Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MGVRN others(1032): Show |
chr20 | 58847716 | 58916192 |
| a0002 | 0/0 | 1049 | 32 | 23 | 6 | 2 | 0 | 1 | 1 | GNAS_chr20_58847716_58916192 | GNAS | MGVRN others(1044): Show |
chr20 | 58847716 | 58916192 |
| a0003 | 0/0 | 1037 | 8 | 1 | 6 | 0 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | MGVRN others(1032): Show |
chr20 | 58847716 | 58916192 |
| a0004 | 0/0 | 1040 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | MGVRN others(1035): Show |
chr20 | 58847716 | 58916192 |
| a0005 | 0/0 | 1049 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | MGVRN others(1044): Show |
chr20 | 58847716 | 58916192 |
| a0006 | 0/0 | 1037 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | MGVRN others(1032): Show |
chr20 | 58847716 | 58916192 |
| a0007 | 0/0 | 1028 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | MGVRN others(1023): Show |
chr20 | 58847716 | 58916192 |
| a0008 | 0/0 | 1037 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | MGVRN others(1032): Show |
chr20 | 58847716 | 58916192 |
| a0009 | 0/0 | 1037 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | MGVRN others(1032): Show |
chr20 | 58847716 | 58916192 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 3111 | 118 | 25 | 33 | 42 | 7 | 11 | GNAS_chr20_58847716_58916192 | GNAS | ATGGG others(3106): Show |
chr20 | 58847716 | 58916192 | ||
| a0001c0002 | 1/1 | 3111 | 100 | 9 | 18 | 52 | 6 | 13 | GNAS_chr20_58847716_58916192 | GNAS | ATGGG others(3106): Show |
chr20 | 58847716 | 58916192 | ||
| a0001c0004 | 0/0 | 3111 | 13 | 12 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | ATGGG others(3106): Show |
chr20 | 58847716 | 58916192 | ||
| a0001c0006 | 0/0 | 3111 | 5 | 5 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | ATGGG others(3106): Show |
chr20 | 58847716 | 58916192 | ||
| a0001c0008 | 0/0 | 3111 | 4 | 1 | 2 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | ATGGG others(3106): Show |
chr20 | 58847716 | 58916192 | ||
| a0001c0013 | 0/0 | 3111 | 2 | 2 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | ATGGG others(3106): Show |
chr20 | 58847716 | 58916192 | ||
| a0001c0014 | 0/0 | 3111 | 2 | 2 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | ATGGG others(3106): Show |
chr20 | 58847716 | 58916192 | ||
| a0001c0020 | 0/0 | 3111 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | ATGGG others(3106): Show |
chr20 | 58847716 | 58916192 | ||
| a0001c0022 | 0/0 | 3111 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | ATGGG others(3106): Show |
chr20 | 58847716 | 58916192 | ||
| a0001c0023 | 0/0 | 3111 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | ATGGG others(3106): Show |
chr20 | 58847716 | 58916192 | ||
| a0001c0025 | 0/0 | 3111 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | ATGGG others(3106): Show |
chr20 | 58847716 | 58916192 | ||
| a0001c0029 | 0/0 | 3111 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | ATGGG others(3106): Show |
chr20 | 58847716 | 58916192 | ||
| a0001c0030 | 0/0 | 3111 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | ATGGG others(3106): Show |
chr20 | 58847716 | 58916192 | ||
| a0002c0003 | 0/0 | 3147 | 17 | 11 | 3 | 2 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | ATGGG others(3142): Show |
chr20 | 58847716 | 58916192 | ||
| a0002c0007 | 0/0 | 3147 | 4 | 2 | 2 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | ATGGG others(3142): Show |
chr20 | 58847716 | 58916192 | ||
| a0002c0009 | 0/0 | 3147 | 3 | 2 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | ATGGG others(3142): Show |
chr20 | 58847716 | 58916192 | ||
| a0002c0010 | 0/0 | 3147 | 3 | 3 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | ATGGG others(3142): Show |
chr20 | 58847716 | 58916192 | ||
| a0002c0012 | 0/0 | 3147 | 2 | 2 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | ATGGG others(3142): Show |
chr20 | 58847716 | 58916192 | ||
| a0002c0018 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | ATGGG others(3142): Show |
chr20 | 58847716 | 58916192 | ||
| a0002c0019 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | ATGGG others(3142): Show |
chr20 | 58847716 | 58916192 | ||
| a0002c0021 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | ATGGG others(3142): Show |
chr20 | 58847716 | 58916192 | ||
| a0003c0005 | 0/0 | 3111 | 6 | 1 | 4 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | ATGGG others(3106): Show |
chr20 | 58847716 | 58916192 | ||
| a0003c0016 | 0/0 | 3111 | 2 | 0 | 2 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | ATGGG others(3106): Show |
chr20 | 58847716 | 58916192 | ||
| a0004c0015 | 0/0 | 3120 | 2 | 2 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | ATGGG others(3115): Show |
chr20 | 58847716 | 58916192 | ||
| a0004c0027 | 0/0 | 3120 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | ATGGG others(3115): Show |
chr20 | 58847716 | 58916192 | ||
| a0004c0028 | 0/0 | 3120 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | ATGGG others(3115): Show |
chr20 | 58847716 | 58916192 | ||
| a0005c0011 | 0/0 | 3147 | 3 | 3 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | ATGGG others(3142): Show |
chr20 | 58847716 | 58916192 | ||
| a0005c0031 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | ATGGG others(3142): Show |
chr20 | 58847716 | 58916192 | ||
| a0006c0017 | 0/0 | 3111 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | ATGGG others(3106): Show |
chr20 | 58847716 | 58916192 | ||
| a0007c0026 | 0/0 | 3084 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | ATGGG others(3079): Show |
chr20 | 58847716 | 58916192 | ||
| a0008c0032 | 0/0 | 3111 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | ATGGG others(3106): Show |
chr20 | 58847716 | 58916192 | ||
| a0009c0024 | 0/0 | 3111 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | ATGGG others(3106): Show |
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 | AGACT others(4022): Show |
chr20 | 58847716 | 58916192 |
| a0001c0001t0003 | 0/0 | 4027 | 7 | 0 | 0 | 7 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | AGACT others(4022): Show |
chr20 | 58847716 | 58916192 |
| a0001c0001t0004 | 0/0 | 4027 | 2 | 2 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | AGACT others(4022): Show |
chr20 | 58847716 | 58916192 |
| a0001c0001t0005 | 0/0 | 4027 | 2 | 0 | 2 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | AGACT others(4022): Show |
chr20 | 58847716 | 58916192 |
| a0001c0002t0001 | 1/1 | 4027 | 87 | 9 | 18 | 39 | 6 | 13 | GNAS_chr20_58847716_58916192 | GNAS | AGACT others(4022): Show |
chr20 | 58847716 | 58916192 |
| a0001c0002t0003 | 0/0 | 4027 | 13 | 0 | 0 | 13 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | AGACT others(4022): Show |
chr20 | 58847716 | 58916192 |
| a0001c0004t0001 | 0/0 | 4027 | 12 | 11 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | AGACT others(4022): Show |
chr20 | 58847716 | 58916192 |
| a0001c0004t0004 | 0/0 | 4027 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | AGACT others(4022): Show |
chr20 | 58847716 | 58916192 |
| a0001c0006t0001 | 0/0 | 4027 | 5 | 5 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | AGACT others(4022): Show |
chr20 | 58847716 | 58916192 |
| a0001c0008t0001 | 0/0 | 4027 | 4 | 1 | 2 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | AGACT others(4022): Show |
chr20 | 58847716 | 58916192 |
| a0001c0013t0001 | 0/0 | 4027 | 2 | 2 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | AGACT others(4022): Show |
chr20 | 58847716 | 58916192 |
| a0001c0014t0001 | 0/0 | 4027 | 2 | 2 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | AGACT others(4022): Show |
chr20 | 58847716 | 58916192 |
| a0001c0020t0001 | 0/0 | 4027 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | AGACT others(4022): Show |
chr20 | 58847716 | 58916192 |
| a0001c0022t0004 | 0/0 | 4027 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | AGACT others(4022): Show |
chr20 | 58847716 | 58916192 |
| a0001c0023t0001 | 0/0 | 4027 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | AGACT others(4022): Show |
chr20 | 58847716 | 58916192 |
| a0001c0025t0001 | 0/0 | 4027 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | AGACT others(4022): Show |
chr20 | 58847716 | 58916192 |
| a0001c0029t0001 | 0/0 | 4027 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | AGACT others(4022): Show |
chr20 | 58847716 | 58916192 |
| a0001c0030t0001 | 0/0 | 4027 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | AGACT others(4022): Show |
chr20 | 58847716 | 58916192 |
| a0002c0003t0002 | 0/0 | 4063 | 17 | 11 | 3 | 2 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | AGACT others(4058): Show |
chr20 | 58847716 | 58916192 |
| a0002c0007t0002 | 0/0 | 4063 | 4 | 2 | 2 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | AGACT others(4058): Show |
chr20 | 58847716 | 58916192 |
| a0002c0009t0002 | 0/0 | 4063 | 3 | 2 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | AGACT others(4058): Show |
chr20 | 58847716 | 58916192 |
| a0002c0010t0002 | 0/0 | 4063 | 3 | 3 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | AGACT others(4058): Show |
chr20 | 58847716 | 58916192 |
| a0002c0012t0002 | 0/0 | 4063 | 2 | 2 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | AGACT others(4058): Show |
chr20 | 58847716 | 58916192 |
| a0002c0018t0002 | 0/0 | 4063 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | AGACT others(4058): Show |
chr20 | 58847716 | 58916192 |
| a0002c0019t0002 | 0/0 | 4063 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | AGACT others(4058): Show |
chr20 | 58847716 | 58916192 |
| a0002c0021t0002 | 0/0 | 4063 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | AGACT others(4058): Show |
chr20 | 58847716 | 58916192 |
| a0003c0005t0001 | 0/0 | 4027 | 6 | 1 | 4 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | AGACT others(4022): Show |
chr20 | 58847716 | 58916192 |
| a0003c0016t0001 | 0/0 | 4027 | 2 | 0 | 2 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | AGACT others(4022): Show |
chr20 | 58847716 | 58916192 |
| a0004c0015t0001 | 0/0 | 4036 | 2 | 2 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | AGACT others(4031): Show |
chr20 | 58847716 | 58916192 |
| a0004c0027t0001 | 0/0 | 4036 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | AGACT others(4031): Show |
chr20 | 58847716 | 58916192 |
| a0004c0028t0001 | 0/0 | 4036 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | AGACT others(4031): Show |
chr20 | 58847716 | 58916192 |
| a0005c0011t0002 | 0/0 | 4063 | 3 | 3 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | AGACT others(4058): Show |
chr20 | 58847716 | 58916192 |
| a0005c0031t0002 | 0/0 | 4063 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | AGACT others(4058): Show |
chr20 | 58847716 | 58916192 |
| a0006c0017t0001 | 0/0 | 4027 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | AGACT others(4022): Show |
chr20 | 58847716 | 58916192 |
| a0007c0026t0006 | 0/0 | 4000 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | AGACT others(3995): Show |
chr20 | 58847716 | 58916192 |
| a0008c0032t0003 | 0/0 | 4027 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | AGACT others(4022): Show |
chr20 | 58847716 | 58916192 |
| a0009c0024t0001 | 0/0 | 4027 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | AGACT others(4022): Show |
chr20 | 58847716 | 58916192 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 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 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 1 | 1 | 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 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0091 | 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 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 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 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 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 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0209 | 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 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0001g0240 | 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 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0003g0111 | 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 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0001t0005g0096 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0005 | 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 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0059 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0100 | 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 |
| a0001c0002t0001g0106 | 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 | 0 | 1 | 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 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0138 | 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 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0002t0001g0144 | 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 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
| 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 |
| a0001c0004t0001g0200 | 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 |
| a0001c0004t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0004t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0004t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0004t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0006t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0006t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0006t0001g0205 | 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 |
| a0001c0006t0001g0221 | 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 |
| a0001c0008t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0008t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0008t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0013t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0013t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0014t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0014t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0020t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0022t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0023t0001g0232 | 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 |
| a0001c0029t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0001c0030t0001g0219 | 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 |
| a0002c0003t0002g0247 | 0/0 | 1 | 1 | 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 |
| a0002c0003t0002g0251 | 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 |
| a0002c0003t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0003t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0003t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0003t0002g0257 | 0/0 | 1 | 0 | 1 | 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 |
| a0002c0003t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0003t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0003t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0002c0007t0002g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0007t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0007t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0009t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0009t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0009t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0010t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0010t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0010t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0012t0002g0268 | 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 |
| a0002c0018t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0019t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0002c0021t0002g0270 | 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 |
| a0003c0005t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0003c0005t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0003c0005t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0003c0005t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0003c0016t0001g0228 | 0/0 | 1 | 0 | 1 | 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 |
| a0004c0015t0001g0185 | 0/0 | 1 | 1 | 0 | 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 |
| a0004c0027t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0004c0028t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0005c0011t0002g0265 | 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 |
| a0005c0031t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0006c0017t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0007c0026t0006g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0008c0032t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| a0009c0024t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | g0212 | EUR | GBR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0060 | EUR | GBR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0113 | EUR | GBR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0235 | EUR | GBR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0063 | 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 | g0162 | 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 | g0134 | 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 | g0079 | EAS | CHS | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0150 | 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 | g0130 | 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 | g0149 | EAS | CHS | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0098 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG00639 | hp2 | a0001 | c0008 | t0001 | g0128 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0170 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0106 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG00735 | hp1 | a0003 | c0005 | t0001 | g0225 | 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 | g0228 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG00738 | hp2 | a0002 | c0007 | t0002 | g0250 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0245 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0090 | 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 | g0236 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01070 | hp1 | a0001 | c0008 | t0001 | g0075 | 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 | g0097 | 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 | g0257 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0058 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0099 | 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 | g0169 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0174 | 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 | g0161 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01243 | hp1 | a0001 | c0004 | t0001 | g0215 | 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 | g0125 | AMR | CLM | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0076 | AMR | CLM | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01256 | hp1 | a0002 | c0003 | t0002 | g0258 | AMR | CLM | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01256 | hp2 | a0003 | c0016 | t0001 | g0229 | AMR | CLM | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0100 | AMR | CLM | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01258 | hp2 | a0002 | c0003 | t0002 | g0259 | AMR | CLM | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01261 | hp2 | a0001 | c0001 | t0005 | g0096 | AMR | CLM | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0246 | AMR | CLM | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01496 | hp1 | a0003 | c0005 | t0001 | g0227 | 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 | g0171 | EUR | IBS | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0194 | 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 | g0172 | EUR | IBS | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01884 | hp1 | a0001 | c0004 | t0001 | g0202 | AFR | ACB | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01884 | hp2 | a0004 | c0027 | t0001 | g0184 | 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 | g0190 | AFR | ACB | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01943 | hp1 | a0002 | c0007 | t0002 | g0253 | AMR | PEL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0101 | AMR | PEL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0243 | AMR | PEL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0204 | 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 | g0107 | AMR | PEL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02027 | hp1 | a0006 | c0017 | t0001 | g0104 | EAS | KHV | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | KHV | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02055 | hp1 | a0007 | c0026 | t0006 | g0231 | AFR | ACB | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0108 | 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 | a0008 | 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 | g0263 | EAS | KHV | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02145 | hp1 | a0002 | c0012 | t0002 | g0268 | AFR | ACB | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02148 | hp1 | a0002 | c0009 | t0002 | g0273 | AMR | PEL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0006 | 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 | g0073 | EAS | CDX | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02258 | hp1 | a0002 | c0012 | t0002 | g0269 | AFR | ACB | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02258 | hp2 | a0002 | c0018 | t0002 | g0260 | AFR | ACB | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0121 | AMR | PEL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02451 | hp2 | a0001 | c0020 | t0001 | g0207 | AFR | ACB | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0136 | EAS | KHV | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0114 | EAS | KHV | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0222 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02615 | hp1 | a0001 | c0014 | t0001 | g0217 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02615 | hp2 | a0002 | c0003 | t0002 | g0274 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02622 | hp2 | a0001 | c0014 | t0001 | g0279 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02630 | hp2 | a0005 | c0031 | t0002 | g0264 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02647 | hp1 | a0004 | c0028 | t0001 | g0187 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0198 | 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 | g0179 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0116 | SAS | PJL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02735 | hp2 | a0003 | c0005 | t0001 | g0226 | SAS | PJL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02738 | hp1 | a0001 | c0029 | t0001 | g0105 | SAS | PJL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0061 | SAS | PJL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02809 | hp1 | a0004 | c0015 | t0001 | g0185 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02809 | hp2 | a0002 | c0003 | t0002 | g0276 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0234 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0176 | 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 | g0247 | 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 | g0262 | AFR | ESN | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ESN | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02965 | hp1 | a0001 | c0006 | t0001 | g0206 | 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 | g0278 | AFR | ESN | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02970 | hp2 | a0005 | c0011 | t0002 | g0267 | AFR | ESN | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02976 | hp1 | a0002 | c0019 | t0002 | g0261 | AFR | ESN | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02976 | hp2 | a0003 | c0005 | t0001 | g0230 | AFR | ESN | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03041 | hp1 | a0002 | c0003 | t0002 | g0248 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03041 | hp2 | a0002 | c0009 | t0002 | g0277 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0203 | 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 | g0275 | 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 | g0208 | 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 | g0156 | AFR | MSL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | MSL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03225 | hp1 | a0001 | c0030 | t0001 | g0219 | AFR | MSL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03225 | hp2 | a0002 | c0003 | t0002 | g0252 | 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 | g0244 | SAS | PJL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03453 | hp1 | a0001 | c0023 | t0001 | g0232 | AFR | MSL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03453 | hp2 | a0002 | c0010 | t0002 | g0271 | AFR | MSL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0123 | 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 | g0064 | 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 | g0183 | SAS | PJL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0137 | 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 | g0251 | 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 | g0191 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03579 | hp1 | a0002 | c0003 | t0002 | g0256 | AFR | MSL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03579 | hp2 | a0001 | c0013 | t0001 | g0192 | AFR | MSL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0087 | SAS | PJL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0159 | SAS | PJL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0066 | SAS | BEB | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0182 | 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 | a0009 | c0024 | t0001 | g0197 | SAS | BEB | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | STU | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0153 | 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 | g0092 | SAS | BEB | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0193 | SAS | STU | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG04204 | hp2 | a0002 | c0003 | t0002 | g0255 | SAS | STU | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18522 | hp1 | a0005 | c0011 | t0002 | g0266 | AFR | YRI | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18522 | hp2 | a0001 | c0006 | t0001 | g0205 | AFR | YRI | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0148 | 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 | g0249 | AFR | YRI | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18906 | hp2 | a0002 | c0021 | t0002 | g0270 | AFR | YRI | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0085 | 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 | g0001 | 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 | g0081 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0088 | 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 | g0163 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0146 | 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 | g0154 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0006 | 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 | g0138 | 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 | g0082 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0109 | 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 | g0155 | 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 | g0151 | 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 | g0112 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0115 | 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 | g0069 | 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 | g0142 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19030 | hp1 | a0001 | c0004 | t0001 | g0233 | AFR | LWK | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | LWK | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0126 | 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 | g0119 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0067 | 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 | g0071 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0147 | 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 | g0089 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0086 | 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 | g0254 | 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 | g0139 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19240 | hp1 | a0001 | c0006 | t0001 | g0199 | AFR | YRI | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0241 | AFR | YRI | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA20129 | hp1 | a0001 | c0004 | t0004 | g0188 | AFR | ASW | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0242 | AFR | ASW | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0181 | EUR | TSI | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0143 | EUR | TSI | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA20805 | hp1 | a0001 | c0008 | t0001 | g0062 | EUR | TSI | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0152 | EUR | TSI | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | GIH | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | GIH | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0102 | AMR | CLM | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02486 | hp1 | a0004 | c0015 | t0001 | g0186 | AFR | ACB | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02486 | hp2 | a0001 | c0004 | t0001 | g0200 | AFR | ACB | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG02559 | hp2 | a0001 | c0006 | t0001 | g0221 | AFR | ACB | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03471 | hp1 | a0002 | c0009 | t0002 | g0272 | AFR | MSL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG03471 | hp2 | a0001 | c0004 | t0001 | g0201 | AFR | MSL | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG06807 | hp1 | a0005 | c0011 | t0002 | g0265 | AFR | USA | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| HG06807 | hp2 | a0001 | c0013 | t0001 | g0175 | 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 | g0196 | AFR | USA | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0072 | AFR | USA | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | LWK | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | LWK | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0059 | REF | REF | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0140 | REF | REF | GNAS_chr20_58847716_58916192 | GNAS | chr20 | 58847716 | 58916192 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:58853551 | C | G | 1 | a0008 | 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 | a0006 | 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 | a0002 a0005 |
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 | a0002 a0005 |
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 | a0009 | 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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:58853790 | T | C | 2 | a0002c0018 a0002c0019 |
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 | a0001c0006 a0001c0020 |
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 | a0001c0023 a0002c0021 |
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 | a0001c0023 a0002c0021 |
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 | a0001c0001 a0001c0004 a0001c0006 others(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 | a0001c0014 a0001c0030 a0002c0012 others(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 | a0001c0004 a0001c0008 a0001c0013 others(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 | a0001c0013 a0002c0019 |
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 | a0001c0004 a0001c0008 a0001c0020 others(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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0002c0003t0002 a0002c0007t0002 a0002c0009t0002 others(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 | a0001c0001t0004 a0001c0004t0004 a0001c0022t0004 |
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 | a0001c0001t0003 a0001c0002t0003 a0008c0032t0003 |
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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:58855372 | C | T | 1 | a0001c0014t0001g0279 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0183 a0001c0001t0001g0189 others(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 | a0002c0003t0002g0020 a0002c0003t0002g0247 a0002c0003t0002g0248 others(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 | a0002c0003t0002g0020 a0002c0003t0002g0274 a0002c0003t0002g0275 others(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 | a0002c0003t0002g0020 a0002c0003t0002g0247 a0002c0003t0002g0248 others(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 | a0001c0001t0001g0183 | 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 | a0001c0002t0001g0242 a0001c0002t0001g0243 a0001c0002t0001g0244 others(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 | a0004c0015t0001g0185 a0004c0015t0001g0186 a0004c0027t0001g0184 others(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 | a0002c0003t0002g0020 a0002c0003t0002g0274 a0002c0003t0002g0275 others(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 | a0001c0001t0004g0241 | 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 | a0001c0001t0001g0183 a0001c0001t0001g0189 a0001c0001t0001g0190 others(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 | a0004c0015t0001g0185 a0004c0015t0001g0186 a0004c0027t0001g0184 others(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 | a0005c0011t0002g0265 a0005c0011t0002g0266 a0005c0011t0002g0267 others(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 | a0001c0001t0001g0182 | 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 | a0005c0011t0002g0265 a0005c0011t0002g0266 a0005c0011t0002g0267 |
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 | a0001c0001t0001g0240 | 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 | a0004c0015t0001g0185 a0004c0015t0001g0186 a0004c0027t0001g0184 others(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 | a0002c0003t0002g0020 a0002c0003t0002g0247 a0002c0003t0002g0248 others(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 | a0002c0010t0002g0278 | 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 | a0001c0002t0001g0198 | 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 | a0001c0001t0001g0035 a0001c0002t0001g0003 a0001c0002t0001g0026 others(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 | a0002c0003t0002g0020 a0002c0003t0002g0274 a0002c0003t0002g0275 others(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 | a0004c0015t0001g0185 a0004c0015t0001g0186 a0004c0027t0001g0184 |
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 | a0001c0001t0001g0183 a0009c0024t0001g0197 |
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 | a0001c0001t0001g0013 a0001c0001t0001g0180 a0001c0001t0001g0181 |
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 | a0002c0021t0002g0270 | 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 | a0001c0022t0004g0196 | 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 | a0002c0003t0002g0020 a0002c0003t0002g0247 a0002c0003t0002g0248 others(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 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0176 others(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 | a0002c0003t0002g0247 a0002c0003t0002g0248 a0002c0003t0002g0251 others(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 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0176 others(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 | a0005c0011t0002g0265 a0005c0011t0002g0266 a0005c0011t0002g0267 others(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 | a0002c0003t0002g0020 a0002c0003t0002g0247 a0002c0003t0002g0248 others(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 | a0001c0001t0001g0042 a0001c0001t0001g0203 a0001c0002t0001g0041 others(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 | a0001c0001t0004g0241 a0001c0004t0004g0188 a0001c0022t0004g0196 |
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 | a0001c0001t0004g0241 a0001c0004t0004g0188 a0001c0022t0004g0196 others(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 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0171 others(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 | a0002c0003t0002g0020 a0002c0003t0002g0247 a0002c0003t0002g0248 others(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 | a0001c0001t0001g0195 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0203 a0001c0001t0001g0209 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 |
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 | a0001c0001t0004g0241 a0001c0004t0004g0188 a0001c0022t0004g0196 |
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 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0171 others(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 | a0001c0001t0004g0241 | 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 | a0001c0001t0001g0239 | 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 | a0002c0012t0002g0268 a0002c0012t0002g0269 |
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 | a0001c0001t0001g0164 | 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 | a0002c0003t0002g0263 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0203 a0001c0001t0001g0209 others(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 | a0002c0003t0002g0262 a0002c0018t0002g0260 a0002c0019t0002g0261 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0183 a0001c0001t0001g0189 others(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 | a0002c0003t0002g0020 a0002c0003t0002g0274 a0002c0003t0002g0275 others(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 | a0001c0001t0001g0163 | 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 | a0001c0001t0004g0241 a0001c0004t0004g0188 a0001c0022t0004g0196 |
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 | a0002c0003t0002g0262 a0002c0018t0002g0260 a0002c0019t0002g0261 |
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 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0239 others(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 | a0001c0001t0001g0237 a0001c0001t0001g0238 |
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 | a0001c0001t0001g0162 | 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 | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(216): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): 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 | a0001c0002t0001g0121 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0203 a0001c0001t0001g0209 others(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 | a0002c0003t0002g0247 a0002c0003t0002g0248 a0002c0003t0002g0251 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0203 a0001c0001t0001g0209 others(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 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0237 others(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 | a0001c0001t0001g0181 | 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 | a0002c0003t0002g0258 a0002c0003t0002g0259 |
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 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(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 | a0001c0002t0001g0014 a0001c0002t0001g0193 a0001c0002t0001g0194 others(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 | a0002c0003t0002g0255 a0002c0003t0002g0256 a0002c0003t0002g0258 |
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 | a0009c0024t0001g0197 | 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 | a0001c0001t0001g0183 | 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 | a0001c0001t0001g0050 a0001c0001t0001g0053 a0001c0001t0001g0054 others(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 | a0002c0003t0002g0254 a0002c0003t0002g0257 a0002c0003t0002g0259 |
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 | a0002c0003t0002g0254 | 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 | a0002c0003t0002g0254 a0002c0003t0002g0257 a0002c0003t0002g0259 |
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 | a0002c0003t0002g0254 a0002c0003t0002g0257 a0002c0003t0002g0259 |
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 | a0001c0001t0001g0161 a0002c0003t0002g0255 a0002c0003t0002g0256 others(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 | a0002c0003t0002g0254 a0002c0003t0002g0257 a0002c0003t0002g0259 |
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 | a0002c0003t0002g0254 a0002c0003t0002g0257 a0002c0003t0002g0259 |
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 | a0002c0003t0002g0247 a0002c0003t0002g0248 a0002c0003t0002g0251 others(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 | a0001c0001t0001g0195 | 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 | a0001c0001t0001g0195 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0183 a0001c0001t0001g0189 others(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 | a0001c0001t0001g0183 a0001c0001t0001g0189 a0001c0001t0001g0190 others(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 | a0005c0011t0002g0265 a0005c0011t0002g0266 a0005c0011t0002g0267 others(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 | a0001c0006t0001g0199 | 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 | a0002c0003t0002g0252 a0002c0007t0002g0019 |
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 | a0005c0011t0002g0265 a0005c0011t0002g0266 a0005c0011t0002g0267 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0183 a0001c0001t0001g0189 others(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 | a0008c0032t0003g0049 | 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 | a0001c0001t0004g0241 a0001c0004t0004g0188 a0001c0022t0004g0196 others(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 | a0001c0001t0001g0183 a0001c0001t0001g0189 a0001c0001t0001g0190 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0160 a0001c0001t0001g0203 others(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 | a0001c0001t0001g0117 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0183 a0001c0001t0001g0189 others(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 | a0001c0002t0001g0116 | 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 | a0001c0022t0004g0196 | 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 | a0001c0001t0001g0224 | 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 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
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 | a0001c0001t0001g0191 | 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 | a0007c0026t0006g0231 | 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 | a0002c0003t0002g0020 a0002c0003t0002g0274 a0002c0003t0002g0275 others(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 | a0001c0001t0001g0183 a0001c0001t0001g0189 a0001c0001t0001g0190 others(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 | a0001c0001t0001g0195 | 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 | a0001c0002t0001g0242 a0001c0002t0001g0243 |
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 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0171 others(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 | a0002c0003t0002g0247 | 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 | a0002c0003t0002g0020 a0002c0003t0002g0274 a0002c0003t0002g0275 others(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 | a0001c0001t0001g0182 | 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 | a0005c0011t0002g0265 | 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 | a0002c0003t0002g0262 a0002c0018t0002g0260 a0002c0019t0002g0261 |
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 | a0002c0003t0002g0247 a0002c0003t0002g0248 a0002c0003t0002g0251 others(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 | a0001c0001t0004g0241 a0001c0002t0001g0045 a0001c0004t0004g0188 others(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 | a0002c0003t0002g0247 a0002c0003t0002g0251 a0002c0003t0002g0252 others(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 | a0005c0011t0002g0265 a0005c0011t0002g0266 a0005c0011t0002g0267 others(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 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(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 | a0001c0001t0001g0183 a0001c0001t0001g0189 a0001c0001t0001g0190 others(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 | a0002c0003t0002g0255 | 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 | a0001c0001t0001g0183 a0001c0001t0001g0189 a0001c0001t0001g0190 others(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 | a0001c0013t0001g0192 a0001c0014t0001g0279 |
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 | a0001c0001t0001g0195 | 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 | a0001c0001t0004g0241 | 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 | a0001c0002t0001g0047 a0001c0002t0003g0056 |
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 | a0001c0001t0001g0183 a0001c0001t0001g0189 a0001c0001t0001g0190 others(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 | a0001c0001t0001g0183 a0001c0001t0001g0189 a0001c0001t0001g0190 others(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 | a0003c0005t0001g0225 | 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 | a0001c0001t0001g0183 a0001c0001t0001g0189 a0001c0001t0001g0190 others(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 | a0002c0021t0002g0270 | 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 | a0001c0001t0001g0183 a0001c0001t0001g0189 a0001c0001t0001g0190 others(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 | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(195): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): 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 | a0001c0001t0001g0183 a0001c0001t0001g0189 a0001c0001t0001g0190 others(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 | a0002c0012t0002g0268 a0002c0012t0002g0269 |
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 | a0002c0003t0002g0020 a0002c0003t0002g0274 a0002c0003t0002g0275 others(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 | a0001c0004t0004g0188 | 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 | a0001c0001t0001g0203 a0001c0001t0001g0223 a0001c0001t0001g0224 others(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 | 113 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(110): 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 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0002c0003t0002g0020 others(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 | a0001c0001t0001g0176 a0004c0015t0001g0185 a0004c0015t0001g0186 others(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 | 105 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(102): 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 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0002c0003t0002g0020 others(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 | a0001c0001t0003g0022 a0001c0001t0003g0111 a0001c0001t0003g0112 |
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 | a0001c0001t0001g0195 | 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 | a0001c0001t0001g0183 a0001c0002t0001g0194 a0001c0002t0001g0222 others(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 | a0001c0001t0001g0224 | 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 | 151 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(148): 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 | a0001c0002t0001g0153 | 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 | a0001c0001t0001g0157 a0001c0001t0001g0189 a0001c0001t0001g0190 others(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 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(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 | a0002c0003t0002g0274 a0002c0003t0002g0275 a0002c0009t0002g0272 others(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 | a0005c0031t0002g0264 | 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 | a0002c0003t0002g0274 a0002c0003t0002g0275 a0002c0009t0002g0272 others(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 | a0001c0001t0001g0117 a0001c0001t0001g0124 a0001c0001t0001g0127 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0152 a0001c0001t0001g0158 others(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 | a0002c0010t0002g0278 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0060 a0001c0001t0001g0067 others(25): Show |
32 | HG00099.hp1 HG00099.hp2 HG01069.hp1 others(29): 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 | a0001c0001t0001g0123 a0001c0001t0001g0195 a0001c0001t0001g0224 others(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 | a0001c0004t0001g0200 | 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 | 95 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(92): 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 | a0001c0001t0001g0163 | 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 | a0001c0006t0001g0221 | 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 | a0001c0001t0001g0183 a0001c0001t0001g0220 a0001c0002t0001g0194 others(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 | a0002c0012t0002g0268 a0002c0012t0002g0269 |
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 | 107 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(104): 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 | a0001c0001t0001g0237 | 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 | a0001c0001t0001g0124 | 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 | 126 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(123): 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 | a0001c0001t0001g0218 a0001c0014t0001g0217 a0001c0030t0001g0219 |
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 | a0001c0001t0001g0224 | 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 | a0001c0001t0001g0123 a0001c0001t0004g0241 |
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 | a0002c0012t0002g0268 | 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 | a0002c0010t0002g0278 | 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 | a0002c0003t0002g0274 a0002c0003t0002g0275 a0002c0009t0002g0272 others(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 | 105 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(102): 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 | a0001c0001t0001g0123 a0001c0001t0001g0158 a0001c0001t0001g0195 others(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 | a0001c0001t0001g0157 a0001c0001t0001g0189 a0001c0001t0001g0190 others(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 | a0001c0001t0001g0123 a0001c0001t0001g0158 a0001c0001t0004g0241 others(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 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(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 | a0001c0022t0004g0196 a0004c0015t0001g0185 a0004c0015t0001g0186 others(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 | 95 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(92): 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 | a0001c0001t0001g0042 a0001c0001t0001g0129 a0001c0001t0001g0130 others(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 | a0001c0001t0001g0157 a0001c0001t0001g0183 a0001c0001t0001g0189 others(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 | a0002c0003t0002g0254 | 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 | a0002c0003t0002g0274 a0002c0003t0002g0275 a0002c0009t0002g0272 others(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 | a0001c0001t0001g0156 | 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 | a0001c0001t0001g0123 a0001c0001t0001g0127 a0001c0001t0004g0241 others(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 | a0001c0001t0001g0157 a0001c0001t0001g0173 a0001c0001t0001g0189 others(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 | a0001c0001t0001g0157 a0001c0001t0001g0173 a0001c0001t0001g0189 others(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 | a0001c0001t0001g0157 a0001c0001t0001g0173 a0001c0001t0001g0189 others(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 | a0001c0001t0001g0158 a0005c0011t0002g0267 |
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 | a0001c0001t0001g0158 a0005c0011t0002g0267 |
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 | a0001c0022t0004g0196 | 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 | a0001c0001t0001g0057 a0001c0001t0001g0174 a0001c0001t0001g0176 others(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 | a0002c0003t0002g0262 | 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 | a0001c0001t0001g0150 | 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 | a0002c0010t0002g0278 | 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 | a0001c0001t0001g0235 | 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 | a0001c0002t0001g0109 a0001c0002t0001g0110 a0001c0002t0003g0056 |
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 | a0002c0003t0002g0255 | 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 | a0001c0001t0001g0023 a0001c0001t0001g0039 a0001c0001t0001g0057 others(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 | a0001c0001t0001g0220 | 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 | a0006c0017t0001g0104 | 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 | 136 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(133): 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 | a0001c0001t0001g0189 a0001c0001t0001g0236 a0001c0001t0001g0237 others(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 | a0001c0001t0001g0067 | 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 | a0001c0001t0001g0117 | 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 | a0001c0001t0001g0040 a0001c0001t0001g0057 a0001c0001t0001g0123 others(73): Show |
80 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(77): 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 | a0001c0002t0001g0076 | 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 | a0002c0003t0002g0256 | 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 | a0001c0001t0001g0216 | 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 | a0007c0026t0006g0231 | 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 | a0001c0004t0004g0188 | 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 | a0001c0002t0001g0005 a0001c0002t0001g0041 a0001c0002t0001g0063 others(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 | a0001c0001t0001g0123 a0001c0001t0004g0241 |
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 | a0001c0001t0001g0123 a0001c0001t0004g0241 |
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 | a0002c0012t0002g0268 a0002c0012t0002g0269 |
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 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0240 |
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 | a0001c0001t0001g0040 a0001c0001t0001g0127 a0001c0001t0001g0189 others(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 | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(100): 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 | a0001c0001t0001g0220 a0005c0031t0002g0264 |
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 | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(177): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(190): 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 | a0001c0001t0001g0158 a0002c0010t0002g0271 a0005c0011t0002g0267 |
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 | a0001c0001t0001g0236 | 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 | a0001c0004t0004g0188 | 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 | a0004c0015t0001g0185 a0004c0015t0001g0186 a0004c0027t0001g0184 others(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 | a0001c0001t0001g0157 a0002c0012t0002g0269 |
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 | a0001c0001t0001g0157 | 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 | a0001c0001t0001g0040 a0001c0001t0001g0057 a0001c0001t0001g0123 others(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 | a0005c0011t0002g0265 a0005c0011t0002g0266 |
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 | a0001c0001t0001g0157 a0001c0001t0001g0195 a0001c0001t0001g0203 others(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 | a0001c0001t0001g0216 a0005c0031t0002g0264 |
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 | a0001c0002t0001g0131 a0001c0002t0001g0132 |
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 | a0001c0001t0001g0123 a0001c0001t0001g0224 a0001c0006t0001g0206 others(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 | a0003c0005t0001g0230 | 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 | a0001c0001t0001g0223 a0001c0002t0001g0058 a0001c0002t0001g0194 others(6): Show |
9 | HG00099.hp1 HG01109.hp1 HG01109.hp2 others(6): 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 | a0001c0001t0001g0223 a0001c0002t0001g0058 a0001c0002t0001g0194 others(6): Show |
9 | HG00099.hp1 HG01109.hp1 HG01109.hp2 others(6): 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 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0006t0001g0221 others(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 | a0002c0009t0002g0272 | 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 | a0001c0006t0001g0205 | 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 | a0001c0001t0001g0223 a0001c0002t0001g0058 a0001c0002t0001g0194 others(6): Show |
9 | HG00099.hp1 HG01109.hp1 HG01109.hp2 others(6): 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 | a0002c0012t0002g0269 | 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 | a0001c0002t0001g0072 a0001c0002t0001g0148 |
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 | a0001c0001t0001g0216 a0005c0031t0002g0264 |
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 | a0001c0001t0001g0067 | 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 | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(149): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(161): 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 | a0001c0001t0001g0123 a0001c0006t0001g0206 a0001c0014t0001g0217 others(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 | a0001c0004t0001g0015 a0001c0004t0001g0200 a0001c0004t0001g0202 |
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 | a0001c0002t0001g0045 a0002c0003t0002g0274 a0002c0009t0002g0272 others(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 | a0001c0001t0001g0223 a0001c0001t0004g0241 a0005c0011t0002g0265 others(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 | a0001c0001t0001g0216 | 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 | a0001c0001t0001g0078 | 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 | a0001c0001t0001g0035 a0001c0001t0001g0057 a0001c0001t0001g0123 others(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 | a0001c0002t0001g0076 | 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 | a0001c0030t0001g0219 | 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 | a0001c0001t0001g0214 | 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 | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(152): Show |
168 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(165): 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 | a0001c0002t0001g0058 a0001c0002t0001g0194 a0001c0002t0001g0204 others(3): Show |
6 | HG00099.hp1 HG01109.hp2 HG01256.hp2 others(3): 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 | a0001c0001t0001g0124 | 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 | a0001c0001t0001g0079 | 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 | a0001c0001t0001g0223 a0005c0011t0002g0265 a0005c0011t0002g0266 |
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 | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(86): 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 | a0001c0002t0001g0012 a0001c0002t0001g0147 |
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 | a0001c0001t0001g0080 | 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 | a0001c0001t0001g0238 a0003c0005t0001g0225 |
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 | a0001c0001t0001g0080 | 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 | a0001c0001t0001g0124 a0001c0001t0001g0236 a0001c0001t0001g0240 others(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 | a0001c0001t0005g0097 | 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 | a0001c0002t0001g0125 | 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 | a0005c0031t0002g0264 | 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 | a0001c0001t0001g0239 a0001c0001t0004g0234 a0001c0002t0001g0044 others(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 | a0001c0002t0001g0198 | 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 | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(156): Show |
172 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(169): 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 | a0001c0001t0001g0239 a0001c0001t0004g0234 a0001c0002t0001g0044 others(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 | a0003c0005t0001g0230 | 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 | a0001c0001t0001g0223 a0001c0002t0001g0058 a0001c0002t0001g0194 others(6): Show |
9 | HG00099.hp1 HG01109.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2069-10929C>T | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 1/12 | chr20 | 58884683 | |||||||
| chr20:58884756 | C | T | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(145): Show |
160 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(157): 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 | a0001c0001t0005g0096 a0001c0001t0005g0097 |
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 | a0001c0001t0001g0124 a0001c0001t0001g0236 a0001c0001t0001g0240 others(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 | a0004c0028t0001g0187 | 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 | a0001c0001t0005g0096 a0001c0001t0005g0097 |
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 | a0001c0001t0001g0068 a0001c0001t0001g0081 a0001c0002t0001g0071 |
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 | a0001c0001t0001g0039 a0001c0001t0001g0068 a0001c0001t0001g0081 others(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 | a0001c0001t0001g0239 a0001c0001t0004g0234 a0001c0002t0001g0044 others(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 | a0001c0001t0001g0223 a0001c0002t0001g0058 a0001c0002t0001g0194 others(6): Show |
9 | HG00099.hp1 HG01109.hp1 HG01109.hp2 others(6): 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 | a0001c0001t0001g0057 a0001c0001t0001g0123 a0001c0001t0001g0124 others(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 | a0005c0031t0002g0264 | 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 | a0001c0001t0004g0241 | 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 | a0001c0001t0001g0223 a0001c0002t0001g0058 a0001c0002t0001g0194 others(6): Show |
9 | HG00099.hp1 HG01109.hp1 HG01109.hp2 others(6): 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 | a0001c0001t0001g0216 | 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 | a0001c0002t0001g0030 a0001c0002t0003g0032 |
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 | a0001c0001t0001g0123 a0001c0001t0001g0216 a0001c0006t0001g0206 others(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 | a0001c0006t0001g0206 a0002c0003t0002g0247 a0002c0003t0002g0248 others(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 | a0001c0001t0001g0040 a0001c0001t0001g0154 a0001c0001t0001g0166 others(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 | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(154): Show |
170 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(167): 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 | a0001c0002t0001g0136 | 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 | a0005c0031t0002g0264 | 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 | a0001c0001t0001g0040 a0001c0001t0001g0099 a0001c0001t0001g0166 others(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 | a0001c0002t0001g0043 a0001c0002t0001g0137 |
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 | a0001c0001t0001g0083 a0001c0001t0001g0235 a0001c0002t0001g0204 |
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 | a0001c0001t0001g0203 | 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 | a0001c0001t0001g0124 a0001c0001t0001g0236 a0001c0001t0001g0240 others(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 | a0001c0001t0001g0074 | 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 | a0001c0001t0001g0157 | 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 | a0001c0001t0003g0115 | 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 | a0001c0001t0001g0195 a0002c0003t0002g0256 |
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 | a0001c0001t0001g0238 | 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 | a0001c0002t0001g0149 | 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 | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(157): Show |
173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): 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 | a0001c0001t0004g0241 | 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 | a0001c0001t0001g0203 | 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 | a0005c0031t0002g0264 | 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 | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(177): Show |
194 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(191): 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 | a0001c0001t0001g0189 | 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 | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(170): Show |
186 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(183): 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 | a0005c0031t0002g0264 | 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 | a0001c0001t0001g0084 | 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 | a0001c0006t0001g0206 a0001c0014t0001g0217 a0001c0014t0001g0279 others(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 | a0001c0022t0004g0196 | 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 | a0004c0027t0001g0184 | 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 | a0001c0001t0001g0035 a0001c0001t0001g0040 a0001c0001t0001g0057 others(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 | a0001c0014t0001g0217 a0001c0014t0001g0279 a0002c0012t0002g0268 others(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 | a0001c0001t0001g0157 a0001c0001t0001g0203 a0002c0010t0002g0271 others(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 | a0002c0012t0002g0268 | 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 | a0001c0001t0001g0124 a0001c0001t0001g0236 a0001c0001t0001g0240 others(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 | a0001c0001t0001g0001 a0001c0020t0001g0207 |
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 | a0001c0001t0001g0067 a0001c0013t0001g0192 a0003c0005t0001g0018 |
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 | a0005c0011t0002g0267 | 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 | a0001c0001t0001g0195 a0001c0001t0001g0203 a0002c0003t0002g0256 |
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 | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(86): 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 | a0002c0019t0002g0261 | 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 | a0001c0002t0001g0058 a0001c0002t0001g0194 a0001c0002t0001g0204 others(3): Show |
6 | HG00099.hp1 HG01109.hp2 HG01256.hp2 others(3): 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 | a0001c0001t0001g0157 | 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 | a0002c0003t0002g0254 | 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 | a0001c0001t0001g0035 a0001c0001t0001g0057 a0001c0001t0001g0134 others(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 | a0001c0022t0004g0196 | 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 | a0001c0002t0001g0071 | 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 | a0001c0022t0004g0196 | 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 | a0001c0002t0001g0116 | 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 | a0003c0005t0001g0225 | 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 | a0001c0002t0001g0058 a0001c0002t0001g0194 a0001c0002t0001g0204 others(3): Show |
6 | HG00099.hp1 HG01109.hp2 HG01256.hp2 others(3): 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 | a0002c0010t0002g0271 a0002c0018t0002g0260 a0002c0019t0002g0261 |
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 | a0001c0001t0001g0094 a0001c0001t0001g0166 a0001c0001t0001g0167 |
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 | a0001c0004t0001g0016 a0001c0004t0001g0017 a0001c0004t0001g0200 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0093 a0002c0007t0002g0253 |
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 | a0001c0001t0001g0073 a0001c0001t0001g0162 a0001c0002t0001g0003 others(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 | a0001c0002t0001g0136 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0042 a0001c0001t0001g0117 |
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 | a0001c0001t0001g0073 a0001c0001t0001g0162 a0001c0002t0001g0003 others(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 | a0001c0002t0001g0136 | 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 | a0001c0001t0001g0160 | 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 | a0001c0001t0001g0189 a0001c0001t0001g0239 a0001c0001t0004g0234 others(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 | a0001c0001t0001g0157 | 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 | a0001c0002t0001g0045 a0002c0003t0002g0274 a0002c0009t0002g0272 others(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 | a0001c0001t0001g0124 a0001c0001t0001g0236 a0001c0001t0001g0240 |
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 | a0001c0006t0001g0206 a0002c0003t0002g0248 a0002c0003t0002g0251 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0237 |
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 | a0001c0002t0001g0243 | 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 | a0001c0001t0001g0023 a0001c0001t0001g0084 a0001c0001t0001g0099 others(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 | a0001c0001t0001g0039 a0001c0001t0001g0068 a0001c0001t0001g0073 others(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 | a0001c0002t0001g0061 | 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 | a0001c0001t0001g0040 a0001c0001t0001g0164 a0001c0001t0001g0166 others(39): Show |
43 | HG00099.hp1 HG00738.hp2 HG01070.hp1 others(40): 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 | a0001c0001t0001g0174 a0001c0001t0001g0176 a0001c0002t0001g0044 others(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 | a0001c0001t0001g0157 a0001c0001t0001g0189 a0001c0001t0001g0239 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0084 others(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 | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(84): 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 | a0001c0001t0001g0195 a0002c0003t0002g0256 |
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 | a0001c0001t0001g0057 a0001c0001t0001g0134 a0001c0001t0001g0154 others(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 | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(174): Show |
190 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(187): 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 | a0001c0001t0001g0083 | 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 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0166 others(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 | a0001c0001t0001g0223 a0005c0011t0002g0266 |
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 | a0001c0001t0001g0195 a0002c0003t0002g0256 |
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 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0166 others(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 | a0001c0002t0001g0144 | 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 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
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 | a0001c0001t0001g0118 | 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 | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(88): 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 | a0001c0001t0001g0236 a0001c0001t0001g0240 |
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 | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(89): 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 | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(194): Show |
211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): 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 | a0007c0026t0006g0231 | 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 | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(193): Show |
210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): 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 | a0001c0001t0001g0218 | 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 | a0001c0001t0001g0157 | 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 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0190 others(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 | a0001c0001t0004g0241 | 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 | a0001c0001t0004g0241 | 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 | a0001c0001t0001g0157 | 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 | a0001c0014t0001g0217 a0001c0014t0001g0279 a0002c0012t0002g0268 others(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 | a0001c0014t0001g0217 a0001c0014t0001g0279 a0002c0012t0002g0268 others(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 | a0001c0001t0001g0156 a0001c0001t0001g0173 a0001c0001t0001g0209 others(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 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0166 others(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 | a0001c0001t0001g0174 a0001c0001t0001g0176 a0001c0006t0001g0179 others(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 | a0001c0004t0001g0200 | 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 | a0001c0002t0001g0100 | 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 | a0002c0010t0002g0271 a0002c0018t0002g0260 a0002c0019t0002g0261 |
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 | a0001c0002t0001g0147 | 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 | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(173): Show |
189 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(186): 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 | a0001c0001t0001g0152 | 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 | a0005c0011t0002g0267 | 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 | a0001c0001t0001g0123 a0001c0001t0001g0166 a0001c0001t0001g0167 others(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 | a0001c0001t0001g0123 | 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 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0173 others(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 | a0001c0001t0001g0084 | 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 | a0001c0002t0001g0107 | 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 | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(198): Show |
215 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(212): 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 | a0001c0023t0001g0232 a0002c0021t0002g0270 |
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 | a0001c0001t0001g0210 | 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 | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(197): Show |
214 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(211): 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 | a0001c0002t0001g0136 a0001c0002t0001g0142 |
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 | a0001c0001t0001g0236 | 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 | a0001c0001t0001g0156 a0001c0001t0001g0173 a0001c0001t0001g0174 others(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 | a0005c0011t0002g0267 | 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 | a0001c0001t0001g0143 a0001c0001t0001g0237 a0001c0004t0001g0015 |
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 | a0001c0001t0001g0123 | 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 | a0001c0001t0001g0216 | 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 | a0002c0003t0002g0263 | 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 | a0001c0014t0001g0217 a0001c0014t0001g0279 a0002c0012t0002g0268 others(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 | a0001c0001t0001g0156 | 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 | a0001c0001t0001g0120 | 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 | a0001c0001t0001g0240 | 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 | a0001c0001t0001g0189 a0001c0001t0001g0239 a0001c0001t0004g0234 others(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 | a0001c0001t0004g0241 | 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 | a0001c0004t0001g0016 a0001c0004t0001g0017 a0001c0004t0001g0200 others(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 | a0002c0003t0002g0276 | 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 | a0007c0026t0006g0231 | 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 | a0001c0001t0001g0073 | 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 | a0001c0001t0004g0241 | 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 | a0001c0004t0001g0046 a0001c0004t0001g0208 a0001c0004t0001g0215 others(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 | a0001c0001t0001g0070 | 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 | a0001c0001t0001g0195 a0002c0003t0002g0256 a0005c0031t0002g0264 |
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 | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(83): 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 | a0001c0001t0001g0054 a0001c0001t0001g0086 a0001c0001t0001g0094 |
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 | a0001c0001t0001g0189 a0001c0001t0001g0239 a0001c0001t0004g0234 others(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 | a0001c0001t0001g0213 a0005c0031t0002g0264 |
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 | a0001c0001t0001g0095 | 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 | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(210): Show |
229 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(226): 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 | a0001c0001t0001g0156 a0001c0001t0001g0173 a0001c0001t0001g0174 others(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 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0161 others(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 | a0001c0001t0004g0241 | 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 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0190 others(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 | a0001c0001t0001g0216 | 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 | a0001c0001t0001g0236 a0001c0001t0001g0240 |
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 | a0001c0008t0001g0075 | 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 | a0001c0001t0001g0191 | 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 | a0005c0031t0002g0264 | 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 | a0001c0001t0001g0189 a0001c0001t0001g0203 a0001c0001t0001g0239 others(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 | a0002c0012t0002g0268 | 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 | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(183): Show |
199 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(196): 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 | a0002c0021t0002g0270 | 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 | a0001c0001t0001g0123 a0001c0006t0001g0206 a0002c0003t0002g0247 others(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 | a0001c0001t0001g0057 a0001c0001t0001g0134 a0001c0001t0001g0154 others(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 | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(130): Show |
143 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(140): 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 | a0001c0014t0001g0279 | 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 | a0001c0001t0001g0123 | 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 | a0001c0001t0001g0174 a0001c0001t0001g0176 a0001c0006t0001g0179 others(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 | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
145 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.2187-1496T>C | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 3/12 | chr20 | 58902035 | |||||||
| chr20:58902049 | A | T | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(141): Show |
157 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(154): 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 | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
145 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(142): 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 | a0001c0001t0001g0057 a0001c0001t0001g0154 a0001c0001t0001g0156 others(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 | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(133): Show |
147 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(144): 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 | a0001c0001t0001g0189 a0001c0001t0001g0203 a0001c0001t0001g0239 others(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 | a0001c0002t0001g0077 | 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 | a0001c0002t0001g0092 a0003c0005t0001g0018 a0003c0005t0001g0227 others(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 | a0001c0001t0001g0239 a0001c0023t0001g0232 a0002c0021t0002g0270 |
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 | a0001c0001t0001g0238 | 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 | a0001c0002t0001g0126 | 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 | a0001c0001t0001g0189 a0001c0001t0001g0220 a0001c0001t0001g0239 others(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 | a0001c0001t0001g0169 a0001c0002t0001g0030 a0001c0002t0001g0044 others(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 | 38 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0024 others(35): 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 | 32 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(29): 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 | a0001c0001t0001g0078 a0001c0001t0001g0083 a0001c0001t0001g0084 others(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 | a0001c0001t0001g0213 a0001c0001t0001g0216 a0001c0001t0001g0223 others(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 | a0001c0001t0001g0123 a0001c0006t0001g0206 a0001c0022t0004g0196 others(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 | a0001c0001t0001g0190 a0001c0002t0001g0007 a0001c0023t0001g0232 others(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 | a0001c0014t0001g0217 a0004c0028t0001g0187 |
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 | a0002c0012t0002g0269 | 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 | a0002c0010t0002g0271 a0002c0012t0002g0268 a0002c0018t0002g0260 others(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 | a0001c0001t0001g0191 | 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 | a0001c0014t0001g0279 a0002c0021t0002g0270 |
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 | a0001c0001t0001g0057 a0001c0001t0001g0134 a0001c0001t0001g0156 others(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 | a0001c0002t0001g0058 a0001c0002t0001g0194 a0001c0002t0001g0204 others(3): Show |
6 | HG00099.hp1 HG01109.hp2 HG01256.hp2 others(3): 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 | a0001c0001t0001g0195 a0001c0002t0001g0198 a0001c0002t0001g0222 others(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 | a0001c0001t0001g0158 | 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 | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(137): Show |
152 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(149): 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 | a0001c0001t0001g0013 a0001c0001t0001g0181 |
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 | a0001c0001t0001g0013 a0001c0001t0001g0181 |
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 | a0001c0001t0001g0239 | 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 | a0001c0006t0001g0179 | 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 | a0001c0001t0001g0220 | 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 | a0001c0001t0001g0035 a0001c0001t0001g0057 a0001c0001t0001g0124 others(66): Show |
70 | HG00099.hp1 HG00423.hp1 HG00738.hp1 others(67): 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 | a0001c0013t0001g0192 | 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 | a0001c0001t0001g0067 | 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 | a0001c0001t0001g0203 | 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 | a0001c0001t0001g0124 a0001c0001t0001g0127 a0001c0001t0001g0156 others(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 | a0001c0001t0005g0096 a0001c0001t0005g0097 |
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 | a0001c0001t0001g0013 a0001c0001t0001g0035 a0001c0001t0001g0040 others(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 | a0001c0001t0001g0035 a0001c0001t0001g0040 a0001c0001t0001g0090 others(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 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0158 others(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 | ||||||
| chr20:58904437 | C | T | 1 | a0001c0001t0001g0161 | 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 | a0001c0001t0001g0158 a0001c0001t0001g0216 a0001c0001t0001g0218 others(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 | a0001c0002t0001g0155 | 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 | a0001c0002t0001g0136 | 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 | a0002c0003t0002g0247 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0211 others(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 | |||||||
| chr20:58904941 | A | AT | 3 | a0001c0002t0001g0198 a0001c0002t0001g0222 a0002c0007t0002g0019 |
4 | HG01891.hp1 HG02572.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2362-434dupT | GNAS | ENSG00000087460.29 | transcript | ENST00000371100.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr20 | 58904941 | ||||||
| chr20:58904961 | C | T | 13 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0158 others(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 | a0001c0001t0001g0158 a0001c0001t0001g0216 a0001c0001t0001g0218 others(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 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0158 others(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 | a0001c0001t0001g0124 a0001c0001t0001g0127 a0001c0001t0001g0173 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0239 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0021 others(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 | a0001c0002t0001g0147 | 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 | a0002c0003t0002g0247 | 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 | a0001c0001t0001g0158 a0001c0001t0001g0216 a0001c0001t0001g0218 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0035 others(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 | a0001c0001t0001g0158 a0001c0001t0001g0216 a0001c0001t0001g0218 others(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 | a0001c0001t0001g0069 a0001c0001t0001g0074 a0001c0001t0001g0085 others(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 | a0001c0023t0001g0232 a0002c0021t0002g0270 |
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 | a0001c0001t0001g0124 | 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 | a0004c0027t0001g0184 | 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 | a0001c0013t0001g0175 a0001c0014t0001g0217 a0001c0014t0001g0279 others(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 | a0001c0004t0001g0017 a0001c0004t0001g0201 a0001c0004t0001g0233 |
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 | a0001c0023t0001g0232 a0002c0021t0002g0270 |
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 | a0001c0001t0001g0240 a0001c0002t0001g0170 |
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 | a0001c0001t0001g0050 a0001c0001t0001g0139 a0001c0001t0001g0183 others(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 | a0001c0002t0001g0010 a0001c0002t0001g0125 a0002c0003t0002g0248 |
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 | a0001c0002t0001g0222 | 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 | a0001c0001t0001g0123 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0035 others(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 | a0001c0001t0001g0209 a0002c0003t0002g0276 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0021 others(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 | a0001c0004t0001g0015 a0001c0004t0001g0016 a0001c0004t0001g0017 others(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 | a0001c0001t0001g0240 a0001c0002t0001g0170 |
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 | a0001c0001t0001g0210 | 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 | a0001c0001t0001g0068 | 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 | a0001c0001t0001g0123 a0001c0001t0001g0143 a0001c0001t0001g0157 others(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 | a0001c0001t0001g0210 | 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 | a0002c0018t0002g0260 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0021 others(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 |