Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2998 |
| ensemblid | ENSG00000111713.3 |
| hgncid | 4707 |
| symbol | GYS2 |
| name | glycogen synthase 2 |
| refseq_nuc | NM_021957.4 |
| refseq_prot | NP_068776.2 |
| ensembl_nuc | ENST00000261195.3 |
| ensembl_prot | ENSP00000261195.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 21536107 |
| end | 21604847 |
| strand | - |
| ver | v1.2 |
| region | chr12:21536107-21604847 |
| region5000 | chr12:21531107-21609847 |
| regionname0 | GYS2_chr12_21536107_21604847 |
| regionname5000 | GYS2_chr12_21531107_21609847 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 703 | 199 | 42 | 35 | 84 | 14 | 24 | 58 | GYS2_chr12_21531107_21609847 | GYS2 | MLRGR others(698): Show |
chr12 | 21531107 | 21609847 |
| a0002 | 1/1 | 703 | 92 | 30 | 16 | 31 | 2 | 11 | 25 | GYS2_chr12_21531107_21609847 | GYS2 | MLRGR others(698): Show |
chr12 | 21531107 | 21609847 |
| a0003 | 0/0 | 703 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | MLRGR others(698): Show |
chr12 | 21531107 | 21609847 |
| a0004 | 0/0 | 703 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | MLRGR others(698): Show |
chr12 | 21531107 | 21609847 |
| a0005 | 0/0 | 703 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | MLRGR others(698): Show |
chr12 | 21531107 | 21609847 |
| a0006 | 0/0 | 703 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | MLRGR others(698): Show |
chr12 | 21531107 | 21609847 |
| a0007 | 0/0 | 703 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | MLRGR others(698): Show |
chr12 | 21531107 | 21609847 |
| a0008 | 0/0 | 703 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GYS2_chr12_21531107_21609847 | GYS2 | MLRGR others(698): Show |
chr12 | 21531107 | 21609847 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2109 | 179 | 31 | 35 | 76 | 14 | 23 | GYS2_chr12_21531107_21609847 | GYS2 | ATGCT others(2104): Show |
chr12 | 21531107 | 21609847 | ||
| a0001c0004 | 0/0 | 2109 | 8 | 0 | 0 | 8 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | ATGCT others(2104): Show |
chr12 | 21531107 | 21609847 | ||
| a0001c0005 | 0/0 | 2109 | 8 | 8 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | ATGCT others(2104): Show |
chr12 | 21531107 | 21609847 | ||
| a0001c0008 | 0/0 | 2109 | 2 | 2 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | ATGCT others(2104): Show |
chr12 | 21531107 | 21609847 | ||
| a0001c0011 | 0/0 | 2109 | 1 | 0 | 0 | 0 | 0 | 1 | GYS2_chr12_21531107_21609847 | GYS2 | ATGCT others(2104): Show |
chr12 | 21531107 | 21609847 | ||
| a0001c0013 | 0/0 | 2109 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | ATGCT others(2104): Show |
chr12 | 21531107 | 21609847 | ||
| a0002c0002 | 1/1 | 2109 | 91 | 30 | 16 | 30 | 2 | 11 | GYS2_chr12_21531107_21609847 | GYS2 | ATGCT others(2104): Show |
chr12 | 21531107 | 21609847 | ||
| a0002c0012 | 0/0 | 2109 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | ATGCT others(2104): Show |
chr12 | 21531107 | 21609847 | ||
| a0003c0003 | 0/0 | 2109 | 10 | 10 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | ATGCT others(2104): Show |
chr12 | 21531107 | 21609847 | ||
| a0004c0006 | 0/0 | 2109 | 5 | 5 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | ATGCT others(2104): Show |
chr12 | 21531107 | 21609847 | ||
| a0005c0007 | 0/0 | 2109 | 3 | 0 | 2 | 0 | 0 | 1 | GYS2_chr12_21531107_21609847 | GYS2 | ATGCT others(2104): Show |
chr12 | 21531107 | 21609847 | ||
| a0006c0014 | 0/0 | 2109 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | ATGCT others(2104): Show |
chr12 | 21531107 | 21609847 | ||
| a0007c0010 | 0/0 | 2109 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | ATGCT others(2104): Show |
chr12 | 21531107 | 21609847 | ||
| a0008c0009 | 0/0 | 2109 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | ATGCT others(2104): Show |
chr12 | 21531107 | 21609847 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3214 | 26 | 13 | 4 | 1 | 5 | 3 | GYS2_chr12_21531107_21609847 | GYS2 | AGATA others(3209): Show |
chr12 | 21531107 | 21609847 |
| a0001c0001t0002 | 0/0 | 3214 | 91 | 4 | 20 | 43 | 7 | 17 | GYS2_chr12_21531107_21609847 | GYS2 | AGATA others(3209): Show |
chr12 | 21531107 | 21609847 |
| a0001c0001t0003 | 0/0 | 3214 | 47 | 3 | 11 | 28 | 2 | 3 | GYS2_chr12_21531107_21609847 | GYS2 | AGATA others(3209): Show |
chr12 | 21531107 | 21609847 |
| a0001c0001t0004 | 0/0 | 3215 | 10 | 10 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | AGATA others(3210): Show |
chr12 | 21531107 | 21609847 |
| a0001c0001t0007 | 0/0 | 3214 | 2 | 0 | 0 | 2 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | AGATA others(3209): Show |
chr12 | 21531107 | 21609847 |
| a0001c0001t0008 | 0/0 | 3214 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | AGATA others(3209): Show |
chr12 | 21531107 | 21609847 |
| a0001c0001t0010 | 0/0 | 3214 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | AGATA others(3209): Show |
chr12 | 21531107 | 21609847 |
| a0001c0001t0011 | 0/0 | 3214 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | AGATA others(3209): Show |
chr12 | 21531107 | 21609847 |
| a0001c0004t0003 | 0/0 | 3214 | 8 | 0 | 0 | 8 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | AGATA others(3209): Show |
chr12 | 21531107 | 21609847 |
| a0001c0005t0001 | 0/0 | 3214 | 8 | 8 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | AGATA others(3209): Show |
chr12 | 21531107 | 21609847 |
| a0001c0008t0001 | 0/0 | 3214 | 2 | 2 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | AGATA others(3209): Show |
chr12 | 21531107 | 21609847 |
| a0001c0011t0002 | 0/0 | 3214 | 1 | 0 | 0 | 0 | 0 | 1 | GYS2_chr12_21531107_21609847 | GYS2 | AGATA others(3209): Show |
chr12 | 21531107 | 21609847 |
| a0001c0013t0001 | 0/0 | 3214 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | AGATA others(3209): Show |
chr12 | 21531107 | 21609847 |
| a0002c0002t0001 | 1/0 | 3214 | 78 | 26 | 14 | 24 | 2 | 11 | GYS2_chr12_21531107_21609847 | GYS2 | AGATA others(3209): Show |
chr12 | 21531107 | 21609847 |
| a0002c0002t0002 | 0/1 | 3214 | 1 | 0 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | AGATA others(3209): Show |
chr12 | 21531107 | 21609847 |
| a0002c0002t0004 | 0/0 | 3215 | 4 | 2 | 0 | 2 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | AGATA others(3210): Show |
chr12 | 21531107 | 21609847 |
| a0002c0002t0005 | 0/0 | 3214 | 5 | 0 | 1 | 4 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | AGATA others(3209): Show |
chr12 | 21531107 | 21609847 |
| a0002c0002t0006 | 0/0 | 3215 | 2 | 2 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | AGATA others(3210): Show |
chr12 | 21531107 | 21609847 |
| a0002c0002t0009 | 0/0 | 3214 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | AGATA others(3209): Show |
chr12 | 21531107 | 21609847 |
| a0002c0012t0001 | 0/0 | 3214 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | AGATA others(3209): Show |
chr12 | 21531107 | 21609847 |
| a0003c0003t0001 | 0/0 | 3214 | 10 | 10 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | AGATA others(3209): Show |
chr12 | 21531107 | 21609847 |
| a0004c0006t0001 | 0/0 | 3214 | 5 | 5 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | AGATA others(3209): Show |
chr12 | 21531107 | 21609847 |
| a0005c0007t0001 | 0/0 | 3214 | 3 | 0 | 2 | 0 | 0 | 1 | GYS2_chr12_21531107_21609847 | GYS2 | AGATA others(3209): Show |
chr12 | 21531107 | 21609847 |
| a0006c0014t0001 | 0/0 | 3214 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | AGATA others(3209): Show |
chr12 | 21531107 | 21609847 |
| a0007c0010t0001 | 0/0 | 3214 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | AGATA others(3209): Show |
chr12 | 21531107 | 21609847 |
| a0008c0009t0002 | 0/0 | 3214 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | AGATA others(3209): Show |
chr12 | 21531107 | 21609847 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0003g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0003g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0003g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0003g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0007g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0007g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0008g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0010g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0001t0011g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0004t0003g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0004t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0004t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0004t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0004t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0004t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0004t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0005t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0005t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0005t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0005t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0005t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0005t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0005t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0005t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0008t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0011t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0001c0013t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0285 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0002g0140 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0004g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0005g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0005g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0005g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0005g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0005g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0006g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0006g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0002t0009g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0002c0012t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0003c0003t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0003c0003t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0003c0003t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0003c0003t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0003c0003t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0003c0003t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0003c0003t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0003c0003t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0003c0003t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0004c0006t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0004c0006t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0004c0006t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0004c0006t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0004c0006t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0005c0007t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0005c0007t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0005c0007t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0006c0014t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0007c0010t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| a0008c0009t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0223 | EUR | GBR | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0210 | EUR | GBR | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0222 | EUR | FIN | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0152 | EUR | FIN | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0155 | EUR | FIN | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0163 | EUR | FIN | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0165 | EAS | CHS | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | CHS | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | CHS | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0265 | EAS | CHS | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | CHS | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | CHS | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | CHS | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG00558 | hp2 | a0001 | c0004 | t0003 | g0123 | EAS | CHS | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | CHS | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | CHS | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0138 | EAS | CHS | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG00621 | hp2 | a0001 | c0001 | t0011 | g0211 | EAS | CHS | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0199 | AMR | PUR | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0144 | AMR | PUR | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0262 | AMR | PUR | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0097 | AMR | PUR | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | CHS | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG00673 | hp2 | a0002 | c0002 | t0005 | g0040 | EAS | CHS | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0146 | AMR | PUR | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | PUR | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0257 | AMR | PUR | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0226 | AMR | PUR | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | PUR | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0191 | AMR | PUR | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | PUR | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0227 | AMR | PUR | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | PUR | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0261 | AMR | PUR | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0208 | AMR | PUR | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0114 | AMR | PUR | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0195 | AMR | PUR | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0197 | AMR | PUR | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01175 | hp1 | a0005 | c0007 | t0001 | g0139 | AMR | PUR | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0263 | AMR | PUR | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | CLM | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0072 | AMR | CLM | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | CLM | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01346 | hp1 | a0002 | c0002 | t0009 | g0224 | AMR | CLM | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0213 | AMR | CLM | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | CLM | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01358 | hp2 | a0006 | c0014 | t0001 | g0086 | AMR | CLM | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | CLM | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01361 | hp2 | a0005 | c0007 | t0001 | g0251 | AMR | CLM | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0147 | AMR | CLM | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0202 | AMR | CLM | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | IBS | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0190 | EUR | IBS | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0170 | EUR | IBS | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | IBS | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0192 | EUR | IBS | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01884 | hp1 | a0001 | c0005 | t0001 | g0034 | AFR | ACB | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01884 | hp2 | a0003 | c0003 | t0001 | g0287 | AFR | ACB | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01891 | hp1 | a0002 | c0002 | t0004 | g0239 | AFR | ACB | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0089 | AFR | ACB | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0196 | AMR | PEL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0150 | AMR | PEL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | PEL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0219 | AMR | PEL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0135 | AMR | PEL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0067 | AMR | PEL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0087 | AMR | PEL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0209 | AMR | PEL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02004 | hp2 | a0002 | c0002 | t0005 | g0055 | AMR | PEL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | KHV | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0113 | EAS | KHV | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0101 | AFR | ACB | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0109 | AFR | ACB | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | KHV | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02056 | hp2 | a0001 | c0004 | t0003 | g0019 | EAS | KHV | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | KHV | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | KHV | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | KHV | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | KHV | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0269 | EAS | KHV | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0200 | EAS | KHV | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | KHV | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02083 | hp2 | a0002 | c0012 | t0001 | g0259 | EAS | KHV | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0248 | AFR | ACB | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0090 | AFR | ACB | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0249 | AMR | PEL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0098 | AMR | PEL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | CDX | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | CDX | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0160 | EAS | CDX | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | CDX | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02257 | hp1 | a0003 | c0003 | t0001 | g0016 | AFR | ACB | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02258 | hp1 | a0003 | c0003 | t0001 | g0233 | AFR | ACB | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02258 | hp2 | a0001 | c0008 | t0001 | g0006 | AFR | ACB | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02280 | hp1 | a0001 | c0005 | t0001 | g0119 | AFR | ACB | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0085 | AFR | ACB | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0168 | AMR | PEL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | ACB | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | ACB | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0126 | AFR | GWD | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0025 | AFR | GWD | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0136 | SAS | PJL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0238 | SAS | PJL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0234 | AFR | GWD | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02622 | hp2 | a0001 | c0005 | t0001 | g0125 | AFR | GWD | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0246 | AFR | GWD | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02630 | hp2 | a0001 | c0005 | t0001 | g0129 | AFR | GWD | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02647 | hp1 | a0004 | c0006 | t0001 | g0274 | AFR | GWD | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0184 | SAS | PJL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | PJL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0099 | AFR | GWD | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02723 | hp1 | a0004 | c0006 | t0001 | g0273 | AFR | GWD | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0161 | AFR | GWD | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0179 | SAS | PJL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0158 | SAS | PJL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0276 | SAS | PJL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02809 | hp1 | a0001 | c0013 | t0001 | g0282 | AFR | GWD | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02809 | hp2 | a0001 | c0005 | t0001 | g0033 | AFR | GWD | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | GWD | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0283 | AFR | GWD | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02886 | hp1 | a0003 | c0003 | t0001 | g0105 | AFR | GWD | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0277 | AFR | GWD | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02895 | hp1 | a0003 | c0003 | t0001 | g0289 | AFR | GWD | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0280 | AFR | GWD | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0281 | AFR | GWD | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0103 | AFR | GWD | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02922 | hp1 | a0003 | c0003 | t0001 | g0286 | AFR | ESN | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02922 | hp2 | a0004 | c0006 | t0001 | g0275 | AFR | ESN | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02965 | hp1 | a0004 | c0006 | t0001 | g0151 | AFR | ESN | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0266 | AFR | ESN | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02970 | hp1 | a0002 | c0002 | t0006 | g0241 | AFR | ESN | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0118 | AFR | ESN | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0214 | SAS | PJL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0171 | SAS | PJL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0284 | AFR | GWD | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0279 | AFR | GWD | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG03098 | hp1 | a0001 | c0005 | t0001 | g0036 | AFR | MSL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | MSL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0108 | AFR | ESN | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG03130 | hp2 | a0004 | c0006 | t0001 | g0092 | AFR | ESN | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG03139 | hp1 | a0002 | c0002 | t0006 | g0240 | AFR | ESN | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ESN | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG03195 | hp1 | a0002 | c0002 | t0004 | g0295 | AFR | ESN | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0120 | AFR | ESN | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0093 | AFR | MSL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG03209 | hp2 | a0001 | c0008 | t0001 | g0006 | AFR | MSL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0053 | SAS | PJL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0183 | SAS | PJL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG03490 | hp1 | a0001 | c0011 | t0002 | g0203 | SAS | PJL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0236 | SAS | PJL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0081 | SAS | PJL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0237 | SAS | PJL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0244 | AFR | ESN | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0256 | AFR | ESN | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0018 | AFR | GWD | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0198 | AFR | GWD | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0243 | AFR | MSL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0247 | AFR | MSL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | STU | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0077 | SAS | STU | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0176 | SAS | PJL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0148 | SAS | PJL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0142 | SAS | PJL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0107 | SAS | BEB | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0063 | SAS | BEB | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0143 | SAS | BEB | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG03927 | hp2 | a0005 | c0007 | t0001 | g0250 | SAS | BEB | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0232 | SAS | STU | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0110 | SAS | STU | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0235 | SAS | STU | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0221 | SAS | STU | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0220 | SAS | STU | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0145 | SAS | STU | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0288 | AFR | YRI | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18522 | hp2 | a0001 | c0005 | t0001 | g0131 | AFR | YRI | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0111 | EAS | CHB | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | CHB | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18906 | hp1 | a0003 | c0003 | t0001 | g0026 | AFR | YRI | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18906 | hp2 | a0001 | c0005 | t0001 | g0031 | AFR | YRI | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0228 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18940 | hp1 | a0008 | c0009 | t0002 | g0260 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18940 | hp2 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18960 | hp1 | a0001 | c0004 | t0003 | g0008 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18969 | hp2 | a0001 | c0004 | t0003 | g0128 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0229 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18975 | hp2 | a0002 | c0002 | t0005 | g0056 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0270 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18978 | hp1 | a0002 | c0002 | t0004 | g0042 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18989 | hp2 | a0002 | c0002 | t0005 | g0230 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18997 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18998 | hp1 | a0001 | c0004 | t0003 | g0117 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA19010 | hp1 | a0001 | c0001 | t0010 | g0064 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA19011 | hp2 | a0001 | c0004 | t0003 | g0008 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | LWK | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA19030 | hp2 | a0001 | c0001 | t0008 | g0292 | AFR | LWK | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA19043 | hp1 | a0003 | c0003 | t0001 | g0016 | AFR | LWK | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | LWK | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA19057 | hp1 | a0001 | c0004 | t0003 | g0127 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA19062 | hp1 | a0001 | c0004 | t0003 | g0124 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA19064 | hp1 | a0001 | c0001 | t0007 | g0216 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA19083 | hp1 | a0002 | c0002 | t0004 | g0041 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA19090 | hp1 | a0002 | c0002 | t0005 | g0046 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0130 | AFR | YRI | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | YRI | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0141 | AFR | ASW | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ASW | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0167 | EUR | TSI | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0154 | EUR | TSI | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0084 | EUR | TSI | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0166 | EUR | TSI | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0218 | SAS | GIH | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0271 | SAS | GIH | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02109 | hp1 | a0007 | c0010 | t0001 | g0022 | AFR | ACB | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02109 | hp2 | a0003 | c0003 | t0001 | g0278 | AFR | ACB | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0217 | AFR | ACB | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0116 | AFR | ACB | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0104 | AFR | ACB | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0102 | AFR | ACB | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | MSL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0100 | AFR | MSL | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA18955 | hp2 | a0001 | c0001 | t0007 | g0207 | EAS | JPT | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0245 | AFR | USA | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA20300 | hp2 | a0003 | c0003 | t0001 | g0255 | AFR | USA | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0290 | AFR | LWK | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0252 | AFR | LWK | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0140 | REF | REF | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0285 | REF | REF | GYS2_chr12_21531107_21609847 | GYS2 | chr12 | 21531107 | 21609847 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:21537101 | C | G | 1 | a0005 | 3 | HG01175.hp1 HG01361.hp2 HG03927.hp2 |
missense_variant | MODERATE | c.1965G>C | p.Gln655His | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 16/16 | 2220/3214 | 1965/2112 | 655/703 | chr12 | 21537101 | |||
| chr12:21542505 | T | C | 1 | a0006 | 1 | HG01358.hp2 | missense_variant | MODERATE | c.1636A>G | p.Thr546Ala | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 13/16 | 1891/3214 | 1636/2112 | 546/703 | chr12 | 21542505 | |||
| chr12:21559154 | G | C | 2 | a0003 a0007 |
11 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(8): Show |
missense_variant | MODERATE | c.1245C>G | p.Asp415Glu | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 10/16 | 1500/3214 | 1245/2112 | 415/703 | chr12 | 21559154 | |||
| chr12:21560468 | T | C | 6 | a0001 a0003 a0004 others(3): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
missense_variant | MODERATE | c.1087A>G | p.Met363Val | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 8/16 | 1342/3214 | 1087/2112 | 363/703 | chr12 | 21560468 | |||
| chr12:21574245 | C | T | 1 | a0007 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.577G>A | p.Ala193Thr | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/16 | 832/3214 | 577/2112 | 193/703 | chr12 | 21574245 | |||
| chr12:21580365 | C | T | 1 | a0004 | 5 | HG02647.hp1 HG02723.hp1 HG02922.hp2 others(2): Show |
missense_variant | MODERATE | c.280G>A | p.Ala94Thr | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 2/16 | 535/3214 | 280/2112 | 94/703 | chr12 | 21580365 | |||
| chr12:21580512 | A | T | 1 | a0008 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.133T>A | p.Tyr45Asn | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 2/16 | 388/3214 | 133/2112 | 45/703 | chr12 | 21580512 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:21536999 | G | A | 1 | a0001c0005 | 8 | HG01884.hp1 HG02280.hp1 HG02622.hp2 others(5): Show |
synonymous_variant | LOW | c.2067C>T | p.His689His | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 16/16 | 2322/3214 | 2067/2112 | 689/703 | chr12 | 21536999 | |||
| chr12:21539276 | T | C | 1 | a0001c0008 | 2 | HG02258.hp2 HG03209.hp2 |
synonymous_variant | LOW | c.1872A>G | p.Glu624Glu | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 15/16 | 2127/3214 | 1872/2112 | 624/703 | chr12 | 21539276 | |||
| chr12:21540452 | A | G | 1 | a0002c0012 | 1 | HG02083.hp2 | synonymous_variant | LOW | c.1767T>C | p.Thr589Thr | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 14/16 | 2022/3214 | 1767/2112 | 589/703 | chr12 | 21540452 | |||
| chr12:21540509 | A | G | 1 | a0001c0013 | 1 | HG02809.hp1 | synonymous_variant | LOW | c.1710T>C | p.Phe570Phe | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 14/16 | 1965/3214 | 1710/2112 | 570/703 | chr12 | 21540509 | |||
| chr12:21546429 | T | C | 1 | a0001c0005 | 8 | HG01884.hp1 HG02280.hp1 HG02622.hp2 others(5): Show |
synonymous_variant | LOW | c.1464A>G | p.Leu488Leu | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 12/16 | 1719/3214 | 1464/2112 | 488/703 | chr12 | 21546429 | |||
| chr12:21558233 | A | G | 1 | a0001c0004 | 8 | HG00558.hp2 HG02056.hp2 NA18960.hp1 others(5): Show |
synonymous_variant | LOW | c.1389T>C | p.Ile463Ile | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/16 | 1644/3214 | 1389/2112 | 463/703 | chr12 | 21558233 | |||
| chr12:21574192 | C | T | 1 | a0001c0011 | 1 | HG03490.hp1 | synonymous_variant | LOW | c.630G>A | p.Gly210Gly | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/16 | 885/3214 | 630/2112 | 210/703 | chr12 | 21574192 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:21536443 | C | T | 1 | a0001c0001t0008 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*511G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 16/16 | 511 | chr12 | 21536443 | ||||||
| chr12:21536496 | T | A | 1 | a0002c0002t0009 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*458A>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 16/16 | 458 | chr12 | 21536496 | ||||||
| chr12:21536516 | T | TA | 3 | a0001c0001t0004 a0002c0002t0004 a0002c0002t0006 |
16 | HG01891.hp1 HG02055.hp1 HG02486.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*437dupT | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 16/16 | 437 | chr12 | 21536516 | ||||||
| chr12:21536522 | A | G | 1 | a0001c0001t0010 | 1 | NA19010.hp1 | 3_prime_UTR_variant | MODIFIER | c.*432T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 16/16 | 432 | chr12 | 21536522 | ||||||
| chr12:21536562 | G | A | 1 | a0002c0002t0006 | 2 | HG02970.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*392C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 16/16 | 392 | chr12 | 21536562 | ||||||
| chr12:21536600 | G | T | 1 | a0001c0001t0011 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*354C>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 16/16 | 354 | chr12 | 21536600 | ||||||
| chr12:21536664 | C | A | 1 | a0001c0001t0007 | 2 | NA18955.hp2 NA19064.hp1 |
3_prime_UTR_variant | MODIFIER | c.*290G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 16/16 | 290 | chr12 | 21536664 | ||||||
| chr12:21536802 | G | A | 8 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(5): Show |
152 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(149): Show |
3_prime_UTR_variant | MODIFIER | c.*152C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 16/16 | 152 | chr12 | 21536802 | ||||||
| chr12:21536873 | G | T | 1 | a0002c0002t0006 | 2 | HG02970.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*81C>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 16/16 | 81 | chr12 | 21536873 | ||||||
| chr12:21536948 | T | A | 6 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0011 others(3): Show |
101 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*6A>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 16/16 | 6 | chr12 | 21536948 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:21537346 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0008g0292 |
2 | HG02647.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1891-171A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 15/15 | chr12 | 21537346 | |||||||
| chr12:21537364 | A | C | 1 | a0001c0001t0002g0268 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1891-189T>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 15/15 | chr12 | 21537364 | |||||||
| chr12:21537443 | A | C | 180 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0039 others(177): Show |
193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.1891-268T>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 15/15 | chr12 | 21537443 | |||||||
| chr12:21537590 | C | G | 2 | a0003c0003t0001g0255 a0003c0003t0001g0278 |
2 | HG02109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1891-415G>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 15/15 | chr12 | 21537590 | |||||||
| chr12:21537649 | T | A | 6 | a0002c0002t0004g0041 a0002c0002t0004g0042 a0002c0002t0004g0239 others(3): Show |
6 | HG01891.hp1 HG02970.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1891-474A>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 15/15 | chr12 | 21537649 | |||||||
| chr12:21537681 | G | C | 7 | a0001c0001t0004g0025 a0001c0001t0004g0100 a0001c0001t0004g0101 others(4): Show |
7 | HG02055.hp1 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1891-506C>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 15/15 | chr12 | 21537681 | |||||||
| chr12:21537768 | C | T | 1 | a0001c0001t0002g0014 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1891-593G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 15/15 | chr12 | 21537768 | |||||||
| chr12:21537829 | G | A | 1 | a0001c0001t0002g0217 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1891-654C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 15/15 | chr12 | 21537829 | |||||||
| chr12:21537840 | A | T | 180 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0039 others(177): Show |
193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.1891-665T>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 15/15 | chr12 | 21537840 | |||||||
| chr12:21537928 | G | A | 2 | a0002c0002t0001g0088 a0002c0002t0001g0229 |
2 | NA18962.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.1891-753C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 15/15 | chr12 | 21537928 | |||||||
| chr12:21538075 | G | A | 5 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0132 others(2): Show |
5 | HG01168.hp1 HG01169.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.1891-900C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 15/15 | chr12 | 21538075 | |||||||
| chr12:21538112 | G | A | 8 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0205 others(5): Show |
9 | HG00642.hp1 HG01069.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1891-937C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 15/15 | chr12 | 21538112 | |||||||
| chr12:21538547 | A | C | 8 | a0001c0005t0001g0031 a0001c0005t0001g0033 a0001c0005t0001g0034 others(5): Show |
8 | HG01884.hp1 HG02280.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1890+711T>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 15/15 | chr12 | 21538547 | |||||||
| chr12:21538694 | C | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0242 a0001c0001t0001g0272 others(2): Show |
6 | HG02257.hp2 HG02451.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1890+564G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 15/15 | chr12 | 21538694 | |||||||
| chr12:21538855 | C | G | 1 | a0002c0002t0001g0114 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1890+403G>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 15/15 | chr12 | 21538855 | |||||||
| chr12:21538957 | T | C | 180 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0039 others(177): Show |
193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.1890+301A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 15/15 | chr12 | 21538957 | |||||||
| chr12:21538958 | T | C | 1 | a0003c0003t0001g0278 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1890+300A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 15/15 | chr12 | 21538958 | |||||||
| chr12:21539013 | AC | A | 3 | a0005c0007t0001g0139 a0005c0007t0001g0250 a0005c0007t0001g0251 |
3 | HG01175.hp1 HG01361.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1890+244delG | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 15/15 | chr12 | 21539013 | |||||||
| chr12:21539024 | C | T | 79 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0032 others(76): Show |
82 | HG00099.hp1 HG00621.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.1890+234G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 15/15 | chr12 | 21539024 | |||||||
| chr12:21539079 | C | A | 25 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0039 others(22): Show |
27 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.1890+179G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 15/15 | chr12 | 21539079 | |||||||
| chr12:21539232 | CA | C | 179 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0039 others(176): Show |
192 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.1890+25delT | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 15/15 | chr12 | 21539232 | |||||||
| chr12:21539584 | G | A | 3 | a0001c0001t0004g0126 a0001c0001t0004g0234 a0001c0001t0004g0252 |
3 | HG02572.hp1 HG02615.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1810-246C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 14/15 | chr12 | 21539584 | |||||||
| chr12:21539871 | T | C | 4 | a0002c0002t0001g0104 a0002c0002t0001g0108 a0002c0002t0001g0109 others(1): Show |
4 | HG00741.hp1 HG02055.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1810-533A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 14/15 | chr12 | 21539871 | |||||||
| chr12:21539884 | A | T | 1 | a0002c0002t0001g0118 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1809+526T>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 14/15 | chr12 | 21539884 | |||||||
| chr12:21539974 | T | C | 25 | a0002c0002t0001g0001 a0002c0002t0001g0024 a0002c0002t0001g0038 others(22): Show |
27 | HG00621.hp1 HG01981.hp2 HG02040.hp2 others(24): Show |
intron_variant | MODIFIER | c.1809+436A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 14/15 | chr12 | 21539974 | |||||||
| chr12:21540015 | A | G | 196 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0039 others(193): Show |
209 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1809+395T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 14/15 | chr12 | 21540015 | |||||||
| chr12:21540309 | A | T | 76 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0134 others(73): Show |
79 | HG00099.hp1 HG00621.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.1809+101T>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 14/15 | chr12 | 21540309 | |||||||
| chr12:21540310 | T | A | 76 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0134 others(73): Show |
79 | HG00099.hp1 HG00621.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.1809+100A>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 14/15 | chr12 | 21540310 | |||||||
| chr12:21540352 | G | A | 1 | a0001c0001t0003g0198 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1809+58C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 14/15 | chr12 | 21540352 | |||||||
| chr12:21540364 | G | A | 1 | a0001c0001t0003g0270 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1809+46C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 14/15 | chr12 | 21540364 | |||||||
| chr12:21540719 | T | C | 2 | a0001c0013t0001g0282 a0007c0010t0001g0022 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1646-146A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 13/15 | chr12 | 21540719 | |||||||
| chr12:21540753 | A | G | 2 | a0001c0001t0001g0023 a0001c0001t0008g0292 |
2 | HG02647.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1646-180T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 13/15 | chr12 | 21540753 | |||||||
| chr12:21540924 | G | A | 2 | a0001c0001t0002g0164 a0001c0001t0002g0180 |
2 | NA18951.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1646-351C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 13/15 | chr12 | 21540924 | |||||||
| chr12:21541006 | C | T | 23 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0084 others(20): Show |
25 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.1646-433G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 13/15 | chr12 | 21541006 | |||||||
| chr12:21541268 | C | CA | 76 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0035 others(73): Show |
81 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.1646-696dupT | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 13/15 | chr12 | 21541268 | |||||||
| chr12:21541268 | C | CAA | 50 | a0001c0001t0001g0032 a0001c0001t0001g0149 a0001c0001t0001g0153 others(47): Show |
53 | HG00438.hp1 HG00558.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.1646-697_1646-696d others(4): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 13/15 | chr12 | 21541268 | |||||||
| chr12:21541268 | C | CAAA | 62 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0002g0009 others(59): Show |
67 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.1646-698_1646-696d others(5): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 13/15 | chr12 | 21541268 | |||||||
| chr12:21541268 | C | CAAAA | 46 | a0001c0001t0001g0205 a0001c0001t0002g0002 a0001c0001t0002g0014 others(43): Show |
50 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.1646-699_1646-696d others(6): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 13/15 | chr12 | 21541268 | |||||||
| chr12:21541268 | C | CAAAAA | 17 | a0001c0001t0002g0069 a0001c0001t0002g0076 a0001c0001t0002g0094 others(14): Show |
17 | HG00621.hp2 HG00673.hp1 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.1646-700_1646-696d others(7): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 13/15 | chr12 | 21541268 | |||||||
| chr12:21541268 | CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0001g0039 a0001c0001t0001g0156 |
2 | HG01255.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1646-708_1646-696d others(15): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 13/15 | chr12 | 21541268 | |||||||
| chr12:21541280 | AAAAAAAA others(5): Show |
A | 3 | a0001c0001t0002g0044 a0001c0001t0002g0048 a0001c0001t0002g0051 |
3 | NA18970.hp1 NA18991.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1646-719_1646-708d others(14): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 13/15 | chr12 | 21541280 | |||||||
| chr12:21541281 | AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0002g0179 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1646-719_1646-709d others(13): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 13/15 | chr12 | 21541281 | |||||||
| chr12:21541282 | AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0002g0132 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1646-719_1646-710d others(12): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 13/15 | chr12 | 21541282 | |||||||
| chr12:21541284 | A | AAC | 7 | a0001c0001t0004g0100 a0002c0002t0004g0041 a0002c0002t0004g0042 others(4): Show |
7 | HG01891.hp1 HG02970.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1646-712_1646-711i others(4): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 13/15 | chr12 | 21541284 | |||||||
| chr12:21541284 | A | AC | 10 | a0001c0001t0001g0204 a0001c0001t0004g0025 a0001c0001t0004g0101 others(7): Show |
10 | HG02055.hp1 HG02486.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1646-712_1646-711i others(3): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 13/15 | chr12 | 21541284 | |||||||
| chr12:21541292 | C | A | 165 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0205 others(162): Show |
177 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.1646-719G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 13/15 | chr12 | 21541292 | |||||||
| chr12:21541475 | A | G | 6 | a0002c0002t0004g0041 a0002c0002t0004g0042 a0002c0002t0004g0239 others(3): Show |
6 | HG01891.hp1 HG02970.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1646-902T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 13/15 | chr12 | 21541475 | |||||||
| chr12:21541512 | C | T | 3 | a0005c0007t0001g0139 a0005c0007t0001g0250 a0005c0007t0001g0251 |
3 | HG01175.hp1 HG01361.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1646-939G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 13/15 | chr12 | 21541512 | |||||||
| chr12:21541873 | C | A | 1 | a0001c0013t0001g0282 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1645+623G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 13/15 | chr12 | 21541873 | |||||||
| chr12:21541975 | G | T | 2 | a0002c0002t0001g0088 a0002c0002t0001g0229 |
2 | NA18962.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.1645+521C>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 13/15 | chr12 | 21541975 | |||||||
| chr12:21542010 | G | A | 1 | a0001c0001t0002g0199 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1645+486C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 13/15 | chr12 | 21542010 | |||||||
| chr12:21542029 | A | T | 1 | a0001c0001t0001g0267 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1645+467T>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 13/15 | chr12 | 21542029 | |||||||
| chr12:21542052 | C | CT | 108 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0205 others(105): Show |
112 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.1645+443dupA | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 13/15 | chr12 | 21542052 | |||||||
| chr12:21542052 | C | CTT | 49 | a0001c0001t0002g0037 a0001c0001t0002g0048 a0001c0001t0002g0050 others(46): Show |
56 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.1645+442_1645+443d others(4): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 13/15 | chr12 | 21542052 | |||||||
| chr12:21542134 | G | A | 1 | a0002c0002t0001g0114 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1645+362C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 13/15 | chr12 | 21542134 | |||||||
| chr12:21542173 | G | C | 157 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0205 others(154): Show |
168 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.1645+323C>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 13/15 | chr12 | 21542173 | |||||||
| chr12:21542214 | AT | A | 8 | a0001c0005t0001g0031 a0001c0005t0001g0033 a0001c0005t0001g0034 others(5): Show |
8 | HG01884.hp1 HG02280.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1645+281delA | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 13/15 | chr12 | 21542214 | |||||||
| chr12:21542262 | C | A | 149 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0205 others(146): Show |
160 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.1645+234G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 13/15 | chr12 | 21542262 | |||||||
| chr12:21542302 | G | A | 3 | a0005c0007t0001g0139 a0005c0007t0001g0250 a0005c0007t0001g0251 |
3 | HG01175.hp1 HG01361.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1645+194C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 13/15 | chr12 | 21542302 | |||||||
| chr12:21542650 | A | G | 71 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0134 others(68): Show |
73 | HG00099.hp1 HG00621.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.1550-59T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 12/15 | chr12 | 21542650 | |||||||
| chr12:21542690 | A | G | 11 | a0001c0001t0001g0204 a0001c0001t0004g0025 a0001c0001t0004g0100 others(8): Show |
11 | HG02055.hp1 HG02486.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1550-99T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 12/15 | chr12 | 21542690 | |||||||
| chr12:21542774 | G | C | 2 | a0001c0001t0001g0023 a0001c0001t0008g0292 |
2 | HG02647.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1550-183C>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 12/15 | chr12 | 21542774 | |||||||
| chr12:21542890 | C | T | 1 | a0002c0002t0001g0147 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1550-299G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 12/15 | chr12 | 21542890 | |||||||
| chr12:21542910 | G | A | 28 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0084 others(25): Show |
30 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.1550-319C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 12/15 | chr12 | 21542910 | |||||||
| chr12:21543165 | T | C | 1 | a0001c0001t0002g0045 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1550-574A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 12/15 | chr12 | 21543165 | |||||||
| chr12:21543308 | A | G | 1 | a0001c0013t0001g0282 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1550-717T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 12/15 | chr12 | 21543308 | |||||||
| chr12:21543317 | T | C | 1 | a0001c0001t0002g0210 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1550-726A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 12/15 | chr12 | 21543317 | |||||||
| chr12:21543351 | G | A | 1 | a0001c0001t0003g0198 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1550-760C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 12/15 | chr12 | 21543351 | |||||||
| chr12:21543515 | A | T | 152 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0205 others(149): Show |
163 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.1550-924T>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 12/15 | chr12 | 21543515 | |||||||
| chr12:21543603 | G | GT | 209 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(206): Show |
223 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.1550-1013dupA | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 12/15 | chr12 | 21543603 | |||||||
| chr12:21543750 | A | G | 209 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(206): Show |
223 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.1550-1159T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 12/15 | chr12 | 21543750 | |||||||
| chr12:21543767 | G | A | 1 | a0002c0002t0001g0147 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1550-1176C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 12/15 | chr12 | 21543767 | |||||||
| chr12:21543839 | G | A | 182 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(179): Show |
195 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.1550-1248C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 12/15 | chr12 | 21543839 | |||||||
| chr12:21543907 | T | C | 5 | a0001c0001t0001g0015 a0001c0001t0001g0242 a0001c0001t0001g0272 others(2): Show |
6 | HG02257.hp2 HG02451.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1550-1316A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 12/15 | chr12 | 21543907 | |||||||
| chr12:21544123 | C | T | 1 | a0001c0001t0003g0195 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1550-1532G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 12/15 | chr12 | 21544123 | |||||||
| chr12:21544152 | A | G | 27 | a0001c0001t0001g0204 a0001c0001t0004g0025 a0001c0001t0004g0100 others(24): Show |
28 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.1550-1561T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 12/15 | chr12 | 21544152 | |||||||
| chr12:21544268 | C | T | 17 | a0001c0001t0001g0204 a0001c0001t0004g0025 a0001c0001t0004g0100 others(14): Show |
17 | HG01891.hp1 HG02055.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1550-1677G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 12/15 | chr12 | 21544268 | |||||||
| chr12:21544281 | G | A | 8 | a0001c0005t0001g0031 a0001c0005t0001g0033 a0001c0005t0001g0034 others(5): Show |
8 | HG01884.hp1 HG02280.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1550-1690C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 12/15 | chr12 | 21544281 | |||||||
| chr12:21544285 | A | C | 182 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(179): Show |
195 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.1550-1694T>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 12/15 | chr12 | 21544285 | |||||||
| chr12:21544448 | T | C | 27 | a0001c0001t0001g0204 a0001c0001t0004g0025 a0001c0001t0004g0100 others(24): Show |
28 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.1550-1857A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 12/15 | chr12 | 21544448 | |||||||
| chr12:21544550 | G | A | 1 | a0002c0002t0001g0135 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1549+1794C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 12/15 | chr12 | 21544550 | |||||||
| chr12:21544822 | A | G | 1 | a0001c0001t0003g0258 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1549+1522T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 12/15 | chr12 | 21544822 | |||||||
| chr12:21544885 | A | G | 3 | a0005c0007t0001g0139 a0005c0007t0001g0250 a0005c0007t0001g0251 |
3 | HG01175.hp1 HG01361.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1549+1459T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 12/15 | chr12 | 21544885 | |||||||
| chr12:21544931 | A | AT | 89 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0205 others(86): Show |
93 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.1549+1412dupA | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 12/15 | chr12 | 21544931 | |||||||
| chr12:21544940 | G | A | 144 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0205 others(141): Show |
155 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.1549+1404C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 12/15 | chr12 | 21544940 | |||||||
| chr12:21545164 | C | A | 5 | a0002c0002t0001g0007 a0002c0002t0001g0136 a0002c0002t0001g0150 others(2): Show |
6 | HG00642.hp1 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1549+1180G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 12/15 | chr12 | 21545164 | |||||||
| chr12:21545334 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1549+1010G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 12/15 | chr12 | 21545334 | |||||||
| chr12:21545335 | A | G | 285 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(282): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.1549+1009T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 12/15 | chr12 | 21545335 | |||||||
| chr12:21545500 | T | C | 285 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(282): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.1549+844A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 12/15 | chr12 | 21545500 | |||||||
| chr12:21545663 | A | G | 5 | a0004c0006t0001g0092 a0004c0006t0001g0151 a0004c0006t0001g0273 others(2): Show |
5 | HG02647.hp1 HG02723.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1549+681T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 12/15 | chr12 | 21545663 | |||||||
| chr12:21545895 | A | C | 2 | a0001c0001t0003g0011 a0001c0001t0003g0202 |
3 | HG01257.hp2 HG01258.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.1549+449T>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 12/15 | chr12 | 21545895 | |||||||
| chr12:21545982 | T | A | 1 | a0001c0001t0001g0204 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1549+362A>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 12/15 | chr12 | 21545982 | |||||||
| chr12:21546050 | T | TA | 13 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0205 others(10): Show |
14 | HG01070.hp2 HG01071.hp1 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.1549+293dupT | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 12/15 | chr12 | 21546050 | |||||||
| chr12:21546128 | A | C | 1 | a0001c0001t0003g0198 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1549+216T>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 12/15 | chr12 | 21546128 | |||||||
| chr12:21546154 | T | A | 1 | a0001c0001t0002g0045 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1549+190A>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 12/15 | chr12 | 21546154 | |||||||
| chr12:21546182 | T | C | 76 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0134 others(73): Show |
79 | HG00099.hp1 HG00621.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.1549+162A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 12/15 | chr12 | 21546182 | |||||||
| chr12:21546265 | T | C | 3 | a0001c0001t0002g0048 a0001c0001t0002g0264 a0001c0001t0003g0270 |
3 | NA18977.hp2 NA18991.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1549+79A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 12/15 | chr12 | 21546265 | |||||||
| chr12:21546491 | T | C | 7 | a0001c0001t0004g0025 a0001c0001t0004g0100 a0001c0001t0004g0101 others(4): Show |
7 | HG02055.hp1 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1423-21A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21546491 | |||||||
| chr12:21546557 | C | G | 41 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0039 others(38): Show |
43 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.1423-87G>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21546557 | |||||||
| chr12:21546574 | T | C | 149 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0205 others(146): Show |
160 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.1423-104A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21546574 | |||||||
| chr12:21546629 | G | A | 2 | a0002c0002t0001g0024 a0002c0002t0001g0043 |
2 | NA18939.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1423-159C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21546629 | |||||||
| chr12:21546661 | G | A | 10 | a0001c0001t0004g0025 a0001c0001t0004g0100 a0001c0001t0004g0101 others(7): Show |
10 | HG02055.hp1 HG02486.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1423-191C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21546661 | |||||||
| chr12:21546730 | A | C | 51 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0039 others(48): Show |
54 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.1423-260T>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21546730 | |||||||
| chr12:21546808 | C | A | 1 | a0001c0001t0001g0023 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1423-338G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21546808 | |||||||
| chr12:21546832 | A | G | 1 | a0002c0002t0001g0135 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1423-362T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21546832 | |||||||
| chr12:21546910 | C | T | 4 | a0001c0001t0003g0068 a0001c0001t0003g0172 a0001c0001t0003g0175 others(1): Show |
4 | HG00438.hp1 HG02080.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.1423-440G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21546910 | |||||||
| chr12:21546982 | G | A | 185 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(182): Show |
198 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.1423-512C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21546982 | |||||||
| chr12:21546994 | C | A | 185 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(182): Show |
198 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.1423-524G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21546994 | |||||||
| chr12:21547005 | G | A | 186 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(183): Show |
199 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.1423-535C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21547005 | |||||||
| chr12:21547022 | C | T | 2 | a0002c0002t0001g0223 a0002c0002t0009g0224 |
2 | HG00099.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.1423-552G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21547022 | |||||||
| chr12:21547384 | G | A | 3 | a0001c0001t0002g0050 a0001c0001t0002g0187 a0001c0001t0002g0231 |
3 | HG02040.hp1 NA18949.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1423-914C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21547384 | |||||||
| chr12:21547561 | T | G | 185 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(182): Show |
198 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.1423-1091A>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21547561 | |||||||
| chr12:21547610 | G | A | 22 | a0001c0001t0002g0014 a0001c0001t0002g0061 a0001c0001t0002g0070 others(19): Show |
23 | HG00735.hp2 HG01069.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.1423-1140C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21547610 | |||||||
| chr12:21548100 | TA | T | 185 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(182): Show |
198 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.1423-1631delT | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21548100 | |||||||
| chr12:21548216 | T | A | 185 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(182): Show |
198 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.1423-1746A>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21548216 | |||||||
| chr12:21548265 | C | T | 9 | a0001c0001t0001g0084 a0001c0001t0001g0149 a0001c0001t0001g0291 others(6): Show |
10 | HG02258.hp2 HG02647.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1423-1795G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21548265 | |||||||
| chr12:21548366 | C | T | 175 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(172): Show |
188 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.1423-1896G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21548366 | |||||||
| chr12:21548434 | C | G | 4 | a0002c0002t0004g0239 a0002c0002t0004g0295 a0002c0002t0006g0240 others(1): Show |
4 | HG01891.hp1 HG02970.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1423-1964G>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21548434 | |||||||
| chr12:21548500 | G | T | 2 | a0001c0001t0002g0236 a0001c0001t0002g0237 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1423-2030C>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21548500 | |||||||
| chr12:21548503 | C | T | 195 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(192): Show |
209 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1423-2033G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21548503 | |||||||
| chr12:21548597 | A | G | 3 | a0001c0001t0004g0126 a0001c0001t0004g0234 a0001c0001t0004g0252 |
3 | HG02572.hp1 HG02615.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1423-2127T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21548597 | |||||||
| chr12:21548630 | A | G | 3 | a0005c0007t0001g0139 a0005c0007t0001g0250 a0005c0007t0001g0251 |
3 | HG01175.hp1 HG01361.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1423-2160T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21548630 | |||||||
| chr12:21548719 | T | C | 195 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(192): Show |
209 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1423-2249A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21548719 | |||||||
| chr12:21548927 | C | A | 1 | a0001c0001t0001g0015 | 2 | HG02257.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1423-2457G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21548927 | |||||||
| chr12:21549043 | T | A | 3 | a0001c0001t0002g0148 a0001c0001t0002g0166 a0001c0001t0002g0179 |
3 | HG02735.hp1 HG03710.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1423-2573A>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21549043 | |||||||
| chr12:21549044 | T | TATTAATA others(4): Show |
3 | a0001c0001t0002g0148 a0001c0001t0002g0166 a0001c0001t0002g0179 |
3 | HG02735.hp1 HG03710.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1423-2575_1423-257 others(15): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21549044 | |||||||
| chr12:21549045 | C | T | 3 | a0001c0001t0002g0148 a0001c0001t0002g0166 a0001c0001t0002g0179 |
3 | HG02735.hp1 HG03710.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1423-2575G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21549045 | |||||||
| chr12:21549071 | C | T | 196 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(193): Show |
210 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.1423-2601G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21549071 | |||||||
| chr12:21549080 | A | G | 6 | a0002c0002t0004g0041 a0002c0002t0004g0042 a0002c0002t0004g0239 others(3): Show |
6 | HG01891.hp1 HG02970.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1423-2610T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21549080 | |||||||
| chr12:21549086 | A | T | 196 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(193): Show |
210 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.1423-2616T>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21549086 | |||||||
| chr12:21549318 | G | A | 2 | a0001c0001t0003g0065 a0001c0001t0003g0174 |
2 | HG00597.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.1423-2848C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21549318 | |||||||
| chr12:21549397 | C | T | 1 | a0002c0002t0004g0295 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1423-2927G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21549397 | |||||||
| chr12:21549545 | C | CAT | 10 | a0003c0003t0001g0016 a0003c0003t0001g0026 a0003c0003t0001g0105 others(7): Show |
11 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1423-3077_1423-307 others(6): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21549545 | |||||||
| chr12:21549562 | T | C | 3 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0155 |
3 | HG00280.hp2 HG00323.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1423-3092A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21549562 | |||||||
| chr12:21549569 | G | C | 196 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(193): Show |
210 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.1423-3099C>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21549569 | |||||||
| chr12:21549638 | G | A | 2 | a0002c0002t0004g0041 a0002c0002t0004g0042 |
2 | NA18978.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1423-3168C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21549638 | |||||||
| chr12:21549672 | G | A | 1 | a0001c0001t0003g0249 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1423-3202C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21549672 | |||||||
| chr12:21549798 | A | T | 2 | a0001c0001t0002g0044 a0001c0001t0002g0051 |
2 | NA18970.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.1423-3328T>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21549798 | |||||||
| chr12:21549827 | G | C | 1 | a0001c0001t0010g0064 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1423-3357C>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21549827 | |||||||
| chr12:21549852 | C | T | 1 | a0001c0001t0003g0161 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1423-3382G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21549852 | |||||||
| chr12:21549912 | C | G | 196 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(193): Show |
210 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.1423-3442G>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21549912 | |||||||
| chr12:21550314 | A | AAC | 9 | a0002c0002t0001g0007 a0002c0002t0001g0136 a0002c0002t0001g0150 others(6): Show |
10 | HG00642.hp1 HG01069.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.1423-3846_1423-384 others(6): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21550314 | |||||||
| chr12:21550314 | A | AACAC | 4 | a0001c0005t0001g0129 a0001c0005t0001g0131 a0002c0002t0001g0090 others(1): Show |
4 | HG02145.hp2 HG02630.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1423-3848_1423-384 others(8): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21550314 | |||||||
| chr12:21550314 | A | AACACAC | 8 | a0001c0005t0001g0031 a0001c0005t0001g0033 a0001c0005t0001g0034 others(5): Show |
8 | HG01884.hp1 HG02280.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1423-3850_1423-384 others(10): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21550314 | |||||||
| chr12:21550314 | AAC | A | 48 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0134 others(45): Show |
50 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.1423-3846_1423-384 others(6): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21550314 | |||||||
| chr12:21550314 | AACAC | A | 5 | a0002c0002t0001g0058 a0002c0002t0001g0111 a0002c0002t0001g0115 others(2): Show |
5 | HG02965.hp2 NA18747.hp1 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.1423-3848_1423-384 others(8): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21550314 | |||||||
| chr12:21550314 | AACACAC | A | 7 | a0001c0001t0002g0059 a0001c0001t0002g0236 a0001c0001t0002g0237 others(4): Show |
7 | HG02559.hp2 HG03490.hp2 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.1423-3850_1423-384 others(10): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21550314 | |||||||
| chr12:21550314 | AACACACA others(1): Show |
A | 148 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0205 others(145): Show |
159 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.1423-3852_1423-384 others(12): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21550314 | |||||||
| chr12:21550314 | AACACACA others(3): Show |
A | 38 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0039 others(35): Show |
41 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.1423-3854_1423-384 others(14): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21550314 | |||||||
| chr12:21550314 | AACACACA others(7): Show |
A | 7 | a0001c0001t0004g0025 a0001c0001t0004g0100 a0001c0001t0004g0101 others(4): Show |
7 | HG02055.hp1 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1423-3858_1423-384 others(18): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21550314 | |||||||
| chr12:21550348 | C | T | 1 | a0001c0001t0004g0234 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1423-3878G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21550348 | |||||||
| chr12:21550351 | A | C | 7 | a0002c0002t0001g0038 a0002c0002t0001g0106 a0002c0002t0001g0112 others(4): Show |
7 | HG01358.hp2 HG02040.hp2 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.1423-3881T>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21550351 | |||||||
| chr12:21550353 | C | A | 3 | a0005c0007t0001g0139 a0005c0007t0001g0250 a0005c0007t0001g0251 |
3 | HG01175.hp1 HG01361.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1423-3883G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21550353 | |||||||
| chr12:21550364 | A | G | 196 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(193): Show |
210 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.1423-3894T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21550364 | |||||||
| chr12:21550562 | C | T | 2 | a0001c0001t0002g0062 a0001c0001t0002g0071 |
2 | HG01358.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.1423-4092G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21550562 | |||||||
| chr12:21550667 | A | G | 205 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(202): Show |
219 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1423-4197T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21550667 | |||||||
| chr12:21550700 | G | A | 3 | a0005c0007t0001g0139 a0005c0007t0001g0250 a0005c0007t0001g0251 |
3 | HG01175.hp1 HG01361.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1423-4230C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21550700 | |||||||
| chr12:21550739 | G | A | 196 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(193): Show |
210 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.1423-4269C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21550739 | |||||||
| chr12:21550795 | G | T | 1 | a0001c0001t0002g0253 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1423-4325C>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21550795 | |||||||
| chr12:21550920 | C | T | 1 | a0002c0002t0001g0102 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1423-4450G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21550920 | |||||||
| chr12:21550953 | A | G | 196 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(193): Show |
210 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.1423-4483T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21550953 | |||||||
| chr12:21551009 | T | A | 149 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0205 others(146): Show |
160 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.1423-4539A>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21551009 | |||||||
| chr12:21551010 | T | A | 181 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(178): Show |
194 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.1423-4540A>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21551010 | |||||||
| chr12:21551011 | T | A | 196 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(193): Show |
210 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.1423-4541A>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21551011 | |||||||
| chr12:21551013 | A | AT | 203 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(200): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1423-4544dupA | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21551013 | |||||||
| chr12:21551013 | AT | A | 65 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0134 others(62): Show |
67 | HG00099.hp1 HG00621.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.1423-4544delA | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21551013 | |||||||
| chr12:21551063 | G | A | 18 | a0002c0002t0001g0058 a0002c0002t0001g0097 a0002c0002t0001g0107 others(15): Show |
18 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.1423-4593C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21551063 | |||||||
| chr12:21551161 | T | C | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1423-4691A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21551161 | |||||||
| chr12:21551193 | A | T | 2 | a0001c0001t0002g0070 a0001c0001t0002g0183 |
2 | HG01070.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1423-4723T>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21551193 | |||||||
| chr12:21551203 | T | A | 4 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0096 others(1): Show |
6 | HG00423.hp2 NA18949.hp1 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.1423-4733A>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21551203 | |||||||
| chr12:21551518 | T | TA | 193 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(190): Show |
207 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.1423-5049dupT | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21551518 | |||||||
| chr12:21551606 | C | G | 5 | a0002c0002t0001g0007 a0002c0002t0001g0136 a0002c0002t0001g0150 others(2): Show |
6 | HG00642.hp1 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1423-5136G>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21551606 | |||||||
| chr12:21551620 | A | G | 191 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(188): Show |
205 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1423-5150T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21551620 | |||||||
| chr12:21551659 | C | T | 1 | a0002c0002t0001g0135 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1423-5189G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21551659 | |||||||
| chr12:21551778 | A | G | 3 | a0005c0007t0001g0139 a0005c0007t0001g0250 a0005c0007t0001g0251 |
3 | HG01175.hp1 HG01361.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1423-5308T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21551778 | |||||||
| chr12:21551822 | C | T | 1 | a0003c0003t0001g0289 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1423-5352G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21551822 | |||||||
| chr12:21551940 | A | C | 3 | a0005c0007t0001g0139 a0005c0007t0001g0250 a0005c0007t0001g0251 |
3 | HG01175.hp1 HG01361.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1423-5470T>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21551940 | |||||||
| chr12:21552122 | T | G | 193 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(190): Show |
207 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.1423-5652A>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21552122 | |||||||
| chr12:21552412 | T | C | 1 | a0001c0001t0002g0214 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1422+5788A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21552412 | |||||||
| chr12:21552425 | CTG | C | 204 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(201): Show |
218 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.1422+5773_1422+577 others(6): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21552425 | |||||||
| chr12:21552449 | C | G | 204 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(201): Show |
218 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.1422+5751G>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21552449 | |||||||
| chr12:21552786 | T | C | 1 | a0002c0002t0001g0099 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1422+5414A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21552786 | |||||||
| chr12:21552811 | G | C | 10 | a0003c0003t0001g0016 a0003c0003t0001g0026 a0003c0003t0001g0105 others(7): Show |
11 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1422+5389C>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21552811 | |||||||
| chr12:21552853 | G | A | 192 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(189): Show |
205 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1422+5347C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21552853 | |||||||
| chr12:21552854 | T | A | 1 | a0001c0005t0001g0031 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1422+5346A>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21552854 | |||||||
| chr12:21552880 | A | G | 24 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0084 others(21): Show |
26 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.1422+5320T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21552880 | |||||||
| chr12:21552905 | G | A | 1 | a0002c0002t0001g0136 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1422+5295C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21552905 | |||||||
| chr12:21552934 | C | T | 1 | a0001c0001t0008g0292 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1422+5266G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21552934 | |||||||
| chr12:21552962 | C | A | 193 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(190): Show |
206 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1422+5238G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21552962 | |||||||
| chr12:21553027 | G | T | 1 | a0001c0001t0001g0205 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1422+5173C>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21553027 | |||||||
| chr12:21553194 | C | G | 1 | a0001c0001t0003g0171 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1422+5006G>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21553194 | |||||||
| chr12:21553235 | C | A | 1 | a0001c0001t0002g0076 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1422+4965G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21553235 | |||||||
| chr12:21553257 | T | A | 1 | a0001c0001t0001g0028 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1422+4943A>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21553257 | |||||||
| chr12:21553325 | G | A | 2 | a0001c0001t0002g0186 a0001c0001t0002g0215 |
2 | HG00423.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.1422+4875C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21553325 | |||||||
| chr12:21553348 | T | G | 203 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(200): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1422+4852A>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21553348 | |||||||
| chr12:21553400 | T | C | 6 | a0002c0002t0004g0041 a0002c0002t0004g0042 a0002c0002t0004g0239 others(3): Show |
6 | HG01891.hp1 HG02970.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1422+4800A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21553400 | |||||||
| chr12:21553506 | T | A | 2 | a0001c0001t0003g0029 a0001c0001t0003g0030 |
2 | NA18952.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.1422+4694A>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21553506 | |||||||
| chr12:21553720 | A | C | 193 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(190): Show |
206 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1422+4480T>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21553720 | |||||||
| chr12:21553793 | T | C | 193 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(190): Show |
206 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1422+4407A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21553793 | |||||||
| chr12:21553796 | A | AAC | 5 | a0002c0002t0001g0007 a0002c0002t0001g0136 a0002c0002t0001g0150 others(2): Show |
6 | HG00642.hp1 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1422+4402_1422+440 others(6): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21553796 | |||||||
| chr12:21553796 | A | AACAC | 28 | a0001c0001t0001g0023 a0001c0001t0001g0032 a0001c0001t0001g0035 others(25): Show |
28 | HG00099.hp1 HG00741.hp1 HG01346.hp1 others(25): Show |
intron_variant | MODIFIER | c.1422+4400_1422+440 others(8): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21553796 | |||||||
| chr12:21553796 | A | AACACAC | 131 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0028 others(128): Show |
137 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.1422+4398_1422+440 others(10): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21553796 | |||||||
| chr12:21553796 | A | AACACACA others(1): Show |
49 | a0001c0001t0002g0020 a0001c0001t0002g0048 a0001c0001t0002g0179 others(46): Show |
56 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.1422+4396_1422+440 others(12): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21553796 | |||||||
| chr12:21553796 | A | AACACACA others(3): Show |
1 | a0001c0001t0003g0121 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1422+4394_1422+440 others(14): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21553796 | |||||||
| chr12:21553796 | AAC | A | 20 | a0002c0002t0001g0078 a0002c0002t0001g0082 a0002c0002t0001g0088 others(17): Show |
21 | HG01884.hp2 HG01891.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1422+4402_1422+440 others(6): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21553796 | |||||||
| chr12:21553930 | A | G | 193 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(190): Show |
206 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1422+4270T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21553930 | |||||||
| chr12:21553988 | G | A | 2 | a0002c0002t0001g0078 a0002c0002t0001g0082 |
2 | NA18953.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1422+4212C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21553988 | |||||||
| chr12:21554078 | T | G | 3 | a0001c0001t0001g0267 a0001c0005t0001g0036 a0001c0005t0001g0125 |
3 | HG02622.hp2 HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1422+4122A>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21554078 | |||||||
| chr12:21554169 | A | G | 193 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(190): Show |
206 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1422+4031T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21554169 | |||||||
| chr12:21554172 | A | G | 193 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(190): Show |
206 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1422+4028T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21554172 | |||||||
| chr12:21554174 | G | T | 193 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(190): Show |
206 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1422+4026C>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21554174 | |||||||
| chr12:21554214 | G | C | 1 | a0002c0002t0001g0118 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1422+3986C>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21554214 | |||||||
| chr12:21554567 | T | TA | 193 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(190): Show |
206 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1422+3632dupT | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21554567 | |||||||
| chr12:21554599 | C | T | 143 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0205 others(140): Show |
154 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.1422+3601G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21554599 | |||||||
| chr12:21554621 | C | T | 1 | a0001c0001t0003g0161 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1422+3579G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21554621 | |||||||
| chr12:21554645 | C | T | 1 | a0001c0001t0002g0133 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1422+3555G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21554645 | |||||||
| chr12:21554699 | G | A | 1 | a0002c0002t0001g0290 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1422+3501C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21554699 | |||||||
| chr12:21554725 | T | C | 3 | a0005c0007t0001g0139 a0005c0007t0001g0250 a0005c0007t0001g0251 |
3 | HG01175.hp1 HG01361.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1422+3475A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21554725 | |||||||
| chr12:21554858 | A | C | 203 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(200): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1422+3342T>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21554858 | |||||||
| chr12:21554873 | C | T | 8 | a0003c0003t0001g0016 a0003c0003t0001g0026 a0003c0003t0001g0105 others(5): Show |
9 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1422+3327G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21554873 | |||||||
| chr12:21554901 | A | G | 291 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(288): Show |
308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.1422+3299T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21554901 | |||||||
| chr12:21554986 | T | C | 163 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0032 others(160): Show |
174 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1422+3214A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21554986 | |||||||
| chr12:21554988 | C | T | 163 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0032 others(160): Show |
174 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1422+3212G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21554988 | |||||||
| chr12:21555144 | C | G | 48 | a0001c0001t0002g0048 a0001c0001t0002g0264 a0001c0001t0003g0003 others(45): Show |
55 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.1422+3056G>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21555144 | |||||||
| chr12:21555222 | G | A | 3 | a0001c0001t0001g0023 a0001c0001t0008g0292 a0001c0013t0001g0282 |
3 | HG02647.hp2 HG02809.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1422+2978C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21555222 | |||||||
| chr12:21555242 | C | A | 1 | a0001c0005t0001g0131 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1422+2958G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21555242 | |||||||
| chr12:21555278 | A | C | 1 | a0001c0001t0011g0211 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1422+2922T>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21555278 | |||||||
| chr12:21555382 | G | A | 2 | a0001c0001t0003g0029 a0001c0001t0003g0030 |
2 | NA18952.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.1422+2818C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21555382 | |||||||
| chr12:21555447 | G | A | 193 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(190): Show |
206 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1422+2753C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21555447 | |||||||
| chr12:21555657 | A | C | 202 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(199): Show |
215 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.1422+2543T>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21555657 | |||||||
| chr12:21555799 | T | C | 193 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(190): Show |
206 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1422+2401A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21555799 | |||||||
| chr12:21556029 | G | T | 2 | a0002c0002t0004g0041 a0002c0002t0004g0042 |
2 | NA18978.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1422+2171C>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21556029 | |||||||
| chr12:21556209 | C | T | 3 | a0005c0007t0001g0139 a0005c0007t0001g0250 a0005c0007t0001g0251 |
3 | HG01175.hp1 HG01361.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1422+1991G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21556209 | |||||||
| chr12:21556247 | C | G | 1 | a0001c0001t0004g0101 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1422+1953G>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21556247 | |||||||
| chr12:21556276 | C | G | 1 | a0002c0002t0001g0102 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1422+1924G>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21556276 | |||||||
| chr12:21556314 | G | T | 3 | a0005c0007t0001g0139 a0005c0007t0001g0250 a0005c0007t0001g0251 |
3 | HG01175.hp1 HG01361.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1422+1886C>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21556314 | |||||||
| chr12:21556408 | C | A | 3 | a0001c0001t0001g0023 a0001c0001t0008g0292 a0001c0013t0001g0282 |
3 | HG02647.hp2 HG02809.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1422+1792G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21556408 | |||||||
| chr12:21556620 | A | G | 193 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(190): Show |
206 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1422+1580T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21556620 | |||||||
| chr12:21556639 | A | C | 196 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(193): Show |
209 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1422+1561T>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21556639 | |||||||
| chr12:21556670 | T | C | 196 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(193): Show |
209 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1422+1530A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21556670 | |||||||
| chr12:21556685 | G | C | 193 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(190): Show |
206 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1422+1515C>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21556685 | |||||||
| chr12:21556718 | T | C | 1 | a0002c0002t0001g0142 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1422+1482A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21556718 | |||||||
| chr12:21556723 | T | A | 193 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(190): Show |
206 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1422+1477A>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21556723 | |||||||
| chr12:21556731 | AAAGCCAA others(3): Show |
A | 193 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(190): Show |
206 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1422+1459_1422+146 others(14): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21556731 | |||||||
| chr12:21556884 | T | C | 163 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0032 others(160): Show |
174 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1422+1316A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21556884 | |||||||
| chr12:21557304 | G | A | 2 | a0002c0002t0001g0280 a0002c0002t0001g0281 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1422+896C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21557304 | |||||||
| chr12:21557397 | C | T | 1 | a0001c0001t0003g0271 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1422+803G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21557397 | |||||||
| chr12:21557451 | A | G | 3 | a0002c0002t0001g0106 a0002c0002t0001g0112 a0002c0002t0001g0137 |
3 | NA19005.hp1 NA19007.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1422+749T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21557451 | |||||||
| chr12:21557591 | G | T | 4 | a0002c0002t0004g0239 a0002c0002t0004g0295 a0002c0002t0006g0240 others(1): Show |
4 | HG01891.hp1 HG02970.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1422+609C>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21557591 | |||||||
| chr12:21557626 | G | A | 3 | a0005c0007t0001g0139 a0005c0007t0001g0250 a0005c0007t0001g0251 |
3 | HG01175.hp1 HG01361.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1422+574C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21557626 | |||||||
| chr12:21557671 | A | G | 193 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(190): Show |
206 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1422+529T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21557671 | |||||||
| chr12:21557721 | A | G | 6 | a0002c0002t0004g0041 a0002c0002t0004g0042 a0002c0002t0004g0239 others(3): Show |
6 | HG01891.hp1 HG02970.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1422+479T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21557721 | |||||||
| chr12:21557812 | T | C | 1 | a0002c0002t0001g0283 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1422+388A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21557812 | |||||||
| chr12:21557815 | T | C | 193 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(190): Show |
206 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1422+385A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21557815 | |||||||
| chr12:21557819 | G | A | 193 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(190): Show |
206 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1422+381C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21557819 | |||||||
| chr12:21557822 | C | A | 1 | a0001c0001t0001g0204 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1422+378G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21557822 | |||||||
| chr12:21557871 | C | G | 3 | a0005c0007t0001g0139 a0005c0007t0001g0250 a0005c0007t0001g0251 |
3 | HG01175.hp1 HG01361.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1422+329G>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21557871 | |||||||
| chr12:21557886 | G | A | 193 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(190): Show |
206 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1422+314C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21557886 | |||||||
| chr12:21557894 | G | A | 193 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(190): Show |
206 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1422+306C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21557894 | |||||||
| chr12:21557919 | T | C | 193 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(190): Show |
206 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1422+281A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21557919 | |||||||
| chr12:21557985 | G | A | 193 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(190): Show |
206 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1422+215C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21557985 | |||||||
| chr12:21557997 | T | G | 193 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(190): Show |
206 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1422+203A>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21557997 | |||||||
| chr12:21558009 | T | G | 1 | a0002c0002t0001g0266 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1422+191A>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21558009 | |||||||
| chr12:21558019 | A | G | 1 | a0001c0004t0003g0123 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1422+181T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21558019 | |||||||
| chr12:21558075 | C | A | 193 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(190): Show |
206 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1422+125G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21558075 | |||||||
| chr12:21558176 | C | T | 1 | a0002c0002t0001g0079 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1422+24G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21558176 | |||||||
| chr12:21558177 | G | C | 193 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(190): Show |
206 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1422+23C>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 11/15 | chr12 | 21558177 | |||||||
| chr12:21558447 | C | T | 27 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0084 others(24): Show |
29 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.1309-134G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 10/15 | chr12 | 21558447 | |||||||
| chr12:21558451 | G | C | 193 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(190): Show |
206 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1309-138C>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 10/15 | chr12 | 21558451 | |||||||
| chr12:21558465 | T | TGC | 5 | a0002c0002t0001g0043 a0002c0002t0001g0058 a0002c0002t0001g0111 others(2): Show |
5 | NA18747.hp1 NA18939.hp1 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.1309-153_1309-152i others(4): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 10/15 | chr12 | 21558465 | |||||||
| chr12:21558502 | G | A | 196 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(193): Show |
209 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1309-189C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 10/15 | chr12 | 21558502 | |||||||
| chr12:21558575 | C | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0242 a0001c0001t0001g0272 others(2): Show |
6 | HG02257.hp2 HG02451.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1309-262G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 10/15 | chr12 | 21558575 | |||||||
| chr12:21558629 | T | C | 1 | a0002c0002t0001g0137 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1309-316A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 10/15 | chr12 | 21558629 | |||||||
| chr12:21558671 | T | C | 193 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(190): Show |
206 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1309-358A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 10/15 | chr12 | 21558671 | |||||||
| chr12:21558692 | C | T | 193 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(190): Show |
206 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1309-379G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 10/15 | chr12 | 21558692 | |||||||
| chr12:21558817 | A | G | 1 | a0002c0002t0001g0102 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1308+274T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 10/15 | chr12 | 21558817 | |||||||
| chr12:21558891 | T | G | 193 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(190): Show |
206 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1308+200A>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 10/15 | chr12 | 21558891 | |||||||
| chr12:21559326 | GTACATAT others(4): Show |
G | 3 | a0005c0007t0001g0139 a0005c0007t0001g0250 a0005c0007t0001g0251 |
3 | HG01175.hp1 HG01361.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1230-168_1230-158d others(13): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 9/15 | chr12 | 21559326 | |||||||
| chr12:21559356 | A | G | 1 | a0001c0001t0004g0101 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1230-187T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 9/15 | chr12 | 21559356 | |||||||
| chr12:21559393 | C | G | 203 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(200): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1230-224G>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 9/15 | chr12 | 21559393 | |||||||
| chr12:21559397 | C | T | 291 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(288): Show |
308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.1230-228G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 9/15 | chr12 | 21559397 | |||||||
| chr12:21559569 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1229+82A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 9/15 | chr12 | 21559569 | |||||||
| chr12:21559611 | A | G | 203 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(200): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1229+40T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 9/15 | chr12 | 21559611 | |||||||
| chr12:21559640 | C | T | 203 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(200): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1229+11G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 9/15 | chr12 | 21559640 | |||||||
| chr12:21559794 | GACATTCT others(8): Show |
G | 203 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(200): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1170-99_1170-85del others(15): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 8/15 | chr12 | 21559794 | |||||||
| chr12:21559952 | A | G | 8 | a0001c0001t0001g0039 a0001c0001t0001g0091 a0001c0001t0001g0152 others(5): Show |
8 | HG00280.hp2 HG00323.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1170-242T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 8/15 | chr12 | 21559952 | |||||||
| chr12:21559962 | G | C | 203 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(200): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1170-252C>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 8/15 | chr12 | 21559962 | |||||||
| chr12:21559996 | A | G | 203 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(200): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1170-286T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 8/15 | chr12 | 21559996 | |||||||
| chr12:21559999 | G | T | 1 | a0001c0001t0004g0126 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1170-289C>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 8/15 | chr12 | 21559999 | |||||||
| chr12:21560016 | C | T | 4 | a0001c0011t0002g0203 a0005c0007t0001g0139 a0005c0007t0001g0250 others(1): Show |
4 | HG01175.hp1 HG01361.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1170-306G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 8/15 | chr12 | 21560016 | |||||||
| chr12:21560058 | C | T | 3 | a0001c0001t0001g0134 a0001c0001t0004g0234 a0001c0001t0004g0252 |
3 | HG02615.hp1 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1169+328G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 8/15 | chr12 | 21560058 | |||||||
| chr12:21560120 | A | T | 203 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(200): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1169+266T>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 8/15 | chr12 | 21560120 | |||||||
| chr12:21560146 | A | T | 3 | a0005c0007t0001g0139 a0005c0007t0001g0250 a0005c0007t0001g0251 |
3 | HG01175.hp1 HG01361.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1169+240T>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 8/15 | chr12 | 21560146 | |||||||
| chr12:21560178 | C | T | 2 | a0001c0001t0003g0270 a0001c0001t0010g0064 |
2 | NA18977.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1169+208G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 8/15 | chr12 | 21560178 | |||||||
| chr12:21560216 | C | A | 200 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(197): Show |
214 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.1169+170G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 8/15 | chr12 | 21560216 | |||||||
| chr12:21560374 | T | A | 206 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(203): Show |
220 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.1169+12A>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 8/15 | chr12 | 21560374 | |||||||
| chr12:21560507 | G | C | 3 | a0001c0001t0002g0044 a0001c0001t0002g0051 a0001c0001t0002g0169 |
3 | NA18970.hp1 NA19005.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1063-15C>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21560507 | |||||||
| chr12:21560714 | A | G | 203 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(200): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1063-222T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21560714 | |||||||
| chr12:21560873 | C | A | 200 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(197): Show |
214 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.1063-381G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21560873 | |||||||
| chr12:21560882 | A | T | 4 | a0002c0002t0004g0239 a0002c0002t0004g0295 a0002c0002t0006g0240 others(1): Show |
4 | HG01891.hp1 HG02970.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1063-390T>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21560882 | |||||||
| chr12:21560908 | G | C | 24 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0084 others(21): Show |
26 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.1063-416C>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21560908 | |||||||
| chr12:21560965 | G | T | 24 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0084 others(21): Show |
26 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.1063-473C>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21560965 | |||||||
| chr12:21561082 | G | A | 5 | a0002c0002t0001g0007 a0002c0002t0001g0136 a0002c0002t0001g0150 others(2): Show |
6 | HG00642.hp1 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1063-590C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21561082 | |||||||
| chr12:21561148 | T | C | 4 | a0001c0001t0002g0170 a0001c0001t0002g0191 a0001c0001t0002g0192 others(1): Show |
4 | HG01069.hp2 HG01516.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.1063-656A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21561148 | |||||||
| chr12:21561240 | C | G | 193 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(190): Show |
206 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1063-748G>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21561240 | |||||||
| chr12:21561331 | T | C | 1 | a0002c0002t0001g0137 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1063-839A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21561331 | |||||||
| chr12:21561384 | G | A | 2 | a0001c0001t0002g0094 a0001c0001t0002g0201 |
2 | NA18978.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.1063-892C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21561384 | |||||||
| chr12:21561404 | G | A | 3 | a0001c0001t0001g0134 a0001c0001t0004g0234 a0001c0001t0004g0252 |
3 | HG02615.hp1 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1063-912C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21561404 | |||||||
| chr12:21561415 | C | T | 201 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(198): Show |
215 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.1063-923G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21561415 | |||||||
| chr12:21561514 | GT | G | 201 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(198): Show |
215 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.1063-1023delA | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21561514 | |||||||
| chr12:21561672 | T | C | 201 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(198): Show |
215 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.1063-1180A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21561672 | |||||||
| chr12:21561807 | A | G | 201 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(198): Show |
215 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.1062+1111T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21561807 | |||||||
| chr12:21561817 | T | C | 201 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(198): Show |
215 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.1062+1101A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21561817 | |||||||
| chr12:21561826 | G | A | 1 | a0001c0001t0002g0037 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1062+1092C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21561826 | |||||||
| chr12:21561840 | T | C | 1 | a0006c0014t0001g0086 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1062+1078A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21561840 | |||||||
| chr12:21561889 | G | A | 22 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0084 others(19): Show |
24 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.1062+1029C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21561889 | |||||||
| chr12:21561966 | T | G | 201 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(198): Show |
215 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.1062+952A>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21561966 | |||||||
| chr12:21562076 | G | T | 2 | a0001c0001t0003g0172 a0001c0001t0003g0175 |
2 | NA18971.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.1062+842C>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21562076 | |||||||
| chr12:21562115 | G | A | 201 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(198): Show |
215 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.1062+803C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21562115 | |||||||
| chr12:21562123 | G | A | 3 | a0001c0001t0001g0134 a0001c0001t0004g0234 a0001c0001t0004g0252 |
3 | HG02615.hp1 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1062+795C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21562123 | |||||||
| chr12:21562133 | A | T | 1 | a0002c0002t0001g0078 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1062+785T>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21562133 | |||||||
| chr12:21562211 | T | C | 1 | a0004c0006t0001g0092 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1062+707A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21562211 | |||||||
| chr12:21562229 | G | A | 18 | a0001c0001t0001g0091 a0001c0001t0001g0204 a0002c0002t0001g0017 others(15): Show |
18 | HG00099.hp1 HG00741.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.1062+689C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21562229 | |||||||
| chr12:21562256 | A | G | 201 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(198): Show |
215 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.1062+662T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21562256 | |||||||
| chr12:21562316 | T | C | 1 | a0001c0001t0002g0188 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1062+602A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21562316 | |||||||
| chr12:21562340 | G | A | 201 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(198): Show |
215 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.1062+578C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21562340 | |||||||
| chr12:21562347 | C | T | 11 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0267 others(8): Show |
11 | HG01884.hp1 HG02280.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1062+571G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21562347 | |||||||
| chr12:21562494 | A | G | 1 | a0001c0001t0003g0171 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1062+424T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21562494 | |||||||
| chr12:21562507 | A | G | 1 | a0002c0002t0001g0138 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1062+411T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21562507 | |||||||
| chr12:21562607 | A | G | 201 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(198): Show |
215 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.1062+311T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21562607 | |||||||
| chr12:21562609 | A | G | 3 | a0005c0007t0001g0139 a0005c0007t0001g0250 a0005c0007t0001g0251 |
3 | HG01175.hp1 HG01361.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1062+309T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21562609 | |||||||
| chr12:21562643 | GGGGAGAA others(1): Show |
G | 201 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(198): Show |
215 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.1062+267_1062+274d others(10): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21562643 | |||||||
| chr12:21562698 | C | CA | 6 | a0002c0002t0001g0038 a0002c0002t0001g0244 a0002c0002t0001g0245 others(3): Show |
6 | HG01346.hp1 HG02630.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1062+219dupT | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21562698 | |||||||
| chr12:21562698 | CA | C | 16 | a0002c0002t0001g0007 a0002c0002t0001g0099 a0002c0002t0001g0136 others(13): Show |
17 | HG00642.hp1 HG01069.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.1062+219delT | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21562698 | |||||||
| chr12:21562698 | CAAAAA | C | 197 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(194): Show |
211 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.1062+215_1062+219d others(7): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21562698 | |||||||
| chr12:21562698 | CAAAAAAA others(7): Show |
C | 2 | a0002c0002t0001g0078 a0002c0002t0001g0082 |
2 | NA18953.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1062+206_1062+219d others(16): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21562698 | |||||||
| chr12:21562841 | G | A | 2 | a0001c0001t0001g0293 a0001c0001t0001g0294 |
2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1062+77C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21562841 | |||||||
| chr12:21562867 | A | G | 201 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(198): Show |
215 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.1062+51T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21562867 | |||||||
| chr12:21562905 | A | G | 1 | a0001c0001t0001g0023 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1062+13T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 7/15 | chr12 | 21562905 | |||||||
| chr12:21563050 | C | T | 1 | a0002c0002t0001g0136 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.942-12G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 6/15 | chr12 | 21563050 | |||||||
| chr12:21563055 | C | T | 49 | a0001c0001t0002g0048 a0001c0001t0002g0264 a0001c0001t0003g0003 others(46): Show |
56 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.942-17G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 6/15 | chr12 | 21563055 | |||||||
| chr12:21563121 | A | C | 201 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(198): Show |
215 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.942-83T>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 6/15 | chr12 | 21563121 | |||||||
| chr12:21563164 | T | C | 201 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(198): Show |
215 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.941+64A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 6/15 | chr12 | 21563164 | |||||||
| chr12:21563566 | G | T | 190 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(187): Show |
203 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.824-221C>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21563566 | |||||||
| chr12:21563692 | G | A | 201 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(198): Show |
215 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.824-347C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21563692 | |||||||
| chr12:21563758 | T | C | 11 | a0001c0001t0008g0292 a0003c0003t0001g0016 a0003c0003t0001g0026 others(8): Show |
12 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.824-413A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21563758 | |||||||
| chr12:21563785 | G | A | 201 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(198): Show |
215 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.824-440C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21563785 | |||||||
| chr12:21563807 | A | G | 202 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(199): Show |
216 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.824-462T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21563807 | |||||||
| chr12:21563881 | C | T | 163 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0032 others(160): Show |
174 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.824-536G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21563881 | |||||||
| chr12:21563922 | G | A | 201 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(198): Show |
215 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.824-577C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21563922 | |||||||
| chr12:21564012 | A | G | 5 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0132 others(2): Show |
5 | HG01168.hp1 HG01169.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.824-667T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21564012 | |||||||
| chr12:21564030 | G | A | 4 | a0002c0002t0001g0007 a0002c0002t0001g0150 a0002c0002t0001g0154 others(1): Show |
5 | HG00642.hp1 HG01069.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.824-685C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21564030 | |||||||
| chr12:21564087 | T | C | 190 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(187): Show |
203 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.824-742A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21564087 | |||||||
| chr12:21564285 | G | C | 191 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(188): Show |
204 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.824-940C>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21564285 | |||||||
| chr12:21564308 | G | T | 169 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0028 others(166): Show |
180 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.824-963C>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21564308 | |||||||
| chr12:21564314 | C | A | 191 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(188): Show |
204 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.824-969G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21564314 | |||||||
| chr12:21564323 | G | A | 48 | a0001c0001t0002g0048 a0001c0001t0002g0264 a0001c0001t0003g0003 others(45): Show |
55 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.824-978C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21564323 | |||||||
| chr12:21564371 | C | T | 3 | a0005c0007t0001g0139 a0005c0007t0001g0250 a0005c0007t0001g0251 |
3 | HG01175.hp1 HG01361.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.824-1026G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21564371 | |||||||
| chr12:21564435 | GA | G | 202 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(199): Show |
216 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.824-1091delT | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21564435 | |||||||
| chr12:21564500 | C | T | 2 | a0002c0002t0004g0041 a0002c0002t0004g0042 |
2 | NA18978.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.824-1155G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21564500 | |||||||
| chr12:21564578 | G | T | 1 | a0002c0002t0001g0058 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.824-1233C>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21564578 | |||||||
| chr12:21564592 | C | T | 5 | a0002c0002t0001g0007 a0002c0002t0001g0136 a0002c0002t0001g0150 others(2): Show |
6 | HG00642.hp1 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.824-1247G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21564592 | |||||||
| chr12:21564674 | A | G | 191 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(188): Show |
204 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.824-1329T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21564674 | |||||||
| chr12:21564850 | G | A | 10 | a0003c0003t0001g0016 a0003c0003t0001g0026 a0003c0003t0001g0105 others(7): Show |
11 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.824-1505C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21564850 | |||||||
| chr12:21564947 | C | T | 3 | a0001c0001t0001g0134 a0001c0001t0004g0234 a0001c0001t0004g0252 |
3 | HG02615.hp1 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.824-1602G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21564947 | |||||||
| chr12:21564974 | C | T | 1 | a0001c0001t0001g0023 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.824-1629G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21564974 | |||||||
| chr12:21565076 | TA | T | 11 | a0001c0001t0008g0292 a0003c0003t0001g0016 a0003c0003t0001g0026 others(8): Show |
12 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.824-1732delT | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21565076 | |||||||
| chr12:21565252 | G | A | 11 | a0001c0001t0008g0292 a0003c0003t0001g0016 a0003c0003t0001g0026 others(8): Show |
12 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.824-1907C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21565252 | |||||||
| chr12:21565260 | T | G | 285 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(282): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.824-1915A>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21565260 | |||||||
| chr12:21565367 | C | T | 11 | a0001c0001t0008g0292 a0003c0003t0001g0016 a0003c0003t0001g0026 others(8): Show |
12 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.824-2022G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21565367 | |||||||
| chr12:21565390 | A | AAT | 19 | a0001c0001t0004g0100 a0001c0001t0004g0130 a0001c0005t0001g0131 others(16): Show |
19 | HG01358.hp2 HG01891.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.824-2047_824-2046d others(4): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21565390 | |||||||
| chr12:21565390 | A | AATAT | 33 | a0001c0001t0001g0015 a0001c0001t0001g0084 a0001c0001t0001g0149 others(30): Show |
34 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.824-2049_824-2046d others(6): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21565390 | |||||||
| chr12:21565390 | A | AATATAT | 13 | a0001c0001t0001g0242 a0001c0008t0001g0006 a0002c0002t0001g0024 others(10): Show |
13 | HG00099.hp1 HG00741.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.824-2051_824-2046d others(8): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21565390 | |||||||
| chr12:21565390 | A | AATATATA others(3): Show |
2 | a0001c0001t0001g0294 a0002c0002t0001g0057 |
2 | HG02451.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.824-2055_824-2046d others(12): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21565390 | |||||||
| chr12:21565390 | A | T | 1 | a0002c0002t0001g0043 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.824-2045T>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21565390 | |||||||
| chr12:21565390 | AAT | A | 8 | a0001c0001t0001g0157 a0001c0001t0001g0222 a0001c0001t0002g0002 others(5): Show |
8 | HG00280.hp1 HG01257.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.824-2047_824-2046d others(4): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21565390 | |||||||
| chr12:21565390 | AATAT | A | 26 | a0001c0001t0001g0091 a0001c0001t0002g0069 a0001c0001t0002g0094 others(23): Show |
26 | HG00408.hp1 HG00597.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.824-2049_824-2046d others(6): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21565390 | |||||||
| chr12:21565390 | AATATAT | A | 56 | a0001c0001t0001g0204 a0001c0001t0001g0267 a0001c0001t0002g0013 others(53): Show |
60 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.824-2051_824-2046d others(8): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21565390 | |||||||
| chr12:21565390 | AATATATA others(1): Show |
A | 82 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0032 others(79): Show |
83 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.824-2053_824-2046d others(10): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21565390 | |||||||
| chr12:21565390 | AATATATA others(3): Show |
A | 2 | a0001c0001t0004g0252 a0001c0005t0001g0129 |
2 | HG02630.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.824-2055_824-2046d others(12): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21565390 | |||||||
| chr12:21565390 | AATATATA others(5): Show |
A | 2 | a0001c0001t0003g0161 a0001c0001t0004g0234 |
2 | HG02615.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.824-2057_824-2046d others(14): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21565390 | |||||||
| chr12:21565390 | AATATATA others(7): Show |
A | 1 | a0001c0001t0001g0134 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.824-2059_824-2046d others(16): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21565390 | |||||||
| chr12:21565390 | AATATATA others(9): Show |
A | 1 | a0002c0002t0001g0283 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.824-2061_824-2046d others(18): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21565390 | |||||||
| chr12:21565390 | AATATATA others(15): Show |
A | 5 | a0002c0002t0001g0007 a0002c0002t0001g0136 a0002c0002t0001g0150 others(2): Show |
6 | HG00642.hp1 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.824-2067_824-2046d others(24): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21565390 | |||||||
| chr12:21565390 | AATATATA others(17): Show |
A | 11 | a0001c0001t0008g0292 a0003c0003t0001g0016 a0003c0003t0001g0026 others(8): Show |
12 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.824-2069_824-2046d others(26): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21565390 | |||||||
| chr12:21565390 | AATATATA others(21): Show |
A | 1 | a0002c0002t0001g0058 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.824-2073_824-2046d others(30): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21565390 | |||||||
| chr12:21565630 | A | G | 1 | a0001c0001t0003g0197 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.824-2285T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21565630 | |||||||
| chr12:21565786 | T | C | 3 | a0005c0007t0001g0139 a0005c0007t0001g0250 a0005c0007t0001g0251 |
3 | HG01175.hp1 HG01361.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.824-2441A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21565786 | |||||||
| chr12:21565813 | A | ACAATGT | 191 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(188): Show |
204 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.824-2474_824-2469d others(8): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21565813 | |||||||
| chr12:21565931 | T | C | 69 | a0001c0001t0001g0091 a0001c0001t0001g0204 a0002c0002t0001g0001 others(66): Show |
71 | HG00099.hp1 HG00621.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.824-2586A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21565931 | |||||||
| chr12:21566068 | T | G | 1 | a0001c0001t0003g0270 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.824-2723A>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21566068 | |||||||
| chr12:21566562 | A | T | 1 | a0002c0002t0001g0038 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.823+2303T>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21566562 | |||||||
| chr12:21566705 | A | G | 6 | a0002c0002t0004g0041 a0002c0002t0004g0042 a0002c0002t0004g0239 others(3): Show |
6 | HG01891.hp1 HG02970.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.823+2160T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21566705 | |||||||
| chr12:21566747 | G | A | 69 | a0001c0001t0001g0091 a0001c0001t0001g0204 a0002c0002t0001g0001 others(66): Show |
71 | HG00099.hp1 HG00621.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.823+2118C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21566747 | |||||||
| chr12:21566937 | G | A | 2 | a0001c0001t0001g0023 a0001c0013t0001g0282 |
2 | HG02647.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.823+1928C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21566937 | |||||||
| chr12:21567160 | C | T | 1 | a0001c0001t0002g0163 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.823+1705G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21567160 | |||||||
| chr12:21567189 | T | C | 1 | a0002c0002t0001g0145 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.823+1676A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21567189 | |||||||
| chr12:21567467 | A | G | 2 | a0001c0001t0001g0023 a0001c0013t0001g0282 |
2 | HG02647.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.823+1398T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21567467 | |||||||
| chr12:21567490 | T | C | 1 | a0001c0001t0001g0293 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.823+1375A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21567490 | |||||||
| chr12:21567531 | GT | G | 34 | a0001c0001t0001g0242 a0001c0001t0002g0072 a0001c0001t0002g0133 others(31): Show |
37 | HG00099.hp1 HG00597.hp1 HG01169.hp2 others(34): Show |
intron_variant | MODIFIER | c.823+1333delA | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21567531 | |||||||
| chr12:21567729 | C | T | 2 | a0002c0002t0001g0146 a0002c0002t0001g0147 |
2 | HG00735.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.823+1136G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21567729 | |||||||
| chr12:21567760 | C | A | 2 | a0002c0002t0001g0280 a0002c0002t0001g0281 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.823+1105G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21567760 | |||||||
| chr12:21567867 | G | T | 1 | a0002c0002t0004g0042 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.823+998C>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21567867 | |||||||
| chr12:21567880 | C | T | 1 | a0008c0009t0002g0260 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.823+985G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21567880 | |||||||
| chr12:21567899 | C | T | 3 | a0001c0001t0003g0195 a0001c0001t0003g0196 a0001c0001t0003g0197 |
3 | HG01081.hp2 HG01169.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.823+966G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21567899 | |||||||
| chr12:21567902 | G | T | 4 | a0001c0001t0002g0048 a0001c0001t0002g0264 a0001c0001t0003g0162 others(1): Show |
4 | NA18977.hp2 NA18991.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.823+963C>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21567902 | |||||||
| chr12:21568071 | C | CA | 10 | a0001c0001t0002g0094 a0001c0001t0002g0201 a0001c0001t0004g0025 others(7): Show |
10 | HG01891.hp1 HG02055.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.823+793dupT | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21568071 | |||||||
| chr12:21568077 | A | G | 3 | a0001c0001t0001g0134 a0001c0001t0004g0234 a0001c0001t0004g0252 |
3 | HG02615.hp1 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.823+788T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21568077 | |||||||
| chr12:21568086 | A | T | 164 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0032 others(161): Show |
175 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.823+779T>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21568086 | |||||||
| chr12:21568092 | G | T | 1 | a0002c0002t0001g0288 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.823+773C>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21568092 | |||||||
| chr12:21568096 | G | A | 3 | a0005c0007t0001g0139 a0005c0007t0001g0250 a0005c0007t0001g0251 |
3 | HG01175.hp1 HG01361.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.823+769C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21568096 | |||||||
| chr12:21568128 | C | T | 1 | a0001c0001t0003g0269 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.823+737G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21568128 | |||||||
| chr12:21568336 | G | A | 1 | a0001c0001t0002g0094 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.823+529C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21568336 | |||||||
| chr12:21568444 | A | G | 212 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(209): Show |
226 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.823+421T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21568444 | |||||||
| chr12:21568450 | A | G | 6 | a0002c0002t0001g0038 a0002c0002t0001g0106 a0002c0002t0001g0112 others(3): Show |
6 | HG02040.hp2 HG02083.hp2 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.823+415T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21568450 | |||||||
| chr12:21568699 | C | T | 192 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(189): Show |
205 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.823+166G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 5/15 | chr12 | 21568699 | |||||||
| chr12:21569030 | A | G | 1 | a0001c0001t0004g0025 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.679-21T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21569030 | |||||||
| chr12:21569080 | C | T | 29 | a0002c0002t0001g0001 a0002c0002t0001g0024 a0002c0002t0001g0038 others(26): Show |
31 | HG00621.hp1 HG00673.hp2 HG01981.hp2 others(28): Show |
intron_variant | MODIFIER | c.679-71G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21569080 | |||||||
| chr12:21569249 | T | C | 3 | a0005c0007t0001g0139 a0005c0007t0001g0250 a0005c0007t0001g0251 |
3 | HG01175.hp1 HG01361.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.679-240A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21569249 | |||||||
| chr12:21569408 | T | G | 11 | a0001c0001t0008g0292 a0003c0003t0001g0016 a0003c0003t0001g0026 others(8): Show |
12 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.679-399A>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21569408 | |||||||
| chr12:21569430 | T | C | 2 | a0001c0001t0001g0157 a0001c0001t0001g0222 |
2 | HG00280.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.679-421A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21569430 | |||||||
| chr12:21569588 | C | T | 212 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(209): Show |
226 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.679-579G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21569588 | |||||||
| chr12:21569592 | A | T | 3 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0096 |
5 | NA18949.hp1 NA18954.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.679-583T>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21569592 | |||||||
| chr12:21569615 | A | G | 2 | a0002c0002t0001g0142 a0002c0002t0001g0145 |
2 | HG03710.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.679-606T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21569615 | |||||||
| chr12:21569719 | A | C | 212 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(209): Show |
226 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.679-710T>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21569719 | |||||||
| chr12:21569823 | C | G | 2 | a0001c0001t0002g0053 a0001c0001t0002g0063 |
2 | HG03239.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.679-814G>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21569823 | |||||||
| chr12:21569924 | G | A | 1 | a0002c0002t0001g0109 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.679-915C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21569924 | |||||||
| chr12:21569969 | T | C | 212 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(209): Show |
226 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.679-960A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21569969 | |||||||
| chr12:21569974 | CA | C | 5 | a0001c0001t0003g0047 a0001c0001t0003g0066 a0001c0001t0003g0121 others(2): Show |
5 | HG00408.hp1 NA18971.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.679-966delT | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21569974 | |||||||
| chr12:21570045 | A | G | 2 | a0002c0002t0004g0041 a0002c0002t0004g0042 |
2 | NA18978.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.679-1036T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21570045 | |||||||
| chr12:21570264 | T | C | 2 | a0001c0001t0007g0207 a0001c0001t0007g0216 |
2 | NA18955.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.679-1255A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21570264 | |||||||
| chr12:21570381 | A | G | 2 | a0002c0002t0001g0081 a0002c0002t0001g0235 |
2 | HG03491.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.679-1372T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21570381 | |||||||
| chr12:21570597 | G | C | 8 | a0001c0001t0002g0002 a0001c0001t0002g0062 a0001c0001t0002g0070 others(5): Show |
9 | HG01070.hp1 HG01071.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.679-1588C>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21570597 | |||||||
| chr12:21570646 | G | C | 2 | a0004c0006t0001g0092 a0004c0006t0001g0151 |
2 | HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.679-1637C>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21570646 | |||||||
| chr12:21570732 | C | G | 11 | a0001c0001t0008g0292 a0003c0003t0001g0016 a0003c0003t0001g0026 others(8): Show |
12 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.679-1723G>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21570732 | |||||||
| chr12:21570733 | G | A | 164 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0032 others(161): Show |
175 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.679-1724C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21570733 | |||||||
| chr12:21571146 | C | G | 1 | a0001c0001t0002g0182 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.679-2137G>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21571146 | |||||||
| chr12:21571196 | T | G | 25 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0039 others(22): Show |
26 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.679-2187A>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21571196 | |||||||
| chr12:21571248 | G | A | 3 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0205 |
3 | HG01255.hp1 HG01516.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.679-2239C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21571248 | |||||||
| chr12:21571258 | T | G | 2 | a0001c0001t0002g0053 a0001c0001t0002g0063 |
2 | HG03239.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.679-2249A>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21571258 | |||||||
| chr12:21571269 | T | C | 2 | a0003c0003t0001g0016 a0003c0003t0001g0286 |
3 | HG02257.hp1 HG02922.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.679-2260A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21571269 | |||||||
| chr12:21571386 | C | T | 1 | a0002c0002t0001g0090 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.679-2377G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21571386 | |||||||
| chr12:21571426 | G | A | 208 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(205): Show |
221 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.679-2417C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21571426 | |||||||
| chr12:21571483 | T | A | 4 | a0002c0002t0001g0104 a0002c0002t0001g0108 a0002c0002t0001g0109 others(1): Show |
4 | HG00741.hp1 HG02055.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.679-2474A>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21571483 | |||||||
| chr12:21571486 | T | C | 6 | a0002c0002t0004g0041 a0002c0002t0004g0042 a0002c0002t0004g0239 others(3): Show |
6 | HG01891.hp1 HG02970.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.679-2477A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21571486 | |||||||
| chr12:21571700 | C | T | 6 | a0002c0002t0001g0001 a0002c0002t0001g0024 a0002c0002t0001g0043 others(3): Show |
8 | HG00621.hp1 HG03704.hp1 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.678+2444G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21571700 | |||||||
| chr12:21571701 | G | T | 3 | a0005c0007t0001g0139 a0005c0007t0001g0250 a0005c0007t0001g0251 |
3 | HG01175.hp1 HG01361.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.678+2443C>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21571701 | |||||||
| chr12:21571848 | C | G | 31 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0039 others(28): Show |
34 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.678+2296G>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21571848 | |||||||
| chr12:21571957 | C | T | 283 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(280): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.678+2187G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21571957 | |||||||
| chr12:21572046 | A | G | 65 | a0001c0001t0001g0091 a0001c0001t0002g0009 a0001c0001t0002g0095 others(62): Show |
67 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.678+2098T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21572046 | |||||||
| chr12:21572282 | A | C | 1 | a0001c0005t0001g0034 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.678+1862T>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21572282 | |||||||
| chr12:21572484 | T | G | 4 | a0002c0002t0001g0104 a0002c0002t0001g0108 a0002c0002t0001g0109 others(1): Show |
4 | HG00741.hp1 HG02055.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.678+1660A>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21572484 | |||||||
| chr12:21572691 | T | C | 4 | a0001c0001t0002g0170 a0001c0001t0002g0191 a0001c0001t0002g0192 others(1): Show |
4 | HG01069.hp2 HG01516.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.678+1453A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21572691 | |||||||
| chr12:21572726 | T | G | 9 | a0001c0001t0001g0242 a0002c0002t0001g0243 a0002c0002t0001g0244 others(6): Show |
9 | HG02630.hp1 HG02895.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.678+1418A>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21572726 | |||||||
| chr12:21572834 | C | G | 2 | a0001c0001t0002g0045 a0001c0001t0002g0194 |
2 | NA19065.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.678+1310G>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21572834 | |||||||
| chr12:21572922 | G | A | 1 | a0001c0001t0002g0217 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.678+1222C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21572922 | |||||||
| chr12:21573026 | C | A | 1 | a0001c0001t0001g0091 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.678+1118G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21573026 | |||||||
| chr12:21573078 | A | G | 181 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0032 others(178): Show |
194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.678+1066T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21573078 | |||||||
| chr12:21573133 | A | G | 1 | a0002c0002t0009g0224 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.678+1011T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21573133 | |||||||
| chr12:21573585 | T | C | 22 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0149 others(19): Show |
25 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.678+559A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21573585 | |||||||
| chr12:21573820 | C | T | 2 | a0002c0002t0001g0280 a0002c0002t0001g0281 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.678+324G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 4/15 | chr12 | 21573820 | |||||||
| chr12:21574380 | G | A | 9 | a0001c0001t0004g0234 a0001c0001t0004g0252 a0002c0002t0001g0017 others(6): Show |
9 | HG01891.hp2 HG02145.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.496-54C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 3/15 | chr12 | 21574380 | |||||||
| chr12:21574381 | C | A | 279 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(276): Show |
296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.496-55G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 3/15 | chr12 | 21574381 | |||||||
| chr12:21574406 | T | C | 1 | a0002c0002t0001g0290 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.496-80A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 3/15 | chr12 | 21574406 | |||||||
| chr12:21574672 | T | C | 12 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0008g0292 others(9): Show |
13 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.496-346A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 3/15 | chr12 | 21574672 | |||||||
| chr12:21574681 | T | G | 175 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0032 others(172): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.496-355A>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 3/15 | chr12 | 21574681 | |||||||
| chr12:21574802 | C | T | 59 | a0001c0001t0001g0091 a0001c0001t0002g0148 a0001c0001t0002g0236 others(56): Show |
59 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.496-476G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 3/15 | chr12 | 21574802 | |||||||
| chr12:21574853 | T | G | 283 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(280): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.496-527A>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 3/15 | chr12 | 21574853 | |||||||
| chr12:21575326 | T | G | 60 | a0001c0001t0001g0091 a0001c0001t0002g0148 a0001c0001t0002g0236 others(57): Show |
61 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.495+540A>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 3/15 | chr12 | 21575326 | |||||||
| chr12:21575411 | T | C | 175 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0032 others(172): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.495+455A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 3/15 | chr12 | 21575411 | |||||||
| chr12:21575579 | A | G | 1 | a0001c0001t0003g0258 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.495+287T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 3/15 | chr12 | 21575579 | |||||||
| chr12:21575587 | T | A | 2 | a0002c0002t0001g0283 a0003c0003t0001g0255 |
2 | HG02818.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.495+279A>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 3/15 | chr12 | 21575587 | |||||||
| chr12:21575839 | G | A | 1 | a0001c0001t0002g0193 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.495+27C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 3/15 | chr12 | 21575839 | |||||||
| chr12:21576074 | A | G | 2 | a0001c0001t0002g0164 a0001c0001t0002g0180 |
2 | NA18951.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.304-17T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 2/15 | chr12 | 21576074 | |||||||
| chr12:21576131 | G | T | 1 | a0001c0001t0001g0084 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.304-74C>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 2/15 | chr12 | 21576131 | |||||||
| chr12:21576162 | A | G | 12 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0008g0292 others(9): Show |
13 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.304-105T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 2/15 | chr12 | 21576162 | |||||||
| chr12:21576305 | A | G | 1 | a0001c0001t0002g0210 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.304-248T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 2/15 | chr12 | 21576305 | |||||||
| chr12:21576765 | C | T | 2 | a0001c0001t0001g0023 a0002c0002t0001g0290 |
2 | HG02647.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.304-708G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 2/15 | chr12 | 21576765 | |||||||
| chr12:21576844 | A | T | 104 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0039 others(101): Show |
109 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(106): Show |
intron_variant | MODIFIER | c.304-787T>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 2/15 | chr12 | 21576844 | |||||||
| chr12:21576925 | G | A | 1 | a0002c0002t0009g0224 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.304-868C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 2/15 | chr12 | 21576925 | |||||||
| chr12:21576998 | A | G | 12 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0008g0292 others(9): Show |
13 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.304-941T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 2/15 | chr12 | 21576998 | |||||||
| chr12:21577073 | T | C | 1 | a0001c0001t0003g0066 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.304-1016A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 2/15 | chr12 | 21577073 | |||||||
| chr12:21577114 | T | C | 1 | a0002c0002t0001g0263 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.304-1057A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 2/15 | chr12 | 21577114 | |||||||
| chr12:21577425 | G | A | 279 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(276): Show |
296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.304-1368C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 2/15 | chr12 | 21577425 | |||||||
| chr12:21577489 | C | A | 1 | a0002c0002t0001g0261 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.304-1432G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 2/15 | chr12 | 21577489 | |||||||
| chr12:21577537 | A | G | 1 | a0002c0002t0001g0246 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.304-1480T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 2/15 | chr12 | 21577537 | |||||||
| chr12:21577590 | T | C | 1 | a0001c0001t0003g0202 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.304-1533A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 2/15 | chr12 | 21577590 | |||||||
| chr12:21577604 | C | T | 1 | a0002c0002t0001g0243 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.304-1547G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 2/15 | chr12 | 21577604 | |||||||
| chr12:21577966 | C | T | 1 | a0001c0001t0002g0179 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.304-1909G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 2/15 | chr12 | 21577966 | |||||||
| chr12:21578588 | C | T | 22 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0149 others(19): Show |
25 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.303+1754G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 2/15 | chr12 | 21578588 | |||||||
| chr12:21578700 | T | C | 8 | a0001c0001t0001g0134 a0001c0001t0004g0025 a0001c0001t0004g0100 others(5): Show |
8 | HG02055.hp1 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.303+1642A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 2/15 | chr12 | 21578700 | |||||||
| chr12:21578706 | T | C | 275 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0028 others(272): Show |
291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.303+1636A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 2/15 | chr12 | 21578706 | |||||||
| chr12:21578759 | T | C | 11 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0008g0292 others(8): Show |
12 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.303+1583A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 2/15 | chr12 | 21578759 | |||||||
| chr12:21578779 | C | T | 11 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0008g0292 others(8): Show |
12 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.303+1563G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 2/15 | chr12 | 21578779 | |||||||
| chr12:21578816 | A | C | 7 | a0002c0002t0001g0093 a0002c0002t0001g0103 a0002c0002t0001g0104 others(4): Show |
7 | HG00741.hp1 HG02055.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.303+1526T>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 2/15 | chr12 | 21578816 | |||||||
| chr12:21578917 | C | G | 1 | a0002c0002t0001g0154 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.303+1425G>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 2/15 | chr12 | 21578917 | |||||||
| chr12:21579001 | A | C | 1 | a0001c0005t0001g0131 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.303+1341T>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 2/15 | chr12 | 21579001 | |||||||
| chr12:21579213 | T | A | 283 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(280): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.303+1129A>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 2/15 | chr12 | 21579213 | |||||||
| chr12:21579249 | G | C | 3 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0096 |
5 | NA18949.hp1 NA18954.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.303+1093C>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 2/15 | chr12 | 21579249 | |||||||
| chr12:21579252 | A | G | 3 | a0001c0001t0002g0208 a0001c0001t0002g0209 a0001c0001t0002g0219 |
3 | HG01074.hp2 HG01981.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.303+1090T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 2/15 | chr12 | 21579252 | |||||||
| chr12:21579261 | A | G | 3 | a0005c0007t0001g0139 a0005c0007t0001g0250 a0005c0007t0001g0251 |
3 | HG01175.hp1 HG01361.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.303+1081T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 2/15 | chr12 | 21579261 | |||||||
| chr12:21579313 | G | A | 1 | a0008c0009t0002g0260 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.303+1029C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 2/15 | chr12 | 21579313 | |||||||
| chr12:21579349 | CT | C | 45 | a0001c0001t0001g0015 a0001c0001t0001g0084 a0001c0001t0001g0149 others(42): Show |
49 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.303+992delA | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 2/15 | chr12 | 21579349 | |||||||
| chr12:21579349 | CTT | C | 233 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0028 others(230): Show |
246 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.303+991_303+992del others(2): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 2/15 | chr12 | 21579349 | |||||||
| chr12:21579379 | G | T | 2 | a0002c0002t0001g0007 a0002c0002t0001g0262 |
3 | HG00642.hp1 HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.303+963C>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 2/15 | chr12 | 21579379 | |||||||
| chr12:21579387 | T | C | 283 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(280): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.303+955A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 2/15 | chr12 | 21579387 | |||||||
| chr12:21579508 | C | A | 1 | a0002c0002t0001g0017 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.303+834G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 2/15 | chr12 | 21579508 | |||||||
| chr12:21579513 | C | T | 22 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0149 others(19): Show |
25 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.303+829G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 2/15 | chr12 | 21579513 | |||||||
| chr12:21579747 | T | C | 3 | a0005c0007t0001g0139 a0005c0007t0001g0250 a0005c0007t0001g0251 |
3 | HG01175.hp1 HG01361.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.303+595A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 2/15 | chr12 | 21579747 | |||||||
| chr12:21580187 | T | G | 279 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(276): Show |
296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.303+155A>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 2/15 | chr12 | 21580187 | |||||||
| chr12:21580322 | T | C | 1 | a0001c0001t0003g0270 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.303+20A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 2/15 | chr12 | 21580322 | |||||||
| chr12:21580554 | T | G | 1 | a0008c0009t0002g0260 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.122-31A>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21580554 | |||||||
| chr12:21580832 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.122-309A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21580832 | |||||||
| chr12:21580883 | C | T | 2 | a0002c0002t0004g0041 a0002c0002t0004g0042 |
2 | NA18978.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.122-360G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21580883 | |||||||
| chr12:21580919 | A | T | 1 | a0001c0001t0001g0293 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.122-396T>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21580919 | |||||||
| chr12:21581158 | A | G | 1 | a0001c0001t0002g0178 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.122-635T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21581158 | |||||||
| chr12:21581225 | G | T | 177 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0032 others(174): Show |
189 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.122-702C>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21581225 | |||||||
| chr12:21581318 | G | A | 102 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0039 others(99): Show |
107 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.122-795C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21581318 | |||||||
| chr12:21581561 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.122-1038G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21581561 | |||||||
| chr12:21581562 | G | A | 1 | a0001c0001t0002g0194 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.122-1039C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21581562 | |||||||
| chr12:21581608 | C | G | 58 | a0001c0001t0001g0091 a0001c0001t0002g0148 a0001c0001t0002g0236 others(55): Show |
58 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.122-1085G>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21581608 | |||||||
| chr12:21581703 | T | C | 99 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0205 others(96): Show |
105 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.122-1180A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21581703 | |||||||
| chr12:21581776 | C | T | 4 | a0002c0002t0004g0041 a0002c0002t0004g0042 a0002c0002t0004g0239 others(1): Show |
4 | HG01891.hp1 HG03195.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.122-1253G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21581776 | |||||||
| chr12:21582040 | C | T | 1 | a0002c0002t0001g0262 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.122-1517G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21582040 | |||||||
| chr12:21582076 | G | GA | 58 | a0001c0001t0001g0091 a0001c0001t0002g0148 a0001c0001t0002g0236 others(55): Show |
58 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.122-1554dupT | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21582076 | |||||||
| chr12:21582086 | T | A | 1 | a0008c0009t0002g0260 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.122-1563A>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21582086 | |||||||
| chr12:21582138 | C | T | 1 | a0002c0002t0001g0176 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.122-1615G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21582138 | |||||||
| chr12:21582153 | C | A | 1 | a0002c0002t0001g0077 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.122-1630G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21582153 | |||||||
| chr12:21582425 | G | T | 1 | a0001c0001t0004g0025 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.122-1902C>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21582425 | |||||||
| chr12:21582447 | T | C | 283 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(280): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.122-1924A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21582447 | |||||||
| chr12:21582448 | G | A | 1 | a0001c0001t0003g0068 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.122-1925C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21582448 | |||||||
| chr12:21582480 | C | T | 102 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0039 others(99): Show |
107 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.122-1957G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21582480 | |||||||
| chr12:21582504 | C | A | 49 | a0001c0001t0001g0204 a0001c0001t0002g0199 a0001c0001t0002g0201 others(46): Show |
55 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.122-1981G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21582504 | |||||||
| chr12:21582513 | T | A | 58 | a0001c0001t0001g0091 a0001c0001t0002g0148 a0001c0001t0002g0236 others(55): Show |
58 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.122-1990A>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21582513 | |||||||
| chr12:21582570 | T | TATAGATA others(5): Show |
1 | a0002c0002t0004g0295 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.122-2059_122-2048d others(14): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21582570 | |||||||
| chr12:21582582 | GATAGATA others(17): Show |
G | 1 | a0001c0008t0001g0006 | 2 | HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.122-2083_122-2060d others(26): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21582582 | |||||||
| chr12:21582594 | G | GATAGAT | 21 | a0001c0001t0001g0023 a0001c0001t0001g0032 a0001c0001t0001g0134 others(18): Show |
21 | HG01884.hp1 HG01891.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.122-2077_122-2072d others(8): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21582594 | |||||||
| chr12:21582594 | GATAGAT | G | 141 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0204 others(138): Show |
152 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.122-2077_122-2072d others(8): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21582594 | |||||||
| chr12:21582594 | GATAGATA others(5): Show |
G | 97 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0084 others(94): Show |
101 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(98): Show |
intron_variant | MODIFIER | c.122-2083_122-2072d others(14): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21582594 | |||||||
| chr12:21582692 | C | A | 1 | a0002c0002t0001g0077 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.122-2169G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21582692 | |||||||
| chr12:21582738 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.122-2215T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21582738 | |||||||
| chr12:21582920 | T | C | 3 | a0005c0007t0001g0139 a0005c0007t0001g0250 a0005c0007t0001g0251 |
3 | HG01175.hp1 HG01361.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.122-2397A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21582920 | |||||||
| chr12:21582985 | GC | G | 8 | a0001c0001t0004g0234 a0001c0001t0004g0252 a0002c0002t0001g0017 others(5): Show |
8 | HG01891.hp2 HG02145.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.122-2463delG | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21582985 | |||||||
| chr12:21583080 | A | C | 1 | a0002c0002t0001g0290 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.122-2557T>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21583080 | |||||||
| chr12:21583084 | G | A | 25 | a0001c0001t0001g0091 a0001c0001t0002g0148 a0002c0002t0001g0038 others(22): Show |
25 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.122-2561C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21583084 | |||||||
| chr12:21583184 | T | C | 102 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0039 others(99): Show |
107 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.122-2661A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21583184 | |||||||
| chr12:21583274 | G | A | 1 | a0002c0002t0001g0144 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.122-2751C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21583274 | |||||||
| chr12:21583310 | G | C | 1 | a0002c0002t0001g0077 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.122-2787C>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21583310 | |||||||
| chr12:21583336 | T | C | 36 | a0001c0001t0001g0091 a0001c0001t0002g0148 a0002c0002t0001g0038 others(33): Show |
36 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.122-2813A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21583336 | |||||||
| chr12:21583359 | C | T | 1 | a0003c0003t0001g0026 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.122-2836G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21583359 | |||||||
| chr12:21583403 | T | C | 1 | a0002c0002t0001g0103 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.122-2880A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21583403 | |||||||
| chr12:21583560 | G | T | 1 | a0001c0001t0002g0054 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.122-3037C>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21583560 | |||||||
| chr12:21583614 | C | T | 1 | a0006c0014t0001g0086 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.122-3091G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21583614 | |||||||
| chr12:21583642 | C | A | 4 | a0001c0001t0003g0011 a0001c0001t0003g0012 a0001c0001t0003g0067 others(1): Show |
6 | HG01099.hp2 HG01168.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.122-3119G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21583642 | |||||||
| chr12:21583657 | C | T | 1 | a0002c0002t0001g0226 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.122-3134G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21583657 | |||||||
| chr12:21583718 | G | A | 4 | a0002c0002t0001g0104 a0002c0002t0001g0108 a0002c0002t0001g0109 others(1): Show |
4 | HG00741.hp1 HG02055.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.122-3195C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21583718 | |||||||
| chr12:21584078 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.122-3555G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21584078 | |||||||
| chr12:21584232 | G | A | 3 | a0005c0007t0001g0139 a0005c0007t0001g0250 a0005c0007t0001g0251 |
3 | HG01175.hp1 HG01361.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.122-3709C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21584232 | |||||||
| chr12:21584253 | T | A | 1 | a0006c0014t0001g0086 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.122-3730A>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21584253 | |||||||
| chr12:21584321 | GA | G | 6 | a0001c0001t0001g0084 a0001c0001t0003g0003 a0001c0001t0003g0085 others(3): Show |
7 | HG01515.hp1 HG01517.hp1 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.122-3799delT | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21584321 | |||||||
| chr12:21584369 | T | C | 102 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0039 others(99): Show |
107 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.122-3846A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21584369 | |||||||
| chr12:21584370 | G | T | 102 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0039 others(99): Show |
107 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.122-3847C>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21584370 | |||||||
| chr12:21584371 | TGAGTGCT others(27): Show |
T | 102 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0039 others(99): Show |
107 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.122-3882_122-3849d others(36): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21584371 | |||||||
| chr12:21584437 | A | G | 8 | a0001c0001t0001g0023 a0001c0001t0001g0084 a0001c0001t0003g0003 others(5): Show |
9 | HG01515.hp1 HG01517.hp1 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.122-3914T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21584437 | |||||||
| chr12:21584620 | C | A | 1 | a0001c0005t0001g0131 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.122-4097G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21584620 | |||||||
| chr12:21584648 | G | T | 2 | a0002c0002t0001g0283 a0003c0003t0001g0255 |
2 | HG02818.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.122-4125C>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21584648 | |||||||
| chr12:21584727 | G | A | 2 | a0001c0001t0002g0218 a0001c0011t0002g0203 |
2 | HG03490.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.122-4204C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21584727 | |||||||
| chr12:21584813 | C | T | 2 | a0002c0002t0004g0041 a0002c0002t0004g0042 |
2 | NA18978.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.122-4290G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21584813 | |||||||
| chr12:21584827 | T | C | 178 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0032 others(175): Show |
190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.122-4304A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21584827 | |||||||
| chr12:21584847 | C | A | 4 | a0002c0002t0001g0099 a0002c0002t0001g0102 a0002c0002t0001g0283 others(1): Show |
4 | HG02559.hp2 HG02717.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-4324G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21584847 | |||||||
| chr12:21584865 | A | G | 1 | a0001c0001t0002g0247 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.122-4342T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21584865 | |||||||
| chr12:21584939 | C | T | 1 | a0001c0001t0003g0270 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.122-4416G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21584939 | |||||||
| chr12:21585008 | G | T | 2 | a0002c0002t0004g0239 a0002c0002t0004g0295 |
2 | HG01891.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.122-4485C>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21585008 | |||||||
| chr12:21585206 | T | C | 2 | a0002c0002t0004g0239 a0002c0002t0004g0295 |
2 | HG01891.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.122-4683A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21585206 | |||||||
| chr12:21585237 | G | A | 3 | a0005c0007t0001g0139 a0005c0007t0001g0250 a0005c0007t0001g0251 |
3 | HG01175.hp1 HG01361.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.122-4714C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21585237 | |||||||
| chr12:21585248 | G | A | 25 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0149 others(22): Show |
28 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.122-4725C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21585248 | |||||||
| chr12:21585348 | G | A | 2 | a0001c0001t0001g0023 a0002c0002t0001g0290 |
2 | HG02647.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.122-4825C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21585348 | |||||||
| chr12:21585364 | C | G | 101 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0039 others(98): Show |
106 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.122-4841G>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21585364 | |||||||
| chr12:21585541 | G | A | 1 | a0002c0002t0001g0226 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.122-5018C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21585541 | |||||||
| chr12:21585560 | G | GA | 16 | a0001c0001t0001g0084 a0001c0001t0001g0242 a0001c0001t0002g0254 others(13): Show |
17 | HG00438.hp1 HG01515.hp1 HG01517.hp1 others(14): Show |
intron_variant | MODIFIER | c.122-5038dupT | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21585560 | |||||||
| chr12:21585560 | G | GAAAAAAA | 20 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0091 others(17): Show |
23 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.122-5044_122-5038d others(9): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21585560 | |||||||
| chr12:21585661 | C | T | 10 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0008g0292 others(7): Show |
11 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.122-5138G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21585661 | |||||||
| chr12:21585667 | C | T | 1 | a0001c0013t0001g0282 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.122-5144G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21585667 | |||||||
| chr12:21585718 | T | C | 1 | a0002c0002t0001g0077 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.122-5195A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21585718 | |||||||
| chr12:21585896 | G | A | 5 | a0002c0002t0001g0001 a0002c0002t0001g0024 a0002c0002t0001g0043 others(2): Show |
7 | HG00621.hp1 HG03704.hp1 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.122-5373C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21585896 | |||||||
| chr12:21585941 | T | A | 1 | a0001c0001t0002g0132 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.122-5418A>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21585941 | |||||||
| chr12:21586032 | A | G | 1 | a0001c0001t0002g0177 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.122-5509T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21586032 | |||||||
| chr12:21586083 | G | A | 1 | a0002c0002t0001g0246 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.122-5560C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21586083 | |||||||
| chr12:21586200 | GA | G | 6 | a0001c0001t0001g0084 a0001c0001t0003g0003 a0001c0001t0003g0085 others(3): Show |
7 | HG01515.hp1 HG01517.hp1 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.122-5678delT | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21586200 | |||||||
| chr12:21586243 | C | T | 6 | a0001c0001t0001g0084 a0001c0001t0003g0003 a0001c0001t0003g0085 others(3): Show |
7 | HG01515.hp1 HG01517.hp1 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.122-5720G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21586243 | |||||||
| chr12:21586276 | C | A | 2 | a0001c0001t0004g0234 a0001c0001t0004g0252 |
2 | HG02615.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.122-5753G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21586276 | |||||||
| chr12:21586337 | C | A | 2 | a0001c0001t0001g0293 a0001c0001t0001g0294 |
2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.122-5814G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21586337 | |||||||
| chr12:21586419 | A | ATATC | 74 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0028 others(71): Show |
81 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.122-5900_122-5897d others(6): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21586419 | |||||||
| chr12:21586419 | A | ATATCTAT others(1): Show |
7 | a0001c0001t0002g0045 a0001c0001t0002g0163 a0001c0001t0002g0264 others(4): Show |
7 | HG00323.hp2 HG03139.hp1 NA18906.hp2 others(4): Show |
intron_variant | MODIFIER | c.122-5904_122-5897d others(10): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21586419 | |||||||
| chr12:21586419 | A | ATATCTAT others(5): Show |
1 | a0002c0002t0001g0017 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.122-5908_122-5897d others(14): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21586419 | |||||||
| chr12:21586419 | ATATC | A | 78 | a0001c0001t0001g0084 a0001c0001t0001g0156 a0001c0001t0001g0204 others(75): Show |
82 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.122-5900_122-5897d others(6): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21586419 | |||||||
| chr12:21586419 | ATATCTAT others(1): Show |
A | 6 | a0001c0001t0001g0039 a0001c0001t0002g0219 a0002c0002t0001g0243 others(3): Show |
6 | HG01255.hp2 HG01981.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.122-5904_122-5897d others(10): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21586419 | |||||||
| chr12:21586419 | ATATCTAT others(5): Show |
A | 1 | a0002c0002t0001g0145 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.122-5908_122-5897d others(14): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21586419 | |||||||
| chr12:21586543 | A | T | 23 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0091 others(20): Show |
26 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.122-6020T>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21586543 | |||||||
| chr12:21586632 | T | C | 1 | a0001c0001t0002g0158 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.122-6109A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21586632 | |||||||
| chr12:21586931 | C | G | 1 | a0003c0003t0001g0026 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.122-6408G>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21586931 | |||||||
| chr12:21586964 | A | G | 1 | a0001c0001t0003g0162 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.122-6441T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21586964 | |||||||
| chr12:21587146 | A | C | 1 | a0001c0001t0004g0116 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.122-6623T>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21587146 | |||||||
| chr12:21587285 | A | G | 1 | a0001c0001t0003g0161 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.122-6762T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21587285 | |||||||
| chr12:21587308 | G | A | 292 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(289): Show |
309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.122-6785C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21587308 | |||||||
| chr12:21587314 | G | A | 3 | a0001c0001t0002g0014 a0001c0001t0002g0220 a0001c0001t0002g0221 |
4 | HG03491.hp2 HG03492.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-6791C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21587314 | |||||||
| chr12:21587539 | T | G | 1 | a0002c0002t0004g0295 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.122-7016A>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21587539 | |||||||
| chr12:21587723 | T | G | 76 | a0001c0001t0001g0023 a0001c0001t0001g0084 a0001c0001t0001g0091 others(73): Show |
78 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.122-7200A>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21587723 | |||||||
| chr12:21588000 | G | A | 2 | a0002c0002t0001g0223 a0002c0002t0009g0224 |
2 | HG00099.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.122-7477C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21588000 | |||||||
| chr12:21588116 | A | G | 2 | a0001c0001t0001g0023 a0002c0002t0001g0290 |
2 | HG02647.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.122-7593T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21588116 | |||||||
| chr12:21588167 | G | A | 2 | a0002c0002t0004g0041 a0002c0002t0004g0042 |
2 | NA18978.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.122-7644C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21588167 | |||||||
| chr12:21588225 | T | C | 1 | a0002c0002t0001g0266 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.122-7702A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21588225 | |||||||
| chr12:21588332 | G | C | 1 | a0001c0001t0002g0225 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.122-7809C>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21588332 | |||||||
| chr12:21588466 | T | C | 1 | a0002c0002t0001g0226 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.122-7943A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21588466 | |||||||
| chr12:21588480 | A | G | 4 | a0002c0002t0001g0097 a0005c0007t0001g0139 a0005c0007t0001g0250 others(1): Show |
4 | HG00642.hp2 HG01175.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-7957T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21588480 | |||||||
| chr12:21588738 | A | T | 4 | a0002c0002t0001g0097 a0005c0007t0001g0139 a0005c0007t0001g0250 others(1): Show |
4 | HG00642.hp2 HG01175.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-8215T>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21588738 | |||||||
| chr12:21588794 | G | A | 1 | a0002c0002t0001g0290 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.122-8271C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21588794 | |||||||
| chr12:21589234 | T | C | 1 | a0001c0001t0003g0270 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.122-8711A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21589234 | |||||||
| chr12:21589366 | T | A | 1 | a0001c0001t0001g0157 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.122-8843A>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21589366 | |||||||
| chr12:21589366 | T | C | 1 | a0001c0001t0002g0159 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.122-8843A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21589366 | |||||||
| chr12:21589372 | T | C | 178 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0032 others(175): Show |
190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.122-8849A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21589372 | |||||||
| chr12:21589422 | C | G | 58 | a0001c0001t0001g0091 a0001c0001t0002g0148 a0001c0001t0002g0236 others(55): Show |
58 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.122-8899G>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21589422 | |||||||
| chr12:21589589 | G | A | 1 | a0001c0001t0002g0227 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.122-9066C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21589589 | |||||||
| chr12:21590080 | A | G | 10 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0008g0292 others(7): Show |
11 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.122-9557T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21590080 | |||||||
| chr12:21590184 | A | G | 179 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0032 others(176): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.122-9661T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21590184 | |||||||
| chr12:21590192 | G | A | 1 | a0001c0001t0004g0234 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.122-9669C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21590192 | |||||||
| chr12:21590523 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.122-10000C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21590523 | |||||||
| chr12:21590557 | C | T | 1 | a0001c0001t0002g0044 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.122-10034G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21590557 | |||||||
| chr12:21590593 | T | C | 285 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(282): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.122-10070A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21590593 | |||||||
| chr12:21590618 | C | T | 3 | a0002c0002t0004g0041 a0002c0002t0004g0042 a0002c0002t0004g0295 |
3 | HG03195.hp1 NA18978.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.122-10095G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21590618 | |||||||
| chr12:21590667 | G | A | 30 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0149 others(27): Show |
34 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.122-10144C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21590667 | |||||||
| chr12:21591003 | A | C | 180 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0032 others(177): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.122-10480T>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21591003 | |||||||
| chr12:21591148 | G | A | 1 | a0003c0003t0001g0026 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.122-10625C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21591148 | |||||||
| chr12:21591156 | T | C | 3 | a0002c0002t0004g0041 a0002c0002t0004g0042 a0002c0002t0004g0295 |
3 | HG03195.hp1 NA18978.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.122-10633A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21591156 | |||||||
| chr12:21591198 | A | G | 1 | a0002c0002t0001g0146 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.122-10675T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21591198 | |||||||
| chr12:21591260 | G | A | 1 | a0003c0003t0001g0026 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.122-10737C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21591260 | |||||||
| chr12:21591262 | T | C | 2 | a0001c0001t0001g0293 a0001c0001t0001g0294 |
2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.122-10739A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21591262 | |||||||
| chr12:21591294 | C | T | 1 | a0002c0002t0001g0102 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.122-10771G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21591294 | |||||||
| chr12:21591295 | A | G | 264 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0028 others(261): Show |
279 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.122-10772T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21591295 | |||||||
| chr12:21591315 | A | T | 1 | a0002c0002t0001g0290 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.122-10792T>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21591315 | |||||||
| chr12:21591454 | GA | G | 25 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0149 others(22): Show |
28 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.122-10932delT | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21591454 | |||||||
| chr12:21591604 | T | C | 1 | a0001c0001t0002g0133 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.122-11081A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21591604 | |||||||
| chr12:21592140 | T | TAAGA | 54 | a0001c0001t0001g0091 a0001c0001t0002g0236 a0001c0001t0002g0237 others(51): Show |
54 | HG00639.hp2 HG00642.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.122-11621_122-1161 others(8): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21592140 | |||||||
| chr12:21592407 | C | G | 2 | a0002c0002t0001g0024 a0002c0002t0001g0043 |
2 | NA18939.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.122-11884G>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21592407 | |||||||
| chr12:21592525 | A | G | 7 | a0001c0001t0001g0084 a0001c0001t0003g0003 a0001c0001t0003g0085 others(4): Show |
8 | HG01515.hp1 HG01517.hp1 HG02148.hp1 others(5): Show |
intron_variant | MODIFIER | c.121+11947T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21592525 | |||||||
| chr12:21592558 | T | C | 1 | a0001c0001t0002g0076 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.121+11914A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21592558 | |||||||
| chr12:21592848 | T | G | 1 | a0004c0006t0001g0275 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.121+11624A>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21592848 | |||||||
| chr12:21592851 | C | T | 1 | a0001c0001t0002g0254 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.121+11621G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21592851 | |||||||
| chr12:21593002 | T | C | 179 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0032 others(176): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.121+11470A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21593002 | |||||||
| chr12:21593033 | G | A | 1 | a0002c0002t0005g0230 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.121+11439C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21593033 | |||||||
| chr12:21593301 | A | AAAC | 263 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0028 others(260): Show |
278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.121+11168_121+1117 others(7): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21593301 | |||||||
| chr12:21593315 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.121+11157C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21593315 | |||||||
| chr12:21593336 | T | C | 3 | a0005c0007t0001g0139 a0005c0007t0001g0250 a0005c0007t0001g0251 |
3 | HG01175.hp1 HG01361.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.121+11136A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21593336 | |||||||
| chr12:21593362 | A | G | 261 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0028 others(258): Show |
276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.121+11110T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21593362 | |||||||
| chr12:21593386 | AAAGAG | A | 79 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0091 others(76): Show |
82 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.121+11081_121+1108 others(9): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21593386 | |||||||
| chr12:21593441 | A | G | 2 | a0001c0001t0004g0234 a0001c0001t0004g0252 |
2 | HG02615.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.121+11031T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21593441 | |||||||
| chr12:21593468 | A | G | 1 | a0001c0001t0002g0158 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.121+11004T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21593468 | |||||||
| chr12:21593618 | G | A | 1 | a0001c0001t0002g0232 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.121+10854C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21593618 | |||||||
| chr12:21593633 | C | T | 95 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0091 others(92): Show |
98 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.121+10839G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21593633 | |||||||
| chr12:21593702 | C | G | 274 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0028 others(271): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.121+10770G>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21593702 | |||||||
| chr12:21593874 | G | T | 1 | a0002c0002t0005g0040 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.121+10598C>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21593874 | |||||||
| chr12:21594121 | T | C | 54 | a0001c0001t0002g0236 a0001c0001t0002g0237 a0001c0001t0002g0268 others(51): Show |
54 | HG00639.hp2 HG00642.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.121+10351A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21594121 | |||||||
| chr12:21594123 | A | T | 25 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0091 others(22): Show |
28 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.121+10349T>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21594123 | |||||||
| chr12:21594209 | C | T | 8 | a0001c0001t0001g0023 a0001c0001t0001g0084 a0001c0001t0003g0003 others(5): Show |
9 | HG01515.hp1 HG01517.hp1 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.121+10263G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21594209 | |||||||
| chr12:21594302 | T | A | 8 | a0001c0001t0001g0023 a0001c0001t0001g0084 a0001c0001t0003g0003 others(5): Show |
9 | HG01515.hp1 HG01517.hp1 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.121+10170A>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21594302 | |||||||
| chr12:21594312 | C | T | 35 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0039 others(32): Show |
39 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.121+10160G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21594312 | |||||||
| chr12:21594328 | A | G | 8 | a0001c0001t0001g0023 a0001c0001t0001g0084 a0001c0001t0003g0003 others(5): Show |
9 | HG01515.hp1 HG01517.hp1 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.121+10144T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21594328 | |||||||
| chr12:21594374 | T | G | 1 | a0001c0001t0001g0091 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.121+10098A>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21594374 | |||||||
| chr12:21594407 | C | G | 8 | a0001c0001t0001g0023 a0001c0001t0001g0084 a0001c0001t0003g0003 others(5): Show |
9 | HG01515.hp1 HG01517.hp1 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.121+10065G>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21594407 | |||||||
| chr12:21594427 | T | C | 8 | a0001c0001t0001g0023 a0001c0001t0001g0084 a0001c0001t0003g0003 others(5): Show |
9 | HG01515.hp1 HG01517.hp1 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.121+10045A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21594427 | |||||||
| chr12:21594652 | G | A | 8 | a0001c0001t0001g0023 a0001c0001t0001g0084 a0001c0001t0003g0003 others(5): Show |
9 | HG01515.hp1 HG01517.hp1 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.121+9820C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21594652 | |||||||
| chr12:21594663 | C | T | 1 | a0001c0001t0001g0023 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.121+9809G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21594663 | |||||||
| chr12:21594699 | C | A | 17 | a0001c0001t0001g0023 a0001c0001t0001g0084 a0001c0001t0001g0242 others(14): Show |
18 | HG01515.hp1 HG01517.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.121+9773G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21594699 | |||||||
| chr12:21594715 | A | C | 32 | a0001c0001t0001g0091 a0001c0001t0002g0037 a0002c0002t0001g0038 others(29): Show |
32 | HG00639.hp2 HG00642.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.121+9757T>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21594715 | |||||||
| chr12:21594903 | G | A | 1 | a0006c0014t0001g0086 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.121+9569C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21594903 | |||||||
| chr12:21595152 | G | A | 2 | a0005c0007t0001g0139 a0005c0007t0001g0251 |
2 | HG01175.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.121+9320C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21595152 | |||||||
| chr12:21595175 | C | A | 2 | a0002c0002t0001g0280 a0002c0002t0001g0281 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.121+9297G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21595175 | |||||||
| chr12:21595233 | G | C | 13 | a0001c0001t0001g0015 a0001c0001t0001g0035 a0001c0001t0002g0247 others(10): Show |
14 | HG01884.hp1 HG02145.hp1 HG02148.hp1 others(11): Show |
intron_variant | MODIFIER | c.121+9239C>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21595233 | |||||||
| chr12:21595243 | T | A | 1 | a0001c0001t0002g0087 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.121+9229A>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21595243 | |||||||
| chr12:21595352 | G | A | 1 | a0002c0002t0001g0138 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.121+9120C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21595352 | |||||||
| chr12:21595392 | T | C | 4 | a0002c0002t0001g0263 a0005c0007t0001g0139 a0005c0007t0001g0250 others(1): Show |
4 | HG01175.hp1 HG01175.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.121+9080A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21595392 | |||||||
| chr12:21595417 | T | C | 1 | a0001c0001t0004g0256 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.121+9055A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21595417 | |||||||
| chr12:21595458 | C | T | 3 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0008g0292 |
3 | HG02451.hp2 HG02818.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.121+9014G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21595458 | |||||||
| chr12:21595488 | A | C | 1 | a0002c0002t0001g0018 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.121+8984T>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21595488 | |||||||
| chr12:21595525 | C | A | 1 | a0001c0001t0004g0256 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.121+8947G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21595525 | |||||||
| chr12:21595662 | C | A | 1 | a0001c0001t0004g0252 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.121+8810G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21595662 | |||||||
| chr12:21595757 | A | G | 1 | a0002c0002t0001g0001 | 3 | NA18951.hp2 NA18964.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.121+8715T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21595757 | |||||||
| chr12:21595898 | G | A | 3 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0008g0292 |
3 | HG02451.hp2 HG02818.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.121+8574C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21595898 | |||||||
| chr12:21595953 | T | A | 280 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(277): Show |
296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.121+8519A>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21595953 | |||||||
| chr12:21595998 | A | T | 2 | a0002c0002t0001g0277 a0003c0003t0001g0278 |
2 | HG02109.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.121+8474T>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21595998 | |||||||
| chr12:21596008 | G | A | 1 | a0003c0003t0001g0289 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.121+8464C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21596008 | |||||||
| chr12:21596044 | C | T | 2 | a0001c0001t0004g0101 a0002c0002t0004g0295 |
2 | HG02055.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.121+8428G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21596044 | |||||||
| chr12:21596142 | C | T | 1 | a0005c0007t0001g0139 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.121+8330G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21596142 | |||||||
| chr12:21596216 | C | A | 1 | a0002c0002t0001g0018 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.121+8256G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21596216 | |||||||
| chr12:21596424 | G | T | 1 | a0001c0001t0004g0100 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.121+8048C>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21596424 | |||||||
| chr12:21596435 | T | C | 1 | a0002c0002t0001g0018 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.121+8037A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21596435 | |||||||
| chr12:21596620 | G | A | 268 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(265): Show |
284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.121+7852C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21596620 | |||||||
| chr12:21596732 | A | C | 1 | a0002c0002t0001g0018 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.121+7740T>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21596732 | |||||||
| chr12:21596927 | C | T | 1 | a0002c0002t0001g0099 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.121+7545G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21596927 | |||||||
| chr12:21597044 | T | G | 146 | a0001c0001t0001g0091 a0001c0001t0001g0149 a0001c0001t0001g0152 others(143): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.121+7428A>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21597044 | |||||||
| chr12:21597086 | C | G | 1 | a0001c0001t0002g0098 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.121+7386G>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21597086 | |||||||
| chr12:21597138 | T | C | 2 | a0001c0001t0002g0253 a0002c0002t0001g0024 |
2 | NA18944.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.121+7334A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21597138 | |||||||
| chr12:21597356 | T | G | 262 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0028 others(259): Show |
278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.121+7116A>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21597356 | |||||||
| chr12:21597450 | A | T | 1 | a0002c0002t0001g0097 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.121+7022T>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21597450 | |||||||
| chr12:21597561 | A | G | 262 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0028 others(259): Show |
278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.121+6911T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21597561 | |||||||
| chr12:21597580 | A | G | 7 | a0001c0001t0002g0095 a0001c0001t0003g0004 a0001c0001t0003g0005 others(4): Show |
9 | HG00423.hp2 HG02056.hp1 NA18949.hp1 others(6): Show |
intron_variant | MODIFIER | c.121+6892T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21597580 | |||||||
| chr12:21597766 | C | T | 199 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0091 others(196): Show |
212 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.121+6706G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21597766 | |||||||
| chr12:21597853 | A | G | 1 | a0001c0013t0001g0282 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.121+6619T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21597853 | |||||||
| chr12:21597867 | C | T | 262 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0028 others(259): Show |
278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.121+6605G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21597867 | |||||||
| chr12:21598043 | A | G | 285 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(282): Show |
301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.121+6429T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21598043 | |||||||
| chr12:21598118 | A | G | 1 | a0002c0002t0001g0018 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.121+6354T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21598118 | |||||||
| chr12:21598261 | C | G | 1 | a0002c0002t0001g0018 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.121+6211G>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21598261 | |||||||
| chr12:21598272 | A | G | 6 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0002c0002t0001g0017 others(3): Show |
6 | HG01168.hp1 HG01169.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.121+6200T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21598272 | |||||||
| chr12:21598318 | A | G | 1 | a0002c0002t0001g0277 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.121+6154T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21598318 | |||||||
| chr12:21598351 | C | T | 1 | a0001c0001t0002g0094 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.121+6121G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21598351 | |||||||
| chr12:21598451 | C | A | 1 | a0002c0002t0001g0088 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.121+6021G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21598451 | |||||||
| chr12:21598661 | G | C | 1 | a0001c0001t0001g0023 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.121+5811C>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21598661 | |||||||
| chr12:21598867 | G | A | 1 | a0002c0002t0001g0257 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.121+5605C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21598867 | |||||||
| chr12:21598881 | C | T | 1 | a0002c0002t0001g0093 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.121+5591G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21598881 | |||||||
| chr12:21599070 | G | GCT | 273 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(270): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.121+5400_121+5401d others(4): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21599070 | |||||||
| chr12:21599070 | G | T | 1 | a0001c0001t0003g0271 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.121+5402C>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21599070 | |||||||
| chr12:21599086 | T | C | 3 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0008g0292 |
3 | HG02451.hp2 HG02818.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.121+5386A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21599086 | |||||||
| chr12:21599097 | T | C | 1 | a0001c0001t0003g0258 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.121+5375A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21599097 | |||||||
| chr12:21599112 | C | A | 262 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0028 others(259): Show |
278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.121+5360G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21599112 | |||||||
| chr12:21599154 | T | A | 1 | a0002c0012t0001g0259 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.121+5318A>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21599154 | |||||||
| chr12:21599174 | G | T | 58 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0028 others(55): Show |
61 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.121+5298C>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21599174 | |||||||
| chr12:21599534 | A | T | 2 | a0001c0013t0001g0282 a0002c0002t0004g0295 |
2 | HG02809.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.121+4938T>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21599534 | |||||||
| chr12:21599668 | A | C | 6 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0005t0001g0031 others(3): Show |
6 | HG01884.hp1 HG02622.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.121+4804T>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21599668 | |||||||
| chr12:21599675 | A | G | 2 | a0001c0001t0003g0029 a0001c0001t0003g0030 |
2 | NA18952.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.121+4797T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21599675 | |||||||
| chr12:21599727 | G | A | 1 | a0008c0009t0002g0260 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.121+4745C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21599727 | |||||||
| chr12:21600224 | T | G | 280 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(277): Show |
296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.121+4248A>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21600224 | |||||||
| chr12:21600379 | C | T | 1 | a0002c0002t0001g0018 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.121+4093G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21600379 | |||||||
| chr12:21600450 | G | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0028 |
2 | HG01255.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.121+4022C>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21600450 | |||||||
| chr12:21600797 | G | A | 1 | a0002c0002t0001g0261 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.121+3675C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21600797 | |||||||
| chr12:21600849 | T | C | 1 | a0001c0001t0001g0291 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.121+3623A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21600849 | |||||||
| chr12:21600906 | C | A | 2 | a0001c0001t0004g0025 a0003c0003t0001g0026 |
2 | HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.121+3566G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21600906 | |||||||
| chr12:21601251 | C | A | 2 | a0002c0002t0001g0262 a0002c0002t0001g0263 |
2 | HG00642.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.121+3221G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21601251 | |||||||
| chr12:21601255 | T | C | 266 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0028 others(263): Show |
282 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.121+3217A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21601255 | |||||||
| chr12:21601296 | C | T | 266 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0028 others(263): Show |
282 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.121+3176G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21601296 | |||||||
| chr12:21601509 | C | T | 7 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0004g0025 others(4): Show |
7 | HG01168.hp1 HG01169.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.121+2963G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21601509 | |||||||
| chr12:21601652 | G | A | 1 | a0001c0001t0002g0264 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.121+2820C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21601652 | |||||||
| chr12:21601833 | G | C | 3 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0008g0292 |
3 | HG02451.hp2 HG02818.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.121+2639C>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21601833 | |||||||
| chr12:21601991 | T | C | 1 | a0001c0001t0003g0265 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.121+2481A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21601991 | |||||||
| chr12:21602528 | A | G | 1 | a0002c0002t0001g0024 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.121+1944T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21602528 | |||||||
| chr12:21602536 | C | A | 1 | a0002c0002t0001g0266 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.121+1936G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21602536 | |||||||
| chr12:21602630 | C | T | 1 | a0001c0001t0001g0023 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.121+1842G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21602630 | |||||||
| chr12:21602707 | C | T | 4 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0002c0002t0001g0017 others(1): Show |
4 | HG01168.hp1 HG01169.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.121+1765G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21602707 | |||||||
| chr12:21602806 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.121+1666C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21602806 | |||||||
| chr12:21603021 | T | C | 2 | a0001c0001t0002g0268 a0001c0001t0003g0269 |
2 | HG02080.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.121+1451A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21603021 | |||||||
| chr12:21603106 | C | G | 1 | a0001c0004t0003g0019 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.121+1366G>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21603106 | |||||||
| chr12:21603235 | G | C | 1 | a0001c0001t0003g0270 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.121+1237C>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21603235 | |||||||
| chr12:21603284 | G | A | 1 | a0001c0001t0003g0271 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.121+1188C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21603284 | |||||||
| chr12:21603526 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0272 |
3 | HG02257.hp2 HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.121+946C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21603526 | |||||||
| chr12:21603622 | A | T | 1 | a0002c0002t0001g0018 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.121+850T>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21603622 | |||||||
| chr12:21603662 | C | T | 5 | a0002c0002t0001g0277 a0002c0002t0001g0279 a0002c0002t0001g0280 others(2): Show |
5 | HG02109.hp2 HG02886.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.121+810G>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21603662 | |||||||
| chr12:21603752 | T | C | 1 | a0002c0002t0004g0295 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.121+720A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21603752 | |||||||
| chr12:21603850 | G | A | 274 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(271): Show |
290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.121+622C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21603850 | |||||||
| chr12:21603919 | A | G | 1 | a0002c0002t0001g0017 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.121+553T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21603919 | |||||||
| chr12:21603941 | T | A | 3 | a0004c0006t0001g0273 a0004c0006t0001g0274 a0004c0006t0001g0275 |
3 | HG02647.hp1 HG02723.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.121+531A>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21603941 | |||||||
| chr12:21604014 | T | C | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+458A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604014 | |||||||
| chr12:21604016 | A | T | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+456T>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604016 | |||||||
| chr12:21604017 | T | C | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+455A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604017 | |||||||
| chr12:21604020 | T | G | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+452A>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604020 | |||||||
| chr12:21604021 | G | A | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+451C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604021 | |||||||
| chr12:21604024 | T | G | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+448A>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604024 | |||||||
| chr12:21604026 | T | A | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+446A>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604026 | |||||||
| chr12:21604033 | T | A | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+439A>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604033 | |||||||
| chr12:21604038 | A | G | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+434T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604038 | |||||||
| chr12:21604042 | A | C | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+430T>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604042 | |||||||
| chr12:21604044 | T | C | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+428A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604044 | |||||||
| chr12:21604045 | T | TGTCCCCC others(4): Show |
1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+426_121+427ins others(11): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604045 | |||||||
| chr12:21604048 | T | G | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+424A>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604048 | |||||||
| chr12:21604049 | A | C | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+423T>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604049 | |||||||
| chr12:21604050 | T | C | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+422A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604050 | |||||||
| chr12:21604053 | T | G | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+419A>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604053 | |||||||
| chr12:21604056 | C | A | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+416G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604056 | |||||||
| chr12:21604059 | A | C | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+413T>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604059 | |||||||
| chr12:21604063 | A | T | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+409T>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604063 | |||||||
| chr12:21604065 | T | C | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+407A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604065 | |||||||
| chr12:21604066 | G | C | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+406C>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604066 | |||||||
| chr12:21604070 | A | T | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+402T>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604070 | |||||||
| chr12:21604072 | T | A | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+400A>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604072 | |||||||
| chr12:21604073 | T | G | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+399A>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604073 | |||||||
| chr12:21604092 | T | A | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+380A>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604092 | |||||||
| chr12:21604094 | A | C | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+378T>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604094 | |||||||
| chr12:21604097 | A | C | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+375T>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604097 | |||||||
| chr12:21604106 | T | A | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+366A>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604106 | |||||||
| chr12:21604109 | T | G | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+363A>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604109 | |||||||
| chr12:21604110 | C | G | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+362G>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604110 | |||||||
| chr12:21604112 | T | A | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+360A>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604112 | |||||||
| chr12:21604114 | A | C | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+358T>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604114 | |||||||
| chr12:21604119 | A | G | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+353T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604119 | |||||||
| chr12:21604120 | A | G | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+352T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604120 | |||||||
| chr12:21604121 | A | G | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+351T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604121 | |||||||
| chr12:21604122 | T | C | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+350A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604122 | |||||||
| chr12:21604125 | T | C | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+347A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604125 | |||||||
| chr12:21604127 | A | C | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+345T>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604127 | |||||||
| chr12:21604130 | T | C | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+342A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604130 | |||||||
| chr12:21604132 | T | A | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+340A>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604132 | |||||||
| chr12:21604134 | C | A | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+338G>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604134 | |||||||
| chr12:21604135 | T | C | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+337A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604135 | |||||||
| chr12:21604140 | T | G | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+332A>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604140 | |||||||
| chr12:21604141 | G | T | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+331C>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604141 | |||||||
| chr12:21604143 | T | A | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+329A>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604143 | |||||||
| chr12:21604148 | A | T | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+324T>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604148 | |||||||
| chr12:21604149 | A | G | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+323T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604149 | |||||||
| chr12:21604150 | A | C | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+322T>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604150 | |||||||
| chr12:21604151 | A | C | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+321T>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604151 | |||||||
| chr12:21604153 | T | A | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+319A>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604153 | |||||||
| chr12:21604154 | T | C | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+318A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604154 | |||||||
| chr12:21604157 | A | T | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+315T>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604157 | |||||||
| chr12:21604159 | A | C | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+313T>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604159 | |||||||
| chr12:21604165 | A | G | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+307T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604165 | |||||||
| chr12:21604168 | G | T | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+304C>A | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604168 | |||||||
| chr12:21604174 | ATTAACTT others(3): Show |
A | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+288_121+297del others(10): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604174 | |||||||
| chr12:21604186 | T | A | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+286A>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604186 | |||||||
| chr12:21604187 | T | A | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+285A>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604187 | |||||||
| chr12:21604190 | T | C | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+282A>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604190 | |||||||
| chr12:21604192 | T | G | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+280A>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604192 | |||||||
| chr12:21604193 | G | C | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+279C>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604193 | |||||||
| chr12:21604194 | T | A | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+278A>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604194 | |||||||
| chr12:21604196 | G | C | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+276C>G | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604196 | |||||||
| chr12:21604201 | A | G | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+271T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604201 | |||||||
| chr12:21604206 | G | A | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+266C>T | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604206 | |||||||
| chr12:21604207 | GATTTTAA others(4): Show |
G | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.121+254_121+264del others(11): Show |
GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604207 | |||||||
| chr12:21604338 | A | G | 274 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0027 others(271): Show |
290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.121+134T>C | GYS2 | ENSG00000111713.3 | transcript | ENST00000261195.3 | protein_coding | 1/15 | chr12 | 21604338 |