Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 26290 |
|---|---|
| ensemblid | ENSG00000130035.9 |
| hgncid | 4130 |
| symbol | GALNT8 |
| name | polypeptide N-acetylgalactosaminyltransferase 8 |
| refseq_nuc | NM_017417.2 |
| refseq_prot | NP_059113.1 |
| ensembl_nuc | ENST00000252318.7 |
| ensembl_prot | ENSP00000252318.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 4720400 |
| end | 4772726 |
| strand | + |
| ver | v1.2 |
| region | chr12:4720400-4772726 |
| region5000 | chr12:4715400-4777726 |
| regionname0 | GALNT8_chr12_4720400_4772726 |
| regionname5000 | GALNT8_chr12_4715400_4777726 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 637 | 188 | 37 | 36 | 80 | 6 | 27 | 67 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0002 | 0/0 | 637 | 97 | 15 | 20 | 49 | 3 | 10 | 43 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0003 | 0/0 | 637 | 17 | 16 | 0 | 1 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0004 | 0/0 | 637 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0005 | 0/0 | 637 | 6 | 3 | 2 | 0 | 0 | 1 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0006 | 0/0 | 637 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0007 | 0/0 | 637 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0008 | 0/0 | 637 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0009 | 0/0 | 637 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0010 | 0/0 | 637 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0011 | 0/0 | 637 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0012 | 0/0 | 637 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0013 | 0/0 | 637 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0014 | 0/0 | 637 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0015 | 0/0 | 637 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0016 | 0/0 | 637 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0017 | 0/0 | 430 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0018 | 0/0 | 637 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0019 | 0/0 | 637 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0020 | 0/0 | 637 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0021 | 0/0 | 637 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1914 | 186 | 36 | 36 | 80 | 6 | 26 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| c0002 | 0/0 | 1914 | 95 | 14 | 20 | 48 | 3 | 10 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| c0003 | 0/0 | 1914 | 10 | 10 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| c0004 | 0/0 | 1914 | 6 | 6 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| c0005 | 0/0 | 1914 | 6 | 6 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| c0006 | 0/0 | 1914 | 4 | 3 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| c0007 | 0/0 | 1914 | 3 | 0 | 2 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| c0008 | 0/0 | 1914 | 3 | 2 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| c0009 | 0/0 | 1914 | 2 | 1 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| c0010 | 0/0 | 1914 | 2 | 0 | 2 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| c0011 | 0/0 | 1914 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| c0012 | 0/0 | 1914 | 2 | 0 | 1 | 0 | 1 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| c0013 | 0/0 | 1914 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| c0014 | 0/0 | 1914 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| c0015 | 0/0 | 1914 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| c0016 | 0/0 | 1914 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| c0017 | 0/0 | 1914 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| c0018 | 0/0 | 1914 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| c0019 | 0/0 | 1914 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| c0020 | 0/0 | 1914 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| c0021 | 0/0 | 1914 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| c0022 | 0/0 | 1914 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| c0023 | 0/0 | 1914 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| c0024 | 0/0 | 1914 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| c0025 | 0/0 | 1914 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| c0026 | 0/0 | 1914 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| c0027 | 0/0 | 1914 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| c0028 | 0/0 | 1914 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 408 | 170 | 42 | 25 | 79 | 4 | 19 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| t0002 | 0/0 | 408 | 125 | 31 | 29 | 47 | 5 | 13 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| t0003 | 0/1 | 408 | 30 | 8 | 10 | 6 | 1 | 4 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| t0004 | 0/0 | 408 | 4 | 0 | 0 | 0 | 0 | 4 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| t0005 | 0/0 | 430 | 4 | 4 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| t0006 | 0/0 | 430 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| t0007 | 0/0 | 408 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| t0008 | 0/0 | 430 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0002 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0003 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0004 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0005 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0007 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0048 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0258 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1914 | 186 | 36 | 36 | 80 | 6 | 26 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0001c0014 | 0/0 | 1914 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0001c0022 | 0/0 | 1914 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0002c0002 | 0/0 | 1914 | 95 | 14 | 20 | 48 | 3 | 10 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0002c0018 | 0/0 | 1914 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0002c0020 | 0/0 | 1914 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0003c0003 | 0/0 | 1914 | 10 | 10 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0003c0004 | 0/0 | 1914 | 6 | 6 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0003c0016 | 0/0 | 1914 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0004c0005 | 0/0 | 1914 | 6 | 6 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0005c0006 | 0/0 | 1914 | 4 | 3 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0005c0010 | 0/0 | 1914 | 2 | 0 | 2 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0006c0007 | 0/0 | 1914 | 3 | 0 | 2 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0007c0008 | 0/0 | 1914 | 3 | 2 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0008c0009 | 0/0 | 1914 | 2 | 1 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0009c0013 | 0/0 | 1914 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0010c0011 | 0/0 | 1914 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0011c0012 | 0/0 | 1914 | 2 | 0 | 1 | 0 | 1 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0012c0017 | 0/0 | 1914 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0013c0019 | 0/0 | 1914 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0014c0015 | 0/0 | 1914 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0015c0021 | 0/0 | 1914 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0016c0027 | 0/0 | 1914 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0017c0026 | 0/0 | 1914 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0018c0023 | 0/0 | 1914 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0019c0025 | 0/0 | 1914 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0020c0024 | 0/0 | 1914 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0021c0028 | 0/0 | 1914 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2321 | 139 | 22 | 22 | 73 | 3 | 18 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0001c0001t0002 | 0/0 | 2321 | 14 | 6 | 4 | 1 | 2 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0001c0001t0003 | 0/1 | 2321 | 30 | 8 | 10 | 6 | 1 | 4 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0001c0001t0004 | 0/0 | 2321 | 3 | 0 | 0 | 0 | 0 | 3 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0001c0014t0001 | 0/0 | 2321 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0001c0022t0002 | 0/0 | 2321 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0002c0002t0001 | 0/0 | 2321 | 5 | 0 | 0 | 5 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0002c0002t0002 | 0/0 | 2321 | 88 | 12 | 20 | 43 | 3 | 10 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0002c0002t0007 | 0/0 | 2321 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0002c0018t0002 | 0/0 | 2321 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0002c0020t0002 | 0/0 | 2321 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0003c0003t0001 | 0/0 | 2321 | 9 | 9 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0003c0003t0002 | 0/0 | 2321 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0003c0004t0001 | 0/0 | 2321 | 6 | 6 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0003c0016t0002 | 0/0 | 2321 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0004c0005t0005 | 0/0 | 2343 | 4 | 4 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0004c0005t0006 | 0/0 | 2343 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0005c0006t0002 | 0/0 | 2321 | 4 | 3 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0005c0010t0002 | 0/0 | 2321 | 2 | 0 | 2 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0006c0007t0002 | 0/0 | 2321 | 3 | 0 | 2 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0007c0008t0001 | 0/0 | 2321 | 3 | 2 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0008c0009t0002 | 0/0 | 2321 | 2 | 1 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0009c0013t0002 | 0/0 | 2321 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0010c0011t0001 | 0/0 | 2321 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0011c0012t0001 | 0/0 | 2321 | 2 | 0 | 1 | 0 | 1 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0012c0017t0002 | 0/0 | 2321 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0013c0019t0008 | 0/0 | 2343 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0014c0015t0002 | 0/0 | 2321 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0015c0021t0002 | 0/0 | 2321 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0016c0027t0002 | 0/0 | 2321 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0017c0026t0001 | 0/0 | 2321 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0018c0023t0001 | 0/0 | 2321 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0019c0025t0004 | 0/0 | 2321 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0020c0024t0002 | 0/0 | 2321 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| a0021c0028t0001 | 0/0 | 2321 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | copy fasta | chr12 | 4715400 | 4777726 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0258 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0003g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0003g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0003g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0003g0048 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0003g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0004g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0014t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0001c0022t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0002 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0003 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0005 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0007g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0002t0007g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0018t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0002c0020t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0003c0003t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0003c0003t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0003c0003t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0003c0003t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0003c0003t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0003c0003t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0003c0003t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0003c0003t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0003c0003t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0003c0004t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0003c0004t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0003c0004t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0003c0004t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0003c0004t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0003c0004t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0003c0016t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0004c0005t0005g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0004c0005t0005g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0004c0005t0005g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0004c0005t0005g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0004c0005t0006g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0004c0005t0006g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0005c0006t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0005c0006t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0005c0006t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0005c0006t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0005c0010t0002g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0006c0007t0002g0007 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0007c0008t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0007c0008t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0007c0008t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0008c0009t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0008c0009t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0009c0013t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0009c0013t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0010c0011t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0010c0011t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0011c0012t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0011c0012t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0012c0017t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0013c0019t0008g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0014c0015t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0015c0021t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0016c0027t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0017c0026t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0018c0023t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0019c0025t0004g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0020c0024t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| a0021c0028t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0002 | c0002 | t0002 | g0005 | EUR | GBR | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0246 | EUR | GBR | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0247 | EUR | FIN | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG00323 | hp2 | a0002 | c0002 | t0002 | g0105 | EUR | FIN | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG00609 | hp1 | a0002 | c0018 | t0002 | g0020 | EAS | CHS | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | CHS | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0152 | EAS | CHS | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0038 | AMR | PUR | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0287 | AMR | PUR | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0288 | AMR | PUR | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0289 | AMR | PUR | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0006 | AMR | PUR | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0057 | AMR | PUR | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG00741 | hp2 | a0002 | c0002 | t0002 | g0120 | AMR | PUR | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0291 | AMR | PUR | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01070 | hp2 | a0002 | c0002 | t0002 | g0006 | AMR | PUR | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01071 | hp1 | a0002 | c0002 | t0002 | g0006 | AMR | PUR | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0035 | AMR | PUR | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01081 | hp1 | a0002 | c0002 | t0002 | g0150 | AMR | PUR | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01081 | hp2 | a0002 | c0002 | t0002 | g0167 | AMR | PUR | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01106 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01109 | hp1 | a0002 | c0002 | t0002 | g0109 | AMR | PUR | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01109 | hp2 | a0007 | c0008 | t0001 | g0188 | AMR | PUR | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01168 | hp1 | a0021 | c0028 | t0001 | g0023 | AMR | PUR | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01192 | hp1 | a0006 | c0007 | t0002 | g0007 | AMR | PUR | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01255 | hp1 | a0011 | c0012 | t0001 | g0244 | AMR | CLM | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0160 | AMR | CLM | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | CLM | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0005 | AMR | CLM | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01261 | hp1 | a0005 | c0010 | t0002 | g0019 | AMR | CLM | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01346 | hp1 | a0006 | c0007 | t0002 | g0007 | AMR | CLM | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01346 | hp2 | a0002 | c0002 | t0002 | g0149 | AMR | CLM | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | CLM | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01358 | hp2 | a0005 | c0010 | t0002 | g0019 | AMR | CLM | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0296 | AMR | CLM | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01433 | hp1 | a0002 | c0002 | t0002 | g0145 | AMR | CLM | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01496 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0027 | EUR | IBS | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01516 | hp2 | a0002 | c0002 | t0002 | g0002 | EUR | IBS | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0027 | EUR | IBS | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01517 | hp2 | a0011 | c0012 | t0001 | g0245 | EUR | IBS | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01884 | hp1 | a0020 | c0024 | t0002 | g0292 | AFR | ACB | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01891 | hp1 | a0004 | c0005 | t0005 | g0272 | AFR | ACB | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01891 | hp2 | a0018 | c0023 | t0001 | g0267 | AFR | ACB | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01928 | hp1 | a0002 | c0002 | t0002 | g0128 | AMR | PEL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0050 | AMR | PEL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01943 | hp2 | a0002 | c0002 | t0002 | g0155 | AMR | PEL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01952 | hp2 | a0008 | c0009 | t0002 | g0029 | AMR | PEL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PEL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0156 | AMR | PEL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02055 | hp1 | a0010 | c0011 | t0001 | g0186 | AFR | ACB | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02055 | hp2 | a0002 | c0002 | t0002 | g0132 | AFR | ACB | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0127 | EAS | KHV | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02056 | hp2 | a0017 | c0026 | t0001 | g0078 | EAS | KHV | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02071 | hp2 | a0002 | c0002 | t0002 | g0158 | EAS | KHV | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02080 | hp1 | a0002 | c0002 | t0002 | g0114 | EAS | KHV | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02129 | hp2 | a0002 | c0002 | t0002 | g0017 | EAS | KHV | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | ACB | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02145 | hp2 | a0002 | c0002 | t0002 | g0112 | AFR | ACB | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02148 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0034 | AMR | PEL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02257 | hp1 | a0002 | c0002 | t0002 | g0147 | AFR | ACB | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02258 | hp1 | a0003 | c0003 | t0001 | g0104 | AFR | ACB | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02258 | hp2 | a0009 | c0013 | t0002 | g0279 | AFR | ACB | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02280 | hp1 | a0003 | c0004 | t0001 | g0108 | AFR | ACB | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02280 | hp2 | a0003 | c0003 | t0001 | g0018 | AFR | ACB | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0130 | AMR | PEL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02451 | hp1 | a0002 | c0002 | t0002 | g0140 | AFR | ACB | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02451 | hp2 | a0003 | c0004 | t0001 | g0141 | AFR | ACB | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0224 | AFR | GWD | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0042 | AFR | GWD | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02615 | hp2 | a0010 | c0011 | t0001 | g0207 | AFR | GWD | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02622 | hp1 | a0005 | c0006 | t0002 | g0060 | AFR | GWD | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02622 | hp2 | a0003 | c0003 | t0001 | g0171 | AFR | GWD | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02630 | hp1 | a0003 | c0004 | t0001 | g0106 | AFR | GWD | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02630 | hp2 | a0002 | c0002 | t0002 | g0131 | AFR | GWD | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | GWD | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | GWD | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0047 | SAS | PJL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0148 | SAS | PJL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02717 | hp1 | a0001 | c0022 | t0002 | g0251 | AFR | GWD | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0046 | SAS | PJL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02738 | hp1 | a0002 | c0002 | t0002 | g0278 | SAS | PJL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0051 | SAS | PJL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0053 | AFR | GWD | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02809 | hp2 | a0003 | c0003 | t0001 | g0173 | AFR | GWD | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02886 | hp1 | a0002 | c0002 | t0002 | g0177 | AFR | GWD | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0036 | AFR | GWD | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02895 | hp1 | a0002 | c0002 | t0007 | g0139 | AFR | GWD | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02896 | hp2 | a0004 | c0005 | t0006 | g0257 | AFR | GWD | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02897 | hp1 | a0004 | c0005 | t0006 | g0256 | AFR | GWD | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02897 | hp2 | a0002 | c0002 | t0007 | g0138 | AFR | GWD | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02922 | hp1 | a0003 | c0004 | t0001 | g0142 | AFR | ESN | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | ESN | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02965 | hp2 | a0009 | c0013 | t0002 | g0295 | AFR | ESN | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | ESN | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0054 | AFR | ESN | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02976 | hp1 | a0002 | c0020 | t0002 | g0144 | AFR | ESN | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0249 | AFR | ESN | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | GWD | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | GWD | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG03098 | hp1 | a0008 | c0009 | t0002 | g0028 | AFR | MSL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | MSL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG03130 | hp1 | a0005 | c0006 | t0002 | g0031 | AFR | ESN | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0055 | AFR | ESN | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG03195 | hp1 | a0004 | c0005 | t0005 | g0276 | AFR | ESN | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG03209 | hp1 | a0002 | c0002 | t0002 | g0159 | AFR | MSL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | MSL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG03225 | hp1 | a0012 | c0017 | t0002 | g0123 | AFR | MSL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG03225 | hp2 | a0002 | c0002 | t0002 | g0124 | AFR | MSL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG03239 | hp1 | a0006 | c0007 | t0002 | g0007 | SAS | PJL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG03453 | hp1 | a0003 | c0003 | t0001 | g0126 | AFR | MSL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG03453 | hp2 | a0004 | c0005 | t0005 | g0271 | AFR | MSL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG03486 | hp1 | a0003 | c0003 | t0001 | g0170 | AFR | MSL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG03486 | hp2 | a0005 | c0006 | t0002 | g0277 | AFR | MSL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG03491 | hp1 | a0002 | c0002 | t0002 | g0003 | SAS | PJL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0014 | SAS | PJL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0049 | SAS | PJL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG03492 | hp2 | a0002 | c0002 | t0002 | g0161 | SAS | PJL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | GWD | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0281 | AFR | GWD | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0280 | AFR | MSL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | MSL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG03669 | hp1 | a0001 | c0014 | t0001 | g0217 | SAS | PJL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0122 | SAS | STU | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | STU | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0056 | SAS | PJL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG03710 | hp1 | a0002 | c0002 | t0002 | g0168 | SAS | PJL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG03834 | hp1 | a0019 | c0025 | t0004 | g0014 | SAS | BEB | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0098 | SAS | BEB | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | BEB | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG03927 | hp2 | a0002 | c0002 | t0002 | g0111 | SAS | BEB | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | BEB | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | STU | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | STU | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | BEB | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0184 | SAS | BEB | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0113 | SAS | STU | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0044 | SAS | STU | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG04204 | hp1 | a0005 | c0006 | t0002 | g0210 | SAS | STU | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | STU | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0285 | SAS | STU | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | STU | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18522 | hp1 | a0003 | c0003 | t0001 | g0174 | AFR | YRI | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | YRI | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18906 | hp1 | a0002 | c0002 | t0002 | g0137 | AFR | YRI | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18906 | hp2 | a0003 | c0003 | t0001 | g0172 | AFR | YRI | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18939 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0165 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0146 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18946 | hp2 | a0002 | c0002 | t0002 | g0163 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18947 | hp1 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18948 | hp2 | a0002 | c0002 | t0002 | g0121 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18949 | hp1 | a0002 | c0002 | t0002 | g0134 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18950 | hp2 | a0002 | c0002 | t0002 | g0133 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18951 | hp1 | a0002 | c0002 | t0002 | g0175 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18953 | hp1 | a0002 | c0002 | t0002 | g0157 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18954 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18959 | hp2 | a0014 | c0015 | t0002 | g0162 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18960 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18962 | hp1 | a0002 | c0002 | t0002 | g0178 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18963 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18965 | hp2 | a0002 | c0002 | t0002 | g0180 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18968 | hp2 | a0002 | c0002 | t0002 | g0166 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18972 | hp2 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18973 | hp2 | a0002 | c0002 | t0002 | g0115 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18977 | hp2 | a0002 | c0002 | t0002 | g0129 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18983 | hp2 | a0002 | c0002 | t0002 | g0101 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18988 | hp1 | a0002 | c0002 | t0002 | g0119 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18992 | hp2 | a0002 | c0002 | t0002 | g0118 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18993 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18995 | hp2 | a0003 | c0016 | t0002 | g0001 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0176 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19001 | hp1 | a0002 | c0002 | t0002 | g0182 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19002 | hp2 | a0002 | c0002 | t0002 | g0164 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19006 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0117 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0154 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19011 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19030 | hp1 | a0003 | c0004 | t0001 | g0107 | AFR | LWK | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19030 | hp2 | a0016 | c0027 | t0002 | g0250 | AFR | LWK | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19043 | hp1 | a0003 | c0004 | t0001 | g0143 | AFR | LWK | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19043 | hp2 | a0002 | c0002 | t0002 | g0179 | AFR | LWK | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19055 | hp1 | a0002 | c0002 | t0002 | g0116 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19060 | hp1 | a0002 | c0002 | t0002 | g0099 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0136 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19075 | hp2 | a0002 | c0002 | t0002 | g0100 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19077 | hp1 | a0002 | c0002 | t0002 | g0183 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19079 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19081 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19086 | hp2 | a0002 | c0002 | t0002 | g0181 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | YRI | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA19240 | hp2 | a0013 | c0019 | t0008 | g0275 | AFR | YRI | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ASW | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | ASW | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0206 | EUR | TSI | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0040 | EUR | TSI | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | GIH | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | GIH | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0110 | AMR | CLM | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0039 | AMR | CLM | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02109 | hp1 | a0007 | c0008 | t0001 | g0208 | AFR | ACB | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | ACB | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | ACB | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | ACB | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG03471 | hp1 | a0007 | c0008 | t0001 | g0209 | AFR | MSL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG03471 | hp2 | a0015 | c0021 | t0002 | g0125 | AFR | MSL | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | USA | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| HG06807 | hp2 | a0003 | c0003 | t0002 | g0169 | AFR | USA | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18955 | hp1 | a0002 | c0002 | t0002 | g0151 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA20300 | hp1 | a0002 | c0002 | t0002 | g0135 | AFR | USA | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA20300 | hp2 | a0003 | c0003 | t0001 | g0018 | AFR | USA | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA21309 | hp1 | a0002 | c0002 | t0002 | g0153 | AFR | LWK | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| NA21309 | hp2 | a0004 | c0005 | t0005 | g0252 | AFR | LWK | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0048 | REF | REF | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0258 | REF | REF | GALNT8_chr12_4715400_4777726 | GALNT8 | chr12 | 4715400 | 4777726 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:4720834
|
T | G | 9 | a0002a0003a0004others(6): Show | 129 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(126): Show |
missense_variant | MODERATE | c.157T>G | p.Tyr53Asp | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/11 | 435/2321 | 157/1914 | 53/637 | chr12 | 4720834 | ||
| chr12:4739170
|
C | T | 1 | a0011 | 2 | HG01255.hp1 HG01517.hp2 |
missense_variant | MODERATE | c.517C>T | p.Arg173Trp | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/11 | 795/2321 | 517/1914 | 173/637 | chr12 | 4739170 | ||
| chr12:4739263
|
A | G | 2 | a0015a0021 | 2 | HG01168.hp1 HG03471.hp2 |
missense_variant | MODERATE | c.610A>G | p.Ile204Val | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/11 | 888/2321 | 610/1914 | 204/637 | chr12 | 4739263 | ||
| chr12:4744540
|
G | A | 1 | a0010 | 2 | HG02055.hp1 HG02615.hp2 |
missense_variant | MODERATE | c.700G>A | p.Glu234Lys | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 4/11 | 978/2321 | 700/1914 | 234/637 | chr12 | 4744540 | ||
| chr12:4744574
|
G | A | 1 | a0007 | 3 | HG01109.hp2 HG02109.hp1 HG03471.hp1 |
missense_variant | MODERATE | c.734G>A | p.Gly245Glu | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 4/11 | 1012/2321 | 734/1914 | 245/637 | chr12 | 4744574 | ||
| chr12:4744600
|
G | A | 1 | a0014 | 1 | NA18959.hp2 | missense_variant | MODERATE | c.760G>A | p.Glu254Lys | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 4/11 | 1038/2321 | 760/1914 | 254/637 | chr12 | 4744600 | ||
| chr12:4744640
|
A | G | 1 | a0006 | 3 | HG01192.hp1 HG01346.hp1 HG03239.hp1 |
missense_variant | MODERATE | c.800A>G | p.Glu267Gly | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 4/11 | 1078/2321 | 800/1914 | 267/637 | chr12 | 4744640 | ||
| chr12:4745503
|
T | C | 2 | a0009a0013 | 3 | HG02258.hp2 HG02965.hp2 NA19240.hp2 |
missense_variant | MODERATE | c.935T>C | p.Phe312Ser | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 5/11 | 1213/2321 | 935/1914 | 312/637 | chr12 | 4745503 | ||
| chr12:4746227
|
A | G | 1 | a0016 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.1142A>G | p.Tyr381Cys | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/11 | 1420/2321 | 1142/1914 | 381/637 | chr12 | 4746227 | ||
| chr12:4761075
|
C | T | 1 | a0017 | 1 | HG02056.hp2 | stop_gained | HIGH | c.1291C>T | p.Arg431* | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/11 | 1569/2321 | 1291/1914 | 431/637 | chr12 | 4761075 | ||
| chr12:4763291
|
G | C | 2 | a0008a0018 | 3 | HG01891.hp2 HG01952.hp2 HG03098.hp1 |
missense_variant | MODERATE | c.1398G>C | p.Met466Ile | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 8/11 | 1676/2321 | 1398/1914 | 466/637 | chr12 | 4763291 | ||
| chr12:4763997
|
G | T | 5 | a0002a0005a0006others(2): Show | 109 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(106): Show |
missense_variant | MODERATE | c.1543G>T | p.Val515Phe | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 9/11 | 1821/2321 | 1543/1914 | 515/637 | chr12 | 4763997 | ||
| chr12:4765448
|
C | T | 1 | a0019 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.1663C>T | p.Arg555Cys | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/11 | 1941/2321 | 1663/1914 | 555/637 | chr12 | 4765448 | ||
| chr12:4765526
|
A | G | 3 | a0012a0013a0020 | 3 | HG01884.hp1 HG03225.hp1 NA19240.hp2 |
missense_variant | MODERATE | c.1741A>G | p.Ile581Val | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/11 | 2019/2321 | 1741/1914 | 581/637 | chr12 | 4765526 | ||
| chr12:4772514
|
G | A | 1 | a0004 | 6 | HG01891.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
missense_variant | MODERATE | c.1831G>A | p.Val611Met | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 11/11 | 2109/2321 | 1831/1914 | 611/637 | chr12 | 4772514 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:4720791
|
G | A | 1 | a0001c0014 | 1 | HG03669.hp1 | synonymous_variant | LOW | c.114G>A | p.Thr38Thr | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/11 | 392/2321 | 114/1914 | 38/637 | chr12 | 4720791 | ||
| chr12:4726647
|
A | G | 3 | a0002c0020a0003c0003a0015c0021 | 12 | HG02258.hp1 HG02280.hp2 HG02622.hp2 others(9): Show |
synonymous_variant | LOW | c.327A>G | p.Thr109Thr | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/11 | 605/2321 | 327/1914 | 109/637 | chr12 | 4726647 | ||
| chr12:4726716
|
T | G | 7 | a0002c0002a0002c0018a0003c0016others(4): Show | 104 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(101): Show |
synonymous_variant | LOW | c.396T>G | p.Leu132Leu | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/11 | 674/2321 | 396/1914 | 132/637 | chr12 | 4726716 | ||
| chr12:4726770
|
C | T | 1 | a0009c0013 | 2 | HG02258.hp2 HG02965.hp2 |
synonymous_variant | LOW | c.450C>T | p.Asn150Asn | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/11 | 728/2321 | 450/1914 | 150/637 | chr12 | 4726770 | ||
| chr12:4744698
|
G | A | 1 | a0001c0022 | 1 | HG02717.hp1 | splice_region_variant&synonymous_variant | LOW | c.858G>A | p.Gly286Gly | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 4/11 | 1136/2321 | 858/1914 | 286/637 | chr12 | 4744698 | ||
| chr12:4761035
|
C | T | 1 | a0013c0019 | 1 | NA19240.hp2 | synonymous_variant | LOW | c.1251C>T | p.Tyr417Tyr | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/11 | 1529/2321 | 1251/1914 | 417/637 | chr12 | 4761035 | ||
| chr12:4763996
|
C | T | 1 | a0004c0005 | 6 | HG01891.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
synonymous_variant | LOW | c.1542C>T | p.Pro514Pro | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 9/11 | 1820/2321 | 1542/1914 | 514/637 | chr12 | 4763996 | ||
| chr12:4765474
|
G | A | 1 | a0002c0018 | 1 | HG00609.hp1 | synonymous_variant | LOW | c.1689G>A | p.Ala563Ala | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/11 | 1967/2321 | 1689/1914 | 563/637 | chr12 | 4765474 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:4720408
|
C | CCTGAGCA others(15): Show |
3 | a0004c0005t0005a0004c0005t0006a0013c0019t0008 | 7 | HG01891.hp1 HG02896.hp2 HG02897.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-241_-220dupAACCTG others(16): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/11 | 219 | INFO_REALIGN_3_PRIME | chr12 | 4720408 | ||||
| chr12:4720420
|
G | A | 3 | a0001c0001t0003a0001c0001t0004a0019c0025t0004 | 34 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(31): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-258G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/11 | chr12 | 4720420 | ||||||
| chr12:4720452
|
G | A | 2 | a0001c0001t0004a0019c0025t0004 | 4 | HG03491.hp2 HG03492.hp1 HG03834.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-226G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/11 | 226 | chr12 | 4720452 | |||||
| chr12:4720507
|
G | C | 1 | a0004c0005t0006 | 2 | HG02896.hp2 HG02897.hp1 |
5_prime_UTR_variant | MODIFIER | c.-171G>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/11 | 171 | chr12 | 4720507 | |||||
| chr12:4772600
|
C | T | 19 | a0001c0001t0002a0001c0022t0002a0002c0002t0002others(16): Show | 128 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*3C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 11/11 | 3 | chr12 | 4772600 | |||||
| chr12:4772609
|
T | C | 19 | a0001c0001t0002a0001c0022t0002a0002c0002t0002others(16): Show | 128 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*12T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 11/11 | 12 | chr12 | 4772609 | |||||
| chr12:4772682
|
G | A | 1 | a0002c0002t0007 | 2 | HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*85G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 11/11 | 85 | chr12 | 4772682 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:4720900
|
A | G | 1 | a0001c0001t0003g0296 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.211+12A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4720900 | ||||||
| chr12:4721042
|
A | C | 1 | a0001c0001t0002g0027 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.211+154A>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4721042 | ||||||
| chr12:4721183
|
C | T | 1 | a0009c0013t0002g0295 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.211+295C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4721183 | ||||||
| chr12:4721286
|
G | C | 2 | a0008c0009t0002g0028a0008c0009t0002g0029 | 2 | HG01952.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.211+398G>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4721286 | ||||||
| chr12:4721357
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.211+469G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4721357 | ||||||
| chr12:4721580
|
C | G | 2 | a0001c0001t0001g0293a0001c0001t0001g0294 | 2 | HG01975.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.211+692C>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4721580 | ||||||
| chr12:4721612
|
A | G | 1 | a0020c0024t0002g0292 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.211+724A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4721612 | ||||||
| chr12:4721684
|
G | T | 1 | a0001c0001t0002g0291 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.211+796G>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4721684 | ||||||
| chr12:4721783
|
G | A | 2 | a0001c0001t0001g0032a0005c0006t0002g0031 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.211+895G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4721783 | ||||||
| chr12:4721802
|
A | C | 2 | a0001c0001t0001g0026a0001c0001t0001g0290 | 3 | HG00544.hp1 HG00558.hp1 HG00621.hp1 |
intron_variant | MODIFIER | c.211+914A>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4721802 | ||||||
| chr12:4722004
|
C | CATAG | 31 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(28): Show | 34 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.211+1117_211+1120d others(6): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 4722004 | |||||
| chr12:4722106
|
A | G | 12 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0286others(9): Show | 13 | HG00642.hp2 HG00733.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.211+1218A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4722106 | ||||||
| chr12:4722200
|
G | A | 12 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0286others(9): Show | 13 | HG00642.hp2 HG00733.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.211+1312G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4722200 | ||||||
| chr12:4722273
|
G | A | 5 | a0001c0001t0001g0032a0001c0001t0002g0058a0001c0001t0002g0059others(2): Show | 5 | HG02622.hp1 HG02647.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.211+1385G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4722273 | ||||||
| chr12:4722570
|
A | C | 2 | a0009c0013t0002g0279a0009c0013t0002g0295 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.211+1682A>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4722570 | ||||||
| chr12:4722581
|
A | G | 1 | a0005c0006t0002g0060 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.211+1693A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4722581 | ||||||
| chr12:4722896
|
G | A | 41 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(38): Show | 45 | HG00544.hp2 HG00558.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.211+2008G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4722896 | ||||||
| chr12:4722943
|
G | A | 1 | a0005c0006t0002g0031 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.211+2055G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4722943 | ||||||
| chr12:4723015
|
G | A | 2 | a0009c0013t0002g0279a0009c0013t0002g0295 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.211+2127G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4723015 | ||||||
| chr12:4723047
|
C | T | 1 | a0002c0002t0002g0278 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.211+2159C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4723047 | ||||||
| chr12:4723081
|
T | C | 1 | a0002c0002t0002g0098 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.211+2193T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4723081 | ||||||
| chr12:4723203
|
G | C | 5 | a0002c0002t0001g0102a0002c0002t0002g0099a0002c0002t0002g0100others(2): Show | 5 | NA18968.hp1 NA18972.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.211+2315G>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4723203 | ||||||
| chr12:4723204
|
T | A | 5 | a0002c0002t0001g0102a0002c0002t0002g0099a0002c0002t0002g0100others(2): Show | 5 | NA18968.hp1 NA18972.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.211+2316T>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4723204 | ||||||
| chr12:4723210
|
T | C | 101 | a0002c0002t0001g0008a0002c0002t0001g0102a0002c0002t0001g0154others(98): Show | 122 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(119): Show |
intron_variant | MODIFIER | c.211+2322T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4723210 | ||||||
| chr12:4723465
|
C | T | 1 | a0002c0002t0002g0184 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.211+2577C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4723465 | ||||||
| chr12:4723614
|
T | C | 101 | a0002c0002t0001g0008a0002c0002t0001g0102a0002c0002t0001g0154others(98): Show | 122 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(119): Show |
intron_variant | MODIFIER | c.211+2726T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4723614 | ||||||
| chr12:4723700
|
T | A | 2 | a0008c0009t0002g0028a0008c0009t0002g0029 | 2 | HG01952.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.211+2812T>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4723700 | ||||||
| chr12:4723750
|
C | CT | 45 | a0001c0001t0001g0097a0001c0001t0001g0269a0001c0001t0001g0270others(42): Show | 48 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.212-2763dupT | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 4723750 | |||||
| chr12:4723750
|
CT | C | 6 | a0001c0001t0001g0061a0001c0001t0001g0185a0001c0001t0001g0293others(3): Show | 6 | HG02622.hp1 HG02647.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.212-2763delT | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 4723750 | |||||
| chr12:4723921
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.212-2611C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4723921 | ||||||
| chr12:4724021
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.212-2511C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4724021 | ||||||
| chr12:4724022
|
G | A | 2 | a0008c0009t0002g0028a0008c0009t0002g0029 | 2 | HG01952.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.212-2510G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4724022 | ||||||
| chr12:4724024
|
C | CT | 56 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(53): Show | 61 | HG00544.hp2 HG00558.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.212-2507dupT | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 4724024 | |||||
| chr12:4724042
|
G | C | 40 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(37): Show | 44 | HG00544.hp2 HG00558.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.212-2490G>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4724042 | ||||||
| chr12:4724124
|
G | A | 1 | a0003c0003t0001g0104 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.212-2408G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4724124 | ||||||
| chr12:4724143
|
C | T | 2 | a0009c0013t0002g0279a0009c0013t0002g0295 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.212-2389C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4724143 | ||||||
| chr12:4724148
|
C | CA | 107 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0022others(104): Show | 119 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.212-2357dupA | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 4724148 | |||||
| chr12:4724148
|
C | CAA | 28 | a0001c0001t0001g0021a0001c0001t0001g0062a0001c0001t0001g0063others(25): Show | 29 | HG00323.hp2 HG00621.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.212-2358_212-2357d others(4): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 4724148 | |||||
| chr12:4724148
|
CA | C | 39 | a0001c0001t0001g0093a0001c0001t0001g0266a0001c0001t0001g0286others(36): Show | 43 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.212-2357delA | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 4724148 | |||||
| chr12:4724280
|
C | T | 2 | a0009c0013t0002g0279a0009c0013t0002g0295 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.212-2252C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4724280 | ||||||
| chr12:4724521
|
G | A | 3 | a0001c0001t0002g0249a0001c0022t0002g0251a0016c0027t0002g0250 | 3 | HG02717.hp1 HG02976.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.212-2011G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4724521 | ||||||
| chr12:4724730
|
G | A | 2 | a0001c0001t0001g0032a0005c0006t0002g0031 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.212-1802G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4724730 | ||||||
| chr12:4724771
|
T | C | 2 | a0001c0001t0002g0249a0016c0027t0002g0250 | 2 | HG02976.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.212-1761T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4724771 | ||||||
| chr12:4724896
|
C | T | 2 | a0001c0001t0001g0293a0001c0001t0001g0294 | 2 | HG01975.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.212-1636C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4724896 | ||||||
| chr12:4724916
|
G | T | 1 | a0001c0001t0001g0070 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.212-1616G>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4724916 | ||||||
| chr12:4725000
|
A | G | 1 | a0001c0001t0001g0206 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.212-1532A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4725000 | ||||||
| chr12:4725159
|
G | C | 2 | a0010c0011t0001g0186a0010c0011t0001g0207 | 2 | HG02055.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.212-1373G>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4725159 | ||||||
| chr12:4725249
|
G | A | 1 | a0004c0005t0005g0252 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.212-1283G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4725249 | ||||||
| chr12:4725371
|
G | C | 12 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0286others(9): Show | 13 | HG00642.hp2 HG00733.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.212-1161G>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4725371 | ||||||
| chr12:4725483
|
C | A | 2 | a0001c0001t0002g0058a0001c0001t0002g0059 | 2 | HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.212-1049C>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4725483 | ||||||
| chr12:4725525
|
G | A | 5 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0002g0249others(2): Show | 5 | HG01884.hp2 HG02717.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.212-1007G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4725525 | ||||||
| chr12:4725548
|
A | G | 5 | a0002c0002t0002g0020a0002c0002t0002g0133a0002c0002t0002g0134others(2): Show | 5 | HG00609.hp1 NA18939.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.212-984A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4725548 | ||||||
| chr12:4725553
|
C | CT | 116 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(113): Show | 138 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.212-959dupT | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 4725553 | |||||
| chr12:4725553
|
C | CTT | 8 | a0002c0002t0002g0130a0002c0002t0002g0131a0002c0002t0002g0132others(5): Show | 8 | HG01884.hp1 HG02055.hp2 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.212-960_212-959dup others(2): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 4725553 | |||||
| chr12:4725579
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.212-953G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4725579 | ||||||
| chr12:4725597
|
C | G | 1 | a0001c0001t0001g0254 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.212-935C>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4725597 | ||||||
| chr12:4725738
|
T | C | 101 | a0002c0002t0001g0008a0002c0002t0001g0102a0002c0002t0001g0154others(98): Show | 122 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(119): Show |
intron_variant | MODIFIER | c.212-794T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4725738 | ||||||
| chr12:4725756
|
A | G | 1 | a0001c0001t0001g0246 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.212-776A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4725756 | ||||||
| chr12:4725839
|
C | T | 1 | a0002c0002t0002g0179 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.212-693C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4725839 | ||||||
| chr12:4725853
|
C | A | 31 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(28): Show | 34 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.212-679C>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4725853 | ||||||
| chr12:4725964
|
G | A | 5 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0002g0249others(2): Show | 5 | HG01884.hp2 HG02717.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.212-568G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4725964 | ||||||
| chr12:4726193
|
C | G | 6 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0002g0249others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.212-339C>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4726193 | ||||||
| chr12:4726441
|
G | A | 1 | a0005c0006t0002g0060 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.212-91G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 1/10 | chr12 | 4726441 | ||||||
| chr12:4726841
|
C | G | 1 | a0002c0002t0002g0098 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.509+12C>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4726841 | ||||||
| chr12:4726877
|
G | A | 1 | a0001c0001t0003g0040 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.509+48G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4726877 | ||||||
| chr12:4726909
|
C | T | 2 | a0001c0001t0002g0058a0001c0001t0002g0059 | 2 | HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.509+80C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4726909 | ||||||
| chr12:4727101
|
G | A | 3 | a0002c0002t0002g0179a0002c0002t0007g0138a0002c0002t0007g0139 | 3 | HG02895.hp1 HG02897.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.509+272G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4727101 | ||||||
| chr12:4727153
|
C | T | 4 | a0002c0002t0002g0128a0002c0002t0002g0129a0002c0002t0002g0175others(1): Show | 4 | HG01928.hp1 NA18951.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.509+324C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4727153 | ||||||
| chr12:4727172
|
A | G | 102 | a0002c0002t0001g0008a0002c0002t0001g0102a0002c0002t0001g0154others(99): Show | 123 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(120): Show |
intron_variant | MODIFIER | c.509+343A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4727172 | ||||||
| chr12:4727291
|
GT | G | 30 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0026others(27): Show | 34 | HG00544.hp1 HG00558.hp1 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.509+472delT | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 4727291 | |||||
| chr12:4727341
|
T | A | 1 | a0001c0001t0003g0011 | 2 | HG01358.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.509+512T>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4727341 | ||||||
| chr12:4727936
|
T | C | 1 | a0002c0002t0002g0140 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.509+1107T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4727936 | ||||||
| chr12:4727937
|
G | T | 1 | a0002c0002t0002g0140 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.509+1108G>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4727937 | ||||||
| chr12:4728059
|
C | T | 1 | a0002c0002t0002g0127 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.509+1230C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4728059 | ||||||
| chr12:4728214
|
AT | A | 205 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(202): Show | 234 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(231): Show |
intron_variant | MODIFIER | c.509+1396delT | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 4728214 | |||||
| chr12:4728480
|
A | C | 2 | a0002c0002t0007g0138a0002c0002t0007g0139 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.509+1651A>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4728480 | ||||||
| chr12:4728482
|
A | G | 1 | a0001c0001t0001g0265 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.509+1653A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4728482 | ||||||
| chr12:4728522
|
T | C | 6 | a0003c0004t0001g0106a0003c0004t0001g0107a0003c0004t0001g0108others(3): Show | 6 | HG02280.hp1 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.509+1693T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4728522 | ||||||
| chr12:4728644
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.509+1815C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4728644 | ||||||
| chr12:4728649
|
A | C | 299 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(296): Show | 337 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(334): Show |
intron_variant | MODIFIER | c.509+1820A>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4728649 | ||||||
| chr12:4728856
|
A | G | 1 | a0001c0001t0003g0039 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.509+2027A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4728856 | ||||||
| chr12:4728877
|
T | TCTTTTTT others(3): Show |
1 | a0001c0001t0001g0204 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.509+2049_509+2050i others(12): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 4728877 | |||||
| chr12:4728929
|
G | A | 1 | a0002c0020t0002g0144 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.509+2100G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4728929 | ||||||
| chr12:4729132
|
CTG | C | 101 | a0002c0002t0001g0008a0002c0002t0001g0102a0002c0002t0001g0154others(98): Show | 122 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(119): Show |
intron_variant | MODIFIER | c.509+2305_509+2306d others(4): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 4729132 | |||||
| chr12:4729140
|
A | T | 1 | a0002c0002t0002g0182 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.509+2311A>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4729140 | ||||||
| chr12:4729171
|
A | G | 5 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0002g0249others(2): Show | 5 | HG01884.hp2 HG02717.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.509+2342A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4729171 | ||||||
| chr12:4729181
|
A | G | 1 | a0005c0006t0002g0060 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.509+2352A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4729181 | ||||||
| chr12:4729191
|
T | C | 90 | a0002c0002t0001g0008a0002c0002t0001g0102a0002c0002t0001g0154others(87): Show | 110 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.509+2362T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4729191 | ||||||
| chr12:4729337
|
T | C | 3 | a0001c0001t0002g0058a0001c0001t0002g0059a0020c0024t0002g0292 | 3 | HG01884.hp1 HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.509+2508T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4729337 | ||||||
| chr12:4729441
|
C | G | 2 | a0011c0012t0001g0244a0011c0012t0001g0245 | 2 | HG01255.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.509+2612C>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4729441 | ||||||
| chr12:4729490
|
T | G | 1 | a0018c0023t0001g0267 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.509+2661T>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4729490 | ||||||
| chr12:4729662
|
C | G | 1 | a0001c0022t0002g0251 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.509+2833C>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4729662 | ||||||
| chr12:4729680
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.509+2851C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4729680 | ||||||
| chr12:4729758
|
C | G | 2 | a0001c0001t0001g0032a0005c0006t0002g0031 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.509+2929C>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4729758 | ||||||
| chr12:4729859
|
C | G | 89 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(86): Show | 98 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.509+3030C>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4729859 | ||||||
| chr12:4729984
|
G | C | 1 | a0001c0001t0002g0284 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.509+3155G>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4729984 | ||||||
| chr12:4729990
|
T | C | 10 | a0001c0001t0001g0032a0004c0005t0005g0252a0004c0005t0005g0271others(7): Show | 10 | HG01891.hp1 HG02622.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.509+3161T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4729990 | ||||||
| chr12:4730439
|
G | A | 1 | a0002c0002t0002g0145 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.509+3610G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4730439 | ||||||
| chr12:4730715
|
A | G | 1 | a0002c0020t0002g0144 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.509+3886A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4730715 | ||||||
| chr12:4730796
|
C | G | 1 | a0001c0001t0001g0254 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.509+3967C>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4730796 | ||||||
| chr12:4730854
|
G | T | 1 | a0001c0001t0001g0219 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.509+4025G>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4730854 | ||||||
| chr12:4730855
|
A | T | 1 | a0001c0001t0001g0219 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.509+4026A>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4730855 | ||||||
| chr12:4730866
|
C | CT | 15 | a0001c0001t0001g0194a0001c0001t0003g0034a0001c0001t0003g0038others(12): Show | 15 | HG00642.hp1 HG00741.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.509+4053dupT | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 4730866 | |||||
| chr12:4730866
|
C | G | 1 | a0001c0001t0001g0243 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.509+4037C>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4730866 | ||||||
| chr12:4730993
|
C | T | 1 | a0012c0017t0002g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.509+4164C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4730993 | ||||||
| chr12:4731050
|
A | G | 2 | a0001c0001t0001g0241a0001c0001t0001g0242 | 2 | NA19007.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.509+4221A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4731050 | ||||||
| chr12:4731125
|
C | T | 12 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0286others(9): Show | 13 | HG00642.hp2 HG00733.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.509+4296C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4731125 | ||||||
| chr12:4731131
|
C | T | 3 | a0001c0001t0003g0037a0001c0001t0003g0054a0001c0001t0003g0055 | 3 | HG02486.hp1 HG02970.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.509+4302C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4731131 | ||||||
| chr12:4731199
|
A | G | 2 | a0002c0002t0002g0167a0002c0002t0002g0168 | 2 | HG01081.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.509+4370A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4731199 | ||||||
| chr12:4731410
|
A | G | 5 | a0002c0002t0001g0102a0002c0002t0002g0099a0002c0002t0002g0100others(2): Show | 5 | NA18968.hp1 NA18972.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.509+4581A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4731410 | ||||||
| chr12:4731415
|
G | A | 1 | a0005c0006t0002g0060 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.509+4586G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4731415 | ||||||
| chr12:4731573
|
G | A | 1 | a0001c0001t0001g0220 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.509+4744G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4731573 | ||||||
| chr12:4731648
|
G | A | 1 | a0005c0006t0002g0060 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.509+4819G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4731648 | ||||||
| chr12:4731896
|
G | A | 208 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(205): Show | 237 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(234): Show |
intron_variant | MODIFIER | c.509+5067G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4731896 | ||||||
| chr12:4732341
|
C | CGGGAGGA others(162): Show |
1 | a0001c0001t0001g0071 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.509+5588_509+5589i others(171): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 4732341 | |||||
| chr12:4732341
|
C | CGGGAGGA others(162): Show |
141 | a0001c0001t0001g0032a0001c0001t0001g0253a0001c0001t0001g0254others(138): Show | 165 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(162): Show |
intron_variant | MODIFIER | c.509+5680_509+5681i others(171): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 4732341 | |||||
| chr12:4732341
|
C | CGGGAGGA others(162): Show |
1 | a0005c0006t0002g0060 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.509+5579_509+5580i others(171): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 4732341 | |||||
| chr12:4732349
|
G | GTGGCTAG others(162): Show |
1 | a0001c0022t0002g0251 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.509+5680_509+5681i others(171): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 4732349 | |||||
| chr12:4732418
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.509+5589T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4732418 | ||||||
| chr12:4732418
|
T | TGTTCAAT others(162): Show |
40 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(37): Show | 44 | HG00558.hp2 HG00738.hp1 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.509+5680_509+5681i others(171): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 4732418 | |||||
| chr12:4732424
|
A | ATATGATA others(162): Show |
15 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0286others(12): Show | 16 | HG00642.hp2 HG00733.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.509+5680_509+5681i others(171): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 4732424 | |||||
| chr12:4732510
|
C | CGGGAGGA others(162): Show |
1 | a0001c0001t0001g0264 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.509+5757_509+5758i others(171): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 4732510 | |||||
| chr12:4732510
|
C | T | 209 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(206): Show | 238 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(235): Show |
intron_variant | MODIFIER | c.509+5681C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4732510 | ||||||
| chr12:4732558
|
A | AAACACTT others(162): Show |
2 | a0001c0001t0002g0058a0001c0001t0002g0059 | 2 | HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.509+5897_509+5898i others(171): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 4732558 | |||||
| chr12:4732587
|
T | C | 2 | a0001c0001t0001g0264a0002c0002t0002g0146 | 2 | HG01167.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.509+5758T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4732587 | ||||||
| chr12:4732587
|
T | TGTTCAAT others(162): Show |
4 | a0001c0001t0003g0056a0002c0002t0002g0109a0008c0009t0002g0028others(1): Show | 4 | HG01109.hp1 HG01952.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.509+5764_509+5932d others(171): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 4732587 | |||||
| chr12:4732593
|
A | ATATGATA others(162): Show |
91 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(88): Show | 100 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.509+6070_510-6096d others(171): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 4732593 | |||||
| chr12:4732593
|
A | G | 18 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0264others(15): Show | 19 | HG00642.hp2 HG00733.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.509+5764A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4732593 | ||||||
| chr12:4732756
|
C | T | 1 | a0001c0001t0003g0053 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.509+5927C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4732756 | ||||||
| chr12:4732762
|
G | A | 1 | a0001c0001t0003g0053 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.509+5933G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4732762 | ||||||
| chr12:4733136
|
G | T | 2 | a0002c0002t0002g0105a0002c0002t0002g0278 | 2 | HG00323.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.510-6027G>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4733136 | ||||||
| chr12:4733249
|
A | G | 1 | a0001c0001t0003g0036 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.510-5914A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4733249 | ||||||
| chr12:4733312
|
A | G | 1 | a0001c0001t0001g0239 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.510-5851A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4733312 | ||||||
| chr12:4733370
|
C | T | 1 | a0005c0010t0002g0019 | 2 | HG01261.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.510-5793C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4733370 | ||||||
| chr12:4733432
|
G | A | 1 | a0001c0001t0001g0220 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.510-5731G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4733432 | ||||||
| chr12:4733476
|
A | T | 1 | a0018c0023t0001g0267 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.510-5687A>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4733476 | ||||||
| chr12:4733590
|
T | C | 1 | a0001c0001t0002g0249 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.510-5573T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4733590 | ||||||
| chr12:4733856
|
G | A | 1 | a0001c0001t0001g0206 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.510-5307G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4733856 | ||||||
| chr12:4733878
|
C | A | 1 | a0002c0002t0002g0147 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.510-5285C>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4733878 | ||||||
| chr12:4734086
|
A | G | 1 | a0001c0001t0001g0264 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.510-5077A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4734086 | ||||||
| chr12:4734411
|
C | G | 14 | a0002c0002t0001g0008a0002c0002t0002g0003a0002c0002t0002g0020others(11): Show | 21 | HG00609.hp1 HG01081.hp2 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.510-4752C>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4734411 | ||||||
| chr12:4734445
|
C | T | 41 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(38): Show | 45 | HG00544.hp2 HG00558.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.510-4718C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4734445 | ||||||
| chr12:4734551
|
G | A | 1 | a0001c0001t0003g0296 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.510-4612G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4734551 | ||||||
| chr12:4734552
|
C | A | 2 | a0009c0013t0002g0279a0009c0013t0002g0295 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.510-4611C>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4734552 | ||||||
| chr12:4734597
|
C | T | 207 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(204): Show | 235 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(232): Show |
intron_variant | MODIFIER | c.510-4566C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4734597 | ||||||
| chr12:4734604
|
C | T | 41 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(38): Show | 45 | HG00544.hp2 HG00558.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.510-4559C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4734604 | ||||||
| chr12:4734647
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.510-4516C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4734647 | ||||||
| chr12:4734671
|
T | TTAAAATG others(214): Show |
2 | a0001c0001t0002g0280a0001c0001t0002g0285 | 2 | HG03579.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.510-4475_510-4474i others(223): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 4734671 | |||||
| chr12:4734671
|
T | TTAAAATG others(213): Show |
4 | a0001c0001t0001g0286a0001c0001t0002g0287a0001c0001t0002g0289others(1): Show | 4 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(1): Show |
intron_variant | MODIFIER | c.510-4475_510-4474i others(222): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 4734671 | |||||
| chr12:4734671
|
T | TTAAAATG others(212): Show |
1 | a0001c0001t0002g0284 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.510-4475_510-4474i others(221): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 4734671 | |||||
| chr12:4734671
|
T | TTAAAATG others(213): Show |
4 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0002g0027others(1): Show | 5 | HG01516.hp1 HG01517.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.510-4475_510-4474i others(222): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 4734671 | |||||
| chr12:4734671
|
T | TTAAAATG others(213): Show |
1 | a0001c0001t0002g0288 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.510-4475_510-4474i others(222): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 4734671 | |||||
| chr12:4734671
|
T | TTAAAATG others(213): Show |
1 | a0008c0009t0002g0028 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.510-4475_510-4474i others(222): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 4734671 | |||||
| chr12:4734671
|
T | TTAAAATG others(212): Show |
1 | a0008c0009t0002g0029 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.510-4475_510-4474i others(221): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 4734671 | |||||
| chr12:4734795
|
G | A | 1 | a0003c0004t0001g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.510-4368G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4734795 | ||||||
| chr12:4734837
|
T | G | 1 | a0001c0001t0001g0286 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.510-4326T>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4734837 | ||||||
| chr12:4734877
|
C | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG00544.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.510-4286C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4734877 | ||||||
| chr12:4734893
|
G | A | 299 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(296): Show | 337 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(334): Show |
intron_variant | MODIFIER | c.510-4270G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4734893 | ||||||
| chr12:4735045
|
G | C | 1 | a0002c0002t0002g0110 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.510-4118G>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4735045 | ||||||
| chr12:4735245
|
C | A | 2 | a0001c0001t0001g0032a0005c0006t0002g0031 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.510-3918C>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4735245 | ||||||
| chr12:4735399
|
T | C | 5 | a0003c0004t0001g0107a0003c0004t0001g0108a0003c0004t0001g0141others(2): Show | 5 | HG02280.hp1 HG02451.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.510-3764T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4735399 | ||||||
| chr12:4735402
|
GC | G | 82 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(79): Show | 91 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.510-3760delC | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4735402 | ||||||
| chr12:4735456
|
A | G | 3 | a0009c0013t0002g0279a0009c0013t0002g0295a0013c0019t0008g0275 | 3 | HG02258.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.510-3707A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4735456 | ||||||
| chr12:4735529
|
A | C | 3 | a0001c0001t0002g0058a0001c0001t0002g0059a0020c0024t0002g0292 | 3 | HG01884.hp1 HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.510-3634A>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4735529 | ||||||
| chr12:4735729
|
G | A | 1 | a0001c0001t0001g0072 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.510-3434G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4735729 | ||||||
| chr12:4735936
|
A | G | 3 | a0002c0002t0002g0122a0002c0002t0002g0167a0002c0002t0002g0168 | 3 | HG01081.hp2 HG03688.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.510-3227A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4735936 | ||||||
| chr12:4735963
|
T | C | 6 | a0001c0001t0002g0058a0001c0001t0002g0059a0009c0013t0002g0279others(3): Show | 6 | HG01884.hp1 HG02258.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.510-3200T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4735963 | ||||||
| chr12:4736323
|
A | G | 141 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(138): Show | 165 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(162): Show |
intron_variant | MODIFIER | c.510-2840A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4736323 | ||||||
| chr12:4736433
|
G | A | 2 | a0001c0001t0002g0058a0001c0001t0002g0059 | 2 | HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.510-2730G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4736433 | ||||||
| chr12:4736472
|
T | A | 35 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(32): Show | 38 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.510-2691T>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4736472 | ||||||
| chr12:4736557
|
G | A | 215 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(212): Show | 244 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(241): Show |
intron_variant | MODIFIER | c.510-2606G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4736557 | ||||||
| chr12:4736595
|
G | GA | 11 | a0001c0001t0001g0221a0001c0001t0001g0253a0001c0001t0001g0254others(8): Show | 11 | HG01884.hp1 HG01884.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.510-2554dupA | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 4736595 | |||||
| chr12:4736596
|
A | G | 14 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0286others(11): Show | 15 | HG00642.hp2 HG00733.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.510-2567A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4736596 | ||||||
| chr12:4736875
|
G | A | 29 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0026others(26): Show | 33 | HG00544.hp1 HG00558.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.510-2288G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4736875 | ||||||
| chr12:4737008
|
C | A | 5 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0002g0249others(2): Show | 5 | HG01884.hp2 HG02717.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.510-2155C>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4737008 | ||||||
| chr12:4737009
|
A | T | 5 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0002g0249others(2): Show | 5 | HG01884.hp2 HG02717.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.510-2154A>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4737009 | ||||||
| chr12:4737028
|
T | C | 1 | a0001c0001t0001g0073 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.510-2135T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4737028 | ||||||
| chr12:4737089
|
G | A | 1 | a0002c0002t0002g0149 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.510-2074G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4737089 | ||||||
| chr12:4737182
|
T | G | 1 | a0001c0001t0001g0206 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.510-1981T>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4737182 | ||||||
| chr12:4737237
|
T | C | 3 | a0001c0001t0001g0032a0005c0006t0002g0031a0012c0017t0002g0123 | 3 | HG03130.hp1 HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.510-1926T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4737237 | ||||||
| chr12:4737277
|
A | G | 60 | a0001c0001t0001g0032a0001c0001t0001g0253a0001c0001t0001g0254others(57): Show | 64 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.510-1886A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4737277 | ||||||
| chr12:4737359
|
T | G | 35 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(32): Show | 38 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.510-1804T>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4737359 | ||||||
| chr12:4737396
|
C | T | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(40): Show | 47 | HG00544.hp2 HG00558.hp2 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.510-1767C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4737396 | ||||||
| chr12:4737454
|
A | G | 17 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0061others(14): Show | 18 | HG00558.hp2 HG01106.hp2 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.510-1709A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4737454 | ||||||
| chr12:4737499
|
A | G | 1 | a0020c0024t0002g0292 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.510-1664A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4737499 | ||||||
| chr12:4737551
|
C | T | 6 | a0004c0005t0005g0252a0004c0005t0005g0271a0004c0005t0005g0272others(3): Show | 6 | HG01891.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.510-1612C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4737551 | ||||||
| chr12:4737597
|
G | A | 215 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(212): Show | 244 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(241): Show |
intron_variant | MODIFIER | c.510-1566G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4737597 | ||||||
| chr12:4737838
|
C | CT | 3 | a0001c0001t0002g0249a0001c0022t0002g0251a0016c0027t0002g0250 | 3 | HG02717.hp1 HG02976.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.510-1323dupT | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 4737838 | |||||
| chr12:4737841
|
C | A | 2 | a0009c0013t0002g0279a0009c0013t0002g0295 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.510-1322C>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4737841 | ||||||
| chr12:4738522
|
A | G | 1 | a0001c0001t0002g0027 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.510-641A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4738522 | ||||||
| chr12:4738533
|
A | C | 1 | a0005c0006t0002g0060 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.510-630A>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4738533 | ||||||
| chr12:4738551
|
C | A | 2 | a0001c0001t0002g0058a0001c0001t0002g0059 | 2 | HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.510-612C>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4738551 | ||||||
| chr12:4738798
|
G | A | 1 | a0001c0001t0002g0284 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.510-365G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4738798 | ||||||
| chr12:4738964
|
C | T | 1 | a0002c0002t0002g0168 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.510-199C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4738964 | ||||||
| chr12:4738965
|
C | A | 1 | a0002c0002t0002g0150 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.510-198C>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4738965 | ||||||
| chr12:4739042
|
G | T | 1 | a0001c0001t0001g0192 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.510-121G>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | chr12 | 4739042 | ||||||
| chr12:4739113
|
GT | G | 3 | a0009c0013t0002g0279a0009c0013t0002g0295a0013c0019t0008g0275 | 3 | HG02258.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.510-48delT | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 4739113 | |||||
| chr12:4739338
|
C | T | 1 | a0001c0001t0003g0053 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.676+9C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4739338 | ||||||
| chr12:4739394
|
G | A | 1 | a0001c0001t0003g0011 | 2 | HG01358.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.676+65G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4739394 | ||||||
| chr12:4739447
|
A | G | 5 | a0003c0004t0001g0107a0003c0004t0001g0108a0003c0004t0001g0141others(2): Show | 5 | HG02280.hp1 HG02451.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.676+118A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4739447 | ||||||
| chr12:4739562
|
C | T | 1 | a0002c0002t0002g0105 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.676+233C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4739562 | ||||||
| chr12:4739656
|
T | G | 3 | a0001c0001t0001g0032a0005c0006t0002g0031a0012c0017t0002g0123 | 3 | HG03130.hp1 HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.676+327T>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4739656 | ||||||
| chr12:4739797
|
T | C | 3 | a0009c0013t0002g0279a0009c0013t0002g0295a0013c0019t0008g0275 | 3 | HG02258.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.676+468T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4739797 | ||||||
| chr12:4739822
|
A | G | 215 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(212): Show | 244 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(241): Show |
intron_variant | MODIFIER | c.676+493A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4739822 | ||||||
| chr12:4739858
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.676+529G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4739858 | ||||||
| chr12:4739960
|
C | T | 1 | a0020c0024t0002g0292 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.676+631C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4739960 | ||||||
| chr12:4740014
|
G | C | 6 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0002g0249others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.676+685G>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4740014 | ||||||
| chr12:4740035
|
A | G | 10 | a0003c0003t0001g0018a0003c0003t0001g0104a0003c0003t0001g0126others(7): Show | 11 | HG02258.hp1 HG02280.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.676+706A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4740035 | ||||||
| chr12:4740193
|
A | G | 14 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0286others(11): Show | 15 | HG00642.hp2 HG00733.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.676+864A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4740193 | ||||||
| chr12:4740227
|
C | T | 3 | a0002c0002t0002g0163a0002c0002t0002g0164a0002c0002t0002g0165 | 3 | NA18942.hp1 NA18946.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.676+898C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4740227 | ||||||
| chr12:4740424
|
CT | C | 14 | a0001c0001t0001g0074a0001c0001t0001g0195a0001c0001t0001g0211others(11): Show | 14 | HG02258.hp2 HG02572.hp1 HG02895.hp2 others(11): Show |
intron_variant | MODIFIER | c.676+1111delT | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 4740424 | |||||
| chr12:4740440
|
T | C | 1 | a0002c0002t0002g0128 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.676+1111T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4740440 | ||||||
| chr12:4740516
|
C | T | 1 | a0002c0002t0002g0105 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.676+1187C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4740516 | ||||||
| chr12:4740724
|
A | G | 1 | a0012c0017t0002g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.676+1395A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4740724 | ||||||
| chr12:4740790
|
G | A | 3 | a0009c0013t0002g0279a0009c0013t0002g0295a0013c0019t0008g0275 | 3 | HG02258.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.676+1461G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4740790 | ||||||
| chr12:4740833
|
A | G | 2 | a0001c0001t0002g0058a0001c0001t0002g0059 | 2 | HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.676+1504A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4740833 | ||||||
| chr12:4741103
|
T | C | 1 | a0002c0002t0002g0098 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.676+1774T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4741103 | ||||||
| chr12:4741243
|
G | A | 5 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0226others(2): Show | 5 | HG01192.hp2 HG02257.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.676+1914G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4741243 | ||||||
| chr12:4741269
|
A | G | 1 | a0001c0001t0001g0219 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.676+1940A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4741269 | ||||||
| chr12:4741319
|
G | T | 1 | a0001c0001t0001g0066 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.676+1990G>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4741319 | ||||||
| chr12:4741570
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.676+2241T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4741570 | ||||||
| chr12:4741579
|
G | GA | 14 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0286others(11): Show | 15 | HG00642.hp2 HG00733.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.676+2261dupA | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 4741579 | |||||
| chr12:4741603
|
C | G | 1 | a0014c0015t0002g0162 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.676+2274C>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4741603 | ||||||
| chr12:4741607
|
A | G | 2 | a0001c0001t0001g0261a0005c0006t0002g0060 | 2 | HG02622.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.676+2278A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4741607 | ||||||
| chr12:4741889
|
G | C | 1 | a0001c0001t0003g0012 | 2 | HG00639.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.676+2560G>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4741889 | ||||||
| chr12:4741914
|
C | T | 1 | a0003c0003t0001g0174 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.676+2585C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4741914 | ||||||
| chr12:4742389
|
G | A | 91 | a0002c0002t0001g0008a0002c0002t0001g0102a0002c0002t0001g0154others(88): Show | 109 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.677-2128G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4742389 | ||||||
| chr12:4742415
|
A | G | 1 | a0002c0002t0002g0161 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.677-2102A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4742415 | ||||||
| chr12:4742479
|
G | A | 3 | a0002c0002t0002g0112a0002c0002t0002g0124a0002c0002t0002g0140 | 3 | HG02145.hp2 HG02451.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.677-2038G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4742479 | ||||||
| chr12:4742500
|
T | G | 2 | a0001c0001t0001g0066a0001c0001t0001g0072 | 2 | HG02074.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.677-2017T>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4742500 | ||||||
| chr12:4742895
|
C | T | 2 | a0001c0001t0002g0058a0001c0001t0002g0059 | 2 | HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.677-1622C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4742895 | ||||||
| chr12:4743108
|
C | T | 1 | a0001c0001t0001g0270 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.677-1409C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4743108 | ||||||
| chr12:4743150
|
A | G | 1 | a0002c0002t0002g0120 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.677-1367A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4743150 | ||||||
| chr12:4743346
|
G | A | 41 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(38): Show | 45 | HG00544.hp2 HG00558.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.677-1171G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4743346 | ||||||
| chr12:4743348
|
C | T | 1 | a0002c0002t0002g0105 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.677-1169C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4743348 | ||||||
| chr12:4743496
|
C | T | 67 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(64): Show | 73 | HG00544.hp2 HG00558.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.677-1021C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4743496 | ||||||
| chr12:4743531
|
C | G | 3 | a0001c0001t0002g0058a0001c0001t0002g0059a0020c0024t0002g0292 | 3 | HG01884.hp1 HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.677-986C>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4743531 | ||||||
| chr12:4743582
|
A | G | 17 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0061others(14): Show | 18 | HG00558.hp2 HG01106.hp2 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.677-935A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4743582 | ||||||
| chr12:4743849
|
G | T | 96 | a0001c0001t0001g0032a0001c0001t0002g0058a0001c0001t0002g0059others(93): Show | 116 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.677-668G>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4743849 | ||||||
| chr12:4744196
|
G | T | 5 | a0001c0001t0001g0032a0001c0001t0002g0058a0001c0001t0002g0059others(2): Show | 5 | HG01884.hp1 HG02647.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.677-321G>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4744196 | ||||||
| chr12:4744277
|
A | G | 1 | a0018c0023t0001g0267 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.677-240A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4744277 | ||||||
| chr12:4744291
|
G | C | 15 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0286others(12): Show | 16 | HG00642.hp2 HG00733.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.677-226G>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4744291 | ||||||
| chr12:4744304
|
G | A | 1 | a0002c0002t0002g0113 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.677-213G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4744304 | ||||||
| chr12:4744312
|
C | A | 5 | a0001c0001t0001g0032a0001c0001t0002g0058a0001c0001t0002g0059others(2): Show | 5 | HG01884.hp1 HG02647.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.677-205C>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4744312 | ||||||
| chr12:4744334
|
C | G | 3 | a0004c0005t0005g0272a0004c0005t0006g0256a0004c0005t0006g0257 | 3 | HG01891.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.677-183C>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4744334 | ||||||
| chr12:4744363
|
T | G | 3 | a0009c0013t0002g0279a0009c0013t0002g0295a0013c0019t0008g0275 | 3 | HG02258.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.677-154T>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4744363 | ||||||
| chr12:4744389
|
A | G | 41 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(38): Show | 45 | HG00544.hp2 HG00558.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.677-128A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4744389 | ||||||
| chr12:4744503
|
C | T | 5 | a0001c0001t0001g0032a0001c0001t0002g0058a0001c0001t0002g0059others(2): Show | 5 | HG01884.hp1 HG02647.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.677-14C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 3/10 | chr12 | 4744503 | ||||||
| chr12:4744732
|
A | G | 46 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(43): Show | 50 | HG00544.hp2 HG00558.hp2 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.860+32A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 4/10 | chr12 | 4744732 | ||||||
| chr12:4744749
|
T | C | 41 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(38): Show | 45 | HG00544.hp2 HG00558.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.860+49T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 4/10 | chr12 | 4744749 | ||||||
| chr12:4744749
|
T | G | 88 | a0002c0002t0001g0008a0002c0002t0001g0102a0002c0002t0001g0154others(85): Show | 108 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(105): Show |
intron_variant | MODIFIER | c.860+49T>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 4/10 | chr12 | 4744749 | ||||||
| chr12:4744760
|
C | T | 1 | a0020c0024t0002g0292 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.860+60C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 4/10 | chr12 | 4744760 | ||||||
| chr12:4745134
|
G | A | 1 | a0001c0001t0003g0043 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.861-295G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 4/10 | chr12 | 4745134 | ||||||
| chr12:4745352
|
T | G | 1 | a0001c0001t0001g0294 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.861-77T>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 4/10 | chr12 | 4745352 | ||||||
| chr12:4745373
|
T | TC | 83 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(80): Show | 92 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.861-52dupC | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 4745373 | |||||
| chr12:4745376
|
C | G | 2 | a0001c0001t0002g0249a0016c0027t0002g0250 | 2 | HG02976.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.861-53C>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 4/10 | chr12 | 4745376 | ||||||
| chr12:4745380
|
C | T | 1 | a0002c0002t0002g0178 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.861-49C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 4/10 | chr12 | 4745380 | ||||||
| chr12:4745705
|
G | C | 2 | a0001c0001t0001g0259a0001c0001t0001g0266 | 2 | HG02717.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1058+79G>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 5/10 | chr12 | 4745705 | ||||||
| chr12:4745753
|
A | G | 1 | a0001c0001t0003g0037 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1058+127A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 5/10 | chr12 | 4745753 | ||||||
| chr12:4746574
|
C | G | 1 | a0001c0001t0001g0032 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1173+316C>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4746574 | ||||||
| chr12:4746628
|
T | C | 299 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(296): Show | 337 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(334): Show |
intron_variant | MODIFIER | c.1173+370T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4746628 | ||||||
| chr12:4747036
|
A | T | 3 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0240 | 3 | NA18994.hp1 NA18994.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1173+778A>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4747036 | ||||||
| chr12:4747125
|
G | A | 1 | a0006c0007t0002g0007 | 3 | HG01192.hp1 HG01346.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1173+867G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4747125 | ||||||
| chr12:4747173
|
T | G | 1 | a0003c0003t0001g0018 | 2 | HG02280.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1173+915T>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4747173 | ||||||
| chr12:4747185
|
C | T | 2 | a0001c0001t0001g0032a0012c0017t0002g0123 | 2 | HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1173+927C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4747185 | ||||||
| chr12:4747327
|
T | G | 1 | a0003c0003t0002g0169 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1173+1069T>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4747327 | ||||||
| chr12:4747333
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1173+1075C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4747333 | ||||||
| chr12:4747428
|
A | G | 1 | a0008c0009t0002g0029 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1173+1170A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4747428 | ||||||
| chr12:4747545
|
C | T | 1 | a0002c0002t0002g0165 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1173+1287C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4747545 | ||||||
| chr12:4747670
|
A | G | 1 | a0018c0023t0001g0267 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1173+1412A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4747670 | ||||||
| chr12:4747903
|
T | C | 46 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(43): Show | 50 | HG00544.hp2 HG00558.hp2 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.1173+1645T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4747903 | ||||||
| chr12:4747965
|
G | C | 7 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0002g0249others(4): Show | 7 | HG01884.hp2 HG02451.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1173+1707G>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4747965 | ||||||
| chr12:4748457
|
G | T | 1 | a0001c0001t0001g0082 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1173+2199G>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4748457 | ||||||
| chr12:4748494
|
G | A | 103 | a0001c0001t0002g0027a0001c0001t0002g0280a0001c0001t0002g0281others(100): Show | 124 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(121): Show |
intron_variant | MODIFIER | c.1173+2236G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4748494 | ||||||
| chr12:4748608
|
GT | G | 4 | a0001c0001t0001g0206a0001c0001t0001g0227a0001c0001t0001g0246others(1): Show | 4 | HG00140.hp2 HG00323.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173+2354delT | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 4748608 | |||||
| chr12:4748763
|
T | C | 299 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(296): Show | 337 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(334): Show |
intron_variant | MODIFIER | c.1173+2505T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4748763 | ||||||
| chr12:4748883
|
A | G | 2 | a0001c0001t0002g0058a0001c0001t0002g0059 | 2 | HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1173+2625A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4748883 | ||||||
| chr12:4749033
|
A | G | 1 | a0001c0001t0001g0204 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1173+2775A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4749033 | ||||||
| chr12:4749092
|
C | T | 3 | a0001c0001t0002g0249a0001c0022t0002g0251a0016c0027t0002g0250 | 3 | HG02717.hp1 HG02976.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1173+2834C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4749092 | ||||||
| chr12:4749100
|
T | C | 2 | a0001c0001t0001g0228a0001c0001t0001g0243 | 2 | NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1173+2842T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4749100 | ||||||
| chr12:4749298
|
A | G | 3 | a0002c0002t0002g0112a0002c0002t0002g0124a0002c0002t0002g0140 | 3 | HG02145.hp2 HG02451.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1173+3040A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4749298 | ||||||
| chr12:4749318
|
G | T | 1 | a0002c0002t0002g0121 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1173+3060G>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4749318 | ||||||
| chr12:4749922
|
A | G | 1 | a0009c0013t0002g0295 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1173+3664A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4749922 | ||||||
| chr12:4750132
|
C | T | 103 | a0001c0001t0002g0027a0001c0001t0002g0280a0001c0001t0002g0281others(100): Show | 124 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(121): Show |
intron_variant | MODIFIER | c.1173+3874C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4750132 | ||||||
| chr12:4750422
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1173+4164C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4750422 | ||||||
| chr12:4750637
|
C | T | 103 | a0001c0001t0002g0027a0001c0001t0002g0280a0001c0001t0002g0281others(100): Show | 124 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(121): Show |
intron_variant | MODIFIER | c.1173+4379C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4750637 | ||||||
| chr12:4750701
|
GCTGGGTT others(11): Show |
G | 1 | a0007c0008t0001g0188 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1173+4447_1173+446 others(22): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 4750701 | |||||
| chr12:4750790
|
A | T | 90 | a0002c0002t0001g0008a0002c0002t0001g0102a0002c0002t0001g0154others(87): Show | 110 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.1173+4532A>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4750790 | ||||||
| chr12:4750800
|
A | G | 1 | a0018c0023t0001g0267 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1173+4542A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4750800 | ||||||
| chr12:4750893
|
A | T | 3 | a0001c0001t0001g0032a0012c0017t0002g0123a0020c0024t0002g0292 | 3 | HG01884.hp1 HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1173+4635A>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4750893 | ||||||
| chr12:4750925
|
C | T | 2 | a0001c0001t0001g0293a0001c0001t0001g0294 | 2 | HG01975.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.1173+4667C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4750925 | ||||||
| chr12:4750939
|
A | G | 1 | a0001c0001t0002g0288 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1173+4681A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4750939 | ||||||
| chr12:4751035
|
C | T | 1 | a0003c0003t0001g0173 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1173+4777C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4751035 | ||||||
| chr12:4751107
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1173+4849C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4751107 | ||||||
| chr12:4751165
|
A | G | 3 | a0001c0001t0001g0032a0012c0017t0002g0123a0020c0024t0002g0292 | 3 | HG01884.hp1 HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1173+4907A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4751165 | ||||||
| chr12:4751435
|
A | C | 3 | a0001c0001t0002g0249a0001c0022t0002g0251a0016c0027t0002g0250 | 3 | HG02717.hp1 HG02976.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1173+5177A>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4751435 | ||||||
| chr12:4751627
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1173+5369C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4751627 | ||||||
| chr12:4752058
|
T | C | 1 | a0001c0001t0001g0082 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1173+5800T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4752058 | ||||||
| chr12:4752186
|
C | T | 5 | a0001c0001t0001g0032a0001c0001t0002g0058a0001c0001t0002g0059others(2): Show | 5 | HG01884.hp1 HG02647.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1173+5928C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4752186 | ||||||
| chr12:4752218
|
C | T | 9 | a0001c0001t0002g0027a0001c0001t0002g0280a0001c0001t0002g0281others(6): Show | 10 | HG00642.hp2 HG00733.hp1 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.1173+5960C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4752218 | ||||||
| chr12:4752365
|
G | A | 2 | a0001c0001t0001g0198a0001c0001t0001g0274 | 2 | NA18988.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1173+6107G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4752365 | ||||||
| chr12:4752424
|
A | C | 5 | a0003c0004t0001g0107a0003c0004t0001g0108a0003c0004t0001g0141others(2): Show | 5 | HG02280.hp1 HG02451.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1173+6166A>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4752424 | ||||||
| chr12:4752534
|
G | GA | 42 | a0001c0001t0001g0075a0001c0001t0001g0241a0001c0001t0001g0282others(39): Show | 46 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.1173+6289dupA | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 4752534 | |||||
| chr12:4752556
|
A | T | 11 | a0001c0001t0002g0027a0001c0001t0002g0280a0001c0001t0002g0281others(8): Show | 12 | HG00642.hp2 HG00733.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.1173+6298A>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4752556 | ||||||
| chr12:4752738
|
G | T | 5 | a0001c0001t0001g0032a0001c0001t0002g0058a0001c0001t0002g0059others(2): Show | 5 | HG01884.hp1 HG02647.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1173+6480G>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4752738 | ||||||
| chr12:4752828
|
A | G | 2 | a0009c0013t0002g0279a0009c0013t0002g0295 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1173+6570A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4752828 | ||||||
| chr12:4752918
|
T | C | 1 | a0018c0023t0001g0267 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1173+6660T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4752918 | ||||||
| chr12:4752935
|
C | G | 8 | a0001c0001t0001g0032a0001c0001t0002g0058a0001c0001t0002g0059others(5): Show | 8 | HG01884.hp1 HG02647.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1173+6677C>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4752935 | ||||||
| chr12:4753260
|
CT | C | 90 | a0002c0002t0001g0008a0002c0002t0001g0102a0002c0002t0001g0154others(87): Show | 110 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.1173+7003delT | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4753260 | ||||||
| chr12:4753274
|
A | G | 2 | a0001c0001t0001g0197a0001c0001t0001g0262 | 2 | HG02257.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1173+7016A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4753274 | ||||||
| chr12:4753443
|
A | G | 1 | a0001c0001t0002g0027 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1173+7185A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4753443 | ||||||
| chr12:4753465
|
G | A | 103 | a0001c0001t0002g0027a0001c0001t0002g0280a0001c0001t0002g0281others(100): Show | 124 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(121): Show |
intron_variant | MODIFIER | c.1173+7207G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4753465 | ||||||
| chr12:4753485
|
G | A | 103 | a0001c0001t0002g0027a0001c0001t0002g0280a0001c0001t0002g0281others(100): Show | 124 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(121): Show |
intron_variant | MODIFIER | c.1173+7227G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4753485 | ||||||
| chr12:4753529
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1173+7271T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4753529 | ||||||
| chr12:4753694
|
G | C | 103 | a0001c0001t0002g0027a0001c0001t0002g0280a0001c0001t0002g0281others(100): Show | 124 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(121): Show |
intron_variant | MODIFIER | c.1174-7264G>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4753694 | ||||||
| chr12:4753811
|
G | T | 1 | a0018c0023t0001g0267 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1174-7147G>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4753811 | ||||||
| chr12:4753931
|
A | T | 2 | a0001c0001t0001g0073a0001c0001t0001g0089 | 2 | HG02683.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1174-7027A>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4753931 | ||||||
| chr12:4753935
|
A | G | 6 | a0004c0005t0005g0252a0004c0005t0005g0271a0004c0005t0005g0272others(3): Show | 6 | HG01891.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1174-7023A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4753935 | ||||||
| chr12:4753970
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1174-6988C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4753970 | ||||||
| chr12:4754020
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1174-6938C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4754020 | ||||||
| chr12:4754100
|
C | G | 41 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(38): Show | 45 | HG00544.hp2 HG00558.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.1174-6858C>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4754100 | ||||||
| chr12:4754142
|
G | C | 106 | a0001c0001t0002g0027a0001c0001t0002g0249a0001c0001t0002g0280others(103): Show | 127 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(124): Show |
intron_variant | MODIFIER | c.1174-6816G>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4754142 | ||||||
| chr12:4754178
|
A | T | 1 | a0002c0002t0002g0160 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1174-6780A>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4754178 | ||||||
| chr12:4754191
|
G | A | 106 | a0001c0001t0002g0027a0001c0001t0002g0249a0001c0001t0002g0280others(103): Show | 127 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(124): Show |
intron_variant | MODIFIER | c.1174-6767G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4754191 | ||||||
| chr12:4754191
|
G | GTA | 3 | a0001c0001t0001g0032a0012c0017t0002g0123a0020c0024t0002g0292 | 3 | HG01884.hp1 HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1174-6766_1174-676 others(6): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 4754191 | |||||
| chr12:4754233
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1174-6725G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4754233 | ||||||
| chr12:4754281
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1174-6677C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4754281 | ||||||
| chr12:4754302
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1174-6656G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4754302 | ||||||
| chr12:4754799
|
A | G | 26 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0034others(23): Show | 28 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1174-6159A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4754799 | ||||||
| chr12:4754835
|
T | C | 106 | a0001c0001t0002g0027a0001c0001t0002g0249a0001c0001t0002g0280others(103): Show | 127 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(124): Show |
intron_variant | MODIFIER | c.1174-6123T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4754835 | ||||||
| chr12:4754911
|
A | G | 106 | a0001c0001t0002g0027a0001c0001t0002g0249a0001c0001t0002g0280others(103): Show | 127 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(124): Show |
intron_variant | MODIFIER | c.1174-6047A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4754911 | ||||||
| chr12:4754951
|
A | G | 103 | a0001c0001t0002g0027a0001c0001t0002g0280a0001c0001t0002g0281others(100): Show | 124 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(121): Show |
intron_variant | MODIFIER | c.1174-6007A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4754951 | ||||||
| chr12:4755025
|
G | C | 103 | a0001c0001t0002g0027a0001c0001t0002g0280a0001c0001t0002g0281others(100): Show | 124 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(121): Show |
intron_variant | MODIFIER | c.1174-5933G>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4755025 | ||||||
| chr12:4755059
|
G | A | 103 | a0001c0001t0002g0027a0001c0001t0002g0280a0001c0001t0002g0281others(100): Show | 124 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(121): Show |
intron_variant | MODIFIER | c.1174-5899G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4755059 | ||||||
| chr12:4755088
|
T | C | 106 | a0001c0001t0002g0027a0001c0001t0002g0249a0001c0001t0002g0280others(103): Show | 127 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(124): Show |
intron_variant | MODIFIER | c.1174-5870T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4755088 | ||||||
| chr12:4755441
|
C | T | 1 | a0002c0002t0002g0183 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1174-5517C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4755441 | ||||||
| chr12:4755613
|
G | A | 1 | a0002c0002t0002g0114 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1174-5345G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4755613 | ||||||
| chr12:4755662
|
A | C | 202 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(199): Show | 231 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(228): Show |
intron_variant | MODIFIER | c.1174-5296A>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4755662 | ||||||
| chr12:4755685
|
C | A | 9 | a0001c0001t0001g0286a0003c0003t0001g0018a0003c0003t0001g0104others(6): Show | 10 | HG02258.hp1 HG02280.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1174-5273C>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4755685 | ||||||
| chr12:4755708
|
A | G | 1 | a0005c0006t0002g0031 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1174-5250A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4755708 | ||||||
| chr12:4755826
|
C | T | 1 | a0001c0001t0003g0012 | 2 | HG00639.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.1174-5132C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4755826 | ||||||
| chr12:4755944
|
A | G | 1 | a0013c0019t0008g0275 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1174-5014A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4755944 | ||||||
| chr12:4756072
|
T | A | 2 | a0001c0001t0001g0032a0012c0017t0002g0123 | 2 | HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1174-4886T>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4756072 | ||||||
| chr12:4756185
|
C | T | 1 | a0002c0002t0002g0006 | 3 | HG00738.hp2 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1174-4773C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4756185 | ||||||
| chr12:4756211
|
C | T | 2 | a0001c0001t0001g0198a0001c0001t0001g0274 | 2 | NA18988.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1174-4747C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4756211 | ||||||
| chr12:4756249
|
C | T | 94 | a0002c0002t0001g0008a0002c0002t0001g0102a0002c0002t0001g0154others(91): Show | 114 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.1174-4709C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4756249 | ||||||
| chr12:4756282
|
G | A | 1 | a0013c0019t0008g0275 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1174-4676G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4756282 | ||||||
| chr12:4756299
|
G | A | 94 | a0002c0002t0001g0008a0002c0002t0001g0102a0002c0002t0001g0154others(91): Show | 114 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.1174-4659G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4756299 | ||||||
| chr12:4756307
|
A | G | 1 | a0002c0002t0002g0103 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1174-4651A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4756307 | ||||||
| chr12:4756457
|
C | T | 1 | a0001c0014t0001g0217 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1174-4501C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4756457 | ||||||
| chr12:4756527
|
G | A | 1 | a0003c0003t0001g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1174-4431G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4756527 | ||||||
| chr12:4756559
|
A | G | 97 | a0001c0001t0002g0249a0001c0022t0002g0251a0002c0002t0001g0008others(94): Show | 117 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.1174-4399A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4756559 | ||||||
| chr12:4756575
|
T | TC | 90 | a0002c0002t0001g0008a0002c0002t0001g0102a0002c0002t0001g0154others(87): Show | 110 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.1174-4378dupC | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 4756575 | |||||
| chr12:4756609
|
C | A | 2 | a0002c0020t0002g0144a0005c0006t0002g0060 | 2 | HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1174-4349C>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4756609 | ||||||
| chr12:4756866
|
G | A | 94 | a0002c0002t0001g0008a0002c0002t0001g0102a0002c0002t0001g0154others(91): Show | 114 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.1174-4092G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4756866 | ||||||
| chr12:4756981
|
C | T | 3 | a0002c0002t0002g0112a0002c0002t0002g0124a0002c0002t0002g0140 | 3 | HG02145.hp2 HG02451.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1174-3977C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4756981 | ||||||
| chr12:4756984
|
A | G | 3 | a0001c0001t0002g0058a0001c0001t0002g0059a0020c0024t0002g0292 | 3 | HG01884.hp1 HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1174-3974A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4756984 | ||||||
| chr12:4756988
|
G | T | 94 | a0002c0002t0001g0008a0002c0002t0001g0102a0002c0002t0001g0154others(91): Show | 114 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.1174-3970G>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4756988 | ||||||
| chr12:4757058
|
G | T | 94 | a0002c0002t0001g0008a0002c0002t0001g0102a0002c0002t0001g0154others(91): Show | 114 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.1174-3900G>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4757058 | ||||||
| chr12:4757468
|
C | T | 1 | a0003c0003t0001g0171 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1174-3490C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4757468 | ||||||
| chr12:4757506
|
G | A | 1 | a0010c0011t0001g0207 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1174-3452G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4757506 | ||||||
| chr12:4757508
|
CT | C | 3 | a0008c0009t0002g0028a0008c0009t0002g0029a0018c0023t0001g0267 | 3 | HG01891.hp2 HG01952.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1174-3446delT | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 4757508 | |||||
| chr12:4757540
|
C | T | 11 | a0001c0001t0001g0286a0003c0003t0001g0018a0003c0003t0001g0104others(8): Show | 12 | HG02258.hp1 HG02280.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1174-3418C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4757540 | ||||||
| chr12:4757672
|
A | G | 97 | a0001c0001t0002g0249a0001c0022t0002g0251a0002c0002t0001g0008others(94): Show | 117 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.1174-3286A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4757672 | ||||||
| chr12:4757762
|
T | C | 1 | a0001c0001t0001g0229 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1174-3196T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4757762 | ||||||
| chr12:4757766
|
GCAGAAT | G | 128 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0032others(125): Show | 150 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(147): Show |
intron_variant | MODIFIER | c.1174-3185_1174-318 others(10): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 4757766 | |||||
| chr12:4757975
|
G | T | 97 | a0001c0001t0002g0249a0001c0022t0002g0251a0002c0002t0001g0008others(94): Show | 117 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.1174-2983G>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4757975 | ||||||
| chr12:4758073
|
T | C | 97 | a0001c0001t0002g0249a0001c0022t0002g0251a0002c0002t0001g0008others(94): Show | 117 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.1174-2885T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4758073 | ||||||
| chr12:4758204
|
T | C | 97 | a0001c0001t0002g0249a0001c0022t0002g0251a0002c0002t0001g0008others(94): Show | 117 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.1174-2754T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4758204 | ||||||
| chr12:4758232
|
T | G | 5 | a0003c0004t0001g0107a0003c0004t0001g0108a0003c0004t0001g0141others(2): Show | 5 | HG02280.hp1 HG02451.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-2726T>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4758232 | ||||||
| chr12:4758300
|
T | A | 1 | a0001c0001t0002g0284 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1174-2658T>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4758300 | ||||||
| chr12:4758333
|
G | A | 94 | a0002c0002t0001g0008a0002c0002t0001g0102a0002c0002t0001g0154others(91): Show | 114 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.1174-2625G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4758333 | ||||||
| chr12:4758454
|
C | T | 94 | a0002c0002t0001g0008a0002c0002t0001g0102a0002c0002t0001g0154others(91): Show | 114 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.1174-2504C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4758454 | ||||||
| chr12:4758559
|
C | T | 208 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(205): Show | 237 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(234): Show |
intron_variant | MODIFIER | c.1174-2399C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4758559 | ||||||
| chr12:4758606
|
CTG | C | 44 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0023others(41): Show | 49 | HG00140.hp2 HG00323.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.1174-2321_1174-232 others(6): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 4758606 | |||||
| chr12:4758606
|
CTGTG | C | 33 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0091others(30): Show | 35 | HG00544.hp1 HG00558.hp1 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.1174-2323_1174-232 others(8): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 4758606 | |||||
| chr12:4758606
|
CTGTGTG | C | 7 | a0001c0001t0001g0030a0001c0001t0001g0097a0001c0001t0001g0253others(4): Show | 8 | HG01884.hp2 HG02280.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1174-2325_1174-232 others(10): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 4758606 | |||||
| chr12:4758606
|
CTGTGTGT others(3): Show |
C | 1 | a0001c0022t0002g0251 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1174-2329_1174-232 others(14): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 4758606 | |||||
| chr12:4758606
|
CTGTGTGT others(5): Show |
C | 2 | a0008c0009t0002g0028a0008c0009t0002g0029 | 2 | HG01952.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1174-2331_1174-232 others(16): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 4758606 | |||||
| chr12:4758619
|
T | C | 1 | a0013c0019t0008g0275 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1174-2339T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4758619 | ||||||
| chr12:4758623
|
TGTGTGTG others(9): Show |
T | 1 | a0013c0019t0008g0275 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1174-2333_1174-231 others(20): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 4758623 | |||||
| chr12:4758627
|
TGTGTGTG others(9): Show |
T | 1 | a0018c0023t0001g0267 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1174-2329_1174-231 others(20): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 4758627 | |||||
| chr12:4758629
|
TGTGTGTG others(3): Show |
T | 1 | a0003c0003t0001g0172 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1174-2327_1174-231 others(14): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 4758629 | |||||
| chr12:4758629
|
TGTGTGTG others(5): Show |
T | 2 | a0001c0001t0002g0249a0016c0027t0002g0250 | 2 | HG02976.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1174-2327_1174-231 others(16): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 4758629 | |||||
| chr12:4758629
|
TGTGTGTG others(7): Show |
T | 8 | a0001c0001t0002g0027a0001c0001t0002g0280a0001c0001t0002g0281others(5): Show | 9 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.1174-2327_1174-231 others(18): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 4758629 | |||||
| chr12:4758630
|
G | C | 1 | a0004c0005t0005g0252 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1174-2328G>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4758630 | ||||||
| chr12:4758631
|
TGTGTGTG others(1): Show |
T | 16 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0067others(13): Show | 17 | HG00558.hp2 HG01106.hp2 HG01943.hp1 others(14): Show |
intron_variant | MODIFIER | c.1174-2325_1174-231 others(12): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 4758631 | |||||
| chr12:4758631
|
TGTGTGTG others(3): Show |
T | 4 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0003g0033others(1): Show | 4 | HG01975.hp1 HG02647.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.1174-2325_1174-231 others(14): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 4758631 | |||||
| chr12:4758631
|
TGTGTGTG others(5): Show |
T | 17 | a0001c0001t0002g0288a0002c0002t0002g0005a0002c0002t0002g0098others(14): Show | 20 | HG00140.hp1 HG00323.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.1174-2325_1174-231 others(16): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 4758631 | |||||
| chr12:4758631
|
TGTGTGTG others(7): Show |
T | 1 | a0002c0002t0002g0183 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1174-2325_1174-231 others(18): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 4758631 | |||||
| chr12:4758631
|
TGTGTGTG others(9): Show |
T | 2 | a0002c0002t0002g0150a0002c0002t0002g0153 | 2 | HG01081.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1174-2325_1174-231 others(20): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 4758631 | |||||
| chr12:4758633
|
T | A | 4 | a0001c0001t0001g0032a0001c0001t0001g0264a0001c0001t0002g0058others(1): Show | 4 | HG01167.hp2 HG01884.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174-2325T>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4758633 | ||||||
| chr12:4758633
|
TGTGTGA | T | 14 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0001g0086others(11): Show | 15 | HG01358.hp1 HG01517.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.1174-2323_1174-231 others(10): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 4758633 | |||||
| chr12:4758633
|
TGTGTGAG others(1): Show |
T | 48 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0062others(45): Show | 53 | HG00544.hp2 HG00639.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.1174-2323_1174-231 others(12): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 4758633 | |||||
| chr12:4758633
|
TGTGTGAG others(3): Show |
T | 6 | a0001c0001t0003g0036a0001c0001t0003g0042a0001c0001t0003g0053others(3): Show | 6 | HG02572.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1174-2323_1174-231 others(14): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 4758633 | |||||
| chr12:4758633
|
TGTGTGAG others(5): Show |
T | 60 | a0002c0002t0001g0008a0002c0002t0001g0102a0002c0002t0001g0154others(57): Show | 75 | HG00621.hp2 HG00738.hp2 HG00741.hp2 others(72): Show |
intron_variant | MODIFIER | c.1174-2323_1174-231 others(16): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 4758633 | |||||
| chr12:4758633
|
TGTGTGAG others(7): Show |
T | 3 | a0002c0002t0002g0020a0002c0002t0002g0134a0002c0018t0002g0020 | 3 | HG00609.hp1 NA18939.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.1174-2323_1174-231 others(18): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 4758633 | |||||
| chr12:4758635
|
T | A | 17 | a0001c0001t0001g0032a0001c0001t0001g0229a0001c0001t0001g0230others(14): Show | 17 | HG00323.hp1 HG00609.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.1174-2323T>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4758635 | ||||||
| chr12:4758635
|
TGTGA | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0191a0001c0001t0001g0216others(1): Show | 6 | NA18942.hp2 NA18973.hp1 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.1174-2321_1174-231 others(8): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 4758635 | |||||
| chr12:4758635
|
TGTGAGAG others(3): Show |
T | 3 | a0002c0002t0002g0149a0002c0020t0002g0144a0006c0007t0002g0007 | 5 | HG01192.hp1 HG01346.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-2321_1174-231 others(14): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 4758635 | |||||
| chr12:4758635
|
TGTGAGAG others(5): Show |
T | 2 | a0002c0002t0002g0159a0005c0006t0002g0060 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1174-2321_1174-231 others(16): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 4758635 | |||||
| chr12:4758637
|
T | A | 68 | a0001c0001t0001g0010a0001c0001t0001g0023a0001c0001t0001g0025others(65): Show | 72 | HG00140.hp2 HG00323.hp1 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.1174-2321T>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4758637 | ||||||
| chr12:4758678
|
T | G | 1 | a0002c0002t0002g0147 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1174-2280T>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4758678 | ||||||
| chr12:4758776
|
CTT | C | 94 | a0002c0002t0001g0008a0002c0002t0001g0102a0002c0002t0001g0154others(91): Show | 114 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.1174-2170_1174-216 others(6): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 4758776 | |||||
| chr12:4758793
|
T | C | 46 | a0002c0002t0001g0008a0002c0002t0001g0102a0002c0002t0001g0154others(43): Show | 61 | HG00609.hp1 HG00621.hp2 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.1174-2165T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4758793 | ||||||
| chr12:4758858
|
C | A | 5 | a0003c0004t0001g0107a0003c0004t0001g0108a0003c0004t0001g0141others(2): Show | 5 | HG02280.hp1 HG02451.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-2100C>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4758858 | ||||||
| chr12:4758977
|
T | C | 11 | a0001c0001t0001g0286a0003c0003t0001g0018a0003c0003t0001g0104others(8): Show | 12 | HG02258.hp1 HG02280.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1174-1981T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4758977 | ||||||
| chr12:4759394
|
G | T | 1 | a0001c0001t0001g0266 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1174-1564G>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4759394 | ||||||
| chr12:4759475
|
C | CT | 90 | a0002c0002t0001g0008a0002c0002t0001g0102a0002c0002t0001g0154others(87): Show | 110 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.1174-1482dupT | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 4759475 | |||||
| chr12:4759549
|
T | G | 2 | a0008c0009t0002g0028a0008c0009t0002g0029 | 2 | HG01952.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1174-1409T>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4759549 | ||||||
| chr12:4759704
|
C | A | 2 | a0001c0001t0001g0032a0012c0017t0002g0123 | 2 | HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1174-1254C>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4759704 | ||||||
| chr12:4760009
|
T | C | 4 | a0001c0001t0002g0249a0001c0022t0002g0251a0013c0019t0008g0275others(1): Show | 4 | HG02717.hp1 HG02976.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174-949T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4760009 | ||||||
| chr12:4760009
|
T | G | 3 | a0001c0001t0001g0074a0001c0001t0001g0077a0017c0026t0001g0078 | 3 | HG02056.hp2 NA18954.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1174-949T>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4760009 | ||||||
| chr12:4760378
|
C | T | 2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | HG01884.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1174-580C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4760378 | ||||||
| chr12:4760387
|
A | G | 3 | a0002c0002t0002g0179a0002c0002t0007g0138a0002c0002t0007g0139 | 3 | HG02895.hp1 HG02897.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1174-571A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4760387 | ||||||
| chr12:4760433
|
A | G | 3 | a0001c0001t0001g0065a0001c0001t0001g0080a0001c0001t0001g0081 | 3 | HG01256.hp1 HG01258.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1174-525A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4760433 | ||||||
| chr12:4760515
|
G | T | 1 | a0003c0004t0001g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1174-443G>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4760515 | ||||||
| chr12:4760594
|
A | G | 2 | a0008c0009t0002g0028a0008c0009t0002g0029 | 2 | HG01952.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1174-364A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4760594 | ||||||
| chr12:4760649
|
C | T | 1 | a0002c0002t0002g0152 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1174-309C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4760649 | ||||||
| chr12:4760680
|
G | A | 4 | a0001c0001t0001g0225a0001c0001t0001g0260a0001c0001t0001g0261others(1): Show | 4 | HG02572.hp1 HG02895.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1174-278G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4760680 | ||||||
| chr12:4760744
|
G | T | 2 | a0008c0009t0002g0028a0008c0009t0002g0029 | 2 | HG01952.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1174-214G>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4760744 | ||||||
| chr12:4760751
|
T | C | 1 | a0018c0023t0001g0267 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1174-207T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4760751 | ||||||
| chr12:4760762
|
A | G | 94 | a0002c0002t0001g0008a0002c0002t0001g0102a0002c0002t0001g0154others(91): Show | 114 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.1174-196A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4760762 | ||||||
| chr12:4760871
|
G | A | 2 | a0009c0013t0002g0279a0009c0013t0002g0295 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1174-87G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4760871 | ||||||
| chr12:4760919
|
G | C | 1 | a0001c0001t0001g0199 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1174-39G>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4760919 | ||||||
| chr12:4760931
|
G | A | 1 | a0001c0001t0003g0043 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1174-27G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 6/10 | chr12 | 4760931 | ||||||
| chr12:4761197
|
G | A | 89 | a0002c0002t0001g0008a0002c0002t0001g0102a0002c0002t0001g0154others(86): Show | 109 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.1359+54G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4761197 | ||||||
| chr12:4761198
|
G | T | 1 | a0002c0002t0002g0182 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1359+55G>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4761198 | ||||||
| chr12:4761257
|
A | G | 1 | a0001c0001t0001g0223 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1359+114A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4761257 | ||||||
| chr12:4761261
|
C | A | 1 | a0001c0001t0001g0223 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1359+118C>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4761261 | ||||||
| chr12:4761262
|
C | A | 1 | a0001c0001t0001g0223 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1359+119C>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4761262 | ||||||
| chr12:4761263
|
T | C | 1 | a0001c0001t0001g0223 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1359+120T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4761263 | ||||||
| chr12:4761264
|
G | T | 1 | a0001c0001t0001g0223 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1359+121G>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4761264 | ||||||
| chr12:4761270
|
G | T | 1 | a0001c0001t0001g0223 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1359+127G>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4761270 | ||||||
| chr12:4761272
|
G | C | 1 | a0001c0001t0001g0223 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1359+129G>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4761272 | ||||||
| chr12:4761286
|
T | G | 1 | a0001c0001t0001g0223 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1359+143T>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4761286 | ||||||
| chr12:4761292
|
T | G | 1 | a0001c0001t0001g0223 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1359+149T>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4761292 | ||||||
| chr12:4761300
|
ACAGTACA others(6): Show |
A | 1 | a0001c0001t0001g0223 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1359+160_1359+172d others(15): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 4761300 | |||||
| chr12:4761318
|
C | A | 1 | a0001c0001t0001g0223 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1359+175C>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4761318 | ||||||
| chr12:4761319
|
C | T | 1 | a0001c0001t0001g0223 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1359+176C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4761319 | ||||||
| chr12:4761327
|
T | A | 1 | a0001c0001t0001g0223 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1359+184T>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4761327 | ||||||
| chr12:4761329
|
T | C | 1 | a0001c0001t0001g0223 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1359+186T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4761329 | ||||||
| chr12:4761330
|
A | T | 1 | a0001c0001t0001g0223 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1359+187A>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4761330 | ||||||
| chr12:4761333
|
T | G | 1 | a0001c0001t0001g0223 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1359+190T>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4761333 | ||||||
| chr12:4761335
|
T | A | 1 | a0001c0001t0001g0223 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1359+192T>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4761335 | ||||||
| chr12:4761339
|
C | A | 1 | a0001c0001t0001g0223 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1359+196C>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4761339 | ||||||
| chr12:4761340
|
T | C | 1 | a0001c0001t0001g0223 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1359+197T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4761340 | ||||||
| chr12:4761357
|
A | T | 1 | a0001c0001t0001g0223 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1359+214A>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4761357 | ||||||
| chr12:4761358
|
T | C | 1 | a0001c0001t0001g0223 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1359+215T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4761358 | ||||||
| chr12:4761359
|
A | T | 1 | a0001c0001t0001g0223 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1359+216A>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4761359 | ||||||
| chr12:4761361
|
G | C | 1 | a0001c0001t0001g0223 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1359+218G>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4761361 | ||||||
| chr12:4761379
|
T | C | 1 | a0001c0001t0001g0223 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1359+236T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4761379 | ||||||
| chr12:4761385
|
T | C | 1 | a0001c0001t0001g0223 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1359+242T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4761385 | ||||||
| chr12:4761388
|
T | A | 1 | a0001c0001t0001g0223 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1359+245T>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4761388 | ||||||
| chr12:4761389
|
C | T | 1 | a0001c0001t0001g0223 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1359+246C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4761389 | ||||||
| chr12:4761390
|
T | A | 1 | a0001c0001t0001g0223 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1359+247T>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4761390 | ||||||
| chr12:4761468
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1359+325A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4761468 | ||||||
| chr12:4761545
|
G | C | 1 | a0002c0002t0002g0128 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1359+402G>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4761545 | ||||||
| chr12:4761614
|
T | A | 1 | a0002c0002t0002g0182 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1359+471T>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4761614 | ||||||
| chr12:4761616
|
A | G | 1 | a0002c0002t0002g0182 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1359+473A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4761616 | ||||||
| chr12:4761617
|
G | GT | 137 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(134): Show | 161 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(158): Show |
intron_variant | MODIFIER | c.1359+484dupT | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 4761617 | |||||
| chr12:4761617
|
G | T | 1 | a0002c0002t0002g0182 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1359+474G>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4761617 | ||||||
| chr12:4761620
|
T | G | 37 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0003g0011others(34): Show | 40 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1359+477T>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4761620 | ||||||
| chr12:4761668
|
G | A | 2 | a0001c0001t0002g0058a0001c0001t0002g0059 | 2 | HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1359+525G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4761668 | ||||||
| chr12:4761710
|
C | G | 2 | a0001c0001t0002g0249a0016c0027t0002g0250 | 2 | HG02976.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1359+567C>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4761710 | ||||||
| chr12:4761728
|
T | A | 150 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(147): Show | 175 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(172): Show |
intron_variant | MODIFIER | c.1359+585T>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4761728 | ||||||
| chr12:4761797
|
C | G | 1 | a0001c0001t0001g0235 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1359+654C>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4761797 | ||||||
| chr12:4761986
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1359+843G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4761986 | ||||||
| chr12:4762159
|
G | A | 1 | a0018c0023t0001g0267 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1359+1016G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4762159 | ||||||
| chr12:4762289
|
T | C | 138 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(135): Show | 162 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(159): Show |
intron_variant | MODIFIER | c.1360-964T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4762289 | ||||||
| chr12:4762428
|
A | C | 4 | a0001c0001t0001g0253a0001c0001t0001g0254a0003c0004t0001g0107others(1): Show | 4 | HG01884.hp2 HG02451.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1360-825A>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4762428 | ||||||
| chr12:4762472
|
G | A | 1 | a0013c0019t0008g0275 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1360-781G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4762472 | ||||||
| chr12:4762506
|
G | A | 2 | a0001c0001t0003g0013a0001c0001t0003g0043 | 3 | NA18947.hp2 NA18983.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.1360-747G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4762506 | ||||||
| chr12:4762593
|
A | G | 3 | a0001c0001t0001g0032a0012c0017t0002g0123a0020c0024t0002g0292 | 3 | HG01884.hp1 HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1360-660A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4762593 | ||||||
| chr12:4762601
|
C | T | 3 | a0001c0001t0001g0032a0012c0017t0002g0123a0020c0024t0002g0292 | 3 | HG01884.hp1 HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1360-652C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4762601 | ||||||
| chr12:4762667
|
T | C | 1 | a0001c0022t0002g0251 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1360-586T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4762667 | ||||||
| chr12:4762746
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1360-507G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4762746 | ||||||
| chr12:4762757
|
A | G | 1 | a0001c0001t0002g0249 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1360-496A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4762757 | ||||||
| chr12:4762824
|
A | G | 37 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0003g0011others(34): Show | 40 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1360-429A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4762824 | ||||||
| chr12:4762838
|
C | G | 1 | a0001c0022t0002g0251 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1360-415C>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4762838 | ||||||
| chr12:4762846
|
C | T | 1 | a0002c0002t0002g0158 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1360-407C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4762846 | ||||||
| chr12:4762880
|
T | C | 2 | a0001c0001t0001g0198a0001c0001t0001g0274 | 2 | NA18988.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1360-373T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4762880 | ||||||
| chr12:4762936
|
G | A | 2 | a0010c0011t0001g0186a0010c0011t0001g0207 | 2 | HG02055.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1360-317G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4762936 | ||||||
| chr12:4763174
|
C | T | 4 | a0008c0009t0002g0028a0008c0009t0002g0029a0013c0019t0008g0275others(1): Show | 4 | HG01891.hp2 HG01952.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1360-79C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 7/10 | chr12 | 4763174 | ||||||
| chr12:4763533
|
A | G | 1 | a0001c0001t0003g0045 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1497+143A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 8/10 | chr12 | 4763533 | ||||||
| chr12:4763606
|
A | G | 46 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(43): Show | 50 | HG00544.hp2 HG00558.hp2 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.1497+216A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 8/10 | chr12 | 4763606 | ||||||
| chr12:4763633
|
C | T | 2 | a0010c0011t0001g0186a0010c0011t0001g0207 | 2 | HG02055.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1497+243C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 8/10 | chr12 | 4763633 | ||||||
| chr12:4763718
|
T | C | 1 | a0001c0001t0001g0270 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1498-234T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 8/10 | chr12 | 4763718 | ||||||
| chr12:4763724
|
G | C | 1 | a0013c0019t0008g0275 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1498-228G>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 8/10 | chr12 | 4763724 | ||||||
| chr12:4763773
|
C | CG | 2 | a0002c0002t0002g0017a0002c0002t0002g0157 | 3 | HG02129.hp2 NA18947.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.1498-177dupG | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 4763773 | |||||
| chr12:4763812
|
C | T | 3 | a0001c0001t0001g0225a0001c0001t0001g0260a0001c0001t0001g0261 | 3 | HG02895.hp2 HG02970.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1498-140C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 8/10 | chr12 | 4763812 | ||||||
| chr12:4763823
|
C | T | 3 | a0002c0002t0002g0105a0002c0002t0002g0110a0002c0002t0002g0278 | 3 | HG00323.hp2 HG01123.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1498-129C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 8/10 | chr12 | 4763823 | ||||||
| chr12:4764071
|
C | T | 9 | a0001c0001t0001g0286a0003c0003t0001g0018a0003c0003t0001g0104others(6): Show | 10 | HG02258.hp1 HG02280.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1593+24C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 9/10 | chr12 | 4764071 | ||||||
| chr12:4764300
|
G | C | 2 | a0008c0009t0002g0028a0008c0009t0002g0029 | 2 | HG01952.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1593+253G>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 9/10 | chr12 | 4764300 | ||||||
| chr12:4764316
|
A | G | 1 | a0001c0001t0001g0032 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1593+269A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 9/10 | chr12 | 4764316 | ||||||
| chr12:4764409
|
G | A | 10 | a0001c0001t0001g0032a0001c0001t0001g0286a0003c0003t0001g0018others(7): Show | 11 | HG02258.hp1 HG02280.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1593+362G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 9/10 | chr12 | 4764409 | ||||||
| chr12:4764524
|
CAG | C | 89 | a0002c0002t0001g0008a0002c0002t0001g0102a0002c0002t0002g0001others(86): Show | 109 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.1593+478_1593+479d others(4): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 9/10 | chr12 | 4764524 | ||||||
| chr12:4764530
|
A | AT | 46 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0025others(43): Show | 49 | HG00544.hp1 HG00558.hp1 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.1593+514dupT | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 4764530 | |||||
| chr12:4764530
|
A | ATT | 9 | a0001c0001t0001g0196a0001c0001t0001g0201a0001c0001t0001g0241others(6): Show | 9 | HG00733.hp1 HG01070.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1593+513_1593+514d others(4): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 4764530 | |||||
| chr12:4764530
|
A | ATTTTT | 7 | a0001c0001t0001g0030a0001c0001t0001g0069a0001c0001t0001g0073others(4): Show | 7 | HG01943.hp1 HG02683.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.1593+510_1593+514d others(7): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 4764530 | |||||
| chr12:4764530
|
A | ATTTTTT | 7 | a0001c0001t0001g0061a0001c0001t0001g0067a0001c0001t0001g0084others(4): Show | 7 | HG01106.hp2 HG01884.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.1593+509_1593+514d others(8): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 4764530 | |||||
| chr12:4764530
|
A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0085 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1593+505_1593+514d others(12): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 4764530 | |||||
| chr12:4764530
|
AT | A | 42 | a0001c0001t0001g0004a0001c0001t0001g0062a0001c0001t0001g0063others(39): Show | 45 | HG00639.hp1 HG00733.hp2 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.1593+514delT | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 4764530 | |||||
| chr12:4764530
|
ATTTTTTT others(1): Show |
A | 9 | a0001c0001t0001g0032a0001c0001t0001g0286a0003c0003t0001g0018others(6): Show | 10 | HG02258.hp1 HG02280.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1593+507_1593+514d others(10): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 4764530 | |||||
| chr12:4764530
|
ATTTTTTT others(6): Show |
A | 3 | a0002c0002t0002g0100a0002c0002t0002g0149a0002c0002t0002g0168 | 3 | HG01346.hp2 HG03710.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.1593+502_1593+514d others(15): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 4764530 | |||||
| chr12:4764530
|
ATTTTTTT others(7): Show |
A | 86 | a0002c0002t0001g0008a0002c0002t0001g0102a0002c0002t0002g0001others(83): Show | 106 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(103): Show |
intron_variant | MODIFIER | c.1593+501_1593+514d others(16): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 4764530 | |||||
| chr12:4764560
|
T | C | 1 | a0002c0002t0002g0131 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1593+513T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 9/10 | chr12 | 4764560 | ||||||
| chr12:4764608
|
G | C | 1 | a0001c0001t0003g0011 | 2 | HG01358.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1593+561G>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 9/10 | chr12 | 4764608 | ||||||
| chr12:4764653
|
C | T | 1 | a0013c0019t0008g0275 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1593+606C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 9/10 | chr12 | 4764653 | ||||||
| chr12:4764687
|
G | A | 1 | a0018c0023t0001g0267 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1593+640G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 9/10 | chr12 | 4764687 | ||||||
| chr12:4764719
|
A | AT | 13 | a0001c0014t0001g0217a0002c0002t0002g0100a0002c0020t0002g0144others(10): Show | 13 | HG01884.hp1 HG01891.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1594-646dupT | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 4764719 | |||||
| chr12:4764719
|
A | ATTTT | 14 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0061others(11): Show | 15 | HG00558.hp2 HG01106.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.1594-649_1594-646d others(6): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 4764719 | |||||
| chr12:4764742
|
C | T | 17 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0061others(14): Show | 18 | HG00558.hp2 HG01106.hp2 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.1594-637C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 9/10 | chr12 | 4764742 | ||||||
| chr12:4764768
|
G | A | 89 | a0001c0001t0001g0259a0001c0001t0001g0266a0002c0002t0001g0008others(86): Show | 109 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.1594-611G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 9/10 | chr12 | 4764768 | ||||||
| chr12:4764800
|
C | T | 3 | a0004c0005t0005g0272a0004c0005t0006g0256a0004c0005t0006g0257 | 3 | HG01891.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1594-579C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 9/10 | chr12 | 4764800 | ||||||
| chr12:4764846
|
C | T | 2 | a0001c0001t0002g0224a0001c0022t0002g0251 | 2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1594-533C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 9/10 | chr12 | 4764846 | ||||||
| chr12:4764857
|
AT | A | 295 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(292): Show | 333 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.1594-507delT | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 4764857 | |||||
| chr12:4765015
|
A | G | 1 | a0003c0004t0001g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1594-364A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 9/10 | chr12 | 4765015 | ||||||
| chr12:4765072
|
C | G | 10 | a0001c0001t0001g0032a0001c0001t0001g0286a0003c0003t0001g0018others(7): Show | 11 | HG02258.hp1 HG02280.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1594-307C>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 9/10 | chr12 | 4765072 | ||||||
| chr12:4765098
|
G | A | 3 | a0003c0004t0001g0108a0003c0004t0001g0142a0003c0004t0001g0143 | 3 | HG02280.hp1 HG02922.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1594-281G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 9/10 | chr12 | 4765098 | ||||||
| chr12:4765215
|
G | T | 2 | a0001c0001t0002g0058a0001c0001t0002g0059 | 2 | HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1594-164G>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 9/10 | chr12 | 4765215 | ||||||
| chr12:4765349
|
C | G | 1 | a0013c0019t0008g0275 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1594-30C>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 9/10 | chr12 | 4765349 | ||||||
| chr12:4765352
|
CT | C | 176 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(173): Show | 193 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(190): Show |
splice_region_variant&intron_variant | LOW | c.1594-3delT | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 4765352 | |||||
| chr12:4765352
|
CTT | C | 101 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0030others(98): Show | 122 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(119): Show |
splice_region_variant&intron_variant | LOW | c.1594-4_1594-3delTT | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 4765352 | |||||
| chr12:4765352
|
CTTT | C | 11 | a0001c0001t0001g0061a0002c0002t0002g0105a0002c0002t0002g0115others(8): Show | 11 | HG00323.hp2 HG01943.hp2 HG02258.hp2 others(8): Show |
splice_region_variant&intron_variant | LOW | c.1594-5_1594-3delTT others(1): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 4765352 | |||||
| chr12:4765376
|
T | A | 2 | a0012c0017t0002g0123a0020c0024t0002g0292 | 2 | HG01884.hp1 HG03225.hp1 |
splice_region_variant&intron_variant | LOW | c.1594-3T>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 9/10 | chr12 | 4765376 | ||||||
| chr12:4765576
|
GTTTGTTT others(3): Show |
G | 2 | a0003c0003t0002g0169a0015c0021t0002g0125 | 2 | HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1761+45_1761+54del others(10): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 4765576 | |||||
| chr12:4765671
|
A | G | 2 | a0008c0009t0002g0028a0008c0009t0002g0029 | 2 | HG01952.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1761+125A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4765671 | ||||||
| chr12:4765821
|
G | A | 4 | a0001c0001t0002g0224a0001c0001t0002g0249a0001c0022t0002g0251others(1): Show | 4 | HG02572.hp1 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1761+275G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4765821 | ||||||
| chr12:4765836
|
G | T | 2 | a0012c0017t0002g0123a0020c0024t0002g0292 | 2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1761+290G>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4765836 | ||||||
| chr12:4765921
|
C | T | 2 | a0001c0001t0002g0058a0001c0001t0002g0059 | 2 | HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1761+375C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4765921 | ||||||
| chr12:4766006
|
C | T | 123 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0061others(120): Show | 145 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(142): Show |
intron_variant | MODIFIER | c.1761+460C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4766006 | ||||||
| chr12:4766089
|
T | G | 125 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0061others(122): Show | 147 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(144): Show |
intron_variant | MODIFIER | c.1761+543T>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4766089 | ||||||
| chr12:4766114
|
T | C | 2 | a0008c0009t0002g0028a0008c0009t0002g0029 | 2 | HG01952.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1761+568T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4766114 | ||||||
| chr12:4766168
|
T | G | 128 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0061others(125): Show | 150 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(147): Show |
intron_variant | MODIFIER | c.1761+622T>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4766168 | ||||||
| chr12:4766449
|
G | T | 61 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0062others(58): Show | 67 | HG00544.hp2 HG00639.hp1 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.1761+903G>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4766449 | ||||||
| chr12:4766577
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1761+1031C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4766577 | ||||||
| chr12:4766697
|
A | G | 3 | a0001c0001t0004g0014a0001c0001t0004g0049a0019c0025t0004g0014 | 3 | HG03491.hp2 HG03492.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1761+1151A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4766697 | ||||||
| chr12:4766765
|
A | G | 1 | a0002c0002t0002g0128 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1761+1219A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4766765 | ||||||
| chr12:4766771
|
C | T | 4 | a0001c0001t0001g0253a0001c0001t0001g0254a0003c0004t0001g0107others(1): Show | 4 | HG01884.hp2 HG02451.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1761+1225C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4766771 | ||||||
| chr12:4766846
|
T | C | 1 | a0002c0002t0002g0146 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1761+1300T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4766846 | ||||||
| chr12:4766867
|
C | G | 104 | a0001c0001t0002g0027a0001c0001t0002g0058a0001c0001t0002g0059others(101): Show | 125 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(122): Show |
intron_variant | MODIFIER | c.1761+1321C>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4766867 | ||||||
| chr12:4767096
|
T | C | 17 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0061others(14): Show | 18 | HG00558.hp2 HG01106.hp2 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.1761+1550T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4767096 | ||||||
| chr12:4767156
|
T | C | 2 | a0001c0001t0001g0233a0001c0001t0001g0236 | 2 | NA18989.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1761+1610T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4767156 | ||||||
| chr12:4767157
|
C | T | 1 | a0012c0017t0002g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1761+1611C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4767157 | ||||||
| chr12:4767196
|
G | A | 3 | a0007c0008t0001g0188a0007c0008t0001g0208a0007c0008t0001g0209 | 3 | HG01109.hp2 HG02109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1761+1650G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4767196 | ||||||
| chr12:4767322
|
G | A | 1 | a0002c0020t0002g0144 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1761+1776G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4767322 | ||||||
| chr12:4767484
|
A | G | 4 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0082others(1): Show | 4 | HG02080.hp2 NA18953.hp2 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.1761+1938A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4767484 | ||||||
| chr12:4767519
|
G | A | 1 | a0013c0019t0008g0275 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1761+1973G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4767519 | ||||||
| chr12:4767597
|
C | T | 6 | a0004c0005t0005g0252a0004c0005t0005g0271a0004c0005t0005g0272others(3): Show | 6 | HG01891.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1761+2051C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4767597 | ||||||
| chr12:4767620
|
A | G | 1 | a0003c0004t0001g0142 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1761+2074A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4767620 | ||||||
| chr12:4767850
|
T | C | 2 | a0001c0001t0001g0202a0001c0001t0001g0240 | 2 | NA18994.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1761+2304T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4767850 | ||||||
| chr12:4767871
|
C | T | 1 | a0002c0002t0002g0120 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1761+2325C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4767871 | ||||||
| chr12:4767932
|
A | G | 1 | a0012c0017t0002g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1761+2386A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4767932 | ||||||
| chr12:4767974
|
C | A | 2 | a0002c0002t0007g0138a0002c0002t0007g0139 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1761+2428C>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4767974 | ||||||
| chr12:4767989
|
T | C | 87 | a0002c0002t0001g0008a0002c0002t0001g0102a0002c0002t0002g0001others(84): Show | 107 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(104): Show |
intron_variant | MODIFIER | c.1761+2443T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4767989 | ||||||
| chr12:4768086
|
A | G | 1 | a0002c0002t0002g0149 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1761+2540A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4768086 | ||||||
| chr12:4768317
|
A | G | 1 | a0001c0001t0001g0225 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1761+2771A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4768317 | ||||||
| chr12:4768517
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1761+2971C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4768517 | ||||||
| chr12:4768523
|
C | G | 13 | a0001c0001t0002g0027a0001c0001t0002g0058a0001c0001t0002g0059others(10): Show | 14 | HG00642.hp2 HG00733.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.1761+2977C>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4768523 | ||||||
| chr12:4768635
|
T | C | 1 | a0001c0001t0001g0259 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1761+3089T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4768635 | ||||||
| chr12:4768802
|
G | C | 1 | a0002c0002t0002g0006 | 3 | HG00738.hp2 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1761+3256G>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4768802 | ||||||
| chr12:4768880
|
G | T | 1 | a0002c0002t0002g0116 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1761+3334G>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4768880 | ||||||
| chr12:4768881
|
T | TACTTTGT others(32): Show |
1 | a0002c0002t0002g0116 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1761+3335_1761+333 others(43): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4768881 | ||||||
| chr12:4768901
|
A | C | 1 | a0002c0002t0002g0116 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1761+3355A>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4768901 | ||||||
| chr12:4768903
|
T | A | 1 | a0002c0002t0002g0116 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1761+3357T>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4768903 | ||||||
| chr12:4768918
|
G | C | 2 | a0002c0020t0002g0144a0005c0006t0002g0060 | 2 | HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1761+3372G>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4768918 | ||||||
| chr12:4768928
|
T | A | 1 | a0002c0002t0002g0116 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1761+3382T>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4768928 | ||||||
| chr12:4768936
|
T | A | 1 | a0002c0002t0002g0116 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1761+3390T>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4768936 | ||||||
| chr12:4768955
|
T | C | 1 | a0002c0002t0002g0116 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1761+3409T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4768955 | ||||||
| chr12:4768956
|
C | T | 1 | a0002c0002t0002g0116 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1761+3410C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4768956 | ||||||
| chr12:4768963
|
T | A | 1 | a0002c0002t0002g0116 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1761+3417T>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4768963 | ||||||
| chr12:4768968
|
T | A | 1 | a0002c0002t0002g0116 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1761+3422T>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4768968 | ||||||
| chr12:4769007
|
A | C | 1 | a0002c0002t0002g0116 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1762-3438A>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4769007 | ||||||
| chr12:4769118
|
A | C | 1 | a0002c0002t0002g0116 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1762-3327A>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4769118 | ||||||
| chr12:4769225
|
T | A | 1 | a0002c0002t0002g0116 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1762-3220T>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4769225 | ||||||
| chr12:4769241
|
T | C | 2 | a0002c0020t0002g0144a0005c0006t0002g0060 | 2 | HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1762-3204T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4769241 | ||||||
| chr12:4769242
|
G | T | 1 | a0002c0002t0002g0116 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1762-3203G>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4769242 | ||||||
| chr12:4769256
|
T | G | 1 | a0002c0002t0002g0116 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1762-3189T>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4769256 | ||||||
| chr12:4769257
|
G | T | 1 | a0002c0002t0002g0116 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1762-3188G>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4769257 | ||||||
| chr12:4769371
|
A | C | 1 | a0002c0002t0002g0116 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1762-3074A>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4769371 | ||||||
| chr12:4769410
|
T | G | 103 | a0001c0001t0002g0027a0001c0001t0002g0058a0001c0001t0002g0059others(100): Show | 124 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(121): Show |
intron_variant | MODIFIER | c.1762-3035T>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4769410 | ||||||
| chr12:4769527
|
A | C | 1 | a0002c0002t0002g0116 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1762-2918A>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4769527 | ||||||
| chr12:4769542
|
T | A | 1 | a0002c0002t0002g0116 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1762-2903T>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4769542 | ||||||
| chr12:4769548
|
A | C | 1 | a0002c0002t0002g0116 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1762-2897A>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4769548 | ||||||
| chr12:4769554
|
A | C | 1 | a0002c0002t0002g0116 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1762-2891A>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4769554 | ||||||
| chr12:4769555
|
T | A | 1 | a0002c0002t0002g0116 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1762-2890T>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4769555 | ||||||
| chr12:4769566
|
T | C | 1 | a0002c0002t0002g0116 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1762-2879T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4769566 | ||||||
| chr12:4769829
|
G | A | 2 | a0001c0001t0001g0066a0001c0001t0001g0072 | 2 | HG02074.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.1762-2616G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4769829 | ||||||
| chr12:4769931
|
T | A | 1 | a0002c0002t0002g0116 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1762-2514T>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4769931 | ||||||
| chr12:4770020
|
C | T | 1 | a0018c0023t0001g0267 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1762-2425C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4770020 | ||||||
| chr12:4770036
|
C | A | 1 | a0002c0002t0002g0165 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1762-2409C>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4770036 | ||||||
| chr12:4770048
|
C | T | 1 | a0002c0002t0002g0122 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1762-2397C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4770048 | ||||||
| chr12:4770090
|
T | C | 4 | a0001c0001t0001g0253a0001c0001t0001g0254a0003c0004t0001g0107others(1): Show | 4 | HG01884.hp2 HG02451.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1762-2355T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4770090 | ||||||
| chr12:4770160
|
G | T | 1 | a0002c0002t0002g0116 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1762-2285G>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4770160 | ||||||
| chr12:4770162
|
T | C | 111 | a0001c0001t0002g0027a0001c0001t0002g0058a0001c0001t0002g0059others(108): Show | 132 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(129): Show |
intron_variant | MODIFIER | c.1762-2283T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4770162 | ||||||
| chr12:4770295
|
G | C | 111 | a0001c0001t0002g0027a0001c0001t0002g0058a0001c0001t0002g0059others(108): Show | 132 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(129): Show |
intron_variant | MODIFIER | c.1762-2150G>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4770295 | ||||||
| chr12:4770309
|
AAAAAAAA others(4): Show |
A | 1 | a0002c0002t0002g0116 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1762-2129_1762-211 others(15): Show |
GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 4770309 | |||||
| chr12:4770313
|
A | C | 3 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0002g0287 | 3 | HG00642.hp2 HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1762-2132A>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4770313 | ||||||
| chr12:4770320
|
C | A | 1 | a0002c0002t0002g0100 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1762-2125C>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4770320 | ||||||
| chr12:4770321
|
A | C | 1 | a0002c0002t0002g0100 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1762-2124A>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4770321 | ||||||
| chr12:4770324
|
A | C | 2 | a0001c0001t0001g0202a0001c0001t0001g0240 | 2 | NA18994.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1762-2121A>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4770324 | ||||||
| chr12:4770328
|
A | G | 6 | a0004c0005t0005g0252a0004c0005t0005g0271a0004c0005t0005g0272others(3): Show | 6 | HG01891.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1762-2117A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4770328 | ||||||
| chr12:4770505
|
A | G | 6 | a0004c0005t0005g0252a0004c0005t0005g0271a0004c0005t0005g0272others(3): Show | 6 | HG01891.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1762-1940A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4770505 | ||||||
| chr12:4770650
|
A | T | 2 | a0003c0003t0002g0169a0015c0021t0002g0125 | 2 | HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1762-1795A>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4770650 | ||||||
| chr12:4770716
|
G | A | 2 | a0002c0002t0007g0138a0002c0002t0007g0139 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1762-1729G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4770716 | ||||||
| chr12:4770942
|
T | C | 1 | a0001c0001t0001g0215 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1762-1503T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4770942 | ||||||
| chr12:4771094
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1762-1351G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4771094 | ||||||
| chr12:4771147
|
C | T | 3 | a0001c0001t0001g0193a0002c0020t0002g0144a0005c0006t0002g0060 | 3 | HG02622.hp1 HG02976.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1762-1298C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4771147 | ||||||
| chr12:4771324
|
C | T | 4 | a0001c0001t0002g0224a0001c0001t0002g0249a0001c0022t0002g0251others(1): Show | 4 | HG02572.hp1 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1762-1121C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4771324 | ||||||
| chr12:4771364
|
G | A | 2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | HG01884.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1762-1081G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4771364 | ||||||
| chr12:4771400
|
G | A | 86 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(83): Show | 97 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.1762-1045G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4771400 | ||||||
| chr12:4771459
|
T | C | 1 | a0001c0001t0001g0238 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1762-986T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4771459 | ||||||
| chr12:4771598
|
T | C | 109 | a0001c0001t0002g0027a0001c0001t0002g0058a0001c0001t0002g0059others(106): Show | 128 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(125): Show |
intron_variant | MODIFIER | c.1762-847T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4771598 | ||||||
| chr12:4771687
|
A | G | 1 | a0001c0001t0001g0083 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1762-758A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4771687 | ||||||
| chr12:4771704
|
C | T | 1 | a0001c0001t0001g0061 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1762-741C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4771704 | ||||||
| chr12:4771714
|
G | C | 17 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0061others(14): Show | 18 | HG00558.hp2 HG01106.hp2 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.1762-731G>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4771714 | ||||||
| chr12:4771719
|
G | A | 1 | a0001c0001t0001g0097 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1762-726G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4771719 | ||||||
| chr12:4771771
|
C | T | 1 | a0001c0001t0003g0056 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1762-674C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4771771 | ||||||
| chr12:4771878
|
G | A | 8 | a0002c0002t0002g0002a0002c0002t0002g0109a0002c0002t0002g0120others(5): Show | 11 | HG00741.hp2 HG01106.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1762-567G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4771878 | ||||||
| chr12:4771879
|
A | T | 126 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0061others(123): Show | 146 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.1762-566A>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4771879 | ||||||
| chr12:4771900
|
A | G | 2 | a0001c0001t0001g0073a0001c0001t0001g0089 | 2 | HG02683.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1762-545A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4771900 | ||||||
| chr12:4771947
|
G | A | 1 | a0005c0006t0002g0031 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1762-498G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4771947 | ||||||
| chr12:4771965
|
G | C | 1 | a0001c0001t0001g0032 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1762-480G>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4771965 | ||||||
| chr12:4771969
|
C | T | 87 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0003others(84): Show | 105 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.1762-476C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4771969 | ||||||
| chr12:4772103
|
C | T | 1 | a0002c0002t0002g0119 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1762-342C>T | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4772103 | ||||||
| chr12:4772341
|
T | C | 4 | a0001c0001t0002g0058a0001c0001t0002g0059a0012c0017t0002g0123others(1): Show | 4 | HG01884.hp1 HG02647.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1762-104T>C | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4772341 | ||||||
| chr12:4772351
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1762-94A>G | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4772351 | ||||||
| chr12:4772406
|
G | A | 1 | a0002c0002t0002g0109 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1762-39G>A | GALNT8 | ENSG00000130035.9 | transcript | ENST00000252318.7 | protein_coding | 10/10 | chr12 | 4772406 |