Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79158 |
| ensemblid | ENSG00000111670.16 |
| hgncid | 29670 |
| symbol | GNPTAB |
| name | N-acetylglucosamine-1-phosphate transferase subunits alpha and beta |
| refseq_nuc | NM_024312.5 |
| refseq_prot | NP_077288.2 |
| ensembl_nuc | ENST00000299314.12 |
| ensembl_prot | ENSP00000299314.7 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 101745499 |
| end | 101830959 |
| strand | - |
| ver | v1.2 |
| region | chr12:101745499-101830959 |
| region5000 | chr12:101740499-101835959 |
| regionname0 | GNPTAB_chr12_101745499_101830959 |
| regionname5000 | GNPTAB_chr12_101740499_101835959 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1256 | 361 | 73 | 56 | 190 | 11 | 29 | 150 | GNPTAB_chr12_101740499_101835959 | GNPTAB | MLFKL others(1251): Show |
chr12 | 101740499 | 101835959 |
| a0002 | 0/0 | 1256 | 7 | 5 | 1 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | MLFKL others(1251): Show |
chr12 | 101740499 | 101835959 |
| a0003 | 0/0 | 1256 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | MLFKL others(1251): Show |
chr12 | 101740499 | 101835959 |
| a0004 | 0/0 | 1256 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | MLFKL others(1251): Show |
chr12 | 101740499 | 101835959 |
| a0005 | 0/0 | 1256 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | MLFKL others(1251): Show |
chr12 | 101740499 | 101835959 |
| a0006 | 0/0 | 1256 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | MLFKL others(1251): Show |
chr12 | 101740499 | 101835959 |
| a0007 | 0/0 | 1256 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | MLFKL others(1251): Show |
chr12 | 101740499 | 101835959 |
| a0008 | 0/0 | 1256 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | MLFKL others(1251): Show |
chr12 | 101740499 | 101835959 |
| a0009 | 0/0 | 1256 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | MLFKL others(1251): Show |
chr12 | 101740499 | 101835959 |
| a0010 | 0/0 | 1256 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | MLFKL others(1251): Show |
chr12 | 101740499 | 101835959 |
| a0011 | 0/0 | 1256 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GNPTAB_chr12_101740499_101835959 | GNPTAB | MLFKL others(1251): Show |
chr12 | 101740499 | 101835959 |
| a0012 | 0/0 | 1256 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GNPTAB_chr12_101740499_101835959 | GNPTAB | MLFKL others(1251): Show |
chr12 | 101740499 | 101835959 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 3768 | 198 | 32 | 22 | 120 | 6 | 18 | GNPTAB_chr12_101740499_101835959 | GNPTAB | ATGCT others(3763): Show |
chr12 | 101740499 | 101835959 | ||
| a0001c0002 | 1/1 | 3768 | 87 | 27 | 23 | 23 | 4 | 8 | GNPTAB_chr12_101740499_101835959 | GNPTAB | ATGCT others(3763): Show |
chr12 | 101740499 | 101835959 | ||
| a0001c0003 | 0/0 | 3768 | 50 | 0 | 9 | 39 | 1 | 1 | GNPTAB_chr12_101740499_101835959 | GNPTAB | ATGCT others(3763): Show |
chr12 | 101740499 | 101835959 | ||
| a0001c0004 | 0/0 | 3768 | 7 | 5 | 2 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | ATGCT others(3763): Show |
chr12 | 101740499 | 101835959 | ||
| a0001c0007 | 0/0 | 3768 | 6 | 6 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | ATGCT others(3763): Show |
chr12 | 101740499 | 101835959 | ||
| a0001c0008 | 0/0 | 3768 | 6 | 0 | 0 | 6 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | ATGCT others(3763): Show |
chr12 | 101740499 | 101835959 | ||
| a0001c0013 | 0/0 | 3768 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | ATGCT others(3763): Show |
chr12 | 101740499 | 101835959 | ||
| a0001c0014 | 0/0 | 3768 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | ATGCT others(3763): Show |
chr12 | 101740499 | 101835959 | ||
| a0001c0015 | 0/0 | 3768 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | ATGCT others(3763): Show |
chr12 | 101740499 | 101835959 | ||
| a0001c0022 | 0/0 | 3768 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTAB_chr12_101740499_101835959 | GNPTAB | ATGCT others(3763): Show |
chr12 | 101740499 | 101835959 | ||
| a0001c0023 | 0/0 | 3768 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | ATGCT others(3763): Show |
chr12 | 101740499 | 101835959 | ||
| a0001c0024 | 0/0 | 3768 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTAB_chr12_101740499_101835959 | GNPTAB | ATGCT others(3763): Show |
chr12 | 101740499 | 101835959 | ||
| a0001c0025 | 0/0 | 3768 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | ATGCT others(3763): Show |
chr12 | 101740499 | 101835959 | ||
| a0002c0009 | 0/0 | 3768 | 5 | 5 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | ATGCT others(3763): Show |
chr12 | 101740499 | 101835959 | ||
| a0002c0012 | 0/0 | 3768 | 2 | 0 | 1 | 0 | 1 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | ATGCT others(3763): Show |
chr12 | 101740499 | 101835959 | ||
| a0003c0005 | 0/0 | 3768 | 7 | 7 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | ATGCT others(3763): Show |
chr12 | 101740499 | 101835959 | ||
| a0004c0006 | 0/0 | 3768 | 6 | 5 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | ATGCT others(3763): Show |
chr12 | 101740499 | 101835959 | ||
| a0005c0010 | 0/0 | 3768 | 2 | 0 | 2 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | ATGCT others(3763): Show |
chr12 | 101740499 | 101835959 | ||
| a0006c0016 | 0/0 | 3768 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | ATGCT others(3763): Show |
chr12 | 101740499 | 101835959 | ||
| a0006c0017 | 0/0 | 3768 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | ATGCT others(3763): Show |
chr12 | 101740499 | 101835959 | ||
| a0007c0011 | 0/0 | 3768 | 2 | 2 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | ATGCT others(3763): Show |
chr12 | 101740499 | 101835959 | ||
| a0008c0018 | 0/0 | 3768 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | ATGCT others(3763): Show |
chr12 | 101740499 | 101835959 | ||
| a0009c0019 | 0/0 | 3768 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | ATGCT others(3763): Show |
chr12 | 101740499 | 101835959 | ||
| a0010c0026 | 0/0 | 3768 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTAB_chr12_101740499_101835959 | GNPTAB | ATGCT others(3763): Show |
chr12 | 101740499 | 101835959 | ||
| a0011c0020 | 0/0 | 3768 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | ATGCT others(3763): Show |
chr12 | 101740499 | 101835959 | ||
| a0012c0021 | 0/0 | 3768 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | ATGCT others(3763): Show |
chr12 | 101740499 | 101835959 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5717 | 90 | 20 | 17 | 42 | 3 | 8 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5712): Show |
chr12 | 101740499 | 101835959 |
| a0001c0001t0002 | 0/0 | 5720 | 13 | 0 | 0 | 13 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5715): Show |
chr12 | 101740499 | 101835959 |
| a0001c0001t0003 | 0/0 | 5719 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5714): Show |
chr12 | 101740499 | 101835959 |
| a0001c0001t0004 | 0/0 | 5717 | 35 | 0 | 0 | 33 | 0 | 2 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5712): Show |
chr12 | 101740499 | 101835959 |
| a0001c0001t0005 | 0/0 | 5717 | 23 | 0 | 1 | 20 | 1 | 1 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5712): Show |
chr12 | 101740499 | 101835959 |
| a0001c0001t0006 | 0/0 | 5717 | 14 | 2 | 3 | 1 | 2 | 6 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5712): Show |
chr12 | 101740499 | 101835959 |
| a0001c0001t0007 | 0/0 | 5717 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5712): Show |
chr12 | 101740499 | 101835959 |
| a0001c0001t0009 | 0/0 | 5717 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5712): Show |
chr12 | 101740499 | 101835959 |
| a0001c0001t0010 | 0/0 | 5717 | 4 | 4 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5712): Show |
chr12 | 101740499 | 101835959 |
| a0001c0001t0011 | 0/0 | 5720 | 4 | 0 | 0 | 4 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5715): Show |
chr12 | 101740499 | 101835959 |
| a0001c0001t0012 | 0/0 | 5751 | 2 | 0 | 0 | 2 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5746): Show |
chr12 | 101740499 | 101835959 |
| a0001c0001t0015 | 0/0 | 5717 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5712): Show |
chr12 | 101740499 | 101835959 |
| a0001c0001t0016 | 0/0 | 5717 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5712): Show |
chr12 | 101740499 | 101835959 |
| a0001c0001t0018 | 0/0 | 5717 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5712): Show |
chr12 | 101740499 | 101835959 |
| a0001c0001t0019 | 0/0 | 5720 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5715): Show |
chr12 | 101740499 | 101835959 |
| a0001c0001t0020 | 0/0 | 5720 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5715): Show |
chr12 | 101740499 | 101835959 |
| a0001c0001t0021 | 0/0 | 5717 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5712): Show |
chr12 | 101740499 | 101835959 |
| a0001c0001t0022 | 0/0 | 5717 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5712): Show |
chr12 | 101740499 | 101835959 |
| a0001c0001t0023 | 0/0 | 5717 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5712): Show |
chr12 | 101740499 | 101835959 |
| a0001c0001t0024 | 0/0 | 5717 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5712): Show |
chr12 | 101740499 | 101835959 |
| a0001c0001t0025 | 0/0 | 5717 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5712): Show |
chr12 | 101740499 | 101835959 |
| a0001c0002t0001 | 0/1 | 5717 | 10 | 7 | 1 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5712): Show |
chr12 | 101740499 | 101835959 |
| a0001c0002t0002 | 1/0 | 5720 | 54 | 11 | 16 | 14 | 4 | 8 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5715): Show |
chr12 | 101740499 | 101835959 |
| a0001c0002t0005 | 0/0 | 5717 | 15 | 1 | 6 | 8 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5712): Show |
chr12 | 101740499 | 101835959 |
| a0001c0002t0008 | 0/0 | 5718 | 8 | 8 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5713): Show |
chr12 | 101740499 | 101835959 |
| a0001c0003t0003 | 0/0 | 5719 | 49 | 0 | 9 | 38 | 1 | 1 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5714): Show |
chr12 | 101740499 | 101835959 |
| a0001c0003t0004 | 0/0 | 5717 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5712): Show |
chr12 | 101740499 | 101835959 |
| a0001c0004t0001 | 0/0 | 5717 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5712): Show |
chr12 | 101740499 | 101835959 |
| a0001c0004t0006 | 0/0 | 5717 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5712): Show |
chr12 | 101740499 | 101835959 |
| a0001c0004t0007 | 0/0 | 5717 | 5 | 4 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5712): Show |
chr12 | 101740499 | 101835959 |
| a0001c0007t0004 | 0/0 | 5717 | 2 | 2 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5712): Show |
chr12 | 101740499 | 101835959 |
| a0001c0007t0009 | 0/0 | 5717 | 4 | 4 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5712): Show |
chr12 | 101740499 | 101835959 |
| a0001c0008t0004 | 0/0 | 5717 | 6 | 0 | 0 | 6 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5712): Show |
chr12 | 101740499 | 101835959 |
| a0001c0013t0003 | 0/0 | 5719 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5714): Show |
chr12 | 101740499 | 101835959 |
| a0001c0014t0001 | 0/0 | 5717 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5712): Show |
chr12 | 101740499 | 101835959 |
| a0001c0015t0008 | 0/0 | 5718 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5713): Show |
chr12 | 101740499 | 101835959 |
| a0001c0022t0006 | 0/0 | 5717 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5712): Show |
chr12 | 101740499 | 101835959 |
| a0001c0023t0001 | 0/0 | 5717 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5712): Show |
chr12 | 101740499 | 101835959 |
| a0001c0024t0004 | 0/0 | 5717 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5712): Show |
chr12 | 101740499 | 101835959 |
| a0001c0025t0001 | 0/0 | 5717 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5712): Show |
chr12 | 101740499 | 101835959 |
| a0002c0009t0001 | 0/0 | 5717 | 5 | 5 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5712): Show |
chr12 | 101740499 | 101835959 |
| a0002c0012t0001 | 0/0 | 5717 | 1 | 0 | 0 | 0 | 1 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5712): Show |
chr12 | 101740499 | 101835959 |
| a0002c0012t0002 | 0/0 | 5720 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5715): Show |
chr12 | 101740499 | 101835959 |
| a0003c0005t0001 | 0/0 | 5717 | 6 | 6 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5712): Show |
chr12 | 101740499 | 101835959 |
| a0003c0005t0017 | 0/0 | 5717 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5712): Show |
chr12 | 101740499 | 101835959 |
| a0004c0006t0007 | 0/0 | 5717 | 5 | 5 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5712): Show |
chr12 | 101740499 | 101835959 |
| a0004c0006t0014 | 0/0 | 5705 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5700): Show |
chr12 | 101740499 | 101835959 |
| a0005c0010t0003 | 0/0 | 5719 | 2 | 0 | 2 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5714): Show |
chr12 | 101740499 | 101835959 |
| a0006c0016t0013 | 0/0 | 5717 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5712): Show |
chr12 | 101740499 | 101835959 |
| a0006c0017t0013 | 0/0 | 5717 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5712): Show |
chr12 | 101740499 | 101835959 |
| a0007c0011t0002 | 0/0 | 5720 | 2 | 2 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5715): Show |
chr12 | 101740499 | 101835959 |
| a0008c0018t0001 | 0/0 | 5717 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5712): Show |
chr12 | 101740499 | 101835959 |
| a0009c0019t0002 | 0/0 | 5720 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5715): Show |
chr12 | 101740499 | 101835959 |
| a0010c0026t0005 | 0/0 | 5717 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5712): Show |
chr12 | 101740499 | 101835959 |
| a0011c0020t0002 | 0/0 | 5720 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5715): Show |
chr12 | 101740499 | 101835959 |
| a0012c0021t0004 | 0/0 | 5717 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | GCAGC others(5712): Show |
chr12 | 101740499 | 101835959 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0001g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0004g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0004g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0004g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0004g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0004g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0004g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0005g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0005g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0005g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0005g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0005g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0005g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0005g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0005g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0005g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0005g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0005g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0005g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0005g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0005g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0005g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0005g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0005g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0005g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0005g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0005g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0005g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0005g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0005g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0006g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0006g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0006g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0006g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0006g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0006g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0006g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0006g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0006g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0006g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0006g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0006g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0006g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0006g0351 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0007g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0009g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0010g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0010g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0010g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0010g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0011g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0011g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0011g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0011g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0012g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0012g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0015g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0016g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0018g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0019g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0020g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0021g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0022g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0023g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0024g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0001t0025g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0001g0222 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0108 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0005g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0005g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0005g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0005g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0005g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0005g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0005g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0005g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0005g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0005g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0005g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0005g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0005g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0005g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0008g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0008g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0008g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0008g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0008g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0008g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0008g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0002t0008g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0003t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0004t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0004t0006g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0004t0007g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0004t0007g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0004t0007g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0004t0007g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0004t0007g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0007t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0007t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0007t0009g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0007t0009g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0007t0009g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0007t0009g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0008t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0008t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0008t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0008t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0008t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0008t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0013t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0014t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0015t0008g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0022t0006g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0023t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0024t0004g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0001c0025t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0002c0009t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0002c0009t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0002c0009t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0002c0009t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0002c0009t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0002c0012t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0002c0012t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0003c0005t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0003c0005t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0003c0005t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0003c0005t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0003c0005t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0003c0005t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0003c0005t0017g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0004c0006t0007g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0004c0006t0007g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0004c0006t0007g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0004c0006t0007g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0004c0006t0007g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0004c0006t0014g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0005c0010t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0005c0010t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0006c0016t0013g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0006c0017t0013g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0007c0011t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0007c0011t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0008c0018t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0009c0019t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0010c0026t0005g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0011c0020t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| a0012c0021t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0003 | t0003 | g0178 | EUR | GBR | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0102 | EUR | GBR | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG00280 | hp1 | a0002 | c0012 | t0001 | g0214 | EUR | FIN | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG00280 | hp2 | a0001 | c0002 | t0002 | g0003 | EUR | FIN | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG00323 | hp1 | a0001 | c0001 | t0006 | g0224 | EUR | FIN | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0096 | EUR | FIN | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | CHS | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG00408 | hp2 | a0001 | c0001 | t0006 | g0225 | EAS | CHS | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0247 | EAS | CHS | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | CHS | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG00544 | hp1 | a0001 | c0008 | t0004 | g0269 | EAS | CHS | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG00544 | hp2 | a0001 | c0003 | t0003 | g0170 | EAS | CHS | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG00558 | hp1 | a0001 | c0001 | t0012 | g0132 | EAS | CHS | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0128 | EAS | CHS | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG00597 | hp1 | a0001 | c0008 | t0004 | g0216 | EAS | CHS | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG00597 | hp2 | a0001 | c0003 | t0003 | g0172 | EAS | CHS | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | CHS | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG00609 | hp2 | a0001 | c0003 | t0003 | g0145 | EAS | CHS | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | CHS | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG00621 | hp2 | a0001 | c0003 | t0003 | g0174 | EAS | CHS | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0359 | AMR | PUR | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0120 | AMR | PUR | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG00741 | hp1 | a0002 | c0012 | t0002 | g0077 | AMR | PUR | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG00741 | hp2 | a0001 | c0001 | t0006 | g0221 | AMR | PUR | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01070 | hp1 | a0001 | c0002 | t0002 | g0110 | AMR | PUR | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01070 | hp2 | a0005 | c0010 | t0003 | g0180 | AMR | PUR | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0103 | AMR | PUR | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01071 | hp2 | a0005 | c0010 | t0003 | g0179 | AMR | PUR | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01081 | hp1 | a0001 | c0004 | t0007 | g0190 | AMR | PUR | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | PUR | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01099 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01106 | hp1 | a0001 | c0001 | t0005 | g0041 | AMR | PUR | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01106 | hp2 | a0001 | c0003 | t0003 | g0152 | AMR | PUR | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01109 | hp1 | a0001 | c0004 | t0006 | g0203 | AMR | PUR | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01109 | hp2 | a0001 | c0002 | t0002 | g0066 | AMR | PUR | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0340 | AMR | PUR | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01167 | hp2 | a0001 | c0001 | t0009 | g0052 | AMR | PUR | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01168 | hp1 | a0001 | c0001 | t0006 | g0228 | AMR | PUR | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0121 | AMR | PUR | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01169 | hp1 | a0001 | c0002 | t0002 | g0123 | AMR | PUR | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0341 | AMR | PUR | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01175 | hp2 | a0001 | c0003 | t0003 | g0167 | AMR | PUR | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01192 | hp1 | a0001 | c0002 | t0002 | g0101 | AMR | PUR | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | PUR | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | PUR | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01243 | hp2 | a0004 | c0006 | t0014 | g0006 | AMR | PUR | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01255 | hp1 | a0001 | c0002 | t0002 | g0126 | AMR | CLM | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01255 | hp2 | a0001 | c0001 | t0006 | g0218 | AMR | CLM | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0329 | AMR | CLM | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | CLM | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01258 | hp1 | a0008 | c0018 | t0001 | g0296 | AMR | CLM | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | CLM | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0119 | AMR | CLM | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01346 | hp2 | a0001 | c0003 | t0003 | g0184 | AMR | CLM | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01358 | hp1 | a0001 | c0003 | t0003 | g0183 | AMR | CLM | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01358 | hp2 | a0009 | c0019 | t0002 | g0064 | AMR | CLM | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | CLM | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0072 | AMR | CLM | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01433 | hp1 | a0001 | c0003 | t0003 | g0166 | AMR | CLM | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | CLM | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0300 | EUR | IBS | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01515 | hp2 | a0001 | c0001 | t0006 | g0351 | EUR | IBS | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0317 | EUR | IBS | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01516 | hp2 | a0001 | c0001 | t0005 | g0010 | EUR | IBS | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01884 | hp1 | a0001 | c0002 | t0008 | g0212 | AFR | ACB | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0079 | AFR | ACB | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0380 | AFR | ACB | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01891 | hp2 | a0004 | c0006 | t0007 | g0193 | AFR | ACB | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01928 | hp1 | a0001 | c0002 | t0002 | g0075 | AMR | PEL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01928 | hp2 | a0001 | c0003 | t0003 | g0165 | AMR | PEL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01943 | hp1 | a0001 | c0003 | t0003 | g0136 | AMR | PEL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | PEL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01975 | hp1 | a0001 | c0003 | t0003 | g0181 | AMR | PEL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | PEL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01981 | hp1 | a0001 | c0002 | t0005 | g0029 | AMR | PEL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PEL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01993 | hp1 | a0001 | c0002 | t0005 | g0027 | AMR | PEL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0332 | AMR | PEL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0375 | EAS | KHV | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02027 | hp2 | a0001 | c0003 | t0003 | g0173 | EAS | KHV | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02040 | hp1 | a0001 | c0001 | t0022 | g0343 | EAS | KHV | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02040 | hp2 | a0001 | c0003 | t0003 | g0151 | EAS | KHV | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02055 | hp1 | a0004 | c0006 | t0007 | g0187 | AFR | ACB | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02056 | hp1 | a0001 | c0008 | t0004 | g0260 | EAS | KHV | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02056 | hp2 | a0001 | c0003 | t0003 | g0155 | EAS | KHV | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | KHV | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | KHV | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02080 | hp1 | a0001 | c0003 | t0003 | g0137 | EAS | KHV | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0113 | EAS | KHV | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02129 | hp1 | a0001 | c0002 | t0002 | g0124 | EAS | KHV | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0354 | EAS | KHV | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0267 | EAS | KHV | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0097 | EAS | KHV | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0242 | EAS | KHV | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | KHV | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02145 | hp1 | a0001 | c0002 | t0008 | g0210 | AFR | ACB | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02145 | hp2 | a0001 | c0002 | t0002 | g0073 | AFR | ACB | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02148 | hp1 | a0001 | c0002 | t0005 | g0036 | AMR | PEL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | PEL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0266 | EAS | CDX | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02155 | hp2 | a0001 | c0003 | t0003 | g0186 | EAS | CDX | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0098 | EAS | CDX | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0246 | EAS | CDX | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02257 | hp1 | a0001 | c0001 | t0010 | g0043 | AFR | ACB | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0382 | AFR | ACB | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02258 | hp1 | a0002 | c0009 | t0001 | g0200 | AFR | ACB | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02258 | hp2 | a0001 | c0001 | t0015 | g0019 | AFR | ACB | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02273 | hp1 | a0001 | c0002 | t0005 | g0030 | AMR | PEL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0319 | AMR | PEL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0362 | AFR | ACB | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02280 | hp2 | a0001 | c0001 | t0006 | g0230 | AFR | ACB | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02293 | hp1 | a0001 | c0002 | t0005 | g0031 | AMR | PEL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0320 | AMR | PEL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02300 | hp1 | a0001 | c0002 | t0005 | g0013 | AMR | PEL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | PEL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02451 | hp1 | a0002 | c0009 | t0001 | g0195 | AFR | ACB | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02451 | hp2 | a0001 | c0023 | t0001 | g0215 | AFR | ACB | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | KHV | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02523 | hp2 | a0001 | c0014 | t0001 | g0161 | EAS | KHV | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02572 | hp1 | a0002 | c0009 | t0001 | g0201 | AFR | GWD | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02572 | hp2 | a0001 | c0002 | t0002 | g0116 | AFR | GWD | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02602 | hp1 | a0001 | c0002 | t0002 | g0078 | SAS | PJL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0109 | SAS | PJL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02615 | hp1 | a0001 | c0002 | t0008 | g0207 | AFR | GWD | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0368 | AFR | GWD | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0364 | AFR | GWD | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0205 | AFR | GWD | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02630 | hp2 | a0001 | c0001 | t0020 | g0117 | AFR | GWD | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02647 | hp1 | a0003 | c0005 | t0001 | g0282 | AFR | GWD | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02647 | hp2 | a0002 | c0009 | t0001 | g0202 | AFR | GWD | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0352 | SAS | PJL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02683 | hp2 | a0001 | c0002 | t0002 | g0115 | SAS | PJL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02698 | hp1 | a0001 | c0001 | t0006 | g0252 | SAS | PJL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0347 | SAS | PJL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02717 | hp2 | a0001 | c0004 | t0007 | g0198 | AFR | GWD | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0361 | AFR | GWD | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02723 | hp2 | a0001 | c0007 | t0009 | g0053 | AFR | GWD | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0105 | SAS | PJL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02735 | hp2 | a0010 | c0026 | t0005 | g0028 | SAS | PJL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02809 | hp1 | a0003 | c0005 | t0001 | g0283 | AFR | GWD | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02809 | hp2 | a0001 | c0001 | t0010 | g0044 | AFR | GWD | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02818 | hp1 | a0001 | c0001 | t0010 | g0045 | AFR | GWD | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02818 | hp2 | a0001 | c0004 | t0007 | g0188 | AFR | GWD | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02886 | hp1 | a0003 | c0005 | t0017 | g0054 | AFR | GWD | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0367 | AFR | GWD | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02895 | hp1 | a0003 | c0005 | t0001 | g0358 | AFR | GWD | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02896 | hp1 | a0002 | c0009 | t0001 | g0204 | AFR | GWD | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02897 | hp1 | a0003 | c0005 | t0001 | g0357 | AFR | GWD | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0374 | AFR | ESN | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02922 | hp2 | a0006 | c0016 | t0013 | g0235 | AFR | ESN | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02965 | hp1 | a0001 | c0001 | t0010 | g0022 | AFR | ESN | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02965 | hp2 | a0001 | c0002 | t0002 | g0112 | AFR | ESN | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0363 | AFR | ESN | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0356 | AFR | ESN | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0099 | SAS | PJL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG03017 | hp2 | a0001 | c0001 | t0006 | g0274 | SAS | PJL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0365 | AFR | GWD | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG03041 | hp2 | a0001 | c0007 | t0009 | g0056 | AFR | GWD | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG03098 | hp1 | a0001 | c0002 | t0002 | g0074 | AFR | MSL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG03098 | hp2 | a0001 | c0002 | t0008 | g0206 | AFR | MSL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0377 | AFR | ESN | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG03130 | hp2 | a0001 | c0025 | t0001 | g0213 | AFR | ESN | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0360 | AFR | ESN | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0381 | AFR | ESN | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG03209 | hp1 | a0001 | c0007 | t0009 | g0055 | AFR | MSL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG03209 | hp2 | a0003 | c0005 | t0001 | g0280 | AFR | MSL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0285 | SAS | PJL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0258 | SAS | PJL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG03453 | hp1 | a0001 | c0002 | t0008 | g0208 | AFR | MSL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG03453 | hp2 | a0001 | c0004 | t0007 | g0197 | AFR | MSL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG03486 | hp1 | a0001 | c0001 | t0007 | g0278 | AFR | MSL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0369 | AFR | MSL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG03491 | hp1 | a0001 | c0002 | t0002 | g0088 | SAS | PJL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0293 | SAS | PJL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0378 | AFR | ESN | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG03516 | hp2 | a0007 | c0011 | t0002 | g0076 | AFR | ESN | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG03540 | hp1 | a0001 | c0002 | t0008 | g0211 | AFR | GWD | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG03540 | hp2 | a0001 | c0004 | t0001 | g0199 | AFR | GWD | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG03579 | hp1 | a0004 | c0006 | t0007 | g0194 | AFR | MSL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG03579 | hp2 | a0001 | c0007 | t0004 | g0231 | AFR | MSL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG03654 | hp1 | a0001 | c0001 | t0006 | g0226 | SAS | PJL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0122 | SAS | PJL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG03669 | hp2 | a0001 | c0001 | t0005 | g0011 | SAS | PJL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG03704 | hp1 | a0001 | c0002 | t0002 | g0106 | SAS | PJL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG03704 | hp2 | a0001 | c0022 | t0006 | g0223 | SAS | PJL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG03710 | hp1 | a0001 | c0003 | t0003 | g0159 | SAS | PJL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG03710 | hp2 | a0001 | c0001 | t0016 | g0009 | SAS | PJL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0327 | SAS | STU | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG04115 | hp2 | a0001 | c0001 | t0006 | g0229 | SAS | STU | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0335 | SAS | BEB | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG04184 | hp2 | a0001 | c0024 | t0004 | g0268 | SAS | BEB | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG04204 | hp1 | a0001 | c0001 | t0006 | g0220 | SAS | STU | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0295 | SAS | STU | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG04228 | hp1 | a0001 | c0001 | t0006 | g0227 | SAS | STU | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0259 | SAS | STU | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18522 | hp1 | a0001 | c0001 | t0024 | g0353 | AFR | YRI | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18522 | hp2 | a0001 | c0002 | t0002 | g0118 | AFR | YRI | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18612 | hp1 | a0001 | c0003 | t0003 | g0138 | EAS | CHB | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | CHB | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18747 | hp1 | a0001 | c0001 | t0011 | g0059 | EAS | CHB | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0233 | EAS | CHB | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18906 | hp1 | a0001 | c0002 | t0002 | g0080 | AFR | YRI | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0379 | AFR | YRI | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18941 | hp2 | a0001 | c0003 | t0003 | g0148 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0301 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18944 | hp2 | a0001 | c0001 | t0004 | g0270 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18945 | hp2 | a0001 | c0003 | t0003 | g0153 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18946 | hp2 | a0001 | c0003 | t0003 | g0154 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0238 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18947 | hp2 | a0001 | c0002 | t0002 | g0085 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18951 | hp2 | a0001 | c0008 | t0004 | g0275 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18953 | hp2 | a0001 | c0002 | t0002 | g0127 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18954 | hp1 | a0001 | c0001 | t0005 | g0035 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18956 | hp1 | a0001 | c0003 | t0003 | g0143 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18956 | hp2 | a0001 | c0001 | t0005 | g0020 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18957 | hp2 | a0001 | c0003 | t0003 | g0163 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18959 | hp1 | a0001 | c0001 | t0004 | g0249 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18960 | hp1 | a0001 | c0002 | t0005 | g0026 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18960 | hp2 | a0001 | c0003 | t0003 | g0176 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0251 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18962 | hp1 | a0001 | c0001 | t0005 | g0018 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18962 | hp2 | a0001 | c0003 | t0003 | g0135 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18963 | hp2 | a0001 | c0001 | t0004 | g0265 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18966 | hp1 | a0001 | c0003 | t0003 | g0150 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18966 | hp2 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18967 | hp1 | a0001 | c0003 | t0003 | g0185 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18967 | hp2 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18968 | hp2 | a0001 | c0002 | t0002 | g0107 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18969 | hp1 | a0001 | c0001 | t0004 | g0254 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18969 | hp2 | a0001 | c0003 | t0003 | g0169 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0384 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18971 | hp1 | a0001 | c0001 | t0019 | g0062 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18973 | hp1 | a0001 | c0001 | t0025 | g0257 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18974 | hp1 | a0001 | c0003 | t0003 | g0146 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18974 | hp2 | a0001 | c0003 | t0004 | g0134 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18975 | hp1 | a0001 | c0003 | t0003 | g0147 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18977 | hp2 | a0001 | c0003 | t0003 | g0133 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18978 | hp1 | a0001 | c0001 | t0004 | g0241 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18979 | hp2 | a0001 | c0001 | t0005 | g0050 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18980 | hp1 | a0001 | c0002 | t0005 | g0038 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18982 | hp1 | a0001 | c0013 | t0003 | g0156 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0239 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18983 | hp2 | a0001 | c0001 | t0005 | g0046 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18984 | hp1 | a0001 | c0001 | t0012 | g0131 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18984 | hp2 | a0001 | c0001 | t0004 | g0261 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18985 | hp1 | a0001 | c0001 | t0005 | g0049 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18985 | hp2 | a0001 | c0002 | t0002 | g0082 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18986 | hp1 | a0001 | c0002 | t0002 | g0111 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0345 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18987 | hp1 | a0001 | c0001 | t0005 | g0023 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18987 | hp2 | a0001 | c0001 | t0004 | g0272 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18988 | hp1 | a0001 | c0001 | t0005 | g0048 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18988 | hp2 | a0001 | c0003 | t0003 | g0177 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18989 | hp2 | a0001 | c0001 | t0004 | g0271 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18991 | hp1 | a0001 | c0001 | t0004 | g0264 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18992 | hp1 | a0001 | c0003 | t0003 | g0158 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18992 | hp2 | a0001 | c0001 | t0004 | g0243 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18993 | hp1 | a0001 | c0003 | t0003 | g0142 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18994 | hp1 | a0001 | c0002 | t0005 | g0034 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18994 | hp2 | a0001 | c0001 | t0004 | g0255 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18998 | hp1 | a0001 | c0002 | t0005 | g0037 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18999 | hp1 | a0001 | c0001 | t0004 | g0273 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18999 | hp2 | a0001 | c0003 | t0003 | g0164 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19001 | hp1 | a0001 | c0008 | t0004 | g0256 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19001 | hp2 | a0011 | c0020 | t0002 | g0086 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19002 | hp1 | a0001 | c0002 | t0002 | g0070 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19003 | hp1 | a0001 | c0003 | t0003 | g0149 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19004 | hp1 | a0001 | c0001 | t0004 | g0263 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0372 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19005 | hp2 | a0001 | c0001 | t0004 | g0376 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19006 | hp2 | a0012 | c0021 | t0004 | g0240 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19007 | hp1 | a0001 | c0001 | t0018 | g0058 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19007 | hp2 | a0001 | c0001 | t0005 | g0024 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0250 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19011 | hp2 | a0001 | c0001 | t0005 | g0033 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19030 | hp1 | a0001 | c0001 | t0006 | g0236 | AFR | LWK | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19030 | hp2 | a0001 | c0002 | t0002 | g0063 | AFR | LWK | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19043 | hp1 | a0007 | c0011 | t0002 | g0114 | AFR | LWK | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19043 | hp2 | a0004 | c0006 | t0007 | g0192 | AFR | LWK | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19055 | hp1 | a0001 | c0002 | t0002 | g0087 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19055 | hp2 | a0001 | c0001 | t0005 | g0017 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19056 | hp1 | a0001 | c0001 | t0005 | g0040 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0383 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19057 | hp1 | a0001 | c0002 | t0002 | g0083 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0245 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19060 | hp2 | a0001 | c0002 | t0005 | g0015 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19062 | hp2 | a0001 | c0001 | t0004 | g0262 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19063 | hp1 | a0001 | c0001 | t0004 | g0217 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19064 | hp1 | a0001 | c0001 | t0005 | g0016 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19064 | hp2 | a0001 | c0001 | t0011 | g0060 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19065 | hp1 | a0001 | c0008 | t0004 | g0253 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19065 | hp2 | a0001 | c0003 | t0003 | g0157 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19066 | hp1 | a0001 | c0001 | t0005 | g0047 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19066 | hp2 | a0001 | c0003 | t0003 | g0141 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19067 | hp1 | a0001 | c0002 | t0005 | g0051 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0244 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19068 | hp2 | a0001 | c0003 | t0003 | g0144 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19070 | hp2 | a0001 | c0003 | t0003 | g0171 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19072 | hp1 | a0001 | c0003 | t0003 | g0139 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19072 | hp2 | a0001 | c0001 | t0011 | g0061 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19074 | hp1 | a0001 | c0003 | t0003 | g0168 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19081 | hp1 | a0001 | c0002 | t0005 | g0042 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19081 | hp2 | a0001 | c0003 | t0003 | g0140 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19082 | hp1 | a0001 | c0001 | t0004 | g0385 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0373 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19083 | hp1 | a0001 | c0001 | t0011 | g0125 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19083 | hp2 | a0001 | c0002 | t0005 | g0014 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0071 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19084 | hp2 | a0001 | c0003 | t0003 | g0175 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19085 | hp2 | a0001 | c0001 | t0005 | g0039 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19086 | hp1 | a0001 | c0003 | t0003 | g0160 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19086 | hp2 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19089 | hp1 | a0001 | c0001 | t0005 | g0032 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19091 | hp2 | a0001 | c0001 | t0005 | g0021 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0370 | AFR | YRI | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA19240 | hp2 | a0001 | c0002 | t0008 | g0237 | AFR | YRI | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA20129 | hp1 | a0001 | c0001 | t0023 | g0371 | AFR | ASW | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA20129 | hp2 | a0004 | c0006 | t0007 | g0191 | AFR | ASW | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0326 | EUR | TSI | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA20805 | hp2 | a0001 | c0002 | t0002 | g0100 | EUR | TSI | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | CLM | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG01123 | hp2 | a0001 | c0003 | t0003 | g0182 | AMR | CLM | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02109 | hp1 | a0001 | c0002 | t0002 | g0084 | AFR | ACB | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02109 | hp2 | a0003 | c0005 | t0001 | g0281 | AFR | ACB | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02486 | hp1 | a0001 | c0007 | t0009 | g0057 | AFR | ACB | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02486 | hp2 | a0006 | c0017 | t0013 | g0234 | AFR | ACB | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0366 | AFR | ACB | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG02559 | hp2 | a0001 | c0015 | t0008 | g0196 | AFR | ACB | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG03471 | hp1 | a0001 | c0007 | t0004 | g0232 | AFR | MSL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG03471 | hp2 | a0001 | c0002 | t0008 | g0209 | AFR | MSL | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG06807 | hp1 | a0001 | c0004 | t0007 | g0189 | AFR | USA | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | USA | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18955 | hp1 | a0001 | c0001 | t0004 | g0248 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA18955 | hp2 | a0001 | c0003 | t0003 | g0162 | EAS | JPT | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA20300 | hp1 | a0001 | c0002 | t0005 | g0025 | AFR | USA | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA20300 | hp2 | a0001 | c0001 | t0021 | g0279 | AFR | USA | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA21309 | hp1 | a0001 | c0002 | t0002 | g0129 | AFR | LWK | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0104 | AFR | LWK | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0222 | REF | REF | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0108 | REF | REF | GNPTAB_chr12_101740499_101835959 | GNPTAB | chr12 | 101740499 | 101835959 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:101753459 | T | A | 1 | a0005 | 2 | HG01070.hp2 HG01071.hp2 |
missense_variant | MODERATE | c.3515A>T | p.Tyr1172Phe | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 19/21 | 3799/5720 | 3515/3771 | 1172/1256 | chr12 | 101753459 | |||
| chr12:101760082 | G | A | 1 | a0003 | 7 | HG02109.hp2 HG02647.hp1 HG02809.hp1 others(4): Show |
missense_variant | MODERATE | c.3197C>T | p.Thr1066Met | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 16/21 | 3481/5720 | 3197/3771 | 1066/1256 | chr12 | 101760082 | |||
| chr12:101764306 | C | T | 1 | a0006 | 2 | HG02486.hp2 HG02922.hp2 |
missense_variant | MODERATE | c.2611G>A | p.Gly871Ser | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 13/21 | 2895/5720 | 2611/3771 | 871/1256 | chr12 | 101764306 | |||
| chr12:101764986 | G | A | 1 | a0002 | 7 | HG00280.hp1 HG00741.hp1 HG02258.hp1 others(4): Show |
missense_variant | MODERATE | c.1931C>T | p.Thr644Ile | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 13/21 | 2215/5720 | 1931/3771 | 644/1256 | chr12 | 101764986 | |||
| chr12:101765091 | G | T | 1 | a0007 | 2 | HG03516.hp2 NA19043.hp1 |
missense_variant | MODERATE | c.1826C>A | p.Thr609Asn | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 13/21 | 2110/5720 | 1826/3771 | 609/1256 | chr12 | 101765091 | |||
| chr12:101765167 | G | T | 1 | a0012 | 1 | NA19006.hp2 | missense_variant | MODERATE | c.1750C>A | p.Pro584Thr | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 13/21 | 2034/5720 | 1750/3771 | 584/1256 | chr12 | 101765167 | |||
| chr12:101770428 | C | T | 1 | a0011 | 1 | NA19001.hp2 | missense_variant | MODERATE | c.1091G>A | p.Arg364Gln | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 9/21 | 1375/5720 | 1091/3771 | 364/1256 | chr12 | 101770428 | |||
| chr12:101770477 | T | G | 1 | a0004 | 6 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(3): Show |
missense_variant | MODERATE | c.1042A>C | p.Ile348Leu | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 9/21 | 1326/5720 | 1042/3771 | 348/1256 | chr12 | 101770477 | |||
| chr12:101770508 | C | G | 1 | a0009 | 1 | HG01358.hp2 | missense_variant | MODERATE | c.1011G>C | p.Glu337Asp | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 9/21 | 1295/5720 | 1011/3771 | 337/1256 | chr12 | 101770508 | |||
| chr12:101786077 | T | C | 1 | a0010 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.506A>G | p.Asn169Ser | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/21 | 790/5720 | 506/3771 | 169/1256 | chr12 | 101786077 | |||
| chr12:101796743 | C | T | 1 | a0008 | 1 | HG01258.hp1 | missense_variant | MODERATE | c.137G>A | p.Arg46Gln | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/21 | 421/5720 | 137/3771 | 46/1256 | chr12 | 101796743 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:101761139 | C | T | 1 | a0001c0023 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.3123G>A | p.Pro1041Pro | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 15/21 | 3407/5720 | 3123/3771 | 1041/1256 | chr12 | 101761139 | |||
| chr12:101764252 | A | G | 1 | a0001c0022 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.2665T>C | p.Leu889Leu | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 13/21 | 2949/5720 | 2665/3771 | 889/1256 | chr12 | 101764252 | |||
| chr12:101764436 | G | A | 1 | a0001c0008 | 6 | HG00544.hp1 HG00597.hp1 HG02056.hp1 others(3): Show |
synonymous_variant | LOW | c.2481C>T | p.Gly827Gly | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 13/21 | 2765/5720 | 2481/3771 | 827/1256 | chr12 | 101764436 | |||
| chr12:101764898 | T | C | 1 | a0001c0024 | 1 | HG04184.hp2 | synonymous_variant | LOW | c.2019A>G | p.Lys673Lys | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 13/21 | 2303/5720 | 2019/3771 | 673/1256 | chr12 | 101764898 | |||
| chr12:101764985 | T | C | 18 | a0001c0001 a0001c0003 a0001c0004 others(15): Show |
297 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(294): Show |
synonymous_variant | LOW | c.1932A>G | p.Thr644Thr | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 13/21 | 2216/5720 | 1932/3771 | 644/1256 | chr12 | 101764985 | |||
| chr12:101764988 | A | C | 1 | a0001c0013 | 1 | NA18982.hp1 | synonymous_variant | LOW | c.1929T>G | p.Ser643Ser | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 13/21 | 2213/5720 | 1929/3771 | 643/1256 | chr12 | 101764988 | |||
| chr12:101765291 | T | C | 1 | a0001c0025 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.1626A>G | p.Glu542Glu | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 13/21 | 1910/5720 | 1626/3771 | 542/1256 | chr12 | 101765291 | |||
| chr12:101766203 | G | A | 1 | a0006c0017 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.1500C>T | p.Asn500Asn | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 12/21 | 1784/5720 | 1500/3771 | 500/1256 | chr12 | 101766203 | |||
| chr12:101766221 | C | T | 1 | a0001c0007 | 6 | HG02486.hp1 HG02723.hp2 HG03041.hp2 others(3): Show |
synonymous_variant | LOW | c.1482G>A | p.Gln494Gln | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 12/21 | 1766/5720 | 1482/3771 | 494/1256 | chr12 | 101766221 | |||
| chr12:101796744 | G | T | 2 | a0006c0016 a0006c0017 |
2 | HG02486.hp2 HG02922.hp2 |
synonymous_variant | LOW | c.136C>A | p.Arg46Arg | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/21 | 420/5720 | 136/3771 | 46/1256 | chr12 | 101796744 | |||
| chr12:101830649 | C | T | 4 | a0001c0004 a0001c0015 a0002c0009 others(1): Show |
19 | HG01081.hp1 HG01109.hp1 HG01243.hp2 others(16): Show |
synonymous_variant | LOW | c.27G>A | p.Gln9Gln | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/21 | 311/5720 | 27/3771 | 9/1256 | chr12 | 101830649 | |||
| chr12:101830658 | C | T | 4 | a0001c0003 a0001c0013 a0001c0014 others(1): Show |
54 | HG00140.hp1 HG00544.hp2 HG00597.hp2 others(51): Show |
synonymous_variant | LOW | c.18G>A | p.Leu6Leu | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/21 | 302/5720 | 18/3771 | 6/1256 | chr12 | 101830658 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:101745692 | T | G | 1 | a0001c0001t0021 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1472A>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 21/21 | 1472 | chr12 | 101745692 | ||||||
| chr12:101745707 | T | C | 13 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0011 others(10): Show |
59 | HG00544.hp1 HG00597.hp1 HG01167.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*1457A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 21/21 | 1457 | chr12 | 101745707 | ||||||
| chr12:101745924 | A | G | 2 | a0001c0001t0009 a0001c0007t0009 |
5 | HG01167.hp2 HG02486.hp1 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1240T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 21/21 | 1240 | chr12 | 101745924 | ||||||
| chr12:101745933 | G | A | 1 | a0001c0001t0022 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1231C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 21/21 | 1231 | chr12 | 101745933 | ||||||
| chr12:101745969 | T | G | 5 | a0001c0001t0006 a0001c0001t0010 a0001c0001t0015 others(2): Show |
21 | HG00323.hp1 HG00408.hp2 HG00741.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1195A>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 21/21 | 1195 | chr12 | 101745969 | ||||||
| chr12:101745985 | T | C | 1 | a0001c0001t0023 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1179A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 21/21 | 1179 | chr12 | 101745985 | ||||||
| chr12:101746272 | C | CCT | 4 | a0001c0001t0003 a0001c0003t0003 a0001c0013t0003 others(1): Show |
53 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*890_*891dupAG | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 21/21 | 891 | chr12 | 101746272 | ||||||
| chr12:101746350 | A | C | 5 | a0001c0001t0007 a0001c0001t0020 a0001c0004t0007 others(2): Show |
13 | HG01081.hp1 HG01243.hp2 HG01891.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*814T>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 21/21 | 814 | chr12 | 101746350 | ||||||
| chr12:101746435 | G | A | 1 | a0001c0001t0024 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*729C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 21/21 | 729 | chr12 | 101746435 | ||||||
| chr12:101746552 | A | G | 2 | a0006c0016t0013 a0006c0017t0013 |
2 | HG02486.hp2 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*612T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 21/21 | 612 | chr12 | 101746552 | ||||||
| chr12:101746744 | G | GA | 2 | a0001c0002t0008 a0001c0015t0008 |
9 | HG01884.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*419dupT | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 21/21 | 419 | chr12 | 101746744 | ||||||
| chr12:101746841 | A | G | 5 | a0001c0001t0007 a0001c0001t0020 a0001c0004t0007 others(2): Show |
13 | HG01081.hp1 HG01243.hp2 HG01891.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*323T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 21/21 | 323 | chr12 | 101746841 | ||||||
| chr12:101746850 | C | T | 1 | a0001c0001t0015 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*314G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 21/21 | 314 | chr12 | 101746850 | ||||||
| chr12:101746957 | G | A | 1 | a0001c0001t0019 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*207C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 21/21 | 207 | chr12 | 101746957 | ||||||
| chr12:101747021 | C | T | 2 | a0006c0016t0013 a0006c0017t0013 |
2 | HG02486.hp2 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*143G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 21/21 | 143 | chr12 | 101747021 | ||||||
| chr12:101747062 | G | A | 1 | a0001c0001t0025 | 1 | NA18973.hp1 | 3_prime_UTR_variant | MODIFIER | c.*102C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 21/21 | 102 | chr12 | 101747062 | ||||||
| chr12:101747121 | G | A | 5 | a0001c0001t0007 a0001c0001t0020 a0001c0004t0007 others(2): Show |
13 | HG01081.hp1 HG01243.hp2 HG01891.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*43C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 21/21 | 43 | chr12 | 101747121 | ||||||
| chr12:101830711 | T | TGAGCCGC others(24): Show |
1 | a0001c0001t0012 | 2 | HG00558.hp1 NA18984.hp1 |
5_prime_UTR_variant | MODIFIER | c.-67_-37dupGCTGAGGC others(23): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/21 | 37 | chr12 | 101830711 | ||||||
| chr12:101830713 | AGCC | A | 46 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(43): Show |
311 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(308): Show |
5_prime_UTR_variant | MODIFIER | c.-41_-39delGGC | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/21 | 39 | chr12 | 101830713 | ||||||
| chr12:101830795 | C | T | 1 | a0001c0001t0018 | 1 | NA19007.hp1 | 5_prime_UTR_variant | MODIFIER | c.-120G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/21 | 120 | chr12 | 101830795 | ||||||
| chr12:101830820 | C | T | 3 | a0001c0001t0009 a0001c0007t0009 a0003c0005t0017 |
6 | HG01167.hp2 HG02486.hp1 HG02723.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-145G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/21 | 145 | chr12 | 101830820 | ||||||
| chr12:101830832 | G | T | 6 | a0001c0001t0005 a0001c0001t0010 a0001c0001t0015 others(3): Show |
45 | HG01106.hp1 HG01516.hp2 HG01981.hp1 others(42): Show |
5_prime_UTR_variant | MODIFIER | c.-157C>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/21 | 157 | chr12 | 101830832 | ||||||
| chr12:101830903 | CTGCGGCC others(5): Show |
C | 1 | a0004c0006t0014 | 1 | HG01243.hp2 | 5_prime_UTR_variant | MODIFIER | c.-240_-229delTCGCCG others(6): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/21 | 229 | chr12 | 101830903 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:101747325 | T | A | 4 | a0001c0001t0001g0327 a0001c0001t0001g0340 a0001c0001t0001g0341 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.3694-84A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 20/20 | chr12 | 101747325 | |||||||
| chr12:101747488 | C | T | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.3694-247G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 20/20 | chr12 | 101747488 | |||||||
| chr12:101747512 | A | T | 1 | a0001c0002t0001g0356 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3694-271T>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 20/20 | chr12 | 101747512 | |||||||
| chr12:101747593 | A | G | 1 | a0001c0025t0001g0213 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3694-352T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 20/20 | chr12 | 101747593 | |||||||
| chr12:101747626 | G | A | 1 | a0001c0001t0001g0345 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.3694-385C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 20/20 | chr12 | 101747626 | |||||||
| chr12:101747636 | T | TTG | 302 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(299): Show |
306 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(303): Show |
intron_variant | MODIFIER | c.3694-396_3694-395i others(4): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 20/20 | chr12 | 101747636 | |||||||
| chr12:101747637 | G | A | 302 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(299): Show |
306 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(303): Show |
intron_variant | MODIFIER | c.3694-396C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 20/20 | chr12 | 101747637 | |||||||
| chr12:101747638 | A | AAAATCAC others(642): Show |
2 | a0001c0001t0004g0233 a0001c0001t0004g0376 |
2 | NA18747.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.3694-398_3694-397i others(651): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 20/20 | chr12 | 101747638 | |||||||
| chr12:101747639 | T | A | 302 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(299): Show |
306 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(303): Show |
intron_variant | MODIFIER | c.3694-398A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 20/20 | chr12 | 101747639 | |||||||
| chr12:101747641 | T | G | 2 | a0001c0001t0004g0233 a0001c0001t0004g0376 |
2 | NA18747.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.3694-400A>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 20/20 | chr12 | 101747641 | |||||||
| chr12:101747643 | A | ACGACATT others(635): Show |
23 | a0001c0001t0001g0001 a0001c0001t0001g0360 a0001c0001t0001g0361 others(20): Show |
26 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.3694-403_3694-402i others(644): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 20/20 | chr12 | 101747643 | |||||||
| chr12:101747643 | A | ACTACATT others(642): Show |
122 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0003g0247 others(119): Show |
123 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.3694-403_3694-402i others(651): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 20/20 | chr12 | 101747643 | |||||||
| chr12:101747643 | A | ACTACATT others(642): Show |
145 | a0001c0001t0001g0219 a0001c0001t0001g0284 a0001c0001t0001g0285 others(142): Show |
145 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.3694-403_3694-402i others(651): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 20/20 | chr12 | 101747643 | |||||||
| chr12:101747643 | A | ACTACATT others(642): Show |
1 | a0001c0001t0001g0291 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.3694-403_3694-402i others(651): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 20/20 | chr12 | 101747643 | |||||||
| chr12:101747643 | A | ACTACATT others(643): Show |
1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.3694-403_3694-402i others(652): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 20/20 | chr12 | 101747643 | |||||||
| chr12:101747643 | A | ACTACATT others(638): Show |
8 | a0001c0001t0001g0322 a0001c0001t0001g0324 a0001c0001t0001g0338 others(5): Show |
8 | NA18943.hp2 NA18973.hp2 NA18986.hp2 others(5): Show |
intron_variant | MODIFIER | c.3694-403_3694-402i others(647): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 20/20 | chr12 | 101747643 | |||||||
| chr12:101747643 | A | ACTACATT others(642): Show |
2 | a0001c0002t0001g0205 a0001c0023t0001g0215 |
2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.3694-403_3694-402i others(651): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 20/20 | chr12 | 101747643 | |||||||
| chr12:101747772 | G | A | 6 | a0004c0006t0007g0187 a0004c0006t0007g0191 a0004c0006t0007g0192 others(3): Show |
6 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.3694-531C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 20/20 | chr12 | 101747772 | |||||||
| chr12:101747806 | T | C | 1 | a0002c0012t0001g0214 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3694-565A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 20/20 | chr12 | 101747806 | |||||||
| chr12:101747852 | C | CCTGCCTC others(54): Show |
113 | a0001c0001t0001g0219 a0001c0001t0001g0284 a0001c0001t0001g0285 others(110): Show |
113 | HG00408.hp1 HG00423.hp2 HG01099.hp1 others(110): Show |
intron_variant | MODIFIER | c.3694-672_3694-612d others(63): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 20/20 | chr12 | 101747852 | |||||||
| chr12:101748297 | C | T | 6 | a0001c0007t0004g0231 a0001c0007t0004g0232 a0001c0007t0009g0053 others(3): Show |
6 | HG02486.hp1 HG02723.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.3693+804G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 20/20 | chr12 | 101748297 | |||||||
| chr12:101748478 | T | C | 1 | a0001c0004t0007g0189 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3693+623A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 20/20 | chr12 | 101748478 | |||||||
| chr12:101748498 | C | A | 1 | a0001c0001t0011g0061 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.3693+603G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 20/20 | chr12 | 101748498 | |||||||
| chr12:101748756 | A | G | 2 | a0001c0002t0001g0356 a0001c0002t0001g0359 |
2 | HG00642.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.3693+345T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 20/20 | chr12 | 101748756 | |||||||
| chr12:101749069 | T | C | 1 | a0001c0002t0002g0126 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3693+32A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 20/20 | chr12 | 101749069 | |||||||
| chr12:101749091 | T | A | 7 | a0002c0009t0001g0195 a0002c0009t0001g0200 a0002c0009t0001g0201 others(4): Show |
7 | HG00280.hp1 HG00741.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.3693+10A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 20/20 | chr12 | 101749091 | |||||||
| chr12:101749430 | A | G | 51 | a0001c0001t0004g0005 a0001c0001t0004g0217 a0001c0001t0004g0233 others(48): Show |
52 | HG00544.hp1 HG00597.hp1 HG02056.hp1 others(49): Show |
intron_variant | MODIFIER | c.3603-239T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 19/20 | chr12 | 101749430 | |||||||
| chr12:101749470 | C | G | 1 | a0001c0001t0004g0259 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3603-279G>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 19/20 | chr12 | 101749470 | |||||||
| chr12:101749486 | C | A | 1 | a0001c0003t0003g0173 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3603-295G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 19/20 | chr12 | 101749486 | |||||||
| chr12:101749532 | T | G | 181 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0284 others(178): Show |
184 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.3603-341A>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 19/20 | chr12 | 101749532 | |||||||
| chr12:101749830 | G | A | 9 | a0001c0002t0008g0206 a0001c0002t0008g0207 a0001c0002t0008g0208 others(6): Show |
9 | HG01884.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.3603-639C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 19/20 | chr12 | 101749830 | |||||||
| chr12:101749830 | G | C | 2 | a0006c0016t0013g0235 a0006c0017t0013g0234 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3603-639C>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 19/20 | chr12 | 101749830 | |||||||
| chr12:101749832 | G | A | 5 | a0001c0001t0007g0278 a0001c0001t0020g0117 a0001c0004t0007g0188 others(2): Show |
5 | HG01081.hp1 HG02630.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.3603-641C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 19/20 | chr12 | 101749832 | |||||||
| chr12:101750281 | C | G | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.3603-1090G>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 19/20 | chr12 | 101750281 | |||||||
| chr12:101750351 | T | A | 6 | a0001c0001t0010g0022 a0001c0001t0010g0043 a0001c0001t0010g0044 others(3): Show |
6 | HG01109.hp1 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.3603-1160A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 19/20 | chr12 | 101750351 | |||||||
| chr12:101750536 | A | G | 9 | a0001c0002t0001g0205 a0001c0023t0001g0215 a0002c0009t0001g0195 others(6): Show |
9 | HG00280.hp1 HG00741.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.3603-1345T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 19/20 | chr12 | 101750536 | |||||||
| chr12:101750550 | T | C | 34 | a0001c0001t0006g0218 a0001c0001t0006g0220 a0001c0001t0006g0221 others(31): Show |
34 | HG00323.hp1 HG00408.hp2 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.3603-1359A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 19/20 | chr12 | 101750550 | |||||||
| chr12:101750612 | T | C | 2 | a0006c0016t0013g0235 a0006c0017t0013g0234 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3603-1421A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 19/20 | chr12 | 101750612 | |||||||
| chr12:101750749 | T | C | 1 | a0001c0001t0006g0228 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.3603-1558A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 19/20 | chr12 | 101750749 | |||||||
| chr12:101750815 | T | C | 1 | a0001c0001t0006g0224 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.3603-1624A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 19/20 | chr12 | 101750815 | |||||||
| chr12:101750840 | C | G | 23 | a0001c0001t0001g0297 a0001c0001t0001g0298 a0001c0001t0001g0322 others(20): Show |
23 | HG00408.hp1 HG00423.hp2 HG02027.hp1 others(20): Show |
intron_variant | MODIFIER | c.3603-1649G>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 19/20 | chr12 | 101750840 | |||||||
| chr12:101751081 | C | T | 1 | a0001c0003t0003g0145 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3603-1890G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 19/20 | chr12 | 101751081 | |||||||
| chr12:101751198 | T | C | 7 | a0001c0001t0009g0052 a0001c0007t0004g0231 a0001c0007t0004g0232 others(4): Show |
7 | HG01167.hp2 HG02486.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.3603-2007A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 19/20 | chr12 | 101751198 | |||||||
| chr12:101751218 | C | T | 1 | a0001c0002t0008g0237 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3603-2027G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 19/20 | chr12 | 101751218 | |||||||
| chr12:101751246 | G | A | 1 | a0001c0025t0001g0213 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3603-2055C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 19/20 | chr12 | 101751246 | |||||||
| chr12:101751427 | T | G | 1 | a0001c0003t0003g0147 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.3602+1945A>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 19/20 | chr12 | 101751427 | |||||||
| chr12:101751460 | C | A | 3 | a0001c0003t0003g0133 a0001c0003t0003g0147 a0001c0003t0003g0160 |
3 | NA18975.hp1 NA18977.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.3602+1912G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 19/20 | chr12 | 101751460 | |||||||
| chr12:101751550 | A | G | 6 | a0001c0001t0001g0300 a0001c0001t0001g0311 a0001c0001t0001g0312 others(3): Show |
6 | HG01192.hp2 HG01258.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.3602+1822T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 19/20 | chr12 | 101751550 | |||||||
| chr12:101751584 | T | C | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.3602+1788A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 19/20 | chr12 | 101751584 | |||||||
| chr12:101751866 | G | A | 1 | a0001c0007t0004g0232 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3602+1506C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 19/20 | chr12 | 101751866 | |||||||
| chr12:101751950 | A | C | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.3602+1422T>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 19/20 | chr12 | 101751950 | |||||||
| chr12:101752019 | TA | T | 250 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(247): Show |
253 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.3602+1352delT | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 19/20 | chr12 | 101752019 | |||||||
| chr12:101752204 | G | A | 1 | a0002c0009t0001g0202 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3602+1168C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 19/20 | chr12 | 101752204 | |||||||
| chr12:101752441 | A | C | 1 | a0001c0008t0004g0216 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3602+931T>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 19/20 | chr12 | 101752441 | |||||||
| chr12:101752600 | G | A | 1 | a0001c0025t0001g0213 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3602+772C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 19/20 | chr12 | 101752600 | |||||||
| chr12:101752627 | T | C | 2 | a0006c0016t0013g0235 a0006c0017t0013g0234 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3602+745A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 19/20 | chr12 | 101752627 | |||||||
| chr12:101752681 | G | A | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.3602+691C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 19/20 | chr12 | 101752681 | |||||||
| chr12:101752780 | C | T | 51 | a0001c0001t0004g0005 a0001c0001t0004g0217 a0001c0001t0004g0233 others(48): Show |
52 | HG00544.hp1 HG00597.hp1 HG02056.hp1 others(49): Show |
intron_variant | MODIFIER | c.3602+592G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 19/20 | chr12 | 101752780 | |||||||
| chr12:101752832 | A | T | 6 | a0004c0006t0007g0187 a0004c0006t0007g0191 a0004c0006t0007g0192 others(3): Show |
6 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.3602+540T>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 19/20 | chr12 | 101752832 | |||||||
| chr12:101753028 | G | A | 9 | a0001c0002t0008g0206 a0001c0002t0008g0207 a0001c0002t0008g0208 others(6): Show |
9 | HG01884.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.3602+344C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 19/20 | chr12 | 101753028 | |||||||
| chr12:101753185 | G | A | 8 | a0001c0002t0008g0206 a0001c0002t0008g0207 a0001c0002t0008g0208 others(5): Show |
8 | HG01884.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.3602+187C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 19/20 | chr12 | 101753185 | |||||||
| chr12:101753197 | G | A | 7 | a0002c0009t0001g0195 a0002c0009t0001g0200 a0002c0009t0001g0201 others(4): Show |
7 | HG00280.hp1 HG00741.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.3602+175C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 19/20 | chr12 | 101753197 | |||||||
| chr12:101753205 | G | A | 180 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0284 others(177): Show |
183 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.3602+167C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 19/20 | chr12 | 101753205 | |||||||
| chr12:101753260 | A | T | 1 | a0001c0007t0009g0057 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3602+112T>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 19/20 | chr12 | 101753260 | |||||||
| chr12:101753310 | T | C | 53 | a0001c0001t0003g0247 a0001c0003t0003g0133 a0001c0003t0003g0135 others(50): Show |
53 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.3602+62A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 19/20 | chr12 | 101753310 | |||||||
| chr12:101753364 | G | T | 1 | a0001c0001t0006g0228 | 1 | HG01168.hp1 | splice_region_variant&intron_variant | LOW | c.3602+8C>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 19/20 | chr12 | 101753364 | |||||||
| chr12:101753785 | T | C | 58 | a0001c0001t0004g0005 a0001c0001t0004g0217 a0001c0001t0004g0233 others(55): Show |
59 | HG00544.hp1 HG00597.hp1 HG01167.hp2 others(56): Show |
intron_variant | MODIFIER | c.3435-246A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101753785 | |||||||
| chr12:101753881 | G | A | 1 | a0001c0004t0007g0198 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3435-342C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101753881 | |||||||
| chr12:101753978 | A | C | 113 | a0001c0001t0001g0219 a0001c0001t0001g0284 a0001c0001t0001g0285 others(110): Show |
113 | HG00408.hp1 HG00423.hp2 HG01099.hp1 others(110): Show |
intron_variant | MODIFIER | c.3435-439T>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101753978 | |||||||
| chr12:101754136 | T | C | 1 | a0001c0002t0002g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3435-597A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101754136 | |||||||
| chr12:101754186 | G | A | 1 | a0001c0025t0001g0213 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3435-647C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101754186 | |||||||
| chr12:101754199 | G | C | 2 | a0006c0016t0013g0235 a0006c0017t0013g0234 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3435-660C>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101754199 | |||||||
| chr12:101754286 | G | A | 1 | a0004c0006t0007g0193 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3435-747C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101754286 | |||||||
| chr12:101754293 | G | A | 5 | a0001c0001t0002g0081 a0001c0001t0002g0089 a0001c0001t0002g0093 others(2): Show |
5 | HG00558.hp1 HG00609.hp1 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.3435-754C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101754293 | |||||||
| chr12:101754299 | T | C | 296 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(293): Show |
300 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.3435-760A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101754299 | |||||||
| chr12:101754337 | G | A | 1 | a0001c0003t0003g0148 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.3435-798C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101754337 | |||||||
| chr12:101754414 | A | T | 1 | a0001c0004t0007g0198 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3435-875T>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101754414 | |||||||
| chr12:101754431 | A | G | 1 | a0001c0001t0005g0047 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.3435-892T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101754431 | |||||||
| chr12:101754439 | TA | T | 51 | a0001c0001t0004g0005 a0001c0001t0004g0217 a0001c0001t0004g0233 others(48): Show |
52 | HG00544.hp1 HG00597.hp1 HG02056.hp1 others(49): Show |
intron_variant | MODIFIER | c.3435-901delT | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101754439 | |||||||
| chr12:101754447 | A | G | 9 | a0001c0002t0008g0206 a0001c0002t0008g0207 a0001c0002t0008g0208 others(6): Show |
9 | HG01884.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.3435-908T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101754447 | |||||||
| chr12:101754503 | A | C | 1 | a0001c0001t0021g0279 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3435-964T>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101754503 | |||||||
| chr12:101754513 | G | A | 180 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0284 others(177): Show |
183 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.3435-974C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101754513 | |||||||
| chr12:101754522 | A | C | 1 | a0001c0001t0004g0242 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3435-983T>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101754522 | |||||||
| chr12:101754541 | G | T | 180 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0284 others(177): Show |
183 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.3435-1002C>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101754541 | |||||||
| chr12:101754608 | G | A | 1 | a0001c0001t0004g0258 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3435-1069C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101754608 | |||||||
| chr12:101754684 | C | T | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.3435-1145G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101754684 | |||||||
| chr12:101754739 | TA | T | 148 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0284 others(145): Show |
151 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.3435-1201delT | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101754739 | |||||||
| chr12:101754739 | TAA | T | 36 | a0001c0001t0001g0334 a0001c0001t0006g0218 a0001c0001t0006g0220 others(33): Show |
36 | HG00323.hp1 HG00408.hp2 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.3435-1202_3435-120 others(6): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101754739 | |||||||
| chr12:101754993 | A | G | 16 | a0001c0001t0001g0360 a0001c0001t0001g0361 a0001c0001t0001g0363 others(13): Show |
16 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.3435-1454T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101754993 | |||||||
| chr12:101755066 | T | C | 2 | a0006c0016t0013g0235 a0006c0017t0013g0234 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3435-1527A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101755066 | |||||||
| chr12:101755130 | GATAC | G | 4 | a0001c0003t0003g0152 a0001c0003t0003g0159 a0001c0003t0003g0166 others(1): Show |
4 | HG01106.hp2 HG01175.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.3435-1595_3435-159 others(8): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101755130 | |||||||
| chr12:101755145 | C | T | 5 | a0004c0006t0007g0187 a0004c0006t0007g0191 a0004c0006t0007g0192 others(2): Show |
5 | HG01891.hp2 HG02055.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.3435-1606G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101755145 | |||||||
| chr12:101755228 | C | T | 1 | a0001c0002t0002g0118 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3435-1689G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101755228 | |||||||
| chr12:101755244 | T | C | 2 | a0006c0016t0013g0235 a0006c0017t0013g0234 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3435-1705A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101755244 | |||||||
| chr12:101755430 | G | T | 1 | a0001c0001t0012g0131 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3434+1782C>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101755430 | |||||||
| chr12:101755730 | C | T | 1 | a0001c0003t0003g0169 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.3434+1482G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101755730 | |||||||
| chr12:101755749 | A | G | 1 | a0004c0006t0014g0006 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3434+1463T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101755749 | |||||||
| chr12:101755776 | C | A | 1 | a0001c0001t0001g0338 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.3434+1436G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101755776 | |||||||
| chr12:101755848 | A | G | 1 | a0001c0001t0001g0307 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.3434+1364T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101755848 | |||||||
| chr12:101755978 | C | T | 53 | a0001c0001t0004g0005 a0001c0001t0004g0217 a0001c0001t0004g0233 others(50): Show |
54 | HG00544.hp1 HG00597.hp1 HG02056.hp1 others(51): Show |
intron_variant | MODIFIER | c.3434+1234G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101755978 | |||||||
| chr12:101756008 | G | C | 51 | a0001c0001t0004g0005 a0001c0001t0004g0217 a0001c0001t0004g0233 others(48): Show |
52 | HG00544.hp1 HG00597.hp1 HG02056.hp1 others(49): Show |
intron_variant | MODIFIER | c.3434+1204C>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101756008 | |||||||
| chr12:101756138 | AGCTTATG others(4): Show |
A | 2 | a0001c0003t0003g0164 a0001c0003t0003g0169 |
2 | NA18969.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.3434+1063_3434+107 others(15): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101756138 | |||||||
| chr12:101756203 | A | G | 182 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0284 others(179): Show |
185 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.3434+1009T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101756203 | |||||||
| chr12:101756286 | A | G | 2 | a0006c0016t0013g0235 a0006c0017t0013g0234 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3434+926T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101756286 | |||||||
| chr12:101756445 | C | T | 43 | a0001c0001t0006g0218 a0001c0001t0006g0220 a0001c0001t0006g0221 others(40): Show |
43 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(40): Show |
intron_variant | MODIFIER | c.3434+767G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101756445 | |||||||
| chr12:101756702 | C | T | 1 | a0001c0001t0021g0279 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3434+510G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101756702 | |||||||
| chr12:101756728 | T | C | 2 | a0006c0016t0013g0235 a0006c0017t0013g0234 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3434+484A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101756728 | |||||||
| chr12:101756899 | A | G | 6 | a0001c0001t0010g0022 a0001c0001t0010g0043 a0001c0001t0010g0044 others(3): Show |
6 | HG01109.hp1 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.3434+313T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101756899 | |||||||
| chr12:101757100 | G | C | 305 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(302): Show |
309 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(306): Show |
intron_variant | MODIFIER | c.3434+112C>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 18/20 | chr12 | 101757100 | |||||||
| chr12:101757335 | A | G | 137 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0284 others(134): Show |
140 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.3336-25T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 17/20 | chr12 | 101757335 | |||||||
| chr12:101757398 | G | A | 1 | a0001c0002t0002g0063 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3336-88C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 17/20 | chr12 | 101757398 | |||||||
| chr12:101757558 | C | T | 1 | a0001c0002t0002g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3335+14G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 17/20 | chr12 | 101757558 | |||||||
| chr12:101757559 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3335+13C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 17/20 | chr12 | 101757559 | |||||||
| chr12:101757799 | C | G | 1 | a0001c0001t0004g0376 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.3250-142G>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 16/20 | chr12 | 101757799 | |||||||
| chr12:101757960 | G | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0284 others(134): Show |
140 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.3250-303C>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 16/20 | chr12 | 101757960 | |||||||
| chr12:101757989 | T | C | 9 | a0001c0002t0008g0206 a0001c0002t0008g0207 a0001c0002t0008g0208 others(6): Show |
9 | HG01884.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.3250-332A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 16/20 | chr12 | 101757989 | |||||||
| chr12:101758021 | A | G | 2 | a0006c0016t0013g0235 a0006c0017t0013g0234 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3250-364T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 16/20 | chr12 | 101758021 | |||||||
| chr12:101758037 | A | AT | 10 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0328 others(7): Show |
10 | HG03654.hp2 HG04184.hp2 NA18978.hp2 others(7): Show |
intron_variant | MODIFIER | c.3250-381dupA | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 16/20 | chr12 | 101758037 | |||||||
| chr12:101758037 | AT | A | 137 | a0001c0001t0001g0001 a0001c0001t0001g0276 a0001c0001t0001g0277 others(134): Show |
140 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.3250-381delA | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 16/20 | chr12 | 101758037 | |||||||
| chr12:101758126 | C | T | 44 | a0001c0001t0006g0218 a0001c0001t0006g0220 a0001c0001t0006g0221 others(41): Show |
44 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.3250-469G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 16/20 | chr12 | 101758126 | |||||||
| chr12:101758156 | A | G | 2 | a0001c0002t0002g0116 a0001c0002t0002g0118 |
2 | HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3250-499T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 16/20 | chr12 | 101758156 | |||||||
| chr12:101758199 | C | T | 53 | a0001c0001t0003g0247 a0001c0003t0003g0133 a0001c0003t0003g0135 others(50): Show |
53 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.3250-542G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 16/20 | chr12 | 101758199 | |||||||
| chr12:101758237 | C | A | 1 | a0001c0001t0001g0284 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3250-580G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 16/20 | chr12 | 101758237 | |||||||
| chr12:101758286 | G | A | 1 | a0001c0007t0009g0055 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3250-629C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 16/20 | chr12 | 101758286 | |||||||
| chr12:101758359 | T | C | 1 | a0001c0002t0002g0127 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3250-702A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 16/20 | chr12 | 101758359 | |||||||
| chr12:101758441 | T | C | 59 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0004g0005 others(56): Show |
60 | HG00544.hp1 HG00597.hp1 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.3250-784A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 16/20 | chr12 | 101758441 | |||||||
| chr12:101758447 | C | T | 308 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(305): Show |
312 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(309): Show |
intron_variant | MODIFIER | c.3250-790G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 16/20 | chr12 | 101758447 | |||||||
| chr12:101758491 | C | T | 1 | a0001c0002t0002g0109 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3250-834G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 16/20 | chr12 | 101758491 | |||||||
| chr12:101758536 | A | G | 1 | a0001c0002t0005g0051 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.3250-879T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 16/20 | chr12 | 101758536 | |||||||
| chr12:101758830 | C | T | 59 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0004g0005 others(56): Show |
60 | HG00544.hp1 HG00597.hp1 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.3250-1173G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 16/20 | chr12 | 101758830 | |||||||
| chr12:101759038 | T | C | 1 | a0001c0002t0001g0359 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3249+992A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 16/20 | chr12 | 101759038 | |||||||
| chr12:101759040 | C | T | 1 | a0001c0001t0001g0360 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3249+990G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 16/20 | chr12 | 101759040 | |||||||
| chr12:101759074 | G | T | 1 | a0001c0002t0008g0237 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3249+956C>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 16/20 | chr12 | 101759074 | |||||||
| chr12:101759102 | G | T | 294 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(291): Show |
298 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.3249+928C>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 16/20 | chr12 | 101759102 | |||||||
| chr12:101759114 | G | A | 1 | a0001c0002t0001g0368 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3249+916C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 16/20 | chr12 | 101759114 | |||||||
| chr12:101759191 | G | A | 53 | a0001c0001t0003g0247 a0001c0003t0003g0133 a0001c0003t0003g0135 others(50): Show |
53 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.3249+839C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 16/20 | chr12 | 101759191 | |||||||
| chr12:101759223 | C | T | 2 | a0001c0002t0001g0205 a0001c0023t0001g0215 |
2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.3249+807G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 16/20 | chr12 | 101759223 | |||||||
| chr12:101759224 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0284 others(135): Show |
141 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(138): Show |
intron_variant | MODIFIER | c.3249+806C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 16/20 | chr12 | 101759224 | |||||||
| chr12:101759232 | G | A | 50 | a0001c0001t0004g0005 a0001c0001t0004g0217 a0001c0001t0004g0233 others(47): Show |
51 | HG00544.hp1 HG00597.hp1 HG02056.hp1 others(48): Show |
intron_variant | MODIFIER | c.3249+798C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 16/20 | chr12 | 101759232 | |||||||
| chr12:101759362 | C | CA | 138 | a0001c0001t0001g0219 a0001c0001t0001g0284 a0001c0001t0001g0285 others(135): Show |
139 | HG00544.hp1 HG00741.hp2 HG01106.hp1 others(136): Show |
intron_variant | MODIFIER | c.3249+667dupT | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 16/20 | chr12 | 101759362 | |||||||
| chr12:101759362 | C | CAA | 12 | a0001c0001t0001g0290 a0001c0001t0001g0304 a0001c0001t0001g0312 others(9): Show |
12 | HG00597.hp1 HG01099.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.3249+666_3249+667d others(4): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 16/20 | chr12 | 101759362 | |||||||
| chr12:101759362 | CA | C | 12 | a0001c0002t0002g0083 a0001c0002t0008g0206 a0001c0002t0008g0207 others(9): Show |
12 | HG01884.hp1 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.3249+667delT | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 16/20 | chr12 | 101759362 | |||||||
| chr12:101759419 | T | TA | 36 | a0001c0001t0001g0290 a0001c0001t0006g0218 a0001c0001t0006g0220 others(33): Show |
36 | HG00323.hp1 HG00408.hp2 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.3249+610dupT | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 16/20 | chr12 | 101759419 | |||||||
| chr12:101759419 | T | TAA | 11 | a0001c0001t0006g0252 a0001c0001t0006g0274 a0001c0002t0008g0206 others(8): Show |
11 | HG01884.hp1 HG02145.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.3249+609_3249+610d others(4): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 16/20 | chr12 | 101759419 | |||||||
| chr12:101759602 | A | G | 2 | a0006c0016t0013g0235 a0006c0017t0013g0234 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3249+428T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 16/20 | chr12 | 101759602 | |||||||
| chr12:101759641 | A | G | 2 | a0006c0016t0013g0235 a0006c0017t0013g0234 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3249+389T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 16/20 | chr12 | 101759641 | |||||||
| chr12:101759718 | T | C | 2 | a0001c0002t0001g0205 a0001c0023t0001g0215 |
2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.3249+312A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 16/20 | chr12 | 101759718 | |||||||
| chr12:101759882 | C | T | 2 | a0006c0016t0013g0235 a0006c0017t0013g0234 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3249+148G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 16/20 | chr12 | 101759882 | |||||||
| chr12:101760292 | C | CCT | 24 | a0001c0001t0001g0001 a0001c0001t0001g0360 a0001c0001t0001g0361 others(21): Show |
27 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.3136-150_3136-149i others(4): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 15/20 | chr12 | 101760292 | |||||||
| chr12:101760400 | G | A | 36 | a0001c0001t0006g0218 a0001c0001t0006g0220 a0001c0001t0006g0221 others(33): Show |
36 | HG00323.hp1 HG00408.hp2 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.3136-257C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 15/20 | chr12 | 101760400 | |||||||
| chr12:101760401 | G | C | 7 | a0003c0005t0001g0280 a0003c0005t0001g0281 a0003c0005t0001g0282 others(4): Show |
7 | HG02109.hp2 HG02647.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.3136-258C>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 15/20 | chr12 | 101760401 | |||||||
| chr12:101760438 | C | T | 24 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0010 others(21): Show |
24 | HG01106.hp1 HG01516.hp2 HG02735.hp2 others(21): Show |
intron_variant | MODIFIER | c.3136-295G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 15/20 | chr12 | 101760438 | |||||||
| chr12:101760605 | T | C | 1 | a0001c0001t0006g0229 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3136-462A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 15/20 | chr12 | 101760605 | |||||||
| chr12:101760690 | C | A | 1 | a0001c0001t0004g0233 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3135+437G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 15/20 | chr12 | 101760690 | |||||||
| chr12:101760703 | T | A | 1 | a0001c0001t0001g0337 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3135+424A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 15/20 | chr12 | 101760703 | |||||||
| chr12:101760772 | T | A | 1 | a0001c0001t0001g0380 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3135+355A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 15/20 | chr12 | 101760772 | |||||||
| chr12:101760781 | C | CT | 60 | a0001c0001t0001g0306 a0001c0001t0003g0247 a0001c0001t0006g0252 others(57): Show |
60 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.3135+345dupA | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 15/20 | chr12 | 101760781 | |||||||
| chr12:101760786 | T | C | 3 | a0001c0001t0005g0007 a0001c0001t0005g0016 a0001c0001t0005g0020 |
3 | NA18956.hp2 NA18967.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.3135+341A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 15/20 | chr12 | 101760786 | |||||||
| chr12:101760882 | C | T | 1 | a0001c0002t0008g0237 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3135+245G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 15/20 | chr12 | 101760882 | |||||||
| chr12:101761122 | A | G | 305 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(302): Show |
309 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(306): Show |
splice_region_variant&intron_variant | LOW | c.3135+5T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 15/20 | chr12 | 101761122 | |||||||
| chr12:101761861 | G | A | 1 | a0001c0001t0004g0266 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2716-98C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 13/20 | chr12 | 101761861 | |||||||
| chr12:101761938 | A | G | 1 | a0001c0002t0002g0110 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2716-175T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 13/20 | chr12 | 101761938 | |||||||
| chr12:101761987 | G | A | 1 | a0001c0001t0006g0220 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2716-224C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 13/20 | chr12 | 101761987 | |||||||
| chr12:101762156 | T | C | 4 | a0001c0007t0009g0053 a0001c0007t0009g0055 a0001c0007t0009g0056 others(1): Show |
4 | HG02486.hp1 HG02723.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2716-393A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 13/20 | chr12 | 101762156 | |||||||
| chr12:101762163 | G | A | 1 | a0001c0001t0021g0279 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2716-400C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 13/20 | chr12 | 101762163 | |||||||
| chr12:101762222 | T | C | 37 | a0001c0001t0006g0218 a0001c0001t0006g0220 a0001c0001t0006g0221 others(34): Show |
37 | HG00323.hp1 HG00408.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.2716-459A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 13/20 | chr12 | 101762222 | |||||||
| chr12:101762425 | C | T | 1 | a0001c0025t0001g0213 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2716-662G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 13/20 | chr12 | 101762425 | |||||||
| chr12:101762522 | G | A | 1 | a0001c0002t0002g0102 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2716-759C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 13/20 | chr12 | 101762522 | |||||||
| chr12:101762524 | G | A | 52 | a0001c0001t0004g0005 a0001c0001t0004g0217 a0001c0001t0004g0233 others(49): Show |
53 | HG00544.hp1 HG00597.hp1 HG02056.hp1 others(50): Show |
intron_variant | MODIFIER | c.2716-761C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 13/20 | chr12 | 101762524 | |||||||
| chr12:101762525 | A | T | 305 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(302): Show |
309 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(306): Show |
intron_variant | MODIFIER | c.2716-762T>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 13/20 | chr12 | 101762525 | |||||||
| chr12:101762726 | C | G | 52 | a0001c0001t0004g0005 a0001c0001t0004g0217 a0001c0001t0004g0233 others(49): Show |
53 | HG00544.hp1 HG00597.hp1 HG02056.hp1 others(50): Show |
intron_variant | MODIFIER | c.2716-963G>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 13/20 | chr12 | 101762726 | |||||||
| chr12:101762734 | T | C | 2 | a0001c0002t0001g0205 a0001c0023t0001g0215 |
2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2716-971A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 13/20 | chr12 | 101762734 | |||||||
| chr12:101762804 | C | T | 1 | a0001c0004t0006g0203 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2716-1041G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 13/20 | chr12 | 101762804 | |||||||
| chr12:101762903 | T | TA | 193 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0284 others(190): Show |
196 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(193): Show |
intron_variant | MODIFIER | c.2716-1141dupT | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 13/20 | chr12 | 101762903 | |||||||
| chr12:101762903 | TA | T | 56 | a0001c0001t0004g0005 a0001c0001t0004g0217 a0001c0001t0004g0233 others(53): Show |
57 | HG00544.hp1 HG00597.hp1 HG01168.hp1 others(54): Show |
intron_variant | MODIFIER | c.2716-1141delT | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 13/20 | chr12 | 101762903 | |||||||
| chr12:101762959 | G | A | 1 | a0001c0002t0002g0113 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2716-1196C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 13/20 | chr12 | 101762959 | |||||||
| chr12:101762963 | G | A | 23 | a0001c0001t0001g0001 a0001c0001t0001g0360 a0001c0001t0001g0361 others(20): Show |
26 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.2716-1200C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 13/20 | chr12 | 101762963 | |||||||
| chr12:101762986 | C | T | 1 | a0001c0025t0001g0213 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2715+1216G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 13/20 | chr12 | 101762986 | |||||||
| chr12:101763049 | C | T | 1 | a0001c0003t0003g0133 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2715+1153G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 13/20 | chr12 | 101763049 | |||||||
| chr12:101763174 | A | G | 9 | a0001c0002t0008g0206 a0001c0002t0008g0207 a0001c0002t0008g0208 others(6): Show |
9 | HG01884.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2715+1028T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 13/20 | chr12 | 101763174 | |||||||
| chr12:101763208 | C | T | 1 | a0001c0001t0009g0052 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2715+994G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 13/20 | chr12 | 101763208 | |||||||
| chr12:101763233 | AAAAAG | A | 112 | a0001c0001t0001g0219 a0001c0001t0001g0284 a0001c0001t0001g0285 others(109): Show |
112 | HG00408.hp1 HG00423.hp2 HG01099.hp1 others(109): Show |
intron_variant | MODIFIER | c.2715+964_2715+968d others(7): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 13/20 | chr12 | 101763233 | |||||||
| chr12:101763234 | AAAAG | A | 26 | a0001c0001t0001g0001 a0001c0001t0001g0360 a0001c0001t0001g0361 others(23): Show |
29 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.2715+964_2715+967d others(6): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 13/20 | chr12 | 101763234 | |||||||
| chr12:101763237 | A | G | 1 | a0001c0001t0024g0353 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2715+965T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 13/20 | chr12 | 101763237 | |||||||
| chr12:101763463 | G | A | 50 | a0001c0001t0004g0005 a0001c0001t0004g0217 a0001c0001t0004g0233 others(47): Show |
51 | HG00544.hp1 HG00597.hp1 HG02056.hp1 others(48): Show |
intron_variant | MODIFIER | c.2715+739C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 13/20 | chr12 | 101763463 | |||||||
| chr12:101763775 | G | C | 114 | a0001c0001t0001g0219 a0001c0001t0001g0284 a0001c0001t0001g0285 others(111): Show |
114 | HG00408.hp1 HG00423.hp2 HG01099.hp1 others(111): Show |
intron_variant | MODIFIER | c.2715+427C>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 13/20 | chr12 | 101763775 | |||||||
| chr12:101763883 | A | G | 2 | a0001c0002t0001g0205 a0001c0023t0001g0215 |
2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2715+319T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 13/20 | chr12 | 101763883 | |||||||
| chr12:101764076 | A | C | 2 | a0001c0007t0004g0231 a0001c0007t0004g0232 |
2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2715+126T>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 13/20 | chr12 | 101764076 | |||||||
| chr12:101764088 | T | C | 2 | a0001c0002t0001g0205 a0001c0023t0001g0215 |
2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2715+114A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 13/20 | chr12 | 101764088 | |||||||
| chr12:101765353 | CCT | C | 2 | a0001c0001t0001g0001 a0001c0001t0001g0362 |
5 | HG02280.hp1 HG02630.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1613-51_1613-50del others(2): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 12/20 | chr12 | 101765353 | |||||||
| chr12:101765614 | T | C | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1613-310A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 12/20 | chr12 | 101765614 | |||||||
| chr12:101765660 | T | C | 1 | a0001c0001t0006g0225 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1613-356A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 12/20 | chr12 | 101765660 | |||||||
| chr12:101765745 | T | C | 53 | a0001c0001t0003g0247 a0001c0003t0003g0133 a0001c0003t0003g0135 others(50): Show |
53 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.1612+346A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 12/20 | chr12 | 101765745 | |||||||
| chr12:101765865 | CAAACA | C | 21 | a0001c0001t0006g0218 a0001c0001t0006g0220 a0001c0001t0006g0221 others(18): Show |
21 | HG00323.hp1 HG00408.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.1612+221_1612+225d others(7): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 12/20 | chr12 | 101765865 | |||||||
| chr12:101766047 | G | A | 1 | a0001c0001t0001g0302 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1612+44C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 12/20 | chr12 | 101766047 | |||||||
| chr12:101766063 | A | G | 7 | a0002c0009t0001g0195 a0002c0009t0001g0200 a0002c0009t0001g0201 others(4): Show |
7 | HG00280.hp1 HG00741.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1612+28T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 12/20 | chr12 | 101766063 | |||||||
| chr12:101766328 | G | A | 3 | a0001c0007t0009g0053 a0001c0007t0009g0056 a0001c0007t0009g0057 |
3 | HG02486.hp1 HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1409-34C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 11/20 | chr12 | 101766328 | |||||||
| chr12:101766563 | G | A | 1 | a0001c0002t0002g0102 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1409-269C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 11/20 | chr12 | 101766563 | |||||||
| chr12:101766584 | G | C | 1 | a0001c0025t0001g0213 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1409-290C>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 11/20 | chr12 | 101766584 | |||||||
| chr12:101766633 | C | T | 1 | a0001c0002t0002g0082 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1409-339G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 11/20 | chr12 | 101766633 | |||||||
| chr12:101766683 | G | A | 6 | a0004c0006t0007g0187 a0004c0006t0007g0191 a0004c0006t0007g0192 others(3): Show |
6 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1409-389C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 11/20 | chr12 | 101766683 | |||||||
| chr12:101766849 | G | T | 59 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0004g0005 others(56): Show |
60 | HG00544.hp1 HG00597.hp1 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.1409-555C>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 11/20 | chr12 | 101766849 | |||||||
| chr12:101766895 | C | T | 9 | a0001c0002t0008g0206 a0001c0002t0008g0207 a0001c0002t0008g0208 others(6): Show |
9 | HG01884.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1409-601G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 11/20 | chr12 | 101766895 | |||||||
| chr12:101767113 | T | C | 7 | a0001c0001t0009g0052 a0001c0007t0004g0231 a0001c0007t0004g0232 others(4): Show |
7 | HG01167.hp2 HG02486.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1409-819A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 11/20 | chr12 | 101767113 | |||||||
| chr12:101767325 | A | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0284 others(187): Show |
193 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.1408+712T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 11/20 | chr12 | 101767325 | |||||||
| chr12:101767351 | C | T | 1 | a0001c0022t0006g0223 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1408+686G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 11/20 | chr12 | 101767351 | |||||||
| chr12:101767435 | G | T | 1 | a0001c0002t0002g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1408+602C>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 11/20 | chr12 | 101767435 | |||||||
| chr12:101767586 | G | T | 50 | a0001c0001t0004g0005 a0001c0001t0004g0217 a0001c0001t0004g0233 others(47): Show |
51 | HG00544.hp1 HG00597.hp1 HG02056.hp1 others(48): Show |
intron_variant | MODIFIER | c.1408+451C>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 11/20 | chr12 | 101767586 | |||||||
| chr12:101767618 | T | C | 53 | a0001c0001t0003g0247 a0001c0003t0003g0133 a0001c0003t0003g0135 others(50): Show |
53 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.1408+419A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 11/20 | chr12 | 101767618 | |||||||
| chr12:101767658 | T | C | 1 | a0001c0001t0021g0279 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1408+379A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 11/20 | chr12 | 101767658 | |||||||
| chr12:101767720 | T | G | 4 | a0001c0002t0002g0003 a0001c0002t0002g0119 a0001c0002t0002g0121 others(1): Show |
5 | HG00280.hp2 HG01123.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.1408+317A>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 11/20 | chr12 | 101767720 | |||||||
| chr12:101767778 | A | G | 1 | a0001c0002t0005g0025 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1408+259T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 11/20 | chr12 | 101767778 | |||||||
| chr12:101767898 | T | C | 1 | a0001c0001t0010g0045 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1408+139A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 11/20 | chr12 | 101767898 | |||||||
| chr12:101767899 | G | A | 4 | a0001c0002t0002g0003 a0001c0002t0002g0119 a0001c0002t0002g0121 others(1): Show |
5 | HG00280.hp2 HG01123.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.1408+138C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 11/20 | chr12 | 101767899 | |||||||
| chr12:101768326 | C | T | 294 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(291): Show |
298 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.1285-166G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 10/20 | chr12 | 101768326 | |||||||
| chr12:101768350 | G | A | 4 | a0001c0001t0011g0059 a0001c0001t0011g0060 a0001c0001t0011g0061 others(1): Show |
4 | NA18747.hp1 NA18971.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.1285-190C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 10/20 | chr12 | 101768350 | |||||||
| chr12:101768397 | G | C | 1 | a0001c0001t0021g0279 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1285-237C>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 10/20 | chr12 | 101768397 | |||||||
| chr12:101768547 | G | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0284 others(178): Show |
184 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.1285-387C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 10/20 | chr12 | 101768547 | |||||||
| chr12:101768595 | G | A | 7 | a0002c0009t0001g0195 a0002c0009t0001g0200 a0002c0009t0001g0201 others(4): Show |
7 | HG00280.hp1 HG00741.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1285-435C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 10/20 | chr12 | 101768595 | |||||||
| chr12:101768742 | ACTC | A | 53 | a0001c0001t0003g0247 a0001c0003t0003g0133 a0001c0003t0003g0135 others(50): Show |
53 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.1285-585_1285-583d others(5): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 10/20 | chr12 | 101768742 | |||||||
| chr12:101769022 | G | A | 2 | a0001c0007t0004g0231 a0001c0007t0004g0232 |
2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1285-862C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 10/20 | chr12 | 101769022 | |||||||
| chr12:101769024 | G | C | 1 | a0001c0007t0009g0056 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1285-864C>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 10/20 | chr12 | 101769024 | |||||||
| chr12:101769128 | G | A | 1 | a0001c0025t0001g0213 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1284+893C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 10/20 | chr12 | 101769128 | |||||||
| chr12:101769144 | CT | C | 50 | a0001c0001t0004g0005 a0001c0001t0004g0217 a0001c0001t0004g0233 others(47): Show |
51 | HG00544.hp1 HG00597.hp1 HG02056.hp1 others(48): Show |
intron_variant | MODIFIER | c.1284+876delA | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 10/20 | chr12 | 101769144 | |||||||
| chr12:101769151 | C | A | 1 | a0001c0001t0001g0361 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1284+870G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 10/20 | chr12 | 101769151 | |||||||
| chr12:101769227 | G | A | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1284+794C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 10/20 | chr12 | 101769227 | |||||||
| chr12:101769229 | C | A | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1284+792G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 10/20 | chr12 | 101769229 | |||||||
| chr12:101769230 | C | T | 1 | a0006c0017t0013g0234 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1284+791G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 10/20 | chr12 | 101769230 | |||||||
| chr12:101769231 | A | T | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1284+790T>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 10/20 | chr12 | 101769231 | |||||||
| chr12:101769234 | G | A | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1284+787C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 10/20 | chr12 | 101769234 | |||||||
| chr12:101769238 | T | G | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1284+783A>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 10/20 | chr12 | 101769238 | |||||||
| chr12:101769240 | C | G | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1284+781G>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 10/20 | chr12 | 101769240 | |||||||
| chr12:101769256 | T | C | 305 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(302): Show |
309 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(306): Show |
intron_variant | MODIFIER | c.1284+765A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 10/20 | chr12 | 101769256 | |||||||
| chr12:101769260 | T | G | 1 | a0001c0003t0003g0169 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1284+761A>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 10/20 | chr12 | 101769260 | |||||||
| chr12:101769273 | C | T | 1 | a0001c0008t0004g0216 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1284+748G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 10/20 | chr12 | 101769273 | |||||||
| chr12:101769453 | T | C | 2 | a0001c0001t0023g0371 a0001c0004t0007g0198 |
2 | HG02717.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1284+568A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 10/20 | chr12 | 101769453 | |||||||
| chr12:101769498 | C | G | 1 | a0001c0001t0001g0298 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1284+523G>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 10/20 | chr12 | 101769498 | |||||||
| chr12:101769735 | C | T | 53 | a0001c0001t0003g0247 a0001c0003t0003g0133 a0001c0003t0003g0135 others(50): Show |
53 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.1284+286G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 10/20 | chr12 | 101769735 | |||||||
| chr12:101769738 | G | A | 2 | a0001c0001t0001g0360 a0001c0001t0001g0363 |
2 | HG02970.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1284+283C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 10/20 | chr12 | 101769738 | |||||||
| chr12:101769782 | C | T | 1 | a0001c0002t0002g0109 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1284+239G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 10/20 | chr12 | 101769782 | |||||||
| chr12:101770208 | A | G | 7 | a0001c0002t0008g0206 a0001c0002t0008g0207 a0001c0002t0008g0208 others(4): Show |
7 | HG01884.hp1 HG02145.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1114-17T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 9/20 | chr12 | 101770208 | |||||||
| chr12:101770352 | C | T | 5 | a0001c0001t0007g0278 a0001c0001t0020g0117 a0001c0004t0007g0188 others(2): Show |
5 | HG01081.hp1 HG02630.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1113+54G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 9/20 | chr12 | 101770352 | |||||||
| chr12:101770727 | A | G | 21 | a0001c0001t0006g0218 a0001c0001t0006g0220 a0001c0001t0006g0221 others(18): Show |
21 | HG00323.hp1 HG00408.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.934-142T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 8/20 | chr12 | 101770727 | |||||||
| chr12:101771221 | T | A | 1 | a0001c0001t0001g0318 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.772-64A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101771221 | |||||||
| chr12:101771240 | T | A | 1 | a0001c0001t0001g0363 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.772-83A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101771240 | |||||||
| chr12:101771246 | C | CT | 30 | a0001c0001t0001g0291 a0001c0001t0001g0297 a0001c0001t0001g0298 others(27): Show |
30 | HG00408.hp1 HG00423.hp2 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.772-90dupA | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101771246 | |||||||
| chr12:101771246 | C | CTT | 9 | a0001c0002t0008g0206 a0001c0002t0008g0207 a0001c0002t0008g0208 others(6): Show |
9 | HG01884.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.772-91_772-90dupAA | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101771246 | |||||||
| chr12:101771246 | CT | C | 7 | a0001c0001t0004g0272 a0001c0001t0005g0011 a0001c0001t0021g0279 others(4): Show |
7 | HG02486.hp2 HG02922.hp2 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.772-90delA | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101771246 | |||||||
| chr12:101771305 | A | G | 306 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(303): Show |
311 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.772-148T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101771305 | |||||||
| chr12:101771330 | G | A | 1 | a0001c0007t0009g0053 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.772-173C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101771330 | |||||||
| chr12:101771393 | A | G | 1 | a0001c0002t0002g0111 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.772-236T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101771393 | |||||||
| chr12:101771523 | C | T | 2 | a0001c0002t0002g0116 a0001c0002t0002g0118 |
2 | HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.772-366G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101771523 | |||||||
| chr12:101771554 | T | G | 2 | a0002c0012t0001g0214 a0002c0012t0002g0077 |
2 | HG00280.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.772-397A>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101771554 | |||||||
| chr12:101771564 | G | A | 106 | a0001c0001t0001g0219 a0001c0001t0001g0284 a0001c0001t0001g0285 others(103): Show |
106 | HG00408.hp1 HG00423.hp2 HG01099.hp1 others(103): Show |
intron_variant | MODIFIER | c.772-407C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101771564 | |||||||
| chr12:101771646 | A | G | 1 | a0009c0019t0002g0064 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.772-489T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101771646 | |||||||
| chr12:101771773 | T | C | 1 | a0001c0001t0004g0217 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.772-616A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101771773 | |||||||
| chr12:101771836 | G | C | 1 | a0001c0002t0002g0116 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.772-679C>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101771836 | |||||||
| chr12:101771989 | G | A | 2 | a0001c0002t0001g0356 a0001c0002t0001g0359 |
2 | HG00642.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.772-832C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101771989 | |||||||
| chr12:101771992 | G | A | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-835C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101771992 | |||||||
| chr12:101771999 | C | T | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-842G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101771999 | |||||||
| chr12:101772000 | G | A | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-843C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772000 | |||||||
| chr12:101772002 | C | A | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-845G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772002 | |||||||
| chr12:101772003 | A | T | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-846T>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772003 | |||||||
| chr12:101772004 | G | C | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-847C>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772004 | |||||||
| chr12:101772006 | A | C | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-849T>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772006 | |||||||
| chr12:101772007 | C | G | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-850G>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772007 | |||||||
| chr12:101772010 | C | T | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-853G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772010 | |||||||
| chr12:101772011 | C | T | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-854G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772011 | |||||||
| chr12:101772013 | G | C | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-856C>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772013 | |||||||
| chr12:101772015 | A | T | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-858T>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772015 | |||||||
| chr12:101772016 | G | T | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-859C>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772016 | |||||||
| chr12:101772018 | G | A | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-861C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772018 | |||||||
| chr12:101772021 | T | A | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-864A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772021 | |||||||
| chr12:101772022 | C | A | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-865G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772022 | |||||||
| chr12:101772026 | G | A | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-869C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772026 | |||||||
| chr12:101772027 | G | T | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-870C>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772027 | |||||||
| chr12:101772028 | G | A | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-871C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772028 | |||||||
| chr12:101772034 | T | G | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-877A>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772034 | |||||||
| chr12:101772035 | A | T | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-878T>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772035 | |||||||
| chr12:101772038 | T | C | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-881A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772038 | |||||||
| chr12:101772039 | T | A | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-882A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772039 | |||||||
| chr12:101772040 | T | G | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-883A>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772040 | |||||||
| chr12:101772041 | T | A | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-884A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772041 | |||||||
| chr12:101772044 | G | A | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-887C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772044 | |||||||
| chr12:101772046 | C | A | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-889G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772046 | |||||||
| chr12:101772047 | A | G | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-890T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772047 | |||||||
| chr12:101772051 | C | A | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-894G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772051 | |||||||
| chr12:101772052 | T | G | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-895A>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772052 | |||||||
| chr12:101772053 | T | A | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-896A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772053 | |||||||
| chr12:101772054 | T | A | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-897A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772054 | |||||||
| chr12:101772055 | T | A | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-898A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772055 | |||||||
| chr12:101772057 | G | A | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-900C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772057 | |||||||
| chr12:101772063 | T | A | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-906A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772063 | |||||||
| chr12:101772064 | C | G | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-907G>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772064 | |||||||
| chr12:101772066 | T | A | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-909A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772066 | |||||||
| chr12:101772067 | A | T | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-910T>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772067 | |||||||
| chr12:101772071 | C | T | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-914G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772071 | |||||||
| chr12:101772072 | T | G | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-915A>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772072 | |||||||
| chr12:101772076 | C | A | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-919G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772076 | |||||||
| chr12:101772077 | G | A | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-920C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772077 | |||||||
| chr12:101772078 | T | A | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-921A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772078 | |||||||
| chr12:101772079 | G | T | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-922C>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772079 | |||||||
| chr12:101772082 | C | T | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-925G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772082 | |||||||
| chr12:101772083 | A | G | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-926T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772083 | |||||||
| chr12:101772084 | T | G | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-927A>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772084 | |||||||
| chr12:101772086 | A | C | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-929T>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772086 | |||||||
| chr12:101772090 | A | T | 50 | a0001c0001t0004g0005 a0001c0001t0004g0217 a0001c0001t0004g0233 others(47): Show |
51 | HG00544.hp1 HG00597.hp1 HG02056.hp1 others(48): Show |
intron_variant | MODIFIER | c.772-933T>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772090 | |||||||
| chr12:101772091 | C | G | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-934G>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772091 | |||||||
| chr12:101772094 | C | G | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-937G>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772094 | |||||||
| chr12:101772105 | A | G | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-948T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772105 | |||||||
| chr12:101772109 | G | T | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-952C>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772109 | |||||||
| chr12:101772111 | C | A | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-954G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772111 | |||||||
| chr12:101772112 | T | A | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-955A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772112 | |||||||
| chr12:101772114 | T | A | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-957A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772114 | |||||||
| chr12:101772115 | G | T | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-958C>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772115 | |||||||
| chr12:101772116 | C | A | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-959G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772116 | |||||||
| chr12:101772120 | C | A | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-963G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772120 | |||||||
| chr12:101772121 | C | T | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-964G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772121 | |||||||
| chr12:101772125 | C | A | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-968G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772125 | |||||||
| chr12:101772131 | T | C | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-974A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772131 | |||||||
| chr12:101772132 | C | T | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-975G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772132 | |||||||
| chr12:101772135 | C | A | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-978G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772135 | |||||||
| chr12:101772137 | C | A | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-980G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772137 | |||||||
| chr12:101772138 | C | A | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-981G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772138 | |||||||
| chr12:101772145 | T | A | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-988A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772145 | |||||||
| chr12:101772147 | T | G | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-990A>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772147 | |||||||
| chr12:101772148 | C | A | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-991G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772148 | |||||||
| chr12:101772150 | G | A | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-993C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772150 | |||||||
| chr12:101772151 | T | A | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-994A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772151 | |||||||
| chr12:101772152 | T | A | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-995A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772152 | |||||||
| chr12:101772153 | T | C | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-996A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772153 | |||||||
| chr12:101772158 | T | G | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-1001A>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772158 | |||||||
| chr12:101772159 | T | A | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-1002A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772159 | |||||||
| chr12:101772160 | C | G | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-1003G>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772160 | |||||||
| chr12:101772161 | T | G | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-1004A>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772161 | |||||||
| chr12:101772163 | A | G | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-1006T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772163 | |||||||
| chr12:101772164 | C | G | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-1007G>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772164 | |||||||
| chr12:101772166 | C | A | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-1009G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772166 | |||||||
| chr12:101772167 | T | C | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-1010A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772167 | |||||||
| chr12:101772204 | T | G | 1 | a0001c0007t0009g0055 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.772-1047A>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772204 | |||||||
| chr12:101772375 | C | A | 6 | a0004c0006t0007g0187 a0004c0006t0007g0191 a0004c0006t0007g0192 others(3): Show |
6 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.772-1218G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772375 | |||||||
| chr12:101772432 | AG | A | 7 | a0002c0009t0001g0195 a0002c0009t0001g0200 a0002c0009t0001g0201 others(4): Show |
7 | HG00280.hp1 HG00741.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.772-1276delC | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772432 | |||||||
| chr12:101772435 | G | A | 7 | a0002c0009t0001g0195 a0002c0009t0001g0200 a0002c0009t0001g0201 others(4): Show |
7 | HG00280.hp1 HG00741.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.772-1278C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772435 | |||||||
| chr12:101772451 | A | T | 58 | a0001c0001t0002g0081 a0001c0001t0002g0089 a0001c0001t0002g0093 others(55): Show |
58 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.772-1294T>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772451 | |||||||
| chr12:101772467 | T | C | 5 | a0001c0002t0001g0364 a0001c0002t0001g0365 a0001c0002t0001g0366 others(2): Show |
5 | HG02559.hp1 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.772-1310A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772467 | |||||||
| chr12:101772749 | C | A | 53 | a0001c0001t0003g0247 a0001c0003t0003g0133 a0001c0003t0003g0135 others(50): Show |
53 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.772-1592G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772749 | |||||||
| chr12:101772908 | C | T | 41 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0010 others(38): Show |
41 | HG01106.hp1 HG01516.hp2 HG01981.hp1 others(38): Show |
intron_variant | MODIFIER | c.772-1751G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772908 | |||||||
| chr12:101772909 | C | T | 23 | a0001c0001t0001g0297 a0001c0001t0001g0298 a0001c0001t0001g0305 others(20): Show |
23 | HG00408.hp1 HG00423.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.772-1752G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772909 | |||||||
| chr12:101772955 | T | G | 5 | a0002c0009t0001g0195 a0002c0009t0001g0200 a0002c0009t0001g0201 others(2): Show |
5 | HG02258.hp1 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.772-1798A>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772955 | |||||||
| chr12:101772984 | T | C | 1 | a0001c0001t0001g0308 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.772-1827A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101772984 | |||||||
| chr12:101773024 | T | C | 97 | a0001c0001t0001g0001 a0001c0001t0001g0297 a0001c0001t0001g0298 others(94): Show |
100 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.772-1867A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101773024 | |||||||
| chr12:101773032 | C | T | 1 | a0006c0017t0013g0234 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.772-1875G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101773032 | |||||||
| chr12:101773091 | G | A | 1 | a0001c0001t0001g0332 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.772-1934C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101773091 | |||||||
| chr12:101773134 | A | C | 321 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(318): Show |
325 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(322): Show |
intron_variant | MODIFIER | c.772-1977T>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101773134 | |||||||
| chr12:101773182 | T | C | 1 | a0001c0001t0005g0007 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.772-2025A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101773182 | |||||||
| chr12:101773200 | C | T | 35 | a0001c0001t0001g0286 a0001c0001t0001g0290 a0001c0001t0001g0313 others(32): Show |
36 | HG00544.hp2 HG02132.hp1 HG02135.hp1 others(33): Show |
intron_variant | MODIFIER | c.772-2043G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101773200 | |||||||
| chr12:101773250 | T | C | 5 | a0001c0001t0001g0369 a0001c0001t0001g0370 a0001c0001t0001g0374 others(2): Show |
5 | HG02895.hp1 HG02897.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.772-2093A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101773250 | |||||||
| chr12:101773284 | A | G | 1 | a0001c0004t0007g0197 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.772-2127T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101773284 | |||||||
| chr12:101773307 | CCATGCTC others(4): Show |
C | 2 | a0001c0002t0008g0237 a0001c0007t0009g0056 |
2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.772-2161_772-2151d others(13): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101773307 | |||||||
| chr12:101773339 | A | G | 121 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0284 others(118): Show |
122 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.772-2182T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101773339 | |||||||
| chr12:101773386 | G | A | 1 | a0001c0004t0007g0197 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.772-2229C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101773386 | |||||||
| chr12:101773660 | C | T | 14 | a0001c0001t0007g0278 a0001c0001t0020g0117 a0001c0004t0007g0188 others(11): Show |
14 | HG01081.hp1 HG01243.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.772-2503G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101773660 | |||||||
| chr12:101773714 | A | AT | 8 | a0001c0002t0008g0206 a0001c0002t0008g0207 a0001c0002t0008g0208 others(5): Show |
8 | HG01884.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.772-2558dupA | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101773714 | |||||||
| chr12:101773777 | T | A | 1 | a0001c0001t0011g0125 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.772-2620A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101773777 | |||||||
| chr12:101774254 | G | A | 1 | a0001c0001t0002g0068 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.772-3097C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101774254 | |||||||
| chr12:101774373 | T | C | 58 | a0001c0001t0003g0247 a0001c0001t0009g0052 a0001c0003t0003g0133 others(55): Show |
58 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.772-3216A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101774373 | |||||||
| chr12:101774434 | G | C | 1 | a0002c0009t0001g0195 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.772-3277C>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101774434 | |||||||
| chr12:101774886 | A | C | 23 | a0001c0001t0001g0001 a0001c0001t0001g0360 a0001c0001t0001g0361 others(20): Show |
26 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.772-3729T>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101774886 | |||||||
| chr12:101775098 | G | A | 1 | a0001c0001t0010g0045 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.772-3941C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101775098 | |||||||
| chr12:101775287 | C | A | 1 | a0001c0001t0002g0067 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.772-4130G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101775287 | |||||||
| chr12:101775303 | C | T | 2 | a0001c0001t0010g0022 a0001c0001t0015g0019 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.772-4146G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101775303 | |||||||
| chr12:101775355 | T | A | 2 | a0001c0002t0001g0205 a0001c0023t0001g0215 |
2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.772-4198A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101775355 | |||||||
| chr12:101775365 | C | CT | 301 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(298): Show |
305 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.772-4209dupA | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101775365 | |||||||
| chr12:101775365 | C | CTT | 21 | a0001c0001t0001g0360 a0001c0001t0001g0361 a0001c0001t0001g0363 others(18): Show |
21 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.772-4210_772-4209d others(4): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101775365 | |||||||
| chr12:101775644 | T | C | 1 | a0001c0002t0002g0078 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.772-4487A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101775644 | |||||||
| chr12:101775658 | C | T | 1 | a0001c0002t0002g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.771+4494G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101775658 | |||||||
| chr12:101775662 | C | T | 1 | a0001c0001t0004g0259 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.771+4490G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101775662 | |||||||
| chr12:101775680 | C | T | 1 | a0001c0001t0021g0279 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.771+4472G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101775680 | |||||||
| chr12:101775721 | G | T | 41 | a0001c0001t0006g0218 a0001c0001t0006g0220 a0001c0001t0006g0221 others(38): Show |
41 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(38): Show |
intron_variant | MODIFIER | c.771+4431C>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101775721 | |||||||
| chr12:101775874 | A | T | 1 | a0001c0002t0002g0105 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.771+4278T>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101775874 | |||||||
| chr12:101775926 | G | T | 19 | a0001c0001t0006g0218 a0001c0001t0006g0220 a0001c0001t0006g0221 others(16): Show |
19 | HG00323.hp1 HG00408.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.771+4226C>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101775926 | |||||||
| chr12:101776070 | C | CTTATAGA others(1): Show |
52 | a0001c0001t0004g0005 a0001c0001t0004g0217 a0001c0001t0004g0233 others(49): Show |
53 | HG00544.hp1 HG00597.hp1 HG02056.hp1 others(50): Show |
intron_variant | MODIFIER | c.771+4081_771+4082i others(10): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101776070 | |||||||
| chr12:101776174 | C | T | 52 | a0001c0001t0004g0005 a0001c0001t0004g0217 a0001c0001t0004g0233 others(49): Show |
53 | HG00544.hp1 HG00597.hp1 HG02056.hp1 others(50): Show |
intron_variant | MODIFIER | c.771+3978G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101776174 | |||||||
| chr12:101776461 | T | C | 1 | a0001c0001t0004g0244 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.771+3691A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101776461 | |||||||
| chr12:101776667 | G | A | 322 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(319): Show |
326 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(323): Show |
intron_variant | MODIFIER | c.771+3485C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101776667 | |||||||
| chr12:101776688 | A | T | 1 | a0001c0001t0005g0011 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.771+3464T>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101776688 | |||||||
| chr12:101776811 | G | A | 1 | a0001c0004t0006g0203 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.771+3341C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101776811 | |||||||
| chr12:101776973 | G | C | 322 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(319): Show |
326 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(323): Show |
intron_variant | MODIFIER | c.771+3179C>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101776973 | |||||||
| chr12:101776999 | C | T | 102 | a0001c0001t0001g0219 a0001c0001t0001g0284 a0001c0001t0001g0285 others(99): Show |
102 | HG00642.hp1 HG01099.hp1 HG01106.hp1 others(99): Show |
intron_variant | MODIFIER | c.771+3153G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101776999 | |||||||
| chr12:101777123 | C | T | 2 | a0001c0001t0001g0360 a0001c0001t0001g0363 |
2 | HG02970.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.771+3029G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101777123 | |||||||
| chr12:101777302 | C | T | 1 | a0001c0001t0006g0221 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.771+2850G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101777302 | |||||||
| chr12:101777698 | T | G | 58 | a0001c0001t0003g0247 a0001c0001t0009g0052 a0001c0003t0003g0133 others(55): Show |
58 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.771+2454A>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101777698 | |||||||
| chr12:101777768 | T | A | 1 | a0001c0001t0003g0247 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.771+2384A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101777768 | |||||||
| chr12:101777809 | C | T | 53 | a0001c0001t0003g0247 a0001c0003t0003g0133 a0001c0003t0003g0135 others(50): Show |
53 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.771+2343G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101777809 | |||||||
| chr12:101777849 | C | G | 1 | a0001c0001t0001g0355 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.771+2303G>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101777849 | |||||||
| chr12:101777898 | A | C | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.771+2254T>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101777898 | |||||||
| chr12:101777928 | G | C | 1 | a0001c0025t0001g0213 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.771+2224C>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101777928 | |||||||
| chr12:101778075 | G | T | 1 | a0001c0002t0002g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.771+2077C>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101778075 | |||||||
| chr12:101778147 | T | C | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.771+2005A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101778147 | |||||||
| chr12:101778354 | T | C | 8 | a0001c0002t0008g0206 a0001c0002t0008g0207 a0001c0002t0008g0208 others(5): Show |
8 | HG01884.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.771+1798A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101778354 | |||||||
| chr12:101778448 | CAT | C | 3 | a0001c0003t0003g0157 a0001c0003t0003g0168 a0001c0003t0003g0170 |
3 | HG00544.hp2 NA19065.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.771+1702_771+1703d others(4): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101778448 | |||||||
| chr12:101778498 | C | T | 1 | a0001c0001t0001g0307 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.771+1654G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101778498 | |||||||
| chr12:101778756 | A | C | 1 | a0001c0001t0004g0385 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.771+1396T>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101778756 | |||||||
| chr12:101778773 | G | A | 1 | a0001c0001t0001g0354 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.771+1379C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101778773 | |||||||
| chr12:101778860 | C | T | 2 | a0001c0002t0002g0070 a0001c0002t0002g0071 |
2 | NA19002.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.771+1292G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101778860 | |||||||
| chr12:101778904 | C | CA | 8 | a0001c0001t0001g0360 a0001c0001t0001g0363 a0001c0007t0004g0231 others(5): Show |
8 | HG02486.hp1 HG02723.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.771+1247dupT | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101778904 | |||||||
| chr12:101778915 | A | G | 1 | a0001c0002t0002g0004 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.771+1237T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101778915 | |||||||
| chr12:101778917 | C | T | 311 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(308): Show |
315 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.771+1235G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101778917 | |||||||
| chr12:101778921 | G | GAAGAAAA others(1495): Show |
1 | a0001c0008t0004g0260 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.771+1230_771+1231i others(1504): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101778921 | |||||||
| chr12:101778921 | G | GAAGAAAA others(1497): Show |
1 | a0001c0008t0004g0275 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.771+1230_771+1231i others(1506): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101778921 | |||||||
| chr12:101778921 | G | GAAGAAAA others(1500): Show |
2 | a0001c0001t0004g0266 a0001c0001t0006g0274 |
2 | HG02155.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.771+1230_771+1231i others(1509): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101778921 | |||||||
| chr12:101778921 | G | GAAGAAAA others(1501): Show |
2 | a0001c0001t0006g0252 a0001c0001t0011g0059 |
2 | HG02698.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.771+1230_771+1231i others(1510): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101778921 | |||||||
| chr12:101778921 | G | GAAGAAAA others(1502): Show |
2 | a0001c0001t0011g0060 a0001c0001t0019g0062 |
2 | NA18971.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.771+1230_771+1231i others(1511): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101778921 | |||||||
| chr12:101778921 | G | GAAGAAAA others(1503): Show |
3 | a0001c0001t0004g0243 a0001c0001t0004g0248 a0001c0008t0004g0253 |
3 | NA18955.hp1 NA18992.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.771+1230_771+1231i others(1512): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101778921 | |||||||
| chr12:101778921 | G | GAAGAAAA others(1504): Show |
5 | a0001c0001t0004g0217 a0001c0001t0004g0244 a0001c0008t0004g0216 others(2): Show |
5 | HG00544.hp1 HG00597.hp1 NA19001.hp1 others(2): Show |
intron_variant | MODIFIER | c.771+1230_771+1231i others(1513): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101778921 | |||||||
| chr12:101778921 | G | GAAGAAAA others(1505): Show |
2 | a0001c0001t0004g0241 a0001c0001t0004g0273 |
2 | NA18978.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.771+1230_771+1231i others(1514): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101778921 | |||||||
| chr12:101778921 | G | GAAGAAAA others(1505): Show |
1 | a0001c0001t0004g0250 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.771+1230_771+1231i others(1514): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101778921 | |||||||
| chr12:101778921 | G | GAGAAAAA others(1500): Show |
1 | a0001c0001t0011g0061 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.771+1230_771+1231i others(1509): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101778921 | |||||||
| chr12:101779033 | GGA | G | 54 | a0001c0001t0004g0005 a0001c0001t0004g0217 a0001c0001t0004g0233 others(51): Show |
55 | HG00544.hp1 HG00597.hp1 HG02056.hp1 others(52): Show |
intron_variant | MODIFIER | c.771+1117_771+1118d others(4): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101779033 | |||||||
| chr12:101779037 | A | T | 54 | a0001c0001t0004g0005 a0001c0001t0004g0217 a0001c0001t0004g0233 others(51): Show |
55 | HG00544.hp1 HG00597.hp1 HG02056.hp1 others(52): Show |
intron_variant | MODIFIER | c.771+1115T>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101779037 | |||||||
| chr12:101779039 | A | T | 54 | a0001c0001t0004g0005 a0001c0001t0004g0217 a0001c0001t0004g0233 others(51): Show |
55 | HG00544.hp1 HG00597.hp1 HG02056.hp1 others(52): Show |
intron_variant | MODIFIER | c.771+1113T>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101779039 | |||||||
| chr12:101779041 | AAGT | A | 54 | a0001c0001t0004g0005 a0001c0001t0004g0217 a0001c0001t0004g0233 others(51): Show |
55 | HG00544.hp1 HG00597.hp1 HG02056.hp1 others(52): Show |
intron_variant | MODIFIER | c.771+1108_771+1110d others(5): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101779041 | |||||||
| chr12:101779049 | AG | A | 54 | a0001c0001t0004g0005 a0001c0001t0004g0217 a0001c0001t0004g0233 others(51): Show |
55 | HG00544.hp1 HG00597.hp1 HG02056.hp1 others(52): Show |
intron_variant | MODIFIER | c.771+1102delC | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101779049 | |||||||
| chr12:101779051 | G | C | 54 | a0001c0001t0004g0005 a0001c0001t0004g0217 a0001c0001t0004g0233 others(51): Show |
55 | HG00544.hp1 HG00597.hp1 HG02056.hp1 others(52): Show |
intron_variant | MODIFIER | c.771+1101C>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101779051 | |||||||
| chr12:101779053 | A | C | 54 | a0001c0001t0004g0005 a0001c0001t0004g0217 a0001c0001t0004g0233 others(51): Show |
55 | HG00544.hp1 HG00597.hp1 HG02056.hp1 others(52): Show |
intron_variant | MODIFIER | c.771+1099T>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101779053 | |||||||
| chr12:101779060 | T | TG | 54 | a0001c0001t0004g0005 a0001c0001t0004g0217 a0001c0001t0004g0233 others(51): Show |
55 | HG00544.hp1 HG00597.hp1 HG02056.hp1 others(52): Show |
intron_variant | MODIFIER | c.771+1091dupC | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101779060 | |||||||
| chr12:101779073 | TA | T | 56 | a0001c0001t0001g0322 a0001c0001t0001g0345 a0001c0001t0004g0005 others(53): Show |
57 | HG00544.hp1 HG00597.hp1 HG02056.hp1 others(54): Show |
intron_variant | MODIFIER | c.771+1078delT | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101779073 | |||||||
| chr12:101779109 | G | A | 1 | a0001c0001t0006g0227 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.771+1043C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101779109 | |||||||
| chr12:101779111 | T | C | 3 | a0001c0002t0002g0003 a0001c0002t0002g0121 a0001c0002t0002g0123 |
4 | HG00280.hp2 HG01123.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.771+1041A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101779111 | |||||||
| chr12:101779138 | C | T | 3 | a0001c0001t0006g0228 a0001c0002t0002g0066 a0001c0002t0002g0100 |
3 | HG01109.hp2 HG01168.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.771+1014G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101779138 | |||||||
| chr12:101779255 | A | G | 53 | a0001c0001t0003g0247 a0001c0003t0003g0133 a0001c0003t0003g0135 others(50): Show |
53 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.771+897T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101779255 | |||||||
| chr12:101779380 | C | T | 1 | a0001c0001t0001g0328 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.771+772G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101779380 | |||||||
| chr12:101779473 | G | A | 53 | a0001c0001t0003g0247 a0001c0003t0003g0133 a0001c0003t0003g0135 others(50): Show |
53 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.771+679C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101779473 | |||||||
| chr12:101779588 | G | T | 9 | a0001c0002t0008g0206 a0001c0002t0008g0207 a0001c0002t0008g0208 others(6): Show |
9 | HG01884.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.771+564C>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101779588 | |||||||
| chr12:101779611 | G | A | 5 | a0001c0002t0001g0364 a0001c0002t0001g0365 a0001c0002t0001g0366 others(2): Show |
5 | HG02559.hp1 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.771+541C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101779611 | |||||||
| chr12:101779634 | T | C | 2 | a0001c0001t0001g0001 a0001c0001t0001g0362 |
5 | HG02280.hp1 HG02630.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.771+518A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101779634 | |||||||
| chr12:101779844 | G | A | 1 | a0006c0016t0013g0235 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.771+308C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101779844 | |||||||
| chr12:101779876 | T | C | 326 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(323): Show |
330 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(327): Show |
intron_variant | MODIFIER | c.771+276A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101779876 | |||||||
| chr12:101780030 | A | C | 1 | a0001c0001t0004g0233 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.771+122T>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101780030 | |||||||
| chr12:101780116 | G | T | 1 | a0001c0003t0003g0183 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.771+36C>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101780116 | |||||||
| chr12:101780117 | T | A | 1 | a0001c0003t0003g0183 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.771+35A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 7/20 | chr12 | 101780117 | |||||||
| chr12:101780493 | C | T | 17 | a0001c0001t0007g0278 a0001c0004t0007g0188 a0001c0004t0007g0189 others(14): Show |
17 | HG01081.hp1 HG01243.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.636+64G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 6/20 | chr12 | 101780493 | |||||||
| chr12:101780673 | T | C | 9 | a0001c0002t0008g0206 a0001c0002t0008g0207 a0001c0002t0008g0208 others(6): Show |
9 | HG01884.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.572-52A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101780673 | |||||||
| chr12:101780709 | G | A | 2 | a0001c0004t0007g0189 a0001c0004t0007g0190 |
2 | HG01081.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.572-88C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101780709 | |||||||
| chr12:101780718 | G | A | 2 | a0001c0007t0004g0231 a0001c0007t0004g0232 |
2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.572-97C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101780718 | |||||||
| chr12:101780807 | T | C | 1 | a0001c0004t0007g0198 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.572-186A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101780807 | |||||||
| chr12:101781142 | T | C | 1 | a0001c0001t0001g0331 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.572-521A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101781142 | |||||||
| chr12:101781318 | T | C | 2 | a0006c0016t0013g0235 a0006c0017t0013g0234 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.572-697A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101781318 | |||||||
| chr12:101781337 | T | C | 1 | a0001c0001t0002g0091 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.572-716A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101781337 | |||||||
| chr12:101781386 | C | G | 1 | a0001c0002t0002g0088 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.572-765G>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101781386 | |||||||
| chr12:101781530 | C | T | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.572-909G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101781530 | |||||||
| chr12:101781548 | G | A | 4 | a0001c0002t0002g0003 a0001c0002t0002g0119 a0001c0002t0002g0121 others(1): Show |
5 | HG00280.hp2 HG01123.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.572-927C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101781548 | |||||||
| chr12:101781679 | G | A | 9 | a0001c0002t0008g0206 a0001c0002t0008g0207 a0001c0002t0008g0208 others(6): Show |
9 | HG01884.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.572-1058C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101781679 | |||||||
| chr12:101781753 | C | T | 1 | a0002c0012t0001g0214 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.572-1132G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101781753 | |||||||
| chr12:101781868 | G | A | 54 | a0001c0001t0004g0005 a0001c0001t0004g0217 a0001c0001t0004g0233 others(51): Show |
55 | HG00544.hp1 HG00597.hp1 HG02056.hp1 others(52): Show |
intron_variant | MODIFIER | c.572-1247C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101781868 | |||||||
| chr12:101781969 | C | A | 1 | a0001c0001t0001g0361 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.572-1348G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101781969 | |||||||
| chr12:101782236 | T | TA | 326 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(323): Show |
330 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(327): Show |
intron_variant | MODIFIER | c.572-1616dupT | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101782236 | |||||||
| chr12:101782238 | T | C | 326 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(323): Show |
330 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(327): Show |
intron_variant | MODIFIER | c.572-1617A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101782238 | |||||||
| chr12:101782239 | A | T | 326 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(323): Show |
330 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(327): Show |
intron_variant | MODIFIER | c.572-1618T>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101782239 | |||||||
| chr12:101782412 | GTA | G | 9 | a0001c0002t0008g0206 a0001c0002t0008g0207 a0001c0002t0008g0208 others(6): Show |
9 | HG01884.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.572-1793_572-1792d others(4): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101782412 | |||||||
| chr12:101782418 | T | C | 1 | a0001c0022t0006g0223 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.572-1797A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101782418 | |||||||
| chr12:101782975 | T | C | 1 | a0001c0001t0006g0226 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.572-2354A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101782975 | |||||||
| chr12:101783076 | G | GTAA | 208 | a0001c0001t0001g0001 a0001c0001t0001g0276 a0001c0001t0001g0277 others(205): Show |
211 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(208): Show |
intron_variant | MODIFIER | c.572-2458_572-2456d others(5): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101783076 | |||||||
| chr12:101783193 | A | G | 1 | a0001c0002t0008g0237 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.572-2572T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101783193 | |||||||
| chr12:101783204 | C | A | 2 | a0001c0001t0001g0339 a0001c0001t0001g0354 |
2 | HG00423.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.572-2583G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101783204 | |||||||
| chr12:101783303 | T | C | 1 | a0001c0003t0003g0135 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.572-2682A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101783303 | |||||||
| chr12:101783323 | T | C | 9 | a0001c0002t0008g0206 a0001c0002t0008g0207 a0001c0002t0008g0208 others(6): Show |
9 | HG01884.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.571+2689A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101783323 | |||||||
| chr12:101783526 | C | A | 4 | a0001c0001t0001g0369 a0001c0001t0001g0370 a0001c0001t0001g0374 others(1): Show |
4 | HG02922.hp1 HG03486.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.571+2486G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101783526 | |||||||
| chr12:101783543 | G | C | 121 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(118): Show |
121 | HG00408.hp1 HG00423.hp2 HG01099.hp1 others(118): Show |
intron_variant | MODIFIER | c.571+2469C>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101783543 | |||||||
| chr12:101783652 | A | C | 2 | a0006c0016t0013g0235 a0006c0017t0013g0234 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.571+2360T>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101783652 | |||||||
| chr12:101783720 | CT | C | 19 | a0001c0001t0001g0219 a0001c0001t0006g0218 a0001c0001t0006g0221 others(16): Show |
19 | HG00323.hp1 HG00408.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.571+2291delA | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101783720 | |||||||
| chr12:101783887 | G | GT | 6 | a0001c0001t0002g0095 a0001c0002t0002g0066 a0001c0002t0002g0073 others(3): Show |
6 | HG00597.hp1 HG01109.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.571+2124dupA | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101783887 | |||||||
| chr12:101784093 | G | C | 3 | a0001c0003t0003g0135 a0001c0003t0003g0144 a0001c0003t0003g0146 |
3 | NA18962.hp2 NA18974.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.571+1919C>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101784093 | |||||||
| chr12:101784204 | T | A | 4 | a0001c0007t0009g0053 a0001c0007t0009g0055 a0001c0007t0009g0056 others(1): Show |
4 | HG02486.hp1 HG02723.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.571+1808A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101784204 | |||||||
| chr12:101784255 | G | C | 1 | a0001c0001t0021g0279 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.571+1757C>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101784255 | |||||||
| chr12:101784277 | C | T | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.571+1735G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101784277 | |||||||
| chr12:101784323 | G | A | 1 | a0001c0004t0007g0198 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.571+1689C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101784323 | |||||||
| chr12:101784405 | C | G | 7 | a0001c0003t0003g0136 a0001c0003t0003g0181 a0001c0003t0003g0182 others(4): Show |
7 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.571+1607G>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101784405 | |||||||
| chr12:101784521 | A | G | 1 | a0001c0001t0021g0279 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.571+1491T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101784521 | |||||||
| chr12:101784529 | A | G | 131 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(128): Show |
131 | HG00408.hp1 HG00423.hp2 HG00642.hp1 others(128): Show |
intron_variant | MODIFIER | c.571+1483T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101784529 | |||||||
| chr12:101784603 | C | T | 6 | a0004c0006t0007g0187 a0004c0006t0007g0191 a0004c0006t0007g0192 others(3): Show |
6 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.571+1409G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101784603 | |||||||
| chr12:101784618 | G | A | 1 | a0001c0001t0001g0293 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.571+1394C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101784618 | |||||||
| chr12:101784680 | G | GA | 141 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(138): Show |
145 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.571+1331dupT | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101784680 | |||||||
| chr12:101784729 | A | G | 3 | a0001c0002t0001g0205 a0001c0023t0001g0215 a0002c0012t0001g0214 |
3 | HG00280.hp1 HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.571+1283T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101784729 | |||||||
| chr12:101784778 | G | T | 50 | a0001c0001t0003g0247 a0001c0003t0003g0133 a0001c0003t0003g0135 others(47): Show |
50 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.571+1234C>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101784778 | |||||||
| chr12:101784836 | G | A | 2 | a0003c0005t0001g0357 a0003c0005t0001g0358 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.571+1176C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101784836 | |||||||
| chr12:101784849 | T | C | 40 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0010 others(37): Show |
40 | HG01106.hp1 HG01516.hp2 HG01981.hp1 others(37): Show |
intron_variant | MODIFIER | c.571+1163A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101784849 | |||||||
| chr12:101784972 | G | A | 50 | a0001c0001t0003g0247 a0001c0003t0003g0133 a0001c0003t0003g0135 others(47): Show |
50 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.571+1040C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101784972 | |||||||
| chr12:101785005 | A | G | 1 | a0001c0001t0001g0373 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.571+1007T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101785005 | |||||||
| chr12:101785188 | T | C | 1 | a0001c0001t0004g0267 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.571+824A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101785188 | |||||||
| chr12:101785253 | G | A | 1 | a0001c0007t0009g0056 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.571+759C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101785253 | |||||||
| chr12:101785363 | C | T | 46 | a0001c0001t0003g0247 a0001c0003t0003g0133 a0001c0003t0003g0135 others(43): Show |
46 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.571+649G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101785363 | |||||||
| chr12:101785522 | A | C | 2 | a0006c0016t0013g0235 a0006c0017t0013g0234 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.571+490T>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101785522 | |||||||
| chr12:101785531 | A | T | 1 | a0001c0003t0003g0157 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.571+481T>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101785531 | |||||||
| chr12:101785709 | T | C | 9 | a0001c0002t0008g0206 a0001c0002t0008g0207 a0001c0002t0008g0208 others(6): Show |
9 | HG01884.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.571+303A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101785709 | |||||||
| chr12:101785780 | G | A | 1 | a0001c0002t0002g0063 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.571+232C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101785780 | |||||||
| chr12:101785957 | T | G | 1 | a0001c0001t0002g0092 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.571+55A>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 5/20 | chr12 | 101785957 | |||||||
| chr12:101786450 | C | T | 331 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(328): Show |
335 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.366-233G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 4/20 | chr12 | 101786450 | |||||||
| chr12:101787042 | A | G | 1 | a0001c0003t0003g0178 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.366-825T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 4/20 | chr12 | 101787042 | |||||||
| chr12:101787084 | A | G | 5 | a0001c0001t0004g0217 a0001c0001t0004g0243 a0001c0001t0004g0244 others(2): Show |
5 | HG02155.hp1 NA18955.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.366-867T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 4/20 | chr12 | 101787084 | |||||||
| chr12:101787239 | G | A | 1 | a0001c0003t0003g0178 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.366-1022C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 4/20 | chr12 | 101787239 | |||||||
| chr12:101787363 | G | C | 1 | a0001c0002t0008g0237 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.366-1146C>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 4/20 | chr12 | 101787363 | |||||||
| chr12:101787377 | C | CA | 46 | a0001c0001t0003g0247 a0001c0003t0003g0133 a0001c0003t0003g0135 others(43): Show |
46 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.366-1161dupT | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 4/20 | chr12 | 101787377 | |||||||
| chr12:101787458 | T | C | 1 | a0001c0002t0002g0115 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.365+1090A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 4/20 | chr12 | 101787458 | |||||||
| chr12:101787506 | T | G | 1 | a0001c0001t0005g0010 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.365+1042A>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 4/20 | chr12 | 101787506 | |||||||
| chr12:101787577 | A | G | 110 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0003g0247 others(107): Show |
111 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.365+971T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 4/20 | chr12 | 101787577 | |||||||
| chr12:101787637 | G | A | 17 | a0001c0001t0007g0278 a0001c0004t0007g0188 a0001c0004t0007g0189 others(14): Show |
17 | HG01081.hp1 HG01243.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.365+911C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 4/20 | chr12 | 101787637 | |||||||
| chr12:101787656 | T | C | 1 | a0001c0002t0002g0063 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.365+892A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 4/20 | chr12 | 101787656 | |||||||
| chr12:101787688 | C | T | 1 | a0001c0004t0007g0197 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.365+860G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 4/20 | chr12 | 101787688 | |||||||
| chr12:101787689 | G | A | 11 | a0002c0009t0001g0195 a0002c0009t0001g0200 a0002c0009t0001g0201 others(8): Show |
11 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.365+859C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 4/20 | chr12 | 101787689 | |||||||
| chr12:101787867 | C | T | 3 | a0001c0001t0002g0081 a0001c0001t0002g0089 a0001c0001t0002g0093 |
3 | HG00609.hp1 NA18943.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.365+681G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 4/20 | chr12 | 101787867 | |||||||
| chr12:101787908 | C | A | 1 | a0001c0001t0021g0279 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.365+640G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 4/20 | chr12 | 101787908 | |||||||
| chr12:101787913 | C | CA | 217 | a0001c0001t0001g0001 a0001c0001t0001g0284 a0001c0001t0001g0285 others(214): Show |
223 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.365+634dupT | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 4/20 | chr12 | 101787913 | |||||||
| chr12:101787913 | C | CAA | 157 | a0001c0001t0001g0219 a0001c0001t0001g0276 a0001c0001t0001g0277 others(154): Show |
158 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.365+633_365+634dup others(2): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 4/20 | chr12 | 101787913 | |||||||
| chr12:101787913 | C | CAAA | 8 | a0001c0001t0001g0328 a0001c0001t0011g0125 a0001c0002t0001g0205 others(5): Show |
8 | HG01106.hp2 HG02145.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.365+632_365+634dup others(3): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 4/20 | chr12 | 101787913 | |||||||
| chr12:101788038 | G | A | 50 | a0001c0001t0003g0247 a0001c0003t0003g0133 a0001c0003t0003g0135 others(47): Show |
50 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.365+510C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 4/20 | chr12 | 101788038 | |||||||
| chr12:101788087 | G | A | 6 | a0001c0007t0009g0055 a0002c0009t0001g0195 a0002c0009t0001g0200 others(3): Show |
6 | HG02258.hp1 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.365+461C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 4/20 | chr12 | 101788087 | |||||||
| chr12:101788239 | G | A | 1 | a0001c0001t0009g0052 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.365+309C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 4/20 | chr12 | 101788239 | |||||||
| chr12:101788264 | C | T | 29 | a0001c0001t0001g0297 a0001c0001t0001g0298 a0001c0001t0001g0305 others(26): Show |
29 | HG00408.hp1 HG00423.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.365+284G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 4/20 | chr12 | 101788264 | |||||||
| chr12:101788374 | A | G | 1 | a0001c0003t0003g0146 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.365+174T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 4/20 | chr12 | 101788374 | |||||||
| chr12:101788403 | G | A | 310 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(307): Show |
314 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.365+145C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 4/20 | chr12 | 101788403 | |||||||
| chr12:101788450 | AAC | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0284 a0001c0001t0001g0285 others(153): Show |
159 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(156): Show |
intron_variant | MODIFIER | c.365+96_365+97delGT | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 4/20 | chr12 | 101788450 | |||||||
| chr12:101788471 | A | C | 2 | a0006c0016t0013g0235 a0006c0017t0013g0234 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.365+77T>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 4/20 | chr12 | 101788471 | |||||||
| chr12:101788791 | A | G | 52 | a0001c0001t0004g0005 a0001c0001t0004g0217 a0001c0001t0004g0233 others(49): Show |
53 | HG00544.hp1 HG00597.hp1 HG02056.hp1 others(50): Show |
intron_variant | MODIFIER | c.324-202T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 3/20 | chr12 | 101788791 | |||||||
| chr12:101788820 | A | T | 1 | a0001c0001t0002g0089 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.324-231T>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 3/20 | chr12 | 101788820 | |||||||
| chr12:101788929 | A | T | 320 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(317): Show |
324 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(321): Show |
intron_variant | MODIFIER | c.324-340T>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 3/20 | chr12 | 101788929 | |||||||
| chr12:101789046 | T | C | 133 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(130): Show |
133 | HG00408.hp1 HG00423.hp2 HG00642.hp1 others(130): Show |
intron_variant | MODIFIER | c.324-457A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 3/20 | chr12 | 101789046 | |||||||
| chr12:101789214 | T | A | 2 | a0001c0001t0007g0278 a0001c0004t0007g0188 |
2 | HG02818.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.324-625A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 3/20 | chr12 | 101789214 | |||||||
| chr12:101789247 | G | A | 9 | a0001c0002t0008g0206 a0001c0002t0008g0207 a0001c0002t0008g0208 others(6): Show |
9 | HG01884.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.324-658C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 3/20 | chr12 | 101789247 | |||||||
| chr12:101789464 | CTA | C | 52 | a0001c0001t0004g0005 a0001c0001t0004g0217 a0001c0001t0004g0233 others(49): Show |
53 | HG00544.hp1 HG00597.hp1 HG02056.hp1 others(50): Show |
intron_variant | MODIFIER | c.323+472_323+473del others(2): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 3/20 | chr12 | 101789464 | |||||||
| chr12:101789648 | C | A | 1 | a0001c0001t0001g0306 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.323+290G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 3/20 | chr12 | 101789648 | |||||||
| chr12:101789703 | T | G | 1 | a0001c0001t0002g0093 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.323+235A>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 3/20 | chr12 | 101789703 | |||||||
| chr12:101789902 | T | C | 6 | a0001c0002t0005g0013 a0001c0002t0005g0027 a0001c0002t0005g0029 others(3): Show |
6 | HG01981.hp1 HG01993.hp1 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.323+36A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 3/20 | chr12 | 101789902 | |||||||
| chr12:101790072 | C | A | 52 | a0001c0001t0004g0005 a0001c0001t0004g0217 a0001c0001t0004g0233 others(49): Show |
53 | HG00544.hp1 HG00597.hp1 HG02056.hp1 others(50): Show |
intron_variant | MODIFIER | c.204-15G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101790072 | |||||||
| chr12:101790078 | C | G | 2 | a0001c0007t0004g0231 a0001c0007t0004g0232 |
2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.204-21G>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101790078 | |||||||
| chr12:101790148 | T | C | 1 | a0001c0004t0001g0199 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.204-91A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101790148 | |||||||
| chr12:101790160 | C | A | 109 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0003g0247 others(106): Show |
110 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.204-103G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101790160 | |||||||
| chr12:101790218 | G | A | 1 | a0001c0002t0008g0237 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.204-161C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101790218 | |||||||
| chr12:101790293 | C | T | 381 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(378): Show |
387 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.204-236G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101790293 | |||||||
| chr12:101790429 | T | G | 52 | a0001c0001t0004g0005 a0001c0001t0004g0217 a0001c0001t0004g0233 others(49): Show |
53 | HG00544.hp1 HG00597.hp1 HG02056.hp1 others(50): Show |
intron_variant | MODIFIER | c.204-372A>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101790429 | |||||||
| chr12:101790470 | A | G | 1 | a0001c0001t0005g0024 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.204-413T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101790470 | |||||||
| chr12:101790471 | G | A | 2 | a0006c0016t0013g0235 a0006c0017t0013g0234 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.204-414C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101790471 | |||||||
| chr12:101790555 | C | T | 46 | a0001c0001t0003g0247 a0001c0003t0003g0133 a0001c0003t0003g0135 others(43): Show |
46 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.204-498G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101790555 | |||||||
| chr12:101790695 | G | A | 2 | a0001c0001t0001g0340 a0001c0001t0001g0341 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.204-638C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101790695 | |||||||
| chr12:101790726 | C | T | 28 | a0001c0001t0001g0001 a0001c0001t0001g0360 a0001c0001t0001g0361 others(25): Show |
31 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.204-669G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101790726 | |||||||
| chr12:101790740 | TA | T | 309 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(306): Show |
313 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.204-684delT | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101790740 | |||||||
| chr12:101790855 | C | A | 1 | a0001c0003t0003g0162 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.204-798G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101790855 | |||||||
| chr12:101790855 | C | T | 2 | a0001c0002t0002g0074 a0001c0002t0002g0112 |
2 | HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.204-798G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101790855 | |||||||
| chr12:101790945 | C | T | 1 | a0001c0001t0005g0011 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.204-888G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101790945 | |||||||
| chr12:101791052 | C | G | 5 | a0001c0002t0008g0206 a0001c0002t0008g0207 a0001c0002t0008g0208 others(2): Show |
5 | HG02145.hp1 HG02615.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.204-995G>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101791052 | |||||||
| chr12:101791208 | T | C | 2 | a0006c0016t0013g0235 a0006c0017t0013g0234 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.204-1151A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101791208 | |||||||
| chr12:101791272 | A | G | 1 | a0001c0003t0003g0171 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.204-1215T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101791272 | |||||||
| chr12:101791305 | T | C | 319 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(316): Show |
323 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.204-1248A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101791305 | |||||||
| chr12:101791334 | C | T | 1 | a0001c0002t0008g0237 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.204-1277G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101791334 | |||||||
| chr12:101791367 | T | C | 62 | a0001c0001t0001g0219 a0001c0001t0005g0007 a0001c0001t0005g0008 others(59): Show |
62 | HG00323.hp1 HG00408.hp2 HG00741.hp2 others(59): Show |
intron_variant | MODIFIER | c.204-1310A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101791367 | |||||||
| chr12:101791405 | A | C | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.204-1348T>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101791405 | |||||||
| chr12:101791460 | C | CAA | 9 | a0001c0002t0008g0206 a0001c0002t0008g0207 a0001c0002t0008g0208 others(6): Show |
9 | HG01884.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.204-1405_204-1404d others(4): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101791460 | |||||||
| chr12:101791460 | CA | C | 18 | a0001c0001t0001g0313 a0001c0001t0007g0278 a0001c0004t0007g0188 others(15): Show |
18 | HG01081.hp1 HG01243.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.204-1404delT | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101791460 | |||||||
| chr12:101791471 | A | T | 9 | a0001c0003t0003g0138 a0001c0003t0003g0143 a0001c0003t0003g0149 others(6): Show |
9 | HG00597.hp2 HG01928.hp2 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.204-1414T>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101791471 | |||||||
| chr12:101791484 | C | T | 2 | a0006c0016t0013g0235 a0006c0017t0013g0234 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.204-1427G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101791484 | |||||||
| chr12:101791486 | C | CA | 53 | a0001c0001t0001g0276 a0001c0001t0001g0328 a0001c0001t0003g0247 others(50): Show |
53 | HG00140.hp1 HG00423.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.204-1430dupT | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101791486 | |||||||
| chr12:101791576 | A | G | 5 | a0001c0001t0004g0217 a0001c0001t0004g0243 a0001c0001t0004g0244 others(2): Show |
5 | HG02155.hp1 NA18955.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.204-1519T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101791576 | |||||||
| chr12:101791654 | T | C | 1 | a0001c0001t0001g0362 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.204-1597A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101791654 | |||||||
| chr12:101791783 | T | G | 1 | a0001c0002t0002g0111 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.204-1726A>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101791783 | |||||||
| chr12:101791864 | C | A | 319 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(316): Show |
323 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.204-1807G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101791864 | |||||||
| chr12:101791971 | C | T | 319 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(316): Show |
323 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.204-1914G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101791971 | |||||||
| chr12:101792071 | T | C | 5 | a0001c0001t0009g0052 a0001c0007t0009g0053 a0001c0007t0009g0055 others(2): Show |
5 | HG01167.hp2 HG02486.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.204-2014A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101792071 | |||||||
| chr12:101792095 | G | A | 3 | a0001c0001t0001g0379 a0001c0001t0001g0381 a0001c0001t0001g0382 |
3 | HG02257.hp2 HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.204-2038C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101792095 | |||||||
| chr12:101792146 | G | A | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.204-2089C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101792146 | |||||||
| chr12:101792161 | A | G | 1 | a0001c0025t0001g0213 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.204-2104T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101792161 | |||||||
| chr12:101792180 | G | A | 3 | a0001c0001t0005g0007 a0001c0001t0005g0016 a0001c0001t0005g0020 |
3 | NA18956.hp2 NA18967.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.204-2123C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101792180 | |||||||
| chr12:101792286 | G | A | 51 | a0001c0001t0003g0247 a0001c0001t0009g0052 a0001c0003t0003g0133 others(48): Show |
51 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.204-2229C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101792286 | |||||||
| chr12:101792389 | A | G | 2 | a0006c0016t0013g0235 a0006c0017t0013g0234 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.204-2332T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101792389 | |||||||
| chr12:101792621 | T | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0284 a0001c0001t0001g0285 others(117): Show |
123 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.204-2564A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101792621 | |||||||
| chr12:101792849 | G | A | 1 | a0001c0003t0003g0146 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.204-2792C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101792849 | |||||||
| chr12:101792882 | G | A | 1 | a0001c0004t0007g0197 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.204-2825C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101792882 | |||||||
| chr12:101792892 | T | C | 1 | a0001c0001t0005g0024 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.204-2835A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101792892 | |||||||
| chr12:101793037 | G | A | 2 | a0001c0007t0004g0231 a0001c0007t0004g0232 |
2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.204-2980C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101793037 | |||||||
| chr12:101793107 | C | T | 1 | a0001c0002t0008g0237 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.204-3050G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101793107 | |||||||
| chr12:101793234 | C | T | 1 | a0012c0021t0004g0240 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.204-3177G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101793234 | |||||||
| chr12:101793435 | T | A | 7 | a0001c0001t0004g0241 a0001c0001t0004g0250 a0001c0001t0004g0273 others(4): Show |
7 | NA18747.hp1 NA18971.hp1 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.203+3242A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101793435 | |||||||
| chr12:101793441 | A | G | 51 | a0001c0001t0003g0247 a0001c0001t0009g0052 a0001c0003t0003g0133 others(48): Show |
51 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.203+3236T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101793441 | |||||||
| chr12:101793535 | C | T | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.203+3142G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101793535 | |||||||
| chr12:101793669 | T | C | 9 | a0001c0002t0008g0206 a0001c0002t0008g0207 a0001c0002t0008g0208 others(6): Show |
9 | HG01884.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.203+3008A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101793669 | |||||||
| chr12:101793676 | T | G | 2 | a0001c0001t0005g0047 a0001c0001t0005g0050 |
2 | NA18979.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.203+3001A>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101793676 | |||||||
| chr12:101793968 | C | G | 1 | a0001c0002t0008g0237 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.203+2709G>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101793968 | |||||||
| chr12:101793999 | G | A | 1 | a0001c0003t0003g0171 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.203+2678C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101793999 | |||||||
| chr12:101794036 | T | C | 1 | a0001c0001t0001g0284 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.203+2641A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101794036 | |||||||
| chr12:101794057 | G | A | 4 | a0001c0001t0001g0369 a0001c0001t0001g0370 a0001c0001t0001g0374 others(1): Show |
4 | HG02922.hp1 HG03486.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.203+2620C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101794057 | |||||||
| chr12:101794133 | G | A | 1 | a0001c0002t0002g0078 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.203+2544C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101794133 | |||||||
| chr12:101794163 | A | G | 80 | a0001c0001t0001g0219 a0001c0001t0005g0007 a0001c0001t0005g0008 others(77): Show |
80 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.203+2514T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101794163 | |||||||
| chr12:101794187 | T | A | 2 | a0001c0007t0004g0231 a0001c0007t0004g0232 |
2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.203+2490A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101794187 | |||||||
| chr12:101794391 | G | C | 23 | a0001c0001t0001g0297 a0001c0001t0001g0298 a0001c0001t0001g0322 others(20): Show |
23 | HG00408.hp1 HG00423.hp2 HG02027.hp1 others(20): Show |
intron_variant | MODIFIER | c.203+2286C>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101794391 | |||||||
| chr12:101794587 | A | C | 2 | a0006c0016t0013g0235 a0006c0017t0013g0234 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.203+2090T>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101794587 | |||||||
| chr12:101794641 | T | C | 51 | a0001c0001t0003g0247 a0001c0001t0009g0052 a0001c0003t0003g0133 others(48): Show |
51 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.203+2036A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101794641 | |||||||
| chr12:101794954 | G | A | 1 | a0003c0005t0001g0283 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.203+1723C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101794954 | |||||||
| chr12:101794969 | G | A | 3 | a0001c0003t0003g0135 a0001c0003t0003g0144 a0001c0003t0003g0146 |
3 | NA18962.hp2 NA18974.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.203+1708C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101794969 | |||||||
| chr12:101795005 | G | A | 1 | a0001c0002t0008g0237 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.203+1672C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101795005 | |||||||
| chr12:101795403 | C | T | 110 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0003g0247 others(107): Show |
111 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.203+1274G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101795403 | |||||||
| chr12:101795480 | C | T | 1 | a0001c0001t0011g0125 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.203+1197G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101795480 | |||||||
| chr12:101795523 | C | T | 2 | a0001c0002t0002g0078 a0002c0012t0002g0077 |
2 | HG00741.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.203+1154G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101795523 | |||||||
| chr12:101795650 | G | A | 16 | a0001c0001t0003g0247 a0001c0003t0003g0137 a0001c0003t0003g0139 others(13): Show |
16 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.203+1027C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101795650 | |||||||
| chr12:101795668 | G | T | 2 | a0001c0007t0004g0231 a0001c0007t0004g0232 |
2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.203+1009C>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101795668 | |||||||
| chr12:101795685 | A | G | 319 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(316): Show |
323 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.203+992T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101795685 | |||||||
| chr12:101795707 | C | T | 1 | a0001c0001t0001g0327 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.203+970G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101795707 | |||||||
| chr12:101795787 | A | C | 1 | a0001c0002t0002g0099 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.203+890T>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101795787 | |||||||
| chr12:101796068 | A | G | 310 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(307): Show |
314 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.203+609T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101796068 | |||||||
| chr12:101796113 | T | C | 52 | a0001c0001t0004g0005 a0001c0001t0004g0217 a0001c0001t0004g0233 others(49): Show |
53 | HG00544.hp1 HG00597.hp1 HG02056.hp1 others(50): Show |
intron_variant | MODIFIER | c.203+564A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101796113 | |||||||
| chr12:101796179 | C | T | 10 | a0001c0001t0004g0248 a0001c0002t0008g0206 a0001c0002t0008g0207 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.203+498G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101796179 | |||||||
| chr12:101796304 | A | G | 1 | a0001c0001t0021g0279 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.203+373T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101796304 | |||||||
| chr12:101796313 | C | T | 1 | a0002c0012t0001g0214 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.203+364G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101796313 | |||||||
| chr12:101796407 | T | A | 2 | a0001c0001t0005g0024 a0001c0001t0005g0040 |
2 | NA19007.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.203+270A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101796407 | |||||||
| chr12:101796422 | C | T | 1 | a0001c0003t0003g0162 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.203+255G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101796422 | |||||||
| chr12:101796429 | C | T | 2 | a0006c0016t0013g0235 a0006c0017t0013g0234 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.203+248G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101796429 | |||||||
| chr12:101796431 | T | G | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.203+246A>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101796431 | |||||||
| chr12:101796476 | CTCTG | C | 4 | a0001c0002t0002g0003 a0001c0002t0002g0119 a0001c0002t0002g0121 others(1): Show |
5 | HG00280.hp2 HG01123.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.203+197_203+200del others(4): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101796476 | |||||||
| chr12:101796601 | G | A | 1 | a0001c0025t0001g0213 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.203+76C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 2/20 | chr12 | 101796601 | |||||||
| chr12:101796798 | A | C | 1 | a0001c0002t0008g0237 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.118-36T>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101796798 | |||||||
| chr12:101796853 | G | T | 1 | a0001c0001t0001g0299 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.118-91C>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101796853 | |||||||
| chr12:101796902 | A | C | 1 | a0001c0001t0001g0377 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.118-140T>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101796902 | |||||||
| chr12:101797103 | T | C | 1 | a0001c0003t0004g0134 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.118-341A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101797103 | |||||||
| chr12:101797279 | G | A | 1 | a0001c0002t0008g0237 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.118-517C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101797279 | |||||||
| chr12:101797346 | C | T | 1 | a0001c0002t0001g0356 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.118-584G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101797346 | |||||||
| chr12:101797422 | C | T | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.118-660G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101797422 | |||||||
| chr12:101797442 | C | T | 2 | a0001c0002t0002g0072 a0001c0002t0002g0075 |
2 | HG01361.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.118-680G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101797442 | |||||||
| chr12:101797508 | C | T | 1 | a0001c0002t0002g0066 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.118-746G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101797508 | |||||||
| chr12:101797537 | T | C | 1 | a0001c0001t0001g0311 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.118-775A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101797537 | |||||||
| chr12:101797699 | T | A | 1 | a0001c0001t0004g0233 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.118-937A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101797699 | |||||||
| chr12:101797708 | G | A | 2 | a0001c0001t0001g0360 a0001c0001t0001g0363 |
2 | HG02970.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.118-946C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101797708 | |||||||
| chr12:101797752 | A | G | 1 | a0001c0002t0002g0004 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.118-990T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101797752 | |||||||
| chr12:101797946 | T | C | 20 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0012 others(17): Show |
20 | NA18954.hp1 NA18956.hp2 NA18962.hp1 others(17): Show |
intron_variant | MODIFIER | c.118-1184A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101797946 | |||||||
| chr12:101797952 | C | T | 1 | a0001c0008t0004g0275 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.118-1190G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101797952 | |||||||
| chr12:101797953 | G | A | 2 | a0001c0004t0007g0197 a0001c0004t0007g0198 |
2 | HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.118-1191C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101797953 | |||||||
| chr12:101798029 | T | A | 2 | a0003c0005t0001g0281 a0003c0005t0017g0054 |
2 | HG02109.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.118-1267A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101798029 | |||||||
| chr12:101798148 | C | T | 2 | a0001c0007t0004g0231 a0001c0007t0004g0232 |
2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.118-1386G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101798148 | |||||||
| chr12:101798197 | CCT | C | 108 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0003g0247 others(105): Show |
109 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.118-1437_118-1436d others(4): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101798197 | |||||||
| chr12:101798230 | C | A | 1 | a0001c0002t0002g0122 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.118-1468G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101798230 | |||||||
| chr12:101798279 | T | C | 52 | a0001c0001t0004g0005 a0001c0001t0004g0217 a0001c0001t0004g0233 others(49): Show |
53 | HG00544.hp1 HG00597.hp1 HG02056.hp1 others(50): Show |
intron_variant | MODIFIER | c.118-1517A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101798279 | |||||||
| chr12:101798354 | C | G | 60 | a0001c0001t0001g0219 a0001c0001t0005g0007 a0001c0001t0005g0008 others(57): Show |
60 | HG00323.hp1 HG00408.hp2 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.118-1592G>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101798354 | |||||||
| chr12:101798367 | C | G | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.118-1605G>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101798367 | |||||||
| chr12:101798569 | A | G | 1 | a0001c0002t0001g0356 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.118-1807T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101798569 | |||||||
| chr12:101798692 | G | T | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.118-1930C>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101798692 | |||||||
| chr12:101798800 | C | T | 1 | a0001c0001t0001g0362 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.118-2038G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101798800 | |||||||
| chr12:101798805 | AAAAGTGA others(9): Show |
A | 1 | a0001c0003t0003g0139 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.118-2059_118-2044d others(18): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101798805 | |||||||
| chr12:101798933 | A | T | 1 | a0001c0002t0002g0122 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.118-2171T>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101798933 | |||||||
| chr12:101799009 | C | T | 6 | a0001c0001t0001g0219 a0001c0001t0006g0220 a0001c0001t0006g0225 others(3): Show |
6 | HG00408.hp2 HG03669.hp1 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.118-2247G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101799009 | |||||||
| chr12:101799025 | G | T | 80 | a0001c0001t0001g0219 a0001c0001t0005g0007 a0001c0001t0005g0008 others(77): Show |
80 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.118-2263C>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101799025 | |||||||
| chr12:101799037 | GAATCATT others(9): Show |
G | 57 | a0001c0001t0003g0247 a0001c0001t0009g0052 a0001c0003t0003g0133 others(54): Show |
57 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.118-2291_118-2276d others(18): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101799037 | |||||||
| chr12:101799045 | GT | G | 5 | a0001c0001t0001g0298 a0001c0001t0001g0340 a0001c0001t0002g0095 others(2): Show |
5 | HG01167.hp1 NA18946.hp1 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.118-2284delA | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101799045 | |||||||
| chr12:101799051 | T | A | 265 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(262): Show |
269 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.118-2289A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101799051 | |||||||
| chr12:101799145 | C | A | 1 | a0001c0001t0001g0288 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.118-2383G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101799145 | |||||||
| chr12:101799198 | A | G | 1 | a0001c0001t0001g0300 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.118-2436T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101799198 | |||||||
| chr12:101799719 | T | C | 9 | a0001c0002t0008g0206 a0001c0002t0008g0207 a0001c0002t0008g0208 others(6): Show |
9 | HG01884.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.118-2957A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101799719 | |||||||
| chr12:101799722 | C | A | 3 | a0001c0001t0005g0007 a0001c0001t0005g0016 a0001c0001t0005g0020 |
3 | NA18956.hp2 NA18967.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.118-2960G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101799722 | |||||||
| chr12:101799727 | A | AG | 326 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(323): Show |
330 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(327): Show |
intron_variant | MODIFIER | c.118-2966_118-2965i others(3): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101799727 | |||||||
| chr12:101799728 | A | G | 341 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(338): Show |
345 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(342): Show |
intron_variant | MODIFIER | c.118-2966T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101799728 | |||||||
| chr12:101799731 | A | AC | 326 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(323): Show |
330 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(327): Show |
intron_variant | MODIFIER | c.118-2970dupG | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101799731 | |||||||
| chr12:101799733 | T | G | 326 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(323): Show |
330 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(327): Show |
intron_variant | MODIFIER | c.118-2971A>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101799733 | |||||||
| chr12:101799734 | T | C | 326 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(323): Show |
330 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(327): Show |
intron_variant | MODIFIER | c.118-2972A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101799734 | |||||||
| chr12:101799990 | T | C | 2 | a0006c0016t0013g0235 a0006c0017t0013g0234 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.118-3228A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101799990 | |||||||
| chr12:101800121 | G | A | 1 | a0001c0013t0003g0156 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.118-3359C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101800121 | |||||||
| chr12:101800196 | T | TATG | 326 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(323): Show |
330 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(327): Show |
intron_variant | MODIFIER | c.118-3435_118-3434i others(5): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101800196 | |||||||
| chr12:101800285 | G | T | 2 | a0001c0007t0004g0231 a0001c0007t0004g0232 |
2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.118-3523C>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101800285 | |||||||
| chr12:101800330 | TATTATAA others(3): Show |
T | 1 | a0001c0003t0003g0139 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.118-3578_118-3569d others(12): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101800330 | |||||||
| chr12:101800362 | T | C | 53 | a0001c0001t0003g0247 a0001c0003t0003g0133 a0001c0003t0003g0135 others(50): Show |
53 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.118-3600A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101800362 | |||||||
| chr12:101800377 | C | T | 1 | a0002c0012t0001g0214 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.118-3615G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101800377 | |||||||
| chr12:101800571 | C | T | 2 | a0001c0002t0001g0205 a0001c0023t0001g0215 |
2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.118-3809G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101800571 | |||||||
| chr12:101800604 | CA | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0285 a0001c0001t0001g0287 others(172): Show |
179 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.118-3843delT | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101800604 | |||||||
| chr12:101800604 | CAA | C | 139 | a0001c0001t0001g0219 a0001c0001t0001g0284 a0001c0001t0001g0286 others(136): Show |
140 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.118-3844_118-3843d others(4): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101800604 | |||||||
| chr12:101800616 | A | T | 1 | a0001c0023t0001g0215 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.118-3854T>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101800616 | |||||||
| chr12:101800705 | G | A | 1 | a0001c0002t0002g0072 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.118-3943C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101800705 | |||||||
| chr12:101800791 | A | G | 2 | a0001c0001t0004g0238 a0001c0001t0025g0257 |
2 | NA18947.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.118-4029T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101800791 | |||||||
| chr12:101800813 | G | A | 58 | a0001c0001t0003g0247 a0001c0001t0009g0052 a0001c0003t0003g0133 others(55): Show |
58 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.118-4051C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101800813 | |||||||
| chr12:101800905 | T | C | 1 | a0004c0006t0014g0006 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.118-4143A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101800905 | |||||||
| chr12:101800914 | C | T | 1 | a0002c0012t0001g0214 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.118-4152G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101800914 | |||||||
| chr12:101800975 | T | G | 40 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0010 others(37): Show |
40 | HG01106.hp1 HG01516.hp2 HG01981.hp1 others(37): Show |
intron_variant | MODIFIER | c.118-4213A>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101800975 | |||||||
| chr12:101801018 | G | A | 1 | a0001c0002t0002g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.118-4256C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101801018 | |||||||
| chr12:101801087 | G | T | 4 | a0001c0001t0001g0369 a0001c0001t0001g0370 a0001c0001t0001g0374 others(1): Show |
4 | HG02922.hp1 HG03486.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-4325C>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101801087 | |||||||
| chr12:101801230 | T | TC | 4 | a0001c0001t0001g0369 a0001c0001t0001g0370 a0001c0001t0001g0374 others(1): Show |
4 | HG02922.hp1 HG03486.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-4469dupG | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101801230 | |||||||
| chr12:101801231 | C | CA | 182 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0001g0289 others(179): Show |
183 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.118-4470dupT | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101801231 | |||||||
| chr12:101801231 | C | CAA | 45 | a0001c0001t0001g0219 a0001c0001t0001g0290 a0001c0001t0001g0294 others(42): Show |
45 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.118-4471_118-4470d others(4): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101801231 | |||||||
| chr12:101801231 | C | CAAA | 14 | a0001c0001t0001g0001 a0001c0001t0001g0284 a0001c0001t0001g0349 others(11): Show |
17 | HG01891.hp1 HG02145.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.118-4472_118-4470d others(5): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101801231 | |||||||
| chr12:101801231 | C | CAAAA | 10 | a0001c0001t0001g0360 a0001c0001t0001g0362 a0001c0001t0001g0363 others(7): Show |
10 | HG00621.hp1 HG01928.hp2 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.118-4473_118-4470d others(6): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101801231 | |||||||
| chr12:101801231 | C | CAAAAA | 11 | a0001c0001t0001g0361 a0001c0001t0002g0081 a0001c0001t0002g0091 others(8): Show |
11 | HG00558.hp1 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.118-4474_118-4470d others(7): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101801231 | |||||||
| chr12:101801231 | CA | C | 8 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0006g0228 others(5): Show |
8 | HG01168.hp1 HG01168.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.118-4470delT | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101801231 | |||||||
| chr12:101801279 | T | C | 2 | a0001c0001t0004g0383 a0001c0001t0004g0384 |
2 | NA18970.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.118-4517A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101801279 | |||||||
| chr12:101801440 | T | A | 1 | a0001c0007t0009g0056 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.118-4678A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101801440 | |||||||
| chr12:101801539 | C | CA | 97 | a0001c0001t0001g0219 a0001c0001t0001g0289 a0001c0001t0001g0298 others(94): Show |
97 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.118-4778dupT | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101801539 | |||||||
| chr12:101801539 | C | CAA | 72 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(69): Show |
72 | HG00423.hp2 HG01081.hp1 HG01099.hp1 others(69): Show |
intron_variant | MODIFIER | c.118-4779_118-4778d others(4): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101801539 | |||||||
| chr12:101801539 | C | CAAA | 17 | a0001c0001t0001g0291 a0001c0001t0001g0294 a0001c0001t0001g0299 others(14): Show |
17 | HG01169.hp2 HG01175.hp1 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.118-4780_118-4778d others(5): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101801539 | |||||||
| chr12:101801539 | C | CAAAA | 31 | a0001c0001t0003g0247 a0001c0002t0008g0207 a0001c0002t0008g0208 others(28): Show |
31 | HG00423.hp1 HG00597.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.118-4781_118-4778d others(6): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101801539 | |||||||
| chr12:101801539 | C | CAAAAA | 20 | a0001c0001t0001g0277 a0001c0003t0003g0136 a0001c0003t0003g0138 others(17): Show |
20 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.118-4782_118-4778d others(7): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101801539 | |||||||
| chr12:101801539 | C | CAAAAAA | 7 | a0001c0001t0001g0335 a0001c0003t0003g0140 a0001c0003t0003g0152 others(4): Show |
7 | HG01106.hp2 HG01433.hp1 HG04184.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-4783_118-4778d others(8): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101801539 | |||||||
| chr12:101801539 | C | CAAAAAAA | 7 | a0001c0001t0001g0276 a0001c0001t0009g0052 a0001c0003t0003g0153 others(4): Show |
7 | HG01167.hp2 HG01175.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.118-4784_118-4778d others(9): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101801539 | |||||||
| chr12:101801539 | CAAAAAAA others(2): Show |
C | 15 | a0001c0001t0001g0001 a0001c0001t0001g0360 a0001c0001t0001g0361 others(12): Show |
18 | HG01891.hp1 HG02257.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.118-4786_118-4778d others(11): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101801539 | |||||||
| chr12:101801539 | CAAAAAAA others(7): Show |
C | 51 | a0001c0001t0004g0005 a0001c0001t0004g0217 a0001c0001t0004g0233 others(48): Show |
52 | HG00544.hp1 HG00597.hp1 HG02056.hp1 others(49): Show |
intron_variant | MODIFIER | c.118-4791_118-4778d others(16): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101801539 | |||||||
| chr12:101801539 | CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0011g0061 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.118-4792_118-4778d others(17): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101801539 | |||||||
| chr12:101801650 | C | T | 5 | a0001c0002t0002g0097 a0001c0002t0002g0098 a0001c0002t0002g0107 others(2): Show |
5 | HG00558.hp2 HG02132.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.118-4888G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101801650 | |||||||
| chr12:101801822 | C | T | 4 | a0001c0001t0007g0278 a0001c0004t0007g0188 a0001c0004t0007g0189 others(1): Show |
4 | HG01081.hp1 HG02818.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-5060G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101801822 | |||||||
| chr12:101801894 | A | T | 1 | a0001c0002t0008g0237 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.118-5132T>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101801894 | |||||||
| chr12:101801895 | T | A | 9 | a0001c0002t0008g0206 a0001c0002t0008g0207 a0001c0002t0008g0208 others(6): Show |
9 | HG01884.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.118-5133A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101801895 | |||||||
| chr12:101801902 | T | C | 1 | a0001c0004t0007g0198 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.118-5140A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101801902 | |||||||
| chr12:101801963 | G | T | 9 | a0001c0002t0008g0206 a0001c0002t0008g0207 a0001c0002t0008g0208 others(6): Show |
9 | HG01884.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.118-5201C>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101801963 | |||||||
| chr12:101802078 | G | A | 77 | a0001c0001t0001g0219 a0001c0001t0005g0007 a0001c0001t0005g0008 others(74): Show |
77 | HG00323.hp1 HG00408.hp2 HG00741.hp2 others(74): Show |
intron_variant | MODIFIER | c.118-5316C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101802078 | |||||||
| chr12:101802189 | C | A | 2 | a0001c0002t0001g0205 a0001c0023t0001g0215 |
2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.118-5427G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101802189 | |||||||
| chr12:101802199 | T | TA | 15 | a0001c0001t0001g0306 a0001c0001t0002g0065 a0001c0001t0002g0068 others(12): Show |
15 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(12): Show |
intron_variant | MODIFIER | c.118-5438dupT | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101802199 | |||||||
| chr12:101802199 | TA | T | 82 | a0001c0001t0001g0219 a0001c0001t0001g0276 a0001c0001t0001g0277 others(79): Show |
82 | HG00408.hp2 HG00741.hp2 HG01081.hp1 others(79): Show |
intron_variant | MODIFIER | c.118-5438delT | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101802199 | |||||||
| chr12:101802199 | TAA | T | 55 | a0001c0001t0003g0247 a0001c0001t0005g0024 a0001c0001t0005g0032 others(52): Show |
55 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.118-5439_118-5438d others(4): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101802199 | |||||||
| chr12:101802212 | AAAAAAG | A | 11 | a0002c0009t0001g0195 a0002c0009t0001g0200 a0002c0009t0001g0201 others(8): Show |
11 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.118-5456_118-5451d others(8): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101802212 | |||||||
| chr12:101802213 | A | G | 2 | a0001c0002t0002g0078 a0002c0012t0002g0077 |
2 | HG00741.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.118-5451T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101802213 | |||||||
| chr12:101802214 | A | G | 11 | a0001c0001t0001g0369 a0001c0001t0001g0370 a0001c0001t0001g0374 others(8): Show |
11 | HG02922.hp1 HG03486.hp2 NA18747.hp1 others(8): Show |
intron_variant | MODIFIER | c.118-5452T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101802214 | |||||||
| chr12:101802297 | C | G | 1 | a0001c0002t0002g0129 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.118-5535G>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101802297 | |||||||
| chr12:101802324 | G | T | 1 | a0002c0012t0001g0214 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.118-5562C>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101802324 | |||||||
| chr12:101802515 | G | A | 2 | a0006c0016t0013g0235 a0006c0017t0013g0234 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.118-5753C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101802515 | |||||||
| chr12:101802589 | C | T | 7 | a0001c0001t0009g0052 a0001c0007t0004g0231 a0001c0007t0004g0232 others(4): Show |
7 | HG01167.hp2 HG02486.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.118-5827G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101802589 | |||||||
| chr12:101802602 | G | A | 8 | a0001c0001t0005g0008 a0001c0001t0005g0012 a0001c0001t0005g0017 others(5): Show |
8 | NA18954.hp1 NA18966.hp2 NA18983.hp2 others(5): Show |
intron_variant | MODIFIER | c.118-5840C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101802602 | |||||||
| chr12:101802753 | C | G | 1 | a0001c0002t0001g0359 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.118-5991G>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101802753 | |||||||
| chr12:101802791 | G | A | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.118-6029C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101802791 | |||||||
| chr12:101802813 | T | C | 326 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(323): Show |
330 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(327): Show |
intron_variant | MODIFIER | c.118-6051A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101802813 | |||||||
| chr12:101803173 | T | C | 91 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(88): Show |
91 | HG00408.hp1 HG00423.hp2 HG00642.hp1 others(88): Show |
intron_variant | MODIFIER | c.118-6411A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101803173 | |||||||
| chr12:101803418 | C | T | 41 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0010 others(38): Show |
41 | HG01106.hp1 HG01516.hp2 HG01943.hp1 others(38): Show |
intron_variant | MODIFIER | c.118-6656G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101803418 | |||||||
| chr12:101803464 | A | T | 1 | a0001c0001t0006g0224 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.118-6702T>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101803464 | |||||||
| chr12:101803484 | G | C | 4 | a0001c0002t0005g0015 a0001c0002t0005g0034 a0001c0002t0005g0037 others(1): Show |
4 | NA18980.hp1 NA18994.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-6722C>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101803484 | |||||||
| chr12:101803620 | TTC | T | 52 | a0001c0001t0003g0247 a0001c0003t0003g0133 a0001c0003t0003g0135 others(49): Show |
52 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.118-6860_118-6859d others(4): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101803620 | |||||||
| chr12:101803628 | C | A | 4 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0002t0001g0205 others(1): Show |
4 | HG02055.hp2 HG02451.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.118-6866G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101803628 | |||||||
| chr12:101803696 | G | A | 5 | a0002c0009t0001g0195 a0002c0009t0001g0200 a0002c0009t0001g0201 others(2): Show |
5 | HG02258.hp1 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.118-6934C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101803696 | |||||||
| chr12:101803836 | G | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0284 a0001c0001t0001g0285 others(117): Show |
123 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.118-7074C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101803836 | |||||||
| chr12:101803951 | T | G | 116 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0003g0247 others(113): Show |
117 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.118-7189A>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101803951 | |||||||
| chr12:101804057 | C | T | 1 | a0001c0025t0001g0213 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.118-7295G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101804057 | |||||||
| chr12:101804081 | A | T | 1 | a0002c0012t0001g0214 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.118-7319T>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101804081 | |||||||
| chr12:101804082 | A | T | 1 | a0002c0012t0001g0214 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.118-7320T>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101804082 | |||||||
| chr12:101804083 | T | A | 1 | a0001c0002t0005g0013 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.118-7321A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101804083 | |||||||
| chr12:101804254 | A | G | 1 | a0002c0012t0001g0214 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.118-7492T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101804254 | |||||||
| chr12:101804477 | G | C | 326 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(323): Show |
330 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(327): Show |
intron_variant | MODIFIER | c.118-7715C>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101804477 | |||||||
| chr12:101804529 | T | C | 1 | a0001c0002t0001g0364 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.118-7767A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101804529 | |||||||
| chr12:101804708 | T | C | 2 | a0001c0007t0004g0231 a0001c0007t0004g0232 |
2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.118-7946A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101804708 | |||||||
| chr12:101804716 | C | T | 1 | a0001c0001t0004g0238 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.118-7954G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101804716 | |||||||
| chr12:101804729 | C | T | 24 | a0001c0001t0007g0278 a0001c0001t0009g0052 a0001c0004t0007g0188 others(21): Show |
24 | HG01081.hp1 HG01167.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.118-7967G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101804729 | |||||||
| chr12:101805075 | G | A | 9 | a0001c0002t0008g0206 a0001c0002t0008g0207 a0001c0002t0008g0208 others(6): Show |
9 | HG01884.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.118-8313C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101805075 | |||||||
| chr12:101805077 | G | GA | 80 | a0001c0001t0001g0219 a0001c0001t0005g0007 a0001c0001t0005g0008 others(77): Show |
80 | HG00323.hp1 HG00408.hp2 HG00741.hp2 others(77): Show |
intron_variant | MODIFIER | c.118-8316dupT | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101805077 | |||||||
| chr12:101805189 | T | C | 91 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(88): Show |
91 | HG00408.hp1 HG00423.hp2 HG00642.hp1 others(88): Show |
intron_variant | MODIFIER | c.118-8427A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101805189 | |||||||
| chr12:101805217 | C | A | 1 | a0001c0002t0002g0087 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.118-8455G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101805217 | |||||||
| chr12:101805448 | C | T | 1 | a0001c0004t0006g0203 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.118-8686G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101805448 | |||||||
| chr12:101805449 | G | A | 5 | a0001c0002t0002g0078 a0001c0002t0002g0079 a0001c0002t0002g0080 others(2): Show |
5 | HG00741.hp1 HG01884.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.118-8687C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101805449 | |||||||
| chr12:101805530 | G | A | 2 | a0001c0004t0007g0197 a0001c0004t0007g0198 |
2 | HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.118-8768C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101805530 | |||||||
| chr12:101805547 | A | C | 7 | a0001c0001t0009g0052 a0001c0007t0004g0231 a0001c0007t0004g0232 others(4): Show |
7 | HG01167.hp2 HG02486.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.118-8785T>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101805547 | |||||||
| chr12:101805551 | C | T | 53 | a0001c0001t0003g0247 a0001c0001t0004g0376 a0001c0003t0003g0133 others(50): Show |
53 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.118-8789G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101805551 | |||||||
| chr12:101805615 | C | T | 2 | a0001c0001t0001g0302 a0001c0001t0001g0373 |
2 | NA18977.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.118-8853G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101805615 | |||||||
| chr12:101805659 | A | G | 1 | a0001c0001t0024g0353 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.118-8897T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101805659 | |||||||
| chr12:101805727 | A | T | 1 | a0001c0001t0001g0379 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.118-8965T>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101805727 | |||||||
| chr12:101805799 | C | T | 1 | a0001c0003t0003g0139 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.118-9037G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101805799 | |||||||
| chr12:101805800 | T | C | 1 | a0001c0003t0003g0139 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.118-9038A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101805800 | |||||||
| chr12:101805934 | G | A | 1 | a0001c0001t0024g0353 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.118-9172C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101805934 | |||||||
| chr12:101806023 | G | A | 52 | a0001c0001t0004g0005 a0001c0001t0004g0217 a0001c0001t0004g0233 others(49): Show |
53 | HG00544.hp1 HG00597.hp1 HG02056.hp1 others(50): Show |
intron_variant | MODIFIER | c.118-9261C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101806023 | |||||||
| chr12:101806148 | G | C | 78 | a0001c0001t0001g0219 a0001c0001t0005g0007 a0001c0001t0005g0008 others(75): Show |
78 | HG00323.hp1 HG00408.hp2 HG00741.hp2 others(75): Show |
intron_variant | MODIFIER | c.118-9386C>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101806148 | |||||||
| chr12:101806152 | T | C | 2 | a0001c0001t0001g0340 a0001c0001t0001g0341 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.118-9390A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101806152 | |||||||
| chr12:101806240 | T | G | 7 | a0001c0003t0003g0178 a0001c0003t0003g0181 a0001c0003t0003g0182 others(4): Show |
7 | HG00140.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.118-9478A>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101806240 | |||||||
| chr12:101806300 | C | T | 1 | a0001c0001t0001g0300 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.118-9538G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101806300 | |||||||
| chr12:101806455 | C | T | 4 | a0001c0001t0007g0278 a0001c0004t0007g0188 a0001c0004t0007g0189 others(1): Show |
4 | HG01081.hp1 HG02818.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-9693G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101806455 | |||||||
| chr12:101806557 | A | G | 120 | a0001c0001t0001g0001 a0001c0001t0001g0284 a0001c0001t0001g0285 others(117): Show |
123 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.118-9795T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101806557 | |||||||
| chr12:101806934 | GGCCAAAA others(6): Show |
G | 1 | a0001c0001t0005g0023 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.118-10185_118-1017 others(17): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101806934 | |||||||
| chr12:101807020 | C | T | 1 | a0001c0002t0008g0207 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.118-10258G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101807020 | |||||||
| chr12:101807185 | T | C | 1 | a0001c0001t0023g0371 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.118-10423A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101807185 | |||||||
| chr12:101807514 | G | GA | 117 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0003g0247 others(114): Show |
118 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.118-10753dupT | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101807514 | |||||||
| chr12:101807796 | G | A | 52 | a0001c0001t0004g0005 a0001c0001t0004g0217 a0001c0001t0004g0233 others(49): Show |
53 | HG00544.hp1 HG00597.hp1 HG02056.hp1 others(50): Show |
intron_variant | MODIFIER | c.118-11034C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101807796 | |||||||
| chr12:101807838 | A | G | 326 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(323): Show |
330 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(327): Show |
intron_variant | MODIFIER | c.118-11076T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101807838 | |||||||
| chr12:101807956 | G | A | 2 | a0001c0007t0004g0231 a0001c0007t0004g0232 |
2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.118-11194C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101807956 | |||||||
| chr12:101808182 | T | C | 1 | a0002c0012t0001g0214 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.118-11420A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101808182 | |||||||
| chr12:101808199 | T | C | 2 | a0001c0002t0001g0205 a0001c0023t0001g0215 |
2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.118-11437A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101808199 | |||||||
| chr12:101808375 | T | TA | 88 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0297 others(85): Show |
89 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.118-11614dupT | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101808375 | |||||||
| chr12:101808375 | T | TAA | 59 | a0001c0001t0001g0334 a0001c0001t0001g0335 a0001c0001t0001g0344 others(56): Show |
59 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.118-11615_118-1161 others(6): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101808375 | |||||||
| chr12:101808491 | G | A | 1 | a0001c0002t0002g0103 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.118-11729C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101808491 | |||||||
| chr12:101808521 | G | A | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.118-11759C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101808521 | |||||||
| chr12:101808536 | C | T | 60 | a0001c0001t0001g0219 a0001c0001t0005g0007 a0001c0001t0005g0008 others(57): Show |
60 | HG00323.hp1 HG00408.hp2 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.118-11774G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101808536 | |||||||
| chr12:101808607 | A | T | 1 | a0001c0003t0003g0139 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.118-11845T>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101808607 | |||||||
| chr12:101808879 | C | T | 4 | a0001c0002t0001g0356 a0001c0002t0001g0359 a0003c0005t0001g0357 others(1): Show |
4 | HG00642.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-12117G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101808879 | |||||||
| chr12:101808915 | T | G | 40 | a0001c0001t0005g0007 a0001c0001t0005g0008 a0001c0001t0005g0010 others(37): Show |
40 | HG01106.hp1 HG01516.hp2 HG01981.hp1 others(37): Show |
intron_variant | MODIFIER | c.118-12153A>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101808915 | |||||||
| chr12:101808999 | T | C | 1 | a0001c0002t0001g0356 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.118-12237A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101808999 | |||||||
| chr12:101809020 | T | A | 1 | a0001c0001t0006g0218 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.118-12258A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101809020 | |||||||
| chr12:101809178 | T | C | 2 | a0001c0001t0006g0221 a0001c0001t0006g0351 |
2 | HG00741.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.118-12416A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101809178 | |||||||
| chr12:101809376 | A | C | 1 | a0001c0001t0001g0318 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.118-12614T>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101809376 | |||||||
| chr12:101809387 | C | A | 117 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0003g0247 others(114): Show |
118 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.118-12625G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101809387 | |||||||
| chr12:101809397 | T | C | 2 | a0001c0001t0001g0360 a0001c0001t0001g0363 |
2 | HG02970.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.118-12635A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101809397 | |||||||
| chr12:101809423 | G | A | 1 | a0001c0001t0004g0271 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.118-12661C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101809423 | |||||||
| chr12:101809430 | C | T | 2 | a0001c0001t0006g0230 a0001c0001t0006g0236 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.118-12668G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101809430 | |||||||
| chr12:101809438 | G | A | 1 | a0001c0001t0001g0318 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.118-12676C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101809438 | |||||||
| chr12:101809623 | G | T | 9 | a0001c0002t0008g0206 a0001c0002t0008g0207 a0001c0002t0008g0208 others(6): Show |
9 | HG01884.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.118-12861C>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101809623 | |||||||
| chr12:101809637 | G | A | 1 | a0001c0002t0008g0237 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.118-12875C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101809637 | |||||||
| chr12:101809672 | A | G | 28 | a0001c0001t0001g0001 a0001c0001t0001g0360 a0001c0001t0001g0361 others(25): Show |
31 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.118-12910T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101809672 | |||||||
| chr12:101809683 | T | C | 59 | a0001c0001t0004g0005 a0001c0001t0004g0217 a0001c0001t0004g0233 others(56): Show |
60 | HG00544.hp1 HG00597.hp1 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.118-12921A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101809683 | |||||||
| chr12:101809829 | T | A | 1 | a0001c0001t0001g0318 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.118-13067A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101809829 | |||||||
| chr12:101809832 | T | C | 1 | a0001c0003t0003g0171 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.118-13070A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101809832 | |||||||
| chr12:101809885 | G | C | 52 | a0001c0001t0004g0005 a0001c0001t0004g0217 a0001c0001t0004g0233 others(49): Show |
53 | HG00544.hp1 HG00597.hp1 HG02056.hp1 others(50): Show |
intron_variant | MODIFIER | c.118-13123C>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101809885 | |||||||
| chr12:101810009 | T | A | 1 | a0001c0001t0001g0318 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.118-13247A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810009 | |||||||
| chr12:101810088 | A | G | 1 | a0002c0012t0001g0214 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.118-13326T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810088 | |||||||
| chr12:101810100 | C | CA | 80 | a0001c0001t0001g0219 a0001c0001t0005g0007 a0001c0001t0005g0008 others(77): Show |
80 | HG00323.hp1 HG00408.hp2 HG00741.hp2 others(77): Show |
intron_variant | MODIFIER | c.118-13339dupT | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810100 | |||||||
| chr12:101810318 | T | C | 1 | a0001c0002t0002g0088 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.118-13556A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810318 | |||||||
| chr12:101810396 | C | CAT | 9 | a0001c0001t0004g0233 a0001c0001t0004g0383 a0001c0001t0004g0384 others(6): Show |
10 | HG01109.hp2 HG01255.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.118-13636_118-1363 others(6): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810396 | |||||||
| chr12:101810396 | CAT | C | 20 | a0001c0001t0001g0293 a0001c0001t0002g0065 a0001c0001t0002g0069 others(17): Show |
20 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.118-13636_118-1363 others(6): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810396 | |||||||
| chr12:101810396 | CATAT | C | 61 | a0001c0001t0001g0219 a0001c0001t0001g0311 a0001c0001t0003g0247 others(58): Show |
61 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.118-13638_118-1363 others(8): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810396 | |||||||
| chr12:101810396 | CATATAT | C | 23 | a0001c0001t0001g0001 a0001c0001t0001g0276 a0001c0001t0001g0277 others(20): Show |
26 | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.118-13640_118-1363 others(10): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810396 | |||||||
| chr12:101810396 | CATATATA others(1): Show |
C | 98 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(95): Show |
98 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.118-13642_118-1363 others(12): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810396 | |||||||
| chr12:101810396 | CATATATA others(3): Show |
C | 4 | a0001c0001t0007g0278 a0001c0004t0007g0188 a0001c0004t0007g0189 others(1): Show |
4 | HG01081.hp1 HG02818.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-13644_118-1363 others(14): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810396 | |||||||
| chr12:101810410 | T | A | 1 | a0001c0001t0001g0318 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.118-13648A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810410 | |||||||
| chr12:101810410 | TATATATA others(9): Show |
T | 7 | a0001c0002t0008g0206 a0001c0002t0008g0207 a0001c0002t0008g0208 others(4): Show |
7 | HG01884.hp1 HG02145.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-13664_118-1364 others(20): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810410 | |||||||
| chr12:101810412 | TATATATA others(9): Show |
T | 2 | a0001c0015t0008g0196 a0001c0025t0001g0213 |
2 | HG02559.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.118-13666_118-1365 others(20): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810412 | |||||||
| chr12:101810414 | T | TAC | 7 | a0001c0001t0005g0010 a0001c0001t0005g0041 a0001c0001t0010g0043 others(4): Show |
7 | HG01106.hp1 HG01109.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.118-13653_118-1365 others(6): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810414 | |||||||
| chr12:101810414 | T | TACAC | 26 | a0001c0001t0005g0007 a0001c0001t0005g0011 a0001c0001t0005g0012 others(23): Show |
26 | HG01943.hp1 HG01981.hp1 HG02148.hp1 others(23): Show |
intron_variant | MODIFIER | c.118-13653_118-1365 others(8): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810414 | |||||||
| chr12:101810414 | T | TACACAC | 11 | a0001c0001t0005g0035 a0001c0001t0005g0047 a0001c0001t0005g0048 others(8): Show |
11 | HG01993.hp1 HG02273.hp1 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.118-13653_118-1365 others(10): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810414 | |||||||
| chr12:101810414 | TATATATA others(5): Show |
T | 1 | a0001c0004t0001g0199 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.118-13664_118-1365 others(16): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810414 | |||||||
| chr12:101810414 | TATATATA others(13): Show |
T | 1 | a0001c0001t0001g0369 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.118-13672_118-1365 others(24): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810414 | |||||||
| chr12:101810416 | T | C | 46 | a0001c0001t0005g0007 a0001c0001t0005g0010 a0001c0001t0005g0011 others(43): Show |
46 | HG01106.hp1 HG01109.hp1 HG01516.hp2 others(43): Show |
intron_variant | MODIFIER | c.118-13654A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810416 | |||||||
| chr12:101810418 | T | C | 40 | a0001c0001t0001g0293 a0001c0001t0005g0007 a0001c0001t0005g0008 others(37): Show |
40 | HG00741.hp2 HG01106.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.118-13656A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810418 | |||||||
| chr12:101810420 | T | C | 38 | a0001c0001t0001g0219 a0001c0001t0001g0293 a0001c0001t0001g0311 others(35): Show |
38 | HG00323.hp1 HG00408.hp2 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.118-13658A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810420 | |||||||
| chr12:101810422 | T | C | 85 | a0001c0001t0001g0219 a0001c0001t0001g0293 a0001c0001t0001g0311 others(82): Show |
85 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.118-13660A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810422 | |||||||
| chr12:101810424 | C | T | 4 | a0001c0001t0005g0032 a0001c0004t0007g0197 a0006c0016t0013g0235 others(1): Show |
4 | HG02486.hp2 HG02922.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.118-13662G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810424 | |||||||
| chr12:101810426 | C | T | 5 | a0001c0001t0001g0293 a0001c0001t0006g0221 a0002c0009t0001g0195 others(2): Show |
5 | HG00741.hp2 HG02451.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.118-13664G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810426 | |||||||
| chr12:101810428 | C | T | 14 | a0001c0001t0001g0219 a0001c0001t0001g0311 a0001c0001t0006g0218 others(11): Show |
14 | HG00323.hp1 HG00408.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.118-13666G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810428 | |||||||
| chr12:101810430 | C | T | 2 | a0001c0001t0002g0081 a0001c0001t0002g0093 |
2 | NA18943.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.118-13668G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810430 | |||||||
| chr12:101810432 | T | C | 135 | a0001c0001t0001g0219 a0001c0001t0001g0289 a0001c0001t0001g0290 others(132): Show |
136 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.118-13670A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810432 | |||||||
| chr12:101810432 | TAC | T | 7 | a0001c0001t0001g0001 a0001c0001t0001g0362 a0001c0001t0011g0125 others(4): Show |
10 | HG00140.hp1 HG01358.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.118-13672_118-1367 others(6): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810432 | |||||||
| chr12:101810432 | TACAC | T | 8 | a0001c0002t0001g0356 a0001c0003t0003g0142 a0001c0003t0003g0181 others(5): Show |
8 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.118-13674_118-1367 others(8): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810432 | |||||||
| chr12:101810432 | TACACAC | T | 46 | a0001c0001t0003g0247 a0001c0001t0021g0279 a0001c0003t0003g0133 others(43): Show |
46 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.118-13676_118-1367 others(10): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810432 | |||||||
| chr12:101810432 | TACACACA others(1): Show |
T | 3 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0284 |
3 | HG02055.hp2 HG02717.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.118-13678_118-1367 others(12): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810432 | |||||||
| chr12:101810434 | C | T | 51 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0313 others(48): Show |
52 | HG00544.hp1 HG02056.hp1 HG02132.hp1 others(49): Show |
intron_variant | MODIFIER | c.118-13672G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810434 | |||||||
| chr12:101810436 | C | T | 6 | a0001c0002t0008g0237 a0001c0007t0004g0231 a0001c0008t0004g0216 others(3): Show |
6 | HG00597.hp1 HG02486.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.118-13674G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810436 | |||||||
| chr12:101810438 | C | T | 3 | a0001c0001t0004g0259 a0001c0004t0001g0199 a0001c0007t0004g0232 |
3 | HG03471.hp1 HG03540.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.118-13676G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810438 | |||||||
| chr12:101810440 | C | T | 9 | a0001c0002t0008g0206 a0001c0002t0008g0207 a0001c0002t0008g0208 others(6): Show |
9 | HG01884.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.118-13678G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810440 | |||||||
| chr12:101810449 | A | G | 1 | a0001c0002t0008g0237 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.118-13687T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810449 | |||||||
| chr12:101810464 | C | T | 1 | a0001c0001t0005g0008 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.118-13702G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810464 | |||||||
| chr12:101810466 | C | CAT | 23 | a0001c0001t0001g0298 a0001c0001t0001g0300 a0001c0001t0001g0312 others(20): Show |
23 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.118-13705_118-1370 others(6): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810466 | |||||||
| chr12:101810466 | C | T | 277 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(274): Show |
281 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.118-13704G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810466 | |||||||
| chr12:101810468 | C | T | 1 | a0001c0001t0005g0008 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.118-13706G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810468 | |||||||
| chr12:101810497 | CTTTT | C | 16 | a0001c0001t0007g0278 a0001c0004t0007g0188 a0001c0004t0007g0189 others(13): Show |
16 | HG01081.hp1 HG01891.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.118-13739_118-1373 others(8): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810497 | |||||||
| chr12:101810729 | T | G | 1 | a0001c0001t0001g0318 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.118-13967A>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810729 | |||||||
| chr12:101810732 | T | C | 1 | a0001c0001t0001g0303 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.118-13970A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810732 | |||||||
| chr12:101810780 | G | A | 2 | a0001c0007t0004g0231 a0001c0007t0004g0232 |
2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.118-14018C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810780 | |||||||
| chr12:101810900 | A | G | 1 | a0002c0009t0001g0200 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.118-14138T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101810900 | |||||||
| chr12:101811024 | T | G | 1 | a0001c0003t0003g0136 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.118-14262A>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101811024 | |||||||
| chr12:101811140 | T | C | 1 | a0001c0002t0008g0237 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.118-14378A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101811140 | |||||||
| chr12:101811211 | C | T | 1 | a0001c0002t0008g0237 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.118-14449G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101811211 | |||||||
| chr12:101811233 | T | C | 1 | a0001c0003t0003g0183 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.118-14471A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101811233 | |||||||
| chr12:101811383 | CT | C | 255 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(252): Show |
258 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.118-14622delA | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101811383 | |||||||
| chr12:101811383 | CTT | C | 60 | a0001c0001t0004g0005 a0001c0001t0004g0217 a0001c0001t0004g0233 others(57): Show |
61 | HG00544.hp1 HG00597.hp1 HG01167.hp2 others(58): Show |
intron_variant | MODIFIER | c.118-14623_118-1462 others(6): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101811383 | |||||||
| chr12:101811396 | T | C | 1 | a0001c0001t0001g0318 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.118-14634A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101811396 | |||||||
| chr12:101811397 | C | T | 1 | a0001c0001t0001g0318 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.118-14635G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101811397 | |||||||
| chr12:101811408 | T | C | 1 | a0001c0001t0009g0052 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.118-14646A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101811408 | |||||||
| chr12:101811597 | C | T | 60 | a0001c0001t0004g0005 a0001c0001t0004g0217 a0001c0001t0004g0233 others(57): Show |
61 | HG00544.hp1 HG00597.hp1 HG01167.hp2 others(58): Show |
intron_variant | MODIFIER | c.118-14835G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101811597 | |||||||
| chr12:101811638 | C | CT | 6 | a0001c0001t0001g0288 a0001c0001t0001g0318 a0001c0002t0002g0063 others(3): Show |
6 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.118-14877dupA | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101811638 | |||||||
| chr12:101811638 | CT | C | 18 | a0001c0001t0004g0249 a0001c0001t0004g0383 a0001c0001t0004g0384 others(15): Show |
18 | HG00323.hp2 HG00558.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.118-14877delA | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101811638 | |||||||
| chr12:101811731 | C | T | 5 | a0001c0001t0004g0217 a0001c0001t0004g0243 a0001c0001t0004g0244 others(2): Show |
5 | HG02155.hp1 NA18955.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.118-14969G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101811731 | |||||||
| chr12:101811891 | G | A | 1 | a0002c0012t0001g0214 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.118-15129C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101811891 | |||||||
| chr12:101811925 | G | A | 46 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(43): Show |
46 | HG01099.hp1 HG01192.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.118-15163C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101811925 | |||||||
| chr12:101811930 | G | A | 1 | a0001c0001t0005g0020 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.118-15168C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101811930 | |||||||
| chr12:101811966 | C | T | 1 | a0001c0002t0002g0096 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.118-15204G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101811966 | |||||||
| chr12:101811978 | G | A | 1 | a0001c0001t0006g0226 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.118-15216C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101811978 | |||||||
| chr12:101812018 | G | A | 2 | a0001c0002t0001g0205 a0001c0023t0001g0215 |
2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.118-15256C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101812018 | |||||||
| chr12:101812049 | C | T | 1 | a0001c0002t0002g0107 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.118-15287G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101812049 | |||||||
| chr12:101812140 | G | A | 1 | a0001c0001t0001g0318 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.118-15378C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101812140 | |||||||
| chr12:101812141 | A | G | 1 | a0001c0001t0001g0318 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.118-15379T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101812141 | |||||||
| chr12:101812143 | G | C | 1 | a0001c0001t0001g0318 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.118-15381C>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101812143 | |||||||
| chr12:101812228 | G | A | 1 | a0001c0001t0001g0292 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.118-15466C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101812228 | |||||||
| chr12:101812378 | G | A | 1 | a0001c0001t0021g0279 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.118-15616C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101812378 | |||||||
| chr12:101812421 | A | G | 52 | a0001c0001t0004g0005 a0001c0001t0004g0217 a0001c0001t0004g0233 others(49): Show |
53 | HG00544.hp1 HG00597.hp1 HG02056.hp1 others(50): Show |
intron_variant | MODIFIER | c.118-15659T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101812421 | |||||||
| chr12:101812469 | A | T | 1 | a0001c0001t0001g0318 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.118-15707T>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101812469 | |||||||
| chr12:101812581 | A | ACC | 49 | a0001c0001t0004g0217 a0001c0001t0004g0233 a0001c0001t0004g0238 others(46): Show |
49 | HG00544.hp1 HG00597.hp1 HG02056.hp1 others(46): Show |
intron_variant | MODIFIER | c.118-15821_118-1582 others(6): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101812581 | |||||||
| chr12:101812588 | C | G | 1 | a0001c0001t0009g0052 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.118-15826G>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101812588 | |||||||
| chr12:101812688 | G | C | 1 | a0001c0002t0002g0120 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.118-15926C>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101812688 | |||||||
| chr12:101812938 | G | T | 3 | a0003c0005t0001g0280 a0003c0005t0001g0282 a0003c0005t0001g0283 |
3 | HG02647.hp1 HG02809.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.118-16176C>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101812938 | |||||||
| chr12:101812971 | G | GGTGGTTT others(10): Show |
1 | a0001c0001t0001g0318 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.118-16210_118-1620 others(21): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101812971 | |||||||
| chr12:101812980 | G | T | 8 | a0001c0001t0009g0052 a0001c0007t0004g0231 a0001c0007t0004g0232 others(5): Show |
8 | HG01167.hp2 HG02486.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.118-16218C>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101812980 | |||||||
| chr12:101812986 | G | GT | 19 | a0001c0001t0001g0276 a0001c0001t0001g0344 a0001c0001t0001g0372 others(16): Show |
19 | HG00408.hp1 HG01109.hp2 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.118-16225dupA | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101812986 | |||||||
| chr12:101812987 | T | TG | 93 | a0001c0001t0001g0219 a0001c0001t0001g0342 a0001c0001t0005g0007 others(90): Show |
93 | HG00323.hp1 HG00408.hp2 HG00741.hp2 others(90): Show |
intron_variant | MODIFIER | c.118-16226_118-1622 others(5): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101812987 | |||||||
| chr12:101813103 | G | A | 1 | a0001c0007t0009g0057 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.118-16341C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101813103 | |||||||
| chr12:101813184 | T | C | 327 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(324): Show |
331 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(328): Show |
intron_variant | MODIFIER | c.118-16422A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101813184 | |||||||
| chr12:101813261 | A | G | 1 | a0001c0002t0002g0115 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.118-16499T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101813261 | |||||||
| chr12:101813479 | A | T | 1 | a0001c0001t0001g0318 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.118-16717T>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101813479 | |||||||
| chr12:101813480 | T | A | 1 | a0001c0001t0001g0318 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.118-16718A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101813480 | |||||||
| chr12:101813550 | T | C | 1 | a0001c0003t0003g0157 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.118-16788A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101813550 | |||||||
| chr12:101813585 | AT | A | 54 | a0001c0001t0003g0247 a0001c0003t0003g0133 a0001c0003t0003g0135 others(51): Show |
54 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.118-16824delA | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101813585 | |||||||
| chr12:101813631 | G | A | 2 | a0001c0007t0004g0231 a0001c0007t0004g0232 |
2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.118-16869C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101813631 | |||||||
| chr12:101813757 | T | C | 3 | a0001c0002t0001g0205 a0001c0023t0001g0215 a0001c0025t0001g0213 |
3 | HG02451.hp2 HG02622.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.117+16802A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101813757 | |||||||
| chr12:101813761 | A | G | 1 | a0001c0001t0001g0318 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.117+16798T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101813761 | |||||||
| chr12:101813762 | G | A | 1 | a0001c0001t0001g0318 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.117+16797C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101813762 | |||||||
| chr12:101813764 | C | G | 1 | a0001c0001t0001g0318 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.117+16795G>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101813764 | |||||||
| chr12:101813970 | T | G | 1 | a0001c0001t0001g0352 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.117+16589A>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101813970 | |||||||
| chr12:101814065 | C | T | 1 | a0008c0018t0001g0296 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.117+16494G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101814065 | |||||||
| chr12:101814078 | CA | C | 11 | a0001c0001t0001g0291 a0001c0002t0001g0205 a0001c0002t0008g0206 others(8): Show |
11 | HG01884.hp1 HG02145.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.117+16480delT | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101814078 | |||||||
| chr12:101814078 | CAA | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0276 a0001c0001t0001g0277 others(104): Show |
110 | HG00408.hp1 HG00423.hp2 HG00642.hp1 others(107): Show |
intron_variant | MODIFIER | c.117+16479_117+1648 others(6): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101814078 | |||||||
| chr12:101814090 | A | G | 79 | a0001c0001t0001g0219 a0001c0001t0001g0342 a0001c0001t0005g0007 others(76): Show |
79 | HG00323.hp1 HG00408.hp2 HG00741.hp2 others(76): Show |
intron_variant | MODIFIER | c.117+16469T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101814090 | |||||||
| chr12:101814179 | G | T | 2 | a0006c0016t0013g0235 a0006c0017t0013g0234 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.117+16380C>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101814179 | |||||||
| chr12:101814315 | T | C | 4 | a0001c0001t0011g0059 a0001c0001t0011g0060 a0001c0001t0011g0061 others(1): Show |
4 | NA18747.hp1 NA18971.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.117+16244A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101814315 | |||||||
| chr12:101814346 | T | C | 1 | a0001c0002t0008g0237 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.117+16213A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101814346 | |||||||
| chr12:101814392 | G | A | 1 | a0001c0007t0004g0232 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.117+16167C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101814392 | |||||||
| chr12:101814463 | G | A | 2 | a0001c0002t0002g0079 a0001c0002t0002g0080 |
2 | HG01884.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.117+16096C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101814463 | |||||||
| chr12:101814554 | G | A | 1 | a0001c0001t0002g0094 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.117+16005C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101814554 | |||||||
| chr12:101814645 | C | T | 1 | a0002c0009t0001g0204 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.117+15914G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101814645 | |||||||
| chr12:101814765 | T | C | 1 | a0001c0001t0021g0279 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.117+15794A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101814765 | |||||||
| chr12:101814786 | A | G | 8 | a0001c0001t0009g0052 a0001c0007t0004g0231 a0001c0007t0004g0232 others(5): Show |
8 | HG01167.hp2 HG02486.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.117+15773T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101814786 | |||||||
| chr12:101814987 | A | G | 3 | a0001c0002t0001g0205 a0001c0023t0001g0215 a0001c0025t0001g0213 |
3 | HG02451.hp2 HG02622.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.117+15572T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101814987 | |||||||
| chr12:101815228 | G | A | 1 | a0002c0012t0001g0214 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.117+15331C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101815228 | |||||||
| chr12:101815237 | T | C | 1 | a0001c0002t0008g0237 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.117+15322A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101815237 | |||||||
| chr12:101815606 | T | C | 2 | a0006c0016t0013g0235 a0006c0017t0013g0234 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.117+14953A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101815606 | |||||||
| chr12:101815608 | G | A | 1 | a0001c0002t0008g0237 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.117+14951C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101815608 | |||||||
| chr12:101815622 | CA | C | 318 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(315): Show |
322 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(319): Show |
intron_variant | MODIFIER | c.117+14936delT | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101815622 | |||||||
| chr12:101815758 | A | G | 1 | a0004c0006t0014g0006 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.117+14801T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101815758 | |||||||
| chr12:101816012 | G | A | 1 | a0001c0002t0002g0122 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.117+14547C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101816012 | |||||||
| chr12:101816016 | C | G | 2 | a0001c0001t0006g0227 a0001c0001t0006g0229 |
2 | HG04115.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.117+14543G>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101816016 | |||||||
| chr12:101816138 | GACTTACG others(11): Show |
G | 1 | a0001c0003t0003g0149 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.117+14403_117+1442 others(22): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101816138 | |||||||
| chr12:101816140 | C | T | 2 | a0001c0003t0003g0144 a0001c0003t0003g0146 |
2 | NA18974.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.117+14419G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101816140 | |||||||
| chr12:101816162 | G | C | 1 | a0001c0004t0007g0198 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.117+14397C>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101816162 | |||||||
| chr12:101816185 | G | T | 1 | a0001c0001t0005g0021 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.117+14374C>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101816185 | |||||||
| chr12:101816202 | C | T | 1 | a0001c0003t0003g0149 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.117+14357G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101816202 | |||||||
| chr12:101816221 | A | G | 1 | a0001c0002t0001g0359 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.117+14338T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101816221 | |||||||
| chr12:101816379 | T | C | 1 | a0001c0002t0008g0237 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.117+14180A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101816379 | |||||||
| chr12:101816432 | T | C | 2 | a0001c0001t0001g0319 a0001c0001t0001g0320 |
2 | HG02273.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.117+14127A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101816432 | |||||||
| chr12:101816443 | A | T | 54 | a0001c0001t0003g0247 a0001c0003t0003g0133 a0001c0003t0003g0135 others(51): Show |
54 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.117+14116T>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101816443 | |||||||
| chr12:101816587 | C | T | 1 | a0006c0017t0013g0234 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.117+13972G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101816587 | |||||||
| chr12:101816691 | T | A | 2 | a0001c0001t0006g0227 a0001c0001t0006g0229 |
2 | HG04115.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.117+13868A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101816691 | |||||||
| chr12:101817239 | C | A | 1 | a0002c0012t0001g0214 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.117+13320G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101817239 | |||||||
| chr12:101817265 | C | CT | 101 | a0001c0001t0002g0065 a0001c0001t0002g0068 a0001c0001t0002g0069 others(98): Show |
102 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.117+13293dupA | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101817265 | |||||||
| chr12:101817265 | C | CTT | 52 | a0001c0001t0001g0219 a0001c0001t0002g0095 a0001c0001t0004g0251 others(49): Show |
52 | HG00323.hp1 HG00408.hp2 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.117+13292_117+1329 others(6): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101817265 | |||||||
| chr12:101817265 | CT | C | 90 | a0001c0001t0001g0277 a0001c0001t0001g0284 a0001c0001t0001g0285 others(87): Show |
90 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.117+13293delA | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101817265 | |||||||
| chr12:101817265 | CTT | C | 18 | a0001c0001t0001g0001 a0001c0001t0001g0287 a0001c0001t0001g0303 others(15): Show |
21 | HG01243.hp2 HG01433.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.117+13292_117+1329 others(6): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101817265 | |||||||
| chr12:101817598 | A | G | 1 | a0001c0007t0004g0232 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.117+12961T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101817598 | |||||||
| chr12:101817698 | T | C | 52 | a0001c0001t0004g0005 a0001c0001t0004g0217 a0001c0001t0004g0233 others(49): Show |
53 | HG00544.hp1 HG00597.hp1 HG02056.hp1 others(50): Show |
intron_variant | MODIFIER | c.117+12861A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101817698 | |||||||
| chr12:101817781 | G | A | 7 | a0001c0002t0008g0206 a0001c0002t0008g0207 a0001c0002t0008g0208 others(4): Show |
7 | HG01884.hp1 HG02145.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+12778C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101817781 | |||||||
| chr12:101817866 | C | G | 2 | a0006c0016t0013g0235 a0006c0017t0013g0234 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.117+12693G>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101817866 | |||||||
| chr12:101817970 | T | C | 1 | a0001c0004t0007g0197 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.117+12589A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101817970 | |||||||
| chr12:101817988 | T | C | 16 | a0001c0001t0001g0001 a0001c0001t0001g0360 a0001c0001t0001g0361 others(13): Show |
19 | HG01243.hp2 HG01891.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.117+12571A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101817988 | |||||||
| chr12:101818068 | C | T | 1 | a0001c0001t0004g0383 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.117+12491G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101818068 | |||||||
| chr12:101818376 | C | CT | 8 | a0001c0001t0001g0306 a0001c0001t0004g0259 a0001c0001t0006g0252 others(5): Show |
8 | HG02300.hp2 HG02572.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.117+12182dupA | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101818376 | |||||||
| chr12:101818376 | CT | C | 136 | a0001c0001t0001g0219 a0001c0001t0001g0329 a0001c0001t0003g0247 others(133): Show |
136 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.117+12182delA | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101818376 | |||||||
| chr12:101818376 | CTT | C | 8 | a0001c0002t0005g0015 a0001c0002t0005g0034 a0001c0002t0005g0037 others(5): Show |
8 | HG02486.hp2 HG02922.hp2 NA18980.hp1 others(5): Show |
intron_variant | MODIFIER | c.117+12181_117+1218 others(6): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101818376 | |||||||
| chr12:101818509 | C | A | 1 | a0001c0001t0004g0383 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.117+12050G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101818509 | |||||||
| chr12:101818643 | T | C | 2 | a0001c0002t0002g0074 a0001c0002t0002g0112 |
2 | HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.117+11916A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101818643 | |||||||
| chr12:101818775 | G | A | 2 | a0006c0016t0013g0235 a0006c0017t0013g0234 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.117+11784C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101818775 | |||||||
| chr12:101818802 | T | A | 1 | a0001c0001t0004g0383 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.117+11757A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101818802 | |||||||
| chr12:101819051 | G | A | 2 | a0001c0002t0001g0205 a0001c0023t0001g0215 |
2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.117+11508C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101819051 | |||||||
| chr12:101819143 | C | T | 77 | a0001c0001t0001g0219 a0001c0001t0005g0007 a0001c0001t0005g0008 others(74): Show |
77 | HG00323.hp1 HG00408.hp2 HG00741.hp2 others(74): Show |
intron_variant | MODIFIER | c.117+11416G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101819143 | |||||||
| chr12:101819346 | G | A | 1 | a0001c0003t0003g0170 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.117+11213C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101819346 | |||||||
| chr12:101819446 | A | G | 1 | a0001c0001t0004g0258 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.117+11113T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101819446 | |||||||
| chr12:101819508 | G | A | 2 | a0001c0002t0008g0211 a0001c0002t0008g0212 |
2 | HG01884.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.117+11051C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101819508 | |||||||
| chr12:101819509 | A | G | 53 | a0001c0001t0003g0247 a0001c0001t0004g0005 a0001c0001t0004g0217 others(50): Show |
54 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.117+11050T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101819509 | |||||||
| chr12:101819749 | G | A | 47 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(44): Show |
47 | HG01099.hp1 HG01192.hp2 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.117+10810C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101819749 | |||||||
| chr12:101819830 | T | C | 1 | a0001c0002t0008g0237 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.117+10729A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101819830 | |||||||
| chr12:101819878 | A | T | 3 | a0001c0001t0001g0327 a0001c0001t0001g0340 a0001c0001t0001g0341 |
3 | HG01167.hp1 HG01169.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.117+10681T>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101819878 | |||||||
| chr12:101820102 | G | C | 2 | a0006c0016t0013g0235 a0006c0017t0013g0234 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.117+10457C>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101820102 | |||||||
| chr12:101820249 | A | G | 53 | a0001c0001t0003g0247 a0001c0001t0004g0005 a0001c0001t0004g0217 others(50): Show |
54 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.117+10310T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101820249 | |||||||
| chr12:101820252 | T | C | 79 | a0001c0001t0001g0219 a0001c0001t0005g0007 a0001c0001t0005g0008 others(76): Show |
79 | HG00323.hp1 HG00408.hp2 HG00741.hp2 others(76): Show |
intron_variant | MODIFIER | c.117+10307A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101820252 | |||||||
| chr12:101820738 | G | T | 52 | a0001c0001t0004g0005 a0001c0001t0004g0217 a0001c0001t0004g0233 others(49): Show |
53 | HG00544.hp1 HG00597.hp1 HG02056.hp1 others(50): Show |
intron_variant | MODIFIER | c.117+9821C>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101820738 | |||||||
| chr12:101820750 | C | T | 1 | a0001c0001t0006g0351 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.117+9809G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101820750 | |||||||
| chr12:101820830 | G | C | 1 | a0001c0002t0002g0113 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.117+9729C>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101820830 | |||||||
| chr12:101820903 | A | T | 1 | a0006c0017t0013g0234 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.117+9656T>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101820903 | |||||||
| chr12:101821036 | C | A | 60 | a0001c0001t0001g0219 a0001c0001t0005g0007 a0001c0001t0005g0008 others(57): Show |
60 | HG00323.hp1 HG00408.hp2 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.117+9523G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101821036 | |||||||
| chr12:101821056 | TC | T | 86 | a0001c0001t0001g0219 a0001c0001t0001g0291 a0001c0001t0001g0294 others(83): Show |
86 | HG00323.hp1 HG00408.hp2 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.117+9502delG | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101821056 | |||||||
| chr12:101821056 | TCA | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0276 a0001c0001t0001g0277 others(92): Show |
98 | HG00408.hp1 HG00423.hp2 HG01099.hp1 others(95): Show |
intron_variant | MODIFIER | c.117+9501_117+9502d others(4): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101821056 | |||||||
| chr12:101821057 | C | A | 5 | a0001c0001t0005g0017 a0001c0001t0006g0228 a0001c0001t0006g0236 others(2): Show |
5 | HG01168.hp1 HG02717.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.117+9502G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101821057 | |||||||
| chr12:101821057 | C | CA | 17 | a0001c0001t0002g0095 a0001c0001t0004g0241 a0001c0001t0004g0248 others(14): Show |
17 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.117+9501dupT | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101821057 | |||||||
| chr12:101821057 | CA | C | 18 | a0001c0001t0002g0093 a0001c0001t0004g0249 a0001c0001t0009g0052 others(15): Show |
18 | HG00140.hp2 HG00280.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.117+9501delT | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101821057 | |||||||
| chr12:101821057 | CAA | C | 8 | a0001c0002t0008g0207 a0001c0002t0008g0208 a0001c0002t0008g0209 others(5): Show |
8 | HG01884.hp1 HG02145.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.117+9500_117+9501d others(4): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101821057 | |||||||
| chr12:101821079 | A | G | 1 | a0001c0001t0021g0279 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.117+9480T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101821079 | |||||||
| chr12:101821087 | T | A | 2 | a0001c0001t0006g0230 a0001c0001t0006g0236 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.117+9472A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101821087 | |||||||
| chr12:101821309 | C | T | 52 | a0001c0001t0004g0005 a0001c0001t0004g0217 a0001c0001t0004g0233 others(49): Show |
53 | HG00544.hp1 HG00597.hp1 HG02056.hp1 others(50): Show |
intron_variant | MODIFIER | c.117+9250G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101821309 | |||||||
| chr12:101821351 | G | A | 1 | a0001c0002t0002g0115 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.117+9208C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101821351 | |||||||
| chr12:101821383 | G | C | 1 | a0001c0002t0001g0366 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.117+9176C>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101821383 | |||||||
| chr12:101821506 | C | T | 2 | a0006c0016t0013g0235 a0006c0017t0013g0234 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.117+9053G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101821506 | |||||||
| chr12:101821514 | C | T | 1 | a0001c0001t0015g0019 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.117+9045G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101821514 | |||||||
| chr12:101821552 | G | A | 1 | a0001c0001t0006g0220 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.117+9007C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101821552 | |||||||
| chr12:101821599 | T | G | 1 | a0001c0002t0008g0237 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.117+8960A>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101821599 | |||||||
| chr12:101821884 | C | T | 1 | a0001c0002t0002g0129 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.117+8675G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101821884 | |||||||
| chr12:101821897 | C | T | 1 | a0002c0012t0001g0214 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.117+8662G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101821897 | |||||||
| chr12:101822162 | C | G | 1 | a0001c0003t0003g0185 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.117+8397G>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101822162 | |||||||
| chr12:101822173 | G | T | 1 | a0001c0003t0003g0185 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.117+8386C>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101822173 | |||||||
| chr12:101822175 | A | T | 1 | a0001c0003t0003g0185 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.117+8384T>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101822175 | |||||||
| chr12:101822176 | G | T | 1 | a0001c0003t0003g0185 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.117+8383C>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101822176 | |||||||
| chr12:101822210 | A | G | 1 | a0001c0001t0004g0242 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.117+8349T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101822210 | |||||||
| chr12:101822221 | G | A | 1 | a0001c0001t0004g0242 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.117+8338C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101822221 | |||||||
| chr12:101822273 | T | C | 327 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(324): Show |
331 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(328): Show |
intron_variant | MODIFIER | c.117+8286A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101822273 | |||||||
| chr12:101822289 | T | C | 1 | a0001c0004t0007g0198 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.117+8270A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101822289 | |||||||
| chr12:101822895 | C | T | 166 | a0001c0001t0001g0219 a0001c0001t0003g0247 a0001c0001t0004g0005 others(163): Show |
167 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.117+7664G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101822895 | |||||||
| chr12:101823034 | C | A | 3 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0021g0279 |
3 | HG02055.hp2 HG02717.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.117+7525G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101823034 | |||||||
| chr12:101823170 | G | C | 60 | a0001c0001t0001g0219 a0001c0001t0005g0007 a0001c0001t0005g0008 others(57): Show |
60 | HG00323.hp1 HG00408.hp2 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.117+7389C>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101823170 | |||||||
| chr12:101823257 | G | A | 1 | a0001c0002t0002g0106 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.117+7302C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101823257 | |||||||
| chr12:101823308 | G | C | 1 | a0001c0007t0009g0055 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.117+7251C>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101823308 | |||||||
| chr12:101823438 | C | T | 8 | a0001c0002t0001g0356 a0001c0002t0001g0359 a0003c0005t0001g0280 others(5): Show |
8 | HG00642.hp1 HG02109.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.117+7121G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101823438 | |||||||
| chr12:101823503 | G | A | 1 | a0002c0012t0001g0214 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.117+7056C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101823503 | |||||||
| chr12:101823544 | A | G | 1 | a0001c0001t0004g0245 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.117+7015T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101823544 | |||||||
| chr12:101823605 | G | A | 1 | a0001c0007t0009g0053 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.117+6954C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101823605 | |||||||
| chr12:101823609 | C | CA | 88 | a0001c0001t0003g0247 a0001c0001t0004g0005 a0001c0001t0004g0217 others(85): Show |
89 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.117+6949dupT | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101823609 | |||||||
| chr12:101823609 | C | CAA | 64 | a0001c0001t0001g0219 a0001c0001t0004g0383 a0001c0001t0004g0384 others(61): Show |
64 | HG00323.hp1 HG00408.hp2 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.117+6948_117+6949d others(4): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101823609 | |||||||
| chr12:101823609 | C | CAAA | 11 | a0001c0001t0004g0385 a0001c0001t0005g0007 a0001c0001t0005g0047 others(8): Show |
11 | HG02148.hp1 HG03579.hp2 HG04115.hp2 others(8): Show |
intron_variant | MODIFIER | c.117+6947_117+6949d others(5): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101823609 | |||||||
| chr12:101823609 | CA | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0276 a0001c0001t0001g0284 others(167): Show |
176 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.117+6949delT | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101823609 | |||||||
| chr12:101823609 | CAA | C | 15 | a0001c0001t0001g0277 a0001c0001t0001g0312 a0001c0001t0001g0369 others(12): Show |
15 | HG00642.hp1 HG01943.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.117+6948_117+6949d others(4): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101823609 | |||||||
| chr12:101823764 | G | C | 1 | a0002c0012t0001g0214 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.117+6795C>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101823764 | |||||||
| chr12:101823794 | G | A | 1 | a0001c0003t0003g0171 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.117+6765C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101823794 | |||||||
| chr12:101823801 | A | G | 8 | a0001c0002t0008g0206 a0001c0002t0008g0207 a0001c0002t0008g0208 others(5): Show |
8 | HG01884.hp1 HG02145.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.117+6758T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101823801 | |||||||
| chr12:101823942 | C | A | 167 | a0001c0001t0001g0219 a0001c0001t0003g0247 a0001c0001t0004g0005 others(164): Show |
168 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.117+6617G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101823942 | |||||||
| chr12:101824216 | T | C | 1 | a0001c0001t0005g0039 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.117+6343A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824216 | |||||||
| chr12:101824328 | G | C | 1 | a0003c0005t0001g0282 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.117+6231C>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824328 | |||||||
| chr12:101824361 | G | A | 1 | a0001c0001t0001g0369 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.117+6198C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824361 | |||||||
| chr12:101824405 | C | CAT | 36 | a0001c0001t0001g0001 a0001c0001t0001g0293 a0001c0001t0001g0360 others(33): Show |
39 | HG00609.hp1 HG00621.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.117+6152_117+6153d others(4): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824405 | |||||||
| chr12:101824405 | C | CATAT | 10 | a0001c0001t0001g0361 a0001c0001t0002g0065 a0001c0002t0001g0366 others(7): Show |
10 | HG00280.hp1 HG02109.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.117+6150_117+6153d others(6): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824405 | |||||||
| chr12:101824405 | C | CATATAT | 3 | a0001c0001t0001g0276 a0001c0002t0001g0205 a0001c0002t0001g0359 |
3 | HG00642.hp1 HG02055.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.117+6148_117+6153d others(8): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824405 | |||||||
| chr12:101824405 | C | CATATATA others(1): Show |
3 | a0001c0003t0003g0139 a0003c0005t0001g0357 a0003c0005t0001g0358 |
3 | HG02895.hp1 HG02897.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.117+6146_117+6153d others(10): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824405 | |||||||
| chr12:101824405 | C | CATATATA others(3): Show |
25 | a0001c0001t0001g0277 a0001c0001t0001g0322 a0001c0001t0001g0323 others(22): Show |
25 | HG00408.hp1 HG01167.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.117+6144_117+6153d others(12): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824405 | |||||||
| chr12:101824405 | C | CATATATA others(5): Show |
26 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(23): Show |
26 | HG00423.hp2 HG01099.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.117+6142_117+6153d others(14): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824405 | |||||||
| chr12:101824405 | C | CATATATA others(7): Show |
16 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0294 others(13): Show |
16 | HG01175.hp1 HG01192.hp2 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.117+6140_117+6153d others(16): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824405 | |||||||
| chr12:101824405 | C | CATATATA others(9): Show |
11 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0302 others(8): Show |
11 | HG01361.hp1 HG02109.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.117+6138_117+6153d others(18): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824405 | |||||||
| chr12:101824405 | C | CATATATA others(11): Show |
5 | a0001c0001t0001g0297 a0001c0001t0001g0298 a0001c0001t0001g0299 others(2): Show |
5 | HG01515.hp1 NA18612.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.117+6136_117+6153d others(20): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824405 | |||||||
| chr12:101824405 | C | CATATATA others(13): Show |
3 | a0001c0001t0001g0335 a0001c0001t0001g0377 a0001c0003t0003g0138 |
3 | HG03130.hp1 HG04184.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.117+6134_117+6153d others(22): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824405 | |||||||
| chr12:101824405 | C | CATATATA others(15): Show |
5 | a0001c0001t0001g0369 a0001c0001t0001g0370 a0001c0001t0004g0273 others(2): Show |
5 | HG03209.hp2 HG03486.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.117+6132_117+6153d others(24): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824405 | |||||||
| chr12:101824405 | C | CATATATA others(17): Show |
2 | a0001c0001t0001g0334 a0001c0001t0004g0272 |
2 | NA18957.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.117+6130_117+6153d others(26): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824405 | |||||||
| chr12:101824405 | C | CATATATA others(19): Show |
1 | a0001c0001t0001g0333 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.117+6128_117+6153d others(28): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824405 | |||||||
| chr12:101824405 | C | CATATATA others(23): Show |
2 | a0006c0016t0013g0235 a0008c0018t0001g0296 |
2 | HG01258.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.117+6153_117+6154i others(32): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824405 | |||||||
| chr12:101824405 | C | CATATATA others(27): Show |
1 | a0001c0002t0001g0364 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.117+6153_117+6154i others(36): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824405 | |||||||
| chr12:101824405 | CAT | C | 8 | a0001c0002t0002g0109 a0001c0002t0008g0207 a0001c0002t0008g0208 others(5): Show |
8 | HG01884.hp1 HG02145.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.117+6152_117+6153d others(4): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824405 | |||||||
| chr12:101824405 | CATATAT | C | 5 | a0001c0001t0005g0018 a0001c0001t0005g0047 a0001c0001t0005g0048 others(2): Show |
5 | NA18962.hp1 NA18979.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.117+6148_117+6153d others(8): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824405 | |||||||
| chr12:101824405 | CATATATA others(1): Show |
C | 51 | a0001c0001t0001g0219 a0001c0001t0005g0007 a0001c0001t0005g0008 others(48): Show |
51 | HG00323.hp1 HG00408.hp2 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.117+6146_117+6153d others(10): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824405 | |||||||
| chr12:101824405 | CATATATA others(3): Show |
C | 3 | a0001c0001t0006g0230 a0001c0002t0002g0110 a0001c0002t0002g0111 |
3 | HG01070.hp1 HG02280.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.117+6144_117+6153d others(12): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824405 | |||||||
| chr12:101824405 | CATATATA others(7): Show |
C | 1 | a0001c0003t0003g0174 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.117+6140_117+6153d others(16): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824405 | |||||||
| chr12:101824405 | CATATATA others(9): Show |
C | 2 | a0001c0001t0004g0270 a0001c0001t0004g0271 |
2 | NA18944.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.117+6138_117+6153d others(18): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824405 | |||||||
| chr12:101824426 | A | T | 1 | a0001c0007t0004g0232 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.117+6133T>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824426 | |||||||
| chr12:101824428 | A | T | 2 | a0001c0007t0004g0231 a0001c0007t0004g0232 |
2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.117+6131T>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824428 | |||||||
| chr12:101824430 | A | T | 2 | a0001c0007t0004g0231 a0001c0007t0004g0232 |
2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.117+6129T>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824430 | |||||||
| chr12:101824432 | A | T | 11 | a0001c0002t0002g0078 a0001c0002t0008g0206 a0001c0002t0008g0207 others(8): Show |
11 | HG00741.hp1 HG01884.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.117+6127T>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824432 | |||||||
| chr12:101824433 | T | TA | 4 | a0001c0001t0012g0132 a0001c0002t0002g0079 a0001c0002t0002g0080 others(1): Show |
4 | HG00558.hp1 HG01884.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.117+6125_117+6126i others(3): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824433 | |||||||
| chr12:101824433 | T | TATATA | 5 | a0001c0001t0004g0245 a0001c0003t0003g0172 a0001c0003t0003g0173 others(2): Show |
5 | HG00544.hp1 HG00597.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.117+6125_117+6126i others(7): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824433 | |||||||
| chr12:101824433 | T | TATATATA | 4 | a0001c0001t0004g0384 a0001c0001t0004g0385 a0001c0001t0018g0058 others(1): Show |
4 | HG03041.hp2 NA18970.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.117+6125_117+6126i others(9): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824433 | |||||||
| chr12:101824433 | T | TATATATA others(4): Show |
2 | a0001c0001t0004g0233 a0001c0024t0004g0268 |
2 | HG04184.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.117+6125_117+6126i others(13): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824433 | |||||||
| chr12:101824433 | T | TATATATA others(6): Show |
9 | a0001c0001t0004g0217 a0001c0001t0004g0243 a0001c0001t0004g0244 others(6): Show |
9 | HG01346.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.117+6125_117+6126i others(15): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824433 | |||||||
| chr12:101824433 | T | TATATATA others(8): Show |
11 | a0001c0001t0004g0261 a0001c0001t0004g0262 a0001c0001t0004g0263 others(8): Show |
11 | HG00544.hp2 HG01943.hp1 NA18963.hp2 others(8): Show |
intron_variant | MODIFIER | c.117+6125_117+6126i others(17): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824433 | |||||||
| chr12:101824433 | T | TATATATA others(10): Show |
21 | a0001c0001t0004g0242 a0001c0001t0004g0258 a0001c0001t0004g0259 others(18): Show |
21 | HG01070.hp2 HG01123.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.117+6125_117+6126i others(19): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824433 | |||||||
| chr12:101824433 | T | TATATATA others(12): Show |
10 | a0001c0001t0011g0059 a0001c0003t0003g0155 a0001c0003t0003g0157 others(7): Show |
10 | HG00597.hp1 HG01071.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.117+6125_117+6126i others(21): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824433 | |||||||
| chr12:101824433 | T | TATATATA others(14): Show |
13 | a0001c0001t0004g0241 a0001c0001t0004g0254 a0001c0001t0004g0255 others(10): Show |
13 | HG01106.hp2 HG02040.hp2 NA18945.hp2 others(10): Show |
intron_variant | MODIFIER | c.117+6125_117+6126i others(23): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824433 | |||||||
| chr12:101824433 | T | TATATATA others(16): Show |
5 | a0001c0001t0004g0005 a0001c0003t0003g0137 a0001c0003t0003g0148 others(2): Show |
6 | HG00140.hp1 HG02080.hp1 NA18941.hp2 others(3): Show |
intron_variant | MODIFIER | c.117+6125_117+6126i others(25): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824433 | |||||||
| chr12:101824433 | T | TATATATA others(18): Show |
9 | a0001c0001t0003g0247 a0001c0001t0006g0252 a0001c0003t0003g0135 others(6): Show |
9 | HG00423.hp1 HG00609.hp2 HG02698.hp1 others(6): Show |
intron_variant | MODIFIER | c.117+6125_117+6126i others(27): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824433 | |||||||
| chr12:101824433 | T | TATATATA others(20): Show |
4 | a0001c0001t0004g0238 a0001c0001t0004g0239 a0001c0001t0004g0251 others(1): Show |
4 | NA18947.hp1 NA18961.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.117+6125_117+6126i others(29): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824433 | |||||||
| chr12:101824433 | T | TATATATA others(22): Show |
3 | a0001c0001t0004g0250 a0001c0003t0003g0133 a0001c0003t0003g0141 |
3 | NA18977.hp2 NA19011.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.117+6125_117+6126i others(31): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824433 | |||||||
| chr12:101824433 | T | TATATATA others(26): Show |
2 | a0001c0001t0004g0249 a0001c0003t0003g0140 |
2 | NA18959.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.117+6125_117+6126i others(35): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824433 | |||||||
| chr12:101824433 | T | TATATATA others(169): Show |
1 | a0012c0021t0004g0240 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.117+6125_117+6126i others(178): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824433 | |||||||
| chr12:101824434 | T | A | 2 | a0001c0001t0004g0246 a0006c0017t0013g0234 |
2 | HG02165.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.117+6125A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824434 | |||||||
| chr12:101824435 | T | A | 3 | a0001c0002t0002g0079 a0001c0002t0002g0080 a0001c0002t0002g0115 |
3 | HG01884.hp2 HG02683.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.117+6124A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824435 | |||||||
| chr12:101824436 | T | C | 3 | a0001c0001t0001g0328 a0001c0001t0011g0125 a0001c0002t0008g0206 |
3 | HG03098.hp2 NA18991.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.117+6123A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824436 | |||||||
| chr12:101824437 | C | CT | 104 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(101): Show |
104 | HG00408.hp1 HG00423.hp2 HG00642.hp1 others(101): Show |
intron_variant | MODIFIER | c.117+6121dupA | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824437 | |||||||
| chr12:101824437 | C | T | 114 | a0001c0001t0001g0328 a0001c0001t0003g0247 a0001c0001t0004g0005 others(111): Show |
115 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.117+6122G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824437 | |||||||
| chr12:101824437 | CT | C | 60 | a0001c0001t0001g0219 a0001c0001t0004g0270 a0001c0001t0004g0271 others(57): Show |
60 | HG00323.hp1 HG00408.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.117+6121delA | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824437 | |||||||
| chr12:101824437 | CTT | C | 6 | a0001c0001t0004g0272 a0001c0001t0004g0273 a0001c0001t0005g0040 others(3): Show |
6 | HG02922.hp2 HG03471.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.117+6120_117+6121d others(4): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824437 | |||||||
| chr12:101824438 | T | A | 1 | a0001c0015t0008g0196 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.117+6121A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824438 | |||||||
| chr12:101824438 | T | C | 103 | a0001c0001t0003g0247 a0001c0001t0004g0005 a0001c0001t0004g0217 others(100): Show |
104 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.117+6121A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824438 | |||||||
| chr12:101824439 | T | C | 3 | a0001c0001t0004g0246 a0001c0001t0006g0230 a0006c0017t0013g0234 |
3 | HG02165.hp2 HG02280.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.117+6120A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824439 | |||||||
| chr12:101824442 | T | C | 1 | a0001c0002t0002g0113 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.117+6117A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824442 | |||||||
| chr12:101824443 | T | C | 1 | a0001c0015t0008g0196 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.117+6116A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824443 | |||||||
| chr12:101824459 | G | T | 2 | a0001c0001t0003g0247 a0001c0001t0004g0233 |
2 | HG00423.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.117+6100C>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824459 | |||||||
| chr12:101824466 | TTTTTGTT others(3): Show |
T | 2 | a0001c0004t0001g0199 a0004c0006t0014g0006 |
2 | HG01243.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.117+6083_117+6092d others(12): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824466 | |||||||
| chr12:101824495 | C | G | 1 | a0001c0001t0005g0016 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.117+6064G>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824495 | |||||||
| chr12:101824496 | T | A | 1 | a0001c0002t0008g0237 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.117+6063A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824496 | |||||||
| chr12:101824553 | G | T | 1 | a0001c0001t0011g0059 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.117+6006C>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824553 | |||||||
| chr12:101824623 | C | T | 20 | a0001c0001t0007g0278 a0001c0004t0001g0199 a0001c0004t0006g0203 others(17): Show |
20 | HG01081.hp1 HG01109.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.117+5936G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824623 | |||||||
| chr12:101824755 | A | T | 8 | a0001c0002t0008g0206 a0001c0002t0008g0207 a0001c0002t0008g0208 others(5): Show |
8 | HG01884.hp1 HG02145.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.117+5804T>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824755 | |||||||
| chr12:101824823 | G | A | 8 | a0001c0002t0008g0206 a0001c0002t0008g0207 a0001c0002t0008g0208 others(5): Show |
8 | HG01884.hp1 HG02145.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.117+5736C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824823 | |||||||
| chr12:101824833 | C | T | 1 | a0001c0001t0004g0246 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.117+5726G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824833 | |||||||
| chr12:101824840 | C | T | 1 | a0002c0012t0001g0214 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.117+5719G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101824840 | |||||||
| chr12:101825028 | A | T | 1 | a0001c0001t0009g0052 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.117+5531T>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101825028 | |||||||
| chr12:101825121 | T | C | 168 | a0001c0001t0001g0219 a0001c0001t0003g0247 a0001c0001t0004g0005 others(165): Show |
169 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.117+5438A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101825121 | |||||||
| chr12:101825251 | C | T | 1 | a0006c0017t0013g0234 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.117+5308G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101825251 | |||||||
| chr12:101825267 | C | T | 1 | a0001c0001t0001g0295 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.117+5292G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101825267 | |||||||
| chr12:101825613 | T | C | 18 | a0001c0001t0001g0001 a0001c0001t0001g0276 a0001c0001t0001g0277 others(15): Show |
21 | HG01891.hp1 HG02055.hp2 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.117+4946A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101825613 | |||||||
| chr12:101825672 | T | C | 3 | a0001c0003t0003g0175 a0007c0011t0002g0076 a0007c0011t0002g0114 |
3 | HG03516.hp2 NA19043.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.117+4887A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101825672 | |||||||
| chr12:101825695 | A | ATCACG | 15 | a0001c0001t0001g0001 a0001c0001t0001g0360 a0001c0001t0001g0361 others(12): Show |
18 | HG01891.hp1 HG02257.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.117+4863_117+4864i others(7): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101825695 | |||||||
| chr12:101825699 | C | CGTTAT | 296 | a0001c0001t0001g0219 a0001c0001t0001g0276 a0001c0001t0001g0277 others(293): Show |
297 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.117+4859_117+4860i others(7): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101825699 | |||||||
| chr12:101825699 | C | T | 15 | a0001c0001t0001g0001 a0001c0001t0001g0360 a0001c0001t0001g0361 others(12): Show |
18 | HG01891.hp1 HG02257.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.117+4860G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101825699 | |||||||
| chr12:101825789 | G | C | 1 | a0002c0012t0001g0214 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.117+4770C>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101825789 | |||||||
| chr12:101825792 | T | C | 1 | a0002c0012t0001g0214 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.117+4767A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101825792 | |||||||
| chr12:101825841 | C | T | 108 | a0001c0001t0001g0001 a0001c0001t0001g0276 a0001c0001t0001g0277 others(105): Show |
111 | HG00408.hp1 HG00423.hp2 HG00642.hp1 others(108): Show |
intron_variant | MODIFIER | c.117+4718G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101825841 | |||||||
| chr12:101825846 | T | C | 2 | a0001c0004t0001g0199 a0004c0006t0014g0006 |
2 | HG01243.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.117+4713A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101825846 | |||||||
| chr12:101825969 | G | A | 1 | a0001c0002t0001g0368 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.117+4590C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101825969 | |||||||
| chr12:101825988 | G | A | 168 | a0001c0001t0001g0219 a0001c0001t0003g0247 a0001c0001t0004g0005 others(165): Show |
169 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.117+4571C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101825988 | |||||||
| chr12:101826225 | C | G | 168 | a0001c0001t0001g0219 a0001c0001t0003g0247 a0001c0001t0004g0005 others(165): Show |
169 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.117+4334G>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101826225 | |||||||
| chr12:101826506 | AT | A | 290 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0276 others(287): Show |
294 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.117+4052delA | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101826506 | |||||||
| chr12:101826506 | ATT | A | 6 | a0001c0001t0001g0332 a0001c0001t0006g0218 a0001c0001t0006g0274 others(3): Show |
6 | HG01255.hp2 HG01993.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.117+4051_117+4052d others(4): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101826506 | |||||||
| chr12:101826735 | G | A | 1 | a0001c0002t0002g0115 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.117+3824C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101826735 | |||||||
| chr12:101826856 | T | C | 1 | a0001c0002t0001g0368 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.117+3703A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101826856 | |||||||
| chr12:101826950 | G | GT | 83 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(80): Show |
83 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.117+3608dupA | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101826950 | |||||||
| chr12:101826950 | G | GTT | 15 | a0001c0001t0001g0219 a0001c0001t0005g0007 a0001c0001t0005g0008 others(12): Show |
15 | HG01516.hp2 HG02257.hp1 HG02300.hp1 others(12): Show |
intron_variant | MODIFIER | c.117+3607_117+3608d others(4): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101826950 | |||||||
| chr12:101826950 | GT | G | 56 | a0001c0001t0001g0001 a0001c0001t0001g0277 a0001c0001t0001g0333 others(53): Show |
59 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.117+3608delA | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101826950 | |||||||
| chr12:101826950 | GTT | G | 10 | a0001c0002t0001g0364 a0001c0002t0001g0365 a0001c0002t0001g0366 others(7): Show |
10 | HG02486.hp2 HG02559.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.117+3607_117+3608d others(4): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101826950 | |||||||
| chr12:101826950 | GTTTTTTT others(4): Show |
G | 3 | a0001c0001t0020g0117 a0001c0002t0002g0116 a0001c0002t0002g0118 |
3 | HG02572.hp2 HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.117+3598_117+3608d others(13): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101826950 | |||||||
| chr12:101826966 | T | G | 52 | a0001c0003t0003g0133 a0001c0003t0003g0135 a0001c0003t0003g0136 others(49): Show |
52 | HG00140.hp1 HG00544.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.117+3593A>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101826966 | |||||||
| chr12:101827005 | C | G | 168 | a0001c0001t0001g0219 a0001c0001t0003g0247 a0001c0001t0004g0005 others(165): Show |
169 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.117+3554G>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101827005 | |||||||
| chr12:101827082 | G | A | 1 | a0001c0025t0001g0213 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.117+3477C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101827082 | |||||||
| chr12:101827259 | A | G | 168 | a0001c0001t0001g0219 a0001c0001t0003g0247 a0001c0001t0004g0005 others(165): Show |
169 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.117+3300T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101827259 | |||||||
| chr12:101827588 | A | G | 168 | a0001c0001t0001g0219 a0001c0001t0003g0247 a0001c0001t0004g0005 others(165): Show |
169 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.117+2971T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101827588 | |||||||
| chr12:101827647 | C | G | 82 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(79): Show |
82 | HG00408.hp1 HG00423.hp2 HG01099.hp1 others(79): Show |
intron_variant | MODIFIER | c.117+2912G>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101827647 | |||||||
| chr12:101827835 | G | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0276 a0001c0001t0001g0277 others(105): Show |
111 | HG00408.hp1 HG00423.hp2 HG00642.hp1 others(108): Show |
intron_variant | MODIFIER | c.117+2724C>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101827835 | |||||||
| chr12:101827837 | G | C | 8 | a0001c0003t0003g0136 a0001c0003t0003g0178 a0001c0003t0003g0181 others(5): Show |
8 | HG00140.hp1 HG01070.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.117+2722C>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101827837 | |||||||
| chr12:101828063 | G | A | 6 | a0001c0002t0002g0003 a0001c0002t0002g0119 a0001c0002t0002g0120 others(3): Show |
7 | HG00280.hp2 HG00642.hp2 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+2496C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101828063 | |||||||
| chr12:101828236 | C | A | 90 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(87): Show |
90 | HG00408.hp1 HG00423.hp2 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.117+2323G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101828236 | |||||||
| chr12:101828307 | T | C | 2 | a0006c0016t0013g0235 a0006c0017t0013g0234 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.117+2252A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101828307 | |||||||
| chr12:101828389 | G | A | 1 | a0001c0004t0007g0198 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.117+2170C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101828389 | |||||||
| chr12:101828448 | A | G | 4 | a0003c0005t0001g0280 a0003c0005t0001g0281 a0003c0005t0001g0282 others(1): Show |
4 | HG02109.hp2 HG02647.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.117+2111T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101828448 | |||||||
| chr12:101828590 | C | T | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.117+1969G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101828590 | |||||||
| chr12:101828651 | T | C | 1 | a0001c0002t0005g0042 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.117+1908A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101828651 | |||||||
| chr12:101828703 | A | AC | 10 | a0001c0002t0008g0206 a0001c0002t0008g0207 a0001c0002t0008g0208 others(7): Show |
10 | HG01243.hp2 HG01884.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.117+1855_117+1856i others(3): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101828703 | |||||||
| chr12:101828704 | A | C | 2 | a0001c0002t0001g0205 a0001c0023t0001g0215 |
2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.117+1855T>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101828704 | |||||||
| chr12:101828712 | C | T | 59 | a0001c0001t0001g0219 a0001c0001t0005g0007 a0001c0001t0005g0008 others(56): Show |
59 | HG00323.hp1 HG00408.hp2 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.117+1847G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101828712 | |||||||
| chr12:101828796 | T | C | 1 | a0001c0002t0002g0124 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.117+1763A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101828796 | |||||||
| chr12:101828874 | A | G | 1 | a0001c0001t0006g0218 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.117+1685T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101828874 | |||||||
| chr12:101828930 | A | G | 1 | a0001c0001t0001g0377 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.117+1629T>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101828930 | |||||||
| chr12:101829160 | T | C | 1 | a0001c0001t0011g0125 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.117+1399A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101829160 | |||||||
| chr12:101829213 | G | A | 1 | a0001c0001t0001g0377 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.117+1346C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101829213 | |||||||
| chr12:101829302 | T | C | 6 | a0001c0001t0009g0052 a0001c0007t0009g0053 a0001c0007t0009g0055 others(3): Show |
6 | HG01167.hp2 HG02486.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.117+1257A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101829302 | |||||||
| chr12:101829358 | G | A | 1 | a0001c0004t0007g0198 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.117+1201C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101829358 | |||||||
| chr12:101829398 | T | C | 1 | a0001c0002t0002g0004 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.117+1161A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101829398 | |||||||
| chr12:101829458 | C | A | 1 | a0001c0001t0009g0052 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.117+1101G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101829458 | |||||||
| chr12:101829840 | G | T | 1 | a0001c0007t0009g0053 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.117+719C>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101829840 | |||||||
| chr12:101830004 | C | A | 1 | a0001c0001t0006g0236 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.117+555G>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101830004 | |||||||
| chr12:101830004 | C | CA | 86 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0360 others(83): Show |
89 | HG00323.hp1 HG00408.hp2 HG00741.hp2 others(86): Show |
intron_variant | MODIFIER | c.117+554dupT | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101830004 | |||||||
| chr12:101830004 | C | CAA | 103 | a0001c0001t0001g0378 a0001c0001t0001g0379 a0001c0001t0001g0380 others(100): Show |
104 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.117+553_117+554dup others(2): Show |
GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101830004 | |||||||
| chr12:101830004 | CA | C | 26 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0007g0278 others(23): Show |
26 | HG00280.hp1 HG01081.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.117+554delT | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101830004 | |||||||
| chr12:101830087 | C | T | 1 | a0001c0002t0001g0205 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.117+472G>A | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101830087 | |||||||
| chr12:101830210 | T | A | 4 | a0001c0001t0005g0047 a0001c0001t0005g0048 a0001c0001t0005g0049 others(1): Show |
4 | NA18979.hp2 NA18985.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.117+349A>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101830210 | |||||||
| chr12:101830210 | T | C | 1 | a0001c0002t0002g0129 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.117+349A>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101830210 | |||||||
| chr12:101830231 | T | G | 2 | a0001c0003t0003g0185 a0001c0003t0003g0186 |
2 | HG02155.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.117+328A>C | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101830231 | |||||||
| chr12:101830324 | G | A | 19 | a0001c0004t0001g0199 a0001c0004t0006g0203 a0001c0004t0007g0188 others(16): Show |
19 | HG01081.hp1 HG01109.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.117+235C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101830324 | |||||||
| chr12:101830330 | G | A | 54 | a0001c0003t0003g0133 a0001c0003t0003g0135 a0001c0003t0003g0136 others(51): Show |
54 | HG00140.hp1 HG00544.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.117+229C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101830330 | |||||||
| chr12:101830344 | G | A | 109 | a0001c0001t0001g0001 a0001c0001t0001g0276 a0001c0001t0001g0277 others(106): Show |
112 | HG00408.hp1 HG00423.hp2 HG00642.hp1 others(109): Show |
intron_variant | MODIFIER | c.117+215C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101830344 | |||||||
| chr12:101830385 | G | C | 4 | a0001c0001t0004g0383 a0001c0001t0004g0384 a0001c0001t0004g0385 others(1): Show |
4 | NA18970.hp1 NA19007.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.117+174C>G | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101830385 | |||||||
| chr12:101830509 | G | A | 1 | a0001c0002t0005g0051 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.117+50C>T | GNPTAB | ENSG00000111670.16 | transcript | ENST00000299314.12 | protein_coding | 1/20 | chr12 | 101830509 |