Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10672 |
| ensemblid | ENSG00000120063.10 |
| hgncid | 4381 |
| symbol | GNA13 |
| name | G protein subunit alpha 13 |
| refseq_nuc | NM_006572.6 |
| refseq_prot | NP_006563.2 |
| ensembl_nuc | ENST00000439174.7 |
| ensembl_prot | ENSP00000400717.2 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 65009289 |
| end | 65056740 |
| strand | - |
| ver | v1.2 |
| region | chr17:65009289-65056740 |
| region5000 | chr17:65004289-65061740 |
| regionname0 | GNA13_chr17_65009289_65056740 |
| regionname5000 | GNA13_chr17_65004289_65061740 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 377 | 178 | 87 | 36 | 26 | 2 | 25 | 22 | GNA13_chr17_65004289_65061740 | GNA13 | MADFL others(372): Show |
chr17 | 65004289 | 65061740 |
| a0002 | 0/0 | 377 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | MADFL others(372): Show |
chr17 | 65004289 | 65061740 |
| a0003 | 0/0 | 377 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | MADFL others(372): Show |
chr17 | 65004289 | 65061740 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1131 | 159 | 76 | 29 | 26 | 2 | 24 | GNA13_chr17_65004289_65061740 | GNA13 | ATGGC others(1126): Show |
chr17 | 65004289 | 65061740 | ||
| a0001c0002 | 0/0 | 1131 | 11 | 10 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | ATGGC others(1126): Show |
chr17 | 65004289 | 65061740 | ||
| a0001c0003 | 0/0 | 1131 | 3 | 0 | 3 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | ATGGC others(1126): Show |
chr17 | 65004289 | 65061740 | ||
| a0001c0004 | 0/0 | 1131 | 2 | 0 | 2 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | ATGGC others(1126): Show |
chr17 | 65004289 | 65061740 | ||
| a0001c0005 | 0/0 | 1131 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | ATGGC others(1126): Show |
chr17 | 65004289 | 65061740 | ||
| a0001c0007 | 0/0 | 1131 | 1 | 0 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | ATGGC others(1126): Show |
chr17 | 65004289 | 65061740 | ||
| a0001c0009 | 0/0 | 1131 | 1 | 0 | 0 | 0 | 0 | 1 | GNA13_chr17_65004289_65061740 | GNA13 | ATGGC others(1126): Show |
chr17 | 65004289 | 65061740 | ||
| a0002c0006 | 0/0 | 1131 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | ATGGC others(1126): Show |
chr17 | 65004289 | 65061740 | ||
| a0003c0008 | 0/0 | 1131 | 1 | 0 | 0 | 0 | 0 | 1 | GNA13_chr17_65004289_65061740 | GNA13 | ATGGC others(1126): Show |
chr17 | 65004289 | 65061740 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6249 | 86 | 29 | 21 | 22 | 1 | 13 | GNA13_chr17_65004289_65061740 | GNA13 | AGTTC others(6244): Show |
chr17 | 65004289 | 65061740 |
| a0001c0001t0002 | 0/1 | 6246 | 13 | 3 | 2 | 1 | 1 | 5 | GNA13_chr17_65004289_65061740 | GNA13 | AGTTC others(6241): Show |
chr17 | 65004289 | 65061740 |
| a0001c0001t0003 | 0/0 | 6249 | 13 | 12 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | AGTTC others(6244): Show |
chr17 | 65004289 | 65061740 |
| a0001c0001t0005 | 0/0 | 6249 | 8 | 8 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | AGTTC others(6244): Show |
chr17 | 65004289 | 65061740 |
| a0001c0001t0006 | 1/0 | 6249 | 5 | 4 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | AGTTC others(6244): Show |
chr17 | 65004289 | 65061740 |
| a0001c0001t0007 | 0/0 | 6246 | 4 | 4 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | AGTTC others(6241): Show |
chr17 | 65004289 | 65061740 |
| a0001c0001t0008 | 0/0 | 6249 | 4 | 2 | 2 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | AGTTC others(6244): Show |
chr17 | 65004289 | 65061740 |
| a0001c0001t0009 | 0/0 | 6245 | 2 | 1 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | AGTTC others(6240): Show |
chr17 | 65004289 | 65061740 |
| a0001c0001t0010 | 0/0 | 6249 | 3 | 3 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | AGTTC others(6244): Show |
chr17 | 65004289 | 65061740 |
| a0001c0001t0011 | 0/0 | 6252 | 3 | 0 | 1 | 0 | 0 | 2 | GNA13_chr17_65004289_65061740 | GNA13 | AGTTC others(6247): Show |
chr17 | 65004289 | 65061740 |
| a0001c0001t0012 | 0/0 | 6249 | 2 | 0 | 0 | 2 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | AGTTC others(6244): Show |
chr17 | 65004289 | 65061740 |
| a0001c0001t0013 | 0/0 | 6249 | 2 | 2 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | AGTTC others(6244): Show |
chr17 | 65004289 | 65061740 |
| a0001c0001t0014 | 0/0 | 6249 | 1 | 0 | 0 | 0 | 0 | 1 | GNA13_chr17_65004289_65061740 | GNA13 | AGTTC others(6244): Show |
chr17 | 65004289 | 65061740 |
| a0001c0001t0015 | 0/0 | 6249 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | AGTTC others(6244): Show |
chr17 | 65004289 | 65061740 |
| a0001c0001t0016 | 0/0 | 6245 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | AGTTC others(6240): Show |
chr17 | 65004289 | 65061740 |
| a0001c0001t0017 | 0/0 | 6249 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | AGTTC others(6244): Show |
chr17 | 65004289 | 65061740 |
| a0001c0001t0018 | 0/0 | 6249 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | AGTTC others(6244): Show |
chr17 | 65004289 | 65061740 |
| a0001c0001t0019 | 0/0 | 6249 | 1 | 0 | 0 | 0 | 0 | 1 | GNA13_chr17_65004289_65061740 | GNA13 | AGTTC others(6244): Show |
chr17 | 65004289 | 65061740 |
| a0001c0001t0020 | 0/0 | 6249 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | AGTTC others(6244): Show |
chr17 | 65004289 | 65061740 |
| a0001c0001t0021 | 0/0 | 6249 | 1 | 0 | 0 | 1 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | AGTTC others(6244): Show |
chr17 | 65004289 | 65061740 |
| a0001c0001t0022 | 0/0 | 6249 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | AGTTC others(6244): Show |
chr17 | 65004289 | 65061740 |
| a0001c0001t0023 | 0/0 | 6249 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | AGTTC others(6244): Show |
chr17 | 65004289 | 65061740 |
| a0001c0001t0024 | 0/0 | 6249 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | AGTTC others(6244): Show |
chr17 | 65004289 | 65061740 |
| a0001c0001t0025 | 0/0 | 6252 | 1 | 0 | 0 | 0 | 0 | 1 | GNA13_chr17_65004289_65061740 | GNA13 | AGTTC others(6247): Show |
chr17 | 65004289 | 65061740 |
| a0001c0001t0026 | 0/0 | 6252 | 1 | 0 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | AGTTC others(6247): Show |
chr17 | 65004289 | 65061740 |
| a0001c0001t0027 | 0/0 | 6249 | 1 | 0 | 0 | 0 | 0 | 1 | GNA13_chr17_65004289_65061740 | GNA13 | AGTTC others(6244): Show |
chr17 | 65004289 | 65061740 |
| a0001c0002t0004 | 0/0 | 6250 | 11 | 10 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | AGTTC others(6245): Show |
chr17 | 65004289 | 65061740 |
| a0001c0003t0001 | 0/0 | 6249 | 3 | 0 | 3 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | AGTTC others(6244): Show |
chr17 | 65004289 | 65061740 |
| a0001c0004t0002 | 0/0 | 6246 | 2 | 0 | 2 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | AGTTC others(6241): Show |
chr17 | 65004289 | 65061740 |
| a0001c0005t0009 | 0/0 | 6245 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | AGTTC others(6240): Show |
chr17 | 65004289 | 65061740 |
| a0001c0007t0007 | 0/0 | 6246 | 1 | 0 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | AGTTC others(6241): Show |
chr17 | 65004289 | 65061740 |
| a0001c0009t0001 | 0/0 | 6249 | 1 | 0 | 0 | 0 | 0 | 1 | GNA13_chr17_65004289_65061740 | GNA13 | AGTTC others(6244): Show |
chr17 | 65004289 | 65061740 |
| a0002c0006t0001 | 0/0 | 6249 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | AGTTC others(6244): Show |
chr17 | 65004289 | 65061740 |
| a0003c0008t0001 | 0/0 | 6249 | 1 | 0 | 0 | 0 | 0 | 1 | GNA13_chr17_65004289_65061740 | GNA13 | AGTTC others(6244): Show |
chr17 | 65004289 | 65061740 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0002g0009 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0003g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0005g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0005g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0006g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0006g0004 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0007g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0007g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0007g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0007g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0008g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0008g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0008g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0008g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0009g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0009g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0010g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0010g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0010g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0011g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0011g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0011g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0012g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0012g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0013g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0013g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0014g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0015g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0016g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0017g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0018g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0019g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0020g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0021g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0022g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0023g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0024g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0025g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0026g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0001t0027g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0002t0004g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0002t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0002t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0002t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0002t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0002t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0002t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0002t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0002t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0002t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0002t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0003t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0003t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0003t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0004t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0004t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0005t0009g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0007t0007g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0001c0009t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0002c0006t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| a0003c0008t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0019 | EUR | GBR | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0102 | EUR | GBR | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG00639 | hp1 | a0001 | c0003 | t0001 | g0112 | AMR | PUR | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG00639 | hp2 | a0001 | c0001 | t0009 | g0155 | AMR | PUR | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG01069 | hp2 | a0001 | c0001 | t0008 | g0149 | AMR | PUR | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG01071 | hp1 | a0001 | c0001 | t0008 | g0152 | AMR | PUR | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0131 | AMR | PUR | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG01109 | hp1 | a0001 | c0007 | t0007 | g0171 | AMR | PUR | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG01109 | hp2 | a0001 | c0001 | t0011 | g0166 | AMR | PUR | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG01167 | hp1 | a0001 | c0004 | t0002 | g0018 | AMR | PUR | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG01169 | hp2 | a0001 | c0004 | t0002 | g0017 | AMR | PUR | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG01346 | hp2 | a0001 | c0002 | t0004 | g0137 | AMR | CLM | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG01433 | hp1 | a0001 | c0003 | t0001 | g0113 | AMR | CLM | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG01496 | hp1 | a0001 | c0001 | t0026 | g0167 | AMR | CLM | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0136 | AFR | ACB | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG01891 | hp1 | a0001 | c0001 | t0013 | g0157 | AFR | ACB | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG01891 | hp2 | a0001 | c0001 | t0022 | g0115 | AFR | ACB | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG01993 | hp2 | a0001 | c0003 | t0001 | g0111 | AMR | PEL | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0114 | AFR | ACB | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02257 | hp2 | a0001 | c0001 | t0007 | g0170 | AFR | ACB | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0120 | AFR | ACB | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0118 | AFR | ACB | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0003 | AFR | GWD | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02622 | hp2 | a0001 | c0002 | t0004 | g0141 | AFR | GWD | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02647 | hp2 | a0001 | c0001 | t0008 | g0150 | AFR | GWD | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02698 | hp1 | a0001 | c0001 | t0025 | g0165 | SAS | PJL | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0119 | AFR | GWD | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0159 | AFR | GWD | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02735 | hp1 | a0001 | c0001 | t0019 | g0103 | SAS | PJL | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02738 | hp2 | a0001 | c0001 | t0011 | g0168 | SAS | PJL | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0132 | AFR | GWD | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0003 | AFR | GWD | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02886 | hp1 | a0001 | c0001 | t0024 | g0134 | AFR | GWD | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0033 | AFR | GWD | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | GWD | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0160 | AFR | GWD | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | GWD | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02922 | hp1 | a0001 | c0002 | t0004 | g0147 | AFR | ESN | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02965 | hp1 | a0001 | c0001 | t0009 | g0154 | AFR | ESN | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02965 | hp2 | a0001 | c0001 | t0010 | g0121 | AFR | ESN | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02976 | hp1 | a0001 | c0002 | t0004 | g0143 | AFR | ESN | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02976 | hp2 | a0001 | c0001 | t0006 | g0004 | AFR | ESN | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0161 | AFR | GWD | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG03041 | hp2 | a0001 | c0001 | t0007 | g0173 | AFR | GWD | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG03098 | hp1 | a0001 | c0002 | t0004 | g0139 | AFR | MSL | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG03130 | hp1 | a0002 | c0006 | t0001 | g0151 | AFR | ESN | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG03130 | hp2 | a0001 | c0002 | t0004 | g0142 | AFR | ESN | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG03195 | hp1 | a0001 | c0002 | t0004 | g0162 | AFR | ESN | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG03209 | hp2 | a0001 | c0001 | t0007 | g0172 | AFR | MSL | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG03225 | hp1 | a0001 | c0001 | t0017 | g0158 | AFR | MSL | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0130 | AFR | MSL | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG03453 | hp1 | a0001 | c0001 | t0010 | g0123 | AFR | MSL | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | MSL | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0117 | AFR | MSL | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0016 | SAS | PJL | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG03516 | hp2 | a0001 | c0001 | t0008 | g0148 | AFR | ESN | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG03540 | hp1 | a0001 | c0001 | t0016 | g0124 | AFR | GWD | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0031 | AFR | GWD | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG03579 | hp1 | a0001 | c0001 | t0010 | g0122 | AFR | MSL | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG03579 | hp2 | a0001 | c0002 | t0004 | g0163 | AFR | MSL | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG03654 | hp1 | a0003 | c0008 | t0001 | g0110 | SAS | PJL | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | STU | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | STU | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG03704 | hp2 | a0001 | c0001 | t0014 | g0062 | SAS | PJL | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG03927 | hp1 | a0001 | c0009 | t0001 | g0164 | SAS | BEB | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG03927 | hp2 | a0001 | c0001 | t0011 | g0169 | SAS | BEB | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG04115 | hp1 | a0001 | c0001 | t0027 | g0175 | SAS | STU | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | STU | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | STU | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0012 | SAS | STU | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | STU | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | STU | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | YRI | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| NA18522 | hp2 | a0001 | c0001 | t0020 | g0097 | AFR | YRI | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| NA18906 | hp1 | a0001 | c0005 | t0009 | g0140 | AFR | YRI | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| NA18906 | hp2 | a0001 | c0001 | t0015 | g0138 | AFR | YRI | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| NA18941 | hp2 | a0001 | c0001 | t0012 | g0087 | EAS | JPT | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| NA18994 | hp2 | a0001 | c0001 | t0021 | g0093 | EAS | JPT | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0127 | AFR | LWK | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| NA19030 | hp2 | a0001 | c0001 | t0023 | g0129 | AFR | LWK | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0133 | AFR | LWK | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | LWK | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| NA19079 | hp2 | a0001 | c0001 | t0012 | g0091 | EAS | JPT | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | YRI | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | YRI | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02109 | hp1 | a0001 | c0001 | t0018 | g0135 | AFR | ACB | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02109 | hp2 | a0001 | c0002 | t0004 | g0145 | AFR | ACB | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02486 | hp1 | a0001 | c0001 | t0013 | g0156 | AFR | ACB | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0174 | AFR | ACB | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0126 | AFR | MSL | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG03471 | hp2 | a0001 | c0002 | t0004 | g0146 | AFR | MSL | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | USA | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0116 | AFR | USA | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | USA | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0128 | AFR | USA | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| NA21309 | hp1 | a0001 | c0002 | t0004 | g0144 | AFR | LWK | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | LWK | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0009 | REF | REF | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0006 | g0004 | REF | REF | GNA13_chr17_65004289_65061740 | GNA13 | chr17 | 65004289 | 65061740 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:65014412 | C | A | 1 | a0002 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.979G>T | p.Val327Leu | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 4/4 | 1126/6249 | 979/1134 | 327/377 | chr17 | 65014412 | |||
| chr17:65053567 | T | C | 1 | a0003 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.445A>G | p.Ile149Val | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/4 | 592/6249 | 445/1134 | 149/377 | chr17 | 65053567 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:65014290 | C | T | 1 | a0001c0004 | 2 | HG01167.hp1 HG01169.hp2 |
synonymous_variant | LOW | c.1101G>A | p.Leu367Leu | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 4/4 | 1248/6249 | 1101/1134 | 367/377 | chr17 | 65014290 | |||
| chr17:65014488 | T | C | 1 | a0001c0007 | 1 | HG01109.hp1 | synonymous_variant | LOW | c.903A>G | p.Gln301Gln | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 4/4 | 1050/6249 | 903/1134 | 301/377 | chr17 | 65014488 | |||
| chr17:65014752 | T | G | 1 | a0001c0005 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.639A>C | p.Ile213Ile | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 4/4 | 786/6249 | 639/1134 | 213/377 | chr17 | 65014752 | |||
| chr17:65053580 | T | C | 1 | a0001c0003 | 3 | HG00639.hp1 HG01433.hp1 HG01993.hp2 |
synonymous_variant | LOW | c.432A>G | p.Gln144Gln | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/4 | 579/6249 | 432/1134 | 144/377 | chr17 | 65053580 | |||
| chr17:65053706 | A | C | 2 | a0001c0002 a0001c0005 |
12 | HG01346.hp2 HG02109.hp2 HG02622.hp2 others(9): Show |
synonymous_variant | LOW | c.306T>G | p.Ala102Ala | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/4 | 453/6249 | 306/1134 | 102/377 | chr17 | 65053706 | |||
| chr17:65056402 | G | A | 1 | a0001c0009 | 1 | HG03927.hp1 | synonymous_variant | LOW | c.192C>T | p.Phe64Phe | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 1/4 | 339/6249 | 192/1134 | 64/377 | chr17 | 65056402 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:65009354 | G | A | 1 | a0001c0001t0020 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4903C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 4/4 | 4903 | chr17 | 65009354 | ||||||
| chr17:65009557 | T | C | 4 | a0001c0001t0003 a0001c0001t0018 a0001c0001t0023 others(1): Show |
16 | HG01099.hp1 HG01884.hp1 HG02109.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*4700A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 4/4 | 4700 | chr17 | 65009557 | ||||||
| chr17:65009559 | T | TA | 1 | a0001c0002t0004 | 11 | HG01346.hp2 HG02109.hp2 HG02622.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4697dupT | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 4/4 | 4697 | chr17 | 65009559 | ||||||
| chr17:65009739 | C | T | 1 | a0001c0001t0016 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4518G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 4/4 | 4518 | chr17 | 65009739 | ||||||
| chr17:65009936 | T | C | 2 | a0001c0001t0005 a0001c0001t0022 |
9 | HG01891.hp2 HG02055.hp1 HG02280.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4321A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 4/4 | 4321 | chr17 | 65009936 | ||||||
| chr17:65010828 | C | T | 1 | a0001c0001t0019 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3429G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 4/4 | 3429 | chr17 | 65010828 | ||||||
| chr17:65010969 | A | G | 1 | a0001c0001t0012 | 2 | NA18941.hp2 NA19079.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3288T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 4/4 | 3288 | chr17 | 65010969 | ||||||
| chr17:65010977 | G | A | 30 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(27): Show |
164 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(161): Show |
3_prime_UTR_variant | MODIFIER | c.*3280C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 4/4 | 3280 | chr17 | 65010977 | ||||||
| chr17:65011291 | G | A | 1 | a0001c0001t0016 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2966C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 4/4 | 2966 | chr17 | 65011291 | ||||||
| chr17:65011804 | C | T | 2 | a0001c0001t0008 a0001c0001t0018 |
5 | HG01069.hp2 HG01071.hp1 HG02109.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2453G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 4/4 | 2453 | chr17 | 65011804 | ||||||
| chr17:65012008 | T | C | 1 | a0001c0001t0016 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2249A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 4/4 | 2249 | chr17 | 65012008 | ||||||
| chr17:65012088 | C | T | 1 | a0001c0001t0025 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2169G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 4/4 | 2169 | chr17 | 65012088 | ||||||
| chr17:65012354 | C | G | 1 | a0001c0001t0015 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1903G>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 4/4 | 1903 | chr17 | 65012354 | ||||||
| chr17:65012355 | G | A | 1 | a0001c0002t0004 | 11 | HG01346.hp2 HG02109.hp2 HG02622.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1902C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 4/4 | 1902 | chr17 | 65012355 | ||||||
| chr17:65012537 | A | T | 2 | a0001c0001t0013 a0001c0001t0017 |
3 | HG01891.hp1 HG02486.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1720T>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 4/4 | 1720 | chr17 | 65012537 | ||||||
| chr17:65012659 | TCAGA | T | 3 | a0001c0001t0009 a0001c0001t0016 a0001c0005t0009 |
4 | HG00639.hp2 HG02965.hp1 HG03540.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1594_*1597delTCTG | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 4/4 | 1594 | chr17 | 65012659 | ||||||
| chr17:65012701 | T | C | 1 | a0001c0001t0021 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1556A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 4/4 | 1556 | chr17 | 65012701 | ||||||
| chr17:65012968 | G | A | 1 | a0001c0001t0022 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1289C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 4/4 | 1289 | chr17 | 65012968 | ||||||
| chr17:65013018 | C | T | 1 | a0001c0001t0015 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1239G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 4/4 | 1239 | chr17 | 65013018 | ||||||
| chr17:65013361 | T | A | 1 | a0001c0001t0010 | 3 | HG02965.hp2 HG03453.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*896A>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 4/4 | 896 | chr17 | 65013361 | ||||||
| chr17:65013440 | T | C | 1 | a0001c0001t0013 | 2 | HG01891.hp1 HG02486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*817A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 4/4 | 817 | chr17 | 65013440 | ||||||
| chr17:65013599 | T | C | 1 | a0001c0001t0026 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*658A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 4/4 | 658 | chr17 | 65013599 | ||||||
| chr17:65013770 | T | C | 2 | a0001c0001t0023 a0001c0002t0004 |
12 | HG01346.hp2 HG02109.hp2 HG02622.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*487A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 4/4 | 487 | chr17 | 65013770 | ||||||
| chr17:65013886 | C | T | 1 | a0001c0001t0014 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*371G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 4/4 | 371 | chr17 | 65013886 | ||||||
| chr17:65014021 | T | C | 1 | a0001c0001t0024 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*236A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 4/4 | 236 | chr17 | 65014021 | ||||||
| chr17:65056596 | T | TGCC | 3 | a0001c0001t0011 a0001c0001t0025 a0001c0001t0026 |
5 | HG01109.hp2 HG01496.hp1 HG02698.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-6_-4dupGGC | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 1/4 | 4 | chr17 | 65056596 | ||||||
| chr17:65056596 | TGCC | T | 2 | a0001c0001t0002 a0001c0004t0002 |
14 | HG00099.hp1 HG01123.hp2 HG01167.hp1 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-6_-4delGGC | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 1/4 | 4 | chr17 | 65056596 | ||||||
| chr17:65056640 | ACCT | A | 2 | a0001c0001t0007 a0001c0007t0007 |
5 | HG01109.hp1 HG02257.hp2 HG02559.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-50_-48delAGG | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 1/4 | 48 | chr17 | 65056640 | ||||||
| chr17:65056674 | G | A | 1 | a0001c0001t0027 | 1 | HG04115.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-81C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 1/4 | chr17 | 65056674 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:65015047 | G | A | 2 | a0001c0001t0009g0154 a0001c0001t0009g0155 |
2 | HG00639.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.562-218C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65015047 | |||||||
| chr17:65015196 | T | C | 1 | a0001c0007t0007g0171 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.562-367A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65015196 | |||||||
| chr17:65015217 | A | C | 15 | a0001c0001t0001g0125 a0001c0001t0001g0153 a0001c0001t0007g0170 others(12): Show |
15 | HG01069.hp2 HG01071.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.562-388T>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65015217 | |||||||
| chr17:65015244 | C | T | 1 | a0001c0001t0001g0042 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.562-415G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65015244 | |||||||
| chr17:65015268 | C | G | 1 | a0001c0001t0016g0124 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.562-439G>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65015268 | |||||||
| chr17:65015378 | G | A | 2 | a0001c0002t0004g0162 a0001c0002t0004g0163 |
2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.562-549C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65015378 | |||||||
| chr17:65015429 | G | A | 7 | a0001c0001t0001g0125 a0001c0001t0001g0153 a0001c0001t0008g0148 others(4): Show |
7 | HG01069.hp2 HG01071.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.562-600C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65015429 | |||||||
| chr17:65015497 | C | A | 1 | a0001c0001t0006g0161 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.562-668G>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65015497 | |||||||
| chr17:65015532 | G | A | 3 | a0001c0001t0009g0154 a0001c0001t0009g0155 a0001c0005t0009g0140 |
3 | HG00639.hp2 HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.562-703C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65015532 | |||||||
| chr17:65015616 | T | C | 11 | a0001c0002t0004g0137 a0001c0002t0004g0139 a0001c0002t0004g0141 others(8): Show |
11 | HG01346.hp2 HG02109.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.562-787A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65015616 | |||||||
| chr17:65015652 | G | C | 101 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(98): Show |
102 | HG00099.hp2 HG00639.hp1 HG00735.hp1 others(99): Show |
intron_variant | MODIFIER | c.562-823C>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65015652 | |||||||
| chr17:65015662 | T | TA | 102 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(99): Show |
105 | HG00099.hp2 HG00639.hp1 HG00735.hp1 others(102): Show |
intron_variant | MODIFIER | c.562-834dupT | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65015662 | |||||||
| chr17:65015662 | T | TAA | 17 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0066 others(14): Show |
17 | HG00639.hp2 HG01123.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.562-835_562-834dup others(2): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65015662 | |||||||
| chr17:65015662 | TA | T | 7 | a0001c0001t0005g0114 a0001c0001t0007g0170 a0001c0001t0007g0172 others(4): Show |
7 | HG01109.hp1 HG02055.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.562-834delT | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65015662 | |||||||
| chr17:65015687 | G | A | 2 | a0001c0001t0009g0154 a0001c0001t0009g0155 |
2 | HG00639.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.562-858C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65015687 | |||||||
| chr17:65015741 | G | C | 15 | a0001c0001t0001g0125 a0001c0001t0001g0153 a0001c0001t0007g0170 others(12): Show |
15 | HG01069.hp2 HG01071.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.562-912C>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65015741 | |||||||
| chr17:65015978 | G | C | 120 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(117): Show |
121 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(118): Show |
intron_variant | MODIFIER | c.562-1149C>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65015978 | |||||||
| chr17:65016176 | A | G | 1 | a0001c0001t0002g0019 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.562-1347T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65016176 | |||||||
| chr17:65016363 | T | C | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | HG01243.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.562-1534A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65016363 | |||||||
| chr17:65016558 | C | T | 3 | a0001c0001t0011g0168 a0001c0001t0011g0169 a0001c0001t0026g0167 |
3 | HG01496.hp1 HG02738.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.561+1695G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65016558 | |||||||
| chr17:65016559 | A | G | 171 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(168): Show |
174 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(171): Show |
intron_variant | MODIFIER | c.561+1694T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65016559 | |||||||
| chr17:65016581 | C | T | 1 | a0001c0001t0015g0138 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.561+1672G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65016581 | |||||||
| chr17:65016632 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.561+1621C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65016632 | |||||||
| chr17:65016904 | C | T | 2 | a0001c0004t0002g0017 a0001c0004t0002g0018 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.561+1349G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65016904 | |||||||
| chr17:65016915 | A | G | 9 | a0001c0002t0004g0137 a0001c0002t0004g0139 a0001c0002t0004g0141 others(6): Show |
9 | HG01346.hp2 HG02109.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.561+1338T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65016915 | |||||||
| chr17:65017137 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.561+1116G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65017137 | |||||||
| chr17:65017201 | C | T | 1 | a0001c0001t0005g0033 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.561+1052G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65017201 | |||||||
| chr17:65017204 | C | T | 117 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(114): Show |
118 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(115): Show |
intron_variant | MODIFIER | c.561+1049G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65017204 | |||||||
| chr17:65017351 | T | C | 118 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(115): Show |
119 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(116): Show |
intron_variant | MODIFIER | c.561+902A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65017351 | |||||||
| chr17:65017524 | C | G | 171 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(168): Show |
174 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(171): Show |
intron_variant | MODIFIER | c.561+729G>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65017524 | |||||||
| chr17:65017604 | G | A | 3 | a0001c0001t0001g0047 a0001c0001t0001g0050 a0001c0001t0001g0051 |
3 | HG02647.hp1 HG02895.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.561+649C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65017604 | |||||||
| chr17:65017725 | C | T | 5 | a0001c0001t0007g0170 a0001c0001t0007g0172 a0001c0001t0007g0173 others(2): Show |
5 | HG01109.hp1 HG02257.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.561+528G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65017725 | |||||||
| chr17:65017910 | A | G | 8 | a0001c0001t0005g0031 a0001c0001t0005g0114 a0001c0001t0005g0116 others(5): Show |
8 | HG01891.hp2 HG02055.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.561+343T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65017910 | |||||||
| chr17:65018092 | T | TAAAAAAA others(3): Show |
1 | a0001c0001t0005g0120 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.561+151_561+160dup others(10): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65018092 | |||||||
| chr17:65018092 | TA | T | 9 | a0001c0001t0001g0028 a0001c0001t0001g0034 a0001c0001t0001g0058 others(6): Show |
9 | HG01123.hp1 HG01167.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.561+160delT | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65018092 | |||||||
| chr17:65018092 | TAA | T | 19 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(16): Show |
19 | HG00738.hp1 HG01109.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.561+159_561+160del others(2): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65018092 | |||||||
| chr17:65018092 | TAAA | T | 22 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0037 others(19): Show |
22 | HG00099.hp2 HG00639.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.561+158_561+160del others(3): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65018092 | |||||||
| chr17:65018092 | TAAAA | T | 30 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(27): Show |
31 | HG00735.hp2 HG00738.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.561+157_561+160del others(4): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65018092 | |||||||
| chr17:65018092 | TAAAAA | T | 11 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0043 others(8): Show |
11 | HG01069.hp1 HG01169.hp1 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.561+156_561+160del others(5): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65018092 | |||||||
| chr17:65018092 | TAAAAAA | T | 8 | a0001c0001t0001g0054 a0001c0001t0001g0086 a0001c0001t0001g0153 others(5): Show |
8 | HG02451.hp1 HG02723.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.561+155_561+160del others(6): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65018092 | |||||||
| chr17:65018092 | TAAAAAAA others(2): Show |
T | 9 | a0001c0001t0002g0005 a0001c0001t0002g0008 a0001c0001t0002g0010 others(6): Show |
9 | HG01167.hp1 HG01169.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.561+152_561+160del others(9): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65018092 | |||||||
| chr17:65018092 | TAAAAAAA others(3): Show |
T | 9 | a0001c0001t0001g0029 a0001c0001t0002g0006 a0001c0001t0002g0013 others(6): Show |
9 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.561+151_561+160del others(10): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65018092 | |||||||
| chr17:65018092 | TAAAAAAA others(4): Show |
T | 2 | a0001c0001t0002g0014 a0001c0001t0002g0019 |
2 | HG00099.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.561+150_561+160del others(11): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65018092 | |||||||
| chr17:65018092 | TAAAAAAA others(8): Show |
T | 1 | a0001c0001t0005g0114 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.561+146_561+160del others(15): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65018092 | |||||||
| chr17:65018092 | TAAAAAAA others(11): Show |
T | 1 | a0001c0005t0009g0140 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.561+143_561+160del others(18): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65018092 | |||||||
| chr17:65018092 | TAAAAAAA others(12): Show |
T | 1 | a0001c0001t0006g0003 | 2 | HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.561+142_561+160del others(19): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65018092 | |||||||
| chr17:65018092 | TAAAAAAA others(13): Show |
T | 4 | a0001c0001t0001g0072 a0001c0001t0006g0161 a0001c0001t0009g0155 others(1): Show |
4 | HG00639.hp2 HG02258.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.561+141_561+160del others(20): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65018092 | |||||||
| chr17:65018092 | TAAAAAAA others(14): Show |
T | 16 | a0001c0001t0001g0064 a0001c0001t0003g0001 a0001c0001t0003g0126 others(13): Show |
18 | HG01099.hp1 HG01884.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.561+140_561+160del others(21): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65018092 | |||||||
| chr17:65018092 | TAAAAAAA others(16): Show |
T | 1 | a0001c0001t0001g0079 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.561+138_561+160del others(23): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65018092 | |||||||
| chr17:65018092 | TAAAAAAA others(19): Show |
T | 1 | a0001c0001t0015g0138 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.561+135_561+160del others(26): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65018092 | |||||||
| chr17:65018117 | A | G | 2 | a0001c0001t0003g0159 a0001c0001t0003g0160 |
2 | HG02723.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.561+136T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65018117 | |||||||
| chr17:65018130 | AAAAAAAA others(3): Show |
A | 2 | a0001c0001t0005g0116 a0001c0001t0005g0118 |
2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.561+113_561+122del others(10): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65018130 | |||||||
| chr17:65018132 | A | G | 12 | a0001c0001t0001g0030 a0001c0001t0001g0042 a0001c0001t0001g0045 others(9): Show |
12 | HG00738.hp2 HG01099.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.561+121T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65018132 | |||||||
| chr17:65018134 | A | G | 46 | a0001c0001t0001g0020 a0001c0001t0001g0024 a0001c0001t0001g0028 others(43): Show |
46 | HG00735.hp1 HG00738.hp2 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.561+119T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65018134 | |||||||
| chr17:65018136 | A | G | 116 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(113): Show |
117 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(114): Show |
intron_variant | MODIFIER | c.561+117T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65018136 | |||||||
| chr17:65018138 | A | G | 133 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(130): Show |
136 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(133): Show |
intron_variant | MODIFIER | c.561+115T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65018138 | |||||||
| chr17:65018140 | G | A | 4 | a0001c0001t0005g0117 a0001c0001t0005g0119 a0001c0001t0005g0120 others(1): Show |
4 | HG01891.hp2 HG02280.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.561+113C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 3/3 | chr17 | 65018140 | |||||||
| chr17:65018595 | A | G | 1 | a0001c0001t0027g0175 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.511-292T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65018595 | |||||||
| chr17:65018706 | G | T | 42 | a0001c0001t0001g0125 a0001c0001t0001g0153 a0001c0001t0003g0001 others(39): Show |
44 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.511-403C>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65018706 | |||||||
| chr17:65018856 | T | G | 1 | a0001c0001t0001g0077 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.511-553A>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65018856 | |||||||
| chr17:65018886 | G | T | 171 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(168): Show |
174 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(171): Show |
intron_variant | MODIFIER | c.511-583C>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65018886 | |||||||
| chr17:65019031 | C | A | 6 | a0001c0001t0001g0125 a0001c0001t0008g0148 a0001c0001t0008g0149 others(3): Show |
6 | HG01069.hp2 HG01071.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.511-728G>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65019031 | |||||||
| chr17:65019242 | C | T | 1 | a0001c0001t0002g0007 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.511-939G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65019242 | |||||||
| chr17:65019287 | A | G | 2 | a0001c0001t0003g0159 a0001c0001t0003g0160 |
2 | HG02723.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.511-984T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65019287 | |||||||
| chr17:65019464 | A | G | 1 | a0001c0001t0002g0007 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.511-1161T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65019464 | |||||||
| chr17:65019881 | C | T | 3 | a0001c0001t0001g0074 a0001c0001t0012g0087 a0001c0001t0012g0091 |
3 | NA18941.hp2 NA18960.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.511-1578G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65019881 | |||||||
| chr17:65020069 | T | G | 1 | a0001c0001t0001g0065 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.511-1766A>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65020069 | |||||||
| chr17:65020236 | T | G | 2 | a0001c0001t0001g0045 a0001c0001t0001g0053 |
2 | HG01099.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.511-1933A>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65020236 | |||||||
| chr17:65020263 | G | C | 1 | a0001c0001t0001g0060 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.511-1960C>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65020263 | |||||||
| chr17:65020397 | T | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0064 |
2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.511-2094A>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65020397 | |||||||
| chr17:65020437 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.511-2134T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65020437 | |||||||
| chr17:65020574 | T | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0036 |
2 | HG00735.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.511-2271A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65020574 | |||||||
| chr17:65020645 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.511-2342G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65020645 | |||||||
| chr17:65020654 | A | AT | 9 | a0001c0001t0003g0159 a0001c0001t0003g0160 a0001c0001t0019g0103 others(6): Show |
9 | HG02109.hp2 HG02723.hp2 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.511-2352dupA | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65020654 | |||||||
| chr17:65020714 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.511-2411C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65020714 | |||||||
| chr17:65021016 | A | G | 1 | a0001c0001t0017g0158 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.511-2713T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65021016 | |||||||
| chr17:65021213 | T | C | 1 | a0001c0001t0015g0138 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.511-2910A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65021213 | |||||||
| chr17:65022415 | A | G | 4 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0088 others(1): Show |
4 | HG00738.hp1 HG01346.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.511-4112T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65022415 | |||||||
| chr17:65022533 | G | A | 4 | a0001c0001t0001g0025 a0001c0001t0001g0066 a0001c0001t0001g0067 others(1): Show |
4 | HG01255.hp2 HG01884.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.511-4230C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65022533 | |||||||
| chr17:65022812 | G | A | 1 | a0001c0001t0010g0123 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.511-4509C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65022812 | |||||||
| chr17:65022882 | C | T | 161 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(158): Show |
164 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(161): Show |
intron_variant | MODIFIER | c.511-4579G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65022882 | |||||||
| chr17:65023111 | A | G | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | HG01243.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.511-4808T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65023111 | |||||||
| chr17:65023286 | C | T | 1 | a0001c0001t0021g0093 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.511-4983G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65023286 | |||||||
| chr17:65023313 | C | T | 3 | a0001c0001t0005g0116 a0001c0001t0005g0117 a0001c0001t0022g0115 |
3 | HG01891.hp2 HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.511-5010G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65023313 | |||||||
| chr17:65023329 | A | G | 12 | a0001c0001t0003g0001 a0001c0001t0003g0126 a0001c0001t0003g0127 others(9): Show |
14 | HG01099.hp1 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.511-5026T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65023329 | |||||||
| chr17:65023594 | C | A | 18 | a0001c0001t0003g0001 a0001c0001t0003g0126 a0001c0001t0003g0127 others(15): Show |
20 | HG00639.hp2 HG01099.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.511-5291G>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65023594 | |||||||
| chr17:65023698 | A | C | 11 | a0001c0002t0004g0137 a0001c0002t0004g0139 a0001c0002t0004g0141 others(8): Show |
11 | HG01346.hp2 HG02109.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.511-5395T>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65023698 | |||||||
| chr17:65023731 | A | C | 1 | a0001c0001t0001g0051 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.511-5428T>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65023731 | |||||||
| chr17:65023925 | A | T | 1 | a0001c0001t0001g0051 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.511-5622T>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65023925 | |||||||
| chr17:65024014 | G | A | 1 | a0001c0002t0004g0141 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.511-5711C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65024014 | |||||||
| chr17:65024182 | G | A | 1 | a0001c0001t0016g0124 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.511-5879C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65024182 | |||||||
| chr17:65024231 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.511-5928C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65024231 | |||||||
| chr17:65024340 | G | A | 6 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0038 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.511-6037C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65024340 | |||||||
| chr17:65024387 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.511-6084T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65024387 | |||||||
| chr17:65024458 | T | C | 2 | a0001c0001t0009g0154 a0001c0001t0009g0155 |
2 | HG00639.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.511-6155A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65024458 | |||||||
| chr17:65025021 | A | G | 1 | a0001c0001t0005g0118 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.511-6718T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65025021 | |||||||
| chr17:65025044 | T | C | 1 | a0001c0001t0002g0015 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.511-6741A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65025044 | |||||||
| chr17:65025105 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.511-6802G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65025105 | |||||||
| chr17:65025149 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.511-6846G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65025149 | |||||||
| chr17:65025241 | C | T | 9 | a0001c0002t0004g0137 a0001c0002t0004g0139 a0001c0002t0004g0141 others(6): Show |
9 | HG01346.hp2 HG02109.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.511-6938G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65025241 | |||||||
| chr17:65025298 | A | C | 26 | a0001c0001t0001g0125 a0001c0001t0001g0153 a0001c0001t0007g0170 others(23): Show |
26 | HG01069.hp2 HG01071.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.511-6995T>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65025298 | |||||||
| chr17:65025593 | A | G | 5 | a0001c0001t0007g0170 a0001c0001t0007g0172 a0001c0001t0007g0173 others(2): Show |
5 | HG01109.hp1 HG02257.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.511-7290T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65025593 | |||||||
| chr17:65025660 | A | C | 117 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(114): Show |
118 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(115): Show |
intron_variant | MODIFIER | c.511-7357T>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65025660 | |||||||
| chr17:65025760 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.511-7457C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65025760 | |||||||
| chr17:65025817 | CA | C | 12 | a0001c0001t0001g0051 a0001c0001t0001g0063 a0001c0001t0001g0096 others(9): Show |
12 | HG01891.hp2 HG02055.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.511-7515delT | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65025817 | |||||||
| chr17:65025817 | CAA | C | 156 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(153): Show |
159 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(156): Show |
intron_variant | MODIFIER | c.511-7516_511-7515d others(4): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65025817 | |||||||
| chr17:65025842 | C | T | 1 | a0001c0001t0003g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.511-7539G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65025842 | |||||||
| chr17:65025847 | G | A | 1 | a0001c0001t0010g0122 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.511-7544C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65025847 | |||||||
| chr17:65026037 | G | C | 1 | a0001c0001t0001g0056 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.511-7734C>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65026037 | |||||||
| chr17:65026111 | ATTAG | A | 2 | a0001c0001t0003g0128 a0001c0001t0003g0133 |
2 | NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.511-7812_511-7809d others(6): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65026111 | |||||||
| chr17:65026198 | C | CA | 8 | a0001c0001t0005g0031 a0001c0001t0005g0114 a0001c0001t0005g0116 others(5): Show |
8 | HG01891.hp2 HG02055.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.511-7896dupT | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65026198 | |||||||
| chr17:65026203 | T | A | 9 | a0001c0001t0005g0031 a0001c0001t0005g0033 a0001c0001t0005g0114 others(6): Show |
9 | HG01891.hp2 HG02055.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.511-7900A>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65026203 | |||||||
| chr17:65026498 | G | A | 1 | a0001c0001t0006g0161 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.511-8195C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65026498 | |||||||
| chr17:65026500 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.511-8197G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65026500 | |||||||
| chr17:65026752 | T | A | 1 | a0001c0001t0010g0123 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.511-8449A>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65026752 | |||||||
| chr17:65026771 | TTTTG | T | 11 | a0001c0002t0004g0137 a0001c0002t0004g0139 a0001c0002t0004g0141 others(8): Show |
11 | HG01346.hp2 HG02109.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.511-8472_511-8469d others(6): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65026771 | |||||||
| chr17:65026870 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.511-8567G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65026870 | |||||||
| chr17:65026993 | G | C | 8 | a0001c0001t0001g0125 a0001c0001t0001g0153 a0001c0001t0008g0148 others(5): Show |
8 | HG01069.hp2 HG01071.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.511-8690C>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65026993 | |||||||
| chr17:65026996 | T | C | 2 | a0001c0001t0001g0002 a0001c0001t0001g0099 |
3 | HG02698.hp2 HG03491.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.511-8693A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65026996 | |||||||
| chr17:65027058 | G | T | 1 | a0001c0001t0001g0024 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.511-8755C>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65027058 | |||||||
| chr17:65027175 | T | G | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.511-8872A>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65027175 | |||||||
| chr17:65027208 | T | C | 1 | a0001c0001t0016g0124 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.511-8905A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65027208 | |||||||
| chr17:65027253 | C | G | 2 | a0001c0001t0001g0034 a0001c0001t0001g0070 |
2 | HG01261.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.511-8950G>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65027253 | |||||||
| chr17:65027314 | C | CT | 119 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(116): Show |
120 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(117): Show |
intron_variant | MODIFIER | c.511-9012dupA | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65027314 | |||||||
| chr17:65027347 | T | A | 1 | a0001c0001t0016g0124 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.511-9044A>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65027347 | |||||||
| chr17:65027441 | C | G | 1 | a0001c0001t0005g0031 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.511-9138G>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65027441 | |||||||
| chr17:65027806 | A | T | 4 | a0001c0001t0009g0154 a0001c0001t0009g0155 a0001c0001t0016g0124 others(1): Show |
4 | HG00639.hp2 HG02965.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.511-9503T>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65027806 | |||||||
| chr17:65027810 | G | A | 11 | a0001c0002t0004g0137 a0001c0002t0004g0139 a0001c0002t0004g0141 others(8): Show |
11 | HG01346.hp2 HG02109.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.511-9507C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65027810 | |||||||
| chr17:65027822 | A | C | 30 | a0001c0001t0001g0125 a0001c0001t0001g0153 a0001c0001t0007g0170 others(27): Show |
30 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.511-9519T>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65027822 | |||||||
| chr17:65027892 | G | A | 9 | a0001c0001t0003g0001 a0001c0001t0003g0126 a0001c0001t0003g0127 others(6): Show |
11 | HG01099.hp1 HG01884.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.511-9589C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65027892 | |||||||
| chr17:65027954 | T | C | 14 | a0001c0001t0003g0001 a0001c0001t0003g0126 a0001c0001t0003g0127 others(11): Show |
16 | HG01099.hp1 HG01884.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.511-9651A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65027954 | |||||||
| chr17:65028010 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.511-9707C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65028010 | |||||||
| chr17:65028021 | G | C | 7 | a0001c0001t0001g0125 a0001c0001t0008g0148 a0001c0001t0008g0149 others(4): Show |
7 | HG01069.hp2 HG01071.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.511-9718C>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65028021 | |||||||
| chr17:65028083 | G | A | 1 | a0001c0001t0010g0123 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.511-9780C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65028083 | |||||||
| chr17:65028131 | CAGG | C | 2 | a0001c0001t0003g0159 a0001c0001t0003g0160 |
2 | HG02723.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.511-9831_511-9829d others(5): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65028131 | |||||||
| chr17:65028143 | G | A | 1 | a0001c0002t0004g0146 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.511-9840C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65028143 | |||||||
| chr17:65028407 | C | CA | 13 | a0001c0001t0001g0021 a0001c0001t0001g0043 a0001c0001t0001g0060 others(10): Show |
13 | HG00735.hp2 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.511-10105dupT | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65028407 | |||||||
| chr17:65028407 | CA | C | 12 | a0001c0001t0001g0034 a0001c0001t0003g0159 a0001c0001t0003g0160 others(9): Show |
12 | HG01891.hp2 HG02055.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.511-10105delT | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65028407 | |||||||
| chr17:65028424 | A | T | 1 | a0001c0001t0001g0125 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.511-10121T>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65028424 | |||||||
| chr17:65028426 | A | T | 21 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0038 others(18): Show |
21 | HG01069.hp2 HG01071.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.511-10123T>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65028426 | |||||||
| chr17:65028456 | G | GA | 8 | a0001c0001t0003g0160 a0001c0001t0008g0148 a0001c0001t0008g0149 others(5): Show |
8 | HG01069.hp2 HG01071.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.511-10154dupT | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65028456 | |||||||
| chr17:65028487 | T | G | 4 | a0001c0001t0009g0154 a0001c0001t0009g0155 a0001c0001t0016g0124 others(1): Show |
4 | HG00639.hp2 HG02965.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.511-10184A>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65028487 | |||||||
| chr17:65028495 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.511-10192G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65028495 | |||||||
| chr17:65028654 | G | C | 1 | a0001c0001t0010g0123 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.511-10351C>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65028654 | |||||||
| chr17:65028678 | T | C | 9 | a0001c0001t0005g0031 a0001c0001t0005g0033 a0001c0001t0005g0114 others(6): Show |
9 | HG01891.hp2 HG02055.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.511-10375A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65028678 | |||||||
| chr17:65028825 | C | T | 8 | a0001c0001t0005g0031 a0001c0001t0005g0114 a0001c0001t0005g0116 others(5): Show |
8 | HG01891.hp2 HG02055.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.511-10522G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65028825 | |||||||
| chr17:65029088 | T | C | 1 | a0001c0009t0001g0164 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.511-10785A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65029088 | |||||||
| chr17:65029125 | C | T | 1 | a0001c0007t0007g0171 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.511-10822G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65029125 | |||||||
| chr17:65029139 | A | G | 1 | a0001c0001t0010g0123 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.511-10836T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65029139 | |||||||
| chr17:65029623 | G | GT | 117 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(114): Show |
118 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(115): Show |
intron_variant | MODIFIER | c.511-11321dupA | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65029623 | |||||||
| chr17:65029844 | C | T | 2 | a0001c0001t0002g0014 a0001c0001t0002g0016 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.511-11541G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65029844 | |||||||
| chr17:65029915 | T | C | 1 | a0001c0001t0001g0061 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.511-11612A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65029915 | |||||||
| chr17:65030023 | A | T | 9 | a0001c0001t0005g0031 a0001c0001t0005g0033 a0001c0001t0005g0114 others(6): Show |
9 | HG01891.hp2 HG02055.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.511-11720T>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65030023 | |||||||
| chr17:65030046 | G | A | 1 | a0001c0001t0005g0033 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.511-11743C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65030046 | |||||||
| chr17:65030131 | A | G | 1 | a0001c0001t0003g0160 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.511-11828T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65030131 | |||||||
| chr17:65030182 | T | C | 2 | a0001c0004t0002g0017 a0001c0004t0002g0018 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.511-11879A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65030182 | |||||||
| chr17:65030615 | C | T | 3 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0020g0097 |
3 | HG02258.hp1 HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.511-12312G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65030615 | |||||||
| chr17:65030986 | T | G | 1 | a0001c0001t0001g0063 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.511-12683A>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65030986 | |||||||
| chr17:65031092 | A | G | 1 | a0001c0001t0001g0029 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.511-12789T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031092 | |||||||
| chr17:65031114 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.511-12811A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031114 | |||||||
| chr17:65031253 | C | T | 14 | a0001c0001t0003g0001 a0001c0001t0003g0126 a0001c0001t0003g0127 others(11): Show |
16 | HG01099.hp1 HG01884.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.511-12950G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031253 | |||||||
| chr17:65031293 | A | T | 4 | a0001c0001t0008g0148 a0001c0001t0008g0149 a0001c0001t0008g0150 others(1): Show |
4 | HG01069.hp2 HG01071.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.511-12990T>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031293 | |||||||
| chr17:65031361 | G | A | 15 | a0001c0001t0001g0125 a0001c0001t0001g0153 a0001c0001t0007g0170 others(12): Show |
15 | HG01069.hp2 HG01071.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.511-13058C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031361 | |||||||
| chr17:65031819 | T | C | 1 | a0001c0001t0014g0062 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.511-13516A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031819 | |||||||
| chr17:65031866 | TAG | T | 14 | a0001c0001t0003g0001 a0001c0001t0003g0126 a0001c0001t0003g0127 others(11): Show |
16 | HG01099.hp1 HG01884.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.511-13565_511-1356 others(6): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031866 | |||||||
| chr17:65031866 | TAGAG | T | 8 | a0001c0002t0004g0137 a0001c0002t0004g0139 a0001c0002t0004g0141 others(5): Show |
8 | HG01346.hp2 HG02109.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.511-13567_511-1356 others(8): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031866 | |||||||
| chr17:65031880 | G | GAGAGAGA others(6): Show |
1 | a0001c0001t0002g0013 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.511-13590_511-1357 others(17): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031880 | |||||||
| chr17:65031886 | G | A | 8 | a0001c0001t0005g0031 a0001c0001t0005g0116 a0001c0001t0005g0117 others(5): Show |
8 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.511-13583C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031886 | |||||||
| chr17:65031886 | G | GAGAGAGA others(1): Show |
2 | a0001c0001t0001g0046 a0001c0001t0001g0067 |
2 | HG03516.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.511-13584_511-1358 others(12): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031886 | |||||||
| chr17:65031888 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.511-13585C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031888 | |||||||
| chr17:65031888 | G | GAGAGAA | 15 | a0001c0001t0001g0021 a0001c0001t0001g0036 a0001c0001t0001g0048 others(12): Show |
15 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.511-13586_511-1358 others(10): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031888 | |||||||
| chr17:65031890 | G | A | 2 | a0001c0001t0001g0096 a0001c0001t0001g0098 |
2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.511-13587C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031890 | |||||||
| chr17:65031890 | G | GAGAA | 47 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0023 others(44): Show |
48 | HG00735.hp1 HG00738.hp1 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.511-13588_511-1358 others(8): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031890 | |||||||
| chr17:65031890 | GAGAGAA | G | 2 | a0001c0002t0004g0162 a0001c0002t0004g0163 |
2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.511-13593_511-1358 others(10): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031890 | |||||||
| chr17:65031892 | G | A | 1 | a0001c0002t0004g0144 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.511-13589C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031892 | |||||||
| chr17:65031892 | G | GAA | 9 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0060 others(6): Show |
9 | HG01993.hp1 HG02258.hp2 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.511-13590_511-1358 others(6): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031892 | |||||||
| chr17:65031892 | GAGAA | G | 2 | a0001c0001t0001g0096 a0001c0001t0001g0098 |
2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.511-13593_511-1359 others(8): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031892 | |||||||
| chr17:65031894 | G | A | 26 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(23): Show |
26 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.511-13591C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031894 | |||||||
| chr17:65031894 | GAA | G | 5 | a0001c0001t0001g0020 a0001c0001t0013g0156 a0001c0001t0013g0157 others(2): Show |
5 | HG01109.hp1 HG01891.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.511-13593_511-1359 others(6): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031894 | |||||||
| chr17:65031896 | A | G | 125 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0022 others(122): Show |
126 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(123): Show |
intron_variant | MODIFIER | c.511-13593T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031896 | |||||||
| chr17:65031898 | G | A | 2 | a0001c0002t0004g0162 a0001c0002t0004g0163 |
2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.511-13595C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031898 | |||||||
| chr17:65031900 | G | A | 1 | a0001c0005t0009g0140 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.511-13597C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031900 | |||||||
| chr17:65031902 | G | A | 6 | a0001c0001t0007g0170 a0001c0001t0007g0172 a0001c0001t0007g0173 others(3): Show |
6 | HG01891.hp1 HG02257.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.511-13599C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031902 | |||||||
| chr17:65031904 | G | A | 1 | a0001c0007t0007g0171 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.511-13601C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031904 | |||||||
| chr17:65031913 | A | T | 1 | a0001c0001t0002g0011 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.511-13610T>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031913 | |||||||
| chr17:65031915 | A | T | 1 | a0001c0001t0002g0011 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.511-13612T>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031915 | |||||||
| chr17:65031917 | A | T | 1 | a0001c0001t0002g0011 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.511-13614T>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031917 | |||||||
| chr17:65031917 | AGAGAGTG others(9): Show |
A | 1 | a0001c0001t0005g0114 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.511-13630_511-1361 others(20): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031917 | |||||||
| chr17:65031919 | A | T | 7 | a0001c0001t0002g0011 a0001c0001t0015g0138 a0001c0002t0004g0139 others(4): Show |
7 | HG01123.hp2 HG02109.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.511-13616T>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031919 | |||||||
| chr17:65031919 | AGAGT | A | 4 | a0001c0001t0001g0153 a0001c0002t0004g0137 a0001c0002t0004g0141 others(1): Show |
4 | HG01346.hp2 HG02622.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.511-13620_511-1361 others(8): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031919 | |||||||
| chr17:65031919 | AGAGTGTG others(1): Show |
A | 6 | a0001c0001t0008g0148 a0001c0001t0008g0149 a0001c0001t0008g0150 others(3): Show |
6 | HG01069.hp2 HG01071.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.511-13624_511-1361 others(12): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031919 | |||||||
| chr17:65031919 | AGAGTGTG others(7): Show |
A | 5 | a0001c0001t0005g0116 a0001c0001t0005g0117 a0001c0001t0005g0119 others(2): Show |
5 | HG01891.hp2 HG02280.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.511-13630_511-1361 others(18): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031919 | |||||||
| chr17:65031919 | AGAGTGTG others(11): Show |
A | 14 | a0001c0001t0003g0001 a0001c0001t0003g0126 a0001c0001t0003g0127 others(11): Show |
16 | HG01099.hp1 HG01884.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.511-13634_511-1361 others(22): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031919 | |||||||
| chr17:65031921 | A | AGAGAGAG others(11): Show |
1 | a0001c0004t0002g0017 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.511-13619_511-1361 others(22): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031921 | |||||||
| chr17:65031921 | A | AGAGAGAG others(13): Show |
1 | a0001c0004t0002g0018 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.511-13619_511-1361 others(24): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031921 | |||||||
| chr17:65031921 | A | AGAGAGAG others(15): Show |
1 | a0001c0001t0002g0005 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.511-13619_511-1361 others(26): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031921 | |||||||
| chr17:65031921 | A | AGAGAGAG others(9): Show |
1 | a0001c0001t0001g0066 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.511-13619_511-1361 others(20): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031921 | |||||||
| chr17:65031921 | A | AGAGAGAG others(11): Show |
2 | a0001c0001t0002g0007 a0001c0001t0002g0015 |
2 | HG02257.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.511-13619_511-1361 others(22): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031921 | |||||||
| chr17:65031921 | A | AGAGAGAG others(13): Show |
1 | a0001c0001t0002g0008 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.511-13619_511-1361 others(24): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031921 | |||||||
| chr17:65031921 | A | AGAGAGAG others(3): Show |
1 | a0001c0001t0001g0024 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.511-13619_511-1361 others(14): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031921 | |||||||
| chr17:65031921 | A | AGAGAGTG others(1): Show |
3 | a0001c0001t0001g0025 a0001c0001t0001g0080 a0001c0001t0001g0086 |
3 | HG01884.hp2 HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.511-13619_511-1361 others(12): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031921 | |||||||
| chr17:65031921 | A | AGAGAGTG others(5): Show |
1 | a0001c0001t0001g0032 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-13619_511-1361 others(16): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031921 | |||||||
| chr17:65031921 | A | AGAGAGTG others(7): Show |
1 | a0001c0001t0002g0012 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.511-13619_511-1361 others(18): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031921 | |||||||
| chr17:65031921 | A | AGAGTGT | 2 | a0001c0001t0001g0057 a0001c0001t0012g0087 |
2 | HG01258.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.511-13619_511-1361 others(10): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031921 | |||||||
| chr17:65031921 | A | AGAGTGTG others(5): Show |
1 | a0001c0001t0002g0006 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.511-13619_511-1361 others(16): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031921 | |||||||
| chr17:65031921 | A | AGAGTGTG others(7): Show |
1 | a0001c0001t0010g0123 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.511-13619_511-1361 others(18): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031921 | |||||||
| chr17:65031921 | A | AGAGTGTG others(9): Show |
1 | a0001c0001t0010g0122 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.511-13619_511-1361 others(20): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031921 | |||||||
| chr17:65031921 | A | AGTGTGT | 2 | a0001c0001t0001g0106 a0001c0001t0002g0013 |
2 | HG01255.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.511-13624_511-1361 others(10): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031921 | |||||||
| chr17:65031921 | A | AGTGTGTG others(1): Show |
3 | a0001c0001t0002g0014 a0001c0001t0002g0016 a0001c0001t0010g0121 |
3 | HG02965.hp2 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.511-13626_511-1361 others(12): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031921 | |||||||
| chr17:65031921 | A | AGTGTGTG others(3): Show |
1 | a0001c0001t0002g0010 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.511-13628_511-1361 others(14): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031921 | |||||||
| chr17:65031921 | A | T | 20 | a0001c0001t0001g0046 a0001c0001t0001g0056 a0001c0001t0001g0058 others(17): Show |
20 | HG00099.hp2 HG01123.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.511-13618T>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031921 | |||||||
| chr17:65031921 | AGTGT | A | 2 | a0001c0003t0001g0113 a0001c0009t0001g0164 |
2 | HG01433.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.511-13622_511-1361 others(8): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031921 | |||||||
| chr17:65031921 | AGTGTGT | A | 5 | a0001c0001t0007g0170 a0001c0001t0007g0172 a0001c0001t0007g0173 others(2): Show |
5 | HG00639.hp1 HG02257.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.511-13624_511-1361 others(10): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031921 | |||||||
| chr17:65031921 | AGTGTGTG others(5): Show |
A | 2 | a0001c0001t0005g0031 a0001c0001t0005g0118 |
2 | HG02451.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.511-13630_511-1361 others(16): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031921 | |||||||
| chr17:65031921 | AGTGTGTG others(11): Show |
A | 4 | a0001c0001t0009g0154 a0001c0001t0009g0155 a0001c0001t0016g0124 others(1): Show |
4 | HG00639.hp2 HG02965.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.511-13636_511-1361 others(22): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031921 | |||||||
| chr17:65031923 | T | A | 25 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0035 others(22): Show |
25 | HG00099.hp1 HG01109.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.511-13620A>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031923 | |||||||
| chr17:65031925 | T | A | 8 | a0001c0001t0001g0027 a0001c0001t0001g0035 a0001c0001t0001g0047 others(5): Show |
8 | HG01169.hp1 HG01993.hp1 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.511-13622A>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031925 | |||||||
| chr17:65031927 | T | A | 2 | a0001c0003t0001g0111 a0001c0003t0001g0113 |
2 | HG01433.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.511-13624A>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031927 | |||||||
| chr17:65031929 | T | A | 3 | a0001c0003t0001g0111 a0001c0003t0001g0112 a0001c0003t0001g0113 |
3 | HG00639.hp1 HG01433.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.511-13626A>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031929 | |||||||
| chr17:65031931 | T | A | 2 | a0001c0003t0001g0111 a0001c0003t0001g0112 |
2 | HG00639.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.511-13628A>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031931 | |||||||
| chr17:65031944 | G | A | 1 | a0001c0001t0007g0173 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.511-13641C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65031944 | |||||||
| chr17:65032333 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.511-14030T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65032333 | |||||||
| chr17:65032539 | C | T | 2 | a0001c0001t0001g0052 a0001c0001t0001g0088 |
2 | NA18944.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.511-14236G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65032539 | |||||||
| chr17:65032721 | G | T | 11 | a0001c0002t0004g0137 a0001c0002t0004g0139 a0001c0002t0004g0141 others(8): Show |
11 | HG01346.hp2 HG02109.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.511-14418C>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65032721 | |||||||
| chr17:65032730 | C | A | 171 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(168): Show |
174 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(171): Show |
intron_variant | MODIFIER | c.511-14427G>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65032730 | |||||||
| chr17:65032810 | GA | G | 162 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(159): Show |
165 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(162): Show |
intron_variant | MODIFIER | c.511-14508delT | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65032810 | |||||||
| chr17:65032838 | C | T | 18 | a0001c0001t0003g0001 a0001c0001t0003g0126 a0001c0001t0003g0127 others(15): Show |
20 | HG00639.hp2 HG01099.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.511-14535G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65032838 | |||||||
| chr17:65033057 | G | T | 2 | a0001c0001t0010g0121 a0001c0001t0010g0122 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.511-14754C>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65033057 | |||||||
| chr17:65033319 | TA | T | 26 | a0001c0001t0001g0125 a0001c0001t0001g0153 a0001c0001t0007g0170 others(23): Show |
26 | HG01069.hp2 HG01071.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.511-15017delT | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65033319 | |||||||
| chr17:65033400 | T | C | 1 | a0001c0001t0001g0082 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.511-15097A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65033400 | |||||||
| chr17:65033415 | T | C | 11 | a0001c0002t0004g0137 a0001c0002t0004g0139 a0001c0002t0004g0141 others(8): Show |
11 | HG01346.hp2 HG02109.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.511-15112A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65033415 | |||||||
| chr17:65033437 | T | G | 1 | a0001c0001t0015g0138 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.511-15134A>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65033437 | |||||||
| chr17:65033569 | A | G | 5 | a0001c0001t0007g0170 a0001c0001t0007g0172 a0001c0001t0007g0173 others(2): Show |
5 | HG01109.hp1 HG02257.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.511-15266T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65033569 | |||||||
| chr17:65033737 | G | A | 2 | a0001c0001t0009g0154 a0001c0001t0009g0155 |
2 | HG00639.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.511-15434C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65033737 | |||||||
| chr17:65034012 | C | CA | 8 | a0001c0001t0001g0153 a0001c0001t0003g0127 a0001c0001t0003g0128 others(5): Show |
8 | HG01069.hp2 HG01071.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.511-15710dupT | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65034012 | |||||||
| chr17:65034012 | C | CAA | 10 | a0001c0001t0001g0037 a0001c0001t0001g0059 a0001c0001t0001g0060 others(7): Show |
10 | HG01099.hp1 HG01109.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.511-15711_511-1571 others(6): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65034012 | |||||||
| chr17:65034012 | C | CAAA | 42 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0029 others(39): Show |
43 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.511-15712_511-1571 others(7): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65034012 | |||||||
| chr17:65034012 | C | CAAAA | 54 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(51): Show |
54 | HG00099.hp2 HG00639.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.511-15713_511-1571 others(8): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65034012 | |||||||
| chr17:65034012 | C | CAAAAA | 21 | a0001c0001t0001g0073 a0001c0001t0001g0085 a0001c0001t0001g0089 others(18): Show |
21 | HG00099.hp1 HG00738.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.511-15714_511-1571 others(9): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65034012 | |||||||
| chr17:65034012 | C | CAAAAAA | 7 | a0001c0001t0002g0005 a0001c0001t0002g0015 a0001c0001t0005g0116 others(4): Show |
7 | HG01167.hp1 HG02055.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.511-15715_511-1571 others(10): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65034012 | |||||||
| chr17:65034254 | G | A | 1 | a0003c0008t0001g0110 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.511-15951C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65034254 | |||||||
| chr17:65034698 | C | CT | 8 | a0001c0001t0001g0125 a0001c0001t0001g0153 a0001c0001t0008g0148 others(5): Show |
8 | HG01069.hp2 HG01071.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.511-16396dupA | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65034698 | |||||||
| chr17:65034930 | C | T | 117 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(114): Show |
118 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(115): Show |
intron_variant | MODIFIER | c.511-16627G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65034930 | |||||||
| chr17:65035012 | C | T | 3 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0020g0097 |
3 | HG02258.hp1 HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.511-16709G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65035012 | |||||||
| chr17:65035421 | A | G | 1 | a0001c0001t0002g0019 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.511-17118T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65035421 | |||||||
| chr17:65035580 | A | G | 1 | a0001c0005t0009g0140 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.511-17277T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65035580 | |||||||
| chr17:65035673 | A | C | 1 | a0001c0001t0001g0057 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.511-17370T>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65035673 | |||||||
| chr17:65035716 | T | C | 41 | a0001c0001t0001g0125 a0001c0001t0001g0153 a0001c0001t0003g0001 others(38): Show |
43 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.511-17413A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65035716 | |||||||
| chr17:65035753 | T | C | 12 | a0001c0001t0005g0031 a0001c0001t0005g0033 a0001c0001t0005g0114 others(9): Show |
12 | HG01346.hp2 HG01891.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.511-17450A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65035753 | |||||||
| chr17:65035781 | A | AT | 16 | a0001c0001t0001g0076 a0001c0001t0002g0006 a0001c0001t0002g0007 others(13): Show |
16 | HG00099.hp1 HG01123.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.511-17479dupA | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65035781 | |||||||
| chr17:65035781 | AT | A | 10 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0040 others(7): Show |
11 | HG02698.hp1 HG02698.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.511-17479delA | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65035781 | |||||||
| chr17:65035813 | C | T | 171 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(168): Show |
174 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(171): Show |
intron_variant | MODIFIER | c.511-17510G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65035813 | |||||||
| chr17:65035846 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.511-17543C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65035846 | |||||||
| chr17:65035858 | C | A | 117 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(114): Show |
118 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(115): Show |
intron_variant | MODIFIER | c.511-17555G>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65035858 | |||||||
| chr17:65035913 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.510+17589C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65035913 | |||||||
| chr17:65035955 | G | A | 117 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(114): Show |
118 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(115): Show |
intron_variant | MODIFIER | c.510+17547C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65035955 | |||||||
| chr17:65036472 | A | G | 1 | a0001c0001t0001g0024 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.510+17030T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65036472 | |||||||
| chr17:65036568 | T | A | 11 | a0001c0001t0005g0031 a0001c0001t0005g0114 a0001c0001t0005g0116 others(8): Show |
11 | HG01346.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.510+16934A>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65036568 | |||||||
| chr17:65036897 | C | T | 2 | a0001c0001t0003g0159 a0001c0001t0003g0160 |
2 | HG02723.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.510+16605G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65036897 | |||||||
| chr17:65036994 | C | A | 14 | a0001c0001t0003g0001 a0001c0001t0003g0126 a0001c0001t0003g0127 others(11): Show |
16 | HG01099.hp1 HG01884.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.510+16508G>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65036994 | |||||||
| chr17:65037100 | A | G | 4 | a0001c0001t0009g0154 a0001c0001t0009g0155 a0001c0001t0016g0124 others(1): Show |
4 | HG00639.hp2 HG02965.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.510+16402T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65037100 | |||||||
| chr17:65037253 | A | G | 1 | a0001c0001t0005g0031 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.510+16249T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65037253 | |||||||
| chr17:65037596 | T | C | 100 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(97): Show |
101 | HG00099.hp2 HG00639.hp1 HG00735.hp1 others(98): Show |
intron_variant | MODIFIER | c.510+15906A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65037596 | |||||||
| chr17:65037686 | C | T | 1 | a0001c0001t0023g0129 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.510+15816G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65037686 | |||||||
| chr17:65037729 | C | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | NA18957.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.510+15773G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65037729 | |||||||
| chr17:65037777 | G | GAA | 3 | a0001c0001t0005g0033 a0001c0001t0016g0124 a0001c0005t0009g0140 |
3 | HG02886.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.510+15724_510+1572 others(6): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65037777 | |||||||
| chr17:65037777 | G | GAAA | 27 | a0001c0001t0001g0153 a0001c0001t0002g0005 a0001c0001t0002g0007 others(24): Show |
27 | HG00099.hp1 HG00639.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.510+15724_510+1572 others(7): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65037777 | |||||||
| chr17:65037777 | G | GAAAA | 23 | a0001c0001t0001g0022 a0001c0001t0001g0036 a0001c0001t0001g0060 others(20): Show |
23 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.510+15724_510+1572 others(8): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65037777 | |||||||
| chr17:65037777 | G | GAAAAA | 86 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0023 others(83): Show |
89 | HG00099.hp2 HG00639.hp1 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.510+15724_510+1572 others(9): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65037777 | |||||||
| chr17:65037777 | G | GAAAAAA | 18 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0035 others(15): Show |
18 | HG00735.hp2 HG01071.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.510+15724_510+1572 others(10): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65037777 | |||||||
| chr17:65037777 | G | GAAAAAAA | 3 | a0001c0001t0001g0044 a0001c0001t0001g0058 a0001c0001t0001g0084 |
3 | HG01243.hp2 HG01496.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.510+15724_510+1572 others(11): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65037777 | |||||||
| chr17:65037777 | G | GAGAAA | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG01346.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.510+15724_510+1572 others(9): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65037777 | |||||||
| chr17:65037778 | G | A | 163 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(160): Show |
166 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(163): Show |
intron_variant | MODIFIER | c.510+15724C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65037778 | |||||||
| chr17:65037778 | G | GAAA | 5 | a0001c0002t0004g0143 a0001c0002t0004g0144 a0001c0002t0004g0145 others(2): Show |
5 | HG02109.hp2 HG02922.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.510+15721_510+1572 others(7): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65037778 | |||||||
| chr17:65037854 | G | A | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG01346.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.510+15648C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65037854 | |||||||
| chr17:65037880 | T | C | 4 | a0001c0001t0003g0159 a0001c0001t0003g0160 a0001c0001t0010g0121 others(1): Show |
4 | HG02723.hp2 HG02896.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+15622A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65037880 | |||||||
| chr17:65037967 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.510+15535T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65037967 | |||||||
| chr17:65038127 | G | A | 1 | a0001c0001t0011g0166 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.510+15375C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65038127 | |||||||
| chr17:65038154 | C | T | 1 | a0001c0001t0005g0033 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.510+15348G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65038154 | |||||||
| chr17:65038260 | G | A | 117 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(114): Show |
118 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(115): Show |
intron_variant | MODIFIER | c.510+15242C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65038260 | |||||||
| chr17:65038402 | CA | C | 20 | a0001c0001t0003g0001 a0001c0001t0003g0126 a0001c0001t0003g0127 others(17): Show |
22 | HG00639.hp2 HG01099.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.510+15099delT | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65038402 | |||||||
| chr17:65038402 | CAA | C | 27 | a0001c0001t0001g0058 a0001c0001t0001g0125 a0001c0001t0001g0153 others(24): Show |
27 | HG01069.hp2 HG01071.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.510+15098_510+1509 others(6): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65038402 | |||||||
| chr17:65038402 | CAAA | C | 124 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(121): Show |
125 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(122): Show |
intron_variant | MODIFIER | c.510+15097_510+1509 others(7): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65038402 | |||||||
| chr17:65038482 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.510+15020C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65038482 | |||||||
| chr17:65038564 | T | C | 171 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(168): Show |
174 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(171): Show |
intron_variant | MODIFIER | c.510+14938A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65038564 | |||||||
| chr17:65038672 | C | T | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | HG01243.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.510+14830G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65038672 | |||||||
| chr17:65038972 | C | T | 1 | a0001c0005t0009g0140 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.510+14530G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65038972 | |||||||
| chr17:65039136 | G | A | 100 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(97): Show |
101 | HG00099.hp2 HG00639.hp1 HG00735.hp1 others(98): Show |
intron_variant | MODIFIER | c.510+14366C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65039136 | |||||||
| chr17:65039216 | C | G | 1 | a0001c0001t0016g0124 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.510+14286G>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65039216 | |||||||
| chr17:65039277 | C | T | 45 | a0001c0001t0001g0125 a0001c0001t0001g0153 a0001c0001t0003g0001 others(42): Show |
47 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.510+14225G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65039277 | |||||||
| chr17:65039502 | C | G | 1 | a0001c0001t0015g0138 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.510+14000G>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65039502 | |||||||
| chr17:65039597 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.510+13905A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65039597 | |||||||
| chr17:65039845 | G | C | 1 | a0001c0001t0001g0020 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.510+13657C>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65039845 | |||||||
| chr17:65040038 | T | C | 1 | a0001c0009t0001g0164 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.510+13464A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65040038 | |||||||
| chr17:65040108 | C | T | 2 | a0001c0001t0001g0056 a0001c0001t0021g0093 |
2 | NA18971.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.510+13394G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65040108 | |||||||
| chr17:65040126 | A | G | 9 | a0001c0002t0004g0137 a0001c0002t0004g0139 a0001c0002t0004g0141 others(6): Show |
9 | HG01346.hp2 HG02109.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.510+13376T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65040126 | |||||||
| chr17:65040246 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.510+13256T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65040246 | |||||||
| chr17:65040472 | T | C | 162 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(159): Show |
165 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(162): Show |
intron_variant | MODIFIER | c.510+13030A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65040472 | |||||||
| chr17:65040793 | T | C | 8 | a0001c0001t0005g0031 a0001c0001t0005g0114 a0001c0001t0005g0116 others(5): Show |
8 | HG01891.hp2 HG02055.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.510+12709A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65040793 | |||||||
| chr17:65040929 | A | G | 11 | a0001c0002t0004g0137 a0001c0002t0004g0139 a0001c0002t0004g0141 others(8): Show |
11 | HG01346.hp2 HG02109.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.510+12573T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65040929 | |||||||
| chr17:65040952 | C | T | 3 | a0001c0001t0005g0116 a0001c0001t0005g0117 a0001c0001t0022g0115 |
3 | HG01891.hp2 HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.510+12550G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65040952 | |||||||
| chr17:65041025 | G | A | 1 | a0001c0001t0017g0158 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.510+12477C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65041025 | |||||||
| chr17:65041065 | CTA | C | 3 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0020g0097 |
3 | HG02258.hp1 HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.510+12435_510+1243 others(6): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65041065 | |||||||
| chr17:65041110 | T | C | 1 | a0001c0001t0003g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.510+12392A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65041110 | |||||||
| chr17:65041370 | CTTT | C | 14 | a0001c0001t0003g0001 a0001c0001t0003g0126 a0001c0001t0003g0127 others(11): Show |
16 | HG01099.hp1 HG01884.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.510+12129_510+1213 others(7): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65041370 | |||||||
| chr17:65041432 | T | C | 1 | a0001c0001t0001g0085 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.510+12070A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65041432 | |||||||
| chr17:65041510 | A | T | 35 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(32): Show |
35 | HG00738.hp2 HG01099.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.510+11992T>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65041510 | |||||||
| chr17:65041920 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.510+11582A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65041920 | |||||||
| chr17:65041930 | T | C | 11 | a0001c0002t0004g0137 a0001c0002t0004g0139 a0001c0002t0004g0141 others(8): Show |
11 | HG01346.hp2 HG02109.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.510+11572A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65041930 | |||||||
| chr17:65041941 | A | C | 1 | a0001c0001t0008g0150 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.510+11561T>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65041941 | |||||||
| chr17:65042068 | T | C | 6 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0038 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+11434A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65042068 | |||||||
| chr17:65042086 | C | T | 1 | a0001c0001t0001g0023 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.510+11416G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65042086 | |||||||
| chr17:65042109 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.510+11393G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65042109 | |||||||
| chr17:65042110 | G | A | 3 | a0001c0003t0001g0111 a0001c0003t0001g0112 a0001c0003t0001g0113 |
3 | HG00639.hp1 HG01433.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.510+11392C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65042110 | |||||||
| chr17:65042198 | A | G | 2 | a0001c0001t0003g0159 a0001c0001t0003g0160 |
2 | HG02723.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.510+11304T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65042198 | |||||||
| chr17:65042287 | G | A | 19 | a0001c0001t0001g0109 a0001c0001t0003g0001 a0001c0001t0003g0126 others(16): Show |
21 | HG00639.hp2 HG01099.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.510+11215C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65042287 | |||||||
| chr17:65042295 | T | C | 1 | a0001c0001t0003g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.510+11207A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65042295 | |||||||
| chr17:65042357 | C | CA | 6 | a0001c0001t0001g0027 a0001c0001t0001g0100 a0001c0001t0009g0154 others(3): Show |
6 | HG00639.hp2 HG00738.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+11144dupT | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65042357 | |||||||
| chr17:65042357 | CA | C | 19 | a0001c0001t0001g0035 a0001c0001t0001g0125 a0001c0001t0001g0153 others(16): Show |
19 | HG01069.hp2 HG01071.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.510+11144delT | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65042357 | |||||||
| chr17:65042465 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.510+11037C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65042465 | |||||||
| chr17:65042512 | A | G | 171 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(168): Show |
174 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(171): Show |
intron_variant | MODIFIER | c.510+10990T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65042512 | |||||||
| chr17:65042726 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.510+10776C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65042726 | |||||||
| chr17:65043063 | T | C | 1 | a0001c0001t0015g0138 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.510+10439A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65043063 | |||||||
| chr17:65043153 | G | A | 6 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0038 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+10349C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65043153 | |||||||
| chr17:65043255 | A | G | 46 | a0001c0001t0001g0109 a0001c0001t0001g0125 a0001c0001t0001g0153 others(43): Show |
48 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.510+10247T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65043255 | |||||||
| chr17:65043291 | AT | A | 158 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(155): Show |
161 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(158): Show |
intron_variant | MODIFIER | c.510+10210delA | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65043291 | |||||||
| chr17:65043375 | C | A | 1 | a0001c0001t0009g0155 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.510+10127G>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65043375 | |||||||
| chr17:65043672 | T | C | 1 | a0001c0001t0001g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.510+9830A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65043672 | |||||||
| chr17:65043719 | T | C | 1 | a0001c0001t0012g0087 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.510+9783A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65043719 | |||||||
| chr17:65043744 | C | A | 159 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(156): Show |
162 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(159): Show |
intron_variant | MODIFIER | c.510+9758G>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65043744 | |||||||
| chr17:65043879 | C | T | 99 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(96): Show |
100 | HG00099.hp2 HG00639.hp1 HG00735.hp1 others(97): Show |
intron_variant | MODIFIER | c.510+9623G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65043879 | |||||||
| chr17:65044407 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.510+9095C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65044407 | |||||||
| chr17:65044667 | C | T | 2 | a0001c0001t0003g0159 a0001c0001t0003g0160 |
2 | HG02723.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.510+8835G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65044667 | |||||||
| chr17:65044689 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.510+8813C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65044689 | |||||||
| chr17:65044824 | C | T | 7 | a0001c0001t0001g0125 a0001c0001t0001g0153 a0001c0001t0008g0148 others(4): Show |
7 | HG01069.hp2 HG01071.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.510+8678G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65044824 | |||||||
| chr17:65044967 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.510+8535A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65044967 | |||||||
| chr17:65045238 | AGC | A | 17 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(14): Show |
17 | HG00099.hp1 HG01123.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.510+8262_510+8263d others(4): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65045238 | |||||||
| chr17:65045318 | G | A | 45 | a0001c0001t0001g0125 a0001c0001t0001g0153 a0001c0001t0003g0001 others(42): Show |
47 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.510+8184C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65045318 | |||||||
| chr17:65045355 | A | G | 2 | a0001c0001t0001g0029 a0001c0001t0001g0030 |
2 | HG00735.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.510+8147T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65045355 | |||||||
| chr17:65045437 | C | G | 2 | a0001c0001t0009g0154 a0001c0001t0009g0155 |
2 | HG00639.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.510+8065G>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65045437 | |||||||
| chr17:65045470 | G | T | 171 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(168): Show |
174 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(171): Show |
intron_variant | MODIFIER | c.510+8032C>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65045470 | |||||||
| chr17:65045502 | T | C | 1 | a0001c0001t0005g0033 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.510+8000A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65045502 | |||||||
| chr17:65045507 | C | CA | 114 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0022 others(111): Show |
117 | HG00099.hp2 HG00639.hp1 HG00735.hp1 others(114): Show |
intron_variant | MODIFIER | c.510+7994dupT | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65045507 | |||||||
| chr17:65045507 | C | CAA | 16 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0092 others(13): Show |
16 | HG00735.hp2 HG01496.hp1 HG02738.hp1 others(13): Show |
intron_variant | MODIFIER | c.510+7993_510+7994d others(4): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65045507 | |||||||
| chr17:65045529 | C | A | 2 | a0001c0002t0004g0162 a0001c0002t0004g0163 |
2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.510+7973G>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65045529 | |||||||
| chr17:65045973 | T | G | 1 | a0001c0001t0002g0019 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.510+7529A>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65045973 | |||||||
| chr17:65046182 | T | C | 100 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(97): Show |
101 | HG00099.hp2 HG00639.hp1 HG00735.hp1 others(98): Show |
intron_variant | MODIFIER | c.510+7320A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65046182 | |||||||
| chr17:65046257 | C | T | 17 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(14): Show |
17 | HG00099.hp1 HG01123.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.510+7245G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65046257 | |||||||
| chr17:65046315 | G | A | 45 | a0001c0001t0001g0125 a0001c0001t0001g0153 a0001c0001t0003g0001 others(42): Show |
47 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.510+7187C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65046315 | |||||||
| chr17:65046370 | A | C | 1 | a0001c0001t0016g0124 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.510+7132T>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65046370 | |||||||
| chr17:65046462 | T | A | 3 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0020g0097 |
3 | HG02258.hp1 HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.510+7040A>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65046462 | |||||||
| chr17:65046528 | G | C | 25 | a0001c0001t0003g0001 a0001c0001t0003g0126 a0001c0001t0003g0127 others(22): Show |
27 | HG01099.hp1 HG01884.hp1 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.510+6974C>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65046528 | |||||||
| chr17:65046595 | G | A | 15 | a0001c0001t0003g0001 a0001c0001t0003g0126 a0001c0001t0003g0127 others(12): Show |
17 | HG01099.hp1 HG01884.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.510+6907C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65046595 | |||||||
| chr17:65046624 | C | A | 1 | a0001c0001t0005g0033 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.510+6878G>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65046624 | |||||||
| chr17:65046689 | G | A | 14 | a0001c0001t0003g0001 a0001c0001t0003g0126 a0001c0001t0003g0127 others(11): Show |
16 | HG01099.hp1 HG01884.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.510+6813C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65046689 | |||||||
| chr17:65046725 | G | A | 171 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(168): Show |
174 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(171): Show |
intron_variant | MODIFIER | c.510+6777C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65046725 | |||||||
| chr17:65046808 | A | C | 1 | a0001c0001t0005g0033 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.510+6694T>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65046808 | |||||||
| chr17:65046857 | T | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0099 |
3 | HG02698.hp2 HG03491.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.510+6645A>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65046857 | |||||||
| chr17:65046961 | C | T | 1 | a0001c0005t0009g0140 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.510+6541G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65046961 | |||||||
| chr17:65046966 | A | G | 1 | a0001c0005t0009g0140 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.510+6536T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65046966 | |||||||
| chr17:65046967 | T | C | 1 | a0001c0001t0001g0029 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.510+6535A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65046967 | |||||||
| chr17:65046991 | C | G | 1 | a0001c0001t0023g0129 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.510+6511G>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65046991 | |||||||
| chr17:65047073 | C | T | 1 | a0001c0001t0001g0042 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.510+6429G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65047073 | |||||||
| chr17:65047109 | A | G | 6 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0038 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+6393T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65047109 | |||||||
| chr17:65047232 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.510+6270T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65047232 | |||||||
| chr17:65047421 | C | A | 1 | a0001c0001t0005g0114 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.510+6081G>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65047421 | |||||||
| chr17:65047661 | C | CT | 100 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(97): Show |
101 | HG00099.hp2 HG00639.hp1 HG00735.hp1 others(98): Show |
intron_variant | MODIFIER | c.510+5840dupA | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65047661 | |||||||
| chr17:65047661 | CT | C | 17 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(14): Show |
17 | HG00099.hp1 HG01123.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.510+5840delA | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65047661 | |||||||
| chr17:65047685 | G | C | 3 | a0001c0001t0013g0156 a0001c0001t0013g0157 a0001c0001t0017g0158 |
3 | HG01891.hp1 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.510+5817C>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65047685 | |||||||
| chr17:65047742 | C | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0036 |
2 | HG00735.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.510+5760G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65047742 | |||||||
| chr17:65048189 | G | A | 1 | a0001c0002t0004g0147 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.510+5313C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65048189 | |||||||
| chr17:65048321 | C | CCCATCTC others(283): Show |
1 | a0001c0001t0015g0138 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.510+5180_510+5181i others(292): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65048321 | |||||||
| chr17:65048392 | G | T | 1 | a0001c0001t0016g0124 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.510+5110C>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65048392 | |||||||
| chr17:65048742 | T | C | 2 | a0001c0001t0009g0154 a0001c0001t0009g0155 |
2 | HG00639.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.510+4760A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65048742 | |||||||
| chr17:65048838 | G | A | 1 | a0001c0001t0005g0033 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.510+4664C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65048838 | |||||||
| chr17:65049322 | T | C | 8 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(5): Show |
8 | HG00099.hp2 HG00639.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.510+4180A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65049322 | |||||||
| chr17:65049611 | A | G | 2 | a0001c0001t0010g0121 a0001c0001t0010g0122 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.510+3891T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65049611 | |||||||
| chr17:65049619 | C | T | 99 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(96): Show |
100 | HG00099.hp2 HG00639.hp1 HG00735.hp1 others(97): Show |
intron_variant | MODIFIER | c.510+3883G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65049619 | |||||||
| chr17:65049649 | G | C | 3 | a0001c0001t0013g0156 a0001c0001t0013g0157 a0001c0001t0017g0158 |
3 | HG01891.hp1 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.510+3853C>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65049649 | |||||||
| chr17:65049709 | G | A | 1 | a0001c0005t0009g0140 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.510+3793C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65049709 | |||||||
| chr17:65049958 | T | C | 111 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(108): Show |
112 | HG00099.hp2 HG00639.hp1 HG00735.hp1 others(109): Show |
intron_variant | MODIFIER | c.510+3544A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65049958 | |||||||
| chr17:65050025 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.510+3477G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65050025 | |||||||
| chr17:65050123 | A | G | 6 | a0001c0001t0001g0125 a0001c0001t0008g0148 a0001c0001t0008g0149 others(3): Show |
6 | HG01069.hp2 HG01071.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+3379T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65050123 | |||||||
| chr17:65050205 | G | T | 1 | a0001c0001t0001g0034 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.510+3297C>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65050205 | |||||||
| chr17:65050401 | T | G | 18 | a0001c0001t0001g0125 a0001c0001t0001g0153 a0001c0001t0005g0033 others(15): Show |
18 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.510+3101A>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65050401 | |||||||
| chr17:65050417 | CTA | C | 99 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(96): Show |
100 | HG00099.hp2 HG00639.hp1 HG00735.hp1 others(97): Show |
intron_variant | MODIFIER | c.510+3083_510+3084d others(4): Show |
GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65050417 | |||||||
| chr17:65050690 | C | T | 17 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(14): Show |
17 | HG00099.hp1 HG01123.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.510+2812G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65050690 | |||||||
| chr17:65050759 | T | C | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | NA18957.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.510+2743A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65050759 | |||||||
| chr17:65050817 | C | A | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG02735.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.510+2685G>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65050817 | |||||||
| chr17:65050941 | C | G | 6 | a0001c0001t0003g0001 a0001c0001t0003g0126 a0001c0001t0003g0127 others(3): Show |
8 | HG01099.hp1 HG02895.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.510+2561G>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65050941 | |||||||
| chr17:65051240 | A | C | 3 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0008 |
3 | HG02055.hp2 HG02257.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.510+2262T>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65051240 | |||||||
| chr17:65051353 | T | C | 171 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(168): Show |
174 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(171): Show |
intron_variant | MODIFIER | c.510+2149A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65051353 | |||||||
| chr17:65051375 | G | A | 2 | a0001c0002t0004g0137 a0001c0002t0004g0142 |
2 | HG01346.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.510+2127C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65051375 | |||||||
| chr17:65051483 | C | T | 11 | a0001c0001t0005g0031 a0001c0001t0005g0114 a0001c0001t0005g0116 others(8): Show |
11 | HG01346.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.510+2019G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65051483 | |||||||
| chr17:65051494 | A | T | 2 | a0001c0001t0009g0154 a0001c0001t0009g0155 |
2 | HG00639.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.510+2008T>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65051494 | |||||||
| chr17:65051521 | A | G | 1 | a0001c0001t0005g0033 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.510+1981T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65051521 | |||||||
| chr17:65051747 | A | G | 11 | a0001c0001t0005g0031 a0001c0001t0005g0114 a0001c0001t0005g0116 others(8): Show |
11 | HG01346.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.510+1755T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65051747 | |||||||
| chr17:65051811 | G | T | 170 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(167): Show |
173 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(170): Show |
intron_variant | MODIFIER | c.510+1691C>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65051811 | |||||||
| chr17:65051824 | T | C | 8 | a0001c0001t0007g0170 a0001c0001t0007g0172 a0001c0001t0007g0173 others(5): Show |
8 | HG01109.hp1 HG01891.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.510+1678A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65051824 | |||||||
| chr17:65051891 | T | C | 17 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(14): Show |
17 | HG00099.hp1 HG01123.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.510+1611A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65051891 | |||||||
| chr17:65052168 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.510+1334A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65052168 | |||||||
| chr17:65052188 | T | C | 1 | a0001c0001t0001g0030 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.510+1314A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65052188 | |||||||
| chr17:65053059 | G | T | 1 | a0001c0001t0001g0032 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.510+443C>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65053059 | |||||||
| chr17:65053334 | A | G | 118 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(115): Show |
119 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(116): Show |
intron_variant | MODIFIER | c.510+168T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65053334 | |||||||
| chr17:65053385 | A | G | 17 | a0001c0001t0001g0125 a0001c0001t0001g0153 a0001c0001t0007g0170 others(14): Show |
17 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.510+117T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 2/3 | chr17 | 65053385 | |||||||
| chr17:65053890 | T | TA | 10 | a0001c0001t0007g0170 a0001c0001t0007g0172 a0001c0001t0007g0173 others(7): Show |
10 | HG00639.hp2 HG01109.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.284-163dupT | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 1/3 | chr17 | 65053890 | |||||||
| chr17:65054218 | T | C | 1 | a0001c0001t0003g0160 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.284-490A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 1/3 | chr17 | 65054218 | |||||||
| chr17:65054609 | C | A | 1 | a0001c0001t0005g0031 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.284-881G>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 1/3 | chr17 | 65054609 | |||||||
| chr17:65054756 | G | A | 159 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(156): Show |
162 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(159): Show |
intron_variant | MODIFIER | c.284-1028C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 1/3 | chr17 | 65054756 | |||||||
| chr17:65055072 | C | CG | 26 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(23): Show |
27 | HG00735.hp1 HG00735.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.283+1238dupC | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 1/3 | chr17 | 65055072 | |||||||
| chr17:65055107 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.283+1204G>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 1/3 | chr17 | 65055107 | |||||||
| chr17:65055234 | T | C | 17 | a0001c0001t0001g0125 a0001c0001t0001g0153 a0001c0001t0007g0170 others(14): Show |
17 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.283+1077A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 1/3 | chr17 | 65055234 | |||||||
| chr17:65055419 | A | T | 1 | a0001c0001t0005g0114 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.283+892T>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 1/3 | chr17 | 65055419 | |||||||
| chr17:65055628 | T | C | 14 | a0001c0001t0003g0001 a0001c0001t0003g0126 a0001c0001t0003g0127 others(11): Show |
16 | HG01099.hp1 HG01884.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.283+683A>G | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 1/3 | chr17 | 65055628 | |||||||
| chr17:65055932 | A | G | 140 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(137): Show |
143 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(140): Show |
intron_variant | MODIFIER | c.283+379T>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 1/3 | chr17 | 65055932 | |||||||
| chr17:65056126 | G | A | 5 | a0001c0001t0007g0170 a0001c0001t0007g0172 a0001c0001t0007g0173 others(2): Show |
5 | HG01109.hp1 HG02257.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+185C>T | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 1/3 | chr17 | 65056126 | |||||||
| chr17:65056226 | G | T | 102 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(99): Show |
103 | HG00099.hp2 HG00639.hp1 HG00735.hp1 others(100): Show |
intron_variant | MODIFIER | c.283+85C>A | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 1/3 | chr17 | 65056226 | |||||||
| chr17:65056243 | C | G | 169 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(166): Show |
172 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(169): Show |
intron_variant | MODIFIER | c.283+68G>C | GNA13 | ENSG00000120063.10 | transcript | ENST00000439174.7 | protein_coding | 1/3 | chr17 | 65056243 |