Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 470 | 170 | 17 | 29 | 93 | 5 | 25 | 72 | GYG2_chrX_2823930_2887818 | GYG2 | MSVTD others(465): Show |
chrX | 2823930 | 2887818 |
| a0002 | 1/0 | 470 | 128 | 56 | 19 | 41 | 5 | 6 | 32 | GYG2_chrX_2823930_2887818 | GYG2 | MSVTD others(465): Show |
chrX | 2823930 | 2887818 |
| a0003 | 0/0 | 470 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | MSVTD others(465): Show |
chrX | 2823930 | 2887818 |
| a0004 | 0/0 | 470 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | MSVTD others(465): Show |
chrX | 2823930 | 2887818 |
| a0005 | 0/0 | 470 | 3 | 0 | 2 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | MSVTD others(465): Show |
chrX | 2823930 | 2887818 |
| a0006 | 0/0 | 470 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | MSVTD others(465): Show |
chrX | 2823930 | 2887818 |
| a0007 | 0/0 | 470 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | MSVTD others(465): Show |
chrX | 2823930 | 2887818 |
| a0008 | 0/0 | 470 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | MSVTD others(465): Show |
chrX | 2823930 | 2887818 |
| a0009 | 0/0 | 470 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | MSVTD others(465): Show |
chrX | 2823930 | 2887818 |
| a0010 | 0/0 | 470 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | MSVTD others(465): Show |
chrX | 2823930 | 2887818 |
| a0011 | 0/0 | 470 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | MSVTD others(465): Show |
chrX | 2823930 | 2887818 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1410 | 152 | 7 | 28 | 86 | 5 | 25 | GYG2_chrX_2823930_2887818 | GYG2 | ATGTC others(1405): Show |
chrX | 2823930 | 2887818 | ||
| a0001c0003 | 0/0 | 1410 | 11 | 10 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | ATGTC others(1405): Show |
chrX | 2823930 | 2887818 | ||
| a0001c0004 | 0/0 | 1410 | 6 | 0 | 0 | 6 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | ATGTC others(1405): Show |
chrX | 2823930 | 2887818 | ||
| a0001c0013 | 0/0 | 1410 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | ATGTC others(1405): Show |
chrX | 2823930 | 2887818 | ||
| a0002c0002 | 1/0 | 1410 | 117 | 47 | 17 | 41 | 5 | 6 | GYG2_chrX_2823930_2887818 | GYG2 | ATGTC others(1405): Show |
chrX | 2823930 | 2887818 | ||
| a0002c0005 | 0/0 | 1410 | 6 | 4 | 2 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | ATGTC others(1405): Show |
chrX | 2823930 | 2887818 | ||
| a0002c0006 | 0/0 | 1410 | 5 | 5 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | ATGTC others(1405): Show |
chrX | 2823930 | 2887818 | ||
| a0003c0007 | 0/0 | 1410 | 4 | 4 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | ATGTC others(1405): Show |
chrX | 2823930 | 2887818 | ||
| a0004c0009 | 0/0 | 1410 | 3 | 0 | 2 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | ATGTC others(1405): Show |
chrX | 2823930 | 2887818 | ||
| a0005c0010 | 0/0 | 1410 | 3 | 0 | 2 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | ATGTC others(1405): Show |
chrX | 2823930 | 2887818 | ||
| a0006c0008 | 0/0 | 1410 | 3 | 2 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | ATGTC others(1405): Show |
chrX | 2823930 | 2887818 | ||
| a0007c0016 | 0/0 | 1410 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | ATGTC others(1405): Show |
chrX | 2823930 | 2887818 | ||
| a0008c0015 | 0/0 | 1410 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | ATGTC others(1405): Show |
chrX | 2823930 | 2887818 | ||
| a0009c0012 | 0/0 | 1410 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | ATGTC others(1405): Show |
chrX | 2823930 | 2887818 | ||
| a0010c0014 | 0/0 | 1410 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | ATGTC others(1405): Show |
chrX | 2823930 | 2887818 | ||
| a0011c0011 | 0/0 | 1410 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | ATGTC others(1405): Show |
chrX | 2823930 | 2887818 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3192 | 59 | 2 | 12 | 29 | 2 | 14 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0001c0001t0002 | 0/1 | 3192 | 38 | 2 | 5 | 26 | 2 | 2 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0001c0001t0003 | 0/0 | 3192 | 25 | 0 | 2 | 23 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0001c0001t0004 | 0/0 | 3192 | 19 | 1 | 7 | 6 | 0 | 5 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0001c0001t0005 | 0/0 | 3192 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0001c0001t0007 | 0/0 | 3192 | 2 | 1 | 0 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0001c0001t0008 | 0/0 | 3192 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0001c0001t0009 | 0/0 | 3192 | 2 | 0 | 2 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0001c0001t0010 | 0/0 | 3192 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0001c0001t0011 | 0/0 | 3192 | 2 | 0 | 0 | 0 | 0 | 2 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0001c0001t0014 | 0/0 | 3192 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0001c0001t0016 | 0/0 | 3192 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0001c0003t0001 | 0/0 | 3192 | 3 | 3 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0001c0003t0002 | 0/0 | 3192 | 2 | 1 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0001c0003t0004 | 0/0 | 3192 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0001c0003t0005 | 0/0 | 3192 | 3 | 3 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0001c0003t0007 | 0/0 | 3192 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0001c0003t0008 | 0/0 | 3192 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0001c0004t0001 | 0/0 | 3192 | 3 | 0 | 0 | 3 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0001c0004t0002 | 0/0 | 3192 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0001c0004t0004 | 0/0 | 3192 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0001c0004t0013 | 0/0 | 3192 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0001c0013t0003 | 0/0 | 3192 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0002c0002t0001 | 0/0 | 3192 | 19 | 3 | 11 | 2 | 2 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0002c0002t0002 | 0/0 | 3192 | 26 | 9 | 4 | 10 | 3 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0002c0002t0003 | 0/0 | 3192 | 16 | 8 | 0 | 6 | 0 | 2 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0002c0002t0004 | 1/0 | 3192 | 26 | 1 | 0 | 21 | 0 | 3 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0002c0002t0005 | 0/0 | 3192 | 16 | 15 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0002c0002t0006 | 0/0 | 3192 | 4 | 4 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0002c0002t0007 | 0/0 | 3192 | 4 | 4 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0002c0002t0008 | 0/0 | 3192 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0002c0002t0010 | 0/0 | 3192 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0002c0002t0012 | 0/0 | 3192 | 2 | 2 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0002c0002t0015 | 0/0 | 3192 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0002c0002t0017 | 0/0 | 3192 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0002c0005t0002 | 0/0 | 3192 | 2 | 2 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0002c0005t0003 | 0/0 | 3192 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0002c0005t0006 | 0/0 | 3192 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0002c0005t0007 | 0/0 | 3192 | 2 | 1 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0002c0006t0002 | 0/0 | 3192 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0002c0006t0003 | 0/0 | 3192 | 2 | 2 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0002c0006t0005 | 0/0 | 3192 | 2 | 2 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0003c0007t0001 | 0/0 | 3192 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0003c0007t0006 | 0/0 | 3192 | 3 | 3 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0004c0009t0001 | 0/0 | 3192 | 1 | 0 | 0 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0004c0009t0002 | 0/0 | 3192 | 2 | 0 | 2 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0005c0010t0003 | 0/0 | 3192 | 3 | 0 | 2 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0006c0008t0006 | 0/0 | 3192 | 3 | 2 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0007c0016t0003 | 0/0 | 3192 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0008c0015t0001 | 0/0 | 3192 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0009c0012t0001 | 0/0 | 3192 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0010c0014t0005 | 0/0 | 3192 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| a0011c0011t0005 | 0/0 | 3192 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | GCCTC others(3187): Show |
chrX | 2823930 | 2887818 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0215 | 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 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0001g0302 | 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 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0142 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0277 | 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 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0198 | 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 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0004g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0004g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0005g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0007g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0007g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0008g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0009g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0009g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0010g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0011g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0011g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0014g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0001t0016g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0003t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0003t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0003t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0003t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0003t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0003t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0003t0005g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0003t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0003t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0003t0007g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0003t0008g0033 | 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 |
| a0001c0004t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0004t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0004t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0004t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0004t0013g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0001c0013t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0249 | 0/0 | 1 | 1 | 0 | 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 |
| a0002c0002t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0003g0147 | 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 |
| a0002c0002t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0130 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0154 | 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 |
| a0002c0002t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0002c0002t0004g0173 | 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 |
| a0002c0002t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0004g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0005g0099 | 0/0 | 1 | 0 | 1 | 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 |
| a0002c0002t0005g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0005g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0005g0120 | 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 |
| a0002c0002t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0005g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0005g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0005g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0005g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0006g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0006g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0006g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0006g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0007g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0007g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0007g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0007g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0008g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0010g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0012g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0012g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0015g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0002t0017g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0005t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0005t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0005t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0005t0006g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0005t0007g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0005t0007g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0006t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0006t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0006t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0006t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0002c0006t0005g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0003c0007t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0003c0007t0006g0030 | 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 |
| a0003c0007t0006g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0004c0009t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0004c0009t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0004c0009t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0005c0010t0003g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0005c0010t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0005c0010t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0006c0008t0006g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0006c0008t0006g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0006c0008t0006g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0007c0016t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0008c0015t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0009c0012t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0010c0014t0005g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| a0011c0011t0005g0042 | 0/0 | 1 | 1 | 0 | 0 | 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 | g0174 | EUR | GBR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0150 | EUR | GBR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0289 | 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 | g0293 | EUR | FIN | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00323 | hp2 | a0002 | c0002 | t0002 | g0264 | EUR | FIN | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00408 | hp1 | a0001 | c0004 | t0001 | g0106 | EAS | CHS | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | CHS | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00423 | hp1 | a0002 | c0002 | t0004 | g0266 | EAS | CHS | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0278 | EAS | CHS | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0167 | EAS | CHS | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0073 | EAS | CHS | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | CHS | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00621 | hp1 | a0002 | c0002 | t0010 | g0163 | EAS | CHS | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | CHS | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0194 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0011 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG00741 | hp2 | a0002 | c0005 | t0006 | g0107 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0125 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01070 | hp2 | a0004 | c0009 | t0002 | g0244 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0126 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01074 | hp1 | a0002 | c0005 | t0007 | g0023 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0297 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0005 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01106 | hp1 | a0002 | c0002 | t0002 | g0298 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01109 | hp1 | a0002 | c0002 | t0005 | g0099 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01167 | hp1 | a0001 | c0001 | t0009 | g0274 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0152 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01169 | hp2 | a0001 | c0001 | t0009 | g0269 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0005 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01243 | hp1 | a0001 | c0003 | t0002 | g0046 | AMR | PUR | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01255 | hp1 | a0005 | c0010 | t0003 | g0017 | AMR | CLM | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0263 | AMR | CLM | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0133 | AMR | CLM | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0131 | AMR | CLM | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01261 | hp1 | a0006 | c0008 | t0006 | g0020 | AMR | CLM | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0153 | AMR | CLM | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01433 | hp1 | a0002 | c0002 | t0017 | g0258 | AMR | CLM | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01515 | hp1 | a0001 | c0001 | t0007 | g0216 | 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 | g0160 | EUR | IBS | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01884 | hp1 | a0002 | c0002 | t0005 | g0120 | AFR | ACB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01884 | hp2 | a0002 | c0005 | t0003 | g0045 | AFR | ACB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01891 | hp1 | a0006 | c0008 | t0006 | g0024 | AFR | ACB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01891 | hp2 | a0001 | c0003 | t0008 | g0033 | AFR | ACB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0188 | AMR | PEL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01934 | hp1 | a0002 | c0002 | t0002 | g0265 | AMR | PEL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0262 | AMR | PEL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | PEL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0067 | AMR | PEL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01981 | hp1 | a0004 | c0009 | t0002 | g0155 | AMR | PEL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0082 | AMR | PEL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0259 | AMR | PEL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0132 | AMR | PEL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02004 | hp1 | a0002 | c0002 | t0002 | g0261 | AMR | PEL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0280 | AMR | PEL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | KHV | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02055 | hp1 | a0001 | c0003 | t0005 | g0013 | AFR | ACB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02056 | hp1 | a0002 | c0002 | t0004 | g0140 | EAS | KHV | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0225 | EAS | KHV | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0218 | EAS | KHV | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02080 | hp1 | a0005 | c0010 | t0003 | g0189 | EAS | KHV | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0165 | EAS | KHV | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02083 | hp1 | a0002 | c0002 | t0004 | g0157 | EAS | KHV | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | KHV | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02132 | hp1 | a0002 | c0002 | t0004 | g0304 | EAS | KHV | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | KHV | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02145 | hp1 | a0001 | c0003 | t0005 | g0027 | AFR | ACB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0226 | EAS | CDX | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02155 | hp2 | a0001 | c0001 | t0016 | g0097 | EAS | CDX | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0237 | EAS | CDX | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02165 | hp2 | a0001 | c0004 | t0013 | g0291 | EAS | CDX | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02257 | hp1 | a0002 | c0002 | t0002 | g0117 | AFR | ACB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0181 | AFR | ACB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02273 | hp1 | a0007 | c0016 | t0003 | g0207 | AMR | PEL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0009 | AMR | PEL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02280 | hp1 | a0002 | c0005 | t0002 | g0178 | AFR | ACB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02280 | hp2 | a0002 | c0006 | t0005 | g0111 | AFR | ACB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0101 | AMR | PEL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0260 | AMR | PEL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02451 | hp1 | a0001 | c0003 | t0007 | g0034 | AFR | ACB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02451 | hp2 | a0002 | c0002 | t0003 | g0116 | AFR | ACB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | KHV | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02523 | hp2 | a0002 | c0002 | t0004 | g0214 | EAS | KHV | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02572 | hp1 | a0002 | c0002 | t0006 | g0022 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02615 | hp1 | a0002 | c0002 | t0002 | g0014 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02615 | hp2 | a0002 | c0005 | t0007 | g0025 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02622 | hp1 | a0002 | c0006 | t0002 | g0113 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02622 | hp2 | a0002 | c0002 | t0006 | g0056 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02630 | hp1 | a0002 | c0002 | t0002 | g0004 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02647 | hp1 | a0002 | c0002 | t0003 | g0012 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02683 | hp1 | a0001 | c0001 | t0004 | g0250 | SAS | PJL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0231 | SAS | PJL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02698 | hp1 | a0001 | c0001 | t0004 | g0088 | SAS | PJL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02717 | hp1 | a0002 | c0002 | t0005 | g0128 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02723 | hp1 | a0003 | c0007 | t0006 | g0036 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02723 | hp2 | a0001 | c0003 | t0004 | g0047 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02738 | hp1 | a0002 | c0002 | t0003 | g0076 | SAS | PJL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02809 | hp1 | a0002 | c0002 | t0002 | g0054 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02809 | hp2 | a0003 | c0007 | t0001 | g0032 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02818 | hp1 | a0002 | c0005 | t0002 | g0124 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02818 | hp2 | a0002 | c0006 | t0005 | g0035 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0037 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02886 | hp2 | a0002 | c0002 | t0002 | g0004 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02895 | hp1 | a0002 | c0002 | t0012 | g0069 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02896 | hp1 | a0002 | c0002 | t0002 | g0044 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02896 | hp2 | a0002 | c0002 | t0006 | g0136 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02897 | hp1 | a0002 | c0002 | t0002 | g0043 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02897 | hp2 | a0002 | c0002 | t0012 | g0070 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02922 | hp1 | a0002 | c0002 | t0003 | g0040 | AFR | ESN | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02922 | hp2 | a0003 | c0007 | t0006 | g0031 | AFR | ESN | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02965 | hp1 | a0002 | c0002 | t0008 | g0248 | AFR | ESN | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02970 | hp1 | a0002 | c0002 | t0005 | g0055 | AFR | ESN | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02970 | hp2 | a0002 | c0002 | t0005 | g0021 | AFR | ESN | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02976 | hp1 | a0002 | c0002 | t0007 | g0048 | AFR | ESN | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02976 | hp2 | a0002 | c0002 | t0003 | g0038 | AFR | ESN | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03017 | hp1 | a0008 | c0015 | t0001 | g0102 | SAS | PJL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03041 | hp1 | a0002 | c0002 | t0005 | g0098 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03041 | hp2 | a0002 | c0002 | t0007 | g0110 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03098 | hp1 | a0001 | c0003 | t0001 | g0123 | AFR | MSL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03130 | hp1 | a0002 | c0002 | t0005 | g0122 | AFR | ESN | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03139 | hp1 | a0002 | c0002 | t0005 | g0305 | AFR | ESN | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03195 | hp1 | a0002 | c0002 | t0004 | g0026 | AFR | ESN | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03195 | hp2 | a0002 | c0002 | t0005 | g0137 | AFR | ESN | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03209 | hp1 | a0002 | c0002 | t0006 | g0050 | AFR | MSL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03225 | hp1 | a0002 | c0006 | t0003 | g0041 | AFR | MSL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03239 | hp1 | a0002 | c0002 | t0004 | g0166 | SAS | PJL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03453 | hp1 | a0002 | c0002 | t0005 | g0300 | AFR | MSL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03453 | hp2 | a0001 | c0003 | t0002 | g0049 | AFR | MSL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03486 | hp1 | a0002 | c0002 | t0005 | g0205 | AFR | MSL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03486 | hp2 | a0002 | c0002 | t0003 | g0134 | AFR | MSL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03491 | hp1 | a0002 | c0002 | t0004 | g0159 | SAS | PJL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03491 | hp2 | a0001 | c0001 | t0011 | g0075 | SAS | PJL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03492 | hp1 | a0001 | c0001 | t0011 | g0064 | SAS | PJL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03516 | hp1 | a0001 | c0003 | t0005 | g0179 | AFR | ESN | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03516 | hp2 | a0002 | c0002 | t0003 | g0039 | AFR | ESN | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03540 | hp1 | a0001 | c0003 | t0001 | g0029 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03540 | hp2 | a0002 | c0002 | t0002 | g0249 | AFR | GWD | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03579 | hp1 | a0002 | c0002 | t0005 | g0180 | AFR | MSL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03669 | hp2 | a0002 | c0002 | t0004 | g0306 | SAS | PJL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | STU | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03704 | hp1 | a0002 | c0002 | t0003 | g0212 | SAS | PJL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03710 | hp1 | a0001 | c0001 | t0005 | g0019 | SAS | PJL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03831 | hp1 | a0001 | c0001 | t0008 | g0068 | SAS | BEB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0169 | SAS | BEB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | BEB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | BEB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | BEB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0015 | SAS | BEB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0192 | SAS | BEB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG04115 | hp1 | a0009 | c0012 | t0001 | g0141 | SAS | STU | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0202 | SAS | BEB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | BEB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | STU | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | STU | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG04228 | hp1 | a0010 | c0014 | t0005 | g0233 | SAS | STU | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0127 | AFR | YRI | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18612 | hp1 | a0002 | c0002 | t0004 | g0175 | EAS | CHB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CHB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0028 | AFR | YRI | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18906 | hp2 | a0002 | c0002 | t0005 | g0114 | AFR | YRI | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18939 | hp2 | a0002 | c0002 | t0002 | g0148 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18941 | hp2 | a0002 | c0002 | t0002 | g0145 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18942 | hp2 | a0002 | c0002 | t0004 | g0158 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18945 | hp1 | a0002 | c0002 | t0004 | g0301 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18947 | hp2 | a0001 | c0013 | t0003 | g0240 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18948 | hp1 | a0002 | c0002 | t0004 | g0272 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0279 | 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 | g0199 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18956 | hp1 | a0001 | c0001 | t0004 | g0200 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18956 | hp2 | a0002 | c0002 | t0002 | g0149 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18959 | hp1 | a0002 | c0002 | t0004 | g0173 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18960 | hp1 | a0002 | c0002 | t0002 | g0151 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18961 | hp1 | a0002 | c0002 | t0004 | g0224 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18965 | hp1 | a0001 | c0004 | t0001 | g0089 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18967 | hp1 | a0002 | c0002 | t0003 | g0303 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18969 | hp2 | a0002 | c0002 | t0004 | g0177 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18971 | hp1 | a0002 | c0002 | t0004 | g0002 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18975 | hp2 | a0002 | c0002 | t0004 | g0171 | 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 | g0086 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18979 | hp2 | a0002 | c0002 | t0003 | g0147 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18986 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18987 | hp1 | a0002 | c0002 | t0004 | g0154 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18989 | hp1 | a0002 | c0002 | t0004 | g0196 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0276 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0223 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18993 | hp1 | a0002 | c0002 | t0004 | g0162 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18994 | hp1 | a0001 | c0001 | t0004 | g0095 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0146 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19001 | hp1 | a0002 | c0002 | t0002 | g0072 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19005 | hp1 | a0002 | c0002 | t0003 | g0172 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19007 | hp1 | a0001 | c0001 | t0004 | g0096 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19009 | hp1 | a0002 | c0002 | t0004 | g0164 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19030 | hp1 | a0003 | c0007 | t0006 | g0030 | AFR | LWK | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19030 | hp2 | a0002 | c0002 | t0007 | g0190 | AFR | LWK | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19043 | hp1 | a0002 | c0002 | t0005 | g0118 | AFR | LWK | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0299 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19058 | hp1 | a0002 | c0002 | t0004 | g0002 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19060 | hp1 | a0002 | c0002 | t0003 | g0138 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19063 | hp1 | a0001 | c0001 | t0010 | g0092 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19075 | hp1 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19080 | hp1 | a0002 | c0002 | t0003 | g0239 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19083 | hp1 | a0002 | c0002 | t0004 | g0156 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19086 | hp1 | a0001 | c0004 | t0004 | g0091 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19087 | hp2 | a0002 | c0002 | t0002 | g0074 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19088 | hp1 | a0001 | c0004 | t0002 | g0053 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19090 | hp2 | a0002 | c0002 | t0015 | g0275 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19091 | hp1 | a0002 | c0002 | t0004 | g0083 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19240 | hp1 | a0002 | c0002 | t0005 | g0108 | AFR | YRI | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA19240 | hp2 | a0002 | c0002 | t0002 | g0121 | AFR | YRI | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA20752 | hp1 | a0004 | c0009 | t0001 | g0065 | EUR | TSI | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA20805 | hp1 | a0002 | c0002 | t0002 | g0161 | EUR | TSI | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0208 | SAS | GIH | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01123 | hp1 | a0005 | c0010 | t0003 | g0206 | AMR | CLM | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0176 | AMR | CLM | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0052 | AFR | ACB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02109 | hp2 | a0006 | c0008 | t0006 | g0129 | AFR | ACB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02486 | hp1 | a0002 | c0002 | t0003 | g0115 | AFR | ACB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02559 | hp1 | a0002 | c0006 | t0003 | g0112 | AFR | ACB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG02559 | hp2 | a0002 | c0002 | t0003 | g0119 | AFR | ACB | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0071 | AFR | MSL | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG06807 | hp1 | a0002 | c0002 | t0005 | g0109 | AFR | USA | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0273 | AFR | USA | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA18955 | hp1 | a0001 | c0001 | t0004 | g0094 | EAS | JPT | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA20300 | hp1 | a0001 | c0001 | t0014 | g0051 | AFR | USA | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA20300 | hp2 | a0011 | c0011 | t0005 | g0042 | AFR | USA | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA21309 | hp1 | a0001 | c0001 | t0007 | g0193 | AFR | LWK | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| NA21309 | hp2 | a0002 | c0002 | t0007 | g0195 | AFR | LWK | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0142 | REF | REF | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0004 | g0130 | REF | REF | GYG2_chrX_2823930_2887818 | GYG2 | chrX | 2823930 | 2887818 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | 7 | a0001 a0003 a0004 others(4): Show |
182 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(179): 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 | 7 | a0001 a0003 a0005 others(4): Show |
180 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(177): 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:2861708 | C | T | 2 | a0005 a0007 |
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 | a0003 a0006 |
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 | a0010 a0011 |
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:2881073 | T | C | 1 | a0008 | 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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0001c0003 a0002c0006 a0003c0007 |
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 | a0001c0013 | 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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:2881438 | A | T | 13 | a0001c0001t0003 a0001c0013t0003 a0002c0002t0003 others(10): 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 | a0002c0002t0017 | 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 | a0001c0004t0013 | 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:2881778 | G | A | 1 | a0001c0001t0014 | 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:2882011 | C | T | 1 | a0001c0001t0016 | 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 | 38 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(35): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): 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:2882583 | G | T | 26 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0008 others(23): 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 | 39 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(36): 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 | a0002c0002t0015 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1534G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 11/11 | 1534 | chrX | 2882747 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:2829473 | C | T | 132 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0182 others(129): 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 | a0001c0003t0005g0179 a0002c0002t0001g0011 a0002c0002t0001g0181 others(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:2829580 | C | T | 1 | a0002c0005t0002g0178 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-128-481C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 1/10 | chrX | 2829580 | |||||||
| chrX:2829662 | C | T | 41 | a0001c0001t0001g0139 a0001c0001t0001g0143 a0001c0001t0001g0144 others(38): Show |
42 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.-128-399C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 1/10 | chrX | 2829662 | |||||||
| chrX:2829786 | C | T | 1 | a0002c0002t0005g0305 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-128-275C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 1/10 | chrX | 2829786 | |||||||
| chrX:2829829 | C | CG | 25 | a0001c0001t0001g0018 a0001c0001t0001g0139 a0001c0001t0001g0182 others(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:2829926 | G | C | 3 | a0002c0005t0007g0023 a0002c0005t0007g0025 a0006c0008t0006g0024 |
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 | 227 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(224): 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:2830027 | G | A | 4 | a0001c0001t0002g0194 a0001c0001t0007g0193 a0002c0002t0005g0305 others(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:2830212 | G | C | 281 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(278): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): 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 | a0002c0002t0004g0196 | 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 | a0002c0002t0005g0108 | 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 | 196 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(193): 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:2830380 | G | A | 186 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(183): 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:2830468 | C | A | 3 | a0001c0001t0014g0051 a0002c0002t0001g0011 a0002c0002t0001g0052 |
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:2830729 | T | G | 1 | a0001c0004t0002g0053 | 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 | a0002c0002t0004g0177 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.7+549G>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2830744 | |||||||
| chrX:2830812 | A | G | 1 | a0002c0002t0001g0181 | 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 | a0001c0003t0002g0046 a0001c0003t0002g0049 a0001c0003t0004g0047 others(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:2831091 | T | G | 1 | a0002c0002t0005g0109 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.7+896T>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2831091 | |||||||
| chrX:2831213 | G | T | 1 | a0001c0004t0001g0106 | 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 | a0001c0004t0001g0106 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.7+1020A>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2831215 | |||||||
| chrX:2831358 | G | C | 2 | a0002c0002t0002g0054 a0002c0005t0002g0178 |
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:2831480 | T | C | 221 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(218): 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:2831522 | G | A | 1 | a0001c0001t0003g0198 | 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 | a0002c0002t0003g0040 a0002c0005t0007g0023 a0002c0005t0007g0025 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0302 |
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:2832019 | G | A | 2 | a0001c0003t0002g0046 a0001c0003t0004g0047 |
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 | 191 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(188): 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 | 194 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(191): 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:2832582 | T | C | 2 | a0001c0001t0002g0194 a0001c0001t0007g0193 |
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:2832647 | G | A | 2 | a0002c0002t0002g0145 a0002c0002t0002g0146 |
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 | 56 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(53): 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 | a0001c0001t0001g0281 a0001c0001t0001g0282 |
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 | a0002c0002t0001g0280 | 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 | a0001c0003t0002g0049 a0002c0002t0002g0014 a0002c0002t0006g0050 others(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:2833119 | T | C | 266 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(263): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): 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 | a0002c0002t0003g0040 | 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 | a0001c0001t0002g0191 a0001c0001t0002g0277 a0001c0001t0003g0278 others(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 | a0001c0001t0001g0135 a0002c0002t0003g0134 a0002c0002t0005g0021 others(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 | 263 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(260): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.7+3464T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2833659 | |||||||
| chrX:2833863 | C | G | 133 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0182 others(130): 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 | a0002c0002t0003g0040 | 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 | a0002c0002t0003g0038 a0002c0002t0003g0039 a0002c0002t0003g0040 others(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 | 77 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(74): 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 | 5 | a0001c0001t0004g0005 a0001c0001t0004g0131 a0001c0001t0004g0132 others(2): 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 | a0002c0002t0007g0190 | 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 | a0001c0001t0005g0019 | 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 | 83 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(80): 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 | a0002c0002t0005g0137 | 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 | 61 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(58): 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 | a0001c0001t0001g0135 a0002c0002t0002g0004 a0002c0002t0003g0134 others(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 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0004g0200 |
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 | 58 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(55): 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 | a0001c0001t0003g0276 | 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 | a0001c0003t0001g0028 a0001c0003t0001g0029 a0001c0003t0002g0046 others(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 | a0001c0001t0001g0135 a0002c0002t0002g0004 a0002c0002t0003g0134 others(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 | a0002c0002t0001g0052 | 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 | a0002c0002t0003g0038 a0002c0002t0003g0039 a0002c0002t0003g0040 others(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 | a0002c0002t0003g0038 a0002c0002t0003g0039 a0002c0002t0003g0040 others(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 | a0002c0002t0003g0038 a0002c0002t0003g0039 a0002c0002t0003g0040 others(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 | a0002c0002t0003g0038 a0002c0002t0003g0039 a0002c0002t0003g0040 others(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 | a0002c0002t0003g0038 a0002c0002t0003g0039 a0002c0002t0003g0040 others(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:2835141 | G | C | 58 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(55): 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 | a0002c0002t0003g0038 a0002c0002t0003g0039 a0002c0002t0003g0040 others(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 | a0002c0005t0006g0107 | 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 | a0002c0006t0003g0041 | 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 | a0002c0002t0015g0275 | 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 | 119 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(116): Show |
123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.7+5291T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2835486 | |||||||
| chrX:2835672 | C | A | 46 | a0001c0001t0001g0139 a0001c0001t0001g0143 a0001c0001t0001g0144 others(43): Show |
47 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(44): 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 | a0001c0001t0001g0135 a0002c0002t0002g0004 a0002c0002t0003g0134 others(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:2835907 | T | A | 2 | a0001c0001t0001g0203 a0001c0001t0004g0202 |
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 | a0001c0001t0001g0057 a0001c0001t0001g0199 a0001c0001t0001g0201 others(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 | a0001c0001t0002g0204 | 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 | a0001c0001t0001g0135 a0002c0002t0002g0004 a0002c0002t0003g0134 others(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 | a0001c0003t0001g0028 a0001c0003t0001g0029 a0001c0003t0005g0013 others(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 | CA | C | 27 | a0001c0001t0001g0135 a0001c0001t0001g0270 a0001c0001t0001g0271 others(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 | 49 | a0001c0001t0001g0077 a0001c0001t0001g0139 a0001c0001t0001g0143 others(46): Show |
50 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(47): 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 | 69 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(66): 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 | 121 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(118): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.8-6461T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2836752 | |||||||
| chrX:2836770 | C | T | 1 | a0001c0001t0004g0005 | 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 | 291 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(288): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): 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 | a0001c0001t0002g0273 a0001c0001t0009g0269 a0001c0001t0009g0274 |
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:2837048 | G | A | 15 | a0001c0003t0001g0028 a0001c0003t0001g0029 a0001c0003t0005g0013 others(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 | a0002c0006t0003g0112 a0002c0006t0005g0111 |
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 | a0002c0005t0006g0107 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.8-5945G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2837268 | |||||||
| chrX:2837553 | G | A | 5 | a0001c0003t0002g0049 a0002c0002t0002g0014 a0002c0002t0006g0050 others(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:2837723 | A | AATTG | 4 | a0001c0001t0007g0193 a0002c0002t0005g0205 a0002c0002t0005g0305 others(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:2837734 | G | A | 1 | a0002c0002t0005g0021 | 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 | a0001c0001t0001g0182 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.8-5462T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2837751 | |||||||
| chrX:2837838 | T | TAC | 15 | a0001c0001t0001g0183 a0001c0001t0002g0127 a0001c0001t0004g0005 others(12): 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 | a0002c0005t0007g0023 a0002c0005t0007g0025 a0006c0008t0006g0024 |
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 | 46 | a0001c0001t0002g0255 a0001c0001t0002g0256 a0001c0001t0004g0071 others(43): 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 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0281 others(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 | a0001c0001t0001g0282 a0001c0003t0001g0028 a0001c0003t0001g0029 others(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 | 103 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0077 others(100): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): 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 | a0001c0001t0001g0018 | 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 | a0002c0006t0003g0041 a0011c0011t0005g0042 |
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 | a0001c0001t0001g0135 a0002c0002t0002g0004 a0002c0002t0003g0012 others(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 | a0002c0006t0003g0041 a0011c0011t0005g0042 |
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 | a0002c0002t0003g0172 a0002c0002t0004g0173 |
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 | T | 153 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0182 others(150): 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 | a0002c0005t0002g0178 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.8-5310G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2837903 | |||||||
| chrX:2838029 | C | CA | 77 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(74): 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 | 41 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0197 others(38): Show |
42 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(39): 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:2838372 | T | C | 119 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(116): Show |
123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): 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 | a0001c0003t0001g0123 a0002c0002t0002g0117 a0002c0002t0002g0121 others(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 | a0001c0001t0002g0081 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.8-4801T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2838412 | |||||||
| chrX:2838452 | C | CCCCTCCC others(14): Show |
2 | a0002c0002t0003g0115 a0002c0002t0005g0114 |
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 |
272 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(269): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): 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 | a0001c0001t0003g0254 | 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 | 58 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(55): 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:2839095 | G | A | 1 | a0002c0002t0002g0148 | 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 | 119 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(116): Show |
123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.8-4021A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2839192 | |||||||
| chrX:2839358 | C | T | 119 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(116): Show |
123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.8-3855C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2839358 | |||||||
| chrX:2839626 | A | G | 21 | a0001c0003t0001g0123 a0001c0003t0002g0049 a0002c0002t0002g0014 others(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 | a0002c0002t0002g0117 a0002c0002t0003g0116 |
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 | 274 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(271): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): 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 | a0002c0002t0007g0195 | 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 | 120 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(117): Show |
124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): 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 | a0002c0002t0002g0004 | 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 | 154 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0182 others(151): 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:2839874 | C | T | 11 | a0001c0001t0001g0135 a0002c0002t0002g0004 a0002c0002t0003g0012 others(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 | a0002c0002t0003g0303 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.8-3338G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2839875 | |||||||
| chrX:2839934 | A | T | 1 | a0001c0001t0002g0187 | 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 | a0002c0002t0004g0026 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.8-3250A>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2839963 | |||||||
| chrX:2840230 | C | T | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
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:2840446 | C | T | 12 | a0001c0003t0001g0028 a0001c0003t0001g0029 a0001c0003t0005g0013 others(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:2840502 | G | C | 1 | a0001c0001t0002g0208 | 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 | a0001c0001t0009g0269 | 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:2840650 | A | G | 2 | a0002c0002t0003g0038 a0002c0002t0003g0039 |
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 | a0001c0001t0001g0135 a0002c0002t0002g0004 a0002c0002t0003g0134 others(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 | a0002c0002t0003g0012 a0002c0002t0004g0026 |
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:2841004 | TATAG | T | 227 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(224): 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 | a0001c0001t0001g0282 | 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 | a0001c0001t0003g0105 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.8-2006G>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2841207 | |||||||
| chrX:2841364 | TGATA | T | 160 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0104 others(157): 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:2841415 | A | AATGG | 6 | a0001c0001t0001g0135 a0002c0002t0003g0134 a0002c0002t0005g0021 others(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 | 121 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(118): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.8-1639C>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2841574 | |||||||
| chrX:2841656 | C | G | 1 | a0002c0002t0003g0040 | 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 | a0002c0006t0005g0111 | 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 | 119 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(116): Show |
123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): 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 | a0002c0002t0003g0040 | 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 | 151 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0182 others(148): 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 | a0002c0002t0005g0128 a0006c0008t0006g0020 a0006c0008t0006g0129 |
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 | 119 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(116): Show |
123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): 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 | a0001c0001t0001g0135 a0002c0002t0002g0004 a0002c0002t0003g0134 others(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 | AT | A | 45 | a0001c0001t0001g0139 a0001c0001t0001g0143 a0001c0001t0001g0144 others(42): Show |
46 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(43): 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 | a0001c0003t0002g0046 a0001c0003t0004g0047 |
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:2842449 | G | A | 73 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(70): 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 | 120 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(117): Show |
124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): 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 | a0001c0003t0005g0179 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.8-660C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2842553 | |||||||
| chrX:2842743 | GTGTTT | G | 155 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0182 others(152): 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 | 125 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0182 others(122): 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 | a0001c0001t0001g0186 a0001c0001t0001g0251 a0001c0001t0002g0187 others(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:2842935 | T | G | 119 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(116): Show |
123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.8-278T>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2842935 | |||||||
| chrX:2843009 | C | T | 45 | a0001c0001t0001g0139 a0001c0001t0001g0143 a0001c0001t0001g0144 others(42): Show |
46 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(43): 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 | a0002c0002t0005g0137 | 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 | a0001c0001t0004g0250 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.8-66C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 2/10 | chrX | 2843147 | |||||||
| chrX:2843371 | C | T | 11 | a0001c0001t0001g0135 a0002c0002t0002g0004 a0002c0002t0003g0012 others(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 | a0001c0003t0001g0123 a0001c0003t0002g0049 a0002c0002t0002g0014 others(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:2843500 | C | T | 4 | a0002c0005t0006g0107 a0002c0005t0007g0023 a0002c0005t0007g0025 others(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:2843683 | A | G | 138 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(135): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.149+329A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2843683 | |||||||
| chrX:2843760 | G | C | 1 | a0001c0001t0003g0254 | 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 | a0003c0007t0006g0036 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.149+412A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2843766 | |||||||
| chrX:2843790 | C | T | 1 | a0008c0015t0001g0102 | 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 | 120 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(117): Show |
124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): 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 | a0002c0002t0003g0040 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.149+533C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2843887 | |||||||
| chrX:2843997 | A | G | 1 | a0001c0001t0001g0211 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.149+643A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2843997 | |||||||
| chrX:2844102 | A | G | 1 | a0006c0008t0006g0129 | 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 | 119 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(116): Show |
123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): 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 | a0001c0001t0004g0071 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.149+867C>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844221 | |||||||
| chrX:2844303 | A | G | 1 | a0002c0005t0002g0178 | 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 | a0002c0002t0005g0305 | 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 | 58 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(55): 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 | a0002c0005t0006g0107 a0002c0005t0007g0023 a0002c0005t0007g0025 others(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 | a0001c0001t0003g0185 | 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 | a0001c0001t0004g0132 a0001c0001t0004g0176 |
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 | a0001c0001t0001g0210 | 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 | 10 | a0001c0001t0002g0194 a0001c0001t0004g0005 a0001c0001t0004g0131 others(7): 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 | a0002c0002t0004g0272 | 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 | a0001c0001t0003g0213 a0002c0002t0003g0212 a0002c0002t0005g0305 |
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 | a0001c0004t0001g0106 a0002c0002t0003g0038 a0002c0002t0003g0039 others(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 | a0002c0006t0002g0113 a0002c0006t0003g0112 a0002c0006t0005g0111 |
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 | 71 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(68): 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 | a0002c0005t0006g0107 | 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 | a0011c0011t0005g0042 | 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 | a0002c0006t0003g0041 | 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 | a0002c0002t0003g0040 | 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 | a0002c0002t0005g0205 | 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 | 4 | a0001c0001t0004g0005 a0001c0001t0004g0131 a0001c0001t0004g0133 others(1): 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 | a0001c0001t0002g0101 | 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 | 6 | a0001c0001t0001g0241 a0001c0001t0004g0005 a0001c0001t0004g0131 others(3): 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 | 48 | a0001c0001t0001g0135 a0001c0001t0001g0139 a0001c0001t0001g0143 others(45): Show |
49 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(46): 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 | a0002c0005t0007g0023 a0002c0005t0007g0025 a0006c0008t0006g0024 |
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 | a0002c0002t0005g0180 a0002c0002t0006g0022 |
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 | a0001c0001t0009g0269 a0002c0002t0001g0125 a0002c0002t0001g0126 others(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 | a0001c0001t0001g0268 a0001c0001t0001g0281 a0005c0010t0003g0189 |
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 | a0001c0001t0001g0267 | 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 | a0002c0002t0005g0128 | 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 | a0001c0001t0004g0131 a0001c0001t0004g0133 |
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 | a0002c0002t0003g0040 | 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 | a0002c0002t0004g0026 | 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 | a0002c0002t0003g0012 | 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 | a0001c0001t0001g0215 a0001c0001t0001g0270 a0001c0001t0003g0218 others(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 | a0001c0001t0002g0127 | 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 | a0002c0002t0005g0021 a0002c0002t0006g0136 |
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 | a0002c0002t0006g0022 | 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 | a0002c0002t0005g0180 | 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 | a0001c0001t0001g0135 a0002c0002t0002g0004 a0002c0002t0003g0012 others(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 | a0002c0002t0003g0134 | 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 | 4 | a0001c0001t0004g0005 a0001c0001t0004g0131 a0001c0001t0004g0133 others(1): 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 | 40 | a0001c0001t0001g0139 a0001c0001t0001g0143 a0001c0001t0001g0144 others(37): Show |
40 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(37): 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 | a0001c0004t0001g0106 a0002c0002t0005g0055 a0002c0002t0006g0056 others(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:2844554 | A | G | 6 | a0001c0001t0001g0241 a0001c0001t0004g0005 a0001c0001t0004g0131 others(3): 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 | 40 | a0001c0001t0001g0139 a0001c0001t0001g0143 a0001c0001t0001g0144 others(37): Show |
40 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.149+1201T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844555 | |||||||
| chrX:2844558 | G | GTA | 3 | a0001c0001t0001g0282 a0001c0001t0004g0005 a0001c0003t0005g0179 |
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 | a0002c0002t0003g0134 a0002c0002t0005g0021 a0002c0002t0006g0022 others(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 | a0001c0001t0001g0135 | 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 | a0001c0001t0001g0135 a0002c0002t0002g0004 a0002c0002t0003g0012 others(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 | 1 | a0001c0001t0004g0005 | 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 | a0001c0001t0001g0139 a0002c0002t0001g0150 |
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 | a0001c0001t0002g0101 a0001c0004t0001g0106 a0002c0002t0005g0055 others(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 | 5 | a0001c0001t0004g0005 a0001c0001t0004g0131 a0001c0001t0004g0132 others(2): 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 | a0001c0001t0001g0135 a0002c0002t0003g0134 a0002c0002t0006g0022 others(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 | a0001c0001t0001g0135 a0002c0002t0002g0004 a0002c0002t0003g0012 others(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 | 1 | a0001c0001t0004g0005 | 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 | a0002c0006t0002g0113 a0002c0006t0003g0112 a0002c0006t0005g0111 |
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 | 53 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(50): 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 | a0001c0004t0001g0106 a0002c0002t0005g0055 a0002c0002t0006g0056 others(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 | 5 | a0001c0001t0004g0005 a0001c0001t0004g0131 a0001c0001t0004g0132 others(2): 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 | a0002c0006t0002g0113 a0002c0006t0003g0112 a0002c0006t0005g0111 |
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 | a0002c0002t0003g0038 a0002c0002t0003g0039 |
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 | a0001c0001t0001g0135 a0002c0002t0003g0134 a0002c0002t0006g0022 |
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 | a0001c0001t0001g0135 a0002c0002t0002g0004 a0002c0002t0003g0012 others(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 | 40 | a0001c0001t0001g0139 a0001c0001t0001g0143 a0001c0001t0001g0144 others(37): Show |
40 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.149+1268A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844622 | |||||||
| chrX:2844628 | A | G | 1 | a0001c0001t0004g0005 | 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 | 59 | a0001c0001t0001g0139 a0001c0001t0001g0143 a0001c0001t0001g0144 others(56): Show |
60 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(57): 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 | a0002c0005t0007g0023 a0002c0005t0007g0025 a0006c0008t0006g0024 |
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 | 55 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(52): 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 | 5 | a0001c0001t0004g0005 a0001c0001t0004g0131 a0001c0001t0004g0132 others(2): 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 | 18 | a0001c0003t0001g0028 a0001c0003t0001g0029 a0001c0003t0002g0046 others(15): 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 | a0003c0007t0006g0036 | 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 | a0001c0001t0001g0135 a0002c0002t0003g0134 a0002c0002t0006g0022 |
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 | a0001c0001t0001g0135 a0002c0002t0002g0004 a0002c0002t0003g0012 others(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 | 41 | a0001c0001t0001g0139 a0001c0001t0001g0143 a0001c0001t0001g0144 others(38): Show |
41 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(38): 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 | 1 | a0001c0001t0004g0005 | 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:2844657 | CAT | C | 52 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(49): 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 | 5 | a0001c0001t0004g0005 a0001c0001t0004g0131 a0001c0001t0004g0132 others(2): 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 | a0002c0002t0006g0022 | 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 | G | 10 | a0001c0001t0001g0135 a0002c0002t0002g0004 a0002c0002t0003g0012 others(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 | a0002c0002t0005g0137 | 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 | a0001c0004t0001g0106 | 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 | 1 | a0001c0001t0004g0005 | 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 | a0002c0002t0005g0055 a0002c0002t0006g0056 a0008c0015t0001g0102 |
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 | 5 | a0001c0001t0004g0005 a0001c0001t0004g0131 a0001c0001t0004g0132 others(2): 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 | G | 9 | a0001c0001t0001g0135 a0002c0002t0002g0004 a0002c0002t0003g0134 others(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 | a0002c0002t0005g0055 a0002c0002t0006g0056 a0008c0015t0001g0102 |
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 | a0001c0003t0002g0049 a0002c0002t0005g0114 |
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 | 6 | a0001c0003t0002g0046 a0001c0003t0004g0047 a0002c0002t0002g0006 others(3): 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 | a0010c0014t0005g0233 | 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 | 1 | a0001c0001t0004g0005 | 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 | 74 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(71): 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 | a0010c0014t0005g0233 | 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 | 5 | a0001c0001t0004g0005 a0001c0001t0004g0131 a0001c0001t0004g0132 others(2): 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 | a0010c0014t0005g0233 | 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 | 61 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(58): 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 | a0001c0001t0001g0135 a0002c0002t0003g0134 a0002c0002t0005g0021 others(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 | a0001c0003t0001g0028 a0001c0003t0001g0029 a0001c0003t0005g0013 others(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 | a0002c0002t0002g0004 | 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 | a0001c0003t0001g0123 a0002c0002t0002g0014 a0002c0002t0002g0117 others(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 | 119 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(116): Show |
123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): 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 | a0001c0001t0001g0271 a0001c0013t0003g0240 |
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 | 1 | a0001c0001t0004g0005 | 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 | 123 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(120): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.149+1381C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2844735 | |||||||
| chrX:2844736 | A | G | 5 | a0001c0001t0004g0005 a0001c0001t0004g0131 a0001c0001t0004g0132 others(2): 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 | a0001c0001t0001g0135 a0002c0002t0003g0012 a0002c0002t0003g0134 others(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 | a0002c0002t0005g0180 a0002c0006t0003g0041 a0011c0011t0005g0042 |
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 | a0002c0002t0002g0043 a0002c0002t0002g0044 a0002c0005t0003g0045 |
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 | a0002c0002t0003g0040 | 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 | a0001c0001t0001g0282 | 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 | a0001c0001t0003g0016 | 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 | a0001c0001t0001g0057 a0001c0001t0001g0182 a0001c0001t0001g0199 others(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 |
71 | a0001c0001t0001g0008 a0001c0001t0001g0183 a0001c0001t0001g0203 others(68): 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 | 166 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(163): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): 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 | a0001c0001t0001g0135 a0002c0002t0002g0004 a0002c0002t0003g0012 others(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 | a0001c0001t0001g0135 a0002c0002t0002g0004 a0002c0002t0002g0072 others(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 | a0002c0002t0003g0038 a0002c0002t0003g0039 a0002c0002t0003g0040 |
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 | a0002c0005t0006g0107 a0002c0005t0007g0023 a0002c0005t0007g0025 others(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:2844783 | CAT | C | 279 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(276): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): 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 | a0002c0005t0006g0107 a0002c0005t0007g0023 a0002c0005t0007g0025 others(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 | 3 | a0002c0002t0002g0006 a0002c0002t0002g0148 a0002c0002t0002g0149 |
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 | 116 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(113): Show |
119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): 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 | 3 | a0002c0002t0002g0006 a0002c0002t0002g0148 a0002c0002t0002g0149 |
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 | a0002c0002t0001g0009 | 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 | a0001c0001t0003g0213 | 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 | a0001c0001t0003g0213 | 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 | a0001c0003t0001g0028 a0001c0003t0001g0029 a0001c0003t0005g0013 others(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 | a0002c0002t0003g0038 a0002c0002t0003g0039 a0002c0002t0003g0040 |
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:2844928 | A | G | 15 | a0001c0003t0001g0028 a0001c0003t0001g0029 a0001c0003t0005g0013 others(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 | 46 | a0001c0001t0001g0139 a0001c0001t0001g0143 a0001c0001t0001g0144 others(43): Show |
47 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(44): 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 | a0002c0002t0002g0298 | 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 | a0001c0001t0001g0100 | 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 | a0001c0001t0002g0194 | 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 | a0002c0002t0002g0117 a0002c0002t0005g0122 |
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 | a0001c0001t0001g0289 | 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 | a0001c0001t0002g0297 a0001c0004t0013g0291 |
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 | a0001c0001t0001g0077 a0001c0001t0001g0093 a0001c0004t0001g0106 |
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 | a0001c0001t0001g0284 a0001c0001t0010g0092 |
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 | a0001c0001t0002g0090 a0001c0001t0002g0101 a0001c0001t0002g0192 others(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 | a0001c0001t0001g0286 a0001c0001t0001g0288 a0001c0001t0002g0293 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0084 a0001c0001t0002g0081 a0001c0001t0002g0287 others(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 | a0001c0001t0002g0078 a0001c0001t0002g0080 a0001c0001t0002g0103 others(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 | a0001c0001t0002g0086 | 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 | 3 | a0001c0001t0004g0005 a0001c0001t0004g0132 a0001c0001t0004g0176 |
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 | a0001c0001t0004g0131 a0001c0001t0004g0133 |
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 | a0001c0001t0004g0131 a0001c0001t0004g0133 |
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 | a0001c0001t0001g0210 | 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 | a0001c0001t0001g0296 a0002c0002t0005g0055 a0002c0002t0006g0056 |
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:2845039 | A | ATGTGTAT others(37): Show |
1 | a0002c0002t0007g0110 | 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 | a0001c0001t0001g0010 | 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 | a0001c0001t0001g0267 a0001c0003t0001g0028 a0001c0003t0001g0029 others(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 | a0001c0001t0001g0209 a0001c0001t0001g0211 a0001c0001t0001g0281 others(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 | a0001c0001t0001g0268 a0002c0002t0005g0137 |
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 | a0001c0003t0004g0047 | 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 | a0001c0003t0002g0046 | 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 | a0002c0005t0002g0178 | 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 | a0001c0001t0001g0144 a0001c0001t0002g0160 a0002c0002t0004g0154 others(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 | 29 | a0001c0001t0001g0139 a0001c0001t0001g0143 a0001c0001t0001g0197 others(26): Show |
30 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(27): 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 | a0002c0002t0001g0150 a0002c0002t0004g0140 a0002c0002t0004g0166 others(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 | a0002c0002t0003g0012 a0002c0002t0004g0026 a0002c0006t0003g0041 others(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 | a0002c0002t0005g0300 | 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 | a0002c0002t0003g0115 a0002c0002t0005g0120 |
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 | a0002c0002t0002g0121 a0002c0002t0003g0119 |
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 | a0001c0003t0001g0123 a0002c0002t0005g0108 |
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:2845052 | T | C | 7 | a0001c0001t0001g0135 a0002c0002t0002g0004 a0002c0002t0003g0134 others(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 | 155 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0135 others(152): 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 | a0001c0001t0001g0135 a0002c0002t0002g0004 a0002c0002t0003g0134 others(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 | a0001c0001t0004g0176 a0002c0002t0003g0012 a0002c0002t0004g0026 others(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 | a0001c0001t0004g0132 | 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 | a0006c0008t0006g0020 | 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 | a0002c0002t0005g0128 | 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 |
1 | a0001c0001t0004g0005 | 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 | a0001c0001t0001g0135 a0002c0002t0005g0021 a0002c0002t0005g0180 others(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 | 4 | a0001c0001t0004g0005 a0002c0002t0002g0004 a0002c0002t0003g0134 others(1): 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 | a0001c0001t0001g0221 a0001c0001t0001g0243 a0001c0001t0002g0191 others(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 | a0002c0002t0001g0260 | 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 | a0002c0002t0003g0012 a0002c0002t0004g0026 a0002c0006t0003g0041 others(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 | a0002c0002t0003g0134 a0002c0002t0006g0022 |
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 | a0002c0002t0002g0004 | 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 | 169 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0135 others(166): 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 | a0002c0002t0003g0012 a0002c0002t0004g0026 a0002c0006t0003g0041 others(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 | a0001c0001t0002g0277 a0001c0001t0004g0176 a0001c0003t0002g0049 others(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 | a0002c0002t0003g0116 | 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 | a0001c0001t0007g0193 | 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 | a0002c0002t0003g0040 | 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 | a0001c0001t0001g0135 a0002c0002t0005g0180 |
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 | a0001c0001t0009g0269 a0001c0001t0009g0274 |
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 | a0002c0002t0003g0012 a0002c0002t0004g0026 a0002c0006t0003g0041 others(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 | a0001c0001t0001g0135 a0001c0001t0009g0269 a0001c0001t0009g0274 others(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 | a0001c0001t0001g0135 a0002c0002t0005g0021 a0002c0002t0005g0180 others(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 | 164 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0135 others(161): 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:2845119 | A | ACATACAC others(9): Show |
2 | a0002c0002t0005g0021 a0002c0002t0006g0136 |
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 | a0002c0002t0003g0012 a0002c0002t0004g0026 a0002c0006t0003g0041 others(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 | a0002c0002t0005g0021 a0002c0002t0006g0136 |
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 | a0002c0002t0005g0021 a0002c0002t0006g0136 |
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 | a0002c0002t0003g0012 a0002c0002t0004g0026 a0002c0006t0003g0041 others(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 | a0002c0002t0003g0012 a0002c0002t0004g0026 a0002c0006t0003g0041 others(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:2845131 | G | A | 163 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0135 others(160): 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 | a0001c0001t0004g0132 a0002c0005t0006g0107 a0002c0005t0007g0023 others(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 | a0001c0001t0003g0185 | 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 | 163 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0135 others(160): 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 | 161 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0135 others(158): 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 | a0002c0006t0003g0041 a0011c0011t0005g0042 |
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 | a0002c0002t0003g0012 a0002c0002t0004g0026 |
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 | a0002c0005t0006g0107 a0002c0005t0007g0023 a0002c0005t0007g0025 others(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:2845203 | G | A | 155 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0135 others(152): 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 | a0002c0005t0006g0107 a0002c0005t0007g0023 a0002c0005t0007g0025 others(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:2845220 | T | C | 4 | a0002c0005t0006g0107 a0002c0005t0007g0023 a0002c0005t0007g0025 others(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:2845227 | G | A | 155 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0135 others(152): 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:2845244 | T | C | 1 | a0002c0002t0002g0004 | 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 | a0001c0001t0003g0227 a0001c0001t0004g0226 a0002c0002t0003g0038 others(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:2845251 | G | A | 151 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0135 others(148): 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 | a0005c0010t0003g0206 | 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 | a0002c0005t0006g0107 a0002c0005t0007g0023 a0002c0005t0007g0025 others(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 | a0002c0005t0006g0107 a0002c0005t0007g0023 a0002c0005t0007g0025 others(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 | a0002c0002t0003g0038 a0002c0002t0003g0039 |
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 | 22 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0222 others(19): 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 | a0002c0002t0003g0134 a0002c0002t0005g0180 a0002c0002t0006g0022 |
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:2845275 | G | A | 133 | a0001c0001t0001g0135 a0001c0001t0001g0182 a0001c0001t0001g0183 others(130): 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 | a0005c0010t0003g0206 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0222 a0002c0002t0003g0212 |
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 | 42 | a0001c0001t0001g0057 a0001c0001t0001g0199 a0001c0001t0001g0201 others(39): 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 | a0001c0001t0001g0135 a0002c0002t0005g0021 a0002c0002t0005g0180 others(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 | 112 | a0001c0001t0001g0135 a0001c0001t0001g0182 a0001c0001t0001g0183 others(109): 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 | a0002c0002t0003g0134 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.149+1955A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845309 | |||||||
| chrX:2845320 | CACGTGTG others(39): Show |
C | 5 | a0001c0001t0001g0219 a0001c0001t0001g0236 a0001c0001t0002g0062 others(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 | a0001c0001t0001g0057 | 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 | 67 | a0001c0001t0001g0183 a0001c0001t0001g0199 a0001c0001t0001g0201 others(64): 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 | a0001c0001t0001g0135 a0002c0002t0002g0004 a0002c0002t0005g0021 others(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 | 84 | a0001c0001t0001g0135 a0001c0001t0001g0182 a0001c0001t0001g0186 others(81): 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 | a0002c0002t0005g0180 a0002c0002t0006g0022 a0002c0006t0003g0041 others(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 | a0002c0002t0005g0180 a0002c0002t0006g0022 a0002c0006t0003g0041 others(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 | a0001c0001t0014g0051 a0002c0002t0002g0249 |
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 | a0001c0001t0003g0276 | 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 | 85 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0199 others(82): 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 | a0002c0002t0002g0004 a0002c0002t0006g0136 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0222 a0002c0002t0003g0212 |
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 | a0001c0001t0001g0135 a0001c0001t0001g0186 a0001c0001t0001g0203 others(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 | a0001c0001t0001g0135 a0002c0002t0003g0134 a0002c0002t0005g0021 |
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 | a0001c0001t0001g0135 a0002c0002t0003g0134 a0002c0002t0005g0021 |
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 | a0002c0002t0012g0069 a0002c0002t0012g0070 |
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 | a0001c0001t0003g0254 a0002c0002t0001g0011 |
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 | a0001c0001t0001g0238 a0001c0001t0003g0198 a0001c0001t0008g0068 others(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 | 96 | a0001c0001t0001g0008 a0001c0001t0001g0182 a0001c0001t0001g0183 others(93): 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 | a0001c0001t0001g0219 a0001c0001t0001g0236 a0001c0001t0002g0062 others(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 | a0001c0001t0001g0135 a0001c0001t0001g0203 a0001c0001t0001g0232 others(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 | a0002c0002t0002g0004 a0002c0002t0005g0180 a0002c0002t0006g0022 others(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 | a0006c0008t0006g0129 | 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 | a0002c0002t0002g0004 a0002c0002t0005g0180 a0002c0002t0006g0022 others(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 | a0001c0001t0001g0229 a0001c0001t0001g0251 |
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 | a0001c0001t0003g0218 | 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 | 108 | a0001c0001t0001g0008 a0001c0001t0001g0182 a0001c0001t0001g0183 others(105): 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 | a0001c0001t0001g0057 a0001c0001t0014g0051 a0002c0002t0002g0249 others(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 | a0001c0001t0001g0135 a0001c0001t0002g0194 a0001c0001t0007g0193 others(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 | a0001c0001t0001g0135 a0002c0002t0003g0134 a0002c0002t0005g0021 others(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 | ATT | A | 6 | a0001c0001t0001g0135 a0002c0002t0003g0134 a0002c0002t0005g0021 others(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 | a0002c0002t0006g0056 | 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 | 113 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0182 others(110): 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 | a0001c0001t0003g0254 a0001c0001t0003g0276 a0002c0002t0001g0011 |
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 | a0001c0001t0001g0135 a0001c0001t0001g0144 a0001c0001t0002g0160 others(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 | a0002c0002t0002g0004 a0002c0002t0003g0012 a0002c0002t0004g0026 others(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 | a0002c0002t0002g0004 a0002c0002t0003g0012 a0002c0002t0004g0026 others(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 | 119 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0182 others(116): 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 | a0001c0001t0001g0229 a0001c0001t0001g0238 a0001c0001t0001g0251 others(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 | 73 | a0001c0001t0001g0135 a0001c0001t0001g0139 a0001c0001t0001g0143 others(70): Show |
75 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.149+2089G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845443 | |||||||
| chrX:2845453 | A | G | 3 | a0001c0001t0001g0135 a0002c0002t0003g0134 a0002c0002t0005g0021 |
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 | a0002c0002t0005g0305 | 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 | a0002c0002t0002g0121 | 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 | a0002c0006t0003g0041 a0011c0011t0005g0042 |
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 | a0001c0001t0001g0135 a0002c0002t0003g0134 a0002c0002t0005g0021 others(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 | a0002c0006t0003g0041 a0011c0011t0005g0042 |
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 | a0002c0005t0007g0023 a0002c0005t0007g0025 a0006c0008t0006g0024 |
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 | a0002c0002t0005g0055 | 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 | a0002c0005t0007g0023 a0002c0005t0007g0025 a0002c0006t0002g0113 others(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 | a0001c0001t0001g0241 | 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 | a0001c0001t0001g0211 a0001c0001t0001g0219 a0001c0001t0002g0246 |
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 | 126 | a0001c0001t0001g0057 a0001c0001t0001g0182 a0001c0001t0001g0183 others(123): 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 | a0001c0001t0003g0218 a0002c0005t0007g0023 a0002c0005t0007g0025 others(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 | 71 | a0001c0001t0001g0008 a0001c0001t0001g0135 a0001c0001t0001g0139 others(68): Show |
74 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(71): 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 | a0002c0006t0003g0041 a0011c0011t0005g0042 |
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:2845473 | ATGTATAT others(97): Show |
A | 1 | a0001c0001t0004g0176 | 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 | a0002c0002t0002g0004 a0002c0002t0003g0012 a0002c0002t0004g0026 others(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 | a0001c0003t0002g0049 a0002c0005t0007g0023 a0002c0005t0007g0025 others(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 | a0002c0002t0002g0121 a0002c0002t0003g0119 |
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 | a0001c0001t0001g0008 | 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 | a0001c0003t0007g0034 a0002c0002t0002g0004 a0002c0002t0003g0012 others(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 | a0001c0001t0001g0008 | 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:2845486 | T | C | 3 | a0001c0003t0007g0034 a0002c0005t0006g0107 a0002c0006t0002g0113 |
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 | 31 | a0001c0001t0001g0182 a0001c0001t0001g0186 a0001c0001t0001g0201 others(28): 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 | 95 | a0001c0001t0001g0057 a0001c0001t0001g0183 a0001c0001t0001g0199 others(92): 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 | a0001c0001t0001g0241 a0001c0003t0007g0034 a0002c0005t0006g0107 others(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 | 72 | a0001c0001t0001g0135 a0001c0001t0001g0139 a0001c0001t0001g0143 others(69): Show |
74 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(71): 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 | a0001c0001t0001g0008 | 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:2845499 | G | A | 2 | a0002c0006t0003g0041 a0011c0011t0005g0042 |
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 | a0001c0001t0001g0135 a0002c0002t0003g0134 a0002c0002t0005g0021 |
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 | a0001c0001t0002g0101 a0002c0006t0003g0112 a0002c0006t0005g0111 |
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 | a0001c0001t0002g0127 a0001c0003t0007g0034 a0002c0002t0006g0050 others(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 | G | 2 | a0002c0002t0002g0257 a0004c0009t0001g0065 |
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 | a0001c0001t0001g0135 a0001c0003t0005g0013 a0001c0003t0008g0033 others(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 | a0002c0002t0002g0257 a0004c0009t0001g0065 |
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 | a0002c0006t0003g0041 a0011c0011t0005g0042 |
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 | a0001c0003t0005g0013 a0001c0003t0008g0033 a0003c0007t0001g0032 others(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 | a0001c0001t0001g0209 | 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 | 93 | a0001c0001t0001g0183 a0001c0001t0001g0199 a0001c0001t0001g0203 others(90): 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 | 40 | a0001c0001t0001g0182 a0001c0001t0001g0186 a0001c0001t0001g0201 others(37): 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 | 68 | a0001c0001t0001g0057 a0001c0001t0001g0135 a0001c0001t0001g0139 others(65): Show |
70 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(67): 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 | a0001c0001t0002g0101 a0002c0002t0002g0257 a0004c0009t0001g0065 |
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:2845521 | A | ATATTTAT others(11): Show |
1 | a0001c0001t0007g0216 | 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 | a0001c0001t0001g0057 | 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 | a0002c0006t0003g0041 a0011c0011t0005g0042 |
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 | a0002c0002t0006g0022 a0002c0002t0006g0136 |
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 | a0001c0003t0005g0013 a0001c0003t0008g0033 a0002c0002t0001g0125 others(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 | ATT | A | 8 | a0001c0003t0001g0029 a0001c0003t0005g0027 a0002c0002t0001g0037 others(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 | a0002c0002t0006g0022 | 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 | a0002c0006t0003g0041 a0011c0011t0005g0042 |
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 | a0001c0003t0001g0029 a0001c0003t0005g0027 a0002c0002t0001g0037 others(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 | 52 | a0001c0001t0001g0183 a0001c0001t0001g0203 a0001c0001t0001g0210 others(49): 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 | a0001c0003t0001g0029 a0001c0003t0005g0027 a0002c0002t0001g0037 others(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 | 142 | a0001c0001t0001g0008 a0001c0001t0001g0135 a0001c0001t0001g0139 others(139): Show |
146 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(143): 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 | a0001c0001t0007g0193 | 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 | 130 | a0001c0001t0001g0139 a0001c0001t0001g0143 a0001c0001t0001g0144 others(127): Show |
133 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(130): 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 | a0001c0001t0001g0008 a0001c0001t0002g0101 a0002c0002t0002g0257 others(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 | a0001c0001t0001g0135 | 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 | 60 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0077 others(57): 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 | a0001c0003t0001g0028 a0002c0006t0003g0112 a0002c0006t0005g0111 |
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 | a0002c0002t0002g0004 a0002c0002t0003g0134 a0002c0002t0005g0180 others(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 | a0001c0001t0001g0135 | 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 | 130 | a0001c0001t0001g0139 a0001c0001t0001g0143 a0001c0001t0001g0144 others(127): Show |
133 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.149+2197A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845551 | |||||||
| chrX:2845553 | T | A | 139 | a0001c0001t0001g0135 a0001c0001t0001g0139 a0001c0001t0001g0143 others(136): Show |
143 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(140): 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 | a0002c0002t0006g0136 | 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 | a0001c0001t0001g0210 a0001c0001t0001g0215 a0001c0001t0001g0221 others(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 | a0002c0002t0005g0021 | 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 | a0002c0002t0017g0258 | 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 |
14 | a0001c0001t0001g0183 a0001c0001t0001g0220 a0001c0001t0002g0204 others(11): 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 | a0001c0001t0001g0203 a0001c0001t0002g0255 a0001c0001t0002g0256 others(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 | a0001c0001t0003g0237 | 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 | a0001c0001t0003g0227 | 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 | a0001c0001t0001g0232 | 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 | a0001c0001t0001g0209 | 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 | a0001c0001t0002g0101 a0001c0001t0002g0194 a0002c0002t0005g0137 |
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 | a0001c0001t0004g0131 a0001c0001t0004g0133 |
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 | 286 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0018 others(283): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): 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 | a0001c0001t0001g0010 | 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 | a0002c0002t0005g0300 | 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 | a0001c0001t0002g0194 | 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 | a0002c0005t0002g0124 | 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 | a0001c0001t0002g0101 | 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 | a0001c0001t0002g0101 | 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 | a0001c0001t0002g0101 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.149+2218C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845572 | |||||||
| chrX:2845577 | G | A | 1 | a0001c0001t0002g0101 | 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 | a0001c0001t0002g0101 | 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 | a0002c0002t0003g0038 a0002c0002t0003g0039 a0002c0002t0003g0040 |
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 | a0001c0001t0002g0101 | 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 | a0001c0001t0002g0194 a0001c0001t0007g0193 |
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 | a0001c0001t0002g0101 | 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 | 118 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(115): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): 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 | a0001c0001t0002g0101 | 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 | a0001c0001t0002g0101 | 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 | a0001c0001t0002g0101 | 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 | 135 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0182 others(132): 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:2845758 | T | C | 3 | a0002c0002t0005g0128 a0006c0008t0006g0020 a0006c0008t0006g0129 |
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 | a0001c0001t0003g0185 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.149+2435A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2845789 | |||||||
| chrX:2845950 | A | G | 1 | a0002c0002t0015g0275 | 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 | a0002c0005t0006g0107 a0002c0005t0007g0023 a0002c0005t0007g0025 others(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 | a0002c0002t0003g0038 a0002c0002t0003g0039 |
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 | a0001c0001t0003g0185 a0002c0005t0006g0107 a0002c0005t0007g0023 others(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 | 76 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(73): 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 | a0002c0006t0003g0041 | 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 | a0011c0011t0005g0042 | 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:2846035 | A | G | 2 | a0002c0005t0007g0025 a0006c0008t0006g0024 |
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 | CAT | 3 | a0002c0002t0002g0257 a0002c0002t0012g0069 a0002c0002t0012g0070 |
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 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0236 others(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 | a0001c0001t0001g0199 a0001c0001t0001g0209 a0001c0001t0001g0210 others(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 |
14 | a0001c0001t0001g0182 a0001c0001t0001g0186 a0001c0001t0001g0221 others(11): 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 | a0001c0001t0001g0217 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0003g0185 others(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 | a0002c0002t0003g0012 | 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 | a0001c0001t0001g0215 a0005c0010t0003g0206 |
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 | a0002c0005t0007g0023 | 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 | a0002c0005t0007g0025 a0006c0008t0006g0024 |
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:2846049 | ATATATAT others(6): Show |
A | 1 | a0002c0002t0008g0248 | 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 | a0001c0001t0001g0135 a0002c0002t0003g0134 a0002c0002t0004g0026 others(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 | 27 | a0001c0001t0001g0139 a0001c0001t0001g0143 a0001c0001t0001g0144 others(24): Show |
27 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(24): 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 | a0001c0004t0004g0091 a0002c0002t0004g0173 |
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 | a0002c0002t0002g0004 a0002c0002t0005g0180 |
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 | 5 | a0001c0003t0002g0046 a0001c0003t0004g0047 a0002c0002t0002g0006 others(2): 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 | a0001c0001t0001g0077 a0001c0001t0001g0197 a0001c0001t0001g0302 others(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 | a0001c0001t0002g0297 | 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 | a0001c0001t0002g0292 | 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 | ATATACAC others(42): Show |
1 | a0002c0002t0004g0026 | 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 | ATATATAT others(6): Show |
1 | a0001c0001t0004g0015 | 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 | a0001c0001t0001g0241 | 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 | T | 4 | a0002c0002t0002g0043 a0002c0002t0002g0044 a0002c0002t0003g0012 others(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 | ATT | A | 6 | a0001c0001t0002g0194 a0001c0001t0004g0005 a0001c0001t0004g0071 others(3): 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 | a0001c0003t0001g0028 | 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 | a0001c0003t0001g0029 a0001c0003t0005g0013 a0001c0003t0005g0027 others(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 | 6 | a0001c0001t0001g0084 a0001c0001t0002g0101 a0001c0001t0004g0082 others(3): 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 | a0001c0001t0001g0093 a0002c0005t0002g0178 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(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 | a0001c0003t0001g0123 a0002c0002t0002g0117 a0002c0002t0002g0121 others(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 | 14 | a0001c0001t0001g0057 a0002c0002t0001g0009 a0002c0002t0001g0188 others(11): 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 | a0001c0001t0001g0135 a0002c0002t0003g0134 a0002c0002t0005g0021 others(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 | a0001c0001t0001g0183 a0001c0001t0001g0201 a0001c0001t0001g0245 others(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 | a0002c0002t0002g0004 a0002c0002t0005g0180 |
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 | a0001c0001t0001g0203 a0001c0001t0001g0238 a0001c0001t0001g0243 others(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 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0002g0061 others(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 | a0001c0001t0008g0068 a0002c0005t0006g0107 |
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 | a0001c0001t0002g0184 a0001c0001t0002g0246 |
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 | a0001c0001t0003g0247 | 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 | 81 | a0001c0001t0001g0008 a0001c0001t0001g0182 a0001c0001t0001g0186 others(78): 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 | 58 | a0001c0001t0001g0057 a0001c0001t0001g0135 a0001c0001t0001g0183 others(55): 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 | 62 | a0001c0001t0001g0008 a0001c0001t0001g0182 a0001c0001t0001g0186 others(59): 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 | a0001c0001t0001g0057 a0001c0001t0001g0135 a0001c0001t0001g0201 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0199 a0001c0001t0001g0215 others(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 | a0001c0001t0001g0135 a0001c0001t0001g0201 a0001c0001t0001g0268 others(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 | a0001c0001t0001g0215 a0001c0001t0003g0276 a0002c0002t0004g0214 others(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 | a0001c0001t0001g0135 a0002c0002t0002g0004 a0002c0002t0003g0134 others(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 | a0002c0002t0002g0004 a0002c0002t0003g0134 a0002c0002t0005g0021 others(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 | a0001c0003t0001g0028 a0002c0002t0002g0004 a0002c0002t0006g0136 |
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 | a0001c0003t0001g0028 a0001c0003t0001g0029 a0001c0003t0005g0013 others(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 | 5 | a0001c0001t0002g0101 a0001c0001t0004g0082 a0002c0002t0004g0002 others(2): 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 | a0001c0003t0001g0028 a0001c0003t0001g0029 a0001c0003t0005g0013 others(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 | a0002c0002t0001g0037 | 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 | 59 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(56): 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 | a0002c0002t0002g0151 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.149+2776G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846130 | |||||||
| chrX:2846206 | A | T | 1 | a0001c0001t0002g0277 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.149+2852A>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846206 | |||||||
| chrX:2846330 | G | C | 1 | a0001c0001t0001g0284 | 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 | a0001c0001t0001g0135 a0002c0002t0002g0004 a0002c0002t0003g0012 others(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 | a0002c0002t0017g0258 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.149+3218T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846572 | |||||||
| chrX:2846610 | T | A | 1 | a0001c0001t0003g0185 | 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 | 137 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(134): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.149+3281G>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846635 | |||||||
| chrX:2846813 | TAGAA | T | 49 | a0001c0001t0001g0139 a0001c0001t0001g0143 a0001c0001t0001g0144 others(46): Show |
51 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(48): 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 | 135 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(132): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.149+3493A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2846847 | |||||||
| chrX:2847182 | T | G | 4 | a0002c0005t0006g0107 a0002c0005t0007g0023 a0002c0005t0007g0025 others(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:2847223 | C | G | 4 | a0002c0005t0006g0107 a0002c0005t0007g0023 a0002c0005t0007g0025 others(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 | 138 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(135): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.149+3924A>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2847278 | |||||||
| chrX:2847321 | A | G | 78 | a0001c0001t0001g0135 a0001c0001t0001g0139 a0001c0001t0001g0143 others(75): Show |
81 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.149+3967A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2847321 | |||||||
| chrX:2847329 | A | T | 138 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(135): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): 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 | a0001c0003t0001g0028 a0001c0003t0001g0029 a0001c0003t0005g0013 others(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 | a0001c0001t0001g0135 a0002c0002t0002g0004 a0002c0002t0003g0012 others(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 | 49 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(46): Show |
51 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(48): 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 | a0001c0001t0001g0084 a0001c0001t0001g0210 a0001c0001t0002g0078 others(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 | 125 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0182 others(122): 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 | a0001c0001t0003g0247 a0001c0001t0007g0216 a0001c0003t0001g0029 others(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 | a0001c0003t0001g0028 a0001c0003t0005g0013 a0001c0003t0005g0027 others(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 | a0001c0001t0001g0135 a0002c0002t0002g0004 a0002c0002t0003g0012 others(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 | a0001c0001t0001g0135 a0002c0002t0002g0004 a0002c0002t0003g0012 others(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 | 95 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0182 others(92): 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 | a0001c0003t0005g0179 a0002c0002t0002g0043 a0002c0002t0002g0044 others(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 | AAAATAAA others(1): Show |
A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(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 | a0001c0003t0001g0123 a0001c0003t0002g0049 a0002c0002t0001g0260 others(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 | a0001c0001t0001g0135 a0002c0002t0002g0004 a0002c0002t0003g0012 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(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 | a0002c0002t0004g0175 | 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 | 43 | a0001c0001t0001g0139 a0001c0001t0001g0143 a0001c0001t0001g0144 others(40): Show |
45 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.149+4379A>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2847733 | |||||||
| chrX:2847784 | T | C | 3 | a0001c0003t0002g0046 a0001c0003t0004g0047 a0002c0005t0002g0178 |
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 | a0001c0001t0007g0216 | 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 | a0001c0001t0001g0135 a0001c0003t0001g0028 a0001c0003t0001g0029 others(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 | a0009c0012t0001g0141 | 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 | a0002c0005t0007g0023 a0002c0005t0007g0025 a0006c0008t0006g0024 |
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 | a0002c0005t0006g0107 a0002c0005t0007g0023 a0002c0005t0007g0025 others(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 | a0001c0001t0009g0269 a0001c0001t0009g0274 |
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 | a0002c0005t0006g0107 a0002c0005t0007g0023 a0002c0005t0007g0025 others(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 | 225 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(222): 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 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(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:2848547 | G | GA | 17 | a0001c0003t0001g0028 a0001c0003t0001g0029 a0001c0003t0005g0013 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(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 | GGA | 5 | a0001c0001t0001g0135 a0002c0002t0002g0004 a0002c0002t0003g0134 others(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 | GA | G | 210 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0077 others(207): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.149+5205delA | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2848547 | ||||||
| chrX:2848559 | A | C | 1 | a0001c0001t0001g0186 | 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 | a0001c0001t0016g0097 | 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 | 153 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(150): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.149+5276G>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2848630 | |||||||
| chrX:2848979 | A | T | 56 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(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 | 55 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(52): Show |
57 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.150-4835T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2849145 | |||||||
| chrX:2849189 | T | C | 56 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(53): Show |
58 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.150-4791T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2849189 | |||||||
| chrX:2849228 | G | T | 11 | a0002c0002t0001g0011 a0002c0002t0001g0052 a0002c0002t0003g0012 others(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 | a0001c0001t0001g0135 a0002c0002t0002g0014 a0002c0002t0003g0134 others(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 | a0001c0001t0001g0219 a0001c0001t0001g0229 |
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 | 86 | a0001c0001t0001g0135 a0001c0001t0001g0139 a0001c0001t0001g0143 others(83): 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 | 55 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(52): Show |
57 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.150-4649G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2849331 | |||||||
| chrX:2849344 | C | T | 55 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(52): Show |
57 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.150-4636C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2849344 | |||||||
| chrX:2849419 | A | G | 1 | a0002c0002t0004g0306 | 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 | a0002c0002t0001g0169 | 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 | 62 | a0001c0001t0001g0139 a0001c0001t0001g0143 a0001c0001t0001g0144 others(59): 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 | a0001c0001t0001g0135 a0002c0002t0002g0004 a0002c0002t0002g0014 others(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 | a0001c0003t0001g0028 a0001c0003t0001g0029 a0001c0003t0005g0013 others(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 | a0001c0001t0002g0194 | 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 | a0002c0002t0003g0012 a0002c0002t0004g0026 a0002c0002t0005g0055 others(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 | a0001c0001t0001g0135 a0002c0002t0002g0004 a0002c0002t0002g0014 others(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 | a0001c0001t0001g0215 a0001c0001t0001g0252 a0001c0001t0001g0253 |
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 | a0001c0001t0008g0068 | 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 | a0001c0001t0001g0135 a0002c0002t0002g0004 a0002c0002t0002g0014 others(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 | AATAATG | A | 59 | a0001c0001t0001g0139 a0001c0001t0001g0143 a0001c0001t0001g0144 others(56): 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 | a0001c0001t0001g0057 | 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 | a0010c0014t0005g0233 | 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 | a0001c0001t0001g0135 a0001c0003t0001g0028 a0001c0003t0001g0029 others(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 | 146 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0077 others(143): 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 | a0001c0001t0001g0135 a0002c0002t0002g0004 a0002c0002t0002g0014 others(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 | a0002c0002t0002g0043 a0002c0002t0002g0044 a0002c0005t0003g0045 |
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 | 286 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(283): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.150-3385G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2850595 | |||||||
| chrX:2850672 | T | C | 145 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0077 others(142): 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 | a0001c0001t0001g0135 a0001c0003t0001g0028 a0001c0003t0001g0029 others(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 | a0001c0003t0001g0028 a0001c0003t0001g0029 a0001c0003t0005g0013 others(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 | a0004c0009t0001g0065 | 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 | 54 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(51): Show |
56 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.150-3170C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2850810 | |||||||
| chrX:2850823 | A | G | 54 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(51): Show |
56 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.150-3157A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2850823 | |||||||
| chrX:2850824 | T | G | 7 | a0002c0002t0002g0006 a0002c0002t0002g0148 a0002c0002t0002g0149 others(4): 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 | 296 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(293): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): 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 | a0001c0003t0001g0028 a0001c0003t0001g0029 a0001c0003t0005g0013 others(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 | 144 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0077 others(141): 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 | a0001c0001t0001g0135 a0001c0003t0001g0028 a0001c0003t0001g0029 others(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 | 60 | a0001c0001t0001g0139 a0001c0001t0001g0143 a0001c0001t0001g0144 others(57): 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 | a0002c0002t0003g0012 a0002c0002t0003g0038 a0002c0002t0003g0039 others(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 | 227 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(224): Show |
234 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(231): 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 | a0002c0002t0003g0012 a0002c0002t0003g0038 a0002c0002t0003g0039 others(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 | a0001c0001t0002g0101 | 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 | a0002c0002t0005g0128 | 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 | a0001c0001t0001g0288 | 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 | a0001c0001t0001g0135 a0001c0003t0001g0028 a0001c0003t0001g0029 others(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 | a0001c0001t0001g0135 a0001c0003t0001g0028 a0001c0003t0001g0029 others(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 | a0001c0001t0002g0194 a0001c0001t0007g0193 a0002c0002t0007g0195 |
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 | a0001c0003t0002g0046 a0001c0003t0002g0049 a0001c0003t0004g0047 |
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:2853110 | G | T | 1 | a0001c0001t0003g0058 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.150-870G>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2853110 | |||||||
| chrX:2853273 | C | T | 172 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(169): Show |
177 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.150-707C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2853273 | |||||||
| chrX:2853274 | G | A | 39 | a0001c0001t0001g0008 a0001c0001t0004g0071 a0001c0001t0014g0051 others(36): 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 | a0002c0002t0004g0159 | 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 | a0010c0014t0005g0233 | 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 | 39 | a0001c0001t0001g0008 a0001c0001t0004g0071 a0001c0001t0014g0051 others(36): 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 | a0002c0002t0002g0249 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.150-154T>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 3/10 | chrX | 2853826 | |||||||
| chrX:2853930 | G | C | 1 | a0001c0001t0002g0080 | 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 | 90 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(87): Show |
93 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(90): 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 | a0001c0001t0001g0003 a0001c0001t0001g0018 |
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 | a0001c0003t0007g0034 a0001c0003t0008g0033 a0003c0007t0006g0036 |
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 | 279 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(276): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.324+203T>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 4/10 | chrX | 2854357 | |||||||
| chrX:2854619 | G | A | 178 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(175): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): 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 | a0002c0002t0003g0040 | 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 | 178 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(175): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.325-340A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 4/10 | chrX | 2854653 | |||||||
| chrX:2854731 | T | C | 222 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0077 others(219): 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 | 202 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(199): Show |
207 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(204): Show |
intron_variant | MODIFIER | c.325-242C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 4/10 | chrX | 2854751 | |||||||
| chrX:2854847 | G | A | 2 | a0001c0001t0002g0192 a0001c0001t0002g0290 |
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 | a0001c0001t0003g0213 a0001c0001t0003g0276 |
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 | 176 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(173): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): 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 | a0002c0006t0002g0113 a0002c0006t0003g0112 a0002c0006t0005g0111 |
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 | 174 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(171): Show |
179 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.487+584A>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 5/10 | chrX | 2855739 | |||||||
| chrX:2855902 | T | G | 288 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(285): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.488-596T>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 5/10 | chrX | 2855902 | |||||||
| chrX:2856005 | A | G | 288 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(285): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): 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 | a0002c0002t0006g0056 | 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 | a0001c0001t0002g0273 | 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 | 290 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(287): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.488-61A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 5/10 | chrX | 2856437 | |||||||
| chrX:2856659 | T | G | 104 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(101): Show |
107 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.614+35T>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2856659 | |||||||
| chrX:2856719 | CTCTA | C | 113 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(110): 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 | a0001c0001t0002g0191 | 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 | 27 | a0001c0003t0001g0028 a0001c0003t0001g0029 a0001c0003t0001g0123 others(24): Show |
27 | HG00099.hp1 HG00733.hp2 HG01243.hp1 others(24): 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 | 25 | a0001c0001t0001g0139 a0002c0002t0001g0037 a0002c0002t0001g0052 others(22): 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 | a0002c0002t0002g0153 | 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 | a0001c0001t0002g0192 a0001c0001t0002g0290 a0002c0002t0002g0117 others(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 | CT | 52 | a0001c0001t0001g0139 a0001c0001t0002g0192 a0001c0001t0002g0290 others(49): Show |
53 | HG00323.hp2 HG00438.hp2 HG00741.hp2 others(50): 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 | a0002c0002t0001g0011 a0002c0002t0001g0165 a0002c0002t0001g0174 others(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 | a0001c0003t0001g0028 a0001c0003t0001g0029 a0001c0003t0001g0123 others(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 | 25 | a0001c0001t0001g0139 a0002c0002t0001g0037 a0002c0002t0001g0052 others(22): 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 | a0001c0001t0002g0192 a0001c0001t0002g0290 a0002c0002t0002g0117 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0183 others(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 | a0002c0002t0001g0037 a0011c0011t0005g0042 |
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 | 101 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0077 others(98): Show |
106 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(103): 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 | a0001c0001t0002g0127 a0002c0002t0002g0004 a0002c0002t0005g0021 others(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 | a0001c0001t0001g0135 a0002c0002t0002g0014 a0002c0002t0003g0134 others(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 | a0002c0002t0002g0054 a0002c0002t0006g0050 |
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:2856754 | A | G | 2 | a0002c0002t0003g0012 a0002c0002t0004g0026 |
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 | a0002c0002t0006g0056 | 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 | a0001c0001t0003g0079 | 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 | a0001c0001t0004g0094 a0001c0001t0004g0095 a0001c0001t0004g0096 |
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 | a0001c0001t0001g0221 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.614+143T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2856767 | |||||||
| chrX:2856777 | T | TATC | 42 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0077 others(39): 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:2856788 | C | CT | 77 | a0001c0001t0001g0010 a0001c0001t0001g0284 a0001c0001t0001g0296 others(74): 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 | a0001c0003t0001g0123 a0001c0003t0002g0046 a0001c0003t0004g0047 others(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 | 46 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0077 others(43): 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 | 95 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0084 others(92): Show |
97 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.614+172delT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2856795 | |||||||
| chrX:2856799 | C | CATCT | 78 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0183 others(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 |
67 | a0001c0001t0001g0010 a0001c0001t0001g0284 a0001c0001t0001g0296 others(64): 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 | 98 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0084 others(95): Show |
100 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(97): 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 | 176 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(173): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): 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 | a0001c0001t0001g0104 a0001c0001t0002g0192 a0001c0001t0002g0294 others(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 | 96 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0084 others(93): 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 | 29 | a0001c0001t0001g0010 a0001c0001t0001g0284 a0001c0001t0001g0296 others(26): Show |
31 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(28): 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 | a0001c0001t0002g0078 a0001c0001t0002g0080 |
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 | a0001c0001t0001g0093 a0002c0002t0003g0116 a0002c0002t0004g0306 |
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 | a0001c0003t0002g0046 a0001c0003t0002g0049 a0001c0003t0004g0047 others(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 | a0001c0003t0001g0028 a0001c0003t0001g0029 a0001c0003t0005g0013 others(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 | a0001c0003t0001g0123 a0002c0002t0001g0037 a0003c0007t0006g0036 |
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 | TTATC | T | 12 | a0001c0001t0001g0135 a0001c0001t0002g0059 a0001c0001t0002g0187 others(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 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0229 others(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 | 92 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0077 others(89): 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 | a0001c0001t0002g0194 a0001c0001t0007g0193 |
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 | 43 | a0001c0001t0001g0139 a0001c0001t0002g0160 a0002c0002t0001g0150 others(40): 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 | a0002c0006t0003g0041 | 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 | 53 | a0001c0001t0001g0139 a0001c0001t0001g0288 a0001c0001t0002g0160 others(50): 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 | 123 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(120): Show |
126 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.614+546G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2857170 | |||||||
| chrX:2857218 | G | A | 176 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(173): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.614+594G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2857218 | |||||||
| chrX:2857289 | CT | C | 176 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(173): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): 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 | 176 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(173): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.614+691C>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2857315 | |||||||
| chrX:2857406 | A | ATATC | 290 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(287): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): 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 | a0002c0006t0003g0041 | 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 | a0005c0010t0003g0206 a0007c0016t0003g0207 |
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 | a0002c0006t0002g0113 a0002c0006t0003g0112 a0002c0006t0005g0111 |
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 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
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 | 176 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(173): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): 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 | a0002c0002t0008g0248 | 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 | a0002c0002t0008g0248 | 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 | a0001c0001t0002g0184 a0001c0001t0002g0246 |
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 | 114 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0077 others(111): 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 | a0001c0001t0001g0271 | 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 | 115 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0077 others(112): 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:2857879 | C | A | 19 | a0001c0003t0001g0028 a0001c0003t0001g0029 a0001c0003t0001g0123 others(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 | 102 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(99): Show |
105 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(102): 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 | a0002c0002t0003g0040 | 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 | 105 | a0001c0001t0001g0008 a0001c0001t0001g0077 a0001c0001t0001g0143 others(102): 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 | 115 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0077 others(112): 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 | a0002c0005t0002g0124 | 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 | 115 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0077 others(112): 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 | 15 | a0001c0001t0002g0059 a0001c0001t0002g0184 a0001c0001t0002g0187 others(12): 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 | 156 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(153): Show |
161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): 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 | a0002c0002t0003g0303 | 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 | a0001c0001t0016g0097 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.615-1370A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2858473 | |||||||
| chrX:2858645 | G | T | 137 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0077 others(134): 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 | a0002c0002t0004g0272 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.615-1154G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2858689 | |||||||
| chrX:2859066 | T | G | 188 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(185): Show |
194 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(191): 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 | a0001c0001t0001g0186 | 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 | 178 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(175): Show |
184 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.615-570A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 6/10 | chrX | 2859273 | |||||||
| chrX:2859279 | ATAG | A | 178 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(175): Show |
184 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(181): 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 | 262 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(259): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): 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 | a0001c0003t0002g0046 a0001c0003t0004g0047 |
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 | a0002c0002t0004g0154 | 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 | 166 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(163): Show |
172 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(169): 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 | a0002c0002t0005g0128 a0006c0008t0006g0020 a0006c0008t0006g0129 |
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 | a0001c0001t0001g0135 a0001c0003t0001g0028 a0001c0003t0001g0029 others(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:2860171 | T | C | 2 | a0002c0005t0002g0124 a0002c0005t0002g0178 |
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 | 176 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(173): Show |
182 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(179): 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 | a0001c0001t0001g0135 a0001c0003t0001g0028 a0001c0003t0001g0029 others(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 | 176 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(173): Show |
182 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(179): 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 | a0001c0001t0001g0100 | 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 | 176 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(173): Show |
182 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.837+420A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 7/10 | chrX | 2860485 | |||||||
| chrX:2860505 | C | A | 176 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(173): Show |
182 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.837+440C>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 7/10 | chrX | 2860505 | |||||||
| chrX:2860546 | A | G | 175 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(172): Show |
181 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.837+481A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 7/10 | chrX | 2860546 | |||||||
| chrX:2860643 | CT | C | 21 | a0001c0001t0001g0251 a0001c0001t0002g0255 a0001c0001t0002g0256 others(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 | 164 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(161): Show |
170 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(167): 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:2860674 | T | C | 5 | a0001c0001t0001g0182 a0001c0001t0001g0234 a0001c0001t0001g0235 others(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 | a0001c0001t0002g0127 a0001c0001t0004g0071 a0001c0003t0001g0123 others(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 | 175 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(172): Show |
181 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.837+690A>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 7/10 | chrX | 2860755 | |||||||
| chrX:2860791 | A | G | 191 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(188): Show |
197 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(194): 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 | a0002c0005t0002g0124 a0002c0005t0002g0178 a0002c0005t0006g0107 others(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 | 175 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(172): Show |
181 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.838-581G>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 7/10 | chrX | 2860941 | |||||||
| chrX:2860955 | T | C | 175 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(172): Show |
181 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(178): 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 | a0002c0002t0003g0012 a0002c0002t0004g0026 |
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 | a0001c0001t0001g0135 a0001c0001t0004g0200 a0001c0003t0001g0028 others(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:2861130 | G | A | 175 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(172): Show |
181 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(178): 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 | a0001c0001t0016g0097 | 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 | 175 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(172): Show |
181 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(178): 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 | a0001c0001t0014g0051 | 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 | a0001c0001t0001g0084 a0001c0001t0002g0085 a0001c0001t0002g0086 others(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 | 177 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(174): Show |
183 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(180): 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 | a0001c0001t0002g0127 a0001c0001t0004g0071 a0001c0003t0001g0123 others(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 | a0002c0002t0001g0037 a0002c0002t0006g0056 a0011c0011t0005g0042 |
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 | a0001c0001t0003g0066 | 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 | a0001c0001t0001g0135 a0001c0001t0014g0051 a0001c0003t0001g0028 others(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 | a0001c0003t0002g0046 a0001c0003t0004g0047 |
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 | a0001c0001t0001g0183 | 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 | 182 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(179): Show |
188 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(185): 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 | a0002c0002t0006g0056 a0002c0005t0002g0124 a0002c0005t0002g0178 others(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 | a0002c0002t0001g0125 a0002c0002t0001g0126 |
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 | a0001c0003t0002g0046 a0001c0003t0004g0047 |
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 | a0002c0002t0006g0056 a0002c0005t0002g0124 a0002c0005t0002g0178 others(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 | 157 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(154): Show |
163 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.1038+502G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2862224 | |||||||
| chrX:2862278 | A | C | 182 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(179): Show |
188 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(185): 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 | a0001c0001t0002g0127 a0001c0001t0004g0071 a0001c0003t0001g0123 others(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 | 9 | a0002c0002t0001g0009 a0002c0002t0001g0188 a0002c0002t0001g0259 others(6): 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 | 182 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(179): Show |
188 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(185): 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 | a0001c0001t0001g0135 a0001c0001t0014g0051 a0001c0003t0001g0028 others(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 | a0002c0002t0002g0004 a0002c0002t0002g0054 a0002c0002t0003g0038 others(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 | 182 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(179): Show |
188 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.1038+984C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2862706 | |||||||
| chrX:2862785 | C | T | 182 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(179): Show |
188 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.1038+1063C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2862785 | |||||||
| chrX:2862788 | T | A | 182 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(179): Show |
188 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(185): 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 | a0002c0002t0001g0037 a0002c0002t0002g0004 a0002c0002t0002g0014 others(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 | a0001c0001t0001g0057 a0001c0001t0001g0077 a0001c0001t0001g0199 others(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 | a0001c0003t0002g0046 a0001c0003t0004g0047 |
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 | a0001c0001t0001g0084 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1038+1325G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2863047 | |||||||
| chrX:2863080 | CT | C | 186 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(183): Show |
192 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(189): 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 | a0001c0003t0002g0046 a0001c0003t0004g0047 |
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 | 180 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(177): Show |
186 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1038+1457G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2863179 | |||||||
| chrX:2863219 | T | C | 194 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(191): Show |
201 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(198): 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 | a0002c0002t0002g0004 a0002c0002t0002g0054 a0002c0002t0003g0038 others(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 | 39 | a0002c0002t0001g0150 a0002c0002t0001g0165 a0002c0002t0001g0169 others(36): 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 | a0001c0001t0001g0222 | 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 | a0001c0001t0002g0127 a0001c0001t0004g0071 a0001c0003t0001g0123 others(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 | a0002c0005t0006g0107 | 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 | a0001c0001t0002g0194 a0001c0001t0007g0193 a0002c0002t0006g0050 others(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:2864264 | A | T | 198 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(195): Show |
204 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(201): 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 | a0001c0001t0002g0160 | 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 | a0001c0001t0001g0203 | 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 | a0002c0002t0003g0012 a0002c0002t0004g0026 |
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 | 29 | a0002c0002t0001g0009 a0002c0002t0001g0011 a0002c0002t0001g0052 others(26): 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 | AT | A | 208 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(205): Show |
214 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.1038+2678delT | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2864385 | ||||||
| chrX:2864414 | T | C | 269 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(266): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.1038+2692T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2864414 | |||||||
| chrX:2864592 | G | A | 172 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(169): Show |
178 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.1038+2870G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2864592 | |||||||
| chrX:2864745 | A | G | 2 | a0002c0002t0003g0012 a0002c0002t0004g0026 |
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:2864763 | TC | T | 14 | a0001c0001t0001g0135 a0001c0001t0014g0051 a0001c0003t0001g0028 others(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:2864879 | C | T | 1 | a0002c0002t0003g0038 | 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 | a0001c0001t0002g0127 a0001c0003t0002g0049 a0002c0002t0003g0134 others(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 | 220 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(217): Show |
227 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(224): 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 | a0001c0001t0002g0127 a0001c0003t0002g0049 a0001c0003t0005g0179 others(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 | a0002c0002t0003g0239 a0002c0002t0007g0048 |
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 | 227 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(224): Show |
234 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(231): 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 | a0001c0001t0003g0213 | 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 | a0001c0001t0001g0286 a0001c0001t0002g0283 a0001c0001t0002g0287 |
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 | 157 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(154): Show |
163 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.1038+4013T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2865735 | |||||||
| chrX:2865874 | T | TCA | 226 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(223): Show |
233 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(230): 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 | a0002c0006t0005g0111 | 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 | a0001c0003t0005g0013 a0002c0002t0002g0004 a0002c0002t0002g0054 others(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 | 226 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(223): Show |
233 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(230): 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 | a0002c0002t0006g0050 a0002c0002t0012g0069 a0002c0002t0012g0070 |
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 | a0001c0001t0014g0051 | 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 | a0002c0005t0003g0045 a0002c0006t0003g0041 |
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 | a0005c0010t0003g0206 | 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 | a0001c0003t0005g0013 a0002c0002t0002g0004 a0002c0002t0002g0054 others(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 | a0001c0001t0002g0194 a0001c0003t0001g0123 a0002c0002t0005g0055 others(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 | a0002c0002t0003g0212 | 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 | a0001c0001t0001g0135 a0001c0001t0002g0127 a0001c0001t0004g0071 others(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 | AT | A | 7 | a0002c0002t0001g0263 a0002c0002t0003g0168 a0002c0002t0004g0154 others(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:2866836 | TTA | T | 186 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(183): Show |
192 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(189): 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 | a0002c0002t0001g0174 | 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 | a0002c0002t0003g0076 a0002c0002t0010g0163 a0006c0008t0006g0024 |
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 | a0002c0002t0002g0145 a0002c0002t0002g0146 a0002c0002t0004g0266 |
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 | 239 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(236): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): 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 | a0004c0009t0002g0155 | 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 | a0001c0003t0005g0013 a0001c0003t0007g0034 a0002c0002t0001g0037 others(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 | a0001c0003t0001g0123 a0002c0002t0002g0014 a0002c0002t0003g0040 others(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 | a0002c0006t0005g0111 | 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 | 284 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(281): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): 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 | a0001c0001t0004g0071 | 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 | 44 | a0001c0001t0004g0088 a0001c0001t0004g0167 a0001c0003t0002g0046 others(41): 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 | 45 | a0001c0001t0004g0088 a0001c0001t0004g0167 a0001c0003t0002g0046 others(42): 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 | 45 | a0001c0001t0004g0088 a0001c0001t0004g0167 a0001c0003t0002g0046 others(42): 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 | 45 | a0001c0001t0004g0088 a0001c0001t0004g0167 a0001c0003t0002g0046 others(42): 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:2867830 | C | G | 2 | a0001c0003t0002g0046 a0001c0003t0004g0047 |
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 | 59 | a0001c0001t0002g0204 a0001c0001t0004g0088 a0001c0001t0004g0167 others(56): 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 | 195 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(192): Show |
203 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(200): 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 | a0001c0001t0002g0293 | 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 | a0002c0002t0005g0205 | 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 | a0002c0002t0001g0037 a0002c0002t0006g0056 a0011c0011t0005g0042 |
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 | a0001c0001t0014g0051 | 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 | 39 | a0001c0001t0002g0204 a0001c0001t0004g0088 a0001c0001t0004g0167 others(36): 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 | a0001c0003t0005g0027 | 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 | a0002c0005t0002g0124 a0002c0005t0002g0178 a0002c0005t0006g0107 others(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 | a0001c0001t0001g0077 a0001c0001t0001g0230 a0001c0001t0001g0289 |
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 | a0001c0001t0001g0093 a0001c0001t0001g0241 a0001c0001t0001g0286 others(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 | 17 | a0001c0001t0001g0209 a0001c0001t0001g0243 a0001c0001t0002g0063 others(14): Show |
17 | HG00099.hp2 HG00323.hp1 HG01109.hp1 others(14): 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 | CAAA | C | 9 | a0002c0002t0005g0021 a0002c0002t0005g0180 a0002c0002t0006g0022 others(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:2868553 | A | G | 2 | a0002c0002t0006g0136 a0002c0006t0005g0111 |
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 | a0002c0002t0001g0037 a0002c0002t0003g0012 a0002c0002t0004g0026 others(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 | a0002c0002t0001g0037 a0002c0002t0005g0098 a0002c0002t0005g0099 others(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:2868722 | C | T | 12 | a0001c0003t0001g0028 a0001c0003t0005g0027 a0001c0003t0008g0033 others(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 | a0006c0008t0006g0024 | 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 | a0002c0002t0002g0043 a0002c0002t0002g0044 a0002c0002t0003g0116 others(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 | 217 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(214): Show |
226 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(223): 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 | a0001c0001t0007g0193 a0001c0001t0009g0274 a0002c0002t0003g0012 others(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 | a0001c0003t0001g0028 a0001c0003t0005g0027 a0001c0003t0008g0033 others(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 | a0003c0007t0006g0031 | 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 | a0001c0003t0001g0123 a0002c0002t0001g0125 a0002c0002t0001g0126 others(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 | a0002c0006t0005g0111 | 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 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0281 others(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 | 257 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(254): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): 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 | a0001c0001t0001g0251 | 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 | a0001c0001t0001g0008 | 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:2869534 | A | G | 1 | a0002c0002t0005g0108 | 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 | a0002c0002t0005g0128 a0002c0002t0005g0137 a0011c0011t0005g0042 |
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 | a0002c0002t0005g0300 a0002c0005t0007g0023 |
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 | 234 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(231): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): 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 | a0001c0001t0002g0194 a0002c0002t0005g0305 a0002c0002t0007g0190 |
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 | 86 | a0001c0001t0002g0127 a0001c0001t0002g0194 a0001c0001t0002g0273 others(83): 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 | a0002c0002t0001g0011 a0002c0002t0003g0012 a0002c0002t0007g0110 |
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 | a0001c0001t0004g0088 | 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 | 54 | a0001c0001t0001g0084 a0001c0001t0002g0103 a0001c0001t0002g0194 others(51): 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 | 52 | a0001c0001t0002g0194 a0001c0001t0004g0015 a0001c0001t0004g0088 others(49): 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 | a0002c0002t0006g0050 | 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 | 52 | a0001c0001t0002g0194 a0001c0001t0004g0015 a0001c0001t0004g0088 others(49): 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 | a0002c0002t0006g0050 | 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 | 53 | a0001c0001t0002g0194 a0001c0001t0004g0015 a0001c0001t0004g0088 others(50): 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 | a0002c0002t0001g0011 a0002c0002t0007g0110 |
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 | 40 | a0001c0001t0004g0015 a0001c0001t0004g0088 a0001c0001t0004g0094 others(37): 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 | 97 | a0001c0001t0002g0194 a0001c0001t0002g0273 a0001c0001t0003g0001 others(94): 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 | a0002c0002t0003g0115 a0002c0002t0003g0116 a0002c0002t0003g0119 others(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 | a0001c0001t0002g0273 a0001c0003t0007g0034 a0002c0002t0012g0069 others(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 | a0002c0002t0005g0128 a0002c0002t0005g0137 |
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 | 63 | a0001c0001t0002g0194 a0001c0001t0004g0015 a0001c0001t0004g0088 others(60): 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:2870928 | C | T | 1 | a0001c0001t0007g0193 | 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 | a0010c0014t0005g0233 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1039-4853G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2870957 | |||||||
| chrX:2871005 | A | AT | 155 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(152): Show |
162 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(159): 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 | a0001c0001t0002g0273 | 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 | a0002c0002t0002g0249 a0002c0002t0002g0257 a0002c0002t0002g0264 others(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 | a0002c0002t0005g0300 a0002c0005t0007g0023 |
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 | a0001c0001t0001g0215 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1039-4668C>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2871142 | |||||||
| chrX:2871373 | C | T | 1 | a0001c0001t0001g0143 | 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 | 286 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(283): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.1039-4427C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2871383 | |||||||
| chrX:2871387 | TA | T | 153 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(150): Show |
160 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(157): 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 | 40 | a0001c0001t0004g0015 a0001c0001t0004g0088 a0001c0001t0004g0094 others(37): 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 | a0001c0001t0003g0227 a0001c0003t0002g0046 a0005c0010t0003g0017 |
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 | a0001c0003t0004g0047 a0002c0002t0003g0212 a0002c0002t0003g0303 |
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(5): Show |
C | 16 | a0001c0001t0002g0273 a0001c0003t0007g0034 a0002c0002t0003g0038 others(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 | 188 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(185): Show |
196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): 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 | 55 | a0001c0001t0002g0194 a0001c0001t0004g0015 a0001c0001t0004g0088 others(52): 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 | a0002c0002t0005g0180 | 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 | a0002c0002t0008g0248 | 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 | 207 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(204): Show |
215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1039-4003T>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 8/10 | chrX | 2871807 | |||||||
| chrX:2872107 | T | C | 207 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(204): Show |
215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): 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 | a0001c0001t0002g0273 a0001c0003t0007g0034 a0001c0003t0008g0033 others(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:2872326 | T | C | 48 | a0001c0001t0002g0194 a0001c0001t0004g0015 a0001c0001t0004g0088 others(45): 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:2872387 | TAA | T | 50 | a0001c0001t0002g0194 a0001c0001t0004g0015 a0001c0001t0004g0088 others(47): 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 | a0002c0002t0001g0260 | 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 | a0001c0001t0007g0193 a0001c0003t0007g0034 a0002c0002t0003g0115 others(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 | a0001c0001t0002g0273 a0002c0002t0012g0069 a0002c0002t0012g0070 others(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 | a0002c0002t0004g0157 | 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 | a0002c0002t0007g0195 | 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 | 56 | a0001c0001t0001g0236 a0001c0001t0002g0194 a0001c0001t0004g0015 others(53): 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:2873040 | T | C | 220 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(217): 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 | 64 | a0001c0001t0001g0236 a0001c0001t0001g0251 a0001c0001t0002g0194 others(61): 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 | a0001c0001t0002g0194 a0001c0001t0004g0071 a0001c0001t0014g0051 others(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:2873179 | C | A | 7 | a0003c0007t0001g0032 a0003c0007t0006g0030 a0003c0007t0006g0031 others(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:2873231 | A | G | 60 | a0001c0001t0001g0236 a0001c0001t0001g0251 a0001c0001t0002g0194 others(57): 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 | 60 | a0001c0001t0001g0236 a0001c0001t0001g0251 a0001c0001t0002g0194 others(57): 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:2873287 | A | C | 1 | a0002c0002t0007g0195 | 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 | 59 | a0001c0001t0001g0236 a0001c0001t0001g0251 a0001c0001t0002g0194 others(56): 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 | 61 | a0001c0001t0001g0236 a0001c0001t0001g0251 a0001c0001t0002g0194 others(58): 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:2873563 | G | C | 64 | a0001c0001t0001g0236 a0001c0001t0001g0251 a0001c0001t0002g0194 others(61): 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 | a0001c0001t0001g0251 a0001c0003t0008g0033 a0002c0002t0001g0052 others(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:2874097 | A | AAAATAAA others(1): Show |
62 | a0001c0001t0001g0236 a0001c0001t0001g0251 a0001c0001t0002g0194 others(59): 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 | a0001c0001t0001g0251 a0002c0002t0001g0052 a0002c0002t0007g0195 others(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:2874275 | T | C | 2 | a0002c0002t0002g0145 a0002c0002t0002g0146 |
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 | a0011c0011t0005g0042 | 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 | 91 | a0001c0001t0001g0236 a0001c0001t0001g0251 a0001c0001t0002g0194 others(88): 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 | a0001c0001t0014g0051 | 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 | a0001c0001t0004g0071 a0002c0002t0005g0055 a0002c0002t0005g0108 others(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 | a0002c0002t0004g0154 | 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 | a0001c0001t0004g0071 a0002c0002t0001g0037 a0002c0002t0001g0125 others(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 | 31 | a0001c0001t0003g0001 a0001c0001t0003g0016 a0001c0001t0003g0058 others(28): 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 | a0001c0001t0002g0194 a0001c0001t0004g0071 a0001c0001t0014g0051 others(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 | a0010c0014t0005g0233 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0215 |
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 | a0001c0001t0007g0193 a0001c0003t0005g0013 a0001c0003t0007g0034 others(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 | a0002c0002t0004g0157 | 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 | a0001c0001t0001g0251 a0001c0001t0002g0194 a0001c0001t0004g0071 others(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 | a0001c0001t0011g0064 a0001c0001t0011g0075 |
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 | 37 | a0001c0001t0004g0015 a0001c0001t0004g0088 a0001c0001t0004g0094 others(34): 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 | a0001c0003t0005g0027 a0002c0002t0005g0099 a0002c0006t0005g0035 |
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:2876033 | C | CT | 61 | a0001c0001t0002g0062 a0001c0001t0002g0080 a0001c0001t0002g0081 others(58): Show |
64 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(61): 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 | 31 | a0001c0001t0002g0090 a0001c0001t0002g0101 a0001c0001t0002g0152 others(28): 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 | a0001c0001t0004g0088 a0002c0002t0001g0181 a0002c0002t0002g0257 others(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 | T | 5 | a0001c0001t0014g0051 a0001c0003t0005g0027 a0002c0002t0005g0098 others(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 | 36 | a0001c0001t0002g0061 a0001c0001t0002g0063 a0001c0001t0003g0001 others(33): 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 | a0001c0001t0001g0251 a0001c0001t0002g0194 a0001c0001t0003g0237 others(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 | CTTTTTTT | C | 10 | a0001c0001t0001g0008 a0001c0001t0001g0100 a0001c0001t0001g0215 others(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 | 82 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0057 others(79): 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 | a0001c0001t0001g0018 a0001c0001t0001g0229 a0001c0001t0001g0252 others(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 | a0002c0002t0007g0195 | 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 | a0001c0001t0001g0251 a0002c0002t0001g0052 a0002c0002t0007g0195 others(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 | a0011c0011t0005g0042 | 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 | a0001c0001t0002g0273 a0002c0002t0012g0069 a0002c0002t0012g0070 others(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 | 221 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(218): 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 | a0001c0001t0001g0104 a0001c0004t0001g0106 a0002c0002t0001g0165 |
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 | a0002c0006t0005g0035 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1143+642T>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 9/10 | chrX | 2876556 | |||||||
| chrX:2876649 | T | A | 9 | a0001c0003t0005g0013 a0002c0002t0001g0181 a0002c0002t0005g0021 others(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 | a0002c0005t0007g0023 | 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 | a0001c0003t0001g0028 a0002c0002t0002g0014 a0002c0002t0002g0121 others(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 | a0001c0001t0001g0251 a0002c0002t0001g0052 a0002c0002t0007g0195 others(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 | a0011c0011t0005g0042 | 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 | 125 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(122): 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 | a0001c0001t0002g0273 a0002c0002t0003g0038 a0002c0002t0003g0039 others(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 | a0010c0014t0005g0233 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1144-357G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 9/10 | chrX | 2876843 | |||||||
| chrX:2876943 | C | T | 1 | a0002c0002t0004g0026 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1144-257C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 9/10 | chrX | 2876943 | |||||||
| chrX:2877607 | G | A | 1 | a0001c0001t0001g0010 | 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 | a0010c0014t0005g0233 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1251+345G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2877652 | |||||||
| chrX:2877696 | C | T | 1 | a0002c0002t0005g0305 | 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 | a0011c0011t0005g0042 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1251+407A>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2877714 | |||||||
| chrX:2878152 | G | A | 3 | a0001c0001t0001g0251 a0002c0002t0001g0052 a0002c0002t0007g0195 |
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 | a0010c0014t0005g0233 | 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 | a0001c0001t0001g0220 | 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 | a0001c0003t0005g0013 a0002c0002t0001g0181 a0002c0002t0005g0021 others(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:2878282 | A | AATT | 4 | a0001c0001t0001g0251 a0002c0002t0003g0116 a0002c0002t0003g0119 others(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:2878559 | C | T | 1 | a0002c0006t0003g0112 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1251+1252C>T | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2878559 | |||||||
| chrX:2878867 | G | A | 3 | a0002c0002t0003g0038 a0002c0002t0003g0039 a0002c0002t0003g0040 |
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:2879217 | A | ATAT | 113 | a0001c0001t0001g0228 a0001c0001t0002g0059 a0001c0001t0002g0061 others(110): Show |
117 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(114): 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 | a0001c0001t0001g0251 a0001c0001t0002g0192 a0001c0001t0002g0290 others(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 | CT | C | 8 | a0001c0001t0002g0080 a0001c0001t0002g0152 a0001c0003t0005g0179 others(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:2879329 | G | A | 4 | a0002c0002t0002g0006 a0002c0002t0002g0148 a0002c0002t0002g0149 others(1): 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 | a0002c0002t0002g0073 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1252-1582G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2879470 | |||||||
| chrX:2879587 | A | G | 2 | a0001c0001t0007g0193 a0001c0003t0007g0034 |
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 | a0002c0002t0003g0115 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1252-1461C>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2879591 | |||||||
| chrX:2879754 | T | C | 65 | a0001c0001t0001g0228 a0001c0001t0002g0059 a0001c0001t0002g0062 others(62): Show |
68 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.1252-1298T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2879754 | |||||||
| chrX:2879854 | T | A | 63 | a0001c0001t0001g0228 a0001c0001t0002g0059 a0001c0001t0002g0062 others(60): Show |
65 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.1252-1198T>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2879854 | |||||||
| chrX:2880164 | A | ATG | 7 | a0001c0001t0001g0215 a0001c0001t0001g0302 a0001c0001t0002g0242 others(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 | 6 | a0001c0001t0002g0090 a0001c0001t0007g0193 a0002c0002t0002g0006 others(3): 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 | 54 | a0001c0001t0001g0228 a0001c0001t0002g0059 a0001c0001t0002g0061 others(51): Show |
54 | HG00323.hp1 HG00544.hp2 HG00621.hp1 others(51): 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 | a0002c0002t0002g0073 a0002c0002t0002g0261 a0004c0009t0002g0244 |
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 | a0001c0001t0001g0186 a0001c0001t0001g0251 a0001c0001t0014g0051 others(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 | 62 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0016 others(59): 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:2880228 | G | A | 1 | a0002c0006t0005g0111 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1252-824G>A | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2880228 | |||||||
| chrX:2880287 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1252-765T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2880287 | |||||||
| chrX:2880415 | AGT | A | 195 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(192): 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 | a0001c0001t0002g0273 a0001c0003t0002g0046 a0001c0004t0002g0053 others(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 | a0001c0001t0002g0078 a0001c0001t0002g0080 |
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 | 72 | a0001c0001t0001g0228 a0001c0001t0002g0061 a0001c0001t0002g0062 others(69): Show |
74 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.1252-613T>C | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2880439 | |||||||
| chrX:2880439 | T | TGTGC | 3 | a0002c0002t0002g0072 a0002c0002t0002g0073 a0002c0002t0002g0074 |
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:2880559 | CA | C | 19 | a0001c0001t0014g0051 a0001c0003t0005g0027 a0001c0003t0005g0179 others(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 | a0002c0002t0001g0280 | 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 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
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 | a0002c0002t0006g0050 | 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 | a0002c0002t0005g0108 a0002c0005t0007g0025 |
2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1252-292C>G | GYG2 | ENSG00000056998.21 | transcript | ENST00000398806.8 | protein_coding | 10/10 | chrX | 2880760 |