| geneid | 8908 |
|---|---|
| ensemblid | ENSG00000056998.21 |
| hgncid | 4700 |
| symbol | GYG2 |
| name | glycogenin 2 |
| refseq_nuc | NM_001079855.2 |
| refseq_prot | NP_001073324.1 |
| ensembl_nuc | ENST00000398806.8 |
| ensembl_prot | ENSP00000381786.3 |
| mane_status | MANE Select |
| chr | chrX |
| start | 2828930 |
| end | 2882818 |
| strand | + |
| ver | v1.2 |
| region | chrX:2828930-2882818 |
| region5000 | chrX:2823930-2887818 |
| regionname0 | GYG2_chrX_2828930_2882818 |
| regionname5000 | GYG2_chrX_2823930_2887818 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 470 | 167 | 17 | 28 | 91 | 5 | 25 | 70 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0002 | 1/0 | 470 | 127 | 56 | 19 | 40 | 5 | 6 | 31 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0003 | 0/0 | 470 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0004 | 0/0 | 470 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0005 | 0/0 | 470 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0006 | 0/0 | 470 | 3 | 0 | 2 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0007 | 0/0 | 470 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0008 | 0/0 | 404 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0009 | 0/0 | 470 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0010 | 0/0 | 470 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0011 | 0/0 | 300 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0012 | 0/0 | 470 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0013 | 0/0 | 470 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0014 | 0/0 | 27 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0015 | 0/0 | 14 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 1413 | 149 | 7 | 27 | 84 | 5 | 25 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| c0002 | 1/0 | 1413 | 116 | 47 | 17 | 40 | 5 | 6 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| c0003 | 0/0 | 1413 | 11 | 10 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| c0004 | 0/0 | 1413 | 6 | 0 | 0 | 6 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| c0005 | 0/0 | 1413 | 6 | 4 | 2 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| c0006 | 0/0 | 1413 | 5 | 5 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| c0007 | 0/0 | 1413 | 4 | 4 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| c0008 | 0/0 | 1413 | 3 | 2 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| c0009 | 0/0 | 1413 | 3 | 0 | 2 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| c0010 | 0/0 | 1413 | 3 | 0 | 2 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| c0011 | 0/0 | 1414 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| c0012 | 0/0 | 1412 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| c0013 | 0/0 | 1413 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| c0014 | 0/0 | 1414 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| c0015 | 0/0 | 1413 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| c0016 | 0/0 | 1413 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| c0017 | 0/0 | 1413 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| c0018 | 0/0 | 1413 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| c0019 | 0/0 | 1414 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| c0020 | 0/0 | 1413 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 1780 | 88 | 9 | 23 | 34 | 5 | 17 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| t0002 | 0/1 | 1780 | 72 | 15 | 12 | 37 | 5 | 2 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| t0003 | 0/0 | 1780 | 48 | 11 | 5 | 30 | 0 | 2 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| t0004 | 1/0 | 1780 | 45 | 3 | 7 | 26 | 0 | 8 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| t0005 | 0/0 | 1780 | 24 | 21 | 1 | 0 | 0 | 2 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| t0006 | 0/0 | 1780 | 11 | 9 | 2 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| t0007 | 0/0 | 1780 | 9 | 7 | 1 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| t0008 | 0/0 | 1780 | 3 | 2 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| t0009 | 0/0 | 1780 | 2 | 0 | 2 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| t0010 | 0/0 | 1780 | 2 | 0 | 0 | 2 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| t0011 | 0/0 | 1780 | 2 | 0 | 0 | 0 | 0 | 2 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| t0012 | 0/0 | 1780 | 2 | 2 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| t0013 | 0/0 | 1779 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| t0014 | 0/0 | 1780 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| t0015 | 0/0 | 1780 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| t0016 | 0/0 | 1780 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| t0017 | 0/0 | 1780 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| t0018 | 0/0 | 1778 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| t0019 | 0/0 | 1781 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| t0020 | 0/0 | 1780 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0128 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0153 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1413 | 149 | 7 | 27 | 84 | 5 | 25 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0001c0003 | 0/0 | 1413 | 11 | 10 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0001c0004 | 0/0 | 1413 | 6 | 0 | 0 | 6 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0001c0016 | 0/0 | 1413 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0002c0002 | 1/0 | 1413 | 116 | 47 | 17 | 40 | 5 | 6 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0002c0005 | 0/0 | 1413 | 6 | 4 | 2 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0002c0006 | 0/0 | 1413 | 5 | 5 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0003c0007 | 0/0 | 1413 | 4 | 4 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0004c0008 | 0/0 | 1413 | 3 | 2 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0005c0009 | 0/0 | 1413 | 3 | 0 | 2 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0006c0010 | 0/0 | 1413 | 3 | 0 | 2 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0007c0020 | 0/0 | 1413 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0008c0014 | 0/0 | 1414 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0009c0013 | 0/0 | 1413 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0010c0015 | 0/0 | 1413 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0011c0019 | 0/0 | 1414 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0012c0018 | 0/0 | 1413 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0013c0017 | 0/0 | 1413 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0014c0012 | 0/0 | 1412 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0015c0011 | 0/0 | 1414 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3192 | 58 | 2 | 12 | 28 | 2 | 14 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0001c0001t0002 | 0/1 | 3192 | 37 | 2 | 5 | 25 | 2 | 2 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0001c0001t0003 | 0/0 | 3192 | 25 | 0 | 2 | 23 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0001c0001t0004 | 0/0 | 3192 | 18 | 1 | 6 | 6 | 0 | 5 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0001c0001t0005 | 0/0 | 3192 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0001c0001t0007 | 0/0 | 3192 | 2 | 1 | 0 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0001c0001t0008 | 0/0 | 3192 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0001c0001t0009 | 0/0 | 3192 | 2 | 0 | 2 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0001c0001t0010 | 0/0 | 3192 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0001c0001t0011 | 0/0 | 3192 | 2 | 0 | 0 | 0 | 0 | 2 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0001c0001t0015 | 0/0 | 3192 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0001c0001t0017 | 0/0 | 3192 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0001c0003t0001 | 0/0 | 3192 | 3 | 3 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0001c0003t0002 | 0/0 | 3192 | 2 | 1 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0001c0003t0004 | 0/0 | 3192 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0001c0003t0005 | 0/0 | 3192 | 3 | 3 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0001c0003t0007 | 0/0 | 3192 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0001c0003t0008 | 0/0 | 3192 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0001c0004t0001 | 0/0 | 3192 | 3 | 0 | 0 | 3 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0001c0004t0002 | 0/0 | 3192 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0001c0004t0004 | 0/0 | 3192 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0001c0004t0014 | 0/0 | 3192 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0001c0016t0003 | 0/0 | 3192 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0002c0002t0001 | 0/0 | 3192 | 19 | 3 | 11 | 2 | 2 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0002c0002t0002 | 0/0 | 3192 | 26 | 9 | 4 | 10 | 3 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0002c0002t0003 | 0/0 | 3192 | 15 | 8 | 0 | 5 | 0 | 2 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0002c0002t0004 | 1/0 | 3192 | 24 | 1 | 0 | 19 | 0 | 3 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0002c0002t0005 | 0/0 | 3192 | 16 | 15 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0002c0002t0006 | 0/0 | 3192 | 4 | 4 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0002c0002t0007 | 0/0 | 3192 | 4 | 4 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0002c0002t0008 | 0/0 | 3192 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0002c0002t0010 | 0/0 | 3192 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0002c0002t0012 | 0/0 | 3192 | 2 | 2 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0002c0002t0013 | 0/0 | 3191 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0002c0002t0016 | 0/0 | 3192 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0002c0002t0019 | 0/0 | 3193 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0002c0002t0020 | 0/0 | 3192 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0002c0005t0002 | 0/0 | 3192 | 2 | 2 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0002c0005t0003 | 0/0 | 3192 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0002c0005t0006 | 0/0 | 3192 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0002c0005t0007 | 0/0 | 3192 | 2 | 1 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0002c0006t0002 | 0/0 | 3192 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0002c0006t0003 | 0/0 | 3192 | 2 | 2 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0002c0006t0005 | 0/0 | 3192 | 2 | 2 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0003c0007t0001 | 0/0 | 3192 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0003c0007t0006 | 0/0 | 3192 | 3 | 3 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0004c0008t0006 | 0/0 | 3192 | 3 | 2 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0005c0009t0001 | 0/0 | 3192 | 1 | 0 | 0 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0005c0009t0002 | 0/0 | 3192 | 2 | 0 | 2 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0006c0010t0003 | 0/0 | 3192 | 3 | 0 | 2 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0007c0020t0003 | 0/0 | 3192 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0008c0014t0018 | 0/0 | 3191 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0009c0013t0005 | 0/0 | 3192 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0010c0015t0001 | 0/0 | 3192 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0011c0019t0004 | 0/0 | 3193 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0012c0018t0001 | 0/0 | 3192 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0013c0017t0005 | 0/0 | 3192 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0014c0012t0001 | 0/0 | 3191 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| a0015c0011t0002 | 0/0 | 3193 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | copy fasta | chrX | 2823930 | 2887818 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0153 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0004g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0004g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0004g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0004g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0004g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0004g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0005g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0007g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0007g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0008g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0009g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0009g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0010g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0011g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0011g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0015g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0017g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0003t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0003t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0003t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0003t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0003t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0003t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0003t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0003t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0003t0005g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0003t0007g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0003t0008g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0004t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0004t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0004t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0004t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0004t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0004t0014g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0016t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0003g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0128 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0005g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0005g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0005g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0005g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0005g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0005g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0005g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0005g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0005g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0006g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0006g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0006g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0006g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0007g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0007g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0007g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0007g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0008g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0010g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0012g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0012g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0013g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0016g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0019g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0020g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0005t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0005t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0005t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0005t0006g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0005t0007g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0005t0007g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0006t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0006t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0006t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0006t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0006t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0003c0007t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0003c0007t0006g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0003c0007t0006g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0003c0007t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0004c0008t0006g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0004c0008t0006g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0004c0008t0006g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0005c0009t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0005c0009t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0005c0009t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0006c0010t0003g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0006c0010t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0006c0010t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0007c0020t0003g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0008c0014t0018g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0009c0013t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0010c0015t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0011c0019t0004g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0012c0018t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0013c0017t0005g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0014c0012t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0015c0011t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0170 | EUR | GBR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0146 | EUR | GBR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0292 | EUR | GBR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00280 | hp1 | a0002 | c0002 | t0002 | g0257 | EUR | FIN | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0286 | EUR | FIN | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00323 | hp2 | a0002 | c0002 | t0002 | g0252 | EUR | FIN | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00408 | hp1 | a0001 | c0004 | t0001 | g0103 | EAS | CHS | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | CHS | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00423 | hp1 | a0002 | c0002 | t0004 | g0265 | EAS | CHS | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0275 | EAS | CHS | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0159 | EAS | CHS | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0071 | EAS | CHS | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | CHS | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00621 | hp1 | a0002 | c0002 | t0010 | g0157 | EAS | CHS | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0054 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0077 | EAS | CHS | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00741 | hp2 | a0002 | c0005 | t0006 | g0104 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0123 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01070 | hp2 | a0005 | c0009 | t0002 | g0212 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0124 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01074 | hp1 | a0002 | c0005 | t0007 | g0018 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0291 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01106 | hp1 | a0002 | c0002 | t0002 | g0294 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01109 | hp1 | a0002 | c0002 | t0005 | g0091 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01167 | hp1 | a0001 | c0001 | t0009 | g0270 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0150 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01169 | hp2 | a0001 | c0001 | t0009 | g0266 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01175 | hp2 | a0011 | c0019 | t0004 | g0003 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01243 | hp1 | a0001 | c0003 | t0002 | g0042 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01255 | hp1 | a0006 | c0010 | t0003 | g0014 | AMR | CLM | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0259 | AMR | CLM | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0131 | AMR | CLM | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0130 | AMR | CLM | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01261 | hp1 | a0004 | c0008 | t0006 | g0009 | AMR | CLM | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0154 | AMR | CLM | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01433 | hp1 | a0002 | c0002 | t0020 | g0255 | AMR | CLM | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01515 | hp1 | a0001 | c0001 | t0007 | g0221 | EUR | IBS | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0217 | EUR | IBS | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0149 | EUR | IBS | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01884 | hp1 | a0002 | c0002 | t0005 | g0116 | AFR | ACB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01884 | hp2 | a0002 | c0005 | t0003 | g0040 | AFR | ACB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01891 | hp1 | a0004 | c0008 | t0006 | g0019 | AFR | ACB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01891 | hp2 | a0001 | c0003 | t0008 | g0026 | AFR | ACB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0186 | AMR | PEL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01934 | hp1 | a0002 | c0002 | t0002 | g0251 | AMR | PEL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0258 | AMR | PEL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0308 | AMR | PEL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0065 | AMR | PEL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01981 | hp1 | a0005 | c0009 | t0002 | g0162 | AMR | PEL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0081 | AMR | PEL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0256 | AMR | PEL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0129 | AMR | PEL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02004 | hp1 | a0002 | c0002 | t0002 | g0253 | AMR | PEL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0277 | AMR | PEL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | KHV | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02055 | hp1 | a0001 | c0003 | t0005 | g0304 | AFR | ACB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02056 | hp1 | a0002 | c0002 | t0004 | g0137 | EAS | KHV | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | KHV | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0242 | EAS | KHV | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02080 | hp1 | a0006 | c0010 | t0003 | g0187 | EAS | KHV | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0158 | EAS | KHV | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02083 | hp1 | a0002 | c0002 | t0004 | g0151 | EAS | KHV | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0231 | EAS | KHV | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02132 | hp1 | a0002 | c0002 | t0004 | g0300 | EAS | KHV | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | KHV | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02145 | hp1 | a0001 | c0003 | t0005 | g0022 | AFR | ACB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0230 | EAS | CDX | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02155 | hp2 | a0001 | c0001 | t0017 | g0094 | EAS | CDX | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0241 | EAS | CDX | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02165 | hp2 | a0001 | c0004 | t0014 | g0290 | EAS | CDX | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02257 | hp1 | a0002 | c0002 | t0002 | g0107 | AFR | ACB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0179 | AFR | ACB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02273 | hp1 | a0007 | c0020 | t0003 | g0007 | AMR | PEL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0260 | AMR | PEL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02280 | hp1 | a0002 | c0005 | t0002 | g0176 | AFR | ACB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02280 | hp2 | a0002 | c0006 | t0005 | g0119 | AFR | ACB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | PEL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0254 | AMR | PEL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02451 | hp1 | a0001 | c0003 | t0007 | g0024 | AFR | ACB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02451 | hp2 | a0002 | c0002 | t0003 | g0110 | AFR | ACB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | KHV | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02523 | hp2 | a0002 | c0002 | t0004 | g0235 | EAS | KHV | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02572 | hp1 | a0002 | c0002 | t0006 | g0017 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02615 | hp1 | a0002 | c0002 | t0002 | g0011 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02615 | hp2 | a0002 | c0005 | t0007 | g0020 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02622 | hp1 | a0002 | c0006 | t0002 | g0121 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02622 | hp2 | a0002 | c0002 | t0006 | g0051 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02630 | hp1 | a0002 | c0002 | t0002 | g0002 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02647 | hp1 | a0002 | c0002 | t0003 | g0010 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02683 | hp1 | a0001 | c0001 | t0004 | g0246 | SAS | PJL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0225 | SAS | PJL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02698 | hp1 | a0001 | c0001 | t0004 | g0084 | SAS | PJL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02717 | hp1 | a0002 | c0002 | t0005 | g0126 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02723 | hp1 | a0003 | c0007 | t0006 | g0031 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02723 | hp2 | a0001 | c0003 | t0004 | g0041 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02738 | hp1 | a0002 | c0002 | t0003 | g0073 | SAS | PJL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02809 | hp1 | a0002 | c0002 | t0002 | g0049 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02809 | hp2 | a0003 | c0007 | t0001 | g0025 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02818 | hp1 | a0002 | c0005 | t0002 | g0115 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02818 | hp2 | a0002 | c0006 | t0005 | g0023 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0032 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02886 | hp2 | a0002 | c0002 | t0002 | g0002 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02895 | hp1 | a0002 | c0002 | t0012 | g0066 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02896 | hp1 | a0002 | c0002 | t0002 | g0039 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02896 | hp2 | a0002 | c0002 | t0006 | g0134 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02897 | hp1 | a0002 | c0002 | t0002 | g0038 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02897 | hp2 | a0002 | c0002 | t0012 | g0067 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02922 | hp1 | a0002 | c0002 | t0003 | g0035 | AFR | ESN | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02922 | hp2 | a0003 | c0007 | t0006 | g0029 | AFR | ESN | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02965 | hp1 | a0002 | c0002 | t0008 | g0219 | AFR | ESN | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02970 | hp1 | a0002 | c0002 | t0005 | g0050 | AFR | ESN | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02970 | hp2 | a0002 | c0002 | t0005 | g0016 | AFR | ESN | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02976 | hp1 | a0002 | c0002 | t0007 | g0044 | AFR | ESN | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02976 | hp2 | a0002 | c0002 | t0003 | g0034 | AFR | ESN | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03017 | hp1 | a0012 | c0018 | t0001 | g0099 | SAS | PJL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03041 | hp1 | a0002 | c0002 | t0005 | g0095 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03041 | hp2 | a0002 | c0002 | t0007 | g0118 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03098 | hp1 | a0001 | c0003 | t0001 | g0114 | AFR | MSL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03130 | hp1 | a0002 | c0002 | t0005 | g0113 | AFR | ESN | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03139 | hp1 | a0002 | c0002 | t0005 | g0301 | AFR | ESN | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03195 | hp1 | a0002 | c0002 | t0004 | g0021 | AFR | ESN | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03195 | hp2 | a0002 | c0002 | t0005 | g0117 | AFR | ESN | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03209 | hp1 | a0002 | c0002 | t0006 | g0043 | AFR | MSL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03225 | hp1 | a0002 | c0006 | t0003 | g0036 | AFR | MSL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03239 | hp1 | a0002 | c0002 | t0004 | g0006 | SAS | PJL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03453 | hp1 | a0002 | c0002 | t0005 | g0296 | AFR | MSL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03453 | hp2 | a0001 | c0003 | t0002 | g0045 | AFR | MSL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03486 | hp1 | a0002 | c0002 | t0005 | g0201 | AFR | MSL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03486 | hp2 | a0002 | c0002 | t0003 | g0132 | AFR | MSL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03491 | hp1 | a0002 | c0002 | t0004 | g0145 | SAS | PJL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03491 | hp2 | a0001 | c0001 | t0011 | g0072 | SAS | PJL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03492 | hp1 | a0001 | c0001 | t0011 | g0056 | SAS | PJL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03516 | hp1 | a0001 | c0003 | t0005 | g0177 | AFR | ESN | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03516 | hp2 | a0002 | c0002 | t0003 | g0033 | AFR | ESN | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03540 | hp1 | a0001 | c0003 | t0001 | g0027 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03540 | hp2 | a0002 | c0002 | t0002 | g0244 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03579 | hp1 | a0002 | c0002 | t0005 | g0178 | AFR | MSL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03669 | hp2 | a0002 | c0002 | t0004 | g0302 | SAS | PJL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | STU | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03704 | hp1 | a0002 | c0002 | t0003 | g0207 | SAS | PJL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03710 | hp1 | a0001 | c0001 | t0005 | g0015 | SAS | PJL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03831 | hp1 | a0001 | c0001 | t0008 | g0064 | SAS | BEB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0160 | SAS | BEB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | BEB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | BEB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0012 | SAS | BEB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0190 | SAS | BEB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG04115 | hp1 | a0010 | c0015 | t0001 | g0138 | SAS | STU | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0199 | SAS | BEB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | BEB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | STU | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | STU | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG04228 | hp1 | a0013 | c0017 | t0005 | g0243 | SAS | STU | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | YRI | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18612 | hp1 | a0002 | c0002 | t0004 | g0169 | EAS | CHB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CHB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0030 | AFR | YRI | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18906 | hp2 | a0002 | c0002 | t0005 | g0108 | AFR | YRI | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18939 | hp2 | a0002 | c0002 | t0002 | g0144 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18941 | hp2 | a0002 | c0002 | t0002 | g0141 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18942 | hp2 | a0002 | c0002 | t0004 | g0148 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18945 | hp1 | a0002 | c0002 | t0004 | g0297 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18947 | hp2 | a0001 | c0016 | t0003 | g0233 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18948 | hp1 | a0002 | c0002 | t0004 | g0269 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18950 | hp2 | a0002 | c0002 | t0003 | g0168 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18956 | hp1 | a0001 | c0001 | t0004 | g0309 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18956 | hp2 | a0002 | c0002 | t0002 | g0163 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18959 | hp1 | a0002 | c0002 | t0004 | g0167 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18960 | hp1 | a0002 | c0002 | t0002 | g0152 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18961 | hp1 | a0002 | c0002 | t0004 | g0215 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18965 | hp1 | a0001 | c0004 | t0001 | g0088 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18967 | hp1 | a0002 | c0002 | t0003 | g0299 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18969 | hp2 | a0002 | c0002 | t0004 | g0171 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18971 | hp1 | a0002 | c0002 | t0004 | g0080 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18975 | hp2 | a0002 | c0002 | t0004 | g0172 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18977 | hp1 | a0001 | c0004 | t0001 | g0087 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18979 | hp2 | a0002 | c0002 | t0019 | g0143 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18985 | hp1 | a0014 | c0012 | t0001 | g0305 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18986 | hp1 | a0002 | c0002 | t0002 | g0164 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18987 | hp1 | a0008 | c0014 | t0018 | g0147 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18989 | hp1 | a0002 | c0002 | t0013 | g0311 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0273 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0229 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18993 | hp1 | a0002 | c0002 | t0004 | g0155 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18994 | hp1 | a0001 | c0001 | t0004 | g0093 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0174 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0142 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19001 | hp1 | a0002 | c0002 | t0002 | g0069 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19005 | hp1 | a0002 | c0002 | t0003 | g0166 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19006 | hp1 | a0015 | c0011 | t0002 | g0185 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19007 | hp1 | a0001 | c0001 | t0004 | g0089 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19009 | hp1 | a0002 | c0002 | t0004 | g0156 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19030 | hp1 | a0003 | c0007 | t0006 | g0028 | AFR | LWK | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19030 | hp2 | a0002 | c0002 | t0007 | g0188 | AFR | LWK | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19043 | hp1 | a0002 | c0002 | t0005 | g0122 | AFR | LWK | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0295 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19058 | hp1 | a0002 | c0002 | t0004 | g0175 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19060 | hp1 | a0002 | c0002 | t0003 | g0136 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19063 | hp1 | a0001 | c0001 | t0010 | g0097 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19075 | hp1 | a0001 | c0001 | t0003 | g0303 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19080 | hp1 | a0002 | c0002 | t0003 | g0237 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19083 | hp1 | a0002 | c0002 | t0004 | g0310 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19086 | hp1 | a0001 | c0004 | t0004 | g0090 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19087 | hp2 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19088 | hp1 | a0001 | c0004 | t0002 | g0048 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19090 | hp2 | a0002 | c0002 | t0016 | g0272 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19091 | hp1 | a0002 | c0002 | t0004 | g0082 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19240 | hp1 | a0002 | c0002 | t0005 | g0105 | AFR | YRI | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19240 | hp2 | a0002 | c0002 | t0002 | g0111 | AFR | YRI | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA20752 | hp1 | a0005 | c0009 | t0001 | g0060 | EUR | TSI | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA20805 | hp1 | a0002 | c0002 | t0002 | g0165 | EUR | TSI | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0203 | SAS | GIH | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01123 | hp1 | a0006 | c0010 | t0003 | g0202 | AMR | CLM | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0173 | AMR | CLM | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0047 | AFR | ACB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02109 | hp2 | a0004 | c0008 | t0006 | g0127 | AFR | ACB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02486 | hp1 | a0002 | c0002 | t0003 | g0109 | AFR | ACB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02559 | hp1 | a0002 | c0006 | t0003 | g0120 | AFR | ACB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02559 | hp2 | a0002 | c0002 | t0003 | g0112 | AFR | ACB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0068 | AFR | MSL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG06807 | hp1 | a0002 | c0002 | t0005 | g0106 | AFR | USA | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0271 | AFR | USA | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18955 | hp1 | a0001 | c0001 | t0004 | g0092 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA20300 | hp1 | a0001 | c0001 | t0015 | g0046 | AFR | USA | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA20300 | hp2 | a0009 | c0013 | t0005 | g0037 | AFR | USA | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA21309 | hp1 | a0001 | c0001 | t0007 | g0191 | AFR | LWK | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA21309 | hp2 | a0002 | c0002 | t0007 | g0193 | AFR | LWK | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0153 | REF | REF | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0004 | g0128 | REF | REF | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:2843234
|
C | CA | 1 | a0015 | 1 | NA19006.hp1 | frameshift_variant | HIGH | c.30dupA | p.Leu11fs | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/11 | 205/3192 | 31/1413 | 11/470 | INFO_REALIGN_3_PRIME | chrX | 2843234 | |
| chrX:2843276
|
TG | T | 1 | a0014 | 1 | NA18985.hp1 | frameshift_variant | HIGH | c.75delG | p.Gln26fs | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/11 | 249/3192 | 75/1413 | 25/470 | INFO_REALIGN_3_PRIME | chrX | 2843276 | |
| chrX:2855045
|
C | T | 1 | a0007 | 1 | HG02273.hp1 | missense_variant | MODERATE | c.377C>T | p.Pro126Leu | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 5/11 | 551/3192 | 377/1413 | 126/470 | chrX | 2855045 | ||
| chrX:2859944
|
C | T | 10 | a0001a0003a0005others(7): Show | 183 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(180): Show |
missense_variant | MODERATE | c.716C>T | p.Ala239Val | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 7/11 | 890/3192 | 716/1413 | 239/470 | chrX | 2859944 | ||
| chrX:2861529
|
A | G | 10 | a0001a0003a0006others(7): Show | 181 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(178): Show |
missense_variant | MODERATE | c.845A>G | p.His282Arg | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/11 | 1019/3192 | 845/1413 | 282/470 | chrX | 2861529 | ||
| chrX:2861538
|
T | TG | 1 | a0011 | 1 | HG01175.hp2 | frameshift_variant | HIGH | c.861dupG | p.Pro288fs | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/11 | 1036/3192 | 862/1413 | 288/470 | INFO_REALIGN_3_PRIME | chrX | 2861538 | |
| chrX:2861708
|
C | T | 2 | a0006a0007 | 4 | HG01123.hp1 HG01255.hp1 HG02080.hp1 others(1): Show |
missense_variant | MODERATE | c.1024C>T | p.Arg342Cys | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/11 | 1198/3192 | 1024/1413 | 342/470 | chrX | 2861708 | ||
| chrX:2875870
|
C | A | 2 | a0003a0004 | 7 | HG01261.hp1 HG01891.hp1 HG02109.hp2 others(4): Show |
missense_variant | MODERATE | c.1099C>A | p.Pro367Thr | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 9/11 | 1273/3192 | 1099/1413 | 367/470 | chrX | 2875870 | ||
| chrX:2875910
|
T | C | 2 | a0009a0013 | 2 | HG04228.hp1 NA20300.hp2 |
missense_variant | MODERATE | c.1139T>C | p.Ile380Thr | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 9/11 | 1313/3192 | 1139/1413 | 380/470 | chrX | 2875910 | ||
| chrX:2877241
|
C | CT | 1 | a0008 | 1 | NA18987.hp1 | frameshift_variant | HIGH | c.1187dupT | p.Glu397fs | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/11 | 1362/3192 | 1188/1413 | 396/470 | INFO_REALIGN_3_PRIME | chrX | 2877241 | |
| chrX:2881073
|
T | C | 1 | a0012 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.1273T>C | p.Ser425Pro | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 11/11 | 1447/3192 | 1273/1413 | 425/470 | chrX | 2881073 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:2855013
|
G | A | 1 | a0001c0004 | 6 | HG00408.hp1 HG02165.hp2 NA18965.hp1 others(3): Show |
synonymous_variant | LOW | c.345G>A | p.Glu115Glu | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 5/11 | 519/3192 | 345/1413 | 115/470 | chrX | 2855013 | ||
| chrX:2856568
|
G | A | 3 | a0001c0003a0002c0006a0003c0007 | 20 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(17): Show |
synonymous_variant | LOW | c.558G>A | p.Pro186Pro | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/11 | 732/3192 | 558/1413 | 186/470 | chrX | 2856568 | ||
| chrX:2860050
|
G | A | 1 | a0001c0016 | 1 | NA18947.hp2 | synonymous_variant | LOW | c.822G>A | p.Ala274Ala | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 7/11 | 996/3192 | 822/1413 | 274/470 | chrX | 2860050 | ||
| chrX:2861554
|
G | A | 1 | a0002c0005 | 6 | HG00741.hp2 HG01074.hp1 HG01884.hp2 others(3): Show |
synonymous_variant | LOW | c.870G>A | p.Ala290Ala | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/11 | 1044/3192 | 870/1413 | 290/470 | chrX | 2861554 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:2830163
|
GC | G | 1 | a0002c0002t0013 | 1 | NA18989.hp1 | 5_prime_UTR_variant | MODIFIER | c.-23delC | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/11 | 23 | INFO_REALIGN_3_PRIME | chrX | 2830163 | ||||
| chrX:2881438
|
A | T | 14 | a0001c0001t0003a0001c0016t0003a0002c0002t0003others(11): Show | 63 | HG00423.hp2 HG00673.hp1 HG00738.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*225A>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 11/11 | 225 | chrX | 2881438 | |||||
| chrX:2881577
|
C | G | 1 | a0002c0002t0020 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*364C>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 11/11 | 364 | chrX | 2881577 | |||||
| chrX:2881603
|
T | A | 1 | a0001c0004t0014 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*390T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 11/11 | 390 | chrX | 2881603 | |||||
| chrX:2881753
|
G | GA | 1 | a0002c0002t0019 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*543dupA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 11/11 | 544 | INFO_REALIGN_3_PRIME | chrX | 2881753 | ||||
| chrX:2881778
|
G | A | 1 | a0001c0001t0015 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*565G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 11/11 | 565 | chrX | 2881778 | |||||
| chrX:2881855
|
G | A | 1 | a0002c0002t0012 | 2 | HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*642G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 11/11 | 642 | chrX | 2881855 | |||||
| chrX:2881886
|
TA | T | 1 | a0008c0014t0018 | 1 | NA18987.hp1 | 3_prime_UTR_variant | MODIFIER | c.*676delA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 11/11 | 676 | INFO_REALIGN_3_PRIME | chrX | 2881886 | ||||
| chrX:2882011
|
C | T | 1 | a0001c0001t0017 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*798C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 11/11 | 798 | chrX | 2882011 | |||||
| chrX:2882254
|
G | C | 41 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(38): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
3_prime_UTR_variant | MODIFIER | c.*1041G>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 11/11 | 1041 | chrX | 2882254 | |||||
| chrX:2882271
|
A | T | 1 | a0001c0001t0011 | 2 | HG03491.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1058A>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 11/11 | 1058 | chrX | 2882271 | |||||
| chrX:2882321
|
AG | A | 1 | a0008c0014t0018 | 1 | NA18987.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1111delG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 11/11 | 1111 | INFO_REALIGN_3_PRIME | chrX | 2882321 | ||||
| chrX:2882583
|
G | T | 28 | a0001c0001t0001a0001c0001t0003a0001c0001t0008others(25): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
3_prime_UTR_variant | MODIFIER | c.*1370G>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 11/11 | 1370 | chrX | 2882583 | |||||
| chrX:2882610
|
G | C | 1 | a0001c0001t0009 | 2 | HG01167.hp1 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1397G>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 11/11 | 1397 | chrX | 2882610 | |||||
| chrX:2882636
|
A | G | 41 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(38): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
3_prime_UTR_variant | MODIFIER | c.*1423A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 11/11 | 1423 | chrX | 2882636 | |||||
| chrX:2882747
|
G | A | 1 | a0002c0002t0016 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1534G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 11/11 | 1534 | chrX | 2882747 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:2828988
|
G | GT | 1 | a0002c0002t0013g0311 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-129+14dupT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2828988 | |||||
| chrX:2829036
|
C | CG | 1 | a0002c0002t0004g0310 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-129+67dupG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2829036 | |||||
| chrX:2829044
|
CG | C | 1 | a0002c0002t0013g0311 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-129+75delG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2829044 | |||||
| chrX:2829102
|
C | CG | 1 | a0001c0001t0004g0309 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-129+131dupG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2829102 | |||||
| chrX:2829107
|
C | CG | 3 | a0001c0001t0001g0306a0001c0001t0002g0307a0002c0002t0001g0308 | 3 | HG01952.hp1 NA18987.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-129+137dupG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2829107 | |||||
| chrX:2829107
|
CG | C | 1 | a0002c0002t0013g0311 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-129+137delG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2829107 | |||||
| chrX:2829146
|
A | AG | 1 | a0014c0012t0001g0305 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-129+175dupG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2829146 | |||||
| chrX:2829243
|
C | CG | 1 | a0001c0001t0004g0309 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-129+271dupG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2829243 | |||||
| chrX:2829318
|
AG | A | 1 | a0002c0002t0004g0006 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-129+345delG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2829318 | |||||
| chrX:2829397
|
T | TG | 1 | a0001c0001t0004g0309 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-129+426dupG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2829397 | |||||
| chrX:2829402
|
A | AG | 2 | a0001c0003t0005g0304a0002c0002t0013g0311 | 2 | HG02055.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.-129+433dupG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2829402 | |||||
| chrX:2829402
|
AG | A | 1 | a0007c0020t0003g0007 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-129+433delG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2829402 | |||||
| chrX:2829466
|
G | GA | 1 | a0014c0012t0001g0305 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-129+492dupA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2829466 | |||||
| chrX:2829467
|
AG | A | 1 | a0001c0001t0003g0303 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-129+497delG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2829467 | |||||
| chrX:2829473
|
C | T | 134 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0181others(131): Show | 136 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.-129+498C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 1/10 | chrX | 2829473 | ||||||
| chrX:2829552
|
G | A | 4 | a0001c0003t0005g0177a0002c0002t0001g0008a0002c0002t0001g0179others(1): Show | 4 | HG00733.hp2 HG02258.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-128-509G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 1/10 | chrX | 2829552 | ||||||
| chrX:2829574
|
A | AG | 1 | a0001c0001t0004g0309 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-128-482dupG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2829574 | |||||
| chrX:2829580
|
C | T | 1 | a0002c0005t0002g0176 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-128-481C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 1/10 | chrX | 2829580 | ||||||
| chrX:2829586
|
GC | G | 1 | a0002c0002t0004g0175 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-128-473delC | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2829586 | |||||
| chrX:2829588
|
C | CG | 1 | a0001c0001t0004g0309 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-128-467dupG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2829588 | |||||
| chrX:2829652
|
A | AG | 2 | a0001c0001t0004g0309a0004c0008t0006g0009 | 2 | HG01261.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.-128-405dupG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2829652 | |||||
| chrX:2829662
|
C | T | 43 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(40): Show | 43 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.-128-399C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 1/10 | chrX | 2829662 | ||||||
| chrX:2829683
|
C | CG | 1 | a0002c0002t0002g0174 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-128-372dupG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2829683 | |||||
| chrX:2829786
|
C | CG | 1 | a0002c0002t0004g0175 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-128-270dupG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2829786 | |||||
| chrX:2829786
|
C | T | 1 | a0002c0002t0005g0301 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-128-275C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 1/10 | chrX | 2829786 | ||||||
| chrX:2829823
|
ACGC | A | 1 | a0001c0001t0004g0309 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-128-237_-128-235d others(5): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 1/10 | chrX | 2829823 | ||||||
| chrX:2829829
|
C | CG | 25 | a0001c0001t0001g0135a0001c0001t0001g0181a0001c0001t0001g0182others(22): Show | 25 | HG00738.hp1 HG01175.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.-128-228dupG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2829829 | |||||
| chrX:2829857
|
A | AG | 1 | a0001c0001t0003g0180 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-128-199dupG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2829857 | |||||
| chrX:2829899
|
TG | T | 1 | a0001c0001t0004g0309 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-128-160delG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2829899 | |||||
| chrX:2829926
|
G | C | 3 | a0002c0005t0007g0018a0002c0005t0007g0020a0004c0008t0006g0019 | 3 | HG01074.hp1 HG01891.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-128-135G>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 1/10 | chrX | 2829926 | ||||||
| chrX:2830010
|
T | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(228): Show | 234 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.-128-51T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 1/10 | chrX | 2830010 | ||||||
| chrX:2830017
|
G | GC | 1 | a0001c0001t0004g0309 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-128-42dupC | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2830017 | |||||
| chrX:2830027
|
G | A | 4 | a0001c0001t0002g0192a0001c0001t0007g0191a0002c0002t0005g0301others(1): Show | 4 | HG00733.hp1 HG03139.hp1 NA21309.hp1 others(1): Show |
intron_variant | MODIFIER | c.-128-34G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 1/10 | chrX | 2830027 | ||||||
| chrX:2830211
|
TG | T | 1 | a0002c0002t0013g0311 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.7+17delG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2830211 | ||||||
| chrX:2830212
|
G | C | 287 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(284): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.7+17G>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2830212 | ||||||
| chrX:2830214
|
T | C | 1 | a0002c0002t0013g0311 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.7+19T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2830214 | ||||||
| chrX:2830249
|
G | A | 1 | a0002c0002t0005g0105 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.7+54G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2830249 | ||||||
| chrX:2830251
|
C | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(197): Show | 203 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.7+56C>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2830251 | ||||||
| chrX:2830256
|
T | TG | 1 | a0001c0001t0004g0309 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.7+63dupG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2830256 | |||||
| chrX:2830313
|
TCCC | T | 1 | a0002c0002t0004g0172 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.7+121_7+123delCCC | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2830313 | |||||
| chrX:2830320
|
TAC | T | 1 | a0002c0002t0004g0172 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.7+126_7+127delAC | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2830320 | ||||||
| chrX:2830380
|
G | A | 190 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(187): Show | 193 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.7+185G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2830380 | ||||||
| chrX:2830383
|
AG | A | 1 | a0014c0012t0001g0305 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.7+193delG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2830383 | |||||
| chrX:2830415
|
T | TG | 1 | a0001c0001t0004g0309 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.7+223dupG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2830415 | |||||
| chrX:2830468
|
C | A | 3 | a0001c0001t0015g0046a0002c0002t0001g0008a0002c0002t0001g0047 | 3 | HG00733.hp2 HG02109.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.7+273C>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2830468 | ||||||
| chrX:2830535
|
T | TC | 1 | a0014c0012t0001g0305 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.7+341dupC | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2830535 | |||||
| chrX:2830583
|
GT | G | 1 | a0001c0001t0003g0303 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.7+390delT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2830583 | |||||
| chrX:2830667
|
TC | T | 1 | a0002c0002t0013g0311 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.7+475delC | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2830667 | |||||
| chrX:2830708
|
G | GC | 1 | a0014c0012t0001g0305 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.7+515dupC | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2830708 | |||||
| chrX:2830729
|
T | G | 1 | a0001c0004t0002g0048 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.7+534T>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2830729 | ||||||
| chrX:2830744
|
G | T | 1 | a0002c0002t0004g0171 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.7+549G>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2830744 | ||||||
| chrX:2830758
|
G | GA | 1 | a0014c0012t0001g0305 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.7+570dupA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2830758 | |||||
| chrX:2830768
|
TA | T | 1 | a0002c0002t0013g0311 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.7+578delA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2830768 | |||||
| chrX:2830812
|
A | G | 1 | a0002c0002t0001g0179 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.7+617A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2830812 | ||||||
| chrX:2830827
|
G | T | 6 | a0001c0003t0002g0042a0001c0003t0002g0045a0001c0003t0004g0041others(3): Show | 6 | HG01243.hp1 HG02615.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.7+632G>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2830827 | ||||||
| chrX:2830970
|
A | AG | 1 | a0014c0012t0001g0305 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.7+778dupG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2830970 | |||||
| chrX:2831003
|
G | GC | 1 | a0014c0012t0001g0305 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.7+813dupC | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2831003 | |||||
| chrX:2831003
|
GC | G | 1 | a0002c0002t0013g0311 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.7+813delC | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2831003 | |||||
| chrX:2831024
|
GC | G | 1 | a0001c0001t0003g0303 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.7+833delC | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2831024 | |||||
| chrX:2831091
|
T | G | 1 | a0002c0002t0005g0106 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.7+896T>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2831091 | ||||||
| chrX:2831165
|
T | TC | 1 | a0014c0012t0001g0305 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.7+972dupC | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2831165 | |||||
| chrX:2831213
|
G | T | 1 | a0001c0004t0001g0103 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.7+1018G>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2831213 | ||||||
| chrX:2831215
|
A | T | 1 | a0001c0004t0001g0103 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.7+1020A>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2831215 | ||||||
| chrX:2831294
|
AG | A | 1 | a0002c0002t0013g0311 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.7+1101delG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2831294 | |||||
| chrX:2831350
|
GC | G | 1 | a0001c0001t0001g0306 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.7+1157delC | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2831350 | |||||
| chrX:2831356
|
A | AC | 1 | a0014c0012t0001g0305 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.7+1162dupC | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2831356 | |||||
| chrX:2831358
|
G | C | 2 | a0002c0002t0002g0049a0002c0005t0002g0176 | 2 | HG02280.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.7+1163G>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2831358 | ||||||
| chrX:2831378
|
TA | T | 1 | a0001c0001t0001g0306 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.7+1187delA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2831378 | |||||
| chrX:2831403
|
CT | C | 2 | a0002c0002t0004g0175a0002c0002t0013g0311 | 2 | NA18989.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.7+1214delT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2831403 | |||||
| chrX:2831480
|
T | C | 225 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(222): Show | 228 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.7+1285T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2831480 | ||||||
| chrX:2831490
|
C | CG | 1 | a0002c0002t0013g0311 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.7+1299dupG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2831490 | |||||
| chrX:2831522
|
G | A | 1 | a0001c0001t0003g0195 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.7+1327G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2831522 | ||||||
| chrX:2831579
|
C | T | 4 | a0002c0002t0003g0035a0002c0005t0007g0018a0002c0005t0007g0020others(1): Show | 4 | HG01074.hp1 HG01891.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.7+1384C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2831579 | ||||||
| chrX:2831808
|
G | A | 3 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0298 | 3 | NA18939.hp1 NA18964.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.7+1613G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2831808 | ||||||
| chrX:2831946
|
G | GT | 1 | a0014c0012t0001g0305 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.7+1756dupT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2831946 | |||||
| chrX:2832019
|
G | A | 2 | a0001c0003t0002g0042a0001c0003t0004g0041 | 2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.7+1824G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2832019 | ||||||
| chrX:2832081
|
C | T | 195 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(192): Show | 198 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.7+1886C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2832081 | ||||||
| chrX:2832413
|
C | CT | 198 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(195): Show | 201 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.7+2219dupT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2832413 | |||||
| chrX:2832487
|
TG | T | 1 | a0001c0001t0001g0306 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.7+2295delG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2832487 | |||||
| chrX:2832542
|
CT | C | 1 | a0002c0002t0006g0134 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.7+2356delT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2832542 | |||||
| chrX:2832582
|
T | C | 2 | a0001c0001t0002g0192a0001c0001t0007g0191 | 2 | HG00733.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.7+2387T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2832582 | ||||||
| chrX:2832618
|
T | TC | 1 | a0001c0001t0003g0303 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.7+2425dupC | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2832618 | |||||
| chrX:2832647
|
G | A | 2 | a0002c0002t0002g0141a0002c0002t0002g0142 | 2 | NA18941.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.7+2452G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2832647 | ||||||
| chrX:2832727
|
G | T | 57 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(54): Show | 59 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.7+2532G>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2832727 | ||||||
| chrX:2832834
|
C | T | 2 | a0001c0001t0001g0278a0014c0012t0001g0305 | 2 | NA18983.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.7+2639C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2832834 | ||||||
| chrX:2832860
|
A | G | 1 | a0002c0002t0001g0277 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.7+2665A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2832860 | ||||||
| chrX:2832992
|
G | A | 4 | a0001c0003t0002g0045a0002c0002t0002g0011a0002c0002t0006g0043others(1): Show | 4 | HG02615.hp1 HG02976.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+2797G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2832992 | ||||||
| chrX:2833109
|
TC | T | 1 | a0001c0001t0003g0303 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.7+2917delC | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2833109 | |||||
| chrX:2833119
|
T | C | 272 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(269): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.7+2924T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2833119 | ||||||
| chrX:2833346
|
A | G | 1 | a0002c0002t0003g0035 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.7+3151A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2833346 | ||||||
| chrX:2833386
|
G | T | 4 | a0001c0001t0002g0189a0001c0001t0002g0276a0001c0001t0003g0274others(1): Show | 4 | HG00423.hp2 NA18950.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+3191G>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2833386 | ||||||
| chrX:2833645
|
G | T | 6 | a0001c0001t0001g0133a0002c0002t0003g0132a0002c0002t0005g0016others(3): Show | 6 | HG02572.hp1 HG02630.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.7+3450G>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2833645 | ||||||
| chrX:2833659
|
T | C | 269 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(266): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.7+3464T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2833659 | ||||||
| chrX:2833863
|
C | G | 136 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0181others(133): Show | 137 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.7+3668C>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2833863 | ||||||
| chrX:2833867
|
A | C | 1 | a0002c0002t0003g0035 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.7+3672A>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2833867 | ||||||
| chrX:2834012
|
A | G | 6 | a0002c0002t0003g0033a0002c0002t0003g0034a0002c0002t0003g0035others(3): Show | 6 | HG01074.hp1 HG01891.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.7+3817A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2834012 | ||||||
| chrX:2834029
|
C | T | 78 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(75): Show | 80 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.7+3834C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2834029 | ||||||
| chrX:2834071
|
C | T | 6 | a0001c0001t0004g0003a0001c0001t0004g0129a0001c0001t0004g0130others(3): Show | 6 | HG01099.hp1 HG01123.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.7+3876C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2834071 | ||||||
| chrX:2834201
|
A | C | 1 | a0002c0002t0007g0188 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.7+4006A>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2834201 | ||||||
| chrX:2834201
|
A | T | 1 | a0001c0001t0005g0015 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.7+4006A>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2834201 | ||||||
| chrX:2834292
|
C | T | 84 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(81): Show | 86 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.7+4097C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2834292 | ||||||
| chrX:2834517
|
C | T | 1 | a0002c0002t0005g0117 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.7+4322C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2834517 | ||||||
| chrX:2834575
|
G | GA | 62 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(59): Show | 64 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.7+4381dupA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2834575 | |||||
| chrX:2834592
|
G | C | 7 | a0001c0001t0001g0133a0002c0002t0002g0002a0002c0002t0003g0132others(4): Show | 8 | HG02572.hp1 HG02630.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.7+4397G>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2834592 | ||||||
| chrX:2834624
|
G | A | 3 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0004g0309 | 3 | NA18952.hp1 NA18956.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.7+4429G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2834624 | ||||||
| chrX:2834666
|
A | G | 59 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(56): Show | 61 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.7+4471A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2834666 | ||||||
| chrX:2834829
|
A | G | 1 | a0001c0001t0003g0273 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.7+4634A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2834829 | ||||||
| chrX:2834952
|
T | C | 19 | a0001c0003t0001g0027a0001c0003t0001g0030a0001c0003t0002g0042others(16): Show | 19 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.7+4757T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2834952 | ||||||
| chrX:2834971
|
A | G | 7 | a0001c0001t0001g0133a0002c0002t0002g0002a0002c0002t0003g0132others(4): Show | 8 | HG02572.hp1 HG02630.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.7+4776A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2834971 | ||||||
| chrX:2835009
|
C | G | 1 | a0002c0002t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.7+4814C>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2835009 | ||||||
| chrX:2835015
|
A | AGG | 6 | a0002c0002t0003g0033a0002c0002t0003g0034a0002c0002t0003g0035others(3): Show | 6 | HG01074.hp1 HG01891.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.7+4821_7+4822insGG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2835015 | |||||
| chrX:2835032
|
G | A | 6 | a0002c0002t0003g0033a0002c0002t0003g0034a0002c0002t0003g0035others(3): Show | 6 | HG01074.hp1 HG01891.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.7+4837G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2835032 | ||||||
| chrX:2835034
|
C | G | 6 | a0002c0002t0003g0033a0002c0002t0003g0034a0002c0002t0003g0035others(3): Show | 6 | HG01074.hp1 HG01891.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.7+4839C>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2835034 | ||||||
| chrX:2835054
|
T | A | 6 | a0002c0002t0003g0033a0002c0002t0003g0034a0002c0002t0003g0035others(3): Show | 6 | HG01074.hp1 HG01891.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.7+4859T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2835054 | ||||||
| chrX:2835075
|
G | A | 6 | a0002c0002t0003g0033a0002c0002t0003g0034a0002c0002t0003g0035others(3): Show | 6 | HG01074.hp1 HG01891.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.7+4880G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2835075 | ||||||
| chrX:2835099
|
CG | C | 1 | a0001c0001t0003g0303 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.7+4910delG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2835099 | |||||
| chrX:2835141
|
G | C | 59 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(56): Show | 61 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.7+4946G>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2835141 | ||||||
| chrX:2835251
|
G | A | 6 | a0002c0002t0003g0033a0002c0002t0003g0034a0002c0002t0003g0035others(3): Show | 6 | HG01074.hp1 HG01891.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.7+5056G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2835251 | ||||||
| chrX:2835335
|
T | G | 1 | a0002c0005t0006g0104 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.7+5140T>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2835335 | ||||||
| chrX:2835418
|
T | C | 1 | a0002c0006t0003g0036 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.7+5223T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2835418 | ||||||
| chrX:2835436
|
C | T | 1 | a0002c0002t0016g0272 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.7+5241C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2835436 | ||||||
| chrX:2835486
|
T | C | 122 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(119): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.7+5291T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2835486 | ||||||
| chrX:2835672
|
C | A | 48 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(45): Show | 48 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.7+5477C>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2835672 | ||||||
| chrX:2835675
|
C | T | 9 | a0001c0001t0001g0133a0002c0002t0002g0002a0002c0002t0003g0132others(6): Show | 10 | HG02572.hp1 HG02630.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.7+5480C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2835675 | ||||||
| chrX:2835839
|
G | GA | 1 | a0014c0012t0001g0305 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.7+5645dupA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2835839 | |||||
| chrX:2835907
|
T | A | 2 | a0001c0001t0001g0198a0001c0001t0004g0199 | 2 | HG02040.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.7+5712T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2835907 | ||||||
| chrX:2835953
|
G | A | 4 | a0001c0001t0001g0052a0001c0001t0001g0196a0001c0001t0001g0197others(1): Show | 4 | NA18747.hp1 NA18952.hp1 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+5758G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2835953 | ||||||
| chrX:2836197
|
T | C | 1 | a0001c0001t0002g0200 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.7+6002T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2836197 | ||||||
| chrX:2836498
|
C | T | 7 | a0001c0001t0001g0133a0002c0002t0002g0002a0002c0002t0003g0132others(4): Show | 8 | HG02572.hp1 HG02630.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.7+6303C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2836498 | ||||||
| chrX:2836533
|
G | A | 15 | a0001c0003t0001g0027a0001c0003t0001g0030a0001c0003t0005g0022others(12): Show | 15 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.7+6338G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2836533 | ||||||
| chrX:2836673
|
C | CA | 5 | a0001c0001t0003g0053a0001c0003t0002g0045a0002c0002t0002g0107others(2): Show | 5 | HG02135.hp1 HG02257.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.7+6498dupA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2836673 | |||||
| chrX:2836673
|
C | CAA | 1 | a0002c0002t0006g0043 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.7+6497_7+6498dupAA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2836673 | |||||
| chrX:2836673
|
CA | C | 27 | a0001c0001t0001g0133a0001c0001t0001g0267a0001c0001t0001g0268others(24): Show | 28 | HG01074.hp1 HG01167.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.7+6498delA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2836673 | |||||
| chrX:2836673
|
CAA | C | 51 | a0001c0001t0001g0074a0001c0001t0001g0135a0001c0001t0001g0139others(48): Show | 51 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.7+6497_7+6498delAA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2836673 | |||||
| chrX:2836673
|
CAAA | C | 70 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0078others(67): Show | 72 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.7+6496_7+6498delAA others(1): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2836673 | |||||
| chrX:2836752
|
T | C | 124 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(121): Show | 126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.8-6461T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2836752 | ||||||
| chrX:2836770
|
C | T | 2 | a0001c0001t0004g0003a0011c0019t0004g0003 | 2 | HG01099.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.8-6443C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2836770 | ||||||
| chrX:2836852
|
T | A | 297 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(294): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.8-6361T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2836852 | ||||||
| chrX:2836859
|
CA | C | 3 | a0001c0001t0002g0271a0001c0001t0009g0266a0001c0001t0009g0270 | 3 | HG01167.hp1 HG01169.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.8-6353delA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2836859 | ||||||
| chrX:2836966
|
C | CA | 1 | a0014c0012t0001g0305 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.8-6242dupA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2836966 | |||||
| chrX:2836998
|
AC | A | 1 | a0001c0001t0003g0303 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.8-6211delC | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2836998 | |||||
| chrX:2837048
|
G | A | 15 | a0001c0003t0001g0027a0001c0003t0001g0030a0001c0003t0005g0022others(12): Show | 15 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.8-6165G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2837048 | ||||||
| chrX:2837127
|
G | A | 2 | a0002c0006t0003g0120a0002c0006t0005g0119 | 2 | HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.8-6086G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2837127 | ||||||
| chrX:2837268
|
G | A | 1 | a0002c0005t0006g0104 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.8-5945G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2837268 | ||||||
| chrX:2837380
|
T | TA | 1 | a0001c0001t0003g0303 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.8-5831dupA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2837380 | |||||
| chrX:2837431
|
CT | C | 1 | a0001c0001t0003g0303 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.8-5779delT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2837431 | |||||
| chrX:2837447
|
A | AG | 1 | a0001c0001t0003g0303 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.8-5765dupG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2837447 | |||||
| chrX:2837553
|
G | A | 5 | a0001c0003t0002g0045a0002c0002t0002g0011a0002c0002t0006g0043others(2): Show | 5 | HG02615.hp1 HG02976.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.8-5660G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2837553 | ||||||
| chrX:2837567
|
GT | G | 1 | a0002c0002t0003g0035 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.8-5644delT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2837567 | |||||
| chrX:2837609
|
CT | C | 1 | a0014c0012t0001g0305 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.8-5600delT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2837609 | |||||
| chrX:2837723
|
A | AATTG | 4 | a0001c0001t0007g0191a0002c0002t0005g0201a0002c0002t0005g0301others(1): Show | 4 | HG03139.hp1 HG03486.hp1 NA21309.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-5489_8-5486dupAT others(2): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2837723 | |||||
| chrX:2837723
|
A | ATG | 1 | a0001c0001t0002g0192 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.8-5490_8-5489insTG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2837723 | ||||||
| chrX:2837734
|
G | A | 1 | a0002c0002t0005g0016 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.8-5479G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2837734 | ||||||
| chrX:2837751
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.8-5462T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2837751 | ||||||
| chrX:2837754
|
CA | C | 1 | a0002c0002t0003g0168 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.8-5458delA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2837754 | ||||||
| chrX:2837838
|
T | TAC | 16 | a0001c0001t0001g0182a0001c0001t0002g0125a0001c0001t0004g0003others(13): Show | 16 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.8-5345_8-5344dupCA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2837838 | |||||
| chrX:2837838
|
T | TACACAC | 3 | a0002c0005t0007g0018a0002c0005t0007g0020a0004c0008t0006g0019 | 3 | HG01074.hp1 HG01891.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.8-5349_8-5344dupCA others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2837838 | |||||
| chrX:2837838
|
TAC | T | 47 | a0001c0001t0002g0261a0001c0001t0002g0262a0001c0001t0004g0068others(44): Show | 47 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.8-5345_8-5344delCA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2837838 | |||||
| chrX:2837838
|
TACAC | T | 12 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0278others(9): Show | 12 | HG00423.hp1 HG00438.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.8-5347_8-5344delCA others(2): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2837838 | |||||
| chrX:2837838
|
TACACAC | T | 17 | a0001c0003t0001g0027a0001c0003t0001g0030a0001c0003t0005g0022others(14): Show | 17 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.8-5349_8-5344delCA others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2837838 | |||||
| chrX:2837838
|
TACACACA others(1): Show |
T | 106 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(103): Show | 108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.8-5351_8-5344delCA others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2837838 | |||||
| chrX:2837838
|
TACACACA others(3): Show |
T | 1 | a0001c0001t0001g0306 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.8-5353_8-5344delCA others(8): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2837838 | |||||
| chrX:2837838
|
TACACACA others(11): Show |
T | 2 | a0002c0006t0003g0036a0009c0013t0005g0037 | 2 | HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.8-5361_8-5344delCA others(16): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2837838 | |||||
| chrX:2837852
|
C | A | 9 | a0001c0001t0001g0133a0002c0002t0002g0002a0002c0002t0003g0010others(6): Show | 10 | HG02572.hp1 HG02630.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.8-5361C>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2837852 | ||||||
| chrX:2837870
|
T | A | 2 | a0002c0006t0003g0036a0009c0013t0005g0037 | 2 | HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.8-5343T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2837870 | ||||||
| chrX:2837875
|
A | G | 2 | a0002c0002t0003g0166a0002c0002t0004g0167 | 2 | NA18959.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.8-5338A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2837875 | ||||||
| chrX:2837884
|
C | CAT | 2 | a0006c0010t0003g0202a0007c0020t0003g0007 | 2 | HG01123.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.8-5329_8-5328insAT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2837884 | ||||||
| chrX:2837884
|
C | T | 156 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0181others(153): Show | 157 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.8-5329C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2837884 | ||||||
| chrX:2837903
|
G | A | 1 | a0002c0005t0002g0176 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.8-5310G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2837903 | ||||||
| chrX:2837936
|
T | TGG | 1 | a0001c0001t0003g0303 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.8-5276_8-5275dupGG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2837936 | |||||
| chrX:2837999
|
TC | T | 1 | a0001c0001t0003g0303 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.8-5211delC | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2837999 | |||||
| chrX:2838029
|
C | CA | 78 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(75): Show | 80 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.8-5171dupA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2838029 | |||||
| chrX:2838029
|
C | CAA | 43 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0194others(40): Show | 43 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.8-5172_8-5171dupAA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2838029 | |||||
| chrX:2838029
|
C | CAAA | 3 | a0001c0001t0001g0135a0002c0002t0004g0172a0002c0005t0002g0176 | 3 | HG02280.hp1 HG03927.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.8-5173_8-5171dupAA others(1): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2838029 | |||||
| chrX:2838029
|
CA | C | 2 | a0001c0001t0003g0303a0002c0002t0005g0116 | 2 | HG01884.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.8-5171delA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2838029 | |||||
| chrX:2838089
|
G | GA | 1 | a0001c0001t0003g0303 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.8-5121dupA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2838089 | |||||
| chrX:2838159
|
G | GA | 1 | a0001c0001t0003g0303 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.8-5051dupA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2838159 | |||||
| chrX:2838372
|
T | C | 122 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(119): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.8-4841T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2838372 | ||||||
| chrX:2838388
|
G | A | 13 | a0001c0003t0001g0114a0002c0002t0002g0107a0002c0002t0002g0111others(10): Show | 13 | HG01884.hp1 HG02257.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.8-4825G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2838388 | ||||||
| chrX:2838412
|
T | C | 1 | a0001c0001t0002g0307 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.8-4801T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2838412 | ||||||
| chrX:2838436
|
T | TCCCCTC | 1 | a0001c0001t0003g0303 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.8-4773_8-4768dupCT others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2838436 | |||||
| chrX:2838452
|
C | CCCCTCCC others(14): Show |
2 | a0002c0002t0003g0109a0002c0002t0005g0108 | 2 | HG02486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.8-4754_8-4753insCT others(19): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2838452 | |||||
| chrX:2838452
|
C | CCCCTCCC others(9): Show |
278 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(275): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.8-4748_8-4747insCT others(14): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2838452 | |||||
| chrX:2838452
|
C | CCCTTCCT others(4): Show |
1 | a0001c0001t0003g0303 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.8-4759_8-4758insTT others(9): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2838452 | |||||
| chrX:2838775
|
AT | A | 59 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(56): Show | 61 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.8-4433delT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2838775 | |||||
| chrX:2838866
|
GA | G | 1 | a0001c0001t0003g0303 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.8-4346delA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2838866 | ||||||
| chrX:2839095
|
G | A | 1 | a0002c0002t0002g0144 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.8-4118G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2839095 | ||||||
| chrX:2839192
|
A | G | 122 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(119): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.8-4021A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2839192 | ||||||
| chrX:2839295
|
GT | G | 1 | a0001c0001t0003g0303 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.8-3914delT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2839295 | |||||
| chrX:2839337
|
T | TG | 1 | a0001c0001t0003g0303 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.8-3876_8-3875insG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2839337 | ||||||
| chrX:2839358
|
C | T | 122 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(119): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.8-3855C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2839358 | ||||||
| chrX:2839377
|
GA | G | 1 | a0001c0001t0003g0303 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.8-3833delA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2839377 | |||||
| chrX:2839502
|
TG | T | 1 | a0001c0001t0003g0303 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.8-3709delG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2839502 | |||||
| chrX:2839626
|
A | G | 21 | a0001c0003t0001g0114a0001c0003t0002g0045a0002c0002t0002g0011others(18): Show | 21 | HG01884.hp1 HG01884.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.8-3587A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2839626 | ||||||
| chrX:2839630
|
G | A | 2 | a0002c0002t0002g0107a0002c0002t0003g0110 | 2 | HG02257.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.8-3583G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2839630 | ||||||
| chrX:2839707
|
G | A | 280 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(277): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.8-3506G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2839707 | ||||||
| chrX:2839708
|
C | T | 1 | a0002c0002t0007g0193 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.8-3505C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2839708 | ||||||
| chrX:2839713
|
T | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(120): Show | 125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.8-3500T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2839713 | ||||||
| chrX:2839732
|
T | C | 1 | a0002c0002t0002g0002 | 2 | HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.8-3481T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2839732 | ||||||
| chrX:2839742
|
G | A | 157 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0181others(154): Show | 158 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.8-3471G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2839742 | ||||||
| chrX:2839790
|
GA | G | 1 | a0001c0001t0003g0303 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.8-3420delA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2839790 | |||||
| chrX:2839874
|
C | T | 11 | a0001c0001t0001g0133a0002c0002t0002g0002a0002c0002t0003g0010others(8): Show | 12 | HG02572.hp1 HG02630.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.8-3339C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2839874 | ||||||
| chrX:2839875
|
G | A | 1 | a0002c0002t0003g0299 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.8-3338G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2839875 | ||||||
| chrX:2839932
|
G | GGGA | 1 | a0015c0011t0002g0185 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.8-3280_8-3279insGA others(1): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2839932 | |||||
| chrX:2839934
|
A | T | 1 | a0015c0011t0002g0185 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.8-3279A>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2839934 | ||||||
| chrX:2839963
|
A | C | 1 | a0002c0002t0004g0021 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.8-3250A>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2839963 | ||||||
| chrX:2840171
|
G | GT | 1 | a0001c0001t0003g0303 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.8-3040dupT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2840171 | |||||
| chrX:2840230
|
C | T | 2 | a0001c0001t0001g0249a0001c0001t0001g0250 | 2 | HG01081.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.8-2983C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2840230 | ||||||
| chrX:2840236
|
A | AG | 1 | a0015c0011t0002g0185 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.8-2975dupG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2840236 | |||||
| chrX:2840302
|
G | GGT | 1 | a0015c0011t0002g0185 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.8-2911_8-2910insGT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2840302 | ||||||
| chrX:2840357
|
TC | T | 1 | a0001c0001t0003g0303 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.8-2853delC | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2840357 | |||||
| chrX:2840446
|
C | T | 12 | a0001c0003t0001g0027a0001c0003t0001g0030a0001c0003t0005g0022others(9): Show | 12 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.8-2767C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2840446 | ||||||
| chrX:2840486
|
T | TG | 1 | a0001c0001t0003g0303 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.8-2727_8-2726insG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2840486 | ||||||
| chrX:2840502
|
G | C | 1 | a0001c0001t0002g0203 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.8-2711G>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2840502 | ||||||
| chrX:2840567
|
GATAATGG others(19): Show |
G | 1 | a0001c0001t0009g0266 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.8-2642_8-2617delAT others(24): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2840567 | |||||
| chrX:2840583
|
ATT | A | 1 | a0014c0012t0001g0305 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.8-2628_8-2627delTT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2840583 | |||||
| chrX:2840650
|
A | G | 2 | a0002c0002t0003g0033a0002c0002t0003g0034 | 2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.8-2563A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2840650 | ||||||
| chrX:2840756
|
TGATA | T | 7 | a0001c0001t0001g0133a0002c0002t0002g0002a0002c0002t0003g0132others(4): Show | 8 | HG02572.hp1 HG02630.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.8-2452_8-2449delGA others(2): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2840756 | |||||
| chrX:2840875
|
T | C | 2 | a0002c0002t0003g0010a0002c0002t0004g0021 | 2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.8-2338T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2840875 | ||||||
| chrX:2840911
|
G | GT | 1 | a0015c0011t0002g0185 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.8-2301dupT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2840911 | |||||
| chrX:2840922
|
G | GA | 1 | a0001c0001t0003g0303 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.8-2290dupA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2840922 | |||||
| chrX:2840982
|
TGATA | T | 1 | a0001c0001t0001g0248 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.8-2223_8-2220delAG others(2): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2840982 | |||||
| chrX:2841004
|
TATAG | T | 231 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(228): Show | 234 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.8-2195_8-2192delTA others(2): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2841004 | |||||
| chrX:2841169
|
G | GATAGACA others(14): Show |
1 | a0014c0012t0001g0305 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.8-2040_8-2020dupGA others(19): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2841169 | |||||
| chrX:2841207
|
G | T | 1 | a0001c0001t0003g0102 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.8-2006G>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2841207 | ||||||
| chrX:2841326
|
TGATA | T | 2 | a0002c0002t0001g0170a0002c0002t0002g0165 | 2 | HG00099.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.8-1881_8-1878delAT others(2): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2841326 | |||||
| chrX:2841364
|
TGATA | T | 163 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0101others(160): Show | 164 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.8-1841_8-1838delAG others(2): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2841364 | |||||
| chrX:2841398
|
TGATA | T | 1 | a0001c0001t0001g0078 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.8-1810_8-1807delGA others(2): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2841398 | |||||
| chrX:2841415
|
A | AATGG | 6 | a0001c0001t0001g0133a0002c0002t0003g0132a0002c0002t0005g0016others(3): Show | 6 | HG02572.hp1 HG02630.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.8-1788_8-1785dupTG others(2): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2841415 | |||||
| chrX:2841574
|
C | G | 124 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(121): Show | 126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.8-1639C>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2841574 | ||||||
| chrX:2841587
|
G | GA | 1 | a0015c0011t0002g0185 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.8-1626_8-1625insA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2841587 | ||||||
| chrX:2841631
|
A | AT | 1 | a0015c0011t0002g0185 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.8-1579dupT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2841631 | |||||
| chrX:2841656
|
C | G | 1 | a0002c0002t0003g0035 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.8-1557C>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2841656 | ||||||
| chrX:2841713
|
G | A | 1 | a0002c0006t0005g0119 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.8-1500G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2841713 | ||||||
| chrX:2842019
|
T | C | 122 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(119): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.8-1194T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2842019 | ||||||
| chrX:2842045
|
A | G | 1 | a0002c0002t0003g0035 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.8-1168A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2842045 | ||||||
| chrX:2842185
|
C | CTTTCTTT | 154 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0181others(151): Show | 155 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.8-1010_8-1004dupCT others(5): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2842185 | |||||
| chrX:2842185
|
CTTTCTTT | C | 3 | a0002c0002t0005g0126a0004c0008t0006g0009a0004c0008t0006g0127 | 3 | HG01261.hp1 HG02109.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.8-1010_8-1004delCT others(5): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2842185 | |||||
| chrX:2842253
|
A | G | 122 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(119): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.8-960A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2842253 | ||||||
| chrX:2842265
|
G | A | 7 | a0001c0001t0001g0133a0002c0002t0002g0002a0002c0002t0003g0132others(4): Show | 8 | HG02572.hp1 HG02630.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.8-948G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2842265 | ||||||
| chrX:2842361
|
A | AT | 2 | a0001c0001t0003g0065a0001c0001t0007g0191 | 2 | HG01978.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.8-839dupT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2842361 | |||||
| chrX:2842361
|
AT | A | 47 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(44): Show | 47 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.8-839delT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2842361 | |||||
| chrX:2842388
|
G | C | 2 | a0001c0003t0002g0042a0001c0003t0004g0041 | 2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.8-825G>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2842388 | ||||||
| chrX:2842437
|
T | TC | 1 | a0014c0012t0001g0305 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.8-771dupC | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2842437 | |||||
| chrX:2842449
|
G | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(71): Show | 76 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.8-764G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2842449 | ||||||
| chrX:2842458
|
A | G | 123 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(120): Show | 125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.8-755A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2842458 | ||||||
| chrX:2842553
|
C | T | 1 | a0001c0003t0005g0177 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.8-660C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2842553 | ||||||
| chrX:2842605
|
G | GGTGA | 1 | a0015c0011t0002g0185 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.8-605_8-602dupGAGT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2842605 | |||||
| chrX:2842736
|
T | TC | 1 | a0015c0011t0002g0185 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.8-475dupC | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2842736 | |||||
| chrX:2842743
|
GTGTTT | G | 158 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0181others(155): Show | 159 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.8-459_8-455delTGTT others(1): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2842743 | |||||
| chrX:2842816
|
A | AT | 128 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0181others(125): Show | 129 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.8-381dupT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2842816 | |||||
| chrX:2842816
|
A | ATT | 7 | a0001c0001t0001g0184a0001c0001t0001g0247a0001c0001t0003g0295others(4): Show | 7 | HG03486.hp1 HG03669.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.8-382_8-381dupTT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2842816 | |||||
| chrX:2842816
|
AT | A | 1 | a0002c0002t0004g0145 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.8-381delT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2842816 | |||||
| chrX:2842935
|
T | G | 122 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(119): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.8-278T>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2842935 | ||||||
| chrX:2842938
|
C | CT | 1 | a0015c0011t0002g0185 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.8-275_8-274insT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2842938 | ||||||
| chrX:2843009
|
C | T | 47 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(44): Show | 47 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.8-204C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2843009 | ||||||
| chrX:2843112
|
C | CATGAATT others(17): Show |
1 | a0002c0002t0005g0117 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.8-101_8-100insATGA others(20): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2843112 | ||||||
| chrX:2843147
|
C | T | 1 | a0001c0001t0004g0246 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.8-66C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2843147 | ||||||
| chrX:2843152
|
G | GC | 1 | a0014c0012t0001g0305 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.8-57dupC | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2843152 | |||||
| chrX:2843371
|
C | T | 11 | a0001c0001t0001g0133a0002c0002t0002g0002a0002c0002t0003g0010others(8): Show | 12 | HG02572.hp1 HG02630.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.149+17C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2843371 | ||||||
| chrX:2843417
|
C | T | 21 | a0001c0003t0001g0114a0001c0003t0002g0045a0002c0002t0002g0011others(18): Show | 21 | HG01884.hp1 HG01884.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.149+63C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2843417 | ||||||
| chrX:2843475
|
GC | G | 1 | a0015c0011t0002g0185 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.149+123delC | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2843475 | |||||
| chrX:2843500
|
C | T | 4 | a0002c0005t0006g0104a0002c0005t0007g0018a0002c0005t0007g0020others(1): Show | 4 | HG00741.hp2 HG01074.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+146C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2843500 | ||||||
| chrX:2843626
|
CT | C | 1 | a0001c0001t0003g0303 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.149+278delT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2843626 | |||||
| chrX:2843683
|
A | G | 141 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(138): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.149+329A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2843683 | ||||||
| chrX:2843704
|
AC | A | 1 | a0014c0012t0001g0305 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.149+352delC | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2843704 | |||||
| chrX:2843760
|
G | C | 1 | a0001c0001t0003g0303 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.149+406G>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2843760 | ||||||
| chrX:2843766
|
A | G | 1 | a0003c0007t0006g0031 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.149+412A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2843766 | ||||||
| chrX:2843779
|
GC | G | 1 | a0015c0011t0002g0185 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.149+430delC | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2843779 | |||||
| chrX:2843790
|
C | T | 1 | a0012c0018t0001g0099 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.149+436C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2843790 | ||||||
| chrX:2843876
|
A | G | 123 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(120): Show | 125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.149+522A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2843876 | ||||||
| chrX:2843887
|
C | T | 1 | a0002c0002t0003g0035 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.149+533C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2843887 | ||||||
| chrX:2843898
|
TC | T | 1 | a0015c0011t0002g0185 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.149+547delC | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2843898 | |||||
| chrX:2843948
|
T | TC | 1 | a0014c0012t0001g0305 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.149+595dupC | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2843948 | |||||
| chrX:2843997
|
A | G | 1 | a0001c0001t0001g0206 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.149+643A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2843997 | ||||||
| chrX:2844051
|
TA | T | 1 | a0014c0012t0001g0305 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.149+700delA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844051 | |||||
| chrX:2844102
|
A | G | 1 | a0004c0008t0006g0127 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.149+748A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844102 | ||||||
| chrX:2844137
|
G | A | 122 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(119): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.149+783G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844137 | ||||||
| chrX:2844221
|
C | G | 1 | a0001c0001t0004g0068 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.149+867C>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844221 | ||||||
| chrX:2844242
|
TA | T | 1 | a0014c0012t0001g0305 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.149+894delA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844242 | |||||
| chrX:2844261
|
T | TC | 1 | a0014c0012t0001g0305 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.149+909dupC | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844261 | |||||
| chrX:2844303
|
A | G | 1 | a0002c0005t0002g0176 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.149+949A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844303 | ||||||
| chrX:2844335
|
A | T | 1 | a0002c0002t0005g0301 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.149+981A>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844335 | ||||||
| chrX:2844366
|
C | G | 59 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(56): Show | 61 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.149+1012C>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844366 | ||||||
| chrX:2844445
|
A | T | 4 | a0002c0005t0006g0104a0002c0005t0007g0018a0002c0005t0007g0020others(1): Show | 4 | HG00741.hp2 HG01074.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+1091A>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844445 | ||||||
| chrX:2844474
|
A | ATATATAT others(21): Show |
1 | a0001c0001t0003g0180 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.149+1135_149+1162d others(30): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844474 | |||||
| chrX:2844489
|
T | TGCACGCG others(21): Show |
2 | a0001c0001t0004g0129a0001c0001t0004g0173 | 2 | HG01123.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.149+1142_149+1143i others(30): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844489 | |||||
| chrX:2844489
|
T | TGCACGCG others(21): Show |
1 | a0001c0001t0001g0205 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.149+1140_149+1167d others(30): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844489 | |||||
| chrX:2844497
|
T | C | 11 | a0001c0001t0002g0192a0001c0001t0004g0003a0001c0001t0004g0129others(8): Show | 11 | HG00733.hp1 HG00741.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.149+1143T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844497 | ||||||
| chrX:2844497
|
T | TGTGCGTA others(21): Show |
1 | a0002c0002t0004g0269 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.149+1144_149+1171d others(30): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844497 | |||||
| chrX:2844498
|
G | GTGCGTAT others(21): Show |
3 | a0001c0001t0003g0208a0002c0002t0003g0207a0002c0002t0005g0301 | 3 | HG03139.hp1 HG03704.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.149+1182_149+1209d others(30): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844498 | |||||
| chrX:2844498
|
GTGCGTAT others(21): Show |
G | 6 | a0001c0004t0001g0103a0002c0002t0003g0033a0002c0002t0003g0034others(3): Show | 6 | HG00408.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.149+1182_149+1209d others(30): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844498 | |||||
| chrX:2844504
|
ATATATGT others(47): Show |
A | 3 | a0002c0006t0002g0121a0002c0006t0003g0120a0002c0006t0005g0119 | 3 | HG02280.hp2 HG02559.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.149+1182_149+1235d others(56): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844504 | |||||
| chrX:2844504
|
ATATATGT others(73): Show |
A | 73 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(70): Show | 75 | HG00140.hp1 HG00323.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.149+1182_149+1261d others(82): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844504 | |||||
| chrX:2844504
|
ATATATGT others(99): Show |
A | 1 | a0002c0005t0006g0104 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.149+1182_149+1287d others(2): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844504 | |||||
| chrX:2844508
|
A | ATGTGTAT others(93): Show |
1 | a0009c0013t0005g0037 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.149+1167_149+1168i others(102): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844508 | |||||
| chrX:2844508
|
A | ATGTGTAT others(117): Show |
1 | a0002c0006t0003g0036 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.149+1167_149+1168i others(126): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844508 | |||||
| chrX:2844516
|
A | T | 1 | a0002c0002t0003g0035 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.149+1162A>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844516 | ||||||
| chrX:2844517
|
C | T | 1 | a0002c0002t0005g0201 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.149+1163C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844517 | ||||||
| chrX:2844522
|
A | G | 5 | a0001c0001t0004g0003a0001c0001t0004g0130a0001c0001t0004g0131others(2): Show | 5 | HG01099.hp1 HG01123.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.149+1168A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844522 | ||||||
| chrX:2844524
|
G | A | 1 | a0001c0001t0002g0085 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.149+1170G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844524 | ||||||
| chrX:2844526
|
A | G | 7 | a0001c0001t0001g0245a0001c0001t0004g0003a0001c0001t0004g0129others(4): Show | 7 | HG01099.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.149+1172A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844526 | ||||||
| chrX:2844530
|
GTA | G | 49 | a0001c0001t0001g0133a0001c0001t0001g0135a0001c0001t0001g0139others(46): Show | 50 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.149+1182_149+1183d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844530 | |||||
| chrX:2844530
|
GTATATAT others(73): Show |
G | 3 | a0002c0005t0007g0018a0002c0005t0007g0020a0004c0008t0006g0019 | 3 | HG01074.hp1 HG01891.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.149+1182_149+1261d others(82): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844530 | |||||
| chrX:2844531
|
T | C | 2 | a0002c0002t0005g0178a0002c0002t0006g0017 | 2 | HG02572.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.149+1177T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844531 | ||||||
| chrX:2844532
|
A | ATATATGT others(19): Show |
4 | a0001c0001t0009g0266a0002c0002t0001g0123a0002c0002t0001g0124others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+1381_149+1406d others(28): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844532 | |||||
| chrX:2844532
|
A | ATATATGT others(73): Show |
3 | a0001c0001t0001g0264a0001c0001t0001g0278a0006c0010t0003g0187 | 3 | HG02015.hp1 HG02080.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.149+1209_149+1210i others(82): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844532 | |||||
| chrX:2844532
|
A | ATATATGT others(99): Show |
1 | a0001c0001t0001g0263 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.149+1209_149+1210i others(108): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844532 | |||||
| chrX:2844532
|
A | ATATATGT others(45): Show |
1 | a0002c0002t0005g0126 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.149+1355_149+1406d others(54): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844532 | |||||
| chrX:2844532
|
A | ATATATGT others(99): Show |
2 | a0001c0001t0004g0130a0001c0001t0004g0131 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.149+1195_149+1196i others(108): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844532 | |||||
| chrX:2844532
|
A | ATATGTGT others(41): Show |
1 | a0002c0002t0003g0035 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.149+1181_149+1182i others(50): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844532 | |||||
| chrX:2844532
|
A | ATATGTGT others(67): Show |
1 | a0002c0002t0004g0021 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.149+1181_149+1182i others(76): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844532 | |||||
| chrX:2844532
|
A | ATATGTGT others(65): Show |
1 | a0002c0002t0003g0010 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.149+1181_149+1182i others(74): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844532 | |||||
| chrX:2844532
|
ATATATGT others(19): Show |
A | 5 | a0001c0001t0001g0240a0001c0001t0001g0268a0001c0001t0003g0241others(2): Show | 5 | HG02074.hp1 HG02165.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.149+1381_149+1406d others(28): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844532 | |||||
| chrX:2844532
|
ATATATGT others(71): Show |
A | 1 | a0001c0001t0002g0125 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.149+1329_149+1406d others(80): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844532 | |||||
| chrX:2844533
|
T | TGTGTGTA others(95): Show |
2 | a0002c0002t0005g0016a0002c0002t0006g0134 | 2 | HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.149+1179_149+1180i others(104): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844533 | ||||||
| chrX:2844533
|
T | TGTGTGTA others(121): Show |
1 | a0002c0002t0006g0017 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.149+1179_149+1180i others(130): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844533 | ||||||
| chrX:2844533
|
T | TGTGTGTA others(147): Show |
1 | a0002c0002t0005g0178 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.149+1179_149+1180i others(156): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844533 | ||||||
| chrX:2844536
|
A | G | 11 | a0001c0001t0001g0133a0002c0002t0002g0002a0002c0002t0003g0010others(8): Show | 12 | HG02572.hp1 HG02630.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.149+1182A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844536 | ||||||
| chrX:2844549
|
C | CACGCATG others(91): Show |
1 | a0002c0002t0003g0132 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.149+1204_149+1205i others(100): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844549 | |||||
| chrX:2844550
|
A | G | 5 | a0001c0001t0004g0003a0001c0001t0004g0130a0001c0001t0004g0131others(2): Show | 5 | HG01099.hp1 HG01123.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.149+1196A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844550 | ||||||
| chrX:2844550
|
ACG | A | 41 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(38): Show | 41 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.149+1198_149+1199d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844550 | |||||
| chrX:2844552
|
G | A | 4 | a0001c0004t0001g0103a0002c0002t0005g0050a0002c0002t0006g0051others(1): Show | 4 | HG00408.hp1 HG02622.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+1198G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844552 | ||||||
| chrX:2844553
|
CAT | C | 1 | a0001c0001t0002g0085 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.149+1200_149+1201d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844553 | ||||||
| chrX:2844554
|
A | G | 7 | a0001c0001t0001g0245a0001c0001t0004g0003a0001c0001t0004g0129others(4): Show | 7 | HG01099.hp1 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.149+1200A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844554 | ||||||
| chrX:2844555
|
T | C | 41 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(38): Show | 41 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.149+1201T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844555 | ||||||
| chrX:2844558
|
G | GTA | 4 | a0001c0001t0004g0003a0001c0003t0005g0177a0011c0019t0004g0003others(1): Show | 4 | HG01099.hp1 HG01175.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+1208_149+1209d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844558 | |||||
| chrX:2844559
|
T | C | 4 | a0002c0002t0003g0132a0002c0002t0005g0016a0002c0002t0006g0017others(1): Show | 4 | HG02572.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+1205T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844559 | ||||||
| chrX:2844559
|
T | TATGTGTG others(117): Show |
1 | a0001c0001t0001g0133 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.149+1207_149+1208i others(126): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844559 | |||||
| chrX:2844562
|
A | G | 11 | a0001c0001t0001g0133a0002c0002t0002g0002a0002c0002t0003g0010others(8): Show | 12 | HG02572.hp1 HG02630.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.149+1208A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844562 | ||||||
| chrX:2844576
|
A | G | 2 | a0001c0001t0004g0003a0011c0019t0004g0003 | 2 | HG01099.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.149+1222A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844576 | ||||||
| chrX:2844578
|
G | A | 2 | a0001c0001t0001g0135a0002c0002t0001g0146 | 2 | HG00099.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.149+1224G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844578 | ||||||
| chrX:2844579
|
CAT | C | 5 | a0001c0001t0002g0085a0001c0004t0001g0103a0002c0002t0005g0050others(2): Show | 5 | HG00408.hp1 HG02293.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.149+1226_149+1227d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844579 | ||||||
| chrX:2844580
|
A | G | 6 | a0001c0001t0004g0003a0001c0001t0004g0129a0001c0001t0004g0130others(3): Show | 6 | HG01099.hp1 HG01123.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.149+1226A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844580 | ||||||
| chrX:2844585
|
T | C | 4 | a0001c0001t0001g0133a0002c0002t0003g0132a0002c0002t0006g0017others(1): Show | 4 | HG02572.hp1 HG02630.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+1231T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844585 | ||||||
| chrX:2844588
|
A | G | 11 | a0001c0001t0001g0133a0002c0002t0002g0002a0002c0002t0003g0010others(8): Show | 12 | HG02572.hp1 HG02630.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.149+1234A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844588 | ||||||
| chrX:2844602
|
A | G | 2 | a0001c0001t0004g0003a0011c0019t0004g0003 | 2 | HG01099.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.149+1248A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844602 | ||||||
| chrX:2844602
|
ACG | A | 3 | a0002c0006t0002g0121a0002c0006t0003g0120a0002c0006t0005g0119 | 3 | HG02280.hp2 HG02559.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.149+1250_149+1251d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844602 | |||||
| chrX:2844604
|
G | A | 54 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(51): Show | 56 | HG00140.hp1 HG00323.hp1 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.149+1250G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844604 | ||||||
| chrX:2844605
|
CAT | C | 4 | a0001c0004t0001g0103a0002c0002t0005g0050a0002c0002t0006g0051others(1): Show | 4 | HG00408.hp1 HG02622.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+1252_149+1253d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844605 | ||||||
| chrX:2844606
|
A | G | 6 | a0001c0001t0004g0003a0001c0001t0004g0129a0001c0001t0004g0130others(3): Show | 6 | HG01099.hp1 HG01123.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.149+1252A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844606 | ||||||
| chrX:2844607
|
T | C | 3 | a0002c0006t0002g0121a0002c0006t0003g0120a0002c0006t0005g0119 | 3 | HG02280.hp2 HG02559.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.149+1253T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844607 | ||||||
| chrX:2844608
|
GCGTATAT others(143): Show |
G | 2 | a0002c0002t0003g0033a0002c0002t0003g0034 | 2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.149+1260_149+1409d others(2): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844608 | |||||
| chrX:2844611
|
T | C | 3 | a0001c0001t0001g0133a0002c0002t0003g0132a0002c0002t0006g0017 | 3 | HG02572.hp1 HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.149+1257T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844611 | ||||||
| chrX:2844614
|
A | G | 11 | a0001c0001t0001g0133a0002c0002t0002g0002a0002c0002t0003g0010others(8): Show | 12 | HG02572.hp1 HG02630.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.149+1260A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844614 | ||||||
| chrX:2844622
|
A | G | 41 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(38): Show | 41 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.149+1268A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844622 | ||||||
| chrX:2844628
|
A | G | 2 | a0001c0001t0004g0003a0011c0019t0004g0003 | 2 | HG01099.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.149+1274A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844628 | ||||||
| chrX:2844628
|
ACG | A | 61 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(58): Show | 61 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.149+1276_149+1277d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844628 | |||||
| chrX:2844630
|
G | A | 3 | a0002c0005t0007g0018a0002c0005t0007g0020a0004c0008t0006g0019 | 3 | HG01074.hp1 HG01891.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.149+1276G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844630 | ||||||
| chrX:2844631
|
CAT | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(53): Show | 58 | HG00140.hp1 HG00323.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.149+1278_149+1279d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844631 | ||||||
| chrX:2844632
|
A | G | 6 | a0001c0001t0004g0003a0001c0001t0004g0129a0001c0001t0004g0130others(3): Show | 6 | HG01099.hp1 HG01123.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.149+1278A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844632 | ||||||
| chrX:2844633
|
T | C | 19 | a0001c0003t0001g0027a0001c0003t0001g0030a0001c0003t0002g0042others(16): Show | 19 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.149+1279T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844633 | ||||||
| chrX:2844635
|
C | T | 1 | a0003c0007t0006g0031 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.149+1281C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844635 | ||||||
| chrX:2844637
|
T | C | 3 | a0001c0001t0001g0133a0002c0002t0003g0132a0002c0002t0006g0017 | 3 | HG02572.hp1 HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.149+1283T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844637 | ||||||
| chrX:2844640
|
A | G | 11 | a0001c0001t0001g0133a0002c0002t0002g0002a0002c0002t0003g0010others(8): Show | 12 | HG02572.hp1 HG02630.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.149+1286A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844640 | ||||||
| chrX:2844642
|
GTGTATAC others(69): Show |
G | 42 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(39): Show | 42 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.149+1292_149+1367d others(78): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844642 | |||||
| chrX:2844654
|
A | G | 2 | a0001c0001t0004g0003a0011c0019t0004g0003 | 2 | HG01099.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.149+1300A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844654 | ||||||
| chrX:2844656
|
GCA | G | 1 | a0001c0001t0003g0077 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.149+1303_149+1304d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844656 | ||||||
| chrX:2844657
|
CAT | C | 53 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(50): Show | 55 | HG00140.hp1 HG00323.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.149+1304_149+1305d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844657 | ||||||
| chrX:2844658
|
A | G | 6 | a0001c0001t0004g0003a0001c0001t0004g0129a0001c0001t0004g0130others(3): Show | 6 | HG01099.hp1 HG01123.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.149+1304A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844658 | ||||||
| chrX:2844663
|
T | C | 1 | a0002c0002t0006g0017 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.149+1309T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844663 | ||||||
| chrX:2844666
|
A | ATG | 1 | a0002c0002t0004g0021 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.149+1316_149+1317d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844666 | |||||
| chrX:2844666
|
A | G | 10 | a0001c0001t0001g0133a0002c0002t0002g0002a0002c0002t0003g0010others(7): Show | 11 | HG02572.hp1 HG02630.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.149+1312A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844666 | ||||||
| chrX:2844668
|
G | GTGTATAC others(17): Show |
1 | a0002c0002t0005g0117 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.149+1318_149+1341d others(26): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844668 | |||||
| chrX:2844668
|
GTGTATAC others(43): Show |
G | 1 | a0001c0004t0001g0103 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.149+1318_149+1367d others(52): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844668 | |||||
| chrX:2844680
|
A | G | 2 | a0001c0001t0004g0003a0011c0019t0004g0003 | 2 | HG01099.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.149+1326A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844680 | ||||||
| chrX:2844680
|
ACG | A | 3 | a0002c0002t0005g0050a0002c0002t0006g0051a0012c0018t0001g0099 | 3 | HG02622.hp2 HG02970.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.149+1328_149+1329d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844680 | |||||
| chrX:2844684
|
A | G | 6 | a0001c0001t0004g0003a0001c0001t0004g0129a0001c0001t0004g0130others(3): Show | 6 | HG01099.hp1 HG01123.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.149+1330A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844684 | ||||||
| chrX:2844692
|
A | ATG | 2 | a0002c0002t0003g0010a0002c0002t0004g0021 | 2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.149+1342_149+1343d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844692 | |||||
| chrX:2844692
|
A | G | 9 | a0001c0001t0001g0133a0002c0002t0002g0002a0002c0002t0003g0132others(6): Show | 10 | HG02572.hp1 HG02630.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.149+1338A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844692 | ||||||
| chrX:2844694
|
GTGTATAC others(17): Show |
G | 3 | a0002c0002t0005g0050a0002c0002t0006g0051a0012c0018t0001g0099 | 3 | HG02622.hp2 HG02970.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.149+1344_149+1367d others(26): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844694 | |||||
| chrX:2844694
|
GTGTATAC others(91): Show |
G | 2 | a0001c0003t0002g0045a0002c0002t0005g0108 | 2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.149+1342_149+1439d others(100): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844694 | |||||
| chrX:2844700
|
A | G | 7 | a0001c0003t0002g0042a0001c0003t0004g0041a0002c0002t0002g0144others(4): Show | 7 | HG01243.hp1 HG02280.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.149+1346A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844700 | ||||||
| chrX:2844703
|
C | T | 1 | a0013c0017t0005g0243 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.149+1349C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844703 | ||||||
| chrX:2844706
|
A | G | 2 | a0001c0001t0004g0003a0011c0019t0004g0003 | 2 | HG01099.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.149+1352A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844706 | ||||||
| chrX:2844706
|
ACG | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(73): Show | 78 | HG00140.hp1 HG00323.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.149+1354_149+1355d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844706 | |||||
| chrX:2844709
|
C | T | 1 | a0013c0017t0005g0243 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.149+1355C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844709 | ||||||
| chrX:2844710
|
A | G | 6 | a0001c0001t0004g0003a0001c0001t0004g0129a0001c0001t0004g0130others(3): Show | 6 | HG01099.hp1 HG01123.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.149+1356A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844710 | ||||||
| chrX:2844713
|
C | T | 1 | a0013c0017t0005g0243 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.149+1359C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844713 | ||||||
| chrX:2844718
|
A | ATG | 63 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(60): Show | 65 | HG00140.hp1 HG00323.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.149+1368_149+1369d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844718 | |||||
| chrX:2844718
|
A | G | 8 | a0001c0001t0001g0133a0002c0002t0003g0132a0002c0002t0005g0016others(5): Show | 8 | HG02572.hp1 HG02630.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+1364A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844718 | ||||||
| chrX:2844719
|
T | TGC | 15 | a0001c0003t0001g0027a0001c0003t0001g0030a0001c0003t0005g0022others(12): Show | 15 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.149+1366_149+1367i others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844719 | |||||
| chrX:2844720
|
GTGTATAC others(17): Show |
G | 1 | a0002c0002t0002g0002 | 2 | HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.149+1370_149+1393d others(26): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844720 | |||||
| chrX:2844720
|
GTGTATAC others(65): Show |
G | 16 | a0001c0003t0001g0114a0002c0002t0002g0011a0002c0002t0002g0107others(13): Show | 16 | HG01884.hp1 HG02257.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.149+1368_149+1439d others(74): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844720 | |||||
| chrX:2844727
|
C | T | 122 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(119): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.149+1373C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844727 | ||||||
| chrX:2844729
|
C | CACACGCA others(19): Show |
2 | a0001c0001t0001g0267a0001c0016t0003g0233 | 2 | NA18947.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.149+1400_149+1401i others(28): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844729 | |||||
| chrX:2844732
|
A | G | 2 | a0001c0001t0004g0003a0011c0019t0004g0003 | 2 | HG01099.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.149+1378A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844732 | ||||||
| chrX:2844735
|
C | T | 126 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(123): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.149+1381C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844735 | ||||||
| chrX:2844736
|
A | G | 6 | a0001c0001t0004g0003a0001c0001t0004g0129a0001c0001t0004g0130others(3): Show | 6 | HG01099.hp1 HG01123.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.149+1382A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844736 | ||||||
| chrX:2844744
|
A | ATG | 7 | a0001c0001t0001g0133a0002c0002t0003g0010a0002c0002t0003g0132others(4): Show | 7 | HG02572.hp1 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.149+1394_149+1395d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844744 | |||||
| chrX:2844744
|
A | G | 3 | a0002c0002t0005g0178a0002c0006t0003g0036a0009c0013t0005g0037 | 3 | HG03225.hp1 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.149+1390A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844744 | ||||||
| chrX:2844746
|
GTGTATAC others(39): Show |
G | 3 | a0002c0002t0002g0038a0002c0002t0002g0039a0002c0005t0003g0040 | 3 | HG01884.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.149+1394_149+1439d others(48): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844746 | |||||
| chrX:2844755
|
C | CACACGCA others(67): Show |
1 | a0002c0002t0003g0035 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.149+1406_149+1407i others(76): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844755 | |||||
| chrX:2844755
|
C | CACACGCA others(72): Show |
1 | a0014c0012t0001g0305 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.149+1406_149+1407i others(81): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844755 | |||||
| chrX:2844755
|
C | CACACGCA others(71): Show |
1 | a0001c0001t0003g0013 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.149+1406_149+1407i others(80): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844755 | |||||
| chrX:2844755
|
C | CACACGCA others(45): Show |
18 | a0001c0001t0001g0052a0001c0001t0001g0181a0001c0001t0001g0196others(15): Show | 18 | HG00323.hp2 HG00639.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.149+1406_149+1407i others(54): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844755 | |||||
| chrX:2844755
|
C | CACACGCA others(19): Show |
74 | a0001c0001t0001g0004a0001c0001t0001g0182a0001c0001t0001g0198others(71): Show | 75 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.149+1406_149+1407i others(28): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844755 | |||||
| chrX:2844755
|
C | T | 169 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(166): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.149+1401C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844755 | ||||||
| chrX:2844761
|
T | C | 12 | a0001c0001t0001g0133a0002c0002t0002g0002a0002c0002t0003g0010others(9): Show | 13 | HG02572.hp1 HG02630.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.149+1407T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844761 | ||||||
| chrX:2844765
|
T | C | 17 | a0001c0001t0001g0133a0002c0002t0002g0002a0002c0002t0002g0069others(14): Show | 18 | HG00423.hp1 HG00438.hp2 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.149+1411T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844765 | ||||||
| chrX:2844771
|
T | C | 3 | a0002c0002t0003g0033a0002c0002t0003g0034a0002c0002t0003g0035 | 3 | HG02922.hp1 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.149+1417T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844771 | ||||||
| chrX:2844778
|
G | A | 4 | a0002c0005t0006g0104a0002c0005t0007g0018a0002c0005t0007g0020others(1): Show | 4 | HG00741.hp2 HG01074.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+1424G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844778 | ||||||
| chrX:2844779
|
T | TA | 1 | a0015c0011t0002g0185 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.149+1426dupA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844779 | |||||
| chrX:2844783
|
CAT | C | 285 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(282): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.149+1439_149+1440d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844783 | |||||
| chrX:2844786
|
A | C | 4 | a0002c0005t0006g0104a0002c0005t0007g0018a0002c0005t0007g0020others(1): Show | 4 | HG00741.hp2 HG01074.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+1432A>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844786 | ||||||
| chrX:2844786
|
A | G | 4 | a0002c0002t0002g0144a0002c0002t0002g0163a0002c0002t0002g0164others(1): Show | 4 | NA18939.hp2 NA18956.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+1432A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844786 | ||||||
| chrX:2844788
|
A | G | 118 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(115): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.149+1434A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844788 | ||||||
| chrX:2844790
|
ATATACAT others(37): Show |
A | 4 | a0002c0002t0002g0144a0002c0002t0002g0163a0002c0002t0002g0164others(1): Show | 4 | NA18939.hp2 NA18956.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+1439_149+1482d others(46): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844790 | |||||
| chrX:2844792
|
A | G | 1 | a0002c0002t0001g0260 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.149+1438A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844792 | ||||||
| chrX:2844810
|
A | T | 1 | a0001c0001t0003g0208 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.149+1456A>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844810 | ||||||
| chrX:2844812
|
T | A | 1 | a0001c0001t0003g0208 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.149+1458T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844812 | ||||||
| chrX:2844827
|
T | C | 15 | a0001c0003t0001g0027a0001c0003t0001g0030a0001c0003t0005g0022others(12): Show | 15 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.149+1473T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844827 | ||||||
| chrX:2844842
|
ATG | A | 3 | a0002c0002t0003g0033a0002c0002t0003g0034a0002c0002t0003g0035 | 3 | HG02922.hp1 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.149+1492_149+1493d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844842 | |||||
| chrX:2844886
|
ATG | A | 1 | a0002c0002t0002g0252 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.149+1536_149+1537d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844886 | |||||
| chrX:2844928
|
A | G | 15 | a0001c0003t0001g0027a0001c0003t0001g0030a0001c0003t0005g0022others(12): Show | 15 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.149+1574A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844928 | ||||||
| chrX:2844954
|
A | G | 48 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(45): Show | 48 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.149+1600A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844954 | ||||||
| chrX:2844999
|
ATATATTT others(61): Show |
A | 1 | a0002c0002t0002g0294 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.149+1661_149+1728d others(70): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844999 | |||||
| chrX:2844999
|
ATATATTT others(253): Show |
A | 1 | a0001c0001t0001g0098 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.149+1661_149+1920d others(2): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2844999 | |||||
| chrX:2845005
|
T | TTATATAC others(13): Show |
1 | a0001c0001t0002g0192 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.149+1655_149+1674d others(22): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845005 | |||||
| chrX:2845005
|
T | TTATATAC others(37): Show |
2 | a0002c0002t0002g0107a0002c0002t0005g0113 | 2 | HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.149+1661_149+1704d others(46): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845005 | |||||
| chrX:2845015
|
ATGTGTAT others(61): Show |
A | 1 | a0001c0001t0001g0292 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.149+1685_149+1752d others(70): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845015 | |||||
| chrX:2845015
|
ATGTGTAT others(85): Show |
A | 2 | a0001c0001t0002g0291a0001c0004t0014g0290 | 2 | HG01081.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.149+1685_149+1776d others(94): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845015 | |||||
| chrX:2845015
|
ATGTGTAT others(109): Show |
A | 3 | a0001c0001t0001g0074a0001c0001t0001g0078a0001c0004t0001g0103 | 3 | HG00408.hp1 HG04204.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.149+1685_149+1800d others(2): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845015 | |||||
| chrX:2845015
|
ATGTGTAT others(133): Show |
A | 2 | a0001c0001t0001g0289a0001c0001t0010g0097 | 2 | HG00642.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.149+1685_149+1824d others(2): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845015 | |||||
| chrX:2845015
|
ATGTGTAT others(157): Show |
A | 5 | a0001c0001t0002g0085a0001c0001t0002g0096a0001c0001t0002g0190others(2): Show | 5 | HG02293.hp1 HG03017.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.149+1685_149+1848d others(2): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845015 | |||||
| chrX:2845015
|
ATGTGTAT others(181): Show |
A | 11 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0002g0286others(8): Show | 11 | HG00323.hp1 HG02155.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.149+1685_149+1872d others(2): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845015 | |||||
| chrX:2845015
|
ATGTGTAT others(205): Show |
A | 13 | a0001c0001t0001g0001a0001c0001t0001g0101a0001c0001t0001g0306others(10): Show | 14 | HG01109.hp1 HG02027.hp1 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.149+1685_149+1896d others(2): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845015 | |||||
| chrX:2845015
|
ATGTGTAT others(229): Show |
A | 11 | a0001c0001t0001g0083a0001c0001t0002g0280a0001c0001t0002g0281others(8): Show | 11 | HG00544.hp2 HG00673.hp1 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.149+1685_149+1920d others(2): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845015 | |||||
| chrX:2845015
|
ATGTGTAT others(253): Show |
A | 4 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0100others(1): Show | 4 | NA18947.hp1 NA18971.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+1685_149+1944d others(2): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845015 | |||||
| chrX:2845015
|
ATGTGTAT others(301): Show |
A | 1 | a0001c0001t0002g0079 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.149+1685_149+1992d others(2): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845015 | |||||
| chrX:2845025
|
ATATT | A | 4 | a0001c0001t0004g0003a0001c0001t0004g0129a0001c0001t0004g0173others(1): Show | 4 | HG01099.hp1 HG01123.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+1675_149+1678d others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845025 | |||||
| chrX:2845027
|
A | ATATACAC others(29): Show |
2 | a0001c0001t0004g0130a0001c0001t0004g0131 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.149+1674_149+1675i others(38): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845027 | |||||
| chrX:2845029
|
T | A | 2 | a0001c0001t0004g0130a0001c0001t0004g0131 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.149+1675T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845029 | ||||||
| chrX:2845029
|
T | TTATATAC others(13): Show |
1 | a0001c0001t0001g0205 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.149+1685_149+1704d others(22): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845029 | |||||
| chrX:2845029
|
TTATATAC others(13): Show |
T | 3 | a0001c0001t0001g0293a0002c0002t0005g0050a0002c0002t0006g0051 | 3 | HG00639.hp1 HG02622.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.149+1685_149+1704d others(22): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845029 | |||||
| chrX:2845038
|
CAT | C | 1 | a0001c0001t0003g0232 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.149+1685_149+1686d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845038 | ||||||
| chrX:2845039
|
A | ATGTGTAT others(37): Show |
1 | a0002c0002t0007g0118 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.149+1704_149+1705i others(46): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845039 | |||||
| chrX:2845039
|
A | G | 1 | a0001c0001t0001g0005 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.149+1685A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845039 | ||||||
| chrX:2845039
|
ATGTGTAT others(13): Show |
A | 25 | a0001c0001t0001g0263a0001c0003t0001g0027a0001c0003t0001g0030others(22): Show | 25 | HG00741.hp2 HG01074.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.149+1699_149+1718d others(22): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845039 | |||||
| chrX:2845039
|
ATGTGTAT others(37): Show |
A | 4 | a0001c0001t0001g0204a0001c0001t0001g0206a0001c0001t0001g0278others(1): Show | 4 | NA18944.hp1 NA18983.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+1699_149+1742d others(46): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845039 | |||||
| chrX:2845039
|
ATGTGTAT others(61): Show |
A | 2 | a0001c0001t0001g0264a0002c0002t0005g0117 | 2 | HG02015.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.149+1699_149+1766d others(70): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845039 | |||||
| chrX:2845039
|
ATGTGTAT others(229): Show |
A | 1 | a0001c0003t0004g0041 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.149+1699_149+1934d others(2): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845039 | |||||
| chrX:2845039
|
ATGTGTAT others(253): Show |
A | 1 | a0001c0003t0002g0042 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.149+1699_149+1958d others(2): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845039 | |||||
| chrX:2845039
|
ATGTGTAT others(301): Show |
A | 1 | a0002c0005t0002g0176 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.149+1699_149+2006d others(2): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845039 | |||||
| chrX:2845039
|
ATGTGTAT others(349): Show |
A | 5 | a0001c0001t0001g0139a0001c0001t0002g0149a0002c0002t0004g0148others(2): Show | 5 | HG01516.hp2 NA18942.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.149+1699_149+2054d others(2): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845039 | |||||
| chrX:2845039
|
ATGTGTAT others(373): Show |
A | 31 | a0001c0001t0001g0135a0001c0001t0001g0140a0001c0001t0001g0194others(28): Show | 31 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.149+1699_149+2078d others(2): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845039 | |||||
| chrX:2845039
|
ATGTGTAT others(397): Show |
A | 9 | a0002c0002t0001g0146a0002c0002t0004g0006a0002c0002t0004g0137others(6): Show | 9 | HG00099.hp2 HG01981.hp1 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.149+1699_149+2102d others(2): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845039 | |||||
| chrX:2845045
|
A | ATG | 4 | a0002c0002t0003g0010a0002c0002t0004g0021a0002c0006t0003g0036others(1): Show | 4 | HG02647.hp1 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+1693_149+1694d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845045 | |||||
| chrX:2845047
|
G | GTATATAT others(17): Show |
1 | a0002c0002t0005g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.149+1704_149+1705i others(26): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845047 | |||||
| chrX:2845049
|
A | ATATATAC others(61): Show |
2 | a0002c0002t0003g0109a0002c0002t0005g0116 | 2 | HG01884.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.149+1704_149+1705i others(70): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845049 | |||||
| chrX:2845049
|
A | ATATATAC others(85): Show |
2 | a0002c0002t0002g0111a0002c0002t0003g0112 | 2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.149+1704_149+1705i others(94): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845049 | |||||
| chrX:2845049
|
A | ATATATAC others(157): Show |
2 | a0001c0003t0001g0114a0002c0002t0005g0105 | 2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.149+1704_149+1705i others(166): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845049 | |||||
| chrX:2845049
|
A | ATATT | 1 | a0001c0001t0001g0005 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.149+1698_149+1699i others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845049 | |||||
| chrX:2845052
|
T | C | 7 | a0001c0001t0001g0133a0002c0002t0002g0002a0002c0002t0003g0132others(4): Show | 8 | HG02572.hp1 HG02630.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+1698T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845052 | ||||||
| chrX:2845059
|
G | A | 159 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0133others(156): Show | 161 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.149+1705G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845059 | ||||||
| chrX:2845069
|
A | G | 7 | a0001c0001t0001g0133a0002c0002t0002g0002a0002c0002t0003g0132others(4): Show | 8 | HG02572.hp1 HG02630.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+1715A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845069 | ||||||
| chrX:2845069
|
ATATT | A | 6 | a0001c0001t0004g0173a0002c0002t0003g0010a0002c0002t0004g0021others(3): Show | 6 | HG01123.hp2 HG02109.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.149+1719_149+1722d others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845069 | |||||
| chrX:2845069
|
ATATTTAT others(45): Show |
A | 1 | a0001c0001t0004g0129 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.149+1719_149+1770d others(54): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845069 | |||||
| chrX:2845069
|
ATATTTAT others(117): Show |
A | 1 | a0004c0008t0006g0009 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.149+1719_149+1842d others(2): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845069 | |||||
| chrX:2845069
|
ATATTTAT others(165): Show |
A | 1 | a0002c0002t0005g0126 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.149+1719_149+1890d others(2): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845069 | |||||
| chrX:2845071
|
A | ATATACAC others(9): Show |
2 | a0001c0001t0004g0003a0011c0019t0004g0003 | 2 | HG01099.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.149+1718_149+1719i others(18): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845071 | |||||
| chrX:2845071
|
ATT | A | 4 | a0001c0001t0001g0133a0002c0002t0005g0016a0002c0002t0005g0178others(1): Show | 4 | HG02630.hp2 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+1719_149+1720d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845071 | |||||
| chrX:2845073
|
T | A | 5 | a0001c0001t0004g0003a0002c0002t0002g0002a0002c0002t0003g0132others(2): Show | 6 | HG01099.hp1 HG01175.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.149+1719T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845073 | ||||||
| chrX:2845073
|
T | TTATATAC others(13): Show |
7 | a0001c0001t0001g0214a0001c0001t0001g0234a0001c0001t0002g0189others(4): Show | 7 | HG00423.hp2 HG02004.hp1 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.149+1728_149+1729i others(22): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845073 | |||||
| chrX:2845073
|
T | TTATATAC others(17): Show |
1 | a0002c0002t0001g0254 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.149+1728_149+1729i others(26): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845073 | |||||
| chrX:2845076
|
T | C | 4 | a0002c0002t0003g0010a0002c0002t0004g0021a0002c0006t0003g0036others(1): Show | 4 | HG02647.hp1 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+1722T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845076 | ||||||
| chrX:2845076
|
T | TACACATG others(11): Show |
2 | a0002c0002t0003g0132a0002c0002t0006g0017 | 2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.149+1723_149+1724i others(20): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845076 | |||||
| chrX:2845076
|
T | TACACATG others(75): Show |
1 | a0002c0002t0002g0002 | 2 | HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.149+1723_149+1724i others(84): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845076 | |||||
| chrX:2845083
|
G | A | 173 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0133others(170): Show | 175 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.149+1729G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845083 | ||||||
| chrX:2845093
|
A | G | 4 | a0002c0002t0003g0010a0002c0002t0004g0021a0002c0006t0003g0036others(1): Show | 4 | HG02647.hp1 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+1739A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845093 | ||||||
| chrX:2845093
|
ATATT | A | 15 | a0001c0001t0002g0276a0001c0001t0004g0173a0001c0003t0002g0045others(12): Show | 15 | HG00741.hp2 HG01074.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.149+1743_149+1746d others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845093 | |||||
| chrX:2845093
|
ATATTTAT others(21): Show |
A | 1 | a0002c0002t0003g0110 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.149+1743_149+1770d others(30): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845093 | |||||
| chrX:2845093
|
ATATTTAT others(45): Show |
A | 1 | a0001c0001t0007g0191 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.149+1743_149+1794d others(54): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845093 | |||||
| chrX:2845093
|
ATATTTAT others(213): Show |
A | 1 | a0002c0002t0003g0035 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.149+1743_149+1962d others(2): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845093 | |||||
| chrX:2845095
|
A | ACATACAC others(9): Show |
2 | a0001c0001t0001g0133a0002c0002t0005g0178 | 2 | HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.149+1741_149+1742i others(18): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845095 | ||||||
| chrX:2845095
|
A | ATATACAC others(33): Show |
2 | a0001c0001t0009g0266a0001c0001t0009g0270 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.149+1742_149+1743i others(42): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845095 | |||||
| chrX:2845095
|
ATT | A | 4 | a0002c0002t0003g0010a0002c0002t0004g0021a0002c0006t0003g0036others(1): Show | 4 | HG02647.hp1 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+1743_149+1744d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845095 | |||||
| chrX:2845097
|
T | A | 4 | a0001c0001t0001g0133a0001c0001t0009g0266a0001c0001t0009g0270others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+1743T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845097 | ||||||
| chrX:2845100
|
T | C | 4 | a0001c0001t0001g0133a0002c0002t0005g0016a0002c0002t0005g0178others(1): Show | 4 | HG02630.hp2 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+1746T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845100 | ||||||
| chrX:2845107
|
G | A | 167 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0133others(164): Show | 169 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.149+1753G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845107 | ||||||
| chrX:2845113
|
A | AT | 1 | a0001c0001t0003g0180 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.149+1760dupT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845113 | |||||
| chrX:2845117
|
ATATT | A | 1 | a0002c0002t0005g0108 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.149+1767_149+1770d others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845117 | |||||
| chrX:2845119
|
A | ACATACAC others(9): Show |
2 | a0002c0002t0005g0016a0002c0002t0006g0134 | 2 | HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.149+1765_149+1766i others(18): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845119 | ||||||
| chrX:2845119
|
ATT | A | 4 | a0002c0002t0003g0010a0002c0002t0004g0021a0002c0006t0003g0036others(1): Show | 4 | HG02647.hp1 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+1767_149+1768d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845119 | |||||
| chrX:2845121
|
T | A | 2 | a0002c0002t0005g0016a0002c0002t0006g0134 | 2 | HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.149+1767T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845121 | ||||||
| chrX:2845124
|
T | C | 2 | a0002c0002t0005g0016a0002c0002t0006g0134 | 2 | HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.149+1770T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845124 | ||||||
| chrX:2845126
|
T | C | 4 | a0002c0002t0003g0010a0002c0002t0004g0021a0002c0006t0003g0036others(1): Show | 4 | HG02647.hp1 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+1772T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845126 | ||||||
| chrX:2845129
|
AC | A | 4 | a0002c0002t0003g0010a0002c0002t0004g0021a0002c0006t0003g0036others(1): Show | 4 | HG02647.hp1 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+1776delC | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845129 | ||||||
| chrX:2845130
|
CGT | C | 1 | a0001c0001t0003g0180 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.149+1781_149+1782d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845130 | |||||
| chrX:2845131
|
G | A | 166 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0133others(163): Show | 168 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.149+1777G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845131 | ||||||
| chrX:2845141
|
ATATT | A | 5 | a0001c0001t0004g0129a0002c0005t0006g0104a0002c0005t0007g0018others(2): Show | 5 | HG00741.hp2 HG01074.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.149+1791_149+1794d others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845141 | |||||
| chrX:2845142
|
T | C | 1 | a0001c0001t0003g0180 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.149+1788T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845142 | ||||||
| chrX:2845155
|
G | A | 166 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0133others(163): Show | 168 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.149+1801G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845155 | ||||||
| chrX:2845179
|
G | A | 164 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0133others(161): Show | 166 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.149+1825G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845179 | ||||||
| chrX:2845185
|
ATGTATAT others(107): Show |
A | 2 | a0002c0006t0003g0036a0009c0013t0005g0037 | 2 | HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.149+1835_149+1948d others(2): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845185 | |||||
| chrX:2845185
|
ATGTATAT others(203): Show |
A | 2 | a0002c0002t0003g0010a0002c0002t0004g0021 | 2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.149+1835_149+2044d others(2): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845185 | |||||
| chrX:2845189
|
ATATT | A | 4 | a0002c0005t0006g0104a0002c0005t0007g0018a0002c0005t0007g0020others(1): Show | 4 | HG00741.hp2 HG01074.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+1839_149+1842d others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845189 | |||||
| chrX:2845202
|
C | CAT | 2 | a0002c0002t0003g0033a0002c0002t0003g0034 | 2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.149+1848_149+1849i others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845202 | ||||||
| chrX:2845203
|
G | A | 158 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0133others(155): Show | 160 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.149+1849G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845203 | ||||||
| chrX:2845213
|
ATATT | A | 4 | a0002c0005t0006g0104a0002c0005t0007g0018a0002c0005t0007g0020others(1): Show | 4 | HG00741.hp2 HG01074.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+1863_149+1866d others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845213 | |||||
| chrX:2845215
|
A | AT | 1 | a0001c0001t0003g0180 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.149+1864dupT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845215 | |||||
| chrX:2845220
|
T | C | 4 | a0002c0005t0006g0104a0002c0005t0007g0018a0002c0005t0007g0020others(1): Show | 4 | HG00741.hp2 HG01074.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+1866T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845220 | ||||||
| chrX:2845226
|
C | CAT | 2 | a0002c0002t0003g0033a0002c0002t0003g0034 | 2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.149+1872_149+1873i others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845226 | ||||||
| chrX:2845227
|
G | A | 158 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0133others(155): Show | 160 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.149+1873G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845227 | ||||||
| chrX:2845237
|
ATATT | A | 1 | a0002c0002t0002g0002 | 2 | HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.149+1887_149+1890d others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845237 | |||||
| chrX:2845244
|
T | C | 1 | a0002c0002t0002g0002 | 2 | HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.149+1890T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845244 | ||||||
| chrX:2845250
|
C | CAT | 5 | a0001c0001t0003g0231a0001c0001t0004g0230a0002c0002t0003g0033others(2): Show | 5 | HG01123.hp1 HG02129.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.149+1896_149+1897i others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845250 | ||||||
| chrX:2845250
|
C | CATGTGT | 1 | a0002c0002t0003g0132 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.149+1896_149+1897i others(8): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845250 | ||||||
| chrX:2845250
|
CGT | C | 1 | a0001c0001t0002g0276 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.149+1901_149+1902d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845250 | |||||
| chrX:2845251
|
G | A | 154 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0133others(151): Show | 156 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.149+1897G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845251 | ||||||
| chrX:2845256
|
T | C | 1 | a0006c0010t0003g0202 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.149+1902T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845256 | ||||||
| chrX:2845258
|
TGTATA | T | 4 | a0002c0005t0006g0104a0002c0005t0007g0018a0002c0005t0007g0020others(1): Show | 4 | HG00741.hp2 HG01074.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+1905_149+1909d others(7): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845258 | ||||||
| chrX:2845265
|
T | A | 4 | a0002c0005t0006g0104a0002c0005t0007g0018a0002c0005t0007g0020others(1): Show | 4 | HG00741.hp2 HG01074.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+1911T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845265 | ||||||
| chrX:2845272
|
CACGTGTG others(231): Show |
C | 2 | a0002c0002t0003g0033a0002c0002t0003g0034 | 2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.149+1921_149+2158d others(2): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845272 | |||||
| chrX:2845274
|
C | CAT | 23 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0228others(20): Show | 24 | HG01069.hp1 HG01071.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.149+1920_149+1921i others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845274 | ||||||
| chrX:2845274
|
C | CATGTGT | 3 | a0002c0002t0003g0132a0002c0002t0005g0178a0002c0002t0006g0017 | 3 | HG02572.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.149+1920_149+1921i others(8): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845274 | ||||||
| chrX:2845274
|
CGT | C | 1 | a0002c0002t0002g0252 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.149+1925_149+1926d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845274 | |||||
| chrX:2845275
|
G | A | 135 | a0001c0001t0001g0133a0001c0001t0001g0181a0001c0001t0001g0182others(132): Show | 136 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.149+1921G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845275 | ||||||
| chrX:2845280
|
T | C | 1 | a0006c0010t0003g0202 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.149+1926T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845280 | ||||||
| chrX:2845296
|
CACGTGTG others(39): Show |
C | 3 | a0001c0001t0001g0004a0001c0001t0001g0228a0002c0002t0003g0207 | 4 | HG01069.hp1 HG01071.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+1945_149+1990d others(48): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845296 | |||||
| chrX:2845298
|
C | CAT | 43 | a0001c0001t0001g0052a0001c0001t0001g0196a0001c0001t0001g0197others(40): Show | 43 | HG00280.hp1 HG00639.hp2 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.149+1944_149+1945i others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845298 | ||||||
| chrX:2845298
|
C | CATGTGT | 4 | a0001c0001t0001g0133a0002c0002t0005g0016a0002c0002t0005g0178others(1): Show | 4 | HG02572.hp1 HG02630.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+1944_149+1945i others(8): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845298 | ||||||
| chrX:2845299
|
G | A | 114 | a0001c0001t0001g0133a0001c0001t0001g0181a0001c0001t0001g0182others(111): Show | 115 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.149+1945G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845299 | ||||||
| chrX:2845309
|
A | G | 1 | a0002c0002t0003g0132 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.149+1955A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845309 | ||||||
| chrX:2845311
|
ATT | A | 1 | a0002c0002t0003g0132 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.149+1959_149+1960d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845311 | |||||
| chrX:2845320
|
CACGTGTG others(39): Show |
C | 5 | a0001c0001t0001g0224a0001c0001t0001g0226a0001c0001t0002g0054others(2): Show | 5 | HG00639.hp2 HG02683.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.149+1969_149+2014d others(48): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845320 | |||||
| chrX:2845320
|
CACGTGTG others(63): Show |
C | 1 | a0001c0001t0001g0052 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.149+1969_149+2038d others(72): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845320 | |||||
| chrX:2845322
|
C | CAT | 68 | a0001c0001t0001g0182a0001c0001t0001g0196a0001c0001t0001g0197others(65): Show | 68 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.149+1968_149+1969i others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845322 | ||||||
| chrX:2845322
|
C | CATGTGT | 4 | a0001c0001t0001g0133a0002c0002t0002g0002a0002c0002t0005g0016others(1): Show | 5 | HG02630.hp1 HG02630.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.149+1968_149+1969i others(8): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845322 | ||||||
| chrX:2845323
|
G | A | 85 | a0001c0001t0001g0133a0001c0001t0001g0181a0001c0001t0001g0184others(82): Show | 86 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.149+1969G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845323 | ||||||
| chrX:2845333
|
A | G | 4 | a0002c0002t0005g0178a0002c0002t0006g0017a0002c0006t0003g0036others(1): Show | 4 | HG02572.hp1 HG03225.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+1979A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845333 | ||||||
| chrX:2845335
|
ATT | A | 4 | a0002c0002t0005g0178a0002c0002t0006g0017a0002c0006t0003g0036others(1): Show | 4 | HG02572.hp1 HG03225.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+1983_149+1984d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845335 | |||||
| chrX:2845344
|
CACGTGTG others(39): Show |
C | 2 | a0001c0001t0015g0046a0002c0002t0002g0244 | 2 | HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.149+1993_149+2038d others(48): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845344 | |||||
| chrX:2845344
|
CACGTGTG others(63): Show |
C | 1 | a0001c0001t0003g0273 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.149+1993_149+2062d others(72): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845344 | |||||
| chrX:2845346
|
C | CAT | 87 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0196others(84): Show | 87 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.149+1992_149+1993i others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845346 | ||||||
| chrX:2845346
|
C | CATGTGT | 2 | a0002c0002t0002g0002a0002c0002t0006g0134 | 3 | HG02630.hp1 HG02886.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.149+1992_149+1993i others(8): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845346 | ||||||
| chrX:2845346
|
C | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0228a0002c0002t0003g0207 | 4 | HG01069.hp1 HG01071.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+1992C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845346 | ||||||
| chrX:2845347
|
G | A | 64 | a0001c0001t0001g0133a0001c0001t0001g0184a0001c0001t0001g0198others(61): Show | 65 | HG00733.hp1 HG00741.hp2 HG01074.hp1 others(62): Show |
intron_variant | MODIFIER | c.149+1993G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845347 | ||||||
| chrX:2845357
|
A | G | 3 | a0001c0001t0001g0133a0002c0002t0003g0132a0002c0002t0005g0016 | 3 | HG02630.hp2 HG02970.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.149+2003A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845357 | ||||||
| chrX:2845359
|
ATT | A | 3 | a0001c0001t0001g0133a0002c0002t0003g0132a0002c0002t0005g0016 | 3 | HG02630.hp2 HG02970.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.149+2007_149+2008d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845359 | |||||
| chrX:2845368
|
CACGTGTG others(15): Show |
C | 2 | a0002c0002t0012g0066a0002c0002t0012g0067 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.149+2017_149+2038d others(24): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845368 | |||||
| chrX:2845368
|
CACGTGTG others(39): Show |
C | 2 | a0001c0001t0003g0303a0002c0002t0001g0008 | 2 | HG00733.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.149+2017_149+2062d others(48): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845368 | |||||
| chrX:2845368
|
CACGTGTG others(63): Show |
C | 4 | a0001c0001t0001g0239a0001c0001t0003g0195a0001c0001t0008g0064others(1): Show | 4 | HG01123.hp1 HG03831.hp1 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+2017_149+2086d others(72): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845368 | |||||
| chrX:2845370
|
C | CAT | 98 | a0001c0001t0001g0004a0001c0001t0001g0181a0001c0001t0001g0182others(95): Show | 99 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.149+2016_149+2017i others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845370 | ||||||
| chrX:2845370
|
C | T | 5 | a0001c0001t0001g0224a0001c0001t0001g0226a0001c0001t0002g0054others(2): Show | 5 | HG00639.hp2 HG02683.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.149+2016C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845370 | ||||||
| chrX:2845371
|
G | A | 49 | a0001c0001t0001g0133a0001c0001t0001g0198a0001c0001t0001g0216others(46): Show | 50 | HG00733.hp1 HG00741.hp2 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.149+2017G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845371 | ||||||
| chrX:2845381
|
A | G | 6 | a0002c0002t0002g0002a0002c0002t0005g0178a0002c0002t0006g0017others(3): Show | 7 | HG02572.hp1 HG02630.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.149+2027A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845381 | ||||||
| chrX:2845381
|
ATATTTAT others(165): Show |
A | 1 | a0004c0008t0006g0127 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.149+2031_149+2202d others(2): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845381 | |||||
| chrX:2845383
|
ATT | A | 6 | a0002c0002t0002g0002a0002c0002t0005g0178a0002c0002t0006g0017others(3): Show | 7 | HG02572.hp1 HG02630.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.149+2031_149+2032d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845383 | |||||
| chrX:2845392
|
CACGTGTG others(39): Show |
C | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | HG03239.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.149+2041_149+2086d others(48): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845392 | |||||
| chrX:2845392
|
CACGTGTG others(63): Show |
C | 1 | a0001c0001t0003g0242 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.149+2041_149+2110d others(72): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845392 | |||||
| chrX:2845394
|
C | CAT | 111 | a0001c0001t0001g0004a0001c0001t0001g0181a0001c0001t0001g0182others(108): Show | 112 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.149+2040_149+2041i others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845394 | ||||||
| chrX:2845394
|
C | T | 5 | a0001c0001t0001g0052a0001c0001t0015g0046a0002c0002t0002g0244others(2): Show | 5 | HG02895.hp1 HG02897.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.149+2040C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845394 | ||||||
| chrX:2845395
|
G | A | 40 | a0001c0001t0001g0133a0001c0001t0002g0192a0001c0001t0007g0191others(37): Show | 41 | HG00733.hp1 HG00741.hp2 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.149+2041G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845395 | ||||||
| chrX:2845405
|
A | G | 6 | a0001c0001t0001g0133a0002c0002t0003g0132a0002c0002t0005g0016others(3): Show | 6 | HG01074.hp1 HG01891.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.149+2051A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845405 | ||||||
| chrX:2845407
|
A | AT | 1 | a0001c0001t0003g0180 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.149+2056dupT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845407 | |||||
| chrX:2845407
|
ATT | A | 6 | a0001c0001t0001g0133a0002c0002t0003g0132a0002c0002t0005g0016others(3): Show | 6 | HG01074.hp1 HG01891.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.149+2055_149+2056d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845407 | |||||
| chrX:2845411
|
ATATACAC others(135): Show |
A | 1 | a0002c0002t0006g0051 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.149+2062_149+2203d others(2): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845411 | |||||
| chrX:2845418
|
C | CAT | 116 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0181others(113): Show | 117 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.149+2064_149+2065i others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845418 | ||||||
| chrX:2845418
|
C | T | 3 | a0001c0001t0003g0273a0001c0001t0003g0303a0002c0002t0001g0008 | 3 | HG00733.hp2 NA18992.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.149+2064C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845418 | ||||||
| chrX:2845419
|
G | A | 45 | a0001c0001t0001g0133a0001c0001t0001g0139a0001c0001t0002g0149others(42): Show | 46 | HG00733.hp1 HG00741.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.149+2065G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845419 | ||||||
| chrX:2845429
|
A | G | 7 | a0002c0002t0002g0002a0002c0002t0003g0010a0002c0002t0004g0021others(4): Show | 8 | HG00741.hp2 HG02572.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.149+2075A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845429 | ||||||
| chrX:2845431
|
ATT | A | 7 | a0002c0002t0002g0002a0002c0002t0003g0010a0002c0002t0004g0021others(4): Show | 8 | HG00741.hp2 HG02572.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.149+2079_149+2080d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845431 | |||||
| chrX:2845442
|
C | CAT | 122 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0181others(119): Show | 123 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.149+2088_149+2089i others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845442 | ||||||
| chrX:2845442
|
C | T | 6 | a0001c0001t0001g0239a0001c0001t0001g0247a0001c0001t0001g0248others(3): Show | 6 | HG01123.hp1 HG03239.hp2 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.149+2088C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845442 | ||||||
| chrX:2845443
|
G | A | 75 | a0001c0001t0001g0133a0001c0001t0001g0135a0001c0001t0001g0139others(72): Show | 76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.149+2089G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845443 | ||||||
| chrX:2845447
|
GTA | G | 2 | a0002c0006t0003g0036a0009c0013t0005g0037 | 2 | HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.149+2095_149+2096d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845447 | |||||
| chrX:2845453
|
A | G | 3 | a0001c0001t0001g0133a0002c0002t0003g0132a0002c0002t0005g0016 | 3 | HG02630.hp2 HG02970.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.149+2099A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845453 | ||||||
| chrX:2845453
|
ATATTTAT others(93): Show |
A | 1 | a0002c0002t0005g0301 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.149+2103_149+2202d others(102): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845453 | |||||
| chrX:2845454
|
T | C | 1 | a0002c0002t0002g0111 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.149+2100T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845454 | ||||||
| chrX:2845455
|
A | G | 2 | a0002c0006t0003g0036a0009c0013t0005g0037 | 2 | HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.149+2101A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845455 | ||||||
| chrX:2845455
|
ATT | A | 5 | a0001c0001t0001g0133a0002c0002t0003g0132a0002c0002t0005g0016others(2): Show | 5 | HG02622.hp1 HG02630.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.149+2103_149+2104d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845455 | |||||
| chrX:2845457
|
T | A | 2 | a0002c0006t0003g0036a0009c0013t0005g0037 | 2 | HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.149+2103T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845457 | ||||||
| chrX:2845457
|
T | TA | 3 | a0002c0005t0007g0018a0002c0005t0007g0020a0004c0008t0006g0019 | 3 | HG01074.hp1 HG01891.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.149+2103_149+2104i others(3): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845457 | ||||||
| chrX:2845459
|
ATATACAC others(87): Show |
A | 1 | a0002c0002t0005g0050 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.149+2110_149+2203d others(96): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845459 | |||||
| chrX:2845462
|
T | C | 5 | a0002c0005t0007g0018a0002c0005t0007g0020a0002c0006t0002g0121others(2): Show | 5 | HG01074.hp1 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.149+2108T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845462 | ||||||
| chrX:2845464
|
CACGTGTG others(15): Show |
C | 1 | a0001c0001t0001g0245 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.149+2113_149+2134d others(24): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845464 | |||||
| chrX:2845464
|
CACGTGTG others(39): Show |
C | 3 | a0001c0001t0001g0206a0001c0001t0001g0224a0001c0001t0002g0220 | 3 | HG03704.hp2 NA19066.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.149+2113_149+2158d others(48): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845464 | |||||
| chrX:2845466
|
C | CAT | 129 | a0001c0001t0001g0052a0001c0001t0001g0181a0001c0001t0001g0182others(126): Show | 129 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.149+2112_149+2113i others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845466 | ||||||
| chrX:2845466
|
C | T | 6 | a0001c0001t0003g0242a0002c0005t0007g0018a0002c0005t0007g0020others(3): Show | 6 | HG01074.hp1 HG01891.hp1 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.149+2112C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845466 | ||||||
| chrX:2845467
|
G | A | 73 | a0001c0001t0001g0004a0001c0001t0001g0133a0001c0001t0001g0135others(70): Show | 75 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.149+2113G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845467 | ||||||
| chrX:2845469
|
GTGTATGT others(5): Show |
G | 2 | a0002c0006t0003g0036a0009c0013t0005g0037 | 2 | HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.149+2117_149+2128d others(14): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845469 | |||||
| chrX:2845471
|
GTA | G | 1 | a0001c0001t0001g0004 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.149+2119_149+2120d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845471 | |||||
| chrX:2845473
|
ATGTATAT others(97): Show |
A | 1 | a0001c0001t0004g0173 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.149+2127_149+2230d others(2): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845473 | |||||
| chrX:2845477
|
A | G | 6 | a0002c0002t0002g0002a0002c0002t0003g0010a0002c0002t0004g0021others(3): Show | 7 | HG02572.hp1 HG02630.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.149+2123A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845477 | ||||||
| chrX:2845477
|
ATATTTAT others(69): Show |
A | 5 | a0001c0003t0002g0045a0002c0005t0007g0018a0002c0005t0007g0020others(2): Show | 5 | HG01074.hp1 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.149+2127_149+2202d others(78): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845477 | |||||
| chrX:2845478
|
T | C | 2 | a0002c0002t0002g0111a0002c0002t0003g0112 | 2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.149+2124T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845478 | ||||||
| chrX:2845479
|
A | G | 1 | a0001c0001t0001g0004 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.149+2125A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845479 | ||||||
| chrX:2845479
|
ATT | A | 8 | a0001c0003t0007g0024a0002c0002t0002g0002a0002c0002t0003g0010others(5): Show | 9 | HG02451.hp1 HG02572.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.149+2127_149+2128d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845479 | |||||
| chrX:2845481
|
T | A | 1 | a0001c0001t0001g0004 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.149+2127T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845481 | ||||||
| chrX:2845481
|
T | TA | 1 | a0002c0005t0006g0104 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.149+2127_149+2128i others(3): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845481 | ||||||
| chrX:2845486
|
T | C | 3 | a0001c0003t0007g0024a0002c0005t0006g0104a0002c0006t0002g0121 | 3 | HG00741.hp2 HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.149+2132T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845486 | ||||||
| chrX:2845488
|
CACGTGTG others(15): Show |
C | 32 | a0001c0001t0001g0181a0001c0001t0001g0184a0001c0001t0001g0196others(29): Show | 32 | HG00323.hp2 HG00438.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.149+2137_149+2158d others(24): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845488 | |||||
| chrX:2845490
|
C | CAT | 97 | a0001c0001t0001g0052a0001c0001t0001g0182a0001c0001t0001g0197others(94): Show | 97 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.149+2136_149+2137i others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845490 | ||||||
| chrX:2845490
|
C | T | 4 | a0001c0001t0001g0245a0001c0003t0007g0024a0002c0005t0006g0104others(1): Show | 4 | HG00741.hp2 HG02451.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+2136C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845490 | ||||||
| chrX:2845491
|
G | A | 74 | a0001c0001t0001g0133a0001c0001t0001g0135a0001c0001t0001g0139others(71): Show | 75 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.149+2137G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845491 | ||||||
| chrX:2845493
|
GTGTATGT others(29): Show |
G | 1 | a0001c0001t0001g0004 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.149+2141_149+2176d others(38): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845493 | |||||
| chrX:2845495
|
GTA | G | 2 | a0002c0002t0002g0257a0005c0009t0001g0060 | 2 | HG00280.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.149+2143_149+2144d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845495 | |||||
| chrX:2845499
|
G | A | 2 | a0002c0006t0003g0036a0009c0013t0005g0037 | 2 | HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.149+2145G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845499 | ||||||
| chrX:2845501
|
A | G | 3 | a0001c0001t0001g0133a0002c0002t0003g0132a0002c0002t0005g0016 | 3 | HG02630.hp2 HG02970.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.149+2147A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845501 | ||||||
| chrX:2845501
|
ATATT | A | 3 | a0001c0001t0002g0085a0002c0006t0003g0120a0002c0006t0005g0119 | 3 | HG02280.hp2 HG02293.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.149+2151_149+2154d others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845501 | |||||
| chrX:2845501
|
ATATTTAT others(45): Show |
A | 6 | a0001c0001t0002g0125a0001c0003t0007g0024a0002c0002t0006g0043others(3): Show | 6 | HG00741.hp2 HG02451.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.149+2151_149+2202d others(54): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845501 | |||||
| chrX:2845503
|
A | ACACG | 2 | a0002c0006t0003g0036a0009c0013t0005g0037 | 2 | HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.149+2149_149+2150i others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845503 | ||||||
| chrX:2845503
|
A | G | 2 | a0002c0002t0002g0257a0005c0009t0001g0060 | 2 | HG00280.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.149+2149A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845503 | ||||||
| chrX:2845503
|
ATT | A | 7 | a0001c0001t0001g0133a0001c0003t0005g0304a0001c0003t0008g0026others(4): Show | 7 | HG01891.hp2 HG02055.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.149+2151_149+2152d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845503 | |||||
| chrX:2845505
|
T | A | 2 | a0002c0002t0002g0257a0005c0009t0001g0060 | 2 | HG00280.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.149+2151T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845505 | ||||||
| chrX:2845505
|
T | G | 2 | a0002c0006t0003g0036a0009c0013t0005g0037 | 2 | HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.149+2151T>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845505 | ||||||
| chrX:2845510
|
T | C | 4 | a0001c0003t0005g0304a0001c0003t0008g0026a0003c0007t0001g0025others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+2156T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845510 | ||||||
| chrX:2845512
|
CACGTGTG others(39): Show |
C | 1 | a0001c0001t0001g0204 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.149+2161_149+2206d others(48): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845512 | |||||
| chrX:2845514
|
C | CAT | 95 | a0001c0001t0001g0182a0001c0001t0001g0197a0001c0001t0001g0198others(92): Show | 95 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.149+2160_149+2161i others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845514 | ||||||
| chrX:2845514
|
C | T | 41 | a0001c0001t0001g0181a0001c0001t0001g0184a0001c0001t0001g0196others(38): Show | 41 | HG00323.hp2 HG00438.hp2 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.149+2160C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845514 | ||||||
| chrX:2845515
|
G | A | 70 | a0001c0001t0001g0052a0001c0001t0001g0133a0001c0001t0001g0135others(67): Show | 71 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.149+2161G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845515 | ||||||
| chrX:2845517
|
GTGTATGT others(5): Show |
G | 3 | a0001c0001t0002g0085a0002c0002t0002g0257a0005c0009t0001g0060 | 3 | HG00280.hp1 HG02293.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.149+2165_149+2176d others(14): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845517 | |||||
| chrX:2845519
|
GTA | G | 1 | a0001c0001t0001g0245 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.149+2167_149+2168d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845519 | |||||
| chrX:2845521
|
A | ATATTTAT others(11): Show |
1 | a0001c0001t0007g0221 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.149+2168_149+2169i others(20): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845521 | |||||
| chrX:2845521
|
ATGTATAT others(25): Show |
A | 1 | a0001c0001t0001g0052 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.149+2169_149+2200d others(34): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845521 | |||||
| chrX:2845523
|
G | A | 2 | a0002c0006t0003g0036a0009c0013t0005g0037 | 2 | HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.149+2169G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845523 | ||||||
| chrX:2845525
|
A | G | 2 | a0002c0002t0006g0017a0002c0002t0006g0134 | 2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.149+2171A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845525 | ||||||
| chrX:2845525
|
ATATTTAT others(21): Show |
A | 8 | a0001c0003t0005g0304a0001c0003t0008g0026a0002c0002t0001g0123others(5): Show | 8 | HG01070.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.149+2175_149+2202d others(30): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845525 | |||||
| chrX:2845527
|
A | ACACG | 2 | a0002c0006t0003g0036a0009c0013t0005g0037 | 2 | HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.149+2173_149+2174i others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845527 | ||||||
| chrX:2845527
|
ATT | A | 8 | a0001c0003t0001g0027a0001c0003t0005g0022a0002c0002t0001g0032others(5): Show | 8 | HG02145.hp1 HG02280.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.149+2175_149+2176d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845527 | |||||
| chrX:2845529
|
T | A | 1 | a0002c0002t0006g0017 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.149+2175T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845529 | ||||||
| chrX:2845529
|
T | G | 2 | a0002c0006t0003g0036a0009c0013t0005g0037 | 2 | HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.149+2175T>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845529 | ||||||
| chrX:2845534
|
T | C | 8 | a0001c0003t0001g0027a0001c0003t0005g0022a0002c0002t0001g0032others(5): Show | 8 | HG02145.hp1 HG02280.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.149+2180T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845534 | ||||||
| chrX:2845538
|
C | CAT | 53 | a0001c0001t0001g0182a0001c0001t0001g0198a0001c0001t0001g0205others(50): Show | 54 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.149+2184_149+2185i others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845538 | ||||||
| chrX:2845538
|
C | T | 8 | a0001c0003t0001g0027a0001c0003t0005g0022a0002c0002t0001g0032others(5): Show | 8 | HG02145.hp1 HG02280.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.149+2184C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845538 | ||||||
| chrX:2845539
|
G | A | 146 | a0001c0001t0001g0004a0001c0001t0001g0133a0001c0001t0001g0135others(143): Show | 147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.149+2185G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845539 | ||||||
| chrX:2845541
|
GTGTATGT others(27): Show |
G | 1 | a0001c0001t0007g0191 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.149+2191_149+2224d others(36): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845541 | |||||
| chrX:2845543
|
GTA | G | 134 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.149+2191_149+2192d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845543 | |||||
| chrX:2845545
|
ATGTATAT others(1): Show |
A | 5 | a0001c0001t0001g0004a0001c0001t0002g0085a0002c0002t0002g0257others(2): Show | 6 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.149+2193_149+2200d others(10): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845545 | |||||
| chrX:2845549
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.149+2195A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845549 | ||||||
| chrX:2845549
|
ATATT | A | 62 | a0001c0001t0001g0001a0001c0001t0001g0074a0001c0001t0001g0078others(59): Show | 63 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.149+2199_149+2202d others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845549 | |||||
| chrX:2845551
|
A | ATATACAC others(11): Show |
3 | a0001c0003t0001g0030a0002c0006t0003g0120a0002c0006t0005g0119 | 3 | HG02280.hp2 HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.149+2198_149+2199i others(20): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845551 | |||||
| chrX:2845551
|
A | ATATACAC others(17): Show |
4 | a0002c0002t0002g0002a0002c0002t0003g0132a0002c0002t0005g0178others(1): Show | 5 | HG02572.hp1 HG02630.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.149+2198_149+2199i others(26): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845551 | |||||
| chrX:2845551
|
A | ATATATAC others(41): Show |
1 | a0001c0001t0001g0133 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.149+2198_149+2199i others(50): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845551 | |||||
| chrX:2845551
|
A | G | 134 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.149+2197A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845551 | ||||||
| chrX:2845553
|
T | A | 143 | a0001c0001t0001g0133a0001c0001t0001g0135a0001c0001t0001g0139others(140): Show | 144 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.149+2199T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845553 | ||||||
| chrX:2845553
|
T | TTATATAC others(67): Show |
1 | a0002c0002t0006g0134 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.149+2208_149+2209i others(76): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845553 | |||||
| chrX:2845553
|
T | TTATATAC others(15): Show |
20 | a0001c0001t0001g0205a0001c0001t0001g0214a0001c0001t0001g0234others(17): Show | 20 | HG00423.hp1 HG00609.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.149+2208_149+2209i others(24): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845553 | |||||
| chrX:2845553
|
T | TTATATAC others(43): Show |
1 | a0002c0002t0005g0016 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.149+2208_149+2209i others(52): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845553 | |||||
| chrX:2845553
|
T | TTATATAC others(113): Show |
1 | a0002c0002t0020g0255 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.149+2208_149+2209i others(122): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845553 | |||||
| chrX:2845553
|
T | TTATATAC others(41): Show |
15 | a0001c0001t0001g0182a0001c0001t0001g0236a0001c0001t0002g0200others(12): Show | 15 | HG00408.hp2 HG00423.hp2 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.149+2208_149+2209i others(50): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845553 | |||||
| chrX:2845553
|
T | TTATATAC others(67): Show |
10 | a0001c0001t0001g0198a0001c0001t0002g0261a0001c0001t0002g0262others(7): Show | 10 | HG02004.hp2 HG02040.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.149+2208_149+2209i others(76): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845553 | |||||
| chrX:2845553
|
T | TTATATAC others(93): Show |
1 | a0001c0001t0003g0241 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.149+2208_149+2209i others(102): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845553 | |||||
| chrX:2845553
|
T | TTATATAC others(119): Show |
1 | a0001c0001t0003g0231 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.149+2208_149+2209i others(128): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845553 | |||||
| chrX:2845553
|
T | TTATATAC others(91): Show |
1 | a0001c0001t0001g0216 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.149+2208_149+2209i others(100): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845553 | |||||
| chrX:2845562
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.149+2208C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845562 | ||||||
| chrX:2845563
|
G | A | 3 | a0001c0001t0002g0085a0001c0001t0002g0192a0002c0002t0005g0117 | 3 | HG00733.hp1 HG02293.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.149+2209G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845563 | ||||||
| chrX:2845565
|
GTGTATAC others(9): Show |
G | 2 | a0001c0001t0004g0130a0001c0001t0004g0131 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.149+2213_149+2228d others(18): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845565 | |||||
| chrX:2845567
|
G | A | 293 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0052others(290): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.149+2213G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845567 | ||||||
| chrX:2845567
|
G | GTATCTAT others(13): Show |
1 | a0001c0001t0001g0005 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.149+2216_149+2217i others(22): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845567 | |||||
| chrX:2845567
|
G | GTATGTAT others(13): Show |
1 | a0002c0002t0005g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.149+2216_149+2217i others(22): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845567 | |||||
| chrX:2845567
|
G | GTATGTAT others(107): Show |
1 | a0001c0001t0002g0192 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.149+2216_149+2217i others(116): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845567 | |||||
| chrX:2845567
|
G | GTATGTAT others(39): Show |
1 | a0001c0001t0001g0217 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.149+2216_149+2217i others(48): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845567 | |||||
| chrX:2845567
|
G | GTATGTAT others(181): Show |
1 | a0002c0005t0002g0115 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.149+2216_149+2217i others(190): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845567 | |||||
| chrX:2845569
|
A | G | 1 | a0001c0001t0002g0085 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.149+2215A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845569 | ||||||
| chrX:2845571
|
A | G | 1 | a0001c0001t0002g0085 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.149+2217A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845571 | ||||||
| chrX:2845572
|
C | T | 1 | a0001c0001t0002g0085 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.149+2218C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845572 | ||||||
| chrX:2845575
|
A | ATG | 1 | a0001c0001t0002g0192 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.149+2225_149+2226d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845575 | |||||
| chrX:2845577
|
G | A | 1 | a0001c0001t0002g0085 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.149+2223G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845577 | ||||||
| chrX:2845579
|
G | A | 1 | a0001c0001t0002g0085 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.149+2225G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845579 | ||||||
| chrX:2845581
|
A | G | 3 | a0002c0002t0003g0033a0002c0002t0003g0034a0002c0002t0003g0035 | 3 | HG02922.hp1 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.149+2227A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845581 | ||||||
| chrX:2845581
|
A | T | 1 | a0001c0001t0002g0085 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.149+2227A>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845581 | ||||||
| chrX:2845583
|
A | G | 2 | a0001c0001t0002g0192a0001c0001t0007g0191 | 2 | HG00733.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.149+2229A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845583 | ||||||
| chrX:2845589
|
A | G | 1 | a0001c0001t0002g0085 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.149+2235A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845589 | ||||||
| chrX:2845597
|
A | G | 121 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(118): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.149+2243A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845597 | ||||||
| chrX:2845599
|
G | T | 1 | a0001c0001t0002g0085 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.149+2245G>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845599 | ||||||
| chrX:2845606
|
T | C | 1 | a0001c0001t0002g0085 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.149+2252T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845606 | ||||||
| chrX:2845627
|
T | G | 1 | a0001c0001t0002g0085 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.149+2273T>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845627 | ||||||
| chrX:2845643
|
A | G | 138 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0181others(135): Show | 139 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.149+2289A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845643 | ||||||
| chrX:2845690
|
CATTT | C | 2 | a0002c0002t0003g0010a0002c0002t0004g0021 | 2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.149+2343_149+2346d others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845690 | |||||
| chrX:2845758
|
T | C | 3 | a0002c0002t0005g0126a0004c0008t0006g0009a0004c0008t0006g0127 | 3 | HG01261.hp1 HG02109.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.149+2404T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845758 | ||||||
| chrX:2845789
|
A | G | 1 | a0001c0001t0003g0180 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.149+2435A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845789 | ||||||
| chrX:2845945
|
CT | C | 1 | a0001c0001t0003g0180 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.149+2593delT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845945 | |||||
| chrX:2845950
|
A | G | 1 | a0002c0002t0016g0272 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.149+2596A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845950 | ||||||
| chrX:2845971
|
AT | A | 4 | a0002c0005t0006g0104a0002c0005t0007g0018a0002c0005t0007g0020others(1): Show | 4 | HG00741.hp2 HG01074.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+2620delT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845971 | |||||
| chrX:2845974
|
T | A | 2 | a0002c0002t0003g0033a0002c0002t0003g0034 | 2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.149+2620T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845974 | ||||||
| chrX:2845982
|
T | A | 5 | a0001c0001t0003g0180a0002c0005t0006g0104a0002c0005t0007g0018others(2): Show | 5 | HG00741.hp2 HG01074.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.149+2628T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845982 | ||||||
| chrX:2845995
|
G | GTA | 77 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(74): Show | 79 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.149+2650_149+2651d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845995 | |||||
| chrX:2845995
|
G | GTATATAT others(39): Show |
1 | a0002c0006t0003g0036 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.149+2671_149+2672i others(48): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2845995 | |||||
| chrX:2846004
|
T | TACATATA others(39): Show |
1 | a0009c0013t0005g0037 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.149+2671_149+2672i others(48): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846004 | |||||
| chrX:2846006
|
C | CA | 1 | a0001c0001t0003g0180 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.149+2653dupA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846006 | |||||
| chrX:2846014
|
T | TAC | 1 | a0001c0001t0001g0184 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.149+2670_149+2671d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846014 | |||||
| chrX:2846032
|
T | TACGC | 1 | a0002c0005t0007g0018 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.149+2680_149+2681i others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846032 | |||||
| chrX:2846033
|
A | ACG | 1 | a0002c0005t0006g0104 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.149+2680_149+2681i others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846033 | |||||
| chrX:2846035
|
A | G | 2 | a0002c0005t0007g0020a0004c0008t0006g0019 | 2 | HG01891.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.149+2681A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846035 | ||||||
| chrX:2846036
|
C | CACATATA others(1): Show |
1 | a0001c0001t0002g0222 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.149+2683_149+2684i others(10): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846036 | |||||
| chrX:2846036
|
C | CAT | 3 | a0002c0002t0002g0257a0002c0002t0012g0066a0002c0002t0012g0067 | 3 | HG00280.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.149+2701_149+2702d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846036 | |||||
| chrX:2846036
|
C | CATAT | 7 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0238others(4): Show | 7 | HG01978.hp2 HG02257.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.149+2699_149+2702d others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846036 | |||||
| chrX:2846036
|
C | CATATAT | 22 | a0001c0001t0001g0197a0001c0001t0001g0204a0001c0001t0001g0205others(19): Show | 22 | HG00609.hp1 HG00738.hp1 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.149+2697_149+2702d others(8): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846036 | |||||
| chrX:2846036
|
C | CATATATA others(1): Show |
15 | a0001c0001t0001g0181a0001c0001t0001g0184a0001c0001t0001g0214others(12): Show | 15 | HG01175.hp1 HG02071.hp1 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.149+2695_149+2702d others(10): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846036 | |||||
| chrX:2846036
|
C | CATATATA others(3): Show |
9 | a0001c0001t0001g0217a0001c0001t0001g0224a0001c0001t0001g0236others(6): Show | 9 | HG01516.hp1 HG02074.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.149+2693_149+2702d others(12): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846036 | |||||
| chrX:2846036
|
C | CATATATA others(5): Show |
5 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0003g0180others(2): Show | 5 | HG01081.hp1 HG01192.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.149+2691_149+2702d others(14): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846036 | |||||
| chrX:2846036
|
C | CATATATA others(43): Show |
1 | a0002c0002t0003g0010 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.149+2695_149+2696i others(52): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846036 | |||||
| chrX:2846036
|
C | CATATATA others(9): Show |
2 | a0001c0001t0001g0240a0006c0010t0003g0202 | 2 | HG01123.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.149+2687_149+2702d others(18): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846036 | |||||
| chrX:2846036
|
C | T | 1 | a0002c0005t0007g0018 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.149+2682C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846036 | ||||||
| chrX:2846038
|
T | C | 2 | a0002c0005t0007g0020a0004c0008t0006g0019 | 2 | HG01891.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.149+2684T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846038 | ||||||
| chrX:2846047
|
A | ATATG | 1 | a0002c0002t0005g0201 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.149+2696_149+2697i others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846047 | |||||
| chrX:2846049
|
ATATATAT others(6): Show |
A | 1 | a0002c0002t0008g0219 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.149+2697_149+2709d others(15): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846049 | |||||
| chrX:2846050
|
T | C | 6 | a0001c0001t0001g0133a0002c0002t0003g0132a0002c0002t0004g0021others(3): Show | 6 | HG02572.hp1 HG02630.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.149+2696T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846050 | ||||||
| chrX:2846051
|
ATATATTT others(9): Show |
A | 28 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(25): Show | 28 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.149+2699_149+2714d others(18): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846051 | |||||
| chrX:2846051
|
ATATATTT others(10): Show |
A | 2 | a0001c0004t0004g0090a0002c0002t0004g0167 | 2 | NA18959.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.149+2699_149+2715d others(19): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846051 | |||||
| chrX:2846052
|
T | C | 2 | a0002c0002t0002g0002a0002c0002t0005g0178 | 3 | HG02630.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.149+2698T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846052 | ||||||
| chrX:2846053
|
ATATTTTT others(8): Show |
A | 6 | a0001c0003t0002g0042a0001c0003t0004g0041a0002c0002t0002g0144others(3): Show | 6 | HG01243.hp1 HG02723.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.149+2701_149+2715d others(17): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846053 | |||||
| chrX:2846053
|
ATATTTTT others(9): Show |
A | 13 | a0001c0001t0001g0074a0001c0001t0001g0194a0001c0001t0001g0298others(10): Show | 13 | HG00099.hp1 HG00408.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.149+2701_149+2716d others(18): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846053 | |||||
| chrX:2846053
|
ATATTTTT others(10): Show |
A | 1 | a0001c0001t0002g0291 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.149+2701_149+2717d others(19): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846053 | |||||
| chrX:2846053
|
ATATTTTT others(11): Show |
A | 1 | a0001c0001t0002g0281 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.149+2701_149+2718d others(20): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846053 | |||||
| chrX:2846055
|
A | AT | 4 | a0002c0002t0003g0109a0002c0002t0005g0105a0002c0002t0005g0108others(1): Show | 4 | HG02486.hp1 HG03130.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+2730dupT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846055 | |||||
| chrX:2846055
|
A | ATATACAC others(42): Show |
1 | a0002c0002t0004g0021 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.149+2702_149+2703i others(51): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846055 | |||||
| chrX:2846055
|
A | ATATAT | 1 | a0001c0001t0003g0275 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.149+2702_149+2703i others(7): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846055 | |||||
| chrX:2846055
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0004g0012 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.149+2702_149+2703i others(15): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846055 | |||||
| chrX:2846055
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0245 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.149+2702_149+2703i others(17): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846055 | |||||
| chrX:2846055
|
A | ATATATAT others(1): Show |
2 | a0001c0001t0004g0246a0002c0002t0003g0207 | 2 | HG02683.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.149+2702_149+2703i others(10): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846055 | |||||
| chrX:2846055
|
A | ATATATT | 1 | a0005c0009t0001g0060 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.149+2702_149+2703i others(8): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846055 | |||||
| chrX:2846055
|
A | ATT | 1 | a0004c0008t0006g0009 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.149+2729_149+2730d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846055 | |||||
| chrX:2846055
|
A | T | 4 | a0002c0002t0002g0038a0002c0002t0002g0039a0002c0002t0003g0010others(1): Show | 4 | HG01884.hp2 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+2701A>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846055 | ||||||
| chrX:2846055
|
AT | A | 4 | a0001c0001t0004g0131a0002c0002t0007g0118a0002c0005t0007g0020others(1): Show | 4 | HG01257.hp1 HG01891.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+2730delT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846055 | |||||
| chrX:2846055
|
ATT | A | 7 | a0001c0001t0002g0192a0001c0001t0004g0003a0001c0001t0004g0068others(4): Show | 7 | HG00733.hp1 HG01099.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.149+2729_149+2730d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846055 | |||||
| chrX:2846055
|
ATTTTTTT others(4): Show |
A | 1 | a0001c0003t0001g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.149+2720_149+2730d others(13): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846055 | |||||
| chrX:2846055
|
ATTTTTTT others(6): Show |
A | 14 | a0001c0003t0001g0027a0001c0003t0005g0022a0001c0003t0005g0304others(11): Show | 14 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.149+2718_149+2730d others(15): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846055 | |||||
| chrX:2846055
|
ATTTTTTT others(7): Show |
A | 7 | a0001c0001t0001g0083a0001c0001t0002g0085a0001c0001t0004g0081others(4): Show | 7 | HG01255.hp1 HG01978.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.149+2717_149+2730d others(16): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846055 | |||||
| chrX:2846055
|
ATTTTTTT others(8): Show |
A | 2 | a0001c0001t0001g0078a0002c0005t0002g0176 | 2 | HG02280.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.149+2716_149+2730d others(17): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846055 | |||||
| chrX:2846055
|
ATTTTTTT others(9): Show |
A | 47 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0098others(44): Show | 49 | HG00140.hp1 HG00323.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.149+2715_149+2730d others(18): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846055 | |||||
| chrX:2846056
|
T | TA | 10 | a0001c0003t0001g0114a0002c0002t0002g0107a0002c0002t0002g0111others(7): Show | 10 | HG01884.hp1 HG02257.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.149+2702_149+2703i others(3): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846056 | ||||||
| chrX:2846056
|
T | TATA | 15 | a0001c0001t0001g0052a0002c0002t0001g0186a0002c0002t0001g0254others(12): Show | 15 | HG00323.hp2 HG00423.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.149+2702_149+2703i others(5): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846056 | ||||||
| chrX:2846056
|
T | TATACACA others(26): Show |
5 | a0001c0001t0001g0133a0002c0002t0003g0132a0002c0002t0005g0016others(2): Show | 5 | HG02572.hp1 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.149+2702_149+2703i others(35): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846056 | ||||||
| chrX:2846056
|
T | TATATA | 12 | a0001c0001t0001g0182a0001c0001t0001g0196a0001c0001t0001g0211others(9): Show | 12 | HG00438.hp2 HG00741.hp1 HG02976.hp2 others(9): Show |
intron_variant | MODIFIER | c.149+2702_149+2703i others(7): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846056 | ||||||
| chrX:2846056
|
T | TATATACA others(28): Show |
2 | a0002c0002t0002g0002a0002c0002t0005g0178 | 3 | HG02630.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.149+2702_149+2703i others(37): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846056 | ||||||
| chrX:2846056
|
T | TATATATA | 17 | a0001c0001t0001g0198a0001c0001t0001g0234a0001c0001t0001g0239others(14): Show | 17 | HG00639.hp2 HG02004.hp2 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.149+2702_149+2703i others(9): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846056 | ||||||
| chrX:2846056
|
T | TATATATA others(2): Show |
7 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0002g0059others(4): Show | 7 | HG02135.hp1 HG02165.hp1 NA18993.hp2 others(4): Show |
intron_variant | MODIFIER | c.149+2702_149+2703i others(11): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846056 | ||||||
| chrX:2846056
|
T | TATATATA others(4): Show |
2 | a0001c0001t0008g0064a0002c0005t0006g0104 | 2 | HG00741.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.149+2702_149+2703i others(13): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846056 | ||||||
| chrX:2846056
|
T | TATATATA others(6): Show |
2 | a0001c0001t0002g0183a0001c0001t0002g0220 | 2 | NA19066.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.149+2702_149+2703i others(15): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846056 | ||||||
| chrX:2846056
|
T | TATATATA others(8): Show |
1 | a0001c0001t0003g0209 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.149+2702_149+2703i others(17): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846056 | ||||||
| chrX:2846057
|
T | A | 82 | a0001c0001t0001g0004a0001c0001t0001g0181a0001c0001t0001g0184others(79): Show | 83 | HG00280.hp1 HG00408.hp2 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.149+2703T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846057 | ||||||
| chrX:2846058
|
T | A | 60 | a0001c0001t0001g0052a0001c0001t0001g0133a0001c0001t0001g0182others(57): Show | 61 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.149+2704T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846058 | ||||||
| chrX:2846059
|
T | A | 63 | a0001c0001t0001g0004a0001c0001t0001g0181a0001c0001t0001g0184others(60): Show | 64 | HG00280.hp1 HG00609.hp1 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.149+2705T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846059 | ||||||
| chrX:2846060
|
T | A | 36 | a0001c0001t0001g0052a0001c0001t0001g0133a0001c0001t0001g0196others(33): Show | 37 | HG00323.hp2 HG00423.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.149+2706T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846060 | ||||||
| chrX:2846061
|
T | A | 25 | a0001c0001t0001g0004a0001c0001t0001g0197a0001c0001t0001g0227others(22): Show | 26 | HG00280.hp1 HG00733.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.149+2707T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846061 | ||||||
| chrX:2846062
|
T | A | 21 | a0001c0001t0001g0133a0001c0001t0001g0196a0001c0001t0001g0264others(18): Show | 22 | HG00323.hp2 HG01891.hp1 HG02015.hp1 others(19): Show |
intron_variant | MODIFIER | c.149+2708T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846062 | ||||||
| chrX:2846063
|
T | A | 5 | a0001c0001t0001g0240a0001c0001t0003g0273a0002c0002t0004g0235others(2): Show | 5 | HG01074.hp1 HG02523.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.149+2709T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846063 | ||||||
| chrX:2846064
|
T | A | 9 | a0001c0001t0001g0133a0002c0002t0002g0002a0002c0002t0003g0132others(6): Show | 10 | HG02572.hp1 HG02630.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.149+2710T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846064 | ||||||
| chrX:2846066
|
T | A | 6 | a0002c0002t0002g0002a0002c0002t0003g0132a0002c0002t0005g0016others(3): Show | 7 | HG02630.hp1 HG02886.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.149+2712T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846066 | ||||||
| chrX:2846068
|
T | A | 3 | a0001c0003t0001g0030a0002c0002t0002g0002a0002c0002t0006g0134 | 4 | HG02630.hp1 HG02886.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+2714T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846068 | ||||||
| chrX:2846070
|
T | A | 15 | a0001c0003t0001g0027a0001c0003t0001g0030a0001c0003t0005g0022others(12): Show | 15 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.149+2716T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846070 | ||||||
| chrX:2846071
|
T | A | 6 | a0001c0001t0002g0085a0001c0001t0004g0081a0002c0002t0004g0080others(3): Show | 6 | HG01255.hp1 HG01981.hp2 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.149+2717T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846071 | ||||||
| chrX:2846072
|
T | A | 12 | a0001c0003t0001g0027a0001c0003t0001g0030a0001c0003t0005g0304others(9): Show | 12 | HG01891.hp2 HG02055.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.149+2718T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846072 | ||||||
| chrX:2846074
|
T | A | 1 | a0002c0002t0001g0032 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.149+2720T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846074 | ||||||
| chrX:2846128
|
G | A | 60 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(57): Show | 62 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.149+2774G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846128 | ||||||
| chrX:2846130
|
G | A | 1 | a0002c0002t0002g0152 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.149+2776G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846130 | ||||||
| chrX:2846159
|
TG | T | 1 | a0001c0001t0003g0180 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.149+2808delG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846159 | |||||
| chrX:2846206
|
A | T | 1 | a0001c0001t0002g0276 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.149+2852A>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846206 | ||||||
| chrX:2846276
|
A | AG | 1 | a0001c0001t0003g0180 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.149+2924dupG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846276 | |||||
| chrX:2846301
|
A | AT | 1 | a0001c0001t0003g0180 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.149+2947_149+2948i others(3): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846301 | ||||||
| chrX:2846330
|
G | C | 1 | a0001c0001t0001g0289 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.149+2976G>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846330 | ||||||
| chrX:2846441
|
G | T | 11 | a0001c0001t0001g0133a0002c0002t0002g0002a0002c0002t0003g0010others(8): Show | 12 | HG02572.hp1 HG02630.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.149+3087G>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846441 | ||||||
| chrX:2846572
|
T | C | 1 | a0002c0002t0020g0255 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.149+3218T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846572 | ||||||
| chrX:2846580
|
C | CA | 1 | a0001c0001t0003g0180 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.149+3232dupA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846580 | |||||
| chrX:2846592
|
A | AG | 1 | a0001c0001t0003g0180 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.149+3239dupG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846592 | |||||
| chrX:2846610
|
T | A | 1 | a0001c0001t0003g0180 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.149+3256T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846610 | ||||||
| chrX:2846635
|
G | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(137): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.149+3281G>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846635 | ||||||
| chrX:2846813
|
TAGAA | T | 52 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(49): Show | 52 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.149+3464_149+3467d others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846813 | |||||
| chrX:2846847
|
A | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(135): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.149+3493A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846847 | ||||||
| chrX:2846912
|
AG | A | 1 | a0014c0012t0001g0305 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.149+3561delG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2846912 | |||||
| chrX:2847182
|
T | G | 4 | a0002c0005t0006g0104a0002c0005t0007g0018a0002c0005t0007g0020others(1): Show | 4 | HG00741.hp2 HG01074.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+3828T>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2847182 | ||||||
| chrX:2847191
|
G | GT | 1 | a0015c0011t0002g0185 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.149+3840dupT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2847191 | |||||
| chrX:2847223
|
C | G | 4 | a0002c0005t0006g0104a0002c0005t0007g0018a0002c0005t0007g0020others(1): Show | 4 | HG00741.hp2 HG01074.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+3869C>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2847223 | ||||||
| chrX:2847278
|
A | C | 141 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(138): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.149+3924A>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2847278 | ||||||
| chrX:2847321
|
A | G | 81 | a0001c0001t0001g0133a0001c0001t0001g0135a0001c0001t0001g0139others(78): Show | 82 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.149+3967A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2847321 | ||||||
| chrX:2847329
|
A | T | 141 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(138): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.149+3975A>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2847329 | ||||||
| chrX:2847435
|
T | A | 15 | a0001c0003t0001g0027a0001c0003t0001g0030a0001c0003t0005g0022others(12): Show | 15 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.149+4081T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2847435 | ||||||
| chrX:2847464
|
G | C | 11 | a0001c0001t0001g0133a0002c0002t0002g0002a0002c0002t0003g0010others(8): Show | 12 | HG02572.hp1 HG02630.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.149+4110G>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2847464 | ||||||
| chrX:2847533
|
C | CA | 50 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(47): Show | 52 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.149+4200dupA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2847533 | |||||
| chrX:2847533
|
C | CAA | 11 | a0001c0001t0001g0083a0001c0001t0001g0205a0001c0001t0002g0075others(8): Show | 11 | HG00609.hp1 HG01255.hp1 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.149+4199_149+4200d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2847533 | |||||
| chrX:2847533
|
CA | C | 128 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0181others(125): Show | 129 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.149+4200delA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2847533 | |||||
| chrX:2847533
|
CAA | C | 10 | a0001c0001t0003g0209a0001c0001t0007g0221a0001c0003t0001g0027others(7): Show | 10 | HG01243.hp1 HG01515.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.149+4199_149+4200d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2847533 | |||||
| chrX:2847533
|
CAAA | C | 15 | a0001c0003t0001g0030a0001c0003t0005g0022a0001c0003t0005g0304others(12): Show | 15 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.149+4198_149+4200d others(5): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2847533 | |||||
| chrX:2847533
|
CAAAAA | C | 11 | a0001c0001t0001g0133a0002c0002t0002g0002a0002c0002t0003g0010others(8): Show | 12 | HG02572.hp1 HG02630.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.149+4196_149+4200d others(7): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2847533 | |||||
| chrX:2847560
|
T | C | 15 | a0001c0001t0001g0133a0002c0002t0002g0002a0002c0002t0003g0010others(12): Show | 16 | HG00741.hp2 HG01074.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.149+4206T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2847560 | ||||||
| chrX:2847703
|
A | AAAAT | 96 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0181others(93): Show | 97 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.149+4393_149+4396d others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2847703 | |||||
| chrX:2847703
|
A | AAAATAAA others(1): Show |
7 | a0001c0003t0005g0177a0002c0002t0002g0038a0002c0002t0002g0039others(4): Show | 7 | HG01884.hp2 HG02280.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.149+4389_149+4396d others(10): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2847703 | |||||
| chrX:2847703
|
AAAAT | A | 2 | a0001c0001t0001g0239a0001c0001t0001g0268 | 2 | NA18968.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.149+4393_149+4396d others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2847703 | |||||
| chrX:2847703
|
AAAATAAA others(1): Show |
A | 57 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(54): Show | 59 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.149+4389_149+4396d others(10): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2847703 | |||||
| chrX:2847703
|
AAAATAAA others(5): Show |
A | 23 | a0001c0003t0001g0114a0001c0003t0002g0045a0002c0002t0001g0254others(20): Show | 23 | HG00741.hp2 HG01074.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.149+4385_149+4396d others(14): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2847703 | |||||
| chrX:2847703
|
AAAATAAA others(13): Show |
A | 11 | a0001c0001t0001g0133a0002c0002t0002g0002a0002c0002t0003g0010others(8): Show | 12 | HG02572.hp1 HG02630.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.149+4377_149+4396d others(22): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2847703 | |||||
| chrX:2847725
|
A | T | 56 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0074others(53): Show | 58 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.149+4371A>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2847725 | ||||||
| chrX:2847733
|
A | AATAAATA others(5): Show |
1 | a0002c0002t0004g0169 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.149+4390_149+4391i others(14): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2847733 | |||||
| chrX:2847733
|
A | C | 46 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(43): Show | 46 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.149+4379A>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2847733 | ||||||
| chrX:2847747
|
T | TAAAA | 3 | a0001c0001t0002g0261a0001c0001t0002g0262a0001c0001t0003g0208 | 3 | NA18988.hp1 NA18999.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.149+4395_149+4398d others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2847747 | |||||
| chrX:2847747
|
T | TAAATAAA others(1): Show |
2 | a0001c0001t0001g0198a0002c0002t0002g0252 | 2 | HG00323.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.149+4396_149+4397i others(10): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2847747 | |||||
| chrX:2847784
|
T | C | 3 | a0001c0003t0002g0042a0001c0003t0004g0041a0002c0005t0002g0176 | 3 | HG01243.hp1 HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.149+4430T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2847784 | ||||||
| chrX:2847791
|
C | T | 1 | a0001c0001t0007g0221 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.149+4437C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2847791 | ||||||
| chrX:2847884
|
C | G | 26 | a0001c0001t0001g0133a0001c0003t0001g0027a0001c0003t0001g0030others(23): Show | 27 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.149+4530C>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2847884 | ||||||
| chrX:2847900
|
A | T | 1 | a0010c0015t0001g0138 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.149+4546A>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2847900 | ||||||
| chrX:2847903
|
G | A | 3 | a0002c0005t0007g0018a0002c0005t0007g0020a0004c0008t0006g0019 | 3 | HG01074.hp1 HG01891.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.149+4549G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2847903 | ||||||
| chrX:2847930
|
G | A | 4 | a0002c0005t0006g0104a0002c0005t0007g0018a0002c0005t0007g0020others(1): Show | 4 | HG00741.hp2 HG01074.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+4576G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2847930 | ||||||
| chrX:2847970
|
A | T | 2 | a0001c0001t0009g0266a0001c0001t0009g0270 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.149+4616A>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2847970 | ||||||
| chrX:2848096
|
TGA | T | 4 | a0002c0005t0006g0104a0002c0005t0007g0018a0002c0005t0007g0020others(1): Show | 4 | HG00741.hp2 HG01074.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+4744_149+4745d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2848096 | |||||
| chrX:2848312
|
A | G | 228 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(225): Show | 232 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.149+4958A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2848312 | ||||||
| chrX:2848359
|
T | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0078others(51): Show | 56 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.149+5005T>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2848359 | ||||||
| chrX:2848498
|
AC | A | 89 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0078others(86): Show | 92 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.149+5146delC | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2848498 | |||||
| chrX:2848504
|
A | C | 89 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0078others(86): Show | 92 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.149+5150A>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2848504 | ||||||
| chrX:2848535
|
CA | C | 1 | a0014c0012t0001g0305 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.149+5187delA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2848535 | |||||
| chrX:2848544
|
A | AG | 1 | a0002c0002t0006g0134 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.149+5193dupG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2848544 | |||||
| chrX:2848547
|
G | GA | 17 | a0001c0003t0001g0027a0001c0003t0001g0030a0001c0003t0005g0022others(14): Show | 17 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.149+5205dupA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2848547 | |||||
| chrX:2848547
|
G | GAA | 58 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0078others(55): Show | 60 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.149+5204_149+5205d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2848547 | |||||
| chrX:2848547
|
G | GAAA | 2 | a0001c0001t0002g0079a0002c0002t0003g0033 | 2 | HG03516.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.149+5203_149+5205d others(5): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2848547 | |||||
| chrX:2848547
|
G | GGA | 5 | a0001c0001t0001g0133a0002c0002t0002g0002a0002c0002t0003g0132others(2): Show | 6 | HG02630.hp1 HG02630.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.149+5193_149+5194i others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2848547 | ||||||
| chrX:2848547
|
G | GGAA | 1 | a0002c0002t0006g0017 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.149+5193_149+5194i others(5): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2848547 | ||||||
| chrX:2848547
|
GA | G | 217 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0074others(214): Show | 218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.149+5205delA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2848547 | |||||
| chrX:2848547
|
GAA | G | 5 | a0001c0001t0002g0189a0001c0001t0002g0276a0001c0001t0003g0274others(2): Show | 5 | HG00423.hp2 NA18950.hp1 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.149+5204_149+5205d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2848547 | |||||
| chrX:2848559
|
A | C | 1 | a0001c0001t0001g0184 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.149+5205A>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2848559 | ||||||
| chrX:2848616
|
A | T | 1 | a0001c0001t0017g0094 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.149+5262A>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2848616 | ||||||
| chrX:2848630
|
G | C | 156 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0078others(153): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.149+5276G>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2848630 | ||||||
| chrX:2848825
|
G | GA | 1 | a0014c0012t0001g0305 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.150-5152dupA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2848825 | |||||
| chrX:2848926
|
A | AG | 1 | a0014c0012t0001g0305 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.150-5051dupG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2848926 | |||||
| chrX:2848979
|
A | T | 56 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0078others(53): Show | 58 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.150-5001A>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2848979 | ||||||
| chrX:2849145
|
T | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0078others(53): Show | 58 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.150-4835T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2849145 | ||||||
| chrX:2849189
|
T | C | 57 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0078others(54): Show | 59 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.150-4791T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2849189 | ||||||
| chrX:2849216
|
T | TC | 1 | a0014c0012t0001g0305 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.150-4758dupC | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2849216 | |||||
| chrX:2849228
|
G | T | 11 | a0002c0002t0001g0008a0002c0002t0001g0047a0002c0002t0003g0010others(8): Show | 11 | HG00733.hp2 HG01261.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.150-4752G>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2849228 | ||||||
| chrX:2849258
|
A | G | 10 | a0001c0001t0001g0133a0002c0002t0002g0011a0002c0002t0003g0132others(7): Show | 10 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.150-4722A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2849258 | ||||||
| chrX:2849312
|
G | A | 2 | a0001c0001t0001g0224a0001c0001t0001g0248 | 2 | HG03239.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.150-4668G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2849312 | ||||||
| chrX:2849325
|
G | T | 88 | a0001c0001t0001g0133a0001c0001t0001g0135a0001c0001t0001g0139others(85): Show | 89 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.150-4655G>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2849325 | ||||||
| chrX:2849331
|
G | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0078others(53): Show | 58 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.150-4649G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2849331 | ||||||
| chrX:2849344
|
C | T | 56 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0078others(53): Show | 58 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.150-4636C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2849344 | ||||||
| chrX:2849379
|
CA | C | 1 | a0014c0012t0001g0305 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.150-4599delA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2849379 | |||||
| chrX:2849419
|
A | G | 1 | a0002c0002t0004g0302 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.150-4561A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2849419 | ||||||
| chrX:2849535
|
A | T | 1 | a0002c0002t0001g0160 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.150-4445A>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2849535 | ||||||
| chrX:2849596
|
A | G | 64 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(61): Show | 64 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.150-4384A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2849596 | ||||||
| chrX:2849680
|
T | C | 12 | a0001c0001t0001g0133a0002c0002t0002g0002a0002c0002t0002g0011others(9): Show | 13 | HG02572.hp1 HG02615.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.150-4300T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2849680 | ||||||
| chrX:2849704
|
A | G | 15 | a0001c0003t0001g0027a0001c0003t0001g0030a0001c0003t0005g0022others(12): Show | 15 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.150-4276A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2849704 | ||||||
| chrX:2849884
|
G | C | 1 | a0001c0001t0002g0192 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.150-4096G>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2849884 | ||||||
| chrX:2849901
|
G | C | 5 | a0002c0002t0003g0010a0002c0002t0004g0021a0002c0002t0005g0050others(2): Show | 5 | HG02622.hp2 HG02647.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-4079G>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2849901 | ||||||
| chrX:2849904
|
C | T | 12 | a0001c0001t0001g0133a0002c0002t0002g0002a0002c0002t0002g0011others(9): Show | 13 | HG02572.hp1 HG02615.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.150-4076C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2849904 | ||||||
| chrX:2849916
|
A | G | 3 | a0001c0001t0001g0240a0001c0001t0001g0249a0001c0001t0001g0250 | 3 | HG01081.hp1 HG01192.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.150-4064A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2849916 | ||||||
| chrX:2849974
|
G | T | 1 | a0001c0001t0008g0064 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.150-4006G>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2849974 | ||||||
| chrX:2850001
|
C | A | 12 | a0001c0001t0001g0133a0002c0002t0002g0002a0002c0002t0002g0011others(9): Show | 13 | HG02572.hp1 HG02615.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.150-3979C>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2850001 | ||||||
| chrX:2850128
|
A | AATAATG | 1 | a0002c0002t0001g0179 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.150-3834_150-3829d others(8): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2850128 | |||||
| chrX:2850128
|
AATAATG | A | 61 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(58): Show | 61 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.150-3834_150-3829d others(8): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2850128 | |||||
| chrX:2850222
|
T | G | 1 | a0001c0001t0001g0052 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.150-3758T>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2850222 | ||||||
| chrX:2850314
|
C | T | 1 | a0013c0017t0005g0243 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.150-3666C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2850314 | ||||||
| chrX:2850374
|
A | G | 29 | a0001c0001t0001g0133a0001c0003t0001g0027a0001c0003t0001g0030others(26): Show | 30 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.150-3606A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2850374 | ||||||
| chrX:2850570
|
C | G | 150 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0074others(147): Show | 151 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.150-3410C>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2850570 | ||||||
| chrX:2850576
|
T | C | 12 | a0001c0001t0001g0133a0002c0002t0002g0002a0002c0002t0002g0011others(9): Show | 13 | HG02572.hp1 HG02615.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.150-3404T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2850576 | ||||||
| chrX:2850583
|
A | C | 3 | a0002c0002t0002g0038a0002c0002t0002g0039a0002c0005t0003g0040 | 3 | HG01884.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.150-3397A>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2850583 | ||||||
| chrX:2850595
|
G | A | 293 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(290): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.150-3385G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2850595 | ||||||
| chrX:2850672
|
T | C | 149 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0074others(146): Show | 150 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.150-3308T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2850672 | ||||||
| chrX:2850697
|
C | T | 27 | a0001c0001t0001g0133a0001c0003t0001g0027a0001c0003t0001g0030others(24): Show | 28 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.150-3283C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2850697 | ||||||
| chrX:2850698
|
A | T | 15 | a0001c0003t0001g0027a0001c0003t0001g0030a0001c0003t0005g0022others(12): Show | 15 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.150-3282A>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2850698 | ||||||
| chrX:2850791
|
C | T | 1 | a0005c0009t0001g0060 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.150-3189C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2850791 | ||||||
| chrX:2850810
|
C | T | 55 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0078others(52): Show | 57 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.150-3170C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2850810 | ||||||
| chrX:2850823
|
A | G | 55 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0078others(52): Show | 57 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.150-3157A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2850823 | ||||||
| chrX:2850824
|
T | G | 8 | a0002c0002t0002g0144a0002c0002t0002g0163a0002c0002t0002g0164others(5): Show | 8 | HG02083.hp1 HG02132.hp1 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.150-3156T>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2850824 | ||||||
| chrX:2850868
|
T | C | 303 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(300): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.150-3112T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2850868 | ||||||
| chrX:2850887
|
T | C | 15 | a0001c0003t0001g0027a0001c0003t0001g0030a0001c0003t0005g0022others(12): Show | 15 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.150-3093T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2850887 | ||||||
| chrX:2851000
|
C | T | 1 | a0002c0002t0003g0168 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.150-2980C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2851000 | ||||||
| chrX:2851062
|
A | T | 148 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0074others(145): Show | 149 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.150-2918A>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2851062 | ||||||
| chrX:2851232
|
C | T | 27 | a0001c0001t0001g0133a0001c0003t0001g0027a0001c0003t0001g0030others(24): Show | 28 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.150-2748C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2851232 | ||||||
| chrX:2851243
|
T | C | 62 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(59): Show | 62 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.150-2737T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2851243 | ||||||
| chrX:2851285
|
G | A | 7 | a0002c0002t0003g0010a0002c0002t0003g0033a0002c0002t0003g0034others(4): Show | 7 | HG02622.hp2 HG02647.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.150-2695G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2851285 | ||||||
| chrX:2851293
|
C | T | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 235 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.150-2687C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2851293 | ||||||
| chrX:2851433
|
G | A | 7 | a0002c0002t0003g0010a0002c0002t0003g0033a0002c0002t0003g0034others(4): Show | 7 | HG02622.hp2 HG02647.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.150-2547G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2851433 | ||||||
| chrX:2851548
|
G | A | 1 | a0002c0002t0003g0168 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.150-2432G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2851548 | ||||||
| chrX:2851782
|
G | A | 1 | a0001c0001t0002g0085 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.150-2198G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2851782 | ||||||
| chrX:2851865
|
G | A | 1 | a0002c0002t0005g0126 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.150-2115G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2851865 | ||||||
| chrX:2852114
|
G | A | 1 | a0001c0001t0001g0285 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.150-1866G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2852114 | ||||||
| chrX:2852126
|
A | G | 34 | a0001c0001t0001g0133a0001c0003t0001g0027a0001c0003t0001g0030others(31): Show | 35 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(32): Show |
intron_variant | MODIFIER | c.150-1854A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2852126 | ||||||
| chrX:2852378
|
C | T | 27 | a0001c0001t0001g0133a0001c0003t0001g0027a0001c0003t0001g0030others(24): Show | 28 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.150-1602C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2852378 | ||||||
| chrX:2852569
|
C | A | 3 | a0001c0001t0002g0192a0001c0001t0007g0191a0002c0002t0007g0193 | 3 | HG00733.hp1 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.150-1411C>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2852569 | ||||||
| chrX:2853088
|
C | T | 3 | a0001c0003t0002g0042a0001c0003t0002g0045a0001c0003t0004g0041 | 3 | HG01243.hp1 HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.150-892C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2853088 | ||||||
| chrX:2853103
|
C | CTT | 1 | a0001c0001t0003g0180 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.150-876_150-875ins others(2): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2853103 | |||||
| chrX:2853110
|
G | T | 1 | a0001c0001t0003g0057 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.150-870G>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2853110 | ||||||
| chrX:2853190
|
T | TTTTG | 1 | a0013c0017t0005g0243 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.150-778_150-775dup others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2853190 | |||||
| chrX:2853273
|
C | T | 176 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0052others(173): Show | 178 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.150-707C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2853273 | ||||||
| chrX:2853274
|
G | A | 40 | a0001c0001t0001g0004a0001c0001t0004g0068a0001c0001t0015g0046others(37): Show | 41 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.150-706G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2853274 | ||||||
| chrX:2853302
|
C | A | 1 | a0002c0002t0004g0145 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.150-678C>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2853302 | ||||||
| chrX:2853450
|
G | A | 1 | a0013c0017t0005g0243 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.150-530G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2853450 | ||||||
| chrX:2853499
|
G | A | 40 | a0001c0001t0001g0004a0001c0001t0004g0068a0001c0001t0015g0046others(37): Show | 41 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.150-481G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2853499 | ||||||
| chrX:2853826
|
T | G | 1 | a0002c0002t0002g0244 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.150-154T>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2853826 | ||||||
| chrX:2853860
|
TG | T | 1 | a0014c0012t0001g0305 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.150-116delG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2853860 | |||||
| chrX:2853930
|
G | C | 1 | a0001c0001t0002g0076 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.150-50G>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2853930 | ||||||
| chrX:2854234
|
G | T | 92 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0078others(89): Show | 94 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.324+80G>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 4/10 | chrX | 2854234 | ||||||
| chrX:2854253
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0306 | 3 | NA18941.hp1 NA18987.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.324+99G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 4/10 | chrX | 2854253 | ||||||
| chrX:2854346
|
C | T | 3 | a0001c0003t0007g0024a0001c0003t0008g0026a0003c0007t0006g0031 | 3 | HG01891.hp2 HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.324+192C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 4/10 | chrX | 2854346 | ||||||
| chrX:2854357
|
T | G | 286 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(283): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.324+203T>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 4/10 | chrX | 2854357 | ||||||
| chrX:2854619
|
G | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(179): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.325-374G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 4/10 | chrX | 2854619 | ||||||
| chrX:2854623
|
A | T | 1 | a0002c0002t0003g0035 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.325-370A>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 4/10 | chrX | 2854623 | ||||||
| chrX:2854653
|
A | G | 182 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(179): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.325-340A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 4/10 | chrX | 2854653 | ||||||
| chrX:2854731
|
T | C | 228 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0074others(225): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.325-262T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 4/10 | chrX | 2854731 | ||||||
| chrX:2854751
|
C | T | 206 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0052others(203): Show | 208 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.325-242C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 4/10 | chrX | 2854751 | ||||||
| chrX:2854813
|
TC | T | 1 | a0001c0001t0003g0180 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.325-177delC | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2854813 | |||||
| chrX:2854847
|
G | A | 2 | a0001c0001t0002g0190a0001c0001t0002g0282 | 2 | HG02523.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.325-146G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 4/10 | chrX | 2854847 | ||||||
| chrX:2855355
|
T | G | 2 | a0001c0001t0003g0208a0001c0001t0003g0273 | 2 | NA18992.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.487+200T>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 5/10 | chrX | 2855355 | ||||||
| chrX:2855480
|
C | T | 180 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0078others(177): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.487+325C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 5/10 | chrX | 2855480 | ||||||
| chrX:2855525
|
T | C | 3 | a0002c0006t0002g0121a0002c0006t0003g0120a0002c0006t0005g0119 | 3 | HG02280.hp2 HG02559.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.487+370T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 5/10 | chrX | 2855525 | ||||||
| chrX:2855739
|
A | C | 178 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0078others(175): Show | 180 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.487+584A>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 5/10 | chrX | 2855739 | ||||||
| chrX:2855902
|
T | G | 295 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(292): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.488-596T>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 5/10 | chrX | 2855902 | ||||||
| chrX:2855998
|
TTGA | T | 1 | a0002c0002t0002g0111 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.488-499_488-497del others(3): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 5/10 | chrX | 2855998 | ||||||
| chrX:2856005
|
A | G | 295 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(292): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.488-493A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 5/10 | chrX | 2856005 | ||||||
| chrX:2856047
|
C | T | 1 | a0002c0002t0006g0051 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.488-451C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 5/10 | chrX | 2856047 | ||||||
| chrX:2856122
|
G | A | 1 | a0001c0001t0002g0271 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.488-376G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 5/10 | chrX | 2856122 | ||||||
| chrX:2856437
|
A | G | 297 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(294): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.488-61A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 5/10 | chrX | 2856437 | ||||||
| chrX:2856659
|
T | G | 106 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0078others(103): Show | 108 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.614+35T>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2856659 | ||||||
| chrX:2856719
|
CTCTA | C | 115 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0078others(112): Show | 117 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.614+110_614+113del others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2856719 | |||||
| chrX:2856725
|
C | T | 1 | a0001c0001t0002g0189 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.614+101C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2856725 | ||||||
| chrX:2856726
|
T | TATCTATC | 28 | a0001c0001t0002g0153a0001c0003t0001g0027a0001c0003t0001g0030others(25): Show | 28 | HG00099.hp1 HG00733.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.614+103_614+109dup others(7): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2856726 | |||||
| chrX:2856730
|
T | TATC | 26 | a0001c0001t0001g0135a0002c0002t0001g0032a0002c0002t0001g0047others(23): Show | 26 | HG00323.hp2 HG00438.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.614+107_614+109dup others(3): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2856730 | |||||
| chrX:2856733
|
C | CATCTATC others(8): Show |
1 | a0002c0002t0002g0154 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.614+109_614+110ins others(15): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2856733 | ||||||
| chrX:2856733
|
CT | C | 10 | a0001c0001t0002g0190a0001c0001t0002g0282a0002c0002t0002g0107others(7): Show | 10 | HG01884.hp2 HG02257.hp1 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.614+110delT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2856733 | ||||||
| chrX:2856737
|
C | CATCT | 1 | a0001c0001t0001g0238 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.614+124_614+127dup others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2856737 | |||||
| chrX:2856737
|
C | CT | 54 | a0001c0001t0001g0135a0001c0001t0002g0153a0001c0001t0002g0190others(51): Show | 54 | HG00323.hp2 HG00438.hp2 HG00741.hp2 others(51): Show |
intron_variant | MODIFIER | c.614+113_614+114ins others(1): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2856737 | ||||||
| chrX:2856737
|
C | CTATGT | 11 | a0002c0002t0001g0008a0002c0002t0001g0158a0002c0002t0001g0170others(8): Show | 11 | HG00099.hp1 HG00733.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.614+113_614+114ins others(5): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2856737 | ||||||
| chrX:2856740
|
C | G | 16 | a0001c0003t0001g0027a0001c0003t0001g0030a0001c0003t0001g0114others(13): Show | 16 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.614+116C>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2856740 | ||||||
| chrX:2856744
|
C | G | 26 | a0001c0001t0001g0135a0002c0002t0001g0032a0002c0002t0001g0047others(23): Show | 26 | HG00323.hp2 HG00438.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.614+120C>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2856744 | ||||||
| chrX:2856748
|
C | G | 14 | a0001c0001t0002g0190a0001c0001t0002g0282a0002c0002t0002g0107others(11): Show | 14 | HG01884.hp2 HG02257.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.614+124C>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2856748 | ||||||
| chrX:2856748
|
CTATG | C | 60 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0182others(57): Show | 60 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.614+128_614+131del others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2856748 | |||||
| chrX:2856750
|
A | G | 2 | a0002c0002t0001g0032a0009c0013t0005g0037 | 2 | HG02886.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.614+126A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2856750 | ||||||
| chrX:2856752
|
G | C | 106 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0074others(103): Show | 107 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.614+128G>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2856752 | ||||||
| chrX:2856752
|
G | GTATC | 6 | a0001c0001t0002g0125a0002c0002t0002g0002a0002c0002t0005g0016others(3): Show | 7 | HG02572.hp1 HG02630.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.614+161_614+164dup others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2856752 | |||||
| chrX:2856752
|
G | GTATCTAT others(1): Show |
5 | a0001c0001t0001g0133a0002c0002t0002g0011a0002c0002t0003g0132others(2): Show | 5 | HG02615.hp1 HG02630.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.614+157_614+164dup others(8): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2856752 | |||||
| chrX:2856752
|
G | GTATCTAT others(5): Show |
2 | a0002c0002t0002g0049a0002c0002t0006g0043 | 2 | HG02809.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.614+153_614+164dup others(12): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2856752 | |||||
| chrX:2856752
|
GTATC | G | 1 | a0001c0001t0002g0086 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.614+161_614+164del others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2856752 | |||||
| chrX:2856754
|
A | G | 2 | a0002c0002t0003g0010a0002c0002t0004g0021 | 2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.614+130A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2856754 | ||||||
| chrX:2856758
|
A | G | 1 | a0002c0002t0006g0051 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.614+134A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2856758 | ||||||
| chrX:2856760
|
C | G | 1 | a0001c0001t0003g0077 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.614+136C>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2856760 | ||||||
| chrX:2856766
|
A | G | 3 | a0001c0001t0004g0089a0001c0001t0004g0092a0001c0001t0004g0093 | 3 | NA18955.hp1 NA18994.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.614+142A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2856766 | ||||||
| chrX:2856767
|
T | A | 1 | a0001c0001t0001g0214 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.614+143T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2856767 | ||||||
| chrX:2856772
|
CTATCT | C | 2 | a0001c0001t0002g0192a0001c0001t0007g0191 | 2 | HG00733.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.614+149_614+153del others(5): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2856772 | ||||||
| chrX:2856776
|
CT | C | 1 | a0001c0001t0001g0217 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.614+153delT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2856776 | ||||||
| chrX:2856777
|
T | TATC | 45 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0074others(42): Show | 46 | HG00738.hp1 HG00741.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.614+154_614+156dup others(3): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2856777 | |||||
| chrX:2856780
|
CT | C | 1 | a0002c0006t0003g0036 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.614+157delT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2856780 | ||||||
| chrX:2856788
|
C | CT | 79 | a0001c0001t0001g0005a0001c0001t0001g0289a0001c0001t0001g0293others(76): Show | 80 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.614+164_614+165ins others(1): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2856788 | ||||||
| chrX:2856792
|
T | TATC | 13 | a0001c0003t0001g0114a0001c0003t0002g0042a0001c0003t0004g0041others(10): Show | 13 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.614+169_614+171dup others(3): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2856792 | |||||
| chrX:2856792
|
TATCTATC | T | 49 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0074others(46): Show | 50 | HG00733.hp1 HG00738.hp1 HG00741.hp1 others(47): Show |
intron_variant | MODIFIER | c.614+176_614+182del others(7): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2856792 | |||||
| chrX:2856795
|
CT | C | 97 | a0001c0001t0001g0001a0001c0001t0001g0078a0001c0001t0001g0083others(94): Show | 98 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.614+172delT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2856795 | ||||||
| chrX:2856799
|
C | CATCT | 78 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0182others(75): Show | 78 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.614+187_614+190dup others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2856799 | |||||
| chrX:2856799
|
C | CATCTATC others(4): Show |
69 | a0001c0001t0001g0005a0001c0001t0001g0289a0001c0001t0001g0293others(66): Show | 70 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.614+182_614+183ins others(11): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2856799 | |||||
| chrX:2856799
|
C | CT | 100 | a0001c0001t0001g0001a0001c0001t0001g0078a0001c0001t0001g0083others(97): Show | 101 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.614+175_614+176ins others(1): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2856799 | ||||||
| chrX:2856874
|
T | C | 1 | a0001c0004t0001g0087 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.614+250T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2856874 | ||||||
| chrX:2856949
|
G | T | 180 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0078others(177): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.614+325G>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2856949 | ||||||
| chrX:2856956
|
CATCTGTT others(1): Show |
C | 20 | a0001c0001t0001g0101a0001c0001t0002g0190a0001c0001t0002g0283others(17): Show | 20 | HG00741.hp2 HG01884.hp1 HG01981.hp2 others(17): Show |
intron_variant | MODIFIER | c.614+337_614+344del others(8): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2856956 | |||||
| chrX:2856956
|
CATCTGTT others(5): Show |
C | 98 | a0001c0001t0001g0001a0001c0001t0001g0083a0001c0001t0001g0098others(95): Show | 99 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.614+337_614+348del others(12): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2856956 | |||||
| chrX:2856956
|
CATCTGTT others(9): Show |
C | 31 | a0001c0001t0001g0005a0001c0001t0001g0289a0001c0001t0001g0293others(28): Show | 32 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.614+337_614+352del others(16): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2856956 | |||||
| chrX:2856956
|
CATCTGTT others(13): Show |
C | 2 | a0001c0001t0002g0075a0001c0001t0002g0076 | 2 | NA18947.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.614+337_614+356del others(20): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2856956 | |||||
| chrX:2856959
|
CTGTT | C | 3 | a0001c0001t0001g0078a0002c0002t0003g0110a0002c0002t0004g0302 | 3 | HG02451.hp2 HG03669.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.614+337_614+340del others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2856959 | |||||
| chrX:2856961
|
GTTTA | G | 12 | a0001c0003t0002g0042a0001c0003t0002g0045a0001c0003t0004g0041others(9): Show | 12 | HG01243.hp1 HG02145.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.614+339_614+342del others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2856961 | |||||
| chrX:2856961
|
GTTTATCT others(1): Show |
G | 11 | a0001c0003t0001g0027a0001c0003t0001g0030a0001c0003t0005g0177others(8): Show | 11 | HG01891.hp2 HG02055.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.614+339_614+346del others(8): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2856961 | |||||
| chrX:2856961
|
GTTTATCT others(5): Show |
G | 3 | a0001c0003t0001g0114a0002c0002t0001g0032a0003c0007t0006g0031 | 3 | HG02723.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.614+339_614+350del others(12): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2856961 | |||||
| chrX:2856963
|
T | TTATC | 1 | a0001c0001t0002g0125 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.614+384_614+387dup others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2856963 | |||||
| chrX:2856963
|
TTATC | T | 12 | a0001c0001t0001g0133a0001c0001t0002g0063a0001c0001t0004g0159others(9): Show | 13 | HG00438.hp1 HG02572.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.614+384_614+387del others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2856963 | |||||
| chrX:2856963
|
TTATCTAT others(1): Show |
T | 19 | a0001c0001t0001g0214a0001c0001t0001g0228a0001c0001t0001g0248others(16): Show | 19 | HG00639.hp2 HG03209.hp1 HG03239.hp2 others(16): Show |
intron_variant | MODIFIER | c.614+380_614+387del others(8): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2856963 | |||||
| chrX:2856963
|
TTATCTAT others(5): Show |
T | 95 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0074others(92): Show | 96 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.614+376_614+387del others(12): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2856963 | |||||
| chrX:2856963
|
TTATCTAT others(9): Show |
T | 2 | a0001c0001t0002g0192a0001c0001t0007g0191 | 2 | HG00733.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.614+372_614+387del others(16): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2856963 | |||||
| chrX:2857107
|
A | G | 45 | a0001c0001t0001g0135a0001c0001t0002g0149a0002c0002t0001g0146others(42): Show | 45 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.614+483A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2857107 | ||||||
| chrX:2857146
|
T | TTATCTAT others(15): Show |
1 | a0002c0006t0003g0036 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.614+524_614+545dup others(22): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2857146 | |||||
| chrX:2857148
|
ATCTATCT others(15): Show |
A | 55 | a0001c0001t0001g0135a0001c0001t0001g0285a0001c0001t0002g0149others(52): Show | 55 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.614+546_614+567del others(22): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2857148 | |||||
| chrX:2857170
|
G | A | 125 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0078others(122): Show | 127 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.614+546G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2857170 | ||||||
| chrX:2857218
|
G | A | 180 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0078others(177): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.614+594G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2857218 | ||||||
| chrX:2857289
|
CT | C | 180 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0078others(177): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.614+667delT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2857289 | |||||
| chrX:2857315
|
C | A | 180 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0078others(177): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.614+691C>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2857315 | ||||||
| chrX:2857406
|
A | ATATC | 297 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(294): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.614+786_614+789dup others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2857406 | |||||
| chrX:2857499
|
T | C | 1 | a0002c0006t0003g0036 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.614+875T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2857499 | ||||||
| chrX:2857510
|
A | G | 2 | a0006c0010t0003g0202a0007c0020t0003g0007 | 2 | HG01123.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.614+886A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2857510 | ||||||
| chrX:2857515
|
G | C | 3 | a0002c0006t0002g0121a0002c0006t0003g0120a0002c0006t0005g0119 | 3 | HG02280.hp2 HG02559.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.614+891G>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2857515 | ||||||
| chrX:2857525
|
T | G | 2 | a0001c0001t0001g0249a0001c0001t0001g0250 | 2 | HG01081.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.614+901T>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2857525 | ||||||
| chrX:2857560
|
A | G | 180 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0078others(177): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.614+936A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2857560 | ||||||
| chrX:2857579
|
T | A | 1 | a0002c0002t0008g0219 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.614+955T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2857579 | ||||||
| chrX:2857580
|
C | T | 1 | a0002c0002t0008g0219 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.614+956C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2857580 | ||||||
| chrX:2857648
|
A | C | 2 | a0001c0001t0002g0183a0001c0001t0002g0220 | 2 | NA19066.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.614+1024A>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2857648 | ||||||
| chrX:2857650
|
G | C | 117 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0074others(114): Show | 118 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.614+1026G>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2857650 | ||||||
| chrX:2857691
|
C | G | 1 | a0001c0001t0001g0267 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.614+1067C>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2857691 | ||||||
| chrX:2857835
|
A | G | 118 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0074others(115): Show | 119 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.614+1211A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2857835 | ||||||
| chrX:2857839
|
T | TA | 1 | a0001c0001t0001g0306 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.614+1222dupA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2857839 | |||||
| chrX:2857879
|
C | A | 19 | a0001c0003t0001g0027a0001c0003t0001g0030a0001c0003t0001g0114others(16): Show | 19 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.614+1255C>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2857879 | ||||||
| chrX:2857957
|
A | T | 104 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0078others(101): Show | 106 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.614+1333A>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2857957 | ||||||
| chrX:2857981
|
C | T | 1 | a0002c0002t0003g0035 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.614+1357C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2857981 | ||||||
| chrX:2858086
|
A | AT | 108 | a0001c0001t0001g0004a0001c0001t0001g0074a0001c0001t0001g0139others(105): Show | 109 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.614+1470dupT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2858086 | |||||
| chrX:2858112
|
T | C | 118 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0074others(115): Show | 119 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.614+1488T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2858112 | ||||||
| chrX:2858240
|
C | G | 1 | a0002c0005t0002g0115 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.615-1603C>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2858240 | ||||||
| chrX:2858277
|
AT | A | 118 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0074others(115): Show | 119 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.615-1565delT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2858277 | ||||||
| chrX:2858322
|
C | T | 16 | a0001c0001t0002g0063a0001c0001t0002g0183a0001c0001t0002g0200others(13): Show | 16 | HG00438.hp1 HG02071.hp1 HG02129.hp1 others(13): Show |
intron_variant | MODIFIER | c.615-1521C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2858322 | ||||||
| chrX:2858331
|
T | C | 160 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0078others(157): Show | 162 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.615-1512T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2858331 | ||||||
| chrX:2858471
|
A | G | 1 | a0002c0002t0003g0299 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.615-1372A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2858471 | ||||||
| chrX:2858473
|
A | G | 1 | a0001c0001t0017g0094 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.615-1370A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2858473 | ||||||
| chrX:2858476
|
AAAAG | A | 2 | a0002c0002t0003g0010a0002c0002t0004g0021 | 2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.615-1360_615-1357d others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2858476 | |||||
| chrX:2858645
|
G | T | 140 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0074others(137): Show | 142 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.615-1198G>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2858645 | ||||||
| chrX:2858689
|
G | A | 1 | a0002c0002t0004g0269 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.615-1154G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2858689 | ||||||
| chrX:2858956
|
TATG | T | 1 | a0001c0001t0002g0086 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.615-881_615-879del others(3): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2858956 | |||||
| chrX:2859066
|
T | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(189): Show | 195 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.615-777T>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2859066 | ||||||
| chrX:2859132
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.615-711A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2859132 | ||||||
| chrX:2859273
|
A | G | 182 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(179): Show | 185 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.615-570A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2859273 | ||||||
| chrX:2859279
|
ATAG | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(179): Show | 185 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.615-559_615-557del others(3): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2859279 | |||||
| chrX:2859314
|
C | T | 268 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(265): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.615-529C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2859314 | ||||||
| chrX:2859327
|
A | G | 2 | a0001c0003t0002g0042a0001c0003t0004g0041 | 2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.615-516A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2859327 | ||||||
| chrX:2859379
|
A | C | 1 | a0008c0014t0018g0147 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.615-464A>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2859379 | ||||||
| chrX:2859519
|
A | G | 170 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(167): Show | 173 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.615-324A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2859519 | ||||||
| chrX:2859522
|
G | C | 3 | a0002c0002t0005g0126a0004c0008t0006g0009a0004c0008t0006g0127 | 3 | HG01261.hp1 HG02109.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.615-321G>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2859522 | ||||||
| chrX:2859805
|
C | T | 11 | a0001c0001t0001g0133a0001c0003t0001g0027a0001c0003t0001g0030others(8): Show | 11 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.615-38C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2859805 | ||||||
| chrX:2860138
|
G | GT | 2 | a0001c0001t0004g0199a0010c0015t0001g0138 | 2 | HG04115.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.837+82dupT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2860138 | |||||
| chrX:2860171
|
T | C | 2 | a0002c0005t0002g0115a0002c0005t0002g0176 | 2 | HG02280.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.837+106T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 7/10 | chrX | 2860171 | ||||||
| chrX:2860281
|
G | A | 180 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(177): Show | 183 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.837+216G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 7/10 | chrX | 2860281 | ||||||
| chrX:2860304
|
T | C | 17 | a0001c0001t0001g0133a0001c0003t0001g0027a0001c0003t0001g0030others(14): Show | 17 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.837+239T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 7/10 | chrX | 2860304 | ||||||
| chrX:2860392
|
C | G | 180 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(177): Show | 183 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.837+327C>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 7/10 | chrX | 2860392 | ||||||
| chrX:2860483
|
A | C | 1 | a0001c0001t0001g0098 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.837+418A>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 7/10 | chrX | 2860483 | ||||||
| chrX:2860485
|
A | G | 180 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(177): Show | 183 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.837+420A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 7/10 | chrX | 2860485 | ||||||
| chrX:2860505
|
C | A | 180 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(177): Show | 183 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.837+440C>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 7/10 | chrX | 2860505 | ||||||
| chrX:2860546
|
A | G | 179 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(176): Show | 182 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.837+481A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 7/10 | chrX | 2860546 | ||||||
| chrX:2860643
|
C | CT | 4 | a0002c0002t0002g0002a0002c0002t0002g0049a0002c0002t0003g0166others(1): Show | 5 | HG02630.hp1 HG02809.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.837+598dupT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2860643 | |||||
| chrX:2860643
|
CT | C | 21 | a0001c0001t0001g0247a0001c0001t0002g0261a0001c0001t0002g0262others(18): Show | 21 | HG01070.hp1 HG01071.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.837+598delT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2860643 | |||||
| chrX:2860643
|
CTT | C | 168 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(165): Show | 171 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.837+597_837+598del others(2): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2860643 | |||||
| chrX:2860643
|
CTTT | C | 5 | a0001c0001t0001g0139a0001c0001t0002g0125a0001c0001t0004g0068others(2): Show | 5 | HG03098.hp1 HG03471.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.837+596_837+598del others(3): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2860643 | |||||
| chrX:2860643
|
CTTTT | C | 1 | a0001c0003t0002g0045 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.837+595_837+598del others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2860643 | |||||
| chrX:2860674
|
T | C | 5 | a0001c0001t0001g0181a0001c0001t0001g0211a0001c0001t0001g0227others(2): Show | 5 | HG00741.hp1 HG01175.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.837+609T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 7/10 | chrX | 2860674 | ||||||
| chrX:2860725
|
TTTTG | T | 5 | a0001c0001t0002g0125a0001c0001t0004g0068a0001c0003t0001g0114others(2): Show | 5 | HG03098.hp1 HG03453.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.837+676_837+679del others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2860725 | |||||
| chrX:2860755
|
A | T | 179 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(176): Show | 182 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.837+690A>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 7/10 | chrX | 2860755 | ||||||
| chrX:2860791
|
A | G | 195 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(192): Show | 198 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.837+726A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 7/10 | chrX | 2860791 | ||||||
| chrX:2860932
|
G | A | 5 | a0002c0005t0002g0115a0002c0005t0002g0176a0002c0005t0006g0104others(2): Show | 5 | HG00741.hp2 HG01074.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.838-590G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 7/10 | chrX | 2860932 | ||||||
| chrX:2860941
|
G | T | 179 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(176): Show | 182 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.838-581G>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 7/10 | chrX | 2860941 | ||||||
| chrX:2860955
|
T | C | 179 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(176): Show | 182 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.838-567T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 7/10 | chrX | 2860955 | ||||||
| chrX:2860993
|
G | T | 2 | a0002c0002t0003g0010a0002c0002t0004g0021 | 2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.838-529G>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 7/10 | chrX | 2860993 | ||||||
| chrX:2861029
|
C | CT | 13 | a0001c0001t0001g0133a0001c0001t0004g0309a0001c0003t0001g0027others(10): Show | 13 | HG00438.hp2 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.838-480dupT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2861029 | |||||
| chrX:2861029
|
CT | C | 1 | a0002c0002t0002g0069 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.838-480delT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2861029 | |||||
| chrX:2861130
|
G | A | 179 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(176): Show | 182 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.838-392G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 7/10 | chrX | 2861130 | ||||||
| chrX:2861168
|
A | G | 1 | a0001c0001t0017g0094 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.838-354A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 7/10 | chrX | 2861168 | ||||||
| chrX:2861170
|
G | A | 179 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(176): Show | 182 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.838-352G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 7/10 | chrX | 2861170 | ||||||
| chrX:2861273
|
GCTAAGTA others(23): Show |
G | 1 | a0001c0001t0015g0046 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.838-233_838-204del others(30): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2861273 | |||||
| chrX:2861274
|
CTAAGTAC others(8): Show |
C | 8 | a0001c0001t0001g0083a0001c0001t0002g0079a0001c0001t0002g0085others(5): Show | 8 | HG01978.hp1 HG01981.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.838-233_838-219del others(15): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2861274 | |||||
| chrX:2861289
|
T | C | 181 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(178): Show | 184 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.838-233T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 7/10 | chrX | 2861289 | ||||||
| chrX:2861293
|
G | A | 5 | a0001c0001t0002g0125a0001c0001t0004g0068a0001c0003t0001g0114others(2): Show | 5 | HG03098.hp1 HG03453.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.838-229G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 7/10 | chrX | 2861293 | ||||||
| chrX:2861319
|
C | CTAAGTAC others(8): Show |
3 | a0002c0002t0001g0032a0002c0002t0006g0051a0009c0013t0005g0037 | 3 | HG02622.hp2 HG02886.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.838-190_838-189ins others(15): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2861319 | |||||
| chrX:2861820
|
A | T | 1 | a0001c0001t0003g0055 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1038+98A>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2861820 | ||||||
| chrX:2861834
|
C | T | 12 | a0001c0001t0001g0133a0001c0001t0015g0046a0001c0003t0001g0027others(9): Show | 12 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1038+112C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2861834 | ||||||
| chrX:2861894
|
C | T | 2 | a0001c0003t0002g0042a0001c0003t0004g0041 | 2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1038+172C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2861894 | ||||||
| chrX:2861995
|
A | T | 1 | a0001c0001t0001g0182 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1038+273A>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2861995 | ||||||
| chrX:2862078
|
T | TGGAA | 186 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(183): Show | 189 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.1038+358_1038+361d others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2862078 | |||||
| chrX:2862137
|
G | C | 8 | a0002c0002t0006g0051a0002c0005t0002g0115a0002c0005t0002g0176others(5): Show | 8 | HG00741.hp2 HG01074.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.1038+415G>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2862137 | ||||||
| chrX:2862149
|
G | A | 2 | a0002c0002t0001g0123a0002c0002t0001g0124 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1038+427G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2862149 | ||||||
| chrX:2862188
|
A | G | 2 | a0001c0003t0002g0042a0001c0003t0004g0041 | 2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1038+466A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2862188 | ||||||
| chrX:2862202
|
G | C | 8 | a0002c0002t0006g0051a0002c0005t0002g0115a0002c0005t0002g0176others(5): Show | 8 | HG00741.hp2 HG01074.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.1038+480G>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2862202 | ||||||
| chrX:2862224
|
G | A | 161 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(158): Show | 164 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.1038+502G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2862224 | ||||||
| chrX:2862278
|
A | C | 186 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(183): Show | 189 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.1038+556A>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2862278 | ||||||
| chrX:2862422
|
C | T | 11 | a0001c0001t0002g0125a0001c0001t0004g0068a0001c0003t0001g0114others(8): Show | 11 | HG02572.hp1 HG02896.hp2 HG02970.hp2 others(8): Show |
intron_variant | MODIFIER | c.1038+700C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2862422 | ||||||
| chrX:2862480
|
C | T | 10 | a0002c0002t0001g0186a0002c0002t0001g0254a0002c0002t0001g0256others(7): Show | 10 | HG01256.hp1 HG01928.hp1 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.1038+758C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2862480 | ||||||
| chrX:2862492
|
C | T | 186 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(183): Show | 189 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.1038+770C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2862492 | ||||||
| chrX:2862580
|
C | T | 12 | a0001c0001t0001g0133a0001c0001t0015g0046a0001c0003t0001g0027others(9): Show | 12 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1038+858C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2862580 | ||||||
| chrX:2862658
|
C | T | 10 | a0002c0002t0002g0002a0002c0002t0002g0049a0002c0002t0003g0033others(7): Show | 11 | HG01109.hp1 HG02630.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.1038+936C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2862658 | ||||||
| chrX:2862706
|
C | T | 186 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(183): Show | 189 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.1038+984C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2862706 | ||||||
| chrX:2862785
|
C | T | 186 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(183): Show | 189 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.1038+1063C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2862785 | ||||||
| chrX:2862788
|
T | A | 186 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(183): Show | 189 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.1038+1066T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2862788 | ||||||
| chrX:2862843
|
G | C | 20 | a0002c0002t0001g0032a0002c0002t0002g0002a0002c0002t0002g0011others(17): Show | 21 | HG01109.hp1 HG01261.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1038+1121G>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2862843 | ||||||
| chrX:2862937
|
G | A | 27 | a0001c0001t0001g0052a0001c0001t0001g0074a0001c0001t0001g0196others(24): Show | 27 | HG00140.hp1 HG00609.hp1 HG01516.hp1 others(24): Show |
intron_variant | MODIFIER | c.1038+1215G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2862937 | ||||||
| chrX:2863030
|
C | T | 2 | a0001c0003t0002g0042a0001c0003t0004g0041 | 2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1038+1308C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2863030 | ||||||
| chrX:2863047
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1038+1325G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2863047 | ||||||
| chrX:2863063
|
G | GA | 1 | a0001c0001t0003g0180 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1038+1352dupA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2863063 | |||||
| chrX:2863063
|
GA | G | 2 | a0002c0005t0002g0115a0002c0005t0002g0176 | 2 | HG02280.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1038+1352delA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2863063 | |||||
| chrX:2863080
|
CT | C | 190 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(187): Show | 193 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.1038+1370delT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2863080 | |||||
| chrX:2863119
|
G | T | 2 | a0001c0003t0002g0042a0001c0003t0004g0041 | 2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1038+1397G>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2863119 | ||||||
| chrX:2863179
|
G | A | 184 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(181): Show | 187 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.1038+1457G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2863179 | ||||||
| chrX:2863219
|
T | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(195): Show | 202 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.1038+1497T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2863219 | ||||||
| chrX:2863236
|
G | A | 10 | a0002c0002t0002g0002a0002c0002t0002g0049a0002c0002t0003g0033others(7): Show | 11 | HG01109.hp1 HG02630.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.1038+1514G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2863236 | ||||||
| chrX:2863316
|
C | T | 41 | a0002c0002t0001g0146a0002c0002t0001g0158a0002c0002t0001g0160others(38): Show | 41 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.1038+1594C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2863316 | ||||||
| chrX:2863483
|
T | G | 1 | a0001c0001t0001g0228 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1038+1761T>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2863483 | ||||||
| chrX:2863484
|
C | T | 11 | a0001c0001t0002g0125a0001c0001t0004g0068a0001c0003t0001g0114others(8): Show | 11 | HG02572.hp1 HG02896.hp2 HG02970.hp2 others(8): Show |
intron_variant | MODIFIER | c.1038+1762C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2863484 | ||||||
| chrX:2863519
|
G | A | 1 | a0002c0005t0006g0104 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1038+1797G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2863519 | ||||||
| chrX:2864104
|
C | G | 5 | a0001c0001t0002g0192a0001c0001t0007g0191a0002c0002t0006g0043others(2): Show | 5 | HG00733.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1038+2382C>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2864104 | ||||||
| chrX:2864197
|
GAC | G | 1 | a0002c0002t0007g0193 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1038+2479_1038+248 others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2864197 | |||||
| chrX:2864264
|
A | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(199): Show | 205 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.1038+2542A>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2864264 | ||||||
| chrX:2864280
|
G | A | 1 | a0001c0001t0002g0149 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1038+2558G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2864280 | ||||||
| chrX:2864292
|
G | C | 1 | a0001c0001t0001g0198 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1038+2570G>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2864292 | ||||||
| chrX:2864302
|
C | A | 2 | a0002c0002t0003g0010a0002c0002t0004g0021 | 2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1038+2580C>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2864302 | ||||||
| chrX:2864343
|
C | T | 30 | a0002c0002t0001g0008a0002c0002t0001g0047a0002c0002t0001g0186others(27): Show | 30 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.1038+2621C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2864343 | ||||||
| chrX:2864385
|
A | AT | 1 | a0002c0002t0001g0160 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1038+2678dupT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2864385 | |||||
| chrX:2864385
|
AT | A | 212 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(209): Show | 215 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.1038+2678delT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2864385 | |||||
| chrX:2864385
|
ATT | A | 2 | a0001c0001t0003g0013a0001c0001t0003g0273 | 2 | HG00738.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.1038+2677_1038+267 others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2864385 | |||||
| chrX:2864414
|
T | C | 275 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(272): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.1038+2692T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2864414 | ||||||
| chrX:2864592
|
G | A | 176 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(173): Show | 179 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.1038+2870G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2864592 | ||||||
| chrX:2864724
|
G | GT | 2 | a0002c0005t0002g0115a0002c0005t0002g0176 | 2 | HG02280.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1038+3007dupT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2864724 | |||||
| chrX:2864745
|
A | G | 2 | a0002c0002t0003g0010a0002c0002t0004g0021 | 2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1038+3023A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2864745 | ||||||
| chrX:2864762
|
TTC | T | 1 | a0001c0003t0001g0027 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1038+3042_1038+304 others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2864762 | |||||
| chrX:2864763
|
TC | T | 14 | a0001c0001t0001g0133a0001c0001t0015g0046a0001c0003t0001g0030others(11): Show | 14 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1038+3042delC | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2864763 | ||||||
| chrX:2864764
|
C | CT | 1 | a0002c0002t0002g0002 | 2 | HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1038+3055dupT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2864764 | |||||
| chrX:2864764
|
CT | C | 2 | a0001c0001t0003g0061a0002c0006t0003g0036 | 2 | HG03225.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.1038+3055delT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2864764 | |||||
| chrX:2864879
|
C | T | 1 | a0002c0002t0003g0034 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1038+3157C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2864879 | ||||||
| chrX:2865029
|
G | A | 9 | a0001c0001t0002g0125a0001c0003t0002g0045a0002c0002t0003g0132others(6): Show | 9 | HG02572.hp1 HG02896.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1038+3307G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2865029 | ||||||
| chrX:2865066
|
A | G | 224 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(221): Show | 228 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.1038+3344A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2865066 | ||||||
| chrX:2865085
|
C | T | 10 | a0001c0001t0002g0125a0001c0003t0002g0045a0001c0003t0005g0177others(7): Show | 10 | HG02572.hp1 HG02896.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.1038+3363C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2865085 | ||||||
| chrX:2865469
|
C | T | 2 | a0002c0002t0003g0237a0002c0002t0007g0044 | 2 | HG02976.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1038+3747C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2865469 | ||||||
| chrX:2865514
|
T | G | 231 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(228): Show | 235 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.1038+3792T>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2865514 | ||||||
| chrX:2865575
|
G | A | 1 | a0001c0001t0003g0208 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1038+3853G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2865575 | ||||||
| chrX:2865661
|
G | A | 3 | a0001c0001t0001g0284a0001c0001t0002g0279a0001c0001t0002g0280 | 3 | HG00544.hp2 HG02027.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1038+3939G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2865661 | ||||||
| chrX:2865735
|
T | C | 161 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(158): Show | 164 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.1038+4013T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2865735 | ||||||
| chrX:2865874
|
T | TCA | 230 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(227): Show | 234 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.1038+4154_1038+415 others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2865874 | |||||
| chrX:2865916
|
T | G | 1 | a0002c0006t0005g0119 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1038+4194T>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2865916 | ||||||
| chrX:2865935
|
C | A | 14 | a0001c0003t0005g0304a0002c0002t0002g0002a0002c0002t0002g0049others(11): Show | 15 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1038+4213C>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2865935 | ||||||
| chrX:2866010
|
G | A | 230 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(227): Show | 234 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.1038+4288G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2866010 | ||||||
| chrX:2866055
|
C | T | 3 | a0002c0002t0006g0043a0002c0002t0012g0066a0002c0002t0012g0067 | 3 | HG02895.hp1 HG02897.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1038+4333C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2866055 | ||||||
| chrX:2866073
|
T | C | 1 | a0001c0001t0015g0046 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1038+4351T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2866073 | ||||||
| chrX:2866349
|
A | G | 2 | a0002c0005t0003g0040a0002c0006t0003g0036 | 2 | HG01884.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1038+4627A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2866349 | ||||||
| chrX:2866452
|
G | A | 1 | a0006c0010t0003g0202 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1038+4730G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2866452 | ||||||
| chrX:2866476
|
C | T | 14 | a0001c0003t0005g0304a0002c0002t0002g0002a0002c0002t0002g0049others(11): Show | 15 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1038+4754C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2866476 | ||||||
| chrX:2866646
|
T | C | 9 | a0001c0001t0002g0192a0001c0003t0001g0114a0002c0002t0005g0050others(6): Show | 9 | HG00733.hp1 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1038+4924T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2866646 | ||||||
| chrX:2866738
|
C | T | 1 | a0002c0002t0003g0207 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1038+5016C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2866738 | ||||||
| chrX:2866825
|
A | AT | 45 | a0001c0001t0001g0133a0001c0001t0002g0125a0001c0001t0004g0068others(42): Show | 46 | HG01109.hp1 HG01243.hp1 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.1038+5115dupT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2866825 | |||||
| chrX:2866825
|
A | ATT | 2 | a0001c0001t0002g0192a0002c0002t0007g0188 | 2 | HG00733.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1038+5114_1038+511 others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2866825 | |||||
| chrX:2866825
|
AT | A | 7 | a0002c0002t0001g0259a0002c0002t0003g0168a0002c0002t0004g0155others(4): Show | 7 | HG01070.hp2 HG01256.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.1038+5115delT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2866825 | |||||
| chrX:2866835
|
TTTA | T | 3 | a0001c0001t0001g0210a0001c0004t0001g0087a0001c0004t0001g0088 | 3 | HG02735.hp1 NA18965.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.1038+5114_1038+511 others(7): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2866835 | ||||||
| chrX:2866836
|
TTA | T | 190 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(187): Show | 193 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.1038+5115_1038+511 others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2866836 | ||||||
| chrX:2866837
|
T | A | 1 | a0002c0002t0001g0170 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1038+5115T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2866837 | ||||||
| chrX:2866838
|
A | T | 3 | a0002c0002t0003g0073a0002c0002t0010g0157a0004c0008t0006g0019 | 3 | HG00621.hp1 HG01891.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1038+5116A>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2866838 | ||||||
| chrX:2867164
|
G | T | 3 | a0002c0002t0002g0141a0002c0002t0002g0142a0002c0002t0004g0265 | 3 | HG00423.hp1 NA18941.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1038+5442G>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2867164 | ||||||
| chrX:2867297
|
C | CA | 244 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(241): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1038+5579dupA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2867297 | |||||
| chrX:2867336
|
C | T | 1 | a0005c0009t0002g0162 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1038+5614C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2867336 | ||||||
| chrX:2867356
|
CTG | C | 14 | a0001c0003t0005g0304a0001c0003t0007g0024a0002c0002t0001g0032others(11): Show | 15 | HG01261.hp1 HG01891.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1038+5636_1038+563 others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2867356 | |||||
| chrX:2867376
|
G | A | 5 | a0001c0003t0001g0114a0002c0002t0002g0011a0002c0002t0003g0035others(2): Show | 5 | HG02559.hp1 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1038+5654G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2867376 | ||||||
| chrX:2867377
|
G | A | 1 | a0002c0006t0005g0119 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1038+5655G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2867377 | ||||||
| chrX:2867387
|
G | T | 291 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(288): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.1038+5665G>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2867387 | ||||||
| chrX:2867470
|
C | T | 1 | a0001c0001t0004g0068 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1038+5748C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2867470 | ||||||
| chrX:2867671
|
G | A | 45 | a0001c0001t0004g0084a0001c0001t0004g0159a0001c0003t0002g0042others(42): Show | 45 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.1038+5949G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2867671 | ||||||
| chrX:2867696
|
G | A | 46 | a0001c0001t0004g0084a0001c0001t0004g0159a0001c0003t0002g0042others(43): Show | 46 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.1038+5974G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2867696 | ||||||
| chrX:2867699
|
G | C | 46 | a0001c0001t0004g0084a0001c0001t0004g0159a0001c0003t0002g0042others(43): Show | 46 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.1038+5977G>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2867699 | ||||||
| chrX:2867708
|
G | A | 46 | a0001c0001t0004g0084a0001c0001t0004g0159a0001c0003t0002g0042others(43): Show | 46 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.1038+5986G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2867708 | ||||||
| chrX:2867826
|
G | GGT | 1 | a0001c0001t0001g0267 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1038+6105_1038+610 others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2867826 | |||||
| chrX:2867830
|
C | G | 2 | a0001c0003t0002g0042a0001c0003t0004g0041 | 2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1038+6108C>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2867830 | ||||||
| chrX:2867988
|
C | T | 60 | a0001c0001t0002g0200a0001c0001t0004g0084a0001c0001t0004g0159others(57): Show | 60 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.1038+6266C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2867988 | ||||||
| chrX:2867997
|
G | A | 201 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(198): Show | 204 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.1038+6275G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2867997 | ||||||
| chrX:2868107
|
A | G | 1 | a0001c0001t0002g0286 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1038+6385A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2868107 | ||||||
| chrX:2868149
|
G | A | 1 | a0002c0002t0005g0201 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1038+6427G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2868149 | ||||||
| chrX:2868230
|
G | A | 3 | a0002c0002t0001g0032a0002c0002t0006g0051a0009c0013t0005g0037 | 3 | HG02622.hp2 HG02886.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1038+6508G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2868230 | ||||||
| chrX:2868327
|
G | T | 1 | a0001c0001t0015g0046 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1038+6605G>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2868327 | ||||||
| chrX:2868393
|
G | A | 40 | a0001c0001t0002g0200a0001c0001t0004g0084a0001c0001t0004g0159others(37): Show | 40 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.1038+6671G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2868393 | ||||||
| chrX:2868411
|
C | T | 1 | a0001c0003t0005g0022 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1038+6689C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2868411 | ||||||
| chrX:2868451
|
C | T | 6 | a0002c0005t0002g0115a0002c0005t0002g0176a0002c0005t0006g0104others(3): Show | 6 | HG00741.hp2 HG01074.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1038+6729C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2868451 | ||||||
| chrX:2868452
|
G | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0210a0001c0001t0001g0292 | 3 | HG00140.hp1 HG02735.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1038+6730G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2868452 | ||||||
| chrX:2868456
|
C | CA | 16 | a0001c0001t0001g0078a0001c0001t0001g0245a0001c0001t0001g0284others(13): Show | 16 | HG01928.hp1 HG02027.hp1 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.1038+6755dupA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2868456 | |||||
| chrX:2868456
|
CA | C | 18 | a0001c0001t0001g0204a0001c0001t0001g0234a0001c0001t0002g0058others(15): Show | 18 | HG00099.hp2 HG00323.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1038+6755delA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2868456 | |||||
| chrX:2868456
|
CAA | C | 1 | a0002c0005t0006g0104 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1038+6754_1038+675 others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2868456 | |||||
| chrX:2868456
|
CAAA | C | 9 | a0002c0002t0005g0016a0002c0002t0005g0178a0002c0002t0006g0017others(6): Show | 9 | HG01074.hp1 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1038+6753_1038+675 others(7): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2868456 | |||||
| chrX:2868456
|
CAAAA | C | 1 | a0002c0002t0006g0134 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1038+6752_1038+675 others(8): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2868456 | |||||
| chrX:2868553
|
A | G | 2 | a0002c0002t0006g0134a0002c0006t0005g0119 | 2 | HG02280.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1038+6831A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2868553 | ||||||
| chrX:2868555
|
G | T | 14 | a0002c0002t0001g0032a0002c0002t0003g0010a0002c0002t0004g0021others(11): Show | 14 | HG00741.hp2 HG01074.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1038+6833G>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2868555 | ||||||
| chrX:2868567
|
C | G | 12 | a0002c0002t0001g0032a0002c0002t0005g0091a0002c0002t0005g0095others(9): Show | 12 | HG00741.hp2 HG01074.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1038+6845C>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2868567 | ||||||
| chrX:2868587
|
TA | T | 1 | a0001c0001t0009g0270 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1038+6872delA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2868587 | |||||
| chrX:2868722
|
C | T | 12 | a0001c0003t0001g0030a0001c0003t0005g0022a0001c0003t0008g0026others(9): Show | 12 | HG01261.hp1 HG01891.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1038+7000C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2868722 | ||||||
| chrX:2868815
|
T | C | 1 | a0004c0008t0006g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1039-6995T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2868815 | ||||||
| chrX:2868900
|
C | T | 4 | a0002c0002t0002g0038a0002c0002t0002g0039a0002c0002t0003g0110others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039-6910C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2868900 | ||||||
| chrX:2869016
|
T | TA | 223 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(220): Show | 227 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.1039-6780dupA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2869016 | |||||
| chrX:2869016
|
TA | T | 6 | a0001c0001t0007g0191a0001c0001t0009g0270a0002c0002t0003g0010others(3): Show | 6 | HG01167.hp1 HG02647.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1039-6780delA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2869016 | |||||
| chrX:2869017
|
A | T | 11 | a0001c0003t0001g0030a0001c0003t0005g0022a0001c0003t0008g0026others(8): Show | 11 | HG01261.hp1 HG01891.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1039-6793A>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2869017 | ||||||
| chrX:2869018
|
A | T | 1 | a0003c0007t0006g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1039-6792A>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2869018 | ||||||
| chrX:2869074
|
C | T | 12 | a0001c0003t0001g0114a0002c0002t0001g0123a0002c0002t0001g0124others(9): Show | 13 | HG01070.hp1 HG01071.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1039-6736C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2869074 | ||||||
| chrX:2869199
|
C | T | 1 | a0002c0006t0005g0119 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1039-6611C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2869199 | ||||||
| chrX:2869384
|
A | G | 4 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0278others(1): Show | 4 | HG02015.hp1 NA18983.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039-6426A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2869384 | ||||||
| chrX:2869414
|
G | A | 263 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(260): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.1039-6396G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2869414 | ||||||
| chrX:2869441
|
C | T | 1 | a0001c0001t0001g0247 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1039-6369C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2869441 | ||||||
| chrX:2869444
|
G | A | 1 | a0001c0001t0001g0004 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1039-6366G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2869444 | ||||||
| chrX:2869522
|
TA | T | 1 | a0002c0002t0003g0034 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1039-6281delA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2869522 | |||||
| chrX:2869534
|
A | G | 1 | a0002c0002t0005g0105 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1039-6276A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2869534 | ||||||
| chrX:2869578
|
T | C | 3 | a0002c0002t0005g0117a0002c0002t0005g0126a0009c0013t0005g0037 | 3 | HG02717.hp1 HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1039-6232T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2869578 | ||||||
| chrX:2869747
|
G | A | 2 | a0002c0002t0005g0296a0002c0005t0007g0018 | 2 | HG01074.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1039-6063G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2869747 | ||||||
| chrX:2869857
|
C | G | 240 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(237): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.1039-5953C>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2869857 | ||||||
| chrX:2869867
|
C | T | 3 | a0001c0001t0002g0192a0002c0002t0005g0301a0002c0002t0007g0188 | 3 | HG00733.hp1 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1039-5943C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2869867 | ||||||
| chrX:2869925
|
G | A | 87 | a0001c0001t0002g0125a0001c0001t0002g0192a0001c0001t0002g0271others(84): Show | 88 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.1039-5885G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2869925 | ||||||
| chrX:2869998
|
GTAT | G | 3 | a0002c0002t0001g0008a0002c0002t0003g0010a0002c0002t0007g0118 | 3 | HG00733.hp2 HG02647.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1039-5809_1039-580 others(7): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2869998 | |||||
| chrX:2870095
|
C | T | 1 | a0001c0001t0004g0084 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1039-5715C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2870095 | ||||||
| chrX:2870100
|
GT | G | 55 | a0001c0001t0001g0083a0001c0001t0002g0100a0001c0001t0002g0192others(52): Show | 55 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1039-5697delT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2870100 | |||||
| chrX:2870196
|
T | A | 53 | a0001c0001t0002g0192a0001c0001t0004g0012a0001c0001t0004g0084others(50): Show | 53 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.1039-5614T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2870196 | ||||||
| chrX:2870224
|
C | G | 1 | a0002c0002t0006g0043 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1039-5586C>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2870224 | ||||||
| chrX:2870233
|
G | A | 53 | a0001c0001t0002g0192a0001c0001t0004g0012a0001c0001t0004g0084others(50): Show | 53 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.1039-5577G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2870233 | ||||||
| chrX:2870241
|
G | A | 1 | a0002c0002t0006g0043 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1039-5569G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2870241 | ||||||
| chrX:2870347
|
A | C | 54 | a0001c0001t0002g0192a0001c0001t0004g0012a0001c0001t0004g0084others(51): Show | 54 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.1039-5463A>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2870347 | ||||||
| chrX:2870392
|
G | A | 2 | a0002c0002t0001g0008a0002c0002t0007g0118 | 2 | HG00733.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1039-5418G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2870392 | ||||||
| chrX:2870439
|
G | A | 41 | a0001c0001t0004g0012a0001c0001t0004g0084a0001c0001t0004g0089others(38): Show | 41 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.1039-5371G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2870439 | ||||||
| chrX:2870454
|
G | C | 99 | a0001c0001t0002g0192a0001c0001t0002g0271a0001c0001t0003g0013others(96): Show | 99 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.1039-5356G>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2870454 | ||||||
| chrX:2870495
|
G | A | 5 | a0002c0002t0003g0109a0002c0002t0003g0110a0002c0002t0003g0112others(2): Show | 5 | HG02451.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1039-5315G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2870495 | ||||||
| chrX:2870498
|
C | T | 5 | a0001c0001t0002g0271a0001c0003t0007g0024a0002c0002t0012g0066others(2): Show | 5 | HG01884.hp2 HG02451.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1039-5312C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2870498 | ||||||
| chrX:2870648
|
G | T | 2 | a0002c0002t0005g0117a0002c0002t0005g0126 | 2 | HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1039-5162G>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2870648 | ||||||
| chrX:2870666
|
C | T | 64 | a0001c0001t0002g0192a0001c0001t0004g0012a0001c0001t0004g0084others(61): Show | 64 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.1039-5144C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2870666 | ||||||
| chrX:2870671
|
GTTA | G | 1 | a0002c0002t0003g0073 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1039-5134_1039-513 others(7): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2870671 | |||||
| chrX:2870928
|
C | T | 1 | a0001c0001t0007g0191 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1039-4882C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2870928 | ||||||
| chrX:2870957
|
G | A | 1 | a0013c0017t0005g0243 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1039-4853G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2870957 | ||||||
| chrX:2870994
|
AC | A | 2 | a0002c0002t0003g0033a0002c0002t0003g0034 | 2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1039-4813delC | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2870994 | |||||
| chrX:2871005
|
A | AT | 160 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(157): Show | 163 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.1039-4794dupT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2871005 | |||||
| chrX:2871016
|
T | A | 1 | a0001c0001t0002g0271 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1039-4794T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2871016 | ||||||
| chrX:2871106
|
A | G | 4 | a0002c0002t0002g0244a0002c0002t0002g0252a0002c0002t0002g0257others(1): Show | 4 | HG00280.hp1 HG00323.hp2 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039-4704A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2871106 | ||||||
| chrX:2871123
|
G | T | 2 | a0002c0002t0005g0296a0002c0005t0007g0018 | 2 | HG01074.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1039-4687G>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2871123 | ||||||
| chrX:2871142
|
C | G | 1 | a0001c0001t0001g0240 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1039-4668C>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2871142 | ||||||
| chrX:2871296
|
TA | T | 1 | a0002c0002t0004g0172 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1039-4512delA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2871296 | |||||
| chrX:2871373
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1039-4437C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2871373 | ||||||
| chrX:2871383
|
C | T | 293 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(290): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.1039-4427C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2871383 | ||||||
| chrX:2871387
|
T | TA | 1 | a0001c0001t0004g0093 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1039-4409dupA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2871387 | |||||
| chrX:2871387
|
TA | T | 158 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(155): Show | 161 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.1039-4409delA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2871387 | |||||
| chrX:2871684
|
C | T | 41 | a0001c0001t0004g0012a0001c0001t0004g0084a0001c0001t0004g0089others(38): Show | 41 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.1039-4126C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2871684 | ||||||
| chrX:2871689
|
C | CAAAT | 3 | a0001c0001t0003g0231a0001c0003t0002g0042a0006c0010t0003g0014 | 3 | HG01243.hp1 HG01255.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.1039-4077_1039-407 others(8): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2871689 | |||||
| chrX:2871689
|
C | CAAATAAA others(1): Show |
3 | a0001c0003t0004g0041a0002c0002t0003g0207a0002c0002t0003g0299 | 3 | HG02723.hp2 HG03704.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1039-4081_1039-407 others(12): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2871689 | |||||
| chrX:2871689
|
CAAATAAA others(1): Show |
C | 1 | a0001c0003t0008g0026 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1039-4081_1039-407 others(12): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2871689 | |||||
| chrX:2871689
|
CAAATAAA others(5): Show |
C | 16 | a0001c0001t0002g0271a0001c0003t0007g0024a0002c0002t0003g0033others(13): Show | 16 | HG01884.hp2 HG02280.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1039-4085_1039-407 others(16): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2871689 | |||||
| chrX:2871689
|
CAAATAAA others(9): Show |
C | 193 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(190): Show | 197 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.1039-4089_1039-407 others(20): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2871689 | |||||
| chrX:2871689
|
CAAATAAA others(13): Show |
C | 56 | a0001c0001t0002g0192a0001c0001t0004g0012a0001c0001t0004g0084others(53): Show | 56 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.1039-4093_1039-407 others(24): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2871689 | |||||
| chrX:2871689
|
CAAATAAA others(17): Show |
C | 1 | a0002c0002t0005g0178 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1039-4097_1039-407 others(28): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2871689 | |||||
| chrX:2871689
|
CAAATAAA others(21): Show |
C | 1 | a0002c0002t0008g0219 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1039-4101_1039-407 others(32): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2871689 | |||||
| chrX:2871807
|
T | G | 212 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(209): Show | 216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1039-4003T>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2871807 | ||||||
| chrX:2872058
|
TC | T | 1 | a0002c0002t0004g0172 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1039-3749delC | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2872058 | |||||
| chrX:2872107
|
T | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(209): Show | 216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1039-3703T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2872107 | ||||||
| chrX:2872153
|
G | T | 15 | a0001c0001t0002g0271a0001c0003t0007g0024a0001c0003t0008g0026others(12): Show | 15 | HG01884.hp2 HG01891.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1039-3657G>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2872153 | ||||||
| chrX:2872295
|
GTTC | G | 1 | a0002c0002t0003g0299 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1039-3512_1039-351 others(7): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2872295 | |||||
| chrX:2872310
|
CT | C | 1 | a0002c0002t0004g0172 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1039-3497delT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2872310 | |||||
| chrX:2872326
|
T | C | 49 | a0001c0001t0002g0192a0001c0001t0004g0012a0001c0001t0004g0084others(46): Show | 49 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.1039-3484T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2872326 | ||||||
| chrX:2872335
|
TA | T | 1 | a0002c0002t0004g0172 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1039-3471delA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2872335 | |||||
| chrX:2872387
|
TAA | T | 51 | a0001c0001t0002g0192a0001c0001t0004g0012a0001c0001t0004g0084others(48): Show | 51 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.1039-3419_1039-341 others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2872387 | |||||
| chrX:2872410
|
C | T | 1 | a0002c0002t0001g0254 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1039-3400C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2872410 | ||||||
| chrX:2872446
|
C | A | 7 | a0001c0001t0007g0191a0001c0003t0007g0024a0002c0002t0003g0109others(4): Show | 7 | HG02451.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1039-3364C>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2872446 | ||||||
| chrX:2872453
|
A | G | 4 | a0001c0001t0002g0271a0002c0002t0012g0066a0002c0002t0012g0067others(1): Show | 4 | HG01884.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1039-3357A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2872453 | ||||||
| chrX:2872512
|
C | T | 1 | a0002c0002t0004g0151 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1039-3298C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2872512 | ||||||
| chrX:2872673
|
T | C | 1 | a0002c0002t0007g0193 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1039-3137T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2872673 | ||||||
| chrX:2872721
|
T | A | 57 | a0001c0001t0001g0226a0001c0001t0002g0192a0001c0001t0004g0012others(54): Show | 57 | HG00099.hp1 HG00438.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.1039-3089T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2872721 | ||||||
| chrX:2872733
|
G | GT | 3 | a0002c0002t0003g0033a0002c0002t0003g0034a0002c0002t0003g0035 | 3 | HG02922.hp1 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1039-3071dupT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2872733 | |||||
| chrX:2872827
|
A | AG | 1 | a0002c0002t0004g0172 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1039-2982dupG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2872827 | |||||
| chrX:2872971
|
AT | A | 1 | a0002c0002t0004g0172 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1039-2833delT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2872971 | |||||
| chrX:2873040
|
T | C | 225 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(222): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1039-2770T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2873040 | ||||||
| chrX:2873072
|
G | C | 65 | a0001c0001t0001g0226a0001c0001t0001g0247a0001c0001t0002g0192others(62): Show | 65 | HG00099.hp1 HG00438.hp1 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.1039-2738G>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2873072 | ||||||
| chrX:2873096
|
G | A | 13 | a0001c0001t0002g0192a0001c0001t0004g0068a0001c0001t0015g0046others(10): Show | 13 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.1039-2714G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2873096 | ||||||
| chrX:2873157
|
G | GT | 1 | a0002c0002t0004g0172 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1039-2650dupT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2873157 | |||||
| chrX:2873179
|
C | A | 7 | a0003c0007t0001g0025a0003c0007t0006g0028a0003c0007t0006g0029others(4): Show | 7 | HG01261.hp1 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1039-2631C>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2873179 | ||||||
| chrX:2873210
|
CTGT | C | 1 | a0002c0002t0004g0172 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1039-2598_1039-259 others(7): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2873210 | |||||
| chrX:2873231
|
A | G | 61 | a0001c0001t0001g0226a0001c0001t0001g0247a0001c0001t0002g0192others(58): Show | 61 | HG00099.hp1 HG00438.hp1 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.1039-2579A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2873231 | ||||||
| chrX:2873237
|
G | C | 61 | a0001c0001t0001g0226a0001c0001t0001g0247a0001c0001t0002g0192others(58): Show | 61 | HG00099.hp1 HG00438.hp1 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.1039-2573G>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2873237 | ||||||
| chrX:2873276
|
CTTAATT | C | 1 | a0002c0002t0002g0253 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1039-2530_1039-252 others(10): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2873276 | |||||
| chrX:2873287
|
A | C | 1 | a0002c0002t0007g0193 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1039-2523A>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2873287 | ||||||
| chrX:2873287
|
A | G | 60 | a0001c0001t0001g0226a0001c0001t0001g0247a0001c0001t0002g0192others(57): Show | 60 | HG00099.hp1 HG00438.hp1 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.1039-2523A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2873287 | ||||||
| chrX:2873359
|
A | AT | 62 | a0001c0001t0001g0226a0001c0001t0001g0247a0001c0001t0002g0192others(59): Show | 62 | HG00099.hp1 HG00438.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.1039-2448dupT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2873359 | |||||
| chrX:2873512
|
TCTC | T | 2 | a0001c0001t0001g0228a0012c0018t0001g0099 | 2 | HG03017.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1039-2282_1039-228 others(7): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2873512 | |||||
| chrX:2873563
|
G | C | 65 | a0001c0001t0001g0226a0001c0001t0001g0247a0001c0001t0002g0192others(62): Show | 65 | HG00099.hp1 HG00438.hp1 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.1039-2247G>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2873563 | ||||||
| chrX:2873738
|
C | T | 5 | a0001c0001t0001g0247a0001c0003t0008g0026a0002c0002t0001g0047others(2): Show | 5 | HG01891.hp2 HG02109.hp1 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.1039-2072C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2873738 | ||||||
| chrX:2873927
|
G | GA | 1 | a0002c0002t0004g0172 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1039-1877dupA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2873927 | |||||
| chrX:2874097
|
A | AAAATAAA others(1): Show |
63 | a0001c0001t0001g0226a0001c0001t0001g0247a0001c0001t0002g0192others(60): Show | 63 | HG00099.hp1 HG00438.hp1 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.1039-1701_1039-169 others(12): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2874097 | |||||
| chrX:2874119
|
C | A | 4 | a0001c0001t0001g0247a0002c0002t0001g0047a0002c0002t0007g0193others(1): Show | 4 | HG02109.hp1 HG03688.hp1 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.1039-1691C>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2874119 | ||||||
| chrX:2874245
|
G | GT | 1 | a0002c0002t0004g0172 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1039-1560dupT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2874245 | |||||
| chrX:2874275
|
T | C | 2 | a0002c0002t0002g0141a0002c0002t0002g0142 | 2 | NA18941.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1039-1535T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2874275 | ||||||
| chrX:2874328
|
C | T | 1 | a0009c0013t0005g0037 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1039-1482C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2874328 | ||||||
| chrX:2874621
|
A | G | 93 | a0001c0001t0001g0226a0001c0001t0001g0247a0001c0001t0002g0192others(90): Show | 93 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.1039-1189A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2874621 | ||||||
| chrX:2874659
|
C | T | 1 | a0001c0001t0015g0046 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1039-1151C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2874659 | ||||||
| chrX:2874663
|
C | T | 5 | a0001c0001t0004g0068a0002c0002t0005g0050a0002c0002t0005g0105others(2): Show | 5 | HG02615.hp2 HG02970.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1039-1147C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2874663 | ||||||
| chrX:2874663
|
CCATAAAC others(47): Show |
C | 1 | a0008c0014t0018g0147 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1039-1146_1039-109 others(58): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2874663 | ||||||
| chrX:2874698
|
C | T | 6 | a0001c0001t0004g0068a0002c0002t0001g0032a0002c0002t0001g0123others(3): Show | 6 | HG01070.hp1 HG01071.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1039-1112C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2874698 | ||||||
| chrX:2874797
|
A | G | 32 | a0001c0001t0003g0013a0001c0001t0003g0055a0001c0001t0003g0057others(29): Show | 32 | HG00423.hp2 HG00673.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.1039-1013A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2874797 | ||||||
| chrX:2874891
|
G | A | 15 | a0001c0001t0002g0192a0001c0001t0004g0068a0001c0001t0015g0046others(12): Show | 15 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.1039-919G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2874891 | ||||||
| chrX:2875150
|
G | C | 1 | a0013c0017t0005g0243 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1039-660G>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2875150 | ||||||
| chrX:2875397
|
T | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0240 | 3 | HG01069.hp1 HG01071.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1039-413T>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2875397 | ||||||
| chrX:2875402
|
G | C | 14 | a0001c0001t0007g0191a0001c0003t0005g0304a0001c0003t0007g0024others(11): Show | 14 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1039-408G>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2875402 | ||||||
| chrX:2875484
|
G | A | 1 | a0002c0002t0004g0151 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1039-326G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2875484 | ||||||
| chrX:2875502
|
GACTCACA others(16): Show |
G | 17 | a0001c0001t0001g0247a0001c0001t0002g0192a0001c0001t0004g0068others(14): Show | 17 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.1039-279_1039-257d others(25): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2875502 | |||||
| chrX:2875629
|
G | A | 2 | a0001c0001t0011g0056a0001c0001t0011g0072 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1039-181G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2875629 | ||||||
| chrX:2875684
|
CTA | C | 38 | a0001c0001t0004g0012a0001c0001t0004g0084a0001c0001t0004g0089others(35): Show | 38 | HG00438.hp1 HG02056.hp1 HG02083.hp1 others(35): Show |
intron_variant | MODIFIER | c.1039-124_1039-123d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2875684 | |||||
| chrX:2876032
|
C | CT | 3 | a0001c0003t0005g0022a0002c0002t0005g0091a0002c0006t0005g0023 | 3 | HG01109.hp1 HG02145.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1143+118_1143+119i others(3): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 9/10 | chrX | 2876032 | ||||||
| chrX:2876032
|
C | CTT | 1 | a0002c0002t0005g0095 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1143+118_1143+119i others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 9/10 | chrX | 2876032 | ||||||
| chrX:2876032
|
C | CTTTT | 1 | a0001c0001t0015g0046 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1143+118_1143+119i others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 9/10 | chrX | 2876032 | ||||||
| chrX:2876033
|
C | CT | 64 | a0001c0001t0002g0054a0001c0001t0002g0076a0001c0001t0002g0079others(61): Show | 65 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.1143+147dupT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 2876033 | |||||
| chrX:2876033
|
C | CTT | 32 | a0001c0001t0002g0085a0001c0001t0002g0096a0001c0001t0002g0150others(29): Show | 32 | HG00323.hp1 HG00323.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.1143+146_1143+147d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 2876033 | |||||
| chrX:2876033
|
C | CTTT | 7 | a0001c0001t0004g0084a0002c0002t0001g0179a0002c0002t0002g0257others(4): Show | 7 | HG00280.hp1 HG02258.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143+145_1143+147d others(5): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 2876033 | |||||
| chrX:2876033
|
C | CTTTT | 3 | a0001c0003t0001g0030a0001c0003t0008g0026a0002c0002t0005g0108 | 3 | HG01891.hp2 NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1143+144_1143+147d others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 2876033 | |||||
| chrX:2876033
|
C | T | 5 | a0001c0001t0015g0046a0001c0003t0005g0022a0002c0002t0005g0091others(2): Show | 5 | HG01109.hp1 HG02145.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1143+119C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 9/10 | chrX | 2876033 | ||||||
| chrX:2876033
|
CT | C | 37 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0003g0013others(34): Show | 37 | HG00423.hp2 HG00673.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.1143+147delT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 2876033 | |||||
| chrX:2876033
|
CTT | C | 6 | a0001c0001t0001g0247a0001c0001t0002g0192a0001c0001t0003g0241others(3): Show | 6 | HG00733.hp1 HG02109.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.1143+146_1143+147d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 2876033 | |||||
| chrX:2876033
|
CTTTTT | C | 5 | a0001c0001t0001g0293a0002c0002t0001g0170a0002c0002t0001g0277others(2): Show | 5 | HG00099.hp1 HG00639.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.1143+143_1143+147d others(7): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 2876033 | |||||
| chrX:2876033
|
CTTTTTT | C | 4 | a0003c0007t0001g0025a0003c0007t0006g0028a0003c0007t0006g0029others(1): Show | 4 | HG02723.hp1 HG02809.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1143+142_1143+147d others(8): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 2876033 | |||||
| chrX:2876033
|
CTTTTTTT | C | 10 | a0001c0001t0001g0004a0001c0001t0001g0098a0001c0001t0001g0214others(7): Show | 11 | HG00544.hp1 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1143+141_1143+147d others(9): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 2876033 | |||||
| chrX:2876033
|
CTTTTTTT others(1): Show |
C | 84 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0052others(81): Show | 86 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1143+140_1143+147d others(10): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 2876033 | |||||
| chrX:2876033
|
CTTTTTTT others(2): Show |
C | 7 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0306others(4): Show | 7 | HG01081.hp1 HG01167.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143+139_1143+147d others(11): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 2876033 | |||||
| chrX:2876033
|
CTTTTTTT others(9): Show |
C | 1 | a0002c0002t0007g0193 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1143+132_1143+147d others(18): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 2876033 | |||||
| chrX:2876176
|
G | C | 4 | a0001c0001t0001g0247a0002c0002t0001g0047a0002c0002t0007g0193others(1): Show | 4 | HG02109.hp1 HG03688.hp1 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.1143+262G>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 9/10 | chrX | 2876176 | ||||||
| chrX:2876300
|
A | G | 1 | a0009c0013t0005g0037 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1143+386A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 9/10 | chrX | 2876300 | ||||||
| chrX:2876345
|
T | C | 11 | a0001c0001t0002g0271a0002c0002t0012g0066a0002c0002t0012g0067others(8): Show | 11 | HG01261.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1143+431T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 9/10 | chrX | 2876345 | ||||||
| chrX:2876420
|
G | T | 225 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(222): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1143+506G>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 9/10 | chrX | 2876420 | ||||||
| chrX:2876467
|
C | T | 3 | a0001c0001t0001g0101a0001c0004t0001g0103a0002c0002t0001g0158 | 3 | HG00408.hp1 HG02080.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.1143+553C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 9/10 | chrX | 2876467 | ||||||
| chrX:2876556
|
T | G | 1 | a0002c0006t0005g0023 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1143+642T>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 9/10 | chrX | 2876556 | ||||||
| chrX:2876642
|
G | GT | 1 | a0008c0014t0018g0147 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1144-551dupT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 2876642 | |||||
| chrX:2876649
|
T | A | 9 | a0001c0003t0005g0304a0002c0002t0001g0179a0002c0002t0005g0016others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1144-551T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 9/10 | chrX | 2876649 | ||||||
| chrX:2876675
|
G | A | 1 | a0002c0005t0007g0018 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1144-525G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 9/10 | chrX | 2876675 | ||||||
| chrX:2876730
|
T | C | 6 | a0001c0003t0001g0030a0002c0002t0002g0011a0002c0002t0002g0111others(3): Show | 6 | HG01074.hp1 HG02559.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1144-470T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 9/10 | chrX | 2876730 | ||||||
| chrX:2876771
|
AC | A | 4 | a0001c0001t0001g0247a0002c0002t0001g0047a0002c0002t0007g0193others(1): Show | 4 | HG02109.hp1 HG03688.hp1 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.1144-424delC | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 2876771 | |||||
| chrX:2876805
|
T | C | 1 | a0009c0013t0005g0037 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1144-395T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 9/10 | chrX | 2876805 | ||||||
| chrX:2876817
|
T | C | 127 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(124): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.1144-383T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 9/10 | chrX | 2876817 | ||||||
| chrX:2876818
|
G | A | 18 | a0001c0001t0002g0271a0002c0002t0003g0033a0002c0002t0003g0034others(15): Show | 18 | HG01261.hp1 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1144-382G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 9/10 | chrX | 2876818 | ||||||
| chrX:2876843
|
G | A | 1 | a0013c0017t0005g0243 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1144-357G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 9/10 | chrX | 2876843 | ||||||
| chrX:2876933
|
A | AT | 1 | a0008c0014t0018g0147 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1144-267_1144-266i others(3): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 9/10 | chrX | 2876933 | ||||||
| chrX:2876943
|
C | T | 1 | a0002c0002t0004g0021 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1144-257C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 9/10 | chrX | 2876943 | ||||||
| chrX:2877109
|
AC | A | 1 | a0008c0014t0018g0147 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1144-87delC | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 2877109 | |||||
| chrX:2877496
|
G | GC | 1 | a0008c0014t0018g0147 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1251+191dupC | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2877496 | |||||
| chrX:2877607
|
G | A | 1 | a0001c0001t0001g0005 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1251+300G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2877607 | ||||||
| chrX:2877652
|
G | A | 1 | a0013c0017t0005g0243 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1251+345G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2877652 | ||||||
| chrX:2877652
|
G | GA | 1 | a0008c0014t0018g0147 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1251+345_1251+346i others(3): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2877652 | ||||||
| chrX:2877696
|
C | T | 1 | a0002c0002t0005g0301 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1251+389C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2877696 | ||||||
| chrX:2877714
|
A | G | 1 | a0009c0013t0005g0037 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1251+407A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2877714 | ||||||
| chrX:2877803
|
G | GA | 1 | a0008c0014t0018g0147 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1251+499dupA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2877803 | |||||
| chrX:2877946
|
C | CT | 1 | a0008c0014t0018g0147 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1251+639_1251+640i others(3): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2877946 | ||||||
| chrX:2878034
|
C | CA | 1 | a0008c0014t0018g0147 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1251+730dupA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2878034 | |||||
| chrX:2878127
|
C | CT | 1 | a0008c0014t0018g0147 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1251+820_1251+821i others(3): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2878127 | ||||||
| chrX:2878152
|
G | A | 3 | a0001c0001t0001g0247a0002c0002t0001g0047a0002c0002t0007g0193 | 3 | HG02109.hp1 HG03688.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1251+845G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2878152 | ||||||
| chrX:2878169
|
T | G | 1 | a0013c0017t0005g0243 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1251+862T>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2878169 | ||||||
| chrX:2878187
|
G | A | 1 | a0001c0001t0001g0236 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1251+880G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2878187 | ||||||
| chrX:2878200
|
G | A | 12 | a0001c0003t0005g0304a0002c0002t0001g0179a0002c0002t0005g0016others(9): Show | 12 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1251+893G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2878200 | ||||||
| chrX:2878267
|
C | CT | 1 | a0008c0014t0018g0147 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1251+965dupT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2878267 | |||||
| chrX:2878278
|
T | TA | 1 | a0008c0014t0018g0147 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1251+976dupA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2878278 | |||||
| chrX:2878282
|
A | AATT | 4 | a0001c0001t0001g0247a0002c0002t0003g0110a0002c0002t0003g0112others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1251+997_1251+999d others(5): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2878282 | |||||
| chrX:2878444
|
A | AT | 1 | a0008c0014t0018g0147 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1251+1143dupT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2878444 | |||||
| chrX:2878559
|
C | T | 1 | a0002c0006t0003g0120 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1251+1252C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2878559 | ||||||
| chrX:2878604
|
G | GT | 1 | a0008c0014t0018g0147 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1251+1297_1251+129 others(5): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2878604 | ||||||
| chrX:2878662
|
T | TA | 1 | a0008c0014t0018g0147 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1251+1356dupA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2878662 | |||||
| chrX:2878696
|
A | AAG | 1 | a0008c0014t0018g0147 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1251+1391_1251+139 others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2878696 | |||||
| chrX:2878867
|
G | A | 3 | a0002c0002t0003g0033a0002c0002t0003g0034a0002c0002t0003g0035 | 3 | HG02922.hp1 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1251+1560G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2878867 | ||||||
| chrX:2878981
|
G | GCT | 1 | a0008c0014t0018g0147 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1251+1677_1251+167 others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2878981 | |||||
| chrX:2879033
|
TTTG | T | 1 | a0001c0001t0002g0200 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1251+1729_1251+173 others(7): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2879033 | |||||
| chrX:2879217
|
A | ATAT | 117 | a0001c0001t0001g0223a0001c0001t0002g0054a0001c0001t0002g0058others(114): Show | 118 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.1252-1834_1252-183 others(7): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2879217 | |||||
| chrX:2879270
|
C | CT | 7 | a0001c0001t0001g0247a0001c0001t0002g0190a0001c0001t0002g0282others(4): Show | 7 | HG02109.hp1 HG02523.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.1252-1765dupT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2879270 | |||||
| chrX:2879270
|
C | CTT | 1 | a0013c0017t0005g0243 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1252-1766_1252-176 others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2879270 | |||||
| chrX:2879270
|
CT | C | 8 | a0001c0001t0002g0076a0001c0001t0002g0150a0001c0003t0005g0177others(5): Show | 8 | HG01070.hp1 HG01168.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.1252-1765delT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2879270 | |||||
| chrX:2879305
|
T | TACAC | 1 | a0008c0014t0018g0147 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1252-1747_1252-174 others(8): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2879305 | ||||||
| chrX:2879307
|
A | AGTCTGG | 1 | a0008c0014t0018g0147 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1252-1745_1252-174 others(10): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2879307 | ||||||
| chrX:2879319
|
GT | G | 1 | a0008c0014t0018g0147 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1252-1732delT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2879319 | ||||||
| chrX:2879329
|
G | A | 5 | a0002c0002t0002g0144a0002c0002t0002g0163a0002c0002t0002g0164others(2): Show | 5 | HG03041.hp2 NA18939.hp2 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.1252-1723G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2879329 | ||||||
| chrX:2879470
|
G | A | 1 | a0002c0002t0002g0071 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1252-1582G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2879470 | ||||||
| chrX:2879476
|
C | CG | 1 | a0008c0014t0018g0147 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1252-1573dupG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2879476 | |||||
| chrX:2879532
|
T | TG | 1 | a0008c0014t0018g0147 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1252-1517dupG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2879532 | |||||
| chrX:2879587
|
A | G | 2 | a0001c0001t0007g0191a0001c0003t0007g0024 | 2 | HG02451.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1252-1465A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2879587 | ||||||
| chrX:2879591
|
C | G | 1 | a0002c0002t0003g0109 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1252-1461C>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2879591 | ||||||
| chrX:2879731
|
A | AT | 1 | a0008c0014t0018g0147 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1252-1317dupT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2879731 | |||||
| chrX:2879754
|
T | C | 68 | a0001c0001t0001g0223a0001c0001t0002g0054a0001c0001t0002g0063others(65): Show | 69 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.1252-1298T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2879754 | ||||||
| chrX:2879854
|
T | A | 65 | a0001c0001t0001g0223a0001c0001t0002g0054a0001c0001t0002g0063others(62): Show | 66 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.1252-1198T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2879854 | ||||||
| chrX:2879908
|
CAGAT | C | 2 | a0001c0001t0004g0230a0002c0002t0004g0300 | 2 | HG02132.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.1252-1143_1252-114 others(8): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2879908 | ||||||
| chrX:2879909
|
AGATG | A | 1 | a0002c0002t0005g0116 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1252-1122_1252-111 others(8): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2879909 | |||||
| chrX:2880017
|
TGATA | T | 1 | a0001c0001t0004g0159 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1252-1020_1252-101 others(8): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2880017 | |||||
| chrX:2880039
|
A | ATG | 1 | a0008c0014t0018g0147 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1252-1003_1252-100 others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2880039 | |||||
| chrX:2880073
|
A | AT | 1 | a0008c0014t0018g0147 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1252-974dupT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2880073 | |||||
| chrX:2880164
|
A | ATG | 7 | a0001c0001t0001g0240a0001c0001t0001g0298a0001c0001t0002g0222others(4): Show | 7 | HG00408.hp2 HG01074.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1252-862_1252-861d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2880164 | |||||
| chrX:2880164
|
A | ATGTG | 7 | a0001c0001t0002g0096a0001c0001t0007g0191a0002c0002t0002g0144others(4): Show | 7 | NA18939.hp2 NA18956.hp2 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.1252-864_1252-861d others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2880164 | |||||
| chrX:2880164
|
A | ATGTGTG | 55 | a0001c0001t0001g0223a0001c0001t0002g0054a0001c0001t0002g0058others(52): Show | 55 | HG00323.hp1 HG00544.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1252-866_1252-861d others(8): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2880164 | |||||
| chrX:2880164
|
A | ATGTGTGT others(1): Show |
3 | a0002c0002t0002g0071a0002c0002t0002g0253a0005c0009t0002g0212 | 3 | HG00438.hp2 HG01070.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.1252-868_1252-861d others(10): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2880164 | |||||
| chrX:2880164
|
ATG | A | 18 | a0001c0001t0001g0184a0001c0001t0001g0247a0001c0001t0015g0046others(15): Show | 18 | HG00280.hp1 HG00323.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1252-862_1252-861d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2880164 | |||||
| chrX:2880164
|
ATGTG | A | 64 | a0001c0001t0003g0013a0001c0001t0003g0053a0001c0001t0003g0055others(61): Show | 64 | HG00423.hp2 HG00673.hp1 HG00738.hp1 others(61): Show |
intron_variant | MODIFIER | c.1252-864_1252-861d others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2880164 | |||||
| chrX:2880164
|
ATGTGTG | A | 1 | a0002c0002t0003g0166 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1252-866_1252-861d others(8): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2880164 | |||||
| chrX:2880164
|
ATGTGTGT others(1): Show |
A | 1 | a0013c0017t0005g0243 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1252-868_1252-861d others(10): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2880164 | |||||
| chrX:2880228
|
G | A | 1 | a0002c0006t0005g0119 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1252-824G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2880228 | ||||||
| chrX:2880243
|
A | AGG | 1 | a0008c0014t0018g0147 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1252-808_1252-807d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2880243 | |||||
| chrX:2880287
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1252-765T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2880287 | ||||||
| chrX:2880396
|
TG | T | 1 | a0002c0002t0001g0229 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1252-653delG | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2880396 | |||||
| chrX:2880415
|
A | AGT | 2 | a0002c0002t0005g0050a0013c0017t0005g0243 | 2 | HG02970.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1252-613_1252-612d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2880415 | |||||
| chrX:2880415
|
A | AGTGTGT | 1 | a0002c0002t0007g0118 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1252-617_1252-612d others(8): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2880415 | |||||
| chrX:2880415
|
AGT | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(197): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1252-613_1252-612d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2880415 | |||||
| chrX:2880415
|
AGTGT | A | 18 | a0001c0001t0002g0271a0001c0003t0002g0042a0001c0004t0002g0048others(15): Show | 19 | HG00280.hp1 HG00323.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.1252-615_1252-612d others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2880415 | |||||
| chrX:2880437
|
T | C | 2 | a0001c0001t0002g0075a0001c0001t0002g0076 | 2 | NA18947.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.1252-615T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2880437 | ||||||
| chrX:2880439
|
T | C | 74 | a0001c0001t0001g0223a0001c0001t0002g0054a0001c0001t0002g0058others(71): Show | 75 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.1252-613T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2880439 | ||||||
| chrX:2880439
|
T | TGC | 2 | a0001c0001t0002g0063a0015c0011t0002g0185 | 2 | NA18970.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1252-612_1252-611d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2880439 | |||||
| chrX:2880439
|
T | TGTGC | 3 | a0002c0002t0002g0069a0002c0002t0002g0070a0002c0002t0002g0071 | 3 | HG00438.hp2 NA19001.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1252-612_1252-611i others(6): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2880439 | |||||
| chrX:2880553
|
CTT | C | 2 | a0001c0001t0007g0191a0001c0003t0007g0024 | 2 | HG02451.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1252-498_1252-497d others(4): Show |
GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2880553 | ||||||
| chrX:2880559
|
CA | C | 19 | a0001c0001t0015g0046a0001c0003t0005g0022a0001c0003t0005g0177others(16): Show | 19 | HG01070.hp1 HG01071.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.1252-485delA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2880559 | |||||
| chrX:2880630
|
G | C | 1 | a0002c0002t0001g0277 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1252-422G>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2880630 | ||||||
| chrX:2880678
|
C | G | 2 | a0001c0001t0001g0249a0001c0001t0001g0250 | 2 | HG01081.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1252-374C>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2880678 | ||||||
| chrX:2880686
|
T | C | 1 | a0002c0002t0006g0043 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1252-366T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2880686 | ||||||
| chrX:2880760
|
C | G | 2 | a0002c0002t0005g0105a0002c0005t0007g0020 | 2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1252-292C>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2880760 |