Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9733 |
| ensemblid | ENSG00000075856.12 |
| hgncid | 16860 |
| symbol | SART3 |
| name | spliceosome associated factor 3, U4/U6 recycling protein |
| refseq_nuc | NM_014706.4 |
| refseq_prot | NP_055521.1 |
| ensembl_nuc | ENST00000546815.6 |
| ensembl_prot | ENSP00000449386.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 108522214 |
| end | 108561173 |
| strand | - |
| ver | v1.2 |
| region | chr12:108522214-108561173 |
| region5000 | chr12:108517214-108566173 |
| regionname0 | SART3_chr12_108522214_108561173 |
| regionname5000 | SART3_chr12_108517214_108566173 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 963 | 262 | 82 | 32 | 110 | 9 | 27 | 93 | SART3_chr12_108517214_108566173 | SART3 | MATAA others(958): Show |
chr12 | 108517214 | 108566173 |
| a0002 | 0/0 | 963 | 122 | 11 | 25 | 70 | 3 | 13 | 54 | SART3_chr12_108517214_108566173 | SART3 | MATAA others(958): Show |
chr12 | 108517214 | 108566173 |
| a0003 | 0/0 | 963 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | SART3_chr12_108517214_108566173 | SART3 | MATAA others(958): Show |
chr12 | 108517214 | 108566173 |
| a0004 | 0/0 | 963 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | MATAA others(958): Show |
chr12 | 108517214 | 108566173 |
| a0005 | 0/0 | 963 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | MATAA others(958): Show |
chr12 | 108517214 | 108566173 |
| a0006 | 0/0 | 963 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | MATAA others(958): Show |
chr12 | 108517214 | 108566173 |
| a0007 | 0/0 | 963 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | MATAA others(958): Show |
chr12 | 108517214 | 108566173 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2889 | 162 | 22 | 22 | 91 | 6 | 20 | SART3_chr12_108517214_108566173 | SART3 | ATGGC others(2884): Show |
chr12 | 108517214 | 108566173 | ||
| a0001c0003 | 1/0 | 2889 | 55 | 30 | 5 | 16 | 2 | 1 | SART3_chr12_108517214_108566173 | SART3 | ATGGC others(2884): Show |
chr12 | 108517214 | 108566173 | ||
| a0001c0005 | 0/0 | 2889 | 18 | 9 | 1 | 2 | 1 | 5 | SART3_chr12_108517214_108566173 | SART3 | ATGGC others(2884): Show |
chr12 | 108517214 | 108566173 | ||
| a0001c0006 | 0/0 | 2889 | 12 | 11 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | ATGGC others(2884): Show |
chr12 | 108517214 | 108566173 | ||
| a0001c0007 | 0/0 | 2889 | 9 | 8 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | ATGGC others(2884): Show |
chr12 | 108517214 | 108566173 | ||
| a0001c0010 | 0/0 | 2889 | 2 | 2 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | ATGGC others(2884): Show |
chr12 | 108517214 | 108566173 | ||
| a0001c0011 | 0/0 | 2889 | 2 | 0 | 2 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | ATGGC others(2884): Show |
chr12 | 108517214 | 108566173 | ||
| a0001c0014 | 0/0 | 2889 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | ATGGC others(2884): Show |
chr12 | 108517214 | 108566173 | ||
| a0001c0015 | 0/0 | 2889 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | ATGGC others(2884): Show |
chr12 | 108517214 | 108566173 | ||
| a0002c0002 | 0/0 | 2889 | 65 | 5 | 15 | 42 | 2 | 1 | SART3_chr12_108517214_108566173 | SART3 | ATGGC others(2884): Show |
chr12 | 108517214 | 108566173 | ||
| a0002c0004 | 0/0 | 2889 | 53 | 3 | 9 | 28 | 1 | 12 | SART3_chr12_108517214_108566173 | SART3 | ATGGC others(2884): Show |
chr12 | 108517214 | 108566173 | ||
| a0002c0009 | 0/0 | 2889 | 3 | 2 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | ATGGC others(2884): Show |
chr12 | 108517214 | 108566173 | ||
| a0002c0017 | 0/0 | 2889 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | ATGGC others(2884): Show |
chr12 | 108517214 | 108566173 | ||
| a0003c0008 | 0/0 | 2889 | 5 | 0 | 0 | 5 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | ATGGC others(2884): Show |
chr12 | 108517214 | 108566173 | ||
| a0004c0012 | 0/0 | 2889 | 2 | 2 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | ATGGC others(2884): Show |
chr12 | 108517214 | 108566173 | ||
| a0005c0018 | 0/0 | 2889 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | ATGGC others(2884): Show |
chr12 | 108517214 | 108566173 | ||
| a0006c0013 | 0/0 | 2889 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | ATGGC others(2884): Show |
chr12 | 108517214 | 108566173 | ||
| a0007c0016 | 0/0 | 2889 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | ATGGC others(2884): Show |
chr12 | 108517214 | 108566173 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4154 | 150 | 17 | 22 | 84 | 6 | 20 | SART3_chr12_108517214_108566173 | SART3 | GAGTC others(4149): Show |
chr12 | 108517214 | 108566173 |
| a0001c0001t0003 | 0/0 | 4154 | 6 | 0 | 0 | 6 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | GAGTC others(4149): Show |
chr12 | 108517214 | 108566173 |
| a0001c0001t0004 | 0/0 | 4154 | 5 | 5 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | GAGTC others(4149): Show |
chr12 | 108517214 | 108566173 |
| a0001c0001t0008 | 0/0 | 4154 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | GAGTC others(4149): Show |
chr12 | 108517214 | 108566173 |
| a0001c0003t0002 | 1/0 | 4154 | 54 | 30 | 4 | 16 | 2 | 1 | SART3_chr12_108517214_108566173 | SART3 | GAGTC others(4149): Show |
chr12 | 108517214 | 108566173 |
| a0001c0003t0007 | 0/0 | 4154 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | GAGTC others(4149): Show |
chr12 | 108517214 | 108566173 |
| a0001c0005t0002 | 0/0 | 4154 | 18 | 9 | 1 | 2 | 1 | 5 | SART3_chr12_108517214_108566173 | SART3 | GAGTC others(4149): Show |
chr12 | 108517214 | 108566173 |
| a0001c0006t0001 | 0/0 | 4154 | 12 | 11 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | GAGTC others(4149): Show |
chr12 | 108517214 | 108566173 |
| a0001c0007t0002 | 0/0 | 4154 | 7 | 6 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | GAGTC others(4149): Show |
chr12 | 108517214 | 108566173 |
| a0001c0007t0006 | 0/0 | 4154 | 2 | 2 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | GAGTC others(4149): Show |
chr12 | 108517214 | 108566173 |
| a0001c0010t0001 | 0/0 | 4154 | 2 | 2 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | GAGTC others(4149): Show |
chr12 | 108517214 | 108566173 |
| a0001c0011t0001 | 0/0 | 4154 | 2 | 0 | 2 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | GAGTC others(4149): Show |
chr12 | 108517214 | 108566173 |
| a0001c0014t0001 | 0/0 | 4154 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | GAGTC others(4149): Show |
chr12 | 108517214 | 108566173 |
| a0001c0015t0002 | 0/0 | 4154 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | GAGTC others(4149): Show |
chr12 | 108517214 | 108566173 |
| a0002c0002t0001 | 0/0 | 4154 | 65 | 5 | 15 | 42 | 2 | 1 | SART3_chr12_108517214_108566173 | SART3 | GAGTC others(4149): Show |
chr12 | 108517214 | 108566173 |
| a0002c0004t0001 | 0/0 | 4154 | 50 | 0 | 9 | 28 | 1 | 12 | SART3_chr12_108517214_108566173 | SART3 | GAGTC others(4149): Show |
chr12 | 108517214 | 108566173 |
| a0002c0004t0005 | 0/0 | 4154 | 3 | 3 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | GAGTC others(4149): Show |
chr12 | 108517214 | 108566173 |
| a0002c0009t0001 | 0/0 | 4154 | 3 | 2 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | GAGTC others(4149): Show |
chr12 | 108517214 | 108566173 |
| a0002c0017t0002 | 0/0 | 4154 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | GAGTC others(4149): Show |
chr12 | 108517214 | 108566173 |
| a0003c0008t0001 | 0/0 | 4154 | 5 | 0 | 0 | 5 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | GAGTC others(4149): Show |
chr12 | 108517214 | 108566173 |
| a0004c0012t0001 | 0/0 | 4154 | 2 | 2 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | GAGTC others(4149): Show |
chr12 | 108517214 | 108566173 |
| a0005c0018t0001 | 0/0 | 4154 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | GAGTC others(4149): Show |
chr12 | 108517214 | 108566173 |
| a0006c0013t0001 | 0/0 | 4154 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | GAGTC others(4149): Show |
chr12 | 108517214 | 108566173 |
| a0007c0016t0001 | 0/0 | 4154 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | GAGTC others(4149): Show |
chr12 | 108517214 | 108566173 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 14 | 0 | 2 | 8 | 1 | 3 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0003 | 0/0 | 8 | 0 | 1 | 6 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0053 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0003g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0004g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0001t0008g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0006 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0175 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0003t0007g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0005t0002g0011 | 0/0 | 4 | 0 | 0 | 0 | 1 | 3 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0005t0002g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0005t0002g0041 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0005t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0005t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0005t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0005t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0005t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0005t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0005t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0005t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0005t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0006t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0006t0001g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0006t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0006t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0006t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0006t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0006t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0006t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0006t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0006t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0007t0002g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0007t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0007t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0007t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0007t0006g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0010t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0010t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0011t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0014t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0001c0015t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0002 | 0/0 | 13 | 0 | 4 | 8 | 1 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0005 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0012 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0043 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0044 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0004 | 0/0 | 8 | 0 | 2 | 5 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0021 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0048 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0005g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0004t0005g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0009t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0009t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0009t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0002c0017t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0003c0008t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0003c0008t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0003c0008t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0004c0012t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0005c0018t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0006c0013t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| a0007c0016t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | GBR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0111 | EUR | GBR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0118 | EUR | FIN | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0043 | EAS | CHS | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00544 | hp2 | a0001 | c0003 | t0002 | g0190 | EAS | CHS | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0218 | EAS | CHS | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00609 | hp2 | a0001 | c0001 | t0008 | g0057 | EAS | CHS | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0217 | EAS | CHS | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | CHS | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00639 | hp2 | a0002 | c0004 | t0001 | g0004 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00673 | hp1 | a0002 | c0004 | t0001 | g0257 | EAS | CHS | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00735 | hp2 | a0001 | c0003 | t0002 | g0037 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00741 | hp1 | a0001 | c0003 | t0002 | g0172 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG00741 | hp2 | a0002 | c0004 | t0001 | g0004 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0241 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0231 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0043 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01109 | hp2 | a0001 | c0006 | t0001 | g0035 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01167 | hp1 | a0001 | c0007 | t0002 | g0159 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01167 | hp2 | a0002 | c0004 | t0001 | g0272 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01168 | hp1 | a0002 | c0004 | t0001 | g0021 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01168 | hp2 | a0001 | c0011 | t0001 | g0031 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01169 | hp1 | a0002 | c0004 | t0001 | g0242 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01169 | hp2 | a0001 | c0011 | t0001 | g0031 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01175 | hp1 | a0002 | c0009 | t0001 | g0214 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0233 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01243 | hp1 | a0001 | c0003 | t0002 | g0164 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01258 | hp1 | a0001 | c0003 | t0007 | g0174 | AMR | CLM | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0232 | AMR | CLM | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0212 | AMR | CLM | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0012 | AMR | CLM | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01496 | hp1 | a0001 | c0003 | t0002 | g0038 | AMR | CLM | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01496 | hp2 | a0005 | c0018 | t0001 | g0282 | AMR | CLM | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0230 | EUR | IBS | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01515 | hp2 | a0001 | c0003 | t0002 | g0173 | EUR | IBS | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0002 | EUR | IBS | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01516 | hp2 | a0001 | c0003 | t0002 | g0188 | EUR | IBS | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01884 | hp2 | a0001 | c0003 | t0002 | g0176 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01891 | hp1 | a0001 | c0003 | t0002 | g0006 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01891 | hp2 | a0002 | c0004 | t0005 | g0049 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01943 | hp1 | a0002 | c0004 | t0001 | g0271 | AMR | PEL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01943 | hp2 | a0001 | c0005 | t0002 | g0041 | AMR | PEL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01952 | hp2 | a0002 | c0004 | t0001 | g0281 | AMR | PEL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02027 | hp1 | a0001 | c0003 | t0002 | g0177 | EAS | KHV | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02055 | hp1 | a0001 | c0003 | t0002 | g0207 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02055 | hp2 | a0001 | c0003 | t0002 | g0194 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0239 | EAS | KHV | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02074 | hp1 | a0002 | c0004 | t0001 | g0276 | EAS | KHV | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02080 | hp1 | a0002 | c0004 | t0001 | g0261 | EAS | KHV | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02080 | hp2 | a0006 | c0013 | t0001 | g0066 | EAS | KHV | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02129 | hp2 | a0002 | c0004 | t0001 | g0266 | EAS | KHV | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0226 | EAS | KHV | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02145 | hp1 | a0001 | c0003 | t0002 | g0186 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02145 | hp2 | a0001 | c0003 | t0002 | g0187 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | CDX | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02155 | hp2 | a0002 | c0004 | t0001 | g0004 | EAS | CDX | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CDX | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02257 | hp1 | a0001 | c0010 | t0001 | g0052 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02257 | hp2 | a0001 | c0006 | t0001 | g0158 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02258 | hp2 | a0007 | c0016 | t0001 | g0280 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0044 | AMR | PEL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02273 | hp2 | a0002 | c0004 | t0001 | g0253 | AMR | PEL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02280 | hp1 | a0001 | c0003 | t0002 | g0006 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02451 | hp2 | a0002 | c0009 | t0001 | g0237 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02523 | hp2 | a0001 | c0014 | t0001 | g0084 | EAS | KHV | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02572 | hp1 | a0001 | c0005 | t0002 | g0206 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02572 | hp2 | a0001 | c0003 | t0002 | g0195 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02602 | hp1 | a0002 | c0004 | t0001 | g0208 | SAS | PJL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02615 | hp1 | a0001 | c0006 | t0001 | g0149 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02615 | hp2 | a0001 | c0003 | t0002 | g0036 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02622 | hp1 | a0001 | c0003 | t0002 | g0006 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02622 | hp2 | a0001 | c0006 | t0001 | g0151 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02630 | hp2 | a0001 | c0006 | t0001 | g0153 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0240 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02647 | hp2 | a0001 | c0003 | t0002 | g0037 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02717 | hp2 | a0002 | c0009 | t0001 | g0228 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02723 | hp1 | a0001 | c0005 | t0002 | g0040 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02723 | hp2 | a0001 | c0007 | t0002 | g0010 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02738 | hp2 | a0002 | c0004 | t0001 | g0278 | SAS | PJL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02809 | hp1 | a0001 | c0007 | t0002 | g0010 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02818 | hp1 | a0001 | c0007 | t0002 | g0010 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02818 | hp2 | a0001 | c0003 | t0002 | g0191 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02886 | hp1 | a0001 | c0003 | t0002 | g0006 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02886 | hp2 | a0002 | c0017 | t0002 | g0221 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02895 | hp1 | a0001 | c0005 | t0002 | g0205 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02895 | hp2 | a0001 | c0003 | t0002 | g0019 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02896 | hp1 | a0004 | c0012 | t0001 | g0047 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02896 | hp2 | a0001 | c0003 | t0002 | g0197 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02897 | hp1 | a0001 | c0005 | t0002 | g0204 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02897 | hp2 | a0004 | c0012 | t0001 | g0047 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02922 | hp1 | a0001 | c0003 | t0002 | g0019 | AFR | ESN | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02970 | hp2 | a0001 | c0003 | t0002 | g0039 | AFR | ESN | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02976 | hp1 | a0001 | c0006 | t0001 | g0150 | AFR | ESN | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02976 | hp2 | a0001 | c0007 | t0006 | g0033 | AFR | ESN | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03041 | hp1 | a0001 | c0003 | t0002 | g0171 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03098 | hp1 | a0001 | c0003 | t0002 | g0192 | AFR | MSL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0100 | AFR | MSL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0210 | AFR | ESN | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03130 | hp2 | a0001 | c0003 | t0002 | g0198 | AFR | ESN | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03139 | hp1 | a0002 | c0004 | t0005 | g0049 | AFR | ESN | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03139 | hp2 | a0001 | c0006 | t0001 | g0035 | AFR | ESN | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0222 | AFR | ESN | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03195 | hp2 | a0001 | c0003 | t0002 | g0196 | AFR | ESN | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03209 | hp1 | a0001 | c0006 | t0001 | g0034 | AFR | MSL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03225 | hp1 | a0001 | c0003 | t0002 | g0039 | AFR | MSL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03225 | hp2 | a0001 | c0003 | t0002 | g0169 | AFR | MSL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03239 | hp2 | a0002 | c0004 | t0001 | g0004 | SAS | PJL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03453 | hp1 | a0001 | c0006 | t0001 | g0156 | AFR | MSL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03453 | hp2 | a0002 | c0004 | t0005 | g0264 | AFR | MSL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03486 | hp1 | a0001 | c0005 | t0002 | g0202 | AFR | MSL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03486 | hp2 | a0001 | c0003 | t0002 | g0165 | AFR | MSL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03490 | hp2 | a0001 | c0005 | t0002 | g0011 | SAS | PJL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03491 | hp1 | a0001 | c0005 | t0002 | g0203 | SAS | PJL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03492 | hp2 | a0001 | c0005 | t0002 | g0011 | SAS | PJL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03540 | hp1 | a0001 | c0006 | t0001 | g0157 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03579 | hp2 | a0001 | c0007 | t0002 | g0155 | AFR | MSL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03669 | hp2 | a0001 | c0005 | t0002 | g0041 | SAS | PJL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03688 | hp1 | a0002 | c0004 | t0001 | g0250 | SAS | STU | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | STU | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0229 | SAS | PJL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03831 | hp2 | a0002 | c0004 | t0001 | g0263 | SAS | BEB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03834 | hp2 | a0001 | c0005 | t0002 | g0011 | SAS | BEB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03927 | hp2 | a0002 | c0004 | t0001 | g0267 | SAS | BEB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03942 | hp2 | a0002 | c0004 | t0001 | g0048 | SAS | BEB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | STU | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG04115 | hp2 | a0002 | c0004 | t0001 | g0048 | SAS | STU | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG04184 | hp1 | a0002 | c0004 | t0001 | g0275 | SAS | BEB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG04184 | hp2 | a0001 | c0015 | t0002 | g0170 | SAS | BEB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG04199 | hp2 | a0002 | c0004 | t0001 | g0021 | SAS | STU | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG04204 | hp1 | a0002 | c0004 | t0001 | g0246 | SAS | STU | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG04204 | hp2 | a0001 | c0003 | t0002 | g0161 | SAS | STU | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18522 | hp1 | a0001 | c0006 | t0001 | g0034 | AFR | YRI | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18522 | hp2 | a0001 | c0007 | t0002 | g0010 | AFR | YRI | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CHB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0238 | EAS | CHB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CHB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0225 | EAS | CHB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18906 | hp1 | a0001 | c0005 | t0002 | g0201 | AFR | YRI | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18906 | hp2 | a0001 | c0007 | t0006 | g0033 | AFR | YRI | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18940 | hp2 | a0001 | c0003 | t0002 | g0168 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18941 | hp2 | a0002 | c0004 | t0001 | g0004 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18943 | hp1 | a0001 | c0003 | t0002 | g0181 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18945 | hp1 | a0001 | c0005 | t0002 | g0042 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18947 | hp2 | a0002 | c0004 | t0001 | g0245 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18951 | hp2 | a0002 | c0004 | t0001 | g0243 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18953 | hp2 | a0002 | c0004 | t0001 | g0265 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18956 | hp2 | a0001 | c0005 | t0002 | g0042 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18959 | hp1 | a0002 | c0004 | t0001 | g0254 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18964 | hp2 | a0001 | c0003 | t0002 | g0162 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18965 | hp1 | a0001 | c0003 | t0002 | g0038 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18970 | hp2 | a0001 | c0003 | t0002 | g0178 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18971 | hp2 | a0001 | c0003 | t0002 | g0180 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18973 | hp2 | a0002 | c0004 | t0001 | g0256 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18974 | hp1 | a0003 | c0008 | t0001 | g0016 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18977 | hp2 | a0002 | c0004 | t0001 | g0269 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18980 | hp2 | a0002 | c0004 | t0001 | g0259 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18982 | hp2 | a0003 | c0008 | t0001 | g0077 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18984 | hp1 | a0001 | c0003 | t0002 | g0189 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0236 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18985 | hp2 | a0002 | c0004 | t0001 | g0046 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18988 | hp2 | a0002 | c0004 | t0001 | g0255 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18989 | hp1 | a0002 | c0004 | t0001 | g0251 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18989 | hp2 | a0002 | c0004 | t0001 | g0260 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18990 | hp1 | a0002 | c0004 | t0001 | g0004 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18991 | hp2 | a0001 | c0003 | t0002 | g0183 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18992 | hp1 | a0002 | c0004 | t0001 | g0258 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18993 | hp1 | a0001 | c0003 | t0002 | g0160 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18994 | hp2 | a0002 | c0004 | t0001 | g0252 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18998 | hp1 | a0002 | c0004 | t0001 | g0004 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19000 | hp2 | a0001 | c0003 | t0002 | g0179 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19003 | hp1 | a0002 | c0004 | t0001 | g0273 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0213 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0234 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0209 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0224 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19011 | hp2 | a0003 | c0008 | t0001 | g0081 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | LWK | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19030 | hp2 | a0001 | c0005 | t0002 | g0200 | AFR | LWK | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19043 | hp1 | a0001 | c0005 | t0002 | g0040 | AFR | LWK | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0220 | AFR | LWK | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19054 | hp1 | a0002 | c0004 | t0001 | g0244 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19054 | hp2 | a0003 | c0008 | t0001 | g0016 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19055 | hp1 | a0001 | c0003 | t0002 | g0166 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19064 | hp1 | a0001 | c0003 | t0002 | g0182 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19070 | hp2 | a0002 | c0004 | t0001 | g0004 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19072 | hp2 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19074 | hp2 | a0002 | c0004 | t0001 | g0270 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19076 | hp2 | a0002 | c0002 | t0001 | g0277 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19078 | hp2 | a0002 | c0004 | t0001 | g0279 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19079 | hp1 | a0003 | c0008 | t0001 | g0016 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0248 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19083 | hp1 | a0002 | c0004 | t0001 | g0268 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0211 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19085 | hp2 | a0001 | c0003 | t0002 | g0184 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19086 | hp1 | a0001 | c0003 | t0002 | g0167 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0249 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19091 | hp1 | a0002 | c0004 | t0001 | g0046 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19240 | hp1 | a0001 | c0003 | t0002 | g0019 | AFR | YRI | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0018 | AFR | YRI | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA20129 | hp1 | a0001 | c0003 | t0002 | g0163 | AFR | ASW | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ASW | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA20752 | hp1 | a0002 | c0004 | t0001 | g0274 | EUR | TSI | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA20752 | hp2 | a0001 | c0005 | t0002 | g0011 | EUR | TSI | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0119 | EUR | TSI | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0130 | EUR | TSI | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA20905 | hp2 | a0002 | c0004 | t0001 | g0262 | SAS | GIH | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0216 | AMR | CLM | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG01123 | hp2 | a0002 | c0004 | t0001 | g0021 | AMR | CLM | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02109 | hp1 | a0001 | c0010 | t0001 | g0051 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02109 | hp2 | a0001 | c0007 | t0002 | g0152 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0101 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02486 | hp2 | a0001 | c0003 | t0002 | g0006 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02559 | hp1 | a0001 | c0003 | t0002 | g0185 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG02559 | hp2 | a0001 | c0003 | t0002 | g0193 | AFR | ACB | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | MSL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG06807 | hp1 | a0001 | c0006 | t0001 | g0154 | AFR | USA | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | USA | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0247 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | USA | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA20300 | hp2 | a0001 | c0003 | t0002 | g0036 | AFR | USA | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0223 | AFR | LWK | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| NA21309 | hp2 | a0001 | c0005 | t0002 | g0199 | AFR | LWK | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0053 | REF | REF | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0002 | g0175 | REF | REF | SART3_chr12_108517214_108566173 | SART3 | chr12 | 108517214 | 108566173 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:108526470 | C | T | 1 | a0006 | 1 | HG02080.hp2 | missense_variant | MODERATE | c.1999G>A | p.Ala667Thr | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 16/19 | 2018/4154 | 1999/2892 | 667/963 | chr12 | 108526470 | |||
| chr12:108530194 | C | A | 1 | a0003 | 5 | NA18974.hp1 NA18982.hp2 NA19011.hp2 others(2): Show |
missense_variant | MODERATE | c.1863G>T | p.Glu621Asp | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/19 | 1882/4154 | 1863/2892 | 621/963 | chr12 | 108530194 | |||
| chr12:108536543 | C | G | 1 | a0004 | 2 | HG02896.hp1 HG02897.hp2 |
missense_variant | MODERATE | c.1417G>C | p.Val473Leu | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 11/19 | 1436/4154 | 1417/2892 | 473/963 | chr12 | 108536543 | |||
| chr12:108547926 | C | T | 1 | a0007 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.505G>A | p.Val169Met | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/19 | 524/4154 | 505/2892 | 169/963 | chr12 | 108547926 | |||
| chr12:108561086 | G | C | 4 | a0002 a0004 a0005 others(1): Show |
126 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(123): Show |
missense_variant | MODERATE | c.69C>G | p.Asp23Glu | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/19 | 88/4154 | 69/2892 | 23/963 | chr12 | 108561086 | |||
| chr12:108561132 | G | A | 1 | a0005 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.23C>T | p.Ser8Leu | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/19 | 42/4154 | 23/2892 | 8/963 | chr12 | 108561132 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:108523541 | C | T | 1 | a0001c0006 | 12 | HG01109.hp2 HG02257.hp2 HG02615.hp1 others(9): Show |
synonymous_variant | LOW | c.2808G>A | p.Ala936Ala | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 19/19 | 2827/4154 | 2808/2892 | 936/963 | chr12 | 108523541 | |||
| chr12:108523553 | G | A | 3 | a0002c0009 a0004c0012 a0007c0016 |
6 | HG01175.hp1 HG02258.hp2 HG02451.hp2 others(3): Show |
synonymous_variant | LOW | c.2796C>T | p.Asn932Asn | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 19/19 | 2815/4154 | 2796/2892 | 932/963 | chr12 | 108523553 | |||
| chr12:108524369 | C | T | 14 | a0001c0001 a0001c0006 a0001c0007 others(11): Show |
318 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(315): Show |
synonymous_variant | LOW | c.2661G>A | p.Pro887Pro | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 18/19 | 2680/4154 | 2661/2892 | 887/963 | chr12 | 108524369 | |||
| chr12:108526396 | G | A | 1 | a0001c0015 | 1 | HG04184.hp2 | synonymous_variant | LOW | c.2073C>T | p.Asp691Asp | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 16/19 | 2092/4154 | 2073/2892 | 691/963 | chr12 | 108526396 | |||
| chr12:108530173 | A | G | 15 | a0001c0001 a0001c0006 a0001c0007 others(12): Show |
319 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(316): Show |
synonymous_variant | LOW | c.1884T>C | p.Asp628Asp | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/19 | 1903/4154 | 1884/2892 | 628/963 | chr12 | 108530173 | |||
| chr12:108532253 | G | A | 1 | a0001c0014 | 1 | HG02523.hp2 | synonymous_variant | LOW | c.1638C>T | p.Cys546Cys | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 13/19 | 1657/4154 | 1638/2892 | 546/963 | chr12 | 108532253 | |||
| chr12:108538156 | G | A | 1 | a0001c0010 | 2 | HG02109.hp1 HG02257.hp1 |
synonymous_variant | LOW | c.1110C>T | p.Arg370Arg | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 8/19 | 1129/4154 | 1110/2892 | 370/963 | chr12 | 108538156 | |||
| chr12:108539045 | G | A | 1 | a0001c0011 | 2 | HG01168.hp2 HG01169.hp2 |
synonymous_variant | LOW | c.951C>T | p.Ile317Ile | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 7/19 | 970/4154 | 951/2892 | 317/963 | chr12 | 108539045 | |||
| chr12:108547903 | G | A | 1 | a0002c0004 | 53 | HG00639.hp2 HG00673.hp1 HG00741.hp2 others(50): Show |
synonymous_variant | LOW | c.528C>T | p.Ala176Ala | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/19 | 547/4154 | 528/2892 | 176/963 | chr12 | 108547903 | |||
| chr12:108547924 | C | G | 1 | a0001c0005 | 18 | HG01943.hp2 HG02572.hp1 HG02723.hp1 others(15): Show |
synonymous_variant | LOW | c.507G>C | p.Val169Val | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/19 | 526/4154 | 507/2892 | 169/963 | chr12 | 108547924 | |||
| chr12:108561047 | C | T | 13 | a0001c0001 a0001c0010 a0001c0011 others(10): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
synonymous_variant | LOW | c.108G>A | p.Arg36Arg | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/19 | 127/4154 | 108/2892 | 36/963 | chr12 | 108561047 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:108522762 | C | T | 1 | a0001c0007t0006 | 2 | HG02976.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*695G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 19/19 | 695 | chr12 | 108522762 | ||||||
| chr12:108522900 | T | G | 18 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(15): Show |
311 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(308): Show |
3_prime_UTR_variant | MODIFIER | c.*557A>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 19/19 | 557 | chr12 | 108522900 | ||||||
| chr12:108523002 | C | T | 1 | a0001c0001t0004 | 5 | HG01884.hp1 HG02486.hp1 HG03098.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*455G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 19/19 | 455 | chr12 | 108523002 | ||||||
| chr12:108523013 | A | T | 1 | a0001c0001t0003 | 6 | NA18966.hp2 NA18984.hp2 NA19063.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*444T>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 19/19 | 444 | chr12 | 108523013 | ||||||
| chr12:108523130 | A | G | 1 | a0001c0001t0008 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*327T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 19/19 | 327 | chr12 | 108523130 | ||||||
| chr12:108523174 | C | T | 1 | a0002c0004t0005 | 3 | HG01891.hp2 HG03139.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*283G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 19/19 | 283 | chr12 | 108523174 | ||||||
| chr12:108523384 | G | T | 1 | a0001c0003t0007 | 1 | HG01258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*73C>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 19/19 | 73 | chr12 | 108523384 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:108523743 | G | GA | 219 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(216): Show |
313 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.2715-110dupT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 18/18 | chr12 | 108523743 | |||||||
| chr12:108523777 | T | G | 3 | a0001c0003t0002g0191 a0001c0003t0002g0192 a0001c0003t0002g0193 |
3 | HG02559.hp2 HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2715-143A>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 18/18 | chr12 | 108523777 | |||||||
| chr12:108523846 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2715-212G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 18/18 | chr12 | 108523846 | |||||||
| chr12:108524553 | G | T | 43 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0027 others(40): Show |
58 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.2524-47C>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 17/18 | chr12 | 108524553 | |||||||
| chr12:108524654 | C | T | 233 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(230): Show |
332 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(329): Show |
intron_variant | MODIFIER | c.2524-148G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 17/18 | chr12 | 108524654 | |||||||
| chr12:108524659 | CCT | C | 45 | a0002c0002t0001g0002 a0002c0002t0001g0005 a0002c0002t0001g0012 others(42): Show |
71 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.2524-155_2524-154d others(4): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 17/18 | chr12 | 108524659 | |||||||
| chr12:108524818 | A | G | 9 | a0001c0001t0001g0030 a0001c0001t0001g0132 a0001c0001t0001g0133 others(6): Show |
11 | HG01168.hp2 HG01169.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.2524-312T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 17/18 | chr12 | 108524818 | |||||||
| chr12:108524897 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2524-391G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 17/18 | chr12 | 108524897 | |||||||
| chr12:108525389 | T | C | 46 | a0002c0002t0001g0002 a0002c0002t0001g0005 a0002c0002t0001g0012 others(43): Show |
72 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.2523+68A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 17/18 | chr12 | 108525389 | |||||||
| chr12:108525613 | T | C | 43 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0027 others(40): Show |
58 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(55): Show |
splice_region_variant&intron_variant | LOW | c.2371-4A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 16/18 | chr12 | 108525613 | |||||||
| chr12:108525759 | G | A | 1 | a0002c0002t0001g0229 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2371-150C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 16/18 | chr12 | 108525759 | |||||||
| chr12:108525763 | C | T | 11 | a0001c0003t0002g0019 a0001c0003t0002g0039 a0001c0003t0002g0191 others(8): Show |
14 | HG02055.hp1 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.2371-154G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 16/18 | chr12 | 108525763 | |||||||
| chr12:108525771 | T | G | 1 | a0001c0007t0002g0152 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2371-162A>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 16/18 | chr12 | 108525771 | |||||||
| chr12:108525897 | G | A | 223 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(220): Show |
319 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(316): Show |
intron_variant | MODIFIER | c.2370+202C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 16/18 | chr12 | 108525897 | |||||||
| chr12:108526755 | CTCGGGT | C | 47 | a0002c0002t0001g0002 a0002c0002t0001g0005 a0002c0002t0001g0012 others(44): Show |
73 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.1916-208_1916-203d others(8): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108526755 | |||||||
| chr12:108526829 | T | C | 223 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(220): Show |
319 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(316): Show |
intron_variant | MODIFIER | c.1916-276A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108526829 | |||||||
| chr12:108526946 | T | C | 11 | a0001c0003t0002g0019 a0001c0003t0002g0039 a0001c0003t0002g0191 others(8): Show |
14 | HG02055.hp1 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1916-393A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108526946 | |||||||
| chr12:108526948 | C | G | 1 | a0001c0007t0006g0033 | 2 | HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1916-395G>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108526948 | |||||||
| chr12:108527014 | A | G | 41 | a0002c0004t0001g0004 a0002c0004t0001g0021 a0002c0004t0001g0046 others(38): Show |
53 | HG00639.hp2 HG00673.hp1 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.1916-461T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108527014 | |||||||
| chr12:108527172 | A | G | 223 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(220): Show |
319 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(316): Show |
intron_variant | MODIFIER | c.1916-619T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108527172 | |||||||
| chr12:108527369 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1916-816A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108527369 | |||||||
| chr12:108527443 | A | C | 1 | a0001c0001t0001g0110 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1916-890T>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108527443 | |||||||
| chr12:108527823 | C | T | 47 | a0002c0002t0001g0002 a0002c0002t0001g0005 a0002c0002t0001g0012 others(44): Show |
73 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.1916-1270G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108527823 | |||||||
| chr12:108527890 | C | T | 1 | a0001c0003t0007g0174 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1916-1337G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108527890 | |||||||
| chr12:108527891 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1916-1338C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108527891 | |||||||
| chr12:108527895 | A | G | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG01243.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1916-1342T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108527895 | |||||||
| chr12:108527928 | A | G | 262 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(259): Show |
373 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(370): Show |
intron_variant | MODIFIER | c.1916-1375T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108527928 | |||||||
| chr12:108527954 | C | G | 1 | a0001c0001t0001g0090 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1916-1401G>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108527954 | |||||||
| chr12:108527970 | T | C | 1 | a0002c0002t0001g0216 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1916-1417A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108527970 | |||||||
| chr12:108528008 | G | A | 1 | a0001c0001t0001g0025 | 2 | NA18983.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1916-1455C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108528008 | |||||||
| chr12:108528034 | G | A | 2 | a0002c0004t0001g0260 a0002c0004t0001g0270 |
2 | NA18989.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1916-1481C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108528034 | |||||||
| chr12:108528070 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1916-1517T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108528070 | |||||||
| chr12:108528106 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1916-1553T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108528106 | |||||||
| chr12:108528125 | G | A | 2 | a0001c0010t0001g0051 a0001c0010t0001g0052 |
2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1916-1572C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108528125 | |||||||
| chr12:108528415 | G | A | 14 | a0001c0005t0002g0011 a0001c0005t0002g0040 a0001c0005t0002g0041 others(11): Show |
20 | HG01943.hp2 HG02109.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1915+1727C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108528415 | |||||||
| chr12:108528444 | C | T | 11 | a0001c0005t0002g0011 a0001c0005t0002g0040 a0001c0005t0002g0041 others(8): Show |
17 | HG01943.hp2 HG02572.hp1 HG02723.hp1 others(14): Show |
intron_variant | MODIFIER | c.1915+1698G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108528444 | |||||||
| chr12:108528462 | G | A | 1 | a0002c0017t0002g0221 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1915+1680C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108528462 | |||||||
| chr12:108528482 | C | CA | 117 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(114): Show |
172 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.1915+1659dupT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108528482 | |||||||
| chr12:108528482 | CA | C | 26 | a0001c0001t0001g0030 a0001c0001t0001g0132 a0001c0001t0001g0133 others(23): Show |
29 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.1915+1659delT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108528482 | |||||||
| chr12:108528508 | G | T | 55 | a0001c0001t0001g0127 a0001c0003t0002g0207 a0001c0005t0002g0011 others(52): Show |
73 | HG00639.hp2 HG00673.hp1 HG00741.hp2 others(70): Show |
intron_variant | MODIFIER | c.1915+1634C>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108528508 | |||||||
| chr12:108528555 | G | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(61): Show |
99 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.1915+1587C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108528555 | |||||||
| chr12:108528692 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1915+1450C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108528692 | |||||||
| chr12:108528891 | G | A | 1 | a0001c0007t0006g0033 | 2 | HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1915+1251C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108528891 | |||||||
| chr12:108528940 | G | A | 1 | a0002c0004t0001g0046 | 2 | NA18985.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1915+1202C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108528940 | |||||||
| chr12:108528989 | G | A | 16 | a0001c0001t0001g0030 a0001c0001t0001g0132 a0001c0001t0001g0133 others(13): Show |
20 | HG01168.hp2 HG01169.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1915+1153C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108528989 | |||||||
| chr12:108529004 | T | G | 39 | a0002c0004t0001g0004 a0002c0004t0001g0021 a0002c0004t0001g0046 others(36): Show |
51 | HG00639.hp2 HG00673.hp1 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.1915+1138A>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108529004 | |||||||
| chr12:108529089 | C | T | 1 | a0004c0012t0001g0047 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1915+1053G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108529089 | |||||||
| chr12:108529205 | A | G | 2 | a0002c0004t0001g0271 a0002c0004t0001g0281 |
2 | HG01943.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.1915+937T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108529205 | |||||||
| chr12:108529301 | A | G | 11 | a0001c0003t0002g0019 a0001c0003t0002g0039 a0001c0003t0002g0191 others(8): Show |
14 | HG02055.hp1 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1915+841T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108529301 | |||||||
| chr12:108529320 | C | T | 11 | a0001c0003t0002g0019 a0001c0003t0002g0039 a0001c0003t0002g0191 others(8): Show |
14 | HG02055.hp1 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1915+822G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108529320 | |||||||
| chr12:108529425 | T | C | 1 | a0001c0001t0001g0129 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1915+717A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108529425 | |||||||
| chr12:108529604 | G | A | 3 | a0002c0004t0001g0257 a0002c0004t0001g0261 a0002c0004t0001g0279 |
3 | HG00673.hp1 HG02080.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1915+538C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108529604 | |||||||
| chr12:108529609 | A | G | 223 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(220): Show |
319 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(316): Show |
intron_variant | MODIFIER | c.1915+533T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108529609 | |||||||
| chr12:108529772 | G | A | 1 | a0002c0002t0001g0229 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1915+370C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108529772 | |||||||
| chr12:108529784 | A | C | 223 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(220): Show |
319 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(316): Show |
intron_variant | MODIFIER | c.1915+358T>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108529784 | |||||||
| chr12:108529806 | TA | T | 47 | a0002c0002t0001g0002 a0002c0002t0001g0005 a0002c0002t0001g0012 others(44): Show |
73 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.1915+335delT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108529806 | |||||||
| chr12:108529838 | C | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(61): Show |
99 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.1915+304G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108529838 | |||||||
| chr12:108529876 | T | A | 1 | a0001c0001t0001g0069 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1915+266A>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 15/18 | chr12 | 108529876 | |||||||
| chr12:108530332 | G | A | 1 | a0002c0004t0001g0245 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1747-22C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 14/18 | chr12 | 108530332 | |||||||
| chr12:108530333 | C | A | 1 | a0002c0004t0001g0245 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1747-23G>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 14/18 | chr12 | 108530333 | |||||||
| chr12:108530380 | A | C | 1 | a0001c0007t0006g0033 | 2 | HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1747-70T>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 14/18 | chr12 | 108530380 | |||||||
| chr12:108530436 | G | A | 1 | a0001c0005t0002g0200 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1747-126C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 14/18 | chr12 | 108530436 | |||||||
| chr12:108530564 | T | C | 88 | a0002c0002t0001g0002 a0002c0002t0001g0005 a0002c0002t0001g0012 others(85): Show |
126 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.1747-254A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 14/18 | chr12 | 108530564 | |||||||
| chr12:108530719 | G | A | 5 | a0001c0001t0001g0027 a0001c0001t0001g0105 a0001c0001t0001g0118 others(2): Show |
6 | HG00099.hp1 HG00323.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.1747-409C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 14/18 | chr12 | 108530719 | |||||||
| chr12:108530733 | C | A | 225 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(222): Show |
321 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(318): Show |
intron_variant | MODIFIER | c.1747-423G>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 14/18 | chr12 | 108530733 | |||||||
| chr12:108530766 | A | T | 1 | a0001c0005t0002g0200 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1746+438T>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 14/18 | chr12 | 108530766 | |||||||
| chr12:108530852 | C | T | 1 | a0001c0003t0002g0186 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1746+352G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 14/18 | chr12 | 108530852 | |||||||
| chr12:108530857 | CA | C | 68 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0024 others(65): Show |
101 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.1746+346delT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 14/18 | chr12 | 108530857 | |||||||
| chr12:108530972 | T | C | 223 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(220): Show |
319 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(316): Show |
intron_variant | MODIFIER | c.1746+232A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 14/18 | chr12 | 108530972 | |||||||
| chr12:108530977 | C | T | 9 | a0001c0006t0001g0034 a0001c0006t0001g0035 a0001c0006t0001g0149 others(6): Show |
11 | HG01109.hp2 HG02257.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1746+227G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 14/18 | chr12 | 108530977 | |||||||
| chr12:108531127 | C | T | 47 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0027 others(44): Show |
62 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.1746+77G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 14/18 | chr12 | 108531127 | |||||||
| chr12:108531154 | G | C | 1 | a0002c0004t0005g0264 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1746+50C>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 14/18 | chr12 | 108531154 | |||||||
| chr12:108531477 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1670-197C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 13/18 | chr12 | 108531477 | |||||||
| chr12:108531492 | C | T | 1 | a0002c0017t0002g0221 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1670-212G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 13/18 | chr12 | 108531492 | |||||||
| chr12:108531638 | C | A | 246 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(243): Show |
351 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(348): Show |
intron_variant | MODIFIER | c.1670-358G>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 13/18 | chr12 | 108531638 | |||||||
| chr12:108531639 | A | C | 1 | a0001c0001t0001g0080 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1670-359T>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 13/18 | chr12 | 108531639 | |||||||
| chr12:108531639 | A | T | 245 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(242): Show |
350 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(347): Show |
intron_variant | MODIFIER | c.1670-359T>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 13/18 | chr12 | 108531639 | |||||||
| chr12:108531640 | A | T | 246 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(243): Show |
351 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(348): Show |
intron_variant | MODIFIER | c.1670-360T>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 13/18 | chr12 | 108531640 | |||||||
| chr12:108531847 | C | T | 2 | a0002c0004t0001g0244 a0002c0004t0001g0251 |
2 | NA18989.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1669+375G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 13/18 | chr12 | 108531847 | |||||||
| chr12:108531875 | A | G | 9 | a0001c0001t0001g0030 a0001c0001t0001g0132 a0001c0001t0001g0133 others(6): Show |
11 | HG01168.hp2 HG01169.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1669+347T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 13/18 | chr12 | 108531875 | |||||||
| chr12:108531976 | C | A | 1 | a0001c0005t0002g0200 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1669+246G>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 13/18 | chr12 | 108531976 | |||||||
| chr12:108531979 | C | G | 1 | a0001c0005t0002g0200 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1669+243G>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 13/18 | chr12 | 108531979 | |||||||
| chr12:108531986 | G | A | 223 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(220): Show |
319 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(316): Show |
intron_variant | MODIFIER | c.1669+236C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 13/18 | chr12 | 108531986 | |||||||
| chr12:108532108 | C | T | 1 | a0001c0003t0002g0172 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1669+114G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 13/18 | chr12 | 108532108 | |||||||
| chr12:108532669 | G | A | 2 | a0001c0010t0001g0051 a0001c0010t0001g0052 |
2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1557-335C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108532669 | |||||||
| chr12:108532678 | G | A | 1 | a0001c0003t0002g0192 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1557-344C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108532678 | |||||||
| chr12:108532747 | G | A | 1 | a0001c0010t0001g0052 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1557-413C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108532747 | |||||||
| chr12:108533048 | G | A | 43 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0027 others(40): Show |
58 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.1557-714C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108533048 | |||||||
| chr12:108533109 | C | T | 9 | a0001c0001t0001g0027 a0001c0001t0001g0105 a0001c0001t0001g0115 others(6): Show |
10 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.1557-775G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108533109 | |||||||
| chr12:108533297 | C | T | 15 | a0001c0006t0001g0034 a0001c0006t0001g0035 a0001c0006t0001g0149 others(12): Show |
21 | HG01109.hp2 HG01167.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1557-963G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108533297 | |||||||
| chr12:108533317 | T | C | 5 | a0002c0002t0001g0211 a0002c0002t0001g0224 a0002c0002t0001g0247 others(2): Show |
5 | NA18955.hp1 NA19011.hp1 NA19076.hp2 others(2): Show |
intron_variant | MODIFIER | c.1557-983A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108533317 | |||||||
| chr12:108533367 | C | A | 1 | a0001c0001t0001g0062 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1557-1033G>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108533367 | |||||||
| chr12:108533388 | C | CA | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(157): Show |
239 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.1557-1055dupT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108533388 | |||||||
| chr12:108533388 | C | CAA | 19 | a0001c0001t0001g0061 a0001c0001t0001g0120 a0001c0001t0001g0121 others(16): Show |
25 | HG01109.hp2 HG01167.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1557-1056_1557-105 others(6): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108533388 | |||||||
| chr12:108533407 | A | G | 41 | a0002c0004t0001g0004 a0002c0004t0001g0021 a0002c0004t0001g0046 others(38): Show |
53 | HG00639.hp2 HG00673.hp1 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.1557-1073T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108533407 | |||||||
| chr12:108533545 | A | G | 1 | a0001c0001t0001g0082 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1557-1211T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108533545 | |||||||
| chr12:108533689 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1557-1355G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108533689 | |||||||
| chr12:108533707 | T | C | 223 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(220): Show |
319 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(316): Show |
intron_variant | MODIFIER | c.1557-1373A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108533707 | |||||||
| chr12:108533764 | G | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0071 a0001c0001t0001g0094 |
6 | NA18965.hp2 NA18968.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1557-1430C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108533764 | |||||||
| chr12:108533833 | T | G | 1 | a0001c0001t0001g0116 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1557-1499A>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108533833 | |||||||
| chr12:108534022 | G | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(70): Show |
110 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.1556+1337C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108534022 | |||||||
| chr12:108534111 | CTA | C | 11 | a0001c0003t0002g0019 a0001c0003t0002g0039 a0001c0003t0002g0191 others(8): Show |
14 | HG02055.hp1 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1556+1246_1556+124 others(6): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108534111 | |||||||
| chr12:108534115 | A | T | 11 | a0001c0003t0002g0019 a0001c0003t0002g0039 a0001c0003t0002g0191 others(8): Show |
14 | HG02055.hp1 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1556+1244T>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108534115 | |||||||
| chr12:108534302 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1556+1057G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108534302 | |||||||
| chr12:108534304 | G | A | 4 | a0001c0003t0002g0039 a0001c0003t0002g0194 a0001c0003t0002g0196 others(1): Show |
5 | HG02055.hp2 HG02896.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1556+1055C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108534304 | |||||||
| chr12:108534321 | G | A | 2 | a0002c0004t0001g0243 a0002c0004t0001g0259 |
2 | NA18951.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.1556+1038C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108534321 | |||||||
| chr12:108534398 | G | A | 34 | a0002c0004t0001g0004 a0002c0004t0001g0021 a0002c0004t0001g0046 others(31): Show |
45 | HG00639.hp2 HG00673.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.1556+961C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108534398 | |||||||
| chr12:108534507 | T | TA | 5 | a0001c0001t0001g0080 a0001c0001t0001g0117 a0001c0003t0002g0019 others(2): Show |
7 | HG02055.hp1 HG02895.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1556+851dupT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108534507 | |||||||
| chr12:108534507 | TA | T | 15 | a0001c0001t0001g0114 a0001c0006t0001g0034 a0001c0006t0001g0035 others(12): Show |
20 | HG01109.hp2 HG01167.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1556+851delT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108534507 | |||||||
| chr12:108534553 | G | C | 11 | a0001c0003t0002g0019 a0001c0003t0002g0039 a0001c0003t0002g0191 others(8): Show |
14 | HG02055.hp1 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1556+806C>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108534553 | |||||||
| chr12:108534599 | G | A | 3 | a0001c0003t0002g0191 a0001c0003t0002g0192 a0001c0003t0002g0193 |
3 | HG02559.hp2 HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1556+760C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108534599 | |||||||
| chr12:108534937 | A | G | 47 | a0002c0002t0001g0002 a0002c0002t0001g0005 a0002c0002t0001g0012 others(44): Show |
73 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.1556+422T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108534937 | |||||||
| chr12:108535048 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1556+311A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108535048 | |||||||
| chr12:108535179 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1556+180T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108535179 | |||||||
| chr12:108535244 | A | G | 5 | a0001c0001t0001g0017 a0001c0001t0001g0070 a0001c0001t0001g0088 others(2): Show |
7 | HG01070.hp1 HG01071.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.1556+115T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108535244 | |||||||
| chr12:108535310 | GTGCA | G | 3 | a0002c0004t0001g0243 a0002c0004t0001g0259 a0002c0004t0001g0268 |
3 | NA18951.hp2 NA18980.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1556+45_1556+48del others(4): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108535310 | |||||||
| chr12:108535340 | C | T | 11 | a0001c0003t0002g0019 a0001c0003t0002g0039 a0001c0003t0002g0191 others(8): Show |
14 | HG02055.hp1 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1556+19G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 12/18 | chr12 | 108535340 | |||||||
| chr12:108535515 | C | T | 11 | a0001c0003t0002g0019 a0001c0003t0002g0039 a0001c0003t0002g0191 others(8): Show |
14 | HG02055.hp1 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1447-47G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 11/18 | chr12 | 108535515 | |||||||
| chr12:108535587 | G | C | 11 | a0001c0003t0002g0019 a0001c0003t0002g0039 a0001c0003t0002g0191 others(8): Show |
14 | HG02055.hp1 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1447-119C>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 11/18 | chr12 | 108535587 | |||||||
| chr12:108535674 | C | T | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(205): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.1447-206G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 11/18 | chr12 | 108535674 | |||||||
| chr12:108535700 | G | T | 9 | a0001c0001t0001g0030 a0001c0001t0001g0132 a0001c0001t0001g0133 others(6): Show |
11 | HG01168.hp2 HG01169.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1447-232C>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 11/18 | chr12 | 108535700 | |||||||
| chr12:108535786 | T | TA | 85 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0027 others(82): Show |
126 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.1447-319dupT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 11/18 | chr12 | 108535786 | |||||||
| chr12:108535786 | TA | T | 12 | a0001c0001t0001g0137 a0001c0003t0002g0019 a0001c0003t0002g0039 others(9): Show |
15 | HG02055.hp1 HG02055.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1447-319delT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 11/18 | chr12 | 108535786 | |||||||
| chr12:108535964 | C | T | 2 | a0002c0004t0001g0252 a0002c0004t0001g0256 |
2 | NA18973.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1447-496G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 11/18 | chr12 | 108535964 | |||||||
| chr12:108535974 | G | A | 3 | a0001c0001t0001g0028 a0001c0001t0001g0099 a0001c0001t0001g0107 |
4 | HG01081.hp1 HG01175.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.1447-506C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 11/18 | chr12 | 108535974 | |||||||
| chr12:108536064 | A | G | 1 | a0001c0001t0001g0062 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1446+450T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 11/18 | chr12 | 108536064 | |||||||
| chr12:108536246 | G | A | 40 | a0002c0004t0001g0004 a0002c0004t0001g0021 a0002c0004t0001g0046 others(37): Show |
52 | HG00639.hp2 HG00673.hp1 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.1446+268C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 11/18 | chr12 | 108536246 | |||||||
| chr12:108536251 | C | T | 1 | a0002c0002t0001g0020 | 3 | NA18957.hp2 NA18968.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.1446+263G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 11/18 | chr12 | 108536251 | |||||||
| chr12:108536258 | A | C | 1 | a0002c0004t0005g0264 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1446+256T>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 11/18 | chr12 | 108536258 | |||||||
| chr12:108536333 | A | G | 220 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(217): Show |
314 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.1446+181T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 11/18 | chr12 | 108536333 | |||||||
| chr12:108536484 | G | A | 4 | a0001c0003t0002g0039 a0001c0003t0002g0194 a0001c0003t0002g0196 others(1): Show |
5 | HG02055.hp2 HG02896.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1446+30C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 11/18 | chr12 | 108536484 | |||||||
| chr12:108536508 | A | T | 13 | a0001c0003t0007g0174 a0001c0005t0002g0011 a0001c0005t0002g0040 others(10): Show |
19 | HG01258.hp1 HG01943.hp2 HG02572.hp1 others(16): Show |
splice_region_variant&intron_variant | LOW | c.1446+6T>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 11/18 | chr12 | 108536508 | |||||||
| chr12:108537014 | G | C | 1 | a0001c0003t0007g0174 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1310-229C>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 9/18 | chr12 | 108537014 | |||||||
| chr12:108537044 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1310-259G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 9/18 | chr12 | 108537044 | |||||||
| chr12:108537055 | G | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(205): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.1310-270C>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 9/18 | chr12 | 108537055 | |||||||
| chr12:108537168 | G | A | 1 | a0002c0004t0001g0267 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1309+320C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 9/18 | chr12 | 108537168 | |||||||
| chr12:108537199 | A | T | 234 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(231): Show |
333 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.1309+289T>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 9/18 | chr12 | 108537199 | |||||||
| chr12:108537367 | C | T | 9 | a0001c0001t0001g0030 a0001c0001t0001g0132 a0001c0001t0001g0133 others(6): Show |
11 | HG01168.hp2 HG01169.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1309+121G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 9/18 | chr12 | 108537367 | |||||||
| chr12:108537428 | C | T | 1 | a0007c0016t0001g0280 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1309+60G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 9/18 | chr12 | 108537428 | |||||||
| chr12:108537670 | C | A | 1 | a0001c0003t0002g0195 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1202-75G>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 8/18 | chr12 | 108537670 | |||||||
| chr12:108537707 | C | T | 1 | a0002c0002t0001g0232 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1202-112G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 8/18 | chr12 | 108537707 | |||||||
| chr12:108537930 | C | G | 1 | a0001c0003t0002g0166 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1201+135G>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 8/18 | chr12 | 108537930 | |||||||
| chr12:108538003 | C | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(70): Show |
110 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.1201+62G>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 8/18 | chr12 | 108538003 | |||||||
| chr12:108538222 | G | A | 1 | a0004c0012t0001g0047 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1063-19C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 7/18 | chr12 | 108538222 | |||||||
| chr12:108538277 | C | T | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(205): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.1063-74G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 7/18 | chr12 | 108538277 | |||||||
| chr12:108538324 | G | A | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(205): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.1063-121C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 7/18 | chr12 | 108538324 | |||||||
| chr12:108538358 | G | A | 5 | a0001c0001t0001g0017 a0001c0001t0001g0070 a0001c0001t0001g0088 others(2): Show |
7 | HG01070.hp1 HG01071.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.1063-155C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 7/18 | chr12 | 108538358 | |||||||
| chr12:108538412 | G | A | 2 | a0002c0002t0001g0230 a0002c0002t0001g0231 |
2 | HG01074.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1063-209C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 7/18 | chr12 | 108538412 | |||||||
| chr12:108538703 | G | T | 223 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(220): Show |
319 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(316): Show |
intron_variant | MODIFIER | c.1062+231C>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 7/18 | chr12 | 108538703 | |||||||
| chr12:108539140 | C | T | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(205): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.907-51G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108539140 | |||||||
| chr12:108539540 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.907-451A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108539540 | |||||||
| chr12:108539594 | C | T | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG01243.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.907-505G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108539594 | |||||||
| chr12:108539603 | A | T | 1 | a0007c0016t0001g0280 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.907-514T>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108539603 | |||||||
| chr12:108539636 | G | A | 1 | a0001c0001t0001g0071 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.907-547C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108539636 | |||||||
| chr12:108539652 | C | T | 2 | a0001c0001t0001g0059 a0001c0001t0008g0057 |
2 | HG00609.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.907-563G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108539652 | |||||||
| chr12:108539783 | T | C | 2 | a0002c0004t0001g0242 a0002c0004t0001g0272 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.907-694A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108539783 | |||||||
| chr12:108540155 | T | TA | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(205): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.907-1067dupT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108540155 | |||||||
| chr12:108540212 | G | A | 1 | a0002c0004t0001g0245 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.907-1123C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108540212 | |||||||
| chr12:108540404 | T | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(205): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.907-1315A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108540404 | |||||||
| chr12:108540459 | T | C | 2 | a0001c0010t0001g0051 a0001c0010t0001g0052 |
2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.907-1370A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108540459 | |||||||
| chr12:108540573 | TA | T | 206 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(203): Show |
296 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.907-1485delT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108540573 | |||||||
| chr12:108540641 | CA | C | 222 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(219): Show |
317 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.907-1553delT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108540641 | |||||||
| chr12:108540643 | A | C | 14 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0024 others(11): Show |
21 | HG00597.hp1 HG00673.hp2 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.907-1554T>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108540643 | |||||||
| chr12:108540659 | C | T | 1 | a0001c0015t0002g0170 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.907-1570G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108540659 | |||||||
| chr12:108540910 | C | T | 1 | a0002c0002t0001g0226 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.907-1821G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108540910 | |||||||
| chr12:108540946 | G | A | 4 | a0001c0007t0002g0010 a0001c0007t0002g0152 a0001c0007t0002g0155 others(1): Show |
7 | HG01167.hp1 HG02109.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.907-1857C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108540946 | |||||||
| chr12:108541045 | C | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(61): Show |
99 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.907-1956G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108541045 | |||||||
| chr12:108541321 | C | T | 1 | a0001c0003t0002g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.906+1707G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108541321 | |||||||
| chr12:108541340 | G | A | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG01243.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.906+1688C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108541340 | |||||||
| chr12:108541543 | T | A | 2 | a0001c0010t0001g0051 a0001c0010t0001g0052 |
2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.906+1485A>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108541543 | |||||||
| chr12:108541670 | C | A | 3 | a0002c0002t0001g0210 a0002c0002t0001g0220 a0002c0002t0001g0222 |
3 | HG03130.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.906+1358G>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108541670 | |||||||
| chr12:108541684 | G | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(117): Show |
172 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.906+1344C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108541684 | |||||||
| chr12:108541712 | G | C | 1 | a0002c0004t0005g0264 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.906+1316C>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108541712 | |||||||
| chr12:108541762 | A | C | 47 | a0002c0002t0001g0002 a0002c0002t0001g0005 a0002c0002t0001g0012 others(44): Show |
73 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.906+1266T>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108541762 | |||||||
| chr12:108541767 | T | C | 6 | a0001c0003t0002g0006 a0001c0003t0002g0036 a0001c0003t0002g0163 others(3): Show |
11 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.906+1261A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108541767 | |||||||
| chr12:108541781 | A | G | 207 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(204): Show |
297 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.906+1247T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108541781 | |||||||
| chr12:108541792 | G | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(61): Show |
99 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.906+1236C>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108541792 | |||||||
| chr12:108541954 | C | T | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(205): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.906+1074G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108541954 | |||||||
| chr12:108541998 | C | CT | 24 | a0001c0003t0002g0036 a0001c0003t0002g0164 a0001c0003t0002g0165 others(21): Show |
25 | HG00544.hp2 HG00741.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.906+1029dupA | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108541998 | |||||||
| chr12:108541998 | C | CTTTTTTT others(2987): Show |
1 | a0001c0005t0002g0042 | 2 | NA18945.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.906+1029_906+1030i others(2996): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108541998 | |||||||
| chr12:108541998 | CTTTTTT | C | 10 | a0001c0001t0001g0113 a0001c0001t0001g0128 a0001c0001t0001g0144 others(7): Show |
12 | HG00673.hp1 HG01123.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.906+1024_906+1029d others(8): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108541998 | |||||||
| chr12:108541998 | CTTTTTTT | C | 87 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0027 others(84): Show |
111 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.906+1023_906+1029d others(9): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108541998 | |||||||
| chr12:108541998 | CTTTTTTT others(1): Show |
C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(96): Show |
160 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.906+1022_906+1029d others(10): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108541998 | |||||||
| chr12:108541998 | CTTTTTTT others(2): Show |
C | 24 | a0001c0001t0001g0030 a0001c0001t0001g0075 a0001c0001t0001g0132 others(21): Show |
31 | HG01070.hp2 HG01109.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.906+1021_906+1029d others(11): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108541998 | |||||||
| chr12:108541998 | CTTTTTTT others(9): Show |
C | 2 | a0002c0004t0001g0048 a0002c0004t0001g0278 |
3 | HG02738.hp2 HG03942.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.906+1014_906+1029d others(18): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108541998 | |||||||
| chr12:108542070 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.906+958G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108542070 | |||||||
| chr12:108542282 | C | A | 1 | a0002c0002t0001g0235 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.906+746G>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108542282 | |||||||
| chr12:108542394 | C | A | 1 | a0001c0007t0006g0033 | 2 | HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.906+634G>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108542394 | |||||||
| chr12:108542473 | C | T | 2 | a0001c0006t0001g0151 a0001c0006t0001g0156 |
2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.906+555G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108542473 | |||||||
| chr12:108542538 | CACAG | C | 43 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0027 others(40): Show |
58 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.906+486_906+489del others(4): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108542538 | |||||||
| chr12:108542573 | C | T | 1 | a0002c0004t0001g0267 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.906+455G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108542573 | |||||||
| chr12:108542574 | G | A | 6 | a0001c0001t0001g0029 a0001c0003t0002g0160 a0001c0003t0002g0168 others(3): Show |
7 | NA18940.hp2 NA18983.hp1 NA18991.hp2 others(4): Show |
intron_variant | MODIFIER | c.906+454C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108542574 | |||||||
| chr12:108542652 | T | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(70): Show |
110 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.906+376A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108542652 | |||||||
| chr12:108542708 | G | A | 88 | a0002c0002t0001g0002 a0002c0002t0001g0005 a0002c0002t0001g0012 others(85): Show |
126 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.906+320C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108542708 | |||||||
| chr12:108542740 | T | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(205): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.906+288A>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108542740 | |||||||
| chr12:108542743 | C | T | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(205): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.906+285G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108542743 | |||||||
| chr12:108542886 | T | G | 1 | a0001c0001t0001g0143 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.906+142A>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108542886 | |||||||
| chr12:108542904 | G | A | 3 | a0001c0003t0002g0160 a0001c0003t0002g0168 a0001c0003t0002g0182 |
3 | NA18940.hp2 NA18993.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.906+124C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 6/18 | chr12 | 108542904 | |||||||
| chr12:108543279 | A | C | 1 | a0001c0001t0004g0100 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.782-127T>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 5/18 | chr12 | 108543279 | |||||||
| chr12:108543352 | C | T | 1 | a0001c0003t0002g0186 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.782-200G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 5/18 | chr12 | 108543352 | |||||||
| chr12:108543466 | C | T | 47 | a0002c0002t0001g0002 a0002c0002t0001g0005 a0002c0002t0001g0012 others(44): Show |
73 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.782-314G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 5/18 | chr12 | 108543466 | |||||||
| chr12:108543617 | G | A | 6 | a0002c0002t0001g0005 a0002c0002t0001g0043 a0002c0002t0001g0212 others(3): Show |
12 | HG00423.hp2 HG00621.hp1 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.782-465C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 5/18 | chr12 | 108543617 | |||||||
| chr12:108543622 | T | A | 2 | a0001c0001t0001g0022 a0001c0001t0001g0054 |
3 | HG01071.hp2 HG01433.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.782-470A>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 5/18 | chr12 | 108543622 | |||||||
| chr12:108543641 | G | A | 16 | a0001c0001t0001g0059 a0001c0006t0001g0034 a0001c0006t0001g0035 others(13): Show |
22 | HG01109.hp2 HG01167.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.782-489C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 5/18 | chr12 | 108543641 | |||||||
| chr12:108544153 | C | T | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(205): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.781+274G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 5/18 | chr12 | 108544153 | |||||||
| chr12:108544391 | T | C | 1 | a0001c0005t0002g0202 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.781+36A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 5/18 | chr12 | 108544391 | |||||||
| chr12:108544714 | C | G | 3 | a0001c0001t0001g0030 a0001c0001t0001g0134 a0001c0001t0001g0136 |
4 | HG02630.hp1 HG02809.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.730-236G>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 4/18 | chr12 | 108544714 | |||||||
| chr12:108544779 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.730-301C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 4/18 | chr12 | 108544779 | |||||||
| chr12:108544823 | C | T | 2 | a0001c0003t0002g0179 a0001c0003t0002g0180 |
2 | NA18971.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.729+316G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 4/18 | chr12 | 108544823 | |||||||
| chr12:108544854 | C | T | 1 | a0002c0004t0005g0049 | 2 | HG01891.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.729+285G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 4/18 | chr12 | 108544854 | |||||||
| chr12:108544974 | T | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(205): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.729+165A>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 4/18 | chr12 | 108544974 | |||||||
| chr12:108545407 | C | T | 1 | a0001c0007t0006g0033 | 2 | HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.545-84G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108545407 | |||||||
| chr12:108545809 | T | C | 43 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0027 others(40): Show |
58 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.545-486A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108545809 | |||||||
| chr12:108545967 | C | CA | 39 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0027 others(36): Show |
54 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.545-645dupT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108545967 | |||||||
| chr12:108545967 | C | CAA | 9 | a0001c0001t0001g0024 a0001c0001t0001g0104 a0001c0001t0001g0112 others(6): Show |
10 | HG02074.hp1 HG02129.hp2 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.545-646_545-645dup others(2): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108545967 | |||||||
| chr12:108545967 | C | CAAA | 106 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(103): Show |
154 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(151): Show |
intron_variant | MODIFIER | c.545-647_545-645dup others(3): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108545967 | |||||||
| chr12:108545967 | C | CAAAA | 49 | a0001c0001t0001g0062 a0001c0001t0001g0073 a0001c0001t0001g0085 others(46): Show |
75 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.545-648_545-645dup others(4): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108545967 | |||||||
| chr12:108545967 | C | CAAAAA | 6 | a0002c0002t0001g0212 a0002c0002t0001g0223 a0002c0002t0001g0233 others(3): Show |
6 | HG01192.hp1 HG01361.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.545-649_545-645dup others(5): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108545967 | |||||||
| chr12:108545967 | CA | C | 11 | a0001c0003t0002g0019 a0001c0003t0002g0039 a0001c0003t0002g0191 others(8): Show |
14 | HG02055.hp1 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.545-645delT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108545967 | |||||||
| chr12:108545985 | C | A | 41 | a0002c0004t0001g0004 a0002c0004t0001g0021 a0002c0004t0001g0046 others(38): Show |
53 | HG00639.hp2 HG00673.hp1 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.545-662G>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108545985 | |||||||
| chr12:108546104 | T | C | 2 | a0001c0010t0001g0051 a0001c0010t0001g0052 |
2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.545-781A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108546104 | |||||||
| chr12:108546125 | T | A | 246 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(243): Show |
351 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(348): Show |
intron_variant | MODIFIER | c.545-802A>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108546125 | |||||||
| chr12:108546137 | T | C | 1 | a0001c0001t0001g0086 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.545-814A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108546137 | |||||||
| chr12:108546231 | G | A | 2 | a0002c0002t0001g0218 a0002c0002t0001g0236 |
2 | HG00609.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.545-908C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108546231 | |||||||
| chr12:108546337 | C | T | 1 | a0001c0001t0001g0062 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.545-1014G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108546337 | |||||||
| chr12:108546367 | T | A | 1 | a0001c0007t0006g0033 | 2 | HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.545-1044A>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108546367 | |||||||
| chr12:108546369 | T | C | 4 | a0001c0003t0002g0039 a0001c0003t0002g0194 a0001c0003t0002g0196 others(1): Show |
5 | HG02055.hp2 HG02896.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.545-1046A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108546369 | |||||||
| chr12:108546522 | CT | C | 31 | a0001c0001t0001g0062 a0001c0003t0002g0195 a0001c0005t0002g0011 others(28): Show |
43 | HG01109.hp2 HG01167.hp1 HG01943.hp2 others(40): Show |
intron_variant | MODIFIER | c.545-1200delA | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108546522 | |||||||
| chr12:108546522 | CTT | C | 205 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(202): Show |
295 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.545-1201_545-1200d others(4): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108546522 | |||||||
| chr12:108546679 | C | T | 1 | a0002c0002t0001g0220 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.544+1208G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108546679 | |||||||
| chr12:108546741 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.544+1146C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108546741 | |||||||
| chr12:108546776 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.544+1111G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108546776 | |||||||
| chr12:108546778 | C | G | 1 | a0001c0001t0001g0061 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.544+1109G>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108546778 | |||||||
| chr12:108546779 | C | G | 1 | a0001c0001t0001g0061 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.544+1108G>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108546779 | |||||||
| chr12:108546780 | C | G | 1 | a0001c0001t0001g0061 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.544+1107G>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108546780 | |||||||
| chr12:108546907 | C | T | 1 | a0001c0003t0002g0195 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.544+980G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108546907 | |||||||
| chr12:108547008 | C | T | 1 | a0002c0002t0001g0212 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.544+879G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108547008 | |||||||
| chr12:108547182 | G | A | 223 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(220): Show |
319 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(316): Show |
intron_variant | MODIFIER | c.544+705C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108547182 | |||||||
| chr12:108547205 | T | C | 1 | a0002c0009t0001g0237 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.544+682A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108547205 | |||||||
| chr12:108547278 | G | A | 4 | a0001c0007t0002g0010 a0001c0007t0002g0152 a0001c0007t0002g0155 others(1): Show |
7 | HG01167.hp1 HG02109.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.544+609C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108547278 | |||||||
| chr12:108547509 | C | G | 1 | a0003c0008t0001g0077 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.544+378G>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108547509 | |||||||
| chr12:108547563 | T | A | 1 | a0001c0005t0002g0042 | 2 | NA18945.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.544+324A>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108547563 | |||||||
| chr12:108547573 | T | C | 15 | a0001c0006t0001g0034 a0001c0006t0001g0035 a0001c0006t0001g0149 others(12): Show |
21 | HG01109.hp2 HG01167.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.544+314A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108547573 | |||||||
| chr12:108547671 | T | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(205): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.544+216A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108547671 | |||||||
| chr12:108547846 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.544+41A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 3/18 | chr12 | 108547846 | |||||||
| chr12:108548252 | C | T | 2 | a0001c0010t0001g0051 a0001c0010t0001g0052 |
2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.440-261G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 2/18 | chr12 | 108548252 | |||||||
| chr12:108548274 | T | C | 1 | a0001c0001t0001g0072 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.440-283A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 2/18 | chr12 | 108548274 | |||||||
| chr12:108548281 | A | G | 1 | a0001c0001t0001g0076 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.440-290T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 2/18 | chr12 | 108548281 | |||||||
| chr12:108548319 | C | T | 5 | a0002c0002t0001g0211 a0002c0002t0001g0224 a0002c0002t0001g0247 others(2): Show |
5 | NA18955.hp1 NA19011.hp1 NA19076.hp2 others(2): Show |
intron_variant | MODIFIER | c.440-328G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 2/18 | chr12 | 108548319 | |||||||
| chr12:108548340 | T | A | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(205): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.440-349A>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 2/18 | chr12 | 108548340 | |||||||
| chr12:108548774 | C | T | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(205): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.439+314G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 2/18 | chr12 | 108548774 | |||||||
| chr12:108548994 | GT | G | 34 | a0002c0004t0001g0004 a0002c0004t0001g0021 a0002c0004t0001g0046 others(31): Show |
45 | HG00639.hp2 HG00673.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.439+93delA | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 2/18 | chr12 | 108548994 | |||||||
| chr12:108548999 | C | G | 34 | a0002c0004t0001g0004 a0002c0004t0001g0021 a0002c0004t0001g0046 others(31): Show |
45 | HG00639.hp2 HG00673.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.439+89G>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 2/18 | chr12 | 108548999 | |||||||
| chr12:108549252 | G | A | 223 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(220): Show |
319 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(316): Show |
intron_variant | MODIFIER | c.313-38C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108549252 | |||||||
| chr12:108549322 | G | C | 15 | a0001c0006t0001g0034 a0001c0006t0001g0035 a0001c0006t0001g0149 others(12): Show |
21 | HG01109.hp2 HG01167.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.313-108C>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108549322 | |||||||
| chr12:108549520 | T | A | 47 | a0002c0002t0001g0002 a0002c0002t0001g0005 a0002c0002t0001g0012 others(44): Show |
73 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.313-306A>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108549520 | |||||||
| chr12:108549595 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.313-381G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108549595 | |||||||
| chr12:108549781 | C | T | 8 | a0001c0005t0002g0204 a0001c0005t0002g0205 a0002c0002t0001g0210 others(5): Show |
8 | HG02647.hp1 HG02886.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.313-567G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108549781 | |||||||
| chr12:108549927 | C | T | 11 | a0001c0003t0002g0019 a0001c0003t0002g0039 a0001c0003t0002g0191 others(8): Show |
14 | HG02055.hp1 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.313-713G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108549927 | |||||||
| chr12:108549956 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.313-742G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108549956 | |||||||
| chr12:108549972 | C | T | 41 | a0002c0004t0001g0004 a0002c0004t0001g0021 a0002c0004t0001g0046 others(38): Show |
53 | HG00639.hp2 HG00673.hp1 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.313-758G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108549972 | |||||||
| chr12:108550013 | CA | C | 19 | a0001c0001t0001g0108 a0001c0001t0001g0145 a0001c0001t0001g0146 others(16): Show |
25 | HG01243.hp2 HG01943.hp2 HG02074.hp1 others(22): Show |
intron_variant | MODIFIER | c.313-800delT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108550013 | |||||||
| chr12:108550013 | CAA | C | 128 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0027 others(125): Show |
180 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.313-801_313-800del others(2): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108550013 | |||||||
| chr12:108550013 | CAAA | C | 69 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0013 others(66): Show |
104 | HG00323.hp1 HG00609.hp2 HG00673.hp2 others(101): Show |
intron_variant | MODIFIER | c.313-802_313-800del others(3): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108550013 | |||||||
| chr12:108550013 | CAAAA | C | 6 | a0001c0001t0001g0007 a0001c0001t0001g0060 a0001c0001t0001g0075 others(3): Show |
9 | HG00597.hp1 HG02809.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.313-803_313-800del others(4): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108550013 | |||||||
| chr12:108550453 | T | A | 246 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(243): Show |
351 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(348): Show |
intron_variant | MODIFIER | c.313-1239A>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108550453 | |||||||
| chr12:108550469 | G | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(205): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.313-1255C>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108550469 | |||||||
| chr12:108550535 | C | A | 11 | a0001c0003t0002g0019 a0001c0003t0002g0039 a0001c0003t0002g0191 others(8): Show |
14 | HG02055.hp1 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.313-1321G>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108550535 | |||||||
| chr12:108550715 | T | C | 12 | a0001c0005t0002g0011 a0001c0005t0002g0040 a0001c0005t0002g0041 others(9): Show |
18 | HG01943.hp2 HG02572.hp1 HG02723.hp1 others(15): Show |
intron_variant | MODIFIER | c.313-1501A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108550715 | |||||||
| chr12:108550721 | G | A | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(205): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.313-1507C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108550721 | |||||||
| chr12:108550740 | G | A | 2 | a0001c0003t0002g0183 a0001c0003t0002g0184 |
2 | NA18991.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.313-1526C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108550740 | |||||||
| chr12:108550776 | T | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(205): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.313-1562A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108550776 | |||||||
| chr12:108550966 | C | T | 1 | a0001c0003t0002g0163 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.313-1752G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108550966 | |||||||
| chr12:108550981 | T | C | 1 | a0001c0001t0001g0073 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.313-1767A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108550981 | |||||||
| chr12:108551183 | G | A | 1 | a0001c0005t0002g0203 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.313-1969C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108551183 | |||||||
| chr12:108551209 | A | G | 15 | a0001c0006t0001g0034 a0001c0006t0001g0035 a0001c0006t0001g0149 others(12): Show |
21 | HG01109.hp2 HG01167.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.313-1995T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108551209 | |||||||
| chr12:108551222 | G | A | 9 | a0001c0001t0001g0030 a0001c0001t0001g0132 a0001c0001t0001g0133 others(6): Show |
11 | HG01168.hp2 HG01169.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.313-2008C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108551222 | |||||||
| chr12:108551457 | G | A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.313-2243C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108551457 | |||||||
| chr12:108551465 | G | A | 1 | a0001c0006t0001g0149 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.313-2251C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108551465 | |||||||
| chr12:108551473 | A | G | 2 | a0001c0003t0002g0177 a0001c0003t0002g0178 |
2 | HG02027.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.313-2259T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108551473 | |||||||
| chr12:108551625 | G | A | 1 | a0001c0005t0002g0200 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.313-2411C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108551625 | |||||||
| chr12:108551676 | G | A | 1 | a0002c0002t0001g0209 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.313-2462C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108551676 | |||||||
| chr12:108551816 | G | A | 11 | a0001c0003t0002g0019 a0001c0003t0002g0039 a0001c0003t0002g0191 others(8): Show |
14 | HG02055.hp1 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.313-2602C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108551816 | |||||||
| chr12:108551834 | A | G | 64 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(61): Show |
99 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.313-2620T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108551834 | |||||||
| chr12:108551934 | G | A | 1 | a0001c0006t0001g0156 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.313-2720C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108551934 | |||||||
| chr12:108551950 | T | TA | 15 | a0001c0006t0001g0034 a0001c0006t0001g0035 a0001c0006t0001g0149 others(12): Show |
21 | HG01109.hp2 HG01167.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.313-2737dupT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108551950 | |||||||
| chr12:108552145 | G | C | 223 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(220): Show |
319 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(316): Show |
intron_variant | MODIFIER | c.313-2931C>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108552145 | |||||||
| chr12:108552206 | G | C | 1 | a0002c0004t0005g0264 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.313-2992C>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108552206 | |||||||
| chr12:108552391 | T | G | 17 | a0001c0003t0002g0038 a0001c0003t0002g0160 a0001c0003t0002g0161 others(14): Show |
18 | HG00544.hp2 HG01496.hp1 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.313-3177A>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108552391 | |||||||
| chr12:108552442 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.313-3228A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108552442 | |||||||
| chr12:108552450 | T | C | 64 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(61): Show |
99 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.313-3236A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108552450 | |||||||
| chr12:108552472 | TA | T | 216 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(213): Show |
309 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(306): Show |
intron_variant | MODIFIER | c.313-3259delT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108552472 | |||||||
| chr12:108552542 | C | A | 1 | a0001c0001t0001g0127 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.313-3328G>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108552542 | |||||||
| chr12:108552542 | C | CA | 93 | a0001c0001t0001g0026 a0001c0001t0001g0145 a0001c0001t0001g0146 others(90): Show |
132 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(129): Show |
intron_variant | MODIFIER | c.313-3329dupT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108552542 | |||||||
| chr12:108552542 | C | CAA | 14 | a0001c0006t0001g0034 a0001c0006t0001g0035 a0001c0006t0001g0149 others(11): Show |
20 | HG01109.hp2 HG02109.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.313-3330_313-3329d others(4): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108552542 | |||||||
| chr12:108552554 | C | A | 15 | a0001c0006t0001g0034 a0001c0006t0001g0035 a0001c0006t0001g0149 others(12): Show |
21 | HG01109.hp2 HG01167.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.313-3340G>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108552554 | |||||||
| chr12:108552676 | T | C | 1 | a0001c0015t0002g0170 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.313-3462A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108552676 | |||||||
| chr12:108552844 | A | G | 12 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0103 others(9): Show |
16 | NA18942.hp1 NA18946.hp1 NA18953.hp1 others(13): Show |
intron_variant | MODIFIER | c.313-3630T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108552844 | |||||||
| chr12:108552942 | C | G | 43 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0027 others(40): Show |
58 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.313-3728G>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108552942 | |||||||
| chr12:108553022 | G | C | 64 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(61): Show |
99 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.313-3808C>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108553022 | |||||||
| chr12:108553099 | G | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(61): Show |
99 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.313-3885C>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108553099 | |||||||
| chr12:108553178 | T | C | 12 | a0001c0005t0002g0011 a0001c0005t0002g0040 a0001c0005t0002g0041 others(9): Show |
18 | HG01943.hp2 HG02572.hp1 HG02723.hp1 others(15): Show |
intron_variant | MODIFIER | c.313-3964A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108553178 | |||||||
| chr12:108553351 | T | C | 1 | a0001c0001t0001g0128 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.313-4137A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108553351 | |||||||
| chr12:108553787 | G | A | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG01243.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.313-4573C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108553787 | |||||||
| chr12:108553876 | G | C | 67 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(64): Show |
103 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.313-4662C>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108553876 | |||||||
| chr12:108553953 | C | A | 1 | a0002c0002t0001g0239 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.313-4739G>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108553953 | |||||||
| chr12:108553984 | C | T | 1 | a0001c0001t0003g0056 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.313-4770G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108553984 | |||||||
| chr12:108554127 | G | C | 1 | a0001c0006t0001g0156 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.313-4913C>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108554127 | |||||||
| chr12:108554131 | C | CCCCCGCC others(5): Show |
234 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(231): Show |
333 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.313-4918_313-4917i others(14): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108554131 | |||||||
| chr12:108554300 | A | G | 1 | a0002c0004t0001g0245 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.313-5086T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108554300 | |||||||
| chr12:108554302 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.313-5088T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108554302 | |||||||
| chr12:108554392 | G | A | 15 | a0001c0006t0001g0034 a0001c0006t0001g0035 a0001c0006t0001g0149 others(12): Show |
21 | HG01109.hp2 HG01167.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.313-5178C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108554392 | |||||||
| chr12:108554844 | T | C | 11 | a0001c0003t0002g0019 a0001c0003t0002g0039 a0001c0003t0002g0191 others(8): Show |
14 | HG02055.hp1 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.313-5630A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108554844 | |||||||
| chr12:108554886 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.313-5672G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108554886 | |||||||
| chr12:108554896 | A | G | 1 | a0001c0006t0001g0157 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.313-5682T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108554896 | |||||||
| chr12:108555231 | T | G | 12 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0103 others(9): Show |
16 | NA18942.hp1 NA18946.hp1 NA18953.hp1 others(13): Show |
intron_variant | MODIFIER | c.312+5612A>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108555231 | |||||||
| chr12:108555431 | G | A | 1 | a0001c0003t0002g0197 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.312+5412C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108555431 | |||||||
| chr12:108555483 | G | T | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(205): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.312+5360C>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108555483 | |||||||
| chr12:108555507 | C | T | 246 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(243): Show |
351 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(348): Show |
intron_variant | MODIFIER | c.312+5336G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108555507 | |||||||
| chr12:108555580 | G | A | 2 | a0001c0005t0002g0204 a0001c0005t0002g0205 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.312+5263C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108555580 | |||||||
| chr12:108555766 | T | G | 14 | a0001c0006t0001g0034 a0001c0006t0001g0035 a0001c0006t0001g0149 others(11): Show |
19 | HG01109.hp2 HG01167.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.312+5077A>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108555766 | |||||||
| chr12:108555781 | C | T | 120 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(117): Show |
172 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.312+5062G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108555781 | |||||||
| chr12:108555820 | T | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(205): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.312+5023A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108555820 | |||||||
| chr12:108555884 | C | G | 47 | a0002c0002t0001g0002 a0002c0002t0001g0005 a0002c0002t0001g0012 others(44): Show |
73 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.312+4959G>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108555884 | |||||||
| chr12:108555929 | G | A | 41 | a0002c0004t0001g0004 a0002c0004t0001g0021 a0002c0004t0001g0046 others(38): Show |
53 | HG00639.hp2 HG00673.hp1 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.312+4914C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108555929 | |||||||
| chr12:108555963 | T | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(205): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.312+4880A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108555963 | |||||||
| chr12:108555989 | T | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG02602.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.312+4854A>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108555989 | |||||||
| chr12:108556100 | CT | C | 206 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(203): Show |
296 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.312+4742delA | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108556100 | |||||||
| chr12:108556190 | C | G | 120 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(117): Show |
172 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.312+4653G>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108556190 | |||||||
| chr12:108556368 | G | T | 1 | a0001c0003t0002g0162 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.312+4475C>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108556368 | |||||||
| chr12:108556441 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.312+4402A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108556441 | |||||||
| chr12:108556574 | C | A | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG01243.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.312+4269G>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108556574 | |||||||
| chr12:108556678 | T | C | 1 | a0001c0001t0001g0129 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.312+4165A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108556678 | |||||||
| chr12:108556793 | T | C | 1 | a0002c0004t0001g0246 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.312+4050A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108556793 | |||||||
| chr12:108556950 | G | A | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(205): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.312+3893C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108556950 | |||||||
| chr12:108557090 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.312+3753A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108557090 | |||||||
| chr12:108557171 | G | A | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(205): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.312+3672C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108557171 | |||||||
| chr12:108557206 | G | GT | 98 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0030 others(95): Show |
122 | HG00544.hp1 HG00597.hp1 HG00673.hp1 others(119): Show |
intron_variant | MODIFIER | c.312+3636dupA | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108557206 | |||||||
| chr12:108557206 | G | GTT | 23 | a0001c0001t0001g0024 a0001c0001t0001g0132 a0001c0003t0002g0194 others(20): Show |
32 | HG00609.hp1 HG00621.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.312+3635_312+3636d others(4): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108557206 | |||||||
| chr12:108557206 | G | GTTT | 9 | a0001c0006t0001g0034 a0001c0006t0001g0035 a0001c0006t0001g0150 others(6): Show |
15 | HG00423.hp2 HG01109.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.312+3634_312+3636d others(5): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108557206 | |||||||
| chr12:108557206 | GTTT | G | 10 | a0001c0005t0002g0011 a0001c0005t0002g0040 a0001c0005t0002g0041 others(7): Show |
16 | HG01943.hp2 HG02723.hp1 HG02895.hp1 others(13): Show |
intron_variant | MODIFIER | c.312+3634_312+3636d others(5): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108557206 | |||||||
| chr12:108557206 | GTTTTTTT others(8): Show |
G | 1 | a0001c0001t0001g0092 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.312+3622_312+3636d others(17): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108557206 | |||||||
| chr12:108557236 | T | C | 1 | a0001c0001t0001g0026 | 2 | NA19012.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.312+3607A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108557236 | |||||||
| chr12:108557309 | G | A | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG01243.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.312+3534C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108557309 | |||||||
| chr12:108557317 | G | A | 2 | a0001c0001t0001g0093 a0001c0003t0002g0185 |
2 | HG02165.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.312+3526C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108557317 | |||||||
| chr12:108557531 | T | C | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | HG01074.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.312+3312A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108557531 | |||||||
| chr12:108557551 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.312+3292C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108557551 | |||||||
| chr12:108557711 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0094 |
5 | NA18965.hp2 NA18968.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.312+3132C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108557711 | |||||||
| chr12:108557739 | C | T | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(205): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.312+3104G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108557739 | |||||||
| chr12:108557765 | G | A | 11 | a0001c0003t0002g0019 a0001c0003t0002g0039 a0001c0003t0002g0191 others(8): Show |
14 | HG02055.hp1 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.312+3078C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108557765 | |||||||
| chr12:108557829 | T | G | 1 | a0001c0001t0001g0095 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.312+3014A>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108557829 | |||||||
| chr12:108557864 | A | T | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(205): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.312+2979T>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108557864 | |||||||
| chr12:108557912 | C | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(61): Show |
99 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.312+2931G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108557912 | |||||||
| chr12:108557981 | T | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(205): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.312+2862A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108557981 | |||||||
| chr12:108558038 | G | T | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(205): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.312+2805C>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108558038 | |||||||
| chr12:108558111 | G | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(205): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.312+2732C>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108558111 | |||||||
| chr12:108558133 | C | G | 1 | a0001c0003t0002g0161 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.312+2710G>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108558133 | |||||||
| chr12:108558140 | A | C | 234 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(231): Show |
333 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.312+2703T>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108558140 | |||||||
| chr12:108558175 | T | A | 223 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(220): Show |
319 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(316): Show |
intron_variant | MODIFIER | c.312+2668A>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108558175 | |||||||
| chr12:108558178 | T | C | 1 | a0001c0007t0006g0033 | 2 | HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.312+2665A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108558178 | |||||||
| chr12:108558295 | A | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(70): Show |
110 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.312+2548T>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108558295 | |||||||
| chr12:108558612 | G | A | 13 | a0001c0003t0002g0193 a0001c0005t0002g0011 a0001c0005t0002g0040 others(10): Show |
19 | HG01943.hp2 HG02559.hp2 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.312+2231C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108558612 | |||||||
| chr12:108558663 | C | T | 3 | a0001c0003t0002g0191 a0001c0003t0002g0192 a0001c0003t0002g0193 |
3 | HG02559.hp2 HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.312+2180G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108558663 | |||||||
| chr12:108558715 | T | A | 3 | a0001c0006t0001g0035 a0001c0006t0001g0149 a0001c0006t0001g0157 |
4 | HG01109.hp2 HG02615.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.312+2128A>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108558715 | |||||||
| chr12:108558737 | T | C | 12 | a0001c0005t0002g0011 a0001c0005t0002g0040 a0001c0005t0002g0041 others(9): Show |
18 | HG01943.hp2 HG02572.hp1 HG02723.hp1 others(15): Show |
intron_variant | MODIFIER | c.312+2106A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108558737 | |||||||
| chr12:108558756 | A | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(205): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.312+2087T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108558756 | |||||||
| chr12:108558815 | C | T | 45 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0027 others(42): Show |
60 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.312+2028G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108558815 | |||||||
| chr12:108558958 | G | A | 1 | a0004c0012t0001g0047 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.312+1885C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108558958 | |||||||
| chr12:108558999 | C | A | 1 | a0002c0004t0001g0275 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.312+1844G>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108558999 | |||||||
| chr12:108559039 | G | GA | 107 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(104): Show |
170 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.312+1803dupT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559039 | |||||||
| chr12:108559039 | G | GAA | 22 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0102 others(19): Show |
26 | HG01070.hp2 HG01169.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.312+1802_312+1803d others(4): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559039 | |||||||
| chr12:108559039 | G | GAAA | 82 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0027 others(79): Show |
112 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.312+1801_312+1803d others(5): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559039 | |||||||
| chr12:108559039 | G | GAAAA | 7 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0145 others(4): Show |
7 | HG01167.hp1 HG01243.hp2 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.312+1800_312+1803d others(6): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559039 | |||||||
| chr12:108559039 | GAA | G | 5 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0002c0004t0001g0046 others(2): Show |
6 | HG02602.hp2 HG03017.hp2 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.312+1802_312+1803d others(4): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559039 | |||||||
| chr12:108559177 | C | T | 1 | a0001c0006t0001g0149 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.312+1666G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559177 | |||||||
| chr12:108559205 | A | C | 1 | a0001c0001t0001g0099 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.312+1638T>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559205 | |||||||
| chr12:108559257 | T | G | 14 | a0001c0006t0001g0034 a0001c0006t0001g0035 a0001c0006t0001g0149 others(11): Show |
19 | HG01109.hp2 HG01167.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.312+1586A>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559257 | |||||||
| chr12:108559321 | A | C | 1 | a0001c0001t0001g0098 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.312+1522T>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559321 | |||||||
| chr12:108559322 | A | C | 64 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(61): Show |
99 | HG00323.hp1 HG00597.hp1 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.312+1521T>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559322 | |||||||
| chr12:108559481 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0055 |
3 | NA18947.hp1 NA18988.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.312+1362G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559481 | |||||||
| chr12:108559495 | G | A | 12 | a0001c0005t0002g0011 a0001c0005t0002g0040 a0001c0005t0002g0041 others(9): Show |
18 | HG01943.hp2 HG02572.hp1 HG02723.hp1 others(15): Show |
intron_variant | MODIFIER | c.312+1348C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559495 | |||||||
| chr12:108559547 | C | G | 3 | a0001c0003t0002g0191 a0001c0003t0002g0192 a0001c0003t0002g0193 |
3 | HG02559.hp2 HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.312+1296G>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559547 | |||||||
| chr12:108559569 | G | A | 2 | a0001c0010t0001g0051 a0001c0010t0001g0052 |
2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.312+1274C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559569 | |||||||
| chr12:108559664 | C | CA | 8 | a0001c0003t0002g0186 a0001c0003t0002g0187 a0001c0003t0002g0188 others(5): Show |
11 | HG00544.hp2 HG01516.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.312+1178dupT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559664 | |||||||
| chr12:108559664 | C | CAA | 5 | a0001c0003t0002g0019 a0001c0003t0002g0039 a0001c0003t0002g0196 others(2): Show |
8 | HG02895.hp2 HG02896.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.312+1177_312+1178d others(4): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559664 | |||||||
| chr12:108559664 | CA | C | 62 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(59): Show |
82 | HG00639.hp2 HG00673.hp1 HG00673.hp2 others(79): Show |
intron_variant | MODIFIER | c.312+1178delT | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559664 | |||||||
| chr12:108559664 | CAA | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(155): Show |
235 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.312+1177_312+1178d others(4): Show |
SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559664 | |||||||
| chr12:108559686 | A | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0054 |
3 | HG01071.hp2 HG01433.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.312+1157T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559686 | |||||||
| chr12:108559693 | A | G | 1 | a0002c0004t0001g0208 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.312+1150T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559693 | |||||||
| chr12:108559780 | C | T | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(205): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.312+1063G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559780 | |||||||
| chr12:108559953 | C | T | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(205): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.312+890G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559953 | |||||||
| chr12:108559991 | G | A | 11 | a0001c0003t0002g0019 a0001c0003t0002g0039 a0001c0003t0002g0191 others(8): Show |
14 | HG02055.hp1 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.312+852C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108559991 | |||||||
| chr12:108560053 | G | A | 1 | a0007c0016t0001g0280 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.312+790C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108560053 | |||||||
| chr12:108560079 | G | A | 12 | a0001c0005t0002g0011 a0001c0005t0002g0040 a0001c0005t0002g0041 others(9): Show |
18 | HG01943.hp2 HG02572.hp1 HG02723.hp1 others(15): Show |
intron_variant | MODIFIER | c.312+764C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108560079 | |||||||
| chr12:108560140 | T | C | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG01243.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.312+703A>G | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108560140 | |||||||
| chr12:108560179 | G | A | 1 | a0002c0004t0001g0281 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.312+664C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108560179 | |||||||
| chr12:108560254 | C | T | 15 | a0001c0006t0001g0034 a0001c0006t0001g0035 a0001c0006t0001g0149 others(12): Show |
21 | HG01109.hp2 HG01167.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.312+589G>A | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108560254 | |||||||
| chr12:108560457 | T | TC | 3 | a0001c0001t0001g0032 a0001c0001t0001g0147 a0001c0001t0001g0148 |
4 | HG02602.hp2 HG03017.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.312+385dupG | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108560457 | |||||||
| chr12:108560570 | A | G | 2 | a0001c0010t0001g0051 a0001c0010t0001g0052 |
2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.312+273T>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108560570 | |||||||
| chr12:108560648 | G | A | 1 | a0001c0003t0002g0207 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.312+195C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108560648 | |||||||
| chr12:108560702 | C | G | 1 | a0001c0001t0001g0050 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.312+141G>C | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108560702 | |||||||
| chr12:108560726 | G | A | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(205): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.312+117C>T | SART3 | ENSG00000075856.12 | transcript | ENST00000546815.6 | protein_coding | 1/18 | chr12 | 108560726 |