| geneid | 2775 |
|---|---|
| ensemblid | ENSG00000087258.16 |
| hgncid | 4389 |
| symbol | GNAO1 |
| name | G protein subunit alpha o1 |
| refseq_nuc | NM_020988.3 |
| refseq_prot | NP_066268.1 |
| ensembl_nuc | ENST00000262493.12 |
| ensembl_prot | ENSP00000262493.6 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 56191489 |
| end | 56357444 |
| strand | + |
| ver | v1.2 |
| region | chr16:56191489-56357444 |
| region5000 | chr16:56186489-56362444 |
| regionname0 | GNAO1_chr16_56191489_56357444 |
| regionname5000 | GNAO1_chr16_56186489_56362444 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 354 | 297 | 70 | 50 | 117 | 18 | 40 | 87 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0002 | 0/0 | 354 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 1065 | 164 | 24 | 28 | 89 | 9 | 14 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| c0002 | 1/1 | 1065 | 128 | 43 | 20 | 28 | 9 | 26 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| c0003 | 0/0 | 1065 | 2 | 0 | 2 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| c0004 | 0/0 | 1065 | 2 | 2 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| c0005 | 0/0 | 1065 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| c0006 | 0/0 | 1065 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 2118 | 110 | 28 | 20 | 39 | 10 | 12 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| t0002 | 0/0 | 2116 | 36 | 10 | 5 | 6 | 5 | 10 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| t0003 | 0/0 | 2116 | 33 | 6 | 4 | 18 | 0 | 5 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| t0004 | 0/0 | 2117 | 32 | 11 | 3 | 10 | 3 | 5 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| t0005 | 0/0 | 2117 | 15 | 1 | 3 | 11 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| t0006 | 0/1 | 2117 | 13 | 0 | 4 | 6 | 0 | 2 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| t0007 | 0/0 | 2118 | 10 | 0 | 10 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| t0008 | 0/0 | 2117 | 7 | 0 | 0 | 7 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| t0009 | 0/0 | 2122 | 6 | 0 | 0 | 6 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| t0010 | 0/0 | 2118 | 4 | 0 | 0 | 2 | 0 | 2 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| t0011 | 0/0 | 2117 | 4 | 0 | 0 | 3 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| t0012 | 0/0 | 2118 | 4 | 4 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| t0013 | 0/0 | 2114 | 3 | 3 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| t0014 | 0/0 | 2118 | 3 | 3 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| t0015 | 0/0 | 2117 | 3 | 0 | 1 | 0 | 0 | 2 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| t0016 | 0/0 | 2121 | 2 | 0 | 0 | 2 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| t0017 | 0/0 | 2118 | 2 | 2 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| t0018 | 0/0 | 2117 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| t0019 | 0/0 | 2121 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| t0020 | 0/0 | 2121 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| t0021 | 0/0 | 2113 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| t0022 | 0/0 | 2113 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| t0023 | 0/0 | 2118 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| t0024 | 0/0 | 2118 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| t0025 | 0/0 | 2118 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| t0026 | 0/0 | 2130 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| t0027 | 0/0 | 2118 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| t0028 | 0/0 | 2117 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0171 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0234 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1065 | 164 | 24 | 28 | 89 | 9 | 14 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0002 | 1/1 | 1065 | 128 | 43 | 20 | 28 | 9 | 26 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0003 | 0/0 | 1065 | 2 | 0 | 2 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0004 | 0/0 | 1065 | 2 | 2 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0006 | 0/0 | 1065 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0002c0005 | 0/0 | 1065 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3182 | 60 | 13 | 8 | 30 | 5 | 4 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0001t0002 | 0/0 | 3180 | 7 | 1 | 1 | 2 | 2 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0001t0003 | 0/0 | 3180 | 19 | 4 | 1 | 13 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0001t0004 | 0/0 | 3181 | 20 | 2 | 3 | 8 | 2 | 5 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0001t0005 | 0/0 | 3181 | 13 | 0 | 2 | 11 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0001t0006 | 0/0 | 3181 | 4 | 0 | 3 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0001t0007 | 0/0 | 3182 | 10 | 0 | 10 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0001t0008 | 0/0 | 3181 | 7 | 0 | 0 | 7 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0001t0009 | 0/0 | 3186 | 6 | 0 | 0 | 6 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0001t0010 | 0/0 | 3182 | 2 | 0 | 0 | 1 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0001t0011 | 0/0 | 3181 | 4 | 0 | 0 | 3 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0001t0013 | 0/0 | 3178 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0001t0014 | 0/0 | 3182 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0001t0015 | 0/0 | 3181 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0001t0016 | 0/0 | 3185 | 2 | 0 | 0 | 2 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0001t0017 | 0/0 | 3182 | 2 | 2 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0001t0019 | 0/0 | 3185 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0001t0020 | 0/0 | 3185 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0001t0024 | 0/0 | 3182 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0001t0026 | 0/0 | 3194 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0001t0028 | 0/0 | 3181 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0002t0001 | 1/0 | 3182 | 50 | 15 | 12 | 9 | 5 | 8 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0002t0002 | 0/0 | 3180 | 25 | 7 | 2 | 4 | 3 | 9 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0002t0003 | 0/0 | 3180 | 13 | 2 | 3 | 4 | 0 | 4 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0002t0004 | 0/0 | 3181 | 12 | 9 | 0 | 2 | 1 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0002t0005 | 0/0 | 3181 | 2 | 1 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0002t0006 | 0/1 | 3181 | 9 | 0 | 1 | 5 | 0 | 2 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0002t0010 | 0/0 | 3182 | 2 | 0 | 0 | 1 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0002t0012 | 0/0 | 3182 | 4 | 4 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0002t0013 | 0/0 | 3178 | 2 | 2 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0002t0014 | 0/0 | 3182 | 2 | 2 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0002t0015 | 0/0 | 3181 | 2 | 0 | 1 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0002t0018 | 0/0 | 3181 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0002t0022 | 0/0 | 3177 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0002t0023 | 0/0 | 3182 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0002t0025 | 0/0 | 3182 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0002t0027 | 0/0 | 3182 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0003t0002 | 0/0 | 3180 | 2 | 0 | 2 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0004t0002 | 0/0 | 3180 | 2 | 2 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0001c0006t0021 | 0/0 | 3177 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| a0002c0005t0003 | 0/0 | 3180 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | copy fasta | chr16 | 56186489 | 56362444 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0004g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0004g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0004g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0004g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0004g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0004g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0005g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0005g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0005g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0005g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0005g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0005g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0005g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0005g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0005g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0005g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0005g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0005g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0005g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0006g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0006g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0006g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0006g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0007g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0007g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0007g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0007g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0007g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0007g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0007g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0007g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0007g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0007g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0008g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0008g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0008g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0008g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0008g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0008g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0008g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0009g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0009g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0009g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0009g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0009g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0009g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0010g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0010g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0011g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0011g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0011g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0011g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0013g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0014g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0015g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0016g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0016g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0017g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0017g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0019g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0020g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0024g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0026g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0001t0028g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0171 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0002g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0002g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0003g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0003g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0003g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0004g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0004g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0004g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0005g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0006g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0006g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0006g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0006g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0006g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0006g0234 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0006g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0006g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0006g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0010g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0010g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0012g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0012g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0012g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0012g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0013g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0013g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0014g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0014g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0015g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0015g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0018g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0022g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0023g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0025g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0002t0027g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0003t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0003t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0004t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0004t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0001c0006t0021g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| a0002c0005t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0175 | EUR | GBR | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0192 | EUR | GBR | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG00140 | hp1 | a0001 | c0002 | t0002 | g0194 | EUR | GBR | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0061 | EUR | GBR | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG00280 | hp1 | a0001 | c0002 | t0004 | g0074 | EUR | FIN | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0185 | EUR | FIN | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0115 | EUR | FIN | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0242 | EUR | FIN | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG00423 | hp1 | a0001 | c0001 | t0010 | g0123 | EAS | CHS | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | CHS | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | CHS | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG00609 | hp2 | a0001 | c0001 | t0020 | g0126 | EAS | CHS | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0120 | AMR | PUR | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG00639 | hp2 | a0001 | c0002 | t0006 | g0193 | AMR | PUR | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG00642 | hp1 | a0001 | c0002 | t0003 | g0137 | AMR | PUR | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG00642 | hp2 | a0001 | c0001 | t0007 | g0038 | AMR | PUR | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG00673 | hp1 | a0001 | c0002 | t0018 | g0229 | EAS | CHS | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | CHS | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG00733 | hp1 | a0001 | c0001 | t0007 | g0039 | AMR | PUR | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG00733 | hp2 | a0001 | c0002 | t0003 | g0233 | AMR | PUR | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG00735 | hp1 | a0001 | c0001 | t0006 | g0080 | AMR | PUR | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG00735 | hp2 | a0001 | c0003 | t0002 | g0103 | AMR | PUR | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0093 | AMR | PUR | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0241 | AMR | PUR | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0104 | AMR | PUR | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0147 | AMR | PUR | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0239 | AMR | PUR | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0245 | AMR | PUR | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0254 | AMR | PUR | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0142 | AMR | PUR | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01255 | hp1 | a0001 | c0003 | t0002 | g0114 | AMR | CLM | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01255 | hp2 | a0001 | c0001 | t0007 | g0158 | AMR | CLM | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01256 | hp1 | a0001 | c0001 | t0007 | g0157 | AMR | CLM | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0246 | AMR | CLM | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01258 | hp1 | a0001 | c0001 | t0007 | g0155 | AMR | CLM | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01261 | hp1 | a0001 | c0001 | t0007 | g0016 | AMR | CLM | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0082 | AMR | CLM | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01346 | hp2 | a0001 | c0001 | t0005 | g0206 | AMR | CLM | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0151 | AMR | CLM | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0099 | AMR | CLM | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01433 | hp2 | a0001 | c0001 | t0005 | g0216 | AMR | CLM | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01496 | hp2 | a0001 | c0002 | t0003 | g0160 | AMR | CLM | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0081 | EUR | IBS | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0107 | EUR | IBS | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0150 | EUR | IBS | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0228 | EUR | IBS | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0025 | EUR | IBS | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0152 | EUR | IBS | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01884 | hp1 | a0001 | c0001 | t0017 | g0290 | AFR | ACB | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0296 | AFR | ACB | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01928 | hp1 | a0001 | c0002 | t0002 | g0118 | AMR | PEL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01934 | hp1 | a0001 | c0001 | t0006 | g0226 | AMR | PEL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01934 | hp2 | a0001 | c0001 | t0007 | g0012 | AMR | PEL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01975 | hp1 | a0001 | c0002 | t0005 | g0162 | AMR | PEL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0105 | AMR | PEL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01978 | hp1 | a0001 | c0001 | t0004 | g0207 | AMR | PEL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01978 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01993 | hp1 | a0001 | c0001 | t0007 | g0156 | AMR | PEL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG01993 | hp2 | a0001 | c0001 | t0007 | g0113 | AMR | PEL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0286 | EAS | KHV | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02015 | hp2 | a0001 | c0001 | t0009 | g0094 | EAS | KHV | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | KHV | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02027 | hp2 | a0001 | c0001 | t0004 | g0237 | EAS | KHV | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02055 | hp2 | a0001 | c0004 | t0002 | g0282 | AFR | ACB | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | KHV | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02074 | hp1 | a0001 | c0002 | t0023 | g0027 | EAS | KHV | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | KHV | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02080 | hp1 | a0001 | c0001 | t0028 | g0125 | EAS | KHV | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02080 | hp2 | a0001 | c0002 | t0006 | g0265 | EAS | KHV | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02083 | hp1 | a0001 | c0001 | t0016 | g0091 | EAS | KHV | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02083 | hp2 | a0001 | c0001 | t0006 | g0255 | EAS | KHV | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02132 | hp1 | a0001 | c0001 | t0011 | g0138 | EAS | KHV | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0227 | EAS | KHV | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02135 | hp1 | a0001 | c0001 | t0009 | g0140 | EAS | KHV | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02135 | hp2 | a0001 | c0001 | t0024 | g0068 | EAS | KHV | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02145 | hp1 | a0001 | c0002 | t0002 | g0029 | AFR | ACB | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0086 | AFR | ACB | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02257 | hp2 | a0001 | c0002 | t0004 | g0053 | AFR | ACB | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0204 | AFR | ACB | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02258 | hp2 | a0001 | c0002 | t0014 | g0058 | AFR | ACB | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02273 | hp1 | a0001 | c0001 | t0007 | g0070 | AMR | PEL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02280 | hp1 | a0001 | c0002 | t0002 | g0087 | AFR | ACB | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02280 | hp2 | a0001 | c0002 | t0012 | g0179 | AFR | ACB | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02293 | hp1 | a0001 | c0002 | t0015 | g0135 | AMR | PEL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02293 | hp2 | a0001 | c0001 | t0006 | g0069 | AMR | PEL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0263 | AMR | PEL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0198 | AMR | PEL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02451 | hp1 | a0001 | c0002 | t0003 | g0148 | AFR | ACB | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02451 | hp2 | a0001 | c0002 | t0012 | g0181 | AFR | ACB | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02523 | hp1 | a0001 | c0002 | t0002 | g0108 | EAS | KHV | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0047 | SAS | PJL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02622 | hp1 | a0001 | c0002 | t0004 | g0067 | AFR | GWD | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02622 | hp2 | a0001 | c0001 | t0017 | g0244 | AFR | GWD | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0247 | AFR | GWD | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02630 | hp2 | a0001 | c0002 | t0004 | g0278 | AFR | GWD | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0065 | SAS | PJL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0232 | SAS | PJL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0190 | SAS | PJL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0052 | AFR | GWD | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0249 | AFR | GWD | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0017 | SAS | PJL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0191 | SAS | PJL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02809 | hp1 | a0001 | c0001 | t0013 | g0187 | AFR | GWD | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02809 | hp2 | a0001 | c0006 | t0021 | g0019 | AFR | GWD | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02965 | hp1 | a0001 | c0002 | t0005 | g0026 | AFR | ESN | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0054 | AFR | ESN | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0294 | AFR | ESN | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG03098 | hp1 | a0001 | c0002 | t0013 | g0293 | AFR | MSL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG03098 | hp2 | a0001 | c0002 | t0004 | g0277 | AFR | MSL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | ESN | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0117 | AFR | ESN | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0056 | AFR | ESN | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ESN | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG03225 | hp1 | a0001 | c0002 | t0027 | g0146 | AFR | MSL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG03225 | hp2 | a0001 | c0002 | t0002 | g0260 | AFR | MSL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG03453 | hp1 | a0001 | c0002 | t0004 | g0063 | AFR | MSL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG03453 | hp2 | a0001 | c0002 | t0012 | g0183 | AFR | MSL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0279 | AFR | MSL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0055 | AFR | MSL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0130 | SAS | PJL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG03490 | hp2 | a0001 | c0002 | t0003 | g0235 | SAS | PJL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG03491 | hp1 | a0001 | c0002 | t0006 | g0197 | SAS | PJL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0002 | SAS | PJL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0002 | SAS | PJL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0111 | SAS | PJL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0289 | AFR | ESN | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG03516 | hp2 | a0001 | c0002 | t0012 | g0180 | AFR | ESN | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG03540 | hp1 | a0001 | c0002 | t0004 | g0144 | AFR | GWD | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0064 | AFR | GWD | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0209 | AFR | MSL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0291 | AFR | MSL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0195 | SAS | PJL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG03654 | hp2 | a0001 | c0002 | t0025 | g0129 | SAS | PJL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG03688 | hp1 | a0001 | c0001 | t0015 | g0251 | SAS | STU | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG03688 | hp2 | a0001 | c0002 | t0010 | g0274 | SAS | STU | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG03704 | hp1 | a0001 | c0001 | t0011 | g0285 | SAS | PJL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0253 | SAS | PJL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0240 | SAS | PJL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0020 | SAS | PJL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG03834 | hp1 | a0001 | c0002 | t0003 | g0136 | SAS | BEB | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | BEB | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0006 | SAS | BEB | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0119 | SAS | BEB | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG03942 | hp1 | a0001 | c0002 | t0006 | g0264 | SAS | BEB | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | BEB | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG04115 | hp1 | a0001 | c0002 | t0003 | g0257 | SAS | STU | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG04115 | hp2 | a0001 | c0002 | t0015 | g0128 | SAS | STU | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0212 | SAS | BEB | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0271 | SAS | BEB | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0236 | SAS | STU | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG04199 | hp2 | a0001 | c0001 | t0010 | g0040 | SAS | STU | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0287 | SAS | STU | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG04204 | hp2 | a0001 | c0002 | t0003 | g0275 | SAS | STU | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0250 | SAS | STU | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG04228 | hp2 | a0001 | c0002 | t0002 | g0214 | SAS | STU | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18522 | hp1 | a0001 | c0002 | t0014 | g0033 | AFR | YRI | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | YRI | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | CHB | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0178 | EAS | CHB | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHB | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHB | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18906 | hp1 | a0001 | c0002 | t0004 | g0143 | AFR | YRI | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | YRI | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18942 | hp2 | a0001 | c0002 | t0006 | g0134 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18945 | hp1 | a0001 | c0001 | t0009 | g0089 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18945 | hp2 | a0001 | c0001 | t0005 | g0222 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18946 | hp1 | a0001 | c0001 | t0005 | g0272 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18949 | hp1 | a0001 | c0002 | t0006 | g0133 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18952 | hp2 | a0001 | c0002 | t0004 | g0124 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18959 | hp2 | a0001 | c0001 | t0005 | g0048 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0269 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0215 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18966 | hp2 | a0001 | c0001 | t0005 | g0186 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18969 | hp1 | a0001 | c0001 | t0004 | g0217 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18973 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18973 | hp2 | a0001 | c0001 | t0008 | g0037 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18975 | hp1 | a0001 | c0001 | t0008 | g0046 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18975 | hp2 | a0001 | c0002 | t0002 | g0102 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18978 | hp2 | a0001 | c0001 | t0008 | g0005 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0161 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18981 | hp2 | a0001 | c0002 | t0002 | g0066 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18983 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18986 | hp1 | a0001 | c0001 | t0009 | g0127 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18986 | hp2 | a0001 | c0001 | t0008 | g0042 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18987 | hp1 | a0001 | c0001 | t0005 | g0230 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18987 | hp2 | a0001 | c0001 | t0011 | g0031 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18994 | hp1 | a0001 | c0002 | t0004 | g0267 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18994 | hp2 | a0001 | c0001 | t0026 | g0003 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA19000 | hp2 | a0001 | c0001 | t0005 | g0256 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA19002 | hp2 | a0001 | c0002 | t0006 | g0243 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0266 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA19004 | hp2 | a0001 | c0001 | t0008 | g0045 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA19005 | hp1 | a0001 | c0001 | t0008 | g0036 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA19009 | hp1 | a0001 | c0001 | t0005 | g0225 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA19009 | hp2 | a0001 | c0001 | t0008 | g0110 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA19011 | hp1 | a0001 | c0001 | t0009 | g0095 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA19011 | hp2 | a0001 | c0001 | t0011 | g0203 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA19030 | hp1 | a0001 | c0001 | t0014 | g0034 | AFR | LWK | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA19030 | hp2 | a0001 | c0002 | t0004 | g0205 | AFR | LWK | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA19043 | hp1 | a0001 | c0004 | t0002 | g0028 | AFR | LWK | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | LWK | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA19057 | hp2 | a0002 | c0005 | t0003 | g0088 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA19060 | hp1 | a0001 | c0001 | t0005 | g0220 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA19060 | hp2 | a0001 | c0002 | t0006 | g0154 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA19065 | hp1 | a0001 | c0001 | t0005 | g0218 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA19070 | hp1 | a0001 | c0001 | t0005 | g0201 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA19079 | hp1 | a0001 | c0001 | t0016 | g0059 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA19079 | hp2 | a0001 | c0001 | t0004 | g0223 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA19080 | hp1 | a0001 | c0002 | t0022 | g0122 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA19080 | hp2 | a0001 | c0001 | t0005 | g0221 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA19081 | hp1 | a0001 | c0001 | t0004 | g0112 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA19083 | hp1 | a0001 | c0001 | t0019 | g0090 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA19083 | hp2 | a0001 | c0002 | t0003 | g0015 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA19084 | hp1 | a0001 | c0002 | t0010 | g0252 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA19084 | hp2 | a0001 | c0001 | t0009 | g0060 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA19085 | hp2 | a0001 | c0002 | t0003 | g0109 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0248 | EUR | TSI | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0023 | EUR | TSI | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0196 | EUR | TSI | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0084 | EUR | TSI | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0173 | SAS | GIH | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0149 | SAS | GIH | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0013 | AFR | ACB | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0283 | AFR | ACB | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02486 | hp1 | a0001 | c0002 | t0003 | g0184 | AFR | ACB | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0085 | AFR | ACB | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | ACB | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG02559 | hp2 | a0001 | c0002 | t0013 | g0032 | AFR | ACB | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | MSL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | MSL | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG06807 | hp1 | a0001 | c0002 | t0002 | g0139 | AFR | USA | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0288 | AFR | USA | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18955 | hp1 | a0001 | c0002 | t0002 | g0213 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA20300 | hp1 | a0001 | c0002 | t0004 | g0021 | AFR | USA | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0292 | AFR | USA | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0259 | AFR | LWK | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0035 | AFR | LWK | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0006 | g0234 | REF | REF | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0171 | REF | REF | GNAO1_chr16_56186489_56362444 | GNAO1 | chr16 | 56186489 | 56362444 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:56336738
|
G | C | 1 | a0002 | 1 | NA19057.hp2 | missense_variant | MODERATE | c.601G>C | p.Asp201His | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/9 | 1348/3182 | 601/1065 | 201/354 | chr16 | 56336738 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:56334777
|
C | T | 1 | a0001c0001 | 164 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(161): Show |
synonymous_variant | LOW | c.513C>T | p.Thr171Thr | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 5/9 | 1260/3182 | 513/1065 | 171/354 | chr16 | 56334777 | ||
| chr16:56354891
|
C | T | 1 | a0001c0006 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.903C>T | p.Ala301Ala | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 8/9 | 1650/3182 | 903/1065 | 301/354 | chr16 | 56354891 | ||
| chr16:56354909
|
A | G | 1 | a0001c0004 | 2 | HG02055.hp2 NA19043.hp1 |
synonymous_variant | LOW | c.921A>G | p.Gln307Gln | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 8/9 | 1668/3182 | 921/1065 | 307/354 | chr16 | 56354909 | ||
| chr16:56354981
|
C | T | 1 | a0001c0003 | 2 | HG00735.hp2 HG01255.hp1 |
synonymous_variant | LOW | c.993C>T | p.Asn331Asn | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 8/9 | 1740/3182 | 993/1065 | 331/354 | chr16 | 56354981 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:56191614
|
G | A | 1 | a0001c0002t0018 | 1 | HG00673.hp1 | 5_prime_UTR_variant | MODIFIER | c.-622G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 1/9 | 622 | chr16 | 56191614 | |||||
| chr16:56191749
|
C | G | 1 | a0001c0001t0028 | 1 | HG02080.hp1 | 5_prime_UTR_variant | MODIFIER | c.-487C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 1/9 | 487 | chr16 | 56191749 | |||||
| chr16:56191842
|
C | T | 1 | a0001c0002t0012 | 4 | HG02280.hp2 HG02451.hp2 HG03453.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-394C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 1/9 | 394 | chr16 | 56191842 | |||||
| chr16:56192140
|
G | GAGCC | 4 | a0001c0001t0009a0001c0001t0016a0001c0001t0019others(1): Show | 10 | HG00609.hp2 HG02015.hp2 HG02083.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-95_-92dupAGCC | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 1/9 | 91 | INFO_REALIGN_3_PRIME | chr16 | 56192140 | ||||
| chr16:56192149
|
C | T | 1 | a0001c0002t0027 | 1 | HG03225.hp1 | 5_prime_UTR_variant | MODIFIER | c.-87C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 1/9 | 87 | chr16 | 56192149 | |||||
| chr16:56356360
|
T | A | 1 | a0001c0001t0026 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*286T>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 9/9 | 1307 | chr16 | 56356360 | |||||
| chr16:56356408
|
C | T | 6 | a0001c0001t0010a0001c0001t0011a0001c0001t0020others(3): Show | 11 | HG00423.hp1 HG00609.hp2 HG02132.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*334C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 9/9 | 1355 | chr16 | 56356408 | |||||
| chr16:56356412
|
C | T | 5 | a0001c0001t0005a0001c0001t0007a0001c0001t0015others(2): Show | 28 | HG00642.hp2 HG00733.hp1 HG01255.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*338C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 9/9 | 1359 | chr16 | 56356412 | |||||
| chr16:56356684
|
C | T | 1 | a0001c0002t0025 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*610C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 9/9 | 1631 | chr16 | 56356684 | |||||
| chr16:56356732
|
C | T | 1 | a0001c0002t0023 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*658C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 9/9 | 1679 | chr16 | 56356732 | |||||
| chr16:56356770
|
T | G | 1 | a0001c0001t0008 | 7 | NA18973.hp2 NA18975.hp1 NA18978.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*696T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 9/9 | 1717 | chr16 | 56356770 | |||||
| chr16:56356772
|
C | T | 1 | a0001c0001t0008 | 7 | NA18973.hp2 NA18975.hp1 NA18978.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*698C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 9/9 | 1719 | chr16 | 56356772 | |||||
| chr16:56356773
|
CT | C | 17 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(14): Show | 96 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*713delT | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 9/9 | 1734 | INFO_REALIGN_3_PRIME | chr16 | 56356773 | ||||
| chr16:56356773
|
CTT | C | 4 | a0001c0001t0002a0001c0002t0002a0001c0003t0002others(1): Show | 36 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*712_*713delTT | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 9/9 | 1733 | INFO_REALIGN_3_PRIME | chr16 | 56356773 | ||||
| chr16:56356774
|
T | C | 1 | a0001c0001t0008 | 7 | NA18973.hp2 NA18975.hp1 NA18978.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*700T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 9/9 | 1721 | chr16 | 56356774 | |||||
| chr16:56356837
|
C | G | 1 | a0001c0001t0017 | 2 | HG01884.hp1 HG02622.hp2 |
3_prime_UTR_variant | MODIFIER | c.*763C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 9/9 | 1784 | chr16 | 56356837 | |||||
| chr16:56357036
|
T | A | 1 | a0001c0001t0026 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*962T>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 9/9 | 1983 | chr16 | 56357036 | |||||
| chr16:56357056
|
GA | G | 10 | a0001c0001t0003a0001c0001t0006a0001c0001t0008others(7): Show | 58 | HG00438.hp2 HG00639.hp2 HG00642.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*992delA | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 9/9 | 2013 | INFO_REALIGN_3_PRIME | chr16 | 56357056 | ||||
| chr16:56357263
|
C | A | 1 | a0001c0001t0024 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1189C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 9/9 | 2210 | chr16 | 56357263 | |||||
| chr16:56357271
|
T | TA | 4 | a0001c0001t0010a0001c0001t0024a0001c0002t0010others(1): Show | 6 | HG00423.hp1 HG02135.hp2 HG03654.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1208dupA | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 9/9 | 2230 | INFO_REALIGN_3_PRIME | chr16 | 56357271 | ||||
| chr16:56357272
|
A | T | 2 | a0001c0001t0014a0001c0002t0014 | 3 | HG02258.hp2 NA18522.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1198A>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 9/9 | 2219 | chr16 | 56357272 | |||||
| chr16:56357391
|
TCTGA | T | 4 | a0001c0001t0013a0001c0002t0013a0001c0002t0022others(1): Show | 5 | HG02559.hp2 HG02809.hp1 HG02809.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1320_*1323delGACT | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 9/9 | 2341 | INFO_REALIGN_3_PRIME | chr16 | 56357391 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:56192405
|
C | G | 6 | a0001c0001t0001g0295a0001c0001t0004g0291a0001c0001t0004g0296others(3): Show | 6 | HG01891.hp1 HG02970.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.118+52C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 1/8 | chr16 | 56192405 | ||||||
| chr16:56192506
|
T | TC | 19 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0014others(16): Show | 19 | HG00438.hp2 HG00673.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.119-61dupC | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 56192506 | |||||
| chr16:56192624
|
C | T | 3 | a0001c0001t0003g0289a0001c0001t0017g0290a0001c0002t0001g0288 | 3 | HG01884.hp1 HG03516.hp1 HG06807.hp2 |
splice_region_variant&intron_variant | LOW | c.161+8C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56192624 | ||||||
| chr16:56192686
|
C | T | 5 | a0001c0001t0004g0002a0001c0001t0004g0287a0001c0001t0011g0285others(2): Show | 6 | HG02015.hp1 HG03491.hp2 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.161+70C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56192686 | ||||||
| chr16:56192723
|
C | CGT | 5 | a0001c0001t0001g0281a0001c0001t0001g0284a0001c0002t0002g0283others(2): Show | 5 | HG01106.hp1 HG02055.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.161+109_161+110dup others(2): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56192723 | |||||
| chr16:56192726
|
G | GCA | 136 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0041others(133): Show | 136 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.161+134_161+135dup others(2): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56192726 | |||||
| chr16:56192726
|
G | GCACA | 8 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0004g0023others(5): Show | 9 | HG01517.hp1 HG02074.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.161+132_161+135dup others(4): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56192726 | |||||
| chr16:56192726
|
GCA | G | 33 | a0001c0001t0001g0258a0001c0001t0001g0262a0001c0001t0001g0270others(30): Show | 34 | HG00423.hp2 HG00673.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.161+134_161+135del others(2): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56192726 | |||||
| chr16:56192750
|
A | ACC | 9 | a0001c0001t0003g0159a0001c0001t0004g0161a0001c0001t0007g0012others(6): Show | 9 | HG01255.hp2 HG01256.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.161+137_161+138dup others(2): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56192750 | |||||
| chr16:56192750
|
A | C | 2 | a0001c0001t0004g0002a0001c0001t0004g0287 | 3 | HG03491.hp2 HG03492.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.161+134A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56192750 | ||||||
| chr16:56192847
|
C | G | 1 | a0001c0002t0003g0257 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.161+231C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56192847 | ||||||
| chr16:56192980
|
G | A | 8 | a0001c0001t0001g0295a0001c0001t0004g0291a0001c0001t0004g0296others(5): Show | 8 | HG01891.hp1 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.161+364G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56192980 | ||||||
| chr16:56193054
|
C | T | 1 | a0001c0002t0006g0154 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.161+438C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56193054 | ||||||
| chr16:56193064
|
T | C | 2 | a0001c0001t0003g0030a0001c0002t0004g0021 | 2 | NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.161+448T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56193064 | ||||||
| chr16:56193069
|
C | G | 8 | a0001c0001t0001g0295a0001c0001t0004g0291a0001c0001t0004g0296others(5): Show | 8 | HG01891.hp1 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.161+453C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56193069 | ||||||
| chr16:56193117
|
A | G | 1 | a0001c0001t0005g0256 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.161+501A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56193117 | ||||||
| chr16:56193368
|
C | G | 1 | a0001c0002t0002g0029 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.161+752C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56193368 | ||||||
| chr16:56193454
|
C | T | 1 | a0001c0001t0006g0255 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.161+838C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56193454 | ||||||
| chr16:56193517
|
G | A | 1 | a0001c0002t0001g0013 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.161+901G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56193517 | ||||||
| chr16:56193826
|
C | G | 5 | a0001c0001t0001g0153a0001c0001t0002g0150a0001c0002t0001g0151others(2): Show | 5 | HG01361.hp2 HG01516.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.161+1210C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56193826 | ||||||
| chr16:56193858
|
T | C | 1 | a0001c0001t0011g0031 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.161+1242T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56193858 | ||||||
| chr16:56193997
|
G | A | 33 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(30): Show | 33 | HG00438.hp1 HG00642.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.161+1381G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56193997 | ||||||
| chr16:56194021
|
G | A | 6 | a0001c0001t0001g0295a0001c0001t0004g0291a0001c0001t0004g0296others(3): Show | 6 | HG01891.hp1 HG02970.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.161+1405G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56194021 | ||||||
| chr16:56194053
|
T | G | 120 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0024others(117): Show | 121 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.161+1437T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56194053 | ||||||
| chr16:56194154
|
A | G | 284 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0014others(281): Show | 286 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.161+1538A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56194154 | ||||||
| chr16:56194202
|
C | T | 1 | a0001c0002t0001g0054 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.161+1586C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56194202 | ||||||
| chr16:56194271
|
G | C | 1 | a0001c0002t0027g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.161+1655G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56194271 | ||||||
| chr16:56194307
|
G | C | 2 | a0001c0001t0001g0177a0001c0001t0004g0178 | 2 | NA18612.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.161+1691G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56194307 | ||||||
| chr16:56194419
|
C | T | 1 | a0001c0002t0005g0162 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.161+1803C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56194419 | ||||||
| chr16:56194609
|
C | T | 3 | a0001c0001t0001g0145a0001c0002t0004g0143a0001c0002t0004g0144 | 3 | HG03540.hp1 NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.161+1993C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56194609 | ||||||
| chr16:56194966
|
C | A | 73 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(70): Show | 74 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.161+2350C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56194966 | ||||||
| chr16:56195024
|
G | A | 8 | a0001c0001t0001g0295a0001c0001t0004g0291a0001c0001t0004g0296others(5): Show | 8 | HG01891.hp1 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.161+2408G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56195024 | ||||||
| chr16:56195074
|
C | CT | 12 | a0001c0001t0001g0176a0001c0001t0002g0253a0001c0001t0002g0254others(9): Show | 12 | HG01109.hp2 HG01169.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.161+2477dupT | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56195074 | |||||
| chr16:56195074
|
CT | C | 10 | a0001c0001t0001g0014a0001c0001t0001g0177a0001c0001t0001g0188others(7): Show | 10 | HG00280.hp2 HG01884.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.161+2477delT | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56195074 | |||||
| chr16:56195089
|
TTTTTC | T | 6 | a0001c0002t0002g0029a0001c0002t0012g0179a0001c0002t0012g0180others(3): Show | 6 | HG02074.hp1 HG02145.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.161+2474_161+2478d others(7): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56195089 | ||||||
| chr16:56195090
|
TTTTC | T | 75 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0049others(72): Show | 76 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.161+2475_161+2478d others(6): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56195090 | ||||||
| chr16:56195091
|
TTTC | T | 120 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(117): Show | 121 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.161+2476_161+2478d others(5): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56195091 | ||||||
| chr16:56195255
|
C | G | 41 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(38): Show | 41 | HG00438.hp1 HG00642.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.161+2639C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56195255 | ||||||
| chr16:56195342
|
G | C | 1 | a0001c0002t0003g0184 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.161+2726G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56195342 | ||||||
| chr16:56195440
|
C | G | 4 | a0001c0002t0012g0179a0001c0002t0012g0180a0001c0002t0012g0181others(1): Show | 4 | HG02280.hp2 HG02451.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.161+2824C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56195440 | ||||||
| chr16:56195513
|
G | A | 32 | a0001c0001t0001g0258a0001c0001t0001g0262a0001c0001t0001g0270others(29): Show | 33 | HG00423.hp2 HG00673.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.161+2897G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56195513 | ||||||
| chr16:56195616
|
G | A | 2 | a0001c0001t0001g0258a0001c0002t0001g0259 | 2 | HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.161+3000G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56195616 | ||||||
| chr16:56195666
|
A | G | 205 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(202): Show | 207 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.161+3050A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56195666 | ||||||
| chr16:56195685
|
C | T | 1 | a0001c0001t0009g0140 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.161+3069C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56195685 | ||||||
| chr16:56195814
|
G | A | 1 | a0001c0002t0001g0245 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.161+3198G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56195814 | ||||||
| chr16:56195969
|
T | C | 11 | a0001c0001t0001g0192a0001c0001t0001g0196a0001c0001t0004g0185others(8): Show | 11 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(8): Show |
intron_variant | MODIFIER | c.161+3353T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56195969 | ||||||
| chr16:56196259
|
C | T | 5 | a0001c0001t0003g0289a0001c0001t0017g0290a0001c0002t0001g0288others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.161+3643C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56196259 | ||||||
| chr16:56196316
|
G | C | 2 | a0001c0001t0001g0177a0001c0001t0004g0178 | 2 | NA18612.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.161+3700G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56196316 | ||||||
| chr16:56196452
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.161+3836A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56196452 | ||||||
| chr16:56196485
|
G | A | 2 | a0001c0001t0009g0060a0001c0001t0016g0059 | 2 | NA19079.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.161+3869G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56196485 | ||||||
| chr16:56196566
|
G | T | 41 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(38): Show | 41 | HG00438.hp1 HG00642.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.161+3950G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56196566 | ||||||
| chr16:56196568
|
G | A | 1 | a0001c0001t0001g0280 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.161+3952G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56196568 | ||||||
| chr16:56196784
|
G | A | 73 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(70): Show | 74 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.161+4168G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56196784 | ||||||
| chr16:56196879
|
A | T | 6 | a0001c0001t0001g0295a0001c0001t0004g0291a0001c0001t0004g0296others(3): Show | 6 | HG01891.hp1 HG02970.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.161+4263A>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56196879 | ||||||
| chr16:56196944
|
C | G | 1 | a0001c0002t0002g0139 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.161+4328C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56196944 | ||||||
| chr16:56196964
|
G | A | 5 | a0001c0001t0001g0295a0001c0001t0004g0291a0001c0002t0001g0294others(2): Show | 5 | HG02970.hp1 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.161+4348G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56196964 | ||||||
| chr16:56197004
|
A | G | 1 | a0001c0001t0001g0050 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.161+4388A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56197004 | ||||||
| chr16:56197020
|
G | A | 1 | a0001c0001t0007g0156 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.161+4404G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56197020 | ||||||
| chr16:56197049
|
T | A | 2 | a0001c0001t0001g0062a0001c0002t0002g0061 | 2 | HG00140.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.161+4433T>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56197049 | ||||||
| chr16:56197132
|
T | A | 39 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(36): Show | 39 | HG00438.hp1 HG00642.hp2 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.161+4516T>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56197132 | ||||||
| chr16:56197183
|
G | A | 1 | a0001c0002t0004g0143 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.161+4567G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56197183 | ||||||
| chr16:56197423
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.161+4807G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56197423 | ||||||
| chr16:56197559
|
G | A | 1 | a0001c0002t0004g0063 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.161+4943G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56197559 | ||||||
| chr16:56197646
|
T | C | 73 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(70): Show | 74 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.161+5030T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56197646 | ||||||
| chr16:56197650
|
A | G | 24 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0049others(21): Show | 24 | HG00438.hp1 HG00642.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.161+5034A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56197650 | ||||||
| chr16:56197774
|
A | G | 1 | a0001c0001t0001g0050 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.161+5158A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56197774 | ||||||
| chr16:56197780
|
C | T | 3 | a0001c0001t0001g0177a0001c0001t0004g0178a0001c0002t0003g0148 | 3 | HG02451.hp1 NA18612.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.161+5164C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56197780 | ||||||
| chr16:56197809
|
A | G | 1 | a0001c0001t0017g0244 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.161+5193A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56197809 | ||||||
| chr16:56197842
|
G | T | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.161+5226G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56197842 | ||||||
| chr16:56197985
|
A | G | 1 | a0001c0002t0027g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.161+5369A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56197985 | ||||||
| chr16:56198073
|
C | A | 1 | a0001c0001t0003g0246 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.161+5457C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56198073 | ||||||
| chr16:56198406
|
G | T | 2 | a0001c0001t0001g0284a0001c0002t0002g0283 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.161+5790G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56198406 | ||||||
| chr16:56198512
|
A | C | 1 | a0001c0002t0006g0243 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.161+5896A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56198512 | ||||||
| chr16:56198585
|
G | A | 1 | a0001c0002t0027g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.161+5969G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56198585 | ||||||
| chr16:56198717
|
C | T | 4 | a0001c0001t0001g0242a0001c0001t0004g0240a0001c0001t0004g0241others(1): Show | 4 | HG00323.hp2 HG01071.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.161+6101C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56198717 | ||||||
| chr16:56198762
|
C | T | 1 | a0001c0001t0011g0138 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.161+6146C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56198762 | ||||||
| chr16:56198788
|
G | C | 1 | a0001c0002t0027g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.161+6172G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56198788 | ||||||
| chr16:56198827
|
G | C | 1 | a0001c0002t0001g0064 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.161+6211G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56198827 | ||||||
| chr16:56199031
|
G | C | 1 | a0001c0002t0027g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.161+6415G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56199031 | ||||||
| chr16:56199036
|
G | A | 205 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(202): Show | 207 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.161+6420G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56199036 | ||||||
| chr16:56199272
|
T | A | 1 | a0001c0002t0001g0065 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.161+6656T>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56199272 | ||||||
| chr16:56199427
|
G | A | 8 | a0001c0001t0001g0295a0001c0001t0004g0291a0001c0001t0004g0296others(5): Show | 8 | HG01891.hp1 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.161+6811G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56199427 | ||||||
| chr16:56199432
|
T | C | 121 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0024others(118): Show | 122 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.161+6816T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56199432 | ||||||
| chr16:56199463
|
A | G | 1 | a0001c0002t0003g0137 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.161+6847A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56199463 | ||||||
| chr16:56199517
|
A | T | 1 | a0001c0001t0003g0238 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.161+6901A>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56199517 | ||||||
| chr16:56199576
|
A | G | 1 | a0001c0002t0023g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.161+6960A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56199576 | ||||||
| chr16:56199950
|
C | G | 1 | a0001c0002t0001g0198 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.161+7334C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56199950 | ||||||
| chr16:56200443
|
A | G | 1 | a0001c0001t0017g0244 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.161+7827A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56200443 | ||||||
| chr16:56201163
|
C | T | 1 | a0001c0001t0004g0296 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.161+8547C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56201163 | ||||||
| chr16:56201646
|
GGGAAAGG others(16): Show |
G | 1 | a0001c0001t0004g0296 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.161+9031_161+9053d others(25): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56201646 | ||||||
| chr16:56201836
|
A | G | 1 | a0001c0002t0004g0063 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.161+9220A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56201836 | ||||||
| chr16:56201864
|
C | G | 1 | a0001c0001t0004g0237 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.161+9248C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56201864 | ||||||
| chr16:56201963
|
G | A | 1 | a0001c0001t0003g0246 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.161+9347G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56201963 | ||||||
| chr16:56201974
|
T | C | 9 | a0001c0001t0001g0258a0001c0001t0004g0002a0001c0001t0004g0287others(6): Show | 10 | HG02015.hp1 HG02717.hp2 HG03225.hp2 others(7): Show |
intron_variant | MODIFIER | c.161+9358T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56201974 | ||||||
| chr16:56202036
|
A | C | 1 | a0001c0002t0014g0058 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.161+9420A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56202036 | ||||||
| chr16:56202319
|
A | C | 1 | a0001c0002t0003g0136 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.161+9703A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56202319 | ||||||
| chr16:56202372
|
C | G | 1 | a0001c0002t0015g0135 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.161+9756C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56202372 | ||||||
| chr16:56202424
|
G | A | 1 | a0001c0002t0002g0066 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.161+9808G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56202424 | ||||||
| chr16:56202536
|
G | A | 41 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(38): Show | 41 | HG00438.hp1 HG00642.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.161+9920G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56202536 | ||||||
| chr16:56202606
|
C | T | 2 | a0001c0001t0001g0177a0001c0001t0004g0178 | 2 | NA18612.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.161+9990C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56202606 | ||||||
| chr16:56202649
|
G | A | 41 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(38): Show | 41 | HG00438.hp1 HG00642.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.161+10033G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56202649 | ||||||
| chr16:56202784
|
A | G | 23 | a0001c0001t0001g0192a0001c0001t0001g0196a0001c0001t0001g0231others(20): Show | 23 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(20): Show |
intron_variant | MODIFIER | c.161+10168A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56202784 | ||||||
| chr16:56202878
|
C | T | 2 | a0001c0002t0006g0133a0001c0002t0006g0134 | 2 | NA18942.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.161+10262C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56202878 | ||||||
| chr16:56202949
|
G | A | 1 | a0001c0002t0002g0283 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.161+10333G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56202949 | ||||||
| chr16:56202951
|
A | C | 1 | a0001c0001t0004g0296 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.161+10335A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56202951 | ||||||
| chr16:56203078
|
A | G | 2 | a0001c0002t0001g0279a0001c0002t0002g0260 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.161+10462A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56203078 | ||||||
| chr16:56203089
|
G | A | 1 | a0001c0001t0002g0261 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.161+10473G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56203089 | ||||||
| chr16:56203153
|
G | A | 1 | a0001c0002t0002g0029 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.161+10537G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56203153 | ||||||
| chr16:56203241
|
C | T | 1 | a0001c0001t0001g0132 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.161+10625C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56203241 | ||||||
| chr16:56203365
|
C | A | 1 | a0001c0002t0004g0067 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.161+10749C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56203365 | ||||||
| chr16:56203365
|
C | G | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.161+10749C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56203365 | ||||||
| chr16:56203425
|
G | A | 1 | a0001c0001t0024g0068 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.161+10809G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56203425 | ||||||
| chr16:56203805
|
G | A | 2 | a0001c0001t0001g0062a0001c0002t0002g0061 | 2 | HG00140.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.161+11189G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56203805 | ||||||
| chr16:56204190
|
A | G | 5 | a0001c0001t0003g0289a0001c0001t0017g0290a0001c0002t0001g0288others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.161+11574A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56204190 | ||||||
| chr16:56204921
|
A | G | 4 | a0001c0001t0001g0153a0001c0001t0002g0150a0001c0002t0001g0151others(1): Show | 4 | HG01361.hp2 HG01516.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.161+12305A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56204921 | ||||||
| chr16:56204993
|
C | G | 1 | a0001c0002t0006g0197 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.161+12377C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56204993 | ||||||
| chr16:56205161
|
G | A | 9 | a0001c0001t0001g0258a0001c0001t0004g0002a0001c0001t0004g0287others(6): Show | 10 | HG02015.hp1 HG02717.hp2 HG03225.hp2 others(7): Show |
intron_variant | MODIFIER | c.161+12545G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56205161 | ||||||
| chr16:56205220
|
G | T | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.161+12604G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56205220 | ||||||
| chr16:56205266
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.161+12650A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56205266 | ||||||
| chr16:56205312
|
G | C | 121 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0024others(118): Show | 122 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.161+12696G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56205312 | ||||||
| chr16:56205355
|
A | C | 1 | a0001c0001t0004g0296 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.161+12739A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56205355 | ||||||
| chr16:56205356
|
G | C | 1 | a0001c0001t0004g0296 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.161+12740G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56205356 | ||||||
| chr16:56205503
|
A | T | 2 | a0001c0001t0001g0011a0001c0001t0003g0131 | 2 | NA18978.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.161+12887A>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56205503 | ||||||
| chr16:56205676
|
GGCCATTG others(8): Show |
G | 41 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(38): Show | 41 | HG00438.hp1 HG00642.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.161+13066_161+1308 others(19): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56205676 | |||||
| chr16:56205741
|
A | T | 1 | a0001c0002t0002g0029 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.161+13125A>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56205741 | ||||||
| chr16:56205855
|
G | C | 32 | a0001c0001t0001g0258a0001c0001t0001g0262a0001c0001t0001g0270others(29): Show | 33 | HG00423.hp2 HG00673.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.161+13239G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56205855 | ||||||
| chr16:56206006
|
A | G | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.161+13390A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56206006 | ||||||
| chr16:56206096
|
G | T | 1 | a0001c0001t0001g0276 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.161+13480G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56206096 | ||||||
| chr16:56206215
|
G | C | 2 | a0001c0001t0001g0177a0001c0001t0004g0178 | 2 | NA18612.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.161+13599G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56206215 | ||||||
| chr16:56206230
|
G | T | 1 | a0001c0004t0002g0028 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.161+13614G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56206230 | ||||||
| chr16:56206260
|
C | T | 1 | a0001c0002t0027g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.161+13644C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56206260 | ||||||
| chr16:56206269
|
G | A | 1 | a0001c0002t0002g0190 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.161+13653G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56206269 | ||||||
| chr16:56206324
|
T | A | 3 | a0001c0001t0003g0289a0001c0001t0017g0290a0001c0002t0001g0288 | 3 | HG01884.hp1 HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.161+13708T>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56206324 | ||||||
| chr16:56206324
|
T | TA | 52 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(49): Show | 52 | HG00438.hp1 HG00642.hp2 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.161+13729dupA | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56206324 | |||||
| chr16:56206324
|
TA | T | 14 | a0001c0001t0001g0024a0001c0001t0001g0164a0001c0001t0001g0242others(11): Show | 14 | HG00323.hp2 HG00609.hp2 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.161+13729delA | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56206324 | |||||
| chr16:56206419
|
C | T | 9 | a0001c0001t0002g0253a0001c0001t0003g0246a0001c0001t0006g0255others(6): Show | 9 | HG00673.hp1 HG01256.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.161+13803C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56206419 | ||||||
| chr16:56206468
|
G | T | 35 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0049others(32): Show | 35 | HG00438.hp1 HG00642.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.161+13852G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56206468 | ||||||
| chr16:56206485
|
A | C | 1 | a0001c0002t0010g0274 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.161+13869A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56206485 | ||||||
| chr16:56206648
|
G | A | 1 | a0001c0004t0002g0028 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.161+14032G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56206648 | ||||||
| chr16:56206693
|
A | C | 1 | a0001c0002t0004g0124 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.161+14077A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56206693 | ||||||
| chr16:56206770
|
C | T | 33 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(30): Show | 33 | HG00438.hp1 HG00642.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.161+14154C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56206770 | ||||||
| chr16:56206973
|
T | C | 3 | a0001c0001t0001g0199a0001c0001t0003g0200a0001c0001t0005g0186 | 3 | NA18942.hp1 NA18960.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.161+14357T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56206973 | ||||||
| chr16:56206982
|
A | T | 2 | a0001c0001t0004g0178a0001c0001t0004g0237 | 2 | HG02027.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.161+14366A>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56206982 | ||||||
| chr16:56206983
|
T | C | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.161+14367T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56206983 | ||||||
| chr16:56207092
|
T | C | 3 | a0001c0001t0008g0036a0001c0001t0008g0037a0001c0001t0026g0003 | 3 | NA18973.hp2 NA18994.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.161+14476T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56207092 | ||||||
| chr16:56207305
|
A | C | 1 | a0001c0004t0002g0028 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.161+14689A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56207305 | ||||||
| chr16:56207558
|
T | G | 197 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(194): Show | 199 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.161+14942T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56207558 | ||||||
| chr16:56207581
|
C | T | 1 | a0001c0004t0002g0028 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.161+14965C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56207581 | ||||||
| chr16:56207586
|
T | C | 75 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(72): Show | 76 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.161+14970T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56207586 | ||||||
| chr16:56207600
|
C | T | 1 | a0001c0002t0023g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.161+14984C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56207600 | ||||||
| chr16:56207738
|
A | G | 1 | a0001c0002t0002g0029 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.161+15122A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56207738 | ||||||
| chr16:56207955
|
C | T | 1 | a0001c0001t0004g0161 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.161+15339C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56207955 | ||||||
| chr16:56208049
|
A | G | 2 | a0001c0001t0001g0062a0001c0002t0002g0061 | 2 | HG00140.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.161+15433A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56208049 | ||||||
| chr16:56208119
|
A | G | 75 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(72): Show | 76 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.161+15503A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56208119 | ||||||
| chr16:56208132
|
T | C | 1 | a0001c0001t0003g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.161+15516T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56208132 | ||||||
| chr16:56208231
|
T | C | 75 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(72): Show | 76 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.161+15615T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56208231 | ||||||
| chr16:56208257
|
A | C | 1 | a0001c0001t0001g0049 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.161+15641A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56208257 | ||||||
| chr16:56208270
|
T | C | 197 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(194): Show | 199 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.161+15654T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56208270 | ||||||
| chr16:56208272
|
C | T | 1 | a0001c0002t0001g0249 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.161+15656C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56208272 | ||||||
| chr16:56208295
|
T | A | 1 | a0001c0002t0001g0239 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.161+15679T>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56208295 | ||||||
| chr16:56208419
|
A | ATG | 11 | a0001c0001t0001g0062a0001c0001t0001g0165a0001c0001t0001g0174others(8): Show | 11 | HG00099.hp1 HG00609.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.161+15832_161+1583 others(6): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56208419 | |||||
| chr16:56208419
|
ATG | A | 15 | a0001c0001t0001g0166a0001c0001t0003g0246a0001c0001t0004g0296others(12): Show | 15 | HG00673.hp1 HG01109.hp2 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.161+15832_161+1583 others(6): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56208419 | |||||
| chr16:56208419
|
ATGTG | A | 6 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0202others(3): Show | 6 | HG01928.hp2 HG02717.hp1 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.161+15830_161+1583 others(8): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56208419 | |||||
| chr16:56208434
|
TGTGTGTG others(21): Show |
T | 1 | a0001c0002t0002g0029 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.161+15833_161+1586 others(32): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56208434 | |||||
| chr16:56208440
|
TGTGTGTG others(3): Show |
T | 3 | a0001c0001t0006g0069a0001c0001t0007g0070a0001c0002t0004g0144 | 3 | HG02273.hp1 HG02293.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.161+15826_161+1583 others(14): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56208440 | |||||
| chr16:56208444
|
TGTGTGC | T | 14 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0071others(11): Show | 15 | HG00280.hp1 HG02027.hp1 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.161+15830_161+1583 others(10): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56208444 | |||||
| chr16:56208446
|
T | C | 3 | a0001c0001t0001g0262a0001c0002t0001g0263a0001c0002t0001g0279 | 3 | HG01109.hp1 HG02300.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.161+15830T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56208446 | ||||||
| chr16:56208446
|
TGTGC | T | 100 | a0001c0001t0001g0024a0001c0001t0001g0057a0001c0001t0001g0083others(97): Show | 100 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.161+15832_161+1583 others(8): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56208446 | |||||
| chr16:56208448
|
T | C | 69 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(66): Show | 70 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.161+15832T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56208448 | ||||||
| chr16:56208449
|
G | A | 3 | a0001c0002t0012g0179a0001c0002t0012g0180a0001c0002t0012g0181 | 3 | HG02280.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.161+15833G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56208449 | ||||||
| chr16:56208450
|
C | T | 3 | a0001c0001t0001g0062a0001c0001t0003g0030a0001c0002t0027g0146 | 3 | HG01496.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.161+15834C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56208450 | ||||||
| chr16:56208451
|
G | A | 1 | a0001c0002t0001g0288 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.161+15835G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56208451 | ||||||
| chr16:56208453
|
G | A | 2 | a0001c0002t0001g0013a0001c0002t0001g0204 | 2 | HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.161+15837G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56208453 | ||||||
| chr16:56208456
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.161+15840C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56208456 | ||||||
| chr16:56208458
|
CGCACGT | C | 35 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(32): Show | 35 | HG00438.hp1 HG00642.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.161+15844_161+1584 others(10): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56208458 | |||||
| chr16:56208460
|
CACGT | C | 19 | a0001c0001t0001g0153a0001c0001t0001g0258a0001c0001t0003g0289others(16): Show | 20 | HG01884.hp1 HG02015.hp1 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.161+15845_161+1584 others(8): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56208460 | ||||||
| chr16:56208460
|
CACGTGT | C | 15 | a0001c0001t0001g0270a0001c0001t0001g0276a0001c0001t0002g0261others(12): Show | 15 | HG00423.hp2 HG02080.hp2 HG02738.hp1 others(12): Show |
intron_variant | MODIFIER | c.161+15845_161+1585 others(10): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56208460 | ||||||
| chr16:56208461
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.161+15845A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56208461 | ||||||
| chr16:56208464
|
T | C | 3 | a0001c0001t0001g0182a0001c0001t0003g0030a0001c0002t0027g0146 | 3 | HG03225.hp1 HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.161+15848T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56208464 | ||||||
| chr16:56208466
|
T | C | 16 | a0001c0001t0001g0258a0001c0001t0003g0030a0001c0001t0003g0289others(13): Show | 17 | HG01884.hp1 HG02015.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.161+15850T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56208466 | ||||||
| chr16:56208565
|
G | A | 197 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(194): Show | 199 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.161+15949G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56208565 | ||||||
| chr16:56208567
|
A | C | 2 | a0001c0001t0004g0178a0001c0001t0004g0237 | 2 | HG02027.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.161+15951A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56208567 | ||||||
| chr16:56208661
|
A | G | 1 | a0001c0002t0002g0149 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.161+16045A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56208661 | ||||||
| chr16:56208887
|
G | A | 1 | a0001c0002t0006g0265 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.161+16271G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56208887 | ||||||
| chr16:56208958
|
A | G | 197 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(194): Show | 199 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.161+16342A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56208958 | ||||||
| chr16:56209136
|
A | C | 1 | a0001c0001t0001g0165 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.161+16520A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56209136 | ||||||
| chr16:56209354
|
A | G | 8 | a0001c0001t0001g0295a0001c0001t0004g0291a0001c0001t0004g0296others(5): Show | 8 | HG01891.hp1 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.161+16738A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56209354 | ||||||
| chr16:56209542
|
G | A | 6 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0002g0081others(3): Show | 6 | HG00735.hp1 HG01169.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.161+16926G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56209542 | ||||||
| chr16:56209589
|
C | T | 1 | a0001c0002t0002g0195 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.161+16973C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56209589 | ||||||
| chr16:56209606
|
A | G | 2 | a0001c0001t0004g0291a0001c0002t0002g0292 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.161+16990A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56209606 | ||||||
| chr16:56209812
|
A | G | 1 | a0001c0001t0001g0050 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.161+17196A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56209812 | ||||||
| chr16:56209832
|
C | G | 1 | a0001c0001t0014g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.161+17216C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56209832 | ||||||
| chr16:56209890
|
C | A | 2 | a0001c0002t0006g0133a0001c0002t0006g0134 | 2 | NA18942.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.161+17274C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56209890 | ||||||
| chr16:56209922
|
CT | C | 3 | a0001c0002t0001g0247a0001c0002t0001g0248a0001c0002t0001g0249 | 3 | HG02630.hp1 HG02723.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.161+17308delT | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56209922 | |||||
| chr16:56210206
|
A | C | 1 | a0001c0006t0021g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.161+17590A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56210206 | ||||||
| chr16:56210249
|
T | C | 2 | a0001c0001t0003g0085a0001c0002t0002g0086 | 2 | HG02257.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.161+17633T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56210249 | ||||||
| chr16:56210330
|
G | A | 1 | a0001c0001t0003g0017 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.161+17714G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56210330 | ||||||
| chr16:56210353
|
A | G | 17 | a0001c0001t0001g0262a0001c0001t0001g0270a0001c0001t0001g0276others(14): Show | 17 | HG00423.hp2 HG01109.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.161+17737A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56210353 | ||||||
| chr16:56210400
|
A | G | 1 | a0001c0001t0010g0123 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.161+17784A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56210400 | ||||||
| chr16:56210506
|
A | G | 2 | a0001c0001t0001g0163a0001c0002t0001g0013 | 2 | HG02109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.161+17890A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56210506 | ||||||
| chr16:56210732
|
G | A | 1 | a0001c0001t0005g0201 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.161+18116G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56210732 | ||||||
| chr16:56210769
|
G | A | 1 | a0001c0001t0003g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.161+18153G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56210769 | ||||||
| chr16:56210801
|
C | G | 75 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(72): Show | 76 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.161+18185C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56210801 | ||||||
| chr16:56210854
|
A | G | 75 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(72): Show | 76 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.161+18238A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56210854 | ||||||
| chr16:56210904
|
T | G | 122 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0024others(119): Show | 123 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.161+18288T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56210904 | ||||||
| chr16:56210911
|
T | C | 2 | a0001c0001t0001g0163a0001c0002t0001g0013 | 2 | HG02109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.161+18295T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56210911 | ||||||
| chr16:56211032
|
G | T | 75 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(72): Show | 76 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.161+18416G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56211032 | ||||||
| chr16:56211393
|
C | T | 3 | a0001c0001t0004g0002a0001c0001t0004g0287a0001c0002t0001g0286 | 4 | HG02015.hp1 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.161+18777C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56211393 | ||||||
| chr16:56211434
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.161+18818G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56211434 | ||||||
| chr16:56211482
|
G | A | 75 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(72): Show | 76 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.161+18866G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56211482 | ||||||
| chr16:56211770
|
C | T | 5 | a0001c0001t0001g0132a0001c0001t0011g0031a0001c0001t0011g0138others(2): Show | 5 | HG02132.hp1 NA18964.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.161+19154C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56211770 | ||||||
| chr16:56212104
|
C | CAG | 75 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(72): Show | 76 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.161+19488_161+1948 others(6): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56212104 | ||||||
| chr16:56212104
|
C | T | 5 | a0001c0002t0001g0236a0001c0002t0002g0190a0001c0002t0003g0233others(2): Show | 5 | HG00733.hp2 HG02698.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.161+19488C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56212104 | ||||||
| chr16:56212170
|
A | G | 1 | a0001c0001t0001g0280 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.161+19554A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56212170 | ||||||
| chr16:56212258
|
C | T | 75 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(72): Show | 76 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.161+19642C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56212258 | ||||||
| chr16:56212279
|
C | T | 1 | a0001c0004t0002g0028 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.161+19663C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56212279 | ||||||
| chr16:56212280
|
G | T | 75 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(72): Show | 76 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.161+19664G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56212280 | ||||||
| chr16:56212293
|
C | T | 1 | a0001c0001t0009g0060 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.161+19677C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56212293 | ||||||
| chr16:56212327
|
G | A | 1 | a0001c0002t0001g0249 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.161+19711G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56212327 | ||||||
| chr16:56212402
|
G | T | 75 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(72): Show | 76 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.161+19786G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56212402 | ||||||
| chr16:56212407
|
G | A | 1 | a0001c0004t0002g0028 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.161+19791G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56212407 | ||||||
| chr16:56212427
|
C | G | 5 | a0001c0001t0001g0132a0001c0001t0011g0031a0001c0001t0011g0138others(2): Show | 5 | HG02132.hp1 NA18964.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.161+19811C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56212427 | ||||||
| chr16:56212458
|
A | T | 205 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(202): Show | 207 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.161+19842A>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56212458 | ||||||
| chr16:56212586
|
G | T | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.161+19970G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56212586 | ||||||
| chr16:56212966
|
G | T | 3 | a0001c0002t0001g0119a0001c0002t0001g0120a0001c0002t0003g0137 | 3 | HG00639.hp1 HG00642.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.161+20350G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56212966 | ||||||
| chr16:56213065
|
G | A | 75 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(72): Show | 76 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.161+20449G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56213065 | ||||||
| chr16:56213209
|
T | G | 2 | a0001c0002t0001g0119a0001c0002t0001g0120 | 2 | HG00639.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.161+20593T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56213209 | ||||||
| chr16:56213246
|
C | T | 75 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(72): Show | 76 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.161+20630C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56213246 | ||||||
| chr16:56213408
|
T | C | 2 | a0001c0001t0001g0163a0001c0002t0001g0013 | 2 | HG02109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.161+20792T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56213408 | ||||||
| chr16:56213419
|
T | C | 1 | a0001c0002t0002g0004 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.161+20803T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56213419 | ||||||
| chr16:56213629
|
C | T | 1 | a0001c0002t0014g0033 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.161+21013C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56213629 | ||||||
| chr16:56213754
|
A | G | 1 | a0001c0004t0002g0028 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.161+21138A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56213754 | ||||||
| chr16:56213833
|
CA | C | 75 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(72): Show | 76 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.161+21226delA | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56213833 | |||||
| chr16:56213909
|
C | A | 2 | a0001c0001t0004g0178a0001c0001t0004g0237 | 2 | HG02027.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.161+21293C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56213909 | ||||||
| chr16:56213919
|
A | G | 17 | a0001c0001t0001g0262a0001c0001t0001g0270a0001c0001t0001g0276others(14): Show | 17 | HG00423.hp2 HG01109.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.161+21303A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56213919 | ||||||
| chr16:56214064
|
T | A | 33 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(30): Show | 33 | HG00438.hp1 HG00642.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.161+21448T>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56214064 | ||||||
| chr16:56214064
|
T | C | 1 | a0001c0002t0002g0087 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.161+21448T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56214064 | ||||||
| chr16:56214202
|
G | A | 1 | a0001c0002t0004g0205 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.161+21586G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56214202 | ||||||
| chr16:56214223
|
C | T | 41 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(38): Show | 41 | HG00438.hp1 HG00642.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.161+21607C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56214223 | ||||||
| chr16:56214273
|
T | C | 2 | a0001c0001t0001g0166a0001c0001t0011g0203 | 2 | NA19011.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.161+21657T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56214273 | ||||||
| chr16:56214358
|
C | T | 1 | a0001c0002t0002g0118 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.161+21742C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56214358 | ||||||
| chr16:56214389
|
G | A | 1 | a0001c0002t0023g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.161+21773G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56214389 | ||||||
| chr16:56214508
|
T | C | 1 | a0002c0005t0003g0088 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.161+21892T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56214508 | ||||||
| chr16:56214566
|
G | A | 1 | a0001c0002t0001g0191 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.161+21950G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56214566 | ||||||
| chr16:56214604
|
A | G | 1 | a0001c0001t0005g0048 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.161+21988A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56214604 | ||||||
| chr16:56214659
|
A | G | 1 | a0001c0002t0001g0013 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.161+22043A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56214659 | ||||||
| chr16:56214872
|
G | A | 1 | a0001c0002t0023g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.161+22256G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56214872 | ||||||
| chr16:56215002
|
A | G | 1 | a0001c0002t0003g0275 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.161+22386A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56215002 | ||||||
| chr16:56215088
|
T | C | 17 | a0001c0001t0001g0262a0001c0001t0001g0270a0001c0001t0001g0276others(14): Show | 17 | HG00423.hp2 HG01109.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.161+22472T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56215088 | ||||||
| chr16:56215624
|
G | T | 197 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(194): Show | 199 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.161+23008G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56215624 | ||||||
| chr16:56215649
|
C | T | 3 | a0001c0001t0001g0079a0001c0002t0001g0117a0001c0002t0004g0067 | 3 | HG02622.hp1 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.161+23033C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56215649 | ||||||
| chr16:56215862
|
G | A | 57 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0071others(54): Show | 57 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.161+23246G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56215862 | ||||||
| chr16:56215909
|
C | A | 2 | a0001c0001t0004g0178a0001c0001t0004g0237 | 2 | HG02027.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.161+23293C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56215909 | ||||||
| chr16:56215975
|
G | A | 121 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0024others(118): Show | 122 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.161+23359G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56215975 | ||||||
| chr16:56216239
|
A | G | 9 | a0001c0001t0001g0258a0001c0001t0004g0002a0001c0001t0004g0287others(6): Show | 10 | HG02015.hp1 HG02717.hp2 HG03225.hp2 others(7): Show |
intron_variant | MODIFIER | c.161+23623A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56216239 | ||||||
| chr16:56216364
|
G | A | 2 | a0001c0002t0004g0277a0001c0002t0004g0278 | 2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.161+23748G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56216364 | ||||||
| chr16:56216543
|
C | T | 1 | a0001c0002t0023g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.161+23927C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56216543 | ||||||
| chr16:56216638
|
G | A | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.161+24022G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56216638 | ||||||
| chr16:56216639
|
A | T | 1 | a0001c0001t0001g0079 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.161+24023A>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56216639 | ||||||
| chr16:56216707
|
A | G | 1 | a0001c0001t0004g0296 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.161+24091A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56216707 | ||||||
| chr16:56216732
|
A | G | 1 | a0001c0001t0001g0024 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.161+24116A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56216732 | ||||||
| chr16:56216785
|
G | A | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG00642.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.161+24169G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56216785 | ||||||
| chr16:56217063
|
A | G | 9 | a0001c0001t0001g0258a0001c0001t0004g0002a0001c0001t0004g0287others(6): Show | 10 | HG02015.hp1 HG02717.hp2 HG03225.hp2 others(7): Show |
intron_variant | MODIFIER | c.161+24447A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56217063 | ||||||
| chr16:56217073
|
A | G | 9 | a0001c0001t0001g0258a0001c0001t0004g0002a0001c0001t0004g0287others(6): Show | 10 | HG02015.hp1 HG02717.hp2 HG03225.hp2 others(7): Show |
intron_variant | MODIFIER | c.161+24457A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56217073 | ||||||
| chr16:56217158
|
A | G | 1 | a0001c0002t0023g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.161+24542A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56217158 | ||||||
| chr16:56217201
|
G | A | 1 | a0001c0002t0001g0064 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.161+24585G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56217201 | ||||||
| chr16:56217273
|
G | A | 1 | a0001c0002t0027g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.161+24657G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56217273 | ||||||
| chr16:56217572
|
T | C | 5 | a0001c0001t0014g0034a0001c0002t0001g0035a0001c0002t0001g0054others(2): Show | 5 | HG02559.hp2 HG02965.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.161+24956T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56217572 | ||||||
| chr16:56217576
|
A | G | 17 | a0001c0001t0001g0262a0001c0001t0001g0270a0001c0001t0001g0276others(14): Show | 17 | HG00423.hp2 HG01109.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.161+24960A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56217576 | ||||||
| chr16:56217675
|
A | G | 17 | a0001c0001t0001g0262a0001c0001t0001g0270a0001c0001t0001g0276others(14): Show | 17 | HG00423.hp2 HG01109.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.161+25059A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56217675 | ||||||
| chr16:56217682
|
G | T | 3 | a0001c0001t0001g0024a0001c0001t0001g0077a0001c0001t0001g0164 | 3 | NA18955.hp2 NA18982.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.161+25066G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56217682 | ||||||
| chr16:56217706
|
C | G | 1 | a0001c0001t0001g0007 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.161+25090C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56217706 | ||||||
| chr16:56217857
|
G | A | 1 | a0001c0001t0001g0167 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.161+25241G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56217857 | ||||||
| chr16:56218017
|
A | G | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.161+25401A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56218017 | ||||||
| chr16:56218518
|
C | T | 1 | a0001c0002t0002g0029 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.161+25902C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56218518 | ||||||
| chr16:56218764
|
G | A | 3 | a0001c0002t0001g0247a0001c0002t0001g0248a0001c0002t0001g0249 | 3 | HG02630.hp1 HG02723.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.161+26148G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56218764 | ||||||
| chr16:56218814
|
A | G | 75 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(72): Show | 76 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.161+26198A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56218814 | ||||||
| chr16:56218986
|
C | T | 5 | a0001c0001t0001g0295a0001c0001t0004g0291a0001c0002t0001g0294others(2): Show | 5 | HG02970.hp1 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.161+26370C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56218986 | ||||||
| chr16:56219006
|
C | T | 1 | a0001c0002t0010g0274 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.161+26390C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56219006 | ||||||
| chr16:56219148
|
G | A | 1 | a0001c0001t0024g0068 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.161+26532G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56219148 | ||||||
| chr16:56219229
|
C | T | 75 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(72): Show | 76 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.161+26613C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56219229 | ||||||
| chr16:56219361
|
G | T | 1 | a0001c0002t0002g0190 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.161+26745G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56219361 | ||||||
| chr16:56219406
|
C | T | 1 | a0001c0001t0003g0246 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.161+26790C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56219406 | ||||||
| chr16:56219723
|
G | C | 1 | a0001c0002t0002g0260 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.161+27107G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56219723 | ||||||
| chr16:56219780
|
C | T | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.161+27164C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56219780 | ||||||
| chr16:56219928
|
G | A | 5 | a0001c0001t0003g0289a0001c0001t0017g0290a0001c0002t0001g0288others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.161+27312G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56219928 | ||||||
| chr16:56219977
|
C | A | 2 | a0001c0002t0004g0277a0001c0002t0004g0278 | 2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.161+27361C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56219977 | ||||||
| chr16:56220146
|
T | C | 2 | a0001c0002t0001g0035a0001c0002t0013g0032 | 2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.161+27530T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56220146 | ||||||
| chr16:56220466
|
C | G | 1 | a0001c0002t0002g0029 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.161+27850C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56220466 | ||||||
| chr16:56220517
|
T | C | 5 | a0001c0001t0003g0289a0001c0001t0017g0290a0001c0002t0001g0288others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.161+27901T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56220517 | ||||||
| chr16:56220570
|
T | TA | 38 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(35): Show | 38 | HG00438.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.161+27960dupA | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56220570 | |||||
| chr16:56220734
|
G | A | 1 | a0001c0001t0005g0206 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.161+28118G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56220734 | ||||||
| chr16:56220738
|
T | G | 14 | a0001c0001t0001g0166a0001c0001t0002g0253a0001c0001t0003g0246others(11): Show | 14 | HG00673.hp1 HG01256.hp2 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.161+28122T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56220738 | ||||||
| chr16:56220738
|
T | TTTG | 7 | a0001c0001t0001g0145a0001c0001t0004g0002a0001c0001t0004g0287others(4): Show | 8 | HG02074.hp1 HG03225.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.161+28146_161+2814 others(7): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56220738 | |||||
| chr16:56220750
|
G | T | 18 | a0001c0001t0001g0192a0001c0001t0001g0196a0001c0001t0001g0231others(15): Show | 18 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.161+28134G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56220750 | ||||||
| chr16:56220845
|
T | A | 1 | a0001c0001t0001g0098 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.161+28229T>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56220845 | ||||||
| chr16:56220937
|
A | G | 1 | a0001c0004t0002g0028 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.161+28321A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56220937 | ||||||
| chr16:56221024
|
G | A | 123 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0024others(120): Show | 124 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.161+28408G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56221024 | ||||||
| chr16:56221025
|
C | G | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.161+28409C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56221025 | ||||||
| chr16:56221249
|
AT | A | 75 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(72): Show | 76 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.161+28641delT | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56221249 | |||||
| chr16:56221441
|
G | A | 23 | a0001c0001t0001g0192a0001c0001t0001g0196a0001c0001t0001g0231others(20): Show | 23 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(20): Show |
intron_variant | MODIFIER | c.161+28825G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56221441 | ||||||
| chr16:56221443
|
A | G | 1 | a0001c0001t0017g0244 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.161+28827A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56221443 | ||||||
| chr16:56221444
|
G | A | 1 | a0001c0001t0017g0244 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.161+28828G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56221444 | ||||||
| chr16:56221558
|
G | A | 5 | a0001c0001t0003g0289a0001c0001t0017g0290a0001c0002t0001g0288others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.161+28942G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56221558 | ||||||
| chr16:56221581
|
C | A | 1 | a0001c0001t0015g0251 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.161+28965C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56221581 | ||||||
| chr16:56221604
|
C | T | 75 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(72): Show | 76 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.161+28988C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56221604 | ||||||
| chr16:56221651
|
C | CA | 9 | a0001c0001t0003g0208a0001c0001t0003g0238a0001c0001t0004g0207others(6): Show | 9 | HG01978.hp1 HG02080.hp1 HG03579.hp1 others(6): Show |
intron_variant | MODIFIER | c.161+29058dupA | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56221651 | |||||
| chr16:56221651
|
CA | C | 103 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0024others(100): Show | 104 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.161+29058delA | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56221651 | |||||
| chr16:56221651
|
CAAAA | C | 10 | a0001c0001t0001g0041a0001c0001t0002g0261a0001c0001t0007g0038others(7): Show | 10 | HG00642.hp2 HG00733.hp1 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.161+29055_161+2905 others(8): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56221651 | |||||
| chr16:56221651
|
CAAAAA | C | 65 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0049others(62): Show | 66 | HG00423.hp2 HG00438.hp1 HG01109.hp1 others(63): Show |
intron_variant | MODIFIER | c.161+29054_161+2905 others(9): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56221651 | |||||
| chr16:56221778
|
A | G | 2 | a0001c0002t0001g0279a0001c0002t0002g0260 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.161+29162A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56221778 | ||||||
| chr16:56221852
|
T | G | 1 | a0001c0001t0001g0182 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.161+29236T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56221852 | ||||||
| chr16:56222029
|
C | T | 1 | a0001c0001t0007g0156 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.161+29413C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56222029 | ||||||
| chr16:56222044
|
T | C | 75 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(72): Show | 76 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.161+29428T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56222044 | ||||||
| chr16:56222214
|
C | A | 3 | a0001c0002t0012g0179a0001c0002t0012g0180a0001c0002t0012g0181 | 3 | HG02280.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.161+29598C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56222214 | ||||||
| chr16:56222231
|
AG | A | 6 | a0001c0001t0001g0295a0001c0001t0004g0291a0001c0001t0004g0296others(3): Show | 6 | HG01891.hp1 HG02970.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.161+29618delG | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56222231 | |||||
| chr16:56222498
|
C | G | 124 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0024others(121): Show | 125 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.161+29882C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56222498 | ||||||
| chr16:56222517
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.161+29901G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56222517 | ||||||
| chr16:56222652
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.161+30036G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56222652 | ||||||
| chr16:56222683
|
G | A | 32 | a0001c0001t0001g0258a0001c0001t0001g0262a0001c0001t0001g0270others(29): Show | 33 | HG00423.hp2 HG01109.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.161+30067G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56222683 | ||||||
| chr16:56222740
|
G | A | 75 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(72): Show | 76 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.161+30124G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56222740 | ||||||
| chr16:56222743
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.161+30127G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56222743 | ||||||
| chr16:56222753
|
C | T | 1 | a0001c0002t0001g0013 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.161+30137C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56222753 | ||||||
| chr16:56222944
|
T | C | 2 | a0001c0001t0003g0030a0001c0002t0004g0021 | 2 | NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.161+30328T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56222944 | ||||||
| chr16:56223087
|
C | T | 75 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(72): Show | 76 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.161+30471C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56223087 | ||||||
| chr16:56223173
|
G | C | 1 | a0001c0002t0002g0029 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.161+30557G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56223173 | ||||||
| chr16:56223173
|
G | T | 2 | a0001c0002t0003g0001a0001c0002t0027g0146 | 3 | HG03225.hp1 NA18973.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.161+30557G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56223173 | ||||||
| chr16:56223270
|
G | C | 76 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(73): Show | 77 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.161+30654G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56223270 | ||||||
| chr16:56223595
|
G | T | 74 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(71): Show | 75 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.161+30979G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56223595 | ||||||
| chr16:56223596
|
C | T | 74 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(71): Show | 75 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.161+30980C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56223596 | ||||||
| chr16:56223669
|
G | T | 1 | a0001c0002t0002g0139 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.161+31053G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56223669 | ||||||
| chr16:56223673
|
A | C | 1 | a0001c0001t0004g0023 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.161+31057A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56223673 | ||||||
| chr16:56223688
|
G | A | 30 | a0001c0001t0001g0258a0001c0001t0001g0262a0001c0001t0001g0270others(27): Show | 31 | HG00423.hp2 HG01109.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.161+31072G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56223688 | ||||||
| chr16:56223756
|
A | G | 1 | a0001c0001t0001g0295 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.161+31140A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56223756 | ||||||
| chr16:56223767
|
C | T | 1 | a0001c0002t0003g0137 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.161+31151C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56223767 | ||||||
| chr16:56223768
|
G | A | 3 | a0001c0002t0001g0055a0001c0002t0001g0056a0001c0002t0014g0058 | 3 | HG02258.hp2 HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.161+31152G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56223768 | ||||||
| chr16:56223869
|
A | G | 1 | a0001c0002t0014g0033 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.161+31253A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56223869 | ||||||
| chr16:56224055
|
C | G | 64 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(61): Show | 65 | HG00438.hp1 HG00642.hp2 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.161+31439C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56224055 | ||||||
| chr16:56224055
|
C | T | 1 | a0001c0004t0002g0028 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.161+31439C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56224055 | ||||||
| chr16:56224061
|
C | G | 1 | a0001c0001t0001g0182 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.161+31445C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56224061 | ||||||
| chr16:56224115
|
G | T | 2 | a0001c0001t0003g0030a0001c0002t0004g0021 | 2 | NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.161+31499G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56224115 | ||||||
| chr16:56224155
|
C | T | 2 | a0001c0002t0001g0198a0001c0002t0002g0194 | 2 | HG00140.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.161+31539C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56224155 | ||||||
| chr16:56224163
|
C | G | 2 | a0001c0001t0001g0078a0001c0002t0015g0135 | 2 | HG01928.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.161+31547C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56224163 | ||||||
| chr16:56224303
|
C | T | 1 | a0001c0002t0001g0236 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.161+31687C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56224303 | ||||||
| chr16:56224371
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0003g0131 | 2 | NA18978.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.161+31755C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56224371 | ||||||
| chr16:56224372
|
C | T | 3 | a0001c0001t0001g0145a0001c0002t0004g0143a0001c0002t0004g0144 | 3 | HG03540.hp1 NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.161+31756C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56224372 | ||||||
| chr16:56224390
|
A | G | 14 | a0001c0001t0001g0166a0001c0001t0002g0253a0001c0001t0003g0246others(11): Show | 14 | HG00673.hp1 HG01256.hp2 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.161+31774A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56224390 | ||||||
| chr16:56224403
|
G | A | 1 | a0001c0002t0003g0275 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.161+31787G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56224403 | ||||||
| chr16:56224504
|
G | A | 4 | a0001c0001t0001g0284a0001c0002t0002g0283a0001c0004t0002g0282others(1): Show | 4 | HG02055.hp2 HG02109.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.161+31888G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56224504 | ||||||
| chr16:56224508
|
C | T | 31 | a0001c0001t0001g0258a0001c0001t0001g0262a0001c0001t0001g0270others(28): Show | 32 | HG00423.hp2 HG01109.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.161+31892C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56224508 | ||||||
| chr16:56224635
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.161+32019A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56224635 | ||||||
| chr16:56224854
|
G | C | 40 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(37): Show | 40 | HG00438.hp1 HG00642.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.161+32238G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56224854 | ||||||
| chr16:56225197
|
G | A | 4 | a0001c0001t0001g0057a0001c0002t0001g0055a0001c0002t0001g0056others(1): Show | 4 | HG02258.hp2 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.161+32581G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56225197 | ||||||
| chr16:56225278
|
G | T | 2 | a0001c0001t0004g0002a0001c0001t0004g0287 | 3 | HG03491.hp2 HG03492.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.161+32662G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56225278 | ||||||
| chr16:56225536
|
T | A | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | NA18998.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.161+32920T>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56225536 | ||||||
| chr16:56225602
|
G | A | 1 | a0001c0002t0001g0266 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.161+32986G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56225602 | ||||||
| chr16:56225860
|
T | C | 1 | a0001c0002t0001g0247 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.161+33244T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56225860 | ||||||
| chr16:56226059
|
G | A | 1 | a0002c0005t0003g0088 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.161+33443G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56226059 | ||||||
| chr16:56226095
|
T | C | 1 | a0001c0002t0004g0267 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.161+33479T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56226095 | ||||||
| chr16:56226108
|
G | A | 2 | a0001c0001t0004g0178a0001c0001t0004g0237 | 2 | HG02027.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.161+33492G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56226108 | ||||||
| chr16:56226126
|
G | A | 1 | a0001c0002t0023g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.161+33510G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56226126 | ||||||
| chr16:56226367
|
T | G | 153 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0024others(150): Show | 155 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.161+33751T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56226367 | ||||||
| chr16:56226556
|
G | A | 1 | a0001c0001t0005g0256 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.161+33940G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56226556 | ||||||
| chr16:56226561
|
C | T | 1 | a0001c0002t0023g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.161+33945C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56226561 | ||||||
| chr16:56226776
|
C | T | 1 | a0001c0004t0002g0028 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.161+34160C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56226776 | ||||||
| chr16:56226863
|
C | A | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.161+34247C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56226863 | ||||||
| chr16:56226980
|
G | A | 75 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(72): Show | 76 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.161+34364G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56226980 | ||||||
| chr16:56227065
|
G | A | 2 | a0001c0001t0001g0163a0001c0002t0001g0013 | 2 | HG02109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.161+34449G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56227065 | ||||||
| chr16:56227128
|
A | G | 1 | a0001c0001t0005g0225 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.161+34512A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56227128 | ||||||
| chr16:56227218
|
G | GC | 5 | a0001c0001t0004g0207a0001c0001t0005g0230a0001c0002t0001g0119others(2): Show | 5 | HG01978.hp1 HG03927.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.161+34607dupC | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56227218 | |||||
| chr16:56227223
|
C | T | 3 | a0001c0002t0001g0247a0001c0002t0001g0248a0001c0002t0001g0249 | 3 | HG02630.hp1 HG02723.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.161+34607C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56227223 | ||||||
| chr16:56227282
|
C | T | 1 | a0001c0002t0001g0173 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.161+34666C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56227282 | ||||||
| chr16:56227319
|
C | T | 2 | a0001c0001t0004g0178a0001c0001t0004g0237 | 2 | HG02027.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.161+34703C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56227319 | ||||||
| chr16:56227347
|
G | A | 1 | a0001c0004t0002g0028 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.161+34731G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56227347 | ||||||
| chr16:56227517
|
T | G | 119 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0024others(116): Show | 120 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.161+34901T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56227517 | ||||||
| chr16:56227629
|
A | G | 1 | a0001c0001t0009g0140 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.161+35013A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56227629 | ||||||
| chr16:56227687
|
C | CA | 13 | a0001c0001t0001g0057a0001c0001t0001g0163a0001c0001t0003g0238others(10): Show | 13 | HG01106.hp2 HG01934.hp1 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.161+35096dupA | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56227687 | |||||
| chr16:56227687
|
C | CAA | 99 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0062others(96): Show | 100 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.161+35095_161+3509 others(6): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56227687 | |||||
| chr16:56227687
|
C | CAAA | 16 | a0001c0001t0001g0024a0001c0001t0001g0077a0001c0001t0001g0164others(13): Show | 16 | HG00735.hp1 HG00735.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.161+35094_161+3509 others(7): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56227687 | |||||
| chr16:56227687
|
CA | C | 53 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0049others(50): Show | 54 | HG00642.hp2 HG00733.hp1 HG01258.hp2 others(51): Show |
intron_variant | MODIFIER | c.161+35096delA | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56227687 | |||||
| chr16:56227687
|
CAA | C | 24 | a0001c0001t0001g0262a0001c0001t0001g0270a0001c0001t0001g0276others(21): Show | 24 | HG00423.hp2 HG01109.hp1 HG01517.hp2 others(21): Show |
intron_variant | MODIFIER | c.161+35095_161+3509 others(6): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56227687 | |||||
| chr16:56227764
|
C | T | 2 | a0001c0001t0004g0178a0001c0001t0004g0237 | 2 | HG02027.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.161+35148C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56227764 | ||||||
| chr16:56227837
|
G | C | 42 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(39): Show | 42 | HG00438.hp1 HG00642.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.161+35221G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56227837 | ||||||
| chr16:56227867
|
T | A | 1 | a0001c0002t0002g0214 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.161+35251T>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56227867 | ||||||
| chr16:56227907
|
C | T | 1 | a0001c0002t0001g0076 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.161+35291C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56227907 | ||||||
| chr16:56228085
|
G | C | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.161+35469G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56228085 | ||||||
| chr16:56228156
|
C | T | 75 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(72): Show | 76 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.161+35540C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56228156 | ||||||
| chr16:56228206
|
A | G | 2 | a0001c0001t0004g0178a0001c0001t0004g0237 | 2 | HG02027.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.161+35590A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56228206 | ||||||
| chr16:56228213
|
A | G | 197 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(194): Show | 199 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.161+35597A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56228213 | ||||||
| chr16:56228254
|
G | A | 1 | a0001c0001t0003g0017 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.161+35638G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56228254 | ||||||
| chr16:56228448
|
T | C | 1 | a0001c0002t0023g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.161+35832T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56228448 | ||||||
| chr16:56228668
|
G | A | 75 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(72): Show | 76 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.161+36052G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56228668 | ||||||
| chr16:56228826
|
GCC | G | 3 | a0001c0001t0003g0289a0001c0001t0017g0290a0001c0002t0001g0288 | 3 | HG01884.hp1 HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.161+36213_161+3621 others(6): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56228826 | |||||
| chr16:56228900
|
T | C | 1 | a0001c0002t0001g0054 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.161+36284T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56228900 | ||||||
| chr16:56228994
|
T | C | 75 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(72): Show | 76 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.161+36378T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56228994 | ||||||
| chr16:56229202
|
TTTTG | T | 17 | a0001c0001t0001g0262a0001c0001t0001g0270a0001c0001t0001g0276others(14): Show | 17 | HG00423.hp2 HG01109.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.161+36598_161+3660 others(8): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56229202 | |||||
| chr16:56229257
|
T | C | 1 | a0001c0002t0023g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.161+36641T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56229257 | ||||||
| chr16:56229287
|
T | C | 75 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(72): Show | 76 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.161+36671T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56229287 | ||||||
| chr16:56229359
|
C | G | 17 | a0001c0001t0001g0262a0001c0001t0001g0270a0001c0001t0001g0276others(14): Show | 17 | HG00423.hp2 HG01109.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.161+36743C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56229359 | ||||||
| chr16:56229609
|
G | GTGGA | 26 | a0001c0001t0001g0014a0001c0001t0001g0096a0001c0001t0001g0163others(23): Show | 27 | HG01884.hp1 HG01975.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.161+37032_161+3703 others(8): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56229609 | |||||
| chr16:56229609
|
GTGGA | G | 57 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(54): Show | 57 | HG00140.hp1 HG00438.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.161+37032_161+3703 others(8): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56229609 | |||||
| chr16:56229803
|
TA | T | 197 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(194): Show | 199 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.161+37190delA | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56229803 | |||||
| chr16:56229916
|
G | A | 1 | a0001c0002t0001g0054 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.161+37300G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56229916 | ||||||
| chr16:56230123
|
TA | T | 78 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(75): Show | 79 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.161+37519delA | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56230123 | |||||
| chr16:56230154
|
C | T | 1 | a0001c0002t0010g0252 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.161+37538C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56230154 | ||||||
| chr16:56230230
|
G | A | 205 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(202): Show | 207 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.161+37614G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56230230 | ||||||
| chr16:56230278
|
C | T | 1 | a0001c0002t0002g0139 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.161+37662C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56230278 | ||||||
| chr16:56230338
|
C | A | 1 | a0001c0001t0024g0068 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.161+37722C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56230338 | ||||||
| chr16:56230401
|
A | C | 6 | a0001c0001t0003g0030a0001c0002t0004g0021a0001c0002t0012g0179others(3): Show | 6 | HG02280.hp2 HG02451.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.161+37785A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56230401 | ||||||
| chr16:56230600
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.161+37984C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56230600 | ||||||
| chr16:56230736
|
C | T | 1 | a0001c0002t0001g0259 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.161+38120C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56230736 | ||||||
| chr16:56230738
|
C | T | 5 | a0001c0001t0003g0289a0001c0001t0017g0290a0001c0002t0001g0288others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.161+38122C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56230738 | ||||||
| chr16:56230859
|
C | G | 75 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(72): Show | 76 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.161+38243C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56230859 | ||||||
| chr16:56230903
|
G | C | 201 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(198): Show | 203 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.161+38287G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56230903 | ||||||
| chr16:56231136
|
T | C | 17 | a0001c0001t0001g0262a0001c0001t0001g0270a0001c0001t0001g0276others(14): Show | 17 | HG00423.hp2 HG01109.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.161+38520T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56231136 | ||||||
| chr16:56231313
|
T | G | 75 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(72): Show | 76 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.161+38697T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56231313 | ||||||
| chr16:56231341
|
C | T | 1 | a0001c0001t0003g0246 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.161+38725C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56231341 | ||||||
| chr16:56231493
|
A | G | 198 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(195): Show | 200 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.161+38877A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56231493 | ||||||
| chr16:56232001
|
C | T | 1 | a0001c0002t0006g0193 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.161+39385C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56232001 | ||||||
| chr16:56232568
|
G | A | 1 | a0001c0002t0001g0104 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.161+39952G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56232568 | ||||||
| chr16:56232798
|
G | A | 9 | a0001c0001t0001g0258a0001c0001t0004g0002a0001c0001t0004g0287others(6): Show | 10 | HG02015.hp1 HG02717.hp2 HG03225.hp2 others(7): Show |
intron_variant | MODIFIER | c.161+40182G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56232798 | ||||||
| chr16:56233010
|
A | G | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.161+40394A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56233010 | ||||||
| chr16:56233135
|
T | C | 1 | a0001c0001t0004g0185 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.161+40519T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56233135 | ||||||
| chr16:56233145
|
C | T | 2 | a0001c0001t0001g0262a0001c0002t0001g0263 | 2 | HG01109.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.161+40529C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56233145 | ||||||
| chr16:56233287
|
A | G | 75 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(72): Show | 76 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.161+40671A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56233287 | ||||||
| chr16:56233379
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.161+40763G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56233379 | ||||||
| chr16:56233426
|
T | C | 75 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(72): Show | 76 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.161+40810T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56233426 | ||||||
| chr16:56233585
|
G | A | 1 | a0001c0001t0028g0125 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.161+40969G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56233585 | ||||||
| chr16:56233600
|
A | T | 1 | a0001c0002t0001g0228 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.161+40984A>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56233600 | ||||||
| chr16:56233720
|
G | A | 1 | a0001c0001t0004g0215 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.161+41104G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56233720 | ||||||
| chr16:56233779
|
G | A | 17 | a0001c0001t0001g0262a0001c0001t0001g0270a0001c0001t0001g0276others(14): Show | 17 | HG00423.hp2 HG01109.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.161+41163G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56233779 | ||||||
| chr16:56233785
|
G | A | 75 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(72): Show | 76 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.161+41169G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56233785 | ||||||
| chr16:56234101
|
C | T | 122 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0024others(119): Show | 123 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.161+41485C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56234101 | ||||||
| chr16:56234125
|
G | A | 1 | a0001c0002t0023g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.161+41509G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56234125 | ||||||
| chr16:56234195
|
A | C | 1 | a0001c0002t0002g0029 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.161+41579A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56234195 | ||||||
| chr16:56234210
|
A | G | 1 | a0001c0002t0023g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.161+41594A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56234210 | ||||||
| chr16:56234422
|
G | A | 1 | a0001c0002t0023g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.162-41509G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56234422 | ||||||
| chr16:56234457
|
C | A | 10 | a0001c0001t0001g0043a0001c0001t0003g0044a0001c0001t0005g0048others(7): Show | 10 | HG00438.hp1 NA18959.hp2 NA18973.hp2 others(7): Show |
intron_variant | MODIFIER | c.162-41474C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56234457 | ||||||
| chr16:56234493
|
C | A | 1 | a0001c0001t0001g0022 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.162-41438C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56234493 | ||||||
| chr16:56234502
|
C | G | 2 | a0001c0001t0001g0258a0001c0002t0001g0259 | 2 | HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.162-41429C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56234502 | ||||||
| chr16:56234898
|
G | T | 1 | a0001c0001t0001g0182 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.162-41033G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56234898 | ||||||
| chr16:56234970
|
A | G | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.162-40961A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56234970 | ||||||
| chr16:56235584
|
T | C | 3 | a0001c0001t0004g0002a0001c0001t0004g0287a0001c0002t0001g0286 | 4 | HG02015.hp1 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.162-40347T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56235584 | ||||||
| chr16:56235980
|
G | A | 121 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0024others(118): Show | 122 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.162-39951G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56235980 | ||||||
| chr16:56236046
|
T | A | 3 | a0001c0002t0003g0136a0001c0002t0015g0128a0001c0002t0025g0129 | 3 | HG03654.hp2 HG03834.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.162-39885T>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56236046 | ||||||
| chr16:56236086
|
T | C | 1 | a0001c0002t0023g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.162-39845T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56236086 | ||||||
| chr16:56236163
|
A | G | 75 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(72): Show | 76 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.162-39768A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56236163 | ||||||
| chr16:56236199
|
G | A | 4 | a0001c0001t0010g0123a0001c0002t0001g0018a0001c0002t0002g0066others(1): Show | 4 | HG00423.hp1 HG00673.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.162-39732G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56236199 | ||||||
| chr16:56236335
|
C | G | 1 | a0001c0004t0002g0028 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.162-39596C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56236335 | ||||||
| chr16:56236335
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.162-39596C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56236335 | ||||||
| chr16:56236391
|
C | T | 1 | a0001c0001t0003g0075 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.162-39540C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56236391 | ||||||
| chr16:56236573
|
C | T | 1 | a0001c0002t0001g0204 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.162-39358C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56236573 | ||||||
| chr16:56236596
|
A | G | 1 | a0001c0002t0003g0137 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.162-39335A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56236596 | ||||||
| chr16:56236637
|
A | C | 1 | a0001c0002t0002g0029 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.162-39294A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56236637 | ||||||
| chr16:56236642
|
G | A | 122 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0024others(119): Show | 123 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.162-39289G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56236642 | ||||||
| chr16:56236724
|
G | A | 33 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(30): Show | 33 | HG00438.hp1 HG00642.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.162-39207G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56236724 | ||||||
| chr16:56236754
|
A | G | 1 | a0001c0002t0003g0233 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.162-39177A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56236754 | ||||||
| chr16:56236856
|
G | A | 1 | a0001c0002t0027g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.162-39075G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56236856 | ||||||
| chr16:56236989
|
G | A | 3 | a0001c0001t0003g0289a0001c0001t0017g0290a0001c0002t0001g0288 | 3 | HG01884.hp1 HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.162-38942G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56236989 | ||||||
| chr16:56237172
|
A | G | 2 | a0001c0002t0001g0054a0001c0002t0014g0033 | 2 | HG02965.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.162-38759A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56237172 | ||||||
| chr16:56237271
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.162-38660G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56237271 | ||||||
| chr16:56237881
|
A | G | 3 | a0001c0001t0001g0231a0001c0001t0002g0254a0001c0002t0001g0232 | 3 | HG01169.hp1 HG01361.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.162-38050A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56237881 | ||||||
| chr16:56237988
|
G | T | 73 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(70): Show | 74 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.162-37943G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56237988 | ||||||
| chr16:56238110
|
C | G | 31 | a0001c0001t0001g0258a0001c0001t0001g0262a0001c0001t0001g0270others(28): Show | 32 | HG00423.hp2 HG01109.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.162-37821C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56238110 | ||||||
| chr16:56238111
|
G | A | 2 | a0001c0001t0001g0163a0001c0002t0001g0013 | 2 | HG02109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.162-37820G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56238111 | ||||||
| chr16:56238279
|
T | G | 1 | a0001c0001t0001g0153 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.162-37652T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56238279 | ||||||
| chr16:56238378
|
C | T | 198 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(195): Show | 200 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.162-37553C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56238378 | ||||||
| chr16:56238488
|
T | C | 73 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(70): Show | 74 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.162-37443T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56238488 | ||||||
| chr16:56238523
|
C | T | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.162-37408C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56238523 | ||||||
| chr16:56238552
|
A | G | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.162-37379A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56238552 | ||||||
| chr16:56238767
|
A | G | 1 | a0001c0004t0002g0028 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.162-37164A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56238767 | ||||||
| chr16:56238985
|
C | G | 6 | a0001c0001t0001g0262a0001c0001t0001g0270a0001c0001t0002g0261others(3): Show | 6 | HG01109.hp1 HG02300.hp1 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.162-36946C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56238985 | ||||||
| chr16:56239041
|
G | T | 1 | a0001c0002t0023g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.162-36890G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56239041 | ||||||
| chr16:56239103
|
A | C | 1 | a0001c0002t0001g0035 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.162-36828A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56239103 | ||||||
| chr16:56239273
|
T | C | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.162-36658T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56239273 | ||||||
| chr16:56239512
|
G | A | 1 | a0001c0002t0023g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.162-36419G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56239512 | ||||||
| chr16:56239544
|
C | T | 2 | a0001c0001t0004g0178a0001c0001t0004g0237 | 2 | HG02027.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.162-36387C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56239544 | ||||||
| chr16:56239620
|
G | A | 58 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0071others(55): Show | 58 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.162-36311G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56239620 | ||||||
| chr16:56239673
|
A | T | 1 | a0001c0001t0001g0098 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.162-36258A>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56239673 | ||||||
| chr16:56239780
|
C | T | 17 | a0001c0001t0001g0262a0001c0001t0001g0270a0001c0001t0001g0276others(14): Show | 17 | HG00423.hp2 HG01109.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.162-36151C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56239780 | ||||||
| chr16:56239974
|
T | C | 219 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(216): Show | 221 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.162-35957T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56239974 | ||||||
| chr16:56240187
|
C | T | 1 | a0001c0001t0003g0075 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.162-35744C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56240187 | ||||||
| chr16:56240492
|
A | G | 1 | a0001c0002t0001g0228 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.162-35439A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56240492 | ||||||
| chr16:56240583
|
G | A | 2 | a0001c0001t0001g0177a0001c0001t0009g0127 | 2 | NA18946.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.162-35348G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56240583 | ||||||
| chr16:56240589
|
C | T | 121 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0024others(118): Show | 122 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.162-35342C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56240589 | ||||||
| chr16:56240815
|
C | T | 18 | a0001c0001t0001g0262a0001c0001t0001g0270a0001c0001t0001g0276others(15): Show | 18 | HG00423.hp2 HG01109.hp1 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.162-35116C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56240815 | ||||||
| chr16:56240865
|
A | G | 5 | a0001c0001t0004g0002a0001c0001t0004g0287a0001c0001t0011g0285others(2): Show | 6 | HG02015.hp1 HG03491.hp2 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.162-35066A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56240865 | ||||||
| chr16:56241014
|
C | G | 2 | a0001c0001t0011g0285a0001c0002t0002g0020 | 2 | HG03704.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.162-34917C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56241014 | ||||||
| chr16:56241080
|
C | G | 1 | a0001c0002t0001g0263 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.162-34851C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56241080 | ||||||
| chr16:56241123
|
T | A | 1 | a0001c0002t0014g0033 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.162-34808T>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56241123 | ||||||
| chr16:56241151
|
G | A | 77 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0057others(74): Show | 77 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.162-34780G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56241151 | ||||||
| chr16:56241158
|
C | T | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.162-34773C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56241158 | ||||||
| chr16:56241353
|
T | C | 74 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(71): Show | 75 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.162-34578T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56241353 | ||||||
| chr16:56241367
|
C | T | 3 | a0001c0001t0009g0089a0001c0001t0009g0094a0001c0001t0009g0095 | 3 | HG02015.hp2 NA18945.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.162-34564C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56241367 | ||||||
| chr16:56241381
|
G | C | 74 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(71): Show | 75 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.162-34550G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56241381 | ||||||
| chr16:56241408
|
T | C | 33 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(30): Show | 33 | HG00438.hp1 HG00642.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.162-34523T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56241408 | ||||||
| chr16:56241460
|
C | T | 1 | a0001c0001t0003g0246 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.162-34471C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56241460 | ||||||
| chr16:56241497
|
A | C | 74 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(71): Show | 75 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.162-34434A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56241497 | ||||||
| chr16:56241545
|
T | G | 2 | a0001c0001t0006g0069a0001c0001t0007g0070 | 2 | HG02273.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.162-34386T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56241545 | ||||||
| chr16:56241581
|
C | T | 1 | a0001c0002t0023g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.162-34350C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56241581 | ||||||
| chr16:56241595
|
C | T | 7 | a0001c0001t0001g0202a0001c0001t0004g0223a0001c0001t0005g0201others(4): Show | 7 | NA18945.hp2 NA19009.hp1 NA19060.hp1 others(4): Show |
intron_variant | MODIFIER | c.162-34336C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56241595 | ||||||
| chr16:56241636
|
T | C | 43 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(40): Show | 43 | HG00438.hp1 HG00642.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.162-34295T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56241636 | ||||||
| chr16:56241669
|
T | C | 1 | a0001c0002t0027g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.162-34262T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56241669 | ||||||
| chr16:56241763
|
A | AGT | 4 | a0001c0001t0001g0153a0001c0001t0002g0150a0001c0002t0001g0151others(1): Show | 4 | HG01361.hp2 HG01516.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.162-34167_162-3416 others(6): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56241763 | |||||
| chr16:56241779
|
G | A | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.162-34152G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56241779 | ||||||
| chr16:56241810
|
G | A | 1 | a0001c0001t0004g0291 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.162-34121G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56241810 | ||||||
| chr16:56241833
|
A | G | 75 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(72): Show | 76 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.162-34098A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56241833 | ||||||
| chr16:56242034
|
C | T | 74 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(71): Show | 75 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.162-33897C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56242034 | ||||||
| chr16:56242097
|
C | T | 1 | a0001c0001t0007g0070 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.162-33834C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56242097 | ||||||
| chr16:56242182
|
G | C | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.162-33749G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56242182 | ||||||
| chr16:56242207
|
G | GGAA | 217 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(214): Show | 219 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.162-33721_162-3371 others(7): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56242207 | |||||
| chr16:56242213
|
T | A | 2 | a0001c0002t0001g0035a0001c0002t0013g0032 | 2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.162-33718T>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56242213 | ||||||
| chr16:56242692
|
C | T | 1 | a0001c0001t0002g0253 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.162-33239C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56242692 | ||||||
| chr16:56242767
|
A | G | 75 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(72): Show | 76 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.162-33164A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56242767 | ||||||
| chr16:56242938
|
G | A | 1 | a0001c0002t0023g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.162-32993G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56242938 | ||||||
| chr16:56242948
|
G | A | 31 | a0001c0001t0001g0258a0001c0001t0001g0262a0001c0001t0001g0270others(28): Show | 32 | HG00423.hp2 HG01109.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.162-32983G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56242948 | ||||||
| chr16:56242998
|
A | C | 45 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0078others(42): Show | 46 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.162-32933A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56242998 | ||||||
| chr16:56243019
|
C | T | 1 | a0001c0002t0023g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.162-32912C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56243019 | ||||||
| chr16:56243280
|
A | G | 153 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0024others(150): Show | 154 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.162-32651A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56243280 | ||||||
| chr16:56243449
|
T | C | 1 | a0001c0002t0018g0229 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.162-32482T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56243449 | ||||||
| chr16:56243684
|
AT | A | 74 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(71): Show | 75 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.162-32237delT | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56243684 | |||||
| chr16:56243882
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.162-32049A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56243882 | ||||||
| chr16:56244050
|
G | C | 1 | a0001c0002t0027g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.162-31881G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56244050 | ||||||
| chr16:56244366
|
T | TA | 81 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0057others(78): Show | 81 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.162-31551dupA | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56244366 | |||||
| chr16:56244366
|
TA | T | 16 | a0001c0001t0001g0262a0001c0001t0001g0270a0001c0001t0001g0276others(13): Show | 16 | HG00423.hp2 HG01109.hp1 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.162-31551delA | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56244366 | |||||
| chr16:56244487
|
G | A | 77 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0057others(74): Show | 77 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.162-31444G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56244487 | ||||||
| chr16:56244530
|
A | T | 8 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0002g0081others(5): Show | 8 | HG00280.hp1 HG00735.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.162-31401A>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56244530 | ||||||
| chr16:56244798
|
G | C | 67 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0071others(64): Show | 67 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.162-31133G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56244798 | ||||||
| chr16:56245082
|
C | T | 74 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(71): Show | 75 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.162-30849C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56245082 | ||||||
| chr16:56245099
|
A | G | 1 | a0001c0002t0027g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.162-30832A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56245099 | ||||||
| chr16:56245138
|
A | T | 3 | a0001c0002t0001g0025a0001c0002t0001g0107a0001c0002t0005g0026 | 3 | HG01515.hp2 HG01517.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.162-30793A>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56245138 | ||||||
| chr16:56245215
|
G | A | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.162-30716G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56245215 | ||||||
| chr16:56245429
|
G | A | 2 | a0001c0001t0004g0291a0001c0002t0002g0292 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.162-30502G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56245429 | ||||||
| chr16:56245776
|
A | G | 1 | a0001c0002t0022g0122 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.162-30155A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56245776 | ||||||
| chr16:56245837
|
T | C | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.162-30094T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56245837 | ||||||
| chr16:56245852
|
T | C | 4 | a0001c0001t0001g0057a0001c0002t0001g0055a0001c0002t0001g0056others(1): Show | 4 | HG02258.hp2 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.162-30079T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56245852 | ||||||
| chr16:56245900
|
A | G | 2 | a0001c0001t0001g0188a0001c0001t0013g0187 | 2 | HG01884.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.162-30031A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56245900 | ||||||
| chr16:56245924
|
GGT | G | 5 | a0001c0001t0004g0002a0001c0001t0004g0287a0001c0001t0011g0285others(2): Show | 6 | HG02015.hp1 HG03491.hp2 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.162-30002_162-3000 others(6): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56245924 | |||||
| chr16:56246166
|
A | G | 3 | a0001c0001t0001g0145a0001c0002t0004g0143a0001c0002t0004g0144 | 3 | HG03540.hp1 NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.162-29765A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56246166 | ||||||
| chr16:56246392
|
A | G | 3 | a0001c0002t0001g0247a0001c0002t0001g0248a0001c0002t0001g0249 | 3 | HG02630.hp1 HG02723.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.162-29539A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56246392 | ||||||
| chr16:56246504
|
C | CA | 39 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(36): Show | 39 | HG00438.hp1 HG00642.hp2 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.162-29425dupA | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56246504 | |||||
| chr16:56246548
|
C | A | 1 | a0001c0002t0023g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.162-29383C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56246548 | ||||||
| chr16:56246703
|
G | A | 1 | a0001c0002t0023g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.162-29228G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56246703 | ||||||
| chr16:56246806
|
C | T | 1 | a0001c0002t0006g0133 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.162-29125C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56246806 | ||||||
| chr16:56247185
|
C | T | 32 | a0001c0001t0001g0182a0001c0001t0001g0258a0001c0001t0001g0262others(29): Show | 33 | HG00423.hp2 HG01109.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.162-28746C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56247185 | ||||||
| chr16:56247195
|
C | A | 1 | a0001c0002t0023g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.162-28736C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56247195 | ||||||
| chr16:56247482
|
G | GT | 27 | a0001c0001t0001g0078a0001c0001t0001g0132a0001c0001t0001g0164others(24): Show | 27 | HG00639.hp1 HG00735.hp2 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.162-28428dupT | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56247482 | |||||
| chr16:56247482
|
GT | G | 16 | a0001c0001t0001g0014a0001c0001t0001g0049a0001c0001t0001g0188others(13): Show | 16 | HG01884.hp2 HG01978.hp2 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.162-28428delT | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56247482 | |||||
| chr16:56247482
|
GTT | G | 33 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(30): Show | 33 | HG00438.hp1 HG00642.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.162-28429_162-2842 others(6): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56247482 | |||||
| chr16:56247482
|
GTTTT | G | 29 | a0001c0001t0001g0182a0001c0001t0001g0258a0001c0001t0001g0262others(26): Show | 30 | HG00423.hp2 HG01109.hp1 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.162-28431_162-2842 others(8): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56247482 | |||||
| chr16:56247489
|
T | G | 1 | a0001c0001t0006g0255 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.162-28442T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56247489 | ||||||
| chr16:56247591
|
C | T | 26 | a0001c0001t0001g0258a0001c0001t0001g0262a0001c0001t0001g0270others(23): Show | 27 | HG00423.hp2 HG01109.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.162-28340C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56247591 | ||||||
| chr16:56247695
|
C | T | 1 | a0001c0002t0004g0063 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.162-28236C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56247695 | ||||||
| chr16:56247771
|
A | G | 73 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(70): Show | 74 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.162-28160A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56247771 | ||||||
| chr16:56247842
|
C | T | 122 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0024others(119): Show | 123 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.162-28089C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56247842 | ||||||
| chr16:56248195
|
A | T | 2 | a0001c0001t0001g0219a0001c0001t0001g0280 | 2 | NA18995.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.162-27736A>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56248195 | ||||||
| chr16:56248280
|
A | G | 123 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0024others(120): Show | 124 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.162-27651A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56248280 | ||||||
| chr16:56248699
|
A | G | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.162-27232A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56248699 | ||||||
| chr16:56248715
|
G | A | 1 | a0001c0002t0023g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.162-27216G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56248715 | ||||||
| chr16:56248725
|
G | A | 2 | a0001c0001t0004g0291a0001c0002t0002g0292 | 2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.162-27206G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56248725 | ||||||
| chr16:56248778
|
G | A | 73 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(70): Show | 74 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.162-27153G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56248778 | ||||||
| chr16:56248988
|
G | A | 73 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(70): Show | 74 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.162-26943G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56248988 | ||||||
| chr16:56249078
|
G | A | 1 | a0001c0001t0013g0187 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.162-26853G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56249078 | ||||||
| chr16:56249153
|
TGA | T | 5 | a0001c0001t0003g0289a0001c0001t0017g0290a0001c0002t0001g0288others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.162-26773_162-2677 others(6): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56249153 | |||||
| chr16:56249244
|
G | C | 1 | a0001c0004t0002g0028 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.162-26687G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56249244 | ||||||
| chr16:56249314
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.162-26617C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56249314 | ||||||
| chr16:56249339
|
G | A | 73 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(70): Show | 74 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.162-26592G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56249339 | ||||||
| chr16:56249374
|
C | T | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.162-26557C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56249374 | ||||||
| chr16:56249375
|
C | A | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.162-26556C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56249375 | ||||||
| chr16:56249436
|
T | C | 117 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0024others(114): Show | 118 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.162-26495T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56249436 | ||||||
| chr16:56249489
|
AGGCTGTT others(12): Show |
A | 1 | a0001c0001t0001g0132 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.162-26438_162-2642 others(23): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56249489 | |||||
| chr16:56249622
|
C | A | 73 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(70): Show | 74 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.162-26309C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56249622 | ||||||
| chr16:56249638
|
A | G | 2 | a0001c0001t0001g0092a0001c0001t0001g0106 | 2 | NA19005.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.162-26293A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56249638 | ||||||
| chr16:56249923
|
G | A | 1 | a0001c0002t0001g0104 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.162-26008G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56249923 | ||||||
| chr16:56249994
|
A | G | 197 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(194): Show | 199 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.162-25937A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56249994 | ||||||
| chr16:56250040
|
C | T | 123 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0024others(120): Show | 124 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.162-25891C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56250040 | ||||||
| chr16:56250190
|
G | A | 3 | a0001c0002t0003g0001a0001c0002t0003g0109a0002c0005t0003g0088 | 4 | NA18973.hp1 NA18983.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.162-25741G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56250190 | ||||||
| chr16:56250602
|
C | T | 5 | a0001c0001t0001g0295a0001c0001t0004g0291a0001c0002t0001g0294others(2): Show | 5 | HG02970.hp1 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.162-25329C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56250602 | ||||||
| chr16:56250745
|
ACT | A | 3 | a0001c0001t0001g0231a0001c0001t0002g0254a0001c0002t0001g0232 | 3 | HG01169.hp1 HG01361.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.162-25182_162-2518 others(6): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56250745 | |||||
| chr16:56250789
|
T | A | 39 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(36): Show | 39 | HG00438.hp1 HG00642.hp2 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.162-25142T>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56250789 | ||||||
| chr16:56250821
|
A | G | 3 | a0001c0002t0001g0247a0001c0002t0001g0248a0001c0002t0001g0249 | 3 | HG02630.hp1 HG02723.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.162-25110A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56250821 | ||||||
| chr16:56250869
|
T | C | 1 | a0001c0002t0002g0195 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.162-25062T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56250869 | ||||||
| chr16:56251303
|
A | G | 1 | a0001c0002t0023g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.162-24628A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56251303 | ||||||
| chr16:56251373
|
A | C | 1 | a0001c0001t0004g0296 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.162-24558A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56251373 | ||||||
| chr16:56251432
|
G | A | 6 | a0001c0001t0001g0295a0001c0001t0004g0291a0001c0001t0004g0296others(3): Show | 6 | HG01891.hp1 HG02970.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.162-24499G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56251432 | ||||||
| chr16:56251607
|
C | T | 1 | a0001c0002t0023g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.162-24324C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56251607 | ||||||
| chr16:56251837
|
C | T | 2 | a0001c0002t0001g0119a0001c0002t0001g0120 | 2 | HG00639.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.162-24094C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56251837 | ||||||
| chr16:56251873
|
A | G | 3 | a0001c0002t0012g0179a0001c0002t0012g0180a0001c0002t0012g0181 | 3 | HG02280.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.162-24058A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56251873 | ||||||
| chr16:56251927
|
T | A | 1 | a0001c0002t0003g0235 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.162-24004T>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56251927 | ||||||
| chr16:56252344
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.162-23587A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56252344 | ||||||
| chr16:56252474
|
C | T | 2 | a0001c0002t0004g0277a0001c0002t0004g0278 | 2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.162-23457C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56252474 | ||||||
| chr16:56252635
|
C | T | 1 | a0001c0002t0003g0137 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.162-23296C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56252635 | ||||||
| chr16:56252667
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.162-23264G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56252667 | ||||||
| chr16:56252719
|
C | T | 1 | a0001c0002t0023g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.162-23212C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56252719 | ||||||
| chr16:56253014
|
A | G | 74 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(71): Show | 75 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.162-22917A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56253014 | ||||||
| chr16:56253075
|
G | A | 1 | a0001c0004t0002g0028 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.162-22856G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56253075 | ||||||
| chr16:56253201
|
C | A | 219 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(216): Show | 221 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.162-22730C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56253201 | ||||||
| chr16:56253246
|
C | T | 1 | a0001c0002t0023g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.162-22685C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56253246 | ||||||
| chr16:56253247
|
G | A | 40 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(37): Show | 40 | HG00438.hp1 HG00642.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.162-22684G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56253247 | ||||||
| chr16:56253266
|
C | T | 1 | a0001c0001t0017g0290 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.162-22665C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56253266 | ||||||
| chr16:56253309
|
A | G | 1 | a0001c0001t0024g0068 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.162-22622A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56253309 | ||||||
| chr16:56253357
|
G | A | 10 | a0001c0001t0001g0043a0001c0001t0003g0044a0001c0001t0005g0048others(7): Show | 10 | HG00438.hp1 NA18959.hp2 NA18973.hp2 others(7): Show |
intron_variant | MODIFIER | c.162-22574G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56253357 | ||||||
| chr16:56253661
|
A | C | 4 | a0001c0001t0004g0223a0001c0001t0005g0221a0001c0001t0005g0222others(1): Show | 4 | NA18945.hp2 NA19009.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.162-22270A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56253661 | ||||||
| chr16:56253933
|
A | G | 7 | a0001c0001t0004g0002a0001c0001t0004g0287a0001c0001t0011g0285others(4): Show | 8 | HG02015.hp1 HG03225.hp2 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.162-21998A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56253933 | ||||||
| chr16:56254026
|
T | TG | 74 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(71): Show | 75 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.162-21905_162-2190 others(5): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56254026 | ||||||
| chr16:56254113
|
A | G | 1 | a0001c0001t0001g0211 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.162-21818A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56254113 | ||||||
| chr16:56254636
|
G | A | 39 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(36): Show | 39 | HG00438.hp1 HG00642.hp2 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.162-21295G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56254636 | ||||||
| chr16:56254651
|
A | T | 73 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(70): Show | 74 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.162-21280A>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56254651 | ||||||
| chr16:56254730
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.162-21201G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56254730 | ||||||
| chr16:56254896
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.162-21035C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56254896 | ||||||
| chr16:56255047
|
C | G | 73 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(70): Show | 74 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.162-20884C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56255047 | ||||||
| chr16:56255362
|
A | G | 2 | a0001c0001t0003g0030a0001c0002t0004g0021 | 2 | NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.162-20569A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56255362 | ||||||
| chr16:56255527
|
T | C | 1 | a0001c0001t0003g0008 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.162-20404T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56255527 | ||||||
| chr16:56255563
|
T | A | 1 | a0001c0001t0001g0211 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.162-20368T>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56255563 | ||||||
| chr16:56255595
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.162-20336A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56255595 | ||||||
| chr16:56255627
|
C | T | 2 | a0001c0001t0004g0178a0001c0001t0004g0237 | 2 | HG02027.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.162-20304C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56255627 | ||||||
| chr16:56255659
|
G | T | 205 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(202): Show | 207 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.162-20272G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56255659 | ||||||
| chr16:56255696
|
T | C | 45 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0078others(42): Show | 46 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.162-20235T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56255696 | ||||||
| chr16:56255781
|
A | C | 1 | a0001c0002t0023g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.162-20150A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56255781 | ||||||
| chr16:56256018
|
A | G | 2 | a0001c0003t0002g0103a0001c0003t0002g0114 | 2 | HG00735.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.162-19913A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56256018 | ||||||
| chr16:56256116
|
C | T | 1 | a0001c0002t0027g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.162-19815C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56256116 | ||||||
| chr16:56256118
|
T | A | 77 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0057others(74): Show | 77 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.162-19813T>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56256118 | ||||||
| chr16:56256138
|
T | A | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.162-19793T>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56256138 | ||||||
| chr16:56256213
|
C | T | 1 | a0001c0002t0002g0260 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.162-19718C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56256213 | ||||||
| chr16:56256307
|
G | A | 2 | a0001c0001t0004g0178a0001c0001t0004g0237 | 2 | HG02027.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.162-19624G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56256307 | ||||||
| chr16:56256418
|
GT | G | 31 | a0001c0001t0001g0258a0001c0001t0001g0262a0001c0001t0001g0270others(28): Show | 32 | HG00423.hp2 HG01109.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.162-19511delT | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56256418 | |||||
| chr16:56256433
|
C | T | 74 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(71): Show | 75 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.162-19498C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56256433 | ||||||
| chr16:56256520
|
G | A | 40 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(37): Show | 40 | HG00438.hp1 HG00642.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.162-19411G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56256520 | ||||||
| chr16:56256678
|
T | TTCTCTCT others(1): Show |
5 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0003g0030others(2): Show | 5 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.162-19245_162-1923 others(12): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56256678 | |||||
| chr16:56256686
|
GTC | G | 10 | a0001c0001t0001g0199a0001c0001t0002g0253a0001c0001t0003g0200others(7): Show | 10 | HG00673.hp1 HG01256.hp2 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.162-19213_162-1921 others(6): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56256686 | |||||
| chr16:56256686
|
GTCTCTC | G | 4 | a0001c0001t0004g0291a0001c0001t0004g0296a0001c0002t0002g0292others(1): Show | 4 | HG01891.hp1 HG02074.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.162-19217_162-1921 others(10): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56256686 | |||||
| chr16:56256690
|
C | CTCTG | 4 | a0001c0002t0001g0054a0001c0002t0002g0006a0001c0002t0004g0021others(1): Show | 4 | HG02965.hp2 HG03927.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.162-19238_162-1923 others(8): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56256690 | |||||
| chr16:56256692
|
C | CTG | 21 | a0001c0001t0001g0043a0001c0001t0001g0049a0001c0001t0001g0050others(18): Show | 21 | HG00438.hp1 HG01258.hp2 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.162-19238_162-1923 others(6): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56256692 | |||||
| chr16:56256694
|
C | G | 86 | a0001c0001t0001g0022a0001c0001t0001g0041a0001c0001t0001g0062others(83): Show | 88 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.162-19237C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56256694 | ||||||
| chr16:56256702
|
C | G | 1 | a0001c0001t0014g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.162-19229C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56256702 | ||||||
| chr16:56256710
|
C | G | 1 | a0001c0004t0002g0028 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.162-19221C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56256710 | ||||||
| chr16:56256710
|
CTCTCTCT others(3): Show |
C | 3 | a0001c0001t0001g0295a0001c0002t0001g0294a0001c0002t0013g0293 | 3 | HG02970.hp1 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.162-19219_162-1921 others(14): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56256710 | |||||
| chr16:56256712
|
C | G | 3 | a0001c0002t0002g0029a0001c0002t0023g0027a0001c0004t0002g0028 | 3 | HG02074.hp1 HG02145.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.162-19219C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56256712 | ||||||
| chr16:56256712
|
CTCTCTCT others(5): Show |
C | 1 | a0001c0002t0003g0136 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.162-19217_162-1920 others(16): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56256712 | |||||
| chr16:56256712
|
CTCTCTCT others(7): Show |
C | 1 | a0001c0002t0015g0128 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.162-19217_162-1920 others(18): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56256712 | |||||
| chr16:56256712
|
CTCTCTCT others(9): Show |
C | 2 | a0001c0001t0001g0281a0001c0002t0025g0129 | 2 | HG01106.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.162-19217_162-1920 others(20): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56256712 | |||||
| chr16:56256714
|
C | G | 3 | a0001c0002t0002g0029a0001c0002t0023g0027a0001c0004t0002g0028 | 3 | HG02074.hp1 HG02145.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.162-19217C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56256714 | ||||||
| chr16:56256714
|
CTCTCTGT others(9): Show |
C | 39 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0078others(36): Show | 40 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(37): Show |
intron_variant | MODIFIER | c.162-19215_162-1920 others(20): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56256714 | |||||
| chr16:56256716
|
C | G | 5 | a0001c0001t0001g0166a0001c0001t0011g0203a0001c0002t0002g0029others(2): Show | 5 | HG02074.hp1 HG02145.hp1 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.162-19215C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56256716 | ||||||
| chr16:56256716
|
CTCTGTGT others(7): Show |
C | 1 | a0001c0006t0021g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.162-19213_162-1920 others(18): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56256716 | |||||
| chr16:56256716
|
CTCTGTGT others(9): Show |
C | 70 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0057others(67): Show | 70 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.162-19213_162-1919 others(20): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56256716 | |||||
| chr16:56256718
|
C | CTG | 6 | a0001c0001t0001g0224a0001c0001t0003g0238a0001c0001t0005g0256others(3): Show | 6 | HG00099.hp1 HG02738.hp2 NA18949.hp2 others(3): Show |
intron_variant | MODIFIER | c.162-19173_162-1917 others(6): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56256718 | |||||
| chr16:56256718
|
C | CTGTG | 3 | a0001c0001t0001g0165a0001c0001t0001g0188a0001c0001t0013g0187 | 3 | HG01884.hp2 HG02809.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.162-19175_162-1917 others(8): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56256718 | |||||
| chr16:56256718
|
C | G | 21 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0051others(18): Show | 21 | HG00733.hp2 HG01516.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.162-19213C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56256718 | ||||||
| chr16:56256718
|
CTG | C | 8 | a0001c0001t0001g0041a0001c0001t0001g0153a0001c0001t0004g0227others(5): Show | 8 | HG00642.hp2 HG00733.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.162-19173_162-1917 others(6): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56256718 | |||||
| chr16:56256718
|
CTGTG | C | 5 | a0001c0002t0001g0247a0001c0002t0001g0248a0001c0002t0001g0249others(2): Show | 5 | HG02280.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.162-19175_162-1917 others(8): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56256718 | |||||
| chr16:56256718
|
CTGTGTG | C | 6 | a0001c0001t0001g0258a0001c0001t0003g0289a0001c0001t0017g0290others(3): Show | 6 | HG01884.hp1 HG02015.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.162-19177_162-1917 others(10): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56256718 | |||||
| chr16:56256718
|
CTGTGTGT others(1): Show |
C | 10 | a0001c0001t0004g0002a0001c0001t0004g0178a0001c0001t0004g0237others(7): Show | 11 | HG02027.hp2 HG02630.hp2 HG03098.hp2 others(8): Show |
intron_variant | MODIFIER | c.162-19179_162-1917 others(12): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56256718 | |||||
| chr16:56256718
|
CTGTGTGT others(3): Show |
C | 17 | a0001c0001t0001g0262a0001c0001t0001g0270a0001c0001t0001g0276others(14): Show | 17 | HG00423.hp2 HG01109.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.162-19181_162-1917 others(14): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56256718 | |||||
| chr16:56256718
|
CTGTGTGT others(5): Show |
C | 1 | a0001c0002t0001g0013 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.162-19183_162-1917 others(16): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56256718 | |||||
| chr16:56256718
|
CTGTGTGT others(7): Show |
C | 6 | a0001c0001t0001g0079a0001c0001t0001g0163a0001c0001t0002g0081others(3): Show | 6 | HG01515.hp1 HG01515.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.162-19185_162-1917 others(18): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56256718 | |||||
| chr16:56256720
|
G | C | 30 | a0001c0001t0001g0043a0001c0001t0001g0049a0001c0001t0001g0050others(27): Show | 30 | HG00438.hp1 HG00609.hp1 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.162-19211G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56256720 | ||||||
| chr16:56256722
|
G | C | 33 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0049others(30): Show | 33 | HG00438.hp1 HG00642.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.162-19209G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56256722 | ||||||
| chr16:56256724
|
G | C | 28 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0049others(25): Show | 28 | HG00438.hp1 HG00642.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.162-19207G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56256724 | ||||||
| chr16:56256726
|
G | C | 10 | a0001c0001t0001g0153a0001c0001t0001g0182a0001c0001t0001g0258others(7): Show | 10 | HG01884.hp1 HG02015.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.162-19205G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56256726 | ||||||
| chr16:56256728
|
G | C | 17 | a0001c0001t0001g0153a0001c0001t0001g0258a0001c0001t0003g0289others(14): Show | 18 | HG01884.hp1 HG02015.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.162-19203G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56256728 | ||||||
| chr16:56256730
|
G | C | 25 | a0001c0001t0001g0258a0001c0001t0001g0262a0001c0001t0001g0270others(22): Show | 26 | HG00423.hp2 HG01109.hp1 HG02015.hp1 others(23): Show |
intron_variant | MODIFIER | c.162-19201G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56256730 | ||||||
| chr16:56256732
|
G | C | 2 | a0001c0002t0001g0013a0001c0002t0001g0286 | 2 | HG02015.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.162-19199G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56256732 | ||||||
| chr16:56256925
|
G | A | 1 | a0001c0001t0001g0284 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.162-19006G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56256925 | ||||||
| chr16:56256942
|
C | G | 2 | a0001c0001t0004g0178a0001c0001t0004g0237 | 2 | HG02027.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.162-18989C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56256942 | ||||||
| chr16:56256972
|
G | T | 2 | a0001c0001t0004g0178a0001c0001t0004g0237 | 2 | HG02027.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.162-18959G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56256972 | ||||||
| chr16:56257061
|
A | G | 1 | a0001c0001t0001g0262 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.162-18870A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56257061 | ||||||
| chr16:56257177
|
G | T | 1 | a0001c0002t0002g0029 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.162-18754G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56257177 | ||||||
| chr16:56257181
|
G | T | 2 | a0001c0001t0004g0178a0001c0001t0004g0237 | 2 | HG02027.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.162-18750G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56257181 | ||||||
| chr16:56257182
|
G | T | 5 | a0001c0001t0004g0178a0001c0001t0004g0237a0001c0002t0012g0179others(2): Show | 5 | HG02027.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.162-18749G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56257182 | ||||||
| chr16:56257300
|
A | G | 44 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0078others(41): Show | 45 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.162-18631A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56257300 | ||||||
| chr16:56257432
|
C | T | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.162-18499C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56257432 | ||||||
| chr16:56257531
|
G | T | 3 | a0001c0001t0001g0079a0001c0002t0001g0117a0001c0002t0004g0067 | 3 | HG02622.hp1 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.162-18400G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56257531 | ||||||
| chr16:56257550
|
G | C | 1 | a0001c0001t0006g0226 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.162-18381G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56257550 | ||||||
| chr16:56257551
|
G | C | 28 | a0001c0001t0001g0258a0001c0001t0001g0262a0001c0001t0001g0270others(25): Show | 29 | HG00423.hp2 HG01109.hp1 HG02015.hp1 others(26): Show |
intron_variant | MODIFIER | c.162-18380G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56257551 | ||||||
| chr16:56258082
|
T | C | 1 | a0001c0001t0015g0251 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.162-17849T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56258082 | ||||||
| chr16:56258131
|
C | A | 44 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0078others(41): Show | 45 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.162-17800C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56258131 | ||||||
| chr16:56258209
|
C | T | 205 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(202): Show | 207 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.162-17722C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56258209 | ||||||
| chr16:56258360
|
T | G | 123 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0024others(120): Show | 124 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.162-17571T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56258360 | ||||||
| chr16:56258447
|
G | A | 171 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(168): Show | 172 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.162-17484G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56258447 | ||||||
| chr16:56258457
|
T | G | 1 | a0001c0001t0001g0210 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.162-17474T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56258457 | ||||||
| chr16:56258673
|
G | C | 9 | a0001c0001t0001g0258a0001c0001t0004g0002a0001c0001t0004g0287others(6): Show | 10 | HG02015.hp1 HG02717.hp2 HG03225.hp2 others(7): Show |
intron_variant | MODIFIER | c.162-17258G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56258673 | ||||||
| chr16:56258684
|
A | G | 26 | a0001c0001t0001g0258a0001c0001t0001g0262a0001c0001t0001g0270others(23): Show | 27 | HG00423.hp2 HG01109.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.162-17247A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56258684 | ||||||
| chr16:56258856
|
A | G | 31 | a0001c0001t0001g0258a0001c0001t0001g0262a0001c0001t0001g0270others(28): Show | 32 | HG00423.hp2 HG01109.hp1 HG02015.hp1 others(29): Show |
intron_variant | MODIFIER | c.162-17075A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56258856 | ||||||
| chr16:56258914
|
T | G | 157 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0024others(154): Show | 159 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.162-17017T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56258914 | ||||||
| chr16:56258952
|
A | C | 1 | a0001c0002t0002g0087 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.162-16979A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56258952 | ||||||
| chr16:56259037
|
A | G | 2 | a0001c0001t0001g0163a0001c0002t0001g0013 | 2 | HG02109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.162-16894A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56259037 | ||||||
| chr16:56259079
|
G | A | 2 | a0001c0001t0004g0178a0001c0001t0004g0237 | 2 | HG02027.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.162-16852G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56259079 | ||||||
| chr16:56259151
|
T | C | 206 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(203): Show | 208 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.162-16780T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56259151 | ||||||
| chr16:56259246
|
G | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0106 | 2 | NA19005.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.162-16685G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56259246 | ||||||
| chr16:56259395
|
G | C | 31 | a0001c0001t0001g0258a0001c0001t0001g0262a0001c0001t0001g0270others(28): Show | 32 | HG00423.hp2 HG01109.hp1 HG02015.hp1 others(29): Show |
intron_variant | MODIFIER | c.162-16536G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56259395 | ||||||
| chr16:56259396
|
T | C | 31 | a0001c0001t0001g0258a0001c0001t0001g0262a0001c0001t0001g0270others(28): Show | 32 | HG00423.hp2 HG01109.hp1 HG02015.hp1 others(29): Show |
intron_variant | MODIFIER | c.162-16535T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56259396 | ||||||
| chr16:56259398
|
T | TTC | 31 | a0001c0001t0001g0258a0001c0001t0001g0262a0001c0001t0001g0270others(28): Show | 32 | HG00423.hp2 HG01109.hp1 HG02015.hp1 others(29): Show |
intron_variant | MODIFIER | c.162-16531_162-1653 others(6): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56259398 | |||||
| chr16:56259404
|
C | G | 45 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0078others(42): Show | 46 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.162-16527C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56259404 | ||||||
| chr16:56259426
|
T | A | 4 | a0001c0002t0002g0118a0001c0002t0002g0139a0001c0003t0002g0103others(1): Show | 4 | HG00735.hp2 HG01255.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.162-16505T>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56259426 | ||||||
| chr16:56259641
|
G | A | 2 | a0001c0001t0001g0163a0001c0002t0001g0013 | 2 | HG02109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.162-16290G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56259641 | ||||||
| chr16:56259682
|
G | A | 11 | a0001c0001t0001g0196a0001c0001t0004g0185a0001c0002t0001g0147others(8): Show | 11 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(8): Show |
intron_variant | MODIFIER | c.162-16249G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56259682 | ||||||
| chr16:56259831
|
A | G | 7 | a0001c0001t0004g0002a0001c0001t0004g0287a0001c0001t0011g0285others(4): Show | 8 | HG02015.hp1 HG03225.hp2 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.162-16100A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56259831 | ||||||
| chr16:56260073
|
A | G | 2 | a0001c0001t0001g0258a0001c0002t0001g0259 | 2 | HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.162-15858A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56260073 | ||||||
| chr16:56260162
|
G | A | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.162-15769G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56260162 | ||||||
| chr16:56260215
|
G | A | 121 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0024others(118): Show | 122 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.162-15716G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56260215 | ||||||
| chr16:56260409
|
C | T | 1 | a0001c0002t0023g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.162-15522C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56260409 | ||||||
| chr16:56260721
|
C | CA | 294 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0014others(291): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.162-15210_162-1520 others(5): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56260721 | ||||||
| chr16:56260795
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.162-15136C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56260795 | ||||||
| chr16:56261185
|
T | C | 205 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(202): Show | 207 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.162-14746T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56261185 | ||||||
| chr16:56261193
|
C | G | 3 | a0001c0001t0001g0262a0001c0001t0001g0270a0001c0002t0001g0263 | 3 | HG01109.hp1 HG02300.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.162-14738C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56261193 | ||||||
| chr16:56261220
|
G | C | 1 | a0001c0001t0001g0258 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.162-14711G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56261220 | ||||||
| chr16:56261377
|
G | A | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.162-14554G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56261377 | ||||||
| chr16:56261508
|
A | G | 1 | a0001c0002t0001g0099 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.162-14423A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56261508 | ||||||
| chr16:56261613
|
G | A | 31 | a0001c0001t0001g0258a0001c0001t0001g0262a0001c0001t0001g0270others(28): Show | 32 | HG00423.hp2 HG01109.hp1 HG02015.hp1 others(29): Show |
intron_variant | MODIFIER | c.162-14318G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56261613 | ||||||
| chr16:56261792
|
T | C | 3 | a0001c0001t0004g0178a0001c0001t0004g0237a0001c0002t0027g0146 | 3 | HG02027.hp2 HG03225.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.162-14139T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56261792 | ||||||
| chr16:56262249
|
C | T | 1 | a0001c0001t0004g0161 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.162-13682C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56262249 | ||||||
| chr16:56262335
|
G | C | 2 | a0001c0001t0001g0166a0001c0001t0011g0203 | 2 | NA19011.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.162-13596G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56262335 | ||||||
| chr16:56262466
|
G | C | 14 | a0001c0001t0001g0166a0001c0001t0002g0253a0001c0001t0003g0246others(11): Show | 14 | HG00673.hp1 HG01256.hp2 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.162-13465G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56262466 | ||||||
| chr16:56262486
|
G | A | 2 | a0001c0001t0001g0166a0001c0001t0011g0203 | 2 | NA19011.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.162-13445G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56262486 | ||||||
| chr16:56262687
|
A | G | 1 | a0001c0006t0021g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.162-13244A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56262687 | ||||||
| chr16:56262880
|
G | A | 153 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0024others(150): Show | 155 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.162-13051G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56262880 | ||||||
| chr16:56262886
|
C | T | 1 | a0001c0001t0005g0256 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.162-13045C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56262886 | ||||||
| chr16:56263134
|
G | T | 1 | a0001c0002t0004g0143 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.162-12797G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56263134 | ||||||
| chr16:56263228
|
G | A | 31 | a0001c0001t0001g0258a0001c0001t0001g0262a0001c0001t0001g0270others(28): Show | 32 | HG00423.hp2 HG01109.hp1 HG02015.hp1 others(29): Show |
intron_variant | MODIFIER | c.162-12703G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56263228 | ||||||
| chr16:56263261
|
G | A | 76 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0057others(73): Show | 76 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.162-12670G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56263261 | ||||||
| chr16:56263843
|
C | T | 1 | a0001c0002t0001g0209 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.162-12088C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56263843 | ||||||
| chr16:56264069
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.162-11862G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56264069 | ||||||
| chr16:56264087
|
G | A | 1 | a0001c0001t0003g0044 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.162-11844G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56264087 | ||||||
| chr16:56264172
|
G | T | 14 | a0001c0001t0001g0166a0001c0001t0002g0253a0001c0001t0003g0246others(11): Show | 14 | HG00673.hp1 HG01256.hp2 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.162-11759G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56264172 | ||||||
| chr16:56264191
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.162-11740A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56264191 | ||||||
| chr16:56264400
|
C | A | 1 | a0001c0002t0001g0209 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.162-11531C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56264400 | ||||||
| chr16:56264530
|
G | C | 1 | a0001c0001t0009g0089 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.162-11401G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56264530 | ||||||
| chr16:56264664
|
A | G | 1 | a0001c0002t0001g0054 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.162-11267A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56264664 | ||||||
| chr16:56264996
|
C | T | 159 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0024others(156): Show | 161 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.162-10935C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56264996 | ||||||
| chr16:56265094
|
A | T | 1 | a0001c0001t0001g0092 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.162-10837A>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56265094 | ||||||
| chr16:56265099
|
C | T | 1 | a0001c0001t0007g0113 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.162-10832C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56265099 | ||||||
| chr16:56265161
|
G | A | 1 | a0001c0002t0002g0029 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.162-10770G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56265161 | ||||||
| chr16:56265404
|
C | G | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.162-10527C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56265404 | ||||||
| chr16:56265588
|
G | C | 1 | a0001c0002t0001g0054 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.162-10343G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56265588 | ||||||
| chr16:56265639
|
T | A | 5 | a0001c0001t0003g0289a0001c0002t0001g0288a0001c0002t0004g0067others(2): Show | 5 | HG02622.hp1 HG02630.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.162-10292T>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56265639 | ||||||
| chr16:56265871
|
G | C | 1 | a0001c0002t0023g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.162-10060G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56265871 | ||||||
| chr16:56265871
|
G | T | 2 | a0001c0001t0001g0163a0001c0002t0001g0013 | 2 | HG02109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.162-10060G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56265871 | ||||||
| chr16:56265897
|
C | G | 31 | a0001c0001t0001g0258a0001c0001t0001g0262a0001c0001t0001g0270others(28): Show | 32 | HG00423.hp2 HG01109.hp1 HG02015.hp1 others(29): Show |
intron_variant | MODIFIER | c.162-10034C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56265897 | ||||||
| chr16:56265975
|
G | A | 1 | a0001c0002t0013g0032 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.162-9956G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56265975 | ||||||
| chr16:56265996
|
G | A | 17 | a0001c0001t0001g0262a0001c0001t0001g0270a0001c0001t0001g0276others(14): Show | 17 | HG00423.hp2 HG01109.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.162-9935G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56265996 | ||||||
| chr16:56266089
|
A | G | 120 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0024others(117): Show | 121 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.162-9842A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56266089 | ||||||
| chr16:56266117
|
A | G | 39 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(36): Show | 39 | HG00438.hp1 HG00642.hp2 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.162-9814A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56266117 | ||||||
| chr16:56266463
|
T | G | 1 | a0001c0002t0012g0181 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.162-9468T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56266463 | ||||||
| chr16:56266513
|
G | C | 1 | a0001c0002t0001g0204 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.162-9418G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56266513 | ||||||
| chr16:56266527
|
C | T | 1 | a0001c0001t0004g0215 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.162-9404C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56266527 | ||||||
| chr16:56266742
|
C | A | 24 | a0001c0001t0001g0258a0001c0001t0001g0262a0001c0001t0001g0270others(21): Show | 25 | HG00423.hp2 HG01109.hp1 HG02015.hp1 others(22): Show |
intron_variant | MODIFIER | c.162-9189C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56266742 | ||||||
| chr16:56266747
|
T | A | 1 | a0001c0002t0023g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.162-9184T>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56266747 | ||||||
| chr16:56266777
|
G | A | 1 | a0001c0002t0004g0144 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.162-9154G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56266777 | ||||||
| chr16:56266810
|
G | A | 3 | a0001c0001t0001g0024a0001c0001t0001g0077a0001c0001t0001g0164 | 3 | NA18955.hp2 NA18982.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.162-9121G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56266810 | ||||||
| chr16:56266921
|
T | G | 1 | a0001c0002t0001g0245 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.162-9010T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56266921 | ||||||
| chr16:56266963
|
C | T | 3 | a0001c0001t0001g0041a0001c0001t0007g0038a0001c0001t0007g0039 | 3 | HG00642.hp2 HG00733.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.162-8968C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56266963 | ||||||
| chr16:56266991
|
A | C | 1 | a0001c0001t0003g0075 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.162-8940A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56266991 | ||||||
| chr16:56267183
|
C | T | 2 | a0001c0001t0003g0030a0001c0002t0004g0021 | 2 | NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.162-8748C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56267183 | ||||||
| chr16:56267364
|
C | A | 1 | a0001c0001t0001g0295 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.162-8567C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56267364 | ||||||
| chr16:56267416
|
C | T | 3 | a0001c0002t0012g0179a0001c0002t0012g0180a0001c0002t0012g0181 | 3 | HG02280.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.162-8515C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56267416 | ||||||
| chr16:56267421
|
G | A | 1 | a0001c0001t0013g0187 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.162-8510G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56267421 | ||||||
| chr16:56267464
|
G | A | 1 | a0001c0004t0002g0028 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.162-8467G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56267464 | ||||||
| chr16:56267544
|
C | T | 17 | a0001c0001t0001g0262a0001c0001t0001g0270a0001c0001t0001g0276others(14): Show | 17 | HG00423.hp2 HG01109.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.162-8387C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56267544 | ||||||
| chr16:56267580
|
C | T | 1 | a0001c0001t0004g0215 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.162-8351C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56267580 | ||||||
| chr16:56267590
|
G | A | 72 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0057others(69): Show | 72 | HG00438.hp2 HG00609.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.162-8341G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56267590 | ||||||
| chr16:56267599
|
G | A | 2 | a0001c0001t0004g0178a0001c0001t0004g0237 | 2 | HG02027.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.162-8332G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56267599 | ||||||
| chr16:56267698
|
A | G | 1 | a0001c0002t0004g0205 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.162-8233A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56267698 | ||||||
| chr16:56267763
|
A | G | 1 | a0001c0001t0004g0227 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.162-8168A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56267763 | ||||||
| chr16:56267800
|
A | G | 1 | a0001c0002t0006g0197 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.162-8131A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56267800 | ||||||
| chr16:56267840
|
A | G | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.162-8091A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56267840 | ||||||
| chr16:56267903
|
A | G | 2 | a0001c0002t0001g0035a0001c0002t0013g0032 | 2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.162-8028A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56267903 | ||||||
| chr16:56267963
|
T | C | 5 | a0001c0001t0014g0034a0001c0002t0001g0035a0001c0002t0001g0054others(2): Show | 5 | HG02559.hp2 HG02965.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.162-7968T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56267963 | ||||||
| chr16:56268063
|
A | G | 1 | a0001c0002t0027g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.162-7868A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56268063 | ||||||
| chr16:56268331
|
A | C | 72 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0057others(69): Show | 72 | HG00438.hp2 HG00609.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.162-7600A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56268331 | ||||||
| chr16:56268390
|
C | T | 2 | a0001c0001t0004g0178a0001c0001t0004g0237 | 2 | HG02027.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.162-7541C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56268390 | ||||||
| chr16:56268411
|
C | T | 1 | a0001c0002t0001g0268 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.162-7520C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56268411 | ||||||
| chr16:56268445
|
T | A | 1 | a0001c0001t0001g0182 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.162-7486T>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56268445 | ||||||
| chr16:56268522
|
C | G | 74 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0057others(71): Show | 74 | HG00438.hp2 HG00609.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.162-7409C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56268522 | ||||||
| chr16:56268528
|
G | T | 74 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0057others(71): Show | 74 | HG00438.hp2 HG00609.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.162-7403G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56268528 | ||||||
| chr16:56268536
|
A | G | 12 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0258others(9): Show | 13 | HG01891.hp2 HG02015.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.162-7395A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56268536 | ||||||
| chr16:56268682
|
T | C | 1 | a0001c0001t0001g0219 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.162-7249T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56268682 | ||||||
| chr16:56268701
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.162-7230A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56268701 | ||||||
| chr16:56269002
|
G | A | 17 | a0001c0001t0001g0153a0001c0001t0001g0166a0001c0001t0002g0150others(14): Show | 17 | HG00280.hp1 HG00673.hp1 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.162-6929G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56269002 | ||||||
| chr16:56269028
|
T | C | 2 | a0001c0001t0001g0163a0001c0002t0001g0013 | 2 | HG02109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.162-6903T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56269028 | ||||||
| chr16:56269063
|
GACCCTAA others(8): Show |
G | 6 | a0001c0001t0003g0030a0001c0002t0004g0021a0001c0002t0012g0179others(3): Show | 6 | HG02280.hp2 HG02451.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.162-6867_162-6853d others(17): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56269063 | ||||||
| chr16:56269074
|
A | G | 17 | a0001c0001t0001g0262a0001c0001t0001g0270a0001c0001t0001g0276others(14): Show | 17 | HG00423.hp2 HG01109.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.162-6857A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56269074 | ||||||
| chr16:56269134
|
C | T | 1 | a0001c0002t0010g0252 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.162-6797C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56269134 | ||||||
| chr16:56269142
|
A | G | 1 | a0001c0002t0004g0143 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.162-6789A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56269142 | ||||||
| chr16:56269189
|
A | G | 28 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0258others(25): Show | 29 | HG00423.hp2 HG01109.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.162-6742A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56269189 | ||||||
| chr16:56269247
|
C | T | 1 | a0001c0001t0004g0161 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.162-6684C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56269247 | ||||||
| chr16:56269298
|
GCTC | G | 3 | a0001c0001t0001g0182a0001c0001t0003g0100a0001c0001t0003g0159 | 3 | HG03471.hp2 NA18979.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.162-6612_162-6610d others(5): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56269298 | |||||
| chr16:56269393
|
C | T | 1 | a0001c0002t0001g0198 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.162-6538C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56269393 | ||||||
| chr16:56269395
|
C | T | 1 | a0001c0001t0001g0219 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.162-6536C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56269395 | ||||||
| chr16:56269422
|
C | T | 1 | a0001c0002t0003g0136 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.162-6509C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56269422 | ||||||
| chr16:56269481
|
G | A | 7 | a0001c0001t0001g0295a0001c0001t0004g0291a0001c0002t0001g0279others(4): Show | 7 | HG02970.hp1 HG03098.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.162-6450G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56269481 | ||||||
| chr16:56269526
|
C | T | 7 | a0001c0001t0001g0202a0001c0001t0001g0280a0001c0001t0004g0223others(4): Show | 7 | NA18945.hp2 NA18995.hp1 NA19009.hp1 others(4): Show |
intron_variant | MODIFIER | c.162-6405C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56269526 | ||||||
| chr16:56269547
|
C | T | 1 | a0001c0002t0023g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.162-6384C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56269547 | ||||||
| chr16:56269571
|
G | A | 1 | a0001c0001t0005g0206 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.162-6360G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56269571 | ||||||
| chr16:56269659
|
C | T | 2 | a0001c0001t0004g0178a0001c0001t0004g0237 | 2 | HG02027.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.162-6272C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56269659 | ||||||
| chr16:56269709
|
C | T | 5 | a0001c0001t0003g0289a0001c0002t0001g0288a0001c0002t0004g0067others(2): Show | 5 | HG02622.hp1 HG02630.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.162-6222C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56269709 | ||||||
| chr16:56269715
|
G | A | 1 | a0001c0001t0001g0177 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.162-6216G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56269715 | ||||||
| chr16:56269969
|
A | G | 28 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0258others(25): Show | 29 | HG00423.hp2 HG01109.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.162-5962A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56269969 | ||||||
| chr16:56270099
|
C | T | 3 | a0001c0001t0001g0231a0001c0001t0002g0254a0001c0002t0001g0232 | 3 | HG01169.hp1 HG01361.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.162-5832C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56270099 | ||||||
| chr16:56270169
|
G | C | 1 | a0001c0001t0010g0040 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.162-5762G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56270169 | ||||||
| chr16:56270177
|
T | G | 2 | a0001c0002t0001g0035a0001c0002t0013g0032 | 2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.162-5754T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56270177 | ||||||
| chr16:56270286
|
G | A | 1 | a0001c0001t0001g0164 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.162-5645G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56270286 | ||||||
| chr16:56270419
|
G | GAC | 15 | a0001c0001t0004g0002a0001c0001t0004g0178a0001c0001t0004g0287others(12): Show | 16 | HG00280.hp1 HG02015.hp1 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.162-5486_162-5485d others(4): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56270419 | |||||
| chr16:56270419
|
G | GACAC | 8 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0258others(5): Show | 8 | HG01891.hp2 HG02027.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.162-5488_162-5485d others(6): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56270419 | |||||
| chr16:56270419
|
GACAC | G | 4 | a0001c0001t0004g0223a0001c0001t0005g0221a0001c0001t0005g0222others(1): Show | 4 | NA18945.hp2 NA19009.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.162-5488_162-5485d others(6): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 56270419 | |||||
| chr16:56270431
|
C | T | 1 | a0001c0002t0004g0205 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.162-5500C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56270431 | ||||||
| chr16:56270469
|
G | A | 1 | a0001c0001t0004g0296 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.162-5462G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56270469 | ||||||
| chr16:56270763
|
A | G | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.162-5168A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56270763 | ||||||
| chr16:56270934
|
G | C | 1 | a0001c0001t0003g0044 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.162-4997G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56270934 | ||||||
| chr16:56270974
|
C | T | 5 | a0001c0001t0007g0113a0001c0002t0001g0116a0001c0002t0003g0160others(2): Show | 5 | HG01496.hp2 HG01975.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.162-4957C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56270974 | ||||||
| chr16:56271070
|
C | G | 3 | a0001c0001t0003g0085a0001c0002t0002g0086a0001c0002t0004g0063 | 3 | HG02257.hp1 HG02486.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.162-4861C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56271070 | ||||||
| chr16:56271081
|
G | A | 1 | a0001c0006t0021g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.162-4850G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56271081 | ||||||
| chr16:56271103
|
T | C | 1 | a0001c0002t0002g0283 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.162-4828T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56271103 | ||||||
| chr16:56271190
|
G | A | 4 | a0001c0002t0002g0190a0001c0002t0003g0233a0001c0002t0003g0235others(1): Show | 4 | HG00733.hp2 HG02698.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.162-4741G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56271190 | ||||||
| chr16:56271191
|
G | A | 1 | a0001c0001t0005g0216 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.162-4740G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56271191 | ||||||
| chr16:56271515
|
G | A | 2 | a0001c0002t0003g0148a0001c0002t0027g0146 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.162-4416G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56271515 | ||||||
| chr16:56271711
|
C | T | 1 | a0001c0002t0001g0018 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.162-4220C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56271711 | ||||||
| chr16:56271740
|
A | G | 23 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0049others(20): Show | 23 | HG00438.hp1 HG00642.hp2 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.162-4191A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56271740 | ||||||
| chr16:56271845
|
G | A | 295 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0014others(292): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.162-4086G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56271845 | ||||||
| chr16:56272178
|
G | A | 2 | a0001c0001t0003g0289a0001c0002t0001g0288 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.162-3753G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56272178 | ||||||
| chr16:56272181
|
C | T | 1 | a0001c0001t0017g0290 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.162-3750C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56272181 | ||||||
| chr16:56272224
|
G | A | 1 | a0001c0001t0028g0125 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.162-3707G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56272224 | ||||||
| chr16:56272245
|
C | T | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.162-3686C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56272245 | ||||||
| chr16:56272295
|
A | G | 29 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0051others(26): Show | 30 | HG00423.hp2 HG00438.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.162-3636A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56272295 | ||||||
| chr16:56272404
|
T | G | 1 | a0001c0002t0013g0293 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.162-3527T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56272404 | ||||||
| chr16:56272548
|
C | T | 1 | a0001c0001t0007g0158 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.162-3383C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56272548 | ||||||
| chr16:56272649
|
C | T | 1 | a0001c0001t0001g0177 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.162-3282C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56272649 | ||||||
| chr16:56272728
|
A | G | 55 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0078others(52): Show | 56 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.162-3203A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56272728 | ||||||
| chr16:56272751
|
C | G | 13 | a0001c0001t0001g0262a0001c0001t0001g0270a0001c0001t0001g0276others(10): Show | 13 | HG00423.hp2 HG01109.hp1 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.162-3180C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56272751 | ||||||
| chr16:56273072
|
T | A | 10 | a0001c0001t0001g0295a0001c0001t0004g0291a0001c0002t0001g0247others(7): Show | 10 | HG02630.hp1 HG02723.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.162-2859T>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56273072 | ||||||
| chr16:56273232
|
C | T | 1 | a0001c0002t0002g0250 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.162-2699C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56273232 | ||||||
| chr16:56273523
|
A | G | 32 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0258others(29): Show | 33 | HG00423.hp2 HG01109.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.162-2408A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56273523 | ||||||
| chr16:56273637
|
G | A | 13 | a0001c0001t0001g0262a0001c0001t0001g0270a0001c0001t0001g0276others(10): Show | 13 | HG00423.hp2 HG01109.hp1 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.162-2294G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56273637 | ||||||
| chr16:56274109
|
G | T | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.162-1822G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56274109 | ||||||
| chr16:56274443
|
C | G | 73 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0057others(70): Show | 73 | HG00438.hp2 HG00609.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.162-1488C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56274443 | ||||||
| chr16:56274519
|
A | C | 173 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(170): Show | 175 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.162-1412A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56274519 | ||||||
| chr16:56274582
|
A | G | 2 | a0001c0001t0003g0101a0001c0001t0004g0112 | 2 | NA18959.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.162-1349A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56274582 | ||||||
| chr16:56274717
|
A | G | 7 | a0001c0001t0001g0202a0001c0001t0001g0280a0001c0001t0004g0223others(4): Show | 7 | NA18945.hp2 NA18995.hp1 NA19009.hp1 others(4): Show |
intron_variant | MODIFIER | c.162-1214A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56274717 | ||||||
| chr16:56274779
|
C | T | 1 | a0001c0002t0023g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.162-1152C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56274779 | ||||||
| chr16:56274942
|
T | C | 10 | a0001c0001t0001g0295a0001c0001t0004g0291a0001c0002t0001g0247others(7): Show | 10 | HG02630.hp1 HG02723.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.162-989T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56274942 | ||||||
| chr16:56275130
|
A | G | 5 | a0001c0001t0003g0289a0001c0002t0001g0288a0001c0002t0004g0067others(2): Show | 5 | HG02622.hp1 HG02630.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.162-801A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56275130 | ||||||
| chr16:56275371
|
G | A | 1 | a0001c0001t0001g0284 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.162-560G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56275371 | ||||||
| chr16:56275404
|
G | A | 3 | a0001c0001t0008g0042a0001c0001t0008g0045a0001c0001t0008g0046 | 3 | NA18975.hp1 NA18986.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.162-527G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56275404 | ||||||
| chr16:56275444
|
A | G | 10 | a0001c0001t0001g0295a0001c0001t0004g0291a0001c0002t0001g0247others(7): Show | 10 | HG02630.hp1 HG02723.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.162-487A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56275444 | ||||||
| chr16:56275446
|
G | T | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.162-485G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56275446 | ||||||
| chr16:56275470
|
T | G | 1 | a0001c0001t0003g0269 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.162-461T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56275470 | ||||||
| chr16:56275843
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.162-88C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56275843 | ||||||
| chr16:56275883
|
A | G | 1 | a0001c0002t0004g0205 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.162-48A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 2/8 | chr16 | 56275883 | ||||||
| chr16:56276261
|
C | CA | 4 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0003g0052others(1): Show | 4 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.303+190dupA | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56276261 | |||||
| chr16:56276277
|
T | C | 2 | a0001c0002t0002g0212a0001c0002t0002g0214 | 2 | HG04184.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.303+205T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56276277 | ||||||
| chr16:56276526
|
G | A | 1 | a0001c0002t0001g0263 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.303+454G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56276526 | ||||||
| chr16:56276837
|
G | A | 1 | a0001c0001t0017g0244 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.303+765G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56276837 | ||||||
| chr16:56277199
|
C | A | 30 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0258others(27): Show | 31 | HG00423.hp2 HG01109.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.303+1127C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56277199 | ||||||
| chr16:56277200
|
G | A | 2 | a0001c0002t0001g0025a0001c0002t0001g0107 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.303+1128G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56277200 | ||||||
| chr16:56277327
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.303+1255G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56277327 | ||||||
| chr16:56277486
|
A | G | 1 | a0001c0001t0007g0158 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.303+1414A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56277486 | ||||||
| chr16:56277714
|
G | C | 132 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0057others(129): Show | 133 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.303+1642G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56277714 | ||||||
| chr16:56277776
|
T | TAC | 25 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0084others(22): Show | 25 | HG00673.hp1 HG01109.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.303+1769_303+1770d others(4): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56277776 | |||||
| chr16:56277776
|
T | TACAC | 19 | a0001c0001t0001g0043a0001c0001t0001g0049a0001c0001t0001g0106others(16): Show | 19 | HG00438.hp1 HG00639.hp1 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.303+1767_303+1770d others(6): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56277776 | |||||
| chr16:56277776
|
T | TACACAC | 6 | a0001c0001t0001g0051a0001c0001t0001g0057a0001c0001t0001g0167others(3): Show | 6 | HG00280.hp1 HG01884.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.303+1765_303+1770d others(8): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56277776 | |||||
| chr16:56277776
|
T | TACACACA others(3): Show |
2 | a0001c0002t0001g0119a0001c0002t0012g0180 | 2 | HG03516.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.303+1761_303+1770d others(12): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56277776 | |||||
| chr16:56277776
|
T | TACACACA others(5): Show |
2 | a0001c0001t0020g0126a0001c0002t0004g0278 | 2 | HG00609.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.303+1759_303+1770d others(14): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56277776 | |||||
| chr16:56277776
|
TAC | T | 33 | a0001c0001t0001g0050a0001c0001t0001g0077a0001c0001t0001g0163others(30): Show | 33 | HG00099.hp2 HG00438.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.303+1769_303+1770d others(4): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56277776 | |||||
| chr16:56277776
|
TACAC | T | 25 | a0001c0001t0001g0041a0001c0001t0001g0132a0001c0001t0001g0166others(22): Show | 25 | HG00423.hp2 HG01106.hp2 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.303+1767_303+1770d others(6): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56277776 | |||||
| chr16:56277776
|
TACACAC | T | 28 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0071others(25): Show | 29 | HG00609.hp1 HG00642.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.303+1765_303+1770d others(8): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56277776 | |||||
| chr16:56277776
|
TACACACA others(1): Show |
T | 18 | a0001c0001t0001g0096a0001c0001t0001g0165a0001c0001t0001g0210others(15): Show | 18 | HG01109.hp1 HG01346.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.303+1763_303+1770d others(10): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56277776 | |||||
| chr16:56277776
|
TACACACA others(3): Show |
T | 9 | a0001c0001t0001g0072a0001c0001t0001g0199a0001c0001t0001g0211others(6): Show | 9 | HG02027.hp1 HG03942.hp1 NA18942.hp1 others(6): Show |
intron_variant | MODIFIER | c.303+1761_303+1770d others(12): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56277776 | |||||
| chr16:56277776
|
TACACACA others(5): Show |
T | 11 | a0001c0001t0001g0284a0001c0001t0003g0208a0001c0001t0003g0238others(8): Show | 11 | HG01261.hp1 HG02055.hp2 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.303+1759_303+1770d others(14): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56277776 | |||||
| chr16:56277776
|
TACACACA others(7): Show |
T | 1 | a0001c0002t0006g0197 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.303+1757_303+1770d others(16): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56277776 | |||||
| chr16:56277776
|
TACACACA others(9): Show |
T | 8 | a0001c0001t0004g0217a0001c0001t0005g0218a0001c0001t0009g0060others(5): Show | 8 | HG02074.hp1 HG04115.hp1 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.303+1755_303+1770d others(18): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56277776 | |||||
| chr16:56277776
|
TACACACA others(11): Show |
T | 19 | a0001c0001t0001g0098a0001c0001t0001g0196a0001c0001t0001g0242others(16): Show | 19 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(16): Show |
intron_variant | MODIFIER | c.303+1753_303+1770d others(20): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56277776 | |||||
| chr16:56277776
|
TACACACA others(13): Show |
T | 12 | a0001c0001t0001g0062a0001c0001t0001g0231a0001c0001t0002g0254others(9): Show | 12 | HG00140.hp2 HG01074.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.303+1751_303+1770d others(22): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56277776 | |||||
| chr16:56277776
|
TACACACA others(15): Show |
T | 27 | a0001c0001t0001g0022a0001c0001t0001g0078a0001c0001t0001g0115others(24): Show | 28 | HG00323.hp1 HG00673.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.303+1749_303+1770d others(24): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56277776 | |||||
| chr16:56277776
|
TACACACA others(17): Show |
T | 11 | a0001c0001t0001g0281a0001c0001t0003g0101a0001c0001t0004g0112others(8): Show | 11 | HG00423.hp1 HG01106.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.303+1747_303+1770d others(26): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56277776 | |||||
| chr16:56277776
|
TACACACA others(19): Show |
T | 12 | a0001c0001t0001g0202a0001c0001t0001g0295a0001c0002t0001g0236others(9): Show | 12 | HG00099.hp1 HG02630.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.303+1745_303+1770d others(28): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56277776 | |||||
| chr16:56277776
|
TACACACA others(21): Show |
T | 1 | a0001c0002t0001g0173 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.303+1743_303+1770d others(30): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56277776 | |||||
| chr16:56277776
|
TACACACA others(25): Show |
T | 1 | a0001c0002t0001g0279 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.303+1739_303+1770d others(34): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56277776 | |||||
| chr16:56277862
|
G | A | 50 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0078others(47): Show | 51 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.303+1790G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56277862 | ||||||
| chr16:56277882
|
C | T | 1 | a0001c0001t0004g0291 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.303+1810C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56277882 | ||||||
| chr16:56277956
|
T | G | 28 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0258others(25): Show | 29 | HG00423.hp2 HG01109.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.303+1884T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56277956 | ||||||
| chr16:56278192
|
G | A | 2 | a0001c0001t0003g0030a0001c0002t0004g0021 | 2 | NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.303+2120G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56278192 | ||||||
| chr16:56278586
|
A | G | 5 | a0001c0001t0001g0284a0001c0001t0017g0290a0001c0002t0002g0283others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.303+2514A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56278586 | ||||||
| chr16:56278652
|
C | G | 73 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0057others(70): Show | 73 | HG00438.hp2 HG00609.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.303+2580C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56278652 | ||||||
| chr16:56278751
|
A | C | 30 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0258others(27): Show | 31 | HG00423.hp2 HG01109.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.303+2679A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56278751 | ||||||
| chr16:56278844
|
T | C | 1 | a0001c0002t0001g0173 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.303+2772T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56278844 | ||||||
| chr16:56278974
|
A | G | 1 | a0001c0002t0003g0184 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.303+2902A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56278974 | ||||||
| chr16:56279125
|
A | C | 28 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0049others(25): Show | 28 | HG00438.hp1 HG00642.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.303+3053A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56279125 | ||||||
| chr16:56279372
|
C | T | 1 | a0001c0002t0002g0213 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.303+3300C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56279372 | ||||||
| chr16:56279393
|
A | C | 1 | a0001c0002t0023g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.303+3321A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56279393 | ||||||
| chr16:56279406
|
C | T | 2 | a0001c0002t0002g0029a0001c0004t0002g0028 | 2 | HG02145.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.303+3334C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56279406 | ||||||
| chr16:56279418
|
C | T | 1 | a0001c0001t0004g0291 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.303+3346C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56279418 | ||||||
| chr16:56279450
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.303+3378C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56279450 | ||||||
| chr16:56279464
|
C | T | 1 | a0001c0002t0002g0213 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.303+3392C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56279464 | ||||||
| chr16:56279522
|
G | A | 1 | a0001c0002t0001g0121 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.303+3450G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56279522 | ||||||
| chr16:56279639
|
C | G | 73 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0057others(70): Show | 73 | HG00438.hp2 HG00609.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.303+3567C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56279639 | ||||||
| chr16:56279833
|
C | A | 1 | a0001c0001t0004g0296 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.303+3761C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56279833 | ||||||
| chr16:56279863
|
C | A | 2 | a0001c0002t0003g0148a0001c0002t0027g0146 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.303+3791C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56279863 | ||||||
| chr16:56279866
|
C | G | 6 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0258others(3): Show | 6 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.303+3794C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56279866 | ||||||
| chr16:56279896
|
G | A | 1 | a0001c0002t0023g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.303+3824G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56279896 | ||||||
| chr16:56279896
|
G | C | 30 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0258others(27): Show | 31 | HG00423.hp2 HG01109.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.303+3824G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56279896 | ||||||
| chr16:56279925
|
C | T | 4 | a0001c0001t0009g0140a0001c0002t0003g0001a0001c0002t0003g0109others(1): Show | 5 | HG02135.hp1 NA18973.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.303+3853C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56279925 | ||||||
| chr16:56279960
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.303+3888A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56279960 | ||||||
| chr16:56280127
|
T | A | 1 | a0001c0001t0004g0296 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.303+4055T>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56280127 | ||||||
| chr16:56280233
|
G | A | 19 | a0001c0001t0001g0262a0001c0001t0001g0270a0001c0001t0001g0276others(16): Show | 19 | HG00423.hp2 HG01109.hp1 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.303+4161G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56280233 | ||||||
| chr16:56280251
|
G | C | 1 | a0001c0002t0023g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.303+4179G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56280251 | ||||||
| chr16:56280307
|
G | A | 1 | a0001c0002t0010g0252 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.303+4235G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56280307 | ||||||
| chr16:56280392
|
G | T | 11 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0258others(8): Show | 12 | HG01891.hp2 HG02015.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.303+4320G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56280392 | ||||||
| chr16:56280632
|
C | T | 5 | a0001c0001t0003g0289a0001c0002t0001g0288a0001c0002t0004g0067others(2): Show | 5 | HG02622.hp1 HG02630.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.303+4560C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56280632 | ||||||
| chr16:56280738
|
T | C | 1 | a0001c0002t0027g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.303+4666T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56280738 | ||||||
| chr16:56280775
|
A | C | 51 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0078others(48): Show | 52 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.303+4703A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56280775 | ||||||
| chr16:56281229
|
G | A | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.303+5157G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56281229 | ||||||
| chr16:56281268
|
C | T | 2 | a0001c0002t0001g0228a0001c0002t0004g0074 | 2 | HG00280.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.303+5196C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56281268 | ||||||
| chr16:56281427
|
G | T | 1 | a0001c0002t0002g0086 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.303+5355G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56281427 | ||||||
| chr16:56281447
|
T | C | 204 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(201): Show | 206 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.303+5375T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56281447 | ||||||
| chr16:56281538
|
C | T | 1 | a0001c0001t0020g0126 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.303+5466C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56281538 | ||||||
| chr16:56281561
|
T | C | 1 | a0001c0002t0027g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.303+5489T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56281561 | ||||||
| chr16:56281632
|
T | G | 2 | a0001c0001t0004g0178a0001c0001t0004g0237 | 2 | HG02027.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.303+5560T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56281632 | ||||||
| chr16:56281683
|
C | G | 2 | a0001c0001t0003g0085a0001c0002t0002g0086 | 2 | HG02257.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.303+5611C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56281683 | ||||||
| chr16:56282103
|
G | A | 1 | a0001c0001t0006g0226 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.303+6031G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56282103 | ||||||
| chr16:56282369
|
AT | A | 222 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(219): Show | 224 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.303+6300delT | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56282369 | |||||
| chr16:56282450
|
T | G | 1 | a0001c0001t0017g0244 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.303+6378T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56282450 | ||||||
| chr16:56282771
|
A | G | 8 | a0001c0001t0001g0182a0001c0001t0001g0295a0001c0001t0004g0291others(5): Show | 8 | HG02970.hp1 HG03098.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.303+6699A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56282771 | ||||||
| chr16:56282803
|
C | A | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | NA18998.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.303+6731C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56282803 | ||||||
| chr16:56282870
|
G | C | 2 | a0001c0002t0001g0111a0001c0002t0001g0130 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.303+6798G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56282870 | ||||||
| chr16:56282943
|
GAAGA | G | 72 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0057others(69): Show | 72 | HG00438.hp2 HG00609.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.303+6876_303+6879d others(6): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56282943 | |||||
| chr16:56282954
|
G | A | 6 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0002g0081others(3): Show | 6 | HG00735.hp1 HG01169.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.303+6882G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56282954 | ||||||
| chr16:56283038
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.303+6966G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56283038 | ||||||
| chr16:56283229
|
A | G | 1 | a0001c0002t0002g0029 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.303+7157A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56283229 | ||||||
| chr16:56283304
|
C | G | 72 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0057others(69): Show | 72 | HG00438.hp2 HG00609.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.303+7232C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56283304 | ||||||
| chr16:56283325
|
G | A | 2 | a0001c0001t0003g0101a0001c0001t0004g0112 | 2 | NA18959.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.303+7253G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56283325 | ||||||
| chr16:56283325
|
G | T | 9 | a0001c0001t0001g0182a0001c0001t0001g0295a0001c0001t0004g0291others(6): Show | 9 | HG02074.hp1 HG02970.hp1 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.303+7253G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56283325 | ||||||
| chr16:56283433
|
C | T | 9 | a0001c0001t0001g0182a0001c0001t0001g0295a0001c0001t0004g0291others(6): Show | 9 | HG02074.hp1 HG02970.hp1 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.303+7361C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56283433 | ||||||
| chr16:56283661
|
G | A | 2 | a0001c0002t0002g0212a0001c0002t0002g0214 | 2 | HG04184.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.303+7589G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56283661 | ||||||
| chr16:56283663
|
T | G | 4 | a0001c0001t0001g0022a0001c0001t0001g0078a0001c0001t0008g0110others(1): Show | 4 | HG01928.hp2 HG02293.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.303+7591T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56283663 | ||||||
| chr16:56283678
|
T | C | 3 | a0001c0001t0001g0295a0001c0002t0001g0294a0001c0002t0013g0293 | 3 | HG02970.hp1 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.303+7606T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56283678 | ||||||
| chr16:56283781
|
A | T | 1 | a0001c0002t0027g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.303+7709A>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56283781 | ||||||
| chr16:56283987
|
T | C | 3 | a0001c0001t0007g0113a0001c0002t0003g0160a0001c0002t0005g0162 | 3 | HG01496.hp2 HG01975.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.303+7915T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56283987 | ||||||
| chr16:56284158
|
G | A | 1 | a0001c0001t0001g0281 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.303+8086G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56284158 | ||||||
| chr16:56284203
|
C | G | 3 | a0001c0002t0001g0025a0001c0002t0001g0107a0001c0002t0005g0026 | 3 | HG01515.hp2 HG01517.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.303+8131C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56284203 | ||||||
| chr16:56284348
|
G | A | 71 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0057others(68): Show | 71 | HG00438.hp2 HG00609.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.303+8276G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56284348 | ||||||
| chr16:56284507
|
G | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0189 | 2 | HG02055.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.303+8435G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56284507 | ||||||
| chr16:56284681
|
C | T | 72 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0057others(69): Show | 72 | HG00438.hp2 HG00609.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.303+8609C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56284681 | ||||||
| chr16:56284683
|
G | A | 1 | a0001c0002t0002g0004 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.303+8611G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56284683 | ||||||
| chr16:56284698
|
C | T | 18 | a0001c0001t0001g0153a0001c0001t0001g0166a0001c0001t0002g0150others(15): Show | 18 | HG00280.hp1 HG00673.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.303+8626C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56284698 | ||||||
| chr16:56284957
|
C | T | 2 | a0001c0001t0005g0272a0001c0002t0002g0271 | 2 | HG04184.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.303+8885C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56284957 | ||||||
| chr16:56284961
|
A | C | 1 | a0001c0002t0003g0275 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.303+8889A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56284961 | ||||||
| chr16:56284985
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.303+8913C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56284985 | ||||||
| chr16:56285034
|
T | A | 31 | a0001c0001t0001g0057a0001c0001t0001g0262a0001c0001t0001g0270others(28): Show | 31 | HG00423.hp2 HG01109.hp1 HG02080.hp2 others(28): Show |
intron_variant | MODIFIER | c.303+8962T>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56285034 | ||||||
| chr16:56285056
|
C | T | 6 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0258others(3): Show | 6 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.303+8984C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56285056 | ||||||
| chr16:56285078
|
A | T | 1 | a0001c0001t0002g0273 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.303+9006A>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56285078 | ||||||
| chr16:56285081
|
C | T | 1 | a0001c0002t0001g0147 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.303+9009C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56285081 | ||||||
| chr16:56285212
|
G | A | 77 | a0001c0001t0001g0022a0001c0001t0001g0041a0001c0001t0001g0043others(74): Show | 78 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.303+9140G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56285212 | ||||||
| chr16:56285411
|
A | C | 202 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(199): Show | 203 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.303+9339A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56285411 | ||||||
| chr16:56285938
|
C | T | 53 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0078others(50): Show | 54 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.303+9866C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56285938 | ||||||
| chr16:56286141
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.303+10069G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56286141 | ||||||
| chr16:56286212
|
G | A | 2 | a0001c0002t0004g0067a0001c0002t0004g0277 | 2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.303+10140G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56286212 | ||||||
| chr16:56286523
|
G | A | 23 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0050others(20): Show | 23 | HG00438.hp1 HG00642.hp2 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.303+10451G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56286523 | ||||||
| chr16:56286695
|
C | CTG | 9 | a0001c0001t0001g0167a0001c0001t0001g0170a0001c0001t0001g0172others(6): Show | 9 | HG01884.hp2 NA18747.hp1 NA18968.hp2 others(6): Show |
intron_variant | MODIFIER | c.303+10659_303+1066 others(6): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56286695 | |||||
| chr16:56286695
|
CTG | C | 81 | a0001c0001t0001g0022a0001c0001t0001g0057a0001c0001t0001g0062others(78): Show | 82 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.303+10659_303+1066 others(6): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56286695 | |||||
| chr16:56286695
|
CTGTG | C | 69 | a0001c0001t0001g0024a0001c0001t0001g0049a0001c0001t0001g0071others(66): Show | 69 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.303+10657_303+1066 others(8): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56286695 | |||||
| chr16:56286695
|
CTGTGTG | C | 6 | a0001c0001t0003g0085a0001c0001t0003g0269a0001c0001t0010g0040others(3): Show | 6 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.303+10655_303+1066 others(10): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56286695 | |||||
| chr16:56286695
|
CTGTGTGT others(1): Show |
C | 43 | a0001c0001t0001g0011a0001c0001t0001g0041a0001c0001t0001g0043others(40): Show | 43 | HG00438.hp1 HG00642.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.303+10653_303+1066 others(12): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56286695 | |||||
| chr16:56286695
|
CTGTGTGT others(3): Show |
C | 17 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0258others(14): Show | 18 | HG01891.hp2 HG02027.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.303+10651_303+1066 others(14): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56286695 | |||||
| chr16:56286695
|
CTGTGTGT others(5): Show |
C | 1 | a0001c0001t0004g0178 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.303+10649_303+1066 others(16): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56286695 | |||||
| chr16:56286695
|
CTGTGTGT others(7): Show |
C | 1 | a0001c0002t0002g0029 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.303+10647_303+1066 others(18): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56286695 | |||||
| chr16:56286731
|
G | A | 1 | a0001c0001t0015g0251 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.303+10659G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56286731 | ||||||
| chr16:56286762
|
T | C | 1 | a0001c0001t0010g0123 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.303+10690T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56286762 | ||||||
| chr16:56286912
|
G | A | 57 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0078others(54): Show | 58 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.303+10840G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56286912 | ||||||
| chr16:56286963
|
A | G | 1 | a0001c0002t0003g0235 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.303+10891A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56286963 | ||||||
| chr16:56286979
|
C | T | 3 | a0001c0002t0001g0025a0001c0002t0001g0107a0001c0002t0005g0026 | 3 | HG01515.hp2 HG01517.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.303+10907C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56286979 | ||||||
| chr16:56287067
|
A | G | 98 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0024others(95): Show | 99 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.303+10995A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56287067 | ||||||
| chr16:56287207
|
A | G | 220 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(217): Show | 222 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.303+11135A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56287207 | ||||||
| chr16:56287249
|
T | G | 1 | a0001c0001t0008g0042 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.303+11177T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56287249 | ||||||
| chr16:56287329
|
C | T | 2 | a0001c0001t0001g0079a0001c0002t0001g0117 | 2 | HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.303+11257C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56287329 | ||||||
| chr16:56287781
|
G | T | 2 | a0001c0001t0001g0295a0001c0002t0001g0294 | 2 | HG02970.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.303+11709G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56287781 | ||||||
| chr16:56287782
|
G | T | 2 | a0001c0001t0001g0295a0001c0002t0001g0294 | 2 | HG02970.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.303+11710G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56287782 | ||||||
| chr16:56287840
|
C | A | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.303+11768C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56287840 | ||||||
| chr16:56288161
|
G | A | 1 | a0001c0002t0004g0074 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.303+12089G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56288161 | ||||||
| chr16:56288423
|
C | A | 69 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0049others(66): Show | 69 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.303+12351C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56288423 | ||||||
| chr16:56288587
|
A | G | 1 | a0001c0001t0005g0256 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.303+12515A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56288587 | ||||||
| chr16:56288651
|
C | T | 18 | a0001c0001t0001g0262a0001c0001t0001g0270a0001c0001t0002g0261others(15): Show | 18 | HG01109.hp1 HG02080.hp2 HG02738.hp1 others(15): Show |
intron_variant | MODIFIER | c.303+12579C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56288651 | ||||||
| chr16:56288740
|
G | C | 101 | a0001c0001t0001g0022a0001c0001t0001g0041a0001c0001t0001g0043others(98): Show | 102 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.303+12668G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56288740 | ||||||
| chr16:56288807
|
A | C | 1 | a0001c0002t0001g0288 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.303+12735A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56288807 | ||||||
| chr16:56288853
|
A | G | 2 | a0001c0001t0004g0178a0001c0001t0004g0237 | 2 | HG02027.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.303+12781A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56288853 | ||||||
| chr16:56288909
|
C | G | 3 | a0001c0001t0004g0002a0001c0001t0004g0287a0001c0001t0011g0285 | 4 | HG03491.hp2 HG03492.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.303+12837C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56288909 | ||||||
| chr16:56288922
|
C | T | 129 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0049others(126): Show | 130 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.303+12850C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56288922 | ||||||
| chr16:56288923
|
G | A | 4 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0003g0052others(1): Show | 4 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.303+12851G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56288923 | ||||||
| chr16:56288964
|
C | G | 1 | a0001c0001t0003g0052 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.303+12892C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56288964 | ||||||
| chr16:56289027
|
CA | C | 109 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0049others(106): Show | 110 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.303+12961delA | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56289027 | |||||
| chr16:56289033
|
A | AAG | 60 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0078others(57): Show | 61 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.303+12961_303+1296 others(6): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56289033 | ||||||
| chr16:56289033
|
A | G | 3 | a0001c0001t0001g0163a0001c0001t0017g0244a0001c0002t0001g0013 | 3 | HG02109.hp1 HG02622.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.303+12961A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56289033 | ||||||
| chr16:56289034
|
G | T | 3 | a0001c0001t0009g0089a0001c0002t0004g0074a0001c0002t0023g0027 | 3 | HG00280.hp1 HG02074.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.303+12962G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56289034 | ||||||
| chr16:56289035
|
G | A | 3 | a0001c0002t0002g0118a0001c0003t0002g0103a0001c0003t0002g0114 | 3 | HG00735.hp2 HG01255.hp1 HG01928.hp1 |
intron_variant | MODIFIER | c.303+12963G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56289035 | ||||||
| chr16:56289035
|
G | C | 31 | a0001c0001t0001g0202a0001c0001t0001g0210a0001c0001t0001g0211others(28): Show | 31 | HG01261.hp1 HG01346.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.303+12963G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56289035 | ||||||
| chr16:56289035
|
G | T | 1 | a0001c0001t0005g0220 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.303+12963G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56289035 | ||||||
| chr16:56289036
|
G | C | 1 | a0001c0001t0001g0176 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.303+12964G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56289036 | ||||||
| chr16:56289037
|
G | C | 7 | a0001c0001t0002g0273a0001c0001t0003g0269a0001c0002t0001g0268others(4): Show | 7 | HG02080.hp2 NA18942.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.303+12965G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56289037 | ||||||
| chr16:56289239
|
C | T | 115 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0041others(112): Show | 116 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.303+13167C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56289239 | ||||||
| chr16:56289240
|
G | A | 3 | a0001c0002t0002g0283a0001c0004t0002g0282a0001c0006t0021g0019 | 3 | HG02055.hp2 HG02109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.303+13168G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56289240 | ||||||
| chr16:56289320
|
A | G | 35 | a0001c0001t0001g0043a0001c0001t0001g0050a0001c0001t0001g0262others(32): Show | 35 | HG00438.hp1 HG01109.hp1 HG01258.hp2 others(32): Show |
intron_variant | MODIFIER | c.303+13248A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56289320 | ||||||
| chr16:56289446
|
C | T | 1 | a0001c0002t0001g0288 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.303+13374C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56289446 | ||||||
| chr16:56289447
|
G | A | 3 | a0001c0002t0002g0283a0001c0004t0002g0282a0001c0006t0021g0019 | 3 | HG02055.hp2 HG02109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.303+13375G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56289447 | ||||||
| chr16:56289455
|
C | T | 15 | a0001c0001t0001g0262a0001c0001t0001g0270a0001c0001t0002g0261others(12): Show | 15 | HG01109.hp1 HG02080.hp2 HG02738.hp1 others(12): Show |
intron_variant | MODIFIER | c.303+13383C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56289455 | ||||||
| chr16:56289546
|
G | C | 2 | a0001c0001t0001g0079a0001c0002t0001g0117 | 2 | HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.303+13474G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56289546 | ||||||
| chr16:56289560
|
C | T | 77 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0041others(74): Show | 77 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.303+13488C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56289560 | ||||||
| chr16:56289596
|
A | G | 295 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0014others(292): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.303+13524A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56289596 | ||||||
| chr16:56289674
|
G | A | 1 | a0001c0001t0002g0141 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.303+13602G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56289674 | ||||||
| chr16:56290132
|
G | A | 3 | a0001c0001t0009g0089a0001c0002t0004g0074a0001c0002t0023g0027 | 3 | HG00280.hp1 HG02074.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.303+14060G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56290132 | ||||||
| chr16:56290214
|
G | C | 1 | a0001c0002t0001g0116 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.303+14142G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56290214 | ||||||
| chr16:56290521
|
C | A | 73 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0041others(70): Show | 73 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.303+14449C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56290521 | ||||||
| chr16:56290666
|
C | T | 1 | a0001c0001t0017g0244 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.303+14594C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56290666 | ||||||
| chr16:56290784
|
C | T | 1 | a0001c0002t0001g0279 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.303+14712C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56290784 | ||||||
| chr16:56290785
|
G | A | 203 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0024others(200): Show | 205 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.303+14713G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56290785 | ||||||
| chr16:56290867
|
T | A | 2 | a0001c0002t0002g0020a0001c0002t0025g0129 | 2 | HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.303+14795T>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56290867 | ||||||
| chr16:56291142
|
A | G | 3 | a0001c0001t0009g0089a0001c0002t0004g0074a0001c0002t0023g0027 | 3 | HG00280.hp1 HG02074.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.303+15070A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56291142 | ||||||
| chr16:56291217
|
G | A | 33 | a0001c0001t0001g0202a0001c0001t0001g0210a0001c0001t0001g0211others(30): Show | 33 | HG01261.hp1 HG01346.hp2 HG01433.hp2 others(30): Show |
intron_variant | MODIFIER | c.303+15145G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56291217 | ||||||
| chr16:56291224
|
A | C | 3 | a0001c0001t0003g0085a0001c0002t0002g0086a0001c0002t0027g0146 | 3 | HG02257.hp1 HG02486.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.303+15152A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56291224 | ||||||
| chr16:56291291
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.303+15219C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56291291 | ||||||
| chr16:56291390
|
G | A | 2 | a0001c0001t0001g0079a0001c0002t0001g0117 | 2 | HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.303+15318G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56291390 | ||||||
| chr16:56291425
|
T | C | 33 | a0001c0001t0001g0202a0001c0001t0001g0210a0001c0001t0001g0211others(30): Show | 33 | HG01261.hp1 HG01346.hp2 HG01433.hp2 others(30): Show |
intron_variant | MODIFIER | c.303+15353T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56291425 | ||||||
| chr16:56291426
|
C | T | 3 | a0001c0001t0003g0085a0001c0002t0002g0086a0001c0002t0027g0146 | 3 | HG02257.hp1 HG02486.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.303+15354C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56291426 | ||||||
| chr16:56291497
|
C | T | 64 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0041others(61): Show | 64 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.303+15425C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56291497 | ||||||
| chr16:56291775
|
G | A | 1 | a0001c0002t0002g0175 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.303+15703G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56291775 | ||||||
| chr16:56291965
|
A | G | 1 | a0001c0001t0006g0069 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.303+15893A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56291965 | ||||||
| chr16:56292175
|
T | C | 1 | a0001c0001t0002g0253 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.303+16103T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56292175 | ||||||
| chr16:56292256
|
C | T | 1 | a0001c0002t0023g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.303+16184C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56292256 | ||||||
| chr16:56292338
|
G | A | 1 | a0001c0001t0026g0003 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.303+16266G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56292338 | ||||||
| chr16:56292688
|
T | G | 25 | a0001c0001t0001g0262a0001c0001t0001g0270a0001c0001t0002g0261others(22): Show | 25 | HG01109.hp1 HG02080.hp2 HG02280.hp2 others(22): Show |
intron_variant | MODIFIER | c.303+16616T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56292688 | ||||||
| chr16:56292700
|
T | C | 30 | a0001c0001t0001g0202a0001c0001t0001g0210a0001c0001t0001g0211others(27): Show | 30 | HG01261.hp1 HG01346.hp2 HG01433.hp2 others(27): Show |
intron_variant | MODIFIER | c.303+16628T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56292700 | ||||||
| chr16:56292776
|
T | C | 1 | a0001c0001t0004g0296 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.303+16704T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56292776 | ||||||
| chr16:56292877
|
C | T | 2 | a0001c0001t0003g0030a0001c0002t0004g0021 | 2 | NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.303+16805C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56292877 | ||||||
| chr16:56292994
|
G | A | 3 | a0001c0002t0012g0179a0001c0002t0012g0180a0001c0002t0012g0181 | 3 | HG02280.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.303+16922G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56292994 | ||||||
| chr16:56293709
|
A | G | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.303+17637A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56293709 | ||||||
| chr16:56293832
|
C | T | 30 | a0001c0001t0001g0202a0001c0001t0001g0210a0001c0001t0001g0211others(27): Show | 30 | HG01261.hp1 HG01346.hp2 HG01433.hp2 others(27): Show |
intron_variant | MODIFIER | c.303+17760C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56293832 | ||||||
| chr16:56294021
|
C | T | 3 | a0001c0002t0002g0283a0001c0004t0002g0282a0001c0006t0021g0019 | 3 | HG02055.hp2 HG02109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.303+17949C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56294021 | ||||||
| chr16:56294062
|
T | G | 4 | a0001c0002t0004g0067a0001c0002t0004g0277a0001c0002t0004g0278others(1): Show | 4 | HG02622.hp1 HG02630.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.303+17990T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56294062 | ||||||
| chr16:56294160
|
T | A | 3 | a0001c0001t0009g0089a0001c0002t0004g0074a0001c0002t0023g0027 | 3 | HG00280.hp1 HG02074.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.303+18088T>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56294160 | ||||||
| chr16:56294294
|
T | C | 1 | a0001c0002t0005g0162 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.303+18222T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56294294 | ||||||
| chr16:56294303
|
T | A | 1 | a0001c0001t0009g0094 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.303+18231T>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56294303 | ||||||
| chr16:56294341
|
T | TA | 157 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0041others(154): Show | 159 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.303+18289dupA | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56294341 | |||||
| chr16:56294341
|
T | TAA | 12 | a0001c0001t0001g0024a0001c0001t0001g0145a0001c0001t0006g0069others(9): Show | 12 | HG01884.hp1 HG02280.hp2 HG02293.hp2 others(9): Show |
intron_variant | MODIFIER | c.303+18288_303+1828 others(6): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56294341 | |||||
| chr16:56294341
|
TA | T | 6 | a0001c0001t0001g0172a0001c0001t0001g0211a0001c0001t0001g0224others(3): Show | 6 | HG01361.hp2 HG03486.hp1 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.303+18289delA | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56294341 | |||||
| chr16:56294363
|
T | G | 1 | a0001c0001t0010g0123 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.303+18291T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56294363 | ||||||
| chr16:56294899
|
G | A | 56 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0078others(53): Show | 57 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.303+18827G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56294899 | ||||||
| chr16:56294901
|
G | T | 56 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0078others(53): Show | 57 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.303+18829G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56294901 | ||||||
| chr16:56294902
|
T | TTAC | 56 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0078others(53): Show | 57 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.303+18830_303+1883 others(7): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56294902 | ||||||
| chr16:56294905
|
AT | A | 56 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0078others(53): Show | 57 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.303+18834delT | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56294905 | ||||||
| chr16:56295022
|
A | G | 1 | a0001c0001t0003g0008 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.303+18950A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56295022 | ||||||
| chr16:56295022
|
AGTTATAT others(5): Show |
A | 1 | a0001c0001t0003g0159 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.303+18951_303+1896 others(16): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56295022 | ||||||
| chr16:56295188
|
T | C | 1 | a0001c0001t0011g0138 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.303+19116T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56295188 | ||||||
| chr16:56295255
|
G | T | 82 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0041others(79): Show | 82 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.303+19183G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56295255 | ||||||
| chr16:56295325
|
G | A | 1 | a0001c0001t0001g0202 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.303+19253G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56295325 | ||||||
| chr16:56295536
|
A | G | 6 | a0001c0001t0003g0030a0001c0001t0014g0034a0001c0002t0001g0035others(3): Show | 6 | HG02559.hp2 HG03098.hp1 NA19030.hp1 others(3): Show |
intron_variant | MODIFIER | c.303+19464A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56295536 | ||||||
| chr16:56295569
|
C | T | 1 | a0001c0002t0002g0175 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.303+19497C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56295569 | ||||||
| chr16:56295826
|
A | T | 2 | a0001c0001t0004g0178a0001c0001t0004g0237 | 2 | HG02027.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.303+19754A>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56295826 | ||||||
| chr16:56295914
|
A | G | 1 | a0001c0002t0004g0205 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.303+19842A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56295914 | ||||||
| chr16:56295939
|
C | T | 1 | a0001c0002t0023g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.303+19867C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56295939 | ||||||
| chr16:56296048
|
T | C | 1 | a0001c0002t0002g0020 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.303+19976T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56296048 | ||||||
| chr16:56296251
|
GTGT | G | 4 | a0001c0002t0004g0067a0001c0002t0004g0277a0001c0002t0004g0278others(1): Show | 4 | HG02622.hp1 HG02630.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.303+20183_303+2018 others(7): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56296251 | |||||
| chr16:56296354
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.303+20282G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56296354 | ||||||
| chr16:56296413
|
T | G | 1 | a0001c0001t0001g0049 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.303+20341T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56296413 | ||||||
| chr16:56296920
|
A | G | 56 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0078others(53): Show | 57 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.303+20848A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56296920 | ||||||
| chr16:56296959
|
G | A | 7 | a0001c0001t0003g0030a0001c0001t0014g0034a0001c0002t0001g0035others(4): Show | 7 | HG02559.hp2 HG03098.hp1 HG06807.hp2 others(4): Show |
intron_variant | MODIFIER | c.303+20887G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56296959 | ||||||
| chr16:56297057
|
G | A | 4 | a0001c0002t0001g0209a0001c0002t0001g0247a0001c0002t0001g0248others(1): Show | 4 | HG02630.hp1 HG02723.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.303+20985G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56297057 | ||||||
| chr16:56297109
|
C | T | 2 | a0001c0001t0001g0096a0001c0002t0001g0097 | 2 | NA18966.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.303+21037C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56297109 | ||||||
| chr16:56297518
|
A | G | 31 | a0001c0001t0001g0202a0001c0001t0001g0210a0001c0001t0001g0211others(28): Show | 31 | HG01261.hp1 HG01346.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.303+21446A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56297518 | ||||||
| chr16:56297522
|
G | GGT | 38 | a0001c0001t0001g0024a0001c0001t0001g0041a0001c0001t0001g0083others(35): Show | 39 | HG00323.hp2 HG00438.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.303+21499_303+2150 others(6): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56297522 | |||||
| chr16:56297522
|
G | GGTGT | 17 | a0001c0001t0001g0049a0001c0001t0001g0167a0001c0001t0003g0044others(14): Show | 17 | HG00280.hp2 HG01261.hp2 HG01993.hp1 others(14): Show |
intron_variant | MODIFIER | c.303+21497_303+2150 others(8): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56297522 | |||||
| chr16:56297522
|
G | GGTGTGT | 10 | a0001c0001t0001g0172a0001c0001t0003g0075a0001c0001t0003g0100others(7): Show | 10 | HG00140.hp1 HG02135.hp2 HG03710.hp1 others(7): Show |
intron_variant | MODIFIER | c.303+21495_303+2150 others(10): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56297522 | |||||
| chr16:56297522
|
G | GGTGTGTG others(1): Show |
3 | a0001c0001t0004g0241a0001c0001t0008g0037a0001c0001t0008g0045 | 3 | HG01071.hp2 NA18973.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.303+21493_303+2150 others(12): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56297522 | |||||
| chr16:56297522
|
G | GGTGTGTG others(3): Show |
3 | a0001c0001t0008g0005a0001c0001t0008g0046a0001c0002t0002g0195 | 3 | HG03654.hp1 NA18975.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.303+21491_303+2150 others(14): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56297522 | |||||
| chr16:56297522
|
G | GGTGTGTG others(7): Show |
1 | a0001c0001t0008g0036 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.303+21487_303+2150 others(18): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56297522 | |||||
| chr16:56297522
|
G | GGTGTGTG others(9): Show |
1 | a0001c0001t0001g0043 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.303+21485_303+2150 others(20): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56297522 | |||||
| chr16:56297522
|
G | GGTGTGTG others(13): Show |
1 | a0001c0001t0026g0003 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.303+21481_303+2150 others(24): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56297522 | |||||
| chr16:56297522
|
GGT | G | 38 | a0001c0001t0001g0011a0001c0001t0001g0077a0001c0001t0001g0079others(35): Show | 38 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.303+21499_303+2150 others(6): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56297522 | |||||
| chr16:56297522
|
GGTGT | G | 43 | a0001c0001t0001g0014a0001c0001t0001g0050a0001c0001t0001g0084others(40): Show | 43 | HG01109.hp1 HG01258.hp2 HG01884.hp2 others(40): Show |
intron_variant | MODIFIER | c.303+21497_303+2150 others(8): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56297522 | |||||
| chr16:56297522
|
GGTGTGT | G | 34 | a0001c0001t0001g0132a0001c0001t0001g0210a0001c0001t0001g0211others(31): Show | 34 | HG01261.hp1 HG01346.hp2 HG01433.hp2 others(31): Show |
intron_variant | MODIFIER | c.303+21495_303+2150 others(10): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56297522 | |||||
| chr16:56297522
|
GGTGTGTG others(1): Show |
G | 47 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0078others(44): Show | 48 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.303+21493_303+2150 others(12): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56297522 | |||||
| chr16:56297522
|
GGTGTGTG others(3): Show |
G | 4 | a0001c0001t0005g0186a0001c0002t0001g0018a0001c0002t0001g0116others(1): Show | 4 | HG00099.hp1 HG00673.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.303+21491_303+2150 others(14): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56297522 | |||||
| chr16:56297522
|
GGTGTGTG others(5): Show |
G | 3 | a0001c0001t0001g0192a0001c0002t0002g0020a0001c0002t0025g0129 | 3 | HG00099.hp2 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.303+21489_303+2150 others(16): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56297522 | |||||
| chr16:56297522
|
GGTGTGTG others(9): Show |
G | 1 | a0001c0002t0001g0232 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.303+21485_303+2150 others(20): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56297522 | |||||
| chr16:56297571
|
G | A | 2 | a0001c0001t0003g0085a0001c0002t0002g0086 | 2 | HG02257.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.303+21499G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56297571 | ||||||
| chr16:56297578
|
T | C | 1 | a0001c0002t0005g0026 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.303+21506T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56297578 | ||||||
| chr16:56297729
|
G | A | 1 | a0001c0002t0001g0065 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.303+21657G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56297729 | ||||||
| chr16:56298150
|
C | G | 1 | a0001c0002t0002g0029 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.303+22078C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56298150 | ||||||
| chr16:56298212
|
T | C | 3 | a0001c0001t0009g0089a0001c0002t0004g0074a0001c0002t0023g0027 | 3 | HG00280.hp1 HG02074.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.303+22140T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56298212 | ||||||
| chr16:56298216
|
G | A | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.303+22144G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56298216 | ||||||
| chr16:56298348
|
G | A | 2 | a0001c0001t0007g0155a0001c0001t0007g0157 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.303+22276G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56298348 | ||||||
| chr16:56298389
|
C | T | 1 | a0001c0002t0003g0001 | 2 | NA18973.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.303+22317C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56298389 | ||||||
| chr16:56298402
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.303+22330C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56298402 | ||||||
| chr16:56298640
|
C | T | 8 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0295others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.303+22568C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56298640 | ||||||
| chr16:56298664
|
G | T | 1 | a0001c0001t0007g0158 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.303+22592G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56298664 | ||||||
| chr16:56298846
|
C | T | 1 | a0001c0001t0011g0285 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.303+22774C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56298846 | ||||||
| chr16:56298908
|
C | CTGTCTCA others(1): Show |
6 | a0001c0001t0001g0011a0001c0001t0001g0071a0001c0001t0001g0072others(3): Show | 6 | HG02027.hp1 HG02074.hp2 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.303+22837_303+2284 others(12): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56298908 | |||||
| chr16:56298914
|
C | CA | 27 | a0001c0001t0001g0043a0001c0001t0001g0050a0001c0001t0001g0182others(24): Show | 27 | HG00438.hp1 HG01258.hp2 HG01978.hp2 others(24): Show |
intron_variant | MODIFIER | c.303+22858dupA | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56298914 | |||||
| chr16:56298964
|
C | T | 5 | a0001c0001t0001g0258a0001c0001t0004g0002a0001c0001t0004g0287others(2): Show | 6 | HG02717.hp2 HG03491.hp2 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.303+22892C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56298964 | ||||||
| chr16:56299246
|
G | A | 1 | a0001c0002t0001g0288 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.303+23174G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56299246 | ||||||
| chr16:56299374
|
G | A | 1 | a0001c0001t0017g0244 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.303+23302G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56299374 | ||||||
| chr16:56299493
|
C | T | 1 | a0001c0001t0004g0223 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.303+23421C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56299493 | ||||||
| chr16:56299597
|
G | A | 1 | a0001c0002t0002g0190 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.303+23525G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56299597 | ||||||
| chr16:56299642
|
C | G | 2 | a0001c0001t0003g0085a0001c0002t0002g0086 | 2 | HG02257.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.303+23570C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56299642 | ||||||
| chr16:56299760
|
C | T | 1 | a0001c0001t0003g0246 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.303+23688C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56299760 | ||||||
| chr16:56300008
|
C | CGT | 24 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0166others(21): Show | 24 | HG00733.hp2 HG01169.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.303+23964_303+2396 others(6): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56300008 | |||||
| chr16:56300008
|
C | CGTGT | 14 | a0001c0001t0001g0196a0001c0001t0001g0242a0001c0001t0004g0185others(11): Show | 14 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(11): Show |
intron_variant | MODIFIER | c.303+23962_303+2396 others(8): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56300008 | |||||
| chr16:56300008
|
C | CGTGTGTG others(1): Show |
8 | a0001c0001t0001g0022a0001c0001t0001g0270a0001c0001t0002g0273others(5): Show | 8 | HG02080.hp2 HG02738.hp1 HG04115.hp2 others(5): Show |
intron_variant | MODIFIER | c.303+23958_303+2396 others(12): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56300008 | |||||
| chr16:56300008
|
C | CGTGTGTG others(3): Show |
11 | a0001c0001t0001g0132a0001c0001t0001g0262a0001c0001t0004g0178others(8): Show | 11 | HG01109.hp1 HG02280.hp2 HG03098.hp2 others(8): Show |
intron_variant | MODIFIER | c.303+23956_303+2396 others(14): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56300008 | |||||
| chr16:56300008
|
C | CGTGTGTG others(5): Show |
26 | a0001c0001t0001g0115a0001c0001t0001g0280a0001c0001t0003g0208others(23): Show | 26 | HG00099.hp1 HG00323.hp1 HG00673.hp2 others(23): Show |
intron_variant | MODIFIER | c.303+23954_303+2396 others(16): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56300008 | |||||
| chr16:56300008
|
C | CGTGTGTG others(7): Show |
33 | a0001c0001t0001g0078a0001c0001t0001g0202a0001c0001t0001g0281others(30): Show | 33 | HG00735.hp2 HG01106.hp1 HG01346.hp2 others(30): Show |
intron_variant | MODIFIER | c.303+23952_303+2396 others(18): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56300008 | |||||
| chr16:56300008
|
C | CGTGTGTG others(9): Show |
25 | a0001c0001t0001g0062a0001c0001t0001g0210a0001c0001t0001g0211others(22): Show | 27 | HG00140.hp2 HG01074.hp1 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.303+23950_303+2396 others(20): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56300008 | |||||
| chr16:56300008
|
C | CGTGTGTG others(11): Show |
2 | a0001c0001t0005g0220a0001c0002t0001g0010 | 2 | HG02071.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.303+23948_303+2396 others(22): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56300008 | |||||
| chr16:56300008
|
C | CGTGTGTG others(13): Show |
2 | a0001c0001t0003g0030a0001c0002t0005g0162 | 2 | HG01975.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.303+23946_303+2396 others(24): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56300008 | |||||
| chr16:56300029
|
GTGTGTGT others(29): Show |
G | 1 | a0001c0001t0019g0090 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.303+23962_303+2399 others(40): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56300029 | |||||
| chr16:56300031
|
GTGTGTGC others(27): Show |
G | 1 | a0001c0001t0001g0163 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.303+23964_303+2399 others(38): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56300031 | |||||
| chr16:56300033
|
GTGTGCGC others(25): Show |
G | 78 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0041others(75): Show | 78 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.303+23966_303+2399 others(36): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56300033 | |||||
| chr16:56300035
|
GTGCGCGC others(23): Show |
G | 4 | a0001c0001t0001g0079a0001c0001t0001g0096a0001c0001t0001g0145others(1): Show | 4 | HG02717.hp1 NA18906.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.303+23966_303+2399 others(34): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56300035 | |||||
| chr16:56300036
|
T | TGTGTGTG others(17): Show |
1 | a0001c0002t0001g0288 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.303+23965_303+2396 others(28): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56300036 | |||||
| chr16:56300036
|
T | TGTGTGTG others(5): Show |
1 | a0001c0002t0001g0259 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.303+23965_303+2396 others(16): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56300036 | |||||
| chr16:56300036
|
T | TGTGTGTG others(7): Show |
1 | a0001c0002t0003g0015 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.303+23965_303+2396 others(18): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56300036 | |||||
| chr16:56300036
|
T | TGTGTGTG others(9): Show |
1 | a0001c0001t0001g0258 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.303+23965_303+2396 others(20): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56300036 | |||||
| chr16:56300036
|
T | TGTGTGTG others(9): Show |
2 | a0001c0001t0006g0226a0001c0002t0002g0108 | 2 | HG01934.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.303+23965_303+2396 others(20): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56300036 | |||||
| chr16:56300036
|
T | TGTGTGTG others(11): Show |
1 | a0001c0002t0004g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.303+23965_303+2396 others(22): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56300036 | |||||
| chr16:56300036
|
T | TGTGTGTG others(11): Show |
1 | a0001c0001t0001g0098 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.303+23965_303+2396 others(22): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56300036 | |||||
| chr16:56300036
|
T | TGTGTGTG others(15): Show |
1 | a0001c0002t0002g0087 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.303+23965_303+2396 others(26): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56300036 | |||||
| chr16:56300037
|
GCGCGCGC others(15): Show |
G | 1 | a0001c0002t0023g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.303+23966_303+2398 others(26): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56300037 | ||||||
| chr16:56300038
|
C | T | 172 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0043others(169): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.303+23966C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56300038 | ||||||
| chr16:56300039
|
GCGCGCGC others(13): Show |
G | 1 | a0001c0002t0004g0074 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.303+23968_303+2398 others(24): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56300039 | ||||||
| chr16:56300040
|
C | T | 25 | a0001c0001t0001g0115a0001c0001t0001g0262a0001c0001t0001g0270others(22): Show | 25 | HG00323.hp1 HG01109.hp1 HG02080.hp2 others(22): Show |
intron_variant | MODIFIER | c.303+23968C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56300040 | ||||||
| chr16:56300041
|
GCGCGCGC others(11): Show |
G | 1 | a0001c0001t0009g0089 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.303+23970_303+2398 others(22): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56300041 | ||||||
| chr16:56300042
|
C | T | 14 | a0001c0001t0001g0262a0001c0001t0001g0270a0001c0001t0002g0273others(11): Show | 14 | HG01109.hp1 HG02080.hp2 HG02738.hp1 others(11): Show |
intron_variant | MODIFIER | c.303+23970C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56300042 | ||||||
| chr16:56300043
|
G | A | 1 | a0001c0002t0001g0288 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.303+23971G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56300043 | ||||||
| chr16:56300055
|
G | A | 4 | a0001c0001t0014g0034a0001c0002t0001g0035a0001c0002t0013g0032others(1): Show | 4 | HG02559.hp2 HG03098.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.303+23983G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56300055 | ||||||
| chr16:56300143
|
T | C | 84 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0041others(81): Show | 84 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.303+24071T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56300143 | ||||||
| chr16:56300214
|
A | G | 2 | a0001c0001t0003g0085a0001c0002t0002g0086 | 2 | HG02257.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.303+24142A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56300214 | ||||||
| chr16:56300294
|
C | T | 13 | a0001c0001t0001g0262a0001c0001t0001g0270a0001c0001t0002g0273others(10): Show | 13 | HG01109.hp1 HG02080.hp2 HG02738.hp1 others(10): Show |
intron_variant | MODIFIER | c.303+24222C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56300294 | ||||||
| chr16:56300649
|
A | T | 3 | a0001c0002t0001g0025a0001c0002t0001g0107a0001c0002t0005g0026 | 3 | HG01515.hp2 HG01517.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.303+24577A>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56300649 | ||||||
| chr16:56300737
|
T | C | 2 | a0001c0001t0001g0284a0001c0001t0003g0289 | 2 | HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.303+24665T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56300737 | ||||||
| chr16:56300791
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.303+24719T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56300791 | ||||||
| chr16:56300845
|
G | A | 1 | a0001c0002t0001g0076 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.303+24773G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56300845 | ||||||
| chr16:56301078
|
A | G | 52 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0078others(49): Show | 53 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.303+25006A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56301078 | ||||||
| chr16:56301223
|
G | A | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | NA18998.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.303+25151G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56301223 | ||||||
| chr16:56301286
|
G | A | 3 | a0001c0001t0003g0101a0001c0001t0003g0131a0001c0001t0004g0112 | 3 | NA18959.hp1 NA18981.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.303+25214G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56301286 | ||||||
| chr16:56301415
|
C | G | 1 | a0001c0001t0001g0084 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.303+25343C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56301415 | ||||||
| chr16:56301444
|
G | T | 1 | a0001c0001t0005g0218 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.303+25372G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56301444 | ||||||
| chr16:56301533
|
G | A | 20 | a0001c0001t0001g0153a0001c0001t0001g0166a0001c0001t0002g0150others(17): Show | 20 | HG00673.hp1 HG01256.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.303+25461G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56301533 | ||||||
| chr16:56301571
|
T | A | 1 | a0001c0001t0003g0159 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.303+25499T>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56301571 | ||||||
| chr16:56301624
|
T | G | 1 | a0001c0001t0003g0159 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.303+25552T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56301624 | ||||||
| chr16:56301729
|
G | A | 88 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0041others(85): Show | 88 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.303+25657G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56301729 | ||||||
| chr16:56301732
|
G | A | 4 | a0001c0002t0012g0179a0001c0002t0012g0180a0001c0002t0012g0181others(1): Show | 4 | HG02280.hp2 HG02451.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.303+25660G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56301732 | ||||||
| chr16:56301810
|
C | T | 30 | a0001c0001t0001g0202a0001c0001t0001g0210a0001c0001t0001g0211others(27): Show | 30 | HG01261.hp1 HG01346.hp2 HG01433.hp2 others(27): Show |
intron_variant | MODIFIER | c.303+25738C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56301810 | ||||||
| chr16:56301948
|
G | A | 2 | a0001c0001t0003g0269a0001c0002t0004g0267 | 2 | NA18960.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.303+25876G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56301948 | ||||||
| chr16:56301966
|
A | T | 1 | a0001c0001t0001g0199 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.303+25894A>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56301966 | ||||||
| chr16:56301998
|
GC | G | 23 | a0001c0001t0001g0262a0001c0001t0001g0270a0001c0001t0002g0273others(20): Show | 23 | HG01109.hp1 HG02080.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.303+25931delC | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56301998 | |||||
| chr16:56302003
|
C | T | 6 | a0001c0001t0001g0281a0001c0002t0001g0065a0001c0002t0001g0099others(3): Show | 6 | HG01074.hp1 HG01106.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.303+25931C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56302003 | ||||||
| chr16:56302012
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.303+25940G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56302012 | ||||||
| chr16:56302041
|
A | T | 13 | a0001c0001t0001g0262a0001c0001t0001g0270a0001c0001t0002g0273others(10): Show | 13 | HG01109.hp1 HG02080.hp2 HG02738.hp1 others(10): Show |
intron_variant | MODIFIER | c.303+25969A>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56302041 | ||||||
| chr16:56302248
|
A | C | 5 | a0001c0001t0001g0057a0001c0002t0001g0055a0001c0002t0001g0056others(2): Show | 5 | HG02258.hp2 HG02970.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.303+26176A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56302248 | ||||||
| chr16:56302255
|
C | T | 1 | a0001c0001t0017g0244 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.303+26183C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56302255 | ||||||
| chr16:56302438
|
G | A | 1 | a0001c0001t0013g0187 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.304-26193G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56302438 | ||||||
| chr16:56302713
|
A | T | 1 | a0001c0001t0001g0168 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.304-25918A>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56302713 | ||||||
| chr16:56303004
|
A | C | 1 | a0001c0001t0001g0182 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.304-25627A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56303004 | ||||||
| chr16:56303217
|
A | G | 1 | a0001c0004t0002g0028 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.304-25414A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56303217 | ||||||
| chr16:56303454
|
C | T | 3 | a0001c0001t0003g0085a0001c0002t0001g0294a0001c0002t0002g0086 | 3 | HG02257.hp1 HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.304-25177C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56303454 | ||||||
| chr16:56303573
|
ACC | A | 23 | a0001c0001t0001g0262a0001c0001t0001g0270a0001c0001t0002g0273others(20): Show | 23 | HG01109.hp1 HG02080.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.304-25056_304-2505 others(6): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56303573 | |||||
| chr16:56303675
|
A | T | 1 | a0001c0001t0008g0045 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.304-24956A>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56303675 | ||||||
| chr16:56303747
|
G | A | 6 | a0001c0001t0001g0153a0001c0002t0001g0151a0001c0002t0001g0152others(3): Show | 6 | HG01361.hp2 HG01516.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.304-24884G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56303747 | ||||||
| chr16:56303811
|
G | GC | 20 | a0001c0001t0001g0262a0001c0001t0001g0270a0001c0001t0002g0273others(17): Show | 20 | HG01109.hp1 HG02080.hp2 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.304-24816dupC | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56303811 | |||||
| chr16:56303889
|
C | G | 1 | a0001c0001t0001g0280 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.304-24742C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56303889 | ||||||
| chr16:56304100
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.304-24531C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56304100 | ||||||
| chr16:56304158
|
C | A | 1 | a0001c0002t0001g0056 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.304-24473C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56304158 | ||||||
| chr16:56304817
|
G | A | 84 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0041others(81): Show | 84 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.304-23814G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56304817 | ||||||
| chr16:56304927
|
G | T | 1 | a0001c0001t0017g0244 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.304-23704G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56304927 | ||||||
| chr16:56304940
|
C | T | 2 | a0001c0001t0004g0296a0001c0002t0027g0146 | 2 | HG01891.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.304-23691C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56304940 | ||||||
| chr16:56305265
|
C | T | 1 | a0001c0001t0001g0170 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.304-23366C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56305265 | ||||||
| chr16:56305314
|
A | G | 24 | a0001c0001t0001g0262a0001c0001t0001g0270a0001c0001t0002g0273others(21): Show | 24 | HG01109.hp1 HG02080.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.304-23317A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56305314 | ||||||
| chr16:56305401
|
G | A | 1 | a0001c0001t0017g0244 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.304-23230G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56305401 | ||||||
| chr16:56305693
|
G | A | 1 | a0001c0002t0012g0183 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.304-22938G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56305693 | ||||||
| chr16:56305696
|
G | A | 3 | a0001c0002t0012g0179a0001c0002t0012g0180a0001c0002t0012g0181 | 3 | HG02280.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.304-22935G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56305696 | ||||||
| chr16:56305718
|
A | T | 2 | a0001c0002t0006g0133a0001c0002t0006g0134 | 2 | NA18942.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.304-22913A>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56305718 | ||||||
| chr16:56306184
|
T | C | 156 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0041others(153): Show | 157 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.304-22447T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56306184 | ||||||
| chr16:56306311
|
C | G | 77 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0041others(74): Show | 77 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.304-22320C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56306311 | ||||||
| chr16:56306373
|
G | T | 1 | a0001c0001t0011g0031 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.304-22258G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56306373 | ||||||
| chr16:56306407
|
A | G | 13 | a0001c0001t0001g0258a0001c0001t0003g0030a0001c0001t0014g0034others(10): Show | 13 | HG02280.hp2 HG02451.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.304-22224A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56306407 | ||||||
| chr16:56306531
|
C | T | 1 | a0001c0001t0004g0291 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.304-22100C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56306531 | ||||||
| chr16:56306725
|
G | A | 1 | a0001c0001t0020g0126 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.304-21906G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56306725 | ||||||
| chr16:56306822
|
C | T | 1 | a0001c0002t0001g0286 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.304-21809C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56306822 | ||||||
| chr16:56306891
|
T | C | 1 | a0001c0001t0011g0031 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.304-21740T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56306891 | ||||||
| chr16:56307045
|
G | T | 2 | a0001c0002t0002g0029a0001c0002t0003g0148 | 2 | HG02145.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.304-21586G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56307045 | ||||||
| chr16:56307125
|
C | T | 162 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0024others(159): Show | 163 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.304-21506C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56307125 | ||||||
| chr16:56307157
|
G | A | 5 | a0001c0001t0001g0258a0001c0002t0001g0259a0001c0002t0001g0288others(2): Show | 5 | HG00280.hp1 HG02451.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.304-21474G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56307157 | ||||||
| chr16:56307175
|
G | C | 1 | a0001c0002t0004g0074 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.304-21456G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56307175 | ||||||
| chr16:56307292
|
T | C | 4 | a0001c0001t0003g0085a0001c0002t0001g0294a0001c0002t0002g0086others(1): Show | 4 | HG02257.hp1 HG02486.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.304-21339T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56307292 | ||||||
| chr16:56307318
|
G | A | 57 | a0001c0001t0001g0062a0001c0001t0001g0078a0001c0001t0001g0098others(54): Show | 58 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(55): Show |
intron_variant | MODIFIER | c.304-21313G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56307318 | ||||||
| chr16:56307347
|
C | A | 1 | a0001c0001t0009g0089 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.304-21284C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56307347 | ||||||
| chr16:56307508
|
G | A | 6 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0295others(3): Show | 6 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.304-21123G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56307508 | ||||||
| chr16:56307670
|
A | G | 5 | a0001c0001t0003g0085a0001c0002t0001g0294a0001c0002t0002g0086others(2): Show | 5 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.304-20961A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56307670 | ||||||
| chr16:56307916
|
C | T | 1 | a0001c0002t0002g0087 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.304-20715C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56307916 | ||||||
| chr16:56307966
|
G | A | 2 | a0001c0001t0001g0079a0001c0002t0001g0117 | 2 | HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.304-20665G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56307966 | ||||||
| chr16:56308000
|
A | G | 1 | a0001c0002t0001g0082 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.304-20631A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56308000 | ||||||
| chr16:56308133
|
C | T | 2 | a0001c0001t0003g0030a0001c0002t0004g0021 | 2 | NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.304-20498C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56308133 | ||||||
| chr16:56308147
|
G | A | 84 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0024others(81): Show | 84 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.304-20484G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56308147 | ||||||
| chr16:56308202
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.304-20429C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56308202 | ||||||
| chr16:56308249
|
A | G | 1 | a0002c0005t0003g0088 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.304-20382A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56308249 | ||||||
| chr16:56308378
|
T | C | 1 | a0001c0002t0002g0190 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.304-20253T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56308378 | ||||||
| chr16:56308403
|
G | A | 14 | a0001c0001t0001g0043a0001c0001t0001g0050a0001c0001t0003g0044others(11): Show | 14 | HG00438.hp1 HG01258.hp2 HG04199.hp2 others(11): Show |
intron_variant | MODIFIER | c.304-20228G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56308403 | ||||||
| chr16:56308462
|
A | T | 5 | a0001c0002t0001g0204a0001c0002t0001g0245a0001c0002t0002g0283others(2): Show | 5 | HG01109.hp2 HG02055.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.304-20169A>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56308462 | ||||||
| chr16:56308463
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.304-20168G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56308463 | ||||||
| chr16:56308470
|
A | G | 11 | a0001c0001t0001g0182a0001c0001t0003g0085a0001c0002t0001g0204others(8): Show | 11 | HG01109.hp2 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.304-20161A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56308470 | ||||||
| chr16:56308532
|
C | T | 11 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(8): Show | 11 | HG01109.hp1 HG02080.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.304-20099C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56308532 | ||||||
| chr16:56308542
|
A | G | 2 | a0001c0002t0001g0259a0001c0002t0001g0288 | 2 | HG06807.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.304-20089A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56308542 | ||||||
| chr16:56308645
|
T | C | 185 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0024others(182): Show | 186 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.304-19986T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56308645 | ||||||
| chr16:56308647
|
C | T | 5 | a0001c0001t0003g0085a0001c0002t0001g0294a0001c0002t0002g0086others(2): Show | 5 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.304-19984C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56308647 | ||||||
| chr16:56308720
|
G | A | 1 | a0001c0001t0003g0009 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.304-19911G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56308720 | ||||||
| chr16:56308877
|
C | G | 4 | a0001c0002t0001g0151a0001c0002t0001g0152a0001c0002t0001g0198others(1): Show | 4 | HG01361.hp2 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.304-19754C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56308877 | ||||||
| chr16:56308895
|
A | T | 3 | a0001c0002t0012g0179a0001c0002t0012g0180a0001c0002t0012g0181 | 3 | HG02280.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.304-19736A>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56308895 | ||||||
| chr16:56308954
|
G | C | 1 | a0001c0001t0001g0051 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.304-19677G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56308954 | ||||||
| chr16:56309042
|
T | C | 11 | a0001c0001t0001g0182a0001c0001t0003g0085a0001c0002t0001g0204others(8): Show | 11 | HG01109.hp2 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.304-19589T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56309042 | ||||||
| chr16:56309172
|
C | T | 1 | a0001c0002t0002g0271 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.304-19459C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56309172 | ||||||
| chr16:56309267
|
TC | T | 3 | a0001c0002t0001g0259a0001c0002t0001g0288a0001c0002t0004g0144 | 3 | HG03540.hp1 HG06807.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.304-19361delC | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56309267 | |||||
| chr16:56309417
|
G | A | 88 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0132others(85): Show | 90 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.304-19214G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56309417 | ||||||
| chr16:56309689
|
G | A | 2 | a0001c0001t0007g0155a0001c0001t0007g0157 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.304-18942G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56309689 | ||||||
| chr16:56309730
|
C | T | 86 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0024others(83): Show | 86 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.304-18901C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56309730 | ||||||
| chr16:56309749
|
C | T | 5 | a0001c0002t0001g0204a0001c0002t0001g0245a0001c0002t0002g0283others(2): Show | 5 | HG01109.hp2 HG02055.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.304-18882C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56309749 | ||||||
| chr16:56309796
|
C | A | 1 | a0001c0001t0001g0182 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.304-18835C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56309796 | ||||||
| chr16:56309798
|
G | GT | 63 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0132others(60): Show | 64 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(61): Show |
intron_variant | MODIFIER | c.304-18832dupT | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56309798 | |||||
| chr16:56309924
|
G | A | 2 | a0001c0002t0001g0119a0001c0002t0001g0120 | 2 | HG00639.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.304-18707G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56309924 | ||||||
| chr16:56310050
|
AC | A | 63 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0132others(60): Show | 64 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(61): Show |
intron_variant | MODIFIER | c.304-18579delC | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56310050 | |||||
| chr16:56310183
|
C | T | 3 | a0001c0002t0012g0179a0001c0002t0012g0180a0001c0002t0012g0181 | 3 | HG02280.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.304-18448C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56310183 | ||||||
| chr16:56310221
|
G | A | 1 | a0001c0002t0002g0194 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.304-18410G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56310221 | ||||||
| chr16:56310475
|
A | G | 6 | a0001c0001t0001g0182a0001c0002t0001g0204a0001c0002t0001g0245others(3): Show | 6 | HG01109.hp2 HG02055.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.304-18156A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56310475 | ||||||
| chr16:56310895
|
A | C | 2 | a0001c0002t0002g0087a0001c0002t0002g0260 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.304-17736A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56310895 | ||||||
| chr16:56311185
|
G | C | 1 | a0001c0001t0002g0150 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.304-17446G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56311185 | ||||||
| chr16:56311199
|
T | G | 1 | a0001c0001t0001g0022 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.304-17432T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56311199 | ||||||
| chr16:56311405
|
G | A | 9 | a0001c0002t0001g0204a0001c0002t0001g0245a0001c0002t0001g0294others(6): Show | 9 | HG01109.hp2 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.304-17226G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56311405 | ||||||
| chr16:56311465
|
G | A | 61 | a0001c0001t0001g0078a0001c0001t0001g0098a0001c0001t0001g0132others(58): Show | 62 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(59): Show |
intron_variant | MODIFIER | c.304-17166G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56311465 | ||||||
| chr16:56311484
|
G | C | 3 | a0001c0001t0001g0177a0001c0001t0001g0276a0001c0001t0009g0127 | 3 | HG00423.hp2 NA18946.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.304-17147G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56311484 | ||||||
| chr16:56311519
|
T | G | 6 | a0001c0001t0004g0291a0001c0002t0002g0292a0001c0002t0003g0148others(3): Show | 6 | HG02280.hp2 HG02451.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.304-17112T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56311519 | ||||||
| chr16:56311673
|
G | C | 1 | a0001c0001t0020g0126 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.304-16958G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56311673 | ||||||
| chr16:56311768
|
G | A | 1 | a0001c0002t0001g0204 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.304-16863G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56311768 | ||||||
| chr16:56311786
|
C | T | 3 | a0001c0002t0012g0179a0001c0002t0012g0180a0001c0002t0012g0181 | 3 | HG02280.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.304-16845C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56311786 | ||||||
| chr16:56311911
|
G | T | 1 | a0001c0001t0001g0098 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.304-16720G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56311911 | ||||||
| chr16:56311913
|
A | G | 1 | a0001c0002t0001g0259 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.304-16718A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56311913 | ||||||
| chr16:56311957
|
G | A | 3 | a0001c0001t0007g0113a0001c0002t0003g0160a0001c0002t0005g0162 | 3 | HG01496.hp2 HG01975.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.304-16674G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56311957 | ||||||
| chr16:56311965
|
C | A | 1 | a0001c0001t0011g0285 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.304-16666C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56311965 | ||||||
| chr16:56311971
|
A | G | 1 | a0001c0001t0011g0285 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.304-16660A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56311971 | ||||||
| chr16:56312010
|
G | A | 6 | a0001c0001t0004g0291a0001c0002t0002g0292a0001c0002t0003g0148others(3): Show | 6 | HG02280.hp2 HG02451.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.304-16621G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56312010 | ||||||
| chr16:56312062
|
C | T | 2 | a0001c0001t0004g0178a0001c0001t0004g0237 | 2 | HG02027.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.304-16569C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56312062 | ||||||
| chr16:56312063
|
T | G | 1 | a0001c0001t0002g0273 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.304-16568T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56312063 | ||||||
| chr16:56312241
|
A | G | 1 | a0001c0001t0001g0270 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.304-16390A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56312241 | ||||||
| chr16:56312256
|
G | A | 1 | a0001c0002t0001g0288 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.304-16375G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56312256 | ||||||
| chr16:56312268
|
C | T | 1 | a0001c0001t0013g0187 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.304-16363C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56312268 | ||||||
| chr16:56312287
|
G | A | 1 | a0001c0001t0001g0072 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.304-16344G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56312287 | ||||||
| chr16:56312337
|
A | G | 1 | a0001c0002t0002g0029 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.304-16294A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56312337 | ||||||
| chr16:56312655
|
G | A | 1 | a0001c0002t0001g0288 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.304-15976G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56312655 | ||||||
| chr16:56312784
|
C | T | 1 | a0001c0004t0002g0028 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.304-15847C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56312784 | ||||||
| chr16:56312785
|
G | A | 1 | a0001c0002t0001g0268 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.304-15846G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56312785 | ||||||
| chr16:56313211
|
A | G | 2 | a0001c0002t0004g0053a0001c0002t0004g0143 | 2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.304-15420A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56313211 | ||||||
| chr16:56313306
|
T | G | 1 | a0001c0001t0004g0296 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.304-15325T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56313306 | ||||||
| chr16:56313309
|
G | A | 2 | a0001c0001t0004g0002a0001c0001t0004g0287 | 3 | HG03491.hp2 HG03492.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.304-15322G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56313309 | ||||||
| chr16:56313374
|
T | C | 1 | a0001c0001t0017g0244 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.304-15257T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56313374 | ||||||
| chr16:56313529
|
C | T | 1 | a0001c0001t0001g0024 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.304-15102C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56313529 | ||||||
| chr16:56313530
|
G | A | 36 | a0001c0001t0001g0041a0001c0001t0001g0078a0001c0001t0001g0196others(33): Show | 36 | HG00280.hp2 HG00642.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.304-15101G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56313530 | ||||||
| chr16:56313550
|
T | C | 1 | a0001c0002t0003g0275 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.304-15081T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56313550 | ||||||
| chr16:56313560
|
T | G | 116 | a0001c0001t0001g0041a0001c0001t0001g0078a0001c0001t0001g0083others(113): Show | 117 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.304-15071T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56313560 | ||||||
| chr16:56313568
|
G | A | 8 | a0001c0001t0002g0273a0001c0002t0001g0076a0001c0002t0001g0268others(5): Show | 8 | HG02074.hp2 HG02080.hp2 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.304-15063G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56313568 | ||||||
| chr16:56313604
|
C | G | 1 | a0001c0001t0009g0127 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.304-15027C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56313604 | ||||||
| chr16:56313626
|
C | G | 1 | a0001c0002t0001g0232 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.304-15005C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56313626 | ||||||
| chr16:56313857
|
G | T | 33 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0051others(30): Show | 33 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.304-14774G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56313857 | ||||||
| chr16:56313970
|
TTC | T | 35 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0051others(32): Show | 35 | HG00642.hp1 HG00733.hp2 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.304-14659_304-1465 others(6): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56313970 | |||||
| chr16:56314134
|
T | G | 88 | a0001c0001t0001g0077a0001c0001t0001g0164a0001c0001t0001g0182others(85): Show | 89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.304-14497T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56314134 | ||||||
| chr16:56314195
|
T | C | 25 | a0001c0001t0001g0050a0001c0001t0001g0078a0001c0001t0001g0196others(22): Show | 25 | HG00280.hp2 HG01109.hp1 HG01258.hp2 others(22): Show |
intron_variant | MODIFIER | c.304-14436T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56314195 | ||||||
| chr16:56314349
|
A | C | 97 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0024others(94): Show | 97 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.304-14282A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56314349 | ||||||
| chr16:56314418
|
A | G | 1 | a0001c0002t0001g0147 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.304-14213A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56314418 | ||||||
| chr16:56314560
|
C | T | 1 | a0001c0001t0003g0075 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.304-14071C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56314560 | ||||||
| chr16:56314641
|
G | A | 1 | a0001c0002t0018g0229 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.304-13990G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56314641 | ||||||
| chr16:56315007
|
A | C | 2 | a0001c0002t0002g0292a0001c0002t0027g0146 | 2 | HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.304-13624A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56315007 | ||||||
| chr16:56315058
|
G | A | 1 | a0001c0001t0007g0012 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.304-13573G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56315058 | ||||||
| chr16:56315224
|
G | A | 1 | a0001c0001t0014g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.304-13407G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56315224 | ||||||
| chr16:56315282
|
C | T | 2 | a0001c0001t0001g0079a0001c0002t0001g0117 | 2 | HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.304-13349C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56315282 | ||||||
| chr16:56315510
|
C | G | 1 | a0001c0002t0002g0029 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.304-13121C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56315510 | ||||||
| chr16:56315522
|
G | C | 4 | a0001c0002t0003g0001a0001c0002t0003g0015a0001c0002t0003g0109others(1): Show | 5 | NA18973.hp1 NA18983.hp1 NA19057.hp2 others(2): Show |
intron_variant | MODIFIER | c.304-13109G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56315522 | ||||||
| chr16:56315625
|
C | A | 3 | a0001c0002t0001g0209a0001c0002t0001g0279a0001c0002t0005g0026 | 3 | HG02965.hp1 HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.304-13006C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56315625 | ||||||
| chr16:56315781
|
C | T | 6 | a0001c0002t0001g0076a0001c0002t0001g0268a0001c0002t0004g0267others(3): Show | 6 | HG02074.hp2 HG02080.hp2 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.304-12850C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56315781 | ||||||
| chr16:56315839
|
CGAGACCA others(10): Show |
C | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.304-12774_304-1275 others(21): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56315839 | |||||
| chr16:56315951
|
C | T | 1 | a0001c0002t0004g0074 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.304-12680C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56315951 | ||||||
| chr16:56315952
|
G | C | 1 | a0001c0001t0001g0295 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.304-12679G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56315952 | ||||||
| chr16:56316120
|
C | G | 3 | a0001c0002t0004g0143a0001c0002t0004g0144a0001c0002t0004g0278 | 3 | HG02630.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.304-12511C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56316120 | ||||||
| chr16:56316350
|
C | T | 2 | a0001c0002t0001g0111a0001c0002t0001g0130 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.304-12281C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56316350 | ||||||
| chr16:56316509
|
C | T | 6 | a0001c0002t0001g0076a0001c0002t0001g0268a0001c0002t0004g0267others(3): Show | 6 | HG02074.hp2 HG02080.hp2 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.304-12122C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56316509 | ||||||
| chr16:56316542
|
C | G | 13 | a0001c0001t0001g0077a0001c0001t0001g0079a0001c0001t0001g0164others(10): Show | 13 | HG00280.hp1 HG00673.hp1 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.304-12089C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56316542 | ||||||
| chr16:56316606
|
C | A | 1 | a0001c0001t0001g0174 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.304-12025C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56316606 | ||||||
| chr16:56316673
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.304-11958C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56316673 | ||||||
| chr16:56316766
|
C | A | 1 | a0001c0002t0004g0144 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.304-11865C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56316766 | ||||||
| chr16:56316876
|
C | T | 1 | a0001c0001t0009g0140 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.304-11755C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56316876 | ||||||
| chr16:56316884
|
G | T | 3 | a0001c0002t0004g0143a0001c0002t0004g0144a0001c0002t0004g0278 | 3 | HG02630.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.304-11747G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56316884 | ||||||
| chr16:56316945
|
G | A | 1 | a0001c0001t0005g0256 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.304-11686G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56316945 | ||||||
| chr16:56317009
|
G | A | 1 | a0001c0001t0001g0132 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.304-11622G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56317009 | ||||||
| chr16:56317097
|
G | A | 5 | a0001c0001t0001g0079a0001c0002t0001g0025a0001c0002t0001g0107others(2): Show | 5 | HG01515.hp2 HG01517.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.304-11534G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56317097 | ||||||
| chr16:56317344
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.304-11287C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56317344 | ||||||
| chr16:56317730
|
G | A | 4 | a0001c0001t0001g0295a0001c0002t0001g0013a0001c0002t0012g0179others(1): Show | 4 | HG02109.hp1 HG02280.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.304-10901G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56317730 | ||||||
| chr16:56317795
|
A | G | 125 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0051others(122): Show | 126 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.304-10836A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56317795 | ||||||
| chr16:56318202
|
G | A | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.304-10429G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56318202 | ||||||
| chr16:56318413
|
G | T | 1 | a0001c0002t0006g0264 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.304-10218G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56318413 | ||||||
| chr16:56318461
|
G | A | 32 | a0001c0001t0001g0043a0001c0001t0001g0078a0001c0001t0001g0115others(29): Show | 33 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.304-10170G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56318461 | ||||||
| chr16:56318671
|
A | G | 1 | a0001c0002t0018g0229 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.304-9960A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56318671 | ||||||
| chr16:56318939
|
G | A | 2 | a0001c0001t0001g0079a0001c0002t0001g0117 | 2 | HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.304-9692G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56318939 | ||||||
| chr16:56318942
|
C | A | 192 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0014others(189): Show | 193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.304-9689C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56318942 | ||||||
| chr16:56318993
|
G | A | 93 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0024others(90): Show | 93 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.304-9638G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56318993 | ||||||
| chr16:56319264
|
A | T | 244 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0014others(241): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.304-9367A>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56319264 | ||||||
| chr16:56319273
|
A | C | 7 | a0001c0002t0001g0013a0001c0002t0001g0035a0001c0002t0001g0055others(4): Show | 7 | HG02109.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.304-9358A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56319273 | ||||||
| chr16:56319363
|
C | G | 5 | a0001c0001t0001g0079a0001c0002t0001g0025a0001c0002t0001g0107others(2): Show | 5 | HG01515.hp2 HG01517.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.304-9268C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56319363 | ||||||
| chr16:56319364
|
G | A | 2 | a0001c0002t0004g0143a0001c0002t0004g0144 | 2 | HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.304-9267G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56319364 | ||||||
| chr16:56319390
|
C | T | 1 | a0001c0002t0012g0180 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.304-9241C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56319390 | ||||||
| chr16:56319441
|
G | T | 6 | a0001c0001t0001g0166a0001c0001t0003g0269a0001c0001t0011g0203others(3): Show | 6 | HG02630.hp1 HG02723.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.304-9190G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56319441 | ||||||
| chr16:56319550
|
C | T | 1 | a0001c0001t0014g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.304-9081C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56319550 | ||||||
| chr16:56319553
|
A | C | 295 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0014others(292): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.304-9078A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56319553 | ||||||
| chr16:56319562
|
G | A | 1 | a0001c0001t0010g0123 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.304-9069G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56319562 | ||||||
| chr16:56319681
|
G | A | 2 | a0001c0001t0001g0079a0001c0002t0001g0117 | 2 | HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.304-8950G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56319681 | ||||||
| chr16:56319927
|
T | G | 1 | a0001c0001t0015g0251 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.304-8704T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56319927 | ||||||
| chr16:56320067
|
A | T | 7 | a0001c0001t0001g0077a0001c0001t0001g0164a0001c0001t0001g0202others(4): Show | 7 | HG00280.hp1 HG00673.hp1 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.304-8564A>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56320067 | ||||||
| chr16:56320156
|
G | A | 2 | a0001c0001t0003g0052a0001c0002t0004g0053 | 2 | HG02257.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.304-8475G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56320156 | ||||||
| chr16:56320167
|
G | A | 241 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0014others(238): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.304-8464G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56320167 | ||||||
| chr16:56320224
|
G | A | 1 | a0001c0002t0001g0245 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.304-8407G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56320224 | ||||||
| chr16:56320227
|
T | C | 6 | a0001c0001t0001g0079a0001c0002t0001g0025a0001c0002t0001g0107others(3): Show | 6 | HG01515.hp2 HG01517.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.304-8404T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56320227 | ||||||
| chr16:56320268
|
A | G | 5 | a0001c0001t0001g0079a0001c0002t0001g0025a0001c0002t0001g0107others(2): Show | 5 | HG01515.hp2 HG01517.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.304-8363A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56320268 | ||||||
| chr16:56320366
|
A | G | 1 | a0001c0001t0009g0140 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.304-8265A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56320366 | ||||||
| chr16:56320677
|
T | G | 1 | a0001c0001t0014g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.304-7954T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56320677 | ||||||
| chr16:56320705
|
A | G | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.304-7926A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56320705 | ||||||
| chr16:56320988
|
A | G | 6 | a0001c0001t0001g0079a0001c0002t0001g0025a0001c0002t0001g0107others(3): Show | 6 | HG01515.hp2 HG01517.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.304-7643A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56320988 | ||||||
| chr16:56321085
|
C | T | 6 | a0001c0001t0001g0079a0001c0002t0001g0025a0001c0002t0001g0107others(3): Show | 6 | HG01515.hp2 HG01517.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.304-7546C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56321085 | ||||||
| chr16:56321112
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.304-7519G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56321112 | ||||||
| chr16:56321130
|
G | C | 1 | a0001c0001t0008g0005 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.304-7501G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56321130 | ||||||
| chr16:56321170
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.304-7461C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56321170 | ||||||
| chr16:56321224
|
C | A | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.304-7407C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56321224 | ||||||
| chr16:56321311
|
G | A | 10 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0051others(7): Show | 10 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.304-7320G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56321311 | ||||||
| chr16:56321384
|
C | T | 3 | a0001c0002t0001g0056a0001c0002t0002g0029a0001c0002t0004g0021 | 3 | HG02145.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.304-7247C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56321384 | ||||||
| chr16:56321532
|
C | G | 1 | a0001c0001t0014g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.304-7099C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56321532 | ||||||
| chr16:56321629
|
C | T | 261 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0014others(258): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.304-7002C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56321629 | ||||||
| chr16:56321776
|
G | A | 7 | a0001c0002t0001g0013a0001c0002t0001g0035a0001c0002t0001g0055others(4): Show | 7 | HG02109.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.304-6855G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56321776 | ||||||
| chr16:56321808
|
G | T | 1 | a0001c0001t0003g0238 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.304-6823G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56321808 | ||||||
| chr16:56321862
|
G | A | 246 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0014others(243): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.304-6769G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56321862 | ||||||
| chr16:56321909
|
C | T | 250 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0014others(247): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.304-6722C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56321909 | ||||||
| chr16:56321927
|
A | T | 261 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0014others(258): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.304-6704A>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56321927 | ||||||
| chr16:56321949
|
A | C | 2 | a0001c0001t0001g0092a0001c0001t0001g0106 | 2 | NA19005.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.304-6682A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56321949 | ||||||
| chr16:56321966
|
A | T | 1 | a0001c0001t0003g0238 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.304-6665A>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56321966 | ||||||
| chr16:56322055
|
G | A | 1 | a0001c0001t0005g0186 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.304-6576G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56322055 | ||||||
| chr16:56322073
|
A | G | 1 | a0001c0001t0003g0238 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.304-6558A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56322073 | ||||||
| chr16:56322122
|
C | G | 252 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0014others(249): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.304-6509C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56322122 | ||||||
| chr16:56322177
|
C | T | 236 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0014others(233): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.304-6454C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56322177 | ||||||
| chr16:56322206
|
T | C | 1 | a0001c0002t0004g0143 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.304-6425T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56322206 | ||||||
| chr16:56322265
|
A | G | 255 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0014others(252): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.304-6366A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56322265 | ||||||
| chr16:56322268
|
A | G | 254 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0014others(251): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.304-6363A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56322268 | ||||||
| chr16:56322272
|
A | G | 255 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0014others(252): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.304-6359A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56322272 | ||||||
| chr16:56322446
|
G | A | 13 | a0001c0001t0001g0079a0001c0001t0001g0295a0001c0002t0001g0013others(10): Show | 13 | HG01515.hp2 HG01517.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.304-6185G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56322446 | ||||||
| chr16:56322466
|
C | T | 1 | a0001c0001t0001g0210 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.304-6165C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56322466 | ||||||
| chr16:56322542
|
G | A | 26 | a0001c0001t0001g0280a0001c0001t0003g0208a0001c0001t0003g0238others(23): Show | 26 | HG01346.hp2 HG01433.hp2 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.304-6089G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56322542 | ||||||
| chr16:56322725
|
G | A | 1 | a0001c0001t0013g0187 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.304-5906G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56322725 | ||||||
| chr16:56322762
|
C | T | 254 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0014others(251): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.304-5869C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56322762 | ||||||
| chr16:56322907
|
C | G | 1 | a0001c0002t0004g0205 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.304-5724C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56322907 | ||||||
| chr16:56322918
|
C | G | 31 | a0001c0001t0001g0043a0001c0001t0001g0078a0001c0001t0001g0115others(28): Show | 32 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.304-5713C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56322918 | ||||||
| chr16:56322932
|
C | T | 7 | a0001c0001t0001g0077a0001c0001t0001g0164a0001c0001t0001g0202others(4): Show | 7 | HG00280.hp1 HG00673.hp1 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.304-5699C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56322932 | ||||||
| chr16:56322952
|
A | G | 244 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0014others(241): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.304-5679A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56322952 | ||||||
| chr16:56322964
|
G | T | 1 | a0001c0002t0006g0264 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.304-5667G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56322964 | ||||||
| chr16:56323041
|
G | A | 2 | a0001c0002t0002g0195a0001c0002t0002g0271 | 2 | HG03654.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.304-5590G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56323041 | ||||||
| chr16:56323093
|
C | T | 1 | a0001c0001t0010g0123 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.304-5538C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56323093 | ||||||
| chr16:56323119
|
C | T | 7 | a0001c0001t0001g0062a0001c0001t0001g0083a0001c0001t0001g0084others(4): Show | 7 | HG00735.hp1 HG01169.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.304-5512C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56323119 | ||||||
| chr16:56323273
|
G | A | 3 | a0001c0002t0004g0067a0001c0002t0014g0033a0001c0002t0014g0058 | 3 | HG02258.hp2 HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.304-5358G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56323273 | ||||||
| chr16:56323312
|
A | G | 1 | a0001c0002t0001g0279 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.304-5319A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56323312 | ||||||
| chr16:56323337
|
G | C | 3 | a0001c0002t0004g0067a0001c0002t0014g0033a0001c0002t0014g0058 | 3 | HG02258.hp2 HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.304-5294G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56323337 | ||||||
| chr16:56323509
|
A | G | 7 | a0001c0002t0001g0013a0001c0002t0001g0035a0001c0002t0001g0055others(4): Show | 7 | HG02109.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.304-5122A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56323509 | ||||||
| chr16:56323658
|
C | CA | 13 | a0001c0002t0001g0013a0001c0002t0001g0035a0001c0002t0001g0055others(10): Show | 13 | HG00735.hp2 HG01255.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.304-4957dupA | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56323658 | |||||
| chr16:56323658
|
CA | C | 177 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0014others(174): Show | 178 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.304-4957delA | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56323658 | |||||
| chr16:56323673
|
A | C | 176 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0014others(173): Show | 177 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.304-4958A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56323673 | ||||||
| chr16:56323833
|
G | T | 15 | a0001c0002t0001g0082a0001c0002t0001g0105a0001c0002t0001g0151others(12): Show | 15 | HG00140.hp2 HG00735.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.304-4798G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56323833 | ||||||
| chr16:56324011
|
G | C | 7 | a0001c0002t0001g0013a0001c0002t0001g0035a0001c0002t0001g0055others(4): Show | 7 | HG02109.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.304-4620G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56324011 | ||||||
| chr16:56324037
|
G | A | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.304-4594G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56324037 | ||||||
| chr16:56324194
|
A | T | 7 | a0001c0002t0001g0013a0001c0002t0001g0035a0001c0002t0001g0055others(4): Show | 7 | HG02109.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.304-4437A>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56324194 | ||||||
| chr16:56324321
|
G | T | 12 | a0001c0001t0001g0077a0001c0001t0001g0164a0001c0001t0001g0202others(9): Show | 12 | HG00280.hp1 HG00673.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.304-4310G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56324321 | ||||||
| chr16:56324385
|
C | G | 1 | a0001c0001t0014g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.304-4246C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56324385 | ||||||
| chr16:56324783
|
C | T | 1 | a0001c0001t0016g0059 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.304-3848C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56324783 | ||||||
| chr16:56324902
|
G | A | 241 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0014others(238): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.304-3729G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56324902 | ||||||
| chr16:56324965
|
C | T | 6 | a0001c0001t0001g0079a0001c0001t0014g0034a0001c0002t0001g0025others(3): Show | 6 | HG01515.hp2 HG01517.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.304-3666C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56324965 | ||||||
| chr16:56324986
|
G | C | 2 | a0001c0002t0001g0056a0001c0002t0004g0021 | 2 | HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.304-3645G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56324986 | ||||||
| chr16:56325126
|
G | T | 2 | a0001c0002t0012g0179a0001c0002t0012g0180 | 2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.304-3505G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56325126 | ||||||
| chr16:56325161
|
G | A | 2 | a0001c0001t0001g0079a0001c0002t0001g0117 | 2 | HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.304-3470G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56325161 | ||||||
| chr16:56325333
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.304-3298G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56325333 | ||||||
| chr16:56325521
|
C | T | 4 | a0001c0002t0001g0056a0001c0002t0002g0029a0001c0002t0003g0148others(1): Show | 4 | HG02145.hp1 HG02451.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.304-3110C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56325521 | ||||||
| chr16:56325576
|
T | C | 266 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0014others(263): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.304-3055T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56325576 | ||||||
| chr16:56325589
|
G | A | 1 | a0001c0002t0002g0194 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.304-3042G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56325589 | ||||||
| chr16:56325619
|
C | T | 7 | a0001c0001t0001g0077a0001c0001t0001g0164a0001c0001t0001g0202others(4): Show | 7 | HG00280.hp1 HG00673.hp1 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.304-3012C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56325619 | ||||||
| chr16:56325818
|
A | G | 1 | a0001c0002t0015g0128 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.304-2813A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56325818 | ||||||
| chr16:56325837
|
C | T | 7 | a0001c0002t0001g0013a0001c0002t0001g0035a0001c0002t0001g0055others(4): Show | 7 | HG02109.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.304-2794C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56325837 | ||||||
| chr16:56325933
|
C | A | 5 | a0001c0001t0001g0079a0001c0002t0001g0025a0001c0002t0001g0107others(2): Show | 5 | HG01515.hp2 HG01517.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.304-2698C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56325933 | ||||||
| chr16:56325991
|
T | C | 5 | a0001c0001t0001g0079a0001c0002t0001g0025a0001c0002t0001g0107others(2): Show | 5 | HG01515.hp2 HG01517.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.304-2640T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56325991 | ||||||
| chr16:56326022
|
C | A | 2 | a0001c0002t0001g0121a0001c0002t0004g0124 | 2 | NA18952.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.304-2609C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56326022 | ||||||
| chr16:56326040
|
C | T | 5 | a0001c0001t0001g0079a0001c0002t0001g0025a0001c0002t0001g0107others(2): Show | 5 | HG01515.hp2 HG01517.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.304-2591C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56326040 | ||||||
| chr16:56326202
|
G | A | 1 | a0001c0001t0001g0145 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.304-2429G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56326202 | ||||||
| chr16:56326399
|
CAG | C | 3 | a0001c0002t0001g0056a0001c0002t0002g0029a0001c0002t0004g0021 | 3 | HG02145.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.304-2231_304-2230d others(4): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56326399 | ||||||
| chr16:56326514
|
A | C | 1 | a0001c0001t0001g0132 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.304-2117A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56326514 | ||||||
| chr16:56326698
|
C | T | 7 | a0001c0002t0001g0013a0001c0002t0001g0035a0001c0002t0001g0055others(4): Show | 7 | HG02109.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.304-1933C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56326698 | ||||||
| chr16:56326786
|
T | TGCTCTGC others(29): Show |
1 | a0001c0001t0003g0008 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.304-1841_304-1806d others(38): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 56326786 | |||||
| chr16:56326839
|
A | G | 2 | a0001c0002t0001g0025a0001c0002t0001g0107 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.304-1792A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56326839 | ||||||
| chr16:56326880
|
G | A | 1 | a0001c0001t0007g0016 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.304-1751G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56326880 | ||||||
| chr16:56327028
|
T | G | 1 | a0001c0001t0008g0005 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.304-1603T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56327028 | ||||||
| chr16:56327222
|
T | C | 5 | a0001c0001t0001g0079a0001c0002t0001g0025a0001c0002t0001g0107others(2): Show | 5 | HG01515.hp2 HG01517.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.304-1409T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56327222 | ||||||
| chr16:56327231
|
C | T | 1 | a0001c0002t0001g0054 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.304-1400C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56327231 | ||||||
| chr16:56327281
|
G | A | 4 | a0001c0002t0001g0105a0001c0002t0002g0118a0001c0003t0002g0103others(1): Show | 4 | HG00735.hp2 HG01255.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.304-1350G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56327281 | ||||||
| chr16:56327296
|
T | C | 20 | a0001c0001t0001g0078a0001c0001t0001g0115a0001c0001t0001g0153others(17): Show | 20 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.304-1335T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56327296 | ||||||
| chr16:56327383
|
C | G | 1 | a0001c0001t0014g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.304-1248C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56327383 | ||||||
| chr16:56327452
|
G | A | 4 | a0001c0002t0004g0074a0001c0002t0010g0274a0001c0002t0015g0128others(1): Show | 4 | HG00280.hp1 HG00673.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.304-1179G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56327452 | ||||||
| chr16:56327645
|
T | C | 59 | a0001c0001t0001g0182a0001c0002t0001g0010a0001c0002t0001g0018others(56): Show | 60 | HG00099.hp1 HG00140.hp2 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.304-986T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56327645 | ||||||
| chr16:56327705
|
C | T | 2 | a0001c0002t0001g0056a0001c0002t0004g0021 | 2 | HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.304-926C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56327705 | ||||||
| chr16:56327760
|
G | T | 2 | a0001c0001t0004g0002a0001c0001t0004g0287 | 3 | HG03491.hp2 HG03492.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.304-871G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56327760 | ||||||
| chr16:56327858
|
T | C | 1 | a0001c0002t0006g0197 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.304-773T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56327858 | ||||||
| chr16:56327864
|
T | C | 2 | a0001c0001t0001g0079a0001c0002t0001g0117 | 2 | HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.304-767T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56327864 | ||||||
| chr16:56327949
|
G | A | 2 | a0001c0001t0001g0079a0001c0002t0001g0117 | 2 | HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.304-682G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56327949 | ||||||
| chr16:56328023
|
T | C | 8 | a0001c0001t0001g0077a0001c0001t0001g0164a0001c0001t0001g0202others(5): Show | 8 | HG00280.hp1 HG00673.hp1 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.304-608T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56328023 | ||||||
| chr16:56328057
|
C | A | 1 | a0001c0001t0001g0092 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.304-574C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56328057 | ||||||
| chr16:56328156
|
A | T | 1 | a0001c0001t0001g0174 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.304-475A>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56328156 | ||||||
| chr16:56328344
|
G | A | 1 | a0001c0001t0007g0156 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.304-287G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56328344 | ||||||
| chr16:56328405
|
T | G | 1 | a0001c0002t0004g0205 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.304-226T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56328405 | ||||||
| chr16:56328419
|
A | G | 8 | a0001c0001t0001g0077a0001c0001t0001g0164a0001c0001t0001g0202others(5): Show | 8 | HG00280.hp1 HG00673.hp1 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.304-212A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56328419 | ||||||
| chr16:56328526
|
T | C | 2 | a0001c0002t0004g0143a0001c0002t0004g0144 | 2 | HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.304-105T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56328526 | ||||||
| chr16:56328536
|
C | T | 8 | a0001c0001t0001g0077a0001c0001t0001g0164a0001c0001t0001g0202others(5): Show | 8 | HG00280.hp1 HG00673.hp1 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.304-95C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56328536 | ||||||
| chr16:56328600
|
G | A | 5 | a0001c0002t0001g0288a0001c0002t0002g0086a0001c0002t0002g0087others(2): Show | 5 | HG02257.hp1 HG02280.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.304-31G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 3/8 | chr16 | 56328600 | ||||||
| chr16:56328813
|
T | C | 174 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0024others(171): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.464+22T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56328813 | ||||||
| chr16:56328889
|
C | T | 1 | a0001c0001t0003g0044 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.464+98C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56328889 | ||||||
| chr16:56328969
|
A | C | 178 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0024others(175): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.464+178A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56328969 | ||||||
| chr16:56329173
|
T | C | 1 | a0001c0001t0020g0126 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.464+382T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56329173 | ||||||
| chr16:56329288
|
T | A | 1 | a0001c0001t0003g0238 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.464+497T>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56329288 | ||||||
| chr16:56329400
|
G | A | 1 | a0001c0002t0004g0143 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.464+609G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56329400 | ||||||
| chr16:56329409
|
G | A | 2 | a0001c0001t0001g0079a0001c0002t0001g0117 | 2 | HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.464+618G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56329409 | ||||||
| chr16:56329487
|
C | T | 2 | a0001c0001t0001g0079a0001c0002t0001g0117 | 2 | HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.464+696C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56329487 | ||||||
| chr16:56329545
|
T | C | 9 | a0001c0001t0001g0079a0001c0002t0001g0013a0001c0002t0001g0035others(6): Show | 9 | HG02109.hp1 HG02280.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.464+754T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56329545 | ||||||
| chr16:56329572
|
G | C | 1 | a0001c0002t0001g0247 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.464+781G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56329572 | ||||||
| chr16:56329616
|
C | G | 52 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0050others(49): Show | 52 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.464+825C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56329616 | ||||||
| chr16:56329668
|
A | G | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.464+877A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56329668 | ||||||
| chr16:56329723
|
C | T | 1 | a0001c0002t0002g0175 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.464+932C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56329723 | ||||||
| chr16:56329825
|
A | G | 2 | a0001c0001t0001g0079a0001c0002t0001g0117 | 2 | HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.464+1034A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56329825 | ||||||
| chr16:56329884
|
G | T | 2 | a0001c0002t0001g0294a0001c0004t0002g0282 | 2 | HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.464+1093G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56329884 | ||||||
| chr16:56329938
|
G | A | 1 | a0001c0001t0002g0150 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.464+1147G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56329938 | ||||||
| chr16:56329964
|
G | T | 2 | a0001c0001t0004g0291a0001c0001t0004g0296 | 2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.464+1173G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56329964 | ||||||
| chr16:56330118
|
G | C | 129 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0024others(126): Show | 130 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.464+1327G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56330118 | ||||||
| chr16:56330166
|
C | A | 2 | a0001c0001t0001g0079a0001c0002t0001g0117 | 2 | HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.464+1375C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56330166 | ||||||
| chr16:56330168
|
C | G | 14 | a0001c0001t0003g0044a0001c0001t0003g0100a0001c0001t0003g0101others(11): Show | 14 | NA18959.hp1 NA18973.hp2 NA18975.hp1 others(11): Show |
intron_variant | MODIFIER | c.464+1377C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56330168 | ||||||
| chr16:56330171
|
G | A | 1 | a0001c0001t0001g0172 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.464+1380G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56330171 | ||||||
| chr16:56330260
|
A | T | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.464+1469A>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56330260 | ||||||
| chr16:56330313
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.464+1522C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56330313 | ||||||
| chr16:56330338
|
G | T | 1 | a0001c0001t0014g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.464+1547G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56330338 | ||||||
| chr16:56330377
|
T | G | 1 | a0001c0001t0005g0186 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.464+1586T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56330377 | ||||||
| chr16:56330449
|
A | G | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.464+1658A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56330449 | ||||||
| chr16:56330479
|
C | CA | 216 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0014others(213): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.464+1697dupA | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 56330479 | |||||
| chr16:56330534
|
T | G | 1 | a0001c0001t0006g0255 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.464+1743T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56330534 | ||||||
| chr16:56330635
|
T | C | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.464+1844T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56330635 | ||||||
| chr16:56330644
|
C | T | 2 | a0001c0001t0001g0166a0001c0001t0011g0203 | 2 | NA19011.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.464+1853C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56330644 | ||||||
| chr16:56330653
|
C | G | 47 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0050others(44): Show | 47 | HG00280.hp2 HG00642.hp1 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.464+1862C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56330653 | ||||||
| chr16:56330654
|
G | A | 1 | a0001c0002t0002g0029 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.464+1863G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56330654 | ||||||
| chr16:56330917
|
C | G | 199 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0014others(196): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.464+2126C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56330917 | ||||||
| chr16:56331036
|
G | A | 2 | a0001c0002t0002g0292a0001c0002t0027g0146 | 2 | HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.464+2245G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56331036 | ||||||
| chr16:56331443
|
C | T | 54 | a0001c0001t0001g0182a0001c0002t0001g0025a0001c0002t0001g0054others(51): Show | 55 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.464+2652C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56331443 | ||||||
| chr16:56331476
|
C | T | 3 | a0001c0002t0010g0252a0001c0002t0015g0128a0001c0002t0018g0229 | 3 | HG00673.hp1 HG04115.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.464+2685C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56331476 | ||||||
| chr16:56331589
|
C | T | 5 | a0001c0001t0003g0208a0001c0001t0003g0238a0001c0001t0004g0207others(2): Show | 5 | HG01978.hp1 NA18949.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.464+2798C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56331589 | ||||||
| chr16:56331590
|
G | A | 1 | a0001c0002t0001g0259 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.464+2799G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56331590 | ||||||
| chr16:56331677
|
T | C | 1 | a0001c0001t0001g0295 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.464+2886T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56331677 | ||||||
| chr16:56331681
|
G | A | 1 | a0001c0001t0005g0220 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.464+2890G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56331681 | ||||||
| chr16:56331810
|
C | T | 2 | a0001c0002t0001g0093a0001c0002t0001g0104 | 2 | HG01071.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.465-2919C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56331810 | ||||||
| chr16:56331847
|
A | G | 1 | a0001c0002t0027g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.465-2882A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56331847 | ||||||
| chr16:56331979
|
G | A | 7 | a0001c0001t0001g0079a0001c0002t0001g0117a0001c0002t0001g0288others(4): Show | 7 | HG02257.hp1 HG02280.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.465-2750G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56331979 | ||||||
| chr16:56332163
|
A | T | 1 | a0001c0002t0003g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.465-2566A>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56332163 | ||||||
| chr16:56332189
|
G | C | 1 | a0001c0002t0004g0277 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.465-2540G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56332189 | ||||||
| chr16:56332373
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.465-2356C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56332373 | ||||||
| chr16:56332513
|
C | G | 6 | a0001c0002t0004g0067a0001c0002t0004g0143a0001c0002t0004g0144others(3): Show | 6 | HG02258.hp2 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.465-2216C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56332513 | ||||||
| chr16:56332521
|
C | G | 2 | a0001c0002t0001g0117a0001c0002t0003g0148 | 2 | HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.465-2208C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56332521 | ||||||
| chr16:56332541
|
C | T | 1 | a0001c0002t0001g0259 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.465-2188C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56332541 | ||||||
| chr16:56332546
|
G | A | 3 | a0001c0002t0004g0143a0001c0002t0004g0144a0001c0002t0004g0278 | 3 | HG02630.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.465-2183G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56332546 | ||||||
| chr16:56332635
|
G | A | 1 | a0001c0001t0003g0008 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.465-2094G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56332635 | ||||||
| chr16:56332636
|
A | T | 1 | a0001c0001t0003g0008 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.465-2093A>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56332636 | ||||||
| chr16:56332662
|
T | C | 8 | a0001c0002t0001g0013a0001c0002t0001g0035a0001c0002t0001g0055others(5): Show | 8 | HG02109.hp1 HG02145.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.465-2067T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56332662 | ||||||
| chr16:56332711
|
A | G | 1 | a0001c0001t0017g0244 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.465-2018A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56332711 | ||||||
| chr16:56332836
|
G | C | 35 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0051others(32): Show | 35 | HG00280.hp2 HG01884.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.465-1893G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56332836 | ||||||
| chr16:56332862
|
T | A | 2 | a0001c0001t0001g0078a0001c0001t0001g0262 | 2 | HG01109.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.465-1867T>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56332862 | ||||||
| chr16:56332958
|
G | A | 235 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0014others(232): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.465-1771G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56332958 | ||||||
| chr16:56332970
|
C | T | 3 | a0001c0002t0010g0252a0001c0002t0015g0128a0001c0002t0018g0229 | 3 | HG00673.hp1 HG04115.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.465-1759C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56332970 | ||||||
| chr16:56333083
|
G | T | 13 | a0001c0002t0001g0013a0001c0002t0001g0035a0001c0002t0001g0055others(10): Show | 13 | HG02109.hp1 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.465-1646G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56333083 | ||||||
| chr16:56333149
|
G | A | 232 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0014others(229): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.465-1580G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56333149 | ||||||
| chr16:56333209
|
T | C | 1 | a0001c0001t0003g0200 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.465-1520T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56333209 | ||||||
| chr16:56333210
|
C | CT | 132 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0024others(129): Show | 133 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.465-1505dupT | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 56333210 | |||||
| chr16:56333210
|
C | T | 1 | a0001c0001t0003g0200 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.465-1519C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56333210 | ||||||
| chr16:56333298
|
C | T | 1 | a0001c0002t0004g0278 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.465-1431C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56333298 | ||||||
| chr16:56333309
|
T | C | 1 | a0001c0002t0010g0274 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.465-1420T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56333309 | ||||||
| chr16:56333345
|
G | A | 66 | a0001c0002t0001g0013a0001c0002t0001g0025a0001c0002t0001g0035others(63): Show | 67 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.465-1384G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56333345 | ||||||
| chr16:56333385
|
C | T | 3 | a0001c0002t0004g0067a0001c0002t0014g0033a0001c0002t0014g0058 | 3 | HG02258.hp2 HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.465-1344C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56333385 | ||||||
| chr16:56333511
|
C | G | 2 | a0001c0002t0001g0025a0001c0002t0001g0107 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.465-1218C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56333511 | ||||||
| chr16:56333694
|
A | C | 3 | a0001c0002t0002g0086a0001c0002t0002g0087a0001c0002t0002g0260 | 3 | HG02257.hp1 HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.465-1035A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56333694 | ||||||
| chr16:56333725
|
G | T | 1 | a0001c0001t0003g0008 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.465-1004G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56333725 | ||||||
| chr16:56333726
|
T | C | 1 | a0001c0001t0003g0008 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.465-1003T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56333726 | ||||||
| chr16:56333727
|
C | A | 1 | a0001c0001t0003g0008 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.465-1002C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56333727 | ||||||
| chr16:56333769
|
A | T | 2 | a0001c0002t0001g0286a0001c0002t0006g0154 | 2 | HG02015.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.465-960A>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56333769 | ||||||
| chr16:56333813
|
C | T | 1 | a0001c0001t0005g0272 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.465-916C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56333813 | ||||||
| chr16:56333934
|
C | T | 1 | a0001c0001t0003g0289 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.465-795C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56333934 | ||||||
| chr16:56334057
|
C | T | 163 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0014others(160): Show | 164 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.465-672C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56334057 | ||||||
| chr16:56334277
|
A | C | 1 | a0001c0001t0003g0008 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.465-452A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56334277 | ||||||
| chr16:56334494
|
C | T | 1 | a0001c0001t0009g0089 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.465-235C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56334494 | ||||||
| chr16:56334495
|
G | A | 3 | a0001c0001t0001g0062a0001c0001t0001g0165a0001c0001t0001g0281 | 3 | HG01106.hp1 HG01496.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.465-234G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56334495 | ||||||
| chr16:56334571
|
G | A | 1 | a0001c0002t0004g0063 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.465-158G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56334571 | ||||||
| chr16:56334583
|
T | C | 70 | a0001c0002t0001g0013a0001c0002t0001g0025a0001c0002t0001g0035others(67): Show | 71 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.465-146T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56334583 | ||||||
| chr16:56334589
|
C | T | 21 | a0001c0001t0001g0050a0001c0001t0001g0078a0001c0001t0001g0115others(18): Show | 21 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.465-140C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 4/8 | chr16 | 56334589 | ||||||
| chr16:56334875
|
C | T | 6 | a0001c0002t0004g0067a0001c0002t0004g0143a0001c0002t0004g0144others(3): Show | 6 | HG02258.hp2 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.593+18C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 5/8 | chr16 | 56334875 | ||||||
| chr16:56334905
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.593+48C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 5/8 | chr16 | 56334905 | ||||||
| chr16:56334971
|
G | A | 1 | a0001c0002t0004g0063 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.593+114G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 5/8 | chr16 | 56334971 | ||||||
| chr16:56334974
|
C | T | 233 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0014others(230): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.593+117C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 5/8 | chr16 | 56334974 | ||||||
| chr16:56335165
|
G | A | 1 | a0001c0001t0003g0008 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.593+308G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 5/8 | chr16 | 56335165 | ||||||
| chr16:56335193
|
G | A | 59 | a0001c0002t0001g0025a0001c0002t0001g0054a0001c0002t0001g0056others(56): Show | 60 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.593+336G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 5/8 | chr16 | 56335193 | ||||||
| chr16:56335194
|
A | C | 59 | a0001c0002t0001g0025a0001c0002t0001g0054a0001c0002t0001g0056others(56): Show | 60 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.593+337A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 5/8 | chr16 | 56335194 | ||||||
| chr16:56335220
|
C | T | 1 | a0001c0002t0003g0184 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.593+363C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 5/8 | chr16 | 56335220 | ||||||
| chr16:56335222
|
C | T | 1 | a0001c0006t0021g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.593+365C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 5/8 | chr16 | 56335222 | ||||||
| chr16:56335253
|
A | C | 233 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0014others(230): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.593+396A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 5/8 | chr16 | 56335253 | ||||||
| chr16:56335404
|
G | A | 1 | a0001c0001t0011g0203 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.593+547G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 5/8 | chr16 | 56335404 | ||||||
| chr16:56335417
|
C | T | 1 | a0001c0002t0002g0029 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.593+560C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 5/8 | chr16 | 56335417 | ||||||
| chr16:56335428
|
G | A | 47 | a0001c0002t0001g0025a0001c0002t0001g0054a0001c0002t0001g0056others(44): Show | 48 | HG00099.hp1 HG00140.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.593+571G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 5/8 | chr16 | 56335428 | ||||||
| chr16:56335451
|
G | C | 1 | a0001c0002t0004g0063 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.593+594G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 5/8 | chr16 | 56335451 | ||||||
| chr16:56335517
|
G | A | 1 | a0001c0002t0001g0279 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.593+660G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 5/8 | chr16 | 56335517 | ||||||
| chr16:56335727
|
C | G | 1 | a0001c0002t0001g0054 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.593+870C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 5/8 | chr16 | 56335727 | ||||||
| chr16:56335814
|
C | T | 1 | a0001c0001t0006g0080 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.594-917C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 5/8 | chr16 | 56335814 | ||||||
| chr16:56335949
|
T | G | 1 | a0001c0001t0001g0182 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.594-782T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 5/8 | chr16 | 56335949 | ||||||
| chr16:56335974
|
T | C | 5 | a0001c0002t0004g0074a0001c0002t0010g0252a0001c0002t0010g0274others(2): Show | 5 | HG00280.hp1 HG00673.hp1 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.594-757T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 5/8 | chr16 | 56335974 | ||||||
| chr16:56335991
|
C | A | 12 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0051others(9): Show | 12 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.594-740C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 5/8 | chr16 | 56335991 | ||||||
| chr16:56336082
|
G | A | 1 | a0001c0001t0004g0207 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.594-649G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 5/8 | chr16 | 56336082 | ||||||
| chr16:56336206
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.594-525C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 5/8 | chr16 | 56336206 | ||||||
| chr16:56336208
|
C | A | 12 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0051others(9): Show | 12 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.594-523C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 5/8 | chr16 | 56336208 | ||||||
| chr16:56336254
|
C | A | 1 | a0001c0001t0009g0094 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.594-477C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 5/8 | chr16 | 56336254 | ||||||
| chr16:56336269
|
G | T | 58 | a0001c0002t0001g0025a0001c0002t0001g0054a0001c0002t0001g0056others(55): Show | 59 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.594-462G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 5/8 | chr16 | 56336269 | ||||||
| chr16:56336462
|
A | C | 2 | a0001c0002t0004g0074a0001c0002t0010g0274 | 2 | HG00280.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.594-269A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 5/8 | chr16 | 56336462 | ||||||
| chr16:56336881
|
G | A | 1 | a0001c0001t0003g0052 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.723+21G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56336881 | ||||||
| chr16:56336929
|
T | A | 1 | a0001c0001t0003g0008 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.723+69T>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56336929 | ||||||
| chr16:56337016
|
G | A | 2 | a0001c0002t0001g0056a0001c0002t0004g0021 | 2 | HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.723+156G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56337016 | ||||||
| chr16:56337287
|
A | G | 79 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0051others(76): Show | 80 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.723+427A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56337287 | ||||||
| chr16:56337365
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.723+505G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56337365 | ||||||
| chr16:56337470
|
C | G | 69 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0051others(66): Show | 70 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.723+610C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56337470 | ||||||
| chr16:56337677
|
AGTGGGGT others(2): Show |
A | 3 | a0001c0002t0001g0035a0001c0002t0013g0032a0001c0002t0013g0293 | 3 | HG02559.hp2 HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.723+821_723+829del others(9): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 56337677 | |||||
| chr16:56337691
|
T | A | 1 | a0001c0001t0009g0094 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.723+831T>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56337691 | ||||||
| chr16:56337694
|
G | A | 6 | a0001c0001t0001g0022a0001c0001t0001g0177a0001c0001t0001g0210others(3): Show | 6 | HG00423.hp2 NA18747.hp2 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.723+834G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56337694 | ||||||
| chr16:56337743
|
G | A | 18 | a0001c0001t0001g0196a0001c0001t0003g0044a0001c0001t0003g0100others(15): Show | 18 | HG00280.hp2 HG04199.hp2 NA18959.hp1 others(15): Show |
intron_variant | MODIFIER | c.723+883G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56337743 | ||||||
| chr16:56337787
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.723+927C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56337787 | ||||||
| chr16:56337812
|
C | T | 3 | a0001c0001t0008g0042a0001c0001t0008g0045a0001c0001t0008g0046 | 3 | NA18975.hp1 NA18986.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.723+952C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56337812 | ||||||
| chr16:56337912
|
A | G | 2 | a0001c0001t0004g0291a0001c0001t0004g0296 | 2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.723+1052A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56337912 | ||||||
| chr16:56337972
|
G | A | 2 | a0001c0002t0001g0056a0001c0002t0004g0021 | 2 | HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.723+1112G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56337972 | ||||||
| chr16:56338224
|
C | T | 1 | a0001c0001t0001g0170 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.723+1364C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56338224 | ||||||
| chr16:56338335
|
C | A | 2 | a0001c0001t0003g0208a0001c0001t0003g0238 | 2 | NA18949.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.723+1475C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56338335 | ||||||
| chr16:56338549
|
T | C | 120 | a0001c0001t0001g0024a0001c0001t0001g0043a0001c0001t0001g0050others(117): Show | 122 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.723+1689T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56338549 | ||||||
| chr16:56338711
|
C | G | 1 | a0001c0001t0001g0079 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.723+1851C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56338711 | ||||||
| chr16:56338823
|
C | CT | 39 | a0001c0001t0001g0166a0001c0001t0001g0199a0001c0001t0002g0150others(36): Show | 40 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.723+1964dupT | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 56338823 | |||||
| chr16:56338830
|
T | C | 1 | a0001c0001t0001g0276 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.723+1970T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56338830 | ||||||
| chr16:56338850
|
G | A | 2 | a0001c0001t0001g0182a0001c0001t0001g0295 | 2 | HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.723+1990G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56338850 | ||||||
| chr16:56338955
|
C | T | 58 | a0001c0001t0001g0041a0001c0001t0001g0079a0001c0001t0002g0253others(55): Show | 59 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(56): Show |
intron_variant | MODIFIER | c.723+2095C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56338955 | ||||||
| chr16:56338995
|
A | C | 103 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0024others(100): Show | 103 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.723+2135A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56338995 | ||||||
| chr16:56339025
|
G | C | 2 | a0001c0001t0002g0141a0001c0001t0017g0290 | 2 | HG01884.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.723+2165G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56339025 | ||||||
| chr16:56339272
|
C | T | 22 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0051others(19): Show | 23 | HG01515.hp1 HG01516.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.723+2412C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56339272 | ||||||
| chr16:56339310
|
G | A | 229 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0014others(226): Show | 231 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.723+2450G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56339310 | ||||||
| chr16:56339381
|
C | A | 1 | a0001c0001t0009g0094 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.723+2521C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56339381 | ||||||
| chr16:56339396
|
G | T | 104 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0024others(101): Show | 104 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.723+2536G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56339396 | ||||||
| chr16:56339690
|
G | C | 1 | a0001c0001t0006g0069 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.723+2830G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56339690 | ||||||
| chr16:56339701
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.723+2841C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56339701 | ||||||
| chr16:56339753
|
C | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0071a0001c0001t0001g0072others(2): Show | 5 | HG02071.hp1 HG02074.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.723+2893C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56339753 | ||||||
| chr16:56339825
|
C | T | 1 | a0001c0002t0004g0205 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.723+2965C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56339825 | ||||||
| chr16:56340008
|
T | A | 51 | a0001c0001t0001g0166a0001c0001t0001g0199a0001c0001t0001g0284others(48): Show | 51 | HG00438.hp2 HG01884.hp1 HG01891.hp1 others(48): Show |
intron_variant | MODIFIER | c.723+3148T>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56340008 | ||||||
| chr16:56340050
|
G | T | 104 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0024others(101): Show | 104 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.723+3190G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56340050 | ||||||
| chr16:56340225
|
C | A | 4 | a0001c0002t0001g0147a0001c0002t0001g0191a0001c0002t0006g0193others(1): Show | 4 | HG00639.hp2 HG01074.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.723+3365C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56340225 | ||||||
| chr16:56340247
|
C | T | 1 | a0001c0001t0005g0220 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.723+3387C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56340247 | ||||||
| chr16:56340286
|
C | CCA | 44 | a0001c0001t0001g0199a0001c0001t0001g0284a0001c0001t0003g0008others(41): Show | 44 | HG00438.hp2 HG01891.hp1 HG02257.hp1 others(41): Show |
intron_variant | MODIFIER | c.723+3429_723+3430d others(4): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 56340286 | |||||
| chr16:56340464
|
G | A | 1 | a0001c0002t0002g0149 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.723+3604G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56340464 | ||||||
| chr16:56340472
|
G | A | 20 | a0001c0001t0001g0050a0001c0001t0001g0078a0001c0001t0001g0115others(17): Show | 20 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.723+3612G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56340472 | ||||||
| chr16:56340491
|
C | T | 6 | a0001c0002t0001g0013a0001c0002t0001g0117a0001c0002t0004g0021others(3): Show | 6 | HG02109.hp1 HG02257.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.723+3631C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56340491 | ||||||
| chr16:56340553
|
ACTGCCCC others(3): Show |
A | 10 | a0001c0001t0001g0098a0001c0001t0001g0231a0001c0001t0001g0242others(7): Show | 10 | HG00323.hp2 HG01071.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.723+3697_723+3706d others(12): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 56340553 | |||||
| chr16:56340625
|
C | T | 4 | a0001c0001t0014g0034a0001c0002t0004g0067a0001c0002t0014g0033others(1): Show | 4 | HG02258.hp2 HG02622.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.723+3765C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56340625 | ||||||
| chr16:56340627
|
C | T | 6 | a0001c0002t0001g0013a0001c0002t0001g0117a0001c0002t0004g0021others(3): Show | 6 | HG02109.hp1 HG02257.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.723+3767C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56340627 | ||||||
| chr16:56340709
|
G | A | 1 | a0001c0002t0001g0064 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.723+3849G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56340709 | ||||||
| chr16:56340736
|
G | A | 1 | a0001c0001t0004g0227 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.723+3876G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56340736 | ||||||
| chr16:56340774
|
C | T | 3 | a0001c0001t0001g0284a0001c0002t0003g0184a0001c0002t0012g0183 | 3 | HG02486.hp1 HG02559.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.723+3914C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56340774 | ||||||
| chr16:56340959
|
G | A | 2 | a0001c0001t0001g0182a0001c0001t0001g0295 | 2 | HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.723+4099G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56340959 | ||||||
| chr16:56341032
|
C | T | 4 | a0001c0001t0001g0145a0001c0002t0001g0209a0001c0002t0001g0245others(1): Show | 4 | HG01109.hp2 HG02965.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.723+4172C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56341032 | ||||||
| chr16:56341081
|
A | T | 3 | a0001c0001t0004g0291a0001c0001t0004g0296a0001c0002t0002g0292 | 3 | HG01891.hp1 HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.723+4221A>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56341081 | ||||||
| chr16:56341132
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.723+4272G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56341132 | ||||||
| chr16:56341187
|
A | G | 122 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0041others(119): Show | 124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.723+4327A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56341187 | ||||||
| chr16:56341218
|
T | G | 4 | a0001c0001t0001g0182a0001c0001t0001g0295a0001c0001t0002g0141others(1): Show | 4 | HG01884.hp1 HG03130.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.723+4358T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56341218 | ||||||
| chr16:56341273
|
T | C | 2 | a0001c0001t0001g0182a0001c0001t0001g0295 | 2 | HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.723+4413T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56341273 | ||||||
| chr16:56341278
|
C | T | 3 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0006t0021g0019 | 3 | HG01891.hp2 HG02145.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.723+4418C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56341278 | ||||||
| chr16:56341283
|
C | T | 1 | a0001c0001t0001g0011 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.723+4423C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56341283 | ||||||
| chr16:56341294
|
C | T | 1 | a0001c0001t0004g0223 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.723+4434C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56341294 | ||||||
| chr16:56341359
|
C | T | 1 | a0001c0001t0008g0110 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.723+4499C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56341359 | ||||||
| chr16:56341360
|
G | C | 4 | a0001c0001t0001g0182a0001c0001t0001g0295a0001c0001t0002g0141others(1): Show | 4 | HG01884.hp1 HG03130.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.723+4500G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56341360 | ||||||
| chr16:56341451
|
G | A | 1 | a0001c0002t0002g0283 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.723+4591G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56341451 | ||||||
| chr16:56341516
|
C | T | 2 | a0001c0002t0004g0074a0001c0002t0010g0274 | 2 | HG00280.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.723+4656C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56341516 | ||||||
| chr16:56341584
|
C | T | 40 | a0001c0001t0001g0041a0001c0001t0002g0253a0001c0001t0002g0254others(37): Show | 41 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(38): Show |
intron_variant | MODIFIER | c.723+4724C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56341584 | ||||||
| chr16:56341708
|
C | T | 20 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0051others(17): Show | 21 | HG01515.hp1 HG01516.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.723+4848C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56341708 | ||||||
| chr16:56341970
|
A | G | 6 | a0001c0001t0001g0182a0001c0001t0014g0034a0001c0001t0017g0244others(3): Show | 6 | HG02258.hp2 HG02622.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.723+5110A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56341970 | ||||||
| chr16:56342121
|
T | C | 1 | a0001c0001t0001g0166 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.723+5261T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56342121 | ||||||
| chr16:56342151
|
C | T | 2 | a0001c0002t0004g0074a0001c0002t0010g0274 | 2 | HG00280.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.723+5291C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56342151 | ||||||
| chr16:56342158
|
G | A | 1 | a0001c0001t0007g0016 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.723+5298G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56342158 | ||||||
| chr16:56342211
|
G | C | 104 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0041others(101): Show | 106 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.723+5351G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56342211 | ||||||
| chr16:56342249
|
G | T | 2 | a0001c0001t0002g0254a0001c0002t0002g0250 | 2 | HG01169.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.723+5389G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56342249 | ||||||
| chr16:56342370
|
C | T | 39 | a0001c0001t0001g0041a0001c0001t0002g0253a0001c0001t0002g0254others(36): Show | 40 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(37): Show |
intron_variant | MODIFIER | c.723+5510C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56342370 | ||||||
| chr16:56342591
|
C | T | 1 | a0001c0002t0013g0032 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.723+5731C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56342591 | ||||||
| chr16:56342592
|
G | A | 17 | a0001c0001t0003g0208a0001c0001t0003g0238a0001c0001t0004g0207others(14): Show | 17 | HG01346.hp2 HG01433.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.723+5732G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56342592 | ||||||
| chr16:56342639
|
G | A | 4 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0070others(1): Show | 4 | HG00642.hp2 HG00733.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.723+5779G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56342639 | ||||||
| chr16:56342725
|
A | G | 39 | a0001c0001t0001g0041a0001c0001t0002g0253a0001c0001t0002g0254others(36): Show | 40 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(37): Show |
intron_variant | MODIFIER | c.723+5865A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56342725 | ||||||
| chr16:56342731
|
T | C | 124 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0041others(121): Show | 126 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.723+5871T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56342731 | ||||||
| chr16:56342734
|
G | A | 5 | a0001c0001t0002g0261a0001c0001t0002g0273a0001c0002t0002g0102others(2): Show | 5 | HG02523.hp1 NA18612.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.723+5874G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56342734 | ||||||
| chr16:56343079
|
C | G | 2 | a0001c0002t0004g0063a0001c0002t0004g0277 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.723+6219C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56343079 | ||||||
| chr16:56343133
|
G | A | 125 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0041others(122): Show | 127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.723+6273G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56343133 | ||||||
| chr16:56343224
|
C | G | 6 | a0001c0002t0001g0013a0001c0002t0001g0117a0001c0002t0004g0021others(3): Show | 6 | HG02109.hp1 HG02257.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.723+6364C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56343224 | ||||||
| chr16:56343326
|
T | TAAAAATA others(312): Show |
1 | a0001c0001t0017g0244 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.723+6482_723+6483i others(321): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 56343326 | |||||
| chr16:56343329
|
A | AAAT | 69 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0051others(66): Show | 70 | HG00438.hp2 HG01515.hp1 HG01884.hp1 others(67): Show |
intron_variant | MODIFIER | c.723+6490_723+6492d others(5): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 56343329 | |||||
| chr16:56343329
|
A | AAATAATA others(318): Show |
1 | a0001c0002t0004g0067 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.723+6482_723+6483i others(327): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 56343329 | |||||
| chr16:56343329
|
A | AAATAATA others(318): Show |
3 | a0001c0001t0014g0034a0001c0002t0014g0033a0001c0002t0014g0058 | 3 | HG02258.hp2 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.723+6482_723+6483i others(327): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 56343329 | |||||
| chr16:56343487
|
C | CA | 128 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0043others(125): Show | 128 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.723+6643dupA | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 56343487 | |||||
| chr16:56343487
|
C | CAA | 37 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0051others(34): Show | 38 | HG00642.hp2 HG00733.hp1 HG01256.hp1 others(35): Show |
intron_variant | MODIFIER | c.723+6642_723+6643d others(4): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 56343487 | |||||
| chr16:56343487
|
C | CAAA | 43 | a0001c0001t0001g0041a0001c0001t0001g0057a0001c0001t0002g0253others(40): Show | 44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.723+6641_723+6643d others(5): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 56343487 | |||||
| chr16:56343684
|
C | T | 1 | a0001c0001t0004g0240 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.723+6824C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56343684 | ||||||
| chr16:56343809
|
C | T | 1 | a0001c0002t0002g0029 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.723+6949C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56343809 | ||||||
| chr16:56343836
|
A | G | 113 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0041others(110): Show | 114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.723+6976A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56343836 | ||||||
| chr16:56343994
|
G | A | 2 | a0001c0001t0002g0141a0001c0001t0017g0290 | 2 | HG01884.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.723+7134G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56343994 | ||||||
| chr16:56343996
|
C | T | 5 | a0001c0001t0014g0034a0001c0001t0017g0244a0001c0002t0004g0067others(2): Show | 5 | HG02258.hp2 HG02622.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.723+7136C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56343996 | ||||||
| chr16:56344132
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.724-7252C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56344132 | ||||||
| chr16:56344185
|
C | T | 1 | a0001c0002t0006g0265 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.724-7199C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56344185 | ||||||
| chr16:56344221
|
C | A | 2 | a0001c0002t0001g0288a0001c0002t0027g0146 | 2 | HG03225.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.724-7163C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56344221 | ||||||
| chr16:56344393
|
G | A | 1 | a0001c0002t0001g0259 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.724-6991G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56344393 | ||||||
| chr16:56344511
|
G | T | 4 | a0001c0001t0001g0284a0001c0002t0001g0294a0001c0002t0003g0184others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.724-6873G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56344511 | ||||||
| chr16:56344563
|
A | G | 1 | a0001c0002t0001g0259 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.724-6821A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56344563 | ||||||
| chr16:56344699
|
A | G | 215 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0014others(212): Show | 217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.724-6685A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56344699 | ||||||
| chr16:56344717
|
C | T | 4 | a0001c0001t0014g0034a0001c0002t0004g0067a0001c0002t0014g0033others(1): Show | 4 | HG02258.hp2 HG02622.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.724-6667C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56344717 | ||||||
| chr16:56344792
|
G | A | 1 | a0001c0002t0004g0063 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.724-6592G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56344792 | ||||||
| chr16:56344945
|
CGAGTTTG others(33): Show |
C | 5 | a0001c0001t0001g0043a0001c0001t0001g0071a0001c0001t0001g0219others(2): Show | 5 | HG00438.hp1 NA18995.hp2 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.724-6436_724-6397d others(42): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 56344945 | |||||
| chr16:56345053
|
C | A | 1 | a0001c0002t0001g0013 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.724-6331C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56345053 | ||||||
| chr16:56345066
|
A | C | 90 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0041others(87): Show | 90 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.724-6318A>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56345066 | ||||||
| chr16:56345070
|
C | G | 2 | a0001c0002t0001g0054a0001c0002t0001g0064 | 2 | HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.724-6314C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56345070 | ||||||
| chr16:56345136
|
C | T | 4 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0224others(1): Show | 4 | HG02015.hp1 HG02523.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.724-6248C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56345136 | ||||||
| chr16:56345160
|
T | G | 5 | a0001c0002t0001g0025a0001c0002t0001g0054a0001c0002t0001g0064others(2): Show | 5 | HG01515.hp2 HG01517.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.724-6224T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56345160 | ||||||
| chr16:56345317
|
C | T | 25 | a0001c0001t0003g0008a0001c0001t0003g0044a0001c0001t0003g0075others(22): Show | 25 | HG01256.hp2 HG02257.hp2 HG03540.hp1 others(22): Show |
intron_variant | MODIFIER | c.724-6067C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56345317 | ||||||
| chr16:56345430
|
C | T | 1 | a0001c0002t0027g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.724-5954C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56345430 | ||||||
| chr16:56345431
|
G | A | 2 | a0001c0001t0001g0049a0001c0001t0001g0174 | 2 | HG00609.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.724-5953G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56345431 | ||||||
| chr16:56345503
|
G | A | 1 | a0001c0002t0001g0279 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.724-5881G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56345503 | ||||||
| chr16:56345539
|
G | C | 22 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0051others(19): Show | 23 | HG00609.hp2 HG00673.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.724-5845G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56345539 | ||||||
| chr16:56345540
|
CCAAATGC others(3): Show |
C | 22 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0051others(19): Show | 23 | HG00609.hp2 HG00673.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.724-5841_724-5832d others(12): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 56345540 | |||||
| chr16:56345584
|
G | A | 23 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0051others(20): Show | 24 | HG00609.hp2 HG00673.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.724-5800G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56345584 | ||||||
| chr16:56345859
|
A | G | 25 | a0001c0001t0003g0008a0001c0001t0003g0044a0001c0001t0003g0075others(22): Show | 25 | HG01256.hp2 HG02257.hp2 HG03540.hp1 others(22): Show |
intron_variant | MODIFIER | c.724-5525A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56345859 | ||||||
| chr16:56345880
|
C | T | 224 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0050others(221): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.724-5504C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56345880 | ||||||
| chr16:56345923
|
T | G | 1 | a0001c0002t0001g0247 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.724-5461T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56345923 | ||||||
| chr16:56346025
|
C | T | 202 | a0001c0001t0001g0050a0001c0001t0001g0077a0001c0001t0001g0078others(199): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.724-5359C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56346025 | ||||||
| chr16:56346353
|
G | A | 1 | a0001c0002t0025g0129 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.724-5031G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56346353 | ||||||
| chr16:56346473
|
T | G | 6 | a0001c0001t0010g0123a0001c0001t0011g0285a0001c0001t0024g0068others(3): Show | 6 | HG00423.hp1 HG02135.hp2 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.724-4911T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56346473 | ||||||
| chr16:56346503
|
G | A | 1 | a0001c0002t0001g0018 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.724-4881G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56346503 | ||||||
| chr16:56346558
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.724-4826C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56346558 | ||||||
| chr16:56346583
|
G | A | 22 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0051others(19): Show | 23 | HG00609.hp2 HG00673.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.724-4801G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56346583 | ||||||
| chr16:56346590
|
G | A | 73 | a0001c0001t0001g0050a0001c0001t0001g0077a0001c0001t0001g0078others(70): Show | 73 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.724-4794G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56346590 | ||||||
| chr16:56346612
|
A | G | 6 | a0001c0001t0010g0123a0001c0001t0011g0285a0001c0001t0024g0068others(3): Show | 6 | HG00423.hp1 HG02135.hp2 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.724-4772A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56346612 | ||||||
| chr16:56346658
|
A | G | 63 | a0001c0001t0001g0199a0001c0001t0003g0008a0001c0001t0003g0009others(60): Show | 63 | HG00438.hp2 HG00642.hp1 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.724-4726A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56346658 | ||||||
| chr16:56346681
|
C | G | 186 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0050others(183): Show | 187 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.724-4703C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56346681 | ||||||
| chr16:56346814
|
G | C | 8 | a0001c0001t0001g0284a0001c0002t0001g0294a0001c0002t0003g0184others(5): Show | 8 | HG02257.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.724-4570G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56346814 | ||||||
| chr16:56347171
|
A | G | 61 | a0001c0001t0001g0199a0001c0001t0003g0008a0001c0001t0003g0009others(58): Show | 61 | HG00438.hp2 HG00642.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.724-4213A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56347171 | ||||||
| chr16:56347175
|
G | C | 4 | a0001c0002t0004g0021a0001c0002t0004g0053a0001c0002t0004g0143others(1): Show | 4 | HG02257.hp2 HG03540.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.724-4209G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56347175 | ||||||
| chr16:56347285
|
G | T | 134 | a0001c0001t0001g0050a0001c0001t0001g0077a0001c0001t0001g0078others(131): Show | 134 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.724-4099G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56347285 | ||||||
| chr16:56347353
|
G | A | 1 | a0001c0006t0021g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.724-4031G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56347353 | ||||||
| chr16:56347365
|
C | T | 74 | a0001c0001t0001g0050a0001c0001t0001g0077a0001c0001t0001g0078others(71): Show | 74 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.724-4019C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56347365 | ||||||
| chr16:56347400
|
G | A | 145 | a0001c0001t0001g0050a0001c0001t0001g0077a0001c0001t0001g0078others(142): Show | 145 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.724-3984G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56347400 | ||||||
| chr16:56347400
|
G | C | 1 | a0001c0001t0001g0167 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.724-3984G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56347400 | ||||||
| chr16:56347568
|
A | G | 1 | a0001c0002t0001g0204 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.724-3816A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56347568 | ||||||
| chr16:56347632
|
CT | C | 145 | a0001c0001t0001g0050a0001c0001t0001g0077a0001c0001t0001g0078others(142): Show | 145 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.724-3751delT | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56347632 | ||||||
| chr16:56347704
|
G | A | 4 | a0001c0001t0004g0291a0001c0001t0004g0296a0001c0002t0002g0029others(1): Show | 4 | HG01891.hp1 HG02145.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.724-3680G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56347704 | ||||||
| chr16:56347705
|
A | T | 4 | a0001c0001t0004g0291a0001c0001t0004g0296a0001c0002t0002g0029others(1): Show | 4 | HG01891.hp1 HG02145.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.724-3679A>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56347705 | ||||||
| chr16:56347721
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.724-3663A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56347721 | ||||||
| chr16:56347769
|
C | T | 7 | a0001c0001t0001g0079a0001c0001t0013g0187a0001c0002t0001g0055others(4): Show | 7 | HG02280.hp2 HG02559.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.724-3615C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56347769 | ||||||
| chr16:56347787
|
C | T | 159 | a0001c0001t0001g0050a0001c0001t0001g0077a0001c0001t0001g0078others(156): Show | 160 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.724-3597C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56347787 | ||||||
| chr16:56347955
|
C | A | 1 | a0001c0001t0003g0200 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.724-3429C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56347955 | ||||||
| chr16:56347978
|
G | A | 1 | a0001c0001t0009g0094 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.724-3406G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56347978 | ||||||
| chr16:56348015
|
G | A | 3 | a0001c0001t0011g0031a0001c0001t0011g0138a0001c0001t0020g0126 | 3 | HG00609.hp2 HG02132.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.724-3369G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56348015 | ||||||
| chr16:56348245
|
T | A | 3 | a0001c0002t0001g0054a0001c0002t0001g0064a0001c0002t0012g0181 | 3 | HG02451.hp2 HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.724-3139T>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56348245 | ||||||
| chr16:56348312
|
A | G | 4 | a0001c0002t0004g0021a0001c0002t0004g0053a0001c0002t0004g0143others(1): Show | 4 | HG02257.hp2 HG03540.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.724-3072A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56348312 | ||||||
| chr16:56348358
|
C | T | 1 | a0001c0002t0001g0056 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.724-3026C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56348358 | ||||||
| chr16:56348381
|
G | A | 3 | a0001c0002t0001g0054a0001c0002t0001g0064a0001c0002t0012g0181 | 3 | HG02451.hp2 HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.724-3003G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56348381 | ||||||
| chr16:56348555
|
G | T | 1 | a0001c0002t0027g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.724-2829G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56348555 | ||||||
| chr16:56348636
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.724-2748C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56348636 | ||||||
| chr16:56348733
|
G | T | 1 | a0001c0001t0004g0296 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.724-2651G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56348733 | ||||||
| chr16:56348734
|
G | GGGGGCTG others(11): Show |
21 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0051others(18): Show | 22 | HG00609.hp2 HG00673.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.724-2649_724-2632d others(20): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 56348734 | |||||
| chr16:56348916
|
C | T | 3 | a0001c0001t0001g0078a0001c0001t0001g0262a0001c0001t0001g0270 | 3 | HG01109.hp1 HG01928.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.724-2468C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56348916 | ||||||
| chr16:56349060
|
G | A | 4 | a0001c0002t0004g0021a0001c0002t0004g0053a0001c0002t0004g0143others(1): Show | 4 | HG02257.hp2 HG03540.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.724-2324G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56349060 | ||||||
| chr16:56349279
|
G | A | 4 | a0001c0001t0019g0090a0001c0002t0006g0154a0001c0002t0006g0243others(1): Show | 4 | NA19002.hp2 NA19060.hp2 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.724-2105G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56349279 | ||||||
| chr16:56349589
|
T | C | 1 | a0001c0001t0009g0060 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.724-1795T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56349589 | ||||||
| chr16:56349766
|
C | T | 32 | a0001c0001t0003g0009a0001c0001t0003g0030a0001c0001t0003g0052others(29): Show | 32 | HG00438.hp2 HG01346.hp2 HG01433.hp2 others(29): Show |
intron_variant | MODIFIER | c.724-1618C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56349766 | ||||||
| chr16:56349907
|
C | G | 3 | a0001c0002t0001g0259a0001c0002t0001g0288a0001c0002t0027g0146 | 3 | HG03225.hp1 HG06807.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.724-1477C>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56349907 | ||||||
| chr16:56349907
|
C | T | 1 | a0001c0001t0005g0048 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.724-1477C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56349907 | ||||||
| chr16:56350324
|
A | G | 4 | a0001c0002t0004g0021a0001c0002t0004g0053a0001c0002t0004g0143others(1): Show | 4 | HG02257.hp2 HG03540.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.724-1060A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56350324 | ||||||
| chr16:56350511
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.724-873C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56350511 | ||||||
| chr16:56350532
|
C | T | 2 | a0001c0001t0001g0098a0001c0001t0001g0242 | 2 | HG00323.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.724-852C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56350532 | ||||||
| chr16:56350541
|
C | T | 7 | a0001c0001t0010g0040a0001c0001t0010g0123a0001c0001t0011g0285others(4): Show | 7 | HG00423.hp1 HG02135.hp2 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.724-843C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56350541 | ||||||
| chr16:56350725
|
G | A | 6 | a0001c0001t0001g0182a0001c0001t0001g0295a0001c0001t0014g0034others(3): Show | 6 | HG02258.hp2 HG02622.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.724-659G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56350725 | ||||||
| chr16:56350775
|
G | T | 4 | a0001c0001t0003g0246a0001c0002t0003g0137a0001c0002t0003g0233others(1): Show | 4 | HG00642.hp1 HG00733.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.724-609G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56350775 | ||||||
| chr16:56350808
|
T | C | 170 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0050others(167): Show | 171 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.724-576T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56350808 | ||||||
| chr16:56350878
|
A | G | 2 | a0001c0002t0014g0033a0001c0002t0014g0058 | 2 | HG02258.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.724-506A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56350878 | ||||||
| chr16:56350909
|
ACACACAG others(5): Show |
A | 1 | a0001c0002t0002g0175 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.724-468_724-457del others(12): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 56350909 | |||||
| chr16:56350920
|
C | T | 1 | a0001c0001t0004g0047 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.724-464C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56350920 | ||||||
| chr16:56350994
|
C | T | 3 | a0001c0001t0013g0187a0001c0002t0013g0032a0001c0002t0013g0293 | 3 | HG02559.hp2 HG02809.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.724-390C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56350994 | ||||||
| chr16:56351019
|
G | A | 24 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0051others(21): Show | 25 | HG00609.hp2 HG00673.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.724-365G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 6/8 | chr16 | 56351019 | ||||||
| chr16:56351560
|
C | T | 1 | a0001c0001t0005g0201 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.877+23C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 7/8 | chr16 | 56351560 | ||||||
| chr16:56351660
|
A | T | 13 | a0001c0001t0001g0182a0001c0001t0001g0295a0001c0001t0010g0040others(10): Show | 13 | HG00423.hp1 HG02135.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.877+123A>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 7/8 | chr16 | 56351660 | ||||||
| chr16:56351729
|
C | T | 1 | a0001c0002t0004g0205 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.877+192C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 7/8 | chr16 | 56351729 | ||||||
| chr16:56352006
|
G | A | 1 | a0001c0002t0006g0154 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.877+469G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 7/8 | chr16 | 56352006 | ||||||
| chr16:56352137
|
G | A | 4 | a0001c0001t0001g0284a0001c0002t0001g0294a0001c0002t0003g0184others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.877+600G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 7/8 | chr16 | 56352137 | ||||||
| chr16:56352274
|
G | A | 2 | a0001c0002t0003g0136a0001c0002t0003g0257 | 2 | HG03834.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.877+737G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 7/8 | chr16 | 56352274 | ||||||
| chr16:56352329
|
T | C | 4 | a0001c0001t0001g0284a0001c0002t0001g0294a0001c0002t0003g0184others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.877+792T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 7/8 | chr16 | 56352329 | ||||||
| chr16:56352408
|
G | T | 68 | a0001c0001t0001g0050a0001c0001t0001g0077a0001c0001t0001g0078others(65): Show | 68 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.877+871G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 7/8 | chr16 | 56352408 | ||||||
| chr16:56352515
|
G | T | 5 | a0001c0001t0001g0079a0001c0002t0001g0055a0001c0002t0001g0117others(2): Show | 5 | HG02280.hp2 HG02717.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.877+978G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 7/8 | chr16 | 56352515 | ||||||
| chr16:56352701
|
G | A | 1 | a0001c0001t0016g0059 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.877+1164G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 7/8 | chr16 | 56352701 | ||||||
| chr16:56352704
|
T | G | 1 | a0001c0002t0001g0013 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.877+1167T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 7/8 | chr16 | 56352704 | ||||||
| chr16:56352748
|
G | C | 7 | a0001c0001t0010g0040a0001c0001t0010g0123a0001c0001t0011g0285others(4): Show | 7 | HG00423.hp1 HG02135.hp2 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.877+1211G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 7/8 | chr16 | 56352748 | ||||||
| chr16:56352771
|
T | C | 1 | a0001c0002t0002g0118 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.877+1234T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 7/8 | chr16 | 56352771 | ||||||
| chr16:56353078
|
G | A | 1 | a0001c0001t0006g0080 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.877+1541G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 7/8 | chr16 | 56353078 | ||||||
| chr16:56353088
|
C | T | 72 | a0001c0001t0001g0050a0001c0001t0001g0077a0001c0001t0001g0078others(69): Show | 72 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.877+1551C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 7/8 | chr16 | 56353088 | ||||||
| chr16:56353125
|
A | G | 72 | a0001c0001t0001g0050a0001c0001t0001g0077a0001c0001t0001g0078others(69): Show | 72 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.877+1588A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 7/8 | chr16 | 56353125 | ||||||
| chr16:56353167
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.877+1630C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 7/8 | chr16 | 56353167 | ||||||
| chr16:56353376
|
T | C | 111 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0050others(108): Show | 112 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.878-1490T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 7/8 | chr16 | 56353376 | ||||||
| chr16:56353467
|
C | T | 24 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0051others(21): Show | 25 | HG00609.hp2 HG00673.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.878-1399C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 7/8 | chr16 | 56353467 | ||||||
| chr16:56353557
|
A | G | 218 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0050others(215): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.878-1309A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 7/8 | chr16 | 56353557 | ||||||
| chr16:56353610
|
G | A | 1 | a0001c0001t0024g0068 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.878-1256G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 7/8 | chr16 | 56353610 | ||||||
| chr16:56353640
|
G | A | 4 | a0001c0001t0001g0284a0001c0002t0001g0294a0001c0002t0003g0184others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.878-1226G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 7/8 | chr16 | 56353640 | ||||||
| chr16:56353652
|
C | T | 7 | a0001c0001t0010g0040a0001c0001t0010g0123a0001c0001t0011g0285others(4): Show | 7 | HG00423.hp1 HG02135.hp2 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.878-1214C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 7/8 | chr16 | 56353652 | ||||||
| chr16:56353722
|
G | A | 2 | a0001c0002t0004g0067a0001c0002t0004g0277 | 2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.878-1144G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 7/8 | chr16 | 56353722 | ||||||
| chr16:56353893
|
C | T | 1 | a0001c0001t0004g0241 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.878-973C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 7/8 | chr16 | 56353893 | ||||||
| chr16:56353918
|
G | A | 3 | a0001c0001t0013g0187a0001c0002t0013g0032a0001c0002t0013g0293 | 3 | HG02559.hp2 HG02809.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.878-948G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 7/8 | chr16 | 56353918 | ||||||
| chr16:56354123
|
G | A | 1 | a0001c0002t0015g0128 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.878-743G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 7/8 | chr16 | 56354123 | ||||||
| chr16:56354132
|
C | T | 57 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0030others(54): Show | 57 | HG00438.hp2 HG00642.hp1 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.878-734C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 7/8 | chr16 | 56354132 | ||||||
| chr16:56354194
|
G | A | 2 | a0001c0002t0004g0063a0001c0006t0021g0019 | 2 | HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.878-672G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 7/8 | chr16 | 56354194 | ||||||
| chr16:56354319
|
A | T | 6 | a0001c0001t0010g0040a0001c0001t0010g0123a0001c0001t0024g0068others(3): Show | 6 | HG00423.hp1 HG02135.hp2 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.878-547A>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 7/8 | chr16 | 56354319 | ||||||
| chr16:56354349
|
AAGTAATT others(2): Show |
A | 107 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0050others(104): Show | 108 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.878-504_878-496del others(9): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr16 | 56354349 | |||||
| chr16:56354484
|
T | G | 21 | a0001c0001t0001g0163a0001c0001t0006g0069a0001c0001t0006g0226others(18): Show | 21 | HG00639.hp2 HG01074.hp2 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.878-382T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 7/8 | chr16 | 56354484 | ||||||
| chr16:56354504
|
C | T | 3 | a0001c0001t0013g0187a0001c0002t0013g0032a0001c0002t0013g0293 | 3 | HG02559.hp2 HG02809.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.878-362C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 7/8 | chr16 | 56354504 | ||||||
| chr16:56354546
|
C | T | 1 | a0001c0002t0001g0054 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.878-320C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 7/8 | chr16 | 56354546 | ||||||
| chr16:56354569
|
A | G | 218 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0050others(215): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.878-297A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 7/8 | chr16 | 56354569 | ||||||
| chr16:56354799
|
G | A | 4 | a0001c0001t0006g0069a0001c0002t0006g0133a0001c0002t0006g0134others(1): Show | 4 | HG02080.hp2 HG02293.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.878-67G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 7/8 | chr16 | 56354799 | ||||||
| chr16:56355074
|
C | CCTATTTG others(5): Show |
1 | a0001c0001t0026g0003 | 1 | NA18994.hp2 | splice_region_variant&intron_variant | LOW | c.*22_*28+5dupCTATTT others(6): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 56355074 | |||||
| chr16:56355125
|
T | TAC | 45 | a0001c0001t0001g0174a0001c0001t0001g0258a0001c0001t0002g0254others(42): Show | 45 | HG00609.hp1 HG00642.hp1 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.*28+73_*28+74dupAC | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 56355125 | |||||
| chr16:56355125
|
T | TACAC | 10 | a0001c0001t0003g0030a0001c0001t0003g0052a0001c0001t0003g0085others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.*28+71_*28+74dupAC others(2): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 56355125 | |||||
| chr16:56355125
|
T | TACACACA others(1): Show |
5 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0017g0290others(2): Show | 5 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.*28+67_*28+74dupAC others(6): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 56355125 | |||||
| chr16:56355125
|
T | TACACACA others(3): Show |
20 | a0001c0001t0001g0014a0001c0001t0001g0057a0001c0001t0001g0182others(17): Show | 20 | HG00609.hp2 HG00673.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.*28+65_*28+74dupAC others(8): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 56355125 | |||||
| chr16:56355125
|
T | TACACACA others(5): Show |
6 | a0001c0001t0001g0295a0001c0001t0004g0217a0001c0001t0011g0285others(3): Show | 6 | HG02622.hp2 HG03130.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.*28+63_*28+74dupAC others(10): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 56355125 | |||||
| chr16:56355125
|
T | TACACACA others(7): Show |
1 | a0001c0001t0010g0123 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.*28+61_*28+74dupAC others(12): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 56355125 | |||||
| chr16:56355125
|
T | TACACACA others(9): Show |
1 | a0001c0002t0025g0129 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.*28+59_*28+74dupAC others(14): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 56355125 | |||||
| chr16:56355125
|
T | TACACACA others(11): Show |
6 | a0001c0001t0004g0002a0001c0001t0004g0287a0001c0001t0010g0040others(3): Show | 7 | HG02135.hp2 HG03491.hp2 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.*28+57_*28+74dupAC others(16): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 56355125 | |||||
| chr16:56355125
|
TAC | T | 58 | a0001c0001t0001g0050a0001c0001t0001g0077a0001c0001t0001g0078others(55): Show | 58 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.*28+73_*28+74delAC | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 56355125 | |||||
| chr16:56355155
|
C | CACACACA others(4): Show |
1 | a0001c0002t0004g0267 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.*28+74_*28+75insAC others(9): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 8/8 | chr16 | 56355155 | ||||||
| chr16:56355184
|
C | T | 1 | a0001c0001t0003g0200 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.*28+103C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 8/8 | chr16 | 56355184 | ||||||
| chr16:56355207
|
T | TTA | 127 | a0001c0001t0001g0050a0001c0001t0001g0077a0001c0001t0001g0078others(124): Show | 127 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.*28+145_*28+146dup others(2): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 56355207 | |||||
| chr16:56355207
|
T | TTATA | 8 | a0001c0001t0005g0186a0001c0001t0005g0256a0001c0001t0005g0272others(5): Show | 8 | HG00639.hp2 HG01975.hp1 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.*28+143_*28+146dup others(4): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 56355207 | |||||
| chr16:56355207
|
T | TTATATAT others(1): Show |
10 | a0001c0001t0005g0048a0001c0001t0005g0201a0001c0001t0005g0206others(7): Show | 10 | HG01346.hp2 HG01433.hp2 NA18945.hp2 others(7): Show |
intron_variant | MODIFIER | c.*28+139_*28+146dup others(8): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 56355207 | |||||
| chr16:56355340
|
CGTGT | C | 7 | a0001c0001t0010g0040a0001c0001t0010g0123a0001c0001t0011g0285others(4): Show | 7 | HG00423.hp1 HG02135.hp2 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.*28+268_*28+271del others(4): Show |
GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | 56355340 | |||||
| chr16:56355501
|
C | T | 1 | a0001c0001t0007g0113 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.*28+420C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 8/8 | chr16 | 56355501 | ||||||
| chr16:56355579
|
T | C | 6 | a0001c0001t0001g0182a0001c0001t0001g0295a0001c0001t0014g0034others(3): Show | 6 | HG02258.hp2 HG02622.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.*28+498T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 8/8 | chr16 | 56355579 | ||||||
| chr16:56355679
|
T | C | 1 | a0001c0001t0001g0258 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.*29-424T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 8/8 | chr16 | 56355679 | ||||||
| chr16:56355778
|
T | C | 58 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0017others(55): Show | 58 | HG00438.hp2 HG00642.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.*29-325T>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 8/8 | chr16 | 56355778 | ||||||
| chr16:56355877
|
G | A | 4 | a0001c0001t0001g0284a0001c0002t0001g0294a0001c0002t0003g0184others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.*29-226G>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 8/8 | chr16 | 56355877 | ||||||
| chr16:56355883
|
C | T | 1 | a0001c0001t0017g0244 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.*29-220C>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 8/8 | chr16 | 56355883 | ||||||
| chr16:56355915
|
CA | C | 90 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0051others(87): Show | 91 | HG00438.hp2 HG00609.hp2 HG00642.hp1 others(88): Show |
intron_variant | MODIFIER | c.*29-187delA | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 8/8 | chr16 | 56355915 | ||||||
| chr16:56355916
|
A | G | 2 | a0001c0001t0003g0052a0001c0002t0014g0033 | 2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.*29-187A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 8/8 | chr16 | 56355916 | ||||||
| chr16:56355918
|
G | C | 1 | a0001c0002t0002g0214 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.*29-185G>C | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 8/8 | chr16 | 56355918 | ||||||
| chr16:56355919
|
G | T | 1 | a0001c0001t0005g0201 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.*29-184G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 8/8 | chr16 | 56355919 | ||||||
| chr16:56355958
|
A | G | 1 | a0001c0002t0002g0194 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.*29-145A>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 8/8 | chr16 | 56355958 | ||||||
| chr16:56355963
|
G | T | 1 | a0001c0002t0004g0205 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.*29-140G>T | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 8/8 | chr16 | 56355963 | ||||||
| chr16:56356053
|
T | G | 1 | a0001c0001t0017g0290 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.*29-50T>G | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 8/8 | chr16 | 56356053 | ||||||
| chr16:56356081
|
C | A | 1 | a0001c0001t0026g0003 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.*29-22C>A | GNAO1 | ENSG00000087258.16 | transcript | ENST00000262493.12 | protein_coding | 8/8 | chr16 | 56356081 |