Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2992 |
| ensemblid | ENSG00000163754.18 |
| hgncid | 4699 |
| symbol | GYG1 |
| name | glycogenin 1 |
| refseq_nuc | NM_004130.4 |
| refseq_prot | NP_004121.2 |
| ensembl_nuc | ENST00000345003.9 |
| ensembl_prot | ENSP00000340736.4 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 148991540 |
| end | 149031775 |
| strand | + |
| ver | v1.2 |
| region | chr3:148991540-149031775 |
| region5000 | chr3:148986540-149036775 |
| regionname0 | GYG1_chr3_148991540_149031775 |
| regionname5000 | GYG1_chr3_148986540_149036775 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 350 | 409 | 95 | 64 | 184 | 18 | 46 | 142 | GYG1_chr3_148986540_149036775 | GYG1 | MTDQA others(345): Show |
chr3 | 148986540 | 149036775 |
| a0002 | 0/0 | 350 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | MTDQA others(345): Show |
chr3 | 148986540 | 149036775 |
| a0003 | 0/0 | 350 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | MTDQA others(345): Show |
chr3 | 148986540 | 149036775 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1050 | 249 | 49 | 44 | 112 | 10 | 32 | GYG1_chr3_148986540_149036775 | GYG1 | ATGAC others(1045): Show |
chr3 | 148986540 | 149036775 | ||
| a0001c0002 | 0/0 | 1050 | 137 | 27 | 16 | 72 | 8 | 14 | GYG1_chr3_148986540_149036775 | GYG1 | ATGAC others(1045): Show |
chr3 | 148986540 | 149036775 | ||
| a0001c0003 | 0/0 | 1050 | 21 | 18 | 3 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | ATGAC others(1045): Show |
chr3 | 148986540 | 149036775 | ||
| a0001c0006 | 0/0 | 1050 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | ATGAC others(1045): Show |
chr3 | 148986540 | 149036775 | ||
| a0001c0007 | 0/0 | 1050 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | ATGAC others(1045): Show |
chr3 | 148986540 | 149036775 | ||
| a0002c0004 | 0/0 | 1050 | 3 | 3 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | ATGAC others(1045): Show |
chr3 | 148986540 | 149036775 | ||
| a0003c0005 | 0/0 | 1050 | 2 | 0 | 2 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | ATGAC others(1045): Show |
chr3 | 148986540 | 149036775 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 5999 | 89 | 1 | 24 | 55 | 3 | 6 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5994): Show |
chr3 | 148986540 | 149036775 |
| a0001c0001t0003 | 1/1 | 5996 | 87 | 10 | 11 | 39 | 5 | 20 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5991): Show |
chr3 | 148986540 | 149036775 |
| a0001c0001t0004 | 0/0 | 5996 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5991): Show |
chr3 | 148986540 | 149036775 |
| a0001c0001t0005 | 0/0 | 5996 | 9 | 8 | 0 | 0 | 1 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5991): Show |
chr3 | 148986540 | 149036775 |
| a0001c0001t0007 | 0/0 | 5998 | 5 | 0 | 1 | 4 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5993): Show |
chr3 | 148986540 | 149036775 |
| a0001c0001t0008 | 0/0 | 5996 | 2 | 0 | 0 | 2 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5991): Show |
chr3 | 148986540 | 149036775 |
| a0001c0001t0009 | 0/0 | 5995 | 5 | 1 | 0 | 2 | 1 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5990): Show |
chr3 | 148986540 | 149036775 |
| a0001c0001t0010 | 0/0 | 5997 | 5 | 0 | 1 | 4 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5992): Show |
chr3 | 148986540 | 149036775 |
| a0001c0001t0011 | 0/0 | 5996 | 5 | 5 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5991): Show |
chr3 | 148986540 | 149036775 |
| a0001c0001t0013 | 0/0 | 5997 | 4 | 4 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5992): Show |
chr3 | 148986540 | 149036775 |
| a0001c0001t0014 | 0/0 | 5996 | 3 | 0 | 2 | 0 | 0 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5991): Show |
chr3 | 148986540 | 149036775 |
| a0001c0001t0015 | 0/0 | 5999 | 3 | 3 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5994): Show |
chr3 | 148986540 | 149036775 |
| a0001c0001t0016 | 0/0 | 5997 | 3 | 3 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5992): Show |
chr3 | 148986540 | 149036775 |
| a0001c0001t0017 | 0/0 | 6000 | 3 | 0 | 1 | 2 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5995): Show |
chr3 | 148986540 | 149036775 |
| a0001c0001t0019 | 0/0 | 5999 | 3 | 0 | 0 | 0 | 0 | 3 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5994): Show |
chr3 | 148986540 | 149036775 |
| a0001c0001t0020 | 0/0 | 5996 | 2 | 2 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5991): Show |
chr3 | 148986540 | 149036775 |
| a0001c0001t0021 | 0/0 | 5999 | 2 | 0 | 0 | 2 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5994): Show |
chr3 | 148986540 | 149036775 |
| a0001c0001t0022 | 0/0 | 5997 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5992): Show |
chr3 | 148986540 | 149036775 |
| a0001c0001t0023 | 0/0 | 5999 | 2 | 2 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5994): Show |
chr3 | 148986540 | 149036775 |
| a0001c0001t0024 | 0/0 | 5999 | 2 | 0 | 2 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5994): Show |
chr3 | 148986540 | 149036775 |
| a0001c0001t0027 | 0/0 | 5999 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5994): Show |
chr3 | 148986540 | 149036775 |
| a0001c0001t0028 | 0/0 | 5995 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5990): Show |
chr3 | 148986540 | 149036775 |
| a0001c0001t0030 | 0/0 | 5995 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5990): Show |
chr3 | 148986540 | 149036775 |
| a0001c0001t0031 | 0/0 | 5996 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5991): Show |
chr3 | 148986540 | 149036775 |
| a0001c0001t0033 | 0/0 | 5996 | 1 | 0 | 0 | 0 | 0 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5991): Show |
chr3 | 148986540 | 149036775 |
| a0001c0001t0034 | 0/0 | 5996 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5991): Show |
chr3 | 148986540 | 149036775 |
| a0001c0001t0035 | 0/0 | 5997 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5992): Show |
chr3 | 148986540 | 149036775 |
| a0001c0001t0036 | 0/0 | 6000 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5995): Show |
chr3 | 148986540 | 149036775 |
| a0001c0001t0037 | 0/0 | 5996 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5991): Show |
chr3 | 148986540 | 149036775 |
| a0001c0001t0038 | 0/0 | 5997 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5992): Show |
chr3 | 148986540 | 149036775 |
| a0001c0001t0043 | 0/0 | 5999 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5994): Show |
chr3 | 148986540 | 149036775 |
| a0001c0001t0051 | 0/0 | 5995 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5990): Show |
chr3 | 148986540 | 149036775 |
| a0001c0001t0052 | 0/0 | 5996 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5991): Show |
chr3 | 148986540 | 149036775 |
| a0001c0002t0001 | 0/0 | 5990 | 115 | 24 | 13 | 67 | 5 | 6 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5985): Show |
chr3 | 148986540 | 149036775 |
| a0001c0002t0006 | 0/0 | 5990 | 7 | 0 | 1 | 0 | 0 | 6 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5985): Show |
chr3 | 148986540 | 149036775 |
| a0001c0002t0008 | 0/0 | 5996 | 4 | 1 | 0 | 2 | 0 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5991): Show |
chr3 | 148986540 | 149036775 |
| a0001c0002t0018 | 0/0 | 5990 | 3 | 0 | 1 | 0 | 1 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5985): Show |
chr3 | 148986540 | 149036775 |
| a0001c0002t0025 | 0/0 | 5990 | 2 | 2 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5985): Show |
chr3 | 148986540 | 149036775 |
| a0001c0002t0026 | 0/0 | 5990 | 2 | 0 | 0 | 0 | 2 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5985): Show |
chr3 | 148986540 | 149036775 |
| a0001c0002t0044 | 0/0 | 5990 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5985): Show |
chr3 | 148986540 | 149036775 |
| a0001c0002t0045 | 0/0 | 5990 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5985): Show |
chr3 | 148986540 | 149036775 |
| a0001c0002t0046 | 0/0 | 5990 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5985): Show |
chr3 | 148986540 | 149036775 |
| a0001c0002t0047 | 0/0 | 5990 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5985): Show |
chr3 | 148986540 | 149036775 |
| a0001c0003t0004 | 0/0 | 5996 | 11 | 10 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5991): Show |
chr3 | 148986540 | 149036775 |
| a0001c0003t0007 | 0/0 | 5998 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5993): Show |
chr3 | 148986540 | 149036775 |
| a0001c0003t0012 | 0/0 | 6000 | 4 | 4 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5995): Show |
chr3 | 148986540 | 149036775 |
| a0001c0003t0022 | 0/0 | 5997 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5992): Show |
chr3 | 148986540 | 149036775 |
| a0001c0003t0039 | 0/0 | 5996 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5991): Show |
chr3 | 148986540 | 149036775 |
| a0001c0003t0040 | 0/0 | 5996 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5991): Show |
chr3 | 148986540 | 149036775 |
| a0001c0003t0041 | 0/0 | 5996 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5991): Show |
chr3 | 148986540 | 149036775 |
| a0001c0003t0042 | 0/0 | 5995 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5990): Show |
chr3 | 148986540 | 149036775 |
| a0001c0006t0029 | 0/0 | 5985 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5980): Show |
chr3 | 148986540 | 149036775 |
| a0001c0007t0032 | 0/0 | 5996 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5991): Show |
chr3 | 148986540 | 149036775 |
| a0002c0004t0048 | 0/0 | 5995 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5990): Show |
chr3 | 148986540 | 149036775 |
| a0002c0004t0049 | 0/0 | 5995 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5990): Show |
chr3 | 148986540 | 149036775 |
| a0002c0004t0050 | 0/0 | 5995 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5990): Show |
chr3 | 148986540 | 149036775 |
| a0003c0005t0001 | 0/0 | 5990 | 2 | 0 | 2 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | TCCCC others(5985): Show |
chr3 | 148986540 | 149036775 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0005 | 0/0 | 5 | 0 | 1 | 3 | 1 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0001 | 0/0 | 7 | 0 | 0 | 6 | 1 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0003 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0004 | 0/0 | 4 | 1 | 0 | 1 | 0 | 2 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0012 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0013 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0112 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0142 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0003g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0004g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0005g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0005g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0005g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0005g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0005g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0005g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0005g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0005g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0007g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0007g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0007g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0007g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0007g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0008g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0009g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0009g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0009g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0009g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0009g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0010g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0010g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0010g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0011g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0011g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0011g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0011g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0013g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0013g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0013g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0013g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0014g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0014g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0014g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0015g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0015g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0016g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0016g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0016g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0017g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0017g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0017g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0019g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0019g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0020g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0020g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0021g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0021g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0022g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0023g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0023g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0024g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0024g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0027g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0028g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0030g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0031g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0033g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0034g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0035g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0036g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0037g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0038g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0043g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0051g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0001t0052g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0002 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0006 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0008 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0006g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0006g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0006g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0006g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0006g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0006g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0006g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0008g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0008g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0008g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0008g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0018g0029 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0018g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0025g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0026g0017 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0044g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0045g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0046g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0002t0047g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0003t0004g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0003t0004g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0003t0004g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0003t0004g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0003t0004g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0003t0004g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0003t0004g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0003t0004g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0003t0007g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0003t0012g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0003t0012g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0003t0012g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0003t0012g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0003t0022g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0003t0039g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0003t0040g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0003t0041g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0003t0042g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0006t0029g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0001c0007t0032g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0002c0004t0048g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0002c0004t0049g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0002c0004t0050g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0003c0005t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| a0003c0005t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0005 | EUR | GBR | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0001 | EUR | GBR | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0138 | EUR | GBR | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0078 | EUR | GBR | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0179 | EUR | FIN | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0008 | EUR | FIN | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG00323 | hp1 | a0001 | c0001 | t0009 | g0113 | EUR | FIN | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG00323 | hp2 | a0001 | c0002 | t0018 | g0029 | EUR | FIN | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0167 | EAS | CHS | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | CHS | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | CHS | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | CHS | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | CHS | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | CHS | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0111 | EAS | CHS | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | CHS | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | CHS | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0327 | EAS | CHS | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | CHS | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0214 | AMR | PUR | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0277 | AMR | PUR | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | CHS | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | CHS | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0080 | AMR | PUR | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0259 | AMR | PUR | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0265 | AMR | PUR | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0060 | AMR | PUR | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG00738 | hp1 | a0001 | c0001 | t0036 | g0009 | AMR | PUR | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0239 | AMR | PUR | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0123 | AMR | PUR | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01070 | hp2 | a0003 | c0005 | t0001 | g0092 | AMR | PUR | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01071 | hp2 | a0003 | c0005 | t0001 | g0093 | AMR | PUR | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0110 | AMR | PUR | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0213 | AMR | PUR | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | PUR | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01081 | hp2 | a0001 | c0002 | t0018 | g0164 | AMR | PUR | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0248 | AMR | PUR | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0258 | AMR | PUR | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0019 | AMR | PUR | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01167 | hp1 | a0001 | c0001 | t0014 | g0146 | AMR | PUR | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01167 | hp2 | a0001 | c0003 | t0042 | g0339 | AMR | PUR | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01169 | hp1 | a0001 | c0003 | t0007 | g0338 | AMR | PUR | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01169 | hp2 | a0001 | c0001 | t0007 | g0225 | AMR | PUR | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01175 | hp1 | a0001 | c0001 | t0017 | g0236 | AMR | PUR | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0102 | AMR | PUR | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01243 | hp2 | a0001 | c0003 | t0004 | g0336 | AMR | PUR | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0137 | AMR | CLM | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01255 | hp2 | a0001 | c0001 | t0022 | g0302 | AMR | CLM | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0263 | AMR | CLM | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0018 | AMR | CLM | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01261 | hp1 | a0001 | c0001 | t0024 | g0281 | AMR | CLM | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0257 | AMR | CLM | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01346 | hp1 | a0001 | c0001 | t0014 | g0147 | AMR | CLM | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0094 | AMR | CLM | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01358 | hp1 | a0001 | c0007 | t0032 | g0148 | AMR | CLM | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0224 | AMR | CLM | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0105 | AMR | CLM | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0324 | AMR | CLM | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0201 | AMR | CLM | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0077 | AMR | CLM | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0222 | EUR | IBS | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0145 | EUR | IBS | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01516 | hp1 | a0001 | c0002 | t0026 | g0017 | EUR | IBS | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01516 | hp2 | a0001 | c0001 | t0005 | g0270 | EUR | IBS | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01517 | hp1 | a0001 | c0002 | t0026 | g0017 | EUR | IBS | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0144 | EUR | IBS | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0316 | AFR | ACB | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0314 | AFR | ACB | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0059 | AFR | ACB | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01891 | hp2 | a0001 | c0001 | t0016 | g0304 | AFR | ACB | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0230 | AMR | PEL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0049 | AMR | PEL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0245 | AMR | PEL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0024 | AMR | PEL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0260 | AMR | PEL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0076 | AMR | PEL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0261 | AMR | PEL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0019 | AMR | PEL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0211 | AMR | PEL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0280 | AMR | PEL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | PEL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0055 | EAS | KHV | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02015 | hp2 | a0001 | c0001 | t0007 | g0039 | EAS | KHV | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | KHV | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | KHV | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | KHV | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | KHV | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02055 | hp1 | a0001 | c0002 | t0008 | g0328 | AFR | ACB | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02055 | hp2 | a0001 | c0001 | t0038 | g0199 | AFR | ACB | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | KHV | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0062 | EAS | KHV | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02074 | hp1 | a0001 | c0001 | t0021 | g0118 | EAS | KHV | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | KHV | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | KHV | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | KHV | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0122 | EAS | KHV | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | KHV | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | KHV | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | KHV | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | KHV | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02135 | hp2 | a0001 | c0001 | t0021 | g0120 | EAS | KHV | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0057 | AFR | ACB | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02145 | hp2 | a0001 | c0001 | t0037 | g0099 | AFR | ACB | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02148 | hp1 | a0001 | c0001 | t0010 | g0299 | AMR | PEL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0262 | AMR | PEL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CDX | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | CDX | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02165 | hp1 | a0001 | c0001 | t0007 | g0247 | EAS | CDX | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0173 | EAS | CDX | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02257 | hp1 | a0001 | c0001 | t0011 | g0205 | AFR | ACB | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0186 | AFR | ACB | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02258 | hp1 | a0002 | c0004 | t0050 | g0194 | AFR | ACB | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0290 | AFR | ACB | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02273 | hp1 | a0001 | c0002 | t0006 | g0292 | AMR | PEL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02273 | hp2 | a0001 | c0002 | t0046 | g0018 | AMR | PEL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02280 | hp1 | a0001 | c0001 | t0023 | g0101 | AFR | ACB | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02280 | hp2 | a0001 | c0003 | t0004 | g0332 | AFR | ACB | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0063 | AMR | PEL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0212 | AMR | PEL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02300 | hp1 | a0001 | c0001 | t0024 | g0233 | AMR | PEL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0206 | AMR | PEL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02451 | hp1 | a0001 | c0002 | t0025 | g0033 | AFR | ACB | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02451 | hp2 | a0001 | c0001 | t0015 | g0009 | AFR | ACB | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | KHV | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | KHV | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02572 | hp1 | a0001 | c0003 | t0012 | g0309 | AFR | GWD | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02572 | hp2 | a0001 | c0001 | t0030 | g0197 | AFR | GWD | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0103 | SAS | PJL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02602 | hp2 | a0001 | c0002 | t0018 | g0029 | SAS | PJL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02615 | hp1 | a0002 | c0004 | t0049 | g0195 | AFR | GWD | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02615 | hp2 | a0001 | c0001 | t0051 | g0157 | AFR | GWD | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02622 | hp1 | a0001 | c0003 | t0040 | g0329 | AFR | GWD | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02622 | hp2 | a0001 | c0001 | t0034 | g0161 | AFR | GWD | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0193 | AFR | GWD | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0040 | AFR | GWD | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02647 | hp1 | a0002 | c0004 | t0048 | g0196 | AFR | GWD | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0317 | AFR | GWD | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02683 | hp1 | a0001 | c0002 | t0006 | g0296 | SAS | PJL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0231 | SAS | PJL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0075 | SAS | PJL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02698 | hp2 | a0001 | c0002 | t0006 | g0298 | SAS | PJL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0318 | AFR | GWD | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0276 | AFR | GWD | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02723 | hp1 | a0001 | c0003 | t0012 | g0306 | AFR | GWD | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02723 | hp2 | a0001 | c0001 | t0016 | g0305 | AFR | GWD | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0068 | SAS | PJL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02735 | hp2 | a0001 | c0002 | t0006 | g0297 | SAS | PJL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0046 | SAS | PJL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0234 | SAS | PJL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02809 | hp1 | a0001 | c0001 | t0052 | g0156 | AFR | GWD | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0162 | AFR | GWD | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02818 | hp1 | a0001 | c0001 | t0031 | g0200 | AFR | GWD | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0288 | AFR | GWD | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02886 | hp1 | a0001 | c0006 | t0029 | g0044 | AFR | GWD | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0271 | AFR | GWD | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02895 | hp1 | a0001 | c0003 | t0004 | g0042 | AFR | GWD | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0040 | AFR | GWD | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02896 | hp1 | a0001 | c0001 | t0015 | g0009 | AFR | GWD | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02896 | hp2 | a0001 | c0003 | t0004 | g0335 | AFR | GWD | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02897 | hp1 | a0001 | c0003 | t0004 | g0334 | AFR | GWD | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02897 | hp2 | a0001 | c0003 | t0004 | g0042 | AFR | GWD | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02922 | hp1 | a0001 | c0001 | t0013 | g0151 | AFR | ESN | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0026 | AFR | ESN | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02965 | hp1 | a0001 | c0001 | t0035 | g0301 | AFR | ESN | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02965 | hp2 | a0001 | c0003 | t0004 | g0331 | AFR | ESN | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02970 | hp1 | a0001 | c0001 | t0013 | g0153 | AFR | ESN | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02970 | hp2 | a0001 | c0001 | t0023 | g0100 | AFR | ESN | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02976 | hp1 | a0001 | c0003 | t0022 | g0330 | AFR | ESN | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0030 | AFR | ESN | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03041 | hp1 | a0001 | c0001 | t0009 | g0319 | AFR | GWD | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0215 | AFR | GWD | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0191 | AFR | MSL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03098 | hp2 | a0001 | c0003 | t0039 | g0340 | AFR | MSL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03130 | hp1 | a0001 | c0003 | t0004 | g0014 | AFR | ESN | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03130 | hp2 | a0001 | c0001 | t0015 | g0198 | AFR | ESN | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0189 | AFR | ESN | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03139 | hp2 | a0001 | c0001 | t0013 | g0155 | AFR | ESN | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0026 | AFR | ESN | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03195 | hp2 | a0001 | c0001 | t0011 | g0036 | AFR | ESN | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0031 | AFR | MSL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0269 | AFR | MSL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0032 | AFR | MSL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0268 | AFR | MSL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03239 | hp1 | a0001 | c0001 | t0014 | g0149 | SAS | PJL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0143 | SAS | PJL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0091 | AFR | MSL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03453 | hp2 | a0001 | c0001 | t0020 | g0154 | AFR | MSL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03486 | hp1 | a0001 | c0001 | t0028 | g0098 | AFR | MSL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0274 | AFR | MSL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03490 | hp1 | a0001 | c0002 | t0006 | g0294 | SAS | PJL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03490 | hp2 | a0001 | c0002 | t0008 | g0006 | SAS | PJL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0140 | SAS | PJL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03491 | hp2 | a0001 | c0001 | t0019 | g0037 | SAS | PJL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03492 | hp1 | a0001 | c0001 | t0019 | g0037 | SAS | PJL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0027 | SAS | PJL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0032 | AFR | ESN | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03516 | hp2 | a0001 | c0001 | t0013 | g0150 | AFR | ESN | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0160 | AFR | MSL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03579 | hp2 | a0001 | c0001 | t0020 | g0152 | AFR | MSL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0237 | SAS | PJL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0013 | SAS | PJL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0321 | SAS | PJL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0141 | SAS | PJL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0133 | SAS | STU | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0246 | SAS | STU | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0130 | SAS | PJL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03704 | hp2 | a0001 | c0001 | t0009 | g0310 | SAS | PJL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0311 | SAS | PJL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0025 | SAS | PJL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0072 | SAS | BEB | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | BEB | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0323 | SAS | BEB | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0132 | SAS | BEB | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0218 | SAS | BEB | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0315 | SAS | BEB | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0114 | SAS | STU | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG04115 | hp2 | a0001 | c0002 | t0006 | g0293 | SAS | STU | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0025 | SAS | BEB | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0074 | SAS | BEB | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0139 | SAS | STU | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG04199 | hp2 | a0001 | c0001 | t0019 | g0226 | SAS | STU | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG04204 | hp1 | a0001 | c0002 | t0006 | g0295 | SAS | STU | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0235 | SAS | STU | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0041 | SAS | STU | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | STU | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18522 | hp1 | a0001 | c0001 | t0011 | g0216 | AFR | YRI | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18522 | hp2 | a0001 | c0003 | t0004 | g0333 | AFR | YRI | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | CHB | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | CHB | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0170 | EAS | CHB | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | CHB | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18906 | hp1 | a0001 | c0003 | t0012 | g0308 | AFR | YRI | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0313 | AFR | YRI | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0325 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18945 | hp2 | a0001 | c0001 | t0043 | g0011 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18946 | hp1 | a0001 | c0001 | t0007 | g0252 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18946 | hp2 | a0001 | c0002 | t0045 | g0089 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18947 | hp2 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0183 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0165 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18963 | hp1 | a0001 | c0001 | t0027 | g0007 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18967 | hp1 | a0001 | c0001 | t0017 | g0221 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18985 | hp2 | a0001 | c0001 | t0010 | g0003 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18987 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18990 | hp2 | a0001 | c0001 | t0009 | g0135 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0190 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18992 | hp1 | a0001 | c0001 | t0009 | g0004 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19000 | hp1 | a0001 | c0002 | t0008 | g0058 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19005 | hp2 | a0001 | c0002 | t0044 | g0002 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19006 | hp1 | a0001 | c0001 | t0007 | g0227 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19012 | hp2 | a0001 | c0001 | t0010 | g0003 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0031 | AFR | LWK | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0129 | AFR | LWK | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19043 | hp1 | a0001 | c0003 | t0041 | g0337 | AFR | LWK | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19043 | hp2 | a0001 | c0001 | t0011 | g0217 | AFR | LWK | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19056 | hp2 | a0001 | c0002 | t0008 | g0051 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19060 | hp1 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19060 | hp2 | a0001 | c0002 | t0047 | g0069 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0159 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0177 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19076 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19077 | hp1 | a0001 | c0001 | t0017 | g0256 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19078 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0326 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0136 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19090 | hp1 | a0001 | c0001 | t0008 | g0021 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0291 | AFR | YRI | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA19240 | hp2 | a0001 | c0003 | t0004 | g0014 | AFR | YRI | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0030 | AFR | ASW | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA20129 | hp2 | a0001 | c0002 | t0025 | g0033 | AFR | ASW | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0079 | EUR | TSI | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0312 | EUR | TSI | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0008 | EUR | TSI | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0279 | EUR | TSI | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA20905 | hp1 | a0001 | c0001 | t0033 | g0041 | SAS | GIH | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0006 | SAS | GIH | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | CLM | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0028 | AMR | CLM | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02109 | hp1 | a0001 | c0001 | t0016 | g0303 | AFR | ACB | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02109 | hp2 | a0001 | c0003 | t0012 | g0307 | AFR | ACB | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0185 | AFR | ACB | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0322 | AFR | ACB | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02559 | hp1 | a0001 | c0003 | t0004 | g0014 | AFR | ACB | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0187 | AFR | ACB | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | MSL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0289 | AFR | MSL | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG06807 | hp1 | a0001 | c0001 | t0011 | g0036 | AFR | USA | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0169 | AFR | USA | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18955 | hp1 | a0001 | c0001 | t0008 | g0021 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | USA | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | USA | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0320 | AFR | LWK | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0188 | AFR | LWK | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0112 | REF | REF | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0142 | REF | REF | GYG1_chr3_148986540_149036775 | GYG1 | chr3 | 148986540 | 149036775 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:148996862 | A | G | 1 | a0003 | 2 | HG01070.hp2 HG01071.hp2 |
missense_variant | MODERATE | c.439A>G | p.Asn147Asp | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/8 | 540/5996 | 439/1053 | 147/350 | chr3 | 148996862 | |||
| chr3:148996875 | A | T | 1 | a0002 | 3 | HG02258.hp1 HG02615.hp1 HG02647.hp1 |
missense_variant | MODERATE | c.452A>T | p.His151Leu | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/8 | 553/5996 | 452/1053 | 151/350 | chr3 | 148996875 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:148994248 | C | T | 1 | a0001c0003 | 21 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(18): Show |
synonymous_variant | LOW | c.114C>T | p.Leu38Leu | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 2/8 | 215/5996 | 114/1053 | 38/350 | chr3 | 148994248 | |||
| chr3:148996317 | A | G | 1 | a0001c0007 | 1 | HG01358.hp1 | synonymous_variant | LOW | c.159A>G | p.Thr53Thr | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 3/8 | 260/5996 | 159/1053 | 53/350 | chr3 | 148996317 | |||
| chr3:149009346 | G | A | 2 | a0001c0002 a0003c0005 |
139 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(136): Show |
synonymous_variant | LOW | c.552G>A | p.Pro184Pro | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/8 | 653/5996 | 552/1053 | 184/350 | chr3 | 149009346 | |||
| chr3:149024053 | G | A | 1 | a0001c0006 | 1 | HG02886.hp1 | splice_region_variant&synonymous_variant | LOW | c.609G>A | p.Val203Val | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 6/8 | 710/5996 | 609/1053 | 203/350 | chr3 | 149024053 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:148991566 | C | T | 1 | a0001c0002t0026 | 2 | HG01516.hp1 HG01517.hp1 |
5_prime_UTR_variant | MODIFIER | c.-75C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 1/8 | 75 | chr3 | 148991566 | ||||||
| chr3:148991568 | C | G | 2 | a0001c0001t0051 a0001c0001t0052 |
2 | HG02615.hp2 HG02809.hp1 |
5_prime_UTR_variant | MODIFIER | c.-73C>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 1/8 | 73 | chr3 | 148991568 | ||||||
| chr3:149027081 | G | GT | 1 | a0001c0001t0013 | 4 | HG02922.hp1 HG02970.hp1 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*149dupT | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 150 | INFO_REALIGN_3_PRIME | chr3 | 149027081 | |||||
| chr3:149027123 | T | C | 1 | a0001c0001t0027 | 1 | NA18963.hp1 | 3_prime_UTR_variant | MODIFIER | c.*190T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 190 | chr3 | 149027123 | ||||||
| chr3:149027334 | C | T | 1 | a0001c0001t0019 | 3 | HG03491.hp2 HG03492.hp1 HG04199.hp2 |
3_prime_UTR_variant | MODIFIER | c.*401C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 401 | chr3 | 149027334 | ||||||
| chr3:149027364 | T | C | 1 | a0001c0001t0013 | 4 | HG02922.hp1 HG02970.hp1 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*431T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 431 | chr3 | 149027364 | ||||||
| chr3:149027449 | A | G | 15 | a0001c0001t0008 a0001c0002t0001 a0001c0002t0006 others(12): Show |
144 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*516A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 516 | chr3 | 149027449 | ||||||
| chr3:149027773 | G | C | 1 | a0001c0001t0028 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*840G>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 840 | chr3 | 149027773 | ||||||
| chr3:149027874 | C | T | 10 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0011 others(7): Show |
111 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*941C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 941 | chr3 | 149027874 | ||||||
| chr3:149027890 | G | C | 1 | a0001c0002t0025 | 2 | HG02451.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*957G>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 957 | chr3 | 149027890 | ||||||
| chr3:149028026 | A | C | 1 | a0002c0004t0050 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1093A>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 1093 | chr3 | 149028026 | ||||||
| chr3:149028117 | A | G | 5 | a0001c0001t0004 a0001c0003t0004 a0001c0003t0039 others(2): Show |
15 | HG01243.hp2 HG02280.hp2 HG02559.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1184A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 1184 | chr3 | 149028117 | ||||||
| chr3:149028170 | T | C | 5 | a0001c0001t0004 a0001c0003t0004 a0001c0003t0039 others(2): Show |
15 | HG01243.hp2 HG02280.hp2 HG02559.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1237T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 1237 | chr3 | 149028170 | ||||||
| chr3:149028316 | A | G | 2 | a0001c0001t0023 a0001c0003t0012 |
6 | HG02109.hp2 HG02280.hp1 HG02572.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1383A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 1383 | chr3 | 149028316 | ||||||
| chr3:149028426 | A | G | 1 | a0001c0003t0041 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1493A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 1493 | chr3 | 149028426 | ||||||
| chr3:149028614 | G | A | 1 | a0001c0001t0014 | 3 | HG01167.hp1 HG01346.hp1 HG03239.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1681G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 1681 | chr3 | 149028614 | ||||||
| chr3:149028705 | A | AT | 12 | a0001c0001t0010 a0001c0001t0016 a0001c0001t0017 others(9): Show |
20 | HG00738.hp1 HG01175.hp1 HG01255.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1795dupT | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 1796 | INFO_REALIGN_3_PRIME | chr3 | 149028705 | |||||
| chr3:149028705 | AT | A | 5 | a0001c0001t0007 a0001c0001t0009 a0001c0001t0051 others(2): Show |
13 | HG00323.hp1 HG01167.hp2 HG01169.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1795delT | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 1795 | INFO_REALIGN_3_PRIME | chr3 | 149028705 | |||||
| chr3:149028705 | ATTTTTT | A | 10 | a0001c0002t0001 a0001c0002t0006 a0001c0002t0018 others(7): Show |
135 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*1790_*1795delTTTT others(2): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 1790 | INFO_REALIGN_3_PRIME | chr3 | 149028705 | |||||
| chr3:149028705 | ATTTTTTT others(4): Show |
A | 1 | a0001c0006t0029 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1785_*1795delTTTT others(7): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 1785 | INFO_REALIGN_3_PRIME | chr3 | 149028705 | |||||
| chr3:149028884 | C | G | 11 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(8): Show |
120 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*1951C>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 1951 | chr3 | 149028884 | ||||||
| chr3:149028963 | G | A | 1 | a0001c0002t0044 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2030G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 2030 | chr3 | 149028963 | ||||||
| chr3:149029099 | G | A | 1 | a0001c0001t0035 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2166G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 2166 | chr3 | 149029099 | ||||||
| chr3:149029332 | A | G | 11 | a0001c0001t0008 a0001c0002t0001 a0001c0002t0008 others(8): Show |
134 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*2399A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 2399 | chr3 | 149029332 | ||||||
| chr3:149029390 | A | G | 1 | a0001c0001t0024 | 2 | HG01261.hp1 HG02300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2457A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 2457 | chr3 | 149029390 | ||||||
| chr3:149029489 | AC | A | 5 | a0001c0001t0015 a0001c0001t0028 a0001c0001t0030 others(2): Show |
7 | HG00738.hp1 HG02145.hp2 HG02451.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2559delC | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 2559 | INFO_REALIGN_3_PRIME | chr3 | 149029489 | |||||
| chr3:149029530 | T | TGAA | 2 | a0001c0001t0023 a0001c0003t0012 |
6 | HG02109.hp2 HG02280.hp1 HG02572.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2599_*2601dupAAG | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 2602 | INFO_REALIGN_3_PRIME | chr3 | 149029530 | |||||
| chr3:149029572 | T | C | 51 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(48): Show |
313 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
3_prime_UTR_variant | MODIFIER | c.*2639T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 2639 | chr3 | 149029572 | ||||||
| chr3:149029722 | C | T | 3 | a0001c0001t0004 a0001c0003t0004 a0001c0003t0040 |
13 | HG01243.hp2 HG02280.hp2 HG02559.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2789C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 2789 | chr3 | 149029722 | ||||||
| chr3:149029958 | A | G | 1 | a0001c0001t0034 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3025A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 3025 | chr3 | 149029958 | ||||||
| chr3:149030014 | C | G | 1 | a0001c0002t0047 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3081C>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 3081 | chr3 | 149030014 | ||||||
| chr3:149030095 | A | C | 1 | a0001c0002t0001 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3162A>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 3162 | chr3 | 149030095 | ||||||
| chr3:149030107 | T | C | 1 | a0001c0002t0045 | 1 | NA18946.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3174T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 3174 | chr3 | 149030107 | ||||||
| chr3:149030292 | C | CT | 1 | a0001c0003t0012 | 4 | HG02109.hp2 HG02572.hp1 HG02723.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3365dupT | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 3366 | INFO_REALIGN_3_PRIME | chr3 | 149030292 | |||||
| chr3:149030415 | A | AACTT | 2 | a0001c0001t0015 a0001c0001t0036 |
4 | HG00738.hp1 HG02451.hp2 HG02896.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3488_*3491dupCTTA | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 3492 | INFO_REALIGN_3_PRIME | chr3 | 149030415 | |||||
| chr3:149030453 | A | C | 1 | a0001c0006t0029 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3520A>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 3520 | chr3 | 149030453 | ||||||
| chr3:149030475 | T | TGTC | 9 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0017 others(6): Show |
107 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*3543_*3545dupGTC | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 3546 | INFO_REALIGN_3_PRIME | chr3 | 149030475 | |||||
| chr3:149030579 | C | T | 4 | a0001c0001t0013 a0001c0001t0020 a0001c0001t0035 others(1): Show |
8 | HG02055.hp2 HG02922.hp1 HG02965.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3646C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 3646 | chr3 | 149030579 | ||||||
| chr3:149030593 | T | C | 12 | a0001c0001t0008 a0001c0002t0001 a0001c0002t0006 others(9): Show |
141 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*3660T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 3660 | chr3 | 149030593 | ||||||
| chr3:149030681 | G | A | 1 | a0001c0002t0046 | 1 | HG02273.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3748G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 3748 | chr3 | 149030681 | ||||||
| chr3:149030713 | C | G | 1 | a0001c0002t0018 | 3 | HG00323.hp2 HG01081.hp2 HG02602.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3780C>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 3780 | chr3 | 149030713 | ||||||
| chr3:149030729 | T | C | 12 | a0001c0001t0013 a0001c0001t0015 a0001c0001t0020 others(9): Show |
18 | HG00738.hp1 HG02055.hp2 HG02145.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3796T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 3796 | chr3 | 149030729 | ||||||
| chr3:149030894 | A | G | 1 | a0001c0001t0016 | 3 | HG01891.hp2 HG02109.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3961A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 3961 | chr3 | 149030894 | ||||||
| chr3:149031224 | T | G | 1 | a0001c0001t0033 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4291T>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 4291 | chr3 | 149031224 | ||||||
| chr3:149031252 | A | G | 1 | a0001c0001t0033 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4319A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 4319 | chr3 | 149031252 | ||||||
| chr3:149031379 | T | G | 1 | a0002c0004t0048 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4446T>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 4446 | chr3 | 149031379 | ||||||
| chr3:149031418 | TTA | T | 3 | a0002c0004t0048 a0002c0004t0049 a0002c0004t0050 |
3 | HG02258.hp1 HG02615.hp1 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4487_*4488delAT | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 4487 | INFO_REALIGN_3_PRIME | chr3 | 149031418 | |||||
| chr3:149031421 | T | C | 1 | a0001c0003t0040 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4488T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 4488 | chr3 | 149031421 | ||||||
| chr3:149031566 | A | G | 1 | a0001c0001t0043 | 1 | NA18945.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4633A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 8/8 | 4633 | chr3 | 149031566 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:148991743 | C | G | 14 | a0001c0003t0004g0014 a0001c0003t0004g0042 a0001c0003t0004g0331 others(11): Show |
17 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.7+96C>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 1/7 | chr3 | 148991743 | |||||||
| chr3:148991897 | G | A | 1 | a0001c0001t0003g0043 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.7+250G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 1/7 | chr3 | 148991897 | |||||||
| chr3:148991963 | G | A | 14 | a0001c0003t0004g0014 a0001c0003t0004g0042 a0001c0003t0004g0331 others(11): Show |
17 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.7+316G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 1/7 | chr3 | 148991963 | |||||||
| chr3:148991993 | G | T | 1 | a0001c0002t0008g0328 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.7+346G>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 1/7 | chr3 | 148991993 | |||||||
| chr3:148992005 | G | C | 1 | a0001c0006t0029g0044 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.7+358G>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 1/7 | chr3 | 148992005 | |||||||
| chr3:148992077 | C | T | 3 | a0001c0001t0003g0325 a0001c0001t0003g0326 a0001c0001t0003g0327 |
3 | HG00621.hp1 NA18939.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.7+430C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 1/7 | chr3 | 148992077 | |||||||
| chr3:148992284 | G | A | 1 | a0001c0002t0001g0045 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.7+637G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 1/7 | chr3 | 148992284 | |||||||
| chr3:148992336 | A | C | 19 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0041 others(16): Show |
23 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.7+689A>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 1/7 | chr3 | 148992336 | |||||||
| chr3:148992379 | G | T | 4 | a0001c0003t0012g0306 a0001c0003t0012g0307 a0001c0003t0012g0308 others(1): Show |
4 | HG02109.hp2 HG02572.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+732G>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 1/7 | chr3 | 148992379 | |||||||
| chr3:148992556 | C | T | 6 | a0001c0001t0016g0303 a0001c0001t0016g0304 a0001c0001t0016g0305 others(3): Show |
6 | HG01255.hp2 HG01891.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.7+909C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 1/7 | chr3 | 148992556 | |||||||
| chr3:148992574 | T | G | 1 | a0001c0001t0003g0046 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.7+927T>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 1/7 | chr3 | 148992574 | |||||||
| chr3:148992736 | A | G | 1 | a0001c0001t0002g0300 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.7+1089A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 1/7 | chr3 | 148992736 | |||||||
| chr3:148992805 | G | T | 1 | a0001c0001t0010g0299 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.7+1158G>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 1/7 | chr3 | 148992805 | |||||||
| chr3:148992896 | C | G | 1 | a0001c0001t0003g0324 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.8-1246C>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 1/7 | chr3 | 148992896 | |||||||
| chr3:148992930 | A | G | 7 | a0001c0002t0006g0292 a0001c0002t0006g0293 a0001c0002t0006g0294 others(4): Show |
7 | HG02273.hp1 HG02683.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-1212A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 1/7 | chr3 | 148992930 | |||||||
| chr3:148992931 | C | T | 1 | a0001c0002t0001g0291 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.8-1211C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 1/7 | chr3 | 148992931 | |||||||
| chr3:148992986 | C | T | 8 | a0001c0001t0016g0303 a0001c0001t0016g0304 a0001c0001t0016g0305 others(5): Show |
8 | HG01255.hp2 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.8-1156C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 1/7 | chr3 | 148992986 | |||||||
| chr3:148993014 | G | A | 61 | a0001c0002t0001g0002 a0001c0002t0001g0008 a0001c0002t0001g0015 others(58): Show |
72 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.8-1128G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 1/7 | chr3 | 148993014 | |||||||
| chr3:148993101 | A | G | 1 | a0001c0002t0001g0288 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.8-1041A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 1/7 | chr3 | 148993101 | |||||||
| chr3:148993116 | C | A | 19 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0041 others(16): Show |
23 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.8-1026C>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 1/7 | chr3 | 148993116 | |||||||
| chr3:148993128 | A | G | 1 | a0001c0002t0001g0096 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.8-1014A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 1/7 | chr3 | 148993128 | |||||||
| chr3:148993225 | G | A | 4 | a0001c0003t0012g0306 a0001c0003t0012g0307 a0001c0003t0012g0308 others(1): Show |
4 | HG02109.hp2 HG02572.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-917G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 1/7 | chr3 | 148993225 | |||||||
| chr3:148993351 | T | A | 1 | a0001c0001t0003g0097 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.8-791T>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 1/7 | chr3 | 148993351 | |||||||
| chr3:148993352 | T | C | 1 | a0001c0001t0003g0097 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.8-790T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 1/7 | chr3 | 148993352 | |||||||
| chr3:148993397 | A | T | 1 | a0001c0001t0003g0323 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.8-745A>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 1/7 | chr3 | 148993397 | |||||||
| chr3:148993774 | G | A | 2 | a0001c0001t0028g0098 a0001c0001t0037g0099 |
2 | HG02145.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.8-368G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 1/7 | chr3 | 148993774 | |||||||
| chr3:148993852 | A | C | 1 | a0001c0003t0039g0340 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.8-290A>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 1/7 | chr3 | 148993852 | |||||||
| chr3:148994016 | AT | A | 18 | a0001c0003t0004g0014 a0001c0003t0004g0042 a0001c0003t0004g0331 others(15): Show |
21 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.8-124delT | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 148994016 | ||||||
| chr3:148994388 | T | C | 2 | a0001c0001t0023g0100 a0001c0001t0023g0101 |
2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.143+111T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 2/7 | chr3 | 148994388 | |||||||
| chr3:148994468 | A | G | 103 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0010 others(100): Show |
118 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.143+191A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 2/7 | chr3 | 148994468 | |||||||
| chr3:148994478 | G | A | 1 | a0001c0003t0040g0329 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.143+201G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 2/7 | chr3 | 148994478 | |||||||
| chr3:148994524 | GA | G | 289 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0010 others(286): Show |
333 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.143+250delA | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 148994524 | ||||||
| chr3:148994869 | A | G | 104 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0010 others(101): Show |
119 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.143+592A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 2/7 | chr3 | 148994869 | |||||||
| chr3:148994920 | C | T | 1 | a0001c0002t0025g0033 | 2 | HG02451.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.143+643C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 2/7 | chr3 | 148994920 | |||||||
| chr3:148994935 | C | G | 13 | a0001c0001t0016g0303 a0001c0001t0016g0304 a0001c0001t0016g0305 others(10): Show |
13 | HG01255.hp2 HG01891.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.143+658C>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 2/7 | chr3 | 148994935 | |||||||
| chr3:148995001 | C | T | 2 | a0001c0001t0002g0286 a0001c0001t0002g0287 |
2 | NA18948.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.143+724C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 2/7 | chr3 | 148995001 | |||||||
| chr3:148995524 | T | C | 4 | a0001c0001t0014g0146 a0001c0001t0014g0147 a0001c0001t0014g0149 others(1): Show |
4 | HG01167.hp1 HG01346.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.144-778T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 2/7 | chr3 | 148995524 | |||||||
| chr3:148995603 | A | G | 1 | a0001c0001t0002g0285 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.144-699A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 2/7 | chr3 | 148995603 | |||||||
| chr3:148995748 | T | C | 1 | a0001c0001t0008g0021 | 2 | NA18955.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.144-554T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 2/7 | chr3 | 148995748 | |||||||
| chr3:148995752 | C | T | 1 | a0001c0001t0002g0284 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.144-550C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 2/7 | chr3 | 148995752 | |||||||
| chr3:148995760 | G | A | 341 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0010 others(338): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(400): Show |
intron_variant | MODIFIER | c.144-542G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 2/7 | chr3 | 148995760 | |||||||
| chr3:148995789 | C | T | 2 | a0001c0001t0002g0282 a0001c0001t0002g0283 |
2 | HG02523.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.144-513C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 2/7 | chr3 | 148995789 | |||||||
| chr3:148995841 | A | G | 1 | a0001c0001t0003g0137 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.144-461A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 2/7 | chr3 | 148995841 | |||||||
| chr3:148996238 | C | G | 103 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0010 others(100): Show |
118 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.144-64C>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 2/7 | chr3 | 148996238 | |||||||
| chr3:148996273 | G | A | 1 | a0001c0002t0001g0047 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.144-29G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 2/7 | chr3 | 148996273 | |||||||
| chr3:148996691 | G | A | 1 | a0001c0003t0040g0329 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.319-51G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 3/7 | chr3 | 148996691 | |||||||
| chr3:148996723 | C | G | 1 | a0001c0003t0039g0340 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.319-19C>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 3/7 | chr3 | 148996723 | |||||||
| chr3:148996730 | C | T | 2 | a0001c0001t0023g0100 a0001c0001t0023g0101 |
2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.319-12C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 3/7 | chr3 | 148996730 | |||||||
| chr3:148996974 | A | G | 1 | a0001c0001t0024g0281 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.481+70A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 148996974 | |||||||
| chr3:148997053 | A | G | 1 | a0002c0004t0048g0196 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.481+149A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 148997053 | |||||||
| chr3:148997054 | T | TTG | 10 | a0001c0001t0003g0004 a0001c0001t0003g0041 a0001c0001t0003g0105 others(7): Show |
10 | HG00558.hp2 HG01074.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.481+178_481+179dup others(2): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 148997054 | ||||||
| chr3:148997054 | T | TTGTGTG | 8 | a0001c0001t0005g0270 a0001c0001t0016g0303 a0001c0001t0016g0304 others(5): Show |
8 | HG01255.hp2 HG01516.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.481+174_481+179dup others(6): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 148997054 | ||||||
| chr3:148997054 | T | TTGTGTGT others(1): Show |
6 | a0001c0001t0005g0040 a0001c0001t0005g0268 a0001c0001t0005g0269 others(3): Show |
7 | HG02630.hp2 HG02717.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.481+172_481+179dup others(8): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 148997054 | ||||||
| chr3:148997054 | T | TTGTGTGT others(7): Show |
1 | a0001c0001t0016g0305 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.481+166_481+179dup others(14): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 148997054 | ||||||
| chr3:148997054 | TTG | T | 123 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0010 others(120): Show |
141 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.481+178_481+179del others(2): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 148997054 | ||||||
| chr3:148997054 | TTGTG | T | 122 | a0001c0001t0002g0243 a0001c0001t0005g0162 a0001c0001t0013g0150 others(119): Show |
142 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.481+176_481+179del others(4): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 148997054 | ||||||
| chr3:148997054 | TTGTGTGT others(3): Show |
T | 1 | a0001c0001t0008g0021 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.481+170_481+179del others(10): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 148997054 | ||||||
| chr3:148997054 | TTGTGTGT others(7): Show |
T | 1 | a0001c0001t0002g0234 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.481+166_481+179del others(14): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 148997054 | ||||||
| chr3:148997100 | A | G | 20 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0041 others(17): Show |
24 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.481+196A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 148997100 | |||||||
| chr3:148997107 | T | C | 166 | a0001c0001t0005g0162 a0001c0001t0013g0150 a0001c0001t0013g0151 others(163): Show |
191 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.481+203T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 148997107 | |||||||
| chr3:148997228 | T | G | 1 | a0001c0002t0001g0048 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.481+324T>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 148997228 | |||||||
| chr3:148997327 | G | T | 19 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0041 others(16): Show |
23 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.481+423G>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 148997327 | |||||||
| chr3:148997370 | A | AAGAT | 12 | a0001c0001t0016g0303 a0001c0001t0016g0304 a0001c0001t0016g0305 others(9): Show |
12 | HG01255.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.481+469_481+470ins others(4): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 148997370 | ||||||
| chr3:148997461 | T | G | 2 | a0001c0001t0003g0041 a0001c0001t0033g0041 |
2 | HG04228.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.481+557T>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 148997461 | |||||||
| chr3:148997481 | T | G | 6 | a0001c0001t0013g0150 a0001c0001t0013g0151 a0001c0001t0013g0153 others(3): Show |
6 | HG02922.hp1 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.481+577T>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 148997481 | |||||||
| chr3:148997508 | T | C | 2 | a0001c0001t0051g0157 a0001c0001t0052g0156 |
2 | HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.481+604T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 148997508 | |||||||
| chr3:148997551 | T | C | 2 | a0001c0002t0001g0158 a0001c0002t0001g0159 |
2 | NA19063.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.481+647T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 148997551 | |||||||
| chr3:148997649 | G | A | 10 | a0001c0003t0004g0014 a0001c0003t0004g0042 a0001c0003t0004g0331 others(7): Show |
13 | HG01243.hp2 HG02280.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.481+745G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 148997649 | |||||||
| chr3:148997794 | A | G | 14 | a0001c0001t0013g0150 a0001c0001t0013g0151 a0001c0001t0013g0153 others(11): Show |
15 | HG00738.hp1 HG02145.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.481+890A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 148997794 | |||||||
| chr3:148998057 | C | T | 1 | a0001c0001t0014g0149 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.481+1153C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 148998057 | |||||||
| chr3:148998157 | A | G | 4 | a0001c0001t0015g0009 a0001c0001t0015g0198 a0001c0001t0030g0197 others(1): Show |
5 | HG00738.hp1 HG02451.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.481+1253A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 148998157 | |||||||
| chr3:148998299 | A | G | 6 | a0001c0001t0013g0150 a0001c0001t0013g0151 a0001c0001t0013g0153 others(3): Show |
6 | HG02922.hp1 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.481+1395A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 148998299 | |||||||
| chr3:148998459 | A | G | 1 | a0001c0002t0001g0095 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.481+1555A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 148998459 | |||||||
| chr3:148998557 | G | A | 103 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0010 others(100): Show |
118 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.481+1653G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 148998557 | |||||||
| chr3:148998638 | CGTG | C | 6 | a0001c0001t0013g0150 a0001c0001t0013g0151 a0001c0001t0013g0153 others(3): Show |
6 | HG02922.hp1 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.481+1737_481+1739d others(5): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 148998638 | ||||||
| chr3:148998639 | G | T | 1 | a0001c0001t0003g0012 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.481+1735G>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 148998639 | |||||||
| chr3:148998705 | C | G | 1 | a0001c0001t0002g0283 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.481+1801C>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 148998705 | |||||||
| chr3:148998819 | G | A | 1 | a0001c0001t0031g0200 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.481+1915G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 148998819 | |||||||
| chr3:148998848 | G | C | 6 | a0001c0001t0023g0100 a0001c0001t0023g0101 a0001c0003t0012g0306 others(3): Show |
6 | HG02109.hp2 HG02280.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.481+1944G>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 148998848 | |||||||
| chr3:148998912 | C | T | 1 | a0001c0001t0038g0199 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.481+2008C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 148998912 | |||||||
| chr3:148999029 | C | T | 3 | a0001c0002t0001g0094 a0003c0005t0001g0092 a0003c0005t0001g0093 |
3 | HG01070.hp2 HG01071.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.481+2125C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 148999029 | |||||||
| chr3:148999131 | C | T | 12 | a0001c0001t0016g0303 a0001c0001t0016g0304 a0001c0001t0016g0305 others(9): Show |
12 | HG01255.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.481+2227C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 148999131 | |||||||
| chr3:148999221 | C | T | 3 | a0002c0004t0048g0196 a0002c0004t0049g0195 a0002c0004t0050g0194 |
3 | HG02258.hp1 HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.481+2317C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 148999221 | |||||||
| chr3:148999222 | G | A | 1 | a0001c0001t0002g0201 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.481+2318G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 148999222 | |||||||
| chr3:148999377 | A | G | 6 | a0001c0001t0023g0100 a0001c0001t0023g0101 a0001c0003t0012g0306 others(3): Show |
6 | HG02109.hp2 HG02280.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.481+2473A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 148999377 | |||||||
| chr3:148999498 | A | G | 1 | a0001c0001t0038g0199 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.481+2594A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 148999498 | |||||||
| chr3:148999562 | A | G | 2 | a0001c0002t0001g0091 a0001c0002t0025g0033 |
3 | HG02451.hp1 HG03453.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.481+2658A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 148999562 | |||||||
| chr3:148999632 | C | T | 2 | a0001c0001t0051g0157 a0001c0001t0052g0156 |
2 | HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.481+2728C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 148999632 | |||||||
| chr3:148999683 | A | G | 113 | a0001c0001t0005g0162 a0001c0001t0008g0021 a0001c0001t0034g0161 others(110): Show |
135 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.481+2779A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 148999683 | |||||||
| chr3:148999721 | C | T | 6 | a0001c0001t0023g0100 a0001c0001t0023g0101 a0001c0003t0012g0306 others(3): Show |
6 | HG02109.hp2 HG02280.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.481+2817C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 148999721 | |||||||
| chr3:148999960 | C | T | 4 | a0001c0001t0014g0146 a0001c0001t0014g0147 a0001c0001t0014g0149 others(1): Show |
4 | HG01167.hp1 HG01346.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.481+3056C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 148999960 | |||||||
| chr3:149000235 | T | C | 2 | a0001c0002t0001g0026 a0001c0002t0001g0160 |
3 | HG02922.hp2 HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.481+3331T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149000235 | |||||||
| chr3:149000300 | G | T | 48 | a0001c0002t0001g0006 a0001c0002t0001g0026 a0001c0002t0001g0027 others(45): Show |
58 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.481+3396G>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149000300 | |||||||
| chr3:149000522 | C | T | 1 | a0001c0001t0009g0135 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.481+3618C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149000522 | |||||||
| chr3:149000608 | G | A | 118 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0008 others(115): Show |
139 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.481+3704G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149000608 | |||||||
| chr3:149000721 | A | G | 1 | a0001c0001t0002g0280 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.481+3817A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149000721 | |||||||
| chr3:149000925 | T | G | 2 | a0002c0004t0049g0195 a0002c0004t0050g0194 |
2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.481+4021T>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149000925 | |||||||
| chr3:149000948 | G | C | 4 | a0001c0003t0012g0306 a0001c0003t0012g0307 a0001c0003t0012g0308 others(1): Show |
4 | HG02109.hp2 HG02572.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.481+4044G>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149000948 | |||||||
| chr3:149001017 | A | G | 1 | a0001c0001t0003g0134 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.481+4113A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149001017 | |||||||
| chr3:149001118 | G | A | 1 | a0001c0001t0002g0201 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.481+4214G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149001118 | |||||||
| chr3:149001129 | A | G | 7 | a0001c0001t0015g0009 a0001c0001t0015g0198 a0001c0001t0028g0098 others(4): Show |
8 | HG00738.hp1 HG02145.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.481+4225A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149001129 | |||||||
| chr3:149001146 | G | T | 1 | a0001c0001t0002g0279 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.481+4242G>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149001146 | |||||||
| chr3:149001192 | G | A | 9 | a0001c0003t0004g0014 a0001c0003t0004g0042 a0001c0003t0004g0331 others(6): Show |
12 | HG01243.hp2 HG02280.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.481+4288G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149001192 | |||||||
| chr3:149001213 | G | A | 4 | a0001c0003t0012g0306 a0001c0003t0012g0307 a0001c0003t0012g0308 others(1): Show |
4 | HG02109.hp2 HG02572.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.481+4309G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149001213 | |||||||
| chr3:149001246 | T | G | 1 | a0001c0002t0001g0049 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.481+4342T>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149001246 | |||||||
| chr3:149001278 | G | A | 6 | a0001c0001t0023g0100 a0001c0001t0023g0101 a0001c0003t0012g0306 others(3): Show |
6 | HG02109.hp2 HG02280.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.481+4374G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149001278 | |||||||
| chr3:149001365 | G | A | 1 | a0001c0002t0001g0050 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.481+4461G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149001365 | |||||||
| chr3:149001410 | T | G | 1 | a0001c0001t0013g0150 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.481+4506T>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149001410 | |||||||
| chr3:149001638 | G | C | 5 | a0001c0001t0016g0303 a0001c0001t0016g0304 a0001c0001t0016g0305 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.481+4734G>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149001638 | |||||||
| chr3:149001696 | G | C | 118 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0008 others(115): Show |
139 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.481+4792G>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149001696 | |||||||
| chr3:149001918 | C | T | 1 | a0001c0002t0001g0193 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.481+5014C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149001918 | |||||||
| chr3:149002145 | A | G | 3 | a0001c0002t0001g0090 a0001c0002t0001g0192 a0001c0002t0045g0089 |
3 | NA18946.hp2 NA19067.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.481+5241A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149002145 | |||||||
| chr3:149002533 | C | T | 5 | a0001c0001t0016g0303 a0001c0001t0016g0304 a0001c0001t0016g0305 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.481+5629C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149002533 | |||||||
| chr3:149002558 | G | C | 2 | a0001c0001t0003g0102 a0001c0001t0003g0103 |
2 | HG01175.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.481+5654G>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149002558 | |||||||
| chr3:149002678 | T | C | 2 | a0001c0001t0002g0034 a0001c0001t0002g0202 |
3 | HG00597.hp1 NA18953.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.481+5774T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149002678 | |||||||
| chr3:149002698 | T | C | 1 | a0001c0001t0003g0104 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.481+5794T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149002698 | |||||||
| chr3:149002701 | A | G | 4 | a0001c0003t0012g0306 a0001c0003t0012g0307 a0001c0003t0012g0308 others(1): Show |
4 | HG02109.hp2 HG02572.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.481+5797A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149002701 | |||||||
| chr3:149002745 | G | T | 1 | a0001c0001t0003g0322 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.481+5841G>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149002745 | |||||||
| chr3:149002779 | G | A | 2 | a0001c0002t0001g0052 a0001c0002t0008g0051 |
2 | NA18965.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.481+5875G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149002779 | |||||||
| chr3:149002878 | G | A | 121 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0008 others(118): Show |
143 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.481+5974G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149002878 | |||||||
| chr3:149003024 | A | G | 1 | a0001c0001t0015g0198 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.481+6120A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149003024 | |||||||
| chr3:149003058 | G | A | 118 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0008 others(115): Show |
139 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.481+6154G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149003058 | |||||||
| chr3:149003114 | AT | A | 156 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0010 others(153): Show |
177 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.482-6144delT | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 149003114 | ||||||
| chr3:149003114 | ATT | A | 121 | a0001c0001t0002g0203 a0001c0001t0003g0322 a0001c0001t0013g0151 others(118): Show |
142 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.482-6145_482-6144d others(4): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 149003114 | ||||||
| chr3:149003258 | G | C | 1 | a0001c0001t0002g0204 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.482-6018G>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149003258 | |||||||
| chr3:149003470 | G | C | 1 | a0001c0001t0003g0104 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.482-5806G>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149003470 | |||||||
| chr3:149003547 | T | C | 15 | a0001c0001t0014g0146 a0001c0001t0014g0147 a0001c0001t0014g0149 others(12): Show |
15 | HG01167.hp1 HG01255.hp2 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.482-5729T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149003547 | |||||||
| chr3:149003608 | A | T | 1 | a0001c0001t0003g0043 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.482-5668A>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149003608 | |||||||
| chr3:149003679 | G | T | 1 | a0001c0001t0037g0099 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.482-5597G>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149003679 | |||||||
| chr3:149003772 | G | A | 1 | a0001c0001t0003g0138 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.482-5504G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149003772 | |||||||
| chr3:149003779 | T | G | 4 | a0001c0001t0015g0009 a0001c0001t0015g0198 a0001c0001t0030g0197 others(1): Show |
5 | HG00738.hp1 HG02451.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.482-5497T>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149003779 | |||||||
| chr3:149004129 | C | A | 1 | a0001c0002t0001g0053 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.482-5147C>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149004129 | |||||||
| chr3:149004177 | C | T | 1 | a0001c0002t0001g0087 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.482-5099C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149004177 | |||||||
| chr3:149004200 | C | T | 1 | a0001c0001t0005g0276 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.482-5076C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149004200 | |||||||
| chr3:149004315 | A | G | 1 | a0001c0001t0003g0320 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.482-4961A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149004315 | |||||||
| chr3:149004320 | G | A | 1 | a0001c0001t0003g0043 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.482-4956G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149004320 | |||||||
| chr3:149004498 | C | T | 10 | a0001c0003t0004g0014 a0001c0003t0004g0042 a0001c0003t0004g0331 others(7): Show |
13 | HG01243.hp2 HG02280.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.482-4778C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149004498 | |||||||
| chr3:149004507 | AT | A | 6 | a0001c0001t0023g0100 a0001c0001t0023g0101 a0001c0003t0012g0306 others(3): Show |
6 | HG02109.hp2 HG02280.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.482-4766delT | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 149004507 | ||||||
| chr3:149004569 | C | T | 5 | a0001c0001t0016g0303 a0001c0001t0016g0304 a0001c0001t0016g0305 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.482-4707C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149004569 | |||||||
| chr3:149004734 | G | A | 2 | a0001c0001t0051g0157 a0001c0001t0052g0156 |
2 | HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.482-4542G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149004734 | |||||||
| chr3:149004738 | T | G | 1 | a0001c0001t0011g0205 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.482-4538T>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149004738 | |||||||
| chr3:149004858 | G | C | 13 | a0001c0001t0002g0010 a0001c0001t0002g0035 a0001c0001t0002g0206 others(10): Show |
16 | HG00621.hp2 HG00639.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.482-4418G>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149004858 | |||||||
| chr3:149004974 | C | A | 1 | a0001c0001t0038g0199 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.482-4302C>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149004974 | |||||||
| chr3:149004985 | C | T | 3 | a0002c0004t0048g0196 a0002c0004t0049g0195 a0002c0004t0050g0194 |
3 | HG02258.hp1 HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.482-4291C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149004985 | |||||||
| chr3:149005039 | T | C | 5 | a0001c0001t0016g0303 a0001c0001t0016g0304 a0001c0001t0016g0305 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.482-4237T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149005039 | |||||||
| chr3:149005089 | C | T | 1 | a0001c0001t0003g0133 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.482-4187C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149005089 | |||||||
| chr3:149005194 | G | C | 1 | a0001c0003t0041g0337 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.482-4082G>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149005194 | |||||||
| chr3:149005236 | A | C | 119 | a0001c0001t0008g0021 a0001c0002t0001g0002 a0001c0002t0001g0006 others(116): Show |
141 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.482-4040A>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149005236 | |||||||
| chr3:149005355 | G | A | 4 | a0001c0003t0012g0306 a0001c0003t0012g0307 a0001c0003t0012g0308 others(1): Show |
4 | HG02109.hp2 HG02572.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.482-3921G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149005355 | |||||||
| chr3:149005442 | G | A | 1 | a0001c0002t0001g0054 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.482-3834G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149005442 | |||||||
| chr3:149005465 | A | T | 270 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0010 others(267): Show |
311 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.482-3811A>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149005465 | |||||||
| chr3:149005466 | G | A | 12 | a0001c0003t0004g0014 a0001c0003t0004g0042 a0001c0003t0004g0331 others(9): Show |
15 | HG01243.hp2 HG02280.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.482-3810G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149005466 | |||||||
| chr3:149005483 | T | A | 106 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0010 others(103): Show |
121 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.482-3793T>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149005483 | |||||||
| chr3:149005528 | A | G | 4 | a0001c0001t0014g0146 a0001c0001t0014g0147 a0001c0001t0014g0149 others(1): Show |
4 | HG01167.hp1 HG01346.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.482-3748A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149005528 | |||||||
| chr3:149005574 | C | T | 1 | a0001c0001t0002g0287 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.482-3702C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149005574 | |||||||
| chr3:149005623 | T | C | 4 | a0001c0001t0014g0146 a0001c0001t0014g0147 a0001c0001t0014g0149 others(1): Show |
4 | HG01167.hp1 HG01346.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.482-3653T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149005623 | |||||||
| chr3:149005709 | A | G | 1 | a0001c0001t0003g0322 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.482-3567A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149005709 | |||||||
| chr3:149005856 | A | T | 1 | a0001c0001t0002g0287 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.482-3420A>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149005856 | |||||||
| chr3:149005903 | A | G | 1 | a0001c0001t0002g0275 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.482-3373A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149005903 | |||||||
| chr3:149005978 | A | G | 1 | a0001c0001t0005g0274 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.482-3298A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149005978 | |||||||
| chr3:149005982 | T | C | 3 | a0002c0004t0048g0196 a0002c0004t0049g0195 a0002c0004t0050g0194 |
3 | HG02258.hp1 HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.482-3294T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149005982 | |||||||
| chr3:149006080 | C | CT | 133 | a0001c0001t0002g0273 a0001c0001t0003g0131 a0001c0001t0003g0132 others(130): Show |
153 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.482-3176dupT | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 149006080 | ||||||
| chr3:149006080 | C | CTT | 10 | a0001c0001t0015g0009 a0001c0001t0015g0198 a0001c0001t0030g0197 others(7): Show |
12 | HG00597.hp2 HG00738.hp1 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.482-3177_482-3176d others(4): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 149006080 | ||||||
| chr3:149006080 | CT | C | 14 | a0001c0001t0002g0215 a0001c0001t0003g0107 a0001c0001t0003g0108 others(11): Show |
17 | HG02280.hp2 HG02559.hp1 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.482-3176delT | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 149006080 | ||||||
| chr3:149006137 | C | T | 4 | a0001c0001t0015g0009 a0001c0001t0015g0198 a0001c0001t0030g0197 others(1): Show |
5 | HG00738.hp1 HG02451.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.482-3139C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149006137 | |||||||
| chr3:149006214 | C | G | 118 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0008 others(115): Show |
139 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.482-3062C>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149006214 | |||||||
| chr3:149006228 | G | A | 1 | a0002c0004t0048g0196 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.482-3048G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149006228 | |||||||
| chr3:149006230 | G | A | 6 | a0001c0001t0013g0150 a0001c0001t0013g0151 a0001c0001t0013g0153 others(3): Show |
6 | HG02922.hp1 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.482-3046G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149006230 | |||||||
| chr3:149006506 | A | G | 2 | a0001c0002t0001g0090 a0001c0002t0045g0089 |
2 | NA18946.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.482-2770A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149006506 | |||||||
| chr3:149006639 | T | C | 1 | a0001c0001t0023g0100 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.482-2637T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149006639 | |||||||
| chr3:149006751 | T | C | 1 | a0001c0001t0009g0310 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.482-2525T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149006751 | |||||||
| chr3:149006824 | G | A | 1 | a0001c0001t0008g0021 | 2 | NA18955.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.482-2452G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149006824 | |||||||
| chr3:149006943 | A | C | 1 | a0001c0001t0002g0272 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.482-2333A>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149006943 | |||||||
| chr3:149006962 | C | T | 2 | a0001c0002t0001g0083 a0001c0002t0001g0084 |
2 | NA18957.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.482-2314C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149006962 | |||||||
| chr3:149006989 | A | G | 1 | a0001c0002t0001g0082 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.482-2287A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149006989 | |||||||
| chr3:149007101 | G | A | 12 | a0001c0003t0004g0014 a0001c0003t0004g0042 a0001c0003t0004g0331 others(9): Show |
15 | HG01243.hp2 HG02280.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.482-2175G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149007101 | |||||||
| chr3:149007224 | C | A | 1 | a0001c0001t0002g0206 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.482-2052C>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149007224 | |||||||
| chr3:149007279 | G | A | 12 | a0001c0003t0004g0014 a0001c0003t0004g0042 a0001c0003t0004g0331 others(9): Show |
15 | HG01243.hp2 HG02280.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.482-1997G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149007279 | |||||||
| chr3:149007414 | C | T | 2 | a0001c0001t0003g0320 a0001c0001t0009g0319 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.482-1862C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149007414 | |||||||
| chr3:149007419 | T | C | 5 | a0001c0001t0016g0303 a0001c0001t0016g0304 a0001c0001t0016g0305 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.482-1857T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149007419 | |||||||
| chr3:149007460 | G | A | 3 | a0001c0003t0004g0014 a0001c0003t0004g0333 a0001c0003t0004g0336 |
5 | HG01243.hp2 HG02559.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.482-1816G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149007460 | |||||||
| chr3:149007511 | G | A | 1 | a0001c0001t0003g0102 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.482-1765G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149007511 | |||||||
| chr3:149007673 | T | C | 1 | a0001c0002t0001g0055 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.482-1603T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149007673 | |||||||
| chr3:149007833 | C | T | 5 | a0001c0001t0016g0303 a0001c0001t0016g0304 a0001c0001t0016g0305 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.482-1443C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149007833 | |||||||
| chr3:149007837 | G | A | 3 | a0001c0002t0001g0015 a0001c0002t0001g0056 a0001c0002t0001g0088 |
4 | HG00408.hp2 HG02083.hp2 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.482-1439G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149007837 | |||||||
| chr3:149007853 | C | G | 1 | a0001c0002t0001g0159 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.482-1423C>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149007853 | |||||||
| chr3:149007867 | C | G | 5 | a0001c0001t0016g0303 a0001c0001t0016g0304 a0001c0001t0016g0305 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.482-1409C>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149007867 | |||||||
| chr3:149007900 | GTC | G | 12 | a0001c0003t0004g0014 a0001c0003t0004g0042 a0001c0003t0004g0331 others(9): Show |
15 | HG01243.hp2 HG02280.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.482-1374_482-1373d others(4): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 149007900 | ||||||
| chr3:149008058 | C | T | 6 | a0001c0001t0015g0009 a0001c0001t0015g0198 a0001c0001t0028g0098 others(3): Show |
7 | HG00738.hp1 HG02145.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.482-1218C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149008058 | |||||||
| chr3:149008092 | C | T | 4 | a0001c0001t0016g0303 a0001c0001t0016g0304 a0001c0001t0016g0305 others(1): Show |
4 | HG01255.hp2 HG01891.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.482-1184C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149008092 | |||||||
| chr3:149008156 | G | A | 8 | a0001c0003t0004g0014 a0001c0003t0004g0042 a0001c0003t0004g0331 others(5): Show |
11 | HG01243.hp2 HG02559.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.482-1120G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149008156 | |||||||
| chr3:149008229 | T | C | 3 | a0002c0004t0048g0196 a0002c0004t0049g0195 a0002c0004t0050g0194 |
3 | HG02258.hp1 HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.482-1047T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149008229 | |||||||
| chr3:149008283 | A | G | 1 | a0001c0002t0001g0094 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.482-993A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149008283 | |||||||
| chr3:149008314 | C | T | 8 | a0001c0001t0005g0040 a0001c0001t0005g0162 a0001c0001t0005g0268 others(5): Show |
9 | HG01516.hp2 HG02630.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.482-962C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149008314 | |||||||
| chr3:149008315 | C | T | 1 | a0001c0002t0001g0159 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.482-961C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149008315 | |||||||
| chr3:149008341 | G | T | 1 | a0001c0001t0003g0130 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.482-935G>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149008341 | |||||||
| chr3:149008434 | G | T | 291 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0010 others(288): Show |
335 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.482-842G>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149008434 | |||||||
| chr3:149008435 | G | A | 291 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0010 others(288): Show |
335 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.482-841G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149008435 | |||||||
| chr3:149008488 | A | G | 3 | a0002c0004t0048g0196 a0002c0004t0049g0195 a0002c0004t0050g0194 |
3 | HG02258.hp1 HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.482-788A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149008488 | |||||||
| chr3:149008536 | A | G | 9 | a0001c0003t0004g0014 a0001c0003t0004g0042 a0001c0003t0004g0331 others(6): Show |
12 | HG01243.hp2 HG02280.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.482-740A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149008536 | |||||||
| chr3:149008837 | T | C | 3 | a0001c0001t0011g0036 a0001c0001t0011g0216 a0001c0001t0011g0217 |
4 | HG03195.hp2 HG06807.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.482-439T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149008837 | |||||||
| chr3:149008838 | T | C | 4 | a0001c0001t0015g0009 a0001c0001t0015g0198 a0001c0001t0030g0197 others(1): Show |
5 | HG00738.hp1 HG02451.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.482-438T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149008838 | |||||||
| chr3:149008884 | G | A | 106 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0010 others(103): Show |
121 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.482-392G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149008884 | |||||||
| chr3:149008896 | G | A | 4 | a0001c0001t0016g0303 a0001c0001t0016g0304 a0001c0001t0016g0305 others(1): Show |
4 | HG01255.hp2 HG01891.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.482-380G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149008896 | |||||||
| chr3:149009060 | TAGAC | T | 111 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0008 others(108): Show |
132 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.482-213_482-210del others(4): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 149009060 | ||||||
| chr3:149009146 | G | A | 118 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0008 others(115): Show |
139 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.482-130G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149009146 | |||||||
| chr3:149009153 | C | T | 4 | a0001c0002t0001g0026 a0001c0002t0001g0160 a0001c0002t0001g0193 others(1): Show |
5 | HG02630.hp1 HG02818.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.482-123C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149009153 | |||||||
| chr3:149009158 | C | CA | 106 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0010 others(103): Show |
121 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.482-102dupA | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 149009158 | ||||||
| chr3:149009158 | C | CAA | 8 | a0001c0001t0002g0207 a0001c0001t0002g0218 a0001c0001t0002g0219 others(5): Show |
8 | HG01169.hp1 HG03225.hp2 HG03942.hp1 others(5): Show |
intron_variant | MODIFIER | c.482-103_482-102dup others(2): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 149009158 | ||||||
| chr3:149009158 | CA | C | 28 | a0001c0001t0003g0106 a0001c0001t0003g0126 a0001c0001t0003g0127 others(25): Show |
30 | HG01243.hp2 HG02109.hp2 HG02280.hp1 others(27): Show |
intron_variant | MODIFIER | c.482-102delA | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 149009158 | ||||||
| chr3:149009180 | T | G | 12 | a0001c0003t0004g0014 a0001c0003t0004g0042 a0001c0003t0004g0331 others(9): Show |
15 | HG01243.hp2 HG02280.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.482-96T>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 4/7 | chr3 | 149009180 | |||||||
| chr3:149009416 | G | C | 2 | a0001c0001t0028g0098 a0001c0001t0037g0099 |
2 | HG02145.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.608+14G>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149009416 | |||||||
| chr3:149009456 | G | A | 1 | a0001c0001t0003g0312 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.608+54G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149009456 | |||||||
| chr3:149009510 | A | G | 1 | a0001c0003t0040g0329 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.608+108A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149009510 | |||||||
| chr3:149009595 | G | A | 1 | a0001c0001t0038g0199 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.608+193G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149009595 | |||||||
| chr3:149009621 | G | T | 1 | a0001c0001t0038g0199 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.608+219G>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149009621 | |||||||
| chr3:149009649 | C | T | 6 | a0001c0001t0015g0009 a0001c0001t0015g0198 a0001c0001t0028g0098 others(3): Show |
7 | HG00738.hp1 HG02145.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.608+247C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149009649 | |||||||
| chr3:149009658 | A | G | 7 | a0001c0002t0006g0292 a0001c0002t0006g0293 a0001c0002t0006g0294 others(4): Show |
7 | HG02273.hp1 HG02683.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.608+256A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149009658 | |||||||
| chr3:149009689 | A | G | 1 | a0001c0001t0003g0128 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.608+287A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149009689 | |||||||
| chr3:149009690 | C | T | 1 | a0001c0001t0008g0021 | 2 | NA18955.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.608+288C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149009690 | |||||||
| chr3:149009691 | T | G | 4 | a0001c0001t0014g0146 a0001c0001t0014g0147 a0001c0001t0014g0149 others(1): Show |
4 | HG01167.hp1 HG01346.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.608+289T>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149009691 | |||||||
| chr3:149009823 | G | C | 5 | a0001c0001t0016g0303 a0001c0001t0016g0304 a0001c0001t0016g0305 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.608+421G>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149009823 | |||||||
| chr3:149009851 | G | T | 13 | a0001c0001t0002g0010 a0001c0001t0002g0035 a0001c0001t0002g0206 others(10): Show |
16 | HG00621.hp2 HG00639.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.608+449G>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149009851 | |||||||
| chr3:149010106 | A | G | 10 | a0001c0002t0001g0030 a0001c0002t0001g0031 a0001c0002t0001g0032 others(7): Show |
13 | HG02257.hp2 HG02486.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.608+704A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149010106 | |||||||
| chr3:149010194 | C | A | 7 | a0001c0001t0005g0040 a0001c0001t0005g0162 a0001c0001t0005g0268 others(4): Show |
8 | HG01516.hp2 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.608+792C>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149010194 | |||||||
| chr3:149010241 | A | G | 2 | a0001c0001t0051g0157 a0001c0001t0052g0156 |
2 | HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.608+839A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149010241 | |||||||
| chr3:149010326 | T | TC | 12 | a0001c0003t0004g0014 a0001c0003t0004g0042 a0001c0003t0004g0331 others(9): Show |
15 | HG01243.hp2 HG02280.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.608+925dupC | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149010326 | ||||||
| chr3:149010327 | C | CT | 31 | a0001c0001t0002g0007 a0001c0001t0002g0258 a0001c0001t0002g0259 others(28): Show |
33 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.608+943dupT | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149010327 | ||||||
| chr3:149010327 | CT | C | 6 | a0001c0001t0002g0222 a0001c0001t0011g0036 a0001c0001t0011g0216 others(3): Show |
7 | HG01167.hp2 HG01169.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.608+943delT | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149010327 | ||||||
| chr3:149010327 | CTTTTT | C | 6 | a0001c0001t0015g0009 a0001c0001t0015g0198 a0001c0001t0030g0197 others(3): Show |
7 | HG00738.hp1 HG02451.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.608+939_608+943del others(5): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149010327 | ||||||
| chr3:149010353 | A | C | 1 | a0001c0002t0001g0080 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.608+951A>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149010353 | |||||||
| chr3:149010418 | C | T | 1 | a0001c0002t0008g0328 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.608+1016C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149010418 | |||||||
| chr3:149010436 | C | T | 5 | a0001c0001t0016g0303 a0001c0001t0016g0304 a0001c0001t0016g0305 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.608+1034C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149010436 | |||||||
| chr3:149010487 | C | T | 3 | a0002c0004t0048g0196 a0002c0004t0049g0195 a0002c0004t0050g0194 |
3 | HG02258.hp1 HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.608+1085C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149010487 | |||||||
| chr3:149010509 | T | C | 19 | a0001c0001t0013g0150 a0001c0001t0013g0151 a0001c0001t0013g0153 others(16): Show |
20 | HG00738.hp1 HG02055.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.608+1107T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149010509 | |||||||
| chr3:149010720 | A | G | 1 | a0001c0001t0003g0123 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.608+1318A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149010720 | |||||||
| chr3:149010849 | A | G | 1 | a0001c0001t0003g0130 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.608+1447A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149010849 | |||||||
| chr3:149010932 | C | T | 1 | a0001c0001t0011g0217 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.608+1530C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149010932 | |||||||
| chr3:149011055 | T | G | 103 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0010 others(100): Show |
118 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.608+1653T>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149011055 | |||||||
| chr3:149011307 | T | A | 5 | a0001c0001t0016g0303 a0001c0001t0016g0304 a0001c0001t0016g0305 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.608+1905T>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149011307 | |||||||
| chr3:149011367 | C | T | 1 | a0001c0001t0031g0200 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.608+1965C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149011367 | |||||||
| chr3:149011444 | T | G | 1 | a0001c0001t0038g0199 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.608+2042T>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149011444 | |||||||
| chr3:149011467 | CA | C | 4 | a0001c0001t0014g0146 a0001c0001t0014g0147 a0001c0001t0014g0149 others(1): Show |
4 | HG01167.hp1 HG01346.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.608+2066delA | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149011467 | |||||||
| chr3:149011528 | T | C | 1 | a0001c0002t0001g0047 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.608+2126T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149011528 | |||||||
| chr3:149011587 | C | G | 3 | a0001c0002t0001g0008 a0001c0002t0001g0078 a0001c0002t0001g0079 |
5 | HG00140.hp2 HG00280.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.608+2185C>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149011587 | |||||||
| chr3:149011719 | G | T | 1 | a0001c0001t0002g0267 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.608+2317G>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149011719 | |||||||
| chr3:149011854 | G | A | 6 | a0001c0001t0023g0100 a0001c0001t0023g0101 a0001c0003t0012g0306 others(3): Show |
6 | HG02109.hp2 HG02280.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.608+2452G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149011854 | |||||||
| chr3:149011895 | A | T | 6 | a0001c0001t0023g0100 a0001c0001t0023g0101 a0001c0003t0012g0306 others(3): Show |
6 | HG02109.hp2 HG02280.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.608+2493A>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149011895 | |||||||
| chr3:149012035 | C | T | 1 | a0001c0002t0001g0082 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.608+2633C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149012035 | |||||||
| chr3:149012085 | TTTCCTTA others(225): Show |
T | 1 | a0001c0002t0001g0060 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.608+2685_608+2916d others(2): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149012085 | ||||||
| chr3:149012312 | A | G | 5 | a0001c0001t0011g0036 a0001c0001t0011g0216 a0001c0001t0011g0217 others(2): Show |
6 | HG01167.hp2 HG01169.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.608+2910A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149012312 | |||||||
| chr3:149012693 | TA | T | 12 | a0001c0003t0004g0014 a0001c0003t0004g0042 a0001c0003t0004g0331 others(9): Show |
15 | HG01243.hp2 HG02280.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.608+3298delA | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149012693 | ||||||
| chr3:149012711 | A | AT | 7 | a0001c0002t0001g0018 a0001c0002t0001g0019 a0001c0002t0001g0074 others(4): Show |
8 | HG01109.hp2 HG01257.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.608+3319dupT | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149012711 | ||||||
| chr3:149012749 | A | G | 3 | a0001c0001t0011g0036 a0001c0001t0011g0216 a0001c0001t0011g0217 |
4 | HG03195.hp2 HG06807.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.608+3347A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149012749 | |||||||
| chr3:149012809 | C | T | 2 | a0001c0002t0018g0029 a0001c0002t0018g0164 |
3 | HG00323.hp2 HG01081.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.608+3407C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149012809 | |||||||
| chr3:149012847 | C | T | 12 | a0001c0003t0004g0014 a0001c0003t0004g0042 a0001c0003t0004g0331 others(9): Show |
15 | HG01243.hp2 HG02280.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.608+3445C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149012847 | |||||||
| chr3:149012997 | T | TGTGTGTG others(4): Show |
1 | a0001c0002t0001g0054 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.608+3595_608+3596i others(13): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149012997 | |||||||
| chr3:149012997 | T | TTG | 13 | a0001c0001t0002g0203 a0001c0001t0002g0208 a0001c0001t0002g0224 others(10): Show |
14 | HG01109.hp1 HG01169.hp2 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.608+3629_608+3630d others(4): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149012997 | ||||||
| chr3:149012997 | T | TTGTG | 13 | a0001c0001t0002g0215 a0001c0001t0002g0222 a0001c0001t0003g0013 others(10): Show |
15 | HG01069.hp1 HG01071.hp1 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.608+3627_608+3630d others(6): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149012997 | ||||||
| chr3:149012997 | T | TTGTGTG | 18 | a0001c0001t0003g0012 a0001c0001t0003g0314 a0001c0001t0003g0318 others(15): Show |
22 | HG01123.hp2 HG01243.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.608+3625_608+3630d others(8): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149012997 | ||||||
| chr3:149012997 | T | TTGTGTGT others(1): Show |
63 | a0001c0001t0002g0223 a0001c0001t0003g0313 a0001c0001t0003g0324 others(60): Show |
77 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.608+3623_608+3630d others(10): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149012997 | ||||||
| chr3:149012997 | T | TTGTGTGT others(3): Show |
32 | a0001c0002t0001g0006 a0001c0002t0001g0026 a0001c0002t0001g0027 others(29): Show |
36 | HG00140.hp2 HG00558.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.608+3621_608+3630d others(12): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149012997 | ||||||
| chr3:149012997 | T | TTGTGTGT others(5): Show |
17 | a0001c0001t0013g0151 a0001c0001t0013g0153 a0001c0001t0020g0154 others(14): Show |
17 | HG00408.hp1 HG01243.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.608+3619_608+3630d others(14): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149012997 | ||||||
| chr3:149012997 | T | TTGTGTGT others(7): Show |
15 | a0001c0001t0013g0150 a0001c0001t0016g0304 a0001c0001t0016g0305 others(12): Show |
17 | HG01358.hp1 HG01891.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.608+3617_608+3630d others(16): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149012997 | ||||||
| chr3:149012997 | T | TTGTGTGT others(9): Show |
7 | a0001c0003t0004g0042 a0001c0003t0004g0332 a0001c0003t0004g0333 others(4): Show |
8 | HG02280.hp2 HG02647.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.608+3615_608+3630d others(18): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149012997 | ||||||
| chr3:149012997 | T | TTGTGTGT others(11): Show |
7 | a0001c0001t0014g0147 a0001c0001t0014g0149 a0001c0001t0016g0303 others(4): Show |
7 | HG01346.hp1 HG02109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.608+3613_608+3630d others(20): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149012997 | ||||||
| chr3:149012997 | T | TTGTGTGT others(15): Show |
2 | a0001c0001t0014g0146 a0001c0001t0022g0302 |
2 | HG01167.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.608+3609_608+3630d others(24): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149012997 | ||||||
| chr3:149012997 | TTG | T | 47 | a0001c0001t0003g0001 a0001c0001t0003g0003 a0001c0001t0003g0004 others(44): Show |
64 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.608+3629_608+3630d others(4): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149012997 | ||||||
| chr3:149012997 | TTGTG | T | 5 | a0001c0001t0003g0122 a0001c0001t0015g0009 a0001c0001t0015g0198 others(2): Show |
6 | HG00738.hp1 HG02083.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.608+3627_608+3630d others(6): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149012997 | ||||||
| chr3:149012997 | TTGTGTGT others(3): Show |
T | 1 | a0001c0003t0012g0309 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.608+3621_608+3630d others(12): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149012997 | ||||||
| chr3:149012997 | TTGTGTGT others(5): Show |
T | 1 | a0001c0001t0003g0325 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.608+3619_608+3630d others(14): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149012997 | ||||||
| chr3:149012997 | TTGTGTGT others(7): Show |
T | 1 | a0001c0002t0026g0017 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.608+3617_608+3630d others(16): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149012997 | ||||||
| chr3:149013154 | A | G | 1 | a0001c0001t0002g0272 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.608+3752A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149013154 | |||||||
| chr3:149013264 | T | C | 12 | a0001c0003t0004g0014 a0001c0003t0004g0042 a0001c0003t0004g0331 others(9): Show |
15 | HG01243.hp2 HG02280.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.608+3862T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149013264 | |||||||
| chr3:149013268 | GGTTTT | G | 12 | a0001c0003t0004g0014 a0001c0003t0004g0042 a0001c0003t0004g0331 others(9): Show |
15 | HG01243.hp2 HG02280.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.608+3871_608+3875d others(7): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149013268 | ||||||
| chr3:149013702 | G | A | 5 | a0001c0001t0016g0303 a0001c0001t0016g0304 a0001c0001t0016g0305 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.608+4300G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149013702 | |||||||
| chr3:149013898 | C | G | 5 | a0001c0002t0001g0018 a0001c0002t0001g0019 a0001c0002t0001g0076 others(2): Show |
6 | HG01109.hp2 HG01257.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.608+4496C>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149013898 | |||||||
| chr3:149014088 | A | C | 1 | a0001c0001t0002g0257 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.608+4686A>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149014088 | |||||||
| chr3:149014482 | GAAGAAGA others(44): Show |
G | 4 | a0001c0001t0003g0114 a0001c0001t0003g0137 a0001c0001t0009g0113 others(1): Show |
4 | HG00323.hp1 HG01255.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.608+5167_608+5217d others(53): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149014482 | ||||||
| chr3:149014513 | G | A | 2 | a0001c0001t0002g0201 a0001c0001t0002g0241 |
2 | HG01081.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.608+5111G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149014513 | |||||||
| chr3:149014635 | C | T | 1 | a0001c0001t0003g0123 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.608+5233C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149014635 | |||||||
| chr3:149014683 | T | TA | 9 | a0001c0001t0002g0202 a0001c0002t0001g0136 a0001c0002t0006g0292 others(6): Show |
9 | HG02273.hp1 HG02683.hp1 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.608+5292dupA | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149014683 | ||||||
| chr3:149014683 | TA | T | 7 | a0001c0001t0015g0009 a0001c0001t0015g0198 a0001c0001t0020g0152 others(4): Show |
8 | HG00738.hp1 HG02280.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.608+5292delA | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149014683 | ||||||
| chr3:149014701 | T | C | 1 | a0001c0001t0014g0147 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.608+5299T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149014701 | |||||||
| chr3:149014794 | G | C | 1 | a0001c0001t0002g0287 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.608+5392G>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149014794 | |||||||
| chr3:149014867 | C | CA | 21 | a0001c0001t0002g0223 a0001c0001t0003g0109 a0001c0001t0003g0115 others(18): Show |
21 | HG01346.hp2 HG01978.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.608+5482dupA | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149014867 | ||||||
| chr3:149014867 | CA | C | 131 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0010 others(128): Show |
150 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.608+5482delA | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149014867 | ||||||
| chr3:149014867 | CAA | C | 37 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0041 others(34): Show |
42 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.608+5481_608+5482d others(4): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149014867 | ||||||
| chr3:149014923 | A | G | 2 | a0001c0001t0023g0100 a0001c0001t0023g0101 |
2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.608+5521A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149014923 | |||||||
| chr3:149014953 | T | C | 16 | a0001c0001t0014g0146 a0001c0001t0014g0147 a0001c0001t0014g0149 others(13): Show |
19 | HG01167.hp1 HG01243.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.608+5551T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149014953 | |||||||
| chr3:149015016 | A | G | 1 | a0001c0003t0004g0336 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.608+5614A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149015016 | |||||||
| chr3:149015036 | T | G | 120 | a0001c0001t0002g0223 a0001c0001t0008g0021 a0001c0002t0001g0002 others(117): Show |
142 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.608+5634T>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149015036 | |||||||
| chr3:149015063 | G | C | 2 | a0001c0003t0007g0338 a0001c0003t0042g0339 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.608+5661G>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149015063 | |||||||
| chr3:149015107 | T | A | 3 | a0002c0004t0048g0196 a0002c0004t0049g0195 a0002c0004t0050g0194 |
3 | HG02258.hp1 HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.608+5705T>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149015107 | |||||||
| chr3:149015192 | C | T | 6 | a0001c0001t0023g0100 a0001c0001t0023g0101 a0001c0003t0012g0306 others(3): Show |
6 | HG02109.hp2 HG02280.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.608+5790C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149015192 | |||||||
| chr3:149015286 | G | A | 2 | a0001c0002t0006g0297 a0001c0002t0006g0298 |
2 | HG02698.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.608+5884G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149015286 | |||||||
| chr3:149015296 | G | A | 1 | a0001c0002t0001g0190 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.608+5894G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149015296 | |||||||
| chr3:149015579 | A | T | 2 | a0001c0001t0023g0100 a0001c0001t0023g0101 |
2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.608+6177A>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149015579 | |||||||
| chr3:149015659 | G | C | 12 | a0001c0003t0004g0014 a0001c0003t0004g0042 a0001c0003t0004g0331 others(9): Show |
15 | HG01243.hp2 HG02280.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.608+6257G>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149015659 | |||||||
| chr3:149015841 | G | A | 6 | a0001c0001t0013g0150 a0001c0001t0013g0151 a0001c0001t0013g0153 others(3): Show |
6 | HG02922.hp1 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.608+6439G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149015841 | |||||||
| chr3:149015927 | G | A | 1 | a0001c0001t0003g0116 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.608+6525G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149015927 | |||||||
| chr3:149016015 | C | T | 1 | a0001c0001t0003g0316 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.608+6613C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149016015 | |||||||
| chr3:149016065 | G | A | 10 | a0001c0003t0004g0014 a0001c0003t0004g0042 a0001c0003t0004g0331 others(7): Show |
13 | HG01243.hp2 HG02280.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.608+6663G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149016065 | |||||||
| chr3:149016104 | C | A | 1 | a0001c0001t0013g0150 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.608+6702C>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149016104 | |||||||
| chr3:149016140 | T | A | 1 | a0001c0001t0002g0229 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.608+6738T>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149016140 | |||||||
| chr3:149016166 | C | G | 2 | a0001c0001t0051g0157 a0001c0001t0052g0156 |
2 | HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.608+6764C>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149016166 | |||||||
| chr3:149016260 | C | CA | 33 | a0001c0001t0002g0229 a0001c0001t0002g0231 a0001c0001t0002g0232 others(30): Show |
34 | HG00438.hp2 HG01167.hp1 HG01358.hp1 others(31): Show |
intron_variant | MODIFIER | c.608+6874dupA | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149016260 | ||||||
| chr3:149016260 | C | CAA | 94 | a0001c0001t0002g0223 a0001c0001t0008g0021 a0001c0001t0014g0147 others(91): Show |
115 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.608+6873_608+6874d others(4): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149016260 | ||||||
| chr3:149016260 | C | CAAA | 20 | a0001c0002t0001g0018 a0001c0002t0001g0019 a0001c0002t0001g0053 others(17): Show |
21 | HG00733.hp1 HG01109.hp2 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.608+6872_608+6874d others(5): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149016260 | ||||||
| chr3:149016277 | C | A | 15 | a0001c0001t0002g0230 a0001c0001t0013g0150 a0001c0001t0013g0151 others(12): Show |
15 | HG01928.hp1 HG02273.hp1 HG02683.hp1 others(12): Show |
intron_variant | MODIFIER | c.608+6875C>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149016277 | |||||||
| chr3:149016288 | A | G | 13 | a0001c0001t0002g0203 a0001c0001t0002g0219 a0001c0001t0002g0220 others(10): Show |
13 | HG02040.hp1 NA18946.hp1 NA18947.hp1 others(10): Show |
intron_variant | MODIFIER | c.608+6886A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149016288 | |||||||
| chr3:149016313 | T | A | 5 | a0001c0001t0016g0303 a0001c0001t0016g0304 a0001c0001t0016g0305 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.608+6911T>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149016313 | |||||||
| chr3:149016368 | T | C | 13 | a0001c0001t0002g0203 a0001c0001t0002g0219 a0001c0001t0002g0220 others(10): Show |
13 | HG02040.hp1 NA18946.hp1 NA18947.hp1 others(10): Show |
intron_variant | MODIFIER | c.608+6966T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149016368 | |||||||
| chr3:149016474 | T | G | 12 | a0001c0003t0004g0014 a0001c0003t0004g0042 a0001c0003t0004g0331 others(9): Show |
15 | HG01243.hp2 HG02280.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.608+7072T>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149016474 | |||||||
| chr3:149016513 | T | G | 4 | a0001c0001t0014g0146 a0001c0001t0014g0147 a0001c0001t0014g0149 others(1): Show |
4 | HG01167.hp1 HG01346.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.608+7111T>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149016513 | |||||||
| chr3:149016555 | G | A | 1 | a0001c0002t0006g0294 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.608+7153G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149016555 | |||||||
| chr3:149016560 | G | A | 4 | a0001c0003t0012g0306 a0001c0003t0012g0307 a0001c0003t0012g0308 others(1): Show |
4 | HG02109.hp2 HG02572.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.608+7158G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149016560 | |||||||
| chr3:149016652 | TG | T | 4 | a0001c0001t0014g0146 a0001c0001t0014g0147 a0001c0001t0014g0149 others(1): Show |
4 | HG01167.hp1 HG01346.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.608+7255delG | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149016652 | ||||||
| chr3:149016654 | G | C | 1 | a0001c0001t0002g0204 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.608+7252G>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149016654 | |||||||
| chr3:149016798 | G | T | 5 | a0001c0001t0016g0303 a0001c0001t0016g0304 a0001c0001t0016g0305 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.609-7255G>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149016798 | |||||||
| chr3:149016896 | G | A | 4 | a0001c0001t0014g0146 a0001c0001t0014g0147 a0001c0001t0014g0149 others(1): Show |
4 | HG01167.hp1 HG01346.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.609-7157G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149016896 | |||||||
| chr3:149016957 | T | C | 271 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0010 others(268): Show |
312 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.609-7096T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149016957 | |||||||
| chr3:149016976 | G | A | 7 | a0001c0001t0013g0150 a0001c0001t0013g0151 a0001c0001t0013g0153 others(4): Show |
7 | HG02818.hp1 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.609-7077G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149016976 | |||||||
| chr3:149016998 | C | A | 5 | a0001c0001t0016g0303 a0001c0001t0016g0304 a0001c0001t0016g0305 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.609-7055C>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149016998 | |||||||
| chr3:149017159 | T | C | 2 | a0001c0001t0028g0098 a0001c0001t0037g0099 |
2 | HG02145.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.609-6894T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149017159 | |||||||
| chr3:149017216 | A | G | 105 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0010 others(102): Show |
120 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.609-6837A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149017216 | |||||||
| chr3:149017394 | T | C | 291 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0010 others(288): Show |
336 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.609-6659T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149017394 | |||||||
| chr3:149017399 | CT | C | 49 | a0001c0001t0002g0209 a0001c0001t0002g0250 a0001c0001t0003g0111 others(46): Show |
59 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.609-6641delT | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149017399 | ||||||
| chr3:149017501 | G | A | 2 | a0001c0002t0001g0072 a0001c0002t0047g0069 |
2 | HG03834.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.609-6552G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149017501 | |||||||
| chr3:149017571 | C | A | 3 | a0001c0002t0001g0015 a0001c0002t0001g0056 a0001c0002t0001g0088 |
4 | HG00408.hp2 HG02083.hp2 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.609-6482C>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149017571 | |||||||
| chr3:149017582 | G | GT | 65 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0097 others(62): Show |
79 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.609-6441dupT | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149017582 | ||||||
| chr3:149017582 | G | GTT | 25 | a0001c0001t0003g0004 a0001c0001t0003g0043 a0001c0001t0003g0046 others(22): Show |
28 | HG01074.hp1 HG01433.hp1 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.609-6442_609-6441d others(4): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149017582 | ||||||
| chr3:149017582 | G | GTTT | 13 | a0001c0001t0003g0121 a0001c0001t0016g0304 a0001c0001t0021g0120 others(10): Show |
13 | HG00280.hp1 HG00597.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.609-6443_609-6441d others(5): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149017582 | ||||||
| chr3:149017582 | G | GTTTT | 9 | a0001c0001t0002g0223 a0001c0001t0003g0115 a0001c0001t0016g0305 others(6): Show |
10 | HG00323.hp2 HG02602.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.609-6444_609-6441d others(6): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149017582 | ||||||
| chr3:149017582 | G | GTTTTTTT others(6): Show |
1 | a0001c0001t0023g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.609-6453_609-6441d others(15): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149017582 | ||||||
| chr3:149017582 | G | GTTTTTTT others(7): Show |
1 | a0001c0001t0023g0100 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.609-6454_609-6441d others(16): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149017582 | ||||||
| chr3:149017582 | G | GTTTTTTT others(28): Show |
1 | a0002c0004t0049g0195 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.609-6441_609-6440i others(37): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149017582 | ||||||
| chr3:149017582 | GT | G | 10 | a0001c0001t0002g0010 a0001c0001t0002g0214 a0001c0001t0002g0283 others(7): Show |
12 | HG00408.hp1 HG00621.hp2 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.609-6441delT | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149017582 | ||||||
| chr3:149017582 | GTT | G | 46 | a0001c0001t0002g0034 a0001c0001t0002g0035 a0001c0001t0002g0202 others(43): Show |
48 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.609-6442_609-6441d others(4): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149017582 | ||||||
| chr3:149017582 | GTTT | G | 69 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0011 others(66): Show |
83 | HG00099.hp1 HG00423.hp1 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.609-6443_609-6441d others(5): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149017582 | ||||||
| chr3:149017582 | GTTTTT | G | 5 | a0001c0001t0005g0040 a0001c0001t0005g0268 a0001c0001t0005g0270 others(2): Show |
6 | HG01516.hp2 HG02630.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.609-6445_609-6441d others(7): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149017582 | ||||||
| chr3:149017582 | GTTTTTTT others(8): Show |
G | 17 | a0001c0001t0013g0150 a0001c0001t0013g0151 a0001c0001t0013g0153 others(14): Show |
18 | HG00738.hp1 HG02055.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.609-6455_609-6441d others(17): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149017582 | ||||||
| chr3:149017582 | GTTTTTTT others(12): Show |
G | 12 | a0001c0003t0004g0014 a0001c0003t0004g0042 a0001c0003t0004g0331 others(9): Show |
15 | HG01243.hp2 HG02280.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.609-6459_609-6441d others(21): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149017582 | ||||||
| chr3:149017728 | C | T | 1 | a0001c0001t0002g0264 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.609-6325C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149017728 | |||||||
| chr3:149017770 | G | GT | 14 | a0001c0001t0002g0220 a0001c0001t0003g0046 a0001c0001t0003g0114 others(11): Show |
16 | HG01243.hp2 HG02145.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.609-6268dupT | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149017770 | ||||||
| chr3:149017794 | G | GT | 6 | a0001c0001t0013g0150 a0001c0001t0013g0151 a0001c0001t0013g0153 others(3): Show |
6 | HG02922.hp1 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.609-6258dupT | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149017794 | ||||||
| chr3:149017847 | A | T | 3 | a0001c0002t0006g0292 a0001c0002t0006g0293 a0001c0002t0006g0295 |
3 | HG02273.hp1 HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.609-6206A>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149017847 | |||||||
| chr3:149017864 | C | T | 4 | a0001c0001t0016g0303 a0001c0001t0016g0304 a0001c0001t0016g0305 others(1): Show |
4 | HG01255.hp2 HG01891.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.609-6189C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149017864 | |||||||
| chr3:149017972 | G | T | 2 | a0001c0001t0002g0277 a0001c0001t0002g0279 |
2 | HG00639.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.609-6081G>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149017972 | |||||||
| chr3:149018069 | T | C | 7 | a0001c0002t0006g0292 a0001c0002t0006g0293 a0001c0002t0006g0294 others(4): Show |
7 | HG02273.hp1 HG02683.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.609-5984T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149018069 | |||||||
| chr3:149018071 | A | G | 1 | a0001c0003t0004g0332 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.609-5982A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149018071 | |||||||
| chr3:149018109 | A | G | 1 | a0001c0002t0001g0047 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.609-5944A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149018109 | |||||||
| chr3:149018212 | C | T | 1 | a0001c0002t0001g0070 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.609-5841C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149018212 | |||||||
| chr3:149018427 | C | G | 160 | a0001c0001t0008g0021 a0001c0001t0013g0150 a0001c0001t0013g0151 others(157): Show |
186 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.609-5626C>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149018427 | |||||||
| chr3:149018621 | C | A | 4 | a0001c0001t0014g0146 a0001c0001t0014g0147 a0001c0001t0014g0149 others(1): Show |
4 | HG01167.hp1 HG01346.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.609-5432C>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149018621 | |||||||
| chr3:149018730 | A | G | 2 | a0001c0003t0039g0340 a0001c0003t0041g0337 |
2 | HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.609-5323A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149018730 | |||||||
| chr3:149018753 | G | A | 5 | a0001c0001t0016g0303 a0001c0001t0016g0304 a0001c0001t0016g0305 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.609-5300G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149018753 | |||||||
| chr3:149018789 | C | A | 166 | a0001c0001t0002g0223 a0001c0001t0013g0150 a0001c0001t0013g0151 others(163): Show |
191 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.609-5264C>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149018789 | |||||||
| chr3:149018916 | G | A | 1 | a0001c0002t0001g0075 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.609-5137G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149018916 | |||||||
| chr3:149019068 | T | TA | 88 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0010 others(85): Show |
103 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.609-4966dupA | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149019068 | ||||||
| chr3:149019068 | T | TAA | 9 | a0001c0001t0002g0201 a0001c0001t0002g0202 a0001c0001t0002g0215 others(6): Show |
9 | HG01081.hp1 HG01109.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.609-4967_609-4966d others(4): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149019068 | ||||||
| chr3:149019068 | TA | T | 16 | a0001c0001t0003g0024 a0001c0001t0003g0119 a0001c0001t0003g0130 others(13): Show |
17 | HG01167.hp1 HG01346.hp1 HG01516.hp2 others(14): Show |
intron_variant | MODIFIER | c.609-4966delA | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149019068 | ||||||
| chr3:149019086 | A | G | 6 | a0001c0001t0023g0100 a0001c0001t0023g0101 a0001c0003t0012g0306 others(3): Show |
6 | HG02109.hp2 HG02280.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.609-4967A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149019086 | |||||||
| chr3:149019312 | T | C | 2 | a0001c0001t0002g0250 a0001c0001t0002g0251 |
2 | NA18947.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.609-4741T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149019312 | |||||||
| chr3:149019404 | C | T | 118 | a0001c0001t0002g0223 a0001c0002t0001g0002 a0001c0002t0001g0006 others(115): Show |
139 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.609-4649C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149019404 | |||||||
| chr3:149019418 | C | T | 1 | a0001c0001t0009g0135 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.609-4635C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149019418 | |||||||
| chr3:149019428 | C | T | 2 | a0001c0001t0028g0098 a0001c0001t0037g0099 |
2 | HG02145.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.609-4625C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149019428 | |||||||
| chr3:149019477 | A | G | 13 | a0001c0002t0001g0028 a0001c0002t0001g0045 a0001c0002t0001g0091 others(10): Show |
16 | HG00280.hp1 HG00323.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.609-4576A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149019477 | |||||||
| chr3:149019761 | G | A | 1 | a0001c0001t0034g0161 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.609-4292G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149019761 | |||||||
| chr3:149019861 | C | T | 2 | a0001c0001t0051g0157 a0001c0001t0052g0156 |
2 | HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.609-4192C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149019861 | |||||||
| chr3:149019915 | G | A | 5 | a0001c0001t0002g0011 a0001c0001t0002g0038 a0001c0001t0002g0275 others(2): Show |
7 | HG00423.hp1 HG02040.hp2 NA18941.hp2 others(4): Show |
intron_variant | MODIFIER | c.609-4138G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149019915 | |||||||
| chr3:149020039 | C | T | 1 | a0001c0003t0022g0330 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.609-4014C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149020039 | |||||||
| chr3:149020096 | T | TTAAGCAC others(181): Show |
1 | a0001c0006t0029g0044 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.609-3938_609-3937i others(190): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149020096 | ||||||
| chr3:149020149 | C | G | 1 | a0001c0002t0001g0169 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.609-3904C>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149020149 | |||||||
| chr3:149020222 | C | T | 2 | a0001c0001t0023g0100 a0001c0001t0023g0101 |
2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.609-3831C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149020222 | |||||||
| chr3:149020282 | T | G | 129 | a0001c0001t0004g0317 a0001c0002t0001g0002 a0001c0002t0001g0006 others(126): Show |
153 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.609-3771T>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149020282 | |||||||
| chr3:149020288 | T | C | 1 | a0001c0003t0040g0329 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.609-3765T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149020288 | |||||||
| chr3:149020431 | G | A | 2 | a0001c0001t0002g0259 a0001c0001t0002g0265 |
2 | HG00733.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.609-3622G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149020431 | |||||||
| chr3:149020716 | T | C | 1 | a0001c0002t0008g0058 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.609-3337T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149020716 | |||||||
| chr3:149020772 | C | T | 1 | a0001c0002t0001g0095 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.609-3281C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149020772 | |||||||
| chr3:149020826 | A | C | 2 | a0001c0001t0002g0282 a0001c0001t0002g0283 |
2 | HG02523.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.609-3227A>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149020826 | |||||||
| chr3:149020850 | G | A | 24 | a0001c0001t0002g0203 a0001c0001t0002g0219 a0001c0001t0002g0220 others(21): Show |
25 | HG00639.hp2 HG01261.hp1 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.609-3203G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149020850 | |||||||
| chr3:149020876 | G | A | 1 | a0001c0001t0003g0115 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.609-3177G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149020876 | |||||||
| chr3:149020958 | G | A | 3 | a0001c0001t0002g0253 a0001c0001t0007g0252 a0001c0001t0017g0221 |
3 | NA18946.hp1 NA18967.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.609-3095G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149020958 | |||||||
| chr3:149021012 | C | T | 1 | a0001c0001t0002g0243 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.609-3041C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149021012 | |||||||
| chr3:149021076 | C | G | 5 | a0001c0003t0004g0014 a0001c0003t0004g0333 a0001c0003t0004g0334 others(2): Show |
7 | HG01243.hp2 HG02559.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.609-2977C>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149021076 | |||||||
| chr3:149021163 | C | T | 1 | a0001c0001t0038g0199 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.609-2890C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149021163 | |||||||
| chr3:149021205 | T | G | 12 | a0001c0001t0004g0317 a0001c0003t0004g0014 a0001c0003t0004g0042 others(9): Show |
15 | HG01243.hp2 HG02280.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.609-2848T>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149021205 | |||||||
| chr3:149021273 | T | C | 5 | a0001c0001t0016g0303 a0001c0001t0016g0304 a0001c0001t0016g0305 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.609-2780T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149021273 | |||||||
| chr3:149021288 | C | T | 2 | a0001c0001t0051g0157 a0001c0001t0052g0156 |
2 | HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.609-2765C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149021288 | |||||||
| chr3:149021353 | C | T | 20 | a0001c0001t0013g0150 a0001c0001t0013g0151 a0001c0001t0013g0153 others(17): Show |
21 | HG00738.hp1 HG02055.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.609-2700C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149021353 | |||||||
| chr3:149021403 | A | T | 2 | a0001c0001t0003g0137 a0001c0003t0039g0340 |
2 | HG01255.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.609-2650A>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149021403 | |||||||
| chr3:149021543 | A | C | 9 | a0001c0001t0013g0150 a0001c0001t0013g0151 a0001c0001t0013g0153 others(6): Show |
9 | HG02055.hp2 HG02818.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.609-2510A>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149021543 | |||||||
| chr3:149021698 | T | C | 19 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0041 others(16): Show |
23 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.609-2355T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149021698 | |||||||
| chr3:149021712 | GGTCTCCA others(6): Show |
G | 1 | a0001c0002t0001g0082 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.609-2338_609-2326d others(15): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149021712 | ||||||
| chr3:149021762 | CT | C | 6 | a0001c0001t0002g0222 a0001c0001t0002g0272 a0001c0001t0003g0129 others(3): Show |
7 | HG01515.hp1 HG03195.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.609-2278delT | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149021762 | ||||||
| chr3:149021782 | C | T | 2 | a0001c0003t0012g0307 a0001c0003t0012g0308 |
2 | HG02109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.609-2271C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149021782 | |||||||
| chr3:149021851 | G | A | 7 | a0001c0001t0013g0150 a0001c0001t0013g0151 a0001c0001t0013g0153 others(4): Show |
7 | HG02818.hp1 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.609-2202G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149021851 | |||||||
| chr3:149021858 | G | A | 2 | a0001c0001t0002g0215 a0001c0001t0002g0222 |
2 | HG01515.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.609-2195G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149021858 | |||||||
| chr3:149021985 | G | A | 2 | a0001c0001t0051g0157 a0001c0001t0052g0156 |
2 | HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.609-2068G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149021985 | |||||||
| chr3:149022062 | T | C | 1 | a0001c0002t0026g0017 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.609-1991T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149022062 | |||||||
| chr3:149022242 | C | T | 2 | a0001c0001t0003g0102 a0001c0001t0003g0103 |
2 | HG01175.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.609-1811C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149022242 | |||||||
| chr3:149022243 | G | A | 122 | a0001c0001t0008g0021 a0001c0002t0001g0002 a0001c0002t0001g0006 others(119): Show |
144 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.609-1810G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149022243 | |||||||
| chr3:149022259 | T | C | 4 | a0001c0001t0015g0009 a0001c0001t0015g0198 a0001c0001t0030g0197 others(1): Show |
5 | HG00738.hp1 HG02451.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.609-1794T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149022259 | |||||||
| chr3:149022416 | C | T | 2 | a0001c0003t0039g0340 a0001c0003t0041g0337 |
2 | HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.609-1637C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149022416 | |||||||
| chr3:149022498 | C | CTTT | 6 | a0001c0001t0013g0151 a0001c0001t0013g0153 a0001c0001t0013g0155 others(3): Show |
6 | HG02818.hp1 HG02922.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.609-1539_609-1537d others(5): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149022498 | ||||||
| chr3:149022498 | C | CTTTTT | 5 | a0001c0001t0015g0009 a0001c0001t0015g0198 a0001c0001t0036g0009 others(2): Show |
6 | HG00738.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.609-1541_609-1537d others(7): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149022498 | ||||||
| chr3:149022498 | C | CTTTTTTT others(1): Show |
38 | a0001c0002t0001g0006 a0001c0002t0001g0026 a0001c0002t0001g0028 others(35): Show |
45 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.609-1544_609-1537d others(10): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149022498 | ||||||
| chr3:149022498 | C | CTTTTTTT others(2): Show |
71 | a0001c0001t0008g0021 a0001c0001t0023g0101 a0001c0002t0001g0002 others(68): Show |
86 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.609-1545_609-1537d others(11): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149022498 | ||||||
| chr3:149022498 | C | CTTTTTTT others(3): Show |
13 | a0001c0001t0023g0100 a0001c0002t0001g0062 a0001c0002t0001g0076 others(10): Show |
13 | HG01346.hp2 HG01978.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.609-1546_609-1537d others(12): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149022498 | ||||||
| chr3:149022498 | C | CTTTTTTT others(5): Show |
1 | a0001c0003t0004g0332 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.609-1548_609-1537d others(14): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149022498 | ||||||
| chr3:149022498 | C | CTTTTTTT others(6): Show |
2 | a0001c0002t0001g0050 a0001c0003t0040g0329 |
2 | HG02622.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.609-1549_609-1537d others(15): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149022498 | ||||||
| chr3:149022498 | C | CTTTTTTT others(7): Show |
4 | a0001c0001t0002g0254 a0001c0001t0016g0304 a0001c0001t0016g0305 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.609-1550_609-1537d others(16): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149022498 | ||||||
| chr3:149022498 | C | CTTTTTTT others(8): Show |
2 | a0001c0001t0016g0303 a0001c0001t0022g0302 |
2 | HG01255.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.609-1551_609-1537d others(17): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149022498 | ||||||
| chr3:149022498 | C | CTTTTTTT others(12): Show |
3 | a0001c0001t0002g0213 a0001c0001t0002g0272 a0001c0001t0007g0225 |
3 | HG01074.hp2 HG01169.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.609-1537_609-1536i others(21): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149022498 | ||||||
| chr3:149022498 | C | CTTTTTTT others(13): Show |
3 | a0001c0001t0002g0201 a0001c0001t0002g0209 a0001c0001t0002g0222 |
3 | HG01496.hp1 HG01515.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.609-1537_609-1536i others(22): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149022498 | ||||||
| chr3:149022498 | C | CTTTTTTT others(14): Show |
32 | a0001c0001t0002g0034 a0001c0001t0002g0035 a0001c0001t0002g0038 others(29): Show |
36 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.609-1537_609-1536i others(23): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149022498 | ||||||
| chr3:149022498 | C | CTTTTTTT others(15): Show |
35 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(32): Show |
43 | HG00099.hp1 HG00423.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.609-1537_609-1536i others(24): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149022498 | ||||||
| chr3:149022498 | C | CTTTTTTT others(16): Show |
21 | a0001c0001t0002g0007 a0001c0001t0002g0206 a0001c0001t0002g0212 others(18): Show |
25 | HG00673.hp1 HG01081.hp1 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.609-1537_609-1536i others(25): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149022498 | ||||||
| chr3:149022498 | C | CTTTTTTT others(17): Show |
6 | a0001c0001t0002g0204 a0001c0001t0002g0237 a0001c0001t0002g0261 others(3): Show |
6 | HG01978.hp2 HG02257.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.609-1537_609-1536i others(26): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149022498 | ||||||
| chr3:149022498 | C | CTTTTTTT others(18): Show |
2 | a0001c0001t0002g0238 a0001c0001t0002g0262 |
2 | HG02148.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.609-1537_609-1536i others(27): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149022498 | ||||||
| chr3:149022498 | C | CTTTTTTT others(19): Show |
2 | a0001c0003t0004g0334 a0001c0003t0004g0335 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.609-1537_609-1536i others(28): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149022498 | ||||||
| chr3:149022498 | C | CTTTTTTT others(20): Show |
1 | a0001c0003t0004g0331 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.609-1537_609-1536i others(29): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149022498 | ||||||
| chr3:149022498 | C | CTTTTTTT others(23): Show |
1 | a0001c0003t0041g0337 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.609-1537_609-1536i others(32): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149022498 | ||||||
| chr3:149022498 | C | CTTTTTTT others(24): Show |
2 | a0001c0003t0004g0014 a0001c0003t0004g0333 |
4 | HG02559.hp1 HG03130.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.609-1537_609-1536i others(33): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149022498 | ||||||
| chr3:149022498 | C | CTTTTTTT others(32): Show |
1 | a0001c0003t0004g0336 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.609-1537_609-1536i others(41): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149022498 | ||||||
| chr3:149022517 | G | T | 1 | a0001c0001t0002g0257 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.609-1536G>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149022517 | |||||||
| chr3:149022518 | A | T | 1 | a0001c0001t0002g0257 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.609-1535A>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149022518 | |||||||
| chr3:149022519 | G | T | 1 | a0001c0001t0002g0257 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.609-1534G>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149022519 | |||||||
| chr3:149022520 | A | T | 1 | a0001c0001t0002g0257 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.609-1533A>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149022520 | |||||||
| chr3:149022522 | G | T | 1 | a0001c0001t0002g0257 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.609-1531G>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149022522 | |||||||
| chr3:149022523 | G | T | 1 | a0001c0001t0002g0257 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.609-1530G>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149022523 | |||||||
| chr3:149022524 | A | T | 1 | a0001c0001t0002g0257 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.609-1529A>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149022524 | |||||||
| chr3:149022525 | G | T | 1 | a0001c0001t0002g0257 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.609-1528G>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149022525 | |||||||
| chr3:149022527 | C | T | 1 | a0001c0001t0002g0257 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.609-1526C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149022527 | |||||||
| chr3:149022529 | C | T | 1 | a0001c0001t0002g0257 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.609-1524C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149022529 | |||||||
| chr3:149022530 | A | T | 1 | a0001c0001t0002g0257 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.609-1523A>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149022530 | |||||||
| chr3:149022531 | C | T | 1 | a0001c0001t0002g0257 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.609-1522C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149022531 | |||||||
| chr3:149022533 | G | T | 1 | a0001c0001t0002g0257 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.609-1520G>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149022533 | |||||||
| chr3:149022535 | C | T | 1 | a0001c0001t0002g0257 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.609-1518C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149022535 | |||||||
| chr3:149022536 | A | T | 1 | a0001c0001t0002g0257 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.609-1517A>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149022536 | |||||||
| chr3:149022537 | C | T | 1 | a0001c0001t0002g0257 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.609-1516C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149022537 | |||||||
| chr3:149022538 | C | T | 1 | a0001c0001t0002g0257 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.609-1515C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149022538 | |||||||
| chr3:149022539 | A | G | 1 | a0001c0001t0002g0257 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.609-1514A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149022539 | |||||||
| chr3:149022540 | G | A | 1 | a0001c0001t0002g0257 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.609-1513G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149022540 | |||||||
| chr3:149022542 | C | A | 1 | a0001c0001t0002g0257 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.609-1511C>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149022542 | |||||||
| chr3:149022549 | G | C | 1 | a0001c0001t0002g0257 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.609-1504G>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149022549 | |||||||
| chr3:149022550 | C | T | 1 | a0001c0001t0002g0257 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.609-1503C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149022550 | |||||||
| chr3:149022551 | A | C | 1 | a0001c0001t0002g0257 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.609-1502A>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149022551 | |||||||
| chr3:149022688 | G | A | 1 | a0001c0001t0003g0103 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.609-1365G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149022688 | |||||||
| chr3:149022752 | G | A | 1 | a0001c0003t0041g0337 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.609-1301G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149022752 | |||||||
| chr3:149022773 | T | C | 1 | a0001c0001t0002g0254 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.609-1280T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149022773 | |||||||
| chr3:149022959 | C | CT | 134 | a0001c0001t0004g0317 a0001c0001t0008g0021 a0001c0002t0001g0002 others(131): Show |
159 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.609-1091dupT | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149022959 | ||||||
| chr3:149023013 | C | G | 5 | a0001c0002t0001g0163 a0001c0002t0001g0171 a0001c0002t0001g0172 others(2): Show |
5 | NA18945.hp1 NA18993.hp2 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.609-1040C>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149023013 | |||||||
| chr3:149023175 | T | C | 9 | a0001c0001t0013g0150 a0001c0001t0013g0151 a0001c0001t0013g0153 others(6): Show |
9 | HG02055.hp2 HG02818.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.609-878T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149023175 | |||||||
| chr3:149023283 | A | G | 122 | a0001c0001t0008g0021 a0001c0002t0001g0002 a0001c0002t0001g0006 others(119): Show |
144 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.609-770A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149023283 | |||||||
| chr3:149023888 | T | TA | 122 | a0001c0001t0008g0021 a0001c0002t0001g0002 a0001c0002t0001g0006 others(119): Show |
144 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.609-164dupA | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 149023888 | ||||||
| chr3:149023922 | C | G | 12 | a0001c0001t0004g0317 a0001c0003t0004g0014 a0001c0003t0004g0042 others(9): Show |
15 | HG01243.hp2 HG02280.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.609-131C>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 5/7 | chr3 | 149023922 | |||||||
| chr3:149024538 | C | A | 1 | a0001c0001t0028g0098 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.828+266C>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 6/7 | chr3 | 149024538 | |||||||
| chr3:149024625 | A | C | 2 | a0001c0001t0051g0157 a0001c0001t0052g0156 |
2 | HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.828+353A>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 6/7 | chr3 | 149024625 | |||||||
| chr3:149024639 | T | A | 1 | a0001c0001t0002g0235 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.828+367T>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 6/7 | chr3 | 149024639 | |||||||
| chr3:149024900 | G | T | 1 | a0001c0003t0022g0330 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.828+628G>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 6/7 | chr3 | 149024900 | |||||||
| chr3:149024971 | C | A | 1 | a0001c0001t0002g0220 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.828+699C>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 6/7 | chr3 | 149024971 | |||||||
| chr3:149025117 | T | C | 5 | a0001c0001t0016g0303 a0001c0001t0016g0304 a0001c0001t0016g0305 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.828+845T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 6/7 | chr3 | 149025117 | |||||||
| chr3:149025155 | G | C | 1 | a0001c0003t0022g0330 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.828+883G>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 6/7 | chr3 | 149025155 | |||||||
| chr3:149025318 | G | C | 1 | a0001c0001t0002g0238 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.828+1046G>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 6/7 | chr3 | 149025318 | |||||||
| chr3:149025350 | C | G | 1 | a0001c0001t0007g0247 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.828+1078C>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 6/7 | chr3 | 149025350 | |||||||
| chr3:149025445 | C | G | 1 | a0001c0002t0001g0063 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.829-1007C>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 6/7 | chr3 | 149025445 | |||||||
| chr3:149025579 | T | C | 1 | a0001c0002t0001g0176 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.829-873T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 6/7 | chr3 | 149025579 | |||||||
| chr3:149025849 | TTTAAG | T | 3 | a0001c0001t0017g0256 a0001c0001t0023g0100 a0001c0001t0023g0101 |
3 | HG02280.hp1 HG02970.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.829-599_829-595del others(5): Show |
GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 149025849 | ||||||
| chr3:149025903 | G | A | 138 | a0001c0001t0004g0317 a0001c0001t0016g0303 a0001c0001t0016g0304 others(135): Show |
162 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.829-549G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 6/7 | chr3 | 149025903 | |||||||
| chr3:149026003 | G | A | 5 | a0001c0001t0016g0303 a0001c0001t0016g0304 a0001c0001t0016g0305 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.829-449G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 6/7 | chr3 | 149026003 | |||||||
| chr3:149026037 | C | T | 3 | a0001c0001t0002g0243 a0001c0001t0024g0233 a0001c0001t0024g0281 |
3 | HG01261.hp1 HG02300.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.829-415C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 6/7 | chr3 | 149026037 | |||||||
| chr3:149026093 | C | T | 1 | a0001c0001t0031g0200 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.829-359C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 6/7 | chr3 | 149026093 | |||||||
| chr3:149026098 | G | A | 1 | a0002c0004t0048g0196 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.829-354G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 6/7 | chr3 | 149026098 | |||||||
| chr3:149026098 | G | C | 6 | a0001c0002t0001g0028 a0001c0002t0001g0179 a0001c0002t0001g0181 others(3): Show |
7 | HG00280.hp1 HG01123.hp2 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.829-354G>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 6/7 | chr3 | 149026098 | |||||||
| chr3:149026105 | C | T | 1 | a0001c0001t0003g0143 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.829-347C>T | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 6/7 | chr3 | 149026105 | |||||||
| chr3:149026279 | A | G | 1 | a0001c0001t0002g0242 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.829-173A>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 6/7 | chr3 | 149026279 | |||||||
| chr3:149026439 | G | A | 2 | a0001c0001t0021g0118 a0001c0001t0021g0120 |
2 | HG02074.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.829-13G>A | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 6/7 | chr3 | 149026439 | |||||||
| chr3:149026535 | T | C | 1 | a0001c0001t0014g0149 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.879+33T>C | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 7/7 | chr3 | 149026535 | |||||||
| chr3:149026617 | T | G | 8 | a0001c0001t0002g0007 a0001c0001t0002g0260 a0001c0001t0002g0261 others(5): Show |
10 | HG01257.hp1 HG01975.hp2 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.879+115T>G | GYG1 | ENSG00000163754.18 | transcript | ENST00000345003.9 | protein_coding | 7/7 | chr3 | 149026617 |