Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 2802 |
|---|---|
| ensemblid | ENSG00000090615.16 |
| hgncid | 4426 |
| symbol | GOLGA3 |
| name | golgin A3 |
| refseq_nuc | NM_001389683.1 |
| refseq_prot | NP_001376612.1 |
| ensembl_nuc | ENST00000450791.8 |
| ensembl_prot | ENSP00000410378.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 132768914 |
| end | 132828869 |
| strand | - |
| ver | v1.2 |
| region | chr12:132768914-132828869 |
| region5000 | chr12:132763914-132833869 |
| regionname0 | GOLGA3_chr12_132768914_132828869 |
| regionname5000 | GOLGA3_chr12_132763914_132833869 |
| 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 | 1498 | 148 | 36 | 25 | 65 | 8 | 12 | 49 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0002 | 0/0 | 1498 | 78 | 16 | 15 | 33 | 0 | 14 | 19 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0003 | 0/0 | 1498 | 26 | 0 | 2 | 18 | 1 | 5 | 15 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0004 | 0/0 | 1498 | 16 | 1 | 6 | 3 | 3 | 3 | 3 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0005 | 0/0 | 1498 | 13 | 13 | 0 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0006 | 0/0 | 1498 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0007 | 0/0 | 1498 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0008 | 0/0 | 1498 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0009 | 0/0 | 1498 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0010 | 0/0 | 1498 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0011 | 0/0 | 1498 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0012 | 0/0 | 1498 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0013 | 0/0 | 1498 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0014 | 0/0 | 1498 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0015 | 0/0 | 1498 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0016 | 0/0 | 1498 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0017 | 0/0 | 1498 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0018 | 0/0 | 1498 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0019 | 0/0 | 1498 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0020 | 0/0 | 1498 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0021 | 0/0 | 1498 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0022 | 0/0 | 1498 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0023 | 0/0 | 85 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0024 | 0/0 | 1498 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 4497 | 96 | 22 | 17 | 45 | 4 | 7 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| c0002 | 0/0 | 4497 | 65 | 14 | 15 | 25 | 0 | 11 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| c0003 | 1/0 | 4497 | 36 | 13 | 6 | 13 | 0 | 3 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| c0004 | 0/0 | 4497 | 18 | 0 | 2 | 10 | 1 | 5 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| c0005 | 0/0 | 4497 | 14 | 1 | 6 | 3 | 2 | 2 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| c0006 | 0/0 | 4497 | 13 | 13 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| c0007 | 0/0 | 4497 | 9 | 1 | 0 | 8 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| c0008 | 0/0 | 4497 | 8 | 0 | 0 | 8 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| c0009 | 0/0 | 4497 | 7 | 0 | 1 | 1 | 3 | 2 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| c0010 | 0/0 | 4497 | 6 | 5 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| c0011 | 0/0 | 4497 | 2 | 0 | 0 | 2 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| c0012 | 0/0 | 4497 | 2 | 0 | 0 | 0 | 0 | 2 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| c0013 | 0/0 | 4497 | 2 | 1 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| c0014 | 0/0 | 4497 | 2 | 0 | 0 | 0 | 0 | 2 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| c0015 | 0/0 | 4497 | 2 | 2 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| c0016 | 0/0 | 4497 | 2 | 0 | 0 | 0 | 0 | 2 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| c0017 | 0/0 | 4497 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| c0018 | 0/0 | 4497 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| c0019 | 0/0 | 4497 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| c0020 | 0/0 | 4497 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| c0021 | 0/0 | 4497 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| c0022 | 0/0 | 4497 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| c0023 | 0/0 | 4497 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| c0024 | 0/0 | 4497 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| c0025 | 0/0 | 4497 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| c0026 | 0/0 | 4497 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| c0027 | 0/0 | 4497 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| c0028 | 0/0 | 4497 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| c0029 | 0/0 | 4497 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| c0030 | 0/0 | 4497 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| c0031 | 0/0 | 4497 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| c0032 | 0/0 | 4497 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| c0033 | 0/0 | 4497 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| c0034 | 0/0 | 4497 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| c0035 | 0/0 | 4497 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| c0036 | 0/0 | 4497 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| c0037 | 0/0 | 4497 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| c0038 | 0/0 | 4497 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| c0039 | 0/0 | 4497 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| c0040 | 0/0 | 4442 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 4434 | 66 | 10 | 11 | 42 | 0 | 3 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0002 | 0/0 | 4442 | 57 | 9 | 16 | 18 | 1 | 13 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0003 | 0/1 | 4442 | 22 | 3 | 6 | 4 | 4 | 4 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0004 | 0/0 | 4441 | 18 | 1 | 1 | 10 | 0 | 6 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0005 | 0/0 | 4439 | 13 | 1 | 4 | 3 | 2 | 3 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0006 | 0/0 | 4441 | 10 | 8 | 0 | 1 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0007 | 0/0 | 4433 | 9 | 0 | 0 | 9 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0008 | 0/0 | 4433 | 8 | 0 | 1 | 4 | 2 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0009 | 0/0 | 4437 | 7 | 7 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0010 | 0/0 | 4435 | 5 | 1 | 1 | 3 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0011 | 0/0 | 4442 | 4 | 0 | 0 | 3 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0012 | 0/0 | 4443 | 4 | 2 | 1 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0013 | 0/0 | 4434 | 4 | 0 | 0 | 4 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0014 | 0/0 | 4441 | 3 | 3 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0015 | 0/0 | 4441 | 2 | 0 | 0 | 2 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0016 | 0/0 | 4442 | 2 | 0 | 0 | 2 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0017 | 0/0 | 4440 | 2 | 2 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0018 | 0/0 | 4441 | 2 | 2 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0019 | 0/0 | 4394 | 2 | 1 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0020 | 0/0 | 4442 | 2 | 0 | 0 | 0 | 0 | 2 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0021 | 0/0 | 4442 | 2 | 0 | 0 | 0 | 0 | 2 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0022 | 0/0 | 4432 | 2 | 0 | 0 | 2 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0023 | 0/0 | 4440 | 2 | 0 | 2 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0024 | 0/0 | 4434 | 2 | 0 | 0 | 1 | 1 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0025 | 0/0 | 4435 | 2 | 0 | 1 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0026 | 0/0 | 4438 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0027 | 0/0 | 4439 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0028 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0029 | 0/0 | 4441 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0030 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0031 | 0/0 | 4441 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0032 | 0/0 | 4442 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0033 | 0/0 | 4442 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0034 | 0/0 | 4443 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0035 | 0/0 | 4438 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0036 | 0/0 | 4434 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0037 | 0/0 | 4442 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0038 | 0/0 | 4441 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0039 | 0/0 | 4436 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0040 | 0/0 | 4441 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0041 | 0/0 | 4441 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0042 | 0/0 | 4442 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0043 | 0/0 | 4442 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0044 | 0/0 | 4442 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0045 | 0/0 | 4442 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0046 | 0/0 | 4441 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0047 | 0/0 | 4441 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0048 | 0/0 | 4441 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0049 | 0/0 | 4441 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0050 | 0/0 | 4442 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0051 | 0/0 | 4442 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0052 | 0/0 | 4442 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0053 | 0/0 | 4441 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0054 | 0/0 | 4443 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0055 | 0/0 | 4442 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0056 | 0/0 | 4441 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0057 | 0/0 | 4442 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0058 | 0/0 | 4442 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0059 | 0/0 | 4443 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0060 | 0/0 | 4444 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0061 | 0/0 | 4443 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0062 | 0/0 | 4437 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0063 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0064 | 0/0 | 4442 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0065 | 0/0 | 4441 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0066 | 0/0 | 4434 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0067 | 0/0 | 4437 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0068 | 0/0 | 4434 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0069 | 0/0 | 4434 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0070 | 0/0 | 4436 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0071 | 0/0 | 4434 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0072 | 0/0 | 4434 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0073 | 0/0 | 4435 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0074 | 0/0 | 4436 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0075 | 0/0 | 4438 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0076 | 0/0 | 4439 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0077 | 1/0 | 4442 | 1 | 0 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0078 | 0/0 | 4442 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0079 | 0/0 | 4439 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0080 | 0/0 | 4443 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| t0081 | 0/0 | 4427 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0104 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0295 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 4497 | 96 | 22 | 17 | 45 | 4 | 7 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0003 | 1/0 | 4497 | 36 | 13 | 6 | 13 | 0 | 3 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0009 | 0/0 | 4497 | 7 | 0 | 1 | 1 | 3 | 2 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0011 | 0/0 | 4497 | 2 | 0 | 0 | 2 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0018 | 0/0 | 4497 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0023 | 0/0 | 4497 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0024 | 0/0 | 4497 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0025 | 0/0 | 4497 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0026 | 0/0 | 4497 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0027 | 0/0 | 4497 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0034 | 0/0 | 4497 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0002c0002 | 0/0 | 4497 | 65 | 14 | 15 | 25 | 0 | 11 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0002c0007 | 0/0 | 4497 | 9 | 1 | 0 | 8 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0002c0012 | 0/0 | 4497 | 2 | 0 | 0 | 0 | 0 | 2 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0002c0013 | 0/0 | 4497 | 2 | 1 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0003c0004 | 0/0 | 4497 | 18 | 0 | 2 | 10 | 1 | 5 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0003c0008 | 0/0 | 4497 | 8 | 0 | 0 | 8 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0004c0005 | 0/0 | 4497 | 14 | 1 | 6 | 3 | 2 | 2 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0004c0036 | 0/0 | 4497 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0004c0037 | 0/0 | 4497 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0005c0006 | 0/0 | 4497 | 13 | 13 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0006c0010 | 0/0 | 4497 | 6 | 5 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0007c0016 | 0/0 | 4497 | 2 | 0 | 0 | 0 | 0 | 2 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0008c0014 | 0/0 | 4497 | 2 | 0 | 0 | 0 | 0 | 2 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0009c0015 | 0/0 | 4497 | 2 | 2 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0010c0039 | 0/0 | 4497 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0011c0017 | 0/0 | 4497 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0012c0019 | 0/0 | 4497 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0013c0035 | 0/0 | 4497 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0014c0020 | 0/0 | 4497 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0015c0021 | 0/0 | 4497 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0016c0032 | 0/0 | 4497 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0017c0022 | 0/0 | 4497 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0018c0029 | 0/0 | 4497 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0019c0028 | 0/0 | 4497 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0020c0030 | 0/0 | 4497 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0021c0031 | 0/0 | 4497 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0022c0033 | 0/0 | 4497 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0023c0040 | 0/0 | 4442 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0024c0038 | 0/0 | 4497 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 8930 | 46 | 8 | 6 | 32 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0001t0002 | 0/0 | 8938 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0001t0003 | 0/1 | 8938 | 20 | 3 | 5 | 4 | 3 | 4 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0001t0004 | 0/0 | 8937 | 3 | 0 | 0 | 1 | 0 | 2 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0001t0010 | 0/0 | 8931 | 4 | 1 | 1 | 2 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0001t0017 | 0/0 | 8936 | 2 | 2 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0001t0024 | 0/0 | 8930 | 2 | 0 | 0 | 1 | 1 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0001t0025 | 0/0 | 8931 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0001t0026 | 0/0 | 8934 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0001t0027 | 0/0 | 8935 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0001t0028 | 0/0 | 8936 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0001t0029 | 0/0 | 8937 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0001t0030 | 0/0 | 8936 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0001t0032 | 0/0 | 8938 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0001t0033 | 0/0 | 8938 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0001t0037 | 0/0 | 8938 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0001t0055 | 0/0 | 8938 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0001t0059 | 0/0 | 8939 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0001t0066 | 0/0 | 8930 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0001t0067 | 0/0 | 8933 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0001t0069 | 0/0 | 8930 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0001t0071 | 0/0 | 8930 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0001t0072 | 0/0 | 8930 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0001t0073 | 0/0 | 8931 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0001t0075 | 0/0 | 8934 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0003t0001 | 0/0 | 8930 | 3 | 0 | 3 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0003t0002 | 0/0 | 8938 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0003t0004 | 0/0 | 8937 | 11 | 1 | 1 | 7 | 0 | 2 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0003t0006 | 0/0 | 8937 | 3 | 3 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0003t0009 | 0/0 | 8933 | 6 | 6 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0003t0011 | 0/0 | 8938 | 3 | 0 | 0 | 3 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0003t0039 | 0/0 | 8932 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0003t0040 | 0/0 | 8937 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0003t0041 | 0/0 | 8937 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0003t0042 | 0/0 | 8938 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0003t0045 | 0/0 | 8938 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0003t0048 | 0/0 | 8937 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0003t0054 | 0/0 | 8939 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0003t0077 | 1/0 | 8938 | 1 | 0 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0003t0079 | 0/0 | 8935 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0009t0002 | 0/0 | 8938 | 5 | 0 | 1 | 1 | 1 | 2 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0009t0049 | 0/0 | 8937 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0009t0058 | 0/0 | 8938 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0011t0001 | 0/0 | 8930 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0011t0074 | 0/0 | 8932 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0018t0019 | 0/0 | 8890 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0023t0004 | 0/0 | 8937 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0024t0002 | 0/0 | 8938 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0025t0003 | 0/0 | 8938 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0026t0001 | 0/0 | 8930 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0027t0001 | 0/0 | 8930 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0001c0034t0001 | 0/0 | 8930 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0002c0002t0002 | 0/0 | 8938 | 46 | 9 | 13 | 14 | 0 | 10 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0002c0002t0003 | 0/0 | 8938 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0002c0002t0006 | 0/0 | 8937 | 2 | 1 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0002c0002t0007 | 0/0 | 8929 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0002c0002t0012 | 0/0 | 8939 | 3 | 2 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0002c0002t0015 | 0/0 | 8937 | 2 | 0 | 0 | 2 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0002c0002t0016 | 0/0 | 8938 | 2 | 0 | 0 | 2 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0002c0002t0034 | 0/0 | 8939 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0002c0002t0050 | 0/0 | 8938 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0002c0002t0051 | 0/0 | 8938 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0002c0002t0052 | 0/0 | 8938 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0002c0002t0053 | 0/0 | 8937 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0002c0002t0056 | 0/0 | 8937 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0002c0002t0057 | 0/0 | 8938 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0002c0002t0060 | 0/0 | 8940 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0002c0007t0001 | 0/0 | 8930 | 6 | 0 | 0 | 6 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0002c0007t0031 | 0/0 | 8937 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0002c0007t0070 | 0/0 | 8932 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0002c0007t0076 | 0/0 | 8935 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0002c0012t0002 | 0/0 | 8938 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0002c0012t0011 | 0/0 | 8938 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0002c0013t0004 | 0/0 | 8937 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0002c0013t0009 | 0/0 | 8933 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0003c0004t0001 | 0/0 | 8930 | 4 | 0 | 1 | 0 | 0 | 3 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0003c0004t0007 | 0/0 | 8929 | 2 | 0 | 0 | 2 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0003c0004t0008 | 0/0 | 8929 | 6 | 0 | 1 | 3 | 1 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0003c0004t0013 | 0/0 | 8930 | 3 | 0 | 0 | 3 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0003c0004t0022 | 0/0 | 8928 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0003c0004t0025 | 0/0 | 8931 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0003c0004t0036 | 0/0 | 8930 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0003c0008t0007 | 0/0 | 8929 | 6 | 0 | 0 | 6 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0003c0008t0013 | 0/0 | 8930 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0003c0008t0022 | 0/0 | 8928 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0004c0005t0005 | 0/0 | 8935 | 12 | 1 | 4 | 3 | 2 | 2 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0004c0005t0023 | 0/0 | 8936 | 2 | 0 | 2 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0004c0036t0008 | 0/0 | 8929 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0004c0037t0005 | 0/0 | 8935 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0005c0006t0001 | 0/0 | 8930 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0005c0006t0014 | 0/0 | 8937 | 3 | 3 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0005c0006t0018 | 0/0 | 8937 | 2 | 2 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0005c0006t0043 | 0/0 | 8938 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0005c0006t0044 | 0/0 | 8938 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0005c0006t0062 | 0/0 | 8933 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0005c0006t0063 | 0/0 | 8936 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0005c0006t0064 | 0/0 | 8938 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0005c0006t0065 | 0/0 | 8937 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0005c0006t0081 | 0/0 | 8923 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0006c0010t0006 | 0/0 | 8937 | 4 | 4 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0006c0010t0046 | 0/0 | 8937 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0006c0010t0047 | 0/0 | 8937 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0007c0016t0020 | 0/0 | 8938 | 2 | 0 | 0 | 0 | 0 | 2 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0008c0014t0021 | 0/0 | 8938 | 2 | 0 | 0 | 0 | 0 | 2 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0009c0015t0078 | 0/0 | 8938 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0009c0015t0080 | 0/0 | 8939 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0010c0039t0010 | 0/0 | 8931 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0011c0017t0008 | 0/0 | 8929 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0012c0019t0038 | 0/0 | 8937 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0013c0035t0035 | 0/0 | 8934 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0014c0020t0019 | 0/0 | 8890 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0015c0021t0068 | 0/0 | 8930 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0016c0032t0001 | 0/0 | 8930 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0017c0022t0001 | 0/0 | 8930 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0018c0029t0061 | 0/0 | 8939 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0019c0028t0004 | 0/0 | 8937 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0020c0030t0012 | 0/0 | 8939 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0021c0031t0006 | 0/0 | 8937 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0022c0033t0002 | 0/0 | 8938 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0023c0040t0002 | 0/0 | 8883 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| a0024c0038t0004 | 0/0 | 8937 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | copy fasta | chr12 | 132763914 | 132833869 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0003g0104 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0010g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0010g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0010g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0010g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0017g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0017g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0024g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0024g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0025g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0026g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0027g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0028g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0029g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0030g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0032g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0033g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0037g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0055g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0059g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0066g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0067g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0069g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0071g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0072g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0073g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0001t0075g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0003t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0003t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0003t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0003t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0003t0004g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0003t0004g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0003t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0003t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0003t0004g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0003t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0003t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0003t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0003t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0003t0004g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0003t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0003t0006g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0003t0006g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0003t0006g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0003t0009g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0003t0009g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0003t0009g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0003t0009g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0003t0009g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0003t0009g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0003t0011g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0003t0011g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0003t0011g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0003t0039g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0003t0040g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0003t0041g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0003t0042g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0003t0045g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0003t0048g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0003t0054g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0003t0077g0295 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0003t0079g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0009t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0009t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0009t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0009t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0009t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0009t0049g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0009t0058g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0011t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0011t0074g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0018t0019g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0023t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0024t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0025t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0026t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0027t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0001c0034t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0003g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0006g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0006g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0007g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0012g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0012g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0012g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0015g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0015g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0016g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0016g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0034g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0050g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0051g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0052g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0053g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0056g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0057g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0002t0060g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0007t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0007t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0007t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0007t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0007t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0007t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0007t0031g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0007t0070g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0007t0076g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0012t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0012t0011g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0013t0004g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0002c0013t0009g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0003c0004t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0003c0004t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0003c0004t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0003c0004t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0003c0004t0007g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0003c0004t0007g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0003c0004t0008g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0003c0004t0008g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0003c0004t0008g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0003c0004t0008g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0003c0004t0008g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0003c0004t0008g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0003c0004t0013g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0003c0004t0013g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0003c0004t0013g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0003c0004t0022g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0003c0004t0025g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0003c0004t0036g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0003c0008t0007g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0003c0008t0007g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0003c0008t0007g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0003c0008t0007g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0003c0008t0007g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0003c0008t0007g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0003c0008t0013g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0003c0008t0022g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0004c0005t0005g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0004c0005t0005g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0004c0005t0005g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0004c0005t0005g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0004c0005t0005g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0004c0005t0005g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0004c0005t0005g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0004c0005t0005g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0004c0005t0005g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0004c0005t0005g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0004c0005t0005g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0004c0005t0005g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0004c0005t0023g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0004c0005t0023g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0004c0036t0008g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0004c0037t0005g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0005c0006t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0005c0006t0014g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0005c0006t0014g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0005c0006t0014g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0005c0006t0018g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0005c0006t0018g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0005c0006t0043g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0005c0006t0044g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0005c0006t0062g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0005c0006t0063g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0005c0006t0064g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0005c0006t0065g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0005c0006t0081g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0006c0010t0006g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0006c0010t0006g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0006c0010t0006g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0006c0010t0006g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0006c0010t0046g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0006c0010t0047g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0007c0016t0020g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0007c0016t0020g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0008c0014t0021g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0008c0014t0021g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0009c0015t0078g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0009c0015t0080g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0010c0039t0010g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0011c0017t0008g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0012c0019t0038g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0013c0035t0035g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0014c0020t0019g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0015c0021t0068g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0016c0032t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0017c0022t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0018c0029t0061g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0019c0028t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0020c0030t0012g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0021c0031t0006g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0022c0033t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0023c0040t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| a0024c0038t0004g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0010 | EUR | FIN | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG00280 | hp2 | a0003 | c0004 | t0008 | g0287 | EUR | FIN | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG00323 | hp1 | a0004 | c0005 | t0005 | g0248 | EUR | FIN | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG00323 | hp2 | a0001 | c0001 | t0024 | g0094 | EUR | FIN | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG00408 | hp2 | a0003 | c0004 | t0013 | g0268 | EAS | CHS | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0215 | EAS | CHS | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG00438 | hp1 | a0001 | c0003 | t0004 | g0150 | EAS | CHS | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | CHS | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG00544 | hp1 | a0003 | c0008 | t0013 | g0264 | EAS | CHS | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG00544 | hp2 | a0011 | c0017 | t0008 | g0267 | EAS | CHS | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0230 | EAS | CHS | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG00609 | hp2 | a0002 | c0007 | t0001 | g0058 | EAS | CHS | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG00642 | hp1 | a0002 | c0002 | t0002 | g0175 | AMR | PUR | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG00642 | hp2 | a0001 | c0003 | t0004 | g0143 | AMR | PUR | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG00673 | hp1 | a0002 | c0002 | t0002 | g0218 | EAS | CHS | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG00673 | hp2 | a0002 | c0007 | t0001 | g0059 | EAS | CHS | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG00735 | hp1 | a0003 | c0004 | t0001 | g0283 | AMR | PUR | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0194 | AMR | PUR | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0122 | AMR | PUR | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0119 | AMR | PUR | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG00741 | hp2 | a0002 | c0002 | t0002 | g0179 | AMR | PUR | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01069 | hp1 | a0002 | c0002 | t0053 | g0239 | AMR | PUR | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0116 | AMR | PUR | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01070 | hp1 | a0004 | c0005 | t0005 | g0249 | AMR | PUR | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01070 | hp2 | a0002 | c0002 | t0002 | g0173 | AMR | PUR | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01071 | hp1 | a0004 | c0005 | t0005 | g0250 | AMR | PUR | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01071 | hp2 | a0002 | c0002 | t0003 | g0240 | AMR | PUR | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01074 | hp1 | a0002 | c0002 | t0002 | g0188 | AMR | PUR | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01074 | hp2 | a0001 | c0009 | t0002 | g0181 | AMR | PUR | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01106 | hp1 | a0006 | c0010 | t0047 | g0134 | AMR | PUR | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01106 | hp2 | a0001 | c0003 | t0045 | g0149 | AMR | PUR | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01167 | hp2 | a0002 | c0002 | t0002 | g0176 | AMR | PUR | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01169 | hp2 | a0003 | c0004 | t0008 | g0285 | AMR | PUR | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01175 | hp1 | a0004 | c0005 | t0005 | g0259 | AMR | PUR | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01175 | hp2 | a0001 | c0001 | t0032 | g0107 | AMR | PUR | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01192 | hp1 | a0022 | c0033 | t0002 | g0186 | AMR | PUR | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01192 | hp2 | a0002 | c0002 | t0002 | g0192 | AMR | PUR | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01243 | hp1 | a0001 | c0001 | t0025 | g0040 | AMR | PUR | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01243 | hp2 | a0004 | c0005 | t0005 | g0252 | AMR | PUR | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01255 | hp1 | a0001 | c0003 | t0001 | g0167 | AMR | CLM | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | CLM | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01256 | hp1 | a0004 | c0005 | t0023 | g0256 | AMR | CLM | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0210 | AMR | CLM | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0112 | AMR | CLM | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01258 | hp1 | a0004 | c0005 | t0023 | g0246 | AMR | CLM | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0111 | AMR | CLM | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0223 | AMR | CLM | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01361 | hp2 | a0002 | c0002 | t0002 | g0180 | AMR | CLM | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01496 | hp2 | a0001 | c0001 | t0037 | g0113 | AMR | CLM | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01515 | hp1 | a0001 | c0009 | t0049 | g0202 | EUR | IBS | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01515 | hp2 | a0004 | c0005 | t0005 | g0247 | EUR | IBS | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01517 | hp1 | a0001 | c0009 | t0058 | g0200 | EUR | IBS | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01517 | hp2 | a0001 | c0025 | t0003 | g0106 | EUR | IBS | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01884 | hp1 | a0001 | c0003 | t0006 | g0291 | AFR | ACB | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01884 | hp2 | a0001 | c0003 | t0004 | g0159 | AFR | ACB | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01891 | hp1 | a0006 | c0010 | t0046 | g0129 | AFR | ACB | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01891 | hp2 | a0002 | c0002 | t0002 | g0014 | AFR | ACB | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01978 | hp1 | a0001 | c0027 | t0001 | g0085 | AMR | PEL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01978 | hp2 | a0020 | c0030 | t0012 | g0228 | AMR | PEL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01981 | hp1 | a0001 | c0003 | t0041 | g0165 | AMR | PEL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01981 | hp2 | a0001 | c0001 | t0010 | g0089 | AMR | PEL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01993 | hp1 | a0001 | c0003 | t0001 | g0151 | AMR | PEL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01993 | hp2 | a0001 | c0001 | t0075 | g0128 | AMR | PEL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02004 | hp2 | a0013 | c0035 | t0035 | g0262 | AMR | PEL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0301 | EAS | KHV | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02015 | hp2 | a0001 | c0001 | t0072 | g0075 | EAS | KHV | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02027 | hp2 | a0003 | c0004 | t0013 | g0284 | EAS | KHV | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02055 | hp1 | a0002 | c0002 | t0012 | g0233 | AFR | ACB | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02055 | hp2 | a0005 | c0006 | t0064 | g0022 | AFR | ACB | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02056 | hp1 | a0001 | c0001 | t0010 | g0082 | EAS | KHV | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02056 | hp2 | a0001 | c0003 | t0039 | g0156 | EAS | KHV | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02074 | hp2 | a0002 | c0002 | t0015 | g0214 | EAS | KHV | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02080 | hp1 | a0002 | c0002 | t0002 | g0226 | EAS | KHV | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02080 | hp2 | a0001 | c0003 | t0011 | g0161 | EAS | KHV | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02129 | hp1 | a0002 | c0002 | t0006 | g0211 | EAS | KHV | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02129 | hp2 | a0001 | c0001 | t0055 | g0009 | EAS | KHV | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02132 | hp1 | a0002 | c0002 | t0015 | g0222 | EAS | KHV | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02132 | hp2 | a0001 | c0018 | t0019 | g0132 | EAS | KHV | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02145 | hp1 | a0002 | c0002 | t0006 | g0182 | AFR | ACB | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02145 | hp2 | a0001 | c0003 | t0009 | g0293 | AFR | ACB | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0207 | EAS | CDX | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02155 | hp2 | a0001 | c0023 | t0004 | g0160 | EAS | CDX | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02258 | hp1 | a0002 | c0002 | t0012 | g0209 | AFR | ACB | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02258 | hp2 | a0002 | c0013 | t0009 | g0133 | AFR | ACB | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02280 | hp1 | a0001 | c0001 | t0073 | g0041 | AFR | ACB | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02280 | hp2 | a0002 | c0002 | t0002 | g0191 | AFR | ACB | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02293 | hp1 | a0001 | c0003 | t0001 | g0148 | AMR | PEL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0177 | AMR | PEL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02523 | hp1 | a0002 | c0007 | t0076 | g0076 | EAS | KHV | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02523 | hp2 | a0001 | c0003 | t0004 | g0155 | EAS | KHV | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0109 | SAS | PJL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02602 | hp2 | a0008 | c0014 | t0021 | g0172 | SAS | PJL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02615 | hp1 | a0005 | c0006 | t0044 | g0005 | AFR | GWD | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02615 | hp2 | a0001 | c0001 | t0017 | g0015 | AFR | GWD | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02622 | hp2 | a0006 | c0010 | t0006 | g0130 | AFR | GWD | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02630 | hp2 | a0001 | c0003 | t0009 | g0297 | AFR | GWD | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02683 | hp1 | a0001 | c0003 | t0004 | g0142 | SAS | PJL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02683 | hp2 | a0002 | c0002 | t0002 | g0198 | SAS | PJL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02698 | hp1 | a0021 | c0031 | t0006 | g0169 | SAS | PJL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02698 | hp2 | a0024 | c0038 | t0004 | g0163 | SAS | PJL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02717 | hp1 | a0014 | c0020 | t0019 | g0003 | AFR | GWD | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02735 | hp1 | a0004 | c0037 | t0005 | g0245 | SAS | PJL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0110 | SAS | PJL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02738 | hp1 | a0001 | c0003 | t0004 | g0164 | SAS | PJL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02738 | hp2 | a0003 | c0004 | t0025 | g0280 | SAS | PJL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0123 | AFR | GWD | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02809 | hp2 | a0006 | c0010 | t0006 | g0012 | AFR | GWD | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02818 | hp1 | a0001 | c0001 | t0028 | g0305 | AFR | GWD | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02818 | hp2 | a0009 | c0015 | t0080 | g0065 | AFR | GWD | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02886 | hp1 | a0001 | c0003 | t0006 | g0298 | AFR | GWD | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02886 | hp2 | a0002 | c0007 | t0031 | g0307 | AFR | GWD | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02895 | hp1 | a0001 | c0001 | t0026 | g0302 | AFR | GWD | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02896 | hp1 | a0009 | c0015 | t0078 | g0066 | AFR | GWD | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02896 | hp2 | a0002 | c0002 | t0002 | g0174 | AFR | GWD | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02897 | hp1 | a0001 | c0001 | t0027 | g0306 | AFR | GWD | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02897 | hp2 | a0002 | c0002 | t0002 | g0168 | AFR | GWD | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02922 | hp1 | a0001 | c0001 | t0067 | g0044 | AFR | ESN | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02922 | hp2 | a0002 | c0002 | t0002 | g0190 | AFR | ESN | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02965 | hp1 | a0001 | c0034 | t0001 | g0062 | AFR | ESN | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02965 | hp2 | a0005 | c0006 | t0062 | g0016 | AFR | ESN | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02976 | hp1 | a0006 | c0010 | t0006 | g0011 | AFR | ESN | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02976 | hp2 | a0001 | c0003 | t0009 | g0294 | AFR | ESN | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG03017 | hp1 | a0008 | c0014 | t0021 | g0171 | SAS | PJL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0126 | SAS | PJL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG03130 | hp1 | a0002 | c0002 | t0060 | g0185 | AFR | ESN | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG03130 | hp2 | a0001 | c0001 | t0030 | g0303 | AFR | ESN | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG03195 | hp1 | a0001 | c0003 | t0009 | g0292 | AFR | ESN | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG03195 | hp2 | a0018 | c0029 | t0061 | g0103 | AFR | ESN | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG03209 | hp2 | a0005 | c0006 | t0043 | g0004 | AFR | MSL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG03225 | hp1 | a0005 | c0006 | t0001 | g0021 | AFR | MSL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG03225 | hp2 | a0006 | c0010 | t0006 | g0131 | AFR | MSL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG03486 | hp1 | a0005 | c0006 | t0018 | g0102 | AFR | MSL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG03486 | hp2 | a0002 | c0002 | t0002 | g0212 | AFR | MSL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG03490 | hp1 | a0004 | c0005 | t0005 | g0251 | SAS | PJL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0139 | SAS | PJL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG03491 | hp1 | a0002 | c0002 | t0002 | g0203 | SAS | PJL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG03491 | hp2 | a0007 | c0016 | t0020 | g0253 | SAS | PJL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG03492 | hp1 | a0007 | c0016 | t0020 | g0254 | SAS | PJL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG03492 | hp2 | a0004 | c0005 | t0005 | g0255 | SAS | PJL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG03516 | hp1 | a0001 | c0001 | t0010 | g0244 | AFR | ESN | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG03516 | hp2 | a0001 | c0003 | t0079 | g0299 | AFR | ESN | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0117 | AFR | GWD | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG03540 | hp2 | a0005 | c0006 | t0014 | g0019 | AFR | GWD | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG03579 | hp1 | a0005 | c0006 | t0018 | g0023 | AFR | MSL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG03579 | hp2 | a0005 | c0006 | t0065 | g0017 | AFR | MSL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG03654 | hp1 | a0001 | c0001 | t0004 | g0127 | SAS | PJL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG03654 | hp2 | a0001 | c0009 | t0002 | g0219 | SAS | PJL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG03669 | hp1 | a0002 | c0002 | t0002 | g0243 | SAS | PJL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG03669 | hp2 | a0002 | c0002 | t0002 | g0242 | SAS | PJL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0224 | SAS | STU | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG03688 | hp2 | a0002 | c0012 | t0011 | g0125 | SAS | STU | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG03710 | hp1 | a0002 | c0002 | t0002 | g0204 | SAS | PJL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG03710 | hp2 | a0001 | c0009 | t0002 | g0199 | SAS | PJL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0217 | SAS | BEB | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG03927 | hp2 | a0002 | c0012 | t0002 | g0124 | SAS | BEB | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG03942 | hp1 | a0003 | c0004 | t0001 | g0282 | SAS | BEB | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG03942 | hp2 | a0001 | c0001 | t0059 | g0120 | SAS | BEB | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG04115 | hp1 | a0003 | c0004 | t0001 | g0279 | SAS | STU | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG04115 | hp2 | a0001 | c0003 | t0054 | g0154 | SAS | STU | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG04199 | hp1 | a0003 | c0004 | t0001 | g0270 | SAS | STU | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0140 | SAS | STU | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG04204 | hp1 | a0002 | c0013 | t0004 | g0141 | SAS | STU | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG04204 | hp2 | a0003 | c0004 | t0008 | g0286 | SAS | STU | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0216 | SAS | STU | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG04228 | hp2 | a0002 | c0002 | t0052 | g0220 | SAS | STU | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18522 | hp1 | a0001 | c0001 | t0071 | g0050 | AFR | YRI | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18522 | hp2 | a0005 | c0006 | t0063 | g0013 | AFR | YRI | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18612 | hp1 | a0002 | c0002 | t0051 | g0238 | EAS | CHB | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18612 | hp2 | a0002 | c0002 | t0007 | g0236 | EAS | CHB | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18747 | hp1 | a0001 | c0009 | t0002 | g0232 | EAS | CHB | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18747 | hp2 | a0001 | c0024 | t0002 | g0100 | EAS | CHB | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0118 | AFR | YRI | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18906 | hp2 | a0005 | c0006 | t0014 | g0018 | AFR | YRI | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18939 | hp1 | a0003 | c0008 | t0007 | g0273 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18939 | hp2 | a0023 | c0040 | t0002 | g0234 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18942 | hp1 | a0003 | c0004 | t0007 | g0266 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18942 | hp2 | a0004 | c0005 | t0005 | g0101 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18946 | hp2 | a0003 | c0008 | t0022 | g0265 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18947 | hp2 | a0003 | c0004 | t0022 | g0277 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18948 | hp1 | a0002 | c0002 | t0056 | g0195 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18948 | hp2 | a0002 | c0007 | t0001 | g0048 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18950 | hp1 | a0002 | c0002 | t0002 | g0197 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18950 | hp2 | a0001 | c0001 | t0066 | g0031 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18951 | hp1 | a0019 | c0028 | t0004 | g0153 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18951 | hp2 | a0002 | c0007 | t0070 | g0060 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18952 | hp1 | a0001 | c0011 | t0001 | g0061 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18952 | hp2 | a0003 | c0008 | t0007 | g0281 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18956 | hp1 | a0001 | c0003 | t0011 | g0147 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18956 | hp2 | a0004 | c0005 | t0005 | g0257 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18957 | hp2 | a0001 | c0003 | t0004 | g0158 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18959 | hp2 | a0003 | c0008 | t0007 | g0271 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18960 | hp1 | a0002 | c0002 | t0002 | g0205 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18960 | hp2 | a0017 | c0022 | t0001 | g0025 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18964 | hp1 | a0015 | c0021 | t0068 | g0072 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0079 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18967 | hp2 | a0004 | c0005 | t0005 | g0049 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18970 | hp1 | a0002 | c0002 | t0002 | g0189 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18975 | hp2 | a0002 | c0002 | t0050 | g0237 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18977 | hp1 | a0003 | c0004 | t0008 | g0278 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18977 | hp2 | a0002 | c0007 | t0001 | g0092 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18979 | hp2 | a0003 | c0004 | t0008 | g0276 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18980 | hp2 | a0002 | c0002 | t0002 | g0193 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18989 | hp2 | a0001 | c0001 | t0010 | g0083 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18991 | hp1 | a0001 | c0011 | t0074 | g0067 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18991 | hp2 | a0003 | c0008 | t0007 | g0272 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18994 | hp1 | a0001 | c0003 | t0042 | g0146 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA18998 | hp2 | a0001 | c0001 | t0033 | g0108 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19002 | hp1 | a0002 | c0007 | t0001 | g0068 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19002 | hp2 | a0002 | c0002 | t0012 | g0183 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19004 | hp1 | a0003 | c0004 | t0007 | g0269 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19005 | hp1 | a0010 | c0039 | t0010 | g0033 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19005 | hp2 | a0002 | c0002 | t0002 | g0231 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19006 | hp2 | a0003 | c0004 | t0036 | g0260 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19009 | hp2 | a0002 | c0002 | t0002 | g0225 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19010 | hp1 | a0003 | c0004 | t0008 | g0288 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19012 | hp1 | a0001 | c0003 | t0002 | g0196 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | LWK | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19043 | hp2 | a0001 | c0003 | t0048 | g0289 | AFR | LWK | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19057 | hp1 | a0016 | c0032 | t0001 | g0034 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19057 | hp2 | a0002 | c0002 | t0002 | g0213 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19058 | hp2 | a0001 | c0003 | t0004 | g0162 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19060 | hp2 | a0002 | c0002 | t0016 | g0221 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19064 | hp1 | a0001 | c0003 | t0004 | g0166 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19064 | hp2 | a0001 | c0003 | t0011 | g0157 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19065 | hp2 | a0003 | c0008 | t0007 | g0275 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19066 | hp1 | a0001 | c0001 | t0069 | g0032 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0229 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19068 | hp1 | a0002 | c0007 | t0001 | g0071 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19077 | hp1 | a0003 | c0008 | t0007 | g0274 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19082 | hp1 | a0002 | c0002 | t0016 | g0170 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19082 | hp2 | a0003 | c0004 | t0013 | g0261 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19083 | hp1 | a0002 | c0002 | t0034 | g0227 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19087 | hp1 | a0001 | c0001 | t0024 | g0095 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19087 | hp2 | a0001 | c0003 | t0004 | g0144 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19088 | hp1 | a0001 | c0003 | t0004 | g0145 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19088 | hp2 | a0001 | c0026 | t0001 | g0099 | EAS | JPT | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19240 | hp1 | a0002 | c0002 | t0002 | g0178 | AFR | YRI | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA19240 | hp2 | a0001 | c0001 | t0029 | g0304 | AFR | YRI | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA20129 | hp1 | a0001 | c0003 | t0040 | g0152 | AFR | ASW | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA20129 | hp2 | a0002 | c0002 | t0002 | g0187 | AFR | ASW | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0115 | EUR | TSI | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA20752 | hp2 | a0001 | c0009 | t0002 | g0201 | EUR | TSI | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0114 | EUR | TSI | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA20805 | hp2 | a0004 | c0036 | t0008 | g0263 | EUR | TSI | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA20905 | hp1 | a0002 | c0002 | t0002 | g0241 | SAS | GIH | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA20905 | hp2 | a0002 | c0002 | t0002 | g0235 | SAS | GIH | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0208 | AMR | CLM | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02109 | hp1 | a0002 | c0002 | t0002 | g0206 | AFR | ACB | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02486 | hp2 | a0005 | c0006 | t0081 | g0308 | AFR | ACB | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02559 | hp1 | a0001 | c0003 | t0009 | g0296 | AFR | ACB | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG02559 | hp2 | a0005 | c0006 | t0014 | g0020 | AFR | ACB | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG03471 | hp1 | a0001 | c0003 | t0006 | g0290 | AFR | MSL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG03471 | hp2 | a0012 | c0019 | t0038 | g0024 | AFR | MSL | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG06807 | hp1 | a0001 | c0003 | t0009 | g0300 | AFR | USA | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| HG06807 | hp2 | a0004 | c0005 | t0005 | g0258 | AFR | USA | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA21309 | hp1 | a0002 | c0002 | t0057 | g0184 | AFR | LWK | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| NA21309 | hp2 | a0001 | c0001 | t0017 | g0001 | AFR | LWK | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0104 | REF | REF | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0077 | g0295 | REF | REF | GOLGA3_chr12_132763914_132833869 | GOLGA3 | chr12 | 132763914 | 132833869 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:132775223
|
G | A | 1 | a0015 | 1 | NA18964.hp1 | missense_variant | MODERATE | c.4061C>T | p.Ser1354Leu | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 22/24 | 4311/8938 | 4061/4497 | 1354/1498 | chr12 | 132775223 | ||
| chr12:132777085
|
C | T | 1 | a0018 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.3728G>A | p.Arg1243Gln | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 20/24 | 3978/8938 | 3728/4497 | 1243/1498 | chr12 | 132777085 | ||
| chr12:132777676
|
C | T | 1 | a0013 | 1 | HG02004.hp2 | missense_variant | MODERATE | c.3712G>A | p.Asp1238Asn | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 19/24 | 3962/8938 | 3712/4497 | 1238/1498 | chr12 | 132777676 | ||
| chr12:132777727
|
T | C | 2 | a0008a0022 | 3 | HG01192.hp1 HG02602.hp2 HG03017.hp1 |
missense_variant | MODERATE | c.3661A>G | p.Lys1221Glu | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 19/24 | 3911/8938 | 3661/4497 | 1221/1498 | chr12 | 132777727 | ||
| chr12:132780826
|
T | C | 10 | a0002a0006a0007others(7): Show | 94 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(91): Show |
missense_variant | MODERATE | c.3554A>G | p.Lys1185Arg | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/24 | 3804/8938 | 3554/4497 | 1185/1498 | chr12 | 132780826 | ||
| chr12:132782399
|
A | C | 1 | a0019 | 1 | NA18951.hp1 | missense_variant | MODERATE | c.3362T>G | p.Leu1121Arg | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 17/24 | 3612/8938 | 3362/4497 | 1121/1498 | chr12 | 132782399 | ||
| chr12:132786407
|
C | G | 1 | a0020 | 1 | HG01978.hp2 | missense_variant | MODERATE | c.3055G>C | p.Ala1019Pro | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 15/24 | 3305/8938 | 3055/4497 | 1019/1498 | chr12 | 132786407 | ||
| chr12:132801840
|
T | C | 1 | a0021 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.1727A>G | p.Gln576Arg | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/24 | 1977/8938 | 1727/4497 | 576/1498 | chr12 | 132801840 | ||
| chr12:132801879
|
G | A | 1 | a0009 | 2 | HG02818.hp2 HG02896.hp1 |
missense_variant | MODERATE | c.1688C>T | p.Ala563Val | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/24 | 1938/8938 | 1688/4497 | 563/1498 | chr12 | 132801879 | ||
| chr12:132807247
|
A | T | 1 | a0017 | 1 | NA18960.hp2 | missense_variant | MODERATE | c.1220T>A | p.Met407Lys | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 6/24 | 1470/8938 | 1220/4497 | 407/1498 | chr12 | 132807247 | ||
| chr12:132807255
|
C | A | 1 | a0016 | 1 | NA19057.hp1 | missense_variant | MODERATE | c.1212G>T | p.Gln404His | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 6/24 | 1462/8938 | 1212/4497 | 404/1498 | chr12 | 132807255 | ||
| chr12:132807918
|
C | T | 1 | a0015 | 1 | NA18964.hp1 | missense_variant | MODERATE | c.1151G>A | p.Arg384Gln | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 5/24 | 1401/8938 | 1151/4497 | 384/1498 | chr12 | 132807918 | ||
| chr12:132807930
|
T | C | 1 | a0022 | 1 | HG01192.hp1 | missense_variant | MODERATE | c.1139A>G | p.Asn380Ser | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 5/24 | 1389/8938 | 1139/4497 | 380/1498 | chr12 | 132807930 | ||
| chr12:132808092
|
C | T | 1 | a0011 | 1 | HG00544.hp2 | missense_variant | MODERATE | c.977G>A | p.Arg326Gln | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 5/24 | 1227/8938 | 977/4497 | 326/1498 | chr12 | 132808092 | ||
| chr12:132808150
|
C | T | 1 | a0014 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.919G>A | p.Val307Met | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 5/24 | 1169/8938 | 919/4497 | 307/1498 | chr12 | 132808150 | ||
| chr12:132808278
|
G | A | 5 | a0003a0004a0007others(2): Show | 46 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(43): Show |
missense_variant | MODERATE | c.791C>T | p.Pro264Leu | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 5/24 | 1041/8938 | 791/4497 | 264/1498 | chr12 | 132808278 | ||
| chr12:132816659
|
CCTGGAGA others(48): Show |
C | 1 | a0023 | 1 | NA18939.hp2 | frameshift_variant | HIGH | c.232_286delCCTCCGTC others(47): Show |
p.Pro78fs | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/24 | 536/8938 | 232/4497 | 78/1498 | chr12 | 132816659 | ||
| chr12:132816704
|
G | C | 2 | a0005a0012 | 14 | HG02055.hp2 HG02486.hp2 HG02559.hp2 others(11): Show |
missense_variant | MODERATE | c.242C>G | p.Ser81Cys | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/24 | 492/8938 | 242/4497 | 81/1498 | chr12 | 132816704 | ||
| chr12:132816705
|
A | G | 2 | a0005a0012 | 14 | HG02055.hp2 HG02486.hp2 HG02559.hp2 others(11): Show |
missense_variant | MODERATE | c.241T>C | p.Ser81Pro | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/24 | 491/8938 | 241/4497 | 81/1498 | chr12 | 132816705 | ||
| chr12:132816710
|
G | T | 1 | a0006 | 6 | HG01106.hp1 HG01891.hp1 HG02622.hp2 others(3): Show |
missense_variant | MODERATE | c.236C>A | p.Pro79Gln | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/24 | 486/8938 | 236/4497 | 79/1498 | chr12 | 132816710 | ||
| chr12:132816737
|
C | T | 2 | a0003a0011 | 27 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(24): Show |
missense_variant | MODERATE | c.209G>A | p.Gly70Glu | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/24 | 459/8938 | 209/4497 | 70/1498 | chr12 | 132816737 | ||
| chr12:132816758
|
T | C | 1 | a0024 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.188A>G | p.Gln63Arg | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/24 | 438/8938 | 188/4497 | 63/1498 | chr12 | 132816758 | ||
| chr12:132816788
|
G | C | 1 | a0010 | 1 | NA19005.hp1 | missense_variant | MODERATE | c.158C>G | p.Thr53Arg | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/24 | 408/8938 | 158/4497 | 53/1498 | chr12 | 132816788 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:132775150
|
C | T | 1 | a0018c0029 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.4134G>A | p.Ala1378Ala | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 22/24 | 4384/8938 | 4134/4497 | 1378/1498 | chr12 | 132775150 | ||
| chr12:132776994
|
G | A | 1 | a0001c0026 | 1 | NA19088.hp2 | synonymous_variant | LOW | c.3819C>T | p.Asp1273Asp | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 20/24 | 4069/8938 | 3819/4497 | 1273/1498 | chr12 | 132776994 | ||
| chr12:132777755
|
C | T | 3 | a0001c0018a0009c0015a0014c0020 | 4 | HG02132.hp2 HG02717.hp1 HG02818.hp2 others(1): Show |
synonymous_variant | LOW | c.3633G>A | p.Ala1211Ala | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 19/24 | 3883/8938 | 3633/4497 | 1211/1498 | chr12 | 132777755 | ||
| chr12:132782398
|
A | G | 1 | a0014c0020 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.3363T>C | p.Leu1121Leu | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 17/24 | 3613/8938 | 3363/4497 | 1121/1498 | chr12 | 132782398 | ||
| chr12:132786420
|
G | A | 9 | a0001c0009a0002c0002a0002c0012others(6): Show | 86 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(83): Show |
synonymous_variant | LOW | c.3042C>T | p.Leu1014Leu | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 15/24 | 3292/8938 | 3042/4497 | 1014/1498 | chr12 | 132786420 | ||
| chr12:132786785
|
C | T | 1 | a0001c0025 | 1 | HG01517.hp2 | splice_region_variant&synonymous_variant | LOW | c.2814G>A | p.Ser938Ser | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 14/24 | 3064/8938 | 2814/4497 | 938/1498 | chr12 | 132786785 | ||
| chr12:132789072
|
G | C | 1 | a0001c0027 | 1 | HG01978.hp1 | synonymous_variant | LOW | c.2766C>G | p.Leu922Leu | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/24 | 3016/8938 | 2766/4497 | 922/1498 | chr12 | 132789072 | ||
| chr12:132789135
|
G | T | 1 | a0001c0024 | 1 | NA18747.hp2 | synonymous_variant | LOW | c.2703C>A | p.Leu901Leu | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/24 | 2953/8938 | 2703/4497 | 901/1498 | chr12 | 132789135 | ||
| chr12:132796094
|
G | A | 1 | a0004c0037 | 1 | HG02735.hp1 | synonymous_variant | LOW | c.2227C>T | p.Leu743Leu | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/24 | 2477/8938 | 2227/4497 | 743/1498 | chr12 | 132796094 | ||
| chr12:132801854
|
C | T | 16 | a0001c0001a0001c0011a0001c0018others(13): Show | 127 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(124): Show |
synonymous_variant | LOW | c.1713G>A | p.Leu571Leu | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/24 | 1963/8938 | 1713/4497 | 571/1498 | chr12 | 132801854 | ||
| chr12:132804840
|
C | T | 1 | a0001c0011 | 2 | NA18952.hp1 NA18991.hp1 |
synonymous_variant | LOW | c.1473G>A | p.Leu491Leu | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/24 | 1723/8938 | 1473/4497 | 491/1498 | chr12 | 132804840 | ||
| chr12:132804909
|
C | T | 1 | a0001c0023 | 1 | HG02155.hp2 | synonymous_variant | LOW | c.1404G>A | p.Ser468Ser | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/24 | 1654/8938 | 1404/4497 | 468/1498 | chr12 | 132804909 | ||
| chr12:132808223
|
G | A | 1 | a0001c0034 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.846C>T | p.Ser282Ser | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 5/24 | 1096/8938 | 846/4497 | 282/1498 | chr12 | 132808223 | ||
| chr12:132808301
|
C | T | 1 | a0003c0008 | 8 | HG00544.hp1 NA18939.hp1 NA18946.hp2 others(5): Show |
synonymous_variant | LOW | c.768G>A | p.Ala256Ala | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 5/24 | 1018/8938 | 768/4497 | 256/1498 | chr12 | 132808301 | ||
| chr12:132813412
|
T | C | 3 | a0004c0005a0004c0037a0007c0016 | 17 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(14): Show |
synonymous_variant | LOW | c.414A>G | p.Thr138Thr | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/24 | 664/8938 | 414/4497 | 138/1498 | chr12 | 132813412 | ||
| chr12:132816709
|
C | T | 1 | a0001c0018 | 1 | HG02132.hp2 | synonymous_variant | LOW | c.237G>A | p.Pro79Pro | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/24 | 487/8938 | 237/4497 | 79/1498 | chr12 | 132816709 | ||
| chr12:132816787
|
C | G | 1 | a0010c0039 | 1 | NA19005.hp1 | synonymous_variant | LOW | c.159G>C | p.Thr53Thr | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/24 | 409/8938 | 159/4497 | 53/1498 | chr12 | 132816787 | ||
| chr12:132816793
|
T | A | 1 | a0023c0040 | 1 | NA18939.hp2 | synonymous_variant | LOW | c.153A>T | p.Ala51Ala | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/24 | 403/8938 | 153/4497 | 51/1498 | chr12 | 132816793 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:132769015
|
A | G | 2 | a0001c0003t0040a0001c0003t0045 | 2 | HG01106.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4090T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 4090 | chr12 | 132769015 | |||||
| chr12:132769170
|
C | T | 1 | a0012c0019t0038 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3935G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 3935 | chr12 | 132769170 | |||||
| chr12:132769223
|
C | G | 1 | a0001c0001t0069 | 1 | NA19066.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3882G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 3882 | chr12 | 132769223 | |||||
| chr12:132769223
|
C | T | 14 | a0001c0001t0004a0001c0003t0004a0001c0003t0011others(11): Show | 28 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*3882G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 3882 | chr12 | 132769223 | |||||
| chr12:132769226
|
CACTCA | C | 12 | a0001c0003t0039a0002c0002t0007a0003c0004t0007others(9): Show | 25 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*3874_*3878delTGAG others(1): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 3874 | chr12 | 132769226 | |||||
| chr12:132769270
|
G | C | 2 | a0001c0018t0019a0014c0020t0019 | 2 | HG02132.hp2 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3835C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 3835 | chr12 | 132769270 | |||||
| chr12:132769271
|
A | G | 3 | a0001c0003t0009a0001c0003t0079a0002c0013t0009 | 8 | HG02145.hp2 HG02258.hp2 HG02559.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3834T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 3834 | chr12 | 132769271 | |||||
| chr12:132769456
|
G | A | 2 | a0009c0015t0078a0009c0015t0080 | 2 | HG02818.hp2 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3649C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 3649 | chr12 | 132769456 | |||||
| chr12:132769536
|
G | T | 1 | a0006c0010t0047 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3569C>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 3569 | chr12 | 132769536 | |||||
| chr12:132769558
|
C | T | 1 | a0007c0016t0020 | 2 | HG03491.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3547G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 3547 | chr12 | 132769558 | |||||
| chr12:132769585
|
C | T | 24 | a0001c0001t0001a0001c0001t0010a0001c0001t0025others(21): Show | 82 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*3520G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 3520 | chr12 | 132769585 | |||||
| chr12:132769586
|
G | A | 1 | a0001c0003t0048 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3519C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 3519 | chr12 | 132769586 | |||||
| chr12:132769626
|
A | G | 105 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(102): Show | 267 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(264): Show |
3_prime_UTR_variant | MODIFIER | c.*3479T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 3479 | chr12 | 132769626 | |||||
| chr12:132769640
|
T | C | 1 | a0001c0003t0041 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3465A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 3465 | chr12 | 132769640 | |||||
| chr12:132769899
|
T | C | 2 | a0009c0015t0078a0009c0015t0080 | 2 | HG02818.hp2 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3206A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 3206 | chr12 | 132769899 | |||||
| chr12:132770053
|
G | A | 28 | a0001c0001t0001a0001c0001t0010a0001c0001t0024others(25): Show | 92 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*3052C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 3052 | chr12 | 132770053 | |||||
| chr12:132770226
|
C | G | 1 | a0002c0002t0057 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2879G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 2879 | chr12 | 132770226 | |||||
| chr12:132770232
|
CA | C | 56 | a0001c0001t0002a0001c0001t0003a0001c0001t0017others(53): Show | 139 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*2872delT | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 2872 | chr12 | 132770232 | |||||
| chr12:132770232
|
CAA | C | 44 | a0001c0001t0001a0001c0001t0004a0001c0001t0010others(41): Show | 123 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*2871_*2872delTT | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 2871 | chr12 | 132770232 | |||||
| chr12:132770284
|
AAGGAAGT others(44): Show |
A | 2 | a0001c0018t0019a0014c0020t0019 | 2 | HG02132.hp2 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2770_*2820delCGGC others(47): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 2770 | chr12 | 132770284 | |||||
| chr12:132770296
|
G | A | 2 | a0009c0015t0078a0009c0015t0080 | 2 | HG02818.hp2 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2809C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 2809 | chr12 | 132770296 | |||||
| chr12:132770336
|
T | C | 2 | a0001c0018t0019a0014c0020t0019 | 2 | HG02132.hp2 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2769A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 2769 | chr12 | 132770336 | |||||
| chr12:132770581
|
AAGG | A | 57 | a0001c0001t0001a0001c0001t0004a0001c0001t0010others(54): Show | 139 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*2521_*2523delCCT | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 2521 | chr12 | 132770581 | |||||
| chr12:132770633
|
A | T | 13 | a0001c0001t0004a0001c0003t0004a0001c0003t0011others(10): Show | 27 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*2472T>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 2472 | chr12 | 132770633 | |||||
| chr12:132770688
|
G | T | 2 | a0001c0018t0019a0014c0020t0019 | 2 | HG02132.hp2 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2417C>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 2417 | chr12 | 132770688 | |||||
| chr12:132770793
|
C | T | 1 | a0015c0021t0068 | 1 | NA18964.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2312G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 2312 | chr12 | 132770793 | |||||
| chr12:132770876
|
C | G | 1 | a0005c0006t0043 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2229G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 2229 | chr12 | 132770876 | |||||
| chr12:132770924
|
C | T | 1 | a0002c0007t0076 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2181G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 2181 | chr12 | 132770924 | |||||
| chr12:132770936
|
G | A | 13 | a0001c0001t0004a0001c0003t0004a0001c0003t0011others(10): Show | 27 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*2169C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 2169 | chr12 | 132770936 | |||||
| chr12:132771013
|
T | C | 1 | a0001c0001t0071 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2092A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 2092 | chr12 | 132771013 | |||||
| chr12:132771073
|
T | C | 2 | a0009c0015t0078a0009c0015t0080 | 2 | HG02818.hp2 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2032A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 2032 | chr12 | 132771073 | |||||
| chr12:132771300
|
C | T | 10 | a0001c0001t0030a0005c0006t0014a0005c0006t0018others(7): Show | 13 | HG02055.hp2 HG02486.hp2 HG02559.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1805G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 1805 | chr12 | 132771300 | |||||
| chr12:132771301
|
G | A | 1 | a0001c0001t0072 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1804C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 1804 | chr12 | 132771301 | |||||
| chr12:132771413
|
T | G | 1 | a0001c0001t0055 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1692A>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 1692 | chr12 | 132771413 | |||||
| chr12:132771414
|
T | C | 2 | a0009c0015t0078a0009c0015t0080 | 2 | HG02818.hp2 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1691A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 1691 | chr12 | 132771414 | |||||
| chr12:132771650
|
A | G | 8 | a0001c0001t0017a0001c0001t0026a0001c0001t0027others(5): Show | 9 | HG01993.hp2 HG02615.hp2 HG02818.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1455T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 1455 | chr12 | 132771650 | |||||
| chr12:132771762
|
T | C | 12 | a0001c0001t0030a0005c0006t0014a0005c0006t0018others(9): Show | 15 | HG02055.hp2 HG02486.hp2 HG02559.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1343A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 1343 | chr12 | 132771762 | |||||
| chr12:132771777
|
C | T | 1 | a0002c0002t0050 | 1 | NA18975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1328G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 1328 | chr12 | 132771777 | |||||
| chr12:132771791
|
A | G | 2 | a0009c0015t0078a0009c0015t0080 | 2 | HG02818.hp2 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1314T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 1314 | chr12 | 132771791 | |||||
| chr12:132771823
|
C | T | 1 | a0001c0001t0037 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1282G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 1282 | chr12 | 132771823 | |||||
| chr12:132771846
|
C | G | 1 | a0018c0029t0061 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1259G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 1259 | chr12 | 132771846 | |||||
| chr12:132771847
|
TCTCCTC | T | 15 | a0002c0002t0007a0003c0004t0007a0003c0004t0008others(12): Show | 40 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1252_*1257delGAGG others(2): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 1252 | chr12 | 132771847 | |||||
| chr12:132771886
|
C | A | 2 | a0001c0009t0049a0001c0009t0058 | 2 | HG01515.hp1 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1219G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 1219 | chr12 | 132771886 | |||||
| chr12:132771913
|
C | T | 25 | a0001c0001t0004a0001c0001t0030a0001c0003t0004others(22): Show | 42 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1192G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 1192 | chr12 | 132771913 | |||||
| chr12:132771987
|
C | T | 11 | a0001c0001t0003a0001c0001t0032a0001c0001t0033others(8): Show | 30 | HG00280.hp1 HG00438.hp2 HG00738.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1118G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 1118 | chr12 | 132771987 | |||||
| chr12:132772265
|
C | T | 3 | a0002c0002t0015a0002c0002t0016a0002c0002t0034 | 5 | HG02074.hp2 HG02132.hp1 NA19060.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*840G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 840 | chr12 | 132772265 | |||||
| chr12:132772270
|
G | A | 1 | a0008c0014t0021 | 2 | HG02602.hp2 HG03017.hp1 |
3_prime_UTR_variant | MODIFIER | c.*835C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 835 | chr12 | 132772270 | |||||
| chr12:132772389
|
CA | C | 15 | a0002c0002t0007a0003c0004t0007a0003c0004t0008others(12): Show | 40 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*715delT | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 715 | chr12 | 132772389 | |||||
| chr12:132772412
|
C | T | 1 | a0002c0002t0052 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*693G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 693 | chr12 | 132772412 | |||||
| chr12:132772491
|
C | T | 2 | a0002c0002t0050a0002c0002t0051 | 2 | NA18612.hp1 NA18975.hp2 |
3_prime_UTR_variant | MODIFIER | c.*614G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 614 | chr12 | 132772491 | |||||
| chr12:132772543
|
C | CA | 30 | a0001c0001t0002a0001c0001t0003a0001c0001t0026others(27): Show | 102 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*561dupT | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 561 | chr12 | 132772543 | |||||
| chr12:132772543
|
C | CAA | 12 | a0001c0001t0017a0001c0001t0030a0001c0001t0059others(9): Show | 15 | HG01978.hp2 HG02055.hp1 HG02258.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*560_*561dupTT | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 561 | chr12 | 132772543 | |||||
| chr12:132772543
|
C | CAAA | 14 | a0001c0001t0029a0002c0002t0007a0003c0004t0007others(11): Show | 28 | HG00280.hp2 HG00544.hp2 HG01169.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*559_*561dupTTT | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 561 | chr12 | 132772543 | |||||
| chr12:132772543
|
C | CAAAA | 20 | a0001c0001t0004a0001c0003t0004a0001c0003t0039others(17): Show | 45 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*558_*561dupTTTT | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 561 | chr12 | 132772543 | |||||
| chr12:132772543
|
C | CAAAAA | 4 | a0001c0003t0011a0001c0003t0045a0002c0012t0011others(1): Show | 7 | HG01106.hp2 HG01256.hp1 HG01258.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*557_*561dupTTTTT | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 561 | chr12 | 132772543 | |||||
| chr12:132772543
|
CAA | C | 4 | a0001c0001t0010a0001c0001t0073a0001c0011t0074others(1): Show | 7 | HG01981.hp2 HG02056.hp1 HG02280.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*560_*561delTT | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 560 | chr12 | 132772543 | |||||
| chr12:132772543
|
CAAA | C | 21 | a0001c0001t0001a0001c0001t0024a0001c0001t0025others(18): Show | 77 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*559_*561delTTT | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 559 | chr12 | 132772543 | |||||
| chr12:132772562
|
A | C | 2 | a0001c0001t0066a0006c0010t0046 | 2 | HG01891.hp1 NA18950.hp2 |
3_prime_UTR_variant | MODIFIER | c.*543T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 543 | chr12 | 132772562 | |||||
| chr12:132772589
|
G | A | 63 | a0001c0001t0002a0001c0001t0003a0001c0001t0017others(60): Show | 169 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*516C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 516 | chr12 | 132772589 | |||||
| chr12:132772720
|
C | T | 1 | a0001c0001t0037 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*385G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 385 | chr12 | 132772720 | |||||
| chr12:132772739
|
C | T | 10 | a0001c0001t0017a0001c0001t0026a0001c0001t0027others(7): Show | 16 | HG00280.hp2 HG00544.hp2 HG01169.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*366G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 366 | chr12 | 132772739 | |||||
| chr12:132772765
|
T | C | 4 | a0005c0006t0014a0005c0006t0062a0005c0006t0063others(1): Show | 6 | HG02055.hp2 HG02559.hp2 HG02965.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*340A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 340 | chr12 | 132772765 | |||||
| chr12:132772828
|
G | C | 1 | a0005c0006t0065 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*277C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 277 | chr12 | 132772828 | |||||
| chr12:132772858
|
G | A | 1 | a0005c0006t0065 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*247C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 247 | chr12 | 132772858 | |||||
| chr12:132773034
|
C | G | 88 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(85): Show | 211 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(208): Show |
3_prime_UTR_variant | MODIFIER | c.*71G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 71 | chr12 | 132773034 | |||||
| chr12:132773037
|
A | G | 3 | a0002c0002t0015a0002c0002t0016a0002c0002t0034 | 5 | HG02074.hp2 HG02132.hp1 NA19060.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*68T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 24/24 | 68 | chr12 | 132773037 | |||||
| chr12:132822140
|
C | T | 1 | a0001c0001t0033 | 1 | NA18998.hp2 | 5_prime_UTR_variant | MODIFIER | c.-12G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/24 | 12 | chr12 | 132822140 | |||||
| chr12:132822170
|
A | G | 7 | a0001c0001t0026a0001c0001t0027a0001c0001t0028others(4): Show | 7 | HG01175.hp2 HG02818.hp1 HG02886.hp2 others(4): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-42T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/24 | chr12 | 132822170 | ||||||
| chr12:132828474
|
AAGGGCCA others(335): Show |
A | 1 | a0005c0006t0081 | 1 | HG02486.hp2 | splice_donor_variant&splice_region_variant&5_prime_UTR_variant&intron_variant | HIGH | c.-197_-184+328del | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/24 | 6347 | chr12 | 132828474 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:132773307
|
A | G | 214 | a0001c0001t0002g0121a0001c0001t0003g0006a0001c0001t0003g0007others(211): Show | 214 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.4308-13T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 23/23 | chr12 | 132773307 | ||||||
| chr12:132773325
|
G | C | 1 | a0014c0020t0019g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4308-31C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 23/23 | chr12 | 132773325 | ||||||
| chr12:132773348
|
C | G | 2 | a0005c0006t0043g0004a0005c0006t0044g0005 | 2 | HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.4308-54G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 23/23 | chr12 | 132773348 | ||||||
| chr12:132773404
|
G | A | 1 | a0001c0003t0041g0165 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.4308-110C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 23/23 | chr12 | 132773404 | ||||||
| chr12:132773469
|
G | A | 15 | a0004c0005t0005g0049a0004c0005t0005g0101a0004c0005t0005g0247others(12): Show | 15 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.4308-175C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 23/23 | chr12 | 132773469 | ||||||
| chr12:132773479
|
C | T | 2 | a0001c0018t0019g0132a0014c0020t0019g0003 | 2 | HG02132.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.4308-185G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 23/23 | chr12 | 132773479 | ||||||
| chr12:132773598
|
T | C | 1 | a0018c0029t0061g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4308-304A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 23/23 | chr12 | 132773598 | ||||||
| chr12:132773660
|
AG | A | 15 | a0004c0005t0005g0049a0004c0005t0005g0101a0004c0005t0005g0247others(12): Show | 15 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.4308-367delC | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 23/23 | chr12 | 132773660 | ||||||
| chr12:132773721
|
C | T | 1 | a0002c0002t0002g0242 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.4308-427G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 23/23 | chr12 | 132773721 | ||||||
| chr12:132773725
|
CCTTTATA others(33): Show |
C | 1 | a0001c0001t0025g0040 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4307+392_4307+431d others(42): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 23/23 | chr12 | 132773725 | ||||||
| chr12:132773777
|
C | A | 1 | a0018c0029t0061g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4307+380G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 23/23 | chr12 | 132773777 | ||||||
| chr12:132773791
|
TGAGTCCC others(33): Show |
T | 1 | a0001c0003t0004g0155 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.4307+326_4307+365d others(42): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 23/23 | chr12 | 132773791 | ||||||
| chr12:132773797
|
CCCCTCCC others(69): Show |
C | 2 | a0001c0018t0019g0132a0014c0020t0019g0003 | 2 | HG02132.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.4307+284_4307+359d others(78): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 23/23 | chr12 | 132773797 | ||||||
| chr12:132774106
|
G | A | 2 | a0009c0015t0078g0066a0009c0015t0080g0065 | 2 | HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.4307+51C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 23/23 | chr12 | 132774106 | ||||||
| chr12:132774143
|
G | C | 2 | a0006c0010t0006g0011a0006c0010t0006g0130 | 2 | HG02622.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.4307+14C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 23/23 | chr12 | 132774143 | ||||||
| chr12:132774366
|
C | T | 2 | a0001c0001t0017g0001a0001c0001t0029g0304 | 2 | NA19240.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.4144-46G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 22/23 | chr12 | 132774366 | ||||||
| chr12:132774442
|
C | T | 2 | a0001c0001t0003g0116a0001c0001t0003g0122 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.4144-122G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 22/23 | chr12 | 132774442 | ||||||
| chr12:132774443
|
C | T | 1 | a0021c0031t0006g0169 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.4144-123G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 22/23 | chr12 | 132774443 | ||||||
| chr12:132774444
|
G | A | 85 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(82): Show | 85 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.4144-124C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 22/23 | chr12 | 132774444 | ||||||
| chr12:132774654
|
G | T | 286 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(283): Show | 286 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.4144-334C>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 22/23 | chr12 | 132774654 | ||||||
| chr12:132775947
|
C | T | 79 | a0001c0001t0002g0121a0001c0003t0002g0196a0001c0009t0002g0181others(76): Show | 79 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.3979-642G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132775947 | ||||||
| chr12:132776052
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3978+582G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776052 | ||||||
| chr12:132776062
|
C | T | 3 | a0001c0001t0001g0069a0001c0001t0001g0070a0005c0006t0001g0021 | 3 | HG02630.hp1 HG02717.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3978+572G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776062 | ||||||
| chr12:132776064
|
G | A | 2 | a0007c0016t0020g0253a0007c0016t0020g0254 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.3978+570C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776064 | ||||||
| chr12:132776084
|
G | GGCCGCAT | 3 | a0003c0004t0007g0269a0003c0004t0013g0268a0003c0004t0022g0277 | 3 | HG00408.hp2 NA18947.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.3978+543_3978+549d others(9): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776084 | ||||||
| chr12:132776105
|
G | C | 29 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0008others(26): Show | 29 | HG00280.hp1 HG00438.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.3978+529C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776105 | ||||||
| chr12:132776116
|
A | C | 69 | a0001c0001t0004g0079a0001c0001t0004g0126a0001c0001t0004g0127others(66): Show | 69 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.3978+518T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776116 | ||||||
| chr12:132776123
|
GTGCTCCC others(72): Show |
G | 158 | a0001c0001t0001g0036a0001c0001t0002g0121a0001c0001t0004g0079others(155): Show | 158 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.3978+432_3978+510d others(81): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776123 | ||||||
| chr12:132776188
|
C | CTCCTTCC others(472): Show |
1 | a0001c0001t0029g0304 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3978+445_3978+446i others(481): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776188 | ||||||
| chr12:132776196
|
T | TG | 112 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(109): Show | 112 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.3978+437_3978+438i others(3): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776196 | ||||||
| chr12:132776216
|
G | GCCCAGCG others(870): Show |
1 | a0018c0029t0061g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3978+417_3978+418i others(879): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776216 | ||||||
| chr12:132776217
|
T | C | 107 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(104): Show | 107 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.3978+417A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776217 | ||||||
| chr12:132776223
|
A | ACCTCATA others(312): Show |
13 | a0001c0001t0030g0303a0005c0006t0014g0018a0005c0006t0014g0019others(10): Show | 13 | HG02055.hp2 HG02486.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.3978+410_3978+411i others(321): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776223 | ||||||
| chr12:132776223
|
A | G | 113 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(110): Show | 113 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.3978+411T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776223 | ||||||
| chr12:132776229
|
T | G | 107 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(104): Show | 107 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.3978+405A>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776229 | ||||||
| chr12:132776231
|
C | CACAGGTA others(630): Show |
4 | a0001c0001t0017g0015a0001c0001t0026g0302a0001c0001t0027g0306others(1): Show | 4 | HG01993.hp2 HG02615.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.3978+402_3978+403i others(639): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776231 | ||||||
| chr12:132776231
|
C | CACAGGTA others(630): Show |
2 | a0001c0001t0017g0001a0001c0001t0028g0305 | 2 | HG02818.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3978+402_3978+403i others(639): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776231 | ||||||
| chr12:132776231
|
C | T | 107 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(104): Show | 107 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.3978+403G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776231 | ||||||
| chr12:132776254
|
G | A | 2 | a0001c0018t0019g0132a0014c0020t0019g0003 | 2 | HG02132.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.3978+380C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776254 | ||||||
| chr12:132776297
|
C | T | 1 | a0001c0001t0059g0120 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3978+337G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776297 | ||||||
| chr12:132776309
|
G | T | 7 | a0001c0001t0017g0001a0001c0001t0017g0015a0001c0001t0026g0302others(4): Show | 7 | HG01993.hp2 HG02615.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.3978+325C>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776309 | ||||||
| chr12:132776311
|
T | C | 7 | a0001c0001t0017g0001a0001c0001t0017g0015a0001c0001t0026g0302others(4): Show | 7 | HG01993.hp2 HG02615.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.3978+323A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776311 | ||||||
| chr12:132776321
|
T | C | 77 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(74): Show | 77 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.3978+313A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776321 | ||||||
| chr12:132776321
|
TGCAGCAG others(70): Show |
T | 2 | a0009c0015t0078g0066a0009c0015t0080g0065 | 2 | HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.3978+236_3978+312d others(79): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776321 | ||||||
| chr12:132776331
|
GCTGTAGC | G | 27 | a0001c0001t0004g0079a0001c0001t0004g0126a0001c0001t0004g0127others(24): Show | 27 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.3978+296_3978+302d others(9): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776331 | ||||||
| chr12:132776338
|
CCCCTCCA others(148): Show |
C | 1 | a0001c0011t0074g0067 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3978+141_3978+295d others(2): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776338 | ||||||
| chr12:132776347
|
CTCCTTCC others(149): Show |
C | 1 | a0020c0030t0012g0228 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.3978+131_3978+286d others(2): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776347 | ||||||
| chr12:132776352
|
T | A | 7 | a0002c0007t0001g0048a0002c0007t0001g0058a0002c0007t0001g0059others(4): Show | 7 | HG00609.hp2 HG00673.hp2 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.3978+282A>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776352 | ||||||
| chr12:132776355
|
T | TG | 15 | a0001c0001t0001g0036a0001c0001t0017g0001a0001c0001t0017g0015others(12): Show | 15 | HG00609.hp2 HG00673.hp2 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.3978+278_3978+279i others(3): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776355 | ||||||
| chr12:132776356
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3978+278G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776356 | ||||||
| chr12:132776375
|
A | G | 15 | a0001c0001t0001g0036a0001c0001t0017g0001a0001c0001t0017g0015others(12): Show | 15 | HG00609.hp2 HG00673.hp2 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.3978+259T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776375 | ||||||
| chr12:132776375
|
ACCCAGAG others(149): Show |
A | 76 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(73): Show | 76 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.3978+103_3978+258d others(2): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776375 | ||||||
| chr12:132776381
|
A | C | 28 | a0001c0001t0001g0036a0001c0001t0017g0001a0001c0001t0017g0015others(25): Show | 28 | HG00609.hp2 HG00673.hp2 HG01993.hp2 others(25): Show |
intron_variant | MODIFIER | c.3978+253T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776381 | ||||||
| chr12:132776386
|
C | CAG | 15 | a0001c0001t0001g0036a0001c0001t0017g0001a0001c0001t0017g0015others(12): Show | 15 | HG00609.hp2 HG00673.hp2 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.3978+247_3978+248i others(4): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776386 | ||||||
| chr12:132776386
|
C | CATACACA others(234): Show |
13 | a0001c0001t0030g0303a0005c0006t0014g0018a0005c0006t0014g0019others(10): Show | 13 | HG02055.hp2 HG02486.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.3978+247_3978+248i others(243): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776386 | ||||||
| chr12:132776388
|
C | T | 28 | a0001c0001t0001g0036a0001c0001t0017g0001a0001c0001t0017g0015others(25): Show | 28 | HG00609.hp2 HG00673.hp2 HG01993.hp2 others(25): Show |
intron_variant | MODIFIER | c.3978+246G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776388 | ||||||
| chr12:132776398
|
C | T | 46 | a0001c0001t0004g0079a0001c0001t0004g0126a0001c0001t0004g0127others(43): Show | 46 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.3978+236G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776398 | ||||||
| chr12:132776452
|
A | ACCCAGAG others(540): Show |
28 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0008others(25): Show | 28 | HG00280.hp1 HG00438.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.3978+181_3978+182i others(549): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776452 | ||||||
| chr12:132776452
|
A | G | 1 | a0018c0029t0061g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3978+182T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776452 | ||||||
| chr12:132776452
|
ACCCAGCG others(72): Show |
A | 1 | a0001c0009t0002g0181 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3978+103_3978+181d others(81): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776452 | ||||||
| chr12:132776458
|
C | A | 21 | a0001c0001t0003g0110a0001c0001t0017g0001a0001c0001t0017g0015others(18): Show | 21 | HG01993.hp2 HG02055.hp2 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.3978+176G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776458 | ||||||
| chr12:132776462
|
TCA | T | 21 | a0001c0001t0003g0110a0001c0001t0017g0001a0001c0001t0017g0015others(18): Show | 21 | HG01993.hp2 HG02055.hp2 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.3978+170_3978+171d others(4): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776462 | ||||||
| chr12:132776464
|
A | ATACACAG others(629): Show |
1 | a0018c0029t0061g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3978+169_3978+170i others(638): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776464 | ||||||
| chr12:132776478
|
G | A | 42 | a0002c0002t0007g0236a0003c0004t0007g0266a0003c0004t0007g0269others(39): Show | 42 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(39): Show |
intron_variant | MODIFIER | c.3978+156C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776478 | ||||||
| chr12:132776503
|
T | C | 79 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0008others(76): Show | 79 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.3978+131A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776503 | ||||||
| chr12:132776503
|
TTCCTTCC others(72): Show |
T | 127 | a0001c0001t0001g0036a0001c0001t0002g0121a0001c0003t0002g0196others(124): Show | 127 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.3978+52_3978+130de others(80): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776503 | ||||||
| chr12:132776531
|
G | A | 77 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0008others(74): Show | 77 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.3978+103C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776531 | ||||||
| chr12:132776544
|
C | G | 3 | a0009c0015t0078g0066a0009c0015t0080g0065a0020c0030t0012g0228 | 3 | HG01978.hp2 HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.3978+90G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776544 | ||||||
| chr12:132776546
|
C | T | 3 | a0009c0015t0078g0066a0009c0015t0080g0065a0020c0030t0012g0228 | 3 | HG01978.hp2 HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.3978+88G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776546 | ||||||
| chr12:132776556
|
C | T | 2 | a0009c0015t0078g0066a0009c0015t0080g0065 | 2 | HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.3978+78G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776556 | ||||||
| chr12:132776557
|
G | A | 41 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0008others(38): Show | 41 | HG00280.hp1 HG00438.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.3978+77C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776557 | ||||||
| chr12:132776582
|
C | CTCCTTCC others(463): Show |
1 | a0001c0001t0003g0110 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3978+51_3978+52ins others(470): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776582 | ||||||
| chr12:132776582
|
C | T | 156 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(153): Show | 156 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.3978+52G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776582 | ||||||
| chr12:132776604
|
G | A | 20 | a0001c0001t0017g0001a0001c0001t0017g0015a0001c0001t0026g0302others(17): Show | 20 | HG01993.hp2 HG02055.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.3978+30C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 21/23 | chr12 | 132776604 | ||||||
| chr12:132776953
|
G | A | 19 | a0001c0001t0017g0001a0001c0001t0017g0015a0001c0001t0026g0302others(16): Show | 19 | HG01993.hp2 HG02055.hp2 HG02486.hp2 others(16): Show |
splice_region_variant&intron_variant | LOW | c.3855+5C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 20/23 | chr12 | 132776953 | ||||||
| chr12:132777096
|
G | A | 7 | a0001c0001t0017g0001a0001c0001t0017g0015a0001c0001t0026g0302others(4): Show | 7 | HG01993.hp2 HG02615.hp2 HG02818.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.3723-6C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 19/23 | chr12 | 132777096 | ||||||
| chr12:132777098
|
A | G | 6 | a0002c0002t0002g0187a0002c0002t0002g0190a0002c0002t0002g0191others(3): Show | 6 | HG02055.hp1 HG02109.hp1 HG02258.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.3723-8T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 19/23 | chr12 | 132777098 | ||||||
| chr12:132777105
|
C | G | 2 | a0001c0018t0019g0132a0014c0020t0019g0003 | 2 | HG02132.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.3723-15G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 19/23 | chr12 | 132777105 | ||||||
| chr12:132777175
|
AGGCGTTC others(7): Show |
A | 1 | a0002c0002t0034g0227 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.3723-99_3723-86del others(14): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 19/23 | chr12 | 132777175 | ||||||
| chr12:132777183
|
G | C | 7 | a0001c0003t0004g0144a0001c0003t0004g0145a0001c0003t0004g0158others(4): Show | 7 | HG02155.hp2 NA18956.hp1 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.3723-93C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 19/23 | chr12 | 132777183 | ||||||
| chr12:132777388
|
AC | A | 107 | a0001c0001t0002g0121a0001c0001t0003g0006a0001c0001t0003g0007others(104): Show | 107 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.3722+277delG | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 19/23 | chr12 | 132777388 | ||||||
| chr12:132777407
|
G | A | 1 | a0001c0003t0004g0166 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.3722+259C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 19/23 | chr12 | 132777407 | ||||||
| chr12:132777470
|
G | C | 4 | a0001c0018t0019g0132a0009c0015t0078g0066a0009c0015t0080g0065others(1): Show | 4 | HG02132.hp2 HG02717.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.3722+196C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 19/23 | chr12 | 132777470 | ||||||
| chr12:132777617
|
C | A | 21 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0008others(18): Show | 21 | HG00280.hp1 HG00438.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.3722+49G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 19/23 | chr12 | 132777617 | ||||||
| chr12:132777649
|
G | A | 4 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0008others(1): Show | 4 | HG00438.hp2 HG02129.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.3722+17C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 19/23 | chr12 | 132777649 | ||||||
| chr12:132777867
|
C | T | 63 | a0001c0001t0002g0121a0001c0003t0002g0196a0001c0009t0002g0199others(60): Show | 63 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.3583-62G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132777867 | ||||||
| chr12:132777874
|
A | AG | 6 | a0001c0001t0001g0096a0002c0002t0034g0227a0003c0004t0001g0279others(3): Show | 6 | HG01978.hp2 HG04115.hp1 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.3583-70dupC | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132777874 | ||||||
| chr12:132777884
|
T | C | 249 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(246): Show | 249 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.3583-79A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132777884 | ||||||
| chr12:132777893
|
G | A | 2 | a0001c0009t0049g0202a0001c0009t0058g0200 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.3583-88C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132777893 | ||||||
| chr12:132777899
|
G | A | 78 | a0001c0001t0002g0121a0001c0003t0002g0196a0001c0009t0002g0199others(75): Show | 78 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.3583-94C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132777899 | ||||||
| chr12:132778340
|
C | T | 1 | a0001c0001t0029g0304 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3583-535G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132778340 | ||||||
| chr12:132778692
|
T | C | 1 | a0002c0002t0002g0208 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3583-887A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132778692 | ||||||
| chr12:132778790
|
G | A | 1 | a0018c0029t0061g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3583-985C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132778790 | ||||||
| chr12:132778824
|
G | A | 1 | a0001c0001t0017g0015 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3583-1019C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132778824 | ||||||
| chr12:132778888
|
C | T | 26 | a0001c0001t0004g0079a0001c0001t0004g0126a0001c0001t0004g0127others(23): Show | 26 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.3583-1083G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132778888 | ||||||
| chr12:132778893
|
G | GA | 46 | a0001c0001t0001g0036a0001c0001t0001g0051a0001c0001t0001g0091others(43): Show | 46 | HG00280.hp1 HG00438.hp2 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.3583-1089dupT | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132778893 | ||||||
| chr12:132778906
|
C | A | 3 | a0001c0001t0017g0001a0001c0001t0028g0305a0001c0001t0029g0304 | 3 | HG02818.hp1 NA19240.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3583-1101G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132778906 | ||||||
| chr12:132778908
|
G | C | 3 | a0001c0001t0017g0001a0001c0001t0028g0305a0001c0001t0029g0304 | 3 | HG02818.hp1 NA19240.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3583-1103C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132778908 | ||||||
| chr12:132778909
|
A | G | 3 | a0001c0001t0017g0001a0001c0001t0028g0305a0001c0001t0029g0304 | 3 | HG02818.hp1 NA19240.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3583-1104T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132778909 | ||||||
| chr12:132778934
|
C | T | 1 | a0001c0001t0073g0041 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3583-1129G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132778934 | ||||||
| chr12:132778972
|
A | C | 1 | a0001c0024t0002g0100 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3583-1167T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132778972 | ||||||
| chr12:132778984
|
G | A | 2 | a0001c0001t0026g0302a0001c0001t0027g0306 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3583-1179C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132778984 | ||||||
| chr12:132778986
|
C | A | 2 | a0001c0009t0002g0201a0001c0009t0002g0219 | 2 | HG03654.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.3583-1181G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132778986 | ||||||
| chr12:132778997
|
GC | G | 27 | a0001c0001t0004g0079a0001c0001t0004g0126a0001c0001t0004g0127others(24): Show | 27 | HG00438.hp1 HG00544.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.3583-1193delG | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132778997 | ||||||
| chr12:132779127
|
C | T | 1 | a0020c0030t0012g0228 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.3583-1322G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132779127 | ||||||
| chr12:132779175
|
G | A | 1 | a0013c0035t0035g0262 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3583-1370C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132779175 | ||||||
| chr12:132779183
|
G | A | 1 | a0001c0003t0041g0165 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.3583-1378C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132779183 | ||||||
| chr12:132779189
|
C | A | 1 | a0021c0031t0006g0169 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3583-1384G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132779189 | ||||||
| chr12:132779220
|
C | T | 81 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(78): Show | 81 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.3583-1415G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132779220 | ||||||
| chr12:132779236
|
C | T | 263 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(260): Show | 263 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.3583-1431G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132779236 | ||||||
| chr12:132779393
|
A | C | 1 | a0002c0002t0002g0207 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3582+1405T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132779393 | ||||||
| chr12:132779476
|
A | G | 2 | a0001c0001t0026g0302a0001c0001t0027g0306 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3582+1322T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132779476 | ||||||
| chr12:132779720
|
CCACAGCC others(263): Show |
C | 1 | a0003c0008t0007g0275 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3582+808_3582+1077 others(3): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132779720 | ||||||
| chr12:132779727
|
C | T | 1 | a0013c0035t0035g0262 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3582+1071G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132779727 | ||||||
| chr12:132779738
|
C | T | 1 | a0005c0006t0044g0005 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3582+1060G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132779738 | ||||||
| chr12:132779766
|
T | C | 2 | a0001c0001t0026g0302a0001c0001t0027g0306 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3582+1032A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132779766 | ||||||
| chr12:132779766
|
T | TGGACACC others(263): Show |
1 | a0001c0003t0004g0166 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.3582+762_3582+1031 others(273): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132779766 | ||||||
| chr12:132779773
|
CCCCCCCG others(63): Show |
C | 2 | a0001c0001t0026g0302a0001c0001t0027g0306 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3582+955_3582+1024 others(73): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132779773 | ||||||
| chr12:132779779
|
C | T | 2 | a0003c0004t0007g0266a0003c0004t0013g0284 | 2 | HG02027.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.3582+1019G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132779779 | ||||||
| chr12:132779808
|
C | T | 3 | a0005c0006t0018g0023a0005c0006t0018g0102a0005c0006t0081g0308 | 3 | HG02486.hp2 HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3582+990G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132779808 | ||||||
| chr12:132779814
|
T | TGCACACA others(124): Show |
1 | a0001c0001t0075g0128 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3582+983_3582+984i others(133): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132779814 | ||||||
| chr12:132779814
|
TGCACACA others(191): Show |
T | 3 | a0001c0001t0071g0050a0009c0015t0078g0066a0009c0015t0080g0065 | 3 | HG02818.hp2 HG02896.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.3582+786_3582+983d others(2): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132779814 | ||||||
| chr12:132779851
|
G | C | 31 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0008others(28): Show | 31 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.3582+947C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132779851 | ||||||
| chr12:132779852
|
C | T | 3 | a0001c0003t0002g0196a0001c0009t0002g0181a0002c0002t0006g0211 | 3 | HG01074.hp2 HG02129.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.3582+946G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132779852 | ||||||
| chr12:132779853
|
G | A | 6 | a0001c0003t0009g0292a0001c0003t0009g0293a0001c0003t0009g0296others(3): Show | 6 | HG02145.hp2 HG02258.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3582+945C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132779853 | ||||||
| chr12:132779855
|
A | G | 31 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0008others(28): Show | 31 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.3582+943T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132779855 | ||||||
| chr12:132779856
|
CAT | C | 31 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0008others(28): Show | 31 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.3582+940_3582+941d others(4): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132779856 | ||||||
| chr12:132779858
|
TACAC | T | 75 | a0001c0001t0002g0121a0001c0001t0026g0302a0001c0001t0027g0306others(72): Show | 75 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.3582+936_3582+939d others(6): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132779858 | ||||||
| chr12:132779862
|
C | T | 31 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0008others(28): Show | 31 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.3582+936G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132779862 | ||||||
| chr12:132779879
|
CGT | C | 72 | a0001c0001t0002g0121a0001c0009t0002g0199a0001c0009t0002g0201others(69): Show | 72 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.3582+917_3582+918d others(4): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132779879 | ||||||
| chr12:132779906
|
A | G | 1 | a0001c0034t0001g0062 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3582+892T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132779906 | ||||||
| chr12:132779973
|
GCACAGCC others(10): Show |
G | 4 | a0005c0006t0014g0018a0005c0006t0014g0019a0005c0006t0014g0020others(1): Show | 4 | HG02559.hp2 HG03540.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.3582+808_3582+824d others(19): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132779973 | ||||||
| chr12:132780008
|
C | T | 1 | a0001c0003t0001g0151 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.3582+790G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132780008 | ||||||
| chr12:132780009
|
G | A | 6 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(3): Show | 6 | NA18947.hp1 NA18967.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.3582+789C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132780009 | ||||||
| chr12:132780104
|
CGCACAGC others(56): Show |
C | 1 | a0002c0002t0052g0220 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3582+631_3582+693d others(65): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132780104 | ||||||
| chr12:132780117
|
G | A | 2 | a0001c0001t0001g0093a0003c0008t0007g0272 | 2 | HG02074.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.3582+681C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132780117 | ||||||
| chr12:132780119
|
G | A | 1 | a0003c0008t0013g0264 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.3582+679C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132780119 | ||||||
| chr12:132780121
|
GCACACAC others(60): Show |
G | 2 | a0004c0036t0008g0263a0013c0035t0035g0262 | 2 | HG02004.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.3582+610_3582+676d others(69): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132780121 | ||||||
| chr12:132780123
|
A | ACAC | 221 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(218): Show | 221 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.3582+672_3582+674d others(5): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132780123 | ||||||
| chr12:132780127
|
A | C | 1 | a0002c0002t0034g0227 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.3582+671T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132780127 | ||||||
| chr12:132780193
|
CCACACCC others(18): Show |
C | 1 | a0001c0003t0004g0166 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.3582+580_3582+604d others(27): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132780193 | ||||||
| chr12:132780378
|
C | T | 17 | a0001c0001t0001g0052a0001c0001t0003g0008a0001c0001t0025g0040others(14): Show | 17 | HG00438.hp2 HG00544.hp2 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.3582+420G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132780378 | ||||||
| chr12:132780585
|
G | A | 1 | a0002c0002t0016g0221 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.3582+213C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132780585 | ||||||
| chr12:132780645
|
C | G | 1 | a0001c0001t0059g0120 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3582+153G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132780645 | ||||||
| chr12:132780711
|
G | A | 1 | a0002c0002t0002g0198 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3582+87C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 18/23 | chr12 | 132780711 | ||||||
| chr12:132781059
|
CA | C | 89 | a0001c0003t0002g0196a0001c0003t0041g0165a0001c0009t0002g0181others(86): Show | 89 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.3466-146delT | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 17/23 | chr12 | 132781059 | ||||||
| chr12:132781120
|
G | A | 93 | a0001c0001t0073g0041a0001c0003t0002g0196a0001c0003t0041g0165others(90): Show | 93 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.3466-206C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 17/23 | chr12 | 132781120 | ||||||
| chr12:132781161
|
C | T | 1 | a0002c0002t0006g0182 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3466-247G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 17/23 | chr12 | 132781161 | ||||||
| chr12:132781204
|
ACCACCGC others(8): Show |
A | 91 | a0001c0003t0002g0196a0001c0009t0002g0181a0001c0009t0002g0201others(88): Show | 91 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(88): Show |
intron_variant | MODIFIER | c.3466-305_3466-291d others(17): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 17/23 | chr12 | 132781204 | ||||||
| chr12:132781290
|
G | A | 1 | a0002c0002t0002g0217 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3466-376C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 17/23 | chr12 | 132781290 | ||||||
| chr12:132781349
|
G | A | 3 | a0002c0002t0016g0170a0002c0002t0016g0221a0002c0002t0034g0227 | 3 | NA19060.hp2 NA19082.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.3466-435C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 17/23 | chr12 | 132781349 | ||||||
| chr12:132781419
|
C | T | 1 | a0002c0002t0002g0002 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.3466-505G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 17/23 | chr12 | 132781419 | ||||||
| chr12:132781462
|
G | A | 1 | a0001c0001t0001g0029 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3466-548C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 17/23 | chr12 | 132781462 | ||||||
| chr12:132781476
|
T | C | 14 | a0005c0006t0001g0021a0005c0006t0014g0018a0005c0006t0014g0019others(11): Show | 14 | HG02055.hp2 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.3466-562A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 17/23 | chr12 | 132781476 | ||||||
| chr12:132781499
|
G | A | 1 | a0018c0029t0061g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3466-585C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 17/23 | chr12 | 132781499 | ||||||
| chr12:132781567
|
C | A | 27 | a0003c0004t0001g0270a0003c0004t0001g0279a0003c0004t0001g0282others(24): Show | 27 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.3466-653G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 17/23 | chr12 | 132781567 | ||||||
| chr12:132781608
|
T | C | 1 | a0001c0001t0003g0139 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.3465+688A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 17/23 | chr12 | 132781608 | ||||||
| chr12:132781622
|
T | C | 1 | a0001c0001t0001g0029 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3465+674A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 17/23 | chr12 | 132781622 | ||||||
| chr12:132781909
|
TCAACTAA others(14): Show |
T | 5 | a0001c0001t0001g0077a0001c0003t0006g0290a0001c0003t0006g0291others(2): Show | 5 | HG01884.hp1 HG02886.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.3465+366_3465+386d others(23): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 17/23 | chr12 | 132781909 | ||||||
| chr12:132782150
|
C | T | 1 | a0001c0003t0011g0147 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.3465+146G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 17/23 | chr12 | 132782150 | ||||||
| chr12:132782284
|
G | A | 27 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0001g0167others(24): Show | 27 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.3465+12C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 17/23 | chr12 | 132782284 | ||||||
| chr12:132782615
|
G | A | 3 | a0001c0001t0071g0050a0009c0015t0078g0066a0009c0015t0080g0065 | 3 | HG02818.hp2 HG02896.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.3268-122C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 16/23 | chr12 | 132782615 | ||||||
| chr12:132782628
|
G | A | 1 | a0001c0001t0033g0108 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.3268-135C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 16/23 | chr12 | 132782628 | ||||||
| chr12:132782836
|
C | A | 1 | a0017c0022t0001g0025 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.3268-343G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 16/23 | chr12 | 132782836 | ||||||
| chr12:132782875
|
CA | C | 106 | a0001c0001t0002g0121a0001c0001t0003g0006a0001c0001t0003g0007others(103): Show | 106 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.3268-383delT | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 16/23 | chr12 | 132782875 | ||||||
| chr12:132782875
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0051 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.3268-394_3268-383d others(14): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 16/23 | chr12 | 132782875 | ||||||
| chr12:132782888
|
A | G | 1 | a0001c0001t0001g0051 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.3268-395T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 16/23 | chr12 | 132782888 | ||||||
| chr12:132783106
|
A | G | 295 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(292): Show | 295 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.3268-613T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 16/23 | chr12 | 132783106 | ||||||
| chr12:132783211
|
A | AATGGACA others(15): Show |
88 | a0001c0009t0002g0181a0001c0009t0002g0199a0001c0009t0002g0201others(85): Show | 88 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.3268-740_3268-719d others(24): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 16/23 | chr12 | 132783211 | ||||||
| chr12:132783224
|
C | T | 1 | a0011c0017t0008g0267 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.3268-731G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 16/23 | chr12 | 132783224 | ||||||
| chr12:132783248
|
A | C | 88 | a0001c0003t0002g0196a0001c0009t0002g0181a0001c0009t0002g0199others(85): Show | 88 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.3268-755T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 16/23 | chr12 | 132783248 | ||||||
| chr12:132783328
|
C | T | 44 | a0003c0004t0001g0270a0003c0004t0001g0279a0003c0004t0001g0282others(41): Show | 44 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.3268-835G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 16/23 | chr12 | 132783328 | ||||||
| chr12:132783477
|
T | C | 38 | a0001c0001t0002g0121a0001c0001t0003g0006a0001c0001t0003g0007others(35): Show | 38 | HG00280.hp1 HG00438.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.3267+687A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 16/23 | chr12 | 132783477 | ||||||
| chr12:132783508
|
T | TGGGGGCG others(26): Show |
4 | a0001c0001t0010g0082a0003c0004t0001g0283a0003c0004t0013g0261others(1): Show | 4 | HG00735.hp1 HG02056.hp1 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.3267+655_3267+656i others(35): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 16/23 | chr12 | 132783508 | ||||||
| chr12:132783509
|
G | GGGGGCGC others(25): Show |
194 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(191): Show | 194 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.3267+654_3267+655i others(34): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 16/23 | chr12 | 132783509 | ||||||
| chr12:132783510
|
G | GGGGCGCC others(24): Show |
2 | a0009c0015t0078g0066a0009c0015t0080g0065 | 2 | HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.3267+653_3267+654i others(33): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 16/23 | chr12 | 132783510 | ||||||
| chr12:132783515
|
C | CCGGGAAG others(24): Show |
1 | a0001c0001t0075g0128 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3267+648_3267+649i others(33): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 16/23 | chr12 | 132783515 | ||||||
| chr12:132783515
|
C | G | 198 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(195): Show | 198 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.3267+649G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 16/23 | chr12 | 132783515 | ||||||
| chr12:132783542
|
G | C | 295 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(292): Show | 295 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.3267+622C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 16/23 | chr12 | 132783542 | ||||||
| chr12:132783544
|
G | A | 2 | a0001c0003t0006g0291a0001c0003t0006g0298 | 2 | HG01884.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.3267+620C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 16/23 | chr12 | 132783544 | ||||||
| chr12:132783671
|
G | C | 1 | a0001c0001t0001g0093 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3267+493C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 16/23 | chr12 | 132783671 | ||||||
| chr12:132783832
|
T | C | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | NA18980.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.3267+332A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 16/23 | chr12 | 132783832 | ||||||
| chr12:132783835
|
C | T | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | NA18980.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.3267+329G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 16/23 | chr12 | 132783835 | ||||||
| chr12:132783878
|
T | C | 1 | a0001c0018t0019g0132 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3267+286A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 16/23 | chr12 | 132783878 | ||||||
| chr12:132783941
|
C | G | 2 | a0001c0001t0017g0001a0001c0001t0029g0304 | 2 | NA19240.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3267+223G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 16/23 | chr12 | 132783941 | ||||||
| chr12:132783944
|
T | C | 295 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(292): Show | 295 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.3267+220A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 16/23 | chr12 | 132783944 | ||||||
| chr12:132784084
|
C | T | 1 | a0001c0011t0001g0061 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.3267+80G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 16/23 | chr12 | 132784084 | ||||||
| chr12:132784138
|
C | T | 1 | a0002c0002t0060g0185 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3267+26G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 16/23 | chr12 | 132784138 | ||||||
| chr12:132784378
|
G | A | 147 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(144): Show | 147 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.3124-71C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 15/23 | chr12 | 132784378 | ||||||
| chr12:132784638
|
A | G | 220 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(217): Show | 220 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.3124-331T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 15/23 | chr12 | 132784638 | ||||||
| chr12:132784664
|
A | G | 79 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(76): Show | 79 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.3124-357T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 15/23 | chr12 | 132784664 | ||||||
| chr12:132784712
|
CCA | C | 46 | a0003c0004t0001g0270a0003c0004t0001g0279a0003c0004t0001g0282others(43): Show | 46 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.3124-407_3124-406d others(4): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 15/23 | chr12 | 132784712 | ||||||
| chr12:132784724
|
G | A | 1 | a0018c0029t0061g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3124-417C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 15/23 | chr12 | 132784724 | ||||||
| chr12:132784727
|
CTCACACC others(29): Show |
C | 5 | a0005c0006t0018g0023a0005c0006t0018g0102a0005c0006t0043g0004others(2): Show | 5 | HG02486.hp2 HG02615.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.3124-456_3124-421d others(38): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 15/23 | chr12 | 132784727 | ||||||
| chr12:132784737
|
ACACGCAC others(12): Show |
A | 1 | a0001c0001t0071g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3124-449_3124-431d others(21): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 15/23 | chr12 | 132784737 | ||||||
| chr12:132784741
|
G | A | 9 | a0001c0001t0001g0051a0001c0001t0001g0053a0001c0001t0001g0055others(6): Show | 9 | HG00408.hp1 NA18947.hp1 NA18960.hp2 others(6): Show |
intron_variant | MODIFIER | c.3124-434C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 15/23 | chr12 | 132784741 | ||||||
| chr12:132784755
|
CCCA | C | 28 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0001g0167others(25): Show | 28 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.3124-451_3124-449d others(5): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 15/23 | chr12 | 132784755 | ||||||
| chr12:132784759
|
C | CAT | 119 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(116): Show | 119 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.3124-453_3124-452i others(4): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 15/23 | chr12 | 132784759 | ||||||
| chr12:132784760
|
G | A | 1 | a0001c0001t0017g0001 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3124-453C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 15/23 | chr12 | 132784760 | ||||||
| chr12:132784778
|
A | C | 2 | a0002c0002t0002g0179a0002c0002t0002g0180 | 2 | HG00741.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.3124-471T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 15/23 | chr12 | 132784778 | ||||||
| chr12:132784787
|
CAT | C | 119 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(116): Show | 119 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.3124-482_3124-481d others(4): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 15/23 | chr12 | 132784787 | ||||||
| chr12:132784790
|
G | C | 2 | a0002c0002t0002g0179a0002c0002t0002g0180 | 2 | HG00741.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.3124-483C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 15/23 | chr12 | 132784790 | ||||||
| chr12:132784873
|
A | C | 207 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(204): Show | 207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.3124-566T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 15/23 | chr12 | 132784873 | ||||||
| chr12:132785080
|
A | C | 2 | a0006c0010t0006g0011a0006c0010t0006g0130 | 2 | HG02622.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.3124-773T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 15/23 | chr12 | 132785080 | ||||||
| chr12:132785148
|
C | T | 6 | a0006c0010t0006g0011a0006c0010t0006g0012a0006c0010t0006g0130others(3): Show | 6 | HG01106.hp1 HG01891.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.3124-841G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 15/23 | chr12 | 132785148 | ||||||
| chr12:132785161
|
T | C | 1 | a0001c0003t0011g0157 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.3124-854A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 15/23 | chr12 | 132785161 | ||||||
| chr12:132785180
|
T | C | 211 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(208): Show | 211 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.3124-873A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 15/23 | chr12 | 132785180 | ||||||
| chr12:132785201
|
C | T | 1 | a0001c0003t0002g0196 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.3124-894G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 15/23 | chr12 | 132785201 | ||||||
| chr12:132785242
|
A | C | 1 | a0001c0001t0002g0121 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3124-935T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 15/23 | chr12 | 132785242 | ||||||
| chr12:132785257
|
G | A | 28 | a0001c0001t0002g0121a0001c0001t0003g0006a0001c0001t0003g0007others(25): Show | 28 | HG00280.hp1 HG00438.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.3124-950C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 15/23 | chr12 | 132785257 | ||||||
| chr12:132785264
|
T | C | 1 | a0002c0002t0006g0211 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.3124-957A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 15/23 | chr12 | 132785264 | ||||||
| chr12:132785296
|
G | C | 1 | a0002c0002t0002g0217 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3124-989C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 15/23 | chr12 | 132785296 | ||||||
| chr12:132785354
|
G | A | 79 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0001g0167others(76): Show | 79 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.3123+985C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 15/23 | chr12 | 132785354 | ||||||
| chr12:132785584
|
A | C | 29 | a0003c0004t0001g0270a0003c0004t0001g0279a0003c0004t0001g0282others(26): Show | 29 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.3123+755T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 15/23 | chr12 | 132785584 | ||||||
| chr12:132785613
|
G | A | 1 | a0001c0001t0001g0029 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3123+726C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 15/23 | chr12 | 132785613 | ||||||
| chr12:132785703
|
T | C | 2 | a0003c0004t0008g0278a0003c0004t0013g0261 | 2 | NA18977.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.3123+636A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 15/23 | chr12 | 132785703 | ||||||
| chr12:132785803
|
G | A | 1 | a0004c0036t0008g0263 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3123+536C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 15/23 | chr12 | 132785803 | ||||||
| chr12:132785890
|
A | T | 1 | a0001c0003t0004g0162 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.3123+449T>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 15/23 | chr12 | 132785890 | ||||||
| chr12:132785913
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.3123+426G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 15/23 | chr12 | 132785913 | ||||||
| chr12:132786027
|
G | A | 1 | a0018c0029t0061g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3123+312C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 15/23 | chr12 | 132786027 | ||||||
| chr12:132786058
|
C | T | 1 | a0014c0020t0019g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3123+281G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 15/23 | chr12 | 132786058 | ||||||
| chr12:132786099
|
G | A | 1 | a0014c0020t0019g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3123+240C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 15/23 | chr12 | 132786099 | ||||||
| chr12:132786133
|
C | T | 1 | a0001c0003t0004g0142 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3123+206G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 15/23 | chr12 | 132786133 | ||||||
| chr12:132786171
|
G | A | 1 | a0014c0020t0019g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3123+168C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 15/23 | chr12 | 132786171 | ||||||
| chr12:132786195
|
G | C | 294 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(291): Show | 294 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.3123+144C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 15/23 | chr12 | 132786195 | ||||||
| chr12:132786200
|
A | C | 1 | a0001c0003t0011g0157 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.3123+139T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 15/23 | chr12 | 132786200 | ||||||
| chr12:132786568
|
G | A | 1 | a0001c0003t0004g0143 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2907-13C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 14/23 | chr12 | 132786568 | ||||||
| chr12:132786626
|
GCCTCCCC others(13): Show |
G | 34 | a0001c0001t0017g0015a0001c0001t0026g0302a0001c0001t0027g0306others(31): Show | 34 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.2906+47_2906+66del others(20): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 14/23 | chr12 | 132786626 | ||||||
| chr12:132786633
|
C | A | 1 | a0018c0029t0061g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2906+60G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 14/23 | chr12 | 132786633 | ||||||
| chr12:132786633
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2906+60G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 14/23 | chr12 | 132786633 | ||||||
| chr12:132786663
|
C | T | 1 | a0002c0002t0051g0238 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2906+30G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 14/23 | chr12 | 132786663 | ||||||
| chr12:132786675
|
G | A | 1 | a0001c0001t0029g0304 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2906+18C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 14/23 | chr12 | 132786675 | ||||||
| chr12:132786678
|
C | T | 42 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0045others(39): Show | 42 | HG00280.hp1 HG00438.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.2906+15G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 14/23 | chr12 | 132786678 | ||||||
| chr12:132786790
|
G | T | 265 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(262): Show | 265 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(262): Show |
splice_region_variant&intron_variant | LOW | c.2812-3C>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132786790 | ||||||
| chr12:132786956
|
C | CT | 18 | a0001c0011t0074g0067a0003c0004t0013g0284a0005c0006t0001g0021others(15): Show | 18 | HG02027.hp2 HG02055.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.2812-170dupA | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132786956 | ||||||
| chr12:132786980
|
G | A | 1 | a0001c0001t0037g0113 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2812-193C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132786980 | ||||||
| chr12:132786986
|
C | T | 1 | a0024c0038t0004g0163 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2812-199G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132786986 | ||||||
| chr12:132787039
|
C | T | 117 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(114): Show | 117 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.2812-252G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787039 | ||||||
| chr12:132787042
|
C | T | 2 | a0001c0001t0003g0111a0001c0001t0003g0112 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.2812-255G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787042 | ||||||
| chr12:132787046
|
C | T | 117 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(114): Show | 117 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.2812-259G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787046 | ||||||
| chr12:132787047
|
A | G | 202 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(199): Show | 202 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.2812-260T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787047 | ||||||
| chr12:132787115
|
A | C | 1 | a0019c0028t0004g0153 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2812-328T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787115 | ||||||
| chr12:132787282
|
G | A | 253 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(250): Show | 253 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.2812-495C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787282 | ||||||
| chr12:132787342
|
G | A | 1 | a0017c0022t0001g0025 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2812-555C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787342 | ||||||
| chr12:132787374
|
T | C | 294 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(291): Show | 294 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.2812-587A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787374 | ||||||
| chr12:132787556
|
A | G | 2 | a0004c0005t0023g0246a0004c0005t0023g0256 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2812-769T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787556 | ||||||
| chr12:132787556
|
AGGACCCT others(167): Show |
A | 2 | a0001c0001t0017g0001a0001c0001t0029g0304 | 2 | NA19240.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2812-943_2812-770d others(2): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787556 | ||||||
| chr12:132787563
|
T | C | 1 | a0001c0001t0003g0110 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2812-776A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787563 | ||||||
| chr12:132787564
|
T | C | 2 | a0001c0001t0004g0126a0001c0001t0004g0127 | 2 | HG03017.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.2812-777A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787564 | ||||||
| chr12:132787564
|
T | TC | 15 | a0001c0001t0075g0128a0005c0006t0001g0021a0005c0006t0014g0018others(12): Show | 15 | HG01993.hp2 HG02055.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.2812-778dupG | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787564 | ||||||
| chr12:132787567
|
T | C | 15 | a0001c0001t0075g0128a0005c0006t0001g0021a0005c0006t0014g0018others(12): Show | 15 | HG01993.hp2 HG02055.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.2812-780A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787567 | ||||||
| chr12:132787567
|
T | G | 3 | a0001c0001t0003g0110a0001c0001t0004g0126a0001c0001t0004g0127 | 3 | HG02735.hp2 HG03017.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.2812-780A>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787567 | ||||||
| chr12:132787567
|
TGAGACCC others(81): Show |
T | 2 | a0001c0001t0003g0008a0001c0001t0055g0009 | 2 | HG00438.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.2812-868_2812-781d others(90): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787567 | ||||||
| chr12:132787567
|
TGAGACCC others(103): Show |
T | 1 | a0001c0001t0003g0006 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2812-890_2812-781d others(2): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787567 | ||||||
| chr12:132787567
|
TGAGACCC others(125): Show |
T | 1 | a0001c0001t0003g0007 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2812-912_2812-781d others(2): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787567 | ||||||
| chr12:132787575
|
C | CGGGACCC others(15): Show |
6 | a0001c0003t0004g0142a0001c0003t0004g0158a0001c0003t0004g0162others(3): Show | 6 | HG02683.hp1 HG04204.hp1 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.2812-810_2812-789d others(24): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787575 | ||||||
| chr12:132787583
|
CTCCCCAG others(15): Show |
C | 6 | a0001c0001t0003g0104a0001c0001t0003g0109a0001c0001t0003g0119others(3): Show | 6 | HG00738.hp2 HG02602.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.2812-818_2812-797d others(24): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787583 | ||||||
| chr12:132787589
|
A | G | 19 | a0001c0001t0002g0121a0001c0001t0003g0010a0001c0001t0003g0105others(16): Show | 19 | HG00280.hp1 HG00738.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.2812-802T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787589 | ||||||
| chr12:132787591
|
A | AGACCCCG others(2): Show |
4 | a0001c0001t0003g0115a0001c0001t0003g0139a0001c0001t0032g0107others(1): Show | 4 | HG01175.hp2 HG03490.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.2812-805_2812-804i others(11): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787591 | ||||||
| chr12:132787592
|
A | G | 15 | a0001c0001t0002g0121a0001c0001t0003g0010a0001c0001t0003g0105others(12): Show | 15 | HG00280.hp1 HG00738.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.2812-805T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787592 | ||||||
| chr12:132787593
|
C | A | 15 | a0001c0001t0002g0121a0001c0001t0003g0010a0001c0001t0003g0105others(12): Show | 15 | HG00280.hp1 HG00738.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.2812-806G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787593 | ||||||
| chr12:132787597
|
T | C | 15 | a0001c0001t0002g0121a0001c0001t0003g0010a0001c0001t0003g0105others(12): Show | 15 | HG00280.hp1 HG00738.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.2812-810A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787597 | ||||||
| chr12:132787597
|
T | TCCCCGGA others(6): Show |
4 | a0001c0001t0003g0115a0001c0001t0003g0139a0001c0001t0032g0107others(1): Show | 4 | HG01175.hp2 HG03490.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.2812-811_2812-810i others(15): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787597 | ||||||
| chr12:132787597
|
T | TGGGACCC others(37): Show |
2 | a0001c0001t0026g0302a0001c0001t0027g0306 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2812-811_2812-810i others(46): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787597 | ||||||
| chr12:132787597
|
TGGGACCC others(15): Show |
T | 5 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0004g0155others(2): Show | 5 | HG01993.hp1 HG02293.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.2812-832_2812-811d others(24): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787597 | ||||||
| chr12:132787597
|
TGGGACCC others(37): Show |
T | 5 | a0001c0001t0030g0303a0001c0003t0001g0167a0001c0003t0004g0143others(2): Show | 5 | HG00642.hp2 HG01255.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.2812-854_2812-811d others(46): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787597 | ||||||
| chr12:132787597
|
TGGGACCC others(59): Show |
T | 2 | a0001c0001t0017g0015a0001c0001t0075g0128 | 2 | HG01993.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.2812-876_2812-811d others(68): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787597 | ||||||
| chr12:132787605
|
T | C | 106 | a0001c0001t0002g0121a0001c0001t0003g0010a0001c0001t0003g0105others(103): Show | 106 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.2812-818A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787605 | ||||||
| chr12:132787605
|
TTCCCCGG others(37): Show |
T | 2 | a0001c0001t0001g0084a0014c0020t0019g0003 | 2 | HG02027.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2812-862_2812-819d others(46): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787605 | ||||||
| chr12:132787605
|
TTCCCCGG others(59): Show |
T | 1 | a0001c0001t0001g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2812-884_2812-819d others(68): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787605 | ||||||
| chr12:132787605
|
TTCCCCGG others(81): Show |
T | 6 | a0001c0009t0002g0181a0001c0009t0002g0201a0001c0009t0002g0219others(3): Show | 6 | HG01074.hp2 HG01515.hp1 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.2812-906_2812-819d others(90): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787605 | ||||||
| chr12:132787611
|
G | A | 9 | a0001c0003t0004g0144a0001c0003t0004g0145a0001c0003t0004g0159others(6): Show | 9 | HG01884.hp2 HG02080.hp2 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.2812-824C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787611 | ||||||
| chr12:132787613
|
AGACCCCG others(2): Show |
A | 3 | a0001c0003t0004g0145a0001c0003t0011g0161a0024c0038t0004g0163 | 3 | HG02080.hp2 HG02698.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.2812-835_2812-827d others(11): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787613 | ||||||
| chr12:132787614
|
G | A | 6 | a0001c0003t0004g0144a0001c0003t0004g0159a0001c0003t0004g0164others(3): Show | 6 | HG01884.hp2 HG02155.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.2812-827C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787614 | ||||||
| chr12:132787615
|
A | C | 6 | a0001c0003t0004g0144a0001c0003t0004g0159a0001c0003t0004g0164others(3): Show | 6 | HG01884.hp2 HG02155.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.2812-828T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787615 | ||||||
| chr12:132787618
|
C | CCGGGACC others(15): Show |
1 | a0001c0003t0006g0291 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2812-853_2812-832d others(24): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787618 | ||||||
| chr12:132787618
|
C | CCGGGACC others(37): Show |
1 | a0001c0001t0003g0114 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2812-832_2812-831i others(46): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787618 | ||||||
| chr12:132787618
|
CCGGGACC others(15): Show |
C | 2 | a0001c0001t0001g0051a0001c0001t0071g0050 | 2 | NA18522.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.2812-853_2812-832d others(24): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787618 | ||||||
| chr12:132787619
|
C | T | 7 | a0001c0001t0001g0086a0001c0003t0004g0144a0001c0003t0004g0159others(4): Show | 7 | HG01884.hp2 HG02155.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.2812-832G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787619 | ||||||
| chr12:132787624
|
CCCCTCCC others(80): Show |
C | 1 | a0001c0001t0001g0137 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2812-924_2812-838d others(89): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787624 | ||||||
| chr12:132787628
|
TCCCCGGA others(6): Show |
T | 3 | a0001c0003t0004g0145a0001c0003t0011g0161a0024c0038t0004g0163 | 3 | HG02080.hp2 HG02698.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.2812-854_2812-842d others(15): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787628 | ||||||
| chr12:132787633
|
G | A | 2 | a0002c0002t0002g0014a0002c0002t0002g0212 | 2 | HG01891.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2812-846C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787633 | ||||||
| chr12:132787638
|
C | CCCCGGGA others(15): Show |
1 | a0001c0018t0019g0132 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2812-852_2812-851i others(24): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787638 | ||||||
| chr12:132787640
|
A | ACGGGACC others(37): Show |
1 | a0001c0003t0048g0289 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2812-854_2812-853i others(46): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787640 | ||||||
| chr12:132787640
|
A | ACGGGACC others(59): Show |
1 | a0001c0003t0006g0290 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2812-854_2812-853i others(68): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787640 | ||||||
| chr12:132787640
|
A | ACGGGACC others(15): Show |
1 | a0001c0003t0079g0299 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2812-875_2812-854d others(24): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787640 | ||||||
| chr12:132787640
|
A | C | 186 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(183): Show | 186 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.2812-853T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787640 | ||||||
| chr12:132787640
|
ACGGGACC others(81): Show |
A | 57 | a0001c0003t0002g0196a0001c0009t0002g0199a0001c0009t0002g0232others(54): Show | 57 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.2812-941_2812-854d others(90): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787640 | ||||||
| chr12:132787649
|
C | CTCCCCGG others(81): Show |
3 | a0004c0005t0005g0257a0004c0005t0023g0246a0004c0005t0023g0256 | 3 | HG01256.hp1 HG01258.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.2812-863_2812-862i others(90): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787649 | ||||||
| chr12:132787655
|
G | A | 1 | a0001c0003t0039g0156 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2812-868C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787655 | ||||||
| chr12:132787658
|
G | A | 1 | a0001c0003t0039g0156 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2812-871C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787658 | ||||||
| chr12:132787659
|
A | ACCACGGG others(37): Show |
1 | a0018c0029t0061g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2812-873_2812-872i others(46): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787659 | ||||||
| chr12:132787659
|
A | C | 1 | a0001c0003t0039g0156 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2812-872T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787659 | ||||||
| chr12:132787662
|
C | A | 12 | a0001c0001t0002g0121a0001c0001t0003g0109a0001c0001t0003g0111others(9): Show | 12 | HG00544.hp2 HG01255.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.2812-875G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787662 | ||||||
| chr12:132787662
|
C | CCGGGACC others(15): Show |
1 | a0002c0007t0031g0307 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2812-876_2812-875i others(24): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787662 | ||||||
| chr12:132787662
|
CCGGGACC others(103): Show |
C | 7 | a0002c0002t0002g0014a0002c0002t0002g0190a0002c0002t0002g0191others(4): Show | 7 | HG01891.hp2 HG02055.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.2812-985_2812-876d others(2): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787662 | ||||||
| chr12:132787663
|
C | T | 2 | a0001c0003t0039g0156a0018c0029t0061g0103 | 2 | HG02056.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2812-876G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787663 | ||||||
| chr12:132787671
|
C | CTCCCCGG others(37): Show |
14 | a0004c0005t0005g0049a0004c0005t0005g0101a0004c0005t0005g0247others(11): Show | 14 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.2812-885_2812-884i others(46): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787671 | ||||||
| chr12:132787671
|
C | CTCCCCGG others(258): Show |
1 | a0003c0004t0025g0280 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2812-885_2812-884i others(267): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787671 | ||||||
| chr12:132787671
|
C | CTCCCCGG others(257): Show |
24 | a0003c0004t0001g0270a0003c0004t0001g0279a0003c0004t0001g0282others(21): Show | 24 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(21): Show |
intron_variant | MODIFIER | c.2812-885_2812-884i others(266): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787671 | ||||||
| chr12:132787671
|
C | CTTCCCAG others(235): Show |
1 | a0011c0017t0008g0267 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2812-885_2812-884i others(244): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787671 | ||||||
| chr12:132787677
|
G | A | 73 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(70): Show | 73 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.2812-890C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787677 | ||||||
| chr12:132787679
|
AG | A | 73 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(70): Show | 73 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.2812-893delC | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787679 | ||||||
| chr12:132787684
|
C | A | 12 | a0001c0001t0003g0104a0001c0001t0003g0119a0001c0001t0003g0140others(9): Show | 12 | HG00735.hp2 HG00738.hp2 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.2812-897G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787684 | ||||||
| chr12:132787684
|
C | CCGGGACC others(15): Show |
1 | a0002c0013t0004g0141 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2812-898_2812-897i others(24): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787684 | ||||||
| chr12:132787684
|
CCGGGACC others(103): Show |
C | 7 | a0002c0002t0002g0178a0002c0002t0002g0179a0002c0002t0002g0180others(4): Show | 7 | HG00741.hp2 HG01106.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.2812-1007_2812-898 others(3): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787684 | ||||||
| chr12:132787685
|
CGGGACCC others(80): Show |
C | 73 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(70): Show | 73 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.2812-985_2812-899d others(89): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787685 | ||||||
| chr12:132787686
|
GGGACCCC others(190): Show |
G | 1 | a0005c0006t0064g0022 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2812-1096_2812-900 others(3): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787686 | ||||||
| chr12:132787693
|
C | CTTCCCAG others(235): Show |
1 | a0003c0004t0008g0278 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2812-907_2812-906i others(244): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787693 | ||||||
| chr12:132787699
|
G | A | 17 | a0001c0001t0001g0051a0001c0001t0001g0084a0001c0001t0071g0050others(14): Show | 17 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.2812-912C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787699 | ||||||
| chr12:132787702
|
G | A | 17 | a0001c0001t0001g0051a0001c0001t0001g0084a0001c0001t0071g0050others(14): Show | 17 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.2812-915C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787702 | ||||||
| chr12:132787703
|
A | C | 17 | a0001c0001t0001g0051a0001c0001t0001g0084a0001c0001t0071g0050others(14): Show | 17 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.2812-916T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787703 | ||||||
| chr12:132787706
|
C | A | 25 | a0001c0001t0003g0114a0001c0001t0003g0116a0001c0001t0003g0122others(22): Show | 25 | HG00738.hp1 HG01069.hp2 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.2812-919G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787706 | ||||||
| chr12:132787706
|
C | CCGGGACC others(15): Show |
2 | a0001c0003t0004g0150a0001c0003t0041g0165 | 2 | HG00438.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.2812-920_2812-919i others(24): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787706 | ||||||
| chr12:132787706
|
C | CCGGGACC others(343): Show |
2 | a0009c0015t0078g0066a0009c0015t0080g0065 | 2 | HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2812-920_2812-919i others(352): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787706 | ||||||
| chr12:132787706
|
CCGGGACC others(81): Show |
C | 3 | a0002c0002t0002g0177a0002c0002t0002g0198a0002c0002t0051g0238 | 3 | HG02293.hp2 HG02683.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.2812-1007_2812-920 others(91): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787706 | ||||||
| chr12:132787707
|
C | T | 17 | a0001c0001t0001g0051a0001c0001t0001g0084a0001c0001t0071g0050others(14): Show | 17 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.2812-920G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787707 | ||||||
| chr12:132787708
|
GGGACCCC others(168): Show |
G | 7 | a0005c0006t0001g0021a0005c0006t0014g0018a0005c0006t0014g0019others(4): Show | 7 | HG02559.hp2 HG02965.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.2812-1096_2812-922 others(3): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787708 | ||||||
| chr12:132787715
|
C | CTTCCCAG others(235): Show |
2 | a0004c0036t0008g0263a0013c0035t0035g0262 | 2 | HG02004.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.2812-929_2812-928i others(244): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787715 | ||||||
| chr12:132787715
|
C | T | 14 | a0004c0005t0005g0049a0004c0005t0005g0101a0004c0005t0005g0247others(11): Show | 14 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.2812-928G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787715 | ||||||
| chr12:132787721
|
G | A | 3 | a0004c0005t0005g0257a0004c0005t0023g0246a0004c0005t0023g0256 | 3 | HG01256.hp1 HG01258.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.2812-934C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787721 | ||||||
| chr12:132787724
|
G | A | 3 | a0004c0005t0005g0257a0004c0005t0023g0246a0004c0005t0023g0256 | 3 | HG01256.hp1 HG01258.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.2812-937C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787724 | ||||||
| chr12:132787725
|
A | C | 3 | a0004c0005t0005g0257a0004c0005t0023g0246a0004c0005t0023g0256 | 3 | HG01256.hp1 HG01258.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.2812-938T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787725 | ||||||
| chr12:132787728
|
C | A | 63 | a0001c0001t0001g0051a0001c0001t0001g0084a0001c0001t0003g0105others(60): Show | 63 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.2812-941G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787728 | ||||||
| chr12:132787728
|
CCGGGACC others(59): Show |
C | 6 | a0002c0002t0002g0168a0002c0002t0002g0173a0002c0002t0002g0174others(3): Show | 6 | HG00735.hp2 HG01070.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.2812-1007_2812-942 others(69): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787728 | ||||||
| chr12:132787729
|
C | T | 3 | a0004c0005t0005g0257a0004c0005t0023g0246a0004c0005t0023g0256 | 3 | HG01256.hp1 HG01258.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.2812-942G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787729 | ||||||
| chr12:132787734
|
CCCCTCCC others(58): Show |
C | 1 | a0002c0002t0006g0182 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2812-1012_2812-948 others(68): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787734 | ||||||
| chr12:132787737
|
C | T | 3 | a0004c0005t0005g0257a0004c0005t0023g0246a0004c0005t0023g0256 | 3 | HG01256.hp1 HG01258.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.2812-950G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787737 | ||||||
| chr12:132787743
|
G | A | 28 | a0001c0001t0017g0001a0001c0001t0029g0304a0003c0004t0001g0270others(25): Show | 28 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.2812-956C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787743 | ||||||
| chr12:132787746
|
G | A | 26 | a0003c0004t0001g0270a0003c0004t0001g0279a0003c0004t0001g0282others(23): Show | 26 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.2812-959C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787746 | ||||||
| chr12:132787747
|
A | C | 26 | a0003c0004t0001g0270a0003c0004t0001g0279a0003c0004t0001g0282others(23): Show | 26 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.2812-960T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787747 | ||||||
| chr12:132787750
|
C | A | 42 | a0001c0001t0002g0121a0001c0001t0003g0111a0001c0001t0003g0112others(39): Show | 42 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(39): Show |
intron_variant | MODIFIER | c.2812-963G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787750 | ||||||
| chr12:132787750
|
CCGGGACC others(15): Show |
C | 2 | a0001c0003t0009g0293a0001c0003t0009g0294 | 2 | HG02145.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2812-985_2812-964d others(24): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787750 | ||||||
| chr12:132787751
|
C | T | 26 | a0003c0004t0001g0270a0003c0004t0001g0279a0003c0004t0001g0282others(23): Show | 26 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.2812-964G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787751 | ||||||
| chr12:132787752
|
GGGACCCC others(124): Show |
G | 5 | a0005c0006t0018g0023a0005c0006t0018g0102a0005c0006t0043g0004others(2): Show | 5 | HG02486.hp2 HG02615.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2812-1096_2812-966 others(3): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787752 | ||||||
| chr12:132787759
|
C | T | 26 | a0003c0004t0001g0270a0003c0004t0001g0279a0003c0004t0001g0282others(23): Show | 26 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.2812-972G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787759 | ||||||
| chr12:132787765
|
G | A | 2 | a0001c0001t0001g0042a0001c0001t0001g0137 | 2 | HG03209.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.2812-978C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787765 | ||||||
| chr12:132787768
|
G | A | 2 | a0001c0001t0001g0042a0001c0001t0001g0137 | 2 | HG03209.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.2812-981C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787768 | ||||||
| chr12:132787769
|
A | C | 2 | a0001c0001t0001g0042a0001c0001t0001g0137 | 2 | HG03209.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.2812-982T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787769 | ||||||
| chr12:132787772
|
A | C | 72 | a0001c0001t0001g0042a0001c0001t0001g0137a0001c0001t0002g0121others(69): Show | 72 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.2812-985T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787772 | ||||||
| chr12:132787773
|
C | T | 75 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(72): Show | 75 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.2812-986G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787773 | ||||||
| chr12:132787774
|
G | A | 1 | a0018c0029t0061g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2812-987C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787774 | ||||||
| chr12:132787774
|
GGGACCCC others(102): Show |
G | 1 | a0012c0019t0038g0024 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2812-1096_2812-988 others(3): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787774 | ||||||
| chr12:132787787
|
G | A | 17 | a0003c0004t0008g0278a0004c0005t0005g0049a0004c0005t0005g0101others(14): Show | 17 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.2812-1000C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787787 | ||||||
| chr12:132787790
|
G | A | 17 | a0003c0004t0008g0278a0004c0005t0005g0049a0004c0005t0005g0101others(14): Show | 17 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.2812-1003C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787790 | ||||||
| chr12:132787791
|
A | C | 17 | a0003c0004t0008g0278a0004c0005t0005g0049a0004c0005t0005g0101others(14): Show | 17 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.2812-1004T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787791 | ||||||
| chr12:132787794
|
A | ACGGGACC others(15): Show |
3 | a0001c0003t0006g0290a0001c0003t0006g0291a0001c0003t0006g0298 | 3 | HG01884.hp1 HG02886.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2812-1029_2812-100 others(26): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787794 | ||||||
| chr12:132787794
|
A | C | 142 | a0001c0001t0002g0121a0001c0001t0003g0006a0001c0001t0003g0007others(139): Show | 142 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.2812-1007T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787794 | ||||||
| chr12:132787794
|
ACGGGACC others(15): Show |
A | 1 | a0001c0001t0028g0305 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2812-1029_2812-100 others(26): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787794 | ||||||
| chr12:132787794
|
ACGGGACC others(59): Show |
A | 3 | a0001c0001t0001g0051a0001c0001t0001g0084a0001c0001t0071g0050 | 3 | HG02027.hp1 NA18522.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.2812-1073_2812-100 others(70): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787794 | ||||||
| chr12:132787795
|
C | T | 17 | a0003c0004t0008g0278a0004c0005t0005g0049a0004c0005t0005g0101others(14): Show | 17 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.2812-1008G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787795 | ||||||
| chr12:132787803
|
C | A | 1 | a0001c0003t0004g0145 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2812-1016G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787803 | ||||||
| chr12:132787803
|
C | T | 17 | a0003c0004t0008g0278a0004c0005t0005g0049a0004c0005t0005g0101others(14): Show | 17 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.2812-1016G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787803 | ||||||
| chr12:132787809
|
G | A | 5 | a0003c0004t0008g0276a0003c0004t0036g0260a0004c0005t0005g0257others(2): Show | 5 | HG01256.hp1 HG01258.hp1 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.2812-1022C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787809 | ||||||
| chr12:132787812
|
G | A | 5 | a0003c0004t0008g0276a0003c0004t0036g0260a0004c0005t0005g0257others(2): Show | 5 | HG01256.hp1 HG01258.hp1 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.2812-1025C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787812 | ||||||
| chr12:132787813
|
A | C | 5 | a0003c0004t0008g0276a0003c0004t0036g0260a0004c0005t0005g0257others(2): Show | 5 | HG01256.hp1 HG01258.hp1 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.2812-1026T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787813 | ||||||
| chr12:132787816
|
C | A | 29 | a0001c0001t0030g0303a0001c0001t0075g0128a0001c0003t0009g0297others(26): Show | 29 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.2812-1029G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787816 | ||||||
| chr12:132787817
|
C | T | 5 | a0003c0004t0008g0276a0003c0004t0036g0260a0004c0005t0005g0257others(2): Show | 5 | HG01256.hp1 HG01258.hp1 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.2812-1030G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787817 | ||||||
| chr12:132787825
|
C | T | 5 | a0003c0004t0008g0276a0003c0004t0036g0260a0004c0005t0005g0257others(2): Show | 5 | HG01256.hp1 HG01258.hp1 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.2812-1038G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787825 | ||||||
| chr12:132787831
|
G | A | 24 | a0003c0004t0001g0270a0003c0004t0001g0279a0003c0004t0001g0282others(21): Show | 24 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(21): Show |
intron_variant | MODIFIER | c.2812-1044C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787831 | ||||||
| chr12:132787834
|
G | A | 24 | a0003c0004t0001g0270a0003c0004t0001g0279a0003c0004t0001g0282others(21): Show | 24 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(21): Show |
intron_variant | MODIFIER | c.2812-1047C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787834 | ||||||
| chr12:132787835
|
A | C | 24 | a0003c0004t0001g0270a0003c0004t0001g0279a0003c0004t0001g0282others(21): Show | 24 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(21): Show |
intron_variant | MODIFIER | c.2812-1048T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787835 | ||||||
| chr12:132787838
|
C | A | 96 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(93): Show | 96 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.2812-1051G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787838 | ||||||
| chr12:132787838
|
C | CCGGGACC others(15): Show |
1 | a0001c0001t0003g0123 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2812-1052_2812-105 others(26): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787838 | ||||||
| chr12:132787839
|
C | T | 24 | a0003c0004t0001g0270a0003c0004t0001g0279a0003c0004t0001g0282others(21): Show | 24 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(21): Show |
intron_variant | MODIFIER | c.2812-1052G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787839 | ||||||
| chr12:132787847
|
C | CTCCCCGG others(37): Show |
3 | a0003c0004t0008g0278a0004c0036t0008g0263a0013c0035t0035g0262 | 3 | HG02004.hp2 NA18977.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2812-1061_2812-106 others(48): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787847 | ||||||
| chr12:132787847
|
C | T | 24 | a0003c0004t0001g0270a0003c0004t0001g0279a0003c0004t0001g0282others(21): Show | 24 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(21): Show |
intron_variant | MODIFIER | c.2812-1060G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787847 | ||||||
| chr12:132787860
|
C | A | 146 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(143): Show | 146 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.2812-1073G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787860 | ||||||
| chr12:132787860
|
C | CCGGGACC others(15): Show |
2 | a0001c0001t0003g0110a0001c0023t0004g0160 | 2 | HG02155.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.2812-1074_2812-107 others(26): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787860 | ||||||
| chr12:132787860
|
C | CCGGGACC others(37): Show |
3 | a0001c0001t0002g0121a0001c0001t0003g0117a0001c0001t0003g0118 | 3 | HG01255.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2812-1074_2812-107 others(48): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787860 | ||||||
| chr12:132787865
|
AC | A | 5 | a0003c0004t0008g0276a0003c0004t0036g0260a0004c0005t0005g0257others(2): Show | 5 | HG01256.hp1 HG01258.hp1 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.2812-1079delG | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787865 | ||||||
| chr12:132787866
|
C | CCCCTCCC others(58): Show |
14 | a0004c0005t0005g0049a0004c0005t0005g0101a0004c0005t0005g0247others(11): Show | 14 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.2812-1080_2812-107 others(69): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787866 | ||||||
| chr12:132787866
|
C | CCCCTCCC others(14): Show |
27 | a0003c0004t0001g0270a0003c0004t0001g0279a0003c0004t0001g0282others(24): Show | 27 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.2812-1080_2812-107 others(25): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787866 | ||||||
| chr12:132787871
|
T | C | 2 | a0009c0015t0078g0066a0009c0015t0080g0065 | 2 | HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2812-1084A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787871 | ||||||
| chr12:132787874
|
C | CG | 3 | a0001c0001t0030g0303a0009c0015t0078g0066a0009c0015t0080g0065 | 3 | HG02818.hp2 HG02896.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2812-1088dupC | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787874 | ||||||
| chr12:132787875
|
G | A | 114 | a0001c0001t0002g0121a0001c0001t0003g0006a0001c0001t0003g0007others(111): Show | 114 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.2812-1088C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787875 | ||||||
| chr12:132787883
|
A | G | 1 | a0001c0001t0003g0010 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2812-1096T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787883 | ||||||
| chr12:132787926
|
C | CT | 117 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(114): Show | 117 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.2811+1100_2811+110 others(5): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787926 | ||||||
| chr12:132787926
|
C | T | 1 | a0001c0001t0017g0015 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2811+1101G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787926 | ||||||
| chr12:132787948
|
C | T | 39 | a0001c0001t0002g0121a0001c0001t0003g0006a0001c0001t0003g0007others(36): Show | 39 | HG00280.hp1 HG00438.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.2811+1079G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787948 | ||||||
| chr12:132787963
|
G | A | 1 | a0002c0002t0002g0242 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2811+1064C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787963 | ||||||
| chr12:132787964
|
C | A | 1 | a0002c0002t0002g0242 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2811+1063G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787964 | ||||||
| chr12:132787968
|
G | A | 2 | a0002c0002t0002g0224a0020c0030t0012g0228 | 2 | HG01978.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.2811+1059C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132787968 | ||||||
| chr12:132788199
|
C | T | 46 | a0003c0004t0001g0270a0003c0004t0001g0279a0003c0004t0001g0282others(43): Show | 46 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.2811+828G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132788199 | ||||||
| chr12:132788214
|
A | G | 3 | a0003c0004t0007g0269a0003c0004t0013g0268a0003c0004t0022g0277 | 3 | HG00408.hp2 NA18947.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.2811+813T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132788214 | ||||||
| chr12:132788386
|
C | A | 1 | a0018c0029t0061g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2811+641G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132788386 | ||||||
| chr12:132788479
|
C | T | 2 | a0001c0003t0040g0152a0001c0003t0045g0149 | 2 | HG01106.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2811+548G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132788479 | ||||||
| chr12:132788510
|
G | A | 7 | a0006c0010t0006g0011a0006c0010t0006g0012a0006c0010t0006g0130others(4): Show | 7 | HG01106.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2811+517C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132788510 | ||||||
| chr12:132788541
|
G | T | 2 | a0001c0003t0011g0147a0001c0003t0011g0157 | 2 | NA18956.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.2811+486C>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132788541 | ||||||
| chr12:132788549
|
T | G | 119 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(116): Show | 119 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.2811+478A>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132788549 | ||||||
| chr12:132788592
|
T | C | 1 | a0012c0019t0038g0024 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2811+435A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132788592 | ||||||
| chr12:132788598
|
A | G | 1 | a0002c0007t0001g0059 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2811+429T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132788598 | ||||||
| chr12:132788599
|
C | T | 27 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0001g0167others(24): Show | 27 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.2811+428G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132788599 | ||||||
| chr12:132788600
|
G | A | 78 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(75): Show | 78 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.2811+427C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132788600 | ||||||
| chr12:132788629
|
C | T | 1 | a0001c0001t0001g0047 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2811+398G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132788629 | ||||||
| chr12:132788630
|
G | A | 2 | a0001c0001t0017g0001a0001c0001t0029g0304 | 2 | NA19240.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2811+397C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132788630 | ||||||
| chr12:132788686
|
G | A | 1 | a0001c0003t0004g0159 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2811+341C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132788686 | ||||||
| chr12:132788731
|
G | A | 4 | a0001c0003t0006g0290a0001c0003t0006g0291a0001c0003t0006g0298others(1): Show | 4 | HG01884.hp1 HG02886.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2811+296C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132788731 | ||||||
| chr12:132788800
|
T | C | 295 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(292): Show | 295 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.2811+227A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132788800 | ||||||
| chr12:132788829
|
C | T | 14 | a0005c0006t0001g0021a0005c0006t0014g0018a0005c0006t0014g0019others(11): Show | 14 | HG02055.hp2 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.2811+198G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132788829 | ||||||
| chr12:132788911
|
A | C | 294 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(291): Show | 294 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.2811+116T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132788911 | ||||||
| chr12:132788912
|
C | G | 1 | a0001c0001t0059g0120 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2811+115G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132788912 | ||||||
| chr12:132788921
|
A | ACCCCGCC others(11): Show |
124 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0001g0167others(121): Show | 124 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(121): Show |
intron_variant | MODIFIER | c.2811+88_2811+105du others(19): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132788921 | ||||||
| chr12:132788925
|
C | CGCCCCAG others(11): Show |
1 | a0018c0029t0061g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2811+101_2811+102i others(20): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132788925 | ||||||
| chr12:132788939
|
G | GCCCCGCC others(12): Show |
1 | a0002c0002t0034g0227 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2811+69_2811+87dup others(19): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132788939 | ||||||
| chr12:132788970
|
G | A | 1 | a0018c0029t0061g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2811+57C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 13/23 | chr12 | 132788970 | ||||||
| chr12:132789328
|
C | T | 27 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0001g0167others(24): Show | 27 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.2548-38G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132789328 | ||||||
| chr12:132789334
|
G | A | 120 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(117): Show | 120 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.2548-44C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132789334 | ||||||
| chr12:132789430
|
A | C | 79 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(76): Show | 79 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.2548-140T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132789430 | ||||||
| chr12:132789556
|
G | A | 1 | a0001c0001t0029g0304 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2548-266C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132789556 | ||||||
| chr12:132789615
|
T | G | 3 | a0001c0001t0026g0302a0001c0001t0027g0306a0002c0007t0031g0307 | 3 | HG02886.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2548-325A>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132789615 | ||||||
| chr12:132789655
|
G | A | 86 | a0001c0003t0002g0196a0001c0009t0002g0181a0001c0009t0002g0199others(83): Show | 86 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.2548-365C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132789655 | ||||||
| chr12:132789673
|
G | GCTCAGAA others(51): Show |
197 | a0001c0001t0002g0121a0001c0001t0003g0006a0001c0001t0003g0007others(194): Show | 197 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.2548-441_2548-384d others(60): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132789673 | ||||||
| chr12:132789673
|
G | GCTCAGAA others(109): Show |
1 | a0001c0018t0019g0132 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2548-499_2548-384d others(118): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132789673 | ||||||
| chr12:132789673
|
G | GCTCAGAA others(51): Show |
1 | a0018c0029t0061g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2548-384_2548-383i others(60): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132789673 | ||||||
| chr12:132789748
|
A | AGCAGGCC others(51): Show |
7 | a0004c0005t0005g0247a0004c0005t0005g0248a0004c0005t0005g0249others(4): Show | 7 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.2548-459_2548-458i others(60): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132789748 | ||||||
| chr12:132789770
|
A | ACACTTGT others(51): Show |
1 | a0001c0001t0033g0108 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2548-481_2548-480i others(60): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132789770 | ||||||
| chr12:132789858
|
C | T | 1 | a0002c0012t0011g0125 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2548-568G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132789858 | ||||||
| chr12:132790040
|
C | A | 207 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(204): Show | 207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.2548-750G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132790040 | ||||||
| chr12:132790045
|
T | A | 207 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(204): Show | 207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.2548-755A>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132790045 | ||||||
| chr12:132790054
|
G | A | 87 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0001g0167others(84): Show | 87 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.2548-764C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132790054 | ||||||
| chr12:132790069
|
T | C | 2 | a0002c0002t0003g0240a0002c0002t0053g0239 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2548-779A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132790069 | ||||||
| chr12:132790070
|
G | A | 2 | a0002c0002t0003g0240a0002c0002t0053g0239 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2548-780C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132790070 | ||||||
| chr12:132790083
|
G | C | 2 | a0002c0002t0002g0190a0002c0002t0002g0191 | 2 | HG02280.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2548-793C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132790083 | ||||||
| chr12:132790090
|
G | C | 87 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0001g0167others(84): Show | 87 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.2548-800C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132790090 | ||||||
| chr12:132790159
|
G | A | 3 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0025g0040 | 3 | HG01243.hp1 HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2548-869C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132790159 | ||||||
| chr12:132790194
|
C | T | 1 | a0002c0012t0002g0124 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2548-904G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132790194 | ||||||
| chr12:132790258
|
T | G | 174 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0001g0167others(171): Show | 174 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.2547+958A>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132790258 | ||||||
| chr12:132790288
|
C | T | 1 | a0001c0003t0004g0164 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2547+928G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132790288 | ||||||
| chr12:132790328
|
C | A | 87 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0001g0167others(84): Show | 87 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.2547+888G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132790328 | ||||||
| chr12:132790506
|
G | A | 295 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(292): Show | 295 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.2547+710C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132790506 | ||||||
| chr12:132790672
|
C | T | 2 | a0002c0002t0002g0179a0002c0002t0002g0180 | 2 | HG00741.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.2547+544G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132790672 | ||||||
| chr12:132790769
|
C | T | 46 | a0003c0004t0001g0270a0003c0004t0001g0279a0003c0004t0001g0282others(43): Show | 46 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.2547+447G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132790769 | ||||||
| chr12:132790937
|
G | GCTA | 17 | a0004c0005t0005g0049a0004c0005t0005g0101a0004c0005t0005g0247others(14): Show | 17 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.2547+276_2547+278d others(5): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132790937 | ||||||
| chr12:132790976
|
G | A | 2 | a0001c0001t0001g0047a0001c0001t0001g0054 | 2 | NA18979.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.2547+240C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132790976 | ||||||
| chr12:132791050
|
C | CA | 40 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0035others(37): Show | 40 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.2547+165dupT | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132791050 | ||||||
| chr12:132791050
|
C | CAA | 70 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0036others(67): Show | 70 | HG00323.hp2 HG00438.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.2547+164_2547+165d others(4): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132791050 | ||||||
| chr12:132791050
|
C | CAAA | 45 | a0001c0001t0001g0026a0001c0001t0001g0043a0001c0001t0001g0047others(42): Show | 45 | HG01106.hp1 HG01123.hp1 HG01123.hp2 others(42): Show |
intron_variant | MODIFIER | c.2547+163_2547+165d others(5): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132791050 | ||||||
| chr12:132791050
|
C | CAAAA | 20 | a0001c0001t0001g0054a0001c0001t0001g0056a0001c0001t0001g0063others(17): Show | 20 | HG00408.hp2 HG00741.hp1 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.2547+162_2547+165d others(6): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132791050 | ||||||
| chr12:132791050
|
C | CAAAAA | 7 | a0002c0002t0002g0175a0002c0002t0002g0198a0002c0002t0002g0213others(4): Show | 7 | HG00423.hp2 HG00642.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.2547+161_2547+165d others(7): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132791050 | ||||||
| chr12:132791050
|
C | CAAAAAAA others(4): Show |
1 | a0001c0003t0002g0196 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2547+155_2547+165d others(13): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132791050 | ||||||
| chr12:132791050
|
C | CAAAAAAA others(15): Show |
1 | a0001c0018t0019g0132 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2547+144_2547+165d others(24): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132791050 | ||||||
| chr12:132791050
|
CAA | C | 12 | a0004c0005t0005g0101a0004c0005t0005g0247a0004c0005t0005g0248others(9): Show | 12 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.2547+164_2547+165d others(4): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132791050 | ||||||
| chr12:132791050
|
CAAAA | C | 10 | a0001c0001t0075g0128a0001c0003t0004g0143a0001c0003t0004g0144others(7): Show | 10 | HG00642.hp2 HG01884.hp2 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.2547+162_2547+165d others(6): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132791050 | ||||||
| chr12:132791050
|
CAAAAA | C | 18 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0001g0167others(15): Show | 18 | HG01255.hp1 HG01981.hp1 HG01993.hp1 others(15): Show |
intron_variant | MODIFIER | c.2547+161_2547+165d others(7): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132791050 | ||||||
| chr12:132791050
|
CAAAAAA | C | 12 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0059g0120others(9): Show | 12 | HG02055.hp2 HG02486.hp2 HG02683.hp1 others(9): Show |
intron_variant | MODIFIER | c.2547+160_2547+165d others(8): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132791050 | ||||||
| chr12:132791050
|
CAAAAAAA | C | 9 | a0001c0001t0003g0105a0001c0001t0003g0112a0001c0001t0003g0115others(6): Show | 9 | HG00738.hp1 HG01175.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.2547+159_2547+165d others(9): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132791050 | ||||||
| chr12:132791050
|
CAAAAAAA others(1): Show |
C | 20 | a0001c0001t0002g0121a0001c0001t0003g0010a0001c0001t0003g0104others(17): Show | 20 | HG00280.hp1 HG00738.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.2547+158_2547+165d others(10): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132791050 | ||||||
| chr12:132791050
|
CAAAAAAA others(3): Show |
C | 1 | a0014c0020t0019g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2547+156_2547+165d others(12): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132791050 | ||||||
| chr12:132791050
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0030g0303 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2547+154_2547+165d others(14): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132791050 | ||||||
| chr12:132791050
|
CAAAAAAA others(6): Show |
C | 2 | a0009c0015t0078g0066a0009c0015t0080g0065 | 2 | HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2547+153_2547+165d others(15): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132791050 | ||||||
| chr12:132791050
|
CAAAAAAA others(7): Show |
C | 1 | a0002c0002t0002g0206 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2547+152_2547+165d others(16): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132791050 | ||||||
| chr12:132791050
|
CAAAAAAA others(11): Show |
C | 2 | a0002c0002t0003g0240a0002c0002t0053g0239 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2547+148_2547+165d others(20): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132791050 | ||||||
| chr12:132791092
|
A | C | 14 | a0005c0006t0001g0021a0005c0006t0014g0018a0005c0006t0014g0019others(11): Show | 14 | HG02055.hp2 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.2547+124T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132791092 | ||||||
| chr12:132791202
|
C | T | 1 | a0001c0001t0075g0128 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2547+14G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 12/23 | chr12 | 132791202 | ||||||
| chr12:132791466
|
C | T | 1 | a0018c0029t0061g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2470-173G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132791466 | ||||||
| chr12:132791559
|
CGATGTTA others(324): Show |
C | 32 | a0001c0001t0002g0121a0001c0001t0003g0006a0001c0001t0003g0007others(29): Show | 32 | HG00280.hp1 HG00438.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.2470-597_2470-267d others(2): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132791559 | ||||||
| chr12:132791594
|
C | CTGCAGAG others(31): Show |
1 | a0001c0001t0001g0137 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2470-339_2470-302d others(40): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132791594 | ||||||
| chr12:132791681
|
C | T | 3 | a0001c0001t0026g0302a0001c0001t0027g0306a0002c0007t0031g0307 | 3 | HG02886.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2470-388G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132791681 | ||||||
| chr12:132791725
|
CAGATGTT others(34): Show |
C | 3 | a0001c0001t0026g0302a0001c0001t0027g0306a0002c0007t0031g0307 | 3 | HG02886.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2470-473_2470-433d others(43): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132791725 | ||||||
| chr12:132791834
|
A | G | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0045others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2470-541T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132791834 | ||||||
| chr12:132791953
|
G | A | 7 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(4): Show | 7 | NA18950.hp2 NA18964.hp2 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.2470-660C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132791953 | ||||||
| chr12:132791998
|
G | C | 87 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0001g0167others(84): Show | 87 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.2470-705C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132791998 | ||||||
| chr12:132792157
|
G | A | 1 | a0001c0001t0028g0305 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2470-864C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132792157 | ||||||
| chr12:132792426
|
C | G | 1 | a0013c0035t0035g0262 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2470-1133G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132792426 | ||||||
| chr12:132792443
|
C | G | 2 | a0004c0036t0008g0263a0013c0035t0035g0262 | 2 | HG02004.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.2470-1150G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132792443 | ||||||
| chr12:132792624
|
C | CGAGGGCT others(353): Show |
1 | a0001c0001t0073g0041 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2470-1332_2470-133 others(364): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132792624 | ||||||
| chr12:132792625
|
G | A | 2 | a0003c0004t0008g0278a0003c0004t0013g0261 | 2 | NA18977.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.2470-1332C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132792625 | ||||||
| chr12:132792647
|
G | A | 1 | a0002c0007t0031g0307 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2470-1354C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132792647 | ||||||
| chr12:132792651
|
G | A | 1 | a0010c0039t0010g0033 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2470-1358C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132792651 | ||||||
| chr12:132792663
|
C | T | 1 | a0001c0003t0004g0159 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2470-1370G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132792663 | ||||||
| chr12:132792687
|
A | G | 1 | a0014c0020t0019g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2470-1394T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132792687 | ||||||
| chr12:132792698
|
G | GCACTCGG others(113): Show |
1 | a0002c0002t0002g0178 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2470-1406_2470-140 others(124): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132792698 | ||||||
| chr12:132792704
|
G | A | 7 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0056others(4): Show | 7 | HG00408.hp1 NA18947.hp1 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.2470-1411C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132792704 | ||||||
| chr12:132792718
|
G | A | 1 | a0003c0004t0022g0277 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2470-1425C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132792718 | ||||||
| chr12:132792723
|
G | C | 1 | a0003c0004t0022g0277 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2470-1430C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132792723 | ||||||
| chr12:132792730
|
C | T | 3 | a0001c0001t0026g0302a0001c0001t0027g0306a0002c0007t0031g0307 | 3 | HG02886.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2470-1437G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132792730 | ||||||
| chr12:132792737
|
TGCACTCG others(633): Show |
T | 3 | a0003c0008t0007g0271a0003c0008t0007g0273a0003c0008t0022g0265 | 3 | NA18939.hp1 NA18946.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.2470-2084_2470-144 others(4): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132792737 | ||||||
| chr12:132792758
|
G | A | 84 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0001g0167others(81): Show | 84 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.2470-1465C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132792758 | ||||||
| chr12:132792762
|
T | C | 205 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(202): Show | 205 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.2470-1469A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132792762 | ||||||
| chr12:132792763
|
G | C | 26 | a0003c0004t0001g0270a0003c0004t0001g0279a0003c0004t0001g0282others(23): Show | 26 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.2470-1470C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132792763 | ||||||
| chr12:132792763
|
G | GACCGCAC others(273): Show |
1 | a0001c0003t0009g0300 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2470-1471_2470-147 others(284): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132792763 | ||||||
| chr12:132792784
|
G | A | 42 | a0001c0001t0072g0075a0001c0003t0001g0148a0001c0003t0001g0151others(39): Show | 42 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(39): Show |
intron_variant | MODIFIER | c.2470-1491C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132792784 | ||||||
| chr12:132792798
|
G | A | 85 | a0001c0001t0001g0026a0001c0003t0001g0148a0001c0003t0001g0151others(82): Show | 85 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.2470-1505C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132792798 | ||||||
| chr12:132792807
|
C | A | 1 | a0001c0003t0004g0142 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2470-1514G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132792807 | ||||||
| chr12:132792815
|
T | C | 120 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(117): Show | 120 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.2470-1522A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132792815 | ||||||
| chr12:132792818
|
C | G | 1 | a0015c0021t0068g0072 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2470-1525G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132792818 | ||||||
| chr12:132792818
|
CCACTCGG others(113): Show |
C | 2 | a0002c0002t0003g0240a0002c0002t0053g0239 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2470-1645_2470-152 others(4): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132792818 | ||||||
| chr12:132792837
|
C | CA | 14 | a0005c0006t0001g0021a0005c0006t0014g0018a0005c0006t0014g0019others(11): Show | 14 | HG02055.hp2 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.2470-1545_2470-154 others(5): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132792837 | ||||||
| chr12:132792838
|
G | A | 203 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(200): Show | 203 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.2470-1545C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132792838 | ||||||
| chr12:132792839
|
G | A | 14 | a0005c0006t0001g0021a0005c0006t0014g0018a0005c0006t0014g0019others(11): Show | 14 | HG02055.hp2 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.2470-1546C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132792839 | ||||||
| chr12:132792842
|
C | T | 2 | a0001c0011t0001g0061a0001c0011t0074g0067 | 2 | NA18952.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.2470-1549G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132792842 | ||||||
| chr12:132792864
|
G | A | 1 | a0001c0003t0011g0161 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2470-1571C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132792864 | ||||||
| chr12:132792887
|
A | C | 84 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0001g0167others(81): Show | 84 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.2470-1594T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132792887 | ||||||
| chr12:132792897
|
TGCACTCG others(633): Show |
T | 1 | a0005c0006t0018g0102 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2470-2244_2470-160 others(4): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132792897 | ||||||
| chr12:132792937
|
T | C | 1 | a0001c0001t0059g0120 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2470-1644A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132792937 | ||||||
| chr12:132792967
|
A | C | 17 | a0004c0005t0005g0049a0004c0005t0005g0101a0004c0005t0005g0247others(14): Show | 17 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.2470-1674T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132792967 | ||||||
| chr12:132792975
|
T | C | 4 | a0001c0003t0004g0142a0002c0002t0003g0240a0002c0002t0053g0239others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.2470-1682A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132792975 | ||||||
| chr12:132792977
|
T | C | 1 | a0017c0022t0001g0025 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2470-1684A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132792977 | ||||||
| chr12:132792979
|
A | C | 3 | a0006c0010t0006g0011a0006c0010t0006g0130a0006c0010t0047g0134 | 3 | HG01106.hp1 HG02622.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2470-1686T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132792979 | ||||||
| chr12:132793002
|
A | C | 2 | a0002c0002t0002g0213a0002c0002t0002g0215 | 2 | HG00423.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.2470-1709T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793002 | ||||||
| chr12:132793002
|
AGACCGCA others(193): Show |
A | 14 | a0004c0005t0005g0049a0004c0005t0005g0101a0004c0005t0005g0247others(11): Show | 14 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.2470-1909_2470-171 others(4): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793002 | ||||||
| chr12:132793002
|
AGACCGCA others(233): Show |
A | 3 | a0004c0005t0005g0257a0007c0016t0020g0253a0007c0016t0020g0254 | 3 | HG03491.hp2 HG03492.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.2470-1949_2470-171 others(4): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793002 | ||||||
| chr12:132793003
|
G | C | 26 | a0003c0004t0001g0270a0003c0004t0001g0279a0003c0004t0001g0282others(23): Show | 26 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.2470-1710C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793003 | ||||||
| chr12:132793003
|
GACCGCAC others(33): Show |
G | 1 | a0018c0029t0061g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2470-1750_2470-171 others(44): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793003 | ||||||
| chr12:132793003
|
GACCGCAC others(233): Show |
G | 1 | a0001c0003t0001g0167 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2470-1950_2470-171 others(4): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793003 | ||||||
| chr12:132793003
|
GACCGCAC others(353): Show |
G | 1 | a0005c0006t0018g0023 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2470-2070_2470-171 others(4): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793003 | ||||||
| chr12:132793007
|
GCACGGGA others(73): Show |
G | 3 | a0005c0006t0043g0004a0005c0006t0044g0005a0005c0006t0081g0308 | 3 | HG02486.hp2 HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2470-1794_2470-171 others(84): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793007 | ||||||
| chr12:132793017
|
C | T | 49 | a0001c0001t0002g0121a0001c0001t0003g0006a0001c0001t0003g0007others(46): Show | 49 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.2470-1724G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793017 | ||||||
| chr12:132793023
|
C | T | 1 | a0002c0002t0002g0203 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2470-1730G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793023 | ||||||
| chr12:132793038
|
AGACCCAC others(193): Show |
A | 16 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0004g0142others(13): Show | 16 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.2470-1945_2470-174 others(4): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793038 | ||||||
| chr12:132793047
|
G | C | 1 | a0002c0002t0002g0204 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2470-1754C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793047 | ||||||
| chr12:132793057
|
C | T | 1 | a0018c0029t0061g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2470-1764G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793057 | ||||||
| chr12:132793071
|
T | C | 1 | a0001c0003t0009g0300 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2470-1778A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793071 | ||||||
| chr12:132793078
|
AGACCCAC others(153): Show |
A | 8 | a0001c0003t0004g0144a0001c0003t0004g0145a0001c0003t0004g0158others(5): Show | 8 | HG02155.hp2 HG02738.hp1 NA18956.hp1 others(5): Show |
intron_variant | MODIFIER | c.2470-1945_2470-178 others(4): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793078 | ||||||
| chr12:132793087
|
C | CCACGGGA others(33): Show |
1 | a0002c0002t0002g0203 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2470-1834_2470-179 others(44): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793087 | ||||||
| chr12:132793087
|
C | CCACGGGA others(433): Show |
1 | a0001c0024t0002g0100 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2470-1795_2470-179 others(444): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793087 | ||||||
| chr12:132793087
|
C | G | 23 | a0001c0001t0001g0035a0001c0001t0001g0063a0001c0001t0001g0087others(20): Show | 23 | HG00741.hp1 HG01123.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.2470-1794G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793087 | ||||||
| chr12:132793118
|
A | AGACCCAC others(153): Show |
2 | a0002c0002t0002g0203a0002c0002t0002g0204 | 2 | HG03491.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.2470-1826_2470-182 others(164): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793118 | ||||||
| chr12:132793118
|
A | AGACCCAC others(33): Show |
8 | a0005c0006t0001g0021a0005c0006t0014g0018a0005c0006t0014g0019others(5): Show | 8 | HG02055.hp2 HG02559.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.2470-1826_2470-182 others(44): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793118 | ||||||
| chr12:132793118
|
AGACCCAC others(113): Show |
A | 1 | a0009c0015t0080g0065 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2470-1945_2470-182 others(4): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793118 | ||||||
| chr12:132793127
|
G | A | 4 | a0001c0001t0001g0043a0002c0002t0002g0235a0002c0002t0002g0243others(1): Show | 4 | HG03669.hp1 NA18960.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.2470-1834C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793127 | ||||||
| chr12:132793127
|
G | C | 5 | a0001c0001t0001g0063a0001c0001t0001g0087a0001c0001t0001g0088others(2): Show | 5 | HG00741.hp1 HG01123.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.2470-1834C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793127 | ||||||
| chr12:132793130
|
C | CGGGACCC others(153): Show |
1 | a0001c0001t0001g0037 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2470-1838_2470-183 others(164): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793130 | ||||||
| chr12:132793135
|
C | T | 1 | a0001c0001t0001g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2470-1842G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793135 | ||||||
| chr12:132793136
|
C | T | 1 | a0001c0018t0019g0132 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2470-1843G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793136 | ||||||
| chr12:132793137
|
C | T | 1 | a0001c0001t0001g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2470-1844G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793137 | ||||||
| chr12:132793139
|
C | A | 1 | a0001c0001t0001g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2470-1846G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793139 | ||||||
| chr12:132793158
|
A | AGACCCAC others(73): Show |
1 | a0001c0001t0001g0093 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2470-1866_2470-186 others(84): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793158 | ||||||
| chr12:132793158
|
AGACCCAC others(73): Show |
A | 1 | a0009c0015t0078g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2470-1945_2470-186 others(84): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793158 | ||||||
| chr12:132793162
|
C | A | 1 | a0001c0001t0001g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2470-1869G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793162 | ||||||
| chr12:132793163
|
C | G | 1 | a0001c0001t0001g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2470-1870G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793163 | ||||||
| chr12:132793165
|
C | T | 28 | a0001c0001t0002g0121a0001c0001t0003g0006a0001c0001t0003g0007others(25): Show | 28 | HG00438.hp2 HG00738.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.2470-1872G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793165 | ||||||
| chr12:132793167
|
G | A | 1 | a0002c0002t0002g0175 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2470-1874C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793167 | ||||||
| chr12:132793167
|
G | C | 62 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(59): Show | 62 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.2470-1874C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793167 | ||||||
| chr12:132793175
|
C | T | 1 | a0002c0002t0002g0175 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2470-1882G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793175 | ||||||
| chr12:132793177
|
C | T | 1 | a0002c0002t0002g0175 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2470-1884G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793177 | ||||||
| chr12:132793179
|
C | A | 1 | a0002c0002t0002g0175 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2470-1886G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793179 | ||||||
| chr12:132793191
|
T | TCCACACA others(73): Show |
1 | a0001c0001t0001g0027 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2470-1899_2470-189 others(84): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793191 | ||||||
| chr12:132793191
|
T | TCCACACA others(33): Show |
5 | a0001c0001t0001g0063a0001c0001t0001g0087a0001c0001t0001g0088others(2): Show | 5 | HG00741.hp1 HG01123.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.2470-1899_2470-189 others(44): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793191 | ||||||
| chr12:132793191
|
T | TCCACACA others(73): Show |
61 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0029others(58): Show | 61 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.2470-1899_2470-189 others(84): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793191 | ||||||
| chr12:132793198
|
A | T | 5 | a0001c0024t0002g0100a0002c0002t0002g0190a0002c0002t0002g0191others(2): Show | 5 | HG01891.hp1 HG02055.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2470-1905T>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793198 | ||||||
| chr12:132793198
|
AGACCCAC others(33): Show |
A | 1 | a0001c0001t0001g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2470-1945_2470-190 others(44): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793198 | ||||||
| chr12:132793207
|
G | A | 1 | a0001c0001t0017g0001 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2470-1914C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793207 | ||||||
| chr12:132793207
|
G | C | 2 | a0002c0002t0002g0203a0002c0002t0002g0204 | 2 | HG03491.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.2470-1914C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793207 | ||||||
| chr12:132793238
|
T | A | 32 | a0001c0001t0001g0037a0001c0001t0001g0093a0001c0003t0004g0166others(29): Show | 32 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.2470-1945A>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793238 | ||||||
| chr12:132793238
|
T | TGACCCAC others(33): Show |
60 | a0001c0003t0002g0196a0001c0009t0002g0181a0001c0009t0002g0201others(57): Show | 60 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.2470-1985_2470-194 others(44): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793238 | ||||||
| chr12:132793238
|
T | TGACCCAC others(73): Show |
5 | a0001c0001t0026g0302a0001c0001t0027g0306a0001c0001t0030g0303others(2): Show | 5 | HG01257.hp2 HG02129.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2470-2025_2470-194 others(84): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793238 | ||||||
| chr12:132793238
|
T | TGACCCAC others(153): Show |
14 | a0001c0001t0017g0015a0001c0001t0028g0305a0001c0003t0006g0290others(11): Show | 14 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.2470-2105_2470-194 others(164): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793238 | ||||||
| chr12:132793238
|
T | TGACCCAC others(193): Show |
2 | a0002c0002t0002g0217a0002c0002t0052g0220 | 2 | HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2470-1946_2470-194 others(204): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793238 | ||||||
| chr12:132793238
|
T | TGACCCAC others(233): Show |
1 | a0001c0009t0002g0199 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2470-1946_2470-194 others(244): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793238 | ||||||
| chr12:132793238
|
T | TGACCCAC others(73): Show |
3 | a0006c0010t0006g0011a0006c0010t0006g0130a0006c0010t0047g0134 | 3 | HG01106.hp1 HG02622.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2470-1946_2470-194 others(84): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793238 | ||||||
| chr12:132793238
|
TGACCCAC others(153): Show |
T | 3 | a0005c0006t0043g0004a0005c0006t0044g0005a0005c0006t0081g0308 | 3 | HG02486.hp2 HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2470-2105_2470-194 others(4): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793238 | ||||||
| chr12:132793238
|
TGACCCAC others(233): Show |
T | 2 | a0004c0036t0008g0263a0013c0035t0035g0262 | 2 | HG02004.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.2470-2185_2470-194 others(4): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793238 | ||||||
| chr12:132793238
|
TGACCCAC others(273): Show |
T | 24 | a0003c0004t0001g0270a0003c0004t0001g0279a0003c0004t0001g0282others(21): Show | 24 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(21): Show |
intron_variant | MODIFIER | c.2470-2225_2470-194 others(4): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793238 | ||||||
| chr12:132793247
|
G | C | 14 | a0004c0005t0005g0049a0004c0005t0005g0101a0004c0005t0005g0247others(11): Show | 14 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.2470-1954C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793247 | ||||||
| chr12:132793255
|
C | T | 14 | a0004c0005t0005g0049a0004c0005t0005g0101a0004c0005t0005g0247others(11): Show | 14 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.2470-1962G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793255 | ||||||
| chr12:132793257
|
C | T | 14 | a0004c0005t0005g0049a0004c0005t0005g0101a0004c0005t0005g0247others(11): Show | 14 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.2470-1964G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793257 | ||||||
| chr12:132793259
|
C | A | 14 | a0004c0005t0005g0049a0004c0005t0005g0101a0004c0005t0005g0247others(11): Show | 14 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.2470-1966G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793259 | ||||||
| chr12:132793282
|
C | A | 14 | a0004c0005t0005g0049a0004c0005t0005g0101a0004c0005t0005g0247others(11): Show | 14 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.2470-1989G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793282 | ||||||
| chr12:132793283
|
C | CACCGCAC others(273): Show |
1 | a0005c0006t0064g0022 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2470-1991_2470-199 others(284): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793283 | ||||||
| chr12:132793287
|
G | C | 3 | a0004c0005t0005g0257a0007c0016t0020g0253a0007c0016t0020g0254 | 3 | HG03491.hp2 HG03492.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.2470-1994C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793287 | ||||||
| chr12:132793295
|
C | T | 3 | a0004c0005t0005g0257a0007c0016t0020g0253a0007c0016t0020g0254 | 3 | HG03491.hp2 HG03492.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.2470-2002G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793295 | ||||||
| chr12:132793297
|
C | T | 3 | a0004c0005t0005g0257a0007c0016t0020g0253a0007c0016t0020g0254 | 3 | HG03491.hp2 HG03492.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.2470-2004G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793297 | ||||||
| chr12:132793299
|
C | A | 3 | a0004c0005t0005g0257a0007c0016t0020g0253a0007c0016t0020g0254 | 3 | HG03491.hp2 HG03492.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.2470-2006G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793299 | ||||||
| chr12:132793318
|
A | AGACCCAC others(73): Show |
1 | a0012c0019t0038g0024 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2470-2026_2470-202 others(84): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793318 | ||||||
| chr12:132793322
|
C | A | 3 | a0004c0005t0005g0257a0007c0016t0020g0253a0007c0016t0020g0254 | 3 | HG03491.hp2 HG03492.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.2470-2029G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793322 | ||||||
| chr12:132793327
|
G | A | 2 | a0002c0002t0002g0217a0009c0015t0078g0066 | 2 | HG02896.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.2470-2034C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793327 | ||||||
| chr12:132793330
|
C | T | 1 | a0004c0005t0005g0252 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2470-2037G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793330 | ||||||
| chr12:132793335
|
C | T | 1 | a0009c0015t0078g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2470-2042G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793335 | ||||||
| chr12:132793337
|
C | T | 1 | a0009c0015t0078g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2470-2044G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793337 | ||||||
| chr12:132793358
|
A | AGACCCAC others(33): Show |
1 | a0001c0001t0073g0041 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2470-2066_2470-206 others(44): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793358 | ||||||
| chr12:132793363
|
C | CACCGCAC others(193): Show |
6 | a0005c0006t0014g0018a0005c0006t0014g0019a0005c0006t0014g0020others(3): Show | 6 | HG02559.hp2 HG02965.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.2470-2071_2470-207 others(204): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793363 | ||||||
| chr12:132793363
|
C | CACCGCAC others(233): Show |
1 | a0005c0006t0001g0021 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2470-2071_2470-207 others(244): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793363 | ||||||
| chr12:132793367
|
G | A | 1 | a0009c0015t0080g0065 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2470-2074C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793367 | ||||||
| chr12:132793367
|
G | C | 14 | a0004c0005t0005g0049a0004c0005t0005g0101a0004c0005t0005g0247others(11): Show | 14 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.2470-2074C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793367 | ||||||
| chr12:132793375
|
C | T | 1 | a0009c0015t0080g0065 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2470-2082G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793375 | ||||||
| chr12:132793377
|
C | T | 1 | a0009c0015t0080g0065 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2470-2084G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793377 | ||||||
| chr12:132793398
|
A | AGACCCAC others(193): Show |
1 | a0001c0001t0001g0039 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2470-2106_2470-210 others(204): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793398 | ||||||
| chr12:132793407
|
G | C | 3 | a0004c0005t0005g0257a0007c0016t0020g0253a0007c0016t0020g0254 | 3 | HG03491.hp2 HG03492.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.2470-2114C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793407 | ||||||
| chr12:132793410
|
C | CGGGACCC others(33): Show |
1 | a0001c0001t0029g0304 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2470-2118_2470-211 others(44): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793410 | ||||||
| chr12:132793417
|
C | T | 3 | a0003c0008t0007g0271a0003c0008t0007g0273a0003c0008t0022g0265 | 3 | NA18939.hp1 NA18946.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.2470-2124G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793417 | ||||||
| chr12:132793438
|
A | T | 2 | a0009c0015t0078g0066a0009c0015t0080g0065 | 2 | HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2470-2145T>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793438 | ||||||
| chr12:132793445
|
C | CCGCACGG others(33): Show |
1 | a0002c0002t0057g0184 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2470-2153_2470-215 others(44): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793445 | ||||||
| chr12:132793447
|
G | C | 3 | a0003c0008t0007g0271a0003c0008t0007g0273a0003c0008t0022g0265 | 3 | NA18939.hp1 NA18946.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.2470-2154C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793447 | ||||||
| chr12:132793447
|
G | CCACGGGA others(153): Show |
1 | a0001c0003t0048g0289 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2470-2154_2470-215 others(164): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793447 | ||||||
| chr12:132793450
|
C | G | 30 | a0001c0001t0002g0121a0001c0001t0003g0006a0001c0001t0003g0007others(27): Show | 30 | HG00280.hp1 HG00438.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.2470-2157G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793450 | ||||||
| chr12:132793457
|
C | T | 3 | a0003c0008t0007g0271a0003c0008t0007g0273a0003c0008t0022g0265 | 3 | NA18939.hp1 NA18946.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.2470-2164G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793457 | ||||||
| chr12:132793458
|
G | C | 3 | a0003c0008t0007g0271a0003c0008t0007g0273a0003c0008t0022g0265 | 3 | NA18939.hp1 NA18946.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.2470-2165C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793458 | ||||||
| chr12:132793478
|
A | AGACCCAC others(193): Show |
1 | a0001c0018t0019g0132 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2470-2186_2470-218 others(204): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793478 | ||||||
| chr12:132793478
|
A | T | 1 | a0001c0024t0002g0100 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2470-2185T>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793478 | ||||||
| chr12:132793483
|
C | G | 3 | a0003c0008t0007g0271a0003c0008t0007g0273a0003c0008t0022g0265 | 3 | NA18939.hp1 NA18946.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.2470-2190G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793483 | ||||||
| chr12:132793487
|
G | A | 3 | a0003c0008t0007g0271a0003c0008t0007g0273a0003c0008t0022g0265 | 3 | NA18939.hp1 NA18946.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.2470-2194C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793487 | ||||||
| chr12:132793487
|
GCACGGGA others(233): Show |
G | 30 | a0001c0001t0002g0121a0001c0001t0003g0006a0001c0001t0003g0007others(27): Show | 30 | HG00280.hp1 HG00438.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.2469+2125_2470-219 others(4): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793487 | ||||||
| chr12:132793518
|
A | AGACCCAC others(113): Show |
2 | a0001c0001t0001g0069a0001c0001t0073g0041 | 2 | HG02280.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.2470-2226_2470-222 others(124): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793518 | ||||||
| chr12:132793518
|
A | AGACCCAC others(73): Show |
65 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(62): Show | 65 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.2470-2226_2470-222 others(84): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793518 | ||||||
| chr12:132793518
|
A | AGACCCAC others(233): Show |
1 | a0001c0001t0001g0070 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2470-2226_2470-222 others(244): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793518 | ||||||
| chr12:132793518
|
A | AGACCCAC others(73): Show |
1 | a0001c0001t0001g0137 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2470-2226_2470-222 others(84): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793518 | ||||||
| chr12:132793518
|
A | T | 28 | a0001c0001t0001g0093a0001c0024t0002g0100a0003c0008t0007g0271others(25): Show | 28 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.2470-2225T>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793518 | ||||||
| chr12:132793527
|
GCACGGGA others(193): Show |
G | 6 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2469+2125_2470-223 others(4): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793527 | ||||||
| chr12:132793530
|
C | CGGGACCC others(73): Show |
1 | a0001c0001t0029g0304 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2470-2238_2470-223 others(84): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793530 | ||||||
| chr12:132793558
|
A | T | 1 | a0004c0005t0005g0257 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2470-2265T>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793558 | ||||||
| chr12:132793571
|
G | A | 10 | a0004c0005t0005g0049a0004c0005t0005g0247a0004c0005t0005g0248others(7): Show | 10 | HG00323.hp1 HG01175.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.2470-2278C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793571 | ||||||
| chr12:132793577
|
CGCACTCG others(153): Show |
C | 2 | a0002c0002t0002g0168a0002c0002t0002g0174 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2469+2115_2469+227 others(4): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793577 | ||||||
| chr12:132793607
|
GCACGGGA others(113): Show |
G | 1 | a0001c0001t0001g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2469+2125_2469+224 others(4): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793607 | ||||||
| chr12:132793610
|
C | CGGGACCC others(33): Show |
3 | a0002c0002t0002g0175a0002c0002t0002g0176a0002c0002t0002g0177 | 3 | HG00642.hp1 HG01167.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.2469+2241_2469+224 others(44): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793610 | ||||||
| chr12:132793617
|
C | T | 1 | a0002c0007t0001g0058 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2469+2235G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793617 | ||||||
| chr12:132793619
|
C | CACTCGGA others(73): Show |
1 | a0002c0007t0031g0307 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2469+2232_2469+223 others(84): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793619 | ||||||
| chr12:132793627
|
G | A | 2 | a0001c0003t0004g0166a0001c0003t0042g0146 | 2 | NA18994.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.2469+2225C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793627 | ||||||
| chr12:132793681
|
C | A | 1 | a0011c0017t0008g0267 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2469+2171G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793681 | ||||||
| chr12:132793687
|
GCACGGGA others(33): Show |
G | 2 | a0001c0001t0075g0128a0001c0003t0001g0167 | 2 | HG01255.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.2469+2125_2469+216 others(44): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793687 | ||||||
| chr12:132793695
|
C | T | 1 | a0001c0001t0017g0001 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2469+2157G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793695 | ||||||
| chr12:132793697
|
C | T | 1 | a0001c0001t0017g0001 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2469+2155G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793697 | ||||||
| chr12:132793715
|
C | CACAGACC others(33): Show |
1 | a0002c0002t0057g0184 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2469+2136_2469+213 others(44): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793715 | ||||||
| chr12:132793727
|
A | C | 1 | a0005c0006t0018g0102 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2469+2125T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793727 | ||||||
| chr12:132793727
|
A | G | 89 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(86): Show | 89 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.2469+2125T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793727 | ||||||
| chr12:132793731
|
G | GGGACCCG others(633): Show |
1 | a0014c0020t0019g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2469+2120_2469+212 others(644): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793731 | ||||||
| chr12:132793735
|
T | C | 1 | a0014c0020t0019g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2469+2117A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793735 | ||||||
| chr12:132793771
|
A | G | 1 | a0018c0029t0061g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2469+2081T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793771 | ||||||
| chr12:132793797
|
G | C | 1 | a0001c0003t0009g0292 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2469+2055C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132793797 | ||||||
| chr12:132794225
|
T | C | 1 | a0001c0001t0017g0001 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2469+1627A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132794225 | ||||||
| chr12:132794331
|
T | C | 2 | a0002c0002t0002g0179a0002c0002t0002g0180 | 2 | HG00741.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.2469+1521A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132794331 | ||||||
| chr12:132794333
|
T | TA | 29 | a0001c0001t0001g0135a0001c0003t0001g0151a0001c0003t0001g0167others(26): Show | 29 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.2469+1518dupT | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132794333 | ||||||
| chr12:132794333
|
TA | T | 15 | a0001c0001t0001g0073a0001c0001t0003g0116a0001c0003t0006g0291others(12): Show | 15 | HG01069.hp2 HG01070.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.2469+1518delT | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132794333 | ||||||
| chr12:132794627
|
A | C | 87 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0001g0167others(84): Show | 87 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.2469+1225T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132794627 | ||||||
| chr12:132794636
|
CAA | C | 27 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0001g0167others(24): Show | 27 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.2469+1214_2469+121 others(6): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132794636 | ||||||
| chr12:132794692
|
C | G | 5 | a0001c0001t0002g0121a0001c0001t0003g0104a0001c0001t0003g0115others(2): Show | 5 | HG00738.hp1 HG01069.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.2469+1160G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132794692 | ||||||
| chr12:132794955
|
G | A | 46 | a0003c0004t0001g0270a0003c0004t0001g0279a0003c0004t0001g0282others(43): Show | 46 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.2469+897C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132794955 | ||||||
| chr12:132794960
|
G | A | 46 | a0003c0004t0001g0270a0003c0004t0001g0279a0003c0004t0001g0282others(43): Show | 46 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.2469+892C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132794960 | ||||||
| chr12:132795069
|
C | T | 1 | a0002c0007t0070g0060 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2469+783G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132795069 | ||||||
| chr12:132795095
|
G | A | 2 | a0001c0001t0003g0116a0001c0001t0003g0122 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.2469+757C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132795095 | ||||||
| chr12:132795185
|
C | CA | 180 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(177): Show | 180 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.2469+666dupT | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132795185 | ||||||
| chr12:132795369
|
A | G | 295 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(292): Show | 295 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.2469+483T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132795369 | ||||||
| chr12:132795397
|
T | C | 208 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(205): Show | 208 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.2469+455A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132795397 | ||||||
| chr12:132795527
|
G | A | 1 | a0001c0001t0017g0015 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2469+325C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132795527 | ||||||
| chr12:132795577
|
A | G | 87 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0001g0167others(84): Show | 87 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.2469+275T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132795577 | ||||||
| chr12:132795629
|
C | T | 1 | a0001c0001t0030g0303 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2469+223G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132795629 | ||||||
| chr12:132795758
|
C | CA | 10 | a0001c0001t0001g0093a0001c0003t0009g0292a0001c0003t0009g0293others(7): Show | 10 | HG02074.hp1 HG02145.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.2469+93dupT | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132795758 | ||||||
| chr12:132795805
|
T | C | 1 | a0018c0029t0061g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2469+47A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132795805 | ||||||
| chr12:132795809
|
A | C | 208 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(205): Show | 208 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.2469+43T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 11/23 | chr12 | 132795809 | ||||||
| chr12:132796337
|
C | T | 46 | a0003c0004t0001g0270a0003c0004t0001g0279a0003c0004t0001g0282others(43): Show | 46 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.2101-117G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 10/23 | chr12 | 132796337 | ||||||
| chr12:132796402
|
G | A | 5 | a0002c0002t0002g0178a0002c0002t0002g0179a0002c0002t0002g0180others(2): Show | 5 | HG00741.hp2 HG01361.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.2100+137C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 10/23 | chr12 | 132796402 | ||||||
| chr12:132796789
|
C | T | 87 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0001g0167others(84): Show | 87 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.1939-89G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 9/23 | chr12 | 132796789 | ||||||
| chr12:132796790
|
G | A | 1 | a0001c0001t0067g0044 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1939-90C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 9/23 | chr12 | 132796790 | ||||||
| chr12:132796918
|
G | A | 100 | a0001c0003t0002g0196a0001c0009t0002g0181a0001c0009t0002g0199others(97): Show | 100 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.1939-218C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 9/23 | chr12 | 132796918 | ||||||
| chr12:132797057
|
C | T | 1 | a0002c0002t0002g0179 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1939-357G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 9/23 | chr12 | 132797057 | ||||||
| chr12:132797790
|
C | T | 1 | a0002c0002t0002g0242 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1938+550G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 9/23 | chr12 | 132797790 | ||||||
| chr12:132797831
|
G | A | 1 | a0002c0007t0001g0048 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1938+509C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 9/23 | chr12 | 132797831 | ||||||
| chr12:132797871
|
T | C | 1 | a0001c0001t0025g0040 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1938+469A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 9/23 | chr12 | 132797871 | ||||||
| chr12:132797950
|
C | T | 1 | a0014c0020t0019g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1938+390G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 9/23 | chr12 | 132797950 | ||||||
| chr12:132798035
|
C | T | 1 | a0001c0001t0028g0305 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1938+305G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 9/23 | chr12 | 132798035 | ||||||
| chr12:132798096
|
A | C | 62 | a0001c0001t0001g0096a0001c0001t0030g0303a0003c0004t0001g0270others(59): Show | 62 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.1938+244T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 9/23 | chr12 | 132798096 | ||||||
| chr12:132798101
|
TGGGGGGG others(73): Show |
T | 3 | a0001c0001t0003g0139a0001c0001t0017g0001a0001c0001t0028g0305 | 3 | HG02818.hp1 HG03490.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1938+159_1938+238d others(82): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 9/23 | chr12 | 132798101 | ||||||
| chr12:132798119
|
C | T | 1 | a0001c0001t0001g0029 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1938+221G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 9/23 | chr12 | 132798119 | ||||||
| chr12:132798125
|
G | A | 1 | a0001c0011t0074g0067 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1938+215C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 9/23 | chr12 | 132798125 | ||||||
| chr12:132798179
|
T | TG | 79 | a0001c0001t0001g0054a0001c0001t0003g0006a0001c0001t0003g0008others(76): Show | 79 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.1938+160dupC | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 9/23 | chr12 | 132798179 | ||||||
| chr12:132798179
|
T | TGG | 52 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(49): Show | 52 | HG00280.hp2 HG00544.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.1938+159_1938+160d others(4): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 9/23 | chr12 | 132798179 | ||||||
| chr12:132798179
|
T | TGGG | 38 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0029others(35): Show | 38 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.1938+158_1938+160d others(5): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 9/23 | chr12 | 132798179 | ||||||
| chr12:132798243
|
G | A | 58 | a0001c0025t0003g0106a0003c0004t0001g0270a0003c0004t0001g0279others(55): Show | 58 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.1938+97C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 9/23 | chr12 | 132798243 | ||||||
| chr12:132798319
|
C | T | 29 | a0003c0004t0001g0270a0003c0004t0001g0279a0003c0004t0001g0282others(26): Show | 29 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.1938+21G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 9/23 | chr12 | 132798319 | ||||||
| chr12:132798329
|
C | T | 1 | a0002c0002t0002g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1938+11G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 9/23 | chr12 | 132798329 | ||||||
| chr12:132798554
|
C | T | 14 | a0005c0006t0001g0021a0005c0006t0014g0018a0005c0006t0014g0019others(11): Show | 14 | HG02055.hp2 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1801-77G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/23 | chr12 | 132798554 | ||||||
| chr12:132798618
|
C | T | 2 | a0001c0009t0002g0201a0001c0009t0002g0219 | 2 | HG03654.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1801-141G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/23 | chr12 | 132798618 | ||||||
| chr12:132798674
|
C | T | 1 | a0001c0001t0030g0303 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1801-197G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/23 | chr12 | 132798674 | ||||||
| chr12:132798693
|
C | A | 1 | a0001c0001t0001g0037 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1801-216G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/23 | chr12 | 132798693 | ||||||
| chr12:132798785
|
GGGTGAGG others(23): Show |
G | 1 | a0002c0002t0002g0177 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1801-338_1801-309d others(32): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/23 | chr12 | 132798785 | ||||||
| chr12:132798825
|
G | C | 294 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(291): Show | 294 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.1801-348C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/23 | chr12 | 132798825 | ||||||
| chr12:132798918
|
T | C | 295 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(292): Show | 295 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.1801-441A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/23 | chr12 | 132798918 | ||||||
| chr12:132798964
|
G | A | 1 | a0006c0010t0047g0134 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1801-487C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/23 | chr12 | 132798964 | ||||||
| chr12:132799003
|
C | T | 89 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(86): Show | 89 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.1801-526G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/23 | chr12 | 132799003 | ||||||
| chr12:132799040
|
G | A | 1 | a0003c0004t0008g0287 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1801-563C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/23 | chr12 | 132799040 | ||||||
| chr12:132799074
|
G | T | 14 | a0005c0006t0001g0021a0005c0006t0014g0018a0005c0006t0014g0019others(11): Show | 14 | HG02055.hp2 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1801-597C>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/23 | chr12 | 132799074 | ||||||
| chr12:132799087
|
G | A | 1 | a0014c0020t0019g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1801-610C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/23 | chr12 | 132799087 | ||||||
| chr12:132799245
|
A | T | 11 | a0001c0001t0017g0001a0005c0006t0001g0021a0005c0006t0014g0018others(8): Show | 11 | HG02055.hp2 HG02486.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1801-768T>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/23 | chr12 | 132799245 | ||||||
| chr12:132799417
|
C | T | 5 | a0001c0003t0006g0290a0001c0003t0006g0298a0001c0003t0048g0289others(2): Show | 5 | HG02717.hp1 HG02886.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1801-940G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/23 | chr12 | 132799417 | ||||||
| chr12:132799463
|
C | A | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | NA18980.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1801-986G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/23 | chr12 | 132799463 | ||||||
| chr12:132799575
|
G | GGCTGCAG others(59): Show |
1 | a0001c0001t0001g0138 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1801-1164_1801-109 others(70): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/23 | chr12 | 132799575 | ||||||
| chr12:132799694
|
C | T | 1 | a0001c0003t0011g0147 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1801-1217G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/23 | chr12 | 132799694 | ||||||
| chr12:132799723
|
T | C | 217 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(214): Show | 217 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.1801-1246A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/23 | chr12 | 132799723 | ||||||
| chr12:132799740
|
T | G | 1 | a0002c0002t0002g0203 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1801-1263A>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/23 | chr12 | 132799740 | ||||||
| chr12:132799795
|
C | T | 2 | a0001c0001t0003g0116a0001c0001t0003g0122 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1801-1318G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/23 | chr12 | 132799795 | ||||||
| chr12:132799801
|
C | T | 47 | a0001c0001t0001g0052a0003c0004t0001g0270a0003c0004t0001g0279others(44): Show | 47 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.1801-1324G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/23 | chr12 | 132799801 | ||||||
| chr12:132799802
|
G | A | 1 | a0014c0020t0019g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1801-1325C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/23 | chr12 | 132799802 | ||||||
| chr12:132799861
|
C | A | 2 | a0003c0004t0001g0282a0003c0004t0001g0283 | 2 | HG00735.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1801-1384G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/23 | chr12 | 132799861 | ||||||
| chr12:132799984
|
G | A | 27 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0001g0167others(24): Show | 27 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.1801-1507C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/23 | chr12 | 132799984 | ||||||
| chr12:132800068
|
C | T | 1 | a0001c0001t0075g0128 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1801-1591G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/23 | chr12 | 132800068 | ||||||
| chr12:132800163
|
A | C | 1 | a0001c0001t0075g0128 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1800+1604T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/23 | chr12 | 132800163 | ||||||
| chr12:132800206
|
T | A | 1 | a0002c0002t0002g0210 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1800+1561A>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/23 | chr12 | 132800206 | ||||||
| chr12:132800350
|
C | T | 1 | a0001c0001t0017g0001 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1800+1417G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/23 | chr12 | 132800350 | ||||||
| chr12:132800402
|
G | A | 3 | a0001c0001t0002g0121a0001c0001t0003g0104a0001c0001t0003g0115 | 3 | HG01255.hp2 NA20752.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1800+1365C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/23 | chr12 | 132800402 | ||||||
| chr12:132800442
|
T | C | 215 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(212): Show | 215 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.1800+1325A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/23 | chr12 | 132800442 | ||||||
| chr12:132800640
|
C | T | 1 | a0001c0001t0003g0010 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1800+1127G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/23 | chr12 | 132800640 | ||||||
| chr12:132800655
|
T | G | 1 | a0011c0017t0008g0267 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1800+1112A>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/23 | chr12 | 132800655 | ||||||
| chr12:132800815
|
C | T | 1 | a0018c0029t0061g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1800+952G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/23 | chr12 | 132800815 | ||||||
| chr12:132800958
|
C | CA | 7 | a0001c0001t0001g0047a0001c0001t0001g0098a0001c0001t0002g0121others(4): Show | 7 | HG00735.hp1 HG01255.hp2 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.1800+808dupT | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/23 | chr12 | 132800958 | ||||||
| chr12:132801061
|
T | G | 295 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(292): Show | 295 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.1800+706A>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/23 | chr12 | 132801061 | ||||||
| chr12:132801219
|
T | C | 2 | a0003c0004t0007g0266a0003c0004t0013g0284 | 2 | HG02027.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.1800+548A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/23 | chr12 | 132801219 | ||||||
| chr12:132801329
|
C | A | 1 | a0002c0002t0002g0225 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1800+438G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/23 | chr12 | 132801329 | ||||||
| chr12:132801385
|
G | A | 1 | a0001c0001t0003g0104 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1800+382C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/23 | chr12 | 132801385 | ||||||
| chr12:132801654
|
A | G | 1 | a0013c0035t0035g0262 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1800+113T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/23 | chr12 | 132801654 | ||||||
| chr12:132801658
|
AC | A | 127 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(124): Show | 127 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.1800+108delG | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/23 | chr12 | 132801658 | ||||||
| chr12:132801751
|
T | C | 14 | a0005c0006t0001g0021a0005c0006t0014g0018a0005c0006t0014g0019others(11): Show | 14 | HG02055.hp2 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1800+16A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 8/23 | chr12 | 132801751 | ||||||
| chr12:132802024
|
G | A | 60 | a0003c0004t0001g0270a0003c0004t0001g0279a0003c0004t0001g0282others(57): Show | 60 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.1598-55C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132802024 | ||||||
| chr12:132802122
|
G | A | 88 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0001g0167others(85): Show | 88 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1598-153C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132802122 | ||||||
| chr12:132802130
|
G | A | 1 | a0001c0001t0010g0244 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1598-161C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132802130 | ||||||
| chr12:132802200
|
C | T | 1 | a0014c0020t0019g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1598-231G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132802200 | ||||||
| chr12:132802217
|
C | G | 188 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(185): Show | 188 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.1598-248G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132802217 | ||||||
| chr12:132802220
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1598-251T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132802220 | ||||||
| chr12:132802227
|
C | T | 14 | a0005c0006t0001g0021a0005c0006t0014g0018a0005c0006t0014g0019others(11): Show | 14 | HG02055.hp2 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1598-258G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132802227 | ||||||
| chr12:132802265
|
C | T | 188 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(185): Show | 188 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.1598-296G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132802265 | ||||||
| chr12:132802266
|
T | C | 188 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(185): Show | 188 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.1598-297A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132802266 | ||||||
| chr12:132802301
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1598-332G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132802301 | ||||||
| chr12:132802367
|
CGGGGGTG others(11): Show |
C | 63 | a0002c0002t0007g0236a0002c0002t0051g0238a0003c0004t0001g0270others(60): Show | 63 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.1598-416_1598-399d others(20): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132802367 | ||||||
| chr12:132802383
|
AT | A | 27 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0001g0167others(24): Show | 27 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.1598-415delA | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132802383 | ||||||
| chr12:132802385
|
G | C | 27 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0001g0167others(24): Show | 27 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.1598-416C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132802385 | ||||||
| chr12:132802386
|
G | A | 27 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0001g0167others(24): Show | 27 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.1598-417C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132802386 | ||||||
| chr12:132802397
|
G | C | 1 | a0002c0002t0006g0211 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1598-428C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132802397 | ||||||
| chr12:132802402
|
C | T | 3 | a0002c0002t0002g0187a0002c0002t0002g0206a0002c0002t0012g0209 | 3 | HG02109.hp1 HG02258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1598-433G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132802402 | ||||||
| chr12:132802463
|
CA | C | 127 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(124): Show | 127 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.1598-495delT | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132802463 | ||||||
| chr12:132802471
|
A | T | 1 | a0001c0034t0001g0062 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1598-502T>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132802471 | ||||||
| chr12:132802531
|
G | A | 1 | a0003c0008t0013g0264 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1598-562C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132802531 | ||||||
| chr12:132802598
|
G | A | 1 | a0001c0018t0019g0132 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1598-629C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132802598 | ||||||
| chr12:132802651
|
G | T | 215 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(212): Show | 215 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.1598-682C>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132802651 | ||||||
| chr12:132802658
|
T | A | 1 | a0014c0020t0019g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1598-689A>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132802658 | ||||||
| chr12:132802666
|
T | C | 1 | a0002c0002t0006g0182 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1598-697A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132802666 | ||||||
| chr12:132802695
|
C | T | 1 | a0018c0029t0061g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1598-726G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132802695 | ||||||
| chr12:132802716
|
C | T | 14 | a0005c0006t0001g0021a0005c0006t0014g0018a0005c0006t0014g0019others(11): Show | 14 | HG02055.hp2 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1598-747G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132802716 | ||||||
| chr12:132802777
|
C | T | 128 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(125): Show | 128 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.1598-808G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132802777 | ||||||
| chr12:132802892
|
A | C | 1 | a0018c0029t0061g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1598-923T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132802892 | ||||||
| chr12:132802909
|
G | A | 1 | a0002c0007t0001g0071 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1598-940C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132802909 | ||||||
| chr12:132802911
|
C | T | 215 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(212): Show | 215 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.1598-942G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132802911 | ||||||
| chr12:132802917
|
C | T | 215 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(212): Show | 215 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.1598-948G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132802917 | ||||||
| chr12:132802937
|
A | G | 1 | a0001c0001t0001g0039 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1598-968T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132802937 | ||||||
| chr12:132803009
|
G | C | 215 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(212): Show | 215 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.1598-1040C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132803009 | ||||||
| chr12:132803073
|
AC | A | 60 | a0003c0004t0001g0270a0003c0004t0001g0279a0003c0004t0001g0282others(57): Show | 60 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.1598-1105delG | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132803073 | ||||||
| chr12:132803077
|
CAACAACA others(1): Show |
C | 154 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(151): Show | 154 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.1598-1116_1598-110 others(12): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132803077 | ||||||
| chr12:132803083
|
CAA | C | 60 | a0003c0004t0001g0270a0003c0004t0001g0279a0003c0004t0001g0282others(57): Show | 60 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.1598-1116_1598-111 others(6): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132803083 | ||||||
| chr12:132803083
|
CAAAACAA others(4): Show |
C | 1 | a0018c0029t0061g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1598-1125_1598-111 others(15): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132803083 | ||||||
| chr12:132803091
|
C | CA | 8 | a0002c0002t0002g0192a0002c0002t0002g0197a0002c0002t0002g0216others(5): Show | 8 | HG01192.hp1 HG01192.hp2 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.1598-1123dupT | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132803091 | ||||||
| chr12:132803094
|
A | C | 187 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(184): Show | 187 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.1598-1125T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132803094 | ||||||
| chr12:132803133
|
C | A | 77 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(74): Show | 77 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.1598-1164G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132803133 | ||||||
| chr12:132803158
|
ATGTAAAC others(3): Show |
A | 2 | a0001c0001t0001g0035a0001c0001t0004g0079 | 2 | NA18966.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.1598-1199_1598-119 others(14): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132803158 | ||||||
| chr12:132803247
|
T | C | 2 | a0001c0001t0001g0047a0001c0001t0001g0054 | 2 | NA18979.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1598-1278A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132803247 | ||||||
| chr12:132803348
|
C | G | 2 | a0003c0004t0008g0287a0003c0004t0008g0288 | 2 | HG00280.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1597+1368G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132803348 | ||||||
| chr12:132803366
|
A | T | 1 | a0018c0029t0061g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1597+1350T>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132803366 | ||||||
| chr12:132803399
|
T | G | 1 | a0018c0029t0061g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1597+1317A>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132803399 | ||||||
| chr12:132803458
|
G | A | 1 | a0001c0001t0001g0052 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1597+1258C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132803458 | ||||||
| chr12:132803548
|
C | A | 1 | a0005c0006t0001g0021 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1597+1168G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132803548 | ||||||
| chr12:132803604
|
G | A | 1 | a0018c0029t0061g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1597+1112C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132803604 | ||||||
| chr12:132803671
|
GCTTT | G | 17 | a0004c0005t0005g0049a0004c0005t0005g0101a0004c0005t0005g0247others(14): Show | 17 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1597+1041_1597+104 others(8): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132803671 | ||||||
| chr12:132803763
|
A | G | 215 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(212): Show | 215 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.1597+953T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132803763 | ||||||
| chr12:132803912
|
G | A | 80 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(77): Show | 80 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.1597+804C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132803912 | ||||||
| chr12:132804088
|
C | T | 2 | a0009c0015t0078g0066a0009c0015t0080g0065 | 2 | HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1597+628G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132804088 | ||||||
| chr12:132804092
|
G | A | 1 | a0022c0033t0002g0186 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1597+624C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132804092 | ||||||
| chr12:132804204
|
G | A | 27 | a0003c0004t0001g0270a0003c0004t0001g0279a0003c0004t0001g0282others(24): Show | 27 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.1597+512C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132804204 | ||||||
| chr12:132804390
|
G | T | 80 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(77): Show | 80 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.1597+326C>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132804390 | ||||||
| chr12:132804403
|
T | C | 47 | a0001c0001t0002g0121a0001c0001t0003g0006a0001c0001t0003g0007others(44): Show | 47 | HG00280.hp1 HG00438.hp2 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.1597+313A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132804403 | ||||||
| chr12:132804442
|
C | T | 215 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(212): Show | 215 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.1597+274G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132804442 | ||||||
| chr12:132804503
|
GAGGAGGG others(22): Show |
G | 1 | a0001c0001t0025g0040 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1597+184_1597+212d others(31): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132804503 | ||||||
| chr12:132804518
|
A | G | 294 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(291): Show | 294 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.1597+198T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132804518 | ||||||
| chr12:132804540
|
C | T | 293 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(290): Show | 293 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.1597+176G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132804540 | ||||||
| chr12:132804574
|
C | T | 27 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0001g0167others(24): Show | 27 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.1597+142G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132804574 | ||||||
| chr12:132804620
|
G | A | 1 | a0001c0001t0075g0128 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1597+96C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 7/23 | chr12 | 132804620 | ||||||
| chr12:132805092
|
A | G | 6 | a0006c0010t0006g0011a0006c0010t0006g0012a0006c0010t0006g0130others(3): Show | 6 | HG01106.hp1 HG01891.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1291-70T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 6/23 | chr12 | 132805092 | ||||||
| chr12:132805196
|
G | A | 2 | a0001c0001t0001g0047a0001c0001t0001g0054 | 2 | NA18979.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1291-174C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 6/23 | chr12 | 132805196 | ||||||
| chr12:132805268
|
G | A | 1 | a0014c0020t0019g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1291-246C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 6/23 | chr12 | 132805268 | ||||||
| chr12:132805296
|
GCCCCGAG others(34): Show |
G | 193 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(190): Show | 193 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.1291-315_1291-275d others(43): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 6/23 | chr12 | 132805296 | ||||||
| chr12:132805296
|
GCCCCGAG others(75): Show |
G | 17 | a0004c0005t0005g0049a0004c0005t0005g0101a0004c0005t0005g0247others(14): Show | 17 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1291-356_1291-275d others(84): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 6/23 | chr12 | 132805296 | ||||||
| chr12:132805296
|
GCCCCGAG others(116): Show |
G | 1 | a0001c0003t0011g0157 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1291-397_1291-275d others(2): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 6/23 | chr12 | 132805296 | ||||||
| chr12:132805305
|
C | A | 3 | a0001c0001t0002g0121a0001c0011t0074g0067a0016c0032t0001g0034 | 3 | HG01255.hp2 NA18991.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1291-283G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 6/23 | chr12 | 132805305 | ||||||
| chr12:132805341
|
C | T | 7 | a0001c0001t0017g0001a0006c0010t0006g0011a0006c0010t0006g0012others(4): Show | 7 | HG01106.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1291-319G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 6/23 | chr12 | 132805341 | ||||||
| chr12:132805342
|
G | A | 1 | a0001c0001t0017g0001 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1291-320C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 6/23 | chr12 | 132805342 | ||||||
| chr12:132805346
|
C | A | 124 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(121): Show | 124 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.1291-324G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 6/23 | chr12 | 132805346 | ||||||
| chr12:132805415
|
GGGGACCC others(33): Show |
G | 1 | a0001c0001t0002g0121 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1291-433_1291-394d others(42): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 6/23 | chr12 | 132805415 | ||||||
| chr12:132805436
|
C | T | 17 | a0004c0005t0005g0049a0004c0005t0005g0101a0004c0005t0005g0247others(14): Show | 17 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1291-414G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 6/23 | chr12 | 132805436 | ||||||
| chr12:132805478
|
G | A | 74 | a0001c0003t0002g0196a0001c0009t0002g0181a0001c0009t0002g0199others(71): Show | 74 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(71): Show |
intron_variant | MODIFIER | c.1291-456C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 6/23 | chr12 | 132805478 | ||||||
| chr12:132805479
|
CTCTCCCA others(33): Show |
C | 1 | a0016c0032t0001g0034 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1291-497_1291-458d others(42): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 6/23 | chr12 | 132805479 | ||||||
| chr12:132805498
|
GGGACCCC others(116): Show |
G | 1 | a0018c0029t0061g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1291-599_1291-477d others(2): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 6/23 | chr12 | 132805498 | ||||||
| chr12:132805510
|
CCCCCAGG others(33): Show |
C | 1 | a0001c0011t0074g0067 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1291-528_1291-489d others(42): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 6/23 | chr12 | 132805510 | ||||||
| chr12:132805514
|
C | A | 1 | a0001c0018t0019g0132 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1291-492G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 6/23 | chr12 | 132805514 | ||||||
| chr12:132805594
|
C | A | 2 | a0002c0002t0007g0236a0002c0002t0051g0238 | 2 | NA18612.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.1291-572G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 6/23 | chr12 | 132805594 | ||||||
| chr12:132805596
|
C | T | 1 | a0001c0003t0048g0289 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1291-574G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 6/23 | chr12 | 132805596 | ||||||
| chr12:132805601
|
G | A | 1 | a0017c0022t0001g0025 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1291-579C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 6/23 | chr12 | 132805601 | ||||||
| chr12:132805723
|
G | A | 1 | a0002c0007t0031g0307 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1291-701C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 6/23 | chr12 | 132805723 | ||||||
| chr12:132805733
|
A | C | 1 | a0018c0029t0061g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1291-711T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 6/23 | chr12 | 132805733 | ||||||
| chr12:132805749
|
G | A | 2 | a0007c0016t0020g0253a0007c0016t0020g0254 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1291-727C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 6/23 | chr12 | 132805749 | ||||||
| chr12:132806013
|
G | C | 2 | a0001c0003t0011g0147a0001c0003t0011g0157 | 2 | NA18956.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1291-991C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 6/23 | chr12 | 132806013 | ||||||
| chr12:132806051
|
G | A | 27 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0001g0167others(24): Show | 27 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.1291-1029C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 6/23 | chr12 | 132806051 | ||||||
| chr12:132806138
|
A | AGGGGGGG others(56): Show |
1 | a0002c0002t0002g0225 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1290+1038_1290+103 others(67): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 6/23 | chr12 | 132806138 | ||||||
| chr12:132806141
|
A | G | 1 | a0002c0002t0002g0225 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1290+1036T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 6/23 | chr12 | 132806141 | ||||||
| chr12:132806348
|
G | A | 46 | a0003c0004t0001g0270a0003c0004t0001g0279a0003c0004t0001g0282others(43): Show | 46 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.1290+829C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 6/23 | chr12 | 132806348 | ||||||
| chr12:132806382
|
A | C | 1 | a0016c0032t0001g0034 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1290+795T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 6/23 | chr12 | 132806382 | ||||||
| chr12:132806523
|
C | G | 1 | a0014c0020t0019g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1290+654G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 6/23 | chr12 | 132806523 | ||||||
| chr12:132806555
|
G | T | 1 | a0005c0006t0014g0018 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1290+622C>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 6/23 | chr12 | 132806555 | ||||||
| chr12:132806560
|
C | T | 1 | a0002c0002t0002g0208 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1290+617G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 6/23 | chr12 | 132806560 | ||||||
| chr12:132806637
|
G | A | 15 | a0001c0001t0017g0015a0001c0001t0026g0302a0001c0001t0027g0306others(12): Show | 15 | HG01106.hp1 HG01891.hp1 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.1290+540C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 6/23 | chr12 | 132806637 | ||||||
| chr12:132806694
|
A | T | 3 | a0001c0001t0002g0121a0001c0001t0003g0104a0001c0001t0003g0115 | 3 | HG01255.hp2 NA20752.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1290+483T>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 6/23 | chr12 | 132806694 | ||||||
| chr12:132806715
|
T | C | 3 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0138 | 3 | NA18975.hp1 NA19065.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.1290+462A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 6/23 | chr12 | 132806715 | ||||||
| chr12:132806921
|
A | T | 9 | a0001c0001t0001g0051a0001c0001t0001g0053a0001c0001t0001g0055others(6): Show | 9 | HG00408.hp1 NA18947.hp1 NA18960.hp2 others(6): Show |
intron_variant | MODIFIER | c.1290+256T>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 6/23 | chr12 | 132806921 | ||||||
| chr12:132806938
|
C | G | 294 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(291): Show | 294 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.1290+239G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 6/23 | chr12 | 132806938 | ||||||
| chr12:132806976
|
T | C | 293 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(290): Show | 293 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.1290+201A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 6/23 | chr12 | 132806976 | ||||||
| chr12:132807127
|
A | G | 1 | a0005c0006t0018g0023 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1290+50T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 6/23 | chr12 | 132807127 | ||||||
| chr12:132807157
|
G | T | 1 | a0001c0001t0003g0010 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1290+20C>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 6/23 | chr12 | 132807157 | ||||||
| chr12:132807337
|
T | C | 294 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(291): Show | 294 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.1179-49A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 5/23 | chr12 | 132807337 | ||||||
| chr12:132807411
|
A | T | 2 | a0002c0002t0002g0235a0002c0002t0002g0243 | 2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1179-123T>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 5/23 | chr12 | 132807411 | ||||||
| chr12:132807452
|
A | C | 2 | a0001c0003t0006g0291a0001c0003t0006g0298 | 2 | HG01884.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1179-164T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 5/23 | chr12 | 132807452 | ||||||
| chr12:132807469
|
T | C | 1 | a0004c0005t0005g0257 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1179-181A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 5/23 | chr12 | 132807469 | ||||||
| chr12:132807469
|
T | G | 1 | a0010c0039t0010g0033 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1179-181A>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 5/23 | chr12 | 132807469 | ||||||
| chr12:132807481
|
G | A | 41 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0008others(38): Show | 41 | HG00280.hp1 HG00438.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.1179-193C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 5/23 | chr12 | 132807481 | ||||||
| chr12:132807481
|
G | T | 6 | a0001c0001t0002g0121a0001c0001t0003g0104a0001c0001t0003g0114others(3): Show | 6 | HG00738.hp1 HG01069.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.1179-193C>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 5/23 | chr12 | 132807481 | ||||||
| chr12:132807531
|
AGTGACAA others(4): Show |
A | 1 | a0001c0001t0001g0137 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1179-254_1179-244d others(13): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 5/23 | chr12 | 132807531 | ||||||
| chr12:132807610
|
G | A | 2 | a0009c0015t0078g0066a0009c0015t0080g0065 | 2 | HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1178+281C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 5/23 | chr12 | 132807610 | ||||||
| chr12:132807614
|
C | T | 1 | a0001c0001t0017g0001 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1178+277G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 5/23 | chr12 | 132807614 | ||||||
| chr12:132807615
|
A | G | 47 | a0001c0001t0002g0121a0001c0001t0003g0006a0001c0001t0003g0007others(44): Show | 47 | HG00280.hp1 HG00438.hp2 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.1178+276T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 5/23 | chr12 | 132807615 | ||||||
| chr12:132807682
|
A | G | 291 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(288): Show | 291 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.1178+209T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 5/23 | chr12 | 132807682 | ||||||
| chr12:132807688
|
TC | T | 4 | a0002c0007t0001g0058a0002c0007t0001g0059a0002c0007t0001g0068others(1): Show | 4 | HG00609.hp2 HG00673.hp2 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.1178+202delG | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 5/23 | chr12 | 132807688 | ||||||
| chr12:132807712
|
G | A | 4 | a0002c0002t0002g0198a0008c0014t0021g0171a0008c0014t0021g0172others(1): Show | 4 | HG01192.hp1 HG02602.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.1178+179C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 5/23 | chr12 | 132807712 | ||||||
| chr12:132807781
|
GGCCCCAC others(14): Show |
G | 17 | a0001c0003t0002g0196a0001c0009t0002g0232a0002c0002t0002g0002others(14): Show | 17 | HG00642.hp1 HG00673.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.1178+89_1178+109de others(22): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 5/23 | chr12 | 132807781 | ||||||
| chr12:132807829
|
A | C | 7 | a0004c0005t0005g0247a0004c0005t0005g0248a0004c0005t0005g0249others(4): Show | 7 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1178+62T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 5/23 | chr12 | 132807829 | ||||||
| chr12:132807866
|
C | T | 1 | a0005c0006t0014g0019 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1178+25G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 5/23 | chr12 | 132807866 | ||||||
| chr12:132808602
|
A | T | 155 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(152): Show | 155 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.520-53T>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132808602 | ||||||
| chr12:132808814
|
A | G | 2 | a0002c0002t0002g0235a0002c0002t0002g0243 | 2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.520-265T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132808814 | ||||||
| chr12:132808886
|
C | A | 17 | a0004c0005t0005g0049a0004c0005t0005g0101a0004c0005t0005g0247others(14): Show | 17 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.520-337G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132808886 | ||||||
| chr12:132808909
|
A | G | 2 | a0003c0008t0007g0273a0003c0008t0022g0265 | 2 | NA18939.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.520-360T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132808909 | ||||||
| chr12:132809040
|
G | A | 46 | a0003c0004t0001g0270a0003c0004t0001g0279a0003c0004t0001g0282others(43): Show | 46 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.520-491C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132809040 | ||||||
| chr12:132809071
|
C | G | 2 | a0009c0015t0078g0066a0009c0015t0080g0065 | 2 | HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.520-522G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132809071 | ||||||
| chr12:132809099
|
C | T | 1 | a0001c0018t0019g0132 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.520-550G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132809099 | ||||||
| chr12:132809135
|
A | G | 79 | a0001c0003t0002g0196a0001c0009t0002g0181a0001c0009t0002g0199others(76): Show | 79 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.520-586T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132809135 | ||||||
| chr12:132809138
|
A | G | 79 | a0001c0003t0002g0196a0001c0009t0002g0181a0001c0009t0002g0199others(76): Show | 79 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.520-589T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132809138 | ||||||
| chr12:132809436
|
G | A | 1 | a0005c0006t0018g0023 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.520-887C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132809436 | ||||||
| chr12:132809436
|
G | C | 3 | a0001c0003t0004g0155a0002c0002t0016g0170a0003c0004t0008g0278 | 3 | HG02523.hp2 NA18977.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.520-887C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132809436 | ||||||
| chr12:132809436
|
G | GC | 130 | a0001c0001t0002g0121a0001c0001t0003g0007a0001c0001t0003g0008others(127): Show | 130 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.520-888dupG | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132809436 | ||||||
| chr12:132809436
|
G | GCC | 17 | a0001c0001t0003g0105a0001c0001t0003g0118a0001c0003t0039g0156others(14): Show | 17 | HG00673.hp1 HG01106.hp1 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.520-889_520-888dup others(2): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132809436 | ||||||
| chr12:132809443
|
C | T | 76 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(73): Show | 76 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.520-894G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132809443 | ||||||
| chr12:132809444
|
G | C | 1 | a0001c0003t0004g0158 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.520-895C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132809444 | ||||||
| chr12:132809513
|
G | A | 32 | a0001c0001t0002g0121a0001c0001t0003g0006a0001c0001t0003g0007others(29): Show | 32 | HG00280.hp1 HG00438.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.520-964C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132809513 | ||||||
| chr12:132809530
|
G | GCGTCTTC others(1): Show |
7 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0056others(4): Show | 7 | HG00408.hp1 NA18947.hp1 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.520-989_520-982dup others(8): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132809530 | ||||||
| chr12:132809564
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.520-1015C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132809564 | ||||||
| chr12:132809851
|
T | C | 1 | a0001c0003t0048g0289 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.520-1302A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132809851 | ||||||
| chr12:132809859
|
C | T | 1 | a0014c0020t0019g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.520-1310G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132809859 | ||||||
| chr12:132809911
|
C | G | 2 | a0004c0036t0008g0263a0013c0035t0035g0262 | 2 | HG02004.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.520-1362G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132809911 | ||||||
| chr12:132809924
|
T | C | 2 | a0004c0005t0005g0049a0004c0005t0005g0101 | 2 | NA18942.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.520-1375A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132809924 | ||||||
| chr12:132809926
|
T | C | 1 | a0002c0002t0002g0002 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.520-1377A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132809926 | ||||||
| chr12:132809971
|
G | A | 1 | a0002c0002t0002g0203 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.520-1422C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132809971 | ||||||
| chr12:132809984
|
C | T | 127 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(124): Show | 127 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.520-1435G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132809984 | ||||||
| chr12:132809985
|
C | G | 127 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(124): Show | 127 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.520-1436G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132809985 | ||||||
| chr12:132810176
|
A | G | 80 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(77): Show | 80 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.520-1627T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132810176 | ||||||
| chr12:132810192
|
A | G | 2 | a0009c0015t0078g0066a0009c0015t0080g0065 | 2 | HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.520-1643T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132810192 | ||||||
| chr12:132810374
|
G | A | 79 | a0001c0003t0002g0196a0001c0009t0002g0181a0001c0009t0002g0199others(76): Show | 79 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.520-1825C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132810374 | ||||||
| chr12:132810378
|
C | A | 79 | a0001c0003t0002g0196a0001c0009t0002g0181a0001c0009t0002g0199others(76): Show | 79 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.520-1829G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132810378 | ||||||
| chr12:132810421
|
T | C | 1 | a0002c0002t0002g0230 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.520-1872A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132810421 | ||||||
| chr12:132810450
|
A | C | 14 | a0005c0006t0001g0021a0005c0006t0014g0018a0005c0006t0014g0019others(11): Show | 14 | HG02055.hp2 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-1901T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132810450 | ||||||
| chr12:132810587
|
GAC | G | 27 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0001g0167others(24): Show | 27 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.520-2040_520-2039d others(4): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132810587 | ||||||
| chr12:132810626
|
C | G | 2 | a0004c0036t0008g0263a0013c0035t0035g0262 | 2 | HG02004.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.520-2077G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132810626 | ||||||
| chr12:132810699
|
T | C | 1 | a0002c0002t0002g0204 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.520-2150A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132810699 | ||||||
| chr12:132810799
|
G | T | 60 | a0003c0004t0001g0270a0003c0004t0001g0279a0003c0004t0001g0282others(57): Show | 60 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.520-2250C>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132810799 | ||||||
| chr12:132810810
|
G | A | 294 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(291): Show | 294 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.520-2261C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132810810 | ||||||
| chr12:132810823
|
G | A | 1 | a0012c0019t0038g0024 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.520-2274C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132810823 | ||||||
| chr12:132810837
|
G | A | 1 | a0001c0001t0001g0097 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.520-2288C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132810837 | ||||||
| chr12:132810859
|
G | A | 2 | a0002c0002t0002g0168a0002c0002t0002g0174 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.520-2310C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132810859 | ||||||
| chr12:132810889
|
T | C | 1 | a0001c0003t0004g0142 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.520-2340A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132810889 | ||||||
| chr12:132810987
|
C | T | 215 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(212): Show | 215 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.519+2320G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132810987 | ||||||
| chr12:132810988
|
G | A | 1 | a0022c0033t0002g0186 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.519+2319C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132810988 | ||||||
| chr12:132811042
|
G | A | 215 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(212): Show | 215 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.519+2265C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132811042 | ||||||
| chr12:132811165
|
G | A | 14 | a0005c0006t0001g0021a0005c0006t0014g0018a0005c0006t0014g0019others(11): Show | 14 | HG02055.hp2 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.519+2142C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132811165 | ||||||
| chr12:132811203
|
C | A | 1 | a0002c0013t0009g0133 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.519+2104G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132811203 | ||||||
| chr12:132811208
|
C | A | 1 | a0001c0001t0017g0001 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.519+2099G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132811208 | ||||||
| chr12:132811208
|
C | G | 294 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(291): Show | 294 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.519+2099G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132811208 | ||||||
| chr12:132811229
|
CTT | C | 93 | a0001c0001t0002g0121a0001c0001t0003g0006a0001c0001t0003g0007others(90): Show | 93 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.519+2076_519+2077d others(4): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132811229 | ||||||
| chr12:132811460
|
C | G | 215 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(212): Show | 215 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.519+1847G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132811460 | ||||||
| chr12:132811482
|
A | T | 16 | a0001c0001t0017g0001a0001c0001t0017g0015a0001c0001t0026g0302others(13): Show | 16 | HG01106.hp1 HG01891.hp1 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.519+1825T>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132811482 | ||||||
| chr12:132811525
|
A | G | 1 | a0001c0001t0003g0117 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.519+1782T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132811525 | ||||||
| chr12:132811551
|
C | T | 47 | a0001c0001t0002g0121a0001c0001t0003g0006a0001c0001t0003g0007others(44): Show | 47 | HG00280.hp1 HG00438.hp2 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.519+1756G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132811551 | ||||||
| chr12:132811621
|
C | T | 1 | a0002c0002t0050g0237 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.519+1686G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132811621 | ||||||
| chr12:132811622
|
G | A | 1 | a0012c0019t0038g0024 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.519+1685C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132811622 | ||||||
| chr12:132811650
|
C | T | 2 | a0001c0003t0006g0291a0001c0003t0006g0298 | 2 | HG01884.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.519+1657G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132811650 | ||||||
| chr12:132811709
|
G | C | 1 | a0001c0001t0001g0137 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.519+1598C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132811709 | ||||||
| chr12:132811797
|
T | A | 1 | a0002c0002t0057g0184 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.519+1510A>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132811797 | ||||||
| chr12:132811808
|
C | T | 1 | a0018c0029t0061g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.519+1499G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132811808 | ||||||
| chr12:132811837
|
T | C | 27 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0001g0167others(24): Show | 27 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.519+1470A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132811837 | ||||||
| chr12:132811873
|
G | A | 79 | a0001c0003t0002g0196a0001c0009t0002g0181a0001c0009t0002g0199others(76): Show | 79 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.519+1434C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132811873 | ||||||
| chr12:132811874
|
C | T | 60 | a0003c0004t0001g0270a0003c0004t0001g0279a0003c0004t0001g0282others(57): Show | 60 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.519+1433G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132811874 | ||||||
| chr12:132811979
|
C | G | 1 | a0001c0001t0003g0115 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.519+1328G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132811979 | ||||||
| chr12:132812002
|
C | CA | 100 | a0001c0001t0026g0302a0001c0001t0027g0306a0001c0001t0028g0305others(97): Show | 100 | HG00609.hp1 HG00673.hp1 HG00735.hp2 others(97): Show |
intron_variant | MODIFIER | c.519+1304dupT | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132812002 | ||||||
| chr12:132812002
|
C | CAA | 104 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0029others(101): Show | 104 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.519+1303_519+1304d others(4): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132812002 | ||||||
| chr12:132812002
|
C | CAAA | 28 | a0001c0001t0001g0027a0001c0001t0001g0038a0001c0001t0001g0047others(25): Show | 28 | HG00438.hp2 HG00673.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.519+1302_519+1304d others(5): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132812002 | ||||||
| chr12:132812006
|
A | C | 1 | a0005c0006t0062g0016 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.519+1301T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132812006 | ||||||
| chr12:132812023
|
AC | A | 14 | a0005c0006t0001g0021a0005c0006t0014g0018a0005c0006t0014g0019others(11): Show | 14 | HG02055.hp2 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.519+1283delG | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132812023 | ||||||
| chr12:132812024
|
C | A | 1 | a0001c0034t0001g0062 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.519+1283G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132812024 | ||||||
| chr12:132812096
|
G | A | 1 | a0002c0002t0002g0243 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.519+1211C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132812096 | ||||||
| chr12:132812192
|
T | TACAC | 47 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(44): Show | 47 | HG00280.hp1 HG00438.hp2 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.519+1111_519+1114d others(6): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132812192 | ||||||
| chr12:132812192
|
T | TACACAC | 100 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(97): Show | 100 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.519+1109_519+1114d others(8): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132812192 | ||||||
| chr12:132812192
|
T | TACACACA others(1): Show |
78 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0046others(75): Show | 78 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.519+1107_519+1114d others(10): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132812192 | ||||||
| chr12:132812192
|
T | TACACACA others(3): Show |
24 | a0001c0001t0001g0045a0002c0002t0002g0197a0002c0002t0002g0198others(21): Show | 24 | HG01169.hp1 HG01192.hp1 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.519+1105_519+1114d others(12): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132812192 | ||||||
| chr12:132812192
|
T | TACACACA others(5): Show |
10 | a0001c0001t0001g0138a0004c0005t0005g0247a0004c0005t0005g0248others(7): Show | 10 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.519+1103_519+1114d others(14): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132812192 | ||||||
| chr12:132812214
|
T | C | 188 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(185): Show | 188 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.519+1093A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132812214 | ||||||
| chr12:132812216
|
T | C | 35 | a0001c0001t0002g0121a0001c0001t0003g0116a0001c0001t0026g0302others(32): Show | 35 | HG00438.hp1 HG00642.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.519+1091A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132812216 | ||||||
| chr12:132812218
|
T | C | 31 | a0001c0001t0002g0121a0001c0001t0003g0116a0001c0003t0001g0148others(28): Show | 31 | HG00438.hp1 HG00642.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.519+1089A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132812218 | ||||||
| chr12:132812220
|
T | C | 5 | a0001c0003t0004g0155a0001c0003t0004g0166a0001c0003t0042g0146others(2): Show | 5 | HG02055.hp2 HG02523.hp2 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.519+1087A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132812220 | ||||||
| chr12:132812226
|
TA | T | 38 | a0001c0001t0001g0045a0001c0001t0001g0093a0001c0001t0001g0138others(35): Show | 38 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.519+1080delT | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132812226 | ||||||
| chr12:132812227
|
A | T | 6 | a0001c0001t0003g0114a0001c0001t0003g0122a0003c0004t0013g0261others(3): Show | 6 | HG00738.hp1 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.519+1080T>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132812227 | ||||||
| chr12:132812228
|
TA | T | 27 | a0001c0001t0001g0053a0001c0001t0075g0128a0001c0003t0001g0148others(24): Show | 27 | HG00408.hp1 HG00438.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.519+1078delT | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132812228 | ||||||
| chr12:132812229
|
A | T | 143 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(140): Show | 143 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.519+1078T>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132812229 | ||||||
| chr12:132812229
|
AT | A | 19 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(16): Show | 19 | HG02486.hp2 HG02559.hp2 HG02615.hp1 others(16): Show |
intron_variant | MODIFIER | c.519+1077delA | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132812229 | ||||||
| chr12:132812231
|
T | A | 71 | a0001c0003t0002g0196a0001c0009t0002g0181a0001c0009t0002g0199others(68): Show | 71 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.519+1076A>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132812231 | ||||||
| chr12:132812481
|
T | A | 2 | a0004c0005t0005g0249a0004c0005t0005g0250 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.519+826A>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132812481 | ||||||
| chr12:132812788
|
C | T | 1 | a0001c0003t0048g0289 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.519+519G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132812788 | ||||||
| chr12:132813054
|
T | C | 14 | a0005c0006t0001g0021a0005c0006t0014g0018a0005c0006t0014g0019others(11): Show | 14 | HG02055.hp2 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.519+253A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132813054 | ||||||
| chr12:132813200
|
A | G | 1 | a0001c0003t0011g0147 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.519+107T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132813200 | ||||||
| chr12:132813232
|
C | T | 1 | a0001c0001t0001g0096 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.519+75G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132813232 | ||||||
| chr12:132813233
|
G | A | 1 | a0002c0002t0002g0208 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.519+74C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 4/23 | chr12 | 132813233 | ||||||
| chr12:132813435
|
G | C | 2 | a0001c0001t0001g0028a0001c0001t0069g0032 | 2 | NA18964.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.407-16C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/23 | chr12 | 132813435 | ||||||
| chr12:132813721
|
CT | C | 224 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(221): Show | 224 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.407-303delA | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/23 | chr12 | 132813721 | ||||||
| chr12:132813721
|
CTT | C | 60 | a0001c0001t0001g0026a0001c0001t0003g0123a0002c0002t0002g0210others(57): Show | 60 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.407-304_407-303del others(2): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/23 | chr12 | 132813721 | ||||||
| chr12:132813971
|
G | A | 27 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0001g0167others(24): Show | 27 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.407-552C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/23 | chr12 | 132813971 | ||||||
| chr12:132814020
|
G | C | 1 | a0001c0001t0001g0098 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.407-601C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/23 | chr12 | 132814020 | ||||||
| chr12:132814022
|
C | G | 1 | a0001c0001t0001g0098 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.407-603G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/23 | chr12 | 132814022 | ||||||
| chr12:132814023
|
CT | C | 155 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(152): Show | 155 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.407-605delA | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/23 | chr12 | 132814023 | ||||||
| chr12:132814023
|
CTT | C | 19 | a0001c0018t0019g0132a0002c0007t0001g0048a0004c0005t0005g0247others(16): Show | 19 | HG01515.hp2 HG02055.hp2 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.407-606_407-605del others(2): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/23 | chr12 | 132814023 | ||||||
| chr12:132814024
|
T | C | 1 | a0001c0001t0001g0098 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.407-605A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/23 | chr12 | 132814024 | ||||||
| chr12:132814032
|
T | A | 1 | a0001c0001t0001g0081 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.407-613A>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/23 | chr12 | 132814032 | ||||||
| chr12:132814069
|
G | T | 1 | a0001c0001t0001g0026 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.407-650C>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/23 | chr12 | 132814069 | ||||||
| chr12:132814084
|
G | A | 155 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(152): Show | 155 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.407-665C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/23 | chr12 | 132814084 | ||||||
| chr12:132814094
|
G | A | 1 | a0018c0029t0061g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.407-675C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/23 | chr12 | 132814094 | ||||||
| chr12:132814113
|
C | T | 1 | a0001c0009t0002g0181 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.407-694G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/23 | chr12 | 132814113 | ||||||
| chr12:132814168
|
G | A | 1 | a0018c0029t0061g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.407-749C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/23 | chr12 | 132814168 | ||||||
| chr12:132814280
|
T | C | 1 | a0018c0029t0061g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.407-861A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/23 | chr12 | 132814280 | ||||||
| chr12:132814314
|
G | A | 1 | a0002c0002t0002g0208 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.407-895C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/23 | chr12 | 132814314 | ||||||
| chr12:132814368
|
G | A | 14 | a0005c0006t0001g0021a0005c0006t0014g0018a0005c0006t0014g0019others(11): Show | 14 | HG02055.hp2 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.407-949C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/23 | chr12 | 132814368 | ||||||
| chr12:132814436
|
G | A | 60 | a0003c0004t0001g0270a0003c0004t0001g0279a0003c0004t0001g0282others(57): Show | 60 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.407-1017C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/23 | chr12 | 132814436 | ||||||
| chr12:132814476
|
C | T | 1 | a0001c0001t0017g0015 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.407-1057G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/23 | chr12 | 132814476 | ||||||
| chr12:132814519
|
G | A | 1 | a0004c0005t0005g0101 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.407-1100C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/23 | chr12 | 132814519 | ||||||
| chr12:132814741
|
C | T | 3 | a0001c0001t0001g0135a0001c0001t0004g0079a0001c0001t0010g0082 | 3 | HG02056.hp1 NA18966.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.407-1322G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/23 | chr12 | 132814741 | ||||||
| chr12:132814927
|
G | GCCTCATC others(8): Show |
1 | a0003c0004t0013g0261 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.407-1523_407-1509d others(17): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/23 | chr12 | 132814927 | ||||||
| chr12:132814940
|
T | G | 1 | a0003c0004t0008g0286 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.407-1521A>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/23 | chr12 | 132814940 | ||||||
| chr12:132814965
|
C | T | 1 | a0021c0031t0006g0169 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.407-1546G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/23 | chr12 | 132814965 | ||||||
| chr12:132814978
|
G | A | 1 | a0002c0012t0011g0125 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.407-1559C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/23 | chr12 | 132814978 | ||||||
| chr12:132815026
|
C | A | 31 | a0001c0001t0002g0121a0001c0001t0003g0006a0001c0001t0003g0007others(28): Show | 31 | HG00280.hp1 HG00438.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.406+1514G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/23 | chr12 | 132815026 | ||||||
| chr12:132815245
|
A | G | 1 | a0018c0029t0061g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.406+1295T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/23 | chr12 | 132815245 | ||||||
| chr12:132815338
|
T | A | 1 | a0018c0029t0061g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.406+1202A>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/23 | chr12 | 132815338 | ||||||
| chr12:132815493
|
C | T | 2 | a0001c0001t0004g0126a0001c0001t0004g0127 | 2 | HG03017.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.406+1047G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/23 | chr12 | 132815493 | ||||||
| chr12:132815573
|
G | T | 1 | a0001c0003t0041g0165 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.406+967C>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/23 | chr12 | 132815573 | ||||||
| chr12:132815684
|
C | T | 1 | a0013c0035t0035g0262 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.406+856G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/23 | chr12 | 132815684 | ||||||
| chr12:132815716
|
T | G | 1 | a0002c0002t0060g0185 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.406+824A>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/23 | chr12 | 132815716 | ||||||
| chr12:132815925
|
C | G | 1 | a0009c0015t0078g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.406+615G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/23 | chr12 | 132815925 | ||||||
| chr12:132815932
|
C | T | 27 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0001g0167others(24): Show | 27 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.406+608G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/23 | chr12 | 132815932 | ||||||
| chr12:132815941
|
G | A | 1 | a0001c0001t0003g0118 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.406+599C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/23 | chr12 | 132815941 | ||||||
| chr12:132815974
|
A | C | 2 | a0002c0002t0003g0240a0002c0002t0053g0239 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.406+566T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/23 | chr12 | 132815974 | ||||||
| chr12:132816026
|
A | G | 295 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(292): Show | 295 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.406+514T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/23 | chr12 | 132816026 | ||||||
| chr12:132816173
|
G | A | 3 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038 | 3 | HG02109.hp2 HG02486.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.406+367C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/23 | chr12 | 132816173 | ||||||
| chr12:132816500
|
G | A | 2 | a0004c0005t0023g0246a0004c0005t0023g0256 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.406+40C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/23 | chr12 | 132816500 | ||||||
| chr12:132816503
|
C | T | 1 | a0003c0008t0007g0273 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.406+37G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 3/23 | chr12 | 132816503 | ||||||
| chr12:132816964
|
C | T | 3 | a0002c0002t0002g0190a0002c0002t0002g0191a0002c0002t0012g0233 | 3 | HG02055.hp1 HG02280.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.134-152G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132816964 | ||||||
| chr12:132816971
|
G | C | 1 | a0023c0040t0002g0234 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.134-159C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132816971 | ||||||
| chr12:132817067
|
ACTCTAAC others(982): Show |
A | 1 | a0002c0002t0051g0238 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.134-1244_134-256de others(1): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817067 | ||||||
| chr12:132817114
|
T | C | 1 | a0014c0020t0019g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.134-302A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817114 | ||||||
| chr12:132817148
|
C | T | 1 | a0002c0007t0001g0092 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.134-336G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817148 | ||||||
| chr12:132817158
|
T | A | 1 | a0021c0031t0006g0169 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.134-346A>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817158 | ||||||
| chr12:132817182
|
G | C | 1 | a0010c0039t0010g0033 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.134-370C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817182 | ||||||
| chr12:132817184
|
C | G | 1 | a0010c0039t0010g0033 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.134-372G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817184 | ||||||
| chr12:132817191
|
ACCTCCAC others(92): Show |
A | 1 | a0001c0003t0001g0148 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.134-478_134-380del others(99): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817191 | ||||||
| chr12:132817204
|
AAGGTGAA others(91): Show |
A | 1 | a0004c0005t0005g0247 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.134-490_134-393del others(98): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817204 | ||||||
| chr12:132817215
|
G | C | 3 | a0001c0003t0004g0144a0001c0003t0004g0145a0002c0002t0002g0231 | 3 | NA19005.hp2 NA19087.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.134-403C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817215 | ||||||
| chr12:132817232
|
GCTCTAAG others(125): Show |
G | 1 | a0002c0002t0002g0231 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.134-552_134-421del | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817232 | ||||||
| chr12:132817248
|
C | A | 3 | a0001c0001t0037g0113a0001c0003t0004g0144a0001c0003t0004g0145 | 3 | HG01496.hp2 NA19087.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.134-436G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817248 | ||||||
| chr12:132817248
|
C | CCCCCTCC others(27): Show |
3 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038 | 3 | HG02109.hp2 HG02486.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.134-437_134-436ins others(34): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817248 | ||||||
| chr12:132817248
|
C | CCCCCTCC others(60): Show |
6 | a0002c0007t0001g0048a0002c0007t0001g0058a0002c0007t0001g0059others(3): Show | 6 | HG00609.hp2 HG00673.hp2 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.134-437_134-436ins others(67): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817248 | ||||||
| chr12:132817248
|
C | CCCCTCCA others(26): Show |
2 | a0001c0003t0004g0166a0001c0003t0042g0146 | 2 | NA18994.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.134-437_134-436ins others(33): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817248 | ||||||
| chr12:132817248
|
C | CCCCTCCA others(26): Show |
6 | a0002c0002t0002g0208a0002c0002t0002g0229a0002c0002t0002g0230others(3): Show | 6 | HG00609.hp1 HG01123.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.134-437_134-436ins others(33): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817248 | ||||||
| chr12:132817248
|
CCCCTCCA others(92): Show |
C | 137 | a0001c0003t0001g0151a0001c0003t0001g0167a0001c0003t0002g0196others(134): Show | 137 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.134-535_134-437del others(99): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817248 | ||||||
| chr12:132817249
|
CCCTCCAC others(91): Show |
C | 112 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(109): Show | 112 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.134-535_134-438del others(98): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817249 | ||||||
| chr12:132817250
|
CCTCCACA others(90): Show |
C | 3 | a0001c0001t0001g0084a0004c0005t0005g0049a0004c0005t0005g0101 | 3 | HG02027.hp1 NA18942.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.134-535_134-439del others(97): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817250 | ||||||
| chr12:132817251
|
CTCCACAC others(89): Show |
C | 1 | a0001c0001t0001g0098 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.134-535_134-440del others(96): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817251 | ||||||
| chr12:132817256
|
CACCTCCA others(93): Show |
C | 1 | a0010c0039t0010g0033 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.134-544_134-445del others(100): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817256 | ||||||
| chr12:132817257
|
A | T | 6 | a0002c0007t0001g0048a0002c0007t0001g0058a0002c0007t0001g0059others(3): Show | 6 | HG00609.hp2 HG00673.hp2 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.134-445T>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817257 | ||||||
| chr12:132817257
|
ACCTCCAC others(26): Show |
A | 7 | a0002c0002t0002g0205a0003c0004t0001g0270a0003c0004t0001g0282others(4): Show | 7 | HG00735.hp1 HG02027.hp2 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.134-478_134-446del others(33): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817257 | ||||||
| chr12:132817257
|
ACCTCCAC others(158): Show |
A | 1 | a0001c0001t0037g0113 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.134-610_134-446del | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817257 | ||||||
| chr12:132817265
|
A | G | 29 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(26): Show | 29 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.134-453T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817265 | ||||||
| chr12:132817270
|
AACGTGAA others(91): Show |
A | 1 | a0023c0040t0002g0234 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.134-556_134-459del others(98): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817270 | ||||||
| chr12:132817272
|
C | G | 15 | a0001c0001t0010g0089a0001c0003t0004g0159a0001c0003t0011g0161others(12): Show | 15 | HG00544.hp1 HG00609.hp2 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.134-460G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817272 | ||||||
| chr12:132817279
|
C | T | 2 | a0003c0008t0013g0264a0021c0031t0006g0169 | 2 | HG00544.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.134-467G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817279 | ||||||
| chr12:132817281
|
G | A | 9 | a0001c0001t0010g0089a0001c0003t0004g0159a0001c0003t0011g0161others(6): Show | 9 | HG00544.hp1 HG01884.hp2 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.134-469C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817281 | ||||||
| chr12:132817290
|
T | A | 15 | a0001c0001t0010g0089a0001c0003t0004g0159a0001c0003t0011g0161others(12): Show | 15 | HG00544.hp1 HG00609.hp2 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.134-478A>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817290 | ||||||
| chr12:132817295
|
C | T | 1 | a0021c0031t0006g0169 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.134-483G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817295 | ||||||
| chr12:132817305
|
G | C | 9 | a0001c0001t0010g0089a0001c0003t0004g0159a0001c0003t0011g0161others(6): Show | 9 | HG00544.hp1 HG01884.hp2 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.134-493C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817305 | ||||||
| chr12:132817312
|
C | T | 7 | a0002c0002t0002g0205a0003c0004t0001g0270a0003c0004t0001g0282others(4): Show | 7 | HG00735.hp1 HG02027.hp2 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.134-500G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817312 | ||||||
| chr12:132817314
|
G | A | 7 | a0002c0002t0002g0205a0003c0004t0001g0270a0003c0004t0001g0282others(4): Show | 7 | HG00735.hp1 HG02027.hp2 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.134-502C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817314 | ||||||
| chr12:132817323
|
A | ACCTCCAC others(26): Show |
1 | a0002c0002t0002g0208 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.134-512_134-511ins others(33): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817323 | ||||||
| chr12:132817323
|
A | T | 15 | a0001c0001t0010g0089a0001c0003t0004g0159a0001c0003t0011g0161others(12): Show | 15 | HG00544.hp1 HG00609.hp2 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.134-511T>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817323 | ||||||
| chr12:132817335
|
TAAGGTGA others(124): Show |
T | 1 | a0003c0008t0013g0264 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.134-654_134-524del | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817335 | ||||||
| chr12:132817338
|
G | C | 7 | a0002c0002t0002g0205a0003c0004t0001g0270a0003c0004t0001g0282others(4): Show | 7 | HG00735.hp1 HG02027.hp2 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.134-526C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817338 | ||||||
| chr12:132817347
|
G | C | 2 | a0004c0005t0005g0247a0024c0038t0004g0163 | 2 | HG01515.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.134-535C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817347 | ||||||
| chr12:132817349
|
C | A | 6 | a0002c0007t0001g0048a0002c0007t0001g0058a0002c0007t0001g0059others(3): Show | 6 | HG00609.hp2 HG00673.hp2 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.134-537G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817349 | ||||||
| chr12:132817349
|
C | CCTCCACT others(26): Show |
2 | a0001c0003t0004g0166a0001c0003t0042g0146 | 2 | NA18994.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.134-538_134-537ins others(33): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817349 | ||||||
| chr12:132817356
|
A | T | 14 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(11): Show | 14 | HG00609.hp1 HG00735.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.134-544T>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817356 | ||||||
| chr12:132817361
|
C | T | 1 | a0002c0002t0002g0205 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.134-549G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817361 | ||||||
| chr12:132817364
|
A | G | 290 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(287): Show | 290 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.134-552T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817364 | ||||||
| chr12:132817367
|
C | CT | 6 | a0003c0004t0001g0270a0003c0004t0001g0282a0003c0004t0001g0283others(3): Show | 6 | HG00735.hp1 HG02027.hp2 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.134-556dupA | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817367 | ||||||
| chr12:132817367
|
C | G | 2 | a0001c0003t0009g0297a0002c0013t0009g0133 | 2 | HG02258.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.134-555G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817367 | ||||||
| chr12:132817369
|
A | G | 1 | a0023c0040t0002g0234 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.134-557T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817369 | ||||||
| chr12:132817371
|
G | C | 1 | a0002c0002t0002g0205 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.134-559C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817371 | ||||||
| chr12:132817378
|
C | T | 123 | a0001c0003t0002g0196a0001c0009t0002g0181a0001c0009t0002g0199others(120): Show | 123 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.134-566G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817378 | ||||||
| chr12:132817380
|
G | A | 271 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(268): Show | 271 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.134-568C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817380 | ||||||
| chr12:132817382
|
C | A | 3 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038 | 3 | HG02109.hp2 HG02486.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.134-570G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817382 | ||||||
| chr12:132817389
|
A | T | 6 | a0001c0001t0010g0089a0001c0003t0004g0159a0001c0003t0011g0161others(3): Show | 6 | HG01884.hp2 HG01981.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.134-577T>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817389 | ||||||
| chr12:132817397
|
A | G | 282 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(279): Show | 282 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.134-585T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817397 | ||||||
| chr12:132817404
|
C | G | 21 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(18): Show | 21 | HG00609.hp1 HG00735.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.134-592G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817404 | ||||||
| chr12:132817404
|
C | T | 1 | a0002c0002t0002g0205 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.134-592G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817404 | ||||||
| chr12:132817413
|
G | A | 7 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(4): Show | 7 | HG00609.hp1 HG01192.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.134-601C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817413 | ||||||
| chr12:132817413
|
G | C | 1 | a0021c0031t0006g0169 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.134-601C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817413 | ||||||
| chr12:132817415
|
C | A | 6 | a0001c0001t0010g0089a0001c0003t0004g0159a0001c0003t0011g0161others(3): Show | 6 | HG01884.hp2 HG01981.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.134-603G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817415 | ||||||
| chr12:132817422
|
T | A | 16 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(13): Show | 16 | HG00609.hp1 HG01192.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.134-610A>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817422 | ||||||
| chr12:132817430
|
G | A | 8 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(5): Show | 8 | HG00609.hp1 HG01192.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.134-618C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817430 | ||||||
| chr12:132817433
|
C | CT | 49 | a0003c0004t0001g0279a0003c0004t0007g0266a0003c0004t0007g0269others(46): Show | 49 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.134-622dupA | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817433 | ||||||
| chr12:132817437
|
G | C | 8 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(5): Show | 8 | HG00609.hp1 HG01192.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.134-625C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817437 | ||||||
| chr12:132817444
|
C | G | 1 | a0010c0039t0010g0033 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.134-632G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817444 | ||||||
| chr12:132817444
|
C | T | 1 | a0021c0031t0006g0169 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.134-632G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817444 | ||||||
| chr12:132817446
|
G | A | 8 | a0001c0001t0010g0089a0001c0001t0037g0113a0001c0003t0004g0159others(5): Show | 8 | HG01496.hp2 HG01884.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.134-634C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817446 | ||||||
| chr12:132817446
|
G | C | 1 | a0010c0039t0010g0033 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.134-634C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817446 | ||||||
| chr12:132817455
|
A | T | 8 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(5): Show | 8 | HG00609.hp1 HG01192.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.134-643T>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817455 | ||||||
| chr12:132817455
|
ACCTCCAC others(224): Show |
A | 3 | a0001c0003t0006g0290a0001c0003t0006g0291a0001c0003t0006g0298 | 3 | HG01884.hp1 HG02886.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.134-874_134-644del | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817455 | ||||||
| chr12:132817463
|
G | A | 7 | a0001c0001t0010g0089a0001c0003t0004g0159a0001c0003t0011g0161others(4): Show | 7 | HG01884.hp2 HG01981.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.134-651C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817463 | ||||||
| chr12:132817470
|
G | C | 6 | a0001c0001t0010g0089a0001c0001t0037g0113a0001c0003t0004g0159others(3): Show | 6 | HG01496.hp2 HG01884.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.134-658C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817470 | ||||||
| chr12:132817477
|
C | CCACCCTC others(92): Show |
1 | a0002c0002t0002g0208 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.134-666_134-665ins others(99): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817477 | ||||||
| chr12:132817479
|
G | A | 22 | a0001c0003t0004g0166a0001c0003t0042g0146a0002c0002t0002g0208others(19): Show | 22 | HG00609.hp2 HG00673.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.134-667C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817479 | ||||||
| chr12:132817479
|
GCCCTCCA others(257): Show |
G | 1 | a0001c0003t0048g0289 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.134-931_134-668del | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817479 | ||||||
| chr12:132817488
|
T | A | 24 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(21): Show | 24 | HG00609.hp1 HG00609.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.134-676A>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817488 | ||||||
| chr12:132817496
|
G | A | 4 | a0003c0004t0001g0270a0003c0004t0013g0284a0003c0008t0022g0265others(1): Show | 4 | HG02027.hp2 HG04199.hp1 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.134-684C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817496 | ||||||
| chr12:132817503
|
G | C | 6 | a0003c0004t0001g0270a0003c0004t0001g0282a0003c0004t0001g0283others(3): Show | 6 | HG00735.hp1 HG02027.hp2 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.134-691C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817503 | ||||||
| chr12:132817503
|
GGTGAACC others(553): Show |
G | 1 | a0005c0006t0018g0023 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.134-1251_134-692de others(1): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817503 | ||||||
| chr12:132817509
|
C | G | 8 | a0001c0003t0004g0166a0001c0003t0042g0146a0002c0007t0001g0048others(5): Show | 8 | HG00609.hp2 HG00673.hp2 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.134-697G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817509 | ||||||
| chr12:132817512
|
G | A | 8 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(5): Show | 8 | HG00609.hp1 HG01192.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.134-700C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817512 | ||||||
| chr12:132817512
|
G | C | 9 | a0001c0003t0004g0166a0001c0003t0042g0146a0002c0002t0002g0205others(6): Show | 9 | HG00609.hp2 HG00673.hp2 NA18948.hp2 others(6): Show |
intron_variant | MODIFIER | c.134-700C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817512 | ||||||
| chr12:132817514
|
A | C | 155 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(152): Show | 155 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.134-702T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817514 | ||||||
| chr12:132817516
|
T | C | 1 | a0002c0002t0002g0208 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.134-704A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817516 | ||||||
| chr12:132817521
|
A | ACCTCCAC others(124): Show |
2 | a0001c0003t0004g0166a0001c0003t0042g0146 | 2 | NA18994.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.134-710_134-709ins others(131): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817521 | ||||||
| chr12:132817521
|
A | T | 6 | a0003c0004t0001g0270a0003c0004t0001g0282a0003c0004t0001g0283others(3): Show | 6 | HG00735.hp1 HG02027.hp2 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.134-709T>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817521 | ||||||
| chr12:132817529
|
G | A | 6 | a0002c0007t0001g0048a0002c0007t0001g0058a0002c0007t0001g0059others(3): Show | 6 | HG00609.hp2 HG00673.hp2 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.134-717C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817529 | ||||||
| chr12:132817536
|
GGTGAACC others(26): Show |
G | 1 | a0021c0031t0006g0169 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.134-757_134-725del others(33): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817536 | ||||||
| chr12:132817542
|
C | G | 9 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(6): Show | 9 | HG00609.hp1 HG01192.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.134-730G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817542 | ||||||
| chr12:132817543
|
CCACCCTC others(59): Show |
C | 3 | a0001c0001t0075g0128a0001c0003t0011g0161a0014c0020t0019g0003 | 3 | HG01993.hp2 HG02080.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.134-797_134-732del others(66): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817543 | ||||||
| chr12:132817545
|
A | C | 9 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(6): Show | 9 | HG00609.hp1 HG01192.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.134-733T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817545 | ||||||
| chr12:132817545
|
A | G | 61 | a0002c0007t0001g0048a0002c0007t0001g0058a0002c0007t0001g0059others(58): Show | 61 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.134-733T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817545 | ||||||
| chr12:132817547
|
CCTCCACA others(257): Show |
C | 1 | a0001c0003t0079g0299 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.134-999_134-736del | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817547 | ||||||
| chr12:132817554
|
ACCTCCAC others(26): Show |
A | 1 | a0001c0003t0041g0165 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.134-775_134-743del others(33): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817554 | ||||||
| chr12:132817554
|
ACCTCCAC others(290): Show |
A | 1 | a0002c0002t0012g0183 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.134-1039_134-743de others(1): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817554 | ||||||
| chr12:132817558
|
C | G | 2 | a0001c0003t0004g0166a0001c0003t0042g0146 | 2 | NA18994.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.134-746G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817558 | ||||||
| chr12:132817559
|
C | T | 2 | a0001c0003t0004g0166a0001c0003t0042g0146 | 2 | NA18994.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.134-747G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817559 | ||||||
| chr12:132817562
|
A | G | 14 | a0001c0001t0001g0137a0001c0001t0010g0089a0001c0003t0004g0166others(11): Show | 14 | HG00609.hp2 HG00673.hp2 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.134-750T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817562 | ||||||
| chr12:132817569
|
C | G | 18 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(15): Show | 18 | HG00609.hp1 HG00609.hp2 HG00673.hp2 others(15): Show |
intron_variant | MODIFIER | c.134-757G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817569 | ||||||
| chr12:132817569
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.134-757G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817569 | ||||||
| chr12:132817575
|
C | G | 2 | a0001c0001t0010g0089a0009c0015t0080g0065 | 2 | HG01981.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.134-763G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817575 | ||||||
| chr12:132817578
|
G | A | 6 | a0002c0007t0001g0048a0002c0007t0001g0058a0002c0007t0001g0059others(3): Show | 6 | HG00609.hp2 HG00673.hp2 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.134-766C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817578 | ||||||
| chr12:132817578
|
G | C | 2 | a0001c0001t0010g0089a0009c0015t0080g0065 | 2 | HG01981.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.134-766C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817578 | ||||||
| chr12:132817578
|
GCCCTCCA others(92): Show |
G | 10 | a0001c0001t0003g0116a0001c0001t0003g0122a0001c0018t0019g0132others(7): Show | 10 | HG00735.hp1 HG00738.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.134-865_134-767del others(99): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817578 | ||||||
| chr12:132817587
|
T | A | 20 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(17): Show | 20 | HG00609.hp1 HG00609.hp2 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.134-775A>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817587 | ||||||
| chr12:132817587
|
TCCTCCAC others(123): Show |
T | 1 | a0004c0005t0005g0247 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.134-905_134-776del | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817587 | ||||||
| chr12:132817587
|
TCCTCCAC others(125): Show |
T | 120 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0069others(117): Show | 120 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.134-907_134-776del | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817587 | ||||||
| chr12:132817590
|
TCCACGCT others(24): Show |
T | 1 | a0001c0001t0001g0026 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.134-809_134-779del others(31): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817590 | ||||||
| chr12:132817595
|
G | A | 10 | a0001c0001t0010g0089a0001c0003t0004g0166a0001c0003t0042g0146others(7): Show | 10 | HG00609.hp1 HG01192.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.134-783C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817595 | ||||||
| chr12:132817608
|
C | G | 7 | a0001c0003t0041g0165a0002c0007t0001g0048a0002c0007t0001g0058others(4): Show | 7 | HG00609.hp2 HG00673.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.134-796G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817608 | ||||||
| chr12:132817609
|
T | C | 148 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(145): Show | 148 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.134-797A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817609 | ||||||
| chr12:132817611
|
A | C | 7 | a0001c0003t0041g0165a0002c0007t0001g0048a0002c0007t0001g0058others(4): Show | 7 | HG00609.hp2 HG00673.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.134-799T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817611 | ||||||
| chr12:132817611
|
A | G | 139 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(136): Show | 139 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.134-799T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817611 | ||||||
| chr12:132817620
|
A | T | 2 | a0005c0006t0018g0102a0005c0006t0081g0308 | 2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.134-808T>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817620 | ||||||
| chr12:132817620
|
ACCTCCAC others(388): Show |
A | 5 | a0001c0001t0017g0015a0001c0001t0028g0305a0001c0001t0029g0304others(2): Show | 5 | HG02615.hp2 HG02818.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.134-1203_134-809de others(1): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817620 | ||||||
| chr12:132817628
|
G | A | 31 | a0001c0003t0041g0165a0002c0007t0001g0048a0002c0007t0001g0058others(28): Show | 31 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(28): Show |
intron_variant | MODIFIER | c.134-816C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817628 | ||||||
| chr12:132817633
|
AAGGTGAA others(124): Show |
A | 1 | a0023c0040t0002g0234 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.134-952_134-822del | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817633 | ||||||
| chr12:132817635
|
G | C | 23 | a0003c0004t0001g0279a0003c0004t0007g0266a0003c0004t0007g0269others(20): Show | 23 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(20): Show |
intron_variant | MODIFIER | c.134-823C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817635 | ||||||
| chr12:132817635
|
GGTGAACC others(191): Show |
G | 10 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0003g0112others(7): Show | 10 | HG00423.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.134-1021_134-824de others(1): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817635 | ||||||
| chr12:132817641
|
C | G | 5 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(2): Show | 5 | HG02080.hp2 HG02109.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.134-829G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817641 | ||||||
| chr12:132817642
|
C | T | 1 | a0009c0015t0080g0065 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.134-830G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817642 | ||||||
| chr12:132817642
|
CCCCCCCC others(26): Show |
C | 2 | a0001c0003t0004g0144a0002c0002t0002g0205 | 2 | NA18960.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.134-863_134-831del others(33): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817642 | ||||||
| chr12:132817642
|
CCCCCCCC others(290): Show |
C | 1 | a0002c0002t0002g0301 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.134-1127_134-831de others(1): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817642 | ||||||
| chr12:132817644
|
C | A | 94 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(91): Show | 94 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.134-832G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817644 | ||||||
| chr12:132817644
|
C | G | 33 | a0001c0001t0001g0026a0001c0003t0041g0165a0002c0007t0001g0048others(30): Show | 33 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.134-832G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817644 | ||||||
| chr12:132817648
|
C | T | 132 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(129): Show | 132 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.134-836G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817648 | ||||||
| chr12:132817653
|
A | T | 23 | a0003c0004t0001g0279a0003c0004t0007g0266a0003c0004t0007g0269others(20): Show | 23 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(20): Show |
intron_variant | MODIFIER | c.134-841T>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817653 | ||||||
| chr12:132817657
|
C | G | 2 | a0001c0001t0026g0302a0001c0001t0027g0306 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.134-845G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817657 | ||||||
| chr12:132817658
|
C | T | 2 | a0001c0001t0026g0302a0001c0001t0027g0306 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.134-846G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817658 | ||||||
| chr12:132817661
|
A | G | 98 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(95): Show | 98 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.134-849T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817661 | ||||||
| chr12:132817667
|
A | C | 1 | a0010c0039t0010g0033 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.134-855T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817667 | ||||||
| chr12:132817668
|
G | C | 26 | a0001c0001t0026g0302a0001c0001t0027g0306a0003c0004t0001g0279others(23): Show | 26 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.134-856C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817668 | ||||||
| chr12:132817668
|
G | GGTGAAGC others(158): Show |
1 | a0002c0002t0002g0208 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.134-857_134-856ins others(165): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817668 | ||||||
| chr12:132817674
|
C | G | 83 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(80): Show | 83 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.134-862G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817674 | ||||||
| chr12:132817675
|
T | C | 125 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(122): Show | 125 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.134-863A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817675 | ||||||
| chr12:132817677
|
A | ACCCTCCA others(257): Show |
1 | a0022c0033t0002g0186 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.134-866_134-865ins others(264): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817677 | ||||||
| chr12:132817677
|
A | C | 84 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(81): Show | 84 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.134-865T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817677 | ||||||
| chr12:132817677
|
A | G | 35 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(32): Show | 35 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.134-865T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817677 | ||||||
| chr12:132817681
|
T | C | 1 | a0009c0015t0080g0065 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.134-869A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817681 | ||||||
| chr12:132817686
|
T | A | 105 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(102): Show | 105 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.134-874A>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817686 | ||||||
| chr12:132817690
|
C | G | 6 | a0006c0010t0006g0011a0006c0010t0006g0012a0006c0010t0006g0130others(3): Show | 6 | HG01106.hp1 HG01891.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.134-878G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817690 | ||||||
| chr12:132817691
|
C | T | 6 | a0006c0010t0006g0011a0006c0010t0006g0012a0006c0010t0006g0130others(3): Show | 6 | HG01106.hp1 HG01891.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.134-879G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817691 | ||||||
| chr12:132817694
|
G | A | 99 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(96): Show | 99 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.134-882C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817694 | ||||||
| chr12:132817701
|
G | C | 13 | a0001c0001t0075g0128a0003c0004t0001g0270a0003c0004t0001g0282others(10): Show | 13 | HG00735.hp1 HG01106.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.134-889C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817701 | ||||||
| chr12:132817707
|
C | G | 2 | a0001c0001t0001g0026a0001c0003t0004g0144 | 2 | NA18957.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.134-895G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817707 | ||||||
| chr12:132817708
|
C | CCACCCTC others(125): Show |
2 | a0001c0003t0004g0166a0001c0003t0042g0146 | 2 | NA18994.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.134-897_134-896ins others(132): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817708 | ||||||
| chr12:132817708
|
C | T | 6 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(3): Show | 6 | HG02080.hp2 HG02109.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.134-896G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817708 | ||||||
| chr12:132817708
|
CCGCCCTC others(158): Show |
C | 1 | a0001c0003t0004g0159 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.134-1061_134-897de others(1): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817708 | ||||||
| chr12:132817709
|
CG | C | 8 | a0001c0003t0009g0292a0001c0003t0009g0293a0001c0003t0009g0294others(5): Show | 8 | HG01981.hp1 HG02145.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.134-898delC | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817709 | ||||||
| chr12:132817709
|
CGCCCTCC others(27): Show |
C | 1 | a0002c0013t0009g0133 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.134-931_134-898del others(34): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817709 | ||||||
| chr12:132817710
|
G | A | 9 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(6): Show | 9 | HG02080.hp2 HG02109.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.134-898C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817710 | ||||||
| chr12:132817710
|
G | C | 2 | a0001c0001t0001g0026a0001c0003t0004g0144 | 2 | NA18957.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.134-898C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817710 | ||||||
| chr12:132817712
|
C | A | 2 | a0005c0006t0018g0102a0005c0006t0081g0308 | 2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.134-900G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817712 | ||||||
| chr12:132817714
|
T | C | 8 | a0001c0003t0009g0292a0001c0003t0009g0293a0001c0003t0009g0294others(5): Show | 8 | HG01981.hp1 HG02145.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.134-902A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817714 | ||||||
| chr12:132817719
|
A | ACCTCCAC others(58): Show |
3 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038 | 3 | HG02109.hp2 HG02486.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.134-908_134-907ins others(65): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817719 | ||||||
| chr12:132817719
|
A | T | 10 | a0001c0001t0075g0128a0001c0003t0004g0166a0001c0003t0042g0146others(7): Show | 10 | HG00735.hp1 HG01993.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.134-907T>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817719 | ||||||
| chr12:132817721
|
C | T | 1 | a0004c0005t0005g0247 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.134-909G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817721 | ||||||
| chr12:132817722
|
T | C | 1 | a0004c0005t0005g0247 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.134-910A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817722 | ||||||
| chr12:132817723
|
C | G | 1 | a0009c0015t0078g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.134-911G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817723 | ||||||
| chr12:132817723
|
C | T | 1 | a0004c0005t0005g0247 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.134-911G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817723 | ||||||
| chr12:132817724
|
C | T | 1 | a0009c0015t0078g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.134-912G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817724 | ||||||
| chr12:132817727
|
G | A | 19 | a0001c0001t0001g0026a0001c0001t0010g0089a0001c0001t0073g0041others(16): Show | 19 | HG00609.hp2 HG00673.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.134-915C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817727 | ||||||
| chr12:132817734
|
G | C | 1 | a0009c0015t0078g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.134-922C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817734 | ||||||
| chr12:132817740
|
C | G | 1 | a0017c0022t0001g0025 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.134-928G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817740 | ||||||
| chr12:132817741
|
C | CCCCCCCC others(26): Show |
2 | a0004c0005t0005g0251a0004c0005t0005g0255 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.134-930_134-929ins others(33): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817741 | ||||||
| chr12:132817741
|
C | T | 32 | a0001c0001t0073g0041a0001c0003t0001g0148a0001c0003t0001g0151others(29): Show | 32 | HG00438.hp1 HG00642.hp2 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.134-929G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817741 | ||||||
| chr12:132817743
|
A | C | 7 | a0006c0010t0006g0011a0006c0010t0006g0012a0006c0010t0006g0130others(4): Show | 7 | HG01106.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.134-931T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817743 | ||||||
| chr12:132817743
|
A | G | 143 | a0001c0001t0001g0026a0001c0001t0001g0042a0001c0001t0001g0043others(140): Show | 143 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.134-931T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817743 | ||||||
| chr12:132817747
|
T | C | 2 | a0001c0003t0011g0161a0002c0013t0009g0133 | 2 | HG02080.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.134-935A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817747 | ||||||
| chr12:132817752
|
A | T | 21 | a0001c0003t0006g0290a0001c0003t0006g0291a0001c0003t0006g0298others(18): Show | 21 | HG00609.hp1 HG01106.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.134-940T>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817752 | ||||||
| chr12:132817756
|
C | G | 5 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(2): Show | 5 | HG02109.hp2 HG02132.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.134-944G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817756 | ||||||
| chr12:132817757
|
C | T | 5 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(2): Show | 5 | HG02109.hp2 HG02132.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.134-945G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817757 | ||||||
| chr12:132817760
|
G | A | 8 | a0001c0003t0011g0161a0002c0002t0002g0205a0002c0002t0002g0208others(5): Show | 8 | HG01123.hp2 HG01192.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.134-948C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817760 | ||||||
| chr12:132817767
|
G | C | 10 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(7): Show | 10 | HG01123.hp2 HG01192.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.134-955C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817767 | ||||||
| chr12:132817772
|
ACCC | A | 26 | a0001c0001t0001g0035a0001c0001t0001g0039a0001c0001t0001g0051others(23): Show | 26 | HG00323.hp2 HG00423.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.134-963_134-961del others(3): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817772 | ||||||
| chr12:132817773
|
C | G | 60 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(57): Show | 60 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.134-961G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817773 | ||||||
| chr12:132817774
|
C | T | 4 | a0001c0003t0004g0144a0001c0003t0009g0292a0001c0003t0011g0161others(1): Show | 4 | HG02080.hp2 HG02258.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.134-962G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817774 | ||||||
| chr12:132817775
|
CGCCCTCC others(27): Show |
C | 1 | a0001c0001t0001g0098 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.134-997_134-964del others(34): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817775 | ||||||
| chr12:132817775
|
CGCCCTCC others(60): Show |
C | 2 | a0001c0001t0026g0302a0001c0001t0027g0306 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.134-1030_134-964de others(68): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817775 | ||||||
| chr12:132817775
|
CGCCCTCC others(93): Show |
C | 1 | a0010c0039t0010g0033 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.134-1063_134-964de others(101): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817775 | ||||||
| chr12:132817776
|
G | A | 146 | a0001c0001t0001g0026a0001c0001t0001g0042a0001c0001t0001g0043others(143): Show | 146 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.134-964C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817776 | ||||||
| chr12:132817776
|
G | C | 87 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(84): Show | 87 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.134-964C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817776 | ||||||
| chr12:132817778
|
C | A | 3 | a0001c0003t0006g0290a0001c0003t0006g0291a0001c0003t0006g0298 | 3 | HG01884.hp1 HG02886.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.134-966G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817778 | ||||||
| chr12:132817778
|
CCTCCACT others(26): Show |
C | 54 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(51): Show | 54 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.134-999_134-967del others(33): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817778 | ||||||
| chr12:132817779
|
CTCCACTC others(27): Show |
C | 22 | a0001c0001t0073g0041a0001c0003t0001g0148a0001c0003t0001g0151others(19): Show | 22 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.134-1001_134-968de others(35): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817779 | ||||||
| chr12:132817779
|
CTCCACTC others(89): Show |
C | 26 | a0001c0001t0001g0035a0001c0001t0001g0039a0001c0001t0001g0051others(23): Show | 26 | HG00323.hp2 HG00423.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.134-1063_134-968de others(97): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817779 | ||||||
| chr12:132817780
|
T | C | 2 | a0002c0002t0002g0188a0002c0002t0002g0210 | 2 | HG01074.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.134-968A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817780 | ||||||
| chr12:132817780
|
TCCACTCC others(125): Show |
T | 1 | a0017c0022t0001g0025 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.134-1100_134-969de others(1): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817780 | ||||||
| chr12:132817785
|
T | A | 167 | a0001c0001t0001g0026a0001c0001t0001g0036a0001c0001t0001g0037others(164): Show | 167 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.134-973A>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817785 | ||||||
| chr12:132817789
|
C | G | 7 | a0001c0003t0009g0292a0001c0003t0009g0293a0001c0003t0009g0294others(4): Show | 7 | HG01981.hp1 HG02145.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.134-977G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817789 | ||||||
| chr12:132817790
|
C | T | 7 | a0001c0003t0009g0292a0001c0003t0009g0293a0001c0003t0009g0294others(4): Show | 7 | HG01981.hp1 HG02145.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.134-978G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817790 | ||||||
| chr12:132817792
|
C | T | 1 | a0009c0015t0078g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.134-980G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817792 | ||||||
| chr12:132817793
|
G | A | 9 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(6): Show | 9 | HG00738.hp1 HG01069.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.134-981C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817793 | ||||||
| chr12:132817800
|
G | C | 7 | a0001c0003t0009g0292a0001c0003t0009g0293a0001c0003t0009g0294others(4): Show | 7 | HG01981.hp1 HG02145.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.134-988C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817800 | ||||||
| chr12:132817800
|
GGTGAACC others(26): Show |
G | 1 | a0009c0015t0078g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.134-1021_134-989de others(34): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817800 | ||||||
| chr12:132817800
|
GGTGAACC others(256): Show |
G | 7 | a0001c0018t0019g0132a0006c0010t0006g0011a0006c0010t0006g0012others(4): Show | 7 | HG01106.hp1 HG01891.hp1 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.134-1251_134-989de others(1): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817800 | ||||||
| chr12:132817806
|
C | G | 135 | a0001c0001t0001g0026a0001c0001t0001g0042a0001c0001t0001g0043others(132): Show | 135 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.134-994G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817806 | ||||||
| chr12:132817807
|
C | T | 2 | a0002c0002t0002g0188a0002c0002t0002g0210 | 2 | HG01074.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.134-995G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817807 | ||||||
| chr12:132817809
|
G | A | 9 | a0001c0003t0006g0290a0001c0003t0006g0291a0001c0003t0006g0298others(6): Show | 9 | HG00609.hp1 HG01074.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.134-997C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817809 | ||||||
| chr12:132817809
|
G | C | 137 | a0001c0001t0001g0026a0001c0001t0001g0042a0001c0001t0001g0043others(134): Show | 137 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.134-997C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817809 | ||||||
| chr12:132817809
|
G | GCCCTCCA others(59): Show |
1 | a0002c0002t0002g0208 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.134-998_134-997ins others(66): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817809 | ||||||
| chr12:132817809
|
GCACTCCA others(190): Show |
G | 2 | a0005c0006t0018g0102a0005c0006t0081g0308 | 2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.134-1194_134-998de others(1): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817809 | ||||||
| chr12:132817811
|
A | C | 168 | a0001c0001t0001g0026a0001c0001t0001g0036a0001c0001t0001g0037others(165): Show | 168 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.134-999T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817811 | ||||||
| chr12:132817813
|
T | C | 1 | a0001c0003t0004g0144 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.134-1001A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817813 | ||||||
| chr12:132817818
|
A | T | 5 | a0002c0002t0002g0188a0002c0002t0002g0190a0002c0002t0002g0191others(2): Show | 5 | HG01074.hp1 HG01256.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.134-1006T>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817818 | ||||||
| chr12:132817818
|
ACCTCCAC others(190): Show |
A | 1 | a0001c0001t0017g0001 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.134-1203_134-1007d others(2): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817818 | ||||||
| chr12:132817822
|
C | G | 2 | a0001c0003t0011g0161a0002c0013t0009g0133 | 2 | HG02080.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.134-1010G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817822 | ||||||
| chr12:132817823
|
C | T | 2 | a0001c0003t0011g0161a0002c0013t0009g0133 | 2 | HG02080.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.134-1011G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817823 | ||||||
| chr12:132817825
|
C | T | 1 | a0009c0015t0080g0065 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.134-1013G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817825 | ||||||
| chr12:132817826
|
A | G | 19 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(16): Show | 19 | HG01074.hp1 HG01192.hp1 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.134-1014T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817826 | ||||||
| chr12:132817833
|
C | G | 236 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(233): Show | 236 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.134-1021G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817833 | ||||||
| chr12:132817840
|
C | T | 27 | a0001c0001t0003g0116a0001c0001t0003g0122a0001c0001t0073g0041others(24): Show | 27 | HG00438.hp1 HG00642.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.134-1028G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817840 | ||||||
| chr12:132817842
|
G | A | 56 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(53): Show | 56 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.134-1030C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817842 | ||||||
| chr12:132817846
|
T | C | 2 | a0001c0001t0026g0302a0001c0001t0027g0306 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.134-1034A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817846 | ||||||
| chr12:132817846
|
TCCACTCC others(59): Show |
T | 102 | a0001c0001t0001g0026a0001c0001t0001g0042a0001c0001t0001g0043others(99): Show | 102 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.134-1100_134-1035d others(68): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817846 | ||||||
| chr12:132817851
|
T | A | 121 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(118): Show | 121 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.134-1039A>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817851 | ||||||
| chr12:132817855
|
C | G | 9 | a0001c0001t0075g0128a0001c0003t0009g0292a0001c0003t0009g0293others(6): Show | 9 | HG01074.hp1 HG01256.hp2 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.134-1043G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817855 | ||||||
| chr12:132817856
|
C | T | 9 | a0001c0001t0075g0128a0001c0003t0009g0292a0001c0003t0009g0293others(6): Show | 9 | HG01074.hp1 HG01256.hp2 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.134-1044G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817856 | ||||||
| chr12:132817858
|
C | T | 2 | a0009c0015t0078g0066a0009c0015t0080g0065 | 2 | HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.134-1046G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817858 | ||||||
| chr12:132817859
|
G | A | 84 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(81): Show | 84 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.134-1047C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817859 | ||||||
| chr12:132817859
|
G | GCTCTAAG others(59): Show |
2 | a0002c0002t0002g0229a0002c0002t0002g0230 | 2 | HG00609.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.134-1048_134-1047i others(68): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817859 | ||||||
| chr12:132817866
|
G | C | 9 | a0001c0001t0075g0128a0001c0003t0009g0292a0001c0003t0009g0293others(6): Show | 9 | HG01074.hp1 HG01256.hp2 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.134-1054C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817866 | ||||||
| chr12:132817872
|
C | G | 16 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0003g0112others(13): Show | 16 | HG00423.hp2 HG01167.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.134-1060G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817872 | ||||||
| chr12:132817872
|
CT | C | 4 | a0001c0001t0003g0116a0001c0001t0003g0122a0001c0003t0041g0165others(1): Show | 4 | HG00738.hp1 HG01069.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.134-1061delA | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817872 | ||||||
| chr12:132817873
|
T | C | 58 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0003g0112others(55): Show | 58 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.134-1061A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817873 | ||||||
| chr12:132817875
|
A | C | 20 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0003g0112others(17): Show | 20 | HG00423.hp2 HG00738.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.134-1063T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817875 | ||||||
| chr12:132817875
|
A | G | 11 | a0001c0001t0075g0128a0001c0003t0009g0292a0001c0003t0009g0293others(8): Show | 11 | HG01074.hp1 HG01256.hp2 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.134-1063T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817875 | ||||||
| chr12:132817879
|
T | C | 4 | a0001c0001t0003g0116a0001c0001t0003g0122a0001c0003t0041g0165others(1): Show | 4 | HG00738.hp1 HG01069.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.134-1067A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817879 | ||||||
| chr12:132817884
|
A | T | 4 | a0001c0001t0026g0302a0001c0001t0027g0306a0009c0015t0078g0066others(1): Show | 4 | HG02818.hp2 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.134-1072T>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817884 | ||||||
| chr12:132817884
|
ACCTCCAC others(59): Show |
A | 1 | a0023c0040t0002g0234 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.134-1138_134-1073d others(68): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817884 | ||||||
| chr12:132817888
|
C | G | 25 | a0001c0001t0073g0041a0001c0003t0001g0148a0001c0003t0001g0151others(22): Show | 25 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.134-1076G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817888 | ||||||
| chr12:132817889
|
C | T | 25 | a0001c0001t0073g0041a0001c0003t0001g0148a0001c0003t0001g0151others(22): Show | 25 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.134-1077G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817889 | ||||||
| chr12:132817892
|
G | A | 49 | a0001c0001t0001g0035a0001c0001t0001g0039a0001c0001t0001g0045others(46): Show | 49 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.134-1080C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817892 | ||||||
| chr12:132817892
|
G | GCTCTAAG others(59): Show |
2 | a0004c0005t0005g0251a0004c0005t0005g0255 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.134-1081_134-1080i others(68): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817892 | ||||||
| chr12:132817892
|
G | GCTCTAAG others(26): Show |
5 | a0002c0007t0001g0058a0002c0007t0001g0059a0002c0007t0001g0068others(2): Show | 5 | HG00609.hp2 HG00673.hp2 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.134-1081_134-1080i others(35): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817892 | ||||||
| chr12:132817899
|
G | C | 31 | a0001c0001t0073g0041a0001c0003t0001g0148a0001c0003t0001g0151others(28): Show | 31 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.134-1087C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817899 | ||||||
| chr12:132817904
|
ACCCCCCC others(59): Show |
A | 31 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(28): Show | 31 | HG00408.hp1 HG01496.hp1 HG01978.hp1 others(28): Show |
intron_variant | MODIFIER | c.134-1158_134-1093d others(68): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817904 | ||||||
| chr12:132817905
|
C | G | 2 | a0002c0002t0002g0235a0002c0002t0002g0243 | 2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.134-1093G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817905 | ||||||
| chr12:132817905
|
CCCCCCCC others(58): Show |
C | 43 | a0001c0001t0001g0047a0001c0001t0025g0040a0003c0004t0001g0270others(40): Show | 43 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.134-1158_134-1094d others(67): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817905 | ||||||
| chr12:132817906
|
C | T | 4 | a0001c0001t0003g0116a0001c0001t0003g0122a0001c0003t0041g0165others(1): Show | 4 | HG00738.hp1 HG01069.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.134-1094G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817906 | ||||||
| chr12:132817908
|
C | A | 8 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0003g0116others(5): Show | 8 | HG00738.hp1 HG01069.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.134-1096G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817908 | ||||||
| chr12:132817908
|
C | G | 82 | a0001c0001t0001g0035a0001c0001t0001g0039a0001c0001t0001g0051others(79): Show | 82 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.134-1096G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817908 | ||||||
| chr12:132817912
|
C | CCACACCT others(91): Show |
2 | a0001c0003t0004g0166a0001c0003t0042g0146 | 2 | NA18994.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.134-1101_134-1100i others(100): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817912 | ||||||
| chr12:132817912
|
C | CCACACCT others(91): Show |
1 | a0002c0002t0002g0208 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.134-1101_134-1100i others(100): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817912 | ||||||
| chr12:132817912
|
C | T | 95 | a0001c0001t0001g0035a0001c0001t0001g0039a0001c0001t0001g0045others(92): Show | 95 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.134-1100G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817912 | ||||||
| chr12:132817917
|
A | T | 6 | a0001c0001t0003g0116a0001c0001t0003g0122a0001c0003t0041g0165others(3): Show | 6 | HG00738.hp1 HG01069.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.134-1105T>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817917 | ||||||
| chr12:132817921
|
C | G | 2 | a0009c0015t0078g0066a0009c0015t0080g0065 | 2 | HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.134-1109G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817921 | ||||||
| chr12:132817922
|
C | T | 2 | a0009c0015t0078g0066a0009c0015t0080g0065 | 2 | HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.134-1110G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817922 | ||||||
| chr12:132817922
|
CACACTCT others(124): Show |
C | 5 | a0001c0003t0009g0292a0001c0003t0009g0293a0001c0003t0009g0294others(2): Show | 5 | HG02145.hp2 HG02559.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.134-1241_134-1111d others(2): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817922 | ||||||
| chr12:132817925
|
A | G | 15 | a0001c0001t0003g0116a0001c0001t0003g0122a0001c0001t0026g0302others(12): Show | 15 | HG00738.hp1 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.134-1113T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817925 | ||||||
| chr12:132817932
|
G | C | 3 | a0002c0013t0009g0133a0009c0015t0078g0066a0009c0015t0080g0065 | 3 | HG02258.hp2 HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.134-1120C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817932 | ||||||
| chr12:132817939
|
T | C | 12 | a0001c0001t0003g0116a0001c0001t0003g0122a0001c0001t0026g0302others(9): Show | 12 | HG00738.hp1 HG01069.hp2 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.134-1127A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817939 | ||||||
| chr12:132817941
|
A | C | 3 | a0001c0001t0026g0302a0001c0001t0027g0306a0001c0003t0009g0297 | 3 | HG02630.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.134-1129T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817941 | ||||||
| chr12:132817941
|
A | G | 3 | a0002c0013t0009g0133a0009c0015t0078g0066a0009c0015t0080g0065 | 3 | HG02258.hp2 HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.134-1129T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817941 | ||||||
| chr12:132817950
|
T | A | 193 | a0001c0001t0001g0026a0001c0001t0001g0035a0001c0001t0001g0036others(190): Show | 193 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.134-1138A>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817950 | ||||||
| chr12:132817954
|
C | G | 5 | a0001c0001t0003g0116a0001c0001t0003g0122a0001c0001t0073g0041others(2): Show | 5 | HG00738.hp1 HG01069.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.134-1142G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817954 | ||||||
| chr12:132817955
|
C | T | 5 | a0001c0001t0003g0116a0001c0001t0003g0122a0001c0001t0073g0041others(2): Show | 5 | HG00738.hp1 HG01069.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.134-1143G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817955 | ||||||
| chr12:132817957
|
C | T | 3 | a0001c0001t0026g0302a0001c0001t0027g0306a0001c0003t0009g0297 | 3 | HG02630.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.134-1145G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817957 | ||||||
| chr12:132817958
|
G | A | 3 | a0002c0002t0002g0187a0002c0002t0002g0206a0002c0002t0012g0209 | 3 | HG02109.hp1 HG02258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.134-1146C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817958 | ||||||
| chr12:132817965
|
G | C | 4 | a0001c0001t0003g0116a0001c0001t0003g0122a0001c0003t0041g0165others(1): Show | 4 | HG00738.hp1 HG01069.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.134-1153C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817965 | ||||||
| chr12:132817973
|
C | CG | 5 | a0001c0001t0003g0116a0001c0001t0003g0122a0001c0003t0009g0297others(2): Show | 5 | HG00738.hp1 HG01069.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.134-1162_134-1161i others(3): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817973 | ||||||
| chr12:132817977
|
C | CT | 3 | a0002c0002t0002g0188a0002c0002t0002g0210a0002c0013t0009g0133 | 3 | HG01074.hp1 HG01256.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.134-1166_134-1165i others(3): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817977 | ||||||
| chr12:132817977
|
C | G | 1 | a0002c0002t0057g0184 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.134-1165G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817977 | ||||||
| chr12:132817977
|
C | T | 8 | a0001c0001t0003g0116a0001c0001t0003g0122a0001c0001t0026g0302others(5): Show | 8 | HG00738.hp1 HG01069.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.134-1165G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817977 | ||||||
| chr12:132817979
|
C | A | 11 | a0005c0006t0001g0021a0005c0006t0014g0018a0005c0006t0014g0019others(8): Show | 11 | HG02055.hp2 HG02559.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.134-1167G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817979 | ||||||
| chr12:132817982
|
A | T | 3 | a0002c0002t0002g0188a0002c0002t0002g0210a0002c0013t0009g0133 | 3 | HG01074.hp1 HG01256.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.134-1170T>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817982 | ||||||
| chr12:132817989
|
C | T | 1 | a0002c0013t0009g0133 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.134-1177G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817989 | ||||||
| chr12:132817990
|
A | G | 7 | a0001c0001t0003g0116a0001c0001t0003g0122a0001c0003t0041g0165others(4): Show | 7 | HG00738.hp1 HG01069.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.134-1178T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817990 | ||||||
| chr12:132817990
|
ACTCTAAG others(26): Show |
A | 1 | a0001c0003t0009g0297 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.134-1211_134-1179d others(35): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132817990 | ||||||
| chr12:132818004
|
T | C | 4 | a0001c0001t0003g0116a0001c0001t0003g0122a0001c0003t0041g0165others(1): Show | 4 | HG00738.hp1 HG01069.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.134-1192A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818004 | ||||||
| chr12:132818006
|
A | C | 3 | a0001c0001t0003g0116a0001c0001t0003g0122a0001c0003t0041g0165 | 3 | HG00738.hp1 HG01069.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.134-1194T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818006 | ||||||
| chr12:132818006
|
A | G | 2 | a0001c0034t0001g0062a0002c0013t0009g0133 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.134-1194T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818006 | ||||||
| chr12:132818015
|
T | A | 3 | a0002c0013t0009g0133a0005c0006t0018g0102a0005c0006t0081g0308 | 3 | HG02258.hp2 HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.134-1203A>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818015 | ||||||
| chr12:132818022
|
C | T | 3 | a0001c0001t0003g0116a0001c0001t0003g0122a0001c0003t0041g0165 | 3 | HG00738.hp1 HG01069.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.134-1210G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818022 | ||||||
| chr12:132818023
|
G | A | 1 | a0002c0013t0009g0133 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.134-1211C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818023 | ||||||
| chr12:132818039
|
A | G | 3 | a0001c0003t0009g0297a0002c0002t0015g0222a0002c0013t0009g0133 | 3 | HG02132.hp1 HG02258.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.134-1227T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818039 | ||||||
| chr12:132818041
|
C | A | 1 | a0002c0002t0015g0222 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.134-1229G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818041 | ||||||
| chr12:132818048
|
A | T | 1 | a0001c0003t0041g0165 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.134-1236T>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818048 | ||||||
| chr12:132818052
|
G | C | 6 | a0001c0001t0003g0116a0001c0001t0003g0122a0001c0003t0009g0297others(3): Show | 6 | HG00738.hp1 HG01069.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.134-1240C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818052 | ||||||
| chr12:132818053
|
T | C | 6 | a0001c0001t0003g0116a0001c0001t0003g0122a0001c0003t0009g0297others(3): Show | 6 | HG00738.hp1 HG01069.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.134-1241A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818053 | ||||||
| chr12:132818055
|
C | T | 1 | a0001c0003t0041g0165 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.134-1243G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818055 | ||||||
| chr12:132818056
|
G | A | 2 | a0001c0003t0009g0297a0002c0013t0009g0133 | 2 | HG02258.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.134-1244C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818056 | ||||||
| chr12:132818063
|
C | G | 8 | a0001c0001t0003g0116a0001c0001t0003g0122a0001c0003t0009g0292others(5): Show | 8 | HG00738.hp1 HG01069.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.134-1251G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818063 | ||||||
| chr12:132818063
|
C | T | 2 | a0002c0002t0002g0187a0002c0002t0012g0209 | 2 | HG02258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.134-1251G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818063 | ||||||
| chr12:132818072
|
G | A | 2 | a0001c0001t0003g0116a0001c0001t0003g0122 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.134-1260C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818072 | ||||||
| chr12:132818072
|
G | C | 2 | a0001c0003t0041g0165a0001c0018t0019g0132 | 2 | HG01981.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.134-1260C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818072 | ||||||
| chr12:132818081
|
A | T | 2 | a0001c0003t0041g0165a0001c0018t0019g0132 | 2 | HG01981.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.134-1269T>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818081 | ||||||
| chr12:132818088
|
C | T | 2 | a0001c0003t0041g0165a0001c0018t0019g0132 | 2 | HG01981.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.134-1276G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818088 | ||||||
| chr12:132818088
|
CGCTCTAA others(26): Show |
C | 2 | a0009c0015t0078g0066a0009c0015t0080g0065 | 2 | HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.134-1309_134-1277d others(35): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818088 | ||||||
| chr12:132818096
|
G | C | 2 | a0001c0003t0009g0297a0002c0013t0009g0133 | 2 | HG02258.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.134-1284C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818096 | ||||||
| chr12:132818101
|
AC | A | 68 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(65): Show | 68 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.134-1290delG | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818101 | ||||||
| chr12:132818103
|
C | A | 69 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(66): Show | 69 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.134-1291G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818103 | ||||||
| chr12:132818105
|
C | G | 2 | a0001c0003t0009g0297a0002c0013t0009g0133 | 2 | HG02258.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.134-1293G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818105 | ||||||
| chr12:132818114
|
T | A | 7 | a0001c0003t0009g0292a0001c0003t0009g0293a0001c0003t0009g0294others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.134-1302A>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818114 | ||||||
| chr12:132818121
|
T | C | 7 | a0001c0003t0009g0292a0001c0003t0009g0293a0001c0003t0009g0294others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.134-1309A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818121 | ||||||
| chr12:132818138
|
A | C | 7 | a0001c0003t0009g0292a0001c0003t0009g0293a0001c0003t0009g0294others(4): Show | 7 | HG01192.hp1 HG02145.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.134-1326T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818138 | ||||||
| chr12:132818154
|
T | C | 1 | a0002c0002t0002g0223 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.134-1342A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818154 | ||||||
| chr12:132818169
|
T | C | 2 | a0008c0014t0021g0171a0022c0033t0002g0186 | 2 | HG01192.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.134-1357A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818169 | ||||||
| chr12:132818171
|
G | A | 2 | a0008c0014t0021g0171a0022c0033t0002g0186 | 2 | HG01192.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.134-1359C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818171 | ||||||
| chr12:132818171
|
GCCCTCCA others(26): Show |
G | 1 | a0008c0014t0021g0172 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.134-1392_134-1360d others(35): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818171 | ||||||
| chr12:132818180
|
A | T | 2 | a0008c0014t0021g0171a0022c0033t0002g0186 | 2 | HG01192.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.134-1368T>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818180 | ||||||
| chr12:132818185
|
T | C | 2 | a0008c0014t0021g0171a0022c0033t0002g0186 | 2 | HG01192.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.134-1373A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818185 | ||||||
| chr12:132818187
|
C | T | 2 | a0008c0014t0021g0171a0022c0033t0002g0186 | 2 | HG01192.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.134-1375G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818187 | ||||||
| chr12:132818188
|
A | G | 2 | a0008c0014t0021g0171a0022c0033t0002g0186 | 2 | HG01192.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.134-1376T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818188 | ||||||
| chr12:132818191
|
A | C | 2 | a0008c0014t0021g0171a0022c0033t0002g0186 | 2 | HG01192.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.134-1379T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818191 | ||||||
| chr12:132818204
|
A | G | 2 | a0008c0014t0021g0171a0022c0033t0002g0186 | 2 | HG01192.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.134-1392T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818204 | ||||||
| chr12:132818250
|
G | A | 1 | a0002c0002t0002g0207 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.134-1438C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818250 | ||||||
| chr12:132818452
|
G | A | 44 | a0003c0004t0001g0270a0003c0004t0001g0279a0003c0004t0001g0282others(41): Show | 44 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.134-1640C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818452 | ||||||
| chr12:132818456
|
T | C | 1 | a0010c0039t0010g0033 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.134-1644A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818456 | ||||||
| chr12:132818457
|
C | T | 1 | a0010c0039t0010g0033 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.134-1645G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818457 | ||||||
| chr12:132818507
|
G | C | 1 | a0010c0039t0010g0033 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.134-1695C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818507 | ||||||
| chr12:132818509
|
C | G | 1 | a0010c0039t0010g0033 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.134-1697G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818509 | ||||||
| chr12:132818510
|
T | C | 1 | a0010c0039t0010g0033 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.134-1698A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818510 | ||||||
| chr12:132818511
|
C | T | 1 | a0010c0039t0010g0033 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.134-1699G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818511 | ||||||
| chr12:132818545
|
C | A | 2 | a0003c0004t0008g0287a0003c0004t0008g0288 | 2 | HG00280.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.134-1733G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818545 | ||||||
| chr12:132818621
|
G | A | 2 | a0002c0002t0002g0168a0002c0002t0002g0174 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.134-1809C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818621 | ||||||
| chr12:132818712
|
A | G | 81 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(78): Show | 81 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.134-1900T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818712 | ||||||
| chr12:132818986
|
A | G | 1 | a0001c0001t0001g0026 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.134-2174T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132818986 | ||||||
| chr12:132819005
|
G | T | 1 | a0001c0001t0001g0026 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.134-2193C>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132819005 | ||||||
| chr12:132819033
|
AACTGCTG others(37): Show |
A | 14 | a0005c0006t0001g0021a0005c0006t0014g0018a0005c0006t0014g0019others(11): Show | 14 | HG02055.hp2 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.134-2265_134-2222d others(46): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132819033 | ||||||
| chr12:132819155
|
C | T | 2 | a0001c0003t0004g0166a0002c0007t0001g0068 | 2 | NA19002.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.134-2343G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132819155 | ||||||
| chr12:132819251
|
C | T | 2 | a0003c0004t0008g0276a0003c0004t0036g0260 | 2 | NA18979.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.134-2439G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132819251 | ||||||
| chr12:132819402
|
G | A | 4 | a0001c0001t0003g0117a0001c0001t0003g0118a0001c0001t0003g0123others(1): Show | 4 | HG01175.hp2 HG02809.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.134-2590C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132819402 | ||||||
| chr12:132819415
|
G | C | 1 | a0010c0039t0010g0033 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.133+2581C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132819415 | ||||||
| chr12:132819416
|
C | G | 1 | a0010c0039t0010g0033 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.133+2580G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132819416 | ||||||
| chr12:132819454
|
T | G | 294 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(291): Show | 294 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.133+2542A>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132819454 | ||||||
| chr12:132819455
|
C | G | 1 | a0012c0019t0038g0024 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.133+2541G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132819455 | ||||||
| chr12:132819458
|
A | G | 1 | a0012c0019t0038g0024 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.133+2538T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132819458 | ||||||
| chr12:132819460
|
T | C | 1 | a0012c0019t0038g0024 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.133+2536A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132819460 | ||||||
| chr12:132819473
|
A | G | 294 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(291): Show | 294 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.133+2523T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132819473 | ||||||
| chr12:132819528
|
C | CA | 6 | a0001c0001t0001g0137a0004c0005t0005g0255a0004c0037t0005g0245others(3): Show | 6 | HG02735.hp1 HG03491.hp2 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.133+2467dupT | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132819528 | ||||||
| chr12:132819536
|
G | A | 122 | a0001c0003t0002g0196a0001c0009t0002g0181a0001c0009t0002g0199others(119): Show | 122 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.133+2460C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132819536 | ||||||
| chr12:132819598
|
C | T | 1 | a0002c0002t0060g0185 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.133+2398G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132819598 | ||||||
| chr12:132819602
|
C | T | 1 | a0001c0001t0075g0128 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.133+2394G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132819602 | ||||||
| chr12:132819638
|
C | T | 16 | a0005c0006t0001g0021a0005c0006t0014g0018a0005c0006t0014g0019others(13): Show | 16 | HG02055.hp2 HG02486.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.133+2358G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132819638 | ||||||
| chr12:132819654
|
G | A | 79 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(76): Show | 79 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.133+2342C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132819654 | ||||||
| chr12:132819698
|
C | T | 1 | a0018c0029t0061g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.133+2298G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132819698 | ||||||
| chr12:132819766
|
G | A | 1 | a0001c0001t0029g0304 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.133+2230C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132819766 | ||||||
| chr12:132819986
|
C | G | 1 | a0001c0001t0075g0128 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.133+2010G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132819986 | ||||||
| chr12:132820088
|
A | G | 1 | a0012c0019t0038g0024 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.133+1908T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132820088 | ||||||
| chr12:132820171
|
C | T | 1 | a0002c0002t0002g0208 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.133+1825G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132820171 | ||||||
| chr12:132820176
|
C | CA | 7 | a0001c0001t0017g0001a0006c0010t0006g0011a0006c0010t0006g0012others(4): Show | 7 | HG01106.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.133+1819dupT | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132820176 | ||||||
| chr12:132820215
|
G | A | 2 | a0002c0002t0002g0179a0002c0002t0002g0180 | 2 | HG00741.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.133+1781C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132820215 | ||||||
| chr12:132820280
|
C | T | 27 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0001g0167others(24): Show | 27 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.133+1716G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132820280 | ||||||
| chr12:132820415
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.133+1581G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132820415 | ||||||
| chr12:132820440
|
G | C | 1 | a0018c0029t0061g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.133+1556C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132820440 | ||||||
| chr12:132820452
|
C | T | 6 | a0006c0010t0006g0011a0006c0010t0006g0012a0006c0010t0006g0130others(3): Show | 6 | HG01106.hp1 HG01891.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.133+1544G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132820452 | ||||||
| chr12:132820750
|
C | CTACGGGA others(6): Show |
1 | a0002c0007t0001g0071 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.133+1233_133+1245d others(15): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132820750 | ||||||
| chr12:132820821
|
C | G | 1 | a0001c0001t0001g0026 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.133+1175G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132820821 | ||||||
| chr12:132820830
|
T | G | 1 | a0001c0001t0001g0093 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.133+1166A>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132820830 | ||||||
| chr12:132820918
|
G | C | 2 | a0001c0011t0001g0061a0001c0011t0074g0067 | 2 | NA18952.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.133+1078C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132820918 | ||||||
| chr12:132820973
|
G | C | 108 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(105): Show | 108 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.133+1023C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132820973 | ||||||
| chr12:132820993
|
G | A | 6 | a0006c0010t0006g0011a0006c0010t0006g0012a0006c0010t0006g0130others(3): Show | 6 | HG01106.hp1 HG01891.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.133+1003C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132820993 | ||||||
| chr12:132821066
|
C | T | 1 | a0001c0018t0019g0132 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.133+930G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821066 | ||||||
| chr12:132821094
|
C | T | 121 | a0001c0003t0002g0196a0001c0009t0002g0181a0001c0009t0002g0199others(118): Show | 121 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.133+902G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821094 | ||||||
| chr12:132821099
|
C | CA | 41 | a0001c0001t0001g0028a0001c0001t0001g0038a0001c0001t0001g0063others(38): Show | 41 | HG00280.hp2 HG00642.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.133+896dupT | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821099 | ||||||
| chr12:132821099
|
C | CAA | 10 | a0001c0001t0017g0015a0001c0001t0026g0302a0001c0001t0028g0305others(7): Show | 10 | HG02132.hp2 HG02615.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.133+895_133+896dup others(2): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821099 | ||||||
| chr12:132821099
|
C | CAAA | 28 | a0001c0001t0003g0006a0001c0001t0003g0008a0001c0001t0003g0109others(25): Show | 28 | HG00438.hp2 HG00738.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.133+894_133+896dup others(3): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821099 | ||||||
| chr12:132821099
|
C | CAAAA | 25 | a0001c0001t0002g0121a0001c0001t0003g0007a0001c0001t0003g0010others(22): Show | 25 | HG00280.hp1 HG01069.hp2 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.133+893_133+896dup others(4): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821099 | ||||||
| chr12:132821099
|
C | CAAAAA | 41 | a0001c0001t0003g0122a0001c0003t0002g0196a0001c0009t0002g0181others(38): Show | 41 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.133+892_133+896dup others(5): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821099 | ||||||
| chr12:132821099
|
C | CAAAAAA | 28 | a0001c0009t0002g0219a0001c0009t0002g0232a0002c0002t0002g0002others(25): Show | 28 | HG00423.hp2 HG00673.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.133+891_133+896dup others(6): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821099 | ||||||
| chr12:132821099
|
C | CAAAAAAA | 9 | a0002c0002t0002g0014a0002c0002t0002g0224a0002c0002t0002g0225others(6): Show | 9 | HG00609.hp1 HG01891.hp2 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.133+890_133+896dup others(7): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821099 | ||||||
| chr12:132821124
|
T | A | 15 | a0005c0006t0001g0021a0005c0006t0014g0018a0005c0006t0014g0019others(12): Show | 15 | HG02055.hp2 HG02486.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.133+872A>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821124 | ||||||
| chr12:132821169
|
T | G | 15 | a0004c0005t0005g0247a0004c0005t0005g0248a0004c0005t0005g0249others(12): Show | 15 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.133+827A>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821169 | ||||||
| chr12:132821201
|
G | A | 15 | a0004c0005t0005g0247a0004c0005t0005g0248a0004c0005t0005g0249others(12): Show | 15 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.133+795C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821201 | ||||||
| chr12:132821205
|
G | A | 5 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0135others(2): Show | 5 | HG00423.hp1 HG02056.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.133+791C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821205 | ||||||
| chr12:132821273
|
A | G | 79 | a0001c0003t0002g0196a0001c0009t0002g0181a0001c0009t0002g0199others(76): Show | 79 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.133+723T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821273 | ||||||
| chr12:132821299
|
C | T | 1 | a0014c0020t0019g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.133+697G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821299 | ||||||
| chr12:132821368
|
T | C | 2 | a0003c0004t0008g0276a0003c0004t0036g0260 | 2 | NA18979.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.133+628A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821368 | ||||||
| chr12:132821408
|
GA | G | 286 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(283): Show | 286 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.133+587delT | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821408 | ||||||
| chr12:132821434
|
G | C | 79 | a0001c0003t0002g0196a0001c0009t0002g0181a0001c0009t0002g0199others(76): Show | 79 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.133+562C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821434 | ||||||
| chr12:132821485
|
G | C | 1 | a0023c0040t0002g0234 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.133+511C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821485 | ||||||
| chr12:132821569
|
G | T | 1 | a0001c0011t0074g0067 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.133+427C>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821569 | ||||||
| chr12:132821572
|
C | G | 1 | a0023c0040t0002g0234 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.133+424G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821572 | ||||||
| chr12:132821573
|
G | C | 1 | a0023c0040t0002g0234 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.133+423C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821573 | ||||||
| chr12:132821579
|
A | G | 176 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(173): Show | 176 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.133+417T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821579 | ||||||
| chr12:132821589
|
A | G | 13 | a0005c0006t0001g0021a0005c0006t0014g0018a0005c0006t0014g0019others(10): Show | 13 | HG02055.hp2 HG02486.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.133+407T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821589 | ||||||
| chr12:132821660
|
T | C | 2 | a0002c0002t0002g0231a0006c0010t0006g0131 | 2 | HG03225.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.133+336A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821660 | ||||||
| chr12:132821671
|
G | A | 1 | a0001c0003t0001g0167 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.133+325C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821671 | ||||||
| chr12:132821677
|
A | C | 7 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(4): Show | 7 | NA18950.hp2 NA18964.hp2 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.133+319T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821677 | ||||||
| chr12:132821681
|
C | T | 1 | a0001c0003t0001g0167 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.133+315G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821681 | ||||||
| chr12:132821734
|
A | G | 2 | a0001c0003t0004g0143a0001c0003t0004g0159 | 2 | HG00642.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.133+262T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821734 | ||||||
| chr12:132821756
|
G | A | 27 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0001g0167others(24): Show | 27 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.133+240C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821756 | ||||||
| chr12:132821761
|
A | G | 26 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0001g0167others(23): Show | 26 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.133+235T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821761 | ||||||
| chr12:132821769
|
G | T | 1 | a0002c0002t0002g0002 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.133+227C>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821769 | ||||||
| chr12:132821771
|
A | G | 26 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0001g0167others(23): Show | 26 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.133+225T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821771 | ||||||
| chr12:132821779
|
G | A | 5 | a0001c0001t0003g0117a0001c0001t0003g0118a0001c0001t0003g0123others(2): Show | 5 | HG01175.hp2 HG02809.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.133+217C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821779 | ||||||
| chr12:132821796
|
G | C | 1 | a0002c0002t0012g0233 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.133+200C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821796 | ||||||
| chr12:132821797
|
C | T | 28 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0001g0167others(25): Show | 28 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.133+199G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821797 | ||||||
| chr12:132821809
|
A | G | 110 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0028g0305others(107): Show | 110 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.133+187T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821809 | ||||||
| chr12:132821810
|
C | T | 2 | a0001c0001t0003g0006a0001c0001t0003g0007 | 2 | NA18946.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.133+186G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821810 | ||||||
| chr12:132821820
|
G | C | 27 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0001g0167others(24): Show | 27 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.133+176C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821820 | ||||||
| chr12:132821833
|
G | A | 1 | a0002c0002t0002g0177 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.133+163C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821833 | ||||||
| chr12:132821835
|
A | C | 27 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0001g0167others(24): Show | 27 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.133+161T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821835 | ||||||
| chr12:132821841
|
G | A | 1 | a0002c0013t0004g0141 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.133+155C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821841 | ||||||
| chr12:132821841
|
GAGACTCC others(14): Show |
G | 1 | a0001c0001t0001g0135 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.133+134_133+154del others(21): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821841 | ||||||
| chr12:132821846
|
T | C | 1 | a0001c0001t0032g0107 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.133+150A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821846 | ||||||
| chr12:132821853
|
C | CA | 6 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0003t0006g0298others(3): Show | 6 | HG02630.hp1 HG02717.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.133+142dupT | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821853 | ||||||
| chr12:132821853
|
CA | C | 248 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(245): Show | 248 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.133+142delT | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821853 | ||||||
| chr12:132821853
|
CAA | C | 6 | a0001c0001t0001g0039a0003c0004t0013g0261a0005c0006t0018g0023others(3): Show | 6 | HG02486.hp2 HG02895.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.133+141_133+142del others(2): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821853 | ||||||
| chr12:132821864
|
A | C | 1 | a0023c0040t0002g0234 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.133+132T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821864 | ||||||
| chr12:132821865
|
A | C | 82 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(79): Show | 82 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.133+131T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821865 | ||||||
| chr12:132821872
|
A | C | 4 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0008others(1): Show | 4 | HG00438.hp2 HG02129.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.133+124T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821872 | ||||||
| chr12:132821919
|
ATCCTCCC others(11): Show |
A | 32 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(29): Show | 32 | HG00423.hp1 HG02015.hp2 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.133+59_133+76delCG others(16): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821919 | ||||||
| chr12:132821937
|
G | A | 5 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(2): Show | 5 | HG01123.hp1 HG01496.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.133+59C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821937 | ||||||
| chr12:132821975
|
C | A | 3 | a0002c0002t0007g0236a0002c0002t0050g0237a0002c0002t0051g0238 | 3 | NA18612.hp1 NA18612.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.133+21G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 2/23 | chr12 | 132821975 | ||||||
| chr12:132822332
|
A | T | 1 | a0001c0001t0001g0026 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-183-21T>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132822332 | ||||||
| chr12:132822403
|
G | A | 2 | a0001c0003t0004g0166a0023c0040t0002g0234 | 2 | NA18939.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-183-92C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132822403 | ||||||
| chr12:132822465
|
T | C | 1 | a0001c0001t0003g0123 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-183-154A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132822465 | ||||||
| chr12:132822648
|
C | T | 6 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(3): Show | 6 | NA18950.hp2 NA18964.hp2 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-183-337G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132822648 | ||||||
| chr12:132822702
|
C | A | 1 | a0001c0001t0001g0026 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-183-391G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132822702 | ||||||
| chr12:132822719
|
A | G | 79 | a0001c0003t0002g0196a0001c0003t0004g0142a0001c0009t0002g0181others(76): Show | 79 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.-183-408T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132822719 | ||||||
| chr12:132822779
|
G | A | 78 | a0001c0003t0002g0196a0001c0009t0002g0181a0001c0009t0002g0199others(75): Show | 78 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.-183-468C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132822779 | ||||||
| chr12:132822877
|
G | A | 4 | a0001c0001t0026g0302a0001c0001t0027g0306a0001c0001t0028g0305others(1): Show | 4 | HG02818.hp1 HG02886.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-183-566C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132822877 | ||||||
| chr12:132822912
|
A | C | 1 | a0001c0001t0001g0135 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-183-601T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132822912 | ||||||
| chr12:132822967
|
T | C | 44 | a0003c0004t0001g0270a0003c0004t0001g0279a0003c0004t0001g0282others(41): Show | 44 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.-183-656A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132822967 | ||||||
| chr12:132823067
|
C | A | 1 | a0001c0001t0001g0026 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-183-756G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132823067 | ||||||
| chr12:132823091
|
C | G | 294 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(291): Show | 294 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.-183-780G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132823091 | ||||||
| chr12:132823160
|
C | T | 44 | a0003c0004t0001g0270a0003c0004t0001g0279a0003c0004t0001g0282others(41): Show | 44 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.-183-849G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132823160 | ||||||
| chr12:132823219
|
C | T | 1 | a0002c0002t0006g0182 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-183-908G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132823219 | ||||||
| chr12:132823425
|
T | G | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | NA18980.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-183-1114A>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132823425 | ||||||
| chr12:132823561
|
G | A | 1 | a0002c0002t0002g0235 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-183-1250C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132823561 | ||||||
| chr12:132823572
|
G | A | 1 | a0002c0007t0001g0092 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-183-1261C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132823572 | ||||||
| chr12:132823647
|
C | T | 1 | a0004c0037t0005g0245 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-183-1336G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132823647 | ||||||
| chr12:132823660
|
G | A | 52 | a0003c0004t0001g0270a0003c0004t0001g0279a0003c0004t0001g0282others(49): Show | 52 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.-183-1349C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132823660 | ||||||
| chr12:132823686
|
C | G | 1 | a0001c0001t0001g0035 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-183-1375G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132823686 | ||||||
| chr12:132823718
|
C | T | 2 | a0004c0036t0008g0263a0013c0035t0035g0262 | 2 | HG02004.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-183-1407G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132823718 | ||||||
| chr12:132823722
|
G | A | 3 | a0002c0002t0007g0236a0002c0002t0050g0237a0002c0002t0051g0238 | 3 | NA18612.hp1 NA18612.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.-183-1411C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132823722 | ||||||
| chr12:132823787
|
T | TA | 45 | a0001c0001t0001g0135a0003c0004t0001g0270a0003c0004t0001g0279others(42): Show | 45 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.-183-1477dupT | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132823787 | ||||||
| chr12:132823833
|
A | G | 2 | a0004c0036t0008g0263a0013c0035t0035g0262 | 2 | HG02004.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-183-1522T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132823833 | ||||||
| chr12:132823837
|
C | T | 7 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(4): Show | 7 | NA18950.hp2 NA18964.hp2 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.-183-1526G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132823837 | ||||||
| chr12:132824020
|
T | C | 2 | a0004c0005t0005g0258a0004c0005t0005g0259 | 2 | HG01175.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-183-1709A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132824020 | ||||||
| chr12:132824119
|
G | A | 1 | a0001c0018t0019g0132 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-183-1808C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132824119 | ||||||
| chr12:132824139
|
T | A | 1 | a0003c0004t0013g0261 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-183-1828A>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132824139 | ||||||
| chr12:132824165
|
C | T | 1 | a0014c0020t0019g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-183-1854G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132824165 | ||||||
| chr12:132824315
|
T | A | 1 | a0003c0004t0013g0261 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-183-2004A>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132824315 | ||||||
| chr12:132824323
|
A | T | 1 | a0001c0001t0001g0135 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-183-2012T>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132824323 | ||||||
| chr12:132824392
|
T | C | 1 | a0001c0001t0017g0015 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-183-2081A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132824392 | ||||||
| chr12:132824456
|
C | A | 1 | a0003c0004t0013g0261 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-183-2145G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132824456 | ||||||
| chr12:132824457
|
A | C | 1 | a0003c0004t0013g0261 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-183-2146T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132824457 | ||||||
| chr12:132824473
|
A | T | 1 | a0003c0004t0013g0261 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-183-2162T>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132824473 | ||||||
| chr12:132824480
|
T | A | 1 | a0003c0004t0013g0261 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-183-2169A>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132824480 | ||||||
| chr12:132824503
|
A | C | 1 | a0003c0004t0013g0261 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-183-2192T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132824503 | ||||||
| chr12:132824508
|
G | A | 143 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(140): Show | 143 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.-183-2197C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132824508 | ||||||
| chr12:132824510
|
A | C | 1 | a0003c0004t0013g0261 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-183-2199T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132824510 | ||||||
| chr12:132824537
|
A | C | 1 | a0003c0004t0013g0261 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-183-2226T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132824537 | ||||||
| chr12:132824594
|
A | T | 1 | a0001c0001t0001g0135 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-183-2283T>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132824594 | ||||||
| chr12:132824598
|
C | A | 78 | a0001c0003t0002g0196a0001c0009t0002g0181a0001c0009t0002g0199others(75): Show | 78 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.-183-2287G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132824598 | ||||||
| chr12:132824659
|
G | T | 8 | a0005c0006t0001g0021a0005c0006t0014g0018a0005c0006t0014g0019others(5): Show | 8 | HG02055.hp2 HG02559.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.-183-2348C>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132824659 | ||||||
| chr12:132824663
|
C | T | 29 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0001g0167others(26): Show | 29 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.-183-2352G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132824663 | ||||||
| chr12:132824698
|
C | G | 4 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0008others(1): Show | 4 | HG00438.hp2 HG02129.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.-183-2387G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132824698 | ||||||
| chr12:132824727
|
C | T | 15 | a0004c0005t0005g0247a0004c0005t0005g0248a0004c0005t0005g0249others(12): Show | 15 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.-183-2416G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132824727 | ||||||
| chr12:132825035
|
C | T | 1 | a0002c0013t0004g0141 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-183-2724G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132825035 | ||||||
| chr12:132825058
|
G | A | 13 | a0005c0006t0001g0021a0005c0006t0014g0018a0005c0006t0014g0019others(10): Show | 13 | HG02055.hp2 HG02486.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-183-2747C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132825058 | ||||||
| chr12:132825160
|
G | A | 4 | a0001c0001t0017g0001a0001c0018t0019g0132a0001c0025t0003g0106others(1): Show | 4 | HG01517.hp2 HG02132.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.-183-2849C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132825160 | ||||||
| chr12:132825200
|
C | T | 1 | a0001c0009t0002g0181 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-183-2889G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132825200 | ||||||
| chr12:132825359
|
G | A | 15 | a0004c0005t0005g0247a0004c0005t0005g0248a0004c0005t0005g0249others(12): Show | 15 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.-183-3048C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132825359 | ||||||
| chr12:132825506
|
T | C | 2 | a0002c0002t0003g0240a0002c0002t0053g0239 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-183-3195A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132825506 | ||||||
| chr12:132825805
|
GTAC | G | 44 | a0003c0004t0001g0270a0003c0004t0001g0279a0003c0004t0001g0282others(41): Show | 44 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.-184+2995_-184+299 others(7): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132825805 | ||||||
| chr12:132826002
|
A | G | 294 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(291): Show | 294 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.-184+2801T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132826002 | ||||||
| chr12:132826025
|
A | C | 3 | a0002c0002t0002g0178a0002c0002t0002g0179a0002c0002t0002g0180 | 3 | HG00741.hp2 HG01361.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-184+2778T>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132826025 | ||||||
| chr12:132826054
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-184+2749C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132826054 | ||||||
| chr12:132826104
|
G | A | 4 | a0001c0001t0001g0027a0001c0001t0001g0096a0001c0001t0024g0094others(1): Show | 4 | HG00323.hp2 HG02004.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.-184+2699C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132826104 | ||||||
| chr12:132826105
|
G | A | 2 | a0005c0006t0018g0102a0018c0029t0061g0103 | 2 | HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-184+2698C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132826105 | ||||||
| chr12:132826202
|
C | T | 3 | a0002c0002t0002g0175a0002c0002t0002g0176a0002c0002t0002g0177 | 3 | HG00642.hp1 HG01167.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.-184+2601G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132826202 | ||||||
| chr12:132826240
|
C | CA | 46 | a0001c0001t0001g0097a0001c0001t0002g0121a0001c0001t0003g0008others(43): Show | 46 | HG00280.hp1 HG00438.hp2 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.-184+2562dupT | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132826240 | ||||||
| chr12:132826240
|
CA | C | 7 | a0001c0001t0001g0026a0001c0001t0001g0027a0002c0002t0002g0173others(4): Show | 7 | HG01070.hp2 HG02004.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-184+2562delT | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132826240 | ||||||
| chr12:132826253
|
A | AG | 43 | a0003c0004t0001g0270a0003c0004t0001g0279a0003c0004t0001g0282others(40): Show | 43 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(40): Show |
intron_variant | MODIFIER | c.-184+2549_-184+255 others(5): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132826253 | ||||||
| chr12:132826253
|
A | G | 1 | a0003c0004t0036g0260 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-184+2550T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132826253 | ||||||
| chr12:132826368
|
ATGCAGAG others(9): Show |
A | 3 | a0001c0001t0004g0126a0001c0001t0004g0127a0002c0012t0011g0125 | 3 | HG03017.hp2 HG03654.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.-184+2419_-184+243 others(20): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132826368 | ||||||
| chr12:132826420
|
G | A | 2 | a0001c0001t0001g0098a0001c0026t0001g0099 | 2 | NA19058.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-184+2383C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132826420 | ||||||
| chr12:132826481
|
G | C | 30 | a0001c0024t0002g0100a0003c0004t0001g0270a0003c0004t0001g0279others(27): Show | 30 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.-184+2322C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132826481 | ||||||
| chr12:132826721
|
G | A | 29 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0001g0167others(26): Show | 29 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.-184+2082C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132826721 | ||||||
| chr12:132826748
|
C | T | 31 | a0001c0001t0002g0121a0001c0001t0003g0006a0001c0001t0003g0007others(28): Show | 31 | HG00280.hp1 HG00438.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.-184+2055G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132826748 | ||||||
| chr12:132826848
|
CGAG | C | 27 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0001g0167others(24): Show | 27 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.-184+1952_-184+195 others(7): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132826848 | ||||||
| chr12:132826886
|
T | G | 1 | a0004c0005t0005g0101 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-184+1917A>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132826886 | ||||||
| chr12:132826956
|
A | G | 27 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0001g0167others(24): Show | 27 | HG00438.hp1 HG00642.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.-184+1847T>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132826956 | ||||||
| chr12:132827040
|
G | A | 1 | a0006c0010t0047g0134 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-184+1763C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132827040 | ||||||
| chr12:132827096
|
T | G | 82 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(79): Show | 82 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.-184+1707A>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132827096 | ||||||
| chr12:132827255
|
T | C | 2 | a0005c0006t0018g0102a0018c0029t0061g0103 | 2 | HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-184+1548A>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132827255 | ||||||
| chr12:132827356
|
G | T | 2 | a0005c0006t0043g0004a0005c0006t0044g0005 | 2 | HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-184+1447C>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132827356 | ||||||
| chr12:132827847
|
C | T | 2 | a0008c0014t0021g0171a0008c0014t0021g0172 | 2 | HG02602.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.-184+956G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132827847 | ||||||
| chr12:132827905
|
T | TA | 47 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(44): Show | 47 | HG00738.hp1 HG00738.hp2 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.-184+897dupT | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132827905 | ||||||
| chr12:132827905
|
T | TAA | 77 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0003t0002g0196others(74): Show | 77 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.-184+896_-184+897d others(4): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132827905 | ||||||
| chr12:132828219
|
C | G | 44 | a0003c0004t0001g0270a0003c0004t0001g0279a0003c0004t0001g0282others(41): Show | 44 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.-184+584G>C | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132828219 | ||||||
| chr12:132828226
|
G | A | 2 | a0003c0004t0008g0285a0003c0004t0008g0286 | 2 | HG01169.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-184+577C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132828226 | ||||||
| chr12:132828242
|
G | A | 105 | a0001c0003t0001g0148a0001c0003t0001g0151a0001c0003t0001g0167others(102): Show | 105 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.-184+561C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132828242 | ||||||
| chr12:132828272
|
C | A | 1 | a0001c0001t0010g0244 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-184+531G>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132828272 | ||||||
| chr12:132828483
|
G | A | 44 | a0003c0004t0001g0270a0003c0004t0001g0279a0003c0004t0001g0282others(41): Show | 44 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.-184+320C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132828483 | ||||||
| chr12:132828500
|
C | T | 1 | a0014c0020t0019g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-184+303G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132828500 | ||||||
| chr12:132828515
|
G | A | 2 | a0003c0004t0008g0287a0003c0004t0008g0288 | 2 | HG00280.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-184+288C>T | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132828515 | ||||||
| chr12:132828589
|
C | T | 1 | a0001c0003t0048g0289 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-184+214G>A | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132828589 | ||||||
| chr12:132828702
|
C | CCCGCCGC others(14): Show |
295 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(292): Show | 295 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.-184+100_-184+101i others(23): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132828702 | ||||||
| chr12:132828739
|
TGCGGGAG others(5): Show |
T | 1 | a0002c0002t0002g0002 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-184+52_-184+63del others(12): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132828739 | ||||||
| chr12:132828742
|
GGGAGCGG others(25): Show |
G | 1 | a0001c0001t0017g0001 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-184+29_-184+60del others(32): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132828742 | ||||||
| chr12:132828748
|
G | C | 1 | a0002c0002t0002g0301 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-184+55C>G | GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132828748 | ||||||
| chr12:132828773
|
CCGAGGCG others(9): Show |
C | 6 | a0001c0001t0026g0302a0001c0001t0027g0306a0001c0001t0028g0305others(3): Show | 6 | HG02818.hp1 HG02886.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-184+14_-184+29del others(16): Show |
GOLGA3 | ENSG00000090615.16 | transcript | ENST00000450791.8 | protein_coding | 1/23 | chr12 | 132828773 |