | 3 | HG02486.hp2 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1411+4214G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39696326 | ||||||
| chr12:39696350
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1411+4238C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39696350 | ||||||
| chr12:39696351
|
G | A | 25 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0043others(22): Show | 26 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.1411+4239G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39696351 | ||||||
| chr12:39696359
|
C | T | 3 | a0001c0001t0001g0071a0001c0001t0001g0311a0001c0001t0001g0312 | 3 | HG03492.hp2 NA18945.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1411+4247C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39696359 | ||||||
| chr12:39696371
|
G | A | 1 | a0001c0001t0001g0285 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1411+4259G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39696371 | ||||||
| chr12:39696399
|
C | T | 12 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(9): Show | 13 | HG00642.hp2 HG00741.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.1411+4287C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39696399 | ||||||
| chr12:39696400
|
G | A | 2 | a0001c0001t0001g0305a0001c0001t0001g0306 | 2 | HG02132.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1411+4288G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39696400 | ||||||
| chr12:39696415
|
C | T | 3 | a0001c0001t0004g0055a0001c0001t0004g0059a0001c0001t0004g0060 | 3 | HG00099.hp1 HG01070.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1411+4303C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39696415 | ||||||
| chr12:39696542
|
C | CA | 106 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0011others(103): Show | 112 | HG00099.hp2 HG00140.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.1411+4468dupA | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39696542 | |||||
| chr12:39696542
|
C | CAA | 42 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0013others(39): Show | 45 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.1411+4467_1411+446 others(6): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39696542 | |||||
| chr12:39696542
|
C | CAAA | 12 | a0001c0001t0001g0113a0001c0001t0001g0166a0001c0001t0001g0173others(9): Show | 12 | HG00280.hp1 HG01943.hp2 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.1411+4466_1411+446 others(7): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39696542 | |||||
| chr12:39696542
|
C | CAAAA | 11 | a0001c0001t0001g0149a0001c0001t0001g0160a0001c0001t0001g0165others(8): Show | 11 | HG00544.hp2 HG01243.hp1 HG02970.hp1 others(8): Show |
intron_variant | MODIFIER | c.1411+4465_1411+446 others(8): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39696542 | |||||
| chr12:39696542
|
C | CAAAAA | 9 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0092others(6): Show | 9 | HG00099.hp1 HG01106.hp2 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.1411+4464_1411+446 others(9): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39696542 | |||||
| chr12:39696542
|
C | CAAAAAAA others(2): Show |
11 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0029others(8): Show | 12 | HG01123.hp2 HG01192.hp2 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.1411+4460_1411+446 others(13): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39696542 | |||||
| chr12:39696542
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0200 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1411+4459_1411+446 others(14): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39696542 | |||||
| chr12:39696542
|
C | CAAAAAAA others(5): Show |
3 | a0001c0001t0001g0036a0009c0008t0001g0068a0011c0011t0001g0073 | 3 | HG01175.hp1 HG03453.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1411+4457_1411+446 others(16): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39696542 | |||||
| chr12:39696542
|
C | CAAAAAAA others(9): Show |
1 | a0001c0001t0001g0070 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1411+4453_1411+446 others(20): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39696542 | |||||
| chr12:39696542
|
CA | C | 11 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0039others(8): Show | 13 | HG01884.hp2 HG02040.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.1411+4468delA | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39696542 | |||||
| chr12:39696542
|
CAAAAAA | C | 7 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0329others(4): Show | 7 | HG02055.hp1 HG02895.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.1411+4463_1411+446 others(10): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39696542 | |||||
| chr12:39696542
|
CAAAAAAA | C | 10 | a0001c0001t0001g0003a0001c0001t0001g0318a0001c0001t0001g0324others(7): Show | 11 | HG01884.hp1 HG02559.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1411+4462_1411+446 others(11): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39696542 | |||||
| chr12:39696542
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0026 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1411+4459_1411+446 others(14): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39696542 | |||||
| chr12:39696542
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0001g0251a0001c0001t0001g0252 | 2 | HG04228.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1411+4457_1411+446 others(16): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39696542 | |||||
| chr12:39696542
|
CAAAAAAA others(7): Show |
C | 5 | a0001c0001t0001g0240a0002c0002t0001g0094a0002c0002t0001g0099others(2): Show | 5 | HG00738.hp2 HG02145.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1411+4455_1411+446 others(18): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39696542 | |||||
| chr12:39696542
|
CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0001g0247 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1411+4453_1411+446 others(20): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39696542 | |||||
| chr12:39696557
|
A | T | 1 | a0001c0001t0001g0308 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1411+4445A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39696557 | ||||||
| chr12:39696564
|
AAAAAAAA others(10): Show |
A | 2 | a0003c0005t0001g0335a0003c0005t0001g0336 | 2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1411+4455_1411+447 others(21): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39696564 | |||||
| chr12:39696581
|
T | A | 5 | a0002c0002t0001g0122a0002c0002t0001g0123a0002c0002t0001g0124others(2): Show | 5 | HG00408.hp1 HG02027.hp1 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1411+4469T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39696581 | ||||||
| chr12:39696673
|
A | T | 1 | a0001c0001t0001g0203 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1411+4561A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39696673 | ||||||
| chr12:39696685
|
G | A | 1 | a0001c0001t0001g0307 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1411+4573G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39696685 | ||||||
| chr12:39696823
|
A | G | 1 | a0002c0002t0001g0094 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1411+4711A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39696823 | ||||||
| chr12:39697061
|
A | G | 2 | a0005c0003t0001g0034a0005c0003t0001g0035 | 2 | HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1411+4949A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39697061 | ||||||
| chr12:39697112
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1411+5000C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39697112 | ||||||
| chr12:39697345
|
T | G | 1 | a0001c0001t0001g0221 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1411+5233T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39697345 | ||||||
| chr12:39697522
|
G | T | 4 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(1): Show | 4 | NA18961.hp1 NA18965.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.1411+5410G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39697522 | ||||||
| chr12:39697544
|
A | C | 1 | a0001c0001t0006g0033 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1411+5432A>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39697544 | ||||||
| chr12:39698011
|
A | G | 4 | a0001c0001t0006g0033a0001c0007t0001g0024a0005c0003t0001g0034others(1): Show | 4 | HG00733.hp1 HG02486.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1411+5899A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39698011 | ||||||
| chr12:39698209
|
A | G | 255 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1411+6097A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39698209 | ||||||
| chr12:39698273
|
G | T | 2 | a0001c0001t0001g0149a0001c0001t0001g0177 | 2 | HG00280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1411+6161G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39698273 | ||||||
| chr12:39698292
|
A | G | 1 | a0001c0007t0001g0024 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1411+6180A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39698292 | ||||||
| chr12:39698418
|
CT | C | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1411+6310delT | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39698418 | |||||
| chr12:39698644
|
T | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0029others(4): Show | 8 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1411+6532T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39698644 | ||||||
| chr12:39698673
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1411+6561G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39698673 | ||||||
| chr12:39698845
|
T | C | 5 | a0001c0001t0001g0146a0001c0001t0001g0151a0001c0001t0001g0163others(2): Show | 5 | HG00639.hp2 HG01069.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1411+6733T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39698845 | ||||||
| chr12:39698937
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1411+6825C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39698937 | ||||||
| chr12:39699138
|
A | G | 1 | a0001c0001t0001g0300 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1411+7026A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39699138 | ||||||
| chr12:39699153
|
G | T | 2 | a0003c0005t0001g0335a0003c0005t0001g0336 | 2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1411+7041G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39699153 | ||||||
| chr12:39699185
|
G | A | 1 | a0001c0001t0001g0237 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1411+7073G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39699185 | ||||||
| chr12:39699225
|
G | A | 18 | a0001c0001t0001g0003a0001c0001t0001g0264a0001c0001t0001g0318others(15): Show | 19 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.1411+7113G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39699225 | ||||||
| chr12:39699242
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1411+7130C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39699242 | ||||||
| chr12:39699299
|
G | A | 1 | a0001c0001t0001g0241 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1411+7187G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39699299 | ||||||
| chr12:39699451
|
C | T | 4 | a0002c0002t0001g0122a0002c0002t0001g0123a0002c0002t0001g0124others(1): Show | 4 | HG00408.hp1 HG02027.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.1411+7339C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39699451 | ||||||
| chr12:39699452
|
G | A | 4 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(1): Show | 4 | HG02970.hp1 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1411+7340G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39699452 | ||||||
| chr12:39699462
|
T | C | 1 | a0002c0002t0001g0116 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1411+7350T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39699462 | ||||||
| chr12:39699570
|
T | A | 1 | a0001c0001t0001g0091 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1411+7458T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39699570 | ||||||
| chr12:39699585
|
G | T | 13 | a0001c0001t0001g0003a0001c0001t0001g0318a0001c0001t0001g0322others(10): Show | 14 | HG01884.hp1 HG02055.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1411+7473G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39699585 | ||||||
| chr12:39699630
|
G | A | 36 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0043others(33): Show | 37 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.1411+7518G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39699630 | ||||||
| chr12:39699651
|
C | CACAG | 12 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(9): Show | 13 | HG00733.hp1 HG01169.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.1411+7542_1411+754 others(8): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39699651 | |||||
| chr12:39699655
|
A | G | 220 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(217): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.1411+7543A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39699655 | ||||||
| chr12:39699731
|
C | T | 2 | a0001c0001t0001g0314a0001c0001t0001g0315 | 2 | HG02683.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1411+7619C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39699731 | ||||||
| chr12:39699732
|
G | A | 2 | a0001c0001t0001g0227a0001c0001t0001g0230 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1411+7620G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39699732 | ||||||
| chr12:39699821
|
A | C | 255 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1411+7709A>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39699821 | ||||||
| chr12:39699830
|
T | C | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1411+7718T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39699830 | ||||||
| chr12:39699982
|
AT | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(5): Show | 9 | HG01169.hp1 HG01192.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1411+7871delT | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39699982 | ||||||
| chr12:39700029
|
C | T | 2 | a0003c0005t0001g0335a0003c0005t0001g0336 | 2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1411+7917C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39700029 | ||||||
| chr12:39700032
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1411+7920C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39700032 | ||||||
| chr12:39700052
|
G | A | 1 | a0001c0007t0001g0024 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1411+7940G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39700052 | ||||||
| chr12:39700088
|
A | G | 1 | a0001c0001t0001g0280 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1411+7976A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39700088 | ||||||
| chr12:39700093
|
G | A | 1 | a0001c0001t0001g0241 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1411+7981G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39700093 | ||||||
| chr12:39700140
|
C | T | 1 | a0002c0002t0001g0103 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1411+8028C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39700140 | ||||||
| chr12:39700189
|
G | GA | 6 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0247others(3): Show | 6 | HG03669.hp2 NA18981.hp2 NA18997.hp1 others(3): Show |
intron_variant | MODIFIER | c.1411+8085dupA | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39700189 | |||||
| chr12:39700218
|
G | A | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1411+8106G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39700218 | ||||||
| chr12:39700279
|
A | T | 1 | a0001c0001t0001g0040 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1411+8167A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39700279 | ||||||
| chr12:39700292
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1411+8180T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39700292 | ||||||
| chr12:39700311
|
G | A | 1 | a0001c0001t0001g0075 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1411+8199G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39700311 | ||||||
| chr12:39700380
|
T | G | 8 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(5): Show | 9 | HG01169.hp1 HG01192.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1411+8268T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39700380 | ||||||
| chr12:39700404
|
C | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1411+8292C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39700404 | ||||||
| chr12:39700438
|
A | G | 1 | a0001c0001t0001g0283 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1411+8326A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39700438 | ||||||
| chr12:39700512
|
G | A | 5 | a0001c0001t0001g0013a0001c0001t0001g0232a0001c0001t0001g0234others(2): Show | 6 | NA18964.hp2 NA18972.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.1411+8400G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39700512 | ||||||
| chr12:39700537
|
CCAATCTA others(725): Show |
C | 2 | a0002c0002t0001g0101a0002c0002t0001g0102 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1411+8426_1411+915 others(4): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39700537 | ||||||
| chr12:39700576
|
C | A | 1 | a0001c0001t0001g0113 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1411+8464C>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39700576 | ||||||
| chr12:39700690
|
G | C | 1 | a0001c0001t0001g0240 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1411+8578G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39700690 | ||||||
| chr12:39700694
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1411+8582G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39700694 | ||||||
| chr12:39700704
|
C | G | 1 | a0002c0002t0001g0313 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1411+8592C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39700704 | ||||||
| chr12:39700727
|
C | G | 3 | a0001c0001t0004g0055a0001c0001t0004g0059a0001c0001t0004g0060 | 3 | HG00099.hp1 HG01070.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1411+8615C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39700727 | ||||||
| chr12:39700730
|
T | C | 4 | a0001c0001t0001g0280a0001c0001t0004g0055a0001c0001t0004g0059others(1): Show | 4 | HG00099.hp1 HG01070.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1411+8618T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39700730 | ||||||
| chr12:39700731
|
G | T | 4 | a0001c0001t0001g0280a0001c0001t0004g0055a0001c0001t0004g0059others(1): Show | 4 | HG00099.hp1 HG01070.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1411+8619G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39700731 | ||||||
| chr12:39700737
|
C | T | 214 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(211): Show | 226 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.1411+8625C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39700737 | ||||||
| chr12:39700740
|
A | G | 3 | a0001c0001t0004g0055a0001c0001t0004g0059a0001c0001t0004g0060 | 3 | HG00099.hp1 HG01070.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1411+8628A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39700740 | ||||||
| chr12:39700767
|
GT | G | 5 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0056others(2): Show | 6 | HG00639.hp1 HG01074.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1411+8656delT | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39700767 | ||||||
| chr12:39700782
|
C | G | 5 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0056others(2): Show | 6 | HG00639.hp1 HG01074.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1411+8670C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39700782 | ||||||
| chr12:39700811
|
C | G | 6 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(3): Show | 6 | HG01884.hp2 HG02055.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1411+8699C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39700811 | ||||||
| chr12:39700835
|
T | A | 2 | a0005c0003t0001g0034a0005c0003t0001g0035 | 2 | HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1411+8723T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39700835 | ||||||
| chr12:39700860
|
C | A | 1 | a0008c0009t0001g0226 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1411+8748C>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39700860 | ||||||
| chr12:39700875
|
C | G | 25 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0043others(22): Show | 26 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.1411+8763C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39700875 | ||||||
| chr12:39700889
|
G | C | 1 | a0010c0010t0001g0096 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1411+8777G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39700889 | ||||||
| chr12:39700960
|
C | T | 2 | a0001c0001t0001g0147a0001c0001t0001g0172 | 2 | NA18989.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1411+8848C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39700960 | ||||||
| chr12:39701001
|
A | T | 230 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(227): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1411+8889A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39701001 | ||||||
| chr12:39701090
|
T | G | 1 | a0001c0001t0006g0033 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1411+8978T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39701090 | ||||||
| chr12:39701094
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1411+8982T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39701094 | ||||||
| chr12:39701104
|
AATGG | A | 217 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(214): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1411+8994_1411+899 others(8): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39701104 | |||||
| chr12:39701109
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1411+8997A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39701109 | ||||||
| chr12:39701111
|
TAAATG | T | 217 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(214): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1411+9000_1411+900 others(9): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39701111 | ||||||
| chr12:39701117
|
C | T | 217 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(214): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1411+9005C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39701117 | ||||||
| chr12:39701119
|
C | T | 217 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(214): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1411+9007C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39701119 | ||||||
| chr12:39701120
|
C | A | 217 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(214): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1411+9008C>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39701120 | ||||||
| chr12:39701143
|
A | C | 1 | a0001c0001t0001g0049 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1411+9031A>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39701143 | ||||||
| chr12:39701188
|
T | A | 1 | a0001c0001t0001g0244 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1411+9076T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39701188 | ||||||
| chr12:39701191
|
C | G | 1 | a0005c0003t0001g0035 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1411+9079C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39701191 | ||||||
| chr12:39701194
|
A | C | 1 | a0001c0001t0001g0244 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1411+9082A>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39701194 | ||||||
| chr12:39701195
|
C | T | 231 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(228): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.1411+9083C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39701195 | ||||||
| chr12:39701196
|
C | G | 1 | a0001c0001t0001g0244 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1411+9084C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39701196 | ||||||
| chr12:39701198
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1411+9086C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39701198 | ||||||
| chr12:39701202
|
C | T | 230 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(227): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1411+9090C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39701202 | ||||||
| chr12:39701203
|
G | A | 5 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246others(2): Show | 5 | HG00673.hp2 NA18997.hp1 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.1411+9091G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39701203 | ||||||
| chr12:39701210
|
C | A | 2 | a0002c0002t0001g0094a0002c0002t0001g0100 | 2 | HG02717.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1411+9098C>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39701210 | ||||||
| chr12:39701235
|
G | A | 1 | a0001c0001t0006g0033 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1411+9123G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39701235 | ||||||
| chr12:39701314
|
T | C | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1411+9202T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39701314 | ||||||
| chr12:39701383
|
C | G | 24 | a0002c0002t0001g0007a0002c0002t0001g0090a0002c0002t0001g0093others(21): Show | 25 | HG00738.hp2 HG01099.hp2 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.1411+9271C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39701383 | ||||||
| chr12:39701465
|
C | T | 220 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(217): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.1411+9353C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39701465 | ||||||
| chr12:39701501
|
C | T | 1 | a0001c0007t0001g0024 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1411+9389C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39701501 | ||||||
| chr12:39701537
|
G | C | 1 | a0001c0001t0001g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1411+9425G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39701537 | ||||||
| chr12:39701545
|
G | A | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1411+9433G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39701545 | ||||||
| chr12:39701554
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1411+9442C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39701554 | ||||||
| chr12:39701640
|
T | C | 1 | a0001c0001t0001g0327 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1411+9528T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39701640 | ||||||
| chr12:39701667
|
A | G | 4 | a0002c0002t0001g0007a0002c0002t0001g0110a0002c0002t0001g0111others(1): Show | 5 | HG02056.hp1 NA18946.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.1411+9555A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39701667 | ||||||
| chr12:39701702
|
C | G | 1 | a0001c0001t0001g0113 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1411+9590C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39701702 | ||||||
| chr12:39701758
|
T | A | 1 | a0001c0001t0001g0229 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1411+9646T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39701758 | ||||||
| chr12:39701794
|
A | G | 220 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(217): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.1411+9682A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39701794 | ||||||
| chr12:39701800
|
C | G | 2 | a0001c0001t0001g0227a0001c0001t0001g0230 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1411+9688C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39701800 | ||||||
| chr12:39701852
|
C | A | 1 | a0001c0001t0001g0280 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1411+9740C>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39701852 | ||||||
| chr12:39701891
|
C | T | 8 | a0001c0001t0001g0013a0001c0001t0001g0154a0001c0001t0001g0204others(5): Show | 9 | HG02132.hp2 HG04115.hp1 NA18964.hp2 others(6): Show |
intron_variant | MODIFIER | c.1411+9779C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39701891 | ||||||
| chr12:39701892
|
G | T | 1 | a0001c0001t0001g0204 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1411+9780G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39701892 | ||||||
| chr12:39701893
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1411+9781A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39701893 | ||||||
| chr12:39701894
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1411+9782G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39701894 | ||||||
| chr12:39701930
|
A | T | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1411+9818A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39701930 | ||||||
| chr12:39701996
|
C | T | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1411+9884C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39701996 | ||||||
| chr12:39701997
|
A | C | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1411+9885A>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39701997 | ||||||
| chr12:39702065
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1411+9953C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39702065 | ||||||
| chr12:39702111
|
G | C | 1 | a0001c0001t0001g0270 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1411+9999G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39702111 | ||||||
| chr12:39702117
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1411+10005C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39702117 | ||||||
| chr12:39702228
|
G | A | 1 | a0001c0001t0001g0334 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1411+10116G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39702228 | ||||||
| chr12:39702286
|
T | A | 3 | a0001c0007t0001g0024a0005c0003t0001g0034a0005c0003t0001g0035 | 3 | HG02486.hp2 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1411+10174T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39702286 | ||||||
| chr12:39702311
|
C | T | 2 | a0003c0005t0001g0335a0003c0005t0001g0336 | 2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1411+10199C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39702311 | ||||||
| chr12:39702312
|
C | G | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1411+10200C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39702312 | ||||||
| chr12:39702769
|
G | C | 1 | a0001c0001t0001g0330 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1411+10657G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39702769 | ||||||
| chr12:39702842
|
T | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(171): Show | 185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.1411+10730T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39702842 | ||||||
| chr12:39702957
|
A | G | 10 | a0002c0002t0001g0007a0002c0002t0001g0093a0002c0002t0001g0095others(7): Show | 11 | HG01099.hp2 HG01934.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.1411+10845A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39702957 | ||||||
| chr12:39703049
|
C | G | 4 | a0001c0001t0006g0033a0001c0007t0001g0024a0005c0003t0001g0034others(1): Show | 4 | HG00733.hp1 HG02486.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1411+10937C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39703049 | ||||||
| chr12:39703175
|
A | C | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1411+11063A>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39703175 | ||||||
| chr12:39703246
|
C | A | 2 | a0003c0005t0001g0335a0003c0005t0001g0336 | 2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1411+11134C>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39703246 | ||||||
| chr12:39703270
|
A | G | 2 | a0001c0001t0001g0279a0001c0001t0001g0329 | 2 | HG03225.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.1411+11158A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39703270 | ||||||
| chr12:39703273
|
A | T | 2 | a0001c0001t0001g0227a0001c0001t0001g0230 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1411+11161A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39703273 | ||||||
| chr12:39703342
|
C | A | 4 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0247others(1): Show | 4 | NA18997.hp1 NA19001.hp2 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.1411+11230C>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39703342 | ||||||
| chr12:39703401
|
T | A | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1411+11289T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39703401 | ||||||
| chr12:39703468
|
A | G | 1 | a0001c0001t0001g0229 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1411+11356A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39703468 | ||||||
| chr12:39703480
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1411+11368A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39703480 | ||||||
| chr12:39703489
|
C | T | 1 | a0001c0001t0001g0008 | 2 | NA18956.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1411+11377C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39703489 | ||||||
| chr12:39703522
|
C | T | 2 | a0001c0001t0001g0162a0001c0001t0001g0310 | 2 | HG00438.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1411+11410C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39703522 | ||||||
| chr12:39703530
|
A | G | 1 | a0001c0001t0001g0314 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1411+11418A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39703530 | ||||||
| chr12:39703607
|
A | G | 5 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0048others(2): Show | 5 | HG00621.hp1 NA18962.hp1 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.1411+11495A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39703607 | ||||||
| chr12:39703756
|
A | G | 1 | a0001c0001t0001g0194 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1411+11644A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39703756 | ||||||
| chr12:39703767
|
A | G | 1 | a0001c0001t0006g0033 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1411+11655A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39703767 | ||||||
| chr12:39703779
|
A | G | 1 | a0002c0002t0001g0116 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1411+11667A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39703779 | ||||||
| chr12:39703892
|
G | T | 1 | a0001c0001t0001g0057 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1411+11780G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39703892 | ||||||
| chr12:39703967
|
A | T | 1 | a0001c0001t0001g0241 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1411+11855A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39703967 | ||||||
| chr12:39704040
|
A | T | 1 | a0001c0001t0001g0014 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1411+11928A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39704040 | ||||||
| chr12:39704064
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1411+11952T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39704064 | ||||||
| chr12:39704074
|
C | T | 1 | a0001c0001t0001g0045 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1411+11962C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39704074 | ||||||
| chr12:39704148
|
G | C | 1 | a0001c0001t0001g0243 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1411+12036G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39704148 | ||||||
| chr12:39704165
|
T | A | 255 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1411+12053T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39704165 | ||||||
| chr12:39704318
|
A | G | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1411+12206A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39704318 | ||||||
| chr12:39704541
|
A | C | 1 | a0002c0002t0001g0136 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1412-12215A>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39704541 | ||||||
| chr12:39704547
|
T | C | 12 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0084others(9): Show | 14 | HG02071.hp2 NA18945.hp2 NA18956.hp1 others(11): Show |
intron_variant | MODIFIER | c.1412-12209T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39704547 | ||||||
| chr12:39704556
|
G | C | 3 | a0001c0001t0001g0219a0001c0001t0001g0222a0001c0001t0001g0224 | 3 | HG01106.hp1 HG01515.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1412-12200G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39704556 | ||||||
| chr12:39704622
|
C | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(5): Show | 9 | HG01169.hp1 HG01192.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1412-12134C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39704622 | ||||||
| chr12:39704623
|
G | A | 209 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(206): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.1412-12133G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39704623 | ||||||
| chr12:39704645
|
T | C | 6 | a0001c0001t0001g0014a0001c0001t0001g0293a0001c0001t0001g0294others(3): Show | 7 | HG00733.hp2 HG01069.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1412-12111T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39704645 | ||||||
| chr12:39704704
|
A | C | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1412-12052A>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39704704 | ||||||
| chr12:39704787
|
T | C | 1 | a0001c0001t0001g0329 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1412-11969T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39704787 | ||||||
| chr12:39704794
|
T | C | 1 | a0001c0001t0001g0329 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1412-11962T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39704794 | ||||||
| chr12:39704826
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1412-11930A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39704826 | ||||||
| chr12:39704827
|
A | G | 1 | a0001c0001t0001g0272 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1412-11929A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39704827 | ||||||
| chr12:39704852
|
C | T | 174 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(171): Show | 185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.1412-11904C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39704852 | ||||||
| chr12:39704860
|
G | T | 1 | a0002c0002t0001g0116 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1412-11896G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39704860 | ||||||
| chr12:39704928
|
G | A | 3 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0208 | 3 | HG00280.hp2 HG03239.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1412-11828G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39704928 | ||||||
| chr12:39704948
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1412-11808G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39704948 | ||||||
| chr12:39704955
|
G | A | 2 | a0001c0001t0001g0227a0001c0001t0001g0230 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1412-11801G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39704955 | ||||||
| chr12:39704983
|
TAGTG | T | 13 | a0001c0001t0001g0003a0001c0001t0001g0318a0001c0001t0001g0322others(10): Show | 14 | HG01884.hp1 HG02055.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1412-11772_1412-11 others(10): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39704983 | ||||||
| chr12:39705075
|
T | G | 1 | a0001c0001t0001g0143 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1412-11681T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39705075 | ||||||
| chr12:39705097
|
AAAAT | A | 9 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(6): Show | 10 | HG00733.hp1 HG01169.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.1412-11647_1412-11 others(10): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39705097 | |||||
| chr12:39705158
|
A | T | 2 | a0001c0001t0001g0089a0001c0001t0001g0228 | 2 | HG00741.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1412-11598A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39705158 | ||||||
| chr12:39705211
|
A | T | 6 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(3): Show | 6 | HG01884.hp2 HG02055.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1412-11545A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39705211 | ||||||
| chr12:39705286
|
T | C | 2 | a0002c0002t0001g0090a0002c0002t0001g0108 | 2 | HG01496.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.1412-11470T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39705286 | ||||||
| chr12:39705397
|
A | G | 3 | a0001c0007t0001g0024a0005c0003t0001g0034a0005c0003t0001g0035 | 3 | HG02486.hp2 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1412-11359A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39705397 | ||||||
| chr12:39705434
|
A | T | 4 | a0001c0001t0006g0033a0001c0007t0001g0024a0005c0003t0001g0034others(1): Show | 4 | HG00733.hp1 HG02486.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1412-11322A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39705434 | ||||||
| chr12:39705706
|
A | G | 2 | a0001c0001t0001g0149a0001c0001t0001g0177 | 2 | HG00280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1412-11050A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39705706 | ||||||
| chr12:39705988
|
G | A | 1 | a0001c0001t0001g0304 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1412-10768G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39705988 | ||||||
| chr12:39706050
|
G | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1412-10706G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39706050 | ||||||
| chr12:39706077
|
T | C | 228 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(225): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.1412-10679T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39706077 | ||||||
| chr12:39706112
|
A | T | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1412-10644A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39706112 | ||||||
| chr12:39706190
|
T | A | 1 | a0001c0001t0001g0113 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1412-10566T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39706190 | ||||||
| chr12:39706279
|
C | G | 220 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(217): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.1412-10477C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39706279 | ||||||
| chr12:39706352
|
A | G | 6 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0029others(3): Show | 7 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1412-10404A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39706352 | ||||||
| chr12:39706429
|
A | T | 2 | a0001c0001t0001g0089a0001c0001t0001g0228 | 2 | HG00741.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1412-10327A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39706429 | ||||||
| chr12:39706505
|
C | T | 1 | a0002c0002t0001g0103 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1412-10251C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39706505 | ||||||
| chr12:39706541
|
T | C | 1 | a0001c0001t0001g0240 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1412-10215T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39706541 | ||||||
| chr12:39706583
|
G | A | 7 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0243others(4): Show | 7 | HG02809.hp1 HG02818.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1412-10173G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39706583 | ||||||
| chr12:39706602
|
C | G | 8 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(5): Show | 9 | HG01169.hp1 HG01192.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1412-10154C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39706602 | ||||||
| chr12:39706716
|
A | C | 1 | a0001c0001t0001g0205 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1412-10040A>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39706716 | ||||||
| chr12:39706734
|
G | T | 1 | a0001c0001t0001g0217 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1412-10022G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39706734 | ||||||
| chr12:39706945
|
G | C | 1 | a0001c0001t0002g0321 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1412-9811G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39706945 | ||||||
| chr12:39706963
|
A | G | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1412-9793A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39706963 | ||||||
| chr12:39707011
|
C | T | 1 | a0001c0001t0001g0265 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1412-9745C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39707011 | ||||||
| chr12:39707151
|
A | G | 2 | a0002c0002t0001g0132a0002c0002t0001g0134 | 2 | HG02080.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.1412-9605A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39707151 | ||||||
| chr12:39707232
|
C | T | 2 | a0001c0001t0001g0305a0001c0001t0001g0306 | 2 | HG02132.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1412-9524C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39707232 | ||||||
| chr12:39707266
|
C | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(5): Show | 9 | HG01169.hp1 HG01192.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1412-9490C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39707266 | ||||||
| chr12:39707313
|
G | A | 1 | a0001c0001t0001g0280 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1412-9443G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39707313 | ||||||
| chr12:39707322
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1412-9434T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39707322 | ||||||
| chr12:39707506
|
G | T | 1 | a0002c0002t0001g0097 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1412-9250G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39707506 | ||||||
| chr12:39707588
|
C | T | 1 | a0001c0001t0003g0081 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1412-9168C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39707588 | ||||||
| chr12:39707749
|
T | A | 1 | a0001c0001t0001g0228 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1412-9007T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39707749 | ||||||
| chr12:39707815
|
C | A | 1 | a0001c0001t0001g0241 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1412-8941C>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39707815 | ||||||
| chr12:39707878
|
G | A | 20 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(17): Show | 20 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.1412-8878G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39707878 | ||||||
| chr12:39708167
|
T | C | 1 | a0001c0001t0006g0033 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1412-8589T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39708167 | ||||||
| chr12:39708201
|
A | G | 3 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0229 | 3 | HG03017.hp1 NA18906.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1412-8555A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39708201 | ||||||
| chr12:39708456
|
A | T | 1 | a0002c0002t0001g0119 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1412-8300A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39708456 | ||||||
| chr12:39708829
|
A | T | 3 | a0001c0007t0001g0024a0005c0003t0001g0034a0005c0003t0001g0035 | 3 | HG02486.hp2 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1412-7927A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39708829 | ||||||
| chr12:39708874
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1412-7882A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39708874 | ||||||
| chr12:39709226
|
GT | G | 227 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(224): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.1412-7516delT | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39709226 | |||||
| chr12:39709280
|
A | T | 1 | a0001c0001t0001g0258 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1412-7476A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39709280 | ||||||
| chr12:39709286
|
C | A | 1 | a0001c0001t0001g0186 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1412-7470C>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39709286 | ||||||
| chr12:39709324
|
AATT | A | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1412-7424_1412-742 others(7): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39709324 | |||||
| chr12:39709344
|
C | T | 1 | a0001c0001t0001g0310 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1412-7412C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39709344 | ||||||
| chr12:39709410
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1412-7346C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39709410 | ||||||
| chr12:39709518
|
C | G | 1 | a0001c0001t0001g0245 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1412-7238C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39709518 | ||||||
| chr12:39709565
|
A | G | 1 | a0001c0001t0001g0151 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1412-7191A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39709565 | ||||||
| chr12:39709570
|
A | C | 255 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1412-7186A>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39709570 | ||||||
| chr12:39709573
|
A | C | 1 | a0002c0002t0001g0098 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1412-7183A>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39709573 | ||||||
| chr12:39709615
|
G | T | 139 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(136): Show | 150 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.1412-7141G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39709615 | ||||||
| chr12:39709664
|
A | G | 1 | a0001c0001t0001g0009 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1412-7092A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39709664 | ||||||
| chr12:39709684
|
G | T | 11 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(8): Show | 11 | HG00738.hp1 HG01106.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.1412-7072G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39709684 | ||||||
| chr12:39709705
|
G | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(5): Show | 9 | HG01169.hp1 HG01192.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1412-7051G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39709705 | ||||||
| chr12:39709718
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1412-7038A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39709718 | ||||||
| chr12:39709840
|
C | G | 1 | a0002c0002t0001g0099 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1412-6916C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39709840 | ||||||
| chr12:39709877
|
T | A | 4 | a0001c0001t0006g0033a0001c0007t0001g0024a0005c0003t0001g0034others(1): Show | 4 | HG00733.hp1 HG02486.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1412-6879T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39709877 | ||||||
| chr12:39709890
|
A | T | 1 | a0001c0001t0001g0241 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1412-6866A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39709890 | ||||||
| chr12:39710096
|
G | A | 13 | a0001c0001t0001g0003a0001c0001t0001g0318a0001c0001t0001g0322others(10): Show | 14 | HG01884.hp1 HG02055.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1412-6660G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39710096 | ||||||
| chr12:39710216
|
A | G | 1 | a0002c0002t0001g0108 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1412-6540A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39710216 | ||||||
| chr12:39710254
|
A | G | 2 | a0001c0001t0001g0193a0001c0001t0001g0214 | 2 | NA18981.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1412-6502A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39710254 | ||||||
| chr12:39710275
|
A | G | 1 | a0001c0001t0001g0241 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1412-6481A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39710275 | ||||||
| chr12:39710440
|
C | T | 1 | a0001c0001t0001g0293 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1412-6316C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39710440 | ||||||
| chr12:39710461
|
TCTAA | T | 17 | a0001c0001t0001g0003a0001c0001t0001g0318a0001c0001t0001g0322others(14): Show | 18 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1412-6292_1412-628 others(8): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39710461 | |||||
| chr12:39710504
|
C | T | 2 | a0001c0001t0001g0253a0001c0001t0001g0279 | 2 | NA18959.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1412-6252C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39710504 | ||||||
| chr12:39710506
|
T | G | 1 | a0002c0002t0001g0097 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1412-6250T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39710506 | ||||||
| chr12:39710607
|
C | G | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1412-6149C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39710607 | ||||||
| chr12:39710658
|
T | C | 1 | a0001c0007t0001g0024 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1412-6098T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39710658 | ||||||
| chr12:39710662
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1412-6094T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39710662 | ||||||
| chr12:39710715
|
G | T | 1 | a0001c0001t0001g0170 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1412-6041G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39710715 | ||||||
| chr12:39710853
|
ATAAAG | A | 3 | a0002c0002t0001g0093a0002c0002t0001g0104a0002c0002t0001g0107 | 3 | HG01934.hp2 HG02683.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1412-5900_1412-589 others(9): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39710853 | |||||
| chr12:39710859
|
T | A | 1 | a0001c0001t0001g0204 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1412-5897T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39710859 | ||||||
| chr12:39710870
|
T | G | 17 | a0001c0001t0001g0003a0001c0001t0001g0318a0001c0001t0001g0322others(14): Show | 18 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1412-5886T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39710870 | ||||||
| chr12:39710907
|
T | G | 2 | a0001c0001t0001g0296a0001c0001t0001g0299 | 2 | NA18972.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1412-5849T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39710907 | ||||||
| chr12:39710993
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1412-5763C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39710993 | ||||||
| chr12:39711009
|
C | T | 5 | a0001c0001t0001g0010a0001c0001t0001g0174a0001c0001t0001g0181others(2): Show | 6 | NA18939.hp2 NA18962.hp2 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.1412-5747C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711009 | ||||||
| chr12:39711079
|
G | T | 1 | a0001c0001t0001g0178 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1412-5677G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711079 | ||||||
| chr12:39711117
|
A | C | 233 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(230): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.1412-5639A>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711117 | ||||||
| chr12:39711229
|
A | T | 1 | a0002c0002t0001g0116 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1412-5527A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711229 | ||||||
| chr12:39711238
|
T | C | 3 | a0001c0001t0001g0047a0001c0001t0001g0061a0001c0001t0001g0063 | 3 | NA18940.hp1 NA18987.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1412-5518T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711238 | ||||||
| chr12:39711296
|
T | A | 2 | a0001c0001t0001g0337a0001c0001t0001g0338 | 2 | NA18946.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1412-5460T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711296 | ||||||
| chr12:39711332
|
C | CACATATA others(19): Show |
5 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0056others(2): Show | 6 | HG00639.hp1 HG01074.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1412-5412_1412-538 others(30): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711332 | |||||
| chr12:39711385
|
ATG | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(7): Show | 11 | HG01169.hp1 HG01192.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1412-5365_1412-536 others(6): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711385 | |||||
| chr12:39711386
|
T | C | 1 | a0009c0008t0001g0068 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1412-5370T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711386 | ||||||
| chr12:39711420
|
C | T | 231 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(228): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.1412-5336C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711420 | ||||||
| chr12:39711423
|
A | T | 1 | a0001c0001t0001g0046 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1412-5333A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711423 | ||||||
| chr12:39711433
|
GTA | G | 5 | a0001c0001t0001g0152a0001c0001t0001g0164a0001c0001t0001g0165others(2): Show | 5 | HG01109.hp2 HG01952.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1412-5319_1412-531 others(6): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711433 | |||||
| chr12:39711452
|
T | TAC | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1412-5300_1412-529 others(6): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711452 | |||||
| chr12:39711466
|
T | TACATATA others(9): Show |
1 | a0001c0001t0001g0329 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1412-5280_1412-527 others(20): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711466 | |||||
| chr12:39711470
|
T | C | 4 | a0002c0002t0001g0127a0002c0002t0001g0129a0002c0002t0001g0137others(1): Show | 4 | HG00642.hp2 HG00741.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.1412-5286T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711470 | ||||||
| chr12:39711478
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1412-5278T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711478 | ||||||
| chr12:39711493
|
A | G | 1 | a0001c0007t0001g0024 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1412-5263A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711493 | ||||||
| chr12:39711497
|
G | GTATGTAT others(11): Show |
1 | a0001c0001t0003g0079 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1412-5253_1412-523 others(22): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711497 | |||||
| chr12:39711497
|
G | T | 17 | a0002c0002t0001g0007a0002c0002t0001g0090a0002c0002t0001g0093others(14): Show | 18 | HG01099.hp2 HG01175.hp2 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1412-5259G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711497 | ||||||
| chr12:39711513
|
ATATATGT others(1): Show |
A | 6 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0029others(3): Show | 7 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1412-5229_1412-522 others(12): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711513 | |||||
| chr12:39711523
|
A | ATATACAT others(5): Show |
1 | a0001c0001t0001g0031 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1412-5230_1412-522 others(16): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711523 | |||||
| chr12:39711525
|
ATG | A | 7 | a0002c0002t0001g0131a0002c0002t0001g0132a0002c0002t0001g0133others(4): Show | 7 | HG02080.hp1 HG02129.hp1 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.1412-5227_1412-522 others(6): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711525 | |||||
| chr12:39711530
|
T | C | 1 | a0001c0001t0001g0031 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1412-5226T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711530 | ||||||
| chr12:39711532
|
TATACATA others(17): Show |
T | 1 | a0001c0001t0001g0265 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1412-5221_1412-519 others(28): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711532 | |||||
| chr12:39711534
|
T | C | 1 | a0001c0001t0001g0031 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1412-5222T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711534 | ||||||
| chr12:39711538
|
T | C | 3 | a0001c0001t0001g0330a0001c0001t0001g0331a0001c0001t0001g0332 | 3 | HG02145.hp2 HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1412-5218T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711538 | ||||||
| chr12:39711539
|
ATATGTAT others(41): Show |
A | 3 | a0001c0001t0001g0196a0003c0005t0001g0335a0003c0005t0001g0336 | 3 | NA18522.hp2 NA19006.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1412-5215_1412-516 others(52): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711539 | |||||
| chr12:39711541
|
A | G | 1 | a0001c0001t0001g0031 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1412-5215A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711541 | ||||||
| chr12:39711543
|
GTATGTGC others(17): Show |
G | 4 | a0001c0001t0006g0033a0001c0007t0001g0024a0005c0003t0001g0034others(1): Show | 4 | HG00733.hp1 HG02486.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1412-5182_1412-515 others(28): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711543 | |||||
| chr12:39711550
|
CATACACA others(41): Show |
C | 2 | a0001c0001t0001g0176a0001c0001t0001g0312 | 2 | HG02004.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.1412-5187_1412-514 others(52): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711550 | |||||
| chr12:39711565
|
GTA | G | 182 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(179): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.1412-5187_1412-518 others(6): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711565 | |||||
| chr12:39711565
|
GTATATGT others(19): Show |
G | 17 | a0001c0001t0001g0013a0001c0001t0001g0028a0001c0001t0001g0036others(14): Show | 18 | HG00597.hp2 HG01123.hp2 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.1412-5187_1412-516 others(30): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711565 | |||||
| chr12:39711567
|
A | ATGTGCAT others(13): Show |
25 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(22): Show | 25 | HG00408.hp1 HG01109.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.1412-5188_1412-518 others(24): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711567 | |||||
| chr12:39711568
|
T | C | 37 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(34): Show | 38 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.1412-5188T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711568 | ||||||
| chr12:39711574
|
C | T | 39 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0074others(36): Show | 41 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.1412-5182C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711574 | ||||||
| chr12:39711589
|
GTA | G | 203 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(200): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.1412-5163_1412-516 others(6): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711589 | |||||
| chr12:39711591
|
A | ATGTGTAT others(13): Show |
4 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0091others(1): Show | 4 | HG02886.hp1 HG02970.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1412-5164_1412-516 others(24): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711591 | |||||
| chr12:39711591
|
A | G | 3 | a0001c0001t0001g0196a0003c0005t0001g0335a0003c0005t0001g0336 | 3 | NA18522.hp2 NA19006.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1412-5165A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711591 | ||||||
| chr12:39711591
|
ATATGTGT others(15): Show |
A | 2 | a0001c0001t0001g0253a0001c0001t0001g0279 | 2 | NA18959.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1412-5151_1412-513 others(26): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711591 | |||||
| chr12:39711592
|
T | C | 3 | a0001c0001t0001g0048a0001c0001t0001g0051a0001c0001t0001g0052 | 3 | HG00621.hp1 NA18963.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.1412-5164T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711592 | ||||||
| chr12:39711598
|
T | C | 15 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0041others(12): Show | 16 | HG00280.hp2 HG01099.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1412-5158T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711598 | ||||||
| chr12:39711620
|
T | C | 6 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0188others(3): Show | 6 | HG01884.hp2 HG02809.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1412-5136T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711620 | ||||||
| chr12:39711627
|
G | A | 8 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0188others(5): Show | 8 | HG01884.hp2 HG02809.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1412-5129G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711627 | ||||||
| chr12:39711627
|
GTATGTGT others(1): Show |
G | 14 | a0001c0001t0001g0002a0001c0001t0001g0250a0001c0001t0001g0254others(11): Show | 16 | HG00438.hp2 HG00673.hp1 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.1412-5118_1412-511 others(12): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711627 | |||||
| chr12:39711629
|
A | G | 8 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0188others(5): Show | 8 | HG01884.hp2 HG02809.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1412-5127A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711629 | ||||||
| chr12:39711630
|
T | C | 8 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0188others(5): Show | 8 | HG01884.hp2 HG02809.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1412-5126T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711630 | ||||||
| chr12:39711631
|
G | A | 8 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0188others(5): Show | 8 | HG01884.hp2 HG02809.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1412-5125G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711631 | ||||||
| chr12:39711633
|
GTA | G | 212 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(209): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.1412-5119_1412-511 others(6): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711633 | |||||
| chr12:39711635
|
A | G | 8 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0188others(5): Show | 8 | HG01884.hp2 HG02809.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1412-5121A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711635 | ||||||
| chr12:39711649
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1412-5107A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711649 | ||||||
| chr12:39711651
|
G | A | 2 | a0001c0001t0001g0211a0002c0002t0001g0119 | 2 | HG00140.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1412-5105G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711651 | ||||||
| chr12:39711651
|
G | GCA | 7 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0188others(4): Show | 7 | HG01884.hp2 HG02809.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1412-5105_1412-510 others(6): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711651 | ||||||
| chr12:39711653
|
A | G | 9 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0188others(6): Show | 9 | HG00140.hp1 HG01884.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1412-5103A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711653 | ||||||
| chr12:39711661
|
C | G | 9 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0188others(6): Show | 9 | HG00140.hp1 HG01884.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1412-5095C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711661 | ||||||
| chr12:39711668
|
C | CGT | 7 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0188others(4): Show | 7 | HG01884.hp2 HG02809.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1412-5088_1412-508 others(6): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711668 | ||||||
| chr12:39711671
|
G | A | 2 | a0001c0001t0001g0089a0001c0001t0001g0228 | 2 | HG00741.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1412-5085G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711671 | ||||||
| chr12:39711673
|
A | G | 7 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0188others(4): Show | 7 | HG01884.hp2 HG02809.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1412-5083A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711673 | ||||||
| chr12:39711675
|
G | A | 7 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0188others(4): Show | 7 | HG01884.hp2 HG02809.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1412-5081G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711675 | ||||||
| chr12:39711675
|
G | GTGTGTAT others(31): Show |
1 | a0001c0001t0001g0326 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1412-5066_1412-502 others(42): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711675 | |||||
| chr12:39711679
|
G | C | 2 | a0001c0001t0001g0211a0002c0002t0001g0119 | 2 | HG00140.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1412-5077G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711679 | ||||||
| chr12:39711683
|
G | A | 9 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0188others(6): Show | 9 | HG00140.hp1 HG01884.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1412-5073G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711683 | ||||||
| chr12:39711691
|
A | ATG | 6 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0001g0286others(3): Show | 6 | HG00438.hp1 HG00544.hp1 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.1412-5061_1412-506 others(6): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711691 | |||||
| chr12:39711691
|
ATG | A | 7 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0188others(4): Show | 7 | HG01884.hp2 HG02809.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1412-5061_1412-506 others(6): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711691 | |||||
| chr12:39711691
|
ATGTGTAT others(33): Show |
A | 19 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(16): Show | 19 | HG00738.hp1 HG01106.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.1412-5053_1412-501 others(44): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711691 | |||||
| chr12:39711697
|
A | ATG | 14 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0025others(11): Show | 16 | HG01070.hp1 HG01099.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.1412-5055_1412-505 others(6): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711697 | |||||
| chr12:39711699
|
GTGTATAC others(7): Show |
G | 189 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(186): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.1412-5053_1412-504 others(18): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711699 | |||||
| chr12:39711701
|
G | C | 7 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0188others(4): Show | 7 | HG01884.hp2 HG02809.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1412-5055G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711701 | ||||||
| chr12:39711705
|
A | G | 3 | a0001c0001t0001g0211a0001c0001t0001g0270a0002c0002t0001g0119 | 3 | HG00140.hp1 HG00609.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1412-5051A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711705 | ||||||
| chr12:39711708
|
CATGCATG others(15): Show |
C | 1 | a0001c0001t0001g0225 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1412-5047_1412-502 others(26): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711708 | ||||||
| chr12:39711709
|
A | G | 14 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0025others(11): Show | 16 | HG01070.hp1 HG01099.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.1412-5047A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711709 | ||||||
| chr12:39711711
|
G | GTGTA | 12 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0027others(9): Show | 14 | HG01099.hp1 HG01192.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.1412-5045_1412-504 others(8): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711711 | ||||||
| chr12:39711712
|
C | T | 23 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0025others(20): Show | 25 | HG00140.hp1 HG01070.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.1412-5044C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711712 | ||||||
| chr12:39711713
|
A | ATG | 7 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0188others(4): Show | 7 | HG01884.hp2 HG02809.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1412-5039_1412-503 others(6): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711713 | |||||
| chr12:39711713
|
A | G | 14 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0025others(11): Show | 16 | HG01070.hp1 HG01099.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.1412-5043A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711713 | ||||||
| chr12:39711721
|
G | A | 189 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(186): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.1412-5035G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711721 | ||||||
| chr12:39711722
|
C | T | 2 | a0001c0001t0001g0211a0002c0002t0001g0119 | 2 | HG00140.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1412-5034C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711722 | ||||||
| chr12:39711723
|
A | G | 2 | a0001c0001t0001g0211a0002c0002t0001g0119 | 2 | HG00140.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1412-5033A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711723 | ||||||
| chr12:39711724
|
C | T | 2 | a0001c0001t0001g0211a0002c0002t0001g0119 | 2 | HG00140.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1412-5032C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711724 | ||||||
| chr12:39711724
|
CATGCAT | C | 165 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(162): Show | 175 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1412-5031_1412-502 others(10): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711724 | ||||||
| chr12:39711724
|
CATGCATG others(1): Show |
C | 23 | a0001c0001t0001g0005a0001c0001t0001g0043a0001c0001t0001g0044others(20): Show | 24 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.1412-5031_1412-502 others(12): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711724 | ||||||
| chr12:39711727
|
G | A | 2 | a0001c0001t0001g0211a0002c0002t0001g0119 | 2 | HG00140.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1412-5029G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711727 | ||||||
| chr12:39711727
|
GCA | G | 7 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0188others(4): Show | 7 | HG01884.hp2 HG02809.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1412-5028_1412-502 others(6): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711727 | ||||||
| chr12:39711729
|
ATG | A | 13 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0025others(10): Show | 15 | HG01070.hp1 HG01192.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.1412-5021_1412-502 others(6): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711729 | |||||
| chr12:39711730
|
T | C | 2 | a0001c0001t0001g0211a0002c0002t0001g0119 | 2 | HG00140.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1412-5026T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711730 | ||||||
| chr12:39711731
|
G | A | 7 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0188others(4): Show | 7 | HG01884.hp2 HG02809.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1412-5025G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711731 | ||||||
| chr12:39711733
|
GTGTATGT others(21): Show |
G | 1 | a0001c0001t0001g0194 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1412-5019_1412-499 others(32): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711733 | |||||
| chr12:39711737
|
A | G | 23 | a0001c0001t0001g0005a0001c0001t0001g0043a0001c0001t0001g0044others(20): Show | 24 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.1412-5019A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711737 | ||||||
| chr12:39711745
|
A | G | 6 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0004g0059others(3): Show | 7 | HG01070.hp1 HG02074.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1412-5011A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711745 | ||||||
| chr12:39711747
|
A | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(189): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1412-5009A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711747 | ||||||
| chr12:39711749
|
ACATG | A | 12 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(9): Show | 12 | HG01884.hp2 HG02055.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1412-5002_1412-499 others(8): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711749 | |||||
| chr12:39711750
|
CATGCAT | C | 10 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(7): Show | 10 | HG00738.hp1 HG01106.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.1412-5005_1412-500 others(10): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711750 | ||||||
| chr12:39711755
|
A | G | 12 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(9): Show | 12 | HG01884.hp2 HG02055.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1412-5001A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711755 | ||||||
| chr12:39711761
|
A | G | 11 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(8): Show | 11 | HG00738.hp1 HG01106.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.1412-4995A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711761 | ||||||
| chr12:39711769
|
G | A | 27 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0038others(24): Show | 27 | HG00738.hp1 HG01106.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.1412-4987G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711769 | ||||||
| chr12:39711771
|
G | A | 206 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(203): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1412-4985G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711771 | ||||||
| chr12:39711771
|
G | GCACATGC others(57): Show |
1 | a0001c0001t0001g0305 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1412-4970_1412-496 others(68): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711771 | |||||
| chr12:39711771
|
G | GCACATGC others(17): Show |
62 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(59): Show | 66 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.1412-4963_1412-494 others(28): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711771 | |||||
| chr12:39711771
|
G | GCACATGC others(41): Show |
1 | a0001c0001t0001g0260 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1412-4940_1412-493 others(52): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711771 | |||||
| chr12:39711791
|
G | A | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1412-4965G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711791 | ||||||
| chr12:39711793
|
G | A | 3 | a0001c0007t0001g0024a0005c0003t0001g0034a0005c0003t0001g0035 | 3 | HG02486.hp2 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1412-4963G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711793 | ||||||
| chr12:39711795
|
A | G | 1 | a0001c0001t0001g0075 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1412-4961A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711795 | ||||||
| chr12:39711809
|
A | ATG | 31 | a0001c0001t0001g0003a0001c0001t0001g0075a0001c0001t0001g0179others(28): Show | 32 | HG00438.hp2 HG01884.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.1412-4941_1412-494 others(6): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711809 | |||||
| chr12:39711809
|
ATG | A | 25 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(22): Show | 26 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.1412-4941_1412-494 others(6): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711809 | |||||
| chr12:39711811
|
G | A | 2 | a0001c0001t0001g0025a0001c0001t0004g0059 | 2 | HG01070.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1412-4945G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711811 | ||||||
| chr12:39711814
|
TGTACACA others(47): Show |
T | 3 | a0001c0001t0001g0025a0001c0001t0004g0059a0001c0001t0006g0033 | 3 | HG00733.hp1 HG01070.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1412-4938_1412-488 others(58): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711814 | |||||
| chr12:39711829
|
GTA | G | 12 | a0001c0001t0001g0003a0001c0001t0001g0075a0001c0001t0001g0318others(9): Show | 13 | HG01884.hp1 HG02055.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1412-4923_1412-492 others(6): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711829 | |||||
| chr12:39711831
|
ATATG | A | 24 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(21): Show | 24 | HG00438.hp2 HG01884.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.1412-4923_1412-492 others(8): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711831 | |||||
| chr12:39711831
|
ATATGTG | A | 10 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(7): Show | 10 | HG00738.hp1 HG01106.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.1412-4923_1412-491 others(10): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711831 | |||||
| chr12:39711833
|
A | G | 1 | a0001c0001t0001g0012 | 2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1412-4923A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711833 | ||||||
| chr12:39711834
|
TGTGTGTA others(27): Show |
T | 1 | a0001c0001t0001g0012 | 2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1412-4919_1412-488 others(38): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711834 | |||||
| chr12:39711836
|
TGTGTATA others(25): Show |
T | 195 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(192): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.1412-4917_1412-488 others(36): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711836 | |||||
| chr12:39711838
|
T | TGTATACA others(23): Show |
2 | a0001c0001t0001g0271a0001c0001t0001g0309 | 2 | HG00609.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.1412-4876_1412-484 others(34): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711838 | |||||
| chr12:39711838
|
TGTATACA others(23): Show |
T | 10 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0029others(7): Show | 11 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1412-4876_1412-484 others(34): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711838 | |||||
| chr12:39711841
|
A | G | 54 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0037others(51): Show | 56 | HG00438.hp2 HG00673.hp2 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.1412-4915A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711841 | ||||||
| chr12:39711859
|
G | A | 36 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0038others(33): Show | 36 | HG00438.hp2 HG00738.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.1412-4897G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711859 | ||||||
| chr12:39711862
|
TATACAC | T | 24 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(21): Show | 24 | HG00738.hp1 HG01106.hp2 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.1412-4893_1412-488 others(10): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711862 | ||||||
| chr12:39711863
|
A | G | 24 | a0001c0001t0001g0003a0001c0001t0001g0028a0001c0001t0001g0075others(21): Show | 25 | HG00438.hp2 HG01169.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.1412-4893A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711863 | ||||||
| chr12:39711864
|
TACAC | T | 12 | a0001c0001t0001g0028a0001c0001t0001g0240a0001c0001t0001g0241others(9): Show | 12 | HG00438.hp2 HG01169.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1412-4891_1412-488 others(8): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711864 | ||||||
| chr12:39711868
|
C | CATGCATG others(11): Show |
11 | a0001c0001t0001g0003a0001c0001t0001g0318a0001c0001t0001g0326others(8): Show | 12 | HG01884.hp1 HG02055.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1412-4888_1412-488 others(22): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711868 | ||||||
| chr12:39711868
|
C | CATGCATG others(33): Show |
1 | a0001c0001t0001g0075 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1412-4888_1412-488 others(44): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711868 | ||||||
| chr12:39711871
|
A | G | 2 | a0001c0001t0001g0227a0001c0001t0001g0230 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1412-4885A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711871 | ||||||
| chr12:39711889
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1412-4867G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711889 | ||||||
| chr12:39711893
|
A | G | 231 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(228): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.1412-4863A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711893 | ||||||
| chr12:39711897
|
A | C | 2 | a0001c0001t0001g0227a0001c0001t0001g0230 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1412-4859A>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711897 | ||||||
| chr12:39711906
|
C | A | 220 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(217): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.1412-4850C>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711906 | ||||||
| chr12:39711927
|
CTATATGT others(3): Show |
C | 1 | a0001c0001t0001g0274 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1412-4826_1412-481 others(14): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711927 | |||||
| chr12:39711959
|
ATATC | A | 8 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(5): Show | 8 | HG01884.hp2 HG02055.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1412-4793_1412-479 others(8): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711959 | |||||
| chr12:39711960
|
T | A | 2 | a0003c0005t0001g0335a0003c0005t0001g0336 | 2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1412-4796T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39711960 | ||||||
| chr12:39711998
|
C | CTGTATAT others(25): Show |
3 | a0001c0001t0001g0144a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | HG03017.hp1 NA18939.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.1412-4713_1412-468 others(36): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39711998 | |||||
| chr12:39712017
|
TATGTATA others(5): Show |
T | 1 | a0001c0001t0001g0160 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1412-4726_1412-471 others(16): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712017 | |||||
| chr12:39712029
|
C | CATGTATA others(13): Show |
217 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(214): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1412-4714_1412-469 others(24): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712029 | |||||
| chr12:39712029
|
C | CATGTATA others(45): Show |
6 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(3): Show | 6 | HG01884.hp2 HG02055.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1412-4682_1412-468 others(56): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712029 | |||||
| chr12:39712031
|
T | TGTATATA others(13): Show |
2 | a0004c0004t0001g0130a0004c0004t0005g0135 | 2 | NA18989.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1412-4706_1412-470 others(24): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712031 | |||||
| chr12:39712047
|
T | G | 1 | a0001c0001t0001g0270 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1412-4709T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712047 | ||||||
| chr12:39712052
|
G | GTATATAT others(13): Show |
2 | a0001c0001t0001g0217a0001c0001t0001g0223 | 2 | NA18955.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1412-4695_1412-469 others(24): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712052 | |||||
| chr12:39712063
|
T | G | 7 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0029others(4): Show | 8 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1412-4693T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712063 | ||||||
| chr12:39712065
|
T | TATATATA others(5): Show |
1 | a0001c0001t0001g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1412-4683_1412-468 others(16): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712065 | |||||
| chr12:39712093
|
CATATATA others(5): Show |
C | 1 | a0001c0001t0001g0258 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1412-4636_1412-462 others(16): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712093 | |||||
| chr12:39712114
|
C | A | 1 | a0008c0009t0001g0226 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1412-4642C>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712114 | ||||||
| chr12:39712119
|
T | TGTAC | 9 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0156others(6): Show | 9 | HG00642.hp1 HG01123.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.1412-4637_1412-463 others(8): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712119 | ||||||
| chr12:39712125
|
C | CATACAT | 9 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0156others(6): Show | 9 | HG00642.hp1 HG01123.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.1412-4631_1412-463 others(10): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712125 | ||||||
| chr12:39712126
|
C | G | 36 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0043others(33): Show | 37 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.1412-4630C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712126 | ||||||
| chr12:39712128
|
G | A | 11 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0156others(8): Show | 11 | HG00642.hp1 HG01123.hp2 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.1412-4628G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712128 | ||||||
| chr12:39712129
|
T | TAC | 9 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0156others(6): Show | 9 | HG00642.hp1 HG01123.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.1412-4626_1412-462 others(6): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712129 | |||||
| chr12:39712135
|
C | T | 9 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0156others(6): Show | 9 | HG00642.hp1 HG01123.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.1412-4621C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712135 | ||||||
| chr12:39712138
|
A | G | 9 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0156others(6): Show | 9 | HG00642.hp1 HG01123.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.1412-4618A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712138 | ||||||
| chr12:39712142
|
A | G | 6 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(3): Show | 6 | HG01884.hp2 HG02055.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1412-4614A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712142 | ||||||
| chr12:39712144
|
A | G | 9 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0156others(6): Show | 9 | HG00642.hp1 HG01123.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.1412-4612A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712144 | ||||||
| chr12:39712145
|
C | T | 9 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0156others(6): Show | 9 | HG00642.hp1 HG01123.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.1412-4611C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712145 | ||||||
| chr12:39712148
|
C | A | 9 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0156others(6): Show | 9 | HG00642.hp1 HG01123.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.1412-4608C>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712148 | ||||||
| chr12:39712153
|
C | CATGTATA others(21): Show |
1 | a0001c0001t0001g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1412-4589_1412-458 others(32): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712153 | |||||
| chr12:39712153
|
C | CATGTATA others(21): Show |
185 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(182): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.1412-4588_1412-456 others(32): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712153 | |||||
| chr12:39712153
|
C | CATGTATA others(49): Show |
4 | a0002c0002t0001g0093a0002c0002t0001g0097a0002c0002t0001g0104others(1): Show | 4 | HG01934.hp2 HG02683.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.1412-4561_1412-456 others(60): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712153 | |||||
| chr12:39712153
|
C | CATGTATG others(21): Show |
1 | a0001c0007t0001g0024 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1412-4597_1412-459 others(32): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712153 | |||||
| chr12:39712153
|
C | CCTGT | 9 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0156others(6): Show | 9 | HG00642.hp1 HG01123.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.1412-4603_1412-460 others(8): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712153 | ||||||
| chr12:39712154
|
A | ATGTATAT others(17): Show |
7 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0029others(4): Show | 8 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1412-4596_1412-457 others(28): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712154 | |||||
| chr12:39712157
|
T | G | 2 | a0001c0001t0001g0331a0001c0001t0001g0332 | 2 | HG02145.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1412-4599T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712157 | ||||||
| chr12:39712162
|
G | GTACATGT others(75): Show |
23 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0043others(20): Show | 24 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.1412-4561_1412-456 others(86): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712162 | |||||
| chr12:39712162
|
G | GTACATGT others(103): Show |
1 | a0001c0001t0001g0052 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1412-4561_1412-456 others(114): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712162 | |||||
| chr12:39712169
|
T | TATATATA others(49): Show |
1 | a0001c0001t0001g0181 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1412-4561_1412-456 others(60): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712169 | |||||
| chr12:39712199
|
T | C | 1 | a0001c0001t0001g0287 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1412-4557T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712199 | ||||||
| chr12:39712221
|
T | A | 1 | a0001c0001t0001g0040 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1412-4535T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712221 | ||||||
| chr12:39712234
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1412-4522A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712234 | ||||||
| chr12:39712235
|
T | C | 7 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0029others(4): Show | 8 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1412-4521T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712235 | ||||||
| chr12:39712285
|
C | A | 220 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(217): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.1412-4471C>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712285 | ||||||
| chr12:39712323
|
CAT | C | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1412-4430_1412-442 others(6): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712323 | |||||
| chr12:39712340
|
G | T | 4 | a0002c0002t0001g0127a0002c0002t0001g0129a0002c0002t0001g0137others(1): Show | 4 | HG00642.hp2 HG00741.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.1412-4416G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712340 | ||||||
| chr12:39712344
|
T | G | 4 | a0001c0007t0001g0024a0002c0002t0001g0098a0005c0003t0001g0034others(1): Show | 4 | HG02486.hp2 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1412-4412T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712344 | ||||||
| chr12:39712349
|
TATAC | T | 224 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.1412-4391_1412-438 others(8): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712349 | |||||
| chr12:39712357
|
C | CATATGTA others(31): Show |
1 | a0005c0003t0001g0035 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1412-4396_1412-439 others(42): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712357 | |||||
| chr12:39712361
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1412-4395C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712361 | ||||||
| chr12:39712365
|
C | T | 7 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0029others(4): Show | 8 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1412-4391C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712365 | ||||||
| chr12:39712366
|
A | G | 7 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0029others(4): Show | 8 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1412-4390A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712366 | ||||||
| chr12:39712368
|
A | ATATATAC others(1): Show |
7 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0029others(4): Show | 8 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1412-4387_1412-438 others(12): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712368 | |||||
| chr12:39712380
|
C | G | 7 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0029others(4): Show | 8 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1412-4376C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712380 | ||||||
| chr12:39712380
|
C | T | 3 | a0001c0001t0001g0188a0001c0001t0001g0190a0001c0001t0001g0212 | 3 | NA18940.hp2 NA18995.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1412-4376C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712380 | ||||||
| chr12:39712382
|
A | ATG | 7 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0029others(4): Show | 8 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1412-4373_1412-437 others(6): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712382 | |||||
| chr12:39712382
|
A | G | 225 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(222): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.1412-4374A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712382 | ||||||
| chr12:39712388
|
A | G | 2 | a0005c0003t0001g0034a0005c0003t0001g0035 | 2 | HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1412-4368A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712388 | ||||||
| chr12:39712389
|
T | TACCTGTA others(23): Show |
2 | a0003c0005t0001g0335a0003c0005t0001g0336 | 2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1412-4365_1412-433 others(34): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712389 | |||||
| chr12:39712392
|
C | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0029others(4): Show | 8 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1412-4364C>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712392 | ||||||
| chr12:39712393
|
T | TAC | 7 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0029others(4): Show | 8 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1412-4363_1412-436 others(6): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712393 | ||||||
| chr12:39712397
|
T | TATACATA others(1): Show |
7 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0029others(4): Show | 8 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1412-4359_1412-435 others(12): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712397 | ||||||
| chr12:39712397
|
T | TGTATATA others(19): Show |
2 | a0001c0001t0001g0046a0001c0001t0001g0203 | 2 | HG03927.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1412-4338_1412-431 others(30): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712397 | |||||
| chr12:39712397
|
TGTATATA others(19): Show |
T | 1 | a0011c0011t0001g0073 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1412-4338_1412-431 others(30): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712397 | |||||
| chr12:39712412
|
G | A | 13 | a0001c0001t0001g0003a0001c0001t0001g0318a0001c0001t0001g0322others(10): Show | 14 | HG01884.hp1 HG02055.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1412-4344G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712412 | ||||||
| chr12:39712419
|
CATACGTA others(33): Show |
C | 1 | a0001c0007t0001g0024 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1412-4328_1412-428 others(44): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712419 | |||||
| chr12:39712423
|
C | A | 1 | a0001c0001t0001g0071 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1412-4333C>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712423 | ||||||
| chr12:39712423
|
C | G | 1 | a0001c0001t0001g0240 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1412-4333C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712423 | ||||||
| chr12:39712438
|
GTATATGT others(11): Show |
G | 3 | a0001c0001t0001g0005a0001c0001t0001g0076a0001c0001t0001g0077 | 4 | HG00639.hp1 HG01074.hp2 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.1412-4312_1412-429 others(22): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712438 | |||||
| chr12:39712454
|
GTA | G | 228 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(225): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.1412-4295_1412-429 others(6): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712454 | |||||
| chr12:39712463
|
C | A | 6 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0001g0286others(3): Show | 6 | HG00438.hp1 HG00544.hp1 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.1412-4293C>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712463 | ||||||
| chr12:39712469
|
T | C | 21 | a0001c0001t0001g0003a0001c0001t0001g0075a0001c0001t0001g0227others(18): Show | 22 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.1412-4287T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712469 | ||||||
| chr12:39712484
|
G | C | 22 | a0001c0001t0001g0003a0001c0001t0001g0075a0001c0001t0001g0227others(19): Show | 23 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.1412-4272G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712484 | ||||||
| chr12:39712497
|
G | A | 14 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0150others(11): Show | 18 | HG00597.hp2 HG03831.hp2 NA18941.hp2 others(15): Show |
intron_variant | MODIFIER | c.1412-4259G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712497 | ||||||
| chr12:39712505
|
G | A | 1 | a0001c0001t0003g0078 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1412-4251G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712505 | ||||||
| chr12:39712547
|
C | T | 231 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(228): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.1412-4209C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712547 | ||||||
| chr12:39712549
|
C | T | 1 | a0010c0010t0001g0096 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1412-4207C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712549 | ||||||
| chr12:39712558
|
T | TGTATATA others(9): Show |
2 | a0005c0003t0001g0034a0005c0003t0001g0035 | 2 | HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1412-4190_1412-417 others(20): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712558 | |||||
| chr12:39712558
|
TGTATATA others(1): Show |
T | 7 | a0001c0001t0001g0028a0001c0001t0001g0152a0001c0001t0001g0159others(4): Show | 7 | HG01109.hp2 HG01169.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.1412-4182_1412-417 others(12): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712558 | |||||
| chr12:39712582
|
T | C | 2 | a0005c0003t0001g0034a0005c0003t0001g0035 | 2 | HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1412-4174T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712582 | ||||||
| chr12:39712599
|
A | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0029others(7): Show | 11 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1412-4157A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712599 | ||||||
| chr12:39712607
|
GTATA | G | 4 | a0001c0001t0001g0001a0001c0001t0001g0150a0001c0001t0001g0191others(1): Show | 7 | NA18951.hp2 NA18957.hp2 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.1412-4144_1412-414 others(8): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712607 | |||||
| chr12:39712638
|
C | T | 1 | a0001c0007t0001g0024 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1412-4118C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712638 | ||||||
| chr12:39712653
|
A | G | 1 | a0001c0001t0006g0033 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1412-4103A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712653 | ||||||
| chr12:39712670
|
T | TGTGTATA others(19): Show |
1 | a0001c0001t0001g0281 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1412-4068_1412-404 others(30): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712670 | |||||
| chr12:39712688
|
TACGTATA others(19): Show |
T | 221 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(218): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.1412-4037_1412-401 others(30): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712688 | |||||
| chr12:39712714
|
G | T | 83 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(80): Show | 89 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.1412-4042G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712714 | ||||||
| chr12:39712719
|
A | G | 35 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0027others(32): Show | 37 | HG00733.hp1 HG01169.hp1 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.1412-4037A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712719 | ||||||
| chr12:39712722
|
CGTGTATA others(17): Show |
C | 35 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0027others(32): Show | 37 | HG00733.hp1 HG01169.hp1 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.1412-4033_1412-401 others(28): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712722 | ||||||
| chr12:39712750
|
C | T | 35 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0027others(32): Show | 37 | HG00733.hp1 HG01169.hp1 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.1412-4006C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712750 | ||||||
| chr12:39712756
|
T | C | 1 | a0001c0001t0001g0329 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1412-4000T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712756 | ||||||
| chr12:39712809
|
T | A | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1412-3947T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712809 | ||||||
| chr12:39712816
|
C | CAT | 231 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(228): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.1412-3939_1412-393 others(6): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712816 | |||||
| chr12:39712819
|
G | A | 1 | a0001c0001t0006g0033 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1412-3937G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712819 | ||||||
| chr12:39712830
|
T | A | 6 | a0001c0001t0001g0014a0001c0001t0001g0293a0001c0001t0001g0294others(3): Show | 7 | HG00733.hp2 HG01069.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1412-3926T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712830 | ||||||
| chr12:39712834
|
C | CAT | 8 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(5): Show | 8 | HG01884.hp2 HG02055.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1412-3918_1412-391 others(6): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712834 | |||||
| chr12:39712856
|
T | TGTATATA others(3): Show |
1 | a0001c0001t0001g0241 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1412-3880_1412-387 others(14): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712856 | |||||
| chr12:39712856
|
TGTATATA others(3): Show |
T | 217 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(214): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1412-3880_1412-387 others(14): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712856 | |||||
| chr12:39712864
|
CACGTATA others(35): Show |
C | 1 | a0007c0012t0001g0171 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1412-3880_1412-383 others(46): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712864 | |||||
| chr12:39712874
|
CACGTATA others(5): Show |
C | 2 | a0003c0005t0001g0335a0003c0005t0001g0336 | 2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1412-3880_1412-386 others(16): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712874 | |||||
| chr12:39712895
|
A | G | 1 | a0004c0004t0001g0130 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1412-3861A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712895 | ||||||
| chr12:39712906
|
T | TACACGTA others(5): Show |
2 | a0001c0001t0001g0015a0001c0001t0001g0307 | 3 | NA18998.hp1 NA19060.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1412-3848_1412-384 others(16): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712906 | |||||
| chr12:39712921
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0307 | 3 | NA18998.hp1 NA19060.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1412-3835G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712921 | ||||||
| chr12:39712940
|
CGT | C | 2 | a0001c0001t0001g0015a0001c0001t0001g0307 | 3 | NA18998.hp1 NA19060.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1412-3813_1412-381 others(6): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712940 | |||||
| chr12:39712955
|
A | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0307 | 3 | NA18998.hp1 NA19060.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1412-3801A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712955 | ||||||
| chr12:39712958
|
CATATACG others(23): Show |
C | 322 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(319): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.1412-3721_1412-369 others(34): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712958 | |||||
| chr12:39712958
|
CATATACG others(53): Show |
C | 8 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0029others(5): Show | 9 | HG01192.hp2 HG01255.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1412-3751_1412-369 others(64): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712958 | |||||
| chr12:39712971
|
A | ATACG | 2 | a0001c0001t0001g0015a0001c0001t0001g0307 | 3 | NA18998.hp1 NA19060.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1412-3784_1412-378 others(8): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712971 | |||||
| chr12:39712975
|
ATATATAC others(35): Show |
A | 1 | a0001c0001t0001g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1412-3773_1412-373 others(46): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39712975 | |||||
| chr12:39712980
|
T | C | 2 | a0001c0001t0001g0015a0001c0001t0001g0307 | 3 | NA18998.hp1 NA19060.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1412-3776T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712980 | ||||||
| chr12:39712982
|
C | T | 2 | a0001c0001t0001g0015a0001c0001t0001g0307 | 3 | NA18998.hp1 NA19060.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1412-3774C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712982 | ||||||
| chr12:39712985
|
G | A | 4 | a0001c0001t0001g0015a0001c0001t0001g0307a0003c0005t0001g0335others(1): Show | 5 | NA18522.hp2 NA18998.hp1 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.1412-3771G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712985 | ||||||
| chr12:39712988
|
T | C | 4 | a0001c0001t0001g0015a0001c0001t0001g0307a0003c0005t0001g0335others(1): Show | 5 | NA18522.hp2 NA18998.hp1 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.1412-3768T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39712988 | ||||||
| chr12:39713012
|
CATGTGTA others(25): Show |
C | 1 | a0001c0001t0001g0241 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1412-3743_1412-371 others(36): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713012 | ||||||
| chr12:39713014
|
T | C | 1 | a0001c0001t0001g0304 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1412-3742T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713014 | ||||||
| chr12:39713025
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1412-3731G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713025 | ||||||
| chr12:39713032
|
T | C | 2 | a0001c0001t0001g0314a0001c0001t0001g0315 | 2 | HG02683.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1412-3724T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713032 | ||||||
| chr12:39713059
|
A | G | 1 | a0001c0001t0001g0240 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1412-3697A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713059 | ||||||
| chr12:39713073
|
G | T | 2 | a0001c0001t0001g0305a0001c0001t0001g0306 | 2 | HG02132.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1412-3683G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713073 | ||||||
| chr12:39713080
|
C | T | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1412-3676C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713080 | ||||||
| chr12:39713107
|
G | A | 25 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0043others(22): Show | 26 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.1412-3649G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713107 | ||||||
| chr12:39713144
|
G | T | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1412-3612G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713144 | ||||||
| chr12:39713151
|
G | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(5): Show | 9 | HG01169.hp1 HG01192.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1412-3605G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713151 | ||||||
| chr12:39713170
|
T | C | 1 | a0001c0001t0001g0022 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1412-3586T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713170 | ||||||
| chr12:39713206
|
CAT | C | 10 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0029others(7): Show | 11 | HG00408.hp2 HG01192.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1412-3545_1412-354 others(6): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39713206 | |||||
| chr12:39713208
|
T | C | 3 | a0001c0001t0001g0070a0009c0008t0001g0068a0011c0011t0001g0073 | 3 | HG01175.hp1 HG02976.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1412-3548T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713208 | ||||||
| chr12:39713221
|
T | TACACATA others(19): Show |
1 | a0001c0001t0001g0241 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1412-3514_1412-351 others(30): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39713221 | |||||
| chr12:39713227
|
T | TATACGTG others(19): Show |
45 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0245others(42): Show | 48 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.1412-3457_1412-343 others(30): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39713227 | |||||
| chr12:39713227
|
T | TATACGTG others(45): Show |
11 | a0001c0001t0001g0026a0001c0001t0001g0244a0001c0001t0001g0251others(8): Show | 11 | HG00438.hp2 HG00673.hp2 HG00733.hp2 others(8): Show |
intron_variant | MODIFIER | c.1412-3483_1412-343 others(56): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39713227 | |||||
| chr12:39713227
|
TATACGTG others(19): Show |
T | 21 | a0001c0001t0001g0003a0001c0001t0001g0075a0001c0001t0001g0227others(18): Show | 22 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.1412-3457_1412-343 others(30): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39713227 | |||||
| chr12:39713227
|
TATACGTG others(45): Show |
T | 8 | a0001c0001t0001g0015a0001c0001t0001g0302a0001c0001t0001g0303others(5): Show | 9 | HG00621.hp2 HG01496.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.1412-3483_1412-343 others(56): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39713227 | |||||
| chr12:39713238
|
A | ATATGTGT others(41): Show |
1 | a0001c0001t0001g0277 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1412-3514_1412-346 others(52): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39713238 | |||||
| chr12:39713239
|
T | G | 5 | a0001c0001t0001g0028a0001c0001t0006g0033a0001c0007t0001g0024others(2): Show | 5 | HG00733.hp1 HG01169.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1412-3517T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713239 | ||||||
| chr12:39713243
|
T | G | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1412-3513T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713243 | ||||||
| chr12:39713245
|
TACACACA others(21): Show |
T | 1 | a0001c0001t0001g0240 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1412-3503_1412-347 others(32): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39713245 | |||||
| chr12:39713247
|
C | T | 222 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(219): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.1412-3509C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713247 | ||||||
| chr12:39713249
|
CACACATA others(25): Show |
C | 1 | a0001c0001t0001g0148 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1412-3504_1412-347 others(36): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39713249 | |||||
| chr12:39713249
|
CACACATA others(51): Show |
C | 2 | a0001c0001t0001g0197a0001c0001t0004g0060 | 2 | HG01515.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1412-3504_1412-344 others(62): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39713249 | |||||
| chr12:39713253
|
C | CGTGTATA others(15): Show |
6 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0029others(3): Show | 7 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1412-3503_1412-350 others(26): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713253 | ||||||
| chr12:39713253
|
C | T | 223 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(220): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.1412-3503C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713253 | ||||||
| chr12:39713257
|
C | G | 1 | a0001c0001t0001g0023 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1412-3499C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713257 | ||||||
| chr12:39713269
|
T | G | 21 | a0001c0001t0001g0003a0001c0001t0001g0075a0001c0001t0001g0227others(18): Show | 22 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.1412-3487T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713269 | ||||||
| chr12:39713273
|
C | T | 28 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0027others(25): Show | 30 | HG01192.hp2 HG01884.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1412-3483C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713273 | ||||||
| chr12:39713275
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1412-3481C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713275 | ||||||
| chr12:39713275
|
CACACAT | C | 11 | a0001c0001t0001g0070a0001c0001t0001g0089a0001c0001t0001g0178others(8): Show | 11 | HG00741.hp2 HG01175.hp1 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.1412-3478_1412-347 others(10): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39713275 | |||||
| chr12:39713275
|
CACACATA others(25): Show |
C | 203 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(200): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.1412-3478_1412-344 others(36): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39713275 | |||||
| chr12:39713277
|
CACAT | C | 4 | a0001c0001t0001g0028a0001c0001t0006g0033a0001c0007t0001g0024others(1): Show | 4 | HG00733.hp1 HG01169.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1412-3476_1412-347 others(8): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39713277 | |||||
| chr12:39713277
|
CACATACG others(23): Show |
C | 1 | a0005c0003t0001g0034 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1412-3476_1412-344 others(34): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39713277 | |||||
| chr12:39713277
|
CACATACG others(27): Show |
C | 1 | a0002c0002t0001g0121 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1412-3478_1412-344 others(38): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713277 | ||||||
| chr12:39713279
|
C | T | 31 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0027others(28): Show | 33 | HG01192.hp2 HG01884.hp1 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.1412-3477C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713279 | ||||||
| chr12:39713299
|
C | T | 22 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(19): Show | 23 | HG00733.hp1 HG00741.hp2 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.1412-3457C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713299 | ||||||
| chr12:39713305
|
C | CATACGTG others(45): Show |
4 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0001g0286others(1): Show | 4 | HG00438.hp1 HG03831.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1412-3432_1412-343 others(56): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39713305 | |||||
| chr12:39713305
|
C | CATACGTG others(45): Show |
1 | a0001c0001t0001g0248 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1412-3432_1412-343 others(56): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39713305 | |||||
| chr12:39713305
|
C | T | 24 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(21): Show | 25 | HG00733.hp1 HG00741.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.1412-3451C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713305 | ||||||
| chr12:39713314
|
A | G | 1 | a0002c0002t0001g0121 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1412-3442A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713314 | ||||||
| chr12:39713325
|
T | C | 7 | a0001c0001t0001g0018a0001c0001t0001g0026a0001c0001t0001g0251others(4): Show | 7 | HG01255.hp2 HG03130.hp1 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.1412-3431T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713325 | ||||||
| chr12:39713331
|
T | C | 2 | a0001c0001t0001g0282a0001c0001t0001g0283 | 2 | HG01358.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1412-3425T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713331 | ||||||
| chr12:39713353
|
CACATATA others(75): Show |
C | 1 | a0011c0011t0001g0073 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1412-3394_1412-331 others(86): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39713353 | |||||
| chr12:39713355
|
CAT | C | 17 | a0001c0001t0001g0003a0001c0001t0001g0318a0001c0001t0001g0322others(14): Show | 18 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1412-3397_1412-339 others(6): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39713355 | |||||
| chr12:39713361
|
C | CGTGTATA others(3): Show |
9 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(6): Show | 10 | HG00733.hp1 HG01169.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.1412-3388_1412-338 others(14): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39713361 | |||||
| chr12:39713368
|
ACACATAT others(7): Show |
A | 1 | a0002c0002t0001g0103 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1412-3387_1412-337 others(18): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713368 | ||||||
| chr12:39713378
|
A | G | 9 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(6): Show | 10 | HG00733.hp1 HG01169.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.1412-3378A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713378 | ||||||
| chr12:39713380
|
A | G | 9 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(6): Show | 10 | HG00733.hp1 HG01169.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.1412-3376A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713380 | ||||||
| chr12:39713382
|
G | A | 9 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(6): Show | 10 | HG00733.hp1 HG01169.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.1412-3374G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713382 | ||||||
| chr12:39713386
|
G | A | 9 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(6): Show | 10 | HG00733.hp1 HG01169.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.1412-3370G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713386 | ||||||
| chr12:39713390
|
G | A | 1 | a0002c0002t0001g0103 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1412-3366G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713390 | ||||||
| chr12:39713393
|
G | C | 1 | a0002c0002t0001g0103 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1412-3363G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713393 | ||||||
| chr12:39713393
|
G | T | 9 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(6): Show | 10 | HG00733.hp1 HG01169.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.1412-3363G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713393 | ||||||
| chr12:39713393
|
GACACATA others(35): Show |
G | 221 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(218): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.1412-3359_1412-331 others(46): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39713393 | |||||
| chr12:39713397
|
C | T | 1 | a0002c0002t0001g0103 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1412-3359C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713397 | ||||||
| chr12:39713401
|
C | T | 9 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(6): Show | 10 | HG00733.hp1 HG01169.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.1412-3355C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713401 | ||||||
| chr12:39713402
|
G | A | 9 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(6): Show | 10 | HG00733.hp1 HG01169.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.1412-3354G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713402 | ||||||
| chr12:39713403
|
T | C | 9 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(6): Show | 10 | HG00733.hp1 HG01169.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.1412-3353T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713403 | ||||||
| chr12:39713404
|
A | G | 9 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(6): Show | 10 | HG00733.hp1 HG01169.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.1412-3352A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713404 | ||||||
| chr12:39713413
|
CAT | C | 6 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0295others(3): Show | 6 | NA18939.hp1 NA18950.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.1412-3339_1412-333 others(6): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39713413 | |||||
| chr12:39713428
|
A | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(7): Show | 11 | HG00733.hp1 HG01169.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.1412-3328A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713428 | ||||||
| chr12:39713430
|
A | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(7): Show | 11 | HG00733.hp1 HG01169.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.1412-3326A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713430 | ||||||
| chr12:39713434
|
G | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(7): Show | 11 | HG00733.hp1 HG01169.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.1412-3322G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713434 | ||||||
| chr12:39713435
|
T | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(7): Show | 11 | HG00733.hp1 HG01169.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.1412-3321T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713435 | ||||||
| chr12:39713460
|
T | G | 1 | a0001c0001t0001g0236 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1412-3296T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713460 | ||||||
| chr12:39713497
|
CAT | C | 3 | a0001c0007t0001g0024a0005c0003t0001g0034a0005c0003t0001g0035 | 3 | HG02486.hp2 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1412-3257_1412-325 others(6): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39713497 | |||||
| chr12:39713505
|
TGTATACA others(29): Show |
T | 1 | a0001c0001t0001g0193 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1412-3224_1412-318 others(40): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39713505 | |||||
| chr12:39713519
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1412-3237C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713519 | ||||||
| chr12:39713531
|
C | T | 1 | a0001c0007t0001g0024 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1412-3225C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713531 | ||||||
| chr12:39713532
|
A | G | 12 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(9): Show | 13 | HG00733.hp1 HG01169.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.1412-3224A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713532 | ||||||
| chr12:39713538
|
A | G | 1 | a0001c0007t0001g0024 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1412-3218A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713538 | ||||||
| chr12:39713543
|
T | A | 1 | a0001c0001t0001g0216 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1412-3213T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713543 | ||||||
| chr12:39713559
|
C | G | 1 | a0001c0001t0001g0067 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1412-3197C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713559 | ||||||
| chr12:39713567
|
C | T | 3 | a0001c0001t0001g0330a0001c0001t0001g0331a0001c0001t0001g0332 | 3 | HG02145.hp2 HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1412-3189C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713567 | ||||||
| chr12:39713568
|
G | A | 1 | a0001c0001t0001g0334 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1412-3188G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713568 | ||||||
| chr12:39713588
|
G | T | 1 | a0001c0001t0001g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1412-3168G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713588 | ||||||
| chr12:39713616
|
A | G | 6 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(3): Show | 6 | HG01884.hp2 HG02055.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1412-3140A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713616 | ||||||
| chr12:39713619
|
C | G | 2 | a0003c0005t0001g0335a0003c0005t0001g0336 | 2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1412-3137C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713619 | ||||||
| chr12:39713619
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1412-3137C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713619 | ||||||
| chr12:39713631
|
G | A | 1 | a0001c0001t0001g0229 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1412-3125G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713631 | ||||||
| chr12:39713647
|
A | ACCTGTAT others(27): Show |
1 | a0001c0001t0001g0053 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1412-3083_1412-305 others(38): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39713647 | |||||
| chr12:39713673
|
GTATGTAT others(27): Show |
G | 7 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0029others(4): Show | 8 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1412-3049_1412-301 others(38): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39713673 | |||||
| chr12:39713695
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1412-3061G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713695 | ||||||
| chr12:39713697
|
A | G | 1 | a0001c0001t0001g0272 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1412-3059A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713697 | ||||||
| chr12:39713716
|
C | T | 22 | a0001c0001t0001g0003a0001c0001t0001g0075a0001c0001t0001g0227others(19): Show | 23 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.1412-3040C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713716 | ||||||
| chr12:39713719
|
G | C | 1 | a0001c0001t0001g0113 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1412-3037G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713719 | ||||||
| chr12:39713729
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1412-3027G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713729 | ||||||
| chr12:39713749
|
A | G | 1 | a0001c0001t0001g0009 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1412-3007A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713749 | ||||||
| chr12:39713750
|
C | T | 1 | a0002c0002t0001g0098 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1412-3006C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713750 | ||||||
| chr12:39713791
|
AGATG | A | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0146 | 3 | HG01358.hp1 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1412-2964_1412-296 others(8): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713791 | ||||||
| chr12:39713795
|
G | A | 229 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(226): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1412-2961G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713795 | ||||||
| chr12:39713797
|
A | G | 6 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(3): Show | 6 | HG01884.hp2 HG02055.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1412-2959A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713797 | ||||||
| chr12:39713803
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1412-2953G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713803 | ||||||
| chr12:39713838
|
CGT | C | 11 | a0001c0001t0001g0011a0001c0001t0001g0149a0001c0001t0001g0160others(8): Show | 12 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1412-2917_1412-291 others(6): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713838 | ||||||
| chr12:39713839
|
G | T | 163 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(160): Show | 173 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.1412-2917G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713839 | ||||||
| chr12:39713880
|
C | T | 1 | a0001c0001t0001g0329 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1412-2876C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713880 | ||||||
| chr12:39713899
|
A | G | 1 | a0001c0001t0001g0051 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1412-2857A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713899 | ||||||
| chr12:39713903
|
A | C | 220 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(217): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.1412-2853A>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713903 | ||||||
| chr12:39713929
|
T | TTATGTGC others(29): Show |
3 | a0001c0001t0001g0193a0001c0001t0001g0213a0001c0001t0001g0214 | 3 | HG02071.hp1 NA18981.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1412-2813_1412-277 others(40): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39713929 | |||||
| chr12:39713937
|
A | G | 13 | a0001c0001t0001g0003a0001c0001t0001g0318a0001c0001t0001g0322others(10): Show | 14 | HG01884.hp1 HG02055.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1412-2819A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713937 | ||||||
| chr12:39713939
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1412-2817A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713939 | ||||||
| chr12:39713948
|
T | C | 1 | a0001c0001t0006g0033 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1412-2808T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713948 | ||||||
| chr12:39713978
|
C | T | 1 | a0001c0001t0001g0233 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1412-2778C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713978 | ||||||
| chr12:39713987
|
A | G | 1 | a0001c0001t0001g0240 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1412-2769A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713987 | ||||||
| chr12:39713996
|
T | G | 1 | a0001c0001t0001g0240 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1412-2760T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39713996 | ||||||
| chr12:39714015
|
G | A | 1 | a0001c0001t0001g0268 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1412-2741G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714015 | ||||||
| chr12:39714027
|
A | T | 7 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0029others(4): Show | 8 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1412-2729A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714027 | ||||||
| chr12:39714032
|
T | TACATGTA others(5): Show |
1 | a0001c0001t0001g0114 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1412-2709_1412-269 others(16): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39714032 | |||||
| chr12:39714051
|
A | G | 1 | a0001c0001t0001g0040 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1412-2705A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714051 | ||||||
| chr12:39714059
|
G | A | 11 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(8): Show | 11 | HG00738.hp1 HG01106.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.1412-2697G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714059 | ||||||
| chr12:39714062
|
T | C | 11 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(8): Show | 11 | HG00738.hp1 HG01106.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.1412-2694T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714062 | ||||||
| chr12:39714073
|
G | T | 2 | a0001c0001t0001g0253a0001c0001t0001g0279 | 2 | NA18959.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1412-2683G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714073 | ||||||
| chr12:39714080
|
TACAC | T | 220 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(217): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.1412-2674_1412-267 others(8): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39714080 | |||||
| chr12:39714081
|
A | ATATGTAC others(87): Show |
11 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(8): Show | 12 | HG01169.hp1 HG01192.hp2 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.1412-2675_1412-267 others(98): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714081 | ||||||
| chr12:39714081
|
A | ATATGTAC others(87): Show |
1 | a0001c0001t0006g0033 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1412-2675_1412-267 others(98): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714081 | ||||||
| chr12:39714082
|
C | T | 12 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(9): Show | 13 | HG00733.hp1 HG01169.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.1412-2674C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714082 | ||||||
| chr12:39714088
|
T | C | 12 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(9): Show | 13 | HG00733.hp1 HG01169.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.1412-2668T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714088 | ||||||
| chr12:39714089
|
A | G | 12 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(9): Show | 13 | HG00733.hp1 HG01169.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.1412-2667A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714089 | ||||||
| chr12:39714091
|
G | A | 12 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(9): Show | 13 | HG00733.hp1 HG01169.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.1412-2665G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714091 | ||||||
| chr12:39714094
|
C | CATGTATA others(43): Show |
1 | a0002c0002t0001g0313 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1412-2651_1412-260 others(54): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39714094 | |||||
| chr12:39714094
|
C | CATGTATA others(93): Show |
192 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(189): Show | 202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.1412-2602_1412-260 others(104): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39714094 | |||||
| chr12:39714094
|
C | CATGTATA others(93): Show |
1 | a0001c0001t0001g0162 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1412-2602_1412-260 others(104): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39714094 | |||||
| chr12:39714094
|
C | CATGTATA others(92): Show |
2 | a0001c0001t0001g0058a0001c0001t0001g0062 | 2 | HG01346.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.1412-2602_1412-260 others(103): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39714094 | |||||
| chr12:39714094
|
C | CATGTATA others(93): Show |
3 | a0001c0007t0001g0024a0005c0003t0001g0034a0005c0003t0001g0035 | 3 | HG02486.hp2 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1412-2644_1412-264 others(104): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39714094 | |||||
| chr12:39714094
|
C | T | 12 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(9): Show | 13 | HG00733.hp1 HG01169.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.1412-2662C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714094 | ||||||
| chr12:39714126
|
T | TATATGTA others(93): Show |
4 | a0001c0001t0001g0010a0001c0001t0001g0174a0001c0001t0001g0181others(1): Show | 5 | NA18939.hp2 NA18962.hp2 NA18991.hp1 others(2): Show |
intron_variant | MODIFIER | c.1412-2602_1412-260 others(104): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39714126 | |||||
| chr12:39714141
|
A | ATATATGT others(119): Show |
3 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0208 | 3 | HG00280.hp2 HG03239.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1412-2602_1412-260 others(130): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39714141 | |||||
| chr12:39714145
|
A | ATGTATAT others(19): Show |
8 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(5): Show | 9 | HG01169.hp1 HG01192.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1412-2586_1412-258 others(30): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39714145 | |||||
| chr12:39714149
|
A | ATATACGT others(93): Show |
3 | a0001c0001t0004g0055a0001c0001t0004g0059a0001c0001t0004g0060 | 3 | HG00099.hp1 HG01070.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1412-2602_1412-260 others(104): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39714149 | |||||
| chr12:39714154
|
C | CGTATGTA others(67): Show |
10 | a0001c0001t0001g0013a0001c0001t0001g0188a0001c0001t0001g0232others(7): Show | 11 | HG00597.hp2 HG03831.hp2 NA18964.hp1 others(8): Show |
intron_variant | MODIFIER | c.1412-2602_1412-260 others(78): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714154 | ||||||
| chr12:39714154
|
C | CGTATGTA others(117): Show |
1 | a0001c0001t0001g0184 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1412-2602_1412-260 others(128): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714154 | ||||||
| chr12:39714158
|
C | T | 11 | a0001c0001t0001g0013a0001c0001t0001g0184a0001c0001t0001g0188others(8): Show | 12 | HG00597.hp2 HG03831.hp2 NA18964.hp1 others(9): Show |
intron_variant | MODIFIER | c.1412-2598C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714158 | ||||||
| chr12:39714160
|
T | C | 11 | a0001c0001t0001g0013a0001c0001t0001g0184a0001c0001t0001g0188others(8): Show | 12 | HG00597.hp2 HG03831.hp2 NA18964.hp1 others(9): Show |
intron_variant | MODIFIER | c.1412-2596T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714160 | ||||||
| chr12:39714164
|
T | C | 11 | a0001c0001t0001g0013a0001c0001t0001g0184a0001c0001t0001g0188others(8): Show | 12 | HG00597.hp2 HG03831.hp2 NA18964.hp1 others(9): Show |
intron_variant | MODIFIER | c.1412-2592T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714164 | ||||||
| chr12:39714166
|
C | T | 14 | a0001c0001t0001g0013a0001c0001t0001g0184a0001c0001t0001g0188others(11): Show | 15 | HG00280.hp2 HG00597.hp2 HG03239.hp1 others(12): Show |
intron_variant | MODIFIER | c.1412-2590C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714166 | ||||||
| chr12:39714167
|
G | A | 14 | a0001c0001t0001g0013a0001c0001t0001g0184a0001c0001t0001g0188others(11): Show | 15 | HG00280.hp2 HG00597.hp2 HG03239.hp1 others(12): Show |
intron_variant | MODIFIER | c.1412-2589G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714167 | ||||||
| chr12:39714167
|
G | C | 3 | a0001c0001t0004g0055a0001c0001t0004g0059a0001c0001t0004g0060 | 3 | HG00099.hp1 HG01070.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1412-2589G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714167 | ||||||
| chr12:39714171
|
A | G | 2 | a0006c0006t0001g0106a0006c0006t0001g0333 | 2 | HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1412-2585A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714171 | ||||||
| chr12:39714179
|
A | ACATGCAT others(37): Show |
1 | a0001c0001t0001g0280 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1412-2549_1412-250 others(48): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39714179 | |||||
| chr12:39714179
|
A | G | 3 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0208 | 3 | HG00280.hp2 HG03239.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1412-2577A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714179 | ||||||
| chr12:39714184
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1412-2572C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714184 | ||||||
| chr12:39714192
|
T | C | 12 | a0001c0001t0001g0013a0001c0001t0001g0184a0001c0001t0001g0188others(9): Show | 13 | HG00597.hp2 HG03225.hp1 HG03831.hp2 others(10): Show |
intron_variant | MODIFIER | c.1412-2564T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714192 | ||||||
| chr12:39714193
|
A | G | 14 | a0001c0001t0001g0013a0001c0001t0001g0184a0001c0001t0001g0188others(11): Show | 15 | HG00597.hp2 HG02486.hp2 HG03139.hp2 others(12): Show |
intron_variant | MODIFIER | c.1412-2563A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714193 | ||||||
| chr12:39714198
|
T | C | 1 | a0001c0007t0001g0024 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1412-2558T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714198 | ||||||
| chr12:39714198
|
TGTATATA others(11): Show |
T | 69 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(66): Show | 78 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.1412-2551_1412-253 others(22): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39714198 | |||||
| chr12:39714205
|
A | G | 152 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0022others(149): Show | 155 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.1412-2551A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714205 | ||||||
| chr12:39714207
|
A | T | 1 | a0001c0001t0001g0072 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1412-2549A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714207 | ||||||
| chr12:39714209
|
G | T | 8 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0247others(5): Show | 8 | HG00558.hp1 HG03669.hp2 NA18981.hp2 others(5): Show |
intron_variant | MODIFIER | c.1412-2547G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714209 | ||||||
| chr12:39714210
|
C | CATATATG others(1): Show |
12 | a0001c0001t0001g0013a0001c0001t0001g0184a0001c0001t0001g0188others(9): Show | 13 | HG00597.hp2 HG03831.hp2 NA18960.hp2 others(10): Show |
intron_variant | MODIFIER | c.1412-2541_1412-254 others(12): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39714210 | |||||
| chr12:39714216
|
C | T | 162 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(159): Show | 166 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.1412-2540C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714216 | ||||||
| chr12:39714225
|
A | T | 1 | a0001c0001t0001g0061 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1412-2531A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714225 | ||||||
| chr12:39714228
|
CATATATG others(1): Show |
C | 3 | a0001c0001t0001g0227a0001c0001t0001g0230a0001c0001t0001g0241 | 3 | HG02280.hp1 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1412-2514_1412-250 others(12): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39714228 | |||||
| chr12:39714230
|
T | C | 8 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(5): Show | 9 | HG01169.hp1 HG01192.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1412-2526T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714230 | ||||||
| chr12:39714234
|
T | C | 1 | a0001c0001t0001g0294 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1412-2522T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714234 | ||||||
| chr12:39714241
|
A | G | 1 | a0002c0002t0001g0123 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1412-2515A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714241 | ||||||
| chr12:39714250
|
C | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(5): Show | 9 | HG01169.hp1 HG01192.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1412-2506C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714250 | ||||||
| chr12:39714251
|
G | A | 1 | a0001c0001t0001g0298 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1412-2505G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714251 | ||||||
| chr12:39714257
|
G | A | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1412-2499G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714257 | ||||||
| chr12:39714268
|
T | C | 3 | a0001c0001t0001g0298a0001c0001t0001g0314a0001c0001t0001g0315 | 3 | HG01074.hp1 HG02683.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1412-2488T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714268 | ||||||
| chr12:39714270
|
T | TATATATG others(45): Show |
1 | a0001c0001t0001g0240 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1412-2466_1412-246 others(56): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39714270 | |||||
| chr12:39714270
|
T | TATATATG others(19): Show |
2 | a0001c0001t0001g0282a0001c0001t0001g0283 | 2 | HG01358.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1412-2465_1412-244 others(30): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39714270 | |||||
| chr12:39714270
|
T | TTTATATG others(19): Show |
22 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0044others(19): Show | 23 | HG00597.hp1 HG00621.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.1412-2486_1412-248 others(30): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714270 | ||||||
| chr12:39714270
|
T | TTTATATG others(45): Show |
4 | a0001c0001t0001g0069a0001c0001t0004g0055a0001c0001t0004g0059others(1): Show | 4 | HG00099.hp1 HG01070.hp1 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.1412-2486_1412-248 others(56): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714270 | ||||||
| chr12:39714270
|
T | TTTATATG others(71): Show |
8 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(5): Show | 8 | HG00738.hp1 HG02129.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1412-2486_1412-248 others(82): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714270 | ||||||
| chr12:39714270
|
T | TTTATATG others(97): Show |
1 | a0009c0008t0001g0068 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1412-2486_1412-248 others(108): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714270 | ||||||
| chr12:39714271
|
A | T | 197 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(194): Show | 209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.1412-2485A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714271 | ||||||
| chr12:39714284
|
C | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(7): Show | 11 | HG01169.hp1 HG01192.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.1412-2472C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714284 | ||||||
| chr12:39714291
|
G | A | 255 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1412-2465G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714291 | ||||||
| chr12:39714294
|
T | G | 1 | a0002c0002t0001g0117 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1412-2462T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714294 | ||||||
| chr12:39714301
|
A | G | 1 | a0001c0007t0001g0024 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1412-2455A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714301 | ||||||
| chr12:39714320
|
G | T | 1 | a0001c0001t0001g0072 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1412-2436G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714320 | ||||||
| chr12:39714336
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1412-2420T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714336 | ||||||
| chr12:39714339
|
C | A | 254 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(251): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.1412-2417C>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714339 | ||||||
| chr12:39714339
|
C | G | 1 | a0001c0001t0001g0225 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1412-2417C>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714339 | ||||||
| chr12:39714340
|
T | TATACATG others(77): Show |
1 | a0001c0001t0001g0072 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1412-2416_1412-241 others(88): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714340 | ||||||
| chr12:39714342
|
A | C | 1 | a0001c0001t0001g0072 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1412-2414A>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714342 | ||||||
| chr12:39714359
|
A | G | 1 | a0001c0001t0001g0280 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1412-2397A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714359 | ||||||
| chr12:39714367
|
G | C | 220 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(217): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.1412-2389G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714367 | ||||||
| chr12:39714397
|
G | GTA | 231 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(228): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.1412-2351_1412-235 others(6): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 39714397 | |||||
| chr12:39714512
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1412-2244A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714512 | ||||||
| chr12:39714551
|
T | A | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1412-2205T>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714551 | ||||||
| chr12:39714569
|
G | A | 13 | a0001c0001t0001g0003a0001c0001t0001g0318a0001c0001t0001g0322others(10): Show | 14 | HG01884.hp1 HG02055.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1412-2187G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714569 | ||||||
| chr12:39714638
|
A | G | 1 | a0002c0002t0001g0127 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1412-2118A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714638 | ||||||
| chr12:39714686
|
G | A | 1 | a0001c0001t0001g0297 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1412-2070G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714686 | ||||||
| chr12:39714709
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1412-2047C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714709 | ||||||
| chr12:39714716
|
A | G | 255 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1412-2040A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714716 | ||||||
| chr12:39714720
|
A | G | 3 | a0001c0001t0001g0330a0001c0001t0001g0331a0001c0001t0001g0332 | 3 | HG02145.hp2 HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1412-2036A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714720 | ||||||
| chr12:39714796
|
G | A | 6 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(3): Show | 6 | HG01884.hp2 HG02055.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1412-1960G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714796 | ||||||
| chr12:39714915
|
G | T | 1 | a0001c0001t0006g0033 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1412-1841G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714915 | ||||||
| chr12:39714963
|
A | C | 11 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(8): Show | 11 | HG00738.hp1 HG01106.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.1412-1793A>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39714963 | ||||||
| chr12:39715298
|
G | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0029others(4): Show | 8 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1412-1458G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39715298 | ||||||
| chr12:39715316
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1412-1440G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39715316 | ||||||
| chr12:39715334
|
T | C | 8 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(5): Show | 9 | HG01169.hp1 HG01192.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1412-1422T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39715334 | ||||||
| chr12:39715341
|
C | T | 1 | a0002c0002t0001g0119 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1412-1415C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39715341 | ||||||
| chr12:39715393
|
G | C | 2 | a0001c0001t0001g0253a0001c0001t0001g0279 | 2 | NA18959.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1412-1363G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39715393 | ||||||
| chr12:39715506
|
G | A | 3 | a0001c0007t0001g0024a0005c0003t0001g0034a0005c0003t0001g0035 | 3 | HG02486.hp2 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1412-1250G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39715506 | ||||||
| chr12:39715587
|
G | A | 255 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1412-1169G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39715587 | ||||||
| chr12:39715936
|
C | T | 7 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0029others(4): Show | 8 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1412-820C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39715936 | ||||||
| chr12:39715943
|
A | G | 1 | a0002c0002t0001g0094 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1412-813A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39715943 | ||||||
| chr12:39716187
|
C | T | 4 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(1): Show | 4 | HG02970.hp1 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1412-569C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39716187 | ||||||
| chr12:39716201
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1412-555C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39716201 | ||||||
| chr12:39716415
|
C | T | 1 | a0001c0007t0001g0024 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1412-341C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 11/12 | chr12 | 39716415 | ||||||
| chr12:39716960
|
A | G | 1 | a0001c0001t0001g0209 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1494+122A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 12/12 | chr12 | 39716960 | ||||||
| chr12:39717041
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1494+203C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 12/12 | chr12 | 39717041 | ||||||
| chr12:39717124
|
C | CATATATA others(14): Show |
23 | a0001c0001t0001g0003a0001c0001t0001g0075a0001c0001t0001g0227others(20): Show | 24 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.1494+298_1494+318d others(23): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 39717124 | |||||
| chr12:39717124
|
CATATATA others(14): Show |
C | 10 | a0001c0001t0001g0013a0001c0001t0001g0232a0001c0001t0001g0233others(7): Show | 11 | HG00597.hp2 HG00733.hp1 HG03831.hp2 others(8): Show |
intron_variant | MODIFIER | c.1494+298_1494+318d others(23): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 39717124 | |||||
| chr12:39717143
|
G | GTT | 8 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(5): Show | 9 | HG01169.hp1 HG01192.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1494+306_1494+307d others(4): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 39717143 | |||||
| chr12:39717165
|
C | T | 1 | a0001c0001t0001g0327 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1494+327C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 12/12 | chr12 | 39717165 | ||||||
| chr12:39717229
|
A | G | 7 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0029others(4): Show | 8 | HG01192.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1494+391A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 12/12 | chr12 | 39717229 | ||||||
| chr12:39717249
|
G | C | 1 | a0001c0001t0001g0049 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1494+411G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 12/12 | chr12 | 39717249 | ||||||
| chr12:39717259
|
C | T | 13 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(10): Show | 13 | HG00738.hp1 HG01106.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.1494+421C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 12/12 | chr12 | 39717259 | ||||||
| chr12:39717311
|
A | C | 1 | a0001c0001t0001g0092 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1494+473A>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 12/12 | chr12 | 39717311 | ||||||
| chr12:39717471
|
C | A | 1 | a0001c0001t0001g0057 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1494+633C>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 12/12 | chr12 | 39717471 | ||||||
| chr12:39717495
|
G | A | 11 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(8): Show | 11 | HG00738.hp1 HG01106.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.1494+657G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 12/12 | chr12 | 39717495 | ||||||
| chr12:39717592
|
A | C | 1 | a0001c0001t0001g0184 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1494+754A>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 12/12 | chr12 | 39717592 | ||||||
| chr12:39717886
|
T | C | 220 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(217): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.1494+1048T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 12/12 | chr12 | 39717886 | ||||||
| chr12:39717959
|
T | G | 218 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(215): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1494+1121T>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 12/12 | chr12 | 39717959 | ||||||
| chr12:39717971
|
CT | C | 11 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0029others(8): Show | 12 | HG00733.hp1 HG01192.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1494+1143delT | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 39717971 | |||||
| chr12:39718016
|
T | C | 1 | a0001c0001t0001g0329 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1494+1178T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 12/12 | chr12 | 39718016 | ||||||
| chr12:39718072
|
C | A | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1494+1234C>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 12/12 | chr12 | 39718072 | ||||||
| chr12:39718148
|
C | A | 1 | a0002c0002t0001g0094 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1494+1310C>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 12/12 | chr12 | 39718148 | ||||||
| chr12:39718287
|
C | T | 1 | a0001c0001t0001g0188 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1494+1449C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 12/12 | chr12 | 39718287 | ||||||
| chr12:39718320
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1494+1482G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 12/12 | chr12 | 39718320 | ||||||
| chr12:39718383
|
G | T | 1 | a0001c0007t0001g0024 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1494+1545G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 12/12 | chr12 | 39718383 | ||||||
| chr12:39718434
|
G | A | 1 | a0001c0007t0001g0024 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1494+1596G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 12/12 | chr12 | 39718434 | ||||||
| chr12:39718668
|
A | AT | 10 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0025others(7): Show | 11 | HG00639.hp1 HG01074.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.1494+1840dupT | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 39718668 | |||||
| chr12:39718741
|
G | T | 2 | a0005c0003t0001g0034a0005c0003t0001g0035 | 2 | HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1494+1903G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 12/12 | chr12 | 39718741 | ||||||
| chr12:39718864
|
G | C | 8 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0028others(5): Show | 9 | HG01169.hp1 HG01192.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1495-1923G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 12/12 | chr12 | 39718864 | ||||||
| chr12:39719006
|
A | G | 1 | a0001c0001t0001g0021 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1495-1781A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 12/12 | chr12 | 39719006 | ||||||
| chr12:39719020
|
A | G | 1 | a0001c0001t0001g0085 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1495-1767A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 12/12 | chr12 | 39719020 | ||||||
| chr12:39719058
|
C | A | 2 | a0001c0001t0001g0075a0008c0009t0001g0226 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1495-1729C>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 12/12 | chr12 | 39719058 | ||||||
| chr12:39719116
|
G | C | 1 | a0001c0001t0001g0203 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1495-1671G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 12/12 | chr12 | 39719116 | ||||||
| chr12:39719329
|
A | G | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1495-1458A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 12/12 | chr12 | 39719329 | ||||||
| chr12:39719631
|
T | C | 3 | a0001c0001t0001g0154a0001c0001t0001g0161a0001c0001t0001g0197 | 3 | HG01515.hp2 HG02132.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1495-1156T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 12/12 | chr12 | 39719631 | ||||||
| chr12:39719901
|
A | T | 3 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0041 | 3 | HG01884.hp2 HG02622.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1495-886A>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 12/12 | chr12 | 39719901 | ||||||
| chr12:39720088
|
G | T | 1 | a0001c0001t0001g0241 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1495-699G>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 12/12 | chr12 | 39720088 | ||||||
| chr12:39720279
|
T | TTA | 9 | a0001c0001t0001g0015a0001c0001t0001g0064a0001c0001t0001g0302others(6): Show | 10 | HG00621.hp2 HG00738.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.1495-494_1495-493d others(4): Show |
C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 39720279 | |||||
| chr12:39720388
|
C | T | 220 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(217): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.1495-399C>T | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 12/12 | chr12 | 39720388 | ||||||
| chr12:39720426
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1495-361G>A | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 12/12 | chr12 | 39720426 | ||||||
| chr12:39720477
|
A | G | 1 | a0001c0001t0001g0240 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1495-310A>G | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 12/12 | chr12 | 39720477 | ||||||
| chr12:39720682
|
G | C | 1 | a0001c0001t0001g0046 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1495-105G>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 12/12 | chr12 | 39720682 | ||||||
| chr12:39720693
|
T | C | 1 | a0001c0001t0003g0080 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1495-94T>C | C12orf40 | ENSG00000180116.15 | transcript | ENST00000324616.9 | protein_coding | 12/12 | chr12 | 39720693 |