Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2710 |
| ensemblid | ENSG00000198814.14 |
| hgncid | 4289 |
| symbol | GK |
| name | glycerol kinase |
| refseq_nuc | NM_001205019.2 |
| refseq_prot | NP_001191948.1 |
| ensembl_nuc | ENST00000427190.6 |
| ensembl_prot | ENSP00000401720.2 |
| mane_status | MANE Select |
| chr | chrX |
| start | 30653423 |
| end | 30731462 |
| strand | + |
| ver | v1.2 |
| region | chrX:30653423-30731462 |
| region5000 | chrX:30648423-30736462 |
| regionname0 | GK_chrX_30653423_30731462 |
| regionname5000 | GK_chrX_30648423_30736462 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1677 | 279 | 69 | 51 | 118 | 11 | 28 | GK_chrX_30648423_30736462 | GK | ATGGC others(1672): Show |
chrX | 30648423 | 30736462 | ||
| a0001c0002 | 0/0 | 1677 | 4 | 0 | 4 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | ATGGC others(1672): Show |
chrX | 30648423 | 30736462 | ||
| a0001c0003 | 0/0 | 1677 | 2 | 2 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | ATGGC others(1672): Show |
chrX | 30648423 | 30736462 | ||
| a0001c0004 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | ATGGC others(1672): Show |
chrX | 30648423 | 30736462 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4514 | 91 | 11 | 16 | 47 | 2 | 14 | GK_chrX_30648423_30736462 | GK | GCGTT others(4509): Show |
chrX | 30648423 | 30736462 |
| a0001c0001t0002 | 0/0 | 4515 | 85 | 14 | 19 | 37 | 6 | 9 | GK_chrX_30648423_30736462 | GK | GCGTT others(4510): Show |
chrX | 30648423 | 30736462 |
| a0001c0001t0003 | 1/0 | 4515 | 69 | 16 | 16 | 30 | 3 | 3 | GK_chrX_30648423_30736462 | GK | GCGTT others(4510): Show |
chrX | 30648423 | 30736462 |
| a0001c0001t0004 | 0/0 | 4515 | 12 | 12 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | GCGTT others(4510): Show |
chrX | 30648423 | 30736462 |
| a0001c0001t0005 | 0/0 | 4514 | 6 | 6 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | GCGTT others(4509): Show |
chrX | 30648423 | 30736462 |
| a0001c0001t0007 | 0/0 | 4514 | 2 | 2 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | GCGTT others(4509): Show |
chrX | 30648423 | 30736462 |
| a0001c0001t0008 | 0/0 | 4514 | 2 | 2 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | GCGTT others(4509): Show |
chrX | 30648423 | 30736462 |
| a0001c0001t0009 | 0/0 | 4514 | 2 | 0 | 0 | 2 | 0 | 0 | GK_chrX_30648423_30736462 | GK | GCGTT others(4509): Show |
chrX | 30648423 | 30736462 |
| a0001c0001t0010 | 0/0 | 4515 | 2 | 2 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | GCGTT others(4510): Show |
chrX | 30648423 | 30736462 |
| a0001c0001t0011 | 0/0 | 4514 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | GCGTT others(4509): Show |
chrX | 30648423 | 30736462 |
| a0001c0001t0012 | 0/0 | 4515 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | GCGTT others(4510): Show |
chrX | 30648423 | 30736462 |
| a0001c0001t0013 | 0/0 | 4515 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | GCGTT others(4510): Show |
chrX | 30648423 | 30736462 |
| a0001c0001t0014 | 0/0 | 4515 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | GCGTT others(4510): Show |
chrX | 30648423 | 30736462 |
| a0001c0001t0016 | 0/0 | 4515 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | GCGTT others(4510): Show |
chrX | 30648423 | 30736462 |
| a0001c0001t0018 | 0/0 | 4515 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | GCGTT others(4510): Show |
chrX | 30648423 | 30736462 |
| a0001c0001t0019 | 0/0 | 4514 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | GCGTT others(4509): Show |
chrX | 30648423 | 30736462 |
| a0001c0001t0020 | 0/0 | 4515 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | GCGTT others(4510): Show |
chrX | 30648423 | 30736462 |
| a0001c0002t0006 | 0/0 | 4515 | 3 | 0 | 3 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | GCGTT others(4510): Show |
chrX | 30648423 | 30736462 |
| a0001c0002t0017 | 0/0 | 4515 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | GCGTT others(4510): Show |
chrX | 30648423 | 30736462 |
| a0001c0003t0003 | 0/0 | 4515 | 2 | 2 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | GCGTT others(4510): Show |
chrX | 30648423 | 30736462 |
| a0001c0004t0015 | 0/0 | 4515 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | GCGTT others(4510): Show |
chrX | 30648423 | 30736462 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 1 | 2 | 1 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0039 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0007 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0003g0226 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0005g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0005g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0005g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0005g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0007g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0007g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0008g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0008g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0009g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0009g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0010g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0010g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0011g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0012g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0013g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0014g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0016g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0018g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0019g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0001t0020g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0002t0006g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0002t0006g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0002t0006g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0002t0017g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0003t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0003t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| a0001c0004t0015g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0224 | EUR | GBR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0117 | EUR | GBR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0245 | EUR | FIN | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0081 | EUR | FIN | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0252 | EUR | FIN | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0115 | EAS | CHS | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | CHS | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | CHS | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | CHS | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | CHS | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | CHS | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | CHS | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0152 | EAS | CHS | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0133 | EAS | CHS | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0154 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0036 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG00741 | hp1 | a0001 | c0002 | t0017 | g0184 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0237 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0248 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0223 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0222 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0128 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01099 | hp1 | a0001 | c0002 | t0006 | g0186 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0122 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0138 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01168 | hp1 | a0001 | c0002 | t0006 | g0185 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0241 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0240 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0129 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0246 | AMR | CLM | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0261 | AMR | CLM | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0130 | AMR | CLM | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0258 | AMR | CLM | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0140 | AMR | CLM | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | CLM | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0019 | EUR | IBS | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0212 | EUR | IBS | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0017 | EUR | IBS | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01884 | hp1 | a0001 | c0004 | t0015 | g0112 | AFR | ACB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0167 | AFR | ACB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | ACB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01891 | hp2 | a0001 | c0001 | t0008 | g0106 | AFR | ACB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | PEL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0215 | AMR | PEL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0148 | AMR | PEL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01981 | hp1 | a0001 | c0002 | t0006 | g0187 | AMR | PEL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0132 | AMR | PEL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0135 | AMR | PEL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0236 | AMR | PEL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0203 | AMR | PEL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0123 | AMR | PEL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | KHV | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | KHV | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | KHV | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0175 | AFR | ACB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | KHV | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | KHV | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02080 | hp2 | a0001 | c0001 | t0009 | g0118 | EAS | KHV | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | KHV | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02135 | hp1 | a0001 | c0001 | t0016 | g0127 | EAS | KHV | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02145 | hp1 | a0001 | c0003 | t0003 | g0166 | AFR | ACB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0131 | AMR | PEL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | ACB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0209 | AMR | PEL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0153 | AMR | PEL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | ACB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | ACB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0095 | AMR | PEL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0139 | AMR | PEL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0178 | AFR | ACB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0155 | EAS | KHV | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0270 | SAS | PJL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0094 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0170 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0107 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0182 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0199 | SAS | PJL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0181 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0096 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0126 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02809 | hp2 | a0001 | c0001 | t0008 | g0165 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0176 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02818 | hp2 | a0001 | c0001 | t0013 | g0108 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0173 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0029 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0219 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0172 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0202 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | ESN | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | ESN | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0169 | AFR | ESN | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0198 | AFR | ESN | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0032 | AFR | ESN | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0197 | AFR | ESN | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0137 | AFR | ESN | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0206 | SAS | PJL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG03098 | hp1 | a0001 | c0001 | t0010 | g0164 | AFR | MSL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG03195 | hp1 | a0001 | c0001 | t0020 | g0171 | AFR | ESN | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG03195 | hp2 | a0001 | c0003 | t0003 | g0168 | AFR | ESN | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0102 | AFR | MSL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG03225 | hp1 | a0001 | c0001 | t0012 | g0183 | AFR | MSL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0007 | SAS | PJL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | MSL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | MSL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | MSL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG03486 | hp2 | a0001 | c0001 | t0010 | g0111 | AFR | MSL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0144 | AFR | ESN | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG03516 | hp2 | a0001 | c0001 | t0011 | g0030 | AFR | ESN | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0105 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0244 | AFR | MSL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0213 | SAS | PJL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0266 | SAS | PJL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0070 | SAS | PJL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0120 | SAS | STU | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG03704 | hp1 | a0001 | c0001 | t0014 | g0263 | SAS | PJL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG03710 | hp1 | a0001 | c0001 | t0019 | g0046 | SAS | PJL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | BEB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0254 | SAS | BEB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0147 | SAS | BEB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0231 | SAS | BEB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | BEB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | STU | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | STU | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0225 | SAS | STU | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | STU | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0174 | AFR | YRI | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | CHB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0136 | EAS | CHB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | YRI | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | YRI | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18961 | hp1 | a0001 | c0001 | t0009 | g0151 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0023 | AFR | LWK | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19079 | hp1 | a0001 | c0001 | t0018 | g0250 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0180 | AFR | YRI | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0220 | AFR | ASW | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA20129 | hp2 | a0001 | c0001 | t0007 | g0104 | AFR | ASW | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0047 | EUR | TSI | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0264 | EUR | TSI | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | GIH | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0124 | AMR | CLM | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0265 | AMR | CLM | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02109 | hp2 | a0001 | c0001 | t0007 | g0103 | AFR | ACB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0159 | AFR | ACB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0101 | AFR | ACB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | USA | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | USA | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0207 | AFR | LWK | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0179 | AFR | LWK | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0039 | REF | REF | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0226 | REF | REF | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
| 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 |
|---|
| 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:30668024 | G | A | 1 | a0001c0002 | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
synonymous_variant | LOW | c.165G>A | p.Gln55Gln | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/21 | 280/4515 | 165/1680 | 55/559 | chrX | 30668024 | |||
| chrX:30668045 | T | C | 1 | a0001c0004 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.186T>C | p.His62His | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/21 | 301/4515 | 186/1680 | 62/559 | chrX | 30668045 | |||
| chrX:30694486 | C | T | 1 | a0001c0003 | 2 | HG02145.hp1 HG03195.hp2 |
synonymous_variant | LOW | c.501C>T | p.Ala167Ala | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 6/21 | 616/4515 | 501/1680 | 167/559 | chrX | 30694486 |
| 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:30728932 | A | T | 1 | a0001c0001t0020 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*190A>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 21/21 | 190 | chrX | 30728932 | ||||||
| chrX:30728939 | G | T | 1 | a0001c0001t0019 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*197G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 21/21 | 197 | chrX | 30728939 | ||||||
| chrX:30728942 | GT | G | 7 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(4): Show |
104 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*214delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 21/21 | 214 | INFO_REALIGN_3_PRIME | chrX | 30728942 | |||||
| chrX:30728982 | A | C | 1 | a0001c0001t0018 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*240A>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 21/21 | 240 | chrX | 30728982 | ||||||
| chrX:30729082 | C | T | 2 | a0001c0002t0006 a0001c0002t0017 |
4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*340C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 21/21 | 340 | chrX | 30729082 | ||||||
| chrX:30729706 | T | C | 1 | a0001c0001t0011 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*964T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 21/21 | 964 | chrX | 30729706 | ||||||
| chrX:30729739 | C | A | 3 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0008 |
10 | HG01891.hp2 HG02109.hp2 HG02559.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*997C>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 21/21 | 997 | chrX | 30729739 | ||||||
| chrX:30729924 | A | C | 1 | a0001c0001t0010 | 2 | HG03098.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1182A>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 21/21 | 1182 | chrX | 30729924 | ||||||
| chrX:30729986 | T | C | 1 | a0001c0001t0012 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1244T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 21/21 | 1244 | chrX | 30729986 | ||||||
| chrX:30730154 | A | G | 1 | a0001c0001t0008 | 2 | HG01891.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1412A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 21/21 | 1412 | chrX | 30730154 | ||||||
| chrX:30730167 | T | C | 11 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(8): Show |
192 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(189): Show |
3_prime_UTR_variant | MODIFIER | c.*1425T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 21/21 | 1425 | chrX | 30730167 | ||||||
| chrX:30730358 | C | A | 1 | a0001c0001t0013 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1616C>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 21/21 | 1616 | chrX | 30730358 | ||||||
| chrX:30730641 | T | C | 1 | a0001c0004t0015 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1899T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 21/21 | 1899 | chrX | 30730641 | ||||||
| chrX:30730870 | A | G | 1 | a0001c0001t0016 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2128A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 21/21 | 2128 | chrX | 30730870 | ||||||
| chrX:30730934 | C | A | 1 | a0001c0001t0007 | 2 | HG02109.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2192C>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 21/21 | 2192 | chrX | 30730934 | ||||||
| chrX:30730964 | T | C | 17 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(14): Show |
211 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(208): Show |
3_prime_UTR_variant | MODIFIER | c.*2222T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 21/21 | 2222 | chrX | 30730964 | ||||||
| chrX:30730966 | T | C | 1 | a0001c0002t0017 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2224T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 21/21 | 2224 | chrX | 30730966 | ||||||
| chrX:30731025 | T | G | 14 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(11): Show |
197 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*2283T>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 21/21 | 2283 | chrX | 30731025 | ||||||
| chrX:30731330 | T | A | 1 | a0001c0001t0014 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2588T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 21/21 | 2588 | chrX | 30731330 |
| 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:30653779 | G | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(192): Show |
208 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.78+164G>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30653779 | |||||||
| chrX:30654004 | G | A | 8 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0016 others(5): Show |
8 | HG01515.hp1 HG01517.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.78+389G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30654004 | |||||||
| chrX:30654069 | C | T | 1 | a0001c0001t0005g0197 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.78+454C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30654069 | |||||||
| chrX:30654390 | T | A | 1 | a0001c0001t0001g0021 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.78+775T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30654390 | |||||||
| chrX:30654610 | T | A | 1 | a0001c0001t0001g0022 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.78+995T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30654610 | |||||||
| chrX:30654624 | G | A | 1 | a0001c0001t0004g0023 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.78+1009G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30654624 | |||||||
| chrX:30654703 | A | T | 1 | a0001c0001t0002g0270 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.78+1088A>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30654703 | |||||||
| chrX:30654983 | T | C | 1 | a0001c0001t0001g0024 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.78+1368T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30654983 | |||||||
| chrX:30655253 | G | A | 3 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 |
3 | HG02109.hp1 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.78+1638G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30655253 | |||||||
| chrX:30655374 | A | G | 2 | a0001c0001t0001g0196 a0001c0001t0001g0269 |
2 | HG03490.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.78+1759A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30655374 | |||||||
| chrX:30655400 | A | AG | 13 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0024 others(10): Show |
15 | HG00597.hp1 HG01346.hp1 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.78+1790dupG | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30655400 | ||||||
| chrX:30655752 | A | G | 28 | a0001c0001t0002g0181 a0001c0001t0003g0014 a0001c0001t0003g0015 others(25): Show |
28 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.78+2137A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30655752 | |||||||
| chrX:30655981 | A | G | 1 | a0001c0003t0003g0168 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.78+2366A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30655981 | |||||||
| chrX:30656003 | A | G | 1 | a0001c0001t0002g0266 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.78+2388A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30656003 | |||||||
| chrX:30656143 | A | G | 91 | a0001c0001t0002g0121 a0001c0001t0002g0156 a0001c0001t0002g0167 others(88): Show |
95 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.78+2528A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30656143 | |||||||
| chrX:30656335 | A | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0110 |
3 | HG02647.hp1 HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.78+2720A>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30656335 | |||||||
| chrX:30656526 | G | A | 1 | a0001c0001t0010g0111 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.78+2911G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30656526 | |||||||
| chrX:30656543 | T | C | 1 | a0001c0001t0002g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.78+2928T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30656543 | |||||||
| chrX:30656587 | G | A | 1 | a0001c0001t0004g0169 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.78+2972G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30656587 | |||||||
| chrX:30656606 | C | G | 1 | a0001c0001t0005g0197 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.78+2991C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30656606 | |||||||
| chrX:30656606 | C | T | 4 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.78+2991C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30656606 | |||||||
| chrX:30656607 | C | G | 1 | a0001c0001t0002g0167 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.78+2992C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30656607 | |||||||
| chrX:30656895 | G | T | 1 | a0001c0001t0012g0183 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.78+3280G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30656895 | |||||||
| chrX:30657129 | G | T | 1 | a0001c0001t0014g0263 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.78+3514G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30657129 | |||||||
| chrX:30657268 | T | C | 1 | a0001c0004t0015g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.78+3653T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30657268 | |||||||
| chrX:30657308 | T | A | 1 | a0001c0001t0005g0029 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.78+3693T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30657308 | |||||||
| chrX:30657417 | A | T | 2 | a0001c0001t0002g0181 a0001c0001t0004g0182 |
2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.78+3802A>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30657417 | |||||||
| chrX:30657676 | G | T | 1 | a0001c0001t0004g0180 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.78+4061G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30657676 | |||||||
| chrX:30657908 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.78+4293A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30657908 | |||||||
| chrX:30657972 | T | C | 1 | a0001c0001t0011g0030 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.78+4357T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30657972 | |||||||
| chrX:30658051 | C | T | 13 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0005g0029 others(10): Show |
13 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.78+4436C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30658051 | |||||||
| chrX:30658325 | T | C | 1 | a0001c0001t0004g0170 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.78+4710T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30658325 | |||||||
| chrX:30658396 | C | A | 4 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.78+4781C>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30658396 | |||||||
| chrX:30658402 | G | A | 7 | a0001c0001t0004g0170 a0001c0001t0004g0172 a0001c0001t0004g0173 others(4): Show |
7 | HG02055.hp1 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.78+4787G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30658402 | |||||||
| chrX:30658507 | G | A | 56 | a0001c0001t0002g0121 a0001c0001t0002g0156 a0001c0001t0003g0002 others(53): Show |
60 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.78+4892G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30658507 | |||||||
| chrX:30658541 | ATCCTGAC others(1424): Show |
A | 1 | a0001c0001t0002g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.78+4938_79-5528del | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30658541 | ||||||
| chrX:30658697 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.78+5082G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30658697 | |||||||
| chrX:30658791 | T | C | 1 | a0001c0001t0001g0069 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.78+5176T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30658791 | |||||||
| chrX:30658903 | T | C | 1 | a0001c0001t0004g0023 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.78+5288T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30658903 | |||||||
| chrX:30659034 | C | T | 4 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.78+5419C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30659034 | |||||||
| chrX:30659069 | T | A | 1 | a0001c0001t0002g0070 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.78+5454T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30659069 | |||||||
| chrX:30659554 | A | G | 1 | a0001c0002t0017g0184 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.78+5939A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30659554 | |||||||
| chrX:30659570 | G | C | 1 | a0001c0004t0015g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.79-5941G>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30659570 | |||||||
| chrX:30659615 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.79-5896G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30659615 | |||||||
| chrX:30659686 | G | A | 2 | a0001c0001t0002g0181 a0001c0001t0004g0182 |
2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.79-5825G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30659686 | |||||||
| chrX:30659705 | C | T | 1 | a0001c0004t0015g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.79-5806C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30659705 | |||||||
| chrX:30659897 | C | G | 2 | a0001c0001t0002g0200 a0001c0001t0002g0201 |
2 | HG02015.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.79-5614C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30659897 | |||||||
| chrX:30659899 | C | G | 2 | a0001c0001t0002g0200 a0001c0001t0002g0201 |
2 | HG02015.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.79-5612C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30659899 | |||||||
| chrX:30660136 | C | T | 3 | a0001c0001t0004g0169 a0001c0001t0004g0178 a0001c0001t0004g0179 |
3 | HG02451.hp1 HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.79-5375C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30660136 | |||||||
| chrX:30660198 | G | GTAA | 5 | a0001c0001t0002g0094 a0001c0001t0002g0095 a0001c0001t0002g0096 others(2): Show |
5 | HG01243.hp1 HG02293.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.79-5291_79-5289dup others(3): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30660198 | ||||||
| chrX:30660198 | GTAA | G | 55 | a0001c0001t0002g0121 a0001c0001t0002g0156 a0001c0001t0003g0002 others(52): Show |
59 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.79-5291_79-5289del others(3): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30660198 | ||||||
| chrX:30660252 | T | C | 3 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 |
4 | HG02970.hp2 HG03540.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-5259T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30660252 | |||||||
| chrX:30660461 | A | C | 4 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-5050A>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30660461 | |||||||
| chrX:30660792 | A | AT | 13 | a0001c0001t0002g0262 a0001c0001t0003g0015 a0001c0001t0003g0016 others(10): Show |
13 | HG01515.hp1 HG01517.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.79-4707dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30660792 | ||||||
| chrX:30660792 | AT | A | 9 | a0001c0001t0001g0033 a0001c0001t0002g0199 a0001c0001t0004g0169 others(6): Show |
9 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.79-4707delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30660792 | ||||||
| chrX:30660812 | C | CT | 7 | a0001c0001t0001g0093 a0001c0001t0001g0195 a0001c0001t0002g0259 others(4): Show |
7 | HG01346.hp2 HG02148.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.79-4682dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30660812 | ||||||
| chrX:30660812 | CT | C | 90 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0002g0121 others(87): Show |
94 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.79-4682delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30660812 | ||||||
| chrX:30660844 | C | T | 1 | a0001c0001t0013g0108 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.79-4667C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30660844 | |||||||
| chrX:30660869 | G | A | 3 | a0001c0001t0004g0169 a0001c0001t0004g0178 a0001c0001t0004g0179 |
3 | HG02451.hp1 HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.79-4642G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30660869 | |||||||
| chrX:30661012 | C | T | 12 | a0001c0001t0005g0029 a0001c0001t0005g0101 a0001c0001t0005g0102 others(9): Show |
12 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.79-4499C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30661012 | |||||||
| chrX:30661079 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.79-4432T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30661079 | |||||||
| chrX:30661087 | T | C | 88 | a0001c0001t0002g0121 a0001c0001t0002g0156 a0001c0001t0002g0181 others(85): Show |
92 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.79-4424T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30661087 | |||||||
| chrX:30661511 | TCAA | T | 58 | a0001c0001t0002g0121 a0001c0001t0002g0156 a0001c0001t0003g0002 others(55): Show |
62 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.79-3996_79-3994del others(3): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30661511 | ||||||
| chrX:30661789 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.79-3722C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30661789 | |||||||
| chrX:30661971 | T | C | 4 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-3540T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30661971 | |||||||
| chrX:30662111 | A | G | 1 | a0001c0001t0002g0092 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.79-3400A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662111 | |||||||
| chrX:30662163 | C | CCAGATTT | 194 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(191): Show |
207 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.79-3346_79-3345ins others(7): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662163 | ||||||
| chrX:30662431 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.79-3080G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662431 | |||||||
| chrX:30662695 | C | T | 2 | a0001c0001t0010g0111 a0001c0001t0010g0164 |
2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.79-2816C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662695 | |||||||
| chrX:30662703 | T | C | 2 | a0001c0001t0010g0111 a0001c0001t0010g0164 |
2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.79-2808T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662703 | |||||||
| chrX:30662707 | C | T | 2 | a0001c0001t0010g0111 a0001c0001t0010g0164 |
2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.79-2804C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662707 | |||||||
| chrX:30662709 | T | C | 2 | a0001c0001t0010g0111 a0001c0001t0010g0164 |
2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.79-2802T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662709 | |||||||
| chrX:30662709 | T | TTTTC | 47 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(44): Show |
54 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.79-2777_79-2774dup others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662709 | ||||||
| chrX:30662709 | T | TTTTCTTT others(1): Show |
9 | a0001c0001t0001g0021 a0001c0001t0001g0086 a0001c0001t0001g0087 others(6): Show |
9 | HG00544.hp1 HG01175.hp1 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.79-2781_79-2774dup others(8): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662709 | ||||||
| chrX:30662709 | T | TTTTCTTT others(9): Show |
1 | a0001c0001t0001g0091 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.79-2789_79-2774dup others(16): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662709 | ||||||
| chrX:30662709 | TTTTC | T | 7 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0204 others(4): Show |
7 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.79-2777_79-2774del others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662709 | ||||||
| chrX:30662711 | T | C | 2 | a0001c0001t0010g0111 a0001c0001t0010g0164 |
2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.79-2800T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662711 | |||||||
| chrX:30662713 | C | T | 2 | a0001c0001t0010g0111 a0001c0001t0010g0164 |
2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.79-2798C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662713 | |||||||
| chrX:30662738 | C | T | 3 | a0001c0001t0001g0057 a0001c0001t0004g0170 a0001c0001t0008g0165 |
3 | HG02622.hp1 HG02809.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.79-2773C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662738 | |||||||
| chrX:30662742 | T | C | 3 | a0001c0001t0001g0057 a0001c0001t0004g0170 a0001c0001t0008g0165 |
3 | HG02622.hp1 HG02809.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.79-2769T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662742 | |||||||
| chrX:30662746 | TTTCC | T | 82 | a0001c0001t0002g0121 a0001c0001t0002g0156 a0001c0001t0002g0181 others(79): Show |
86 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.79-2745_79-2742del others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662746 | ||||||
| chrX:30662750 | C | T | 3 | a0001c0001t0001g0057 a0001c0001t0004g0170 a0001c0001t0008g0165 |
3 | HG02622.hp1 HG02809.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.79-2761C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662750 | |||||||
| chrX:30662767 | T | TTC | 12 | a0001c0001t0005g0029 a0001c0001t0005g0105 a0001c0001t0005g0107 others(9): Show |
12 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.79-2724_79-2723dup others(2): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662767 | ||||||
| chrX:30662767 | TTC | T | 12 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0002g0028 others(9): Show |
12 | HG01243.hp1 HG01884.hp1 HG02293.hp1 others(9): Show |
intron_variant | MODIFIER | c.79-2724_79-2723del others(2): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662767 | ||||||
| chrX:30662767 | TTCTC | T | 3 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0014g0263 |
3 | HG02015.hp1 HG03704.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.79-2726_79-2723del others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662767 | ||||||
| chrX:30662789 | T | C | 2 | a0001c0001t0004g0169 a0001c0001t0004g0178 |
2 | HG02451.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.79-2722T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662789 | |||||||
| chrX:30662792 | T | C | 1 | a0001c0001t0004g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.79-2719T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662792 | |||||||
| chrX:30662808 | C | T | 1 | a0001c0004t0015g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.79-2703C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662808 | |||||||
| chrX:30662809 | T | C | 1 | a0001c0004t0015g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.79-2702T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662809 | |||||||
| chrX:30662809 | T | TTC | 4 | a0001c0001t0002g0208 a0001c0001t0002g0258 a0001c0001t0002g0260 others(1): Show |
4 | HG00408.hp2 HG01433.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-2678_79-2677dup others(2): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662809 | ||||||
| chrX:30662809 | T | TTCTCTCT others(3): Show |
1 | a0001c0002t0006g0186 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.79-2686_79-2677dup others(10): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662809 | ||||||
| chrX:30662809 | TTC | T | 3 | a0001c0001t0003g0014 a0001c0001t0003g0017 a0001c0001t0003g0019 |
3 | HG01515.hp1 HG01517.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.79-2678_79-2677del others(2): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662809 | ||||||
| chrX:30662825 | CTCTCTCT others(35): Show |
C | 1 | a0001c0001t0012g0183 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.79-2680_79-2639del others(42): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662825 | ||||||
| chrX:30662827 | C | T | 1 | a0001c0004t0015g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.79-2684C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662827 | |||||||
| chrX:30662829 | CTCTCTTT others(3): Show |
C | 2 | a0001c0001t0003g0015 a0001c0001t0003g0016 |
2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.79-2678_79-2669del others(10): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662829 | ||||||
| chrX:30662829 | CTCTCTTT others(7): Show |
C | 1 | a0001c0001t0004g0182 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.79-2678_79-2665del others(14): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662829 | ||||||
| chrX:30662829 | CTCTCTTT others(11): Show |
C | 4 | a0001c0001t0003g0018 a0001c0001t0003g0130 a0001c0001t0003g0136 others(1): Show |
4 | HG01361.hp1 HG03195.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-2678_79-2661del others(18): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662829 | ||||||
| chrX:30662829 | CTCTCTTT others(19): Show |
C | 1 | a0001c0001t0001g0057 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.79-2678_79-2653del others(26): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662829 | ||||||
| chrX:30662829 | CTCTCTTT others(31): Show |
C | 1 | a0001c0001t0010g0164 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.79-2654_79-2617del others(38): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662829 | ||||||
| chrX:30662831 | C | CTCTCTCT others(4): Show |
1 | a0001c0001t0001g0204 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.79-2677_79-2676ins others(11): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662831 | ||||||
| chrX:30662831 | C | CTCTTCTT | 3 | a0001c0001t0002g0012 a0001c0001t0002g0243 a0001c0001t0002g0256 |
3 | HG02027.hp1 HG02129.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.79-2676_79-2675ins others(7): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662831 | ||||||
| chrX:30662831 | C | T | 4 | a0001c0001t0001g0041 a0001c0001t0002g0167 a0001c0001t0010g0111 others(1): Show |
4 | HG01884.hp1 HG01884.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-2680C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662831 | |||||||
| chrX:30662833 | CTTTCTT | C | 4 | a0001c0001t0002g0028 a0001c0001t0003g0122 a0001c0001t0003g0132 others(1): Show |
4 | HG00609.hp1 HG01106.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-2676_79-2671del others(6): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662833 | ||||||
| chrX:30662833 | CTTTCTTT others(3): Show |
C | 4 | a0001c0001t0003g0129 a0001c0001t0003g0140 a0001c0001t0003g0157 others(1): Show |
4 | HG01192.hp1 HG01496.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-2676_79-2667del others(10): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662833 | ||||||
| chrX:30662833 | CTTTCTTT others(7): Show |
C | 35 | a0001c0001t0001g0025 a0001c0001t0002g0156 a0001c0001t0003g0002 others(32): Show |
38 | HG00408.hp1 HG00621.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.79-2676_79-2663del others(14): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662833 | ||||||
| chrX:30662833 | CTTTCTTT others(11): Show |
C | 8 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0040 others(5): Show |
8 | HG01074.hp1 HG01175.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.79-2676_79-2659del others(18): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662833 | ||||||
| chrX:30662833 | CTTTCTTT others(15): Show |
C | 12 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0045 others(9): Show |
12 | HG01167.hp1 HG01358.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.79-2676_79-2655del others(22): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662833 | ||||||
| chrX:30662833 | CTTTCTTT others(19): Show |
C | 4 | a0001c0001t0004g0172 a0001c0001t0004g0174 a0001c0001t0005g0029 others(1): Show |
4 | HG02886.hp2 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-2676_79-2651del others(26): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662833 | ||||||
| chrX:30662835 | T | C | 97 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(94): Show |
104 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(101): Show |
intron_variant | MODIFIER | c.79-2676T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662835 | |||||||
| chrX:30662839 | T | C | 3 | a0001c0001t0001g0027 a0001c0001t0005g0105 a0001c0001t0011g0030 |
3 | HG02615.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.79-2672T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662839 | |||||||
| chrX:30662839 | TTCTTTCT others(23): Show |
T | 5 | a0001c0001t0001g0041 a0001c0001t0001g0189 a0001c0001t0004g0169 others(2): Show |
5 | HG00597.hp1 HG02451.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.79-2646_79-2617del others(30): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662839 | ||||||
| chrX:30662842 | T | C | 1 | a0001c0004t0015g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.79-2669T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662842 | |||||||
| chrX:30662843 | TTCTTTCT others(19): Show |
T | 11 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0051 others(8): Show |
11 | HG02280.hp2 HG02451.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.79-2642_79-2617del others(26): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662843 | ||||||
| chrX:30662847 | T | C | 1 | a0001c0001t0003g0140 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.79-2664T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662847 | |||||||
| chrX:30662847 | TTCTTTCT others(15): Show |
T | 71 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(68): Show |
77 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.79-2640_79-2619del others(22): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662847 | ||||||
| chrX:30662851 | T | C | 1 | a0001c0001t0001g0025 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.79-2660T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662851 | |||||||
| chrX:30662851 | TTCTTTCT others(11): Show |
T | 10 | a0001c0001t0002g0094 a0001c0001t0002g0167 a0001c0001t0002g0225 others(7): Show |
10 | HG00099.hp2 HG01884.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.79-2640_79-2623del others(18): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662851 | ||||||
| chrX:30662855 | T | C | 2 | a0001c0001t0001g0004 a0001c0001t0001g0040 |
2 | HG03834.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.79-2656T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662855 | |||||||
| chrX:30662855 | TTCTTTCT others(7): Show |
T | 17 | a0001c0001t0001g0027 a0001c0001t0002g0056 a0001c0001t0002g0095 others(14): Show |
17 | HG00558.hp1 HG00642.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.79-2640_79-2627del others(14): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662855 | ||||||
| chrX:30662859 | T | C | 1 | a0001c0001t0001g0061 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.79-2652T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662859 | |||||||
| chrX:30662859 | TTCTTTCT others(3): Show |
T | 2 | a0001c0001t0001g0217 a0001c0001t0003g0020 |
2 | HG02280.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.79-2640_79-2631del others(10): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662859 | ||||||
| chrX:30662863 | TTCTTTC | T | 8 | a0001c0001t0002g0201 a0001c0001t0002g0214 a0001c0001t0002g0215 others(5): Show |
8 | HG01496.hp2 HG01891.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.79-2640_79-2635del others(6): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662863 | ||||||
| chrX:30662867 | TTC | T | 100 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0025 others(97): Show |
103 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.79-2640_79-2639del others(2): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662867 | ||||||
| chrX:30662869 | C | CTT | 23 | a0001c0001t0001g0204 a0001c0001t0002g0012 a0001c0001t0002g0202 others(20): Show |
24 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(21): Show |
intron_variant | MODIFIER | c.79-2641_79-2640ins others(2): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662869 | ||||||
| chrX:30662869 | C | CTTTCTT | 13 | a0001c0001t0002g0011 a0001c0001t0002g0203 a0001c0001t0002g0234 others(10): Show |
14 | HG00544.hp2 HG00597.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.79-2641_79-2640ins others(6): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662869 | ||||||
| chrX:30662869 | C | CTTTCTTT others(3): Show |
7 | a0001c0001t0002g0229 a0001c0001t0002g0230 a0001c0001t0002g0231 others(4): Show |
7 | HG00741.hp1 HG02040.hp1 HG03927.hp2 others(4): Show |
intron_variant | MODIFIER | c.79-2641_79-2640ins others(10): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662869 | ||||||
| chrX:30662869 | C | CTTTCTTT others(7): Show |
1 | a0001c0002t0006g0187 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.79-2641_79-2640ins others(14): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662869 | ||||||
| chrX:30662869 | C | CTTTCTTT others(11): Show |
2 | a0001c0001t0002g0227 a0001c0001t0002g0228 |
2 | NA18988.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.79-2641_79-2640ins others(18): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662869 | ||||||
| chrX:30662869 | C | CTTTCTTT others(91): Show |
1 | a0001c0004t0015g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.79-2641_79-2640ins others(98): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662869 | ||||||
| chrX:30662869 | C | T | 1 | a0001c0001t0010g0164 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.79-2642C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662869 | |||||||
| chrX:30662944 | G | A | 4 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-2567G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662944 | |||||||
| chrX:30663023 | C | T | 11 | a0001c0001t0005g0029 a0001c0001t0005g0101 a0001c0001t0005g0102 others(8): Show |
11 | HG01891.hp2 HG02109.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.79-2488C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30663023 | |||||||
| chrX:30663255 | CA | C | 6 | a0001c0001t0002g0056 a0001c0001t0002g0094 a0001c0001t0002g0095 others(3): Show |
6 | HG01243.hp1 HG02293.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.79-2255delA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30663255 | |||||||
| chrX:30663374 | T | C | 1 | a0001c0001t0001g0040 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.79-2137T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30663374 | |||||||
| chrX:30663384 | G | A | 1 | a0001c0001t0002g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.79-2127G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30663384 | |||||||
| chrX:30663525 | G | C | 1 | a0001c0001t0002g0205 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.79-1986G>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30663525 | |||||||
| chrX:30663579 | G | A | 1 | a0001c0001t0002g0092 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.79-1932G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30663579 | |||||||
| chrX:30663591 | A | G | 1 | a0001c0001t0001g0055 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.79-1920A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30663591 | |||||||
| chrX:30663923 | G | GCT | 4 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-1575_79-1574dup others(2): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30663923 | ||||||
| chrX:30663964 | T | TATATATA others(29): Show |
79 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(76): Show |
85 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.79-1517_79-1516ins others(36): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30663964 | ||||||
| chrX:30663964 | T | TATATATA others(65): Show |
2 | a0001c0001t0005g0101 a0001c0001t0005g0102 |
2 | HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.79-1517_79-1516ins others(72): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30663964 | ||||||
| chrX:30663964 | T | TATATATA others(65): Show |
7 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0033 others(4): Show |
9 | HG01934.hp1 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.79-1517_79-1516ins others(72): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30663964 | ||||||
| chrX:30663964 | T | TATATATA others(171): Show |
1 | a0001c0001t0002g0092 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.79-1480_79-1479ins others(178): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30663964 | ||||||
| chrX:30663964 | T | TATATATA others(65): Show |
1 | a0001c0001t0002g0056 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.79-1458_79-1387dup others(72): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30663964 | ||||||
| chrX:30663964 | T | TATATATA others(278): Show |
1 | a0001c0001t0002g0206 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.79-1444_79-1443ins others(285): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30663964 | ||||||
| chrX:30663964 | T | TATATATA others(207): Show |
5 | a0001c0001t0002g0203 a0001c0001t0002g0205 a0001c0001t0002g0207 others(2): Show |
5 | HG01346.hp2 HG02004.hp1 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.79-1444_79-1443ins others(214): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30663964 | ||||||
| chrX:30663964 | T | TATATATA others(243): Show |
45 | a0001c0001t0001g0217 a0001c0001t0002g0011 a0001c0001t0002g0012 others(42): Show |
47 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.79-1444_79-1443ins others(250): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30663964 | ||||||
| chrX:30663964 | T | TATATATA others(279): Show |
16 | a0001c0001t0001g0204 a0001c0001t0002g0199 a0001c0001t0002g0221 others(13): Show |
16 | HG00099.hp1 HG00423.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.79-1444_79-1443ins others(286): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30663964 | ||||||
| chrX:30663964 | T | TATATATA others(208): Show |
1 | a0001c0001t0002g0233 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.79-1444_79-1443ins others(215): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30663964 | ||||||
| chrX:30663964 | T | TATATATA others(101): Show |
1 | a0001c0001t0002g0167 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.79-1494_79-1387dup others(108): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30663964 | ||||||
| chrX:30663964 | T | TATATATA others(278): Show |
2 | a0001c0001t0002g0264 a0001c0001t0002g0265 |
2 | HG01123.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.79-1408_79-1407ins others(285): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30663964 | ||||||
| chrX:30663964 | T | TATATATA others(279): Show |
1 | a0001c0001t0002g0225 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.79-1408_79-1407ins others(286): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30663964 | ||||||
| chrX:30663964 | T | TATATATA others(137): Show |
2 | a0001c0001t0002g0094 a0001c0001t0002g0095 |
2 | HG02293.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.79-1530_79-1387dup others(144): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30663964 | ||||||
| chrX:30663964 | T | TATATATA others(173): Show |
1 | a0001c0001t0002g0096 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.79-1387_79-1386ins others(180): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30663964 | ||||||
| chrX:30663964 | T | TATATATA others(209): Show |
2 | a0001c0001t0002g0097 a0001c0001t0002g0098 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.79-1387_79-1386ins others(216): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30663964 | ||||||
| chrX:30663964 | T | TATATATT others(29): Show |
1 | a0001c0001t0001g0006 | 2 | HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.79-1541_79-1540ins others(36): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30663964 | ||||||
| chrX:30663982 | A | C | 4 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-1529A>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30663982 | |||||||
| chrX:30663995 | T | G | 13 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(10): Show |
13 | HG02109.hp1 HG02109.hp2 HG02148.hp1 others(10): Show |
intron_variant | MODIFIER | c.79-1516T>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30663995 | |||||||
| chrX:30664000 | G | GATATATA others(86): Show |
1 | a0001c0001t0011g0030 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.79-1445_79-1444ins others(93): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664000 | ||||||
| chrX:30664015 | T | G | 1 | a0001c0003t0003g0168 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.79-1496T>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30664015 | |||||||
| chrX:30664028 | AT | A | 15 | a0001c0001t0002g0181 a0001c0001t0003g0014 a0001c0001t0003g0015 others(12): Show |
15 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.79-1479delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664028 | ||||||
| chrX:30664031 | T | TTATAGAT others(183): Show |
1 | a0001c0001t0002g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.79-1444_79-1443ins others(190): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664031 | ||||||
| chrX:30664053 | T | TATCTATA others(278): Show |
1 | a0001c0001t0014g0263 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.79-1444_79-1443ins others(285): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664053 | ||||||
| chrX:30664064 | ATTTTATA others(30): Show |
A | 1 | a0001c0001t0003g0036 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.79-1443_79-1407del others(37): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664064 | ||||||
| chrX:30664065 | T | TTTTATAG others(28): Show |
7 | a0001c0001t0005g0105 a0001c0001t0005g0197 a0001c0001t0007g0103 others(4): Show |
7 | HG01891.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.79-1442_79-1408dup others(35): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664065 | ||||||
| chrX:30664089 | T | G | 9 | a0001c0001t0001g0204 a0001c0001t0002g0206 a0001c0001t0002g0221 others(6): Show |
9 | HG01070.hp2 HG01071.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.79-1422T>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30664089 | |||||||
| chrX:30664089 | TATCTATA others(29): Show |
T | 4 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-1383_79-1348del others(36): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664089 | ||||||
| chrX:30664090 | A | G | 1 | a0001c0001t0003g0018 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.79-1421A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30664090 | |||||||
| chrX:30664100 | AT | A | 68 | a0001c0001t0002g0121 a0001c0001t0002g0156 a0001c0001t0003g0002 others(65): Show |
72 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.79-1407delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664100 | ||||||
| chrX:30664101 | T | TTTATAGA others(27): Show |
1 | a0001c0001t0003g0176 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.79-1408_79-1407ins others(34): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664101 | ||||||
| chrX:30664101 | T | TTTATAGA others(63): Show |
1 | a0001c0001t0004g0180 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.79-1408_79-1407ins others(70): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664101 | ||||||
| chrX:30664101 | T | TTTTATAG others(28): Show |
10 | a0001c0001t0002g0181 a0001c0001t0003g0014 a0001c0001t0003g0015 others(7): Show |
10 | HG01515.hp1 HG01517.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.79-1387_79-1386ins others(35): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664101 | ||||||
| chrX:30664101 | T | TTTTATAG others(64): Show |
1 | a0001c0001t0003g0159 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.79-1387_79-1386ins others(71): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664101 | ||||||
| chrX:30664103 | T | TTATAGAT others(173): Show |
1 | a0001c0001t0001g0025 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.79-1387_79-1386ins others(180): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664103 | ||||||
| chrX:30664103 | T | TTATAGAT others(137): Show |
2 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
2 | HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.79-1387_79-1386ins others(144): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664103 | ||||||
| chrX:30664108 | G | GATATATA others(29): Show |
1 | a0001c0001t0005g0029 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.79-1387_79-1386ins others(36): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664108 | ||||||
| chrX:30664111 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.79-1400A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30664111 | |||||||
| chrX:30664119 | T | TATATATA others(28): Show |
1 | a0001c0001t0004g0013 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.79-1387_79-1386ins others(35): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664119 | ||||||
| chrX:30664125 | G | GATATATA others(28): Show |
1 | a0001c0001t0003g0020 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.79-1384_79-1383ins others(35): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664125 | ||||||
| chrX:30664125 | G | T | 204 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(201): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.79-1386G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30664125 | |||||||
| chrX:30664128 | C | A | 1 | a0001c0004t0015g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.79-1383C>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30664128 | |||||||
| chrX:30664702 | C | CT | 55 | a0001c0001t0002g0121 a0001c0001t0002g0167 a0001c0001t0002g0206 others(52): Show |
58 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.79-787dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664702 | ||||||
| chrX:30664702 | C | CTT | 30 | a0001c0001t0002g0156 a0001c0001t0002g0232 a0001c0001t0003g0008 others(27): Show |
31 | HG00609.hp1 HG00642.hp1 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.79-788_79-787dupTT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664702 | ||||||
| chrX:30664702 | CT | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(82): Show |
94 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.79-787delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664702 | ||||||
| chrX:30664860 | C | T | 1 | a0001c0001t0002g0214 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.79-651C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30664860 | |||||||
| chrX:30665035 | G | A | 3 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 |
3 | HG02109.hp1 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.79-476G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30665035 | |||||||
| chrX:30665071 | C | T | 11 | a0001c0001t0005g0029 a0001c0001t0005g0101 a0001c0001t0005g0102 others(8): Show |
11 | HG01891.hp2 HG02109.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.79-440C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30665071 | |||||||
| chrX:30665337 | T | A | 1 | a0001c0001t0002g0229 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.79-174T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30665337 | |||||||
| chrX:30665613 | C | T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 |
3 | HG02109.hp1 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.152+29C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 2/20 | chrX | 30665613 | |||||||
| chrX:30665620 | T | C | 2 | a0001c0001t0003g0116 a0001c0001t0003g0141 |
2 | NA18983.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.152+36T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 2/20 | chrX | 30665620 | |||||||
| chrX:30665681 | A | G | 1 | a0001c0001t0005g0029 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.152+97A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 2/20 | chrX | 30665681 | |||||||
| chrX:30665833 | G | C | 8 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0016 others(5): Show |
8 | HG01515.hp1 HG01517.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.152+249G>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 2/20 | chrX | 30665833 | |||||||
| chrX:30666178 | G | A | 1 | a0001c0001t0005g0107 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.152+594G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 2/20 | chrX | 30666178 | |||||||
| chrX:30666191 | A | G | 10 | a0001c0001t0002g0214 a0001c0001t0002g0227 a0001c0001t0002g0232 others(7): Show |
10 | HG00597.hp2 NA18612.hp1 NA18940.hp1 others(7): Show |
intron_variant | MODIFIER | c.152+607A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 2/20 | chrX | 30666191 | |||||||
| chrX:30666222 | G | A | 1 | a0001c0001t0005g0197 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.152+638G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 2/20 | chrX | 30666222 | |||||||
| chrX:30666325 | C | T | 1 | a0001c0001t0002g0092 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.152+741C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 2/20 | chrX | 30666325 | |||||||
| chrX:30666593 | C | T | 6 | a0001c0001t0002g0056 a0001c0001t0002g0094 a0001c0001t0002g0095 others(3): Show |
6 | HG01243.hp1 HG02293.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.152+1009C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 2/20 | chrX | 30666593 | |||||||
| chrX:30666654 | T | C | 61 | a0001c0001t0002g0121 a0001c0001t0002g0156 a0001c0001t0002g0264 others(58): Show |
65 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.152+1070T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 2/20 | chrX | 30666654 | |||||||
| chrX:30666970 | T | C | 2 | a0001c0001t0002g0264 a0001c0001t0002g0265 |
2 | HG01123.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.153-1042T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 2/20 | chrX | 30666970 | |||||||
| chrX:30667029 | C | T | 4 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-983C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 2/20 | chrX | 30667029 | |||||||
| chrX:30667108 | T | C | 2 | a0001c0001t0003g0142 a0001c0001t0003g0143 |
2 | NA18993.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.153-904T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 2/20 | chrX | 30667108 | |||||||
| chrX:30667118 | C | T | 2 | a0001c0001t0005g0197 a0001c0001t0013g0108 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.153-894C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 2/20 | chrX | 30667118 | |||||||
| chrX:30667238 | C | G | 1 | a0001c0001t0001g0090 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.153-774C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 2/20 | chrX | 30667238 | |||||||
| chrX:30667402 | C | T | 4 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-610C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 2/20 | chrX | 30667402 | |||||||
| chrX:30667709 | G | A | 4 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-303G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 2/20 | chrX | 30667709 | |||||||
| chrX:30667920 | A | C | 6 | a0001c0001t0002g0056 a0001c0001t0002g0094 a0001c0001t0002g0095 others(3): Show |
6 | HG01243.hp1 HG02293.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.153-92A>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 2/20 | chrX | 30667920 | |||||||
| chrX:30668607 | A | G | 63 | a0001c0001t0001g0085 a0001c0001t0002g0121 a0001c0001t0002g0156 others(60): Show |
67 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.259+489A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30668607 | |||||||
| chrX:30668903 | G | T | 11 | a0001c0001t0005g0029 a0001c0001t0005g0101 a0001c0001t0005g0102 others(8): Show |
11 | HG01891.hp2 HG02109.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.259+785G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30668903 | |||||||
| chrX:30668942 | G | A | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | HG02683.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.259+824G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30668942 | |||||||
| chrX:30669071 | T | G | 1 | a0001c0004t0015g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.259+953T>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30669071 | |||||||
| chrX:30669176 | C | T | 2 | a0001c0001t0003g0116 a0001c0001t0003g0141 |
2 | NA18983.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.259+1058C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30669176 | |||||||
| chrX:30669183 | G | GT | 24 | a0001c0001t0001g0051 a0001c0001t0001g0091 a0001c0001t0002g0251 others(21): Show |
24 | HG00423.hp2 HG00738.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.259+1081dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30669183 | ||||||
| chrX:30669340 | G | T | 1 | a0001c0001t0003g0020 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.259+1222G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30669340 | |||||||
| chrX:30669364 | T | C | 2 | a0001c0001t0003g0015 a0001c0001t0003g0016 |
2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.259+1246T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30669364 | |||||||
| chrX:30669393 | A | C | 1 | a0001c0001t0001g0050 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.259+1275A>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30669393 | |||||||
| chrX:30669404 | G | A | 1 | a0001c0001t0003g0117 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.259+1286G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30669404 | |||||||
| chrX:30669472 | G | A | 85 | a0001c0001t0002g0121 a0001c0001t0002g0156 a0001c0001t0002g0167 others(82): Show |
89 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.259+1354G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30669472 | |||||||
| chrX:30669710 | G | T | 11 | a0001c0001t0005g0029 a0001c0001t0005g0101 a0001c0001t0005g0102 others(8): Show |
11 | HG01891.hp2 HG02109.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.259+1592G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30669710 | |||||||
| chrX:30669751 | G | A | 1 | a0001c0001t0002g0216 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.259+1633G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30669751 | |||||||
| chrX:30669859 | G | A | 1 | a0001c0001t0002g0227 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.259+1741G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30669859 | |||||||
| chrX:30670115 | C | A | 3 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 |
3 | HG02109.hp1 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.259+1997C>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30670115 | |||||||
| chrX:30670451 | G | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
95 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.259+2333G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30670451 | |||||||
| chrX:30670598 | AT | A | 13 | a0001c0001t0002g0181 a0001c0001t0003g0014 a0001c0001t0003g0015 others(10): Show |
13 | HG01515.hp1 HG01517.hp2 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.259+2491delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30670598 | ||||||
| chrX:30670598 | ATT | A | 56 | a0001c0001t0002g0121 a0001c0001t0002g0156 a0001c0001t0003g0002 others(53): Show |
60 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.259+2490_259+2491d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30670598 | ||||||
| chrX:30670850 | G | A | 3 | a0001c0001t0004g0169 a0001c0001t0004g0178 a0001c0001t0004g0179 |
3 | HG02451.hp1 HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.259+2732G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30670850 | |||||||
| chrX:30670968 | A | G | 211 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(208): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.259+2850A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30670968 | |||||||
| chrX:30671008 | C | T | 1 | a0001c0001t0002g0249 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.259+2890C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30671008 | |||||||
| chrX:30671135 | C | T | 2 | a0001c0001t0001g0192 a0001c0001t0001g0195 |
2 | NA18992.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.259+3017C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30671135 | |||||||
| chrX:30671160 | G | A | 8 | a0001c0001t0005g0105 a0001c0001t0005g0107 a0001c0001t0005g0197 others(5): Show |
8 | HG01891.hp2 HG02109.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.259+3042G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30671160 | |||||||
| chrX:30671291 | C | CA | 54 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0054 others(51): Show |
54 | HG00423.hp2 HG00558.hp1 HG01175.hp1 others(51): Show |
intron_variant | MODIFIER | c.259+3197dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30671291 | ||||||
| chrX:30671291 | CA | C | 15 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(12): Show |
15 | HG00741.hp1 HG01515.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.259+3197delA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30671291 | ||||||
| chrX:30671316 | C | A | 1 | a0001c0001t0001g0053 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.259+3198C>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30671316 | |||||||
| chrX:30671509 | TTTC | T | 3 | a0001c0001t0004g0169 a0001c0001t0004g0178 a0001c0001t0004g0179 |
3 | HG02451.hp1 HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.259+3394_259+3396d others(5): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30671509 | ||||||
| chrX:30671629 | T | C | 1 | a0001c0001t0002g0092 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.259+3511T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30671629 | |||||||
| chrX:30672094 | G | A | 4 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.259+3976G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30672094 | |||||||
| chrX:30672159 | C | CA | 97 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(94): Show |
106 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.259+4066dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30672159 | ||||||
| chrX:30672159 | C | CAA | 19 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(16): Show |
19 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.259+4065_259+4066d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30672159 | ||||||
| chrX:30672159 | C | CAAAA | 7 | a0001c0001t0002g0181 a0001c0001t0003g0014 a0001c0001t0003g0017 others(4): Show |
7 | HG01515.hp1 HG01517.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.259+4063_259+4066d others(6): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30672159 | ||||||
| chrX:30672159 | CA | C | 56 | a0001c0001t0002g0121 a0001c0001t0002g0156 a0001c0001t0002g0213 others(53): Show |
60 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.259+4066delA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30672159 | ||||||
| chrX:30672159 | CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0008g0106 a0001c0001t0008g0165 |
2 | HG01891.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.259+4056_259+4066d others(13): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30672159 | ||||||
| chrX:30672310 | A | G | 4 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.259+4192A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30672310 | |||||||
| chrX:30672363 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.259+4245C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30672363 | |||||||
| chrX:30672540 | G | A | 1 | a0001c0004t0015g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.259+4422G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30672540 | |||||||
| chrX:30672727 | T | G | 12 | a0001c0001t0002g0181 a0001c0001t0003g0014 a0001c0001t0003g0015 others(9): Show |
12 | HG01515.hp1 HG01517.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.259+4609T>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30672727 | |||||||
| chrX:30672753 | G | T | 1 | a0001c0001t0003g0141 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.260-4622G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30672753 | |||||||
| chrX:30672919 | T | C | 1 | a0001c0001t0001g0027 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.260-4456T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30672919 | |||||||
| chrX:30672951 | TTA | T | 6 | a0001c0001t0001g0081 a0001c0001t0001g0086 a0001c0001t0001g0088 others(3): Show |
6 | HG00323.hp1 HG01175.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.260-4420_260-4419d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30672951 | ||||||
| chrX:30672958 | T | A | 4 | a0001c0001t0002g0207 a0001c0001t0002g0224 a0001c0001t0002g0252 others(1): Show |
4 | HG00099.hp1 HG00323.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-4417T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30672958 | |||||||
| chrX:30673168 | G | C | 11 | a0001c0001t0002g0181 a0001c0001t0003g0014 a0001c0001t0003g0015 others(8): Show |
11 | HG01515.hp1 HG01517.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.260-4207G>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30673168 | |||||||
| chrX:30673199 | G | A | 1 | a0001c0001t0003g0123 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.260-4176G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30673199 | |||||||
| chrX:30673235 | C | T | 1 | a0001c0001t0012g0183 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.260-4140C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30673235 | |||||||
| chrX:30673389 | G | A | 1 | a0001c0001t0003g0124 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.260-3986G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30673389 | |||||||
| chrX:30673536 | A | G | 59 | a0001c0001t0002g0121 a0001c0001t0002g0156 a0001c0001t0002g0264 others(56): Show |
63 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.260-3839A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30673536 | |||||||
| chrX:30673621 | C | T | 85 | a0001c0001t0002g0121 a0001c0001t0002g0156 a0001c0001t0002g0167 others(82): Show |
89 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.260-3754C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30673621 | |||||||
| chrX:30673649 | T | C | 1 | a0001c0001t0004g0023 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.260-3726T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30673649 | |||||||
| chrX:30673760 | T | C | 1 | a0001c0001t0001g0033 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.260-3615T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30673760 | |||||||
| chrX:30673945 | A | G | 63 | a0001c0001t0002g0121 a0001c0001t0002g0156 a0001c0001t0002g0167 others(60): Show |
67 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.260-3430A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30673945 | |||||||
| chrX:30674077 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.260-3298T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30674077 | |||||||
| chrX:30674342 | G | A | 1 | a0001c0001t0005g0107 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.260-3033G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30674342 | |||||||
| chrX:30674681 | T | A | 4 | a0001c0001t0001g0033 a0001c0001t0002g0028 a0001c0001t0009g0118 others(1): Show |
4 | HG02080.hp2 HG02451.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-2694T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30674681 | |||||||
| chrX:30674775 | G | A | 1 | a0001c0001t0003g0125 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.260-2600G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30674775 | |||||||
| chrX:30674975 | T | A | 1 | a0001c0001t0003g0141 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.260-2400T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30674975 | |||||||
| chrX:30674976 | G | T | 1 | a0001c0001t0003g0141 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.260-2399G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30674976 | |||||||
| chrX:30674977 | T | G | 1 | a0001c0001t0003g0141 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.260-2398T>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30674977 | |||||||
| chrX:30675161 | T | C | 1 | a0001c0001t0002g0244 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.260-2214T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30675161 | |||||||
| chrX:30675198 | A | AT | 19 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0077 others(16): Show |
19 | HG00423.hp1 HG01069.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.260-2162dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30675198 | ||||||
| chrX:30675265 | G | A | 1 | a0001c0001t0004g0169 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.260-2110G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30675265 | |||||||
| chrX:30675320 | C | T | 1 | a0001c0004t0015g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.260-2055C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30675320 | |||||||
| chrX:30675341 | G | A | 4 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-2034G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30675341 | |||||||
| chrX:30675399 | G | A | 4 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-1976G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30675399 | |||||||
| chrX:30675453 | T | C | 1 | a0001c0001t0003g0141 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.260-1922T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30675453 | |||||||
| chrX:30675454 | C | T | 1 | a0001c0001t0003g0141 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.260-1921C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30675454 | |||||||
| chrX:30675519 | CT | C | 21 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(18): Show |
21 | HG00323.hp1 HG01515.hp1 HG01517.hp2 others(18): Show |
intron_variant | MODIFIER | c.260-1839delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30675519 | ||||||
| chrX:30675725 | C | T | 1 | a0001c0001t0003g0125 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.260-1650C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30675725 | |||||||
| chrX:30675816 | G | A | 12 | a0001c0001t0005g0029 a0001c0001t0005g0101 a0001c0001t0005g0102 others(9): Show |
12 | HG01891.hp2 HG02109.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.260-1559G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30675816 | |||||||
| chrX:30675880 | C | G | 5 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0190 others(2): Show |
7 | HG01934.hp1 NA18942.hp1 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.260-1495C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30675880 | |||||||
| chrX:30676082 | C | T | 59 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(56): Show |
66 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.260-1293C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30676082 | |||||||
| chrX:30676106 | A | T | 1 | a0001c0001t0011g0030 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.260-1269A>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30676106 | |||||||
| chrX:30676118 | A | G | 2 | a0001c0001t0002g0264 a0001c0001t0002g0265 |
2 | HG01123.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.260-1257A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30676118 | |||||||
| chrX:30676279 | C | T | 7 | a0001c0001t0004g0170 a0001c0001t0004g0172 a0001c0001t0004g0173 others(4): Show |
7 | HG02055.hp1 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.260-1096C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30676279 | |||||||
| chrX:30676468 | T | A | 1 | a0001c0001t0001g0099 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.260-907T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30676468 | |||||||
| chrX:30676621 | T | C | 1 | a0001c0001t0009g0118 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.260-754T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30676621 | |||||||
| chrX:30676790 | T | C | 5 | a0001c0001t0002g0056 a0001c0001t0002g0094 a0001c0001t0002g0096 others(2): Show |
5 | HG01243.hp1 HG02615.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.260-585T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30676790 | |||||||
| chrX:30676879 | A | G | 3 | a0001c0001t0003g0014 a0001c0001t0003g0017 a0001c0001t0003g0019 |
3 | HG01515.hp1 HG01517.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.260-496A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30676879 | |||||||
| chrX:30676888 | C | T | 1 | a0001c0004t0015g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.260-487C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30676888 | |||||||
| chrX:30676943 | G | GCA | 9 | a0001c0001t0002g0167 a0001c0001t0003g0014 a0001c0001t0003g0017 others(6): Show |
9 | HG01515.hp1 HG01517.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.260-413_260-412dup others(2): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30676943 | ||||||
| chrX:30676948 | C | A | 4 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-427C>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30676948 | |||||||
| chrX:30677216 | CACTCAAA others(6): Show |
C | 1 | a0001c0001t0001g0061 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.260-157_260-145del others(13): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30677216 | ||||||
| chrX:30677247 | A | T | 1 | a0001c0001t0003g0157 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.260-128A>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30677247 | |||||||
| chrX:30677648 | A | T | 1 | a0001c0001t0002g0092 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.337+196A>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30677648 | |||||||
| chrX:30677655 | T | G | 1 | a0001c0001t0003g0149 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.337+203T>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30677655 | |||||||
| chrX:30677806 | G | A | 1 | a0001c0001t0004g0178 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.337+354G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30677806 | |||||||
| chrX:30677824 | C | CA | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(192): Show |
208 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.337+385dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30677824 | ||||||
| chrX:30677844 | A | G | 5 | a0001c0001t0002g0056 a0001c0001t0002g0094 a0001c0001t0002g0096 others(2): Show |
5 | HG01243.hp1 HG02615.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.337+392A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30677844 | |||||||
| chrX:30677853 | A | G | 5 | a0001c0001t0002g0056 a0001c0001t0002g0094 a0001c0001t0002g0096 others(2): Show |
5 | HG01243.hp1 HG02615.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.337+401A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30677853 | |||||||
| chrX:30678176 | G | T | 1 | a0001c0001t0003g0177 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.337+724G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30678176 | |||||||
| chrX:30678632 | T | C | 2 | a0001c0001t0010g0111 a0001c0001t0010g0164 |
2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.337+1180T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30678632 | |||||||
| chrX:30678671 | G | GT | 28 | a0001c0001t0001g0026 a0001c0001t0001g0037 a0001c0001t0001g0038 others(25): Show |
28 | HG00323.hp1 HG01167.hp1 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.337+1233dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30678671 | ||||||
| chrX:30678671 | GT | G | 59 | a0001c0001t0002g0121 a0001c0001t0002g0156 a0001c0001t0002g0264 others(56): Show |
63 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.337+1233delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30678671 | ||||||
| chrX:30678685 | T | C | 4 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.337+1233T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30678685 | |||||||
| chrX:30678695 | G | GT | 11 | a0001c0001t0002g0216 a0001c0001t0002g0225 a0001c0001t0005g0105 others(8): Show |
11 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.337+1256dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30678695 | ||||||
| chrX:30678701 | T | C | 2 | a0001c0001t0003g0142 a0001c0001t0003g0143 |
2 | NA18993.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.337+1249T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30678701 | |||||||
| chrX:30678821 | G | A | 1 | a0001c0001t0012g0183 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.337+1369G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30678821 | |||||||
| chrX:30678841 | C | T | 3 | a0001c0001t0003g0008 a0001c0001t0003g0115 a0001c0001t0003g0157 |
4 | HG00408.hp1 NA18984.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.337+1389C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30678841 | |||||||
| chrX:30678852 | A | AT | 69 | a0001c0001t0001g0022 a0001c0001t0001g0049 a0001c0001t0001g0054 others(66): Show |
73 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.337+1419dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30678852 | ||||||
| chrX:30678852 | AT | A | 16 | a0001c0001t0002g0047 a0001c0001t0002g0208 a0001c0001t0002g0253 others(13): Show |
16 | HG00408.hp2 HG01515.hp1 HG01517.hp2 others(13): Show |
intron_variant | MODIFIER | c.337+1419delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30678852 | ||||||
| chrX:30678852 | ATT | A | 6 | a0001c0001t0002g0181 a0001c0001t0004g0182 a0001c0002t0006g0185 others(3): Show |
6 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.337+1418_337+1419d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30678852 | ||||||
| chrX:30679293 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.337+1841C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30679293 | |||||||
| chrX:30679321 | G | A | 3 | a0001c0001t0004g0169 a0001c0001t0004g0178 a0001c0001t0004g0179 |
3 | HG02451.hp1 HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.337+1869G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30679321 | |||||||
| chrX:30679379 | G | A | 1 | a0001c0004t0015g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.337+1927G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30679379 | |||||||
| chrX:30679446 | G | A | 2 | a0001c0001t0002g0240 a0001c0001t0002g0241 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.337+1994G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30679446 | |||||||
| chrX:30679694 | G | A | 56 | a0001c0001t0002g0121 a0001c0001t0002g0156 a0001c0001t0003g0002 others(53): Show |
60 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.337+2242G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30679694 | |||||||
| chrX:30680035 | C | T | 2 | a0001c0001t0001g0204 a0001c0001t0002g0255 |
2 | NA18942.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.337+2583C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30680035 | |||||||
| chrX:30680036 | G | A | 1 | a0001c0001t0016g0127 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.337+2584G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30680036 | |||||||
| chrX:30680046 | T | A | 1 | a0001c0001t0002g0224 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.337+2594T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30680046 | |||||||
| chrX:30680197 | A | G | 1 | a0001c0002t0017g0184 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.337+2745A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30680197 | |||||||
| chrX:30680399 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.337+2947C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30680399 | |||||||
| chrX:30680491 | C | T | 1 | a0001c0001t0009g0118 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.337+3039C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30680491 | |||||||
| chrX:30680581 | A | C | 1 | a0001c0001t0002g0092 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.337+3129A>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30680581 | |||||||
| chrX:30680601 | A | T | 70 | a0001c0001t0001g0204 a0001c0001t0001g0217 a0001c0001t0002g0011 others(67): Show |
72 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.337+3149A>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30680601 | |||||||
| chrX:30680761 | A | T | 2 | a0001c0001t0002g0181 a0001c0001t0004g0182 |
2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.337+3309A>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30680761 | |||||||
| chrX:30680866 | A | G | 1 | a0001c0001t0003g0198 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.337+3414A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30680866 | |||||||
| chrX:30681008 | T | C | 1 | a0001c0001t0004g0023 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.337+3556T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30681008 | |||||||
| chrX:30681050 | A | G | 181 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(178): Show |
192 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.337+3598A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30681050 | |||||||
| chrX:30681149 | C | T | 1 | a0001c0001t0004g0180 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.337+3697C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30681149 | |||||||
| chrX:30681416 | C | G | 3 | a0001c0001t0002g0224 a0001c0001t0002g0252 a0001c0001t0002g0258 |
3 | HG00099.hp1 HG00323.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.337+3964C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30681416 | |||||||
| chrX:30681475 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.337+4023G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30681475 | |||||||
| chrX:30681492 | A | G | 1 | a0001c0001t0002g0167 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.337+4040A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30681492 | |||||||
| chrX:30681533 | C | T | 1 | a0001c0001t0003g0177 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.337+4081C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30681533 | |||||||
| chrX:30681660 | T | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(212): Show |
226 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.337+4208T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30681660 | |||||||
| chrX:30681682 | G | C | 1 | a0001c0001t0002g0167 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.337+4230G>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30681682 | |||||||
| chrX:30681826 | T | C | 2 | a0001c0001t0001g0110 a0001c0001t0002g0028 |
2 | HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.337+4374T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30681826 | |||||||
| chrX:30681963 | A | C | 1 | a0001c0001t0005g0102 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.337+4511A>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30681963 | |||||||
| chrX:30681968 | A | T | 8 | a0001c0001t0004g0023 a0001c0001t0004g0170 a0001c0001t0004g0172 others(5): Show |
8 | HG02055.hp1 HG02622.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.337+4516A>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30681968 | |||||||
| chrX:30682360 | A | G | 1 | a0001c0001t0019g0046 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.337+4908A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30682360 | |||||||
| chrX:30682732 | T | C | 1 | a0001c0001t0007g0104 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.337+5280T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30682732 | |||||||
| chrX:30682944 | GTA | G | 9 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0016 others(6): Show |
9 | HG01515.hp1 HG01517.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.337+5493_337+5494d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30682944 | |||||||
| chrX:30683192 | A | G | 1 | a0001c0001t0011g0030 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.337+5740A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30683192 | |||||||
| chrX:30683225 | T | G | 1 | a0001c0004t0015g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.337+5773T>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30683225 | |||||||
| chrX:30683287 | C | T | 1 | a0001c0004t0015g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.337+5835C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30683287 | |||||||
| chrX:30683308 | G | A | 1 | a0001c0001t0002g0255 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.337+5856G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30683308 | |||||||
| chrX:30683351 | C | T | 6 | a0001c0001t0002g0203 a0001c0001t0002g0212 a0001c0001t0002g0237 others(3): Show |
6 | HG00741.hp2 HG01070.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.337+5899C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30683351 | |||||||
| chrX:30683538 | C | A | 1 | a0001c0001t0002g0230 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.337+6086C>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30683538 | |||||||
| chrX:30683542 | G | T | 1 | a0001c0001t0002g0230 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.337+6090G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30683542 | |||||||
| chrX:30683543 | G | A | 1 | a0001c0001t0002g0230 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.337+6091G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30683543 | |||||||
| chrX:30683544 | C | G | 1 | a0001c0001t0002g0230 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.337+6092C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30683544 | |||||||
| chrX:30683547 | A | T | 1 | a0001c0001t0002g0230 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.337+6095A>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30683547 | |||||||
| chrX:30683549 | G | T | 1 | a0001c0001t0002g0230 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.337+6097G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30683549 | |||||||
| chrX:30683550 | C | T | 1 | a0001c0001t0002g0230 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.337+6098C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30683550 | |||||||
| chrX:30683886 | G | A | 1 | a0001c0001t0001g0062 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.337+6434G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30683886 | |||||||
| chrX:30683887 | G | A | 1 | a0001c0001t0001g0062 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.337+6435G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30683887 | |||||||
| chrX:30683888 | CCTTGGGC others(4): Show |
C | 1 | a0001c0001t0001g0062 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.337+6441_337+6451d others(13): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30683888 | ||||||
| chrX:30684063 | T | TCTAA | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(192): Show |
206 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.337+6614_337+6615i others(6): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30684063 | ||||||
| chrX:30684216 | C | T | 8 | a0001c0001t0001g0073 a0001c0001t0001g0081 a0001c0001t0001g0084 others(5): Show |
8 | HG00323.hp1 HG01175.hp1 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.337+6764C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30684216 | |||||||
| chrX:30684432 | C | T | 1 | a0001c0001t0002g0227 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.338-6691C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30684432 | |||||||
| chrX:30684527 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.338-6596G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30684527 | |||||||
| chrX:30684580 | C | T | 3 | a0001c0001t0001g0005 a0001c0001t0001g0071 a0001c0001t0001g0072 |
4 | NA18956.hp1 NA18982.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.338-6543C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30684580 | |||||||
| chrX:30684666 | C | CA | 24 | a0001c0001t0003g0002 a0001c0001t0003g0008 a0001c0001t0003g0014 others(21): Show |
27 | HG00408.hp1 HG01074.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.338-6429dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30684666 | ||||||
| chrX:30684666 | CAAAA | C | 33 | a0001c0001t0001g0044 a0001c0001t0001g0049 a0001c0001t0001g0055 others(30): Show |
33 | HG00544.hp2 HG01175.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.338-6432_338-6429d others(6): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30684666 | ||||||
| chrX:30684666 | CAAAAA | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(146): Show |
160 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.338-6433_338-6429d others(7): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30684666 | ||||||
| chrX:30684926 | T | C | 11 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0016 others(8): Show |
11 | HG01515.hp1 HG01517.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.338-6197T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30684926 | |||||||
| chrX:30684966 | C | T | 1 | a0001c0004t0015g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.338-6157C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30684966 | |||||||
| chrX:30685134 | T | C | 1 | a0001c0001t0001g0061 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.338-5989T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30685134 | |||||||
| chrX:30685366 | C | G | 1 | a0001c0001t0004g0169 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.338-5757C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30685366 | |||||||
| chrX:30685519 | C | T | 1 | a0001c0001t0003g0020 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.338-5604C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30685519 | |||||||
| chrX:30685769 | G | T | 1 | a0001c0001t0003g0020 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.338-5354G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30685769 | |||||||
| chrX:30686030 | T | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(187): Show |
201 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.338-5093T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30686030 | |||||||
| chrX:30686125 | T | C | 1 | a0001c0003t0003g0166 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.338-4998T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30686125 | |||||||
| chrX:30686367 | A | G | 1 | a0001c0001t0003g0131 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.338-4756A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30686367 | |||||||
| chrX:30686388 | A | G | 4 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.338-4735A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30686388 | |||||||
| chrX:30686451 | T | C | 1 | a0001c0001t0002g0213 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.338-4672T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30686451 | |||||||
| chrX:30686716 | T | C | 1 | a0001c0001t0001g0033 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.338-4407T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30686716 | |||||||
| chrX:30686797 | A | C | 2 | a0001c0001t0007g0103 a0001c0001t0007g0104 |
2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.338-4326A>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30686797 | |||||||
| chrX:30686969 | C | T | 4 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.338-4154C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30686969 | |||||||
| chrX:30687165 | C | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(79): Show |
91 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.338-3958C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30687165 | |||||||
| chrX:30687696 | T | A | 4 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.338-3427T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30687696 | |||||||
| chrX:30687978 | C | T | 2 | a0001c0003t0003g0166 a0001c0003t0003g0168 |
2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.338-3145C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30687978 | |||||||
| chrX:30688306 | C | T | 1 | a0001c0001t0003g0018 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.338-2817C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30688306 | |||||||
| chrX:30688397 | G | T | 57 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(54): Show |
64 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.338-2726G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30688397 | |||||||
| chrX:30688501 | C | CA | 16 | a0001c0001t0001g0059 a0001c0001t0001g0073 a0001c0001t0001g0079 others(13): Show |
16 | HG00099.hp1 HG00741.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.338-2601dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30688501 | ||||||
| chrX:30688501 | CA | C | 16 | a0001c0001t0001g0193 a0001c0001t0002g0203 a0001c0001t0003g0117 others(13): Show |
16 | HG00099.hp2 HG01496.hp1 HG02004.hp1 others(13): Show |
intron_variant | MODIFIER | c.338-2601delA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30688501 | ||||||
| chrX:30688911 | G | A | 1 | a0001c0001t0001g0190 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.338-2212G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30688911 | |||||||
| chrX:30688926 | A | G | 4 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.338-2197A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30688926 | |||||||
| chrX:30688929 | G | A | 7 | a0001c0001t0004g0170 a0001c0001t0004g0172 a0001c0001t0004g0173 others(4): Show |
7 | HG02055.hp1 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.338-2194G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30688929 | |||||||
| chrX:30688932 | T | C | 1 | a0001c0004t0015g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.338-2191T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30688932 | |||||||
| chrX:30688956 | T | C | 1 | a0001c0003t0003g0166 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.338-2167T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30688956 | |||||||
| chrX:30689158 | G | A | 1 | a0001c0001t0002g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.338-1965G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30689158 | |||||||
| chrX:30689330 | T | A | 1 | a0001c0001t0003g0124 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.338-1793T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30689330 | |||||||
| chrX:30689337 | G | A | 1 | a0001c0001t0010g0164 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.338-1786G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30689337 | |||||||
| chrX:30689767 | G | A | 213 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(210): Show |
224 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.338-1356G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30689767 | |||||||
| chrX:30689837 | C | T | 11 | a0001c0001t0005g0029 a0001c0001t0005g0101 a0001c0001t0005g0102 others(8): Show |
11 | HG01891.hp2 HG02109.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.338-1286C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30689837 | |||||||
| chrX:30689888 | C | G | 2 | a0001c0002t0006g0186 a0001c0002t0006g0187 |
2 | HG01099.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.338-1235C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30689888 | |||||||
| chrX:30690035 | A | G | 1 | a0001c0001t0005g0102 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.338-1088A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30690035 | |||||||
| chrX:30690222 | T | G | 1 | a0001c0001t0002g0230 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.338-901T>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30690222 | |||||||
| chrX:30690223 | G | A | 1 | a0001c0001t0002g0230 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.338-900G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30690223 | |||||||
| chrX:30690226 | A | C | 1 | a0001c0001t0002g0230 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.338-897A>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30690226 | |||||||
| chrX:30690313 | G | A | 1 | a0001c0001t0002g0206 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.338-810G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30690313 | |||||||
| chrX:30690631 | G | A | 1 | a0001c0001t0002g0225 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.338-492G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30690631 | |||||||
| chrX:30691327 | G | A | 82 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(79): Show |
90 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.414+128G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | chrX | 30691327 | |||||||
| chrX:30691432 | C | T | 1 | a0001c0001t0003g0150 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.414+233C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | chrX | 30691432 | |||||||
| chrX:30691468 | C | CT | 14 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0053 others(11): Show |
14 | HG01109.hp1 HG01175.hp2 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.414+290dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30691468 | ||||||
| chrX:30691468 | CT | C | 33 | a0001c0001t0001g0033 a0001c0001t0001g0042 a0001c0001t0001g0064 others(30): Show |
33 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.414+290delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30691468 | ||||||
| chrX:30691600 | G | T | 1 | a0001c0001t0002g0230 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.414+401G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | chrX | 30691600 | |||||||
| chrX:30691643 | T | C | 3 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 |
3 | HG02109.hp1 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.414+444T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | chrX | 30691643 | |||||||
| chrX:30691888 | TATTGA | T | 11 | a0001c0001t0005g0029 a0001c0001t0005g0101 a0001c0001t0005g0102 others(8): Show |
11 | HG01891.hp2 HG02109.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.414+691_414+695del others(5): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30691888 | ||||||
| chrX:30691961 | A | C | 1 | a0001c0001t0001g0059 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.414+762A>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | chrX | 30691961 | |||||||
| chrX:30692068 | TTTTCTGT others(19): Show |
T | 72 | a0001c0001t0001g0204 a0001c0001t0001g0217 a0001c0001t0002g0011 others(69): Show |
74 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.414+872_414+897del others(26): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30692068 | ||||||
| chrX:30692437 | C | A | 1 | a0001c0004t0015g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.414+1238C>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | chrX | 30692437 | |||||||
| chrX:30692502 | A | T | 1 | a0001c0001t0002g0230 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.414+1303A>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | chrX | 30692502 | |||||||
| chrX:30692731 | T | G | 1 | a0001c0001t0002g0230 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.414+1532T>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | chrX | 30692731 | |||||||
| chrX:30692784 | A | AT | 8 | a0001c0001t0004g0023 a0001c0001t0004g0170 a0001c0001t0004g0172 others(5): Show |
8 | HG02055.hp1 HG02622.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.414+1597dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30692784 | ||||||
| chrX:30692966 | A | AATC | 4 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.415-1431_415-1429d others(5): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30692966 | ||||||
| chrX:30693006 | CTTTTCTT others(5): Show |
C | 2 | a0001c0001t0002g0238 a0001c0001t0002g0242 |
2 | HG00597.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.415-1389_415-1378d others(14): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30693006 | ||||||
| chrX:30693011 | C | CT | 28 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0055 others(25): Show |
28 | HG00597.hp1 HG00621.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.415-1366dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30693011 | ||||||
| chrX:30693011 | CT | C | 14 | a0001c0001t0002g0056 a0001c0001t0002g0094 a0001c0001t0002g0095 others(11): Show |
14 | HG00099.hp1 HG00323.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.415-1366delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30693011 | ||||||
| chrX:30693016 | T | C | 3 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 |
4 | HG02970.hp2 HG03540.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.415-1384T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | chrX | 30693016 | |||||||
| chrX:30693688 | G | A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(136): Show |
148 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.415-712G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | chrX | 30693688 | |||||||
| chrX:30694151 | G | A | 2 | a0001c0001t0001g0110 a0001c0001t0002g0028 |
2 | HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.415-249G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | chrX | 30694151 | |||||||
| chrX:30694578 | A | G | 2 | a0001c0001t0003g0146 a0001c0001t0003g0155 |
2 | HG02523.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.552+41A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 6/20 | chrX | 30694578 | |||||||
| chrX:30694679 | G | C | 211 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(208): Show |
221 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.552+142G>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 6/20 | chrX | 30694679 | |||||||
| chrX:30694732 | T | G | 3 | a0001c0001t0004g0172 a0001c0001t0020g0171 a0001c0004t0015g0112 |
3 | HG01884.hp1 HG02897.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.552+195T>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 6/20 | chrX | 30694732 | |||||||
| chrX:30695318 | G | T | 1 | a0001c0001t0003g0117 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.553-724G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 6/20 | chrX | 30695318 | |||||||
| chrX:30695592 | A | C | 1 | a0001c0001t0003g0018 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.553-450A>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 6/20 | chrX | 30695592 | |||||||
| chrX:30695798 | G | A | 6 | a0001c0001t0002g0056 a0001c0001t0002g0094 a0001c0001t0002g0095 others(3): Show |
6 | HG01243.hp1 HG02293.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.553-244G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 6/20 | chrX | 30695798 | |||||||
| chrX:30695846 | A | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(80): Show |
92 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.553-196A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 6/20 | chrX | 30695846 | |||||||
| chrX:30695940 | C | T | 4 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.553-102C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 6/20 | chrX | 30695940 | |||||||
| chrX:30696336 | C | CA | 17 | a0001c0001t0002g0181 a0001c0001t0002g0237 a0001c0001t0002g0248 others(14): Show |
18 | HG00741.hp2 HG01070.hp1 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.662+188dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 30696336 | ||||||
| chrX:30696399 | T | A | 1 | a0001c0001t0004g0023 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.663-218T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 7/20 | chrX | 30696399 | |||||||
| chrX:30696443 | A | T | 4 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.663-174A>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 7/20 | chrX | 30696443 | |||||||
| chrX:30696700 | C | A | 4 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.729+17C>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 8/20 | chrX | 30696700 | |||||||
| chrX:30696723 | C | A | 2 | a0001c0001t0001g0033 a0001c0001t0002g0246 |
2 | HG01258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.729+40C>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 8/20 | chrX | 30696723 | |||||||
| chrX:30696744 | A | C | 1 | a0001c0001t0001g0033 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.729+61A>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 8/20 | chrX | 30696744 | |||||||
| chrX:30696963 | T | C | 1 | a0001c0001t0002g0181 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.729+280T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 8/20 | chrX | 30696963 | |||||||
| chrX:30697008 | G | A | 8 | a0001c0001t0004g0023 a0001c0001t0004g0170 a0001c0001t0004g0172 others(5): Show |
8 | HG02055.hp1 HG02622.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.729+325G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 8/20 | chrX | 30697008 | |||||||
| chrX:30697334 | G | A | 1 | a0001c0001t0003g0123 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.730-398G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 8/20 | chrX | 30697334 | |||||||
| chrX:30697385 | T | G | 4 | a0001c0001t0007g0103 a0001c0001t0007g0104 a0001c0001t0008g0106 others(1): Show |
4 | HG01891.hp2 HG02109.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.730-347T>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 8/20 | chrX | 30697385 | |||||||
| chrX:30697480 | T | C | 4 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.730-252T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 8/20 | chrX | 30697480 | |||||||
| chrX:30697710 | C | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(192): Show |
205 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.730-22C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 8/20 | chrX | 30697710 | |||||||
| chrX:30697923 | T | C | 3 | a0001c0001t0003g0113 a0001c0001t0003g0150 a0001c0001t0009g0151 |
3 | HG00558.hp1 HG02071.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.747+174T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30697923 | |||||||
| chrX:30697968 | G | A | 6 | a0001c0001t0002g0056 a0001c0001t0002g0094 a0001c0001t0002g0095 others(3): Show |
6 | HG01243.hp1 HG02293.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.747+219G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30697968 | |||||||
| chrX:30698004 | A | G | 3 | a0001c0001t0004g0169 a0001c0001t0004g0178 a0001c0001t0004g0179 |
3 | HG02451.hp1 HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.747+255A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30698004 | |||||||
| chrX:30698319 | T | G | 1 | a0001c0001t0002g0231 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.747+570T>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30698319 | |||||||
| chrX:30698464 | G | A | 1 | a0001c0004t0015g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.747+715G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30698464 | |||||||
| chrX:30698599 | G | T | 74 | a0001c0001t0001g0204 a0001c0001t0001g0217 a0001c0001t0002g0011 others(71): Show |
76 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.747+850G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30698599 | |||||||
| chrX:30698680 | G | A | 1 | a0001c0001t0004g0023 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.747+931G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30698680 | |||||||
| chrX:30698683 | G | A | 1 | a0001c0004t0015g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.747+934G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30698683 | |||||||
| chrX:30698701 | C | CA | 9 | a0001c0001t0002g0239 a0001c0001t0003g0198 a0001c0001t0004g0013 others(6): Show |
9 | HG02258.hp1 HG02451.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.747+967dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 30698701 | ||||||
| chrX:30698701 | C | CAA | 184 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(181): Show |
195 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.747+966_747+967dup others(2): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 30698701 | ||||||
| chrX:30698701 | C | CAAA | 10 | a0001c0001t0001g0043 a0001c0001t0001g0059 a0001c0001t0001g0065 others(7): Show |
10 | HG00597.hp2 HG00741.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.747+965_747+967dup others(3): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 30698701 | ||||||
| chrX:30698823 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0109 |
2 | HG00423.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.747+1074G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30698823 | |||||||
| chrX:30698866 | C | CAA | 174 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(171): Show |
185 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.747+1134_747+1135d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 30698866 | ||||||
| chrX:30698866 | C | CAAA | 14 | a0001c0001t0001g0052 a0001c0001t0001g0058 a0001c0001t0002g0056 others(11): Show |
14 | HG01243.hp1 HG01433.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.747+1133_747+1135d others(5): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 30698866 | ||||||
| chrX:30698881 | A | G | 3 | a0001c0001t0003g0014 a0001c0001t0003g0017 a0001c0001t0003g0019 |
3 | HG01515.hp1 HG01517.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.747+1132A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30698881 | |||||||
| chrX:30698885 | G | A | 1 | a0001c0001t0012g0183 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.747+1136G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30698885 | |||||||
| chrX:30699161 | C | G | 1 | a0001c0001t0005g0029 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.748-1253C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30699161 | |||||||
| chrX:30699175 | T | TTA | 3 | a0001c0001t0001g0204 a0001c0001t0002g0221 a0001c0001t0002g0255 |
3 | NA18942.hp2 NA18999.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.748-1225_748-1224d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 30699175 | ||||||
| chrX:30699214 | T | TACATGTT others(20): Show |
15 | a0001c0001t0001g0217 a0001c0001t0002g0200 a0001c0001t0002g0201 others(12): Show |
15 | HG01361.hp1 HG01891.hp1 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.748-1166_748-1140d others(29): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 30699214 | ||||||
| chrX:30699214 | TACATGTT others(20): Show |
T | 6 | a0001c0001t0003g0014 a0001c0001t0003g0017 a0001c0001t0003g0019 others(3): Show |
6 | HG01515.hp1 HG01517.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.748-1166_748-1140d others(29): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 30699214 | ||||||
| chrX:30699220 | T | TTA | 3 | a0001c0001t0004g0169 a0001c0001t0004g0178 a0001c0001t0004g0179 |
3 | HG02451.hp1 HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.748-1187_748-1186d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 30699220 | ||||||
| chrX:30699249 | A | G | 2 | a0001c0001t0001g0083 a0001c0001t0001g0191 |
2 | HG03704.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.748-1165A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30699249 | |||||||
| chrX:30699267 | TAACATGT others(8): Show |
T | 3 | a0001c0001t0004g0169 a0001c0001t0004g0178 a0001c0001t0004g0179 |
3 | HG02451.hp1 HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.748-1139_748-1125d others(17): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 30699267 | ||||||
| chrX:30699273 | G | GTTATATA others(18): Show |
1 | a0001c0001t0001g0010 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.748-1140_748-1139i others(27): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 30699273 | ||||||
| chrX:30699273 | GTA | G | 81 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(78): Show |
88 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.748-1134_748-1133d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 30699273 | ||||||
| chrX:30699275 | A | G | 1 | a0001c0001t0001g0010 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.748-1139A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30699275 | |||||||
| chrX:30699298 | A | T | 2 | a0001c0001t0003g0017 a0001c0001t0003g0019 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.748-1116A>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30699298 | |||||||
| chrX:30699317 | G | GTT | 187 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(184): Show |
197 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.748-1096_748-1095d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 30699317 | ||||||
| chrX:30699320 | A | T | 84 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(81): Show |
92 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.748-1094A>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30699320 | |||||||
| chrX:30699331 | T | C | 5 | a0001c0001t0003g0116 a0001c0001t0003g0133 a0001c0001t0003g0136 others(2): Show |
5 | HG00621.hp1 HG02897.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.748-1083T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30699331 | |||||||
| chrX:30699368 | C | CT | 179 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(176): Show |
189 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.748-1031dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 30699368 | ||||||
| chrX:30699552 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.748-862T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30699552 | |||||||
| chrX:30699555 | G | T | 5 | a0001c0001t0002g0207 a0001c0002t0006g0185 a0001c0002t0006g0186 others(2): Show |
5 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.748-859G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30699555 | |||||||
| chrX:30699595 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.748-819C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30699595 | |||||||
| chrX:30699630 | C | T | 1 | a0001c0001t0004g0013 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.748-784C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30699630 | |||||||
| chrX:30699660 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.748-754G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30699660 | |||||||
| chrX:30699931 | T | C | 2 | a0001c0001t0002g0202 a0001c0001t0002g0219 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.748-483T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30699931 | |||||||
| chrX:30700126 | C | T | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | HG02683.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.748-288C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30700126 | |||||||
| chrX:30700248 | A | G | 2 | a0001c0001t0003g0122 a0001c0001t0003g0129 |
2 | HG01106.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.748-166A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30700248 | |||||||
| chrX:30700367 | G | C | 1 | a0001c0004t0015g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.748-47G>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30700367 | |||||||
| chrX:30700409 | A | T | 2 | a0001c0001t0002g0237 a0001c0001t0002g0248 |
2 | HG00741.hp2 HG01070.hp1 |
splice_region_variant&intron_variant | LOW | c.748-5A>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30700409 | |||||||
| chrX:30700759 | A | AAAAT | 200 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(197): Show |
210 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.784-78_784-75dupAA others(2): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chrX | 30700759 | ||||||
| chrX:30700953 | T | C | 1 | a0001c0001t0003g0162 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.851+48T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30700953 | |||||||
| chrX:30701239 | A | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(191): Show |
204 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.851+334A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30701239 | |||||||
| chrX:30701375 | T | C | 198 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(195): Show |
208 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.851+470T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30701375 | |||||||
| chrX:30701376 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.851+471G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30701376 | |||||||
| chrX:30701463 | T | C | 1 | a0001c0004t0015g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.851+558T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30701463 | |||||||
| chrX:30701606 | T | C | 1 | a0001c0001t0002g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.851+701T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30701606 | |||||||
| chrX:30701639 | G | T | 1 | a0001c0003t0003g0166 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.851+734G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30701639 | |||||||
| chrX:30701653 | C | G | 1 | a0001c0001t0004g0169 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.851+748C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30701653 | |||||||
| chrX:30702051 | T | A | 4 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.851+1146T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30702051 | |||||||
| chrX:30702078 | T | C | 1 | a0001c0001t0004g0023 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.851+1173T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30702078 | |||||||
| chrX:30702191 | C | T | 6 | a0001c0001t0002g0056 a0001c0001t0002g0094 a0001c0001t0002g0095 others(3): Show |
6 | HG01243.hp1 HG02293.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.851+1286C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30702191 | |||||||
| chrX:30702233 | A | G | 1 | a0001c0004t0015g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.851+1328A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30702233 | |||||||
| chrX:30702261 | C | T | 178 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
188 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.851+1356C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30702261 | |||||||
| chrX:30702288 | C | T | 7 | a0001c0001t0004g0170 a0001c0001t0004g0172 a0001c0001t0004g0173 others(4): Show |
7 | HG02055.hp1 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.851+1383C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30702288 | |||||||
| chrX:30702322 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0110 |
3 | HG02647.hp1 HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.851+1417G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30702322 | |||||||
| chrX:30702378 | A | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(176): Show |
189 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.851+1473A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30702378 | |||||||
| chrX:30702433 | A | G | 4 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.851+1528A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30702433 | |||||||
| chrX:30702641 | T | C | 4 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.851+1736T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30702641 | |||||||
| chrX:30702685 | A | G | 1 | a0001c0001t0004g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.851+1780A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30702685 | |||||||
| chrX:30702707 | T | C | 1 | a0001c0001t0005g0107 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.851+1802T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30702707 | |||||||
| chrX:30702951 | A | G | 1 | a0001c0001t0002g0167 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.851+2046A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30702951 | |||||||
| chrX:30702981 | C | T | 7 | a0001c0001t0005g0105 a0001c0001t0005g0107 a0001c0001t0005g0197 others(4): Show |
7 | HG01891.hp2 HG02109.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.851+2076C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30702981 | |||||||
| chrX:30703012 | C | A | 1 | a0001c0001t0004g0178 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.851+2107C>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30703012 | |||||||
| chrX:30703097 | T | C | 1 | a0001c0001t0004g0023 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.851+2192T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30703097 | |||||||
| chrX:30703417 | C | G | 1 | a0001c0001t0005g0197 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.851+2512C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30703417 | |||||||
| chrX:30703511 | G | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(173): Show |
186 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.851+2606G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30703511 | |||||||
| chrX:30703777 | A | G | 1 | a0001c0001t0002g0167 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.851+2872A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30703777 | |||||||
| chrX:30703781 | C | G | 4 | a0001c0001t0002g0207 a0001c0001t0002g0224 a0001c0001t0002g0252 others(1): Show |
4 | HG00099.hp1 HG00323.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.851+2876C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30703781 | |||||||
| chrX:30703956 | C | CA | 6 | a0001c0001t0002g0232 a0001c0001t0003g0120 a0001c0001t0003g0162 others(3): Show |
6 | HG02451.hp1 HG02965.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.851+3063dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30703956 | ||||||
| chrX:30704128 | T | TATATATA others(24): Show |
2 | a0001c0001t0005g0101 a0001c0001t0007g0103 |
2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.851+3223_851+3224i others(33): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30704128 | |||||||
| chrX:30704128 | T | TTA | 72 | a0001c0001t0001g0204 a0001c0001t0001g0217 a0001c0001t0002g0011 others(69): Show |
74 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.851+3243_851+3244d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704128 | ||||||
| chrX:30704128 | T | TTATA | 3 | a0001c0001t0002g0232 a0001c0001t0002g0237 a0001c0001t0002g0248 |
3 | HG00741.hp2 HG01070.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.851+3241_851+3244d others(6): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704128 | ||||||
| chrX:30704128 | T | TTATATA | 3 | a0001c0001t0002g0238 a0001c0001t0010g0111 a0001c0001t0010g0164 |
3 | HG00597.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.851+3239_851+3244d others(8): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704128 | ||||||
| chrX:30704128 | T | TTATATAT others(3): Show |
1 | a0001c0002t0006g0185 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.851+3235_851+3244d others(12): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704128 | ||||||
| chrX:30704128 | T | TTATATAT others(5): Show |
2 | a0001c0002t0006g0187 a0001c0002t0017g0184 |
2 | HG00741.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.851+3233_851+3244d others(14): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704128 | ||||||
| chrX:30704128 | T | TTATATAT others(7): Show |
51 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(48): Show |
58 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.851+3231_851+3244d others(16): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704128 | ||||||
| chrX:30704128 | T | TTATATAT others(9): Show |
13 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0051 others(10): Show |
14 | HG00597.hp1 HG01255.hp1 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.851+3229_851+3244d others(18): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704128 | ||||||
| chrX:30704128 | T | TTATATAT others(11): Show |
9 | a0001c0001t0001g0041 a0001c0001t0001g0052 a0001c0001t0001g0055 others(6): Show |
9 | HG02572.hp1 HG02683.hp1 HG02698.hp1 others(6): Show |
intron_variant | MODIFIER | c.851+3227_851+3244d others(20): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704128 | ||||||
| chrX:30704128 | T | TTATATAT others(13): Show |
7 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0050 others(4): Show |
7 | HG02109.hp1 HG02559.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.851+3225_851+3244d others(22): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704128 | ||||||
| chrX:30704128 | T | TTATATAT others(15): Show |
3 | a0001c0001t0001g0040 a0001c0001t0001g0048 a0001c0001t0002g0167 |
3 | HG01884.hp2 HG03834.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.851+3244_851+3245i others(24): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704128 | ||||||
| chrX:30704128 | T | TTATATAT others(17): Show |
1 | a0001c0001t0001g0059 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.851+3244_851+3245i others(26): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704128 | ||||||
| chrX:30704128 | T | TTATATAT others(19): Show |
3 | a0001c0001t0001g0027 a0001c0001t0004g0174 a0001c0001t0012g0183 |
3 | HG02615.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.851+3244_851+3245i others(28): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704128 | ||||||
| chrX:30704128 | T | TTATATAT others(21): Show |
2 | a0001c0001t0005g0197 a0001c0001t0020g0171 |
2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.851+3244_851+3245i others(30): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704128 | ||||||
| chrX:30704128 | T | TTATATAT others(23): Show |
7 | a0001c0001t0001g0033 a0001c0001t0002g0096 a0001c0001t0004g0169 others(4): Show |
7 | HG01891.hp2 HG02451.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.851+3244_851+3245i others(32): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704128 | ||||||
| chrX:30704128 | T | TTATATAT others(25): Show |
3 | a0001c0001t0002g0095 a0001c0001t0004g0173 a0001c0001t0004g0175 |
3 | HG02055.hp1 HG02293.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.851+3244_851+3245i others(34): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704128 | ||||||
| chrX:30704128 | T | TTATATAT others(27): Show |
6 | a0001c0001t0002g0056 a0001c0001t0002g0094 a0001c0001t0002g0097 others(3): Show |
6 | HG01243.hp1 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.851+3244_851+3245i others(36): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704128 | ||||||
| chrX:30704128 | T | TTATATAT others(29): Show |
4 | a0001c0001t0004g0172 a0001c0001t0004g0179 a0001c0001t0005g0105 others(1): Show |
4 | HG02809.hp2 HG02897.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.851+3244_851+3245i others(38): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704128 | ||||||
| chrX:30704128 | T | TTATATAT others(31): Show |
1 | a0001c0001t0004g0023 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.851+3244_851+3245i others(40): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704128 | ||||||
| chrX:30704128 | T | TTATATAT others(33): Show |
1 | a0001c0001t0002g0098 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.851+3244_851+3245i others(42): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704128 | ||||||
| chrX:30704149 | T | TATATATA others(37): Show |
1 | a0001c0004t0015g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.851+3244_851+3245i others(46): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30704149 | |||||||
| chrX:30704243 | C | G | 1 | a0001c0001t0001g0033 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.852-3313C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30704243 | |||||||
| chrX:30704417 | C | G | 1 | a0001c0001t0001g0040 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.852-3139C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30704417 | |||||||
| chrX:30704495 | C | T | 4 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.852-3061C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30704495 | |||||||
| chrX:30704576 | A | G | 1 | a0001c0001t0004g0174 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.852-2980A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30704576 | |||||||
| chrX:30704577 | C | CT | 18 | a0001c0001t0002g0097 a0001c0001t0002g0237 a0001c0001t0002g0248 others(15): Show |
19 | HG00621.hp1 HG00741.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.852-2966dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704577 | ||||||
| chrX:30704604 | G | A | 1 | a0001c0001t0003g0134 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.852-2952G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30704604 | |||||||
| chrX:30704612 | A | C | 1 | a0001c0001t0003g0134 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.852-2944A>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30704612 | |||||||
| chrX:30704696 | C | T | 183 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(180): Show |
193 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.852-2860C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30704696 | |||||||
| chrX:30704855 | C | A | 82 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(79): Show |
90 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.852-2701C>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30704855 | |||||||
| chrX:30704859 | C | T | 183 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(180): Show |
193 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.852-2697C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30704859 | |||||||
| chrX:30704870 | G | A | 197 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(194): Show |
207 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.852-2686G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30704870 | |||||||
| chrX:30705096 | A | C | 3 | a0001c0001t0004g0169 a0001c0001t0004g0178 a0001c0001t0004g0179 |
3 | HG02451.hp1 HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.852-2460A>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30705096 | |||||||
| chrX:30705262 | A | G | 1 | a0001c0001t0012g0183 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.852-2294A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30705262 | |||||||
| chrX:30705345 | A | G | 1 | a0001c0001t0004g0169 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.852-2211A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30705345 | |||||||
| chrX:30705374 | C | T | 4 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.852-2182C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30705374 | |||||||
| chrX:30705851 | A | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(77): Show |
88 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.852-1705A>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30705851 | |||||||
| chrX:30705876 | C | G | 196 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(193): Show |
206 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.852-1680C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30705876 | |||||||
| chrX:30705910 | C | T | 1 | a0001c0001t0002g0224 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.852-1646C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30705910 | |||||||
| chrX:30706055 | G | A | 8 | a0001c0001t0005g0105 a0001c0001t0005g0107 a0001c0001t0005g0197 others(5): Show |
8 | HG01891.hp2 HG02109.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.852-1501G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30706055 | |||||||
| chrX:30706057 | C | T | 1 | a0001c0004t0015g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.852-1499C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30706057 | |||||||
| chrX:30706065 | C | T | 1 | a0001c0001t0004g0182 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.852-1491C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30706065 | |||||||
| chrX:30706209 | G | A | 190 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(187): Show |
200 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.852-1347G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30706209 | |||||||
| chrX:30706272 | G | A | 1 | a0001c0001t0003g0117 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.852-1284G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30706272 | |||||||
| chrX:30706286 | C | T | 1 | a0001c0001t0003g0128 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.852-1270C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30706286 | |||||||
| chrX:30706434 | C | T | 1 | a0001c0001t0002g0206 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.852-1122C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30706434 | |||||||
| chrX:30706500 | C | G | 2 | a0001c0001t0010g0111 a0001c0001t0010g0164 |
2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.852-1056C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30706500 | |||||||
| chrX:30706546 | A | G | 1 | a0001c0001t0002g0258 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.852-1010A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30706546 | |||||||
| chrX:30706699 | G | A | 1 | a0001c0001t0002g0092 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.852-857G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30706699 | |||||||
| chrX:30706767 | C | T | 3 | a0001c0001t0001g0048 a0001c0001t0001g0052 a0001c0001t0001g0055 |
3 | HG02572.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.852-789C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30706767 | |||||||
| chrX:30706850 | C | T | 1 | a0001c0001t0003g0032 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.852-706C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30706850 | |||||||
| chrX:30706898 | A | T | 1 | a0001c0001t0003g0036 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.852-658A>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30706898 | |||||||
| chrX:30706985 | C | T | 1 | a0001c0004t0015g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.852-571C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30706985 | |||||||
| chrX:30707105 | T | C | 1 | a0001c0001t0004g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.852-451T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30707105 | |||||||
| chrX:30707307 | T | A | 6 | a0001c0001t0002g0056 a0001c0001t0002g0094 a0001c0001t0002g0095 others(3): Show |
6 | HG01243.hp1 HG02293.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.852-249T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30707307 | |||||||
| chrX:30707328 | C | CA | 18 | a0001c0001t0001g0082 a0001c0001t0003g0008 a0001c0001t0003g0114 others(15): Show |
19 | HG00408.hp1 HG00609.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.852-211dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30707328 | ||||||
| chrX:30707677 | C | T | 177 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(174): Show |
187 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.894+79C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 12/20 | chrX | 30707677 | |||||||
| chrX:30707755 | A | G | 2 | a0001c0001t0007g0103 a0001c0001t0007g0104 |
2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.894+157A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 12/20 | chrX | 30707755 | |||||||
| chrX:30707806 | C | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(194): Show |
207 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.894+208C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 12/20 | chrX | 30707806 | |||||||
| chrX:30707936 | A | T | 1 | a0001c0001t0002g0167 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.895-118A>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 12/20 | chrX | 30707936 | |||||||
| chrX:30707997 | T | A | 1 | a0001c0001t0002g0216 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.895-57T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 12/20 | chrX | 30707997 | |||||||
| chrX:30708400 | GT | G | 13 | a0001c0001t0002g0056 a0001c0001t0002g0094 a0001c0001t0002g0095 others(10): Show |
13 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.975+280delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30708400 | ||||||
| chrX:30708715 | A | G | 2 | a0001c0001t0002g0206 a0001c0001t0014g0263 |
2 | HG03017.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.975+581A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30708715 | |||||||
| chrX:30708988 | C | A | 192 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(189): Show |
202 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.975+854C>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30708988 | |||||||
| chrX:30709171 | G | A | 1 | a0001c0001t0004g0023 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.975+1037G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30709171 | |||||||
| chrX:30709258 | A | G | 1 | a0001c0001t0005g0101 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.975+1124A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30709258 | |||||||
| chrX:30709304 | G | T | 1 | a0001c0001t0001g0021 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.975+1170G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30709304 | |||||||
| chrX:30709426 | G | A | 4 | a0001c0001t0002g0209 a0001c0001t0002g0211 a0001c0001t0002g0215 others(1): Show |
4 | HG01928.hp1 HG01952.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.975+1292G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30709426 | |||||||
| chrX:30710385 | G | A | 3 | a0001c0001t0004g0169 a0001c0001t0004g0178 a0001c0001t0004g0179 |
3 | HG02451.hp1 HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.975+2251G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30710385 | |||||||
| chrX:30710461 | T | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(185): Show |
198 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.975+2327T>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30710461 | |||||||
| chrX:30710861 | T | C | 3 | a0001c0001t0003g0008 a0001c0001t0003g0115 a0001c0001t0003g0157 |
4 | HG00408.hp1 NA18984.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.975+2727T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30710861 | |||||||
| chrX:30711053 | G | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(185): Show |
198 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.975+2919G>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30711053 | |||||||
| chrX:30711116 | T | C | 1 | a0001c0004t0015g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.975+2982T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30711116 | |||||||
| chrX:30711127 | C | CT | 186 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(183): Show |
196 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.975+3004dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30711127 | ||||||
| chrX:30711225 | A | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(186): Show |
199 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.975+3091A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30711225 | |||||||
| chrX:30711238 | G | A | 1 | a0001c0001t0002g0092 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.975+3104G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30711238 | |||||||
| chrX:30711292 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.975+3158G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30711292 | |||||||
| chrX:30712556 | CT | C | 5 | a0001c0001t0002g0202 a0001c0001t0002g0218 a0001c0001t0002g0219 others(2): Show |
5 | HG00741.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.975+4432delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30712556 | ||||||
| chrX:30712625 | G | A | 4 | a0001c0001t0002g0207 a0001c0001t0002g0224 a0001c0001t0002g0252 others(1): Show |
4 | HG00099.hp1 HG00323.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.975+4491G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30712625 | |||||||
| chrX:30712717 | C | CT | 23 | a0001c0001t0001g0072 a0001c0001t0001g0078 a0001c0001t0001g0088 others(20): Show |
23 | HG00597.hp1 HG00597.hp2 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.975+4608dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30712717 | ||||||
| chrX:30712717 | CT | C | 23 | a0001c0001t0001g0065 a0001c0001t0001g0188 a0001c0001t0001g0192 others(20): Show |
24 | HG01515.hp1 HG01517.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.975+4608delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30712717 | ||||||
| chrX:30712717 | CTTTTT | C | 8 | a0001c0001t0005g0029 a0001c0001t0005g0101 a0001c0001t0005g0102 others(5): Show |
8 | HG02559.hp1 HG02630.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.975+4604_975+4608d others(7): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30712717 | ||||||
| chrX:30712717 | CTTTTTTT others(5): Show |
C | 4 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.975+4597_975+4608d others(14): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30712717 | ||||||
| chrX:30712964 | G | A | 1 | a0001c0001t0001g0024 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.975+4830G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30712964 | |||||||
| chrX:30713063 | C | T | 4 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.975+4929C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30713063 | |||||||
| chrX:30713185 | T | C | 187 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(184): Show |
197 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.975+5051T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30713185 | |||||||
| chrX:30713206 | C | A | 1 | a0001c0001t0003g0162 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.975+5072C>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30713206 | |||||||
| chrX:30713402 | T | C | 3 | a0001c0001t0004g0169 a0001c0001t0004g0178 a0001c0001t0004g0179 |
3 | HG02451.hp1 HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.976-5136T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30713402 | |||||||
| chrX:30714141 | G | A | 3 | a0001c0001t0003g0008 a0001c0001t0003g0115 a0001c0001t0003g0157 |
4 | HG00408.hp1 NA18984.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.976-4397G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30714141 | |||||||
| chrX:30714219 | A | G | 2 | a0001c0003t0003g0166 a0001c0003t0003g0168 |
2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.976-4319A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30714219 | |||||||
| chrX:30714542 | C | A | 1 | a0001c0001t0001g0033 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.976-3996C>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30714542 | |||||||
| chrX:30714551 | T | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(192): Show |
205 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.976-3987T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30714551 | |||||||
| chrX:30714619 | T | C | 3 | a0001c0001t0003g0003 a0001c0001t0003g0031 a0001c0001t0003g0032 |
4 | HG02970.hp2 HG03540.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.976-3919T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30714619 | |||||||
| chrX:30714828 | T | A | 1 | a0001c0001t0003g0162 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.976-3710T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30714828 | |||||||
| chrX:30714832 | G | A | 4 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.976-3706G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30714832 | |||||||
| chrX:30714859 | G | A | 1 | a0001c0001t0012g0183 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.976-3679G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30714859 | |||||||
| chrX:30714926 | T | C | 1 | a0001c0001t0003g0147 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.976-3612T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30714926 | |||||||
| chrX:30715326 | C | A | 1 | a0001c0001t0002g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.976-3212C>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30715326 | |||||||
| chrX:30715354 | T | A | 1 | a0001c0001t0002g0258 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.976-3184T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30715354 | |||||||
| chrX:30715552 | A | G | 1 | a0001c0001t0001g0042 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.976-2986A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30715552 | |||||||
| chrX:30715637 | G | A | 6 | a0001c0001t0002g0056 a0001c0001t0002g0094 a0001c0001t0002g0095 others(3): Show |
6 | HG01243.hp1 HG02293.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.976-2901G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30715637 | |||||||
| chrX:30715752 | T | C | 3 | a0001c0001t0004g0169 a0001c0001t0004g0178 a0001c0001t0004g0179 |
3 | HG02451.hp1 HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.976-2786T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30715752 | |||||||
| chrX:30715796 | G | A | 1 | a0001c0001t0005g0107 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.976-2742G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30715796 | |||||||
| chrX:30716251 | G | A | 1 | a0001c0001t0002g0243 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.976-2287G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30716251 | |||||||
| chrX:30716627 | A | G | 1 | a0001c0001t0002g0203 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.976-1911A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30716627 | |||||||
| chrX:30716771 | T | TA | 3 | a0001c0001t0004g0013 a0001c0001t0004g0182 a0001c0001t0013g0108 |
3 | HG02258.hp1 HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.976-1765dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30716771 | ||||||
| chrX:30716832 | C | G | 191 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(188): Show |
201 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.976-1706C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30716832 | |||||||
| chrX:30716886 | C | T | 1 | a0001c0001t0004g0182 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.976-1652C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30716886 | |||||||
| chrX:30717128 | T | C | 1 | a0001c0001t0002g0245 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.976-1410T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30717128 | |||||||
| chrX:30717227 | T | C | 1 | a0001c0001t0003g0153 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.976-1311T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30717227 | |||||||
| chrX:30717424 | C | G | 1 | a0001c0001t0005g0101 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.976-1114C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30717424 | |||||||
| chrX:30717476 | A | C | 2 | a0001c0001t0010g0111 a0001c0001t0010g0164 |
2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.976-1062A>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30717476 | |||||||
| chrX:30718167 | A | T | 1 | a0001c0001t0003g0143 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.976-371A>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30718167 | |||||||
| chrX:30718262 | AAGAAGCA others(4): Show |
A | 1 | a0001c0001t0001g0060 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.976-275_976-265del others(11): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30718262 | |||||||
| chrX:30718638 | G | T | 4 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.1054+22G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 14/20 | chrX | 30718638 | |||||||
| chrX:30719092 | T | C | 187 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(184): Show |
197 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.1055-327T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 14/20 | chrX | 30719092 | |||||||
| chrX:30719162 | G | A | 1 | a0001c0001t0003g0126 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1055-257G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 14/20 | chrX | 30719162 | |||||||
| chrX:30719225 | G | A | 2 | a0001c0001t0004g0172 a0001c0001t0020g0171 |
2 | HG02897.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1055-194G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 14/20 | chrX | 30719225 | |||||||
| chrX:30719278 | G | A | 1 | a0001c0001t0009g0118 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1055-141G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 14/20 | chrX | 30719278 | |||||||
| chrX:30719284 | A | G | 1 | a0001c0001t0005g0029 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1055-135A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 14/20 | chrX | 30719284 | |||||||
| chrX:30719355 | G | T | 1 | a0001c0001t0003g0126 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1055-64G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 14/20 | chrX | 30719355 | |||||||
| chrX:30719552 | T | C | 2 | a0001c0001t0002g0267 a0001c0001t0002g0268 |
2 | NA19056.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1151+37T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 15/20 | chrX | 30719552 | |||||||
| chrX:30719640 | G | A | 1 | a0001c0001t0004g0013 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1151+125G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 15/20 | chrX | 30719640 | |||||||
| chrX:30720761 | T | C | 4 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.1357+20T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 17/20 | chrX | 30720761 | |||||||
| chrX:30721038 | C | G | 2 | a0001c0001t0002g0237 a0001c0001t0002g0248 |
2 | HG00741.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.1501+43C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30721038 | |||||||
| chrX:30721125 | G | A | 1 | a0001c0001t0012g0183 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1501+130G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30721125 | |||||||
| chrX:30721176 | T | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(80): Show |
91 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.1501+181T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30721176 | |||||||
| chrX:30721244 | A | G | 8 | a0001c0001t0004g0023 a0001c0001t0004g0170 a0001c0001t0004g0172 others(5): Show |
8 | HG02055.hp1 HG02622.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1501+249A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30721244 | |||||||
| chrX:30721296 | C | CT | 181 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(178): Show |
191 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.1501+314dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chrX | 30721296 | ||||||
| chrX:30721296 | C | CTT | 6 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0085 others(3): Show |
6 | HG01433.hp1 NA18946.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.1501+313_1501+314d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chrX | 30721296 | ||||||
| chrX:30721377 | C | T | 2 | a0001c0001t0001g0037 a0001c0001t0001g0038 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1501+382C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30721377 | |||||||
| chrX:30721448 | C | T | 3 | a0001c0001t0004g0013 a0001c0001t0004g0182 a0001c0001t0012g0183 |
3 | HG02258.hp1 HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1501+453C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30721448 | |||||||
| chrX:30721458 | A | AT | 9 | a0001c0001t0001g0188 a0001c0001t0002g0056 a0001c0001t0003g0116 others(6): Show |
9 | HG02080.hp2 HG02486.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1501+482dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chrX | 30721458 | ||||||
| chrX:30721458 | AT | A | 172 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(169): Show |
182 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1501+482delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chrX | 30721458 | ||||||
| chrX:30721506 | G | A | 1 | a0001c0001t0004g0169 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1501+511G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30721506 | |||||||
| chrX:30721508 | G | A | 1 | a0001c0001t0005g0107 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1501+513G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30721508 | |||||||
| chrX:30722093 | G | A | 11 | a0001c0001t0001g0004 a0001c0001t0001g0057 a0001c0001t0001g0058 others(8): Show |
12 | NA18941.hp1 NA18966.hp1 NA18971.hp1 others(9): Show |
intron_variant | MODIFIER | c.1501+1098G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30722093 | |||||||
| chrX:30722334 | A | G | 1 | a0001c0001t0002g0070 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1501+1339A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30722334 | |||||||
| chrX:30722395 | G | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(191): Show |
204 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.1501+1400G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30722395 | |||||||
| chrX:30722780 | A | G | 2 | a0001c0001t0003g0116 a0001c0001t0003g0141 |
2 | NA18983.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.1502-1321A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30722780 | |||||||
| chrX:30723116 | C | T | 1 | a0001c0001t0002g0214 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1502-985C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30723116 | |||||||
| chrX:30723178 | G | A | 4 | a0001c0001t0003g0125 a0001c0001t0004g0169 a0001c0001t0004g0178 others(1): Show |
4 | HG02074.hp1 HG02451.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1502-923G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30723178 | |||||||
| chrX:30723272 | G | A | 1 | a0001c0001t0005g0029 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1502-829G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30723272 | |||||||
| chrX:30723322 | G | A | 1 | a0001c0001t0004g0023 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1502-779G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30723322 | |||||||
| chrX:30723344 | G | A | 1 | a0001c0001t0003g0139 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1502-757G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30723344 | |||||||
| chrX:30723452 | C | G | 1 | a0001c0001t0003g0134 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1502-649C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30723452 | |||||||
| chrX:30723461 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1502-640G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30723461 | |||||||
| chrX:30723514 | C | T | 2 | a0001c0001t0010g0111 a0001c0001t0010g0164 |
2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1502-587C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30723514 | |||||||
| chrX:30723562 | A | G | 1 | a0001c0001t0005g0101 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1502-539A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30723562 | |||||||
| chrX:30723611 | TTTTGTTT others(1): Show |
T | 57 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(54): Show |
64 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1502-470_1502-463d others(10): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chrX | 30723611 | ||||||
| chrX:30723839 | A | C | 4 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.1502-262A>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30723839 | |||||||
| chrX:30724475 | GA | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(163): Show |
176 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.1582+305delA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 30724475 | ||||||
| chrX:30724574 | T | G | 89 | a0001c0001t0001g0204 a0001c0001t0001g0217 a0001c0001t0002g0011 others(86): Show |
91 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.1582+393T>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 19/20 | chrX | 30724574 | |||||||
| chrX:30724678 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1582+497G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 19/20 | chrX | 30724678 | |||||||
| chrX:30724828 | G | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0069 |
2 | NA18941.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.1582+647G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 19/20 | chrX | 30724828 | |||||||
| chrX:30724966 | C | T | 6 | a0001c0001t0003g0123 a0001c0001t0003g0132 a0001c0001t0003g0135 others(3): Show |
6 | HG01496.hp1 HG01978.hp2 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.1582+785C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 19/20 | chrX | 30724966 | |||||||
| chrX:30724976 | G | T | 4 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.1582+795G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 19/20 | chrX | 30724976 | |||||||
| chrX:30725473 | T | A | 11 | a0001c0001t0005g0029 a0001c0001t0005g0101 a0001c0001t0005g0102 others(8): Show |
11 | HG01891.hp2 HG02109.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1582+1292T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 19/20 | chrX | 30725473 | |||||||
| chrX:30725857 | C | G | 1 | a0001c0001t0001g0194 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1583-1609C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 19/20 | chrX | 30725857 | |||||||
| chrX:30725893 | T | C | 1 | a0001c0001t0004g0178 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1583-1573T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 19/20 | chrX | 30725893 | |||||||
| chrX:30726072 | A | G | 1 | a0001c0001t0003g0125 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1583-1394A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 19/20 | chrX | 30726072 | |||||||
| chrX:30726090 | C | T | 2 | a0001c0001t0001g0059 a0001c0001t0001g0066 |
2 | HG02738.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1583-1376C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 19/20 | chrX | 30726090 | |||||||
| chrX:30726189 | C | G | 1 | a0001c0001t0001g0021 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1583-1277C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 19/20 | chrX | 30726189 | |||||||
| chrX:30726286 | AT | A | 9 | a0001c0001t0002g0121 a0001c0001t0002g0203 a0001c0001t0002g0212 others(6): Show |
9 | HG00738.hp1 HG00741.hp2 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.1583-1162delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 30726286 | ||||||
| chrX:30726437 | G | A | 2 | a0001c0001t0004g0013 a0001c0001t0004g0182 |
2 | HG02258.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1583-1029G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 19/20 | chrX | 30726437 | |||||||
| chrX:30726566 | C | T | 1 | a0001c0001t0004g0175 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1583-900C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 19/20 | chrX | 30726566 | |||||||
| chrX:30727649 | T | G | 2 | a0001c0001t0001g0059 a0001c0001t0001g0066 |
2 | HG02738.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1669+97T>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 20/20 | chrX | 30727649 | |||||||
| chrX:30727673 | A | T | 185 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(182): Show |
195 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.1669+121A>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 20/20 | chrX | 30727673 | |||||||
| chrX:30727694 | C | A | 1 | a0001c0001t0012g0183 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1669+142C>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 20/20 | chrX | 30727694 | |||||||
| chrX:30727749 | T | A | 3 | a0001c0001t0004g0013 a0001c0001t0004g0182 a0001c0001t0013g0108 |
3 | HG02258.hp1 HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1669+197T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 20/20 | chrX | 30727749 | |||||||
| chrX:30728024 | A | G | 1 | a0001c0001t0012g0183 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1669+472A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 20/20 | chrX | 30728024 | |||||||
| chrX:30728042 | C | T | 1 | a0001c0004t0015g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1669+490C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 20/20 | chrX | 30728042 | |||||||
| chrX:30728335 | C | CT | 182 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(179): Show |
192 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.1670-395dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chrX | 30728335 | ||||||
| chrX:30728348 | T | A | 1 | a0001c0004t0015g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1670-384T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 20/20 | chrX | 30728348 | |||||||
| chrX:30728384 | A | G | 1 | a0001c0001t0003g0159 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1670-348A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 20/20 | chrX | 30728384 | |||||||
| chrX:30728543 | G | A | 1 | a0001c0001t0003g0152 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1670-189G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 20/20 | chrX | 30728543 | |||||||
| chrX:30728616 | T | C | 1 | a0001c0001t0009g0118 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1670-116T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 20/20 | chrX | 30728616 |