Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 2778 |
|---|---|
| ensemblid | ENSG00000087460.29 |
| hgncid | 4392 |
| symbol | GNAS |
| name | GNAS complex locus |
| refseq_nuc | NM_080425.4 |
| refseq_prot | NP_536350.2 |
| ensembl_nuc | ENST00000371100.9 |
| ensembl_prot | ENSP00000360141.3 |
| mane_status | MANE Plus Clinical |
| chr | chr20 |
| start | 58852716 |
| end | 58911192 |
| strand | + |
| ver | v1.2 |
| region | chr20:58852716-58911192 |
| region5000 | chr20:58847716-58916192 |
| regionname0 | GNAS_chr20_58852716_58911192 |
| regionname5000 | GNAS_chr20_58847716_58916192 |
| 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 | 1037 | 250 | 61 | 54 | 94 | 14 | 25 | 71 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0002 | 0/0 | 1049 | 32 | 23 | 6 | 2 | 0 | 1 | 1 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0003 | 0/0 | 1037 | 8 | 1 | 6 | 0 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0004 | 0/0 | 1040 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0005 | 0/0 | 1049 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0006 | 0/0 | 1037 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0007 | 0/0 | 1028 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0008 | 0/0 | 1037 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0009 | 0/0 | 1037 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| 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 | 3114 | 118 | 25 | 33 | 42 | 7 | 11 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| c0002 | 1/1 | 3114 | 100 | 9 | 18 | 52 | 6 | 13 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| c0003 | 0/0 | 3150 | 17 | 11 | 3 | 2 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| c0004 | 0/0 | 3114 | 13 | 12 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| c0005 | 0/0 | 3114 | 6 | 1 | 4 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| c0006 | 0/0 | 3114 | 5 | 5 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| c0007 | 0/0 | 3150 | 4 | 2 | 2 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| c0008 | 0/0 | 3114 | 4 | 1 | 2 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| c0009 | 0/0 | 3150 | 3 | 2 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| c0010 | 0/0 | 3150 | 3 | 3 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| c0011 | 0/0 | 3150 | 3 | 3 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| c0012 | 0/0 | 3150 | 2 | 2 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| c0013 | 0/0 | 3114 | 2 | 2 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| c0014 | 0/0 | 3114 | 2 | 2 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| c0015 | 0/0 | 3123 | 2 | 2 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| c0016 | 0/0 | 3114 | 2 | 0 | 2 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| c0017 | 0/0 | 3114 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| c0018 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| c0019 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| c0020 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| c0021 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| c0022 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| c0023 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| c0024 | 0/0 | 3114 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| c0025 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| c0026 | 0/0 | 3087 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| c0027 | 0/0 | 3123 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| c0028 | 0/0 | 3123 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| c0029 | 0/0 | 3114 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| c0030 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| c0031 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| c0032 | 0/0 | 3114 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| 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 | 1/1 | 914 | 238 | 62 | 58 | 75 | 14 | 27 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| t0002 | 0/0 | 914 | 36 | 27 | 6 | 2 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| t0003 | 0/0 | 914 | 21 | 0 | 0 | 21 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| t0004 | 0/0 | 914 | 4 | 4 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| t0005 | 0/0 | 914 | 2 | 0 | 2 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| t0006 | 0/0 | 914 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| 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 | 3 | 0 | 0 | 3 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0005 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0006 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0140 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| 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 | 3114 | 118 | 25 | 33 | 42 | 7 | 11 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0001c0002 | 1/1 | 3114 | 100 | 9 | 18 | 52 | 6 | 13 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0001c0004 | 0/0 | 3114 | 13 | 12 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0001c0006 | 0/0 | 3114 | 5 | 5 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0001c0008 | 0/0 | 3114 | 4 | 1 | 2 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0001c0013 | 0/0 | 3114 | 2 | 2 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0001c0014 | 0/0 | 3114 | 2 | 2 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0001c0020 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0001c0022 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0001c0023 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0001c0025 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0001c0029 | 0/0 | 3114 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0001c0030 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0002c0003 | 0/0 | 3150 | 17 | 11 | 3 | 2 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0002c0007 | 0/0 | 3150 | 4 | 2 | 2 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0002c0009 | 0/0 | 3150 | 3 | 2 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0002c0010 | 0/0 | 3150 | 3 | 3 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0002c0012 | 0/0 | 3150 | 2 | 2 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0002c0018 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0002c0019 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0002c0021 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0003c0005 | 0/0 | 3114 | 6 | 1 | 4 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0003c0016 | 0/0 | 3114 | 2 | 0 | 2 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0004c0015 | 0/0 | 3123 | 2 | 2 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0004c0027 | 0/0 | 3123 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0004c0028 | 0/0 | 3123 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0005c0011 | 0/0 | 3150 | 3 | 3 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0005c0031 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0006c0032 | 0/0 | 3114 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0007c0026 | 0/0 | 3087 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0008c0024 | 0/0 | 3114 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0009c0017 | 0/0 | 3114 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4027 | 107 | 23 | 31 | 35 | 7 | 11 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0001c0001t0003 | 0/0 | 4027 | 7 | 0 | 0 | 7 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0001c0001t0004 | 0/0 | 4027 | 2 | 2 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0001c0001t0005 | 0/0 | 4027 | 2 | 0 | 2 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0001c0002t0001 | 1/1 | 4027 | 87 | 9 | 18 | 39 | 6 | 13 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0001c0002t0003 | 0/0 | 4027 | 13 | 0 | 0 | 13 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0001c0004t0001 | 0/0 | 4027 | 12 | 11 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0001c0004t0004 | 0/0 | 4027 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0001c0006t0001 | 0/0 | 4027 | 5 | 5 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0001c0008t0001 | 0/0 | 4027 | 4 | 1 | 2 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0001c0013t0001 | 0/0 | 4027 | 2 | 2 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0001c0014t0001 | 0/0 | 4027 | 2 | 2 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0001c0020t0001 | 0/0 | 4027 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0001c0022t0004 | 0/0 | 4027 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0001c0023t0001 | 0/0 | 4027 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0001c0025t0001 | 0/0 | 4027 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0001c0029t0001 | 0/0 | 4027 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0001c0030t0001 | 0/0 | 4027 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0002c0003t0002 | 0/0 | 4063 | 17 | 11 | 3 | 2 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0002c0007t0002 | 0/0 | 4063 | 4 | 2 | 2 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0002c0009t0002 | 0/0 | 4063 | 3 | 2 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0002c0010t0002 | 0/0 | 4063 | 3 | 3 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0002c0012t0002 | 0/0 | 4063 | 2 | 2 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0002c0018t0002 | 0/0 | 4063 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0002c0019t0002 | 0/0 | 4063 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0002c0021t0002 | 0/0 | 4063 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0003c0005t0001 | 0/0 | 4027 | 6 | 1 | 4 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0003c0016t0001 | 0/0 | 4027 | 2 | 0 | 2 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0004c0015t0001 | 0/0 | 4036 | 2 | 2 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0004c0027t0001 | 0/0 | 4036 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0004c0028t0001 | 0/0 | 4036 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0005c0011t0002 | 0/0 | 4063 | 3 | 3 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0005c0031t0002 | 0/0 | 4063 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0006c0032t0003 | 0/0 | 4027 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0007c0026t0006 | 0/0 | 4000 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0008c0024t0001 | 0/0 | 4027 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| a0009c0017t0001 | 0/0 | 4027 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | copy fasta | chr20 | 58847716 | 58916192 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0004g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0005g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0005g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0005 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0006 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0140 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0004t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0004t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0004t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0004t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0004t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0004t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0004t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0004t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0004t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0004t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0004t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0006t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0006t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0006t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0006t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0006t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0008t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0008t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0008t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0008t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0013t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0013t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0014t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0014t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0020t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0022t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0023t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0025t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0029t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0030t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0003t0002g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0003t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0003t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0003t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0003t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0003t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0003t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0003t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0003t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0003t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0003t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0003t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0003t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0003t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0003t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0003t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0007t0002g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0007t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0007t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0009t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0009t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0009t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0010t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0010t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0010t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0012t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0012t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0018t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0019t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0021t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0003c0005t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0003c0005t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0003c0005t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0003c0005t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0003c0005t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0003c0016t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0003c0016t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0004c0015t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0004c0015t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0004c0027t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0004c0028t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0005c0011t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0005c0011t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0005c0011t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0005c0031t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0006c0032t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0007c0026t0006g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0008c0024t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0009c0017t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0213 | EUR | GBR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0058 | EUR | GBR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0114 | EUR | GBR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0236 | EUR | GBR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0061 | EUR | FIN | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0014 | EUR | FIN | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | CHS | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | CHS | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG00558 | hp1 | a0001 | c0002 | t0003 | g0032 | EAS | CHS | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0150 | EAS | CHS | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0099 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG00639 | hp2 | a0001 | c0008 | t0001 | g0129 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0171 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0107 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG00735 | hp1 | a0003 | c0005 | t0001 | g0226 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG00738 | hp1 | a0003 | c0016 | t0001 | g0229 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG00738 | hp2 | a0002 | c0007 | t0002 | g0251 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0246 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01070 | hp1 | a0001 | c0008 | t0001 | g0073 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01070 | hp2 | a0003 | c0005 | t0001 | g0018 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01071 | hp2 | a0003 | c0005 | t0001 | g0018 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01081 | hp1 | a0001 | c0001 | t0005 | g0098 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0014 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01106 | hp1 | a0002 | c0003 | t0002 | g0258 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01243 | hp1 | a0001 | c0004 | t0001 | g0216 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0103 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0126 | AMR | CLM | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0074 | AMR | CLM | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01256 | hp1 | a0002 | c0003 | t0002 | g0259 | AMR | CLM | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01256 | hp2 | a0003 | c0016 | t0001 | g0230 | AMR | CLM | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0101 | AMR | CLM | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01258 | hp2 | a0002 | c0003 | t0002 | g0260 | AMR | CLM | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01261 | hp2 | a0001 | c0001 | t0005 | g0097 | AMR | CLM | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0247 | AMR | CLM | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01496 | hp1 | a0003 | c0005 | t0001 | g0228 | AMR | CLM | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0172 | EUR | IBS | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0195 | EUR | IBS | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0041 | EUR | IBS | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0173 | EUR | IBS | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01884 | hp1 | a0001 | c0004 | t0001 | g0203 | AFR | ACB | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01884 | hp2 | a0004 | c0027 | t0001 | g0185 | AFR | ACB | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01891 | hp1 | a0002 | c0007 | t0002 | g0019 | AFR | ACB | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01943 | hp1 | a0002 | c0007 | t0002 | g0254 | AMR | PEL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0102 | AMR | PEL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0244 | AMR | PEL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0205 | AMR | PEL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0108 | AMR | PEL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02027 | hp1 | a0009 | c0017 | t0001 | g0105 | EAS | KHV | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | KHV | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02055 | hp1 | a0007 | c0026 | t0006 | g0232 | AFR | ACB | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | KHV | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | KHV | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02083 | hp1 | a0006 | c0032 | t0003 | g0049 | EAS | KHV | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02135 | hp2 | a0002 | c0003 | t0002 | g0264 | EAS | KHV | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02145 | hp1 | a0002 | c0012 | t0002 | g0269 | AFR | ACB | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02148 | hp1 | a0002 | c0009 | t0002 | g0274 | AMR | PEL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | CDX | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CDX | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | CDX | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | CDX | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02258 | hp1 | a0002 | c0012 | t0002 | g0270 | AFR | ACB | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02258 | hp2 | a0002 | c0018 | t0002 | g0261 | AFR | ACB | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0122 | AMR | PEL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02451 | hp2 | a0001 | c0020 | t0001 | g0208 | AFR | ACB | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0137 | EAS | KHV | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0115 | EAS | KHV | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0223 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02615 | hp1 | a0001 | c0014 | t0001 | g0218 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02615 | hp2 | a0002 | c0003 | t0002 | g0275 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02622 | hp2 | a0001 | c0014 | t0001 | g0280 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02630 | hp2 | a0005 | c0031 | t0002 | g0265 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02647 | hp1 | a0004 | c0028 | t0001 | g0188 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0199 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02717 | hp2 | a0001 | c0004 | t0001 | g0015 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02723 | hp1 | a0001 | c0006 | t0001 | g0180 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0117 | SAS | PJL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02735 | hp2 | a0003 | c0005 | t0001 | g0227 | SAS | PJL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02738 | hp1 | a0001 | c0029 | t0001 | g0106 | SAS | PJL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0059 | SAS | PJL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02809 | hp1 | a0004 | c0015 | t0001 | g0186 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02809 | hp2 | a0002 | c0003 | t0002 | g0277 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0235 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02895 | hp2 | a0002 | c0003 | t0002 | g0248 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02896 | hp1 | a0002 | c0007 | t0002 | g0019 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02896 | hp2 | a0002 | c0003 | t0002 | g0020 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02897 | hp1 | a0002 | c0003 | t0002 | g0020 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02922 | hp1 | a0002 | c0003 | t0002 | g0263 | AFR | ESN | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02965 | hp1 | a0001 | c0006 | t0001 | g0207 | AFR | ESN | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02965 | hp2 | a0001 | c0004 | t0001 | g0046 | AFR | ESN | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02970 | hp1 | a0002 | c0010 | t0002 | g0279 | AFR | ESN | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02970 | hp2 | a0005 | c0011 | t0002 | g0268 | AFR | ESN | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02976 | hp1 | a0002 | c0019 | t0002 | g0262 | AFR | ESN | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02976 | hp2 | a0003 | c0005 | t0001 | g0231 | AFR | ESN | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03041 | hp1 | a0002 | c0003 | t0002 | g0249 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03041 | hp2 | a0002 | c0009 | t0002 | g0278 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | MSL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03098 | hp2 | a0001 | c0004 | t0001 | g0016 | AFR | MSL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03130 | hp1 | a0001 | c0004 | t0001 | g0015 | AFR | ESN | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0045 | AFR | ESN | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03139 | hp1 | a0002 | c0003 | t0002 | g0276 | AFR | ESN | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03139 | hp2 | a0001 | c0004 | t0001 | g0017 | AFR | ESN | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03195 | hp1 | a0001 | c0004 | t0001 | g0209 | AFR | ESN | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03195 | hp2 | a0001 | c0004 | t0001 | g0017 | AFR | ESN | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | MSL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03225 | hp1 | a0001 | c0030 | t0001 | g0220 | AFR | MSL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03225 | hp2 | a0002 | c0003 | t0002 | g0253 | AFR | MSL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0245 | SAS | PJL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03453 | hp1 | a0001 | c0023 | t0001 | g0233 | AFR | MSL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03453 | hp2 | a0002 | c0010 | t0002 | g0272 | AFR | MSL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03486 | hp2 | a0001 | c0025 | t0001 | g0037 | AFR | MSL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0062 | SAS | PJL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0043 | SAS | PJL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0138 | SAS | PJL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03516 | hp1 | a0002 | c0003 | t0002 | g0252 | AFR | ESN | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0044 | AFR | ESN | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03579 | hp1 | a0002 | c0003 | t0002 | g0257 | AFR | MSL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03579 | hp2 | a0001 | c0013 | t0001 | g0193 | AFR | MSL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0085 | SAS | PJL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0006 | SAS | PJL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0160 | SAS | PJL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0064 | SAS | BEB | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | BEB | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | BEB | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03834 | hp2 | a0008 | c0024 | t0001 | g0198 | SAS | BEB | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | STU | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0154 | SAS | STU | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | BEB | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0091 | SAS | BEB | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0194 | SAS | STU | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG04204 | hp2 | a0002 | c0003 | t0002 | g0256 | SAS | STU | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18522 | hp1 | a0005 | c0011 | t0002 | g0267 | AFR | YRI | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18522 | hp2 | a0001 | c0006 | t0001 | g0206 | AFR | YRI | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | CHB | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18747 | hp2 | a0001 | c0002 | t0003 | g0055 | EAS | CHB | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18906 | hp1 | a0002 | c0010 | t0002 | g0250 | AFR | YRI | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18906 | hp2 | a0002 | c0021 | t0002 | g0271 | AFR | YRI | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18944 | hp1 | a0001 | c0002 | t0003 | g0011 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18945 | hp1 | a0001 | c0002 | t0003 | g0011 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18947 | hp1 | a0001 | c0002 | t0003 | g0034 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18950 | hp1 | a0001 | c0002 | t0003 | g0056 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18965 | hp2 | a0001 | c0002 | t0003 | g0025 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18968 | hp1 | a0001 | c0002 | t0003 | g0052 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18973 | hp2 | a0001 | c0002 | t0003 | g0033 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18979 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18984 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18995 | hp1 | a0001 | c0002 | t0003 | g0051 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19030 | hp1 | a0001 | c0004 | t0001 | g0234 | AFR | LWK | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | LWK | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0127 | AFR | LWK | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19043 | hp2 | a0001 | c0008 | t0001 | g0016 | AFR | LWK | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19090 | hp1 | a0002 | c0003 | t0002 | g0255 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19240 | hp1 | a0001 | c0006 | t0001 | g0200 | AFR | YRI | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0242 | AFR | YRI | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA20129 | hp1 | a0001 | c0004 | t0004 | g0189 | AFR | ASW | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0243 | AFR | ASW | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0182 | EUR | TSI | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0144 | EUR | TSI | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA20805 | hp1 | a0001 | c0008 | t0001 | g0060 | EUR | TSI | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0153 | EUR | TSI | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | GIH | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | GIH | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0104 | AMR | CLM | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02486 | hp1 | a0004 | c0015 | t0001 | g0187 | AFR | ACB | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02486 | hp2 | a0001 | c0004 | t0001 | g0201 | AFR | ACB | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02559 | hp2 | a0001 | c0006 | t0001 | g0222 | AFR | ACB | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03471 | hp1 | a0002 | c0009 | t0002 | g0273 | AFR | MSL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03471 | hp2 | a0001 | c0004 | t0001 | g0202 | AFR | MSL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG06807 | hp1 | a0005 | c0011 | t0002 | g0266 | AFR | USA | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG06807 | hp2 | a0001 | c0013 | t0001 | g0176 | AFR | USA | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18955 | hp1 | a0001 | c0002 | t0003 | g0135 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA20300 | hp1 | a0001 | c0022 | t0004 | g0197 | AFR | USA | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0070 | AFR | USA | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | LWK | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | LWK | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0005 | REF | REF | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0140 | REF | REF | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:58853551
|
C | G | 1 | a0006 | 1 | HG02083.hp1 | missense_variant | MODERATE | c.286C>G | p.Pro96Ala | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/13 | 836/4027 | 286/3114 | 96/1037 | chr20 | 58853551 | ||
| chr20:58853578
|
G | A | 1 | a0009 | 1 | HG02027.hp1 | missense_variant | MODERATE | c.313G>A | p.Glu105Lys | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/13 | 863/4027 | 313/3114 | 105/1037 | chr20 | 58853578 | ||
| chr20:58853765
|
A | G | 1 | a0005 | 4 | HG02630.hp2 HG02970.hp2 HG06807.hp1 others(1): Show |
missense_variant | MODERATE | c.500A>G | p.Asp167Gly | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/13 | 1050/4027 | 500/3114 | 167/1037 | chr20 | 58853765 | ||
| chr20:58854392
|
C | T | 1 | a0003 | 8 | HG00735.hp1 HG00738.hp1 HG01070.hp2 others(5): Show |
missense_variant | MODERATE | c.1127C>T | p.Pro376Leu | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/13 | 1677/4027 | 1127/3114 | 376/1037 | chr20 | 58854392 | ||
| chr20:58854444
|
G | GGCAGCCC others(2): Show |
1 | a0004 | 4 | HG01884.hp2 HG02486.hp1 HG02647.hp1 others(1): Show |
disruptive_inframe_insertion | MODERATE | c.1188_1196dupTGCAGC others(3): Show |
p.Pro399_Ala400insAl others(7): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/13 | 1747/4027 | 1197/3114 | 399/1037 | INFO_REALIGN_3_PRIME | chr20 | 58854444 | |
| chr20:58854492
|
AGATCCCG others(20): Show |
A | 1 | a0007 | 1 | HG02055.hp1 | disruptive_inframe_deletion | MODERATE | c.1233_1259delCGACTC others(21): Show |
p.Asp412_Pro420del | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/13 | 1783/4027 | 1233/3114 | 411/1037 | INFO_REALIGN_3_PRIME | chr20 | 58854492 | |
| chr20:58854572
|
C | A | 2 | a0002a0005 | 36 | HG00738.hp2 HG01106.hp1 HG01256.hp1 others(33): Show |
missense_variant | MODERATE | c.1307C>A | p.Ala436Asp | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/13 | 1857/4027 | 1307/3114 | 436/1037 | chr20 | 58854572 | ||
| chr20:58854641
|
C | CTGACGCC others(29): Show |
2 | a0002a0005 | 36 | HG00738.hp2 HG01106.hp1 HG01256.hp1 others(33): Show |
disruptive_inframe_insertion | MODERATE | c.1394_1395insCGACTC others(30): Show |
p.Pro465_Asp466insAs others(34): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/13 | 1945/4027 | 1395/3114 | 465/1037 | INFO_REALIGN_3_PRIME | chr20 | 58854641 | |
| chr20:58855063
|
C | G | 1 | a0008 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.1798C>G | p.Arg600Gly | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/13 | 2348/4027 | 1798/3114 | 600/1037 | chr20 | 58855063 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:58853790
|
T | C | 2 | a0002c0018a0002c0019 | 2 | HG02258.hp2 HG02976.hp1 |
synonymous_variant | LOW | c.525T>C | p.Ser175Ser | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/13 | 1075/4027 | 525/3114 | 175/1037 | chr20 | 58853790 | ||
| chr20:58853892
|
G | A | 2 | a0001c0006a0001c0020 | 6 | HG02451.hp2 HG02559.hp2 HG02723.hp1 others(3): Show |
synonymous_variant | LOW | c.627G>A | p.Lys209Lys | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/13 | 1177/4027 | 627/3114 | 209/1037 | chr20 | 58853892 | ||
| chr20:58853988
|
G | T | 1 | a0001c0030 | 1 | HG03225.hp1 | synonymous_variant | LOW | c.723G>T | p.Gly241Gly | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/13 | 1273/4027 | 723/3114 | 241/1037 | chr20 | 58853988 | ||
| chr20:58854255
|
C | T | 1 | a0001c0029 | 1 | HG02738.hp1 | synonymous_variant | LOW | c.990C>T | p.Ile330Ile | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/13 | 1540/4027 | 990/3114 | 330/1037 | chr20 | 58854255 | ||
| chr20:58854486
|
C | G | 1 | a0007c0026 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.1221C>G | p.Thr407Thr | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/13 | 1771/4027 | 1221/3114 | 407/1037 | chr20 | 58854486 | ||
| chr20:58854687
|
C | T | 1 | a0001c0025 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.1422C>T | p.Pro474Pro | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/13 | 1972/4027 | 1422/3114 | 474/1037 | chr20 | 58854687 | ||
| chr20:58903725
|
C | T | 2 | a0001c0023a0002c0021 | 2 | HG03453.hp1 NA18906.hp2 |
synonymous_variant | LOW | c.2295C>T | p.Pro765Pro | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 5/13 | 2845/4027 | 2295/3114 | 765/1037 | chr20 | 58903725 | ||
| chr20:58903743
|
G | A | 2 | a0001c0023a0002c0021 | 2 | HG03453.hp1 NA18906.hp2 |
synonymous_variant | LOW | c.2313G>A | p.Val771Val | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 5/13 | 2863/4027 | 2313/3114 | 771/1037 | chr20 | 58903743 | ||
| chr20:58903752
|
C | T | 19 | a0001c0001a0001c0004a0001c0006others(16): Show | 181 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(178): Show |
synonymous_variant | LOW | c.2322C>T | p.Ile774Ile | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 5/13 | 2872/4027 | 2322/3114 | 774/1037 | chr20 | 58903752 | ||
| chr20:58903791
|
C | T | 4 | a0001c0014a0001c0030a0002c0012others(1): Show | 7 | HG02145.hp1 HG02258.hp1 HG02486.hp1 others(4): Show |
splice_region_variant&synonymous_variant | LOW | c.2361C>T | p.Pro787Pro | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 5/13 | 2911/4027 | 2361/3114 | 787/1037 | chr20 | 58903791 | ||
| chr20:58909186
|
C | T | 14 | a0001c0004a0001c0008a0001c0013others(11): Show | 37 | HG00639.hp2 HG01070.hp1 HG01243.hp1 others(34): Show |
synonymous_variant | LOW | c.2484C>T | p.Ile828Ile | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 7/13 | 3034/4027 | 2484/3114 | 828/1037 | chr20 | 58909186 | ||
| chr20:58910062
|
C | T | 2 | a0001c0013a0002c0019 | 3 | HG02976.hp1 HG03579.hp2 HG06807.hp2 |
synonymous_variant | LOW | c.2880C>T | p.Arg960Arg | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 11/13 | 3430/4027 | 2880/3114 | 960/1037 | chr20 | 58910062 | ||
| chr20:58910757
|
C | T | 6 | a0001c0004a0001c0008a0001c0020others(3): Show | 25 | HG00639.hp2 HG01070.hp1 HG01243.hp1 others(22): Show |
synonymous_variant | LOW | c.3042C>T | p.Asn1014Asn | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 13/13 | 3592/4027 | 3042/3114 | 1014/1037 | chr20 | 58910757 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:58852896
|
C | A | 1 | a0001c0001t0005 | 2 | HG01081.hp1 HG01261.hp2 |
5_prime_UTR_variant | MODIFIER | c.-370C>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/13 | 370 | chr20 | 58852896 | |||||
| chr20:58853000
|
G | T | 1 | a0007c0026t0006 | 1 | HG02055.hp1 | 5_prime_UTR_variant | MODIFIER | c.-266G>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/13 | 266 | chr20 | 58853000 | |||||
| chr20:58853160
|
T | G | 10 | a0002c0003t0002a0002c0007t0002a0002c0009t0002others(7): Show | 36 | HG00738.hp2 HG01106.hp1 HG01256.hp1 others(33): Show |
5_prime_UTR_variant | MODIFIER | c.-106T>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/13 | 106 | chr20 | 58853160 | |||||
| chr20:58853245
|
T | C | 3 | a0001c0001t0004a0001c0004t0004a0001c0022t0004 | 4 | HG02818.hp2 NA19240.hp2 NA20129.hp1 others(1): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-21T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/13 | chr20 | 58853245 | ||||||
| chr20:58910965
|
G | A | 3 | a0001c0001t0003a0001c0002t0003a0006c0032t0003 | 21 | HG00558.hp1 HG02083.hp1 NA18747.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*136G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 13/13 | 136 | chr20 | 58910965 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:58855372
|
C | T | 1 | a0001c0014t0001g0280 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2068+39C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58855372 | ||||||
| chr20:58855381
|
G | C | 1 | a0001c0001t0001g0021 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2068+48G>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58855381 | ||||||
| chr20:58855422
|
C | G | 106 | a0001c0001t0001g0002a0001c0001t0001g0184a0001c0001t0001g0190others(103): Show | 114 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.2068+89C>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58855422 | ||||||
| chr20:58855474
|
T | A | 1 | a0001c0001t0003g0022 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2068+141T>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58855474 | ||||||
| chr20:58855492
|
C | CTT | 34 | a0002c0003t0002g0020a0002c0003t0002g0248a0002c0003t0002g0249others(31): Show | 36 | HG00738.hp2 HG01106.hp1 HG01256.hp1 others(33): Show |
intron_variant | MODIFIER | c.2068+160_2068+161i others(4): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58855492 | |||||
| chr20:58855502
|
A | T | 9 | a0002c0003t0002g0020a0002c0003t0002g0275a0002c0003t0002g0276others(6): Show | 10 | HG02148.hp1 HG02615.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.2068+169A>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58855502 | ||||||
| chr20:58855513
|
A | T | 34 | a0002c0003t0002g0020a0002c0003t0002g0248a0002c0003t0002g0249others(31): Show | 36 | HG00738.hp2 HG01106.hp1 HG01256.hp1 others(33): Show |
intron_variant | MODIFIER | c.2068+180A>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58855513 | ||||||
| chr20:58855532
|
G | C | 1 | a0001c0001t0001g0184 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2068+199G>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58855532 | ||||||
| chr20:58855687
|
C | T | 5 | a0001c0002t0001g0243a0001c0002t0001g0244a0001c0002t0001g0245others(2): Show | 5 | HG00741.hp1 HG01361.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.2068+354C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58855687 | ||||||
| chr20:58855731
|
T | C | 4 | a0004c0015t0001g0186a0004c0015t0001g0187a0004c0027t0001g0185others(1): Show | 4 | HG01884.hp2 HG02486.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.2068+398T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58855731 | ||||||
| chr20:58855962
|
ACT | A | 12 | a0002c0003t0002g0020a0002c0003t0002g0275a0002c0003t0002g0276others(9): Show | 13 | HG02145.hp1 HG02148.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.2068+632_2068+633d others(4): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58855962 | |||||
| chr20:58855969
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2068+636T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58855969 | ||||||
| chr20:58856028
|
C | T | 1 | a0001c0001t0004g0242 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2068+695C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58856028 | ||||||
| chr20:58856110
|
T | C | 57 | a0001c0001t0001g0184a0001c0001t0001g0190a0001c0001t0001g0191others(54): Show | 60 | HG00280.hp2 HG00738.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.2068+777T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58856110 | ||||||
| chr20:58856178
|
C | G | 4 | a0004c0015t0001g0186a0004c0015t0001g0187a0004c0027t0001g0185others(1): Show | 4 | HG01884.hp2 HG02486.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.2068+845C>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58856178 | ||||||
| chr20:58856610
|
A | G | 4 | a0005c0011t0002g0266a0005c0011t0002g0267a0005c0011t0002g0268others(1): Show | 4 | HG02630.hp2 HG02970.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2068+1277A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58856610 | ||||||
| chr20:58856788
|
T | C | 1 | a0001c0001t0001g0024 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2068+1455T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58856788 | ||||||
| chr20:58856800
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2068+1467C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58856800 | ||||||
| chr20:58857111
|
A | C | 3 | a0005c0011t0002g0266a0005c0011t0002g0267a0005c0011t0002g0268 | 3 | HG02970.hp2 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2068+1778A>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58857111 | ||||||
| chr20:58857124
|
A | G | 1 | a0001c0001t0001g0241 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2068+1791A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58857124 | ||||||
| chr20:58857138
|
C | T | 4 | a0004c0015t0001g0186a0004c0015t0001g0187a0004c0027t0001g0185others(1): Show | 4 | HG01884.hp2 HG02486.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.2068+1805C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58857138 | ||||||
| chr20:58857156
|
T | C | 34 | a0002c0003t0002g0020a0002c0003t0002g0248a0002c0003t0002g0249others(31): Show | 36 | HG00738.hp2 HG01106.hp1 HG01256.hp1 others(33): Show |
intron_variant | MODIFIER | c.2068+1823T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58857156 | ||||||
| chr20:58857263
|
G | T | 1 | a0002c0010t0002g0279 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2068+1930G>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58857263 | ||||||
| chr20:58857412
|
C | A | 1 | a0001c0002t0001g0199 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2068+2079C>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58857412 | ||||||
| chr20:58857551
|
T | A | 14 | a0001c0001t0001g0035a0001c0002t0001g0003a0001c0002t0001g0026others(11): Show | 16 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(13): Show |
intron_variant | MODIFIER | c.2068+2218T>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58857551 | ||||||
| chr20:58857666
|
T | C | 12 | a0002c0003t0002g0020a0002c0003t0002g0275a0002c0003t0002g0276others(9): Show | 13 | HG02145.hp1 HG02148.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.2068+2333T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58857666 | ||||||
| chr20:58857828
|
T | C | 3 | a0004c0015t0001g0186a0004c0015t0001g0187a0004c0027t0001g0185 | 3 | HG01884.hp2 HG02486.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2068+2495T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58857828 | ||||||
| chr20:58857837
|
A | C | 2 | a0001c0001t0001g0184a0008c0024t0001g0198 | 2 | HG03491.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.2068+2504A>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58857837 | ||||||
| chr20:58858073
|
C | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0181a0001c0001t0001g0182 | 4 | HG03490.hp2 HG03492.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.2068+2740C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58858073 | ||||||
| chr20:58858089
|
C | G | 1 | a0002c0021t0002g0271 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2068+2756C>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58858089 | ||||||
| chr20:58858122
|
A | G | 1 | a0001c0022t0004g0197 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2068+2789A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58858122 | ||||||
| chr20:58858287
|
A | G | 34 | a0002c0003t0002g0020a0002c0003t0002g0248a0002c0003t0002g0249others(31): Show | 36 | HG00738.hp2 HG01106.hp1 HG01256.hp1 others(33): Show |
intron_variant | MODIFIER | c.2068+2954A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58858287 | ||||||
| chr20:58858434
|
TAA | T | 7 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0177others(4): Show | 7 | HG01175.hp1 HG02723.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2068+3103_2068+310 others(6): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58858434 | |||||
| chr20:58858510
|
G | A | 5 | a0002c0003t0002g0248a0002c0003t0002g0249a0002c0003t0002g0252others(2): Show | 5 | HG00738.hp2 HG02895.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2068+3177G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58858510 | ||||||
| chr20:58859065
|
T | G | 1 | a0001c0025t0001g0037 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2068+3732T>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58859065 | ||||||
| chr20:58859113
|
T | C | 4 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0177others(1): Show | 4 | HG01175.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2068+3780T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58859113 | ||||||
| chr20:58859214
|
G | A | 4 | a0005c0011t0002g0266a0005c0011t0002g0267a0005c0011t0002g0268others(1): Show | 4 | HG02630.hp2 HG02970.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2068+3881G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58859214 | ||||||
| chr20:58859245
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2068+3912G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58859245 | ||||||
| chr20:58859280
|
A | G | 1 | a0003c0005t0001g0018 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2068+3947A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58859280 | ||||||
| chr20:58859362
|
G | A | 1 | a0001c0001t0001g0039 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2068+4029G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58859362 | ||||||
| chr20:58859405
|
T | G | 1 | a0001c0001t0001g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2068+4072T>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58859405 | ||||||
| chr20:58859454
|
CCCAAAGT others(6): Show |
C | 34 | a0002c0003t0002g0020a0002c0003t0002g0248a0002c0003t0002g0249others(31): Show | 36 | HG00738.hp2 HG01106.hp1 HG01256.hp1 others(33): Show |
intron_variant | MODIFIER | c.2068+4122_2068+413 others(17): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58859454 | ||||||
| chr20:58859628
|
CT | C | 43 | a0001c0001t0001g0042a0001c0001t0001g0204a0001c0002t0001g0041others(40): Show | 46 | HG00738.hp2 HG01106.hp1 HG01256.hp1 others(43): Show |
intron_variant | MODIFIER | c.2068+4311delT | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58859628 | |||||
| chr20:58859669
|
C | A | 1 | a0001c0002t0001g0044 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2068+4336C>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58859669 | ||||||
| chr20:58859780
|
C | A | 3 | a0001c0001t0004g0242a0001c0004t0004g0189a0001c0022t0004g0197 | 3 | NA19240.hp2 NA20129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2068+4447C>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58859780 | ||||||
| chr20:58859803
|
G | T | 36 | a0001c0001t0004g0242a0001c0004t0004g0189a0001c0022t0004g0197others(33): Show | 38 | HG00738.hp2 HG01106.hp1 HG01256.hp1 others(35): Show |
intron_variant | MODIFIER | c.2068+4470G>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58859803 | ||||||
| chr20:58859845
|
C | G | 5 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0172others(2): Show | 5 | HG00733.hp1 HG01168.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.2068+4512C>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58859845 | ||||||
| chr20:58859867
|
G | A | 33 | a0002c0003t0002g0020a0002c0003t0002g0248a0002c0003t0002g0249others(30): Show | 35 | HG00738.hp2 HG01106.hp1 HG01256.hp1 others(32): Show |
intron_variant | MODIFIER | c.2068+4534G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58859867 | ||||||
| chr20:58859919
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2068+4586C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58859919 | ||||||
| chr20:58859981
|
C | CAGATA | 88 | a0001c0001t0001g0002a0001c0001t0001g0204a0001c0001t0001g0210others(85): Show | 95 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.2068+4650_2068+465 others(9): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58859981 | |||||
| chr20:58860013
|
C | T | 3 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168 | 3 | HG01123.hp2 HG03239.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.2068+4680C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58860013 | ||||||
| chr20:58860091
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2068+4758C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58860091 | ||||||
| chr20:58860097
|
G | A | 3 | a0001c0001t0004g0242a0001c0004t0004g0189a0001c0022t0004g0197 | 3 | NA19240.hp2 NA20129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2068+4764G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58860097 | ||||||
| chr20:58860097
|
G | T | 5 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0172others(2): Show | 5 | HG00733.hp1 HG01168.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.2068+4764G>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58860097 | ||||||
| chr20:58860120
|
T | C | 1 | a0001c0001t0004g0242 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2068+4787T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58860120 | ||||||
| chr20:58860316
|
C | T | 1 | a0001c0001t0001g0240 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2068+4983C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58860316 | ||||||
| chr20:58860326
|
T | A | 2 | a0002c0012t0002g0269a0002c0012t0002g0270 | 2 | HG02145.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.2068+4993T>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58860326 | ||||||
| chr20:58860327
|
A | T | 1 | a0001c0001t0001g0165 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2068+4994A>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58860327 | ||||||
| chr20:58860339
|
G | T | 1 | a0002c0003t0002g0264 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2068+5006G>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58860339 | ||||||
| chr20:58860477
|
C | T | 74 | a0001c0001t0001g0002a0001c0001t0001g0204a0001c0001t0001g0210others(71): Show | 80 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.2068+5144C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58860477 | ||||||
| chr20:58860658
|
AGTT | A | 3 | a0002c0003t0002g0263a0002c0018t0002g0261a0002c0019t0002g0262 | 3 | HG02258.hp2 HG02922.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2068+5341_2068+534 others(7): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58860658 | |||||
| chr20:58860985
|
C | A | 105 | a0001c0001t0001g0002a0001c0001t0001g0184a0001c0001t0001g0190others(102): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.2068+5652C>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58860985 | ||||||
| chr20:58861167
|
C | T | 8 | a0002c0003t0002g0020a0002c0003t0002g0275a0002c0003t0002g0276others(5): Show | 9 | HG02148.hp1 HG02615.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2068+5834C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58861167 | ||||||
| chr20:58861595
|
A | G | 1 | a0001c0001t0001g0164 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2068+6262A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58861595 | ||||||
| chr20:58861728
|
G | A | 1 | a0001c0002t0001g0047 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2068+6395G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58861728 | ||||||
| chr20:58862073
|
T | C | 1 | a0001c0002t0001g0026 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2068+6740T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58862073 | ||||||
| chr20:58862117
|
T | G | 3 | a0001c0001t0004g0242a0001c0004t0004g0189a0001c0022t0004g0197 | 3 | NA19240.hp2 NA20129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2068+6784T>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58862117 | ||||||
| chr20:58862333
|
T | A | 3 | a0002c0003t0002g0263a0002c0018t0002g0261a0002c0019t0002g0262 | 3 | HG02258.hp2 HG02922.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2068+7000T>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58862333 | ||||||
| chr20:58862961
|
T | TG | 22 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0240others(19): Show | 24 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.2068+7629dupG | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58862961 | |||||
| chr20:58862963
|
A | G | 2 | a0001c0001t0001g0238a0001c0001t0001g0239 | 2 | HG01261.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.2068+7630A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58862963 | ||||||
| chr20:58863040
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2068+7707A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58863040 | ||||||
| chr20:58863399
|
G | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(218): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.2068+8066G>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58863399 | ||||||
| chr20:58863674
|
C | T | 1 | a0001c0002t0001g0122 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2068+8341C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58863674 | ||||||
| chr20:58863763
|
A | G | 30 | a0001c0001t0001g0002a0001c0001t0001g0204a0001c0001t0001g0210others(27): Show | 33 | HG00099.hp1 HG00642.hp1 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.2068+8430A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58863763 | ||||||
| chr20:58863866
|
G | A | 15 | a0002c0003t0002g0248a0002c0003t0002g0249a0002c0003t0002g0252others(12): Show | 16 | HG00738.hp2 HG01106.hp1 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.2068+8533G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58863866 | ||||||
| chr20:58863885
|
G | A | 30 | a0001c0001t0001g0002a0001c0001t0001g0204a0001c0001t0001g0210others(27): Show | 33 | HG00099.hp1 HG00642.hp1 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.2068+8552G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58863885 | ||||||
| chr20:58864253
|
T | A | 28 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(25): Show | 30 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.2068+8920T>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58864253 | ||||||
| chr20:58864342
|
G | T | 1 | a0001c0001t0001g0182 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2068+9009G>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58864342 | ||||||
| chr20:58864807
|
C | T | 2 | a0002c0003t0002g0259a0002c0003t0002g0260 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.2068+9474C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58864807 | ||||||
| chr20:58864856
|
G | A | 1 | a0001c0002t0001g0048 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2068+9523G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58864856 | ||||||
| chr20:58864928
|
G | GAC | 8 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(5): Show | 8 | HG00408.hp2 HG01069.hp2 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.2068+9623_2068+962 others(6): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58864928 | |||||
| chr20:58864928
|
G | GACAC | 20 | a0001c0002t0001g0014a0001c0002t0001g0194a0001c0002t0001g0195others(17): Show | 22 | HG00280.hp2 HG00738.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.2068+9621_2068+962 others(8): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58864928 | |||||
| chr20:58864928
|
G | GACACAC | 3 | a0002c0003t0002g0256a0002c0003t0002g0257a0002c0003t0002g0259 | 3 | HG01256.hp1 HG03579.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.2068+9619_2068+962 others(10): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58864928 | |||||
| chr20:58864928
|
G | GACACACA others(3): Show |
1 | a0008c0024t0001g0198 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2068+9615_2068+962 others(14): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58864928 | |||||
| chr20:58864928
|
G | GACACACA others(5): Show |
1 | a0001c0001t0001g0184 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2068+9613_2068+962 others(16): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58864928 | |||||
| chr20:58864928
|
GAC | G | 18 | a0001c0001t0001g0050a0001c0001t0001g0053a0001c0001t0001g0054others(15): Show | 19 | HG00735.hp1 HG00738.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.2068+9623_2068+962 others(6): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58864928 | |||||
| chr20:58864958
|
A | C | 3 | a0002c0003t0002g0255a0002c0003t0002g0258a0002c0003t0002g0260 | 3 | HG01106.hp1 HG01258.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.2068+9625A>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58864958 | ||||||
| chr20:58864962
|
C | A | 1 | a0002c0003t0002g0255 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2068+9629C>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58864962 | ||||||
| chr20:58864967
|
G | A | 3 | a0002c0003t0002g0255a0002c0003t0002g0258a0002c0003t0002g0260 | 3 | HG01106.hp1 HG01258.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.2068+9634G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58864967 | ||||||
| chr20:58864975
|
A | G | 3 | a0002c0003t0002g0255a0002c0003t0002g0258a0002c0003t0002g0260 | 3 | HG01106.hp1 HG01258.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.2068+9642A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58864975 | ||||||
| chr20:58864975
|
ACTCT | A | 6 | a0001c0001t0001g0162a0002c0003t0002g0256a0002c0003t0002g0257others(3): Show | 6 | HG01192.hp1 HG01256.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.2068+9657_2068+966 others(8): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58864975 | |||||
| chr20:58864977
|
T | A | 3 | a0002c0003t0002g0255a0002c0003t0002g0258a0002c0003t0002g0260 | 3 | HG01106.hp1 HG01258.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.2068+9644T>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58864977 | ||||||
| chr20:58864979
|
T | A | 3 | a0002c0003t0002g0255a0002c0003t0002g0258a0002c0003t0002g0260 | 3 | HG01106.hp1 HG01258.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.2068+9646T>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58864979 | ||||||
| chr20:58865029
|
C | T | 17 | a0002c0003t0002g0248a0002c0003t0002g0249a0002c0003t0002g0252others(14): Show | 18 | HG00738.hp2 HG01106.hp1 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.2068+9696C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58865029 | ||||||
| chr20:58865040
|
G | C | 1 | a0001c0001t0001g0196 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2068+9707G>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58865040 | ||||||
| chr20:58865091
|
A | C | 1 | a0001c0001t0001g0196 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2068+9758A>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58865091 | ||||||
| chr20:58865133
|
T | C | 108 | a0001c0001t0001g0002a0001c0001t0001g0184a0001c0001t0001g0190others(105): Show | 116 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.2068+9800T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58865133 | ||||||
| chr20:58865200
|
C | T | 20 | a0001c0001t0001g0184a0001c0001t0001g0190a0001c0001t0001g0191others(17): Show | 21 | HG00280.hp2 HG00741.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.2068+9867C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58865200 | ||||||
| chr20:58865332
|
C | T | 4 | a0005c0011t0002g0266a0005c0011t0002g0267a0005c0011t0002g0268others(1): Show | 4 | HG02630.hp2 HG02970.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2068+9999C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58865332 | ||||||
| chr20:58865343
|
G | A | 1 | a0001c0006t0001g0200 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2068+10010G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58865343 | ||||||
| chr20:58865425
|
T | A | 2 | a0002c0003t0002g0253a0002c0007t0002g0019 | 3 | HG01891.hp1 HG02896.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2068+10092T>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58865425 | ||||||
| chr20:58865432
|
AT | A | 4 | a0005c0011t0002g0266a0005c0011t0002g0267a0005c0011t0002g0268others(1): Show | 4 | HG02630.hp2 HG02970.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2068+10100delT | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58865432 | ||||||
| chr20:58865435
|
C | T | 107 | a0001c0001t0001g0002a0001c0001t0001g0184a0001c0001t0001g0190others(104): Show | 115 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.2068+10102C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58865435 | ||||||
| chr20:58865453
|
T | G | 1 | a0006c0032t0003g0049 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2068+10120T>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58865453 | ||||||
| chr20:58865529
|
C | A | 20 | a0001c0001t0004g0242a0001c0004t0004g0189a0001c0022t0004g0197others(17): Show | 21 | HG00738.hp2 HG01106.hp1 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.2068+10196C>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58865529 | ||||||
| chr20:58865531
|
A | G | 40 | a0001c0001t0001g0184a0001c0001t0001g0190a0001c0001t0001g0191others(37): Show | 42 | HG00280.hp2 HG00738.hp2 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.2068+10198A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58865531 | ||||||
| chr20:58865544
|
C | CT | 59 | a0001c0001t0001g0002a0001c0001t0001g0161a0001c0001t0001g0204others(56): Show | 64 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.2068+10221dupT | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58865544 | |||||
| chr20:58865682
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2068+10349C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58865682 | ||||||
| chr20:58865690
|
T | C | 108 | a0001c0001t0001g0002a0001c0001t0001g0184a0001c0001t0001g0190others(105): Show | 116 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.2068+10357T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58865690 | ||||||
| chr20:58865788
|
GACCCTAA others(5): Show |
G | 1 | a0001c0002t0001g0117 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2068+10457_2068+10 others(18): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58865788 | |||||
| chr20:58865816
|
A | G | 1 | a0001c0002t0003g0055 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2068+10483A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58865816 | ||||||
| chr20:58866224
|
A | C | 1 | a0001c0022t0004g0197 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2068+10891A>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58866224 | ||||||
| chr20:58866287
|
A | T | 1 | a0001c0001t0001g0225 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2068+10954A>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58866287 | ||||||
| chr20:58866328
|
G | A | 2 | a0001c0001t0001g0169a0001c0001t0001g0170 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2068+10995G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58866328 | ||||||
| chr20:58866351
|
A | C | 1 | a0001c0001t0001g0192 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2068+11018A>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58866351 | ||||||
| chr20:58866674
|
A | G | 1 | a0007c0026t0006g0232 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2068+11341A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58866674 | ||||||
| chr20:58866688
|
CTCA | C | 8 | a0002c0003t0002g0020a0002c0003t0002g0275a0002c0003t0002g0276others(5): Show | 9 | HG02148.hp1 HG02615.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2068+11359_2068+11 others(9): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58866688 | |||||
| chr20:58866779
|
CT | C | 35 | a0001c0001t0001g0184a0001c0001t0001g0190a0001c0001t0001g0191others(32): Show | 37 | HG00280.hp2 HG00741.hp1 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.2068+11458delT | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58866779 | |||||
| chr20:58866780
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2068+11447T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58866780 | ||||||
| chr20:58866915
|
T | C | 2 | a0001c0002t0001g0243a0001c0002t0001g0244 | 2 | HG01952.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2068+11582T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58866915 | ||||||
| chr20:58866917
|
C | G | 5 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0172others(2): Show | 5 | HG00733.hp1 HG01168.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.2068+11584C>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58866917 | ||||||
| chr20:58866918
|
T | C | 1 | a0002c0003t0002g0248 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2068+11585T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58866918 | ||||||
| chr20:58866929
|
C | A | 8 | a0002c0003t0002g0020a0002c0003t0002g0275a0002c0003t0002g0276others(5): Show | 9 | HG02148.hp1 HG02615.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2068+11596C>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58866929 | ||||||
| chr20:58867430
|
T | C | 1 | a0001c0001t0001g0183 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2068+12097T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58867430 | ||||||
| chr20:58867489
|
G | A | 1 | a0005c0011t0002g0266 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2068+12156G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58867489 | ||||||
| chr20:58867635
|
G | A | 3 | a0002c0003t0002g0263a0002c0018t0002g0261a0002c0019t0002g0262 | 3 | HG02258.hp2 HG02922.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2068+12302G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58867635 | ||||||
| chr20:58867639
|
A | G | 17 | a0002c0003t0002g0248a0002c0003t0002g0249a0002c0003t0002g0252others(14): Show | 18 | HG00738.hp2 HG01106.hp1 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.2068+12306A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58867639 | ||||||
| chr20:58868022
|
C | CTT | 6 | a0001c0001t0004g0242a0001c0002t0001g0045a0001c0004t0004g0189others(3): Show | 6 | HG02451.hp2 HG03130.hp2 NA19240.hp1 others(3): Show |
intron_variant | MODIFIER | c.2068+12704_2068+12 others(8): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58868022 | |||||
| chr20:58868022
|
C | CTTTT | 14 | a0002c0003t0002g0248a0002c0003t0002g0252a0002c0003t0002g0253others(11): Show | 15 | HG00738.hp2 HG01106.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.2068+12702_2068+12 others(10): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58868022 | |||||
| chr20:58868023
|
T | C | 4 | a0005c0011t0002g0266a0005c0011t0002g0267a0005c0011t0002g0268others(1): Show | 4 | HG02630.hp2 HG02970.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2068+12690T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58868023 | ||||||
| chr20:58868024
|
T | TC | 28 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(25): Show | 30 | HG00280.hp2 HG00741.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.2068+12691_2068+12 others(7): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58868024 | ||||||
| chr20:58868075
|
A | T | 29 | a0001c0001t0001g0184a0001c0001t0001g0190a0001c0001t0001g0191others(26): Show | 31 | HG00280.hp2 HG00741.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.2068+12742A>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58868075 | ||||||
| chr20:58868166
|
G | A | 1 | a0002c0003t0002g0256 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2068+12833G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58868166 | ||||||
| chr20:58868189
|
T | C | 29 | a0001c0001t0001g0184a0001c0001t0001g0190a0001c0001t0001g0191others(26): Show | 31 | HG00280.hp2 HG00741.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.2068+12856T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58868189 | ||||||
| chr20:58868213
|
T | C | 2 | a0001c0013t0001g0193a0001c0014t0001g0280 | 2 | HG02622.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2068+12880T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58868213 | ||||||
| chr20:58868261
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2068+12928C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58868261 | ||||||
| chr20:58868351
|
A | C | 1 | a0001c0001t0004g0242 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2068+13018A>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58868351 | ||||||
| chr20:58868373
|
C | A | 2 | a0001c0002t0001g0047a0001c0002t0003g0056 | 2 | NA18950.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.2068+13040C>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58868373 | ||||||
| chr20:58868438
|
A | G | 29 | a0001c0001t0001g0184a0001c0001t0001g0190a0001c0001t0001g0191others(26): Show | 31 | HG00280.hp2 HG00741.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.2068+13105A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58868438 | ||||||
| chr20:58868544
|
C | CT | 49 | a0001c0001t0001g0184a0001c0001t0001g0190a0001c0001t0001g0191others(46): Show | 52 | HG00280.hp2 HG00738.hp2 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.2068+13211_2068+13 others(7): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58868544 | ||||||
| chr20:58868659
|
G | A | 1 | a0003c0005t0001g0226 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2068+13326G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58868659 | ||||||
| chr20:58868776
|
A | G | 29 | a0001c0001t0001g0184a0001c0001t0001g0190a0001c0001t0001g0191others(26): Show | 31 | HG00280.hp2 HG00741.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.2068+13443A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58868776 | ||||||
| chr20:58868951
|
C | T | 1 | a0001c0004t0001g0046 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2068+13618C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58868951 | ||||||
| chr20:58869004
|
G | A | 1 | a0002c0021t0002g0271 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2068+13671G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58869004 | ||||||
| chr20:58869091
|
G | C | 20 | a0001c0001t0001g0184a0001c0001t0001g0190a0001c0001t0001g0191others(17): Show | 21 | HG00280.hp2 HG00741.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.2068+13758G>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58869091 | ||||||
| chr20:58869154
|
C | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(197): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.2068+13821C>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58869154 | ||||||
| chr20:58869173
|
T | C | 32 | a0001c0001t0001g0184a0001c0001t0001g0190a0001c0001t0001g0191others(29): Show | 34 | HG00280.hp2 HG00741.hp1 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.2068+13840T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58869173 | ||||||
| chr20:58869434
|
C | A | 2 | a0002c0012t0002g0269a0002c0012t0002g0270 | 2 | HG02145.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.2068+14101C>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58869434 | ||||||
| chr20:58869506
|
T | C | 8 | a0002c0003t0002g0020a0002c0003t0002g0275a0002c0003t0002g0276others(5): Show | 9 | HG02148.hp1 HG02615.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2068+14173T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58869506 | ||||||
| chr20:58869737
|
C | T | 1 | a0001c0004t0004g0189 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2068+14404C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58869737 | ||||||
| chr20:58869770
|
C | T | 12 | a0001c0001t0001g0204a0001c0001t0001g0224a0001c0001t0001g0225others(9): Show | 13 | HG00738.hp2 HG01109.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.2068+14437C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58869770 | ||||||
| chr20:58869860
|
A | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0013others(112): Show | 123 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.2068+14527A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58869860 | ||||||
| chr20:58869886
|
C | T | 9 | a0001c0001t0001g0158a0001c0001t0001g0159a0002c0003t0002g0020others(6): Show | 10 | HG02145.hp2 HG02148.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.2068+14553C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58869886 | ||||||
| chr20:58870011
|
A | G | 5 | a0001c0001t0001g0177a0004c0015t0001g0186a0004c0015t0001g0187others(2): Show | 5 | HG01884.hp2 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.2068+14678A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58870011 | ||||||
| chr20:58870158
|
G | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0013others(104): Show | 113 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.2068+14825G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58870158 | ||||||
| chr20:58870207
|
G | A | 9 | a0001c0001t0001g0158a0001c0001t0001g0159a0002c0003t0002g0020others(6): Show | 10 | HG02145.hp2 HG02148.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.2068+14874G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58870207 | ||||||
| chr20:58870250
|
A | T | 3 | a0001c0001t0003g0022a0001c0001t0003g0112a0001c0001t0003g0113 | 3 | NA18947.hp2 NA18999.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.2068+14917A>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58870250 | ||||||
| chr20:58870432
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2068+15099T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58870432 | ||||||
| chr20:58870570
|
T | C | 1 | a0001c0002t0001g0047 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2068+15237T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58870570 | ||||||
| chr20:58870572
|
C | A | 1 | a0001c0002t0001g0047 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2068+15239C>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58870572 | ||||||
| chr20:58870573
|
A | G | 1 | a0001c0002t0001g0047 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2068+15240A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58870573 | ||||||
| chr20:58870670
|
G | T | 11 | a0001c0001t0001g0184a0001c0002t0001g0195a0001c0002t0001g0223others(8): Show | 13 | HG01516.hp2 HG01891.hp1 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.2068+15337G>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58870670 | ||||||
| chr20:58870731
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2068+15398C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58870731 | ||||||
| chr20:58870916
|
A | G | 153 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0013others(150): Show | 161 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.2068+15583A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58870916 | ||||||
| chr20:58871050
|
C | T | 1 | a0001c0002t0001g0154 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2068+15717C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58871050 | ||||||
| chr20:58871131
|
G | A | 9 | a0001c0001t0001g0158a0001c0001t0001g0190a0001c0001t0001g0191others(6): Show | 9 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.2068+15798G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58871131 | ||||||
| chr20:58871154
|
G | A | 8 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(5): Show | 8 | HG01891.hp2 HG02258.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2068+15821G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58871154 | ||||||
| chr20:58871254
|
T | C | 5 | a0002c0003t0002g0275a0002c0003t0002g0276a0002c0009t0002g0273others(2): Show | 5 | HG02148.hp1 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2068+15921T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58871254 | ||||||
| chr20:58871271
|
C | T | 1 | a0005c0031t0002g0265 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2068+15938C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58871271 | ||||||
| chr20:58871563
|
G | A | 5 | a0002c0003t0002g0275a0002c0003t0002g0276a0002c0009t0002g0273others(2): Show | 5 | HG02148.hp1 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2068+16230G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58871563 | ||||||
| chr20:58871613
|
G | GA | 20 | a0001c0001t0001g0118a0001c0001t0001g0125a0001c0001t0001g0128others(17): Show | 21 | HG00140.hp2 HG00738.hp2 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.2068+16296dupA | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58871613 | |||||
| chr20:58871613
|
GA | G | 7 | a0001c0001t0001g0008a0001c0001t0001g0153a0001c0001t0001g0159others(4): Show | 8 | HG01074.hp1 HG01169.hp1 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.2068+16296delA | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58871613 | |||||
| chr20:58871614
|
A | G | 1 | a0002c0010t0002g0279 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2068+16281A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58871614 | ||||||
| chr20:58871637
|
C | CA | 28 | a0001c0001t0001g0002a0001c0001t0001g0058a0001c0001t0001g0065others(25): Show | 33 | HG00099.hp1 HG00099.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.2068+16314dupA | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58871637 | |||||
| chr20:58871647
|
A | C | 5 | a0001c0001t0001g0124a0001c0001t0001g0196a0001c0001t0001g0225others(2): Show | 5 | HG02451.hp1 HG02572.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2068+16314A>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58871647 | ||||||
| chr20:58871648
|
C | A | 1 | a0001c0004t0001g0201 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2068+16315C>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58871648 | ||||||
| chr20:58871658
|
T | G | 97 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0013others(94): Show | 102 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.2068+16325T>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58871658 | ||||||
| chr20:58871670
|
A | G | 1 | a0001c0004t0001g0017 | 2 | HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2068+16337A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58871670 | ||||||
| chr20:58871738
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2068+16405G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58871738 | ||||||
| chr20:58871739
|
A | C | 1 | a0001c0001t0001g0164 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2068+16406A>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58871739 | ||||||
| chr20:58871841
|
A | C | 1 | a0001c0006t0001g0222 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2068+16508A>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58871841 | ||||||
| chr20:58871911
|
G | A | 9 | a0001c0001t0001g0184a0001c0001t0001g0221a0001c0002t0001g0195others(6): Show | 10 | HG01516.hp2 HG01952.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.2068+16578G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58871911 | ||||||
| chr20:58871941
|
C | T | 2 | a0002c0012t0002g0269a0002c0012t0002g0270 | 2 | HG02145.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.2068+16608C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58871941 | ||||||
| chr20:58871967
|
C | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0013others(106): Show | 116 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.2068+16634C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58871967 | ||||||
| chr20:58872185
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2068+16852C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58872185 | ||||||
| chr20:58872268
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2068+16935G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58872268 | ||||||
| chr20:58872348
|
T | TA | 128 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0013others(125): Show | 135 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.2068+17026dupA | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58872348 | |||||
| chr20:58872535
|
C | T | 3 | a0001c0001t0001g0219a0001c0014t0001g0218a0001c0030t0001g0220 | 3 | HG02615.hp1 HG03225.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2068+17202C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58872535 | ||||||
| chr20:58872691
|
G | T | 1 | a0001c0001t0001g0225 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2068+17358G>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58872691 | ||||||
| chr20:58872741
|
G | A | 2 | a0001c0001t0001g0124a0001c0001t0004g0242 | 2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2068+17408G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58872741 | ||||||
| chr20:58872751
|
G | C | 1 | a0002c0012t0002g0269 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2068+17418G>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58872751 | ||||||
| chr20:58872755
|
G | A | 1 | a0002c0010t0002g0279 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2068+17422G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58872755 | ||||||
| chr20:58872756
|
CAG | C | 5 | a0002c0003t0002g0275a0002c0003t0002g0276a0002c0009t0002g0273others(2): Show | 5 | HG02148.hp1 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2068+17431_2068+17 others(8): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58872756 | |||||
| chr20:58872835
|
G | A | 1 | a0001c0025t0001g0037 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2068+17502G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58872835 | ||||||
| chr20:58872856
|
T | C | 107 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0013others(104): Show | 112 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.2068+17523T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58872856 | ||||||
| chr20:58873238
|
T | C | 5 | a0001c0001t0001g0124a0001c0001t0001g0159a0001c0001t0001g0196others(2): Show | 5 | HG02559.hp1 HG02572.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2068+17905T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58873238 | ||||||
| chr20:58873265
|
G | T | 9 | a0001c0001t0001g0158a0001c0001t0001g0190a0001c0001t0001g0191others(6): Show | 9 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.2068+17932G>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58873265 | ||||||
| chr20:58873430
|
G | A | 4 | a0001c0001t0001g0124a0001c0001t0001g0159a0001c0001t0004g0242others(1): Show | 4 | HG02559.hp1 HG02970.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2068+18097G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58873430 | ||||||
| chr20:58873516
|
C | T | 8 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(5): Show | 8 | HG01891.hp2 HG02258.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2068+18183C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58873516 | ||||||
| chr20:58873630
|
C | T | 1 | a0001c0002t0001g0047 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2068+18297C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58873630 | ||||||
| chr20:58873670
|
G | A | 5 | a0001c0022t0004g0197a0004c0015t0001g0186a0004c0015t0001g0187others(2): Show | 5 | HG01884.hp2 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.2068+18337G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58873670 | ||||||
| chr20:58873691
|
C | T | 97 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0013others(94): Show | 102 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.2068+18358C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58873691 | ||||||
| chr20:58873752
|
T | A | 5 | a0001c0001t0001g0042a0001c0001t0001g0130a0001c0001t0001g0131others(2): Show | 5 | HG00558.hp2 HG00639.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.2068+18419T>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58873752 | ||||||
| chr20:58873782
|
C | T | 29 | a0001c0001t0001g0158a0001c0001t0001g0184a0001c0001t0001g0190others(26): Show | 30 | HG01516.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.2068+18449C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58873782 | ||||||
| chr20:58873910
|
C | T | 1 | a0002c0003t0002g0255 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2068+18577C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58873910 | ||||||
| chr20:58874135
|
C | T | 5 | a0002c0003t0002g0275a0002c0003t0002g0276a0002c0009t0002g0273others(2): Show | 5 | HG02148.hp1 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2068+18802C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58874135 | ||||||
| chr20:58874327
|
G | T | 1 | a0001c0001t0001g0157 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2068+18994G>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58874327 | ||||||
| chr20:58874640
|
T | TATCTTAG others(41): Show |
9 | a0001c0001t0001g0124a0001c0001t0001g0128a0001c0001t0004g0242others(6): Show | 10 | HG01255.hp1 HG01928.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.2068+19351_2068+19 others(54): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58874640 | |||||
| chr20:58874685
|
T | C | 25 | a0001c0001t0001g0158a0001c0001t0001g0174a0001c0001t0001g0190others(22): Show | 25 | HG01069.hp2 HG01433.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.2068+19352T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58874685 | ||||||
| chr20:58874688
|
T | C | 25 | a0001c0001t0001g0158a0001c0001t0001g0174a0001c0001t0001g0190others(22): Show | 25 | HG01069.hp2 HG01433.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.2068+19355T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58874688 | ||||||
| chr20:58874694
|
T | A | 25 | a0001c0001t0001g0158a0001c0001t0001g0174a0001c0001t0001g0190others(22): Show | 25 | HG01069.hp2 HG01433.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.2068+19361T>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58874694 | ||||||
| chr20:58874830
|
T | C | 2 | a0001c0001t0001g0159a0005c0011t0002g0268 | 2 | HG02559.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2068+19497T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58874830 | ||||||
| chr20:58874875
|
G | A | 2 | a0001c0001t0001g0159a0005c0011t0002g0268 | 2 | HG02559.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2068+19542G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58874875 | ||||||
| chr20:58875204
|
G | A | 1 | a0001c0022t0004g0197 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2068+19871G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58875204 | ||||||
| chr20:58875360
|
C | T | 14 | a0001c0001t0001g0057a0001c0001t0001g0175a0001c0001t0001g0177others(11): Show | 14 | HG01106.hp1 HG01175.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.2068+20027C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58875360 | ||||||
| chr20:58875693
|
C | G | 1 | a0002c0003t0002g0263 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2069-19919C>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58875693 | ||||||
| chr20:58875695
|
C | T | 1 | a0001c0002t0003g0032 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2069-19917C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58875695 | ||||||
| chr20:58875849
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2069-19763C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58875849 | ||||||
| chr20:58876040
|
G | C | 1 | a0002c0010t0002g0279 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2069-19572G>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58876040 | ||||||
| chr20:58876254
|
A | C | 1 | a0001c0001t0001g0236 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2069-19358A>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58876254 | ||||||
| chr20:58876389
|
CG | C | 3 | a0001c0002t0001g0110a0001c0002t0001g0111a0001c0002t0003g0056 | 3 | HG02027.hp2 NA18950.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.2069-19220delG | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58876389 | |||||
| chr20:58876423
|
A | G | 1 | a0002c0003t0002g0256 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2069-19189A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58876423 | ||||||
| chr20:58876538
|
A | AC | 18 | a0001c0001t0001g0023a0001c0001t0001g0039a0001c0001t0001g0057others(15): Show | 18 | HG00597.hp2 HG00733.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.2069-19067dupC | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58876538 | |||||
| chr20:58876539
|
C | A | 1 | a0001c0001t0001g0221 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2069-19073C>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58876539 | ||||||
| chr20:58876762
|
C | T | 1 | a0009c0017t0001g0105 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2069-18850C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58876762 | ||||||
| chr20:58877148
|
A | AT | 138 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0013others(135): Show | 144 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.2069-18454dupT | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58877148 | |||||
| chr20:58877161
|
G | A | 7 | a0001c0001t0001g0190a0001c0001t0001g0237a0001c0001t0001g0238others(4): Show | 7 | HG01069.hp2 HG01433.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.2069-18451G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58877161 | ||||||
| chr20:58877341
|
C | A | 1 | a0001c0001t0001g0057 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2069-18271C>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58877341 | ||||||
| chr20:58877642
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2069-17970G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58877642 | ||||||
| chr20:58877769
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2069-17843G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58877769 | ||||||
| chr20:58877826
|
C | T | 76 | a0001c0001t0001g0040a0001c0001t0001g0057a0001c0001t0001g0124others(73): Show | 81 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.2069-17786C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58877826 | ||||||
| chr20:58877975
|
G | A | 1 | a0001c0002t0001g0074 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2069-17637G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58877975 | ||||||
| chr20:58877997
|
C | T | 1 | a0002c0003t0002g0257 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2069-17615C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58877997 | ||||||
| chr20:58878009
|
A | G | 1 | a0001c0001t0001g0217 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2069-17603A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58878009 | ||||||
| chr20:58878015
|
A | G | 1 | a0007c0026t0006g0232 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2069-17597A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58878015 | ||||||
| chr20:58878098
|
G | T | 1 | a0001c0004t0004g0189 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2069-17514G>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58878098 | ||||||
| chr20:58878128
|
C | G | 1 | a0001c0002t0003g0052 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2069-17484C>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58878128 | ||||||
| chr20:58878337
|
C | G | 5 | a0001c0002t0001g0006a0001c0002t0001g0041a0001c0002t0001g0061others(2): Show | 6 | HG00280.hp1 HG00642.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.2069-17275C>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58878337 | ||||||
| chr20:58878413
|
T | G | 2 | a0001c0001t0001g0124a0001c0001t0004g0242 | 2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2069-17199T>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58878413 | ||||||
| chr20:58878464
|
A | C | 2 | a0001c0001t0001g0124a0001c0001t0004g0242 | 2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2069-17148A>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58878464 | ||||||
| chr20:58878508
|
C | T | 2 | a0002c0012t0002g0269a0002c0012t0002g0270 | 2 | HG02145.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.2069-17104C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58878508 | ||||||
| chr20:58878786
|
G | A | 3 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0241 | 3 | HG01069.hp2 HG01433.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.2069-16826G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58878786 | ||||||
| chr20:58878797
|
C | G | 18 | a0001c0001t0001g0040a0001c0001t0001g0128a0001c0001t0001g0190others(15): Show | 19 | HG01070.hp1 HG01109.hp1 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.2069-16815C>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58878797 | ||||||
| chr20:58878849
|
C | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(102): Show | 112 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.2069-16763C>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58878849 | ||||||
| chr20:58878908
|
C | T | 2 | a0001c0001t0001g0221a0005c0031t0002g0265 | 2 | HG02055.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2069-16704C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58878908 | ||||||
| chr20:58878912
|
TG | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(179): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.2069-16691delG | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58878912 | |||||
| chr20:58878914
|
G | T | 3 | a0001c0001t0001g0159a0002c0010t0002g0272a0005c0011t0002g0268 | 3 | HG02559.hp1 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2069-16698G>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58878914 | ||||||
| chr20:58878952
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2069-16660G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58878952 | ||||||
| chr20:58879173
|
G | T | 1 | a0001c0004t0004g0189 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2069-16439G>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58879173 | ||||||
| chr20:58879211
|
A | G | 4 | a0004c0015t0001g0186a0004c0015t0001g0187a0004c0027t0001g0185others(1): Show | 4 | HG01884.hp2 HG02486.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.2069-16401A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58879211 | ||||||
| chr20:58879400
|
A | G | 2 | a0001c0001t0001g0158a0002c0012t0002g0270 | 2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.2069-16212A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58879400 | ||||||
| chr20:58879624
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2069-15988G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58879624 | ||||||
| chr20:58879685
|
A | T | 28 | a0001c0001t0001g0040a0001c0001t0001g0057a0001c0001t0001g0124others(25): Show | 29 | HG00140.hp1 HG00280.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.2069-15927A>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58879685 | ||||||
| chr20:58879839
|
T | C | 2 | a0005c0011t0002g0266a0005c0011t0002g0267 | 2 | HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2069-15773T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58879839 | ||||||
| chr20:58879921
|
A | C | 4 | a0001c0001t0001g0158a0001c0001t0001g0196a0001c0001t0001g0204others(1): Show | 4 | HG02145.hp2 HG02572.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2069-15691A>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58879921 | ||||||
| chr20:58880042
|
C | T | 2 | a0001c0001t0001g0217a0005c0031t0002g0265 | 2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2069-15570C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58880042 | ||||||
| chr20:58880062
|
G | A | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | NA18962.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.2069-15550G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58880062 | ||||||
| chr20:58880084
|
C | G | 7 | a0001c0001t0001g0124a0001c0001t0001g0225a0001c0006t0001g0207others(4): Show | 7 | HG00738.hp2 HG02451.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.2069-15528C>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58880084 | ||||||
| chr20:58880191
|
A | T | 1 | a0003c0005t0001g0231 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2069-15421A>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58880191 | ||||||
| chr20:58880218
|
A | G | 9 | a0001c0001t0001g0224a0001c0002t0001g0005a0001c0002t0001g0195others(6): Show | 10 | HG00099.hp1 HG01109.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2069-15394A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58880218 | ||||||
| chr20:58880273
|
C | T | 9 | a0001c0001t0001g0224a0001c0002t0001g0005a0001c0002t0001g0195others(6): Show | 10 | HG00099.hp1 HG01109.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2069-15339C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58880273 | ||||||
| chr20:58880311
|
G | A | 4 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0006t0001g0222others(1): Show | 5 | HG02559.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.2069-15301G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58880311 | ||||||
| chr20:58880433
|
G | A | 1 | a0002c0009t0002g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2069-15179G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58880433 | ||||||
| chr20:58880501
|
C | T | 1 | a0001c0006t0001g0206 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2069-15111C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58880501 | ||||||
| chr20:58880521
|
T | C | 9 | a0001c0001t0001g0224a0001c0002t0001g0005a0001c0002t0001g0195others(6): Show | 10 | HG00099.hp1 HG01109.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2069-15091T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58880521 | ||||||
| chr20:58880577
|
G | A | 1 | a0002c0012t0002g0270 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2069-15035G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58880577 | ||||||
| chr20:58880965
|
C | T | 2 | a0001c0002t0001g0070a0001c0002t0001g0149 | 2 | NA18747.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2069-14647C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58880965 | ||||||
| chr20:58881018
|
C | T | 2 | a0001c0001t0001g0217a0005c0031t0002g0265 | 2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2069-14594C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58881018 | ||||||
| chr20:58881426
|
A | T | 1 | a0001c0001t0001g0065 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2069-14186A>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58881426 | ||||||
| chr20:58881440
|
T | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(151): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.2069-14172T>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58881440 | ||||||
| chr20:58881586
|
G | A | 18 | a0001c0001t0001g0124a0001c0006t0001g0207a0001c0014t0001g0218others(15): Show | 18 | HG00738.hp2 HG01884.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.2069-14026G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58881586 | ||||||
| chr20:58881629
|
G | C | 3 | a0001c0004t0001g0015a0001c0004t0001g0201a0001c0004t0001g0203 | 4 | HG01884.hp1 HG02486.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.2069-13983G>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58881629 | ||||||
| chr20:58881859
|
T | C | 5 | a0001c0002t0001g0045a0002c0003t0002g0275a0002c0009t0002g0273others(2): Show | 5 | HG02148.hp1 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2069-13753T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58881859 | ||||||
| chr20:58882037
|
T | C | 4 | a0001c0001t0001g0224a0001c0001t0004g0242a0005c0011t0002g0266others(1): Show | 4 | HG01109.hp1 HG06807.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2069-13575T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58882037 | ||||||
| chr20:58882091
|
C | G | 1 | a0001c0001t0001g0217 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2069-13521C>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58882091 | ||||||
| chr20:58882138
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2069-13474G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58882138 | ||||||
| chr20:58882245
|
A | G | 44 | a0001c0001t0001g0035a0001c0001t0001g0057a0001c0001t0001g0124others(41): Show | 45 | HG00423.hp1 HG00738.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.2069-13367A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58882245 | ||||||
| chr20:58882343
|
C | G | 1 | a0001c0002t0001g0074 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2069-13269C>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58882343 | ||||||
| chr20:58882394
|
C | T | 1 | a0001c0030t0001g0220 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2069-13218C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58882394 | ||||||
| chr20:58882696
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2069-12916C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58882696 | ||||||
| chr20:58882714
|
G | A | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(154): Show | 169 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.2069-12898G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58882714 | ||||||
| chr20:58882764
|
C | T | 6 | a0001c0002t0001g0005a0001c0002t0001g0195a0001c0002t0001g0205others(3): Show | 7 | HG00099.hp1 HG01109.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.2069-12848C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58882764 | ||||||
| chr20:58882853
|
G | T | 1 | a0001c0001t0001g0125 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2069-12759G>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58882853 | ||||||
| chr20:58882905
|
T | G | 1 | a0001c0001t0001g0077 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2069-12707T>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58882905 | ||||||
| chr20:58882929
|
G | T | 3 | a0001c0001t0001g0224a0005c0011t0002g0266a0005c0011t0002g0267 | 3 | HG01109.hp1 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2069-12683G>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58882929 | ||||||
| chr20:58883049
|
G | T | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(88): Show | 100 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.2069-12563G>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58883049 | ||||||
| chr20:58883188
|
G | GT | 2 | a0001c0002t0001g0012a0001c0002t0001g0148 | 3 | NA18982.hp1 NA19083.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.2069-12423dupT | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58883188 | |||||
| chr20:58883265
|
T | G | 1 | a0001c0001t0001g0078 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2069-12347T>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58883265 | ||||||
| chr20:58883332
|
G | A | 2 | a0001c0001t0001g0239a0003c0005t0001g0226 | 2 | HG00735.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.2069-12280G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58883332 | ||||||
| chr20:58883407
|
C | T | 1 | a0001c0001t0001g0078 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2069-12205C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58883407 | ||||||
| chr20:58883469
|
A | G | 4 | a0001c0001t0001g0125a0001c0001t0001g0237a0001c0001t0001g0241others(1): Show | 4 | HG01069.hp2 HG01361.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.2069-12143A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58883469 | ||||||
| chr20:58883707
|
C | T | 1 | a0001c0001t0005g0098 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2069-11905C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58883707 | ||||||
| chr20:58883761
|
G | A | 1 | a0001c0002t0001g0126 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2069-11851G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58883761 | ||||||
| chr20:58883773
|
A | G | 1 | a0005c0031t0002g0265 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2069-11839A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58883773 | ||||||
| chr20:58884029
|
T | C | 8 | a0001c0001t0001g0240a0001c0001t0004g0235a0001c0002t0001g0044others(5): Show | 9 | HG01884.hp1 HG02451.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2069-11583T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58884029 | ||||||
| chr20:58884110
|
C | G | 1 | a0001c0002t0001g0199 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2069-11502C>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58884110 | ||||||
| chr20:58884112
|
A | G | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(158): Show | 173 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.2069-11500A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58884112 | ||||||
| chr20:58884487
|
T | C | 8 | a0001c0001t0001g0240a0001c0001t0004g0235a0001c0002t0001g0044others(5): Show | 9 | HG01884.hp1 HG02451.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2069-11125T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58884487 | ||||||
| chr20:58884511
|
T | C | 1 | a0003c0005t0001g0231 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2069-11101T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58884511 | ||||||
| chr20:58884683
|
C | T | 9 | a0001c0001t0001g0224a0001c0002t0001g0005a0001c0002t0001g0195others(6): Show | 10 | HG00099.hp1 HG01109.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2069-10929C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58884683 | ||||||
| chr20:58884756
|
C | T | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(147): Show | 161 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.2069-10856C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58884756 | ||||||
| chr20:58884807
|
A | G | 2 | a0001c0001t0005g0097a0001c0001t0005g0098 | 2 | HG01081.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.2069-10805A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58884807 | ||||||
| chr20:58884894
|
A | AG | 4 | a0001c0001t0001g0125a0001c0001t0001g0237a0001c0001t0001g0241others(1): Show | 4 | HG01069.hp2 HG01361.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.2069-10717dupG | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58884894 | |||||
| chr20:58885043
|
T | C | 1 | a0004c0028t0001g0188 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2069-10569T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58885043 | ||||||
| chr20:58885043
|
T | G | 2 | a0001c0001t0005g0097a0001c0001t0005g0098 | 2 | HG01081.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.2069-10569T>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58885043 | ||||||
| chr20:58885072
|
T | C | 3 | a0001c0001t0001g0066a0001c0001t0001g0079a0001c0002t0001g0069 | 3 | NA18945.hp2 NA19081.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.2069-10540T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58885072 | ||||||
| chr20:58885087
|
C | G | 5 | a0001c0001t0001g0039a0001c0001t0001g0066a0001c0001t0001g0079others(2): Show | 5 | NA18945.hp2 NA19005.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.2069-10525C>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58885087 | ||||||
| chr20:58885356
|
C | G | 8 | a0001c0001t0001g0240a0001c0001t0004g0235a0001c0002t0001g0044others(5): Show | 9 | HG01884.hp1 HG02451.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2069-10256C>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58885356 | ||||||
| chr20:58885457
|
T | C | 9 | a0001c0001t0001g0224a0001c0002t0001g0005a0001c0002t0001g0195others(6): Show | 10 | HG00099.hp1 HG01109.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2069-10155T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58885457 | ||||||
| chr20:58885620
|
GA | G | 44 | a0001c0001t0001g0057a0001c0001t0001g0124a0001c0001t0001g0125others(41): Show | 45 | HG00423.hp1 HG00738.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.2069-9983delA | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58885620 | |||||
| chr20:58885947
|
C | T | 1 | a0005c0031t0002g0265 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2069-9665C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58885947 | ||||||
| chr20:58886254
|
C | T | 1 | a0001c0001t0004g0242 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2069-9358C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58886254 | ||||||
| chr20:58886255
|
G | C | 9 | a0001c0001t0001g0224a0001c0002t0001g0005a0001c0002t0001g0195others(6): Show | 10 | HG00099.hp1 HG01109.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2069-9357G>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58886255 | ||||||
| chr20:58886307
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2069-9305C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58886307 | ||||||
| chr20:58886377
|
A | C | 2 | a0001c0002t0001g0030a0001c0002t0003g0032 | 2 | HG00423.hp2 HG00558.hp1 |
intron_variant | MODIFIER | c.2069-9235A>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58886377 | ||||||
| chr20:58886496
|
C | T | 20 | a0001c0001t0001g0124a0001c0001t0001g0217a0001c0006t0001g0207others(17): Show | 20 | HG00738.hp2 HG01884.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.2069-9116C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58886496 | ||||||
| chr20:58886611
|
AC | A | 5 | a0001c0006t0001g0207a0002c0003t0002g0248a0002c0003t0002g0249others(2): Show | 5 | HG00738.hp2 HG02895.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2069-9000delC | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58886611 | ||||||
| chr20:58886659
|
G | GA | 32 | a0001c0001t0001g0040a0001c0001t0001g0155a0001c0001t0001g0167others(29): Show | 33 | HG00738.hp2 HG01070.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.2069-8942dupA | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58886659 | |||||
| chr20:58886860
|
G | A | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(156): Show | 171 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.2069-8752G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58886860 | ||||||
| chr20:58887062
|
T | C | 1 | a0001c0002t0001g0137 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2069-8550T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58887062 | ||||||
| chr20:58887276
|
T | C | 1 | a0005c0031t0002g0265 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2069-8336T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58887276 | ||||||
| chr20:58887364
|
T | G | 16 | a0001c0001t0001g0040a0001c0001t0001g0100a0001c0001t0001g0167others(13): Show | 17 | HG01070.hp1 HG01123.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.2069-8248T>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58887364 | ||||||
| chr20:58887435
|
T | C | 2 | a0001c0002t0001g0043a0001c0002t0001g0138 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2069-8177T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58887435 | ||||||
| chr20:58887550
|
G | C | 3 | a0001c0001t0001g0081a0001c0001t0001g0236a0001c0002t0001g0205 | 3 | HG00140.hp2 HG01192.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.2069-8062G>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58887550 | ||||||
| chr20:58887572
|
T | C | 1 | a0001c0001t0001g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2069-8040T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58887572 | ||||||
| chr20:58887573
|
G | A | 4 | a0001c0001t0001g0125a0001c0001t0001g0237a0001c0001t0001g0241others(1): Show | 4 | HG01069.hp2 HG01361.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.2069-8039G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58887573 | ||||||
| chr20:58887773
|
T | A | 1 | a0001c0001t0001g0072 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2069-7839T>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58887773 | ||||||
| chr20:58887889
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2069-7723T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58887889 | ||||||
| chr20:58888114
|
C | G | 1 | a0001c0001t0003g0116 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2069-7498C>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58888114 | ||||||
| chr20:58888121
|
C | G | 2 | a0001c0001t0001g0196a0002c0003t0002g0257 | 2 | HG02572.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2069-7491C>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58888121 | ||||||
| chr20:58888186
|
T | G | 1 | a0001c0001t0001g0239 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2069-7426T>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58888186 | ||||||
| chr20:58888274
|
T | C | 1 | a0001c0002t0001g0150 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2069-7338T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58888274 | ||||||
| chr20:58888417
|
C | G | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(159): Show | 174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.2069-7195C>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58888417 | ||||||
| chr20:58888433
|
C | T | 1 | a0001c0001t0004g0242 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2069-7179C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58888433 | ||||||
| chr20:58888522
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2069-7090C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58888522 | ||||||
| chr20:58888631
|
C | A | 1 | a0005c0031t0002g0265 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2069-6981C>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58888631 | ||||||
| chr20:58888938
|
C | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(179): Show | 195 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.2069-6674C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58888938 | ||||||
| chr20:58888975
|
C | T | 1 | a0001c0002t0001g0047 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2069-6637C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58888975 | ||||||
| chr20:58889127
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2069-6485G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58889127 | ||||||
| chr20:58889222
|
C | CCGGCG | 175 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(172): Show | 187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.2069-6383_2069-637 others(9): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58889222 | |||||
| chr20:58889420
|
G | A | 1 | a0005c0031t0002g0265 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2069-6192G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58889420 | ||||||
| chr20:58889512
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2069-6100T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58889512 | ||||||
| chr20:58889561
|
C | T | 13 | a0001c0006t0001g0207a0001c0014t0001g0218a0001c0014t0001g0280others(10): Show | 13 | HG00738.hp2 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.2069-6051C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58889561 | ||||||
| chr20:58889571
|
G | A | 1 | a0001c0022t0004g0197 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2069-6041G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58889571 | ||||||
| chr20:58889593
|
G | C | 1 | a0004c0027t0001g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2069-6019G>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58889593 | ||||||
| chr20:58889777
|
G | GC | 65 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0057others(62): Show | 67 | HG00423.hp1 HG00597.hp2 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.2069-5829dupC | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58889777 | |||||
| chr20:58889854
|
C | A | 8 | a0001c0014t0001g0218a0001c0014t0001g0280a0002c0012t0002g0269others(5): Show | 8 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2069-5758C>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58889854 | ||||||
| chr20:58890197
|
TGAA | T | 6 | a0001c0001t0001g0158a0001c0001t0001g0204a0002c0010t0002g0272others(3): Show | 6 | HG02145.hp2 HG02258.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2069-5398_2069-539 others(7): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58890197 | |||||
| chr20:58890209
|
A | G | 1 | a0002c0012t0002g0269 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2069-5403A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58890209 | ||||||
| chr20:58890223
|
G | A | 4 | a0001c0001t0001g0125a0001c0001t0001g0237a0001c0001t0001g0241others(1): Show | 4 | HG01069.hp2 HG01361.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.2069-5389G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58890223 | ||||||
| chr20:58890278
|
A | C | 2 | a0001c0001t0001g0095a0001c0020t0001g0208 | 2 | HG02451.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.2069-5334A>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58890278 | ||||||
| chr20:58890287
|
AGGGCGCC others(17): Show |
A | 3 | a0001c0001t0001g0065a0001c0013t0001g0193a0003c0005t0001g0018 | 4 | HG01070.hp2 HG01071.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2069-5304_2069-528 others(28): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58890287 | |||||
| chr20:58890309
|
C | T | 1 | a0005c0011t0002g0268 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2069-5303C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58890309 | ||||||
| chr20:58890311
|
GGGGCGCC others(5): Show |
G | 3 | a0001c0001t0001g0196a0001c0001t0001g0204a0002c0003t0002g0257 | 3 | HG02572.hp1 HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2069-5292_2069-528 others(16): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58890311 | |||||
| chr20:58890516
|
G | A | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(88): Show | 100 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.2069-5096G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58890516 | ||||||
| chr20:58890548
|
C | T | 1 | a0002c0019t0002g0262 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2069-5064C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58890548 | ||||||
| chr20:58890888
|
T | G | 6 | a0001c0002t0001g0005a0001c0002t0001g0195a0001c0002t0001g0205others(3): Show | 7 | HG00099.hp1 HG01109.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.2069-4724T>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58890888 | ||||||
| chr20:58890894
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2069-4718C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58890894 | ||||||
| chr20:58890939
|
G | C | 1 | a0002c0003t0002g0255 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2069-4673G>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58890939 | ||||||
| chr20:58890991
|
G | C | 27 | a0001c0001t0001g0035a0001c0001t0001g0057a0001c0001t0001g0136others(24): Show | 28 | HG00423.hp1 HG00597.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.2069-4621G>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58890991 | ||||||
| chr20:58891092
|
C | G | 1 | a0001c0022t0004g0197 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2069-4520C>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58891092 | ||||||
| chr20:58891092
|
C | T | 1 | a0001c0002t0001g0069 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2069-4520C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58891092 | ||||||
| chr20:58891120
|
C | G | 1 | a0001c0022t0004g0197 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2069-4492C>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58891120 | ||||||
| chr20:58891129
|
G | C | 1 | a0001c0002t0001g0117 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2069-4483G>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58891129 | ||||||
| chr20:58891205
|
G | C | 1 | a0001c0002t0003g0034 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2069-4407G>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58891205 | ||||||
| chr20:58891206
|
G | C | 1 | a0003c0005t0001g0226 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2069-4406G>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58891206 | ||||||
| chr20:58891240
|
A | AGCCGCC | 6 | a0001c0002t0001g0005a0001c0002t0001g0195a0001c0002t0001g0205others(3): Show | 7 | HG00099.hp1 HG01109.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.2069-4360_2069-435 others(10): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58891240 | |||||
| chr20:58891271
|
CCCT | C | 3 | a0002c0010t0002g0272a0002c0018t0002g0261a0002c0019t0002g0262 | 3 | HG02258.hp2 HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2069-4322_2069-432 others(7): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58891271 | |||||
| chr20:58891271
|
CCCTCCT | C | 3 | a0001c0001t0001g0094a0001c0001t0001g0167a0001c0001t0001g0168 | 3 | HG01123.hp2 HG02155.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.2069-4325_2069-432 others(10): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58891271 | |||||
| chr20:58891291
|
C | T | 8 | a0001c0004t0001g0016a0001c0004t0001g0017a0001c0004t0001g0201others(5): Show | 9 | HG01884.hp1 HG02486.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.2069-4321C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58891291 | ||||||
| chr20:58891301
|
C | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0093a0002c0007t0002g0254 | 4 | HG01074.hp1 HG01169.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.2069-4311C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58891301 | ||||||
| chr20:58891314
|
G | GCCT | 21 | a0001c0001t0001g0071a0001c0001t0001g0163a0001c0002t0001g0003others(18): Show | 23 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(20): Show |
intron_variant | MODIFIER | c.2069-4289_2069-428 others(7): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58891314 | |||||
| chr20:58891320
|
TCCTCCCC others(3): Show |
T | 1 | a0001c0002t0001g0137 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2069-4279_2069-427 others(14): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58891320 | |||||
| chr20:58891321
|
C | T | 3 | a0001c0001t0001g0042a0001c0001t0001g0092a0001c0001t0001g0118 | 3 | HG01496.hp2 HG01928.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.2069-4291C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58891321 | ||||||
| chr20:58891412
|
A | G | 21 | a0001c0001t0001g0071a0001c0001t0001g0163a0001c0002t0001g0003others(18): Show | 23 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(20): Show |
intron_variant | MODIFIER | c.2069-4200A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58891412 | ||||||
| chr20:58891735
|
C | T | 1 | a0001c0002t0001g0137 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2069-3877C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58891735 | ||||||
| chr20:58891967
|
C | T | 1 | a0001c0001t0001g0161 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2069-3645C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58891967 | ||||||
| chr20:58892131
|
CTT | C | 6 | a0001c0001t0001g0190a0001c0001t0001g0240a0001c0001t0004g0235others(3): Show | 6 | HG02451.hp2 HG02818.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.2069-3480_2069-347 others(6): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58892131 | ||||||
| chr20:58892137
|
C | G | 1 | a0001c0001t0001g0158 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2069-3475C>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58892137 | ||||||
| chr20:58892151
|
C | T | 5 | a0001c0002t0001g0045a0002c0003t0002g0275a0002c0009t0002g0273others(2): Show | 5 | HG02148.hp1 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2069-3461C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58892151 | ||||||
| chr20:58892153
|
C | T | 3 | a0001c0001t0001g0125a0001c0001t0001g0237a0001c0001t0001g0241 | 3 | HG01069.hp2 HG01361.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.2069-3459C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58892153 | ||||||
| chr20:58892161
|
C | T | 4 | a0001c0006t0001g0207a0002c0003t0002g0249a0002c0003t0002g0252others(1): Show | 4 | HG00738.hp2 HG02965.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2069-3451C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58892161 | ||||||
| chr20:58892182
|
C | T | 2 | a0001c0001t0001g0144a0001c0001t0001g0238 | 2 | HG01433.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.2069-3430C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58892182 | ||||||
| chr20:58892216
|
G | T | 1 | a0001c0002t0001g0244 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2069-3396G>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58892216 | ||||||
| chr20:58892310
|
G | T | 5 | a0001c0001t0001g0023a0001c0001t0001g0082a0001c0001t0001g0100others(2): Show | 5 | HG00735.hp1 HG01168.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.2069-3302G>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58892310 | ||||||
| chr20:58892348
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2069-3264G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58892348 | ||||||
| chr20:58892610
|
G | C | 6 | a0001c0001t0001g0039a0001c0001t0001g0066a0001c0001t0001g0071others(3): Show | 6 | HG02165.hp2 NA18945.hp2 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.2069-3002G>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58892610 | ||||||
| chr20:58892922
|
A | C | 1 | a0001c0002t0001g0059 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2069-2690A>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58892922 | ||||||
| chr20:58893066
|
C | CT | 42 | a0001c0001t0001g0040a0001c0001t0001g0165a0001c0001t0001g0168others(39): Show | 44 | HG00099.hp1 HG00738.hp2 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.2069-2523dupT | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58893066 | |||||
| chr20:58893066
|
CTT | C | 6 | a0001c0001t0001g0175a0001c0001t0001g0177a0001c0002t0001g0044others(3): Show | 6 | HG01175.hp1 HG02723.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2069-2524_2069-252 others(6): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58893066 | |||||
| chr20:58893066
|
CTTT | C | 7 | a0001c0001t0001g0158a0001c0001t0001g0190a0001c0001t0001g0240others(4): Show | 7 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.2069-2525_2069-252 others(7): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58893066 | |||||
| chr20:58893066
|
CTTTTTT | C | 9 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0082others(6): Show | 9 | HG00735.hp1 HG00735.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.2069-2528_2069-252 others(10): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58893066 | |||||
| chr20:58893066
|
CTTTTTTT | C | 89 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(86): Show | 98 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.2069-2529_2069-252 others(11): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58893066 | |||||
| chr20:58893066
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0001g0196a0002c0003t0002g0257 | 2 | HG02572.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2069-2532_2069-252 others(14): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58893066 | |||||
| chr20:58893066
|
CTTTTTTT others(4): Show |
C | 20 | a0001c0001t0001g0057a0001c0001t0001g0136a0001c0001t0001g0155others(17): Show | 21 | HG00423.hp1 HG01106.hp1 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.2069-2533_2069-252 others(15): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58893066 | |||||
| chr20:58893095
|
C | T | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(176): Show | 191 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.2069-2517C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58893095 | ||||||
| chr20:58893246
|
T | A | 1 | a0001c0001t0001g0081 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2069-2366T>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58893246 | ||||||
| chr20:58893251
|
AAAT | A | 40 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0167others(37): Show | 41 | HG00738.hp2 HG01069.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.2069-2352_2069-235 others(7): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58893251 | |||||
| chr20:58893256
|
A | G | 2 | a0001c0001t0001g0224a0005c0011t0002g0267 | 2 | HG01109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2069-2356A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58893256 | ||||||
| chr20:58893338
|
A | T | 2 | a0001c0001t0001g0196a0002c0003t0002g0257 | 2 | HG02572.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2069-2274A>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58893338 | ||||||
| chr20:58893423
|
A | C | 40 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0167others(37): Show | 41 | HG00738.hp2 HG01069.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.2069-2189A>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58893423 | ||||||
| chr20:58893545
|
T | C | 1 | a0001c0002t0001g0146 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2069-2067T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58893545 | ||||||
| chr20:58893553
|
C | T | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2069-2059C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58893553 | ||||||
| chr20:58893643
|
A | G | 1 | a0001c0001t0001g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2069-1969A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58893643 | ||||||
| chr20:58893702
|
G | A | 1 | a0001c0001t0001g0119 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2069-1910G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58893702 | ||||||
| chr20:58893752
|
G | A | 93 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(90): Show | 102 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.2069-1860G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58893752 | ||||||
| chr20:58893918
|
C | T | 2 | a0001c0001t0001g0237a0001c0001t0001g0241 | 2 | HG01069.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.2069-1694C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58893918 | ||||||
| chr20:58894000
|
C | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(91): Show | 103 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.2069-1612C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58894000 | ||||||
| chr20:58894018
|
T | C | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(196): Show | 212 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.2069-1594T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58894018 | ||||||
| chr20:58894113
|
T | C | 1 | a0007c0026t0006g0232 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2069-1499T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58894113 | ||||||
| chr20:58894172
|
C | G | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(195): Show | 211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.2069-1440C>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58894172 | ||||||
| chr20:58894328
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2069-1284C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58894328 | ||||||
| chr20:58894387
|
A | C | 1 | a0001c0001t0001g0158 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2069-1225A>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58894387 | ||||||
| chr20:58894425
|
T | C | 16 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0191others(13): Show | 17 | HG01070.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.2069-1187T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58894425 | ||||||
| chr20:58894752
|
T | G | 1 | a0001c0001t0004g0242 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2069-860T>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58894752 | ||||||
| chr20:58894802
|
G | A | 1 | a0001c0001t0004g0242 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2069-810G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58894802 | ||||||
| chr20:58894857
|
C | G | 1 | a0001c0001t0001g0158 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2069-755C>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58894857 | ||||||
| chr20:58894936
|
T | A | 7 | a0001c0014t0001g0218a0001c0014t0001g0280a0002c0012t0002g0269others(4): Show | 7 | HG02145.hp1 HG02258.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2069-676T>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58894936 | ||||||
| chr20:58894965
|
G | T | 7 | a0001c0014t0001g0218a0001c0014t0001g0280a0002c0012t0002g0269others(4): Show | 7 | HG02145.hp1 HG02258.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2069-647G>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58894965 | ||||||
| chr20:58895361
|
AAAATT | A | 8 | a0001c0001t0001g0157a0001c0001t0001g0174a0001c0001t0001g0210others(5): Show | 8 | HG02630.hp1 HG02723.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.2069-247_2069-243d others(7): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58895361 | |||||
| chr20:58895462
|
G | A | 38 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0167others(35): Show | 39 | HG00738.hp2 HG01069.hp2 HG01123.hp2 others(36): Show |
intron_variant | MODIFIER | c.2069-150G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58895462 | ||||||
| chr20:58895534
|
AAAC | A | 5 | a0001c0001t0001g0175a0001c0001t0001g0177a0001c0006t0001g0180others(2): Show | 5 | HG01175.hp1 HG02723.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2069-70_2069-68del others(3): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 58895534 | |||||
| chr20:58895710
|
G | C | 1 | a0001c0004t0001g0201 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2141+26G>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 2/12 | chr20 | 58895710 | ||||||
| chr20:58896020
|
G | A | 1 | a0001c0002t0001g0101 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.2141+336G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 2/12 | chr20 | 58896020 | ||||||
| chr20:58896063
|
C | T | 3 | a0002c0010t0002g0272a0002c0018t0002g0261a0002c0019t0002g0262 | 3 | HG02258.hp2 HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2141+379C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 2/12 | chr20 | 58896063 | ||||||
| chr20:58896113
|
G | C | 1 | a0001c0002t0001g0148 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2141+429G>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 2/12 | chr20 | 58896113 | ||||||
| chr20:58896228
|
A | AT | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(175): Show | 190 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.2141+552dupT | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr20 | 58896228 | |||||
| chr20:58896496
|
C | T | 1 | a0001c0001t0001g0153 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2141+812C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 2/12 | chr20 | 58896496 | ||||||
| chr20:58896612
|
C | CAAAACGT others(5): Show |
1 | a0005c0011t0002g0268 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2141+933_2141+944d others(14): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr20 | 58896612 | |||||
| chr20:58896621
|
TAAA | T | 33 | a0001c0001t0001g0124a0001c0001t0001g0167a0001c0001t0001g0168others(30): Show | 34 | HG00738.hp2 HG01123.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.2141+948_2141+950d others(5): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr20 | 58896621 | |||||
| chr20:58896703
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2141+1019C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 2/12 | chr20 | 58896703 | ||||||
| chr20:58896755
|
G | A | 25 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0174others(22): Show | 26 | HG01175.hp1 HG02145.hp2 HG02148.hp1 others(23): Show |
intron_variant | MODIFIER | c.2141+1071G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 2/12 | chr20 | 58896755 | ||||||
| chr20:58896789
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2141+1105C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 2/12 | chr20 | 58896789 | ||||||
| chr20:58896912
|
C | T | 1 | a0001c0002t0001g0108 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2141+1228C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 2/12 | chr20 | 58896912 | ||||||
| chr20:58896988
|
A | G | 203 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(200): Show | 216 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.2141+1304A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 2/12 | chr20 | 58896988 | ||||||
| chr20:58897088
|
C | T | 2 | a0001c0023t0001g0233a0002c0021t0002g0271 | 2 | HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2141+1404C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 2/12 | chr20 | 58897088 | ||||||
| chr20:58897090
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2141+1406C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 2/12 | chr20 | 58897090 | ||||||
| chr20:58897119
|
C | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(199): Show | 215 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(212): Show |
intron_variant | MODIFIER | c.2141+1435C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 2/12 | chr20 | 58897119 | ||||||
| chr20:58897291
|
T | A | 1 | a0001c0001t0001g0053 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2141+1607T>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 2/12 | chr20 | 58897291 | ||||||
| chr20:58897424
|
C | T | 2 | a0001c0002t0001g0137a0001c0002t0001g0143 | 2 | HG02523.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.2142-1517C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 2/12 | chr20 | 58897424 | ||||||
| chr20:58897612
|
GCCAGCCT others(6): Show |
G | 1 | a0001c0001t0001g0237 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2142-1324_2142-131 others(17): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr20 | 58897612 | |||||
| chr20:58897812
|
C | T | 22 | a0001c0001t0001g0157a0001c0001t0001g0174a0001c0001t0001g0175others(19): Show | 23 | HG01175.hp1 HG02148.hp1 HG02559.hp2 others(20): Show |
intron_variant | MODIFIER | c.2142-1129C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 2/12 | chr20 | 58897812 | ||||||
| chr20:58897875
|
C | T | 1 | a0005c0011t0002g0268 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2142-1066C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 2/12 | chr20 | 58897875 | ||||||
| chr20:58897994
|
C | T | 3 | a0001c0001t0001g0144a0001c0001t0001g0238a0001c0004t0001g0015 | 4 | HG01433.hp2 HG02717.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2142-947C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 2/12 | chr20 | 58897994 | ||||||
| chr20:58898188
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2142-753G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 2/12 | chr20 | 58898188 | ||||||
| chr20:58898221
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2142-720C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 2/12 | chr20 | 58898221 | ||||||
| chr20:58898280
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2142-661G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 2/12 | chr20 | 58898280 | ||||||
| chr20:58898376
|
C | T | 1 | a0002c0003t0002g0264 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2142-565C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 2/12 | chr20 | 58898376 | ||||||
| chr20:58898577
|
G | A | 7 | a0001c0014t0001g0218a0001c0014t0001g0280a0002c0012t0002g0269others(4): Show | 7 | HG02145.hp1 HG02258.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2142-364G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 2/12 | chr20 | 58898577 | ||||||
| chr20:58898590
|
C | A | 1 | a0001c0001t0001g0157 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2142-351C>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 2/12 | chr20 | 58898590 | ||||||
| chr20:58898643
|
A | T | 1 | a0001c0001t0001g0121 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2142-298A>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 2/12 | chr20 | 58898643 | ||||||
| chr20:58898673
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2142-268C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 2/12 | chr20 | 58898673 | ||||||
| chr20:58899144
|
A | G | 6 | a0001c0001t0001g0190a0001c0001t0001g0240a0001c0001t0004g0235others(3): Show | 6 | HG02451.hp2 HG02818.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.2186+159A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58899144 | ||||||
| chr20:58899148
|
T | A | 1 | a0001c0001t0004g0242 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2186+163T>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58899148 | ||||||
| chr20:58899369
|
CTGA | C | 8 | a0001c0004t0001g0016a0001c0004t0001g0017a0001c0004t0001g0201others(5): Show | 9 | HG01884.hp1 HG02486.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.2186+386_2186+388d others(5): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr20 | 58899369 | |||||
| chr20:58899439
|
G | A | 1 | a0002c0003t0002g0277 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2186+454G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58899439 | ||||||
| chr20:58899468
|
C | T | 1 | a0007c0026t0006g0232 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2186+483C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58899468 | ||||||
| chr20:58899495
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2186+510C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58899495 | ||||||
| chr20:58899519
|
A | G | 1 | a0001c0001t0004g0242 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2186+534A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58899519 | ||||||
| chr20:58899586
|
A | T | 4 | a0001c0004t0001g0046a0001c0004t0001g0209a0001c0004t0001g0216others(1): Show | 4 | HG01243.hp1 HG02965.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2186+601A>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58899586 | ||||||
| chr20:58899604
|
C | T | 1 | a0001c0001t0001g0068 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2186+619C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58899604 | ||||||
| chr20:58899649
|
TCACA | T | 3 | a0001c0001t0001g0196a0002c0003t0002g0257a0005c0031t0002g0265 | 3 | HG02572.hp1 HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2186+676_2186+679d others(6): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr20 | 58899649 | |||||
| chr20:58899665
|
GCA | G | 88 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(85): Show | 97 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.2186+687_2186+688d others(4): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr20 | 58899665 | |||||
| chr20:58899695
|
G | A | 3 | a0001c0001t0001g0054a0001c0001t0001g0084a0001c0001t0001g0094 | 3 | HG02155.hp2 NA18950.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.2186+710G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58899695 | ||||||
| chr20:58899733
|
GCA | G | 6 | a0001c0001t0001g0190a0001c0001t0001g0240a0001c0001t0004g0235others(3): Show | 6 | HG02451.hp2 HG02818.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.2186+758_2186+759d others(4): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr20 | 58899733 | |||||
| chr20:58899735
|
A | G | 2 | a0001c0001t0001g0214a0005c0031t0002g0265 | 2 | HG00642.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2186+750A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58899735 | ||||||
| chr20:58900036
|
A | T | 1 | a0001c0002t0001g0103 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2186+1051A>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58900036 | ||||||
| chr20:58900067
|
T | C | 1 | a0001c0001t0001g0096 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2186+1082T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58900067 | ||||||
| chr20:58900136
|
A | G | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(212): Show | 230 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.2186+1151A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58900136 | ||||||
| chr20:58900277
|
T | C | 23 | a0001c0001t0001g0157a0001c0001t0001g0174a0001c0001t0001g0175others(20): Show | 24 | HG01175.hp1 HG02148.hp1 HG02559.hp2 others(21): Show |
intron_variant | MODIFIER | c.2186+1292T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58900277 | ||||||
| chr20:58900297
|
AAACCCTT others(1): Show |
A | 4 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0162others(1): Show | 4 | HG00558.hp2 HG00639.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.2186+1319_2186+132 others(12): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr20 | 58900297 | |||||
| chr20:58900327
|
T | C | 1 | a0001c0001t0004g0242 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2186+1342T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58900327 | ||||||
| chr20:58900528
|
G | A | 14 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0191others(11): Show | 15 | HG01123.hp2 HG01884.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.2186+1543G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58900528 | ||||||
| chr20:58900579
|
C | A | 1 | a0001c0001t0001g0217 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2186+1594C>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58900579 | ||||||
| chr20:58901050
|
C | T | 2 | a0001c0001t0001g0237a0001c0001t0001g0241 | 2 | HG01069.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.2186+2065C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58901050 | ||||||
| chr20:58901081
|
A | T | 1 | a0001c0008t0001g0073 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2186+2096A>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58901081 | ||||||
| chr20:58901143
|
A | T | 1 | a0001c0001t0001g0192 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2186+2158A>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58901143 | ||||||
| chr20:58901466
|
C | T | 1 | a0005c0031t0002g0265 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2187-2065C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58901466 | ||||||
| chr20:58901606
|
G | T | 7 | a0001c0001t0001g0190a0001c0001t0001g0204a0001c0001t0001g0240others(4): Show | 7 | HG02451.hp2 HG02818.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.2187-1925G>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58901606 | ||||||
| chr20:58901696
|
C | T | 1 | a0002c0012t0002g0269 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2187-1835C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58901696 | ||||||
| chr20:58901754
|
T | C | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(185): Show | 200 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(197): Show |
intron_variant | MODIFIER | c.2187-1777T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58901754 | ||||||
| chr20:58901774
|
A | G | 1 | a0002c0021t0002g0271 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2187-1757A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58901774 | ||||||
| chr20:58901780
|
G | C | 6 | a0001c0001t0001g0124a0001c0006t0001g0207a0002c0003t0002g0248others(3): Show | 6 | HG00738.hp2 HG02895.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.2187-1751G>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58901780 | ||||||
| chr20:58901816
|
G | A | 44 | a0001c0001t0001g0057a0001c0001t0001g0136a0001c0001t0001g0155others(41): Show | 46 | HG00423.hp1 HG01106.hp1 HG01175.hp1 others(43): Show |
intron_variant | MODIFIER | c.2187-1715G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58901816 | ||||||
| chr20:58901835
|
G | A | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(132): Show | 144 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.2187-1696G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58901835 | ||||||
| chr20:58901901
|
G | A | 1 | a0001c0014t0001g0280 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2187-1630G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58901901 | ||||||
| chr20:58901932
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2187-1599C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58901932 | ||||||
| chr20:58901961
|
TTA | T | 5 | a0001c0001t0001g0175a0001c0001t0001g0177a0001c0006t0001g0180others(2): Show | 5 | HG01175.hp1 HG02723.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2187-1566_2187-156 others(6): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr20 | 58901961 | |||||
| chr20:58902035
|
T | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(133): Show | 146 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.2187-1496T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58902035 | ||||||
| chr20:58902049
|
A | T | 146 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(143): Show | 158 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.2187-1482A>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58902049 | ||||||
| chr20:58902105
|
G | T | 1 | a0001c0002t0003g0052 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2187-1426G>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58902105 | ||||||
| chr20:58902122
|
TC | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(133): Show | 146 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.2187-1402delC | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr20 | 58902122 | |||||
| chr20:58902129
|
CT | C | 50 | a0001c0001t0001g0057a0001c0001t0001g0155a0001c0001t0001g0157others(47): Show | 52 | HG01106.hp1 HG01175.hp1 HG01256.hp1 others(49): Show |
intron_variant | MODIFIER | c.2187-1401delT | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58902129 | ||||||
| chr20:58902156
|
A | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(135): Show | 148 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.2187-1375A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58902156 | ||||||
| chr20:58902256
|
G | T | 7 | a0001c0001t0001g0190a0001c0001t0001g0204a0001c0001t0001g0240others(4): Show | 7 | HG02451.hp2 HG02818.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.2187-1275G>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58902256 | ||||||
| chr20:58902324
|
G | A | 1 | a0001c0002t0001g0075 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2187-1207G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58902324 | ||||||
| chr20:58902464
|
C | T | 4 | a0001c0002t0001g0091a0003c0005t0001g0018a0003c0005t0001g0228others(1): Show | 5 | HG00738.hp1 HG01070.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.2187-1067C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58902464 | ||||||
| chr20:58902589
|
C | A | 3 | a0001c0001t0001g0240a0001c0023t0001g0233a0002c0021t0002g0271 | 3 | HG03453.hp1 NA18906.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2187-942C>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58902589 | ||||||
| chr20:58902636
|
C | A | 1 | a0001c0001t0001g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2187-895C>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58902636 | ||||||
| chr20:58902640
|
T | C | 1 | a0001c0001t0001g0239 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2187-891T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58902640 | ||||||
| chr20:58902715
|
G | A | 1 | a0001c0002t0001g0127 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2187-816G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58902715 | ||||||
| chr20:58902725
|
C | CT | 18 | a0001c0001t0001g0190a0001c0001t0001g0221a0001c0001t0001g0240others(15): Show | 18 | HG00558.hp1 HG00597.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.2187-778dupT | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr20 | 58902725 | |||||
| chr20:58902725
|
C | CTT | 7 | a0001c0001t0001g0170a0001c0002t0001g0030a0001c0002t0001g0044others(4): Show | 7 | HG00423.hp2 HG01070.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.2187-779_2187-778d others(4): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr20 | 58902725 | |||||
| chr20:58902725
|
C | CTTTTT | 39 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0024others(36): Show | 42 | HG00597.hp1 HG00733.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.2187-782_2187-778d others(7): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr20 | 58902725 | |||||
| chr20:58902725
|
C | CTTTTTT | 33 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0013others(30): Show | 37 | HG00438.hp1 HG00438.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.2187-783_2187-778d others(8): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr20 | 58902725 | |||||
| chr20:58902725
|
C | CTTTTTTT | 17 | a0001c0001t0001g0076a0001c0001t0001g0081a0001c0001t0001g0082others(14): Show | 18 | HG00140.hp2 HG00558.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.2187-784_2187-778d others(9): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr20 | 58902725 | |||||
| chr20:58902725
|
C | CTTTTTTT others(2): Show |
6 | a0001c0001t0001g0214a0001c0001t0001g0217a0001c0001t0001g0224others(3): Show | 6 | HG00642.hp1 HG01109.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.2187-786_2187-778d others(11): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr20 | 58902725 | |||||
| chr20:58902725
|
C | CTTTTTTT others(3): Show |
6 | a0001c0001t0001g0124a0001c0006t0001g0207a0001c0022t0004g0197others(3): Show | 6 | HG02055.hp1 HG02895.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.2187-787_2187-778d others(12): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr20 | 58902725 | |||||
| chr20:58902725
|
C | CTTTTTTT others(5): Show |
5 | a0001c0001t0001g0191a0001c0002t0001g0007a0001c0023t0001g0233others(2): Show | 6 | HG01891.hp2 HG02809.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.2187-789_2187-778d others(14): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr20 | 58902725 | |||||
| chr20:58902725
|
C | CTTTTTTT others(6): Show |
2 | a0001c0014t0001g0218a0004c0028t0001g0188 | 2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.2187-790_2187-778d others(15): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr20 | 58902725 | |||||
| chr20:58902725
|
C | CTTTTTTT others(7): Show |
1 | a0002c0012t0002g0270 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2187-791_2187-778d others(16): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr20 | 58902725 | |||||
| chr20:58902725
|
C | CTTTTTTT others(8): Show |
5 | a0002c0010t0002g0272a0002c0012t0002g0269a0002c0018t0002g0261others(2): Show | 5 | HG02145.hp1 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2187-792_2187-778d others(17): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr20 | 58902725 | |||||
| chr20:58902725
|
C | CTTTTTTT others(9): Show |
1 | a0001c0001t0001g0192 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2187-793_2187-778d others(18): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr20 | 58902725 | |||||
| chr20:58902725
|
C | CTTTTTTT others(10): Show |
2 | a0001c0014t0001g0280a0002c0021t0002g0271 | 2 | HG02622.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2187-794_2187-778d others(19): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr20 | 58902725 | |||||
| chr20:58902725
|
CT | C | 35 | a0001c0001t0001g0057a0001c0001t0001g0136a0001c0001t0001g0157others(32): Show | 38 | HG00423.hp1 HG01106.hp1 HG01256.hp1 others(35): Show |
intron_variant | MODIFIER | c.2187-778delT | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr20 | 58902725 | |||||
| chr20:58902725
|
CTTTT | C | 6 | a0001c0002t0001g0005a0001c0002t0001g0195a0001c0002t0001g0205others(3): Show | 7 | HG00099.hp1 HG01109.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.2187-781_2187-778d others(6): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr20 | 58902725 | |||||
| chr20:58902725
|
CTTTTTTT others(2): Show |
C | 6 | a0001c0001t0001g0196a0001c0002t0001g0199a0001c0002t0001g0223others(3): Show | 7 | HG01891.hp1 HG02572.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2187-786_2187-778d others(11): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr20 | 58902725 | |||||
| chr20:58902725
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0159 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2187-788_2187-778d others(13): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr20 | 58902725 | |||||
| chr20:58902757
|
A | G | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(139): Show | 153 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.2187-774A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58902757 | ||||||
| chr20:58902881
|
G | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0182 | 3 | HG03490.hp2 HG03492.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2187-650G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58902881 | ||||||
| chr20:58902882
|
C | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0182 | 3 | HG03490.hp2 HG03492.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2187-649C>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58902882 | ||||||
| chr20:58902982
|
C | G | 1 | a0001c0002t0001g0047 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2187-549C>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58902982 | ||||||
| chr20:58902983
|
G | C | 1 | a0001c0002t0001g0047 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2187-548G>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58902983 | ||||||
| chr20:58903020
|
G | C | 1 | a0001c0001t0003g0022 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2187-511G>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58903020 | ||||||
| chr20:58903221
|
T | G | 1 | a0001c0001t0001g0240 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2187-310T>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58903221 | ||||||
| chr20:58903324
|
C | T | 1 | a0001c0006t0001g0180 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2187-207C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58903324 | ||||||
| chr20:58903341
|
A | G | 1 | a0001c0001t0001g0221 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2187-190A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58903341 | ||||||
| chr20:58903393
|
A | T | 69 | a0001c0001t0001g0035a0001c0001t0001g0057a0001c0001t0001g0125others(66): Show | 71 | HG00099.hp1 HG00423.hp1 HG00738.hp1 others(68): Show |
intron_variant | MODIFIER | c.2187-138A>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58903393 | ||||||
| chr20:58903642
|
T | C | 1 | a0001c0013t0001g0193 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2242-30T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 4/12 | chr20 | 58903642 | ||||||
| chr20:58903806
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2361+15G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 5/12 | chr20 | 58903806 | ||||||
| chr20:58903826
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2361+35C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 5/12 | chr20 | 58903826 | ||||||
| chr20:58903884
|
G | A | 104 | a0001c0001t0001g0125a0001c0001t0001g0128a0001c0001t0001g0157others(101): Show | 110 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.2361+93G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 5/12 | chr20 | 58903884 | ||||||
| chr20:58904019
|
C | T | 2 | a0001c0001t0005g0097a0001c0001t0005g0098 | 2 | HG01081.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.2361+228C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 5/12 | chr20 | 58904019 | ||||||
| chr20:58904078
|
A | G | 78 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0040others(75): Show | 82 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.2361+287A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 5/12 | chr20 | 58904078 | ||||||
| chr20:58904221
|
C | T | 71 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0089others(68): Show | 74 | HG00099.hp1 HG00558.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.2361+430C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 5/12 | chr20 | 58904221 | ||||||
| chr20:58904303
|
T | TTTAACA | 14 | a0001c0001t0001g0040a0001c0001t0001g0157a0001c0001t0001g0159others(11): Show | 15 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.2361+514_2361+515i others(8): Show |
GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr20 | 58904303 | |||||
| chr20:58904382
|
C | T | 280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(277): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.2361+591C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 5/12 | chr20 | 58904382 | ||||||
| chr20:58904437
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2361+646C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 5/12 | chr20 | 58904437 | ||||||
| chr20:58904438
|
G | A | 8 | a0001c0001t0001g0159a0001c0001t0001g0217a0001c0001t0001g0219others(5): Show | 9 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.2361+647G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 5/12 | chr20 | 58904438 | ||||||
| chr20:58904507
|
T | C | 1 | a0001c0002t0001g0156 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2361+716T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 5/12 | chr20 | 58904507 | ||||||
| chr20:58904547
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2361+756G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 5/12 | chr20 | 58904547 | ||||||
| chr20:58904745
|
T | A | 1 | a0001c0002t0001g0045 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2362-638T>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 5/12 | chr20 | 58904745 | ||||||
| chr20:58904794
|
T | C | 1 | a0001c0002t0001g0137 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2362-589T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 5/12 | chr20 | 58904794 | ||||||
| chr20:58904818
|
T | C | 1 | a0002c0003t0002g0248 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2362-565T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 5/12 | chr20 | 58904818 | ||||||
| chr20:58904870
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0212others(1): Show | 6 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.2362-513G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 5/12 | chr20 | 58904870 | ||||||
| chr20:58904961
|
C | T | 13 | a0001c0001t0001g0040a0001c0001t0001g0157a0001c0001t0001g0159others(10): Show | 14 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.2362-422C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 5/12 | chr20 | 58904961 | ||||||
| chr20:58904980
|
T | A | 1 | a0001c0002t0001g0047 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2362-403T>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 5/12 | chr20 | 58904980 | ||||||
| chr20:58904988
|
C | T | 8 | a0001c0001t0001g0159a0001c0001t0001g0217a0001c0001t0001g0219others(5): Show | 9 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.2362-395C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 5/12 | chr20 | 58904988 | ||||||
| chr20:58905312
|
G | T | 13 | a0001c0001t0001g0040a0001c0001t0001g0157a0001c0001t0001g0159others(10): Show | 14 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.2362-71G>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 5/12 | chr20 | 58905312 | ||||||
| chr20:58905365
|
T | C | 31 | a0001c0001t0001g0125a0001c0001t0001g0128a0001c0001t0001g0174others(28): Show | 31 | HG00558.hp1 HG00597.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.2362-18T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 5/12 | chr20 | 58905365 | ||||||
| chr20:58905878
|
T | C | 183 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0021others(180): Show | 197 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.2459+398T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 6/12 | chr20 | 58905878 | ||||||
| chr20:58905921
|
G | A | 1 | a0001c0001t0001g0240 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2459+441G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 6/12 | chr20 | 58905921 | ||||||
| chr20:58906093
|
A | G | 182 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0021others(179): Show | 196 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.2459+613A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 6/12 | chr20 | 58906093 | ||||||
| chr20:58906093
|
A | T | 1 | a0001c0002t0001g0148 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2459+613A>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 6/12 | chr20 | 58906093 | ||||||
| chr20:58906176
|
C | T | 1 | a0002c0003t0002g0248 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2459+696C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 6/12 | chr20 | 58906176 | ||||||
| chr20:58906425
|
G | A | 8 | a0001c0001t0001g0159a0001c0001t0001g0217a0001c0001t0001g0219others(5): Show | 9 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.2459+945G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 6/12 | chr20 | 58906425 | ||||||
| chr20:58906532
|
C | G | 133 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0035others(130): Show | 143 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.2459+1052C>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 6/12 | chr20 | 58906532 | ||||||
| chr20:58906819
|
C | T | 9 | a0001c0001t0001g0159a0001c0001t0001g0217a0001c0001t0001g0219others(6): Show | 10 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.2459+1339C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 6/12 | chr20 | 58906819 | ||||||
| chr20:58907015
|
T | G | 7 | a0001c0001t0001g0067a0001c0001t0001g0072a0001c0001t0001g0083others(4): Show | 7 | HG00639.hp1 HG00733.hp2 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.2459+1535T>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 6/12 | chr20 | 58907015 | ||||||
| chr20:58907296
|
G | A | 2 | a0001c0023t0001g0233a0002c0021t0002g0271 | 2 | HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2459+1816G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 6/12 | chr20 | 58907296 | ||||||
| chr20:58907311
|
A | T | 1 | a0001c0001t0001g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2459+1831A>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 6/12 | chr20 | 58907311 | ||||||
| chr20:58907385
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2460-1777T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 6/12 | chr20 | 58907385 | ||||||
| chr20:58907453
|
A | G | 1 | a0004c0027t0001g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2460-1709A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 6/12 | chr20 | 58907453 | ||||||
| chr20:58907535
|
G | T | 11 | a0001c0013t0001g0176a0001c0014t0001g0218a0001c0014t0001g0280others(8): Show | 11 | HG02145.hp1 HG02258.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2460-1627G>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 6/12 | chr20 | 58907535 | ||||||
| chr20:58907590
|
T | C | 1 | a0001c0001t0001g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2460-1572T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 6/12 | chr20 | 58907590 | ||||||
| chr20:58907950
|
T | C | 3 | a0001c0004t0001g0017a0001c0004t0001g0202a0001c0004t0001g0234 | 4 | HG03139.hp2 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2460-1212T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 6/12 | chr20 | 58907950 | ||||||
| chr20:58908246
|
T | C | 2 | a0001c0023t0001g0233a0002c0021t0002g0271 | 2 | HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2460-916T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 6/12 | chr20 | 58908246 | ||||||
| chr20:58908484
|
A | G | 2 | a0001c0001t0001g0241a0001c0002t0001g0171 | 2 | HG00733.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.2460-678A>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 6/12 | chr20 | 58908484 | ||||||
| chr20:58908600
|
T | C | 47 | a0001c0001t0001g0050a0001c0001t0001g0141a0001c0001t0001g0184others(44): Show | 51 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.2460-562T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 6/12 | chr20 | 58908600 | ||||||
| chr20:58908800
|
G | T | 3 | a0001c0002t0001g0010a0001c0002t0001g0126a0002c0003t0002g0249 | 4 | HG01255.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2460-362G>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 6/12 | chr20 | 58908800 | ||||||
| chr20:58908864
|
G | A | 1 | a0001c0002t0001g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2460-298G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 6/12 | chr20 | 58908864 | ||||||
| chr20:58908867
|
C | G | 1 | a0001c0001t0001g0124 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2460-295C>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 6/12 | chr20 | 58908867 | ||||||
| chr20:58908893
|
G | A | 184 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0035others(181): Show | 198 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.2460-269G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 6/12 | chr20 | 58908893 | ||||||
| chr20:58908902
|
A | C | 2 | a0001c0001t0001g0210a0002c0003t0002g0277 | 2 | HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2460-260A>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 6/12 | chr20 | 58908902 | ||||||
| chr20:58909030
|
T | C | 76 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0021others(73): Show | 83 | HG00099.hp1 HG00558.hp1 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.2460-132T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 6/12 | chr20 | 58909030 | ||||||
| chr20:58909062
|
C | T | 1 | a0001c0002t0001g0103 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2460-100C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 6/12 | chr20 | 58909062 | ||||||
| chr20:58909271
|
C | G | 23 | a0001c0004t0001g0015a0001c0004t0001g0016a0001c0004t0001g0017others(20): Show | 25 | HG00639.hp2 HG01070.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.2514+55C>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 7/12 | chr20 | 58909271 | ||||||
| chr20:58909308
|
G | A | 2 | a0001c0001t0001g0241a0001c0002t0001g0171 | 2 | HG00733.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.2515-42G>A | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 7/12 | chr20 | 58909308 | ||||||
| chr20:58909474
|
T | G | 1 | a0001c0001t0001g0211 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2589-47T>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 8/12 | chr20 | 58909474 | ||||||
| chr20:58909828
|
C | G | 1 | a0001c0001t0001g0066 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2768+24C>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 10/12 | chr20 | 58909828 | ||||||
| chr20:58909879
|
C | T | 17 | a0001c0001t0001g0124a0001c0001t0001g0144a0001c0001t0001g0158others(14): Show | 19 | HG01255.hp1 HG01433.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.2769-72C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 10/12 | chr20 | 58909879 | ||||||
| chr20:58909892
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2769-59C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 10/12 | chr20 | 58909892 | ||||||
| chr20:58910464
|
T | G | 1 | a0002c0018t0002g0261 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2967+63T>G | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 12/12 | chr20 | 58910464 | ||||||
| chr20:58910556
|
T | C | 185 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0021others(182): Show | 200 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.2968-127T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 12/12 | chr20 | 58910556 |