Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2769 |
| ensemblid | ENSG00000060558.4 |
| hgncid | 4383 |
| symbol | GNA15 |
| name | G protein subunit alpha 15 |
| refseq_nuc | NM_002068.4 |
| refseq_prot | NP_002059.3 |
| ensembl_nuc | ENST00000262958.4 |
| ensembl_prot | ENSP00000262958.2 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 3136033 |
| end | 3163749 |
| strand | + |
| ver | v1.2 |
| region | chr19:3136033-3163749 |
| region5000 | chr19:3131033-3168749 |
| regionname0 | GNA15_chr19_3136033_3163749 |
| regionname5000 | GNA15_chr19_3131033_3168749 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 374 | 439 | 96 | 82 | 191 | 18 | 50 | 149 | GNA15_chr19_3131033_3168749 | GNA15 | MARSL others(369): Show |
chr19 | 3131033 | 3168749 |
| a0002 | 0/0 | 374 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | MARSL others(369): Show |
chr19 | 3131033 | 3168749 |
| a0003 | 0/0 | 374 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | GNA15_chr19_3131033_3168749 | GNA15 | MARSL others(369): Show |
chr19 | 3131033 | 3168749 |
| a0004 | 0/0 | 374 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | MARSL others(369): Show |
chr19 | 3131033 | 3168749 |
| a0005 | 0/0 | 374 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | MARSL others(369): Show |
chr19 | 3131033 | 3168749 |
| a0006 | 0/0 | 374 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | MARSL others(369): Show |
chr19 | 3131033 | 3168749 |
| a0007 | 0/0 | 374 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | MARSL others(369): Show |
chr19 | 3131033 | 3168749 |
| a0008 | 0/0 | 374 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | MAHSL others(369): Show |
chr19 | 3131033 | 3168749 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1122 | 194 | 47 | 37 | 75 | 9 | 24 | GNA15_chr19_3131033_3168749 | GNA15 | ATGGC others(1117): Show |
chr19 | 3131033 | 3168749 | ||
| a0001c0002 | 0/0 | 1122 | 172 | 21 | 22 | 109 | 4 | 16 | GNA15_chr19_3131033_3168749 | GNA15 | ATGGC others(1117): Show |
chr19 | 3131033 | 3168749 | ||
| a0001c0003 | 0/0 | 1122 | 60 | 16 | 23 | 7 | 5 | 9 | GNA15_chr19_3131033_3168749 | GNA15 | ATGGC others(1117): Show |
chr19 | 3131033 | 3168749 | ||
| a0001c0004 | 0/0 | 1122 | 6 | 6 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | ATGGC others(1117): Show |
chr19 | 3131033 | 3168749 | ||
| a0001c0007 | 0/0 | 1122 | 2 | 2 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | ATGGC others(1117): Show |
chr19 | 3131033 | 3168749 | ||
| a0001c0008 | 0/0 | 1122 | 2 | 2 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | ATGGC others(1117): Show |
chr19 | 3131033 | 3168749 | ||
| a0001c0009 | 0/0 | 1122 | 2 | 2 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | ATGGC others(1117): Show |
chr19 | 3131033 | 3168749 | ||
| a0001c0012 | 0/0 | 1122 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | ATGGC others(1117): Show |
chr19 | 3131033 | 3168749 | ||
| a0002c0005 | 0/0 | 1122 | 3 | 3 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | ATGGC others(1117): Show |
chr19 | 3131033 | 3168749 | ||
| a0003c0006 | 0/0 | 1122 | 3 | 0 | 0 | 3 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | ATGGC others(1117): Show |
chr19 | 3131033 | 3168749 | ||
| a0004c0013 | 0/0 | 1122 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | ATGGC others(1117): Show |
chr19 | 3131033 | 3168749 | ||
| a0005c0011 | 0/0 | 1122 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | ATGGC others(1117): Show |
chr19 | 3131033 | 3168749 | ||
| a0006c0014 | 0/0 | 1122 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | ATGGC others(1117): Show |
chr19 | 3131033 | 3168749 | ||
| a0007c0015 | 0/0 | 1122 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | ATGGC others(1117): Show |
chr19 | 3131033 | 3168749 | ||
| a0008c0010 | 0/0 | 1122 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | ATGGC others(1117): Show |
chr19 | 3131033 | 3168749 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2273 | 164 | 30 | 31 | 75 | 4 | 23 | GNA15_chr19_3131033_3168749 | GNA15 | AGAAG others(2268): Show |
chr19 | 3131033 | 3168749 |
| a0001c0001t0002 | 0/0 | 2273 | 9 | 7 | 2 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | AGAAG others(2268): Show |
chr19 | 3131033 | 3168749 |
| a0001c0001t0003 | 0/1 | 2273 | 3 | 0 | 1 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | AGAAG others(2268): Show |
chr19 | 3131033 | 3168749 |
| a0001c0001t0004 | 0/0 | 2273 | 4 | 4 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | AGAAG others(2268): Show |
chr19 | 3131033 | 3168749 |
| a0001c0001t0005 | 0/0 | 2273 | 5 | 0 | 2 | 0 | 3 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | AGAAG others(2268): Show |
chr19 | 3131033 | 3168749 |
| a0001c0001t0006 | 0/0 | 2273 | 4 | 1 | 1 | 0 | 2 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | AGAAG others(2268): Show |
chr19 | 3131033 | 3168749 |
| a0001c0001t0009 | 0/0 | 2273 | 2 | 2 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | AGAAG others(2268): Show |
chr19 | 3131033 | 3168749 |
| a0001c0001t0010 | 0/0 | 2273 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | AGAAG others(2268): Show |
chr19 | 3131033 | 3168749 |
| a0001c0001t0011 | 0/0 | 2273 | 2 | 2 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | AGAAG others(2268): Show |
chr19 | 3131033 | 3168749 |
| a0001c0002t0001 | 0/0 | 2273 | 162 | 20 | 22 | 102 | 4 | 14 | GNA15_chr19_3131033_3168749 | GNA15 | AGAAG others(2268): Show |
chr19 | 3131033 | 3168749 |
| a0001c0002t0007 | 0/0 | 2273 | 3 | 0 | 0 | 3 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | AGAAG others(2268): Show |
chr19 | 3131033 | 3168749 |
| a0001c0002t0008 | 0/0 | 2273 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | AGAAG others(2268): Show |
chr19 | 3131033 | 3168749 |
| a0001c0002t0013 | 0/0 | 2273 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | AGAAG others(2268): Show |
chr19 | 3131033 | 3168749 |
| a0001c0002t0014 | 0/0 | 2273 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | AGAAG others(2268): Show |
chr19 | 3131033 | 3168749 |
| a0001c0002t0016 | 0/0 | 2273 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | AGAAG others(2268): Show |
chr19 | 3131033 | 3168749 |
| a0001c0002t0018 | 0/0 | 2273 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | AGAAG others(2268): Show |
chr19 | 3131033 | 3168749 |
| a0001c0002t0019 | 0/0 | 2273 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | AGAAG others(2268): Show |
chr19 | 3131033 | 3168749 |
| a0001c0002t0021 | 0/0 | 2273 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | AGAAG others(2268): Show |
chr19 | 3131033 | 3168749 |
| a0001c0003t0001 | 0/0 | 2273 | 51 | 13 | 18 | 7 | 5 | 8 | GNA15_chr19_3131033_3168749 | GNA15 | AGAAG others(2268): Show |
chr19 | 3131033 | 3168749 |
| a0001c0003t0003 | 0/0 | 2273 | 6 | 0 | 5 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | AGAAG others(2268): Show |
chr19 | 3131033 | 3168749 |
| a0001c0003t0004 | 0/0 | 2273 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | AGAAG others(2268): Show |
chr19 | 3131033 | 3168749 |
| a0001c0003t0008 | 0/0 | 2273 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | AGAAG others(2268): Show |
chr19 | 3131033 | 3168749 |
| a0001c0003t0015 | 0/0 | 2273 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | AGAAG others(2268): Show |
chr19 | 3131033 | 3168749 |
| a0001c0004t0001 | 0/0 | 2273 | 5 | 5 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | AGAAG others(2268): Show |
chr19 | 3131033 | 3168749 |
| a0001c0004t0004 | 0/0 | 2273 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | AGAAG others(2268): Show |
chr19 | 3131033 | 3168749 |
| a0001c0007t0010 | 0/0 | 2273 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | AGAAG others(2268): Show |
chr19 | 3131033 | 3168749 |
| a0001c0007t0012 | 0/0 | 2273 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | AGAAG others(2268): Show |
chr19 | 3131033 | 3168749 |
| a0001c0008t0001 | 0/0 | 2273 | 2 | 2 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | AGAAG others(2268): Show |
chr19 | 3131033 | 3168749 |
| a0001c0009t0001 | 0/0 | 2273 | 2 | 2 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | AGAAG others(2268): Show |
chr19 | 3131033 | 3168749 |
| a0001c0012t0005 | 0/0 | 2273 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | AGAAG others(2268): Show |
chr19 | 3131033 | 3168749 |
| a0002c0005t0001 | 0/0 | 2273 | 2 | 2 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | AGAAG others(2268): Show |
chr19 | 3131033 | 3168749 |
| a0002c0005t0017 | 0/0 | 2273 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | AGAAG others(2268): Show |
chr19 | 3131033 | 3168749 |
| a0003c0006t0001 | 0/0 | 2273 | 3 | 0 | 0 | 3 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | AGAAG others(2268): Show |
chr19 | 3131033 | 3168749 |
| a0004c0013t0001 | 0/0 | 2273 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | AGAAG others(2268): Show |
chr19 | 3131033 | 3168749 |
| a0005c0011t0020 | 0/0 | 2273 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | AGAAG others(2268): Show |
chr19 | 3131033 | 3168749 |
| a0006c0014t0001 | 0/0 | 2273 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | AGAAG others(2268): Show |
chr19 | 3131033 | 3168749 |
| a0007c0015t0001 | 0/0 | 2273 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | AGAAG others(2268): Show |
chr19 | 3131033 | 3168749 |
| a0008c0010t0001 | 0/0 | 2273 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | AGAAG others(2268): Show |
chr19 | 3131033 | 3168749 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0384 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0385 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0388 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0390 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0392 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0393 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0397 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0399 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0402 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0403 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0001g0418 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0002g0404 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0002g0406 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0002g0407 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0002g0409 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0002g0410 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0002g0411 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0002g0413 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0003g0221 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0004g0405 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0004g0415 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0004g0416 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0004g0417 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0005g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0005g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0005g0347 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0005g0348 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0005g0349 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0006g0021 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0006g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0006g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0009g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0009g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0010g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0011g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0001t0011g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0001 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0391 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0394 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0396 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0001g0398 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0007g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0007g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0008g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0013g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0014g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0016g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0018g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0019g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0002t0021g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0395 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0400 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0001g0401 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0003g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0004g0412 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0008g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0003t0015g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0004t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0004t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0004t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0004t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0004t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0004t0004g0414 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0007t0010g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0007t0012g0408 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0008t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0008t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0009t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0009t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0001c0012t0005g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0002c0005t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0002c0005t0001g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0002c0005t0017g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0003c0006t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0003c0006t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0004c0013t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0005c0011t0020g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0006c0014t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0007c0015t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| a0008c0010t0001g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0005 | g0348 | EUR | GBR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG00099 | hp2 | a0001 | c0003 | t0001 | g0286 | EUR | GBR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG00140 | hp1 | a0001 | c0003 | t0001 | g0227 | EUR | GBR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0222 | EUR | GBR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG00280 | hp1 | a0001 | c0003 | t0001 | g0207 | EUR | FIN | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG00280 | hp2 | a0001 | c0003 | t0001 | g0085 | EUR | FIN | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG00323 | hp1 | a0001 | c0001 | t0005 | g0349 | EUR | FIN | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0031 | EUR | FIN | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0365 | EAS | CHS | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0325 | EAS | CHS | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0154 | EAS | CHS | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0054 | EAS | CHS | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0368 | EAS | CHS | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | CHS | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0358 | EAS | CHS | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG00639 | hp2 | a0001 | c0003 | t0001 | g0008 | AMR | PUR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG00642 | hp1 | a0001 | c0003 | t0001 | g0016 | AMR | PUR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | PUR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0353 | EAS | CHS | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0387 | EAS | CHS | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG00733 | hp1 | a0001 | c0003 | t0001 | g0010 | AMR | PUR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG00735 | hp2 | a0001 | c0003 | t0001 | g0336 | AMR | PUR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG00738 | hp1 | a0001 | c0003 | t0001 | g0010 | AMR | PUR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0371 | AMR | PUR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0370 | AMR | PUR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01070 | hp1 | a0001 | c0003 | t0001 | g0219 | AMR | PUR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01074 | hp1 | a0001 | c0003 | t0003 | g0214 | AMR | PUR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01081 | hp2 | a0004 | c0013 | t0001 | g0182 | AMR | PUR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01099 | hp1 | a0001 | c0003 | t0001 | g0022 | AMR | PUR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0241 | AMR | PUR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01106 | hp2 | a0001 | c0003 | t0001 | g0082 | AMR | PUR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0407 | AMR | PUR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01167 | hp1 | a0001 | c0003 | t0001 | g0224 | AMR | PUR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0303 | AMR | PUR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01168 | hp2 | a0005 | c0011 | t0020 | g0023 | AMR | PUR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01175 | hp2 | a0001 | c0003 | t0001 | g0076 | AMR | PUR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0175 | AMR | PUR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0406 | AMR | PUR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01255 | hp1 | a0001 | c0003 | t0003 | g0017 | AMR | CLM | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01255 | hp2 | a0001 | c0003 | t0001 | g0022 | AMR | CLM | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01256 | hp2 | a0001 | c0003 | t0001 | g0018 | AMR | CLM | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01257 | hp1 | a0001 | c0003 | t0001 | g0295 | AMR | CLM | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01257 | hp2 | a0001 | c0003 | t0003 | g0064 | AMR | CLM | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01258 | hp1 | a0001 | c0003 | t0001 | g0018 | AMR | CLM | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01258 | hp2 | a0001 | c0003 | t0003 | g0017 | AMR | CLM | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0166 | AMR | CLM | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01261 | hp2 | a0001 | c0003 | t0001 | g0120 | AMR | CLM | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01358 | hp2 | a0001 | c0001 | t0006 | g0287 | AMR | CLM | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0215 | AMR | CLM | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01433 | hp2 | a0001 | c0003 | t0003 | g0226 | AMR | CLM | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01496 | hp1 | a0001 | c0001 | t0005 | g0346 | AMR | CLM | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01515 | hp1 | a0001 | c0001 | t0005 | g0347 | EUR | IBS | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01515 | hp2 | a0001 | c0001 | t0006 | g0021 | EUR | IBS | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01516 | hp1 | a0001 | c0003 | t0001 | g0008 | EUR | IBS | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0236 | EUR | IBS | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01517 | hp1 | a0001 | c0001 | t0006 | g0021 | EUR | IBS | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0173 | EUR | IBS | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01884 | hp1 | a0001 | c0003 | t0015 | g0233 | AFR | ACB | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | ACB | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | ACB | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0055 | AMR | PEL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01934 | hp2 | a0001 | c0003 | t0001 | g0023 | AMR | PEL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0041 | AMR | PEL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0359 | AMR | PEL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0012 | AMR | PEL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0051 | AMR | PEL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0220 | AMR | PEL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0385 | AMR | PEL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02004 | hp1 | a0001 | c0003 | t0001 | g0032 | AMR | PEL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0012 | AMR | PEL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02015 | hp2 | a0001 | c0002 | t0013 | g0043 | EAS | KHV | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0333 | EAS | KHV | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0397 | EAS | KHV | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0301 | AFR | ACB | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02055 | hp2 | a0001 | c0003 | t0001 | g0038 | AFR | ACB | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | KHV | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0134 | EAS | KHV | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0375 | EAS | KHV | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0078 | EAS | KHV | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | KHV | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0165 | EAS | KHV | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02083 | hp1 | a0001 | c0003 | t0001 | g0229 | EAS | KHV | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0402 | EAS | KHV | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02132 | hp2 | a0001 | c0002 | t0021 | g0046 | EAS | KHV | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0362 | EAS | KHV | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02145 | hp1 | a0001 | c0008 | t0001 | g0252 | AFR | ACB | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02145 | hp2 | a0002 | c0005 | t0001 | g0062 | AFR | ACB | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0360 | AMR | PEL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0418 | AFR | ACB | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02258 | hp1 | a0002 | c0005 | t0001 | g0377 | AFR | ACB | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0067 | AFR | ACB | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0391 | AMR | PEL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | ACB | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0390 | AMR | PEL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02293 | hp2 | a0001 | c0003 | t0001 | g0016 | AMR | PEL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02300 | hp1 | a0001 | c0001 | t0005 | g0345 | AMR | PEL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0300 | AFR | ACB | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02451 | hp2 | a0001 | c0004 | t0001 | g0186 | AFR | ACB | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0124 | EAS | KHV | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0063 | EAS | KHV | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0404 | AFR | GWD | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02602 | hp1 | a0001 | c0012 | t0005 | g0354 | SAS | PJL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0158 | SAS | PJL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | GWD | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | GWD | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0270 | AFR | GWD | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0411 | AFR | GWD | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0416 | AFR | GWD | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0208 | AFR | GWD | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02647 | hp1 | a0001 | c0001 | t0011 | g0037 | AFR | GWD | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0276 | AFR | GWD | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0169 | SAS | PJL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02683 | hp2 | a0001 | c0003 | t0001 | g0225 | SAS | PJL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0296 | SAS | PJL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0285 | AFR | GWD | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02717 | hp2 | a0001 | c0004 | t0001 | g0185 | AFR | GWD | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02723 | hp1 | a0001 | c0003 | t0001 | g0279 | AFR | GWD | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0268 | AFR | GWD | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0393 | SAS | PJL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0292 | SAS | PJL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0144 | SAS | PJL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0399 | SAS | PJL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02809 | hp1 | a0001 | c0003 | t0001 | g0274 | AFR | GWD | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | GWD | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0284 | AFR | GWD | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02886 | hp1 | a0001 | c0003 | t0001 | g0278 | AFR | GWD | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | GWD | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0341 | AFR | GWD | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02896 | hp1 | a0001 | c0003 | t0001 | g0280 | AFR | GWD | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0415 | AFR | GWD | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | GWD | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0417 | AFR | GWD | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02922 | hp1 | a0001 | c0003 | t0001 | g0096 | AFR | ESN | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02965 | hp1 | a0001 | c0009 | t0001 | g0298 | AFR | ESN | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0242 | AFR | ESN | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ESN | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02970 | hp2 | a0001 | c0003 | t0001 | g0317 | AFR | ESN | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0209 | AFR | ESN | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | ESN | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0171 | SAS | PJL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03017 | hp2 | a0001 | c0003 | t0001 | g0029 | SAS | PJL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | GWD | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03041 | hp2 | a0001 | c0004 | t0001 | g0282 | AFR | GWD | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03098 | hp1 | a0001 | c0004 | t0001 | g0243 | AFR | MSL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03098 | hp2 | a0001 | c0003 | t0001 | g0240 | AFR | MSL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ESN | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0024 | AFR | ESN | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | ESN | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03139 | hp2 | a0001 | c0004 | t0001 | g0146 | AFR | ESN | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0024 | AFR | ESN | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03195 | hp2 | a0001 | c0008 | t0001 | g0065 | AFR | ESN | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03209 | hp1 | a0001 | c0007 | t0010 | g0373 | AFR | MSL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0269 | AFR | MSL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03225 | hp1 | a0001 | c0003 | t0001 | g0275 | AFR | MSL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03225 | hp2 | a0001 | c0007 | t0012 | g0408 | AFR | MSL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0403 | SAS | PJL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03239 | hp2 | a0001 | c0003 | t0001 | g0251 | SAS | PJL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | MSL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | MSL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0409 | AFR | MSL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03486 | hp2 | a0001 | c0003 | t0001 | g0395 | AFR | MSL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03491 | hp2 | a0001 | c0003 | t0001 | g0400 | SAS | PJL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03492 | hp2 | a0001 | c0003 | t0001 | g0401 | SAS | PJL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0140 | AFR | ESN | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03516 | hp2 | a0001 | c0009 | t0001 | g0264 | AFR | ESN | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0289 | AFR | GWD | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0410 | AFR | GWD | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0405 | AFR | MSL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | MSL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03654 | hp1 | a0001 | c0002 | t0019 | g0328 | SAS | PJL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0086 | SAS | PJL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03688 | hp1 | a0001 | c0003 | t0001 | g0138 | SAS | STU | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0367 | SAS | STU | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0366 | SAS | PJL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03704 | hp2 | a0001 | c0003 | t0001 | g0084 | SAS | PJL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0172 | SAS | PJL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0372 | SAS | PJL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03831 | hp1 | a0001 | c0003 | t0003 | g0228 | SAS | BEB | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | BEB | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0026 | SAS | BEB | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0394 | SAS | BEB | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0217 | SAS | BEB | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0113 | SAS | BEB | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0056 | SAS | BEB | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | STU | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | STU | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0048 | SAS | BEB | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG04184 | hp2 | a0001 | c0003 | t0001 | g0081 | SAS | BEB | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | STU | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG04199 | hp2 | a0001 | c0002 | t0016 | g0155 | SAS | STU | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | STU | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0163 | SAS | STU | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | STU | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | STU | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18522 | hp1 | a0001 | c0001 | t0009 | g0315 | AFR | YRI | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18522 | hp2 | a0001 | c0001 | t0011 | g0267 | AFR | YRI | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0153 | EAS | CHB | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | CHB | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0195 | EAS | CHB | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | CHB | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18906 | hp1 | a0001 | c0002 | t0008 | g0350 | AFR | YRI | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | YRI | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18940 | hp1 | a0001 | c0002 | t0001 | g0199 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0383 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18942 | hp2 | a0001 | c0003 | t0001 | g0361 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18944 | hp1 | a0001 | c0003 | t0001 | g0223 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0381 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0201 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18950 | hp2 | a0003 | c0006 | t0001 | g0197 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0190 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18951 | hp2 | a0001 | c0003 | t0001 | g0253 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0363 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0320 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0389 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0378 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0382 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0374 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0202 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0396 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18962 | hp1 | a0001 | c0003 | t0001 | g0230 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18968 | hp2 | a0001 | c0002 | t0007 | g0143 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0323 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0369 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0246 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18981 | hp2 | a0006 | c0014 | t0001 | g0126 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0327 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18984 | hp2 | a0001 | c0002 | t0014 | g0161 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18990 | hp1 | a0003 | c0006 | t0001 | g0014 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0343 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18994 | hp2 | a0001 | c0002 | t0007 | g0003 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19000 | hp1 | a0001 | c0003 | t0001 | g0247 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0398 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19004 | hp2 | a0001 | c0003 | t0001 | g0231 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0357 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0191 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0380 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0351 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0079 | AFR | LWK | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0379 | AFR | LWK | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19043 | hp1 | a0002 | c0005 | t0017 | g0311 | AFR | LWK | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19043 | hp2 | a0001 | c0003 | t0001 | g0281 | AFR | LWK | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0356 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0249 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19062 | hp2 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0332 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19063 | hp2 | a0001 | c0002 | t0007 | g0003 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19067 | hp1 | a0001 | c0002 | t0018 | g0093 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0386 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19075 | hp1 | a0007 | c0015 | t0001 | g0288 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19078 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19079 | hp1 | a0003 | c0006 | t0001 | g0014 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0189 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0340 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0259 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0337 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0326 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0305 | AFR | YRI | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA19240 | hp2 | a0008 | c0010 | t0001 | g0376 | AFR | YRI | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA20129 | hp1 | a0001 | c0004 | t0004 | g0414 | AFR | ASW | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0097 | AFR | ASW | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0125 | EUR | TSI | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0384 | EUR | TSI | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0330 | EUR | TSI | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0206 | EUR | TSI | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | GIH | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | GIH | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0050 | AMR | CLM | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0388 | AMR | CLM | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02109 | hp1 | a0001 | c0003 | t0004 | g0412 | AFR | ACB | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | ACB | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | ACB | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02559 | hp1 | a0001 | c0001 | t0009 | g0310 | AFR | ACB | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | ACB | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0355 | AFR | MSL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0413 | AFR | MSL | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | USA | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| HG06807 | hp2 | a0001 | c0003 | t0008 | g0316 | AFR | USA | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0364 | AFR | USA | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA20300 | hp2 | a0001 | c0003 | t0001 | g0211 | AFR | USA | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA21309 | hp1 | a0001 | c0003 | t0001 | g0139 | AFR | LWK | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| NA21309 | hp2 | a0001 | c0001 | t0010 | g0105 | AFR | LWK | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0221 | REF | REF | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0392 | REF | REF | GNA15_chr19_3131033_3168749 | GNA15 | chr19 | 3131033 | 3168749 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:3136458 | G | A | 1 | a0008 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.8G>A | p.Arg3His | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/7 | 426/2273 | 8/1125 | 3/374 | chr19 | 3136458 | |||
| chr19:3136473 | G | A | 1 | a0005 | 1 | HG01168.hp2 | missense_variant | MODERATE | c.23G>A | p.Arg8His | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/7 | 441/2273 | 23/1125 | 8/374 | chr19 | 3136473 | |||
| chr19:3150132 | A | T | 1 | a0003 | 3 | NA18950.hp2 NA18990.hp1 NA19079.hp1 |
missense_variant&splice_region_variant | MODERATE | c.332A>T | p.His111Leu | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 3/7 | 750/2273 | 332/1125 | 111/374 | chr19 | 3150132 | |||
| chr19:3150141 | G | A | 1 | a0002 | 3 | HG02145.hp2 HG02258.hp1 NA19043.hp1 |
missense_variant | MODERATE | c.341G>A | p.Ser114Asn | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 3/7 | 759/2273 | 341/1125 | 114/374 | chr19 | 3150141 | |||
| chr19:3151725 | G | T | 1 | a0007 | 1 | NA19075.hp1 | missense_variant | MODERATE | c.504G>T | p.Glu168Asp | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/7 | 922/2273 | 504/1125 | 168/374 | chr19 | 3151725 | |||
| chr19:3157731 | C | T | 1 | a0004 | 1 | HG01081.hp2 | missense_variant | MODERATE | c.748C>T | p.Arg250Cys | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/7 | 1166/2273 | 748/1125 | 250/374 | chr19 | 3157731 | |||
| chr19:3157741 | A | C | 1 | a0006 | 1 | NA18981.hp2 | missense_variant | MODERATE | c.758A>C | p.Glu253Ala | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/7 | 1176/2273 | 758/1125 | 253/374 | chr19 | 3157741 | |||
| chr19:3157787 | A | T | 1 | a0006 | 1 | NA18981.hp2 | missense_variant | MODERATE | c.804A>T | p.Lys268Asn | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/7 | 1222/2273 | 804/1125 | 268/374 | chr19 | 3157787 | |||
| chr19:3157840 | T | C | 1 | a0006 | 1 | NA18981.hp2 | missense_variant | MODERATE | c.857T>C | p.Ile286Thr | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/7 | 1275/2273 | 857/1125 | 286/374 | chr19 | 3157840 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:3148763 | G | A | 1 | a0001c0007 | 2 | HG03209.hp1 HG03225.hp2 |
synonymous_variant | LOW | c.318G>A | p.Arg106Arg | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 2/7 | 736/2273 | 318/1125 | 106/374 | chr19 | 3148763 | |||
| chr19:3150199 | G | A | 1 | a0001c0012 | 1 | HG02602.hp1 | synonymous_variant | LOW | c.399G>A | p.Ala133Ala | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 3/7 | 817/2273 | 399/1125 | 133/374 | chr19 | 3150199 | |||
| chr19:3150226 | C | G | 1 | a0001c0009 | 2 | HG02965.hp1 HG03516.hp2 |
synonymous_variant | LOW | c.426C>G | p.Ala142Ala | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 3/7 | 844/2273 | 426/1125 | 142/374 | chr19 | 3150226 | |||
| chr19:3150271 | C | G | 1 | a0001c0008 | 2 | HG02145.hp1 HG03195.hp2 |
synonymous_variant | LOW | c.471C>G | p.Leu157Leu | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 3/7 | 889/2273 | 471/1125 | 157/374 | chr19 | 3150271 | |||
| chr19:3155904 | G | A | 7 | a0001c0002 a0001c0009 a0001c0012 others(4): Show |
183 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(180): Show |
synonymous_variant | LOW | c.696G>A | p.Leu232Leu | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/7 | 1114/2273 | 696/1125 | 232/374 | chr19 | 3155904 | |||
| chr19:3157868 | C | T | 1 | a0006c0014 | 1 | NA18981.hp2 | synonymous_variant | LOW | c.885C>T | p.Phe295Phe | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/7 | 1303/2273 | 885/1125 | 295/374 | chr19 | 3157868 | |||
| chr19:3162911 | C | T | 2 | a0001c0003 a0005c0011 |
61 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(58): Show |
synonymous_variant | LOW | c.1017C>T | p.Leu339Leu | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 7/7 | 1435/2273 | 1017/1125 | 339/374 | chr19 | 3162911 | |||
| chr19:3162986 | C | T | 2 | a0001c0004 a0001c0008 |
8 | HG02145.hp1 HG02451.hp2 HG02717.hp2 others(5): Show |
synonymous_variant | LOW | c.1092C>T | p.Leu364Leu | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 7/7 | 1510/2273 | 1092/1125 | 364/374 | chr19 | 3162986 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:3136093 | C | T | 2 | a0001c0001t0003 a0001c0003t0003 |
8 | HG01074.hp1 HG01255.hp1 HG01257.hp2 others(5): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-358C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/7 | chr19 | 3136093 | |||||||
| chr19:3136127 | C | T | 1 | a0001c0002t0021 | 1 | HG02132.hp2 | 5_prime_UTR_variant | MODIFIER | c.-324C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/7 | 324 | chr19 | 3136127 | ||||||
| chr19:3136261 | C | T | 2 | a0001c0001t0005 a0001c0012t0005 |
6 | HG00099.hp1 HG00323.hp1 HG01496.hp1 others(3): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-190C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/7 | chr19 | 3136261 | |||||||
| chr19:3136283 | T | C | 5 | a0001c0001t0002 a0001c0001t0004 a0001c0003t0004 others(2): Show |
16 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-168T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/7 | 168 | chr19 | 3136283 | ||||||
| chr19:3136288 | C | T | 1 | a0005c0011t0020 | 1 | HG01168.hp2 | 5_prime_UTR_variant | MODIFIER | c.-163C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/7 | 163 | chr19 | 3136288 | ||||||
| chr19:3136351 | T | C | 5 | a0001c0001t0002 a0001c0001t0004 a0001c0003t0004 others(2): Show |
16 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(13): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-100T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/7 | chr19 | 3136351 | |||||||
| chr19:3136375 | G | A | 1 | a0001c0002t0013 | 1 | HG02015.hp2 | 5_prime_UTR_variant | MODIFIER | c.-76G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/7 | 76 | chr19 | 3136375 | ||||||
| chr19:3136391 | G | A | 3 | a0001c0001t0009 a0001c0002t0008 a0001c0003t0008 |
4 | HG02559.hp1 HG06807.hp2 NA18522.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-60G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/7 | 60 | chr19 | 3136391 | ||||||
| chr19:3163027 | C | T | 1 | a0001c0002t0019 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 7/7 | 8 | chr19 | 3163027 | ||||||
| chr19:3163052 | G | A | 1 | a0001c0002t0014 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*33G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 7/7 | 33 | chr19 | 3163052 | ||||||
| chr19:3163108 | T | C | 1 | a0001c0001t0002 | 9 | HG01109.hp1 HG01243.hp1 HG02559.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*89T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 7/7 | 89 | chr19 | 3163108 | ||||||
| chr19:3163177 | C | T | 1 | a0001c0002t0018 | 1 | NA19067.hp1 | 3_prime_UTR_variant | MODIFIER | c.*158C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 7/7 | 158 | chr19 | 3163177 | ||||||
| chr19:3163187 | G | A | 1 | a0001c0001t0006 | 4 | HG01358.hp2 HG01515.hp2 HG01517.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*168G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 7/7 | 168 | chr19 | 3163187 | ||||||
| chr19:3163458 | C | T | 2 | a0001c0001t0009 a0001c0001t0011 |
4 | HG02559.hp1 HG02647.hp1 NA18522.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*439C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 7/7 | 439 | chr19 | 3163458 | ||||||
| chr19:3163460 | C | T | 1 | a0002c0005t0017 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*441C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 7/7 | 441 | chr19 | 3163460 | ||||||
| chr19:3163462 | C | A | 1 | a0001c0003t0015 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*443C>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 7/7 | 443 | chr19 | 3163462 | ||||||
| chr19:3163556 | T | C | 1 | a0001c0002t0007 | 3 | NA18968.hp2 NA18994.hp2 NA19063.hp2 |
3_prime_UTR_variant | MODIFIER | c.*537T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 7/7 | 537 | chr19 | 3163556 | ||||||
| chr19:3163571 | T | C | 1 | a0001c0002t0016 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*552T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 7/7 | 552 | chr19 | 3163571 | ||||||
| chr19:3163605 | G | A | 3 | a0001c0001t0010 a0001c0007t0010 a0001c0007t0012 |
3 | HG03209.hp1 HG03225.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*586G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 7/7 | 586 | chr19 | 3163605 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:3136616 | C | T | 1 | a0001c0001t0001g0418 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.145+21C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3136616 | |||||||
| chr19:3136694 | T | C | 278 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(275): Show |
301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.145+99T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3136694 | |||||||
| chr19:3136771 | T | C | 278 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(275): Show |
301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.145+176T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3136771 | |||||||
| chr19:3136800 | T | C | 278 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(275): Show |
301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.145+205T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3136800 | |||||||
| chr19:3136803 | G | T | 1 | a0001c0002t0001g0285 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.145+208G>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3136803 | |||||||
| chr19:3136847 | T | C | 278 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(275): Show |
301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.145+252T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3136847 | |||||||
| chr19:3136852 | T | C | 2 | a0001c0001t0006g0287 a0001c0003t0001g0286 |
2 | HG00099.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.145+257T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3136852 | |||||||
| chr19:3136871 | G | A | 1 | a0007c0015t0001g0288 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.145+276G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3136871 | |||||||
| chr19:3136882 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.145+287G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3136882 | |||||||
| chr19:3136896 | C | T | 10 | a0001c0001t0001g0277 a0001c0001t0001g0283 a0001c0002t0001g0276 others(7): Show |
10 | HG01884.hp2 HG02647.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.145+301C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3136896 | |||||||
| chr19:3136931 | G | A | 1 | a0001c0003t0001g0029 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.145+336G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3136931 | |||||||
| chr19:3136964 | A | G | 293 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(290): Show |
317 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.145+369A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3136964 | |||||||
| chr19:3136969 | T | C | 370 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(367): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.145+374T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3136969 | |||||||
| chr19:3137018 | G | A | 3 | a0001c0001t0006g0287 a0001c0001t0006g0289 a0001c0003t0001g0286 |
3 | HG00099.hp2 HG01358.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.145+423G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3137018 | |||||||
| chr19:3137139 | G | A | 293 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(290): Show |
317 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.145+544G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3137139 | |||||||
| chr19:3137464 | C | T | 1 | a0001c0003t0001g0274 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.145+869C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3137464 | |||||||
| chr19:3137550 | G | A | 2 | a0001c0001t0001g0290 a0001c0001t0001g0291 |
2 | HG02129.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.145+955G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3137550 | |||||||
| chr19:3137571 | C | A | 25 | a0001c0001t0001g0020 a0001c0001t0001g0293 a0001c0001t0001g0294 others(22): Show |
29 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.145+976C>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3137571 | |||||||
| chr19:3137571 | C | T | 273 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(270): Show |
296 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.145+976C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3137571 | |||||||
| chr19:3137603 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.145+1008G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3137603 | |||||||
| chr19:3137626 | C | A | 1 | a0001c0001t0001g0036 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.145+1031C>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3137626 | |||||||
| chr19:3137652 | C | T | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG00639.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.145+1057C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3137652 | |||||||
| chr19:3137835 | G | C | 79 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(76): Show |
84 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.145+1240G>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3137835 | |||||||
| chr19:3137869 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.145+1274G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3137869 | |||||||
| chr19:3137870 | A | T | 1 | a0001c0001t0001g0035 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.145+1275A>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3137870 | |||||||
| chr19:3137905 | G | A | 276 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(273): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.145+1310G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3137905 | |||||||
| chr19:3137993 | A | G | 5 | a0001c0001t0001g0271 a0001c0001t0011g0267 a0001c0002t0001g0268 others(2): Show |
5 | HG02486.hp2 HG02622.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.145+1398A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3137993 | |||||||
| chr19:3138035 | G | A | 1 | a0001c0001t0002g0404 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.145+1440G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3138035 | |||||||
| chr19:3138064 | A | G | 370 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(367): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.145+1469A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3138064 | |||||||
| chr19:3138079 | C | T | 4 | a0001c0001t0001g0263 a0001c0001t0001g0265 a0001c0001t0001g0266 others(1): Show |
4 | HG01891.hp2 HG02486.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.145+1484C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3138079 | |||||||
| chr19:3138093 | G | A | 79 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(76): Show |
84 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.145+1498G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3138093 | |||||||
| chr19:3138196 | G | A | 1 | a0001c0003t0001g0038 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.145+1601G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3138196 | |||||||
| chr19:3138261 | C | T | 1 | a0001c0001t0001g0403 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.145+1666C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3138261 | |||||||
| chr19:3138266 | CA | C | 20 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0260 others(17): Show |
21 | HG01109.hp1 HG01169.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.145+1684delA | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3138266 | ||||||
| chr19:3138299 | G | A | 1 | a0001c0001t0001g0308 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.145+1704G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3138299 | |||||||
| chr19:3138333 | T | C | 87 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(84): Show |
92 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.145+1738T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3138333 | |||||||
| chr19:3138370 | C | CG | 370 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(367): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.145+1778dupG | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3138370 | ||||||
| chr19:3138418 | G | A | 22 | a0001c0001t0001g0045 a0001c0001t0001g0057 a0001c0002t0001g0001 others(19): Show |
26 | HG00558.hp1 HG01123.hp1 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.145+1823G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3138418 | |||||||
| chr19:3138489 | G | A | 1 | a0001c0001t0001g0058 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.145+1894G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3138489 | |||||||
| chr19:3138489 | G | T | 78 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(75): Show |
83 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.145+1894G>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3138489 | |||||||
| chr19:3138514 | C | T | 1 | a0001c0002t0001g0255 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.145+1919C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3138514 | |||||||
| chr19:3138544 | A | C | 15 | a0001c0001t0002g0027 a0001c0001t0002g0404 a0001c0001t0002g0406 others(12): Show |
16 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.145+1949A>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3138544 | |||||||
| chr19:3138570 | T | A | 77 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(74): Show |
82 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.145+1975T>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3138570 | |||||||
| chr19:3138570 | T | G | 1 | a0007c0015t0001g0288 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.145+1975T>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3138570 | |||||||
| chr19:3138653 | C | T | 78 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(75): Show |
83 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.145+2058C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3138653 | |||||||
| chr19:3138689 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0059 |
2 | HG01099.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.145+2094G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3138689 | |||||||
| chr19:3138693 | C | T | 78 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(75): Show |
83 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.145+2098C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3138693 | |||||||
| chr19:3138724 | G | A | 1 | a0001c0002t0001g0060 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.145+2129G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3138724 | |||||||
| chr19:3138795 | TA | T | 15 | a0001c0001t0002g0027 a0001c0001t0002g0404 a0001c0001t0002g0406 others(12): Show |
16 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.145+2202delA | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3138795 | ||||||
| chr19:3138797 | A | AT | 41 | a0001c0001t0001g0045 a0001c0001t0001g0263 a0001c0001t0001g0265 others(38): Show |
45 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.145+2216dupT | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3138797 | ||||||
| chr19:3138797 | A | ATT | 240 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(237): Show |
259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.145+2215_145+2216d others(4): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3138797 | ||||||
| chr19:3138797 | A | ATTT | 10 | a0001c0001t0001g0248 a0001c0001t0001g0250 a0001c0001t0001g0254 others(7): Show |
10 | HG01433.hp1 HG02027.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.145+2214_145+2216d others(5): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3138797 | ||||||
| chr19:3138798 | T | C | 15 | a0001c0001t0002g0027 a0001c0001t0002g0404 a0001c0001t0002g0406 others(12): Show |
16 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.145+2203T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3138798 | |||||||
| chr19:3138831 | G | A | 78 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(75): Show |
83 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.145+2236G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3138831 | |||||||
| chr19:3138884 | C | T | 15 | a0001c0001t0002g0027 a0001c0001t0002g0404 a0001c0001t0002g0406 others(12): Show |
16 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.145+2289C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3138884 | |||||||
| chr19:3138897 | C | G | 15 | a0001c0001t0002g0027 a0001c0001t0002g0404 a0001c0001t0002g0406 others(12): Show |
16 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.145+2302C>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3138897 | |||||||
| chr19:3138898 | G | A | 78 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(75): Show |
83 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.145+2303G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3138898 | |||||||
| chr19:3138937 | C | A | 1 | a0001c0001t0001g0020 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.145+2342C>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3138937 | |||||||
| chr19:3138939 | C | CT | 72 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0025 others(69): Show |
78 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.145+2359dupT | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3138939 | ||||||
| chr19:3138939 | C | CTT | 7 | a0001c0001t0001g0306 a0001c0001t0001g0341 a0001c0001t0001g0342 others(4): Show |
7 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(4): Show |
intron_variant | MODIFIER | c.145+2358_145+2359d others(4): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3138939 | ||||||
| chr19:3138939 | CT | C | 28 | a0001c0001t0001g0045 a0001c0001t0001g0057 a0001c0001t0001g0066 others(25): Show |
33 | HG00558.hp1 HG01123.hp1 HG01256.hp1 others(30): Show |
intron_variant | MODIFIER | c.145+2359delT | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3138939 | ||||||
| chr19:3138955 | C | T | 78 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(75): Show |
83 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.145+2360C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3138955 | |||||||
| chr19:3139001 | A | G | 1 | a0001c0001t0001g0308 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.145+2406A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3139001 | |||||||
| chr19:3139032 | G | A | 78 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(75): Show |
83 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.145+2437G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3139032 | |||||||
| chr19:3139180 | A | G | 33 | a0001c0001t0001g0025 a0001c0001t0001g0030 a0001c0001t0001g0290 others(30): Show |
34 | HG00408.hp2 HG00621.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.145+2585A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3139180 | |||||||
| chr19:3139366 | T | C | 78 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(75): Show |
83 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.145+2771T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3139366 | |||||||
| chr19:3139413 | C | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0059 |
2 | HG01099.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.145+2818C>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3139413 | |||||||
| chr19:3139426 | A | T | 3 | a0001c0001t0006g0287 a0001c0001t0006g0289 a0001c0003t0001g0286 |
3 | HG00099.hp2 HG01358.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.145+2831A>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3139426 | |||||||
| chr19:3139461 | G | T | 1 | a0001c0002t0001g0054 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.145+2866G>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3139461 | |||||||
| chr19:3139469 | A | C | 78 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(75): Show |
83 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.145+2874A>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3139469 | |||||||
| chr19:3139492 | G | T | 78 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(75): Show |
83 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.145+2897G>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3139492 | |||||||
| chr19:3139523 | A | C | 1 | a0001c0001t0006g0289 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.145+2928A>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3139523 | |||||||
| chr19:3139598 | C | CA | 40 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0364 others(37): Show |
41 | HG00408.hp1 HG00558.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.145+3022dupA | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3139598 | ||||||
| chr19:3139598 | CA | C | 257 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(254): Show |
280 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.145+3022delA | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3139598 | ||||||
| chr19:3139598 | CAA | C | 51 | a0001c0001t0001g0045 a0001c0001t0001g0057 a0001c0001t0001g0239 others(48): Show |
56 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.145+3021_145+3022d others(4): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3139598 | ||||||
| chr19:3139668 | G | C | 25 | a0001c0001t0001g0020 a0001c0001t0001g0293 a0001c0001t0001g0294 others(22): Show |
29 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.145+3073G>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3139668 | |||||||
| chr19:3139715 | C | T | 2 | a0001c0002t0001g0237 a0001c0002t0001g0238 |
2 | NA18980.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.145+3120C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3139715 | |||||||
| chr19:3139717 | A | G | 372 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(369): Show |
401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.145+3122A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3139717 | |||||||
| chr19:3139727 | G | A | 78 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(75): Show |
83 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.145+3132G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3139727 | |||||||
| chr19:3139739 | A | T | 4 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0306 others(1): Show |
4 | HG00642.hp2 HG00735.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.145+3144A>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3139739 | |||||||
| chr19:3139755 | G | T | 78 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(75): Show |
83 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.145+3160G>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3139755 | |||||||
| chr19:3139761 | T | C | 372 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(369): Show |
401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.145+3166T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3139761 | |||||||
| chr19:3139763 | C | T | 1 | a0001c0001t0001g0319 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.145+3168C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3139763 | |||||||
| chr19:3139773 | C | T | 78 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(75): Show |
83 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.145+3178C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3139773 | |||||||
| chr19:3139799 | G | A | 22 | a0001c0001t0001g0045 a0001c0001t0001g0057 a0001c0002t0001g0001 others(19): Show |
26 | HG00558.hp1 HG01123.hp1 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.145+3204G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3139799 | |||||||
| chr19:3139804 | G | A | 1 | a0001c0003t0001g0082 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.145+3209G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3139804 | |||||||
| chr19:3139849 | T | C | 78 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(75): Show |
83 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.145+3254T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3139849 | |||||||
| chr19:3139905 | G | A | 11 | a0001c0001t0001g0390 a0001c0002t0001g0026 a0001c0002t0001g0356 others(8): Show |
12 | HG00621.hp2 HG01978.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.145+3310G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3139905 | |||||||
| chr19:3139981 | C | G | 3 | a0001c0003t0001g0081 a0001c0003t0001g0400 a0001c0003t0001g0401 |
3 | HG03491.hp2 HG03492.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.145+3386C>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3139981 | |||||||
| chr19:3140013 | A | G | 1 | a0001c0008t0001g0065 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.145+3418A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3140013 | |||||||
| chr19:3140033 | CA | C | 12 | a0001c0001t0002g0027 a0001c0001t0002g0404 a0001c0001t0002g0406 others(9): Show |
13 | HG01109.hp1 HG01243.hp1 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.145+3450delA | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3140033 | ||||||
| chr19:3140044 | A | AAAAAAAA others(27): Show |
1 | a0001c0001t0001g0309 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.145+3450_145+3451i others(36): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3140044 | ||||||
| chr19:3140044 | A | AAAAAAAT others(26): Show |
1 | a0001c0001t0001g0312 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.145+3450_145+3451i others(35): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3140044 | ||||||
| chr19:3140044 | A | AAAAAAAT others(38): Show |
1 | a0007c0015t0001g0288 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.145+3450_145+3451i others(47): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3140044 | ||||||
| chr19:3140044 | A | AAAAAAAT others(30): Show |
3 | a0001c0001t0001g0313 a0001c0001t0001g0319 a0001c0001t0001g0341 |
3 | HG02615.hp2 HG02809.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.145+3450_145+3451i others(39): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3140044 | ||||||
| chr19:3140044 | A | AAAAAATC others(17): Show |
2 | a0001c0002t0008g0350 a0001c0002t0019g0328 |
2 | HG03654.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.145+3450_145+3451i others(26): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3140044 | ||||||
| chr19:3140044 | A | AAAAAATC others(21): Show |
5 | a0001c0001t0001g0314 a0001c0001t0001g0329 a0001c0001t0001g0339 others(2): Show |
5 | HG02056.hp2 HG02559.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.145+3450_145+3451i others(30): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3140044 | ||||||
| chr19:3140044 | A | AAAAAATC others(25): Show |
12 | a0001c0001t0001g0025 a0001c0001t0001g0030 a0001c0001t0001g0290 others(9): Show |
13 | HG02027.hp2 HG02083.hp2 HG02129.hp2 others(10): Show |
intron_variant | MODIFIER | c.145+3450_145+3451i others(34): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3140044 | ||||||
| chr19:3140044 | A | AAAAAATC others(29): Show |
3 | a0001c0001t0001g0294 a0001c0001t0001g0324 a0001c0002t0001g0325 |
3 | HG00408.hp2 HG01243.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.145+3450_145+3451i others(38): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3140044 | ||||||
| chr19:3140044 | A | AAAAAATC others(33): Show |
1 | a0001c0001t0001g0342 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.145+3450_145+3451i others(42): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3140044 | ||||||
| chr19:3140044 | A | AAAAAATC others(41): Show |
2 | a0001c0001t0001g0020 a0001c0001t0001g0293 |
3 | HG01070.hp2 HG01071.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.145+3450_145+3451i others(50): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3140044 | ||||||
| chr19:3140044 | A | AAAAAATC others(45): Show |
1 | a0001c0002t0001g0323 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.145+3450_145+3451i others(54): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3140044 | ||||||
| chr19:3140044 | A | AAAAAATC others(33): Show |
10 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0306 others(7): Show |
12 | HG00642.hp2 HG00673.hp1 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.145+3450_145+3451i others(42): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3140044 | ||||||
| chr19:3140044 | A | AAAAAATC others(37): Show |
4 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0002t0001g0326 others(1): Show |
4 | HG02698.hp1 HG03490.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.145+3450_145+3451i others(46): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3140044 | ||||||
| chr19:3140044 | A | AAAAAATC others(41): Show |
3 | a0001c0002t0001g0320 a0001c0002t0001g0327 a0001c0003t0001g0286 |
3 | HG00099.hp2 NA18953.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.145+3450_145+3451i others(50): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3140044 | ||||||
| chr19:3140044 | A | AAAAAATC others(29): Show |
14 | a0001c0001t0001g0291 a0001c0001t0001g0318 a0001c0001t0001g0321 others(11): Show |
15 | HG01358.hp2 HG02129.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.145+3450_145+3451i others(38): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3140044 | ||||||
| chr19:3140044 | A | AAAAAATC others(33): Show |
6 | a0001c0001t0001g0302 a0001c0001t0001g0338 a0001c0002t0001g0300 others(3): Show |
6 | HG00735.hp2 HG02055.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.145+3450_145+3451i others(42): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3140044 | ||||||
| chr19:3140044 | A | AAAAATCT others(20): Show |
1 | a0001c0001t0005g0345 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.145+3450_145+3451i others(29): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3140044 | ||||||
| chr19:3140044 | A | AAAAATCT others(24): Show |
1 | a0001c0002t0001g0351 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.145+3450_145+3451i others(33): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3140044 | ||||||
| chr19:3140044 | A | AAAAATCT others(28): Show |
1 | a0001c0002t0001g0340 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.145+3450_145+3451i others(37): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3140044 | ||||||
| chr19:3140044 | A | AAAAATCT others(24): Show |
2 | a0001c0001t0005g0346 a0001c0001t0005g0347 |
2 | HG01496.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.145+3450_145+3451i others(33): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3140044 | ||||||
| chr19:3140044 | A | AAAAATCT others(32): Show |
3 | a0001c0001t0001g0308 a0001c0001t0005g0348 a0001c0012t0005g0354 |
3 | HG00099.hp1 HG02602.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.145+3450_145+3451i others(41): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3140044 | ||||||
| chr19:3140044 | A | AAAATCTA others(19): Show |
1 | a0001c0001t0005g0349 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.145+3450_145+3451i others(28): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3140044 | ||||||
| chr19:3140044 | A | AATCT | 111 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0034 others(108): Show |
116 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.145+3488_145+3491d others(6): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3140044 | ||||||
| chr19:3140044 | A | AATCTATC others(1): Show |
189 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0019 others(186): Show |
207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.145+3484_145+3491d others(10): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3140044 | ||||||
| chr19:3140044 | A | AATCTATC others(5): Show |
2 | a0001c0002t0001g0235 a0001c0002t0001g0389 |
2 | NA18948.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.145+3480_145+3491d others(14): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3140044 | ||||||
| chr19:3140044 | A | ATCT | 4 | a0001c0001t0004g0415 a0001c0001t0004g0416 a0001c0001t0004g0417 others(1): Show |
4 | HG02630.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.145+3449_145+3450i others(5): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3140044 | |||||||
| chr19:3140044 | AATCTATC others(5): Show |
A | 1 | a0001c0001t0001g0083 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.145+3480_145+3491d others(14): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3140044 | ||||||
| chr19:3140047 | C | G | 21 | a0001c0001t0001g0025 a0001c0001t0001g0030 a0001c0001t0001g0290 others(18): Show |
22 | HG00323.hp1 HG00408.hp2 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.145+3452C>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3140047 | |||||||
| chr19:3140051 | C | G | 6 | a0001c0001t0001g0030 a0001c0001t0001g0314 a0001c0001t0001g0329 others(3): Show |
6 | HG02056.hp2 HG02559.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.145+3456C>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3140051 | |||||||
| chr19:3140055 | C | G | 3 | a0001c0001t0001g0339 a0001c0002t0008g0350 a0001c0002t0019g0328 |
3 | HG03654.hp1 NA18906.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.145+3460C>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3140055 | |||||||
| chr19:3140126 | C | T | 93 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(90): Show |
99 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.145+3531C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3140126 | |||||||
| chr19:3140180 | C | A | 1 | a0001c0001t0001g0296 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.145+3585C>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3140180 | |||||||
| chr19:3140343 | G | A | 1 | a0001c0001t0001g0308 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.145+3748G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3140343 | |||||||
| chr19:3140419 | A | C | 77 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(74): Show |
82 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.145+3824A>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3140419 | |||||||
| chr19:3140425 | T | A | 1 | a0001c0002t0001g0041 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.145+3830T>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3140425 | |||||||
| chr19:3140516 | C | T | 1 | a0001c0002t0001g0041 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.145+3921C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3140516 | |||||||
| chr19:3140742 | CTGAA | C | 71 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(68): Show |
76 | HG00099.hp2 HG00408.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.145+4173_145+4176d others(6): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3140742 | ||||||
| chr19:3140788 | T | C | 71 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(68): Show |
76 | HG00099.hp2 HG00408.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.145+4193T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3140788 | |||||||
| chr19:3140867 | C | A | 1 | a0001c0002t0001g0098 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.145+4272C>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3140867 | |||||||
| chr19:3140911 | A | T | 370 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(367): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.145+4316A>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3140911 | |||||||
| chr19:3141043 | T | TA | 71 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(68): Show |
76 | HG00099.hp2 HG00408.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.145+4448_145+4449i others(3): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3141043 | |||||||
| chr19:3141054 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.145+4459C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3141054 | |||||||
| chr19:3141055 | C | A | 6 | a0001c0001t0005g0345 a0001c0001t0005g0346 a0001c0001t0005g0347 others(3): Show |
6 | HG00099.hp1 HG00323.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.145+4460C>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3141055 | |||||||
| chr19:3141084 | T | C | 6 | a0001c0001t0005g0345 a0001c0001t0005g0346 a0001c0001t0005g0347 others(3): Show |
6 | HG00099.hp1 HG00323.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.145+4489T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3141084 | |||||||
| chr19:3141102 | TG | T | 71 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(68): Show |
76 | HG00099.hp2 HG00408.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.145+4512delG | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3141102 | ||||||
| chr19:3141135 | C | G | 1 | a0001c0001t0001g0234 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.145+4540C>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3141135 | |||||||
| chr19:3141171 | G | A | 1 | a0001c0001t0001g0341 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.145+4576G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3141171 | |||||||
| chr19:3141213 | C | T | 1 | a0001c0002t0001g0141 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.145+4618C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3141213 | |||||||
| chr19:3141408 | A | T | 71 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(68): Show |
76 | HG00099.hp2 HG00408.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.145+4813A>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3141408 | |||||||
| chr19:3141459 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.145+4864G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3141459 | |||||||
| chr19:3141464 | C | T | 5 | a0001c0001t0001g0263 a0001c0001t0001g0265 a0001c0001t0001g0266 others(2): Show |
5 | HG01891.hp2 HG02486.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.145+4869C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3141464 | |||||||
| chr19:3141552 | T | C | 71 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(68): Show |
76 | HG00099.hp2 HG00408.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.145+4957T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3141552 | |||||||
| chr19:3141572 | T | C | 6 | a0001c0001t0005g0345 a0001c0001t0005g0346 a0001c0001t0005g0347 others(3): Show |
6 | HG00099.hp1 HG00323.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.145+4977T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3141572 | |||||||
| chr19:3141642 | T | A | 174 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(171): Show |
189 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.145+5047T>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3141642 | |||||||
| chr19:3141712 | G | A | 15 | a0001c0001t0002g0027 a0001c0001t0002g0404 a0001c0001t0002g0406 others(12): Show |
16 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.145+5117G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3141712 | |||||||
| chr19:3141890 | A | C | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.145+5295A>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3141890 | |||||||
| chr19:3142007 | C | A | 72 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(69): Show |
77 | HG00099.hp2 HG00408.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.145+5412C>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3142007 | |||||||
| chr19:3142135 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.145+5540G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3142135 | |||||||
| chr19:3142180 | A | T | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.145+5585A>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3142180 | |||||||
| chr19:3142208 | G | A | 1 | a0001c0004t0001g0243 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.145+5613G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3142208 | |||||||
| chr19:3142235 | A | C | 349 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(346): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.145+5640A>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3142235 | |||||||
| chr19:3142237 | C | G | 6 | a0001c0001t0001g0263 a0001c0001t0001g0265 a0001c0001t0001g0266 others(3): Show |
6 | HG01884.hp2 HG01891.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.145+5642C>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3142237 | |||||||
| chr19:3142267 | G | C | 5 | a0001c0001t0001g0263 a0001c0001t0001g0265 a0001c0001t0001g0266 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.145+5672G>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3142267 | |||||||
| chr19:3142275 | G | A | 38 | a0001c0001t0001g0025 a0001c0001t0001g0030 a0001c0001t0001g0290 others(35): Show |
39 | HG00408.hp2 HG00621.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.145+5680G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3142275 | |||||||
| chr19:3142293 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.145+5698C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3142293 | |||||||
| chr19:3142496 | C | T | 15 | a0001c0001t0002g0027 a0001c0001t0002g0404 a0001c0001t0002g0406 others(12): Show |
16 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.145+5901C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3142496 | |||||||
| chr19:3142497 | A | G | 78 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(75): Show |
83 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.145+5902A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3142497 | |||||||
| chr19:3142504 | A | C | 93 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(90): Show |
99 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.145+5909A>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3142504 | |||||||
| chr19:3142520 | C | CT | 93 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(90): Show |
99 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.145+5928dupT | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3142520 | ||||||
| chr19:3142570 | G | T | 1 | a0001c0003t0015g0233 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.145+5975G>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3142570 | |||||||
| chr19:3142731 | G | T | 24 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0068 others(21): Show |
27 | HG02074.hp2 NA18747.hp1 NA18940.hp1 others(24): Show |
intron_variant | MODIFIER | c.146-5860G>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3142731 | |||||||
| chr19:3142786 | C | T | 72 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(69): Show |
77 | HG00099.hp2 HG00408.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.146-5805C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3142786 | |||||||
| chr19:3142803 | A | T | 137 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(134): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.146-5788A>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3142803 | |||||||
| chr19:3142813 | G | A | 1 | a0001c0003t0001g0295 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.146-5778G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3142813 | |||||||
| chr19:3142863 | C | T | 131 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(128): Show |
140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.146-5728C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3142863 | |||||||
| chr19:3142874 | A | T | 137 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(134): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.146-5717A>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3142874 | |||||||
| chr19:3142929 | G | GT | 2 | a0001c0001t0001g0015 a0001c0001t0001g0203 |
3 | NA18981.hp1 NA19058.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.146-5662_146-5661i others(3): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3142929 | |||||||
| chr19:3142945 | C | T | 1 | a0001c0002t0001g0053 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.146-5646C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3142945 | |||||||
| chr19:3142969 | C | T | 2 | a0001c0008t0001g0065 a0002c0005t0001g0062 |
2 | HG02145.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.146-5622C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3142969 | |||||||
| chr19:3142970 | G | C | 1 | a0001c0003t0003g0214 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.146-5621G>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3142970 | |||||||
| chr19:3143015 | C | T | 4 | a0001c0002t0001g0134 a0001c0002t0001g0187 a0001c0002t0001g0188 others(1): Show |
4 | HG02071.hp2 NA18941.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-5576C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3143015 | |||||||
| chr19:3143033 | T | C | 330 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(327): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.146-5558T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3143033 | |||||||
| chr19:3143041 | C | T | 15 | a0001c0001t0002g0027 a0001c0001t0002g0404 a0001c0001t0002g0406 others(12): Show |
16 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.146-5550C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3143041 | |||||||
| chr19:3143046 | G | A | 316 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(313): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.146-5545G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3143046 | |||||||
| chr19:3143071 | G | T | 131 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(128): Show |
140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.146-5520G>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3143071 | |||||||
| chr19:3143156 | A | G | 137 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(134): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.146-5435A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3143156 | |||||||
| chr19:3143157 | T | G | 137 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(134): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.146-5434T>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3143157 | |||||||
| chr19:3143158 | T | C | 137 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(134): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.146-5433T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3143158 | |||||||
| chr19:3143184 | T | C | 348 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(345): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.146-5407T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3143184 | |||||||
| chr19:3143241 | G | A | 2 | a0001c0003t0001g0084 a0001c0003t0001g0085 |
2 | HG00280.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.146-5350G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3143241 | |||||||
| chr19:3143264 | G | A | 137 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(134): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.146-5327G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3143264 | |||||||
| chr19:3143285 | T | G | 59 | a0001c0001t0001g0058 a0001c0001t0001g0080 a0001c0001t0001g0136 others(56): Show |
63 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.146-5306T>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3143285 | |||||||
| chr19:3143322 | C | T | 137 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(134): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.146-5269C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3143322 | |||||||
| chr19:3143514 | C | T | 11 | a0001c0001t0001g0390 a0001c0002t0001g0026 a0001c0002t0001g0356 others(8): Show |
12 | HG00621.hp2 HG01978.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.146-5077C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3143514 | |||||||
| chr19:3143535 | A | C | 131 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(128): Show |
140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.146-5056A>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3143535 | |||||||
| chr19:3143566 | C | T | 9 | a0001c0001t0001g0239 a0001c0001t0001g0271 a0001c0001t0011g0267 others(6): Show |
9 | HG01106.hp1 HG02148.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.146-5025C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3143566 | |||||||
| chr19:3143584 | T | C | 369 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(366): Show |
398 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(395): Show |
intron_variant | MODIFIER | c.146-5007T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3143584 | |||||||
| chr19:3143619 | C | T | 1 | a0001c0001t0001g0036 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.146-4972C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3143619 | |||||||
| chr19:3143650 | C | A | 1 | a0001c0001t0001g0314 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.146-4941C>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3143650 | |||||||
| chr19:3143657 | A | C | 2 | a0001c0004t0001g0185 a0001c0004t0001g0186 |
2 | HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.146-4934A>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3143657 | |||||||
| chr19:3143673 | A | T | 56 | a0001c0001t0001g0058 a0001c0001t0001g0080 a0001c0001t0001g0136 others(53): Show |
60 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.146-4918A>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3143673 | |||||||
| chr19:3143695 | A | G | 102 | a0001c0001t0001g0020 a0001c0001t0001g0058 a0001c0001t0001g0080 others(99): Show |
110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.146-4896A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3143695 | |||||||
| chr19:3143760 | C | T | 3 | a0001c0001t0006g0287 a0001c0001t0006g0289 a0001c0003t0001g0286 |
3 | HG00099.hp2 HG01358.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.146-4831C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3143760 | |||||||
| chr19:3143848 | C | T | 139 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(136): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.146-4743C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3143848 | |||||||
| chr19:3143935 | A | G | 1 | a0001c0002t0001g0305 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.146-4656A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3143935 | |||||||
| chr19:3143956 | TA | T | 154 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(151): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.146-4626delA | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3143956 | ||||||
| chr19:3143975 | T | G | 1 | a0001c0001t0001g0291 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.146-4616T>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3143975 | |||||||
| chr19:3143992 | T | C | 1 | a0001c0001t0001g0308 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.146-4599T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3143992 | |||||||
| chr19:3144005 | T | A | 60 | a0001c0001t0001g0058 a0001c0001t0001g0080 a0001c0001t0001g0136 others(57): Show |
64 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.146-4586T>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144005 | |||||||
| chr19:3144079 | G | A | 136 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(133): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.146-4512G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144079 | |||||||
| chr19:3144127 | C | CA | 17 | a0001c0001t0002g0027 a0001c0001t0002g0404 a0001c0001t0002g0406 others(14): Show |
18 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.146-4449dupA | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3144127 | ||||||
| chr19:3144127 | C | CAA | 8 | a0001c0001t0001g0302 a0001c0001t0001g0309 a0001c0002t0001g0024 others(5): Show |
9 | HG00408.hp2 HG00673.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.146-4450_146-4449d others(4): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3144127 | ||||||
| chr19:3144127 | C | CAAA | 125 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(122): Show |
133 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.146-4451_146-4449d others(5): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3144127 | ||||||
| chr19:3144247 | T | C | 59 | a0001c0001t0001g0058 a0001c0001t0001g0080 a0001c0001t0001g0136 others(56): Show |
62 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.146-4344T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144247 | |||||||
| chr19:3144358 | C | T | 177 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(174): Show |
193 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(190): Show |
intron_variant | MODIFIER | c.146-4233C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144358 | |||||||
| chr19:3144380 | G | A | 1 | a0001c0002t0001g0190 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.146-4211G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144380 | |||||||
| chr19:3144510 | G | A | 153 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0030 others(150): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.146-4081G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144510 | |||||||
| chr19:3144537 | A | AT | 10 | a0001c0001t0001g0263 a0001c0001t0001g0265 a0001c0001t0001g0266 others(7): Show |
10 | HG00099.hp1 HG00323.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.146-4045dupT | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3144537 | ||||||
| chr19:3144538 | T | C | 16 | a0001c0001t0002g0027 a0001c0001t0002g0404 a0001c0001t0002g0406 others(13): Show |
17 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.146-4053T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144538 | |||||||
| chr19:3144559 | C | G | 1 | a0001c0001t0001g0344 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.146-4032C>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144559 | |||||||
| chr19:3144567 | C | T | 1 | a0001c0002t0001g0095 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.146-4024C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144567 | |||||||
| chr19:3144568 | A | C | 14 | a0001c0001t0001g0009 a0001c0001t0001g0073 a0001c0001t0001g0094 others(11): Show |
15 | HG00609.hp2 NA18952.hp2 NA18956.hp1 others(12): Show |
intron_variant | MODIFIER | c.146-4023A>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144568 | |||||||
| chr19:3144568 | A | G | 1 | a0001c0002t0001g0095 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.146-4023A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144568 | |||||||
| chr19:3144591 | T | A | 3 | a0001c0002t0001g0078 a0001c0002t0001g0190 a0001c0002t0001g0191 |
3 | HG02074.hp2 NA18951.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.146-4000T>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144591 | |||||||
| chr19:3144604 | T | C | 2 | a0001c0002t0001g0031 a0001c0003t0001g0032 |
2 | HG00323.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.146-3987T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144604 | |||||||
| chr19:3144622 | C | G | 1 | a0004c0013t0001g0182 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.146-3969C>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144622 | |||||||
| chr19:3144630 | G | A | 1 | a0001c0001t0001g0297 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.146-3961G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144630 | |||||||
| chr19:3144674 | G | A | 1 | a0001c0003t0015g0233 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.146-3917G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144674 | |||||||
| chr19:3144678 | G | A | 3 | a0001c0004t0001g0146 a0001c0004t0001g0185 a0001c0004t0001g0186 |
3 | HG02451.hp2 HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.146-3913G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144678 | |||||||
| chr19:3144685 | T | C | 15 | a0001c0001t0001g0069 a0001c0001t0001g0104 a0001c0001t0001g0390 others(12): Show |
16 | HG00621.hp2 HG01891.hp1 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.146-3906T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144685 | |||||||
| chr19:3144690 | G | A | 4 | a0001c0001t0005g0345 a0001c0001t0005g0346 a0001c0001t0005g0349 others(1): Show |
4 | HG00323.hp1 HG01496.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.146-3901G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144690 | |||||||
| chr19:3144692 | T | C | 1 | a0001c0002t0001g0106 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.146-3899T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144692 | |||||||
| chr19:3144704 | A | G | 1 | a0001c0001t0001g0318 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.146-3887A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144704 | |||||||
| chr19:3144718 | C | T | 20 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0283 others(17): Show |
21 | HG00280.hp2 HG01109.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.146-3873C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144718 | |||||||
| chr19:3144721 | G | A | 1 | a0001c0001t0003g0217 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.146-3870G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144721 | |||||||
| chr19:3144730 | G | A | 2 | a0001c0001t0001g0216 a0001c0001t0001g0218 |
2 | HG01346.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.146-3861G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144730 | |||||||
| chr19:3144735 | A | G | 1 | a0001c0001t0001g0045 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.146-3856A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144735 | |||||||
| chr19:3144739 | A | G | 38 | a0001c0001t0001g0181 a0001c0001t0001g0212 a0001c0001t0001g0213 others(35): Show |
38 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.146-3852A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144739 | |||||||
| chr19:3144741 | G | C | 1 | a0001c0003t0001g0274 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.146-3850G>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144741 | |||||||
| chr19:3144745 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.146-3846G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144745 | |||||||
| chr19:3144750 | G | C | 1 | a0001c0001t0001g0308 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.146-3841G>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144750 | |||||||
| chr19:3144760 | C | T | 2 | a0001c0002t0001g0079 a0002c0005t0001g0377 |
2 | HG02258.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.146-3831C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144760 | |||||||
| chr19:3144771 | G | A | 1 | a0001c0002t0001g0284 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.146-3820G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144771 | |||||||
| chr19:3144774 | C | T | 3 | a0001c0002t0001g0005 a0001c0002t0001g0067 a0001c0002t0001g0141 |
4 | HG02080.hp1 HG02258.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.146-3817C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144774 | |||||||
| chr19:3144775 | G | A | 69 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0020 others(66): Show |
75 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.146-3816G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144775 | |||||||
| chr19:3144779 | T | C | 5 | a0001c0001t0001g0107 a0001c0001t0001g0148 a0001c0002t0001g0147 others(2): Show |
5 | HG02818.hp1 HG03831.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.146-3812T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144779 | |||||||
| chr19:3144789 | T | A | 3 | a0001c0001t0001g0107 a0001c0001t0001g0148 a0001c0002t0001g0147 |
3 | HG03831.hp2 NA18995.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.146-3802T>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144789 | |||||||
| chr19:3144797 | A | G | 3 | a0001c0001t0001g0107 a0001c0001t0001g0148 a0001c0002t0001g0147 |
3 | HG03831.hp2 NA18995.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.146-3794A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144797 | |||||||
| chr19:3144815 | A | G | 3 | a0001c0001t0001g0213 a0001c0001t0001g0272 a0001c0001t0001g0273 |
3 | HG00609.hp1 HG00639.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.146-3776A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144815 | |||||||
| chr19:3144815 | A | T | 4 | a0001c0001t0001g0250 a0001c0001t0001g0302 a0001c0001t0001g0418 others(1): Show |
4 | HG02257.hp1 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-3776A>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144815 | |||||||
| chr19:3144817 | C | T | 4 | a0001c0001t0001g0250 a0001c0001t0001g0302 a0001c0001t0001g0418 others(1): Show |
4 | HG02257.hp1 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-3774C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144817 | |||||||
| chr19:3144819 | G | C | 134 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0020 others(131): Show |
146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.146-3772G>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144819 | |||||||
| chr19:3144819 | G | T | 4 | a0001c0001t0001g0250 a0001c0001t0001g0302 a0001c0001t0001g0418 others(1): Show |
4 | HG02257.hp1 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-3772G>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144819 | |||||||
| chr19:3144823 | C | T | 135 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0020 others(132): Show |
147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.146-3768C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144823 | |||||||
| chr19:3144885 | G | A | 137 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0020 others(134): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.146-3706G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144885 | |||||||
| chr19:3144897 | C | T | 4 | a0001c0001t0001g0136 a0001c0001t0001g0232 a0001c0001t0001g0271 others(1): Show |
4 | HG02486.hp2 HG02572.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-3694C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144897 | |||||||
| chr19:3144969 | C | T | 1 | a0001c0002t0001g0375 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.146-3622C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144969 | |||||||
| chr19:3144975 | C | T | 2 | a0001c0001t0001g0314 a0001c0009t0001g0298 |
2 | HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.146-3616C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3144975 | |||||||
| chr19:3145177 | C | CT | 69 | a0001c0001t0001g0058 a0001c0001t0001g0080 a0001c0001t0001g0136 others(66): Show |
72 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.146-3404dupT | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145177 | ||||||
| chr19:3145266 | C | T | 12 | a0001c0001t0001g0216 a0001c0001t0001g0250 a0001c0001t0001g0302 others(9): Show |
12 | HG00323.hp1 HG01496.hp1 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.146-3325C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3145266 | |||||||
| chr19:3145274 | A | G | 1 | a0001c0001t0001g0302 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.146-3317A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3145274 | |||||||
| chr19:3145277 | C | T | 10 | a0001c0001t0001g0136 a0001c0001t0001g0232 a0001c0001t0001g0271 others(7): Show |
10 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.146-3314C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3145277 | |||||||
| chr19:3145326 | C | T | 7 | a0001c0001t0001g0216 a0001c0001t0001g0250 a0001c0001t0001g0302 others(4): Show |
7 | HG02257.hp1 HG02258.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.146-3265C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3145326 | |||||||
| chr19:3145336 | A | AAT | 15 | a0001c0001t0001g0057 a0001c0002t0001g0001 a0001c0002t0001g0004 others(12): Show |
19 | HG00558.hp1 HG01256.hp1 HG01928.hp1 others(16): Show |
intron_variant | MODIFIER | c.146-3232_146-3231d others(4): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145336 | ||||||
| chr19:3145336 | A | AATAT | 12 | a0001c0002t0001g0047 a0001c0002t0001g0048 a0001c0002t0001g0052 others(9): Show |
12 | HG02074.hp2 HG02132.hp2 HG04184.hp1 others(9): Show |
intron_variant | MODIFIER | c.146-3234_146-3231d others(6): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145336 | ||||||
| chr19:3145336 | A | AATATAT | 4 | a0001c0002t0001g0024 a0001c0002t0001g0300 a0001c0002t0001g0301 others(1): Show |
5 | HG02055.hp1 HG02451.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.146-3236_146-3231d others(8): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145336 | ||||||
| chr19:3145336 | A | AATATATA others(7): Show |
1 | a0001c0003t0001g0084 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.146-3244_146-3231d others(16): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145336 | ||||||
| chr19:3145336 | A | AATATATA others(9): Show |
13 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0073 others(10): Show |
15 | HG00423.hp1 HG00438.hp2 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.146-3246_146-3231d others(18): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145336 | ||||||
| chr19:3145336 | A | AATATATA others(11): Show |
4 | a0001c0001t0001g0108 a0001c0001t0001g0128 a0001c0001t0001g0254 others(1): Show |
4 | HG02027.hp1 NA18954.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-3248_146-3231d others(20): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145336 | ||||||
| chr19:3145336 | A | AATATATA others(15): Show |
3 | a0001c0001t0001g0104 a0001c0001t0001g0151 a0006c0014t0001g0126 |
3 | HG02056.hp1 NA18964.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.146-3252_146-3231d others(24): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145336 | ||||||
| chr19:3145336 | A | AATATATA others(17): Show |
3 | a0001c0001t0001g0007 a0001c0001t0001g0150 a0001c0003t0001g0274 |
4 | HG02809.hp1 NA18945.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-3254_146-3231d others(26): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145336 | ||||||
| chr19:3145355 | A | AT | 3 | a0001c0001t0005g0345 a0001c0001t0005g0346 a0001c0001t0005g0349 |
3 | HG00323.hp1 HG01496.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.146-3235dupT | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145355 | ||||||
| chr19:3145357 | A | ATTTT | 6 | a0001c0001t0001g0297 a0001c0001t0001g0304 a0001c0001t0001g0306 others(3): Show |
7 | HG00735.hp1 HG01169.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.146-3233_146-3232i others(6): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145357 | ||||||
| chr19:3145357 | A | T | 4 | a0001c0001t0001g0308 a0001c0001t0005g0345 a0001c0001t0005g0346 others(1): Show |
4 | HG00323.hp1 HG01496.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.146-3234A>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3145357 | |||||||
| chr19:3145358 | T | C | 4 | a0001c0001t0001g0250 a0001c0001t0001g0302 a0001c0001t0001g0418 others(1): Show |
4 | HG02257.hp1 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-3233T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3145358 | |||||||
| chr19:3145358 | TA | T | 13 | a0001c0001t0001g0263 a0001c0001t0001g0265 a0001c0001t0001g0266 others(10): Show |
14 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.146-3232delA | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3145358 | |||||||
| chr19:3145359 | A | AT | 6 | a0001c0001t0001g0121 a0001c0001t0001g0180 a0001c0001t0001g0250 others(3): Show |
6 | HG00741.hp1 HG02257.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.146-3219dupT | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145359 | A | ATATATAT | 22 | a0001c0001t0001g0058 a0001c0001t0001g0137 a0001c0001t0001g0218 others(19): Show |
22 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.146-3231_146-3230i others(9): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145359 | A | ATATATAT others(5): Show |
2 | a0001c0002t0001g0079 a0002c0005t0001g0377 |
2 | HG02258.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.146-3231_146-3230i others(14): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145359 | A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0216 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.146-3231_146-3230i others(13): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145359 | A | ATATATAT others(4): Show |
5 | a0001c0001t0001g0355 a0001c0003t0001g0275 a0001c0003t0001g0278 others(2): Show |
5 | HG02886.hp1 HG02965.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.146-3231_146-3230i others(13): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145359 | A | ATATATAT others(6): Show |
14 | a0001c0001t0001g0122 a0001c0001t0001g0170 a0001c0001t0001g0181 others(11): Show |
15 | HG01074.hp1 HG01106.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.146-3231_146-3230i others(15): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145359 | A | ATATATAT others(8): Show |
8 | a0001c0001t0001g0028 a0001c0001t0001g0177 a0001c0002t0001g0026 others(5): Show |
8 | HG00280.hp2 HG01175.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.146-3231_146-3230i others(17): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145359 | A | ATATATAT others(10): Show |
10 | a0001c0001t0001g0089 a0001c0001t0001g0309 a0001c0002t0001g0026 others(7): Show |
10 | HG00099.hp2 HG00280.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.146-3231_146-3230i others(19): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145359 | A | ATATATAT others(12): Show |
2 | a0001c0001t0001g0115 a0001c0002t0001g0091 |
2 | HG03491.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.146-3231_146-3230i others(21): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145359 | A | ATATATAT others(14): Show |
1 | a0001c0002t0001g0362 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.146-3231_146-3230i others(23): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145359 | A | ATATATAT others(16): Show |
2 | a0001c0001t0001g0176 a0001c0003t0001g0022 |
2 | HG01099.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.146-3231_146-3230i others(25): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145359 | A | ATATATAT others(18): Show |
2 | a0001c0001t0001g0074 a0001c0003t0001g0022 |
2 | HG01192.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.146-3231_146-3230i others(27): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145359 | A | ATATATAT others(20): Show |
2 | a0001c0002t0001g0134 a0001c0002t0018g0093 |
2 | HG02071.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.146-3231_146-3230i others(29): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145359 | A | ATATATAT others(24): Show |
1 | a0001c0001t0001g0059 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.146-3231_146-3230i others(33): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145359 | A | ATATATAT others(23): Show |
1 | a0001c0001t0001g0178 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.146-3231_146-3230i others(32): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145359 | A | ATATATAT others(22): Show |
1 | a0001c0001t0001g0077 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.146-3231_146-3230i others(31): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145359 | A | ATATATAT others(20): Show |
1 | a0001c0002t0001g0117 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.146-3231_146-3230i others(29): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145359 | A | ATATATAT others(22): Show |
1 | a0001c0001t0001g0262 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.146-3231_146-3230i others(31): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145359 | A | ATATATAT others(18): Show |
3 | a0001c0002t0001g0072 a0001c0002t0001g0118 a0001c0002t0001g0259 |
3 | NA18977.hp2 NA18985.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.146-3231_146-3230i others(27): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145359 | A | ATATATAT others(11): Show |
2 | a0001c0001t0001g0131 a0001c0002t0001g0102 |
2 | HG00609.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.146-3231_146-3230i others(20): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145359 | A | ATATATAT others(12): Show |
7 | a0001c0001t0001g0116 a0001c0001t0001g0123 a0001c0001t0001g0174 others(4): Show |
7 | HG01074.hp2 HG01975.hp1 HG04184.hp2 others(4): Show |
intron_variant | MODIFIER | c.146-3231_146-3230i others(21): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145359 | A | ATATATAT others(9): Show |
6 | a0001c0001t0001g0092 a0001c0001t0001g0132 a0001c0001t0001g0244 others(3): Show |
6 | HG02071.hp1 NA18980.hp2 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.146-3231_146-3230i others(18): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145359 | A | ATATATAT others(10): Show |
6 | a0001c0001t0001g0119 a0001c0002t0001g0101 a0001c0002t0001g0175 others(3): Show |
6 | HG00741.hp2 HG01192.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.146-3231_146-3230i others(19): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145359 | A | ATATATAT others(11): Show |
2 | a0001c0002t0001g0090 a0001c0002t0001g0396 |
2 | NA18960.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.146-3231_146-3230i others(20): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145359 | A | ATATATAT others(7): Show |
2 | a0001c0004t0001g0185 a0005c0011t0020g0023 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.146-3231_146-3230i others(16): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145359 | A | ATATATAT others(9): Show |
1 | a0001c0002t0001g0236 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.146-3231_146-3230i others(18): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145359 | A | ATATATAT others(10): Show |
3 | a0001c0001t0001g0397 a0001c0002t0001g0173 a0001c0002t0001g0333 |
3 | HG01517.hp2 HG02027.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.146-3231_146-3230i others(19): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145359 | A | ATATATAT others(5): Show |
2 | a0001c0004t0001g0146 a0008c0010t0001g0376 |
2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.146-3231_146-3230i others(14): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145359 | A | ATATATAT others(6): Show |
5 | a0001c0001t0001g0341 a0001c0001t0009g0310 a0001c0001t0009g0315 others(2): Show |
5 | HG02559.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.146-3231_146-3230i others(15): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145359 | A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0379 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.146-3231_146-3230i others(17): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145359 | A | ATATATAT others(3): Show |
4 | a0001c0001t0001g0136 a0001c0001t0001g0232 a0001c0001t0001g0271 others(1): Show |
4 | HG02486.hp2 HG02572.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.146-3231_146-3230i others(12): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145359 | A | ATATATAT others(4): Show |
2 | a0001c0001t0001g0069 a0001c0003t0001g0280 |
2 | HG01891.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.146-3231_146-3230i others(13): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145359 | A | ATATATAT others(5): Show |
1 | a0001c0004t0001g0282 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.146-3231_146-3230i others(14): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145359 | A | ATATATAT others(6): Show |
2 | a0001c0003t0001g0008 a0001c0003t0001g0120 |
2 | HG00639.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.146-3231_146-3230i others(15): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145359 | A | ATATATAT others(7): Show |
1 | a0001c0004t0001g0243 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.146-3231_146-3230i others(16): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145359 | A | ATATATAT others(2): Show |
6 | a0001c0001t0001g0066 a0001c0001t0001g0071 a0001c0001t0001g0159 others(3): Show |
6 | HG00099.hp1 HG03209.hp2 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.146-3231_146-3230i others(11): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145359 | A | ATATATTT | 13 | a0001c0001t0001g0148 a0001c0001t0001g0248 a0001c0001t0011g0267 others(10): Show |
13 | HG00738.hp1 HG01361.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.146-3231_146-3230i others(9): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145359 | A | ATATATTT others(6): Show |
1 | a0001c0008t0001g0252 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.146-3231_146-3230i others(15): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145359 | A | ATATT | 5 | a0001c0001t0006g0289 a0001c0002t0001g0050 a0001c0002t0001g0051 others(2): Show |
6 | HG01123.hp1 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.146-3231_146-3230i others(6): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145359 | A | ATATTT | 44 | a0001c0001t0001g0107 a0001c0001t0001g0114 a0001c0001t0001g0160 others(41): Show |
48 | HG00438.hp1 HG01081.hp1 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.146-3231_146-3230i others(7): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145359 | A | ATATTTTT others(4): Show |
2 | a0001c0001t0001g0314 a0001c0008t0001g0065 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.146-3231_146-3230i others(13): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145359 | A | ATTTT | 7 | a0001c0001t0001g0020 a0001c0001t0001g0293 a0001c0001t0001g0294 others(4): Show |
8 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.146-3222_146-3219d others(6): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145359 | A | T | 80 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0025 others(77): Show |
83 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.146-3232A>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3145359 | |||||||
| chr19:3145359 | AT | A | 7 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0002g0410 others(4): Show |
8 | HG01069.hp2 HG01071.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.146-3219delT | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145359 | ||||||
| chr19:3145360 | T | TATATA | 6 | a0001c0001t0001g0142 a0001c0002t0001g0097 a0001c0002t0001g0153 others(3): Show |
6 | HG02647.hp2 HG02922.hp1 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.146-3231_146-3230i others(7): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3145360 | |||||||
| chr19:3145360 | T | TATATATA | 7 | a0001c0001t0001g0080 a0001c0001t0001g0318 a0001c0002t0001g0220 others(4): Show |
8 | HG00642.hp1 HG01070.hp1 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.146-3231_146-3230i others(9): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3145360 | |||||||
| chr19:3145360 | T | TATATATA others(4): Show |
1 | a0001c0001t0002g0406 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.146-3231_146-3230i others(13): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3145360 | |||||||
| chr19:3145360 | T | TATATATA others(6): Show |
1 | a0001c0001t0001g0390 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.146-3231_146-3230i others(15): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3145360 | |||||||
| chr19:3145360 | T | TATATATA others(10): Show |
7 | a0001c0001t0001g0036 a0001c0002t0001g0060 a0001c0002t0001g0332 others(4): Show |
7 | HG00621.hp2 HG01978.hp1 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.146-3231_146-3230i others(19): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3145360 | |||||||
| chr19:3145360 | T | TATATATA others(12): Show |
3 | a0001c0001t0001g0034 a0001c0002t0001g0033 a0001c0002t0001g0391 |
3 | HG02273.hp1 NA18994.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.146-3231_146-3230i others(21): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3145360 | |||||||
| chr19:3145360 | T | TATATATA others(14): Show |
3 | a0001c0001t0001g0045 a0001c0002t0001g0356 a0001c0002t0008g0350 |
3 | NA18906.hp1 NA19004.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.146-3231_146-3230i others(23): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3145360 | |||||||
| chr19:3145360 | T | TATATATA others(18): Show |
4 | a0001c0001t0001g0075 a0001c0001t0001g0083 a0001c0001t0001g0312 others(1): Show |
4 | HG02300.hp2 HG03139.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.146-3231_146-3230i others(27): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3145360 | |||||||
| chr19:3145360 | T | TATATATA others(22): Show |
1 | a0001c0001t0001g0035 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.146-3231_146-3230i others(31): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3145360 | |||||||
| chr19:3145361 | T | A | 5 | a0001c0001t0001g0104 a0001c0001t0001g0127 a0001c0001t0001g0254 others(2): Show |
5 | HG02027.hp1 HG02809.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.146-3230T>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3145361 | |||||||
| chr19:3145362 | T | A | 8 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(5): Show |
8 | HG00621.hp2 HG01099.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.146-3229T>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3145362 | |||||||
| chr19:3145363 | T | A | 1 | a0001c0003t0001g0274 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.146-3228T>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3145363 | |||||||
| chr19:3145422 | G | A | 2 | a0001c0002t0001g0270 a0001c0002t0001g0305 |
2 | HG02622.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.146-3169G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3145422 | |||||||
| chr19:3145431 | G | A | 39 | a0001c0001t0001g0058 a0001c0001t0001g0080 a0001c0001t0001g0137 others(36): Show |
42 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.146-3160G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3145431 | |||||||
| chr19:3145432 | C | T | 1 | a0001c0003t0001g0139 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.146-3159C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3145432 | |||||||
| chr19:3145577 | T | TCTCACTC others(497): Show |
5 | a0001c0001t0011g0267 a0001c0002t0001g0242 a0001c0002t0001g0268 others(2): Show |
5 | HG02723.hp2 HG02965.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.146-2988_146-2987i others(506): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145577 | ||||||
| chr19:3145577 | T | TCTCACTC others(498): Show |
1 | a0001c0002t0001g0241 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.146-2988_146-2987i others(507): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145577 | ||||||
| chr19:3145577 | T | TCTCACTC others(498): Show |
2 | a0001c0001t0001g0137 a0001c0003t0001g0010 |
3 | HG00733.hp1 HG00733.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.146-2988_146-2987i others(507): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145577 | ||||||
| chr19:3145577 | T | TCTCACTC others(488): Show |
1 | a0001c0001t0005g0349 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.146-2988_146-2987i others(497): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145577 | ||||||
| chr19:3145577 | T | TCTCACTC others(489): Show |
13 | a0001c0001t0001g0136 a0001c0001t0001g0232 a0001c0001t0001g0271 others(10): Show |
13 | HG01496.hp1 HG01515.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.146-2988_146-2987i others(498): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145577 | ||||||
| chr19:3145577 | T | TCTCACTC others(490): Show |
4 | a0001c0001t0001g0303 a0001c0001t0005g0345 a0001c0002t0001g0005 others(1): Show |
5 | HG01168.hp1 HG02258.hp2 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.146-2988_146-2987i others(499): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145577 | ||||||
| chr19:3145577 | T | TCTCACTC others(491): Show |
77 | a0001c0001t0001g0020 a0001c0001t0001g0066 a0001c0001t0001g0071 others(74): Show |
83 | HG00438.hp1 HG00642.hp2 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.146-2988_146-2987i others(500): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145577 | ||||||
| chr19:3145577 | T | TCTCACTC others(492): Show |
11 | a0001c0001t0001g0265 a0001c0002t0001g0052 a0001c0002t0001g0098 others(8): Show |
11 | HG01891.hp2 HG02132.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.146-2988_146-2987i others(501): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145577 | ||||||
| chr19:3145577 | T | TCTCACTC others(493): Show |
3 | a0001c0002t0001g0047 a0001c0002t0001g0078 a0001c0002t0001g0246 |
3 | HG02074.hp2 NA18979.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.146-2988_146-2987i others(502): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145577 | ||||||
| chr19:3145577 | T | TCTCACTC others(494): Show |
1 | a0001c0003t0001g0139 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.146-2988_146-2987i others(503): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145577 | ||||||
| chr19:3145577 | T | TCTCACTC others(495): Show |
3 | a0001c0001t0001g0216 a0001c0002t0001g0079 a0002c0005t0001g0377 |
3 | HG02258.hp1 HG02922.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.146-2988_146-2987i others(504): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145577 | ||||||
| chr19:3145577 | T | TCTCACTC others(497): Show |
2 | a0001c0002t0001g0097 a0001c0003t0001g0219 |
2 | HG01070.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.146-2988_146-2987i others(506): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145577 | ||||||
| chr19:3145577 | T | TCTCACTC others(498): Show |
50 | a0001c0001t0001g0058 a0001c0001t0001g0080 a0001c0001t0001g0218 others(47): Show |
53 | HG00140.hp2 HG00621.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.146-2988_146-2987i others(507): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145577 | ||||||
| chr19:3145577 | T | TCTCACTC others(499): Show |
30 | a0001c0001t0001g0057 a0001c0001t0001g0248 a0001c0001t0001g0263 others(27): Show |
34 | HG00140.hp1 HG00558.hp1 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.146-2988_146-2987i others(508): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145577 | ||||||
| chr19:3145577 | T | TCTCACTC others(500): Show |
5 | a0001c0001t0001g0283 a0001c0002t0001g0051 a0001c0002t0001g0276 others(2): Show |
5 | HG01884.hp2 HG01981.hp1 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.146-2988_146-2987i others(509): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145577 | ||||||
| chr19:3145577 | T | TCTCACTC others(506): Show |
2 | a0001c0001t0001g0302 a0001c0001t0001g0418 |
2 | HG02257.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.146-2988_146-2987i others(515): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145577 | ||||||
| chr19:3145577 | T | TCTCACTC others(508): Show |
2 | a0001c0001t0001g0250 a0001c0003t0001g0211 |
2 | HG03130.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.146-2988_146-2987i others(517): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145577 | ||||||
| chr19:3145577 | T | TCTCACTC others(499): Show |
3 | a0001c0001t0001g0369 a0001c0002t0001g0063 a0001c0002t0001g0368 |
3 | HG00558.hp2 HG02523.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.146-2988_146-2987i others(508): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145577 | ||||||
| chr19:3145577 | T | TCTCACTC others(500): Show |
25 | a0001c0001t0001g0087 a0001c0001t0001g0206 a0001c0001t0001g0212 others(22): Show |
25 | HG00323.hp2 HG00609.hp1 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.146-2988_146-2987i others(509): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145577 | ||||||
| chr19:3145577 | T | TCTCACTC others(501): Show |
30 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0025 others(27): Show |
33 | HG00408.hp1 HG00408.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.146-2988_146-2987i others(510): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145577 | ||||||
| chr19:3145577 | T | TCTCACTC others(502): Show |
11 | a0001c0001t0001g0068 a0001c0001t0001g0203 a0001c0001t0001g0324 others(8): Show |
11 | HG00621.hp1 HG02056.hp2 NA18612.hp2 others(8): Show |
intron_variant | MODIFIER | c.146-2988_146-2987i others(511): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145577 | ||||||
| chr19:3145577 | T | TCTCACTC others(491): Show |
11 | a0001c0001t0001g0167 a0001c0001t0001g0364 a0001c0002t0001g0002 others(8): Show |
16 | HG01081.hp1 HG01081.hp2 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.146-2988_146-2987i others(500): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145577 | ||||||
| chr19:3145577 | T | TCTCACTC others(498): Show |
1 | a0001c0002t0001g0169 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.146-2988_146-2987i others(507): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145577 | ||||||
| chr19:3145577 | T | TCTCACTC others(499): Show |
11 | a0001c0001t0001g0073 a0001c0001t0001g0089 a0001c0001t0001g0115 others(8): Show |
11 | HG00741.hp2 HG01346.hp1 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.146-2988_146-2987i others(508): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145577 | ||||||
| chr19:3145577 | T | TCTCACTC others(501): Show |
26 | a0001c0001t0001g0028 a0001c0001t0001g0059 a0001c0001t0001g0074 others(23): Show |
27 | HG00609.hp2 HG00741.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.146-2988_146-2987i others(510): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145577 | ||||||
| chr19:3145577 | T | TCTCACTC others(502): Show |
6 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0001c0001t0001g0123 others(3): Show |
6 | HG00423.hp2 HG01192.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.146-2988_146-2987i others(511): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145577 | ||||||
| chr19:3145577 | T | TCTCACTC others(503): Show |
1 | a0001c0001t0001g0176 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.146-2988_146-2987i others(512): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3145577 | ||||||
| chr19:3145642 | A | G | 22 | a0001c0001t0001g0136 a0001c0001t0001g0216 a0001c0001t0001g0232 others(19): Show |
22 | HG00323.hp1 HG01496.hp1 HG01515.hp1 others(19): Show |
intron_variant | MODIFIER | c.146-2949A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3145642 | |||||||
| chr19:3145654 | T | A | 1 | a0001c0001t0010g0105 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.146-2937T>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3145654 | |||||||
| chr19:3145677 | A | T | 1 | a0001c0001t0001g0030 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.146-2914A>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3145677 | |||||||
| chr19:3145692 | C | G | 54 | a0001c0001t0001g0057 a0001c0001t0001g0277 a0001c0001t0001g0390 others(51): Show |
59 | HG00558.hp1 HG00621.hp2 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.146-2899C>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3145692 | |||||||
| chr19:3145828 | G | A | 19 | a0001c0001t0001g0390 a0001c0001t0001g0397 a0001c0002t0001g0026 others(16): Show |
20 | HG00621.hp2 HG01978.hp1 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.146-2763G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3145828 | |||||||
| chr19:3145885 | A | G | 2 | a0001c0001t0001g0318 a0001c0003t0001g0317 |
2 | HG02970.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.146-2706A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3145885 | |||||||
| chr19:3145889 | C | T | 71 | a0001c0001t0001g0066 a0001c0001t0001g0071 a0001c0001t0001g0099 others(68): Show |
80 | HG00438.hp1 HG01081.hp1 HG01081.hp2 others(77): Show |
intron_variant | MODIFIER | c.146-2702C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3145889 | |||||||
| chr19:3145901 | C | T | 7 | a0001c0001t0001g0216 a0001c0001t0001g0250 a0001c0001t0001g0302 others(4): Show |
7 | HG02257.hp1 HG02258.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.146-2690C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3145901 | |||||||
| chr19:3145917 | C | A | 3 | a0001c0002t0001g0024 a0001c0002t0001g0300 a0001c0002t0001g0301 |
4 | HG02055.hp1 HG02451.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-2674C>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3145917 | |||||||
| chr19:3145954 | A | G | 4 | a0001c0001t0001g0250 a0001c0001t0001g0302 a0001c0001t0001g0418 others(1): Show |
4 | HG02257.hp1 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-2637A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3145954 | |||||||
| chr19:3146031 | C | A | 1 | a0001c0001t0010g0105 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.146-2560C>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3146031 | |||||||
| chr19:3146118 | C | T | 4 | a0001c0001t0001g0216 a0001c0001t0001g0418 a0001c0003t0001g0211 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-2473C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3146118 | |||||||
| chr19:3146171 | G | A | 3 | a0001c0001t0001g0216 a0001c0002t0001g0079 a0002c0005t0001g0377 |
3 | HG02258.hp1 HG02922.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.146-2420G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3146171 | |||||||
| chr19:3146215 | T | A | 97 | a0001c0001t0001g0020 a0001c0001t0001g0066 a0001c0001t0001g0071 others(94): Show |
104 | HG00323.hp1 HG00438.hp1 HG00642.hp2 others(101): Show |
intron_variant | MODIFIER | c.146-2376T>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3146215 | |||||||
| chr19:3146270 | C | G | 102 | a0001c0001t0001g0020 a0001c0001t0001g0066 a0001c0001t0001g0071 others(99): Show |
110 | HG00323.hp1 HG00438.hp1 HG00642.hp2 others(107): Show |
intron_variant | MODIFIER | c.146-2321C>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3146270 | |||||||
| chr19:3146283 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.146-2308C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3146283 | |||||||
| chr19:3146336 | G | A | 9 | a0001c0001t0001g0136 a0001c0001t0001g0232 a0001c0001t0001g0271 others(6): Show |
9 | HG02486.hp2 HG02572.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.146-2255G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3146336 | |||||||
| chr19:3146463 | C | T | 5 | a0001c0001t0005g0345 a0001c0001t0005g0346 a0001c0001t0005g0347 others(2): Show |
5 | HG00323.hp1 HG01496.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.146-2128C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3146463 | |||||||
| chr19:3146503 | G | A | 9 | a0001c0002t0001g0222 a0001c0003t0001g0138 a0001c0003t0001g0240 others(6): Show |
10 | HG00140.hp2 HG01074.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.146-2088G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3146503 | |||||||
| chr19:3146516 | G | T | 1 | a0001c0002t0001g0168 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.146-2075G>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3146516 | |||||||
| chr19:3146539 | CTG | C | 3 | a0001c0002t0001g0124 a0001c0002t0001g0134 a0001c0002t0001g0340 |
3 | HG02071.hp2 HG02523.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.146-2049_146-2048d others(4): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3146539 | ||||||
| chr19:3146703 | C | G | 1 | a0001c0001t0003g0215 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.146-1888C>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3146703 | |||||||
| chr19:3146746 | C | T | 1 | a0001c0001t0001g0318 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.146-1845C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3146746 | |||||||
| chr19:3146763 | G | A | 2 | a0001c0003t0001g0274 a0001c0009t0001g0264 |
2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.146-1828G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3146763 | |||||||
| chr19:3146818 | C | T | 6 | a0001c0001t0001g0299 a0001c0001t0001g0309 a0001c0001t0001g0312 others(3): Show |
6 | HG02280.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.146-1773C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3146818 | |||||||
| chr19:3146855 | C | A | 1 | a0001c0002t0001g0163 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.146-1736C>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3146855 | |||||||
| chr19:3146886 | G | A | 1 | a0001c0009t0001g0264 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.146-1705G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3146886 | |||||||
| chr19:3146903 | C | T | 2 | a0001c0003t0001g0225 a0001c0003t0001g0227 |
2 | HG00140.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.146-1688C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3146903 | |||||||
| chr19:3146918 | C | T | 9 | a0001c0001t0001g0181 a0001c0001t0002g0027 a0001c0001t0002g0404 others(6): Show |
10 | HG01109.hp1 HG01243.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.146-1673C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3146918 | |||||||
| chr19:3147073 | T | C | 252 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(249): Show |
275 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.146-1518T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3147073 | |||||||
| chr19:3147144 | C | T | 1 | a0001c0001t0001g0019 | 2 | HG00438.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.146-1447C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3147144 | |||||||
| chr19:3147262 | A | G | 1 | a0001c0001t0001g0397 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.146-1329A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3147262 | |||||||
| chr19:3147328 | G | A | 260 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(257): Show |
283 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.146-1263G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3147328 | |||||||
| chr19:3147423 | C | T | 299 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(296): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.146-1168C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3147423 | |||||||
| chr19:3147426 | G | A | 2 | a0001c0001t0001g0283 a0001c0004t0001g0185 |
2 | HG01884.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.146-1165G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3147426 | |||||||
| chr19:3147528 | G | A | 2 | a0001c0007t0010g0373 a0001c0007t0012g0408 |
2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.146-1063G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3147528 | |||||||
| chr19:3147552 | AAAAAG | A | 263 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(260): Show |
285 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.146-1034_146-1030d others(7): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3147552 | ||||||
| chr19:3147563 | A | G | 1 | a0001c0002t0018g0093 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.146-1028A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3147563 | |||||||
| chr19:3147564 | A | G | 263 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(260): Show |
286 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.146-1027A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3147564 | |||||||
| chr19:3147565 | G | A | 264 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(261): Show |
287 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.146-1026G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3147565 | |||||||
| chr19:3147636 | G | A | 2 | a0001c0007t0010g0373 a0001c0007t0012g0408 |
2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.146-955G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3147636 | |||||||
| chr19:3147645 | G | A | 265 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(262): Show |
288 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.146-946G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3147645 | |||||||
| chr19:3147680 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.146-911G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3147680 | |||||||
| chr19:3147714 | G | T | 1 | a0001c0002t0019g0328 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.146-877G>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3147714 | |||||||
| chr19:3147759 | T | C | 332 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(329): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.146-832T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3147759 | |||||||
| chr19:3147766 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.146-825A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3147766 | |||||||
| chr19:3147800 | A | G | 264 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(261): Show |
287 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.146-791A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3147800 | |||||||
| chr19:3147871 | G | C | 42 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0025 others(39): Show |
45 | HG00323.hp2 HG00408.hp1 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.146-720G>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3147871 | |||||||
| chr19:3147887 | C | CA | 146 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(143): Show |
156 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.146-687dupA | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3147887 | ||||||
| chr19:3147887 | C | CAA | 13 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0001g0260 others(10): Show |
13 | HG00733.hp2 HG01106.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.146-688_146-687dup others(2): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3147887 | ||||||
| chr19:3147887 | CA | C | 103 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0025 others(100): Show |
110 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.146-687delA | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3147887 | ||||||
| chr19:3148071 | T | G | 265 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(262): Show |
288 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.146-520T>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3148071 | |||||||
| chr19:3148075 | G | GT | 5 | a0001c0001t0001g0210 a0001c0001t0001g0277 a0001c0001t0004g0415 others(2): Show |
5 | HG02630.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.146-508dupT | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3148075 | ||||||
| chr19:3148075 | GT | G | 265 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(262): Show |
288 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.146-508delT | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3148075 | ||||||
| chr19:3148079 | T | G | 1 | a0001c0001t0001g0418 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.146-512T>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3148079 | |||||||
| chr19:3148097 | G | GT | 7 | a0001c0001t0001g0074 a0001c0001t0001g0107 a0001c0001t0001g0250 others(4): Show |
7 | HG01192.hp2 HG01884.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.146-485dupT | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 3148097 | ||||||
| chr19:3148098 | T | G | 3 | a0001c0001t0001g0136 a0001c0001t0001g0232 a0001c0001t0001g0271 |
3 | HG02486.hp2 HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.146-493T>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3148098 | |||||||
| chr19:3148122 | C | T | 183 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(180): Show |
201 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.146-469C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3148122 | |||||||
| chr19:3148127 | C | T | 55 | a0001c0001t0001g0058 a0001c0001t0001g0080 a0001c0001t0001g0181 others(52): Show |
59 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.146-464C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3148127 | |||||||
| chr19:3148131 | C | G | 1 | a0001c0001t0001g0250 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.146-460C>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3148131 | |||||||
| chr19:3148284 | C | T | 27 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0073 others(24): Show |
29 | HG00423.hp1 HG00438.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.146-307C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3148284 | |||||||
| chr19:3148298 | G | T | 83 | a0001c0001t0001g0162 a0001c0001t0001g0262 a0001c0001t0001g0379 others(80): Show |
88 | HG00438.hp1 HG01358.hp2 HG01515.hp2 others(85): Show |
intron_variant | MODIFIER | c.146-293G>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3148298 | |||||||
| chr19:3148496 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.146-95C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3148496 | |||||||
| chr19:3148554 | C | G | 7 | a0001c0001t0001g0020 a0001c0001t0001g0248 a0001c0001t0001g0293 others(4): Show |
9 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.146-37C>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | chr19 | 3148554 | |||||||
| chr19:3148783 | GCCAGGGC others(10): Show |
G | 1 | a0001c0003t0001g0224 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.330+36_330+52delCA others(15): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 3148783 | ||||||
| chr19:3148821 | G | T | 265 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(262): Show |
288 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.330+46G>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 2/6 | chr19 | 3148821 | |||||||
| chr19:3148846 | C | T | 1 | a0001c0002t0001g0113 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.330+71C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 2/6 | chr19 | 3148846 | |||||||
| chr19:3148867 | T | TCAGGG | 11 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0001c0001t0001g0123 others(8): Show |
11 | HG00323.hp1 HG00423.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.330+117_330+121dup others(5): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 3148867 | ||||||
| chr19:3148871 | G | A | 12 | a0001c0003t0001g0008 a0001c0003t0001g0022 a0001c0003t0001g0023 others(9): Show |
14 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.330+96G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 2/6 | chr19 | 3148871 | |||||||
| chr19:3149018 | G | T | 2 | a0001c0002t0001g0097 a0001c0003t0001g0096 |
2 | HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.330+243G>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 2/6 | chr19 | 3149018 | |||||||
| chr19:3149038 | C | CACAT | 328 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(325): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.330+265_330+266ins others(4): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 3149038 | ||||||
| chr19:3149058 | TACAC | T | 7 | a0001c0001t0001g0020 a0001c0001t0001g0248 a0001c0001t0001g0293 others(4): Show |
9 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.330+286_330+289del others(4): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 3149058 | ||||||
| chr19:3149390 | C | T | 265 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(262): Show |
288 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.330+615C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 2/6 | chr19 | 3149390 | |||||||
| chr19:3149421 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.330+646T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 2/6 | chr19 | 3149421 | |||||||
| chr19:3149451 | C | G | 1 | a0001c0001t0001g0148 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.330+676C>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 2/6 | chr19 | 3149451 | |||||||
| chr19:3149497 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.331-634C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 2/6 | chr19 | 3149497 | |||||||
| chr19:3149543 | T | C | 415 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(412): Show |
445 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(442): Show |
intron_variant | MODIFIER | c.331-588T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 2/6 | chr19 | 3149543 | |||||||
| chr19:3149580 | G | A | 1 | a0001c0003t0001g0082 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.331-551G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 2/6 | chr19 | 3149580 | |||||||
| chr19:3149588 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.331-543A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 2/6 | chr19 | 3149588 | |||||||
| chr19:3149595 | AAC | A | 3 | a0001c0001t0006g0021 a0001c0001t0006g0287 a0001c0001t0006g0289 |
4 | HG01358.hp2 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.331-532_331-531del others(2): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 3149595 | ||||||
| chr19:3149697 | A | G | 338 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(335): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.331-434A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 2/6 | chr19 | 3149697 | |||||||
| chr19:3149742 | A | G | 7 | a0001c0001t0001g0020 a0001c0001t0001g0248 a0001c0001t0001g0293 others(4): Show |
9 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.331-389A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 2/6 | chr19 | 3149742 | |||||||
| chr19:3149754 | C | T | 1 | a0001c0001t0003g0217 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.331-377C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 2/6 | chr19 | 3149754 | |||||||
| chr19:3149800 | G | C | 87 | a0001c0001t0001g0258 a0001c0001t0001g0364 a0001c0001t0010g0105 others(84): Show |
98 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.331-331G>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 2/6 | chr19 | 3149800 | |||||||
| chr19:3149852 | G | C | 1 | a0001c0001t0002g0406 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.331-279G>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 2/6 | chr19 | 3149852 | |||||||
| chr19:3149992 | G | C | 343 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(340): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.331-139G>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 2/6 | chr19 | 3149992 | |||||||
| chr19:3150073 | G | T | 86 | a0001c0001t0001g0162 a0001c0001t0001g0250 a0001c0001t0001g0262 others(83): Show |
91 | HG00438.hp1 HG01358.hp2 HG01515.hp2 others(88): Show |
intron_variant | MODIFIER | c.331-58G>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 2/6 | chr19 | 3150073 | |||||||
| chr19:3150097 | G | C | 7 | a0001c0001t0001g0299 a0001c0001t0001g0309 a0001c0001t0001g0312 others(4): Show |
7 | HG02280.hp1 HG02615.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.331-34G>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 2/6 | chr19 | 3150097 | |||||||
| chr19:3150110 | G | T | 3 | a0002c0005t0001g0062 a0002c0005t0001g0377 a0002c0005t0017g0311 |
3 | HG02145.hp2 HG02258.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.331-21G>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 2/6 | chr19 | 3150110 | |||||||
| chr19:3150302 | C | T | 6 | a0001c0004t0001g0146 a0001c0004t0001g0185 a0001c0004t0001g0186 others(3): Show |
6 | HG02451.hp2 HG02717.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.485+17C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 3/6 | chr19 | 3150302 | |||||||
| chr19:3150307 | G | A | 5 | a0001c0001t0001g0250 a0001c0001t0001g0263 a0001c0001t0001g0283 others(2): Show |
5 | HG01884.hp2 HG02486.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+22G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 3/6 | chr19 | 3150307 | |||||||
| chr19:3150420 | C | A | 186 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(183): Show |
198 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.485+135C>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 3/6 | chr19 | 3150420 | |||||||
| chr19:3150466 | C | A | 1 | a0001c0002t0008g0350 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.485+181C>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 3/6 | chr19 | 3150466 | |||||||
| chr19:3150576 | A | C | 6 | a0001c0004t0001g0146 a0001c0004t0001g0185 a0001c0004t0001g0186 others(3): Show |
6 | HG02451.hp2 HG02717.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.485+291A>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 3/6 | chr19 | 3150576 | |||||||
| chr19:3150579 | G | A | 42 | a0001c0001t0001g0216 a0001c0003t0001g0010 a0001c0003t0001g0016 others(39): Show |
45 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.485+294G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 3/6 | chr19 | 3150579 | |||||||
| chr19:3150653 | C | A | 1 | a0001c0002t0001g0124 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.485+368C>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 3/6 | chr19 | 3150653 | |||||||
| chr19:3150683 | T | G | 166 | a0001c0001t0001g0020 a0001c0001t0001g0075 a0001c0001t0001g0077 others(163): Show |
177 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.485+398T>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 3/6 | chr19 | 3150683 | |||||||
| chr19:3150702 | C | A | 2 | a0001c0009t0001g0264 a0001c0009t0001g0298 |
2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.485+417C>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 3/6 | chr19 | 3150702 | |||||||
| chr19:3150726 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.485+441C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 3/6 | chr19 | 3150726 | |||||||
| chr19:3150820 | G | A | 1 | a0001c0002t0001g0031 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.485+535G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 3/6 | chr19 | 3150820 | |||||||
| chr19:3150941 | T | A | 2 | a0001c0002t0001g0356 a0001c0002t0001g0357 |
2 | NA19005.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.485+656T>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 3/6 | chr19 | 3150941 | |||||||
| chr19:3150995 | C | G | 1 | a0001c0002t0008g0350 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.485+710C>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 3/6 | chr19 | 3150995 | |||||||
| chr19:3151046 | CTGTTCCT others(10): Show |
C | 1 | a0008c0010t0001g0376 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.486-648_486-632del others(17): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 3151046 | ||||||
| chr19:3151100 | T | G | 7 | a0001c0001t0001g0299 a0001c0001t0001g0309 a0001c0001t0001g0312 others(4): Show |
7 | HG02280.hp1 HG02615.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.486-607T>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 3/6 | chr19 | 3151100 | |||||||
| chr19:3151123 | C | T | 6 | a0001c0004t0001g0146 a0001c0004t0001g0185 a0001c0004t0001g0186 others(3): Show |
6 | HG02451.hp2 HG02717.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.486-584C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 3/6 | chr19 | 3151123 | |||||||
| chr19:3151426 | G | T | 1 | a0001c0001t0001g0109 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.486-281G>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 3/6 | chr19 | 3151426 | |||||||
| chr19:3151442 | C | T | 59 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(56): Show |
69 | HG00140.hp2 HG00558.hp1 HG01069.hp2 others(66): Show |
intron_variant | MODIFIER | c.486-265C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 3/6 | chr19 | 3151442 | |||||||
| chr19:3151460 | G | A | 186 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(183): Show |
198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.486-247G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 3/6 | chr19 | 3151460 | |||||||
| chr19:3151482 | C | T | 3 | a0001c0002t0001g0173 a0001c0002t0001g0175 a0001c0002t0001g0236 |
3 | HG01192.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.486-225C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 3/6 | chr19 | 3151482 | |||||||
| chr19:3151615 | C | T | 1 | a0001c0001t0001g0294 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.486-92C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 3/6 | chr19 | 3151615 | |||||||
| chr19:3151618 | A | T | 2 | a0001c0008t0001g0065 a0001c0008t0001g0252 |
2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.486-89A>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 3/6 | chr19 | 3151618 | |||||||
| chr19:3151632 | T | C | 2 | a0001c0001t0001g0393 a0001c0001t0003g0217 |
2 | HG02735.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.486-75T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 3/6 | chr19 | 3151632 | |||||||
| chr19:3151633 | G | A | 2 | a0001c0001t0001g0393 a0001c0001t0003g0217 |
2 | HG02735.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.486-74G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 3/6 | chr19 | 3151633 | |||||||
| chr19:3151678 | G | C | 23 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0025 others(20): Show |
26 | HG00408.hp1 HG02056.hp2 HG02083.hp2 others(23): Show |
intron_variant | MODIFIER | c.486-29G>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 3/6 | chr19 | 3151678 | |||||||
| chr19:3151688 | A | C | 7 | a0001c0001t0001g0020 a0001c0001t0001g0248 a0001c0001t0001g0293 others(4): Show |
9 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.486-19A>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 3/6 | chr19 | 3151688 | |||||||
| chr19:3151841 | C | T | 1 | a0001c0001t0001g0330 | 1 | NA20805.hp1 | splice_region_variant&intron_variant | LOW | c.614+6C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3151841 | |||||||
| chr19:3151849 | C | G | 3 | a0002c0005t0001g0062 a0002c0005t0001g0377 a0002c0005t0017g0311 |
3 | HG02145.hp2 HG02258.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.614+14C>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3151849 | |||||||
| chr19:3151850 | T | G | 6 | a0001c0004t0001g0146 a0001c0004t0001g0185 a0001c0004t0001g0186 others(3): Show |
6 | HG02451.hp2 HG02717.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.614+15T>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3151850 | |||||||
| chr19:3151986 | C | G | 2 | a0001c0008t0001g0065 a0001c0008t0001g0252 |
2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.614+151C>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3151986 | |||||||
| chr19:3152019 | C | A | 1 | a0001c0001t0001g0283 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.614+184C>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3152019 | |||||||
| chr19:3152103 | C | T | 87 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(84): Show |
92 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.614+268C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3152103 | |||||||
| chr19:3152141 | C | T | 10 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0001c0001t0001g0123 others(7): Show |
10 | HG00323.hp1 HG00423.hp2 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.614+306C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3152141 | |||||||
| chr19:3152184 | G | A | 3 | a0002c0005t0001g0062 a0002c0005t0001g0377 a0002c0005t0017g0311 |
3 | HG02145.hp2 HG02258.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.614+349G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3152184 | |||||||
| chr19:3152300 | C | T | 379 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(376): Show |
409 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(406): Show |
intron_variant | MODIFIER | c.614+465C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3152300 | |||||||
| chr19:3152365 | G | A | 4 | a0001c0001t0001g0250 a0001c0001t0001g0283 a0001c0001t0001g0302 others(1): Show |
4 | HG01884.hp2 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.614+530G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3152365 | |||||||
| chr19:3152498 | T | C | 1 | a0001c0003t0001g0274 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.614+663T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3152498 | |||||||
| chr19:3152544 | G | A | 3 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0338 |
3 | HG02129.hp1 HG02132.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.614+709G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3152544 | |||||||
| chr19:3152670 | G | A | 6 | a0001c0004t0001g0146 a0001c0004t0001g0185 a0001c0004t0001g0186 others(3): Show |
6 | HG02451.hp2 HG02717.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.614+835G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3152670 | |||||||
| chr19:3152702 | T | C | 2 | a0001c0007t0010g0373 a0001c0007t0012g0408 |
2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.614+867T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3152702 | |||||||
| chr19:3152774 | C | T | 2 | a0001c0009t0001g0264 a0001c0009t0001g0298 |
2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.614+939C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3152774 | |||||||
| chr19:3152807 | C | A | 2 | a0001c0001t0009g0310 a0001c0001t0009g0315 |
2 | HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.614+972C>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3152807 | |||||||
| chr19:3152828 | A | G | 6 | a0001c0004t0001g0146 a0001c0004t0001g0185 a0001c0004t0001g0186 others(3): Show |
6 | HG02451.hp2 HG02717.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.614+993A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3152828 | |||||||
| chr19:3152984 | G | A | 86 | a0001c0001t0001g0258 a0001c0002t0001g0001 a0001c0002t0001g0002 others(83): Show |
97 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.614+1149G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3152984 | |||||||
| chr19:3153004 | G | A | 1 | a0001c0001t0001g0418 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.614+1169G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3153004 | |||||||
| chr19:3153095 | A | G | 2 | a0001c0008t0001g0065 a0001c0008t0001g0252 |
2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.614+1260A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3153095 | |||||||
| chr19:3153117 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.614+1282C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3153117 | |||||||
| chr19:3153182 | C | G | 1 | a0001c0003t0001g0361 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.614+1347C>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3153182 | |||||||
| chr19:3153232 | G | A | 1 | a0001c0002t0001g0154 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.614+1397G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3153232 | |||||||
| chr19:3153257 | TA | T | 159 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(156): Show |
170 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.614+1437delA | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 3153257 | ||||||
| chr19:3153466 | GTGGA | G | 4 | a0001c0001t0001g0262 a0001c0001t0004g0405 a0001c0002t0001g0268 others(1): Show |
4 | HG02723.hp2 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.614+1651_614+1654d others(6): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 3153466 | ||||||
| chr19:3153484 | G | A | 8 | a0001c0001t0002g0027 a0001c0001t0002g0404 a0001c0001t0002g0406 others(5): Show |
9 | HG01109.hp1 HG01243.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.614+1649G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3153484 | |||||||
| chr19:3153531 | G | A | 1 | a0001c0002t0001g0195 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.614+1696G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3153531 | |||||||
| chr19:3153701 | GGGATGGA others(5): Show |
G | 1 | a0001c0001t0001g0418 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.614+1881_614+1892d others(14): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 3153701 | ||||||
| chr19:3153728 | G | GT | 66 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(63): Show |
69 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.614+1894dupT | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 3153728 | ||||||
| chr19:3153754 | G | A | 66 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(63): Show |
69 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.614+1919G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3153754 | |||||||
| chr19:3153763 | G | A | 1 | a0002c0005t0017g0311 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.614+1928G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3153763 | |||||||
| chr19:3153776 | A | G | 66 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0001c0001t0001g0123 others(63): Show |
72 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.614+1941A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3153776 | |||||||
| chr19:3153872 | G | GATGAATG others(140): Show |
1 | a0001c0001t0001g0393 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.615-1818_615-1817i others(149): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 3153872 | ||||||
| chr19:3153887 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.615-1936G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3153887 | |||||||
| chr19:3153942 | T | C | 2 | a0001c0004t0001g0185 a0001c0004t0001g0186 |
2 | HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.615-1881T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3153942 | |||||||
| chr19:3153944 | G | A | 1 | a0001c0001t0001g0370 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.615-1879G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3153944 | |||||||
| chr19:3154015 | G | A | 2 | a0001c0001t0001g0265 a0001c0001t0001g0266 |
2 | HG01891.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.615-1808G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3154015 | |||||||
| chr19:3154062 | TGATG | T | 74 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(71): Show |
77 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.615-1752_615-1749d others(6): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 3154062 | ||||||
| chr19:3154146 | AGATG | A | 7 | a0001c0001t0001g0162 a0001c0001t0001g0379 a0001c0001t0009g0310 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.615-1667_615-1664d others(6): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 3154146 | ||||||
| chr19:3154162 | G | GGGAT | 51 | a0001c0001t0001g0216 a0001c0003t0001g0008 a0001c0003t0001g0010 others(48): Show |
56 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.615-1639_615-1636d others(6): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 3154162 | ||||||
| chr19:3154162 | GGGATGGA others(5): Show |
G | 74 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(71): Show |
77 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.615-1647_615-1636d others(14): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 3154162 | ||||||
| chr19:3154416 | C | G | 238 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(235): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.615-1407C>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3154416 | |||||||
| chr19:3154418 | T | C | 1 | a0001c0001t0001g0318 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.615-1405T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3154418 | |||||||
| chr19:3154492 | A | G | 1 | a0001c0002t0001g0157 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.615-1331A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3154492 | |||||||
| chr19:3154549 | G | A | 1 | a0001c0002t0001g0268 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.615-1274G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3154549 | |||||||
| chr19:3154563 | AGGTGGAT others(80): Show |
A | 2 | a0001c0002t0001g0292 a0001c0002t0001g0372 |
2 | HG02735.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.615-1176_615-1090d others(89): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 3154563 | ||||||
| chr19:3154587 | G | A | 1 | a0001c0001t0001g0418 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.615-1236G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3154587 | |||||||
| chr19:3154689 | GGATA | G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0150 |
4 | NA18945.hp1 NA18962.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.615-1130_615-1127d others(6): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 3154689 | ||||||
| chr19:3154751 | G | A | 1 | a0001c0002t0001g0091 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.615-1072G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3154751 | |||||||
| chr19:3154945 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.615-878C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3154945 | |||||||
| chr19:3154980 | G | A | 21 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0306 others(18): Show |
21 | HG00642.hp2 HG00735.hp1 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.615-843G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3154980 | |||||||
| chr19:3155165 | C | T | 1 | a0001c0001t0006g0289 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.615-658C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3155165 | |||||||
| chr19:3155204 | C | T | 16 | a0001c0002t0001g0003 a0001c0002t0001g0039 a0001c0002t0001g0063 others(13): Show |
17 | HG02523.hp2 NA18612.hp1 NA18944.hp2 others(14): Show |
intron_variant | MODIFIER | c.615-619C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3155204 | |||||||
| chr19:3155369 | G | A | 1 | a0001c0001t0011g0037 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.615-454G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3155369 | |||||||
| chr19:3155396 | C | T | 66 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(63): Show |
69 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.615-427C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3155396 | |||||||
| chr19:3155461 | G | T | 6 | a0001c0001t0001g0020 a0001c0001t0001g0248 a0001c0001t0001g0293 others(3): Show |
7 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.615-362G>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3155461 | |||||||
| chr19:3155463 | AAACTGAG others(15): Show |
A | 1 | a0006c0014t0001g0126 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.615-359_615-338del others(22): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3155463 | |||||||
| chr19:3155489 | A | G | 2 | a0001c0009t0001g0264 a0001c0009t0001g0298 |
2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.615-334A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3155489 | |||||||
| chr19:3155498 | G | A | 1 | a0001c0002t0001g0391 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.615-325G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3155498 | |||||||
| chr19:3155571 | A | G | 1 | a0001c0002t0001g0024 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.615-252A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3155571 | |||||||
| chr19:3155692 | T | C | 1 | a0001c0002t0001g0194 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.615-131T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3155692 | |||||||
| chr19:3155696 | C | T | 6 | a0001c0004t0001g0146 a0001c0004t0001g0185 a0001c0004t0001g0186 others(3): Show |
6 | HG02451.hp2 HG02717.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.615-127C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3155696 | |||||||
| chr19:3155727 | A | G | 2 | a0001c0001t0001g0265 a0001c0001t0001g0266 |
2 | HG01891.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.615-96A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3155727 | |||||||
| chr19:3155738 | T | C | 83 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(80): Show |
87 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.615-85T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3155738 | |||||||
| chr19:3155765 | G | T | 1 | a0006c0014t0001g0126 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.615-58G>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3155765 | |||||||
| chr19:3155804 | G | A | 1 | a0001c0002t0001g0063 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.615-19G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 4/6 | chr19 | 3155804 | |||||||
| chr19:3155963 | GCCTCCCT others(5): Show |
G | 1 | a0001c0001t0001g0104 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.744+12_744+23delCC others(10): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3155963 | |||||||
| chr19:3155997 | A | C | 1 | a0006c0014t0001g0126 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.744+45A>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3155997 | |||||||
| chr19:3156027 | G | T | 1 | a0001c0001t0001g0418 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.744+75G>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3156027 | |||||||
| chr19:3156163 | G | GAC | 106 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0025 others(103): Show |
115 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.744+250_744+251dup others(2): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 3156163 | ||||||
| chr19:3156163 | G | GACAC | 53 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0035 others(50): Show |
55 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.744+248_744+251dup others(4): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 3156163 | ||||||
| chr19:3156163 | G | GACACAC | 9 | a0001c0001t0002g0409 a0001c0002t0001g0133 a0001c0002t0001g0235 others(6): Show |
9 | HG02135.hp2 HG02145.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.744+246_744+251dup others(6): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 3156163 | ||||||
| chr19:3156163 | G | GACACACA others(1): Show |
12 | a0001c0001t0001g0181 a0001c0001t0001g0250 a0001c0001t0002g0027 others(9): Show |
13 | HG01167.hp1 HG02280.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.744+244_744+251dup others(8): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 3156163 | ||||||
| chr19:3156163 | G | GACACACA others(3): Show |
6 | a0001c0001t0002g0406 a0001c0001t0002g0407 a0001c0001t0002g0410 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.744+242_744+251dup others(10): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 3156163 | ||||||
| chr19:3156163 | GAC | G | 31 | a0001c0001t0001g0087 a0001c0001t0001g0107 a0001c0001t0001g0179 others(28): Show |
33 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.744+250_744+251del others(2): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 3156163 | ||||||
| chr19:3156163 | GACAC | G | 10 | a0001c0001t0001g0088 a0001c0001t0001g0119 a0001c0001t0001g0174 others(7): Show |
10 | HG00673.hp2 HG00741.hp2 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.744+248_744+251del others(4): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 3156163 | ||||||
| chr19:3156193 | C | CT | 3 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0002t0001g0005 |
4 | HG00639.hp1 HG01109.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.744+241_744+242ins others(1): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3156193 | |||||||
| chr19:3156195 | C | CTACAGT | 7 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0001c0001t0001g0123 others(4): Show |
7 | HG00423.hp2 HG01515.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.744+243_744+244ins others(6): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3156195 | |||||||
| chr19:3156196 | A | ACTACAGT others(1): Show |
23 | a0001c0001t0001g0318 a0001c0002t0001g0024 a0001c0002t0001g0044 others(20): Show |
24 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.744+245_744+246ins others(8): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 3156196 | ||||||
| chr19:3156196 | A | AGTG | 3 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0002t0001g0005 |
4 | HG00639.hp1 HG01109.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.744+244_744+245ins others(3): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3156196 | |||||||
| chr19:3156196 | A | G | 7 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0001c0001t0001g0123 others(4): Show |
7 | HG00423.hp2 HG01515.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.744+244A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3156196 | |||||||
| chr19:3156199 | C | CT | 25 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0001g0162 others(22): Show |
26 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(23): Show |
intron_variant | MODIFIER | c.744+247_744+248ins others(1): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3156199 | |||||||
| chr19:3156200 | A | G | 1 | a0001c0002t0001g0086 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.744+248A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3156200 | |||||||
| chr19:3156202 | A | ACACACT | 4 | a0001c0001t0001g0020 a0001c0001t0001g0248 a0001c0001t0001g0293 others(1): Show |
5 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.744+251_744+252ins others(6): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 3156202 | ||||||
| chr19:3156202 | A | ACT | 11 | a0001c0002t0001g0095 a0001c0002t0001g0135 a0001c0002t0001g0188 others(8): Show |
12 | NA18747.hp1 NA18940.hp1 NA18941.hp2 others(9): Show |
intron_variant | MODIFIER | c.744+251_744+252dup others(2): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 3156202 | ||||||
| chr19:3156202 | A | T | 1 | a0001c0002t0001g0238 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.744+250A>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3156202 | |||||||
| chr19:3156203 | C | CG | 33 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0001c0001t0001g0123 others(30): Show |
35 | HG00423.hp2 HG00639.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.744+251_744+252ins others(1): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3156203 | |||||||
| chr19:3156203 | C | G | 25 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0001g0162 others(22): Show |
26 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(23): Show |
intron_variant | MODIFIER | c.744+251C>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3156203 | |||||||
| chr19:3156204 | T | C | 33 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0001c0001t0001g0123 others(30): Show |
35 | HG00423.hp2 HG00639.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.744+252T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3156204 | |||||||
| chr19:3156205 | A | G | 25 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0001g0162 others(22): Show |
26 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(23): Show |
intron_variant | MODIFIER | c.744+253A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3156205 | |||||||
| chr19:3156207 | A | ACACACGC others(2): Show |
25 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0001g0162 others(22): Show |
26 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(23): Show |
intron_variant | MODIFIER | c.744+255_744+256ins others(9): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3156207 | |||||||
| chr19:3156207 | AG | A | 33 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0001c0001t0001g0123 others(30): Show |
35 | HG00423.hp2 HG00639.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.744+256delG | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3156207 | |||||||
| chr19:3156208 | G | A | 26 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0001g0162 others(23): Show |
27 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(24): Show |
intron_variant | MODIFIER | c.744+256G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3156208 | |||||||
| chr19:3156208 | G | GTGCACAC others(7): Show |
280 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(277): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.744+258_744+271dup others(14): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 3156208 | ||||||
| chr19:3156261 | A | G | 10 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0001c0001t0001g0123 others(7): Show |
10 | HG00323.hp1 HG00423.hp2 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.744+309A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3156261 | |||||||
| chr19:3156325 | A | T | 56 | a0001c0001t0001g0216 a0001c0003t0001g0008 a0001c0003t0001g0010 others(53): Show |
62 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.744+373A>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3156325 | |||||||
| chr19:3156337 | G | A | 14 | a0001c0001t0001g0020 a0001c0001t0001g0248 a0001c0001t0001g0293 others(11): Show |
15 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.744+385G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3156337 | |||||||
| chr19:3156409 | GCACACAC others(5): Show |
G | 23 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0001c0001t0001g0123 others(20): Show |
24 | HG00323.hp1 HG00423.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.744+468_744+479del others(12): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 3156409 | ||||||
| chr19:3156411 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.744+459A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3156411 | |||||||
| chr19:3156430 | T | C | 28 | a0001c0002t0001g0026 a0001c0002t0001g0031 a0001c0002t0001g0042 others(25): Show |
29 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.744+478T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3156430 | |||||||
| chr19:3156451 | T | C | 1 | a0001c0002t0001g0086 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.744+499T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3156451 | |||||||
| chr19:3156458 | G | A | 1 | a0001c0002t0001g0171 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.744+506G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3156458 | |||||||
| chr19:3156458 | GCACACAC others(5): Show |
G | 10 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0001c0001t0001g0123 others(7): Show |
10 | HG00323.hp1 HG00423.hp2 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.744+514_744+525del others(12): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 3156458 | ||||||
| chr19:3156464 | A | G | 56 | a0001c0001t0001g0216 a0001c0003t0001g0008 a0001c0003t0001g0010 others(53): Show |
62 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.744+512A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3156464 | |||||||
| chr19:3156467 | G | T | 371 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(368): Show |
401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.744+515G>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3156467 | |||||||
| chr19:3156468 | GCA | G | 13 | a0001c0001t0001g0162 a0001c0001t0001g0262 a0001c0001t0001g0379 others(10): Show |
14 | HG01358.hp2 HG01515.hp2 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.744+524_744+525del others(2): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 3156468 | ||||||
| chr19:3156470 | A | G | 2 | a0001c0002t0001g0268 a0001c0002t0001g0269 |
2 | HG02723.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.744+518A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3156470 | |||||||
| chr19:3156475 | C | G | 1 | a0001c0001t0001g0181 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.744+523C>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3156475 | |||||||
| chr19:3156478 | G | A | 2 | a0001c0001t0001g0308 a0001c0003t0001g0336 |
2 | HG00735.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.744+526G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3156478 | |||||||
| chr19:3156507 | C | A | 107 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(104): Show |
112 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.744+555C>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3156507 | |||||||
| chr19:3156532 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0148 |
2 | HG01099.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.744+580G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3156532 | |||||||
| chr19:3156585 | C | G | 1 | a0001c0001t0001g0104 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.744+633C>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3156585 | |||||||
| chr19:3156585 | C | T | 59 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(56): Show |
62 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.744+633C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3156585 | |||||||
| chr19:3156642 | G | A | 172 | a0001c0001t0001g0210 a0001c0001t0001g0277 a0001c0001t0004g0415 others(169): Show |
187 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.744+690G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3156642 | |||||||
| chr19:3156659 | AT | A | 9 | a0001c0001t0001g0181 a0001c0001t0002g0027 a0001c0001t0002g0404 others(6): Show |
10 | HG01109.hp1 HG01243.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.744+717delT | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 3156659 | ||||||
| chr19:3156698 | A | G | 3 | a0001c0001t0006g0021 a0001c0001t0006g0287 a0001c0001t0006g0289 |
4 | HG01358.hp2 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.744+746A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3156698 | |||||||
| chr19:3156718 | A | G | 1 | a0001c0002t0001g0051 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.744+766A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3156718 | |||||||
| chr19:3156798 | T | C | 1 | a0001c0001t0001g0324 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.744+846T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3156798 | |||||||
| chr19:3156856 | C | T | 9 | a0001c0001t0001g0181 a0001c0001t0002g0027 a0001c0001t0002g0404 others(6): Show |
10 | HG01109.hp1 HG01243.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.745-872C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3156856 | |||||||
| chr19:3156879 | C | A | 1 | a0001c0002t0001g0056 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.745-849C>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3156879 | |||||||
| chr19:3157159 | G | A | 2 | a0001c0004t0001g0146 a0001c0004t0004g0414 |
2 | HG03139.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.745-569G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3157159 | |||||||
| chr19:3157246 | G | A | 6 | a0001c0004t0001g0146 a0001c0004t0001g0185 a0001c0004t0001g0186 others(3): Show |
6 | HG02451.hp2 HG02717.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.745-482G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3157246 | |||||||
| chr19:3157262 | G | A | 1 | a0001c0002t0001g0358 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.745-466G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3157262 | |||||||
| chr19:3157348 | G | A | 12 | a0001c0002t0001g0095 a0001c0002t0001g0135 a0001c0002t0001g0188 others(9): Show |
13 | NA18747.hp1 NA18940.hp1 NA18941.hp2 others(10): Show |
intron_variant | MODIFIER | c.745-380G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3157348 | |||||||
| chr19:3157420 | C | T | 1 | a0001c0001t0001g0418 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.745-308C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3157420 | |||||||
| chr19:3157437 | C | G | 1 | a0006c0014t0001g0126 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.745-291C>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3157437 | |||||||
| chr19:3157438 | T | C | 1 | a0006c0014t0001g0126 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.745-290T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3157438 | |||||||
| chr19:3157439 | G | T | 1 | a0006c0014t0001g0126 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.745-289G>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3157439 | |||||||
| chr19:3157456 | A | T | 1 | a0006c0014t0001g0126 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.745-272A>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3157456 | |||||||
| chr19:3157510 | C | T | 4 | a0001c0003t0001g0229 a0001c0003t0001g0230 a0001c0003t0001g0231 others(1): Show |
4 | HG02083.hp1 NA18951.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.745-218C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3157510 | |||||||
| chr19:3157584 | C | A | 1 | a0006c0014t0001g0126 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.745-144C>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3157584 | |||||||
| chr19:3157587 | G | A | 2 | a0001c0001t0001g0099 a0001c0001t0001g0403 |
2 | HG02698.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.745-141G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3157587 | |||||||
| chr19:3157653 | C | A | 1 | a0006c0014t0001g0126 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.745-75C>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 5/6 | chr19 | 3157653 | |||||||
| chr19:3157887 | T | C | 29 | a0001c0001t0001g0020 a0001c0001t0001g0075 a0001c0001t0001g0077 others(26): Show |
31 | HG00323.hp1 HG00423.hp2 HG00639.hp1 others(28): Show |
splice_region_variant&intron_variant | LOW | c.898+6T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3157887 | |||||||
| chr19:3157889 | A | G | 29 | a0001c0001t0001g0020 a0001c0001t0001g0075 a0001c0001t0001g0077 others(26): Show |
31 | HG00323.hp1 HG00423.hp2 HG00639.hp1 others(28): Show |
splice_region_variant&intron_variant | LOW | c.898+8A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3157889 | |||||||
| chr19:3157918 | C | T | 29 | a0001c0001t0001g0020 a0001c0001t0001g0075 a0001c0001t0001g0077 others(26): Show |
31 | HG00323.hp1 HG00423.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.898+37C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3157918 | |||||||
| chr19:3157976 | G | A | 1 | a0001c0002t0019g0328 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.898+95G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3157976 | |||||||
| chr19:3158043 | T | G | 1 | a0006c0014t0001g0126 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.898+162T>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3158043 | |||||||
| chr19:3158117 | A | AGACGTAG others(5): Show |
1 | a0001c0002t0001g0199 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.898+236_898+237ins others(12): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3158117 | |||||||
| chr19:3158118 | C | G | 242 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(239): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.898+237C>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3158118 | |||||||
| chr19:3158365 | G | C | 26 | a0001c0001t0001g0020 a0001c0001t0001g0075 a0001c0001t0001g0077 others(23): Show |
27 | HG00323.hp1 HG00423.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.898+484G>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3158365 | |||||||
| chr19:3158394 | C | T | 3 | a0001c0001t0006g0021 a0001c0001t0006g0287 a0001c0001t0006g0289 |
4 | HG01358.hp2 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.898+513C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3158394 | |||||||
| chr19:3158500 | G | A | 56 | a0001c0001t0001g0216 a0001c0003t0001g0008 a0001c0003t0001g0010 others(53): Show |
62 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.898+619G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3158500 | |||||||
| chr19:3158513 | T | C | 1 | a0001c0001t0001g0192 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.898+632T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3158513 | |||||||
| chr19:3158533 | C | A | 1 | a0001c0002t0001g0056 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.898+652C>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3158533 | |||||||
| chr19:3158549 | T | A | 382 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(379): Show |
412 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(409): Show |
intron_variant | MODIFIER | c.898+668T>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3158549 | |||||||
| chr19:3158715 | C | G | 29 | a0001c0001t0001g0020 a0001c0001t0001g0075 a0001c0001t0001g0077 others(26): Show |
31 | HG00323.hp1 HG00423.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.898+834C>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3158715 | |||||||
| chr19:3158738 | T | C | 29 | a0001c0001t0001g0020 a0001c0001t0001g0075 a0001c0001t0001g0077 others(26): Show |
31 | HG00323.hp1 HG00423.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.898+857T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3158738 | |||||||
| chr19:3158770 | T | A | 1 | a0001c0001t0001g0250 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.898+889T>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3158770 | |||||||
| chr19:3158803 | C | T | 29 | a0001c0001t0001g0020 a0001c0001t0001g0075 a0001c0001t0001g0077 others(26): Show |
31 | HG00323.hp1 HG00423.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.898+922C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3158803 | |||||||
| chr19:3158859 | C | G | 1 | a0001c0001t0001g0283 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.898+978C>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3158859 | |||||||
| chr19:3158884 | C | CAGCCTCC others(42): Show |
1 | a0001c0002t0001g0049 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.898+1004_898+1052d others(51): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 3158884 | ||||||
| chr19:3158896 | G | C | 29 | a0001c0001t0001g0020 a0001c0001t0001g0075 a0001c0001t0001g0077 others(26): Show |
31 | HG00323.hp1 HG00423.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.898+1015G>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3158896 | |||||||
| chr19:3158922 | C | T | 2 | a0001c0002t0001g0241 a0001c0002t0001g0242 |
2 | HG01106.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.898+1041C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3158922 | |||||||
| chr19:3159007 | T | C | 1 | a0001c0003t0001g0022 | 2 | HG01099.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.898+1126T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3159007 | |||||||
| chr19:3159008 | C | G | 1 | a0001c0001t0001g0137 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.898+1127C>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3159008 | |||||||
| chr19:3159022 | AT | A | 29 | a0001c0001t0001g0020 a0001c0001t0001g0075 a0001c0001t0001g0077 others(26): Show |
31 | HG00323.hp1 HG00423.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.898+1150delT | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 3159022 | ||||||
| chr19:3159170 | G | A | 13 | a0001c0001t0001g0162 a0001c0001t0001g0262 a0001c0001t0001g0379 others(10): Show |
14 | HG01358.hp2 HG01515.hp2 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.898+1289G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3159170 | |||||||
| chr19:3159173 | C | T | 7 | a0001c0001t0001g0020 a0001c0001t0001g0248 a0001c0001t0001g0293 others(4): Show |
8 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.898+1292C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3159173 | |||||||
| chr19:3159178 | G | C | 31 | a0001c0001t0001g0020 a0001c0001t0001g0075 a0001c0001t0001g0077 others(28): Show |
33 | HG00323.hp1 HG00423.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.898+1297G>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3159178 | |||||||
| chr19:3159179 | A | C | 31 | a0001c0001t0001g0020 a0001c0001t0001g0075 a0001c0001t0001g0077 others(28): Show |
33 | HG00323.hp1 HG00423.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.898+1298A>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3159179 | |||||||
| chr19:3159182 | G | A | 2 | a0001c0002t0001g0171 a0001c0002t0001g0172 |
2 | HG03017.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.898+1301G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3159182 | |||||||
| chr19:3159191 | G | A | 305 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(302): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.898+1310G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3159191 | |||||||
| chr19:3159226 | A | G | 31 | a0001c0001t0001g0020 a0001c0001t0001g0075 a0001c0001t0001g0077 others(28): Show |
33 | HG00323.hp1 HG00423.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.898+1345A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3159226 | |||||||
| chr19:3159263 | A | G | 10 | a0001c0003t0001g0096 a0001c0003t0001g0211 a0001c0003t0001g0275 others(7): Show |
10 | HG01884.hp1 HG02109.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.898+1382A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3159263 | |||||||
| chr19:3159322 | T | C | 163 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(160): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.898+1441T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3159322 | |||||||
| chr19:3159346 | C | CT | 84 | a0001c0001t0001g0107 a0001c0001t0001g0181 a0001c0001t0001g0206 others(81): Show |
89 | HG00438.hp1 HG02055.hp1 HG02080.hp1 others(86): Show |
intron_variant | MODIFIER | c.898+1482dupT | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 3159346 | ||||||
| chr19:3159346 | CT | C | 35 | a0001c0001t0001g0020 a0001c0001t0001g0075 a0001c0001t0001g0077 others(32): Show |
41 | HG00323.hp1 HG00423.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.898+1482delT | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 3159346 | ||||||
| chr19:3159346 | CTT | C | 128 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(125): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.898+1481_898+1482d others(4): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 3159346 | ||||||
| chr19:3159365 | A | G | 1 | a0001c0001t0001g0314 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.898+1484A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3159365 | |||||||
| chr19:3159416 | G | A | 2 | a0001c0001t0001g0265 a0001c0001t0001g0266 |
2 | HG01891.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.898+1535G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3159416 | |||||||
| chr19:3159439 | C | T | 59 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(56): Show |
62 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.898+1558C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3159439 | |||||||
| chr19:3159471 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.898+1590C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3159471 | |||||||
| chr19:3159534 | G | A | 1 | a0001c0001t0003g0217 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.898+1653G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3159534 | |||||||
| chr19:3159552 | T | C | 1 | a0001c0001t0001g0418 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.898+1671T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3159552 | |||||||
| chr19:3159714 | T | C | 31 | a0001c0001t0001g0020 a0001c0001t0001g0075 a0001c0001t0001g0077 others(28): Show |
33 | HG00323.hp1 HG00423.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.898+1833T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3159714 | |||||||
| chr19:3159771 | A | G | 31 | a0001c0001t0001g0020 a0001c0001t0001g0075 a0001c0001t0001g0077 others(28): Show |
33 | HG00323.hp1 HG00423.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.898+1890A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3159771 | |||||||
| chr19:3159788 | C | T | 31 | a0001c0001t0001g0020 a0001c0001t0001g0075 a0001c0001t0001g0077 others(28): Show |
33 | HG00323.hp1 HG00423.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.898+1907C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3159788 | |||||||
| chr19:3159789 | G | A | 1 | a0003c0006t0001g0014 | 2 | NA18990.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.898+1908G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3159789 | |||||||
| chr19:3159890 | C | A | 1 | a0001c0002t0001g0196 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.898+2009C>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3159890 | |||||||
| chr19:3159969 | G | T | 1 | a0001c0002t0001g0165 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.898+2088G>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3159969 | |||||||
| chr19:3160004 | G | A | 1 | a0001c0001t0001g0302 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.898+2123G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3160004 | |||||||
| chr19:3160030 | C | T | 70 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(67): Show |
73 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.898+2149C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3160030 | |||||||
| chr19:3160182 | A | G | 8 | a0001c0004t0001g0146 a0001c0004t0001g0185 a0001c0004t0001g0186 others(5): Show |
8 | HG02145.hp1 HG02451.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.898+2301A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3160182 | |||||||
| chr19:3160185 | A | T | 1 | a0001c0001t0001g0418 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.898+2304A>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3160185 | |||||||
| chr19:3160238 | ACTCTTGG others(3): Show |
A | 63 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(60): Show |
66 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.898+2362_898+2371d others(12): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 3160238 | ||||||
| chr19:3160282 | A | G | 1 | a0001c0002t0001g0158 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.898+2401A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3160282 | |||||||
| chr19:3160286 | C | G | 8 | a0001c0004t0001g0146 a0001c0004t0001g0185 a0001c0004t0001g0186 others(5): Show |
8 | HG02145.hp1 HG02451.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.898+2405C>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3160286 | |||||||
| chr19:3160295 | C | T | 1 | a0001c0001t0010g0105 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.898+2414C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3160295 | |||||||
| chr19:3160317 | G | A | 1 | a0001c0003t0001g0336 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.898+2436G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3160317 | |||||||
| chr19:3160387 | A | G | 69 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(66): Show |
72 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.899-2406A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3160387 | |||||||
| chr19:3160423 | G | C | 1 | a0001c0002t0008g0350 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.899-2370G>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3160423 | |||||||
| chr19:3160442 | G | C | 55 | a0001c0001t0001g0216 a0001c0003t0001g0008 a0001c0003t0001g0010 others(52): Show |
61 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.899-2351G>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3160442 | |||||||
| chr19:3160474 | A | G | 69 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(66): Show |
72 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.899-2319A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3160474 | |||||||
| chr19:3160530 | C | T | 69 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(66): Show |
72 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.899-2263C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3160530 | |||||||
| chr19:3160531 | G | A | 2 | a0001c0001t0001g0262 a0001c0001t0004g0405 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.899-2262G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3160531 | |||||||
| chr19:3160537 | A | G | 3 | a0001c0001t0006g0021 a0001c0001t0006g0287 a0001c0001t0006g0289 |
4 | HG01358.hp2 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.899-2256A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3160537 | |||||||
| chr19:3160711 | G | A | 69 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(66): Show |
72 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.899-2082G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3160711 | |||||||
| chr19:3160741 | C | T | 8 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0058 others(5): Show |
9 | HG00621.hp1 HG02015.hp1 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.899-2052C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3160741 | |||||||
| chr19:3160763 | T | C | 69 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(66): Show |
72 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.899-2030T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3160763 | |||||||
| chr19:3160790 | C | T | 8 | a0001c0004t0001g0146 a0001c0004t0001g0185 a0001c0004t0001g0186 others(5): Show |
8 | HG02145.hp1 HG02451.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.899-2003C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3160790 | |||||||
| chr19:3160791 | C | T | 8 | a0001c0004t0001g0146 a0001c0004t0001g0185 a0001c0004t0001g0186 others(5): Show |
8 | HG02145.hp1 HG02451.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.899-2002C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3160791 | |||||||
| chr19:3160937 | CT | C | 184 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0020 others(181): Show |
199 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.899-1833delT | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 3160937 | ||||||
| chr19:3160937 | CTT | C | 31 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0162 others(28): Show |
32 | HG01109.hp1 HG01243.hp1 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.899-1834_899-1833d others(4): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 3160937 | ||||||
| chr19:3160937 | CTTT | C | 80 | a0001c0001t0001g0418 a0001c0002t0001g0001 a0001c0002t0001g0002 others(77): Show |
91 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.899-1835_899-1833d others(5): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 3160937 | ||||||
| chr19:3160937 | CTTTTTT | C | 67 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(64): Show |
70 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.899-1838_899-1833d others(8): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 3160937 | ||||||
| chr19:3161087 | C | T | 2 | a0001c0008t0001g0065 a0001c0008t0001g0252 |
2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.899-1706C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3161087 | |||||||
| chr19:3161088 | G | A | 56 | a0001c0001t0001g0216 a0001c0003t0001g0008 a0001c0003t0001g0010 others(53): Show |
62 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.899-1705G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3161088 | |||||||
| chr19:3161200 | T | A | 21 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0073 others(18): Show |
23 | HG00423.hp1 HG00438.hp2 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.899-1593T>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3161200 | |||||||
| chr19:3161468 | T | G | 8 | a0001c0004t0001g0146 a0001c0004t0001g0185 a0001c0004t0001g0186 others(5): Show |
8 | HG02145.hp1 HG02451.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.899-1325T>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3161468 | |||||||
| chr19:3161536 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.899-1257T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3161536 | |||||||
| chr19:3161617 | A | G | 55 | a0001c0001t0001g0216 a0001c0003t0001g0008 a0001c0003t0001g0010 others(52): Show |
61 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.899-1176A>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3161617 | |||||||
| chr19:3161688 | C | G | 1 | a0001c0001t0001g0263 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.899-1105C>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3161688 | |||||||
| chr19:3161804 | G | A | 1 | a0001c0001t0001g0318 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.899-989G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3161804 | |||||||
| chr19:3161907 | C | T | 10 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0001c0001t0001g0123 others(7): Show |
10 | HG00323.hp1 HG00423.hp2 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.899-886C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3161907 | |||||||
| chr19:3162006 | C | T | 29 | a0001c0001t0001g0020 a0001c0001t0001g0075 a0001c0001t0001g0077 others(26): Show |
31 | HG00323.hp1 HG00423.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.899-787C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3162006 | |||||||
| chr19:3162011 | T | C | 106 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(103): Show |
111 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.899-782T>C | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3162011 | |||||||
| chr19:3162034 | AAAT | A | 96 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(93): Show |
101 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.899-740_899-738del others(3): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 3162034 | ||||||
| chr19:3162074 | G | A | 69 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(66): Show |
72 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.899-719G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3162074 | |||||||
| chr19:3162098 | C | T | 3 | a0001c0002t0001g0031 a0001c0002t0001g0106 a0001c0002t0014g0161 |
3 | HG00323.hp2 NA18984.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.899-695C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3162098 | |||||||
| chr19:3162099 | G | T | 60 | a0001c0001t0001g0402 a0001c0002t0001g0001 a0001c0002t0001g0002 others(57): Show |
70 | HG00140.hp2 HG00558.hp1 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.899-694G>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3162099 | |||||||
| chr19:3162198 | G | T | 1 | a0001c0003t0001g0274 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.899-595G>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3162198 | |||||||
| chr19:3162303 | G | A | 1 | a0001c0003t0001g0207 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.899-490G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3162303 | |||||||
| chr19:3162364 | C | T | 1 | a0001c0001t0001g0418 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.899-429C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3162364 | |||||||
| chr19:3162365 | G | A | 4 | a0001c0003t0003g0017 a0001c0003t0003g0064 a0001c0003t0003g0214 others(1): Show |
5 | HG01074.hp1 HG01255.hp1 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.899-428G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3162365 | |||||||
| chr19:3162388 | G | GAAA | 95 | a0001c0001t0001g0020 a0001c0001t0001g0075 a0001c0001t0001g0077 others(92): Show |
103 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.899-396_899-394dup others(3): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 3162388 | ||||||
| chr19:3162388 | G | GAAAA | 66 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(63): Show |
69 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.899-397_899-394dup others(4): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 3162388 | ||||||
| chr19:3162433 | C | T | 49 | a0001c0001t0001g0402 a0001c0002t0001g0001 a0001c0002t0001g0002 others(46): Show |
58 | HG00558.hp1 HG01081.hp1 HG01081.hp2 others(55): Show |
intron_variant | MODIFIER | c.899-360C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3162433 | |||||||
| chr19:3162434 | G | A | 1 | a0001c0001t0001g0418 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.899-359G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3162434 | |||||||
| chr19:3162534 | C | G | 69 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(66): Show |
72 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.899-259C>G | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3162534 | |||||||
| chr19:3162540 | G | A | 341 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(338): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.899-253G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3162540 | |||||||
| chr19:3162567 | C | T | 1 | a0001c0001t0001g0297 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.899-226C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3162567 | |||||||
| chr19:3162635 | G | GA | 10 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0001c0001t0001g0123 others(7): Show |
10 | HG00323.hp1 HG00423.hp2 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.899-157dupA | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 3162635 | ||||||
| chr19:3162672 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.899-121G>A | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3162672 | |||||||
| chr19:3162704 | C | T | 1 | a0001c0001t0001g0297 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.899-89C>T | GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 6/6 | chr19 | 3162704 |