Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4810 |
| ensemblid | ENSG00000188158.17 |
| hgncid | 7820 |
| symbol | NHS |
| name | NHS actin remodeling regulator |
| refseq_nuc | NM_001291867.2 |
| refseq_prot | NP_001278796.1 |
| ensembl_nuc | ENST00000676302.1 |
| ensembl_prot | ENSP00000502262.1 |
| mane_status | MANE Select |
| chr | chrX |
| start | 17375200 |
| end | 17735994 |
| strand | + |
| ver | v1.2 |
| region | chrX:17375200-17735994 |
| region5000 | chrX:17370200-17740994 |
| regionname0 | NHS_chrX_17375200_17735994 |
| regionname5000 | NHS_chrX_17370200_17740994 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1651 | 73 | 28 | 12 | 32 | 0 | 1 | 25 | NHS_chrX_17370200_17740994 | NHS | MPFAK others(1646): Show |
chrX | 17370200 | 17740994 |
| a0002 | 0/0 | 1651 | 66 | 4 | 13 | 30 | 5 | 14 | 20 | NHS_chrX_17370200_17740994 | NHS | MPFAK others(1646): Show |
chrX | 17370200 | 17740994 |
| a0003 | 0/0 | 1650 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | MPFAK others(1645): Show |
chrX | 17370200 | 17740994 |
| a0004 | 0/0 | 1651 | 5 | 0 | 2 | 3 | 0 | 0 | 3 | NHS_chrX_17370200_17740994 | NHS | MPFAK others(1646): Show |
chrX | 17370200 | 17740994 |
| a0005 | 0/0 | 1651 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | MPFAK others(1646): Show |
chrX | 17370200 | 17740994 |
| a0006 | 0/0 | 1651 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | MPFAK others(1646): Show |
chrX | 17370200 | 17740994 |
| a0007 | 0/0 | 1651 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | MPFAK others(1646): Show |
chrX | 17370200 | 17740994 |
| a0008 | 0/0 | 1651 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | MPFAK others(1646): Show |
chrX | 17370200 | 17740994 |
| a0009 | 0/0 | 1639 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | MPFAK others(1634): Show |
chrX | 17370200 | 17740994 |
| a0010 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | MPFAK others(1645): Show |
chrX | 17370200 | 17740994 |
| a0011 | 0/0 | 1651 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | MPFAK others(1646): Show |
chrX | 17370200 | 17740994 |
| a0012 | 0/0 | 1651 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | MPFAK others(1646): Show |
chrX | 17370200 | 17740994 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 4953 | 68 | 24 | 11 | 32 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | ATGCC others(4948): Show |
chrX | 17370200 | 17740994 | ||
| a0001c0003 | 0/0 | 4953 | 5 | 4 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | ATGCC others(4948): Show |
chrX | 17370200 | 17740994 | ||
| a0002c0002 | 0/0 | 4953 | 65 | 4 | 13 | 30 | 4 | 14 | NHS_chrX_17370200_17740994 | NHS | ATGCC others(4948): Show |
chrX | 17370200 | 17740994 | ||
| a0002c0015 | 0/0 | 4953 | 1 | 0 | 0 | 0 | 1 | 0 | NHS_chrX_17370200_17740994 | NHS | ATGCC others(4948): Show |
chrX | 17370200 | 17740994 | ||
| a0003c0006 | 0/0 | 4950 | 4 | 3 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | ATGCC others(4945): Show |
chrX | 17370200 | 17740994 | ||
| a0003c0009 | 0/0 | 4950 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | ATGCC others(4945): Show |
chrX | 17370200 | 17740994 | ||
| a0004c0004 | 0/0 | 4953 | 5 | 0 | 2 | 3 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | ATGCC others(4948): Show |
chrX | 17370200 | 17740994 | ||
| a0005c0005 | 0/0 | 4953 | 5 | 5 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | ATGCC others(4948): Show |
chrX | 17370200 | 17740994 | ||
| a0006c0007 | 0/0 | 4953 | 2 | 2 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | ATGCC others(4948): Show |
chrX | 17370200 | 17740994 | ||
| a0006c0008 | 0/0 | 4953 | 2 | 2 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | ATGCC others(4948): Show |
chrX | 17370200 | 17740994 | ||
| a0007c0014 | 0/0 | 4953 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | ATGCC others(4948): Show |
chrX | 17370200 | 17740994 | ||
| a0008c0011 | 0/0 | 4953 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | ATGCC others(4948): Show |
chrX | 17370200 | 17740994 | ||
| a0009c0016 | 0/0 | 4917 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | ATGCC others(4912): Show |
chrX | 17370200 | 17740994 | ||
| a0010c0010 | 0/0 | 4950 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | ATGCC others(4945): Show |
chrX | 17370200 | 17740994 | ||
| a0011c0012 | 0/0 | 4953 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | ATGCC others(4948): Show |
chrX | 17370200 | 17740994 | ||
| a0012c0013 | 0/0 | 4953 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | ATGCC others(4948): Show |
chrX | 17370200 | 17740994 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 9044 | 38 | 7 | 4 | 26 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | AGAGC others(9039): Show |
chrX | 17370200 | 17740994 |
| a0001c0001t0002 | 0/0 | 9044 | 17 | 12 | 5 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | AGAGC others(9039): Show |
chrX | 17370200 | 17740994 |
| a0001c0001t0004 | 0/0 | 9044 | 3 | 0 | 1 | 2 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | AGAGC others(9039): Show |
chrX | 17370200 | 17740994 |
| a0001c0001t0005 | 0/0 | 9049 | 2 | 2 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | AGAGC others(9044): Show |
chrX | 17370200 | 17740994 |
| a0001c0001t0006 | 0/0 | 9044 | 2 | 0 | 0 | 2 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | AGAGC others(9039): Show |
chrX | 17370200 | 17740994 |
| a0001c0001t0007 | 0/0 | 9044 | 2 | 2 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | AGAGC others(9039): Show |
chrX | 17370200 | 17740994 |
| a0001c0001t0010 | 0/0 | 9044 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | AGAGC others(9039): Show |
chrX | 17370200 | 17740994 |
| a0001c0001t0011 | 0/0 | 9057 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | AGAGC others(9052): Show |
chrX | 17370200 | 17740994 |
| a0001c0001t0012 | 0/0 | 9044 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | AGAGC others(9039): Show |
chrX | 17370200 | 17740994 |
| a0001c0001t0013 | 0/0 | 9044 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | AGAGC others(9039): Show |
chrX | 17370200 | 17740994 |
| a0001c0003t0002 | 0/0 | 9044 | 5 | 4 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | AGAGC others(9039): Show |
chrX | 17370200 | 17740994 |
| a0002c0002t0001 | 0/0 | 9044 | 64 | 3 | 13 | 30 | 4 | 14 | NHS_chrX_17370200_17740994 | NHS | AGAGC others(9039): Show |
chrX | 17370200 | 17740994 |
| a0002c0002t0009 | 0/0 | 9044 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | AGAAC others(9039): Show |
chrX | 17370200 | 17740994 |
| a0002c0015t0001 | 0/0 | 9044 | 1 | 0 | 0 | 0 | 1 | 0 | NHS_chrX_17370200_17740994 | NHS | AGAGC others(9039): Show |
chrX | 17370200 | 17740994 |
| a0003c0006t0001 | 0/0 | 9041 | 2 | 1 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | AGAGC others(9036): Show |
chrX | 17370200 | 17740994 |
| a0003c0006t0002 | 0/0 | 9041 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | AGAGC others(9036): Show |
chrX | 17370200 | 17740994 |
| a0003c0006t0005 | 0/0 | 9046 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | AGAGC others(9041): Show |
chrX | 17370200 | 17740994 |
| a0003c0009t0002 | 0/0 | 9041 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | AGAGC others(9036): Show |
chrX | 17370200 | 17740994 |
| a0004c0004t0001 | 0/0 | 9044 | 5 | 0 | 2 | 3 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | AGAGC others(9039): Show |
chrX | 17370200 | 17740994 |
| a0005c0005t0003 | 0/0 | 9044 | 3 | 3 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | AGAGC others(9039): Show |
chrX | 17370200 | 17740994 |
| a0005c0005t0008 | 0/0 | 9044 | 2 | 2 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | AGAGC others(9039): Show |
chrX | 17370200 | 17740994 |
| a0006c0007t0002 | 0/0 | 9044 | 2 | 2 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | AGAGC others(9039): Show |
chrX | 17370200 | 17740994 |
| a0006c0008t0001 | 0/0 | 9044 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | AGAGC others(9039): Show |
chrX | 17370200 | 17740994 |
| a0006c0008t0002 | 0/0 | 9044 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | AGAGC others(9039): Show |
chrX | 17370200 | 17740994 |
| a0007c0014t0003 | 0/0 | 9044 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | AGAGC others(9039): Show |
chrX | 17370200 | 17740994 |
| a0008c0011t0002 | 0/0 | 9044 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | AGAGC others(9039): Show |
chrX | 17370200 | 17740994 |
| a0009c0016t0002 | 0/0 | 9008 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | AGAGC others(9003): Show |
chrX | 17370200 | 17740994 |
| a0010c0010t0003 | 0/0 | 9041 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | AGAGC others(9036): Show |
chrX | 17370200 | 17740994 |
| a0011c0012t0001 | 0/0 | 9044 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | AGAGC others(9039): Show |
chrX | 17370200 | 17740994 |
| a0012c0013t0001 | 0/0 | 9044 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | AGAGC others(9039): Show |
chrX | 17370200 | 17740994 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0002g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0005g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0005g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0006g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0006g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0007g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0007g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0010g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0011g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0012g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0001t0013g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0003t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0003t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0003t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0003t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0001c0003t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0002t0009g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0002c0015t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0003c0006t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0003c0006t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0003c0006t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0003c0006t0005g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0003c0009t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0004c0004t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0004c0004t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0004c0004t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0004c0004t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0004c0004t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0005c0005t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0005c0005t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0005c0005t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0005c0005t0008g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0005c0005t0008g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0006c0007t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0006c0007t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0006c0008t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0006c0008t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0007c0014t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0008c0011t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0009c0016t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0010c0010t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0011c0012t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| a0012c0013t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0046 | EUR | GBR | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0020 | EUR | FIN | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | CHS | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | CHS | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0123 | AMR | PUR | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0152 | AMR | PUR | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0139 | EAS | CHS | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0130 | AMR | PUR | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0093 | AMR | PUR | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01071 | hp2 | a0007 | c0014 | t0003 | g0092 | AMR | PUR | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0018 | AMR | PUR | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0031 | AMR | PUR | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01106 | hp1 | a0003 | c0006 | t0001 | g0157 | AMR | PUR | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0040 | AMR | PUR | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0032 | AMR | PUR | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0100 | AMR | PUR | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0028 | AMR | CLM | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01258 | hp1 | a0001 | c0003 | t0002 | g0014 | AMR | CLM | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0163 | AMR | CLM | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0075 | AMR | CLM | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | CLM | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0007 | EUR | IBS | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0030 | AMR | PEL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01952 | hp1 | a0004 | c0004 | t0001 | g0132 | AMR | PEL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01975 | hp1 | a0001 | c0001 | t0012 | g0154 | AMR | PEL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0019 | AMR | PEL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0067 | EAS | KHV | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | KHV | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02055 | hp1 | a0005 | c0005 | t0003 | g0101 | AFR | ACB | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0054 | EAS | KHV | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0138 | EAS | KHV | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0023 | EAS | KHV | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0090 | EAS | KHV | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02145 | hp1 | a0006 | c0008 | t0002 | g0113 | AFR | ACB | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02257 | hp1 | a0002 | c0002 | t0009 | g0015 | AFR | ACB | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02257 | hp2 | a0008 | c0011 | t0002 | g0147 | AFR | ACB | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0106 | AFR | ACB | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | ACB | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02280 | hp2 | a0001 | c0003 | t0002 | g0128 | AFR | ACB | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0078 | AMR | PEL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02300 | hp1 | a0004 | c0004 | t0001 | g0012 | AMR | PEL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02572 | hp1 | a0001 | c0003 | t0002 | g0142 | AFR | GWD | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0131 | SAS | PJL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02615 | hp1 | a0006 | c0007 | t0002 | g0118 | AFR | GWD | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02615 | hp2 | a0001 | c0001 | t0007 | g0122 | AFR | GWD | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0027 | AFR | GWD | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02622 | hp2 | a0003 | c0006 | t0005 | g0159 | AFR | GWD | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0146 | AFR | GWD | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02630 | hp2 | a0009 | c0016 | t0002 | g0119 | AFR | GWD | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02647 | hp1 | a0005 | c0005 | t0003 | g0136 | AFR | GWD | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0164 | AFR | GWD | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0096 | AFR | GWD | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02723 | hp2 | a0010 | c0010 | t0003 | g0158 | AFR | GWD | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0033 | SAS | PJL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0084 | SAS | PJL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02809 | hp2 | a0006 | c0007 | t0002 | g0115 | AFR | GWD | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0091 | AFR | GWD | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02922 | hp1 | a0003 | c0006 | t0001 | g0162 | AFR | ESN | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02922 | hp2 | a0001 | c0003 | t0002 | g0102 | AFR | ESN | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02965 | hp1 | a0005 | c0005 | t0008 | g0087 | AFR | ESN | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0072 | SAS | PJL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG03041 | hp1 | a0006 | c0008 | t0001 | g0114 | AFR | GWD | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG03041 | hp2 | a0001 | c0003 | t0002 | g0155 | AFR | GWD | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | MSL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0116 | AFR | MSL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0104 | AFR | MSL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | MSL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG03453 | hp2 | a0003 | c0009 | t0002 | g0160 | AFR | MSL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0043 | SAS | PJL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0063 | SAS | PJL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG03516 | hp1 | a0005 | c0005 | t0003 | g0117 | AFR | ESN | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG03516 | hp2 | a0001 | c0001 | t0007 | g0125 | AFR | ESN | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | MSL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0077 | SAS | PJL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0109 | SAS | STU | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0141 | SAS | BEB | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0034 | SAS | STU | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0062 | SAS | STU | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0079 | SAS | STU | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0076 | SAS | STU | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | YRI | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0052 | EAS | CHB | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CHB | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0111 | AFR | YRI | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0110 | AFR | YRI | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18940 | hp1 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18948 | hp1 | a0011 | c0012 | t0001 | g0150 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18952 | hp1 | a0001 | c0001 | t0011 | g0081 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18965 | hp1 | a0001 | c0001 | t0010 | g0059 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0058 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18977 | hp1 | a0012 | c0013 | t0001 | g0038 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18990 | hp1 | a0004 | c0004 | t0001 | g0149 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19007 | hp1 | a0004 | c0004 | t0001 | g0055 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | LWK | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19030 | hp2 | a0001 | c0001 | t0013 | g0045 | AFR | LWK | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0016 | AFR | LWK | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19063 | hp1 | a0001 | c0001 | t0004 | g0071 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19067 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19068 | hp1 | a0004 | c0004 | t0001 | g0065 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19076 | hp1 | a0001 | c0001 | t0006 | g0103 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA20752 | hp1 | a0002 | c0015 | t0001 | g0039 | EUR | TSI | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0017 | EUR | TSI | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0082 | SAS | GIH | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG02486 | hp1 | a0005 | c0005 | t0008 | g0097 | AFR | ACB | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG03471 | hp1 | a0003 | c0006 | t0002 | g0161 | AFR | MSL | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | USA | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0143 | AFR | USA | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| NA18955 | hp1 | a0001 | c0001 | t0006 | g0074 | EAS | JPT | NHS_chrX_17370200_17740994 | NHS | chrX | 17370200 | 17740994 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:17375961 | ACCG | A | 2 | a0003 a0010 |
6 | HG01106.hp1 HG02622.hp2 HG02723.hp2 others(3): Show |
disruptive_inframe_deletion | MODERATE | c.216_218delGCC | p.Pro73del | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/9 | 774/9044 | 216/4956 | 72/1651 | INFO_REALIGN_3_PRIME | chrX | 17375961 | ||
| chrX:17375968 | C | T | 2 | a0006 a0009 |
5 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
missense_variant | MODERATE | c.211C>T | p.Pro71Ser | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/9 | 769/9044 | 211/4956 | 71/1651 | chrX | 17375968 | |||
| chrX:17376059 | AGGCGGCG others(29): Show |
A | 1 | a0009 | 1 | HG02630.hp2 | conservative_inframe_deletion | MODERATE | c.310_345delCCCGCAGC others(28): Show |
p.Pro104_Ala115del | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/9 | 868/9044 | 310/4956 | 104/1651 | INFO_REALIGN_3_PRIME | chrX | 17376059 | ||
| chrX:17725820 | C | T | 3 | a0005 a0007 a0010 |
7 | HG01071.hp2 HG02055.hp1 HG02486.hp1 others(4): Show |
missense_variant | MODERATE | c.1714C>T | p.Pro572Ser | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 7/9 | 2272/9044 | 1714/4956 | 572/1651 | chrX | 17725820 | |||
| chrX:17725829 | A | G | 1 | a0007 | 1 | HG01071.hp2 | missense_variant | MODERATE | c.1723A>G | p.Lys575Glu | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 7/9 | 2281/9044 | 1723/4956 | 575/1651 | chrX | 17725829 | |||
| chrX:17726716 | G | C | 1 | a0003 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.2610G>C | p.Lys870Asn | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 7/9 | 3168/9044 | 2610/4956 | 870/1651 | chrX | 17726716 | |||
| chrX:17726838 | A | G | 1 | a0012 | 1 | NA18977.hp1 | missense_variant | MODERATE | c.2732A>G | p.Glu911Gly | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 7/9 | 3290/9044 | 2732/4956 | 911/1651 | chrX | 17726838 | |||
| chrX:17726937 | A | T | 2 | a0004 a0011 |
6 | HG01952.hp1 HG02300.hp1 NA18948.hp1 others(3): Show |
missense_variant | MODERATE | c.2831A>T | p.His944Leu | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 7/9 | 3389/9044 | 2831/4956 | 944/1651 | chrX | 17726937 | |||
| chrX:17727651 | C | T | 1 | a0011 | 1 | NA18948.hp1 | missense_variant | MODERATE | c.3545C>T | p.Pro1182Leu | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 7/9 | 4103/9044 | 3545/4956 | 1182/1651 | chrX | 17727651 | |||
| chrX:17728124 | T | C | 10 | a0001 a0003 a0004 others(7): Show |
97 | HG00408.hp1 HG00609.hp1 HG00639.hp2 others(94): Show |
missense_variant | MODERATE | c.4018T>C | p.Phe1340Leu | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 7/9 | 4576/9044 | 4018/4956 | 1340/1651 | chrX | 17728124 | |||
| chrX:17732340 | G | C | 1 | a0008 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.4832G>C | p.Ser1611Thr | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 9/9 | 5390/9044 | 4832/4956 | 1611/1651 | chrX | 17732340 |
| 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:17692381 | C | G | 1 | a0002c0015 | 1 | NA20752.hp1 | synonymous_variant | LOW | c.765C>G | p.Pro255Pro | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/9 | 1323/9044 | 765/4956 | 255/1651 | chrX | 17692381 | |||
| chrX:17727307 | T | C | 2 | a0001c0003 a0006c0007 |
7 | HG01258.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
synonymous_variant | LOW | c.3201T>C | p.Ser1067Ser | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 7/9 | 3759/9044 | 3201/4956 | 1067/1651 | chrX | 17727307 | |||
| chrX:17727310 | A | G | 2 | a0001c0003 a0006c0007 |
7 | HG01258.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
synonymous_variant | LOW | c.3204A>G | p.Leu1068Leu | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 7/9 | 3762/9044 | 3204/4956 | 1068/1651 | chrX | 17727310 |
| 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:17375203 | G | A | 1 | a0002c0002t0009 | 1 | HG02257.hp1 | 5_prime_UTR_variant | MODIFIER | c.-555G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/9 | 555 | chrX | 17375203 | ||||||
| chrX:17733118 | G | A | 1 | a0001c0001t0006 | 2 | NA18955.hp1 NA19076.hp1 |
3_prime_UTR_variant | MODIFIER | c.*654G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 9/9 | 654 | chrX | 17733118 | ||||||
| chrX:17733838 | A | T | 15 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0013 others(12): Show |
40 | HG01069.hp1 HG01071.hp1 HG01071.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1374A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 9/9 | 1374 | chrX | 17733838 | ||||||
| chrX:17733999 | C | T | 1 | a0001c0001t0004 | 3 | HG01261.hp1 NA18970.hp1 NA19063.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1535C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 9/9 | 1535 | chrX | 17733999 | ||||||
| chrX:17734655 | C | T | 17 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(14): Show |
43 | HG01069.hp1 HG01071.hp1 HG01071.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*2191C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 9/9 | 2191 | chrX | 17734655 | ||||||
| chrX:17734817 | T | C | 1 | a0001c0001t0010 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2353T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 9/9 | 2353 | chrX | 17734817 | ||||||
| chrX:17734891 | T | C | 2 | a0001c0001t0005 a0003c0006t0005 |
3 | HG02622.hp2 HG03225.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2427T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 9/9 | 2427 | chrX | 17734891 | ||||||
| chrX:17734989 | A | ATTAAT | 2 | a0001c0001t0005 a0003c0006t0005 |
3 | HG02622.hp2 HG03225.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2529_*2530insTTTA others(1): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 9/9 | 2530 | INFO_REALIGN_3_PRIME | chrX | 17734989 | |||||
| chrX:17735280 | T | G | 6 | a0001c0001t0012 a0001c0001t0013 a0005c0005t0003 others(3): Show |
9 | HG01071.hp2 HG01975.hp1 HG02055.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2816T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 9/9 | 2816 | chrX | 17735280 | ||||||
| chrX:17735303 | T | G | 1 | a0001c0001t0011 | 1 | NA18952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2839T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 9/9 | 2839 | chrX | 17735303 | ||||||
| chrX:17735304 | T | TTAAGCCG others(6): Show |
1 | a0001c0001t0011 | 1 | NA18952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2840_*2841insTAAG others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 9/9 | 2841 | chrX | 17735304 | ||||||
| chrX:17735306 | G | C | 1 | a0001c0001t0011 | 1 | NA18952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2842G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 9/9 | 2842 | chrX | 17735306 | ||||||
| chrX:17735472 | T | A | 4 | a0005c0005t0003 a0005c0005t0008 a0007c0014t0003 others(1): Show |
7 | HG01071.hp2 HG02055.hp1 HG02486.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3008T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 9/9 | 3008 | chrX | 17735472 | ||||||
| chrX:17735718 | T | C | 3 | a0005c0005t0003 a0007c0014t0003 a0010c0010t0003 |
5 | HG01071.hp2 HG02055.hp1 HG02647.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3254T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 9/9 | 3254 | chrX | 17735718 |
| 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:17376857 | C | G | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+535C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17376857 | |||||||
| chrX:17376951 | T | C | 1 | a0002c0002t0001g0001 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.565+629T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17376951 | |||||||
| chrX:17377378 | C | A | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.565+1056C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17377378 | |||||||
| chrX:17377548 | C | G | 1 | a0001c0001t0004g0163 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.565+1226C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17377548 | |||||||
| chrX:17377688 | C | G | 6 | a0003c0006t0001g0157 a0003c0006t0001g0162 a0003c0006t0002g0161 others(3): Show |
6 | HG01106.hp1 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.565+1366C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17377688 | |||||||
| chrX:17378059 | C | CGT | 61 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(58): Show |
61 | HG00609.hp1 HG01069.hp1 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.565+1763_565+1764d others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17378059 | ||||||
| chrX:17378059 | C | CGTGT | 11 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0110 others(8): Show |
11 | HG02258.hp1 HG02622.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.565+1761_565+1764d others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17378059 | ||||||
| chrX:17378059 | C | CGTGTGT | 2 | a0001c0001t0002g0002 a0003c0006t0001g0162 |
2 | HG02293.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.565+1759_565+1764d others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17378059 | ||||||
| chrX:17378059 | C | CGTGTGTG others(5): Show |
4 | a0001c0001t0001g0112 a0006c0007t0002g0115 a0006c0008t0001g0114 others(1): Show |
4 | HG02145.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+1753_565+1764d others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17378059 | ||||||
| chrX:17378059 | C | CGTGTGTG others(7): Show |
1 | a0001c0001t0002g0116 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.565+1751_565+1764d others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17378059 | ||||||
| chrX:17378059 | C | CGTGTGTG others(9): Show |
3 | a0005c0005t0003g0117 a0006c0007t0002g0118 a0009c0016t0002g0119 |
3 | HG02615.hp1 HG02630.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.565+1749_565+1764d others(18): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17378059 | ||||||
| chrX:17378059 | C | CGTGTGTG others(11): Show |
1 | a0001c0001t0002g0120 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.565+1747_565+1764d others(20): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17378059 | ||||||
| chrX:17378059 | C | CGTGTGTG others(13): Show |
4 | a0001c0001t0001g0124 a0001c0001t0002g0121 a0001c0001t0007g0122 others(1): Show |
4 | HG00639.hp1 HG01943.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+1745_565+1764d others(22): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17378059 | ||||||
| chrX:17378059 | C | CGTGTGTG others(15): Show |
11 | a0001c0001t0001g0127 a0001c0001t0001g0129 a0001c0001t0001g0133 others(8): Show |
11 | HG00738.hp1 HG01071.hp1 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.565+1743_565+1764d others(24): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17378059 | ||||||
| chrX:17378059 | C | CGTGTGTG others(17): Show |
12 | a0001c0001t0001g0137 a0001c0001t0001g0140 a0001c0001t0001g0144 others(9): Show |
12 | HG00639.hp2 HG00673.hp1 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.565+1741_565+1764d others(26): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17378059 | ||||||
| chrX:17378059 | C | CGTGTGTG others(19): Show |
7 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0001t0012g0154 others(4): Show |
7 | HG00408.hp1 HG00642.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.565+1739_565+1764d others(28): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17378059 | ||||||
| chrX:17378059 | C | CGTGTGTG others(23): Show |
1 | a0001c0003t0002g0155 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.565+1764_565+1765i others(32): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17378059 | ||||||
| chrX:17378059 | C | CGTGTGTG others(25): Show |
1 | a0002c0002t0001g0156 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.565+1764_565+1765i others(34): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17378059 | ||||||
| chrX:17378059 | CGT | C | 31 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0021 others(28): Show |
31 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.565+1763_565+1764d others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17378059 | ||||||
| chrX:17378099 | CCTT | C | 5 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(2): Show |
5 | HG02280.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+1778_565+1780d others(5): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17378099 | |||||||
| chrX:17378144 | ATG | A | 4 | a0001c0001t0001g0127 a0001c0001t0002g0126 a0001c0001t0007g0125 others(1): Show |
4 | HG01071.hp1 HG02647.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+1825_565+1826d others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17378144 | ||||||
| chrX:17378918 | A | G | 7 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(4): Show |
7 | HG02257.hp2 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.565+2596A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17378918 | |||||||
| chrX:17379337 | C | T | 2 | a0001c0001t0002g0146 a0008c0011t0002g0147 |
2 | HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+3015C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17379337 | |||||||
| chrX:17379380 | T | G | 1 | a0001c0001t0002g0121 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.565+3058T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17379380 | |||||||
| chrX:17379555 | G | A | 5 | a0006c0007t0002g0115 a0006c0007t0002g0118 a0006c0008t0001g0114 others(2): Show |
5 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.565+3233G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17379555 | |||||||
| chrX:17379634 | G | A | 1 | a0006c0007t0002g0118 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.565+3312G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17379634 | |||||||
| chrX:17379905 | G | C | 5 | a0006c0007t0002g0115 a0006c0007t0002g0118 a0006c0008t0001g0114 others(2): Show |
5 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.565+3583G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17379905 | |||||||
| chrX:17380038 | G | C | 1 | a0002c0002t0001g0033 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.565+3716G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17380038 | |||||||
| chrX:17380378 | C | CT | 38 | a0001c0001t0001g0112 a0001c0001t0001g0124 a0001c0001t0001g0127 others(35): Show |
38 | HG00408.hp1 HG00639.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.565+4071dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17380378 | ||||||
| chrX:17380378 | CT | C | 51 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(48): Show |
51 | HG00609.hp1 HG01358.hp1 HG02015.hp1 others(48): Show |
intron_variant | MODIFIER | c.565+4071delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17380378 | ||||||
| chrX:17380608 | A | G | 1 | a0001c0001t0001g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.565+4286A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17380608 | |||||||
| chrX:17381118 | G | A | 6 | a0003c0006t0001g0157 a0003c0006t0001g0162 a0003c0006t0002g0161 others(3): Show |
6 | HG01106.hp1 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.565+4796G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17381118 | |||||||
| chrX:17381259 | G | A | 33 | a0001c0001t0001g0124 a0001c0001t0001g0127 a0001c0001t0001g0129 others(30): Show |
33 | HG00408.hp1 HG00639.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.565+4937G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17381259 | |||||||
| chrX:17381336 | C | T | 1 | a0002c0002t0001g0032 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.565+5014C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17381336 | |||||||
| chrX:17381347 | G | A | 1 | a0002c0002t0001g0156 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.565+5025G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17381347 | |||||||
| chrX:17381462 | A | G | 3 | a0002c0002t0001g0088 a0002c0002t0001g0089 a0002c0002t0001g0090 |
3 | HG02129.hp1 NA18945.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.565+5140A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17381462 | |||||||
| chrX:17381743 | A | T | 1 | a0001c0001t0005g0104 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.565+5421A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17381743 | |||||||
| chrX:17381977 | C | T | 1 | a0001c0003t0002g0155 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.565+5655C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17381977 | |||||||
| chrX:17382025 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.565+5703C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17382025 | |||||||
| chrX:17382184 | G | A | 1 | a0002c0002t0001g0105 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.565+5862G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17382184 | |||||||
| chrX:17383069 | A | T | 4 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0144 others(1): Show |
4 | NA18994.hp1 NA18995.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+6747A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17383069 | |||||||
| chrX:17383107 | T | C | 5 | a0006c0007t0002g0115 a0006c0007t0002g0118 a0006c0008t0001g0114 others(2): Show |
5 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.565+6785T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17383107 | |||||||
| chrX:17383846 | G | T | 1 | a0001c0001t0002g0143 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.565+7524G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17383846 | |||||||
| chrX:17384154 | G | A | 4 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0002c0002t0001g0091 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+7832G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17384154 | |||||||
| chrX:17384545 | A | G | 5 | a0006c0007t0002g0115 a0006c0007t0002g0118 a0006c0008t0001g0114 others(2): Show |
5 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.565+8223A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17384545 | |||||||
| chrX:17384813 | AATTTT | A | 6 | a0003c0006t0001g0157 a0003c0006t0001g0162 a0003c0006t0002g0161 others(3): Show |
6 | HG01106.hp1 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.565+8496_565+8500d others(7): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17384813 | ||||||
| chrX:17385041 | T | C | 38 | a0001c0001t0001g0124 a0001c0001t0001g0127 a0001c0001t0001g0129 others(35): Show |
38 | HG00408.hp1 HG00639.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.565+8719T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17385041 | |||||||
| chrX:17385674 | A | G | 5 | a0006c0007t0002g0115 a0006c0007t0002g0118 a0006c0008t0001g0114 others(2): Show |
5 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.565+9352A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17385674 | |||||||
| chrX:17385701 | G | A | 1 | a0001c0003t0002g0128 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.565+9379G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17385701 | |||||||
| chrX:17386222 | G | A | 9 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(6): Show |
9 | HG02056.hp1 NA18612.hp1 NA18961.hp1 others(6): Show |
intron_variant | MODIFIER | c.565+9900G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17386222 | |||||||
| chrX:17386263 | A | G | 2 | a0002c0002t0001g0054 a0004c0004t0001g0055 |
2 | HG02056.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.565+9941A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17386263 | |||||||
| chrX:17386331 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.565+10009G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17386331 | |||||||
| chrX:17386534 | C | T | 2 | a0001c0001t0002g0086 a0005c0005t0008g0087 |
2 | HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.565+10212C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17386534 | |||||||
| chrX:17386629 | C | T | 6 | a0003c0006t0001g0157 a0003c0006t0001g0162 a0003c0006t0002g0161 others(3): Show |
6 | HG01106.hp1 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.565+10307C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17386629 | |||||||
| chrX:17386663 | C | CA | 58 | a0001c0001t0001g0008 a0001c0001t0001g0094 a0001c0001t0001g0095 others(55): Show |
58 | HG00408.hp1 HG00621.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.565+10362dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17386663 | ||||||
| chrX:17387616 | G | A | 1 | a0002c0002t0001g0010 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.565+11294G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17387616 | |||||||
| chrX:17388145 | C | T | 1 | a0003c0006t0002g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.565+11823C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17388145 | |||||||
| chrX:17388294 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.565+11972G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17388294 | |||||||
| chrX:17388483 | G | C | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.565+12161G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17388483 | |||||||
| chrX:17388829 | A | C | 5 | a0006c0007t0002g0115 a0006c0007t0002g0118 a0006c0008t0001g0114 others(2): Show |
5 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.565+12507A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17388829 | |||||||
| chrX:17388836 | G | A | 3 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0110 |
3 | HG02258.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.565+12514G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17388836 | |||||||
| chrX:17388921 | A | C | 1 | a0001c0001t0002g0121 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.565+12599A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17388921 | |||||||
| chrX:17388947 | T | TA | 2 | a0001c0001t0002g0146 a0008c0011t0002g0147 |
2 | HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+12626dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17388947 | ||||||
| chrX:17389498 | A | G | 2 | a0001c0001t0002g0002 a0001c0001t0002g0096 |
2 | HG02293.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.565+13176A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17389498 | |||||||
| chrX:17389581 | A | T | 1 | a0002c0002t0001g0009 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.565+13259A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17389581 | |||||||
| chrX:17389586 | C | CTTAT | 97 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0037 others(94): Show |
97 | HG00408.hp1 HG00621.hp1 HG00639.hp1 others(94): Show |
intron_variant | MODIFIER | c.565+13291_565+1329 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17389586 | ||||||
| chrX:17389586 | C | CTTATTTA others(1): Show |
9 | a0001c0001t0001g0057 a0001c0001t0001g0129 a0001c0001t0002g0086 others(6): Show |
9 | HG00609.hp1 HG00738.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.565+13287_565+1329 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17389586 | ||||||
| chrX:17389586 | C | CTTATTTA others(5): Show |
12 | a0001c0001t0001g0112 a0001c0001t0001g0137 a0001c0001t0002g0002 others(9): Show |
12 | HG01106.hp1 HG02293.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.565+13283_565+1329 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17389586 | ||||||
| chrX:17389586 | C | CTTATTTA others(9): Show |
6 | a0001c0001t0002g0096 a0003c0006t0001g0162 a0006c0008t0001g0114 others(3): Show |
6 | HG02257.hp2 HG02630.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.565+13279_565+1329 others(20): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17389586 | ||||||
| chrX:17389586 | C | CTTATTTA others(13): Show |
2 | a0001c0001t0002g0146 a0006c0008t0002g0113 |
2 | HG02145.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.565+13275_565+1329 others(24): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17389586 | ||||||
| chrX:17389666 | A | G | 1 | a0002c0002t0001g0046 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.565+13344A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17389666 | |||||||
| chrX:17389813 | G | T | 1 | a0001c0001t0001g0085 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.565+13491G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17389813 | |||||||
| chrX:17389848 | C | A | 2 | a0001c0001t0010g0059 a0002c0002t0001g0060 |
2 | NA18965.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.565+13526C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17389848 | |||||||
| chrX:17389919 | C | T | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0005g0104 others(1): Show |
4 | HG02280.hp2 HG03139.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+13597C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17389919 | |||||||
| chrX:17389943 | A | T | 2 | a0001c0001t0002g0002 a0001c0001t0002g0096 |
2 | HG02293.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.565+13621A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17389943 | |||||||
| chrX:17389944 | A | T | 2 | a0001c0001t0002g0002 a0001c0001t0002g0096 |
2 | HG02293.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.565+13622A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17389944 | |||||||
| chrX:17389952 | G | GA | 6 | a0003c0006t0001g0157 a0003c0006t0001g0162 a0003c0006t0002g0161 others(3): Show |
6 | HG01106.hp1 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.565+13642dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17389952 | ||||||
| chrX:17390052 | T | C | 1 | a0002c0002t0001g0131 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.565+13730T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17390052 | |||||||
| chrX:17390060 | G | A | 2 | a0001c0001t0010g0059 a0002c0002t0001g0060 |
2 | NA18965.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.565+13738G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17390060 | |||||||
| chrX:17390323 | G | A | 4 | a0001c0001t0001g0061 a0001c0001t0001g0098 a0001c0001t0001g0099 others(1): Show |
4 | NA18967.hp1 NA18983.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+14001G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17390323 | |||||||
| chrX:17390460 | G | A | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+14138G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17390460 | |||||||
| chrX:17390512 | T | C | 35 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0124 others(32): Show |
35 | HG00408.hp1 HG00621.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.565+14190T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17390512 | |||||||
| chrX:17390848 | C | T | 34 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0124 others(31): Show |
34 | HG00408.hp1 HG00621.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.565+14526C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17390848 | |||||||
| chrX:17391001 | T | C | 1 | a0002c0002t0001g0108 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.565+14679T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17391001 | |||||||
| chrX:17391023 | G | T | 1 | a0001c0001t0001g0008 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.565+14701G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17391023 | |||||||
| chrX:17391117 | A | G | 2 | a0001c0001t0002g0002 a0001c0001t0002g0096 |
2 | HG02293.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.565+14795A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17391117 | |||||||
| chrX:17391214 | G | T | 4 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0002c0002t0001g0091 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+14892G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17391214 | |||||||
| chrX:17391516 | A | C | 2 | a0001c0001t0002g0002 a0001c0001t0002g0096 |
2 | HG02293.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.565+15194A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17391516 | |||||||
| chrX:17392070 | G | A | 1 | a0002c0002t0001g0108 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.565+15748G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17392070 | |||||||
| chrX:17392246 | G | A | 7 | a0001c0001t0002g0002 a0001c0001t0002g0096 a0006c0007t0002g0115 others(4): Show |
7 | HG02145.hp1 HG02293.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.565+15924G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17392246 | |||||||
| chrX:17392717 | C | A | 1 | a0004c0004t0001g0012 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.565+16395C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17392717 | |||||||
| chrX:17393028 | A | G | 1 | a0002c0002t0001g0007 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.565+16706A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17393028 | |||||||
| chrX:17393102 | TG | T | 5 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(2): Show |
5 | HG02280.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+16783delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17393102 | ||||||
| chrX:17393194 | C | G | 1 | a0002c0002t0001g0084 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.565+16872C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17393194 | |||||||
| chrX:17393363 | G | A | 4 | a0001c0001t0001g0127 a0001c0001t0002g0126 a0001c0001t0007g0125 others(1): Show |
4 | HG01071.hp1 HG02647.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+17041G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17393363 | |||||||
| chrX:17393386 | G | A | 5 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(2): Show |
5 | HG02280.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+17064G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17393386 | |||||||
| chrX:17393556 | C | T | 2 | a0001c0001t0002g0002 a0001c0001t0002g0096 |
2 | HG02293.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.565+17234C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17393556 | |||||||
| chrX:17393726 | G | T | 2 | a0001c0001t0002g0002 a0001c0001t0002g0096 |
2 | HG02293.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.565+17404G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17393726 | |||||||
| chrX:17393956 | C | T | 1 | a0001c0001t0013g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.565+17634C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17393956 | |||||||
| chrX:17394085 | A | G | 1 | a0001c0001t0002g0044 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.565+17763A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17394085 | |||||||
| chrX:17394274 | T | C | 1 | a0006c0008t0001g0114 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.565+17952T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17394274 | |||||||
| chrX:17394321 | T | C | 2 | a0001c0001t0002g0002 a0001c0001t0002g0096 |
2 | HG02293.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.565+17999T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17394321 | |||||||
| chrX:17394637 | C | T | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+18315C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17394637 | |||||||
| chrX:17394726 | C | G | 1 | a0001c0001t0006g0103 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.565+18404C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17394726 | |||||||
| chrX:17394771 | G | T | 10 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(7): Show |
10 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.565+18449G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17394771 | |||||||
| chrX:17394772 | A | AT | 10 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(7): Show |
10 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.565+18456dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17394772 | ||||||
| chrX:17394997 | A | G | 1 | a0001c0003t0002g0142 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.565+18675A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17394997 | |||||||
| chrX:17395179 | GA | G | 6 | a0001c0001t0001g0083 a0001c0001t0001g0112 a0001c0001t0002g0116 others(3): Show |
6 | HG02280.hp1 HG03098.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.565+18869delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17395179 | ||||||
| chrX:17396318 | C | CT | 5 | a0006c0007t0002g0115 a0006c0007t0002g0118 a0006c0008t0001g0114 others(2): Show |
5 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.565+20002dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17396318 | ||||||
| chrX:17396463 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.565+20141G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17396463 | |||||||
| chrX:17396781 | C | T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0124 a0002c0002t0001g0030 others(1): Show |
4 | HG01099.hp1 HG01928.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+20459C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17396781 | |||||||
| chrX:17397143 | A | G | 1 | a0002c0002t0001g0082 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.565+20821A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17397143 | |||||||
| chrX:17397331 | T | C | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.565+21009T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17397331 | |||||||
| chrX:17397611 | G | A | 5 | a0001c0001t0002g0002 a0001c0001t0002g0100 a0001c0001t0002g0146 others(2): Show |
5 | HG01243.hp1 HG02257.hp2 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.565+21289G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17397611 | |||||||
| chrX:17398874 | C | G | 1 | a0005c0005t0003g0117 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.565+22552C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17398874 | |||||||
| chrX:17398938 | A | G | 5 | a0006c0007t0002g0115 a0006c0007t0002g0118 a0006c0008t0001g0114 others(2): Show |
5 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.565+22616A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17398938 | |||||||
| chrX:17399180 | C | T | 1 | a0002c0002t0001g0141 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.565+22858C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17399180 | |||||||
| chrX:17400043 | A | G | 1 | a0001c0001t0001g0083 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.565+23721A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17400043 | |||||||
| chrX:17400064 | C | A | 5 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(2): Show |
5 | HG02280.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+23742C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17400064 | |||||||
| chrX:17400200 | T | C | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.565+23878T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17400200 | |||||||
| chrX:17400367 | T | C | 9 | a0001c0001t0002g0002 a0001c0001t0002g0100 a0001c0001t0002g0146 others(6): Show |
9 | HG01243.hp1 HG02145.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.565+24045T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17400367 | |||||||
| chrX:17400511 | G | A | 5 | a0006c0007t0002g0115 a0006c0007t0002g0118 a0006c0008t0001g0114 others(2): Show |
5 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.565+24189G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17400511 | |||||||
| chrX:17401192 | A | C | 1 | a0001c0001t0002g0143 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.565+24870A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17401192 | |||||||
| chrX:17401289 | A | G | 5 | a0006c0007t0002g0115 a0006c0007t0002g0118 a0006c0008t0001g0114 others(2): Show |
5 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.565+24967A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17401289 | |||||||
| chrX:17401913 | T | C | 5 | a0006c0007t0002g0115 a0006c0007t0002g0118 a0006c0008t0001g0114 others(2): Show |
5 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.565+25591T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17401913 | |||||||
| chrX:17402010 | T | C | 4 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0144 others(1): Show |
4 | NA18994.hp1 NA18995.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+25688T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17402010 | |||||||
| chrX:17402223 | T | C | 9 | a0001c0001t0002g0002 a0001c0001t0002g0100 a0001c0001t0002g0146 others(6): Show |
9 | HG01243.hp1 HG02145.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.565+25901T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17402223 | |||||||
| chrX:17402320 | G | C | 1 | a0006c0007t0002g0118 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.565+25998G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17402320 | |||||||
| chrX:17402553 | A | G | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.565+26231A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17402553 | |||||||
| chrX:17402629 | G | T | 1 | a0002c0002t0001g0043 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.565+26307G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17402629 | |||||||
| chrX:17402894 | G | C | 1 | a0002c0002t0001g0013 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.565+26572G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17402894 | |||||||
| chrX:17403025 | C | G | 2 | a0006c0008t0001g0114 a0006c0008t0002g0113 |
2 | HG02145.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.565+26703C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17403025 | |||||||
| chrX:17403448 | A | G | 8 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0006c0007t0002g0115 others(5): Show |
8 | HG01243.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.565+27126A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17403448 | |||||||
| chrX:17403893 | A | G | 8 | a0001c0001t0005g0111 a0001c0003t0002g0102 a0003c0006t0001g0157 others(5): Show |
8 | HG01106.hp1 HG02622.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.565+27571A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17403893 | |||||||
| chrX:17404024 | A | T | 1 | a0001c0001t0001g0137 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.565+27702A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17404024 | |||||||
| chrX:17404482 | T | C | 1 | a0002c0002t0001g0013 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.565+28160T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17404482 | |||||||
| chrX:17404652 | C | T | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+28330C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17404652 | |||||||
| chrX:17404792 | C | T | 8 | a0001c0001t0005g0111 a0001c0003t0002g0102 a0003c0006t0001g0157 others(5): Show |
8 | HG01106.hp1 HG02622.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.565+28470C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17404792 | |||||||
| chrX:17404801 | CTG | C | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+28481_565+2848 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17404801 | ||||||
| chrX:17404803 | G | GTC | 15 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0144 others(12): Show |
15 | HG01106.hp1 HG01975.hp2 HG02300.hp1 others(12): Show |
intron_variant | MODIFIER | c.565+28508_565+2850 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17404803 | ||||||
| chrX:17404803 | G | GTCTC | 3 | a0001c0001t0002g0086 a0001c0001t0004g0163 a0005c0005t0008g0087 |
3 | HG01261.hp1 HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.565+28506_565+2850 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17404803 | ||||||
| chrX:17405033 | A | G | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+28711A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17405033 | |||||||
| chrX:17405105 | G | A | 6 | a0003c0006t0001g0157 a0003c0006t0001g0162 a0003c0006t0002g0161 others(3): Show |
6 | HG01106.hp1 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.565+28783G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17405105 | |||||||
| chrX:17405593 | T | G | 1 | a0002c0002t0001g0062 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.565+29271T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17405593 | |||||||
| chrX:17405594 | C | T | 1 | a0002c0002t0001g0062 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.565+29272C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17405594 | |||||||
| chrX:17405645 | A | AT | 5 | a0001c0001t0001g0011 a0001c0001t0001g0029 a0001c0001t0001g0124 others(2): Show |
5 | HG01099.hp1 HG01928.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+29329dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17405645 | ||||||
| chrX:17405835 | A | G | 4 | a0001c0001t0002g0002 a0001c0001t0002g0100 a0001c0001t0002g0146 others(1): Show |
4 | HG01243.hp1 HG02257.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.565+29513A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17405835 | |||||||
| chrX:17405885 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.565+29563A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17405885 | |||||||
| chrX:17405996 | C | T | 64 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(61): Show |
64 | HG00609.hp1 HG01069.hp1 HG01071.hp2 others(61): Show |
intron_variant | MODIFIER | c.565+29674C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17405996 | |||||||
| chrX:17406558 | A | C | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+30236A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17406558 | |||||||
| chrX:17406600 | C | T | 1 | a0002c0002t0001g0031 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.565+30278C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17406600 | |||||||
| chrX:17406689 | G | A | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+30367G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17406689 | |||||||
| chrX:17407232 | T | C | 1 | a0001c0001t0012g0154 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.565+30910T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17407232 | |||||||
| chrX:17407438 | C | G | 4 | a0001c0001t0002g0002 a0001c0001t0002g0100 a0001c0001t0002g0146 others(1): Show |
4 | HG01243.hp1 HG02257.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.565+31116C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17407438 | |||||||
| chrX:17407568 | T | G | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+31246T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17407568 | |||||||
| chrX:17408103 | G | A | 1 | a0001c0001t0007g0122 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.565+31781G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17408103 | |||||||
| chrX:17408162 | T | C | 37 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0021 others(34): Show |
37 | HG00280.hp1 HG00408.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.565+31840T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17408162 | |||||||
| chrX:17408576 | C | T | 11 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(8): Show |
11 | HG01256.hp1 HG02145.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.565+32254C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17408576 | |||||||
| chrX:17408711 | G | A | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.565+32389G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17408711 | |||||||
| chrX:17408806 | C | T | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.565+32484C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17408806 | |||||||
| chrX:17408951 | AGAG | A | 2 | a0001c0001t0002g0086 a0005c0005t0008g0087 |
2 | HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.565+32633_565+3263 others(7): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17408951 | ||||||
| chrX:17408954 | G | GGA | 10 | a0001c0001t0001g0127 a0001c0001t0002g0100 a0001c0001t0002g0106 others(7): Show |
10 | HG01071.hp1 HG01243.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.565+32656_565+3265 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17408954 | ||||||
| chrX:17408954 | GGAGA | G | 18 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(15): Show |
18 | HG01106.hp1 HG02145.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.565+32654_565+3265 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17408954 | ||||||
| chrX:17409374 | G | GT | 7 | a0001c0001t0001g0099 a0001c0001t0001g0133 a0001c0001t0002g0002 others(4): Show |
7 | HG01243.hp1 HG01975.hp1 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.565+33068dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17409374 | ||||||
| chrX:17409374 | GT | G | 27 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0029 others(24): Show |
27 | HG00280.hp1 HG00408.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.565+33068delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17409374 | ||||||
| chrX:17409531 | C | T | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+33209C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17409531 | |||||||
| chrX:17409868 | T | C | 1 | a0002c0002t0001g0108 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.565+33546T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17409868 | |||||||
| chrX:17410139 | G | C | 1 | a0001c0001t0001g0066 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.565+33817G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17410139 | |||||||
| chrX:17410218 | G | A | 1 | a0001c0001t0007g0125 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.565+33896G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17410218 | |||||||
| chrX:17410386 | G | A | 1 | a0002c0002t0001g0023 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.565+34064G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17410386 | |||||||
| chrX:17410463 | T | C | 1 | a0002c0002t0001g0054 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.565+34141T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17410463 | |||||||
| chrX:17410516 | C | CT | 27 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(24): Show |
27 | HG00609.hp1 HG00639.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.565+34215dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17410516 | ||||||
| chrX:17410516 | C | CTT | 6 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0001c0001t0011g0081 others(3): Show |
6 | HG01243.hp1 HG02257.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.565+34214_565+3421 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17410516 | ||||||
| chrX:17410516 | CT | C | 13 | a0001c0001t0001g0035 a0001c0001t0002g0164 a0001c0001t0013g0045 others(10): Show |
13 | HG01106.hp1 HG02280.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.565+34215delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17410516 | ||||||
| chrX:17410538 | C | T | 4 | a0001c0001t0002g0002 a0001c0001t0002g0100 a0001c0001t0002g0146 others(1): Show |
4 | HG01243.hp1 HG02257.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.565+34216C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17410538 | |||||||
| chrX:17410555 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.565+34233A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17410555 | |||||||
| chrX:17410850 | A | G | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+34528A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17410850 | |||||||
| chrX:17411275 | A | C | 23 | a0001c0001t0001g0112 a0001c0001t0002g0002 a0001c0001t0002g0100 others(20): Show |
23 | HG01106.hp1 HG01243.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.565+34953A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17411275 | |||||||
| chrX:17411411 | A | G | 1 | a0002c0002t0001g0022 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.565+35089A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17411411 | |||||||
| chrX:17411572 | C | T | 3 | a0001c0001t0001g0085 a0002c0002t0001g0001 a0002c0002t0001g0078 |
3 | HG02040.hp1 HG02293.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.565+35250C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17411572 | |||||||
| chrX:17411610 | A | T | 1 | a0002c0002t0001g0148 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.565+35288A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17411610 | |||||||
| chrX:17411768 | A | G | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.565+35446A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17411768 | |||||||
| chrX:17411888 | G | A | 10 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(7): Show |
10 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.565+35566G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17411888 | |||||||
| chrX:17411944 | T | G | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+35622T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17411944 | |||||||
| chrX:17412145 | G | C | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35823G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412145 | |||||||
| chrX:17412146 | G | T | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35824G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412146 | |||||||
| chrX:17412147 | A | C | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35825A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412147 | |||||||
| chrX:17412149 | G | C | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35827G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412149 | |||||||
| chrX:17412151 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35829G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412151 | |||||||
| chrX:17412152 | T | C | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35830T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412152 | |||||||
| chrX:17412157 | T | A | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35835T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412157 | |||||||
| chrX:17412158 | T | C | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35836T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412158 | |||||||
| chrX:17412160 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35838G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412160 | |||||||
| chrX:17412161 | T | C | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35839T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412161 | |||||||
| chrX:17412163 | T | G | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35841T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412163 | |||||||
| chrX:17412164 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35842G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412164 | |||||||
| chrX:17412166 | C | G | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35844C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412166 | |||||||
| chrX:17412167 | T | A | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35845T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412167 | |||||||
| chrX:17412168 | C | G | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35846C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412168 | |||||||
| chrX:17412169 | C | G | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35847C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412169 | |||||||
| chrX:17412172 | T | G | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35850T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412172 | |||||||
| chrX:17412173 | T | G | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35851T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412173 | |||||||
| chrX:17412174 | C | A | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35852C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412174 | |||||||
| chrX:17412177 | T | A | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35855T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412177 | |||||||
| chrX:17412180 | T | G | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35858T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412180 | |||||||
| chrX:17412182 | T | G | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35860T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412182 | |||||||
| chrX:17412183 | T | A | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35861T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412183 | |||||||
| chrX:17412184 | T | G | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35862T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412184 | |||||||
| chrX:17412188 | T | C | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35866T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412188 | |||||||
| chrX:17412194 | A | G | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35872A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412194 | |||||||
| chrX:17412197 | A | C | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35875A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412197 | |||||||
| chrX:17412198 | A | G | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35876A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412198 | |||||||
| chrX:17412199 | T | C | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35877T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412199 | |||||||
| chrX:17412202 | A | T | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35880A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412202 | |||||||
| chrX:17412210 | A | C | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35888A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412210 | |||||||
| chrX:17412212 | A | C | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35890A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412212 | |||||||
| chrX:17412213 | A | C | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35891A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412213 | |||||||
| chrX:17412215 | A | C | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35893A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412215 | |||||||
| chrX:17412217 | A | C | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35895A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412217 | |||||||
| chrX:17412218 | T | C | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35896T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412218 | |||||||
| chrX:17412219 | A | G | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35897A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412219 | |||||||
| chrX:17412222 | A | G | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35900A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412222 | |||||||
| chrX:17412226 | A | G | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35904A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412226 | |||||||
| chrX:17412232 | A | T | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35910A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412232 | |||||||
| chrX:17412234 | A | G | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35912A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412234 | |||||||
| chrX:17412236 | T | G | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35914T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412236 | |||||||
| chrX:17412238 | T | G | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35916T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412238 | |||||||
| chrX:17412240 | T | G | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35918T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412240 | |||||||
| chrX:17412243 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35921G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412243 | |||||||
| chrX:17412244 | T | C | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35922T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412244 | |||||||
| chrX:17412246 | T | C | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35924T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412246 | |||||||
| chrX:17412248 | C | A | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35926C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412248 | |||||||
| chrX:17412249 | T | G | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35927T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412249 | |||||||
| chrX:17412253 | A | G | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35931A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412253 | |||||||
| chrX:17412254 | T | C | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35932T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412254 | |||||||
| chrX:17412255 | C | G | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35933C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412255 | |||||||
| chrX:17412256 | A | T | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35934A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412256 | |||||||
| chrX:17412257 | T | G | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35935T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412257 | |||||||
| chrX:17412258 | A | T | 1 | a0001c0001t0001g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+35936A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412258 | |||||||
| chrX:17412262 | A | G | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.565+35940A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412262 | |||||||
| chrX:17412343 | C | G | 1 | a0001c0001t0012g0154 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.565+36021C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412343 | |||||||
| chrX:17412366 | C | T | 1 | a0002c0002t0001g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.565+36044C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412366 | |||||||
| chrX:17412423 | C | T | 1 | a0001c0001t0002g0096 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.565+36101C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412423 | |||||||
| chrX:17412481 | C | T | 1 | a0001c0001t0002g0143 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.565+36159C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412481 | |||||||
| chrX:17412559 | T | G | 1 | a0002c0002t0001g0009 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.565+36237T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412559 | |||||||
| chrX:17412827 | G | T | 1 | a0003c0009t0002g0160 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.565+36505G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412827 | |||||||
| chrX:17412893 | C | T | 1 | a0002c0002t0001g0062 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.565+36571C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412893 | |||||||
| chrX:17412902 | C | T | 7 | a0001c0003t0002g0128 a0003c0006t0001g0157 a0003c0006t0001g0162 others(4): Show |
7 | HG01106.hp1 HG02280.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.565+36580C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17412902 | |||||||
| chrX:17413526 | A | G | 19 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(16): Show |
19 | HG01106.hp1 HG02145.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.565+37204A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17413526 | |||||||
| chrX:17413781 | A | C | 1 | a0002c0002t0001g0077 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.565+37459A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17413781 | |||||||
| chrX:17413982 | T | C | 2 | a0002c0002t0001g0054 a0004c0004t0001g0055 |
2 | HG02056.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.565+37660T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17413982 | |||||||
| chrX:17414089 | A | G | 1 | a0001c0001t0002g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.565+37767A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17414089 | |||||||
| chrX:17414386 | C | T | 1 | a0002c0002t0001g0062 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.565+38064C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17414386 | |||||||
| chrX:17414986 | G | C | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+38664G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17414986 | |||||||
| chrX:17414988 | C | T | 7 | a0001c0003t0002g0128 a0003c0006t0001g0157 a0003c0006t0001g0162 others(4): Show |
7 | HG01106.hp1 HG02280.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.565+38666C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17414988 | |||||||
| chrX:17415194 | G | A | 23 | a0001c0001t0001g0112 a0001c0001t0002g0002 a0001c0001t0002g0100 others(20): Show |
23 | HG01106.hp1 HG01243.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.565+38872G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17415194 | |||||||
| chrX:17415279 | T | C | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.565+38957T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17415279 | |||||||
| chrX:17415349 | A | C | 1 | a0002c0002t0001g0034 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.565+39027A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17415349 | |||||||
| chrX:17415769 | A | C | 4 | a0001c0001t0002g0002 a0001c0001t0002g0100 a0001c0001t0002g0146 others(1): Show |
4 | HG01243.hp1 HG02257.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.565+39447A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17415769 | |||||||
| chrX:17416030 | C | T | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.565+39708C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17416030 | |||||||
| chrX:17416551 | T | A | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.565+40229T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17416551 | |||||||
| chrX:17416671 | C | T | 49 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(46): Show |
49 | HG00609.hp1 HG01358.hp1 HG02015.hp1 others(46): Show |
intron_variant | MODIFIER | c.565+40349C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17416671 | |||||||
| chrX:17416792 | A | ATG | 3 | a0001c0001t0002g0143 a0002c0002t0001g0053 a0002c0002t0001g0076 |
3 | HG04228.hp1 HG06807.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.565+40497_565+4049 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17416792 | ||||||
| chrX:17416817 | T | A | 1 | a0001c0001t0002g0121 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.565+40495T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17416817 | |||||||
| chrX:17416817 | T | TGA | 14 | a0001c0001t0001g0112 a0001c0001t0001g0133 a0001c0001t0002g0120 others(11): Show |
14 | HG01106.hp1 HG02071.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.565+40496_565+4049 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17416817 | ||||||
| chrX:17416819 | T | A | 36 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0112 others(33): Show |
36 | HG00408.hp1 HG00621.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.565+40497T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17416819 | |||||||
| chrX:17416819 | T | TGA | 6 | a0001c0001t0002g0116 a0001c0001t0005g0111 a0001c0003t0002g0102 others(3): Show |
6 | HG02280.hp2 HG02602.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.565+40520_565+4052 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17416819 | ||||||
| chrX:17416819 | T | TGTGTGTG others(5): Show |
1 | a0001c0001t0002g0100 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.565+40498_565+4049 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17416819 | ||||||
| chrX:17416819 | T | TGTGTGTG others(9): Show |
1 | a0008c0011t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.565+40498_565+4049 others(20): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17416819 | ||||||
| chrX:17416819 | T | TGTGTGTG others(9): Show |
1 | a0001c0001t0002g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.565+40498_565+4049 others(20): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17416819 | ||||||
| chrX:17416821 | A | T | 1 | a0001c0001t0001g0029 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.565+40499A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17416821 | |||||||
| chrX:17417091 | T | TAC | 13 | a0001c0001t0002g0086 a0001c0001t0002g0164 a0002c0002t0001g0007 others(10): Show |
13 | HG01106.hp1 HG01515.hp1 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.565+40797_565+4079 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17417091 | ||||||
| chrX:17417091 | T | TACAC | 4 | a0001c0001t0005g0111 a0001c0003t0002g0102 a0001c0003t0002g0128 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.565+40795_565+4079 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17417091 | ||||||
| chrX:17417091 | T | TACACACA others(3): Show |
2 | a0001c0001t0002g0100 a0008c0011t0002g0147 |
2 | HG01243.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.565+40789_565+4079 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17417091 | ||||||
| chrX:17417091 | T | TACACACA others(5): Show |
1 | a0001c0001t0002g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.565+40787_565+4079 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17417091 | ||||||
| chrX:17417091 | TAC | T | 11 | a0001c0001t0002g0044 a0001c0001t0002g0116 a0001c0001t0002g0120 others(8): Show |
11 | HG01109.hp1 HG02145.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.565+40797_565+4079 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17417091 | ||||||
| chrX:17417184 | G | A | 1 | a0001c0001t0004g0058 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.565+40862G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17417184 | |||||||
| chrX:17417786 | T | G | 1 | a0001c0001t0001g0068 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.565+41464T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17417786 | |||||||
| chrX:17418999 | T | C | 1 | a0005c0005t0003g0101 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.565+42677T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17418999 | |||||||
| chrX:17419203 | C | T | 41 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0127 others(38): Show |
41 | HG00140.hp1 HG00408.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.565+42881C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17419203 | |||||||
| chrX:17419232 | C | T | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+42910C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17419232 | |||||||
| chrX:17419450 | T | G | 1 | a0001c0001t0002g0096 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.565+43128T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17419450 | |||||||
| chrX:17419554 | A | G | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+43232A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17419554 | |||||||
| chrX:17419701 | C | T | 1 | a0001c0001t0004g0058 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.565+43379C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17419701 | |||||||
| chrX:17419771 | T | C | 2 | a0001c0001t0010g0059 a0002c0002t0001g0105 |
2 | NA18965.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.565+43449T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17419771 | |||||||
| chrX:17419886 | C | G | 1 | a0002c0002t0001g0031 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.565+43564C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17419886 | |||||||
| chrX:17420024 | G | T | 1 | a0002c0002t0001g0031 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.565+43702G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17420024 | |||||||
| chrX:17420194 | G | A | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+43872G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17420194 | |||||||
| chrX:17420376 | A | T | 5 | a0001c0001t0001g0008 a0001c0001t0001g0061 a0001c0001t0001g0098 others(2): Show |
5 | NA18960.hp1 NA18967.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+44054A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17420376 | |||||||
| chrX:17420598 | C | G | 10 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(7): Show |
10 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.565+44276C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17420598 | |||||||
| chrX:17420691 | C | T | 19 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(16): Show |
19 | HG01106.hp1 HG02145.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.565+44369C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17420691 | |||||||
| chrX:17420802 | A | G | 1 | a0002c0002t0001g0084 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.565+44480A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17420802 | |||||||
| chrX:17421266 | C | CAT | 22 | a0001c0001t0001g0112 a0001c0001t0002g0100 a0001c0001t0002g0116 others(19): Show |
22 | HG01106.hp1 HG01243.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.565+44944_565+4494 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17421266 | |||||||
| chrX:17421267 | G | A | 1 | a0001c0001t0002g0126 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.565+44945G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17421267 | |||||||
| chrX:17421725 | C | T | 1 | a0002c0002t0001g0001 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.565+45403C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17421725 | |||||||
| chrX:17421819 | C | T | 3 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0005g0104 |
3 | HG03139.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.565+45497C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17421819 | |||||||
| chrX:17421930 | GACAT | G | 33 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0127 others(30): Show |
33 | HG00140.hp1 HG00408.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.565+45612_565+4561 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17421930 | ||||||
| chrX:17422086 | G | A | 3 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0144 |
3 | NA18994.hp1 NA18995.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.565+45764G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17422086 | |||||||
| chrX:17422437 | C | A | 3 | a0001c0001t0001g0112 a0001c0001t0002g0121 a0005c0005t0003g0117 |
3 | HG02280.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.565+46115C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17422437 | |||||||
| chrX:17422468 | G | A | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+46146G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17422468 | |||||||
| chrX:17422512 | G | C | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+46190G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17422512 | |||||||
| chrX:17422540 | G | A | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+46218G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17422540 | |||||||
| chrX:17423050 | G | A | 2 | a0002c0002t0001g0062 a0002c0002t0001g0079 |
2 | HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.565+46728G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17423050 | |||||||
| chrX:17423128 | G | A | 1 | a0002c0002t0001g0082 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.565+46806G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17423128 | |||||||
| chrX:17423295 | CTGTCT | C | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+46975_565+4697 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17423295 | ||||||
| chrX:17423301 | T | A | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+46979T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17423301 | |||||||
| chrX:17423446 | A | G | 10 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(7): Show |
10 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.565+47124A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17423446 | |||||||
| chrX:17423559 | G | T | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+47237G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17423559 | |||||||
| chrX:17424317 | C | T | 10 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(7): Show |
10 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.565+47995C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17424317 | |||||||
| chrX:17424371 | A | G | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+48049A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17424371 | |||||||
| chrX:17424697 | A | G | 1 | a0001c0001t0001g0021 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.565+48375A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17424697 | |||||||
| chrX:17425115 | C | T | 22 | a0001c0001t0001g0112 a0001c0001t0002g0100 a0001c0001t0002g0116 others(19): Show |
22 | HG01106.hp1 HG01243.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.565+48793C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17425115 | |||||||
| chrX:17425492 | T | TGCTG | 51 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(48): Show |
51 | HG00609.hp1 HG01358.hp1 HG02015.hp1 others(48): Show |
intron_variant | MODIFIER | c.565+49171_565+4917 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425492 | ||||||
| chrX:17425522 | CA | C | 17 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0037 others(14): Show |
17 | HG00642.hp1 HG00738.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.565+49249delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425522 | ||||||
| chrX:17425522 | CAA | C | 11 | a0001c0001t0001g0135 a0001c0001t0001g0140 a0001c0001t0001g0145 others(8): Show |
11 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.565+49248_565+4924 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425522 | ||||||
| chrX:17425522 | CAAA | C | 6 | a0001c0001t0001g0021 a0001c0001t0002g0086 a0001c0001t0012g0154 others(3): Show |
6 | HG01975.hp1 HG02083.hp1 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.565+49247_565+4924 others(7): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425522 | ||||||
| chrX:17425522 | CAAAA | C | 5 | a0001c0001t0001g0098 a0002c0002t0001g0007 a0002c0002t0001g0016 others(2): Show |
5 | HG01192.hp1 HG01515.hp1 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+49246_565+4924 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425522 | ||||||
| chrX:17425522 | CAAAAA | C | 17 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0061 others(14): Show |
17 | HG01099.hp1 HG01109.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.565+49245_565+4924 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425522 | ||||||
| chrX:17425522 | CAAAAAA | C | 10 | a0001c0001t0001g0041 a0001c0001t0001g0094 a0001c0001t0001g0095 others(7): Show |
10 | HG00408.hp2 HG01074.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.565+49244_565+4924 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425522 | ||||||
| chrX:17425522 | CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0002g0106 a0001c0001t0002g0110 |
2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.565+49237_565+4924 others(17): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425522 | ||||||
| chrX:17425522 | CAAAAAAA others(8): Show |
C | 2 | a0002c0002t0001g0006 a0008c0011t0002g0147 |
2 | HG02257.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.565+49235_565+4924 others(19): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425522 | ||||||
| chrX:17425522 | CAAAAAAA others(10): Show |
C | 1 | a0001c0001t0002g0100 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.565+49233_565+4924 others(21): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425522 | ||||||
| chrX:17425522 | CAAAAAAA others(12): Show |
C | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+49231_565+4924 others(23): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425522 | ||||||
| chrX:17425522 | CAAAAAAA others(13): Show |
C | 11 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(8): Show |
11 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.565+49230_565+4924 others(24): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425522 | ||||||
| chrX:17425522 | CAAAAAAA others(14): Show |
C | 2 | a0001c0001t0002g0002 a0001c0001t0004g0163 |
2 | HG01261.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.565+49229_565+4924 others(25): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425522 | ||||||
| chrX:17425522 | CAAAAAAA others(15): Show |
C | 1 | a0002c0002t0001g0042 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.565+49228_565+4924 others(26): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425522 | ||||||
| chrX:17425522 | CAAAAAAA others(16): Show |
C | 1 | a0001c0003t0002g0128 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.565+49227_565+4924 others(27): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425522 | ||||||
| chrX:17425522 | CAAAAAAA others(17): Show |
C | 9 | a0001c0001t0002g0146 a0001c0001t0005g0111 a0001c0003t0002g0102 others(6): Show |
9 | HG01106.hp1 HG02622.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.565+49226_565+4924 others(28): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425522 | ||||||
| chrX:17425522 | CAAAAAAA others(18): Show |
C | 1 | a0002c0002t0001g0020 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.565+49225_565+4924 others(29): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425522 | ||||||
| chrX:17425522 | CAAAAAAA others(20): Show |
C | 3 | a0001c0001t0004g0058 a0002c0002t0001g0088 a0002c0002t0001g0089 |
3 | NA18945.hp1 NA18970.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.565+49223_565+4924 others(31): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425522 | ||||||
| chrX:17425522 | CAAAAAAA others(21): Show |
C | 35 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(32): Show |
35 | HG00609.hp1 HG01358.hp1 HG02015.hp1 others(32): Show |
intron_variant | MODIFIER | c.565+49222_565+4924 others(32): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425522 | ||||||
| chrX:17425522 | CAAAAAAA others(22): Show |
C | 1 | a0004c0004t0001g0065 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.565+49221_565+4924 others(33): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425522 | ||||||
| chrX:17425551 | AAAAAAAA others(18): Show |
A | 1 | a0001c0001t0002g0107 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.565+49233_565+4925 others(29): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425551 | ||||||
| chrX:17425563 | AAAAAAAA others(10): Show |
A | 1 | a0001c0001t0001g0011 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.565+49245_565+4926 others(21): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425563 | ||||||
| chrX:17425564 | A | G | 10 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(7): Show |
10 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.565+49242A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17425564 | |||||||
| chrX:17425568 | A | AAAAAAAA others(15): Show |
1 | a0001c0001t0004g0071 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.565+49249_565+4925 others(26): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425568 | ||||||
| chrX:17425568 | A | AAAAAAAA others(8): Show |
1 | a0005c0005t0003g0101 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.565+49249_565+4925 others(19): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425568 | ||||||
| chrX:17425568 | A | AAAAAAAA others(4): Show |
1 | a0001c0001t0001g0070 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.565+49249_565+4925 others(15): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17425568 | ||||||
| chrX:17425568 | A | G | 105 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0037 others(102): Show |
105 | HG00140.hp1 HG00408.hp1 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.565+49246A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17425568 | |||||||
| chrX:17425616 | A | G | 1 | a0002c0002t0001g0089 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.565+49294A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17425616 | |||||||
| chrX:17425939 | G | A | 1 | a0001c0001t0012g0154 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.565+49617G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17425939 | |||||||
| chrX:17426202 | T | C | 1 | a0005c0005t0003g0101 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.565+49880T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17426202 | |||||||
| chrX:17426457 | T | C | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+50135T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17426457 | |||||||
| chrX:17426766 | C | T | 10 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(7): Show |
10 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.565+50444C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17426766 | |||||||
| chrX:17426769 | G | C | 6 | a0001c0001t0001g0026 a0002c0002t0001g0023 a0002c0002t0001g0024 others(3): Show |
6 | HG02083.hp1 NA18747.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.565+50447G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17426769 | |||||||
| chrX:17427422 | T | C | 1 | a0002c0002t0001g0004 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.565+51100T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17427422 | |||||||
| chrX:17427743 | A | T | 2 | a0002c0002t0001g0019 a0004c0004t0001g0012 |
2 | HG01975.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.565+51421A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17427743 | |||||||
| chrX:17427860 | A | G | 1 | a0001c0003t0002g0155 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.565+51538A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17427860 | |||||||
| chrX:17427922 | C | T | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+51600C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17427922 | |||||||
| chrX:17427943 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.565+51621C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17427943 | |||||||
| chrX:17428142 | G | A | 22 | a0001c0001t0001g0112 a0001c0001t0002g0100 a0001c0001t0002g0116 others(19): Show |
22 | HG01106.hp1 HG01243.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.565+51820G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17428142 | |||||||
| chrX:17428579 | A | G | 1 | a0001c0001t0001g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.565+52257A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17428579 | |||||||
| chrX:17428850 | C | G | 4 | a0001c0001t0001g0021 a0001c0001t0002g0100 a0001c0001t0002g0146 others(1): Show |
4 | HG01243.hp1 HG02135.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.565+52528C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17428850 | |||||||
| chrX:17428908 | T | A | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.565+52586T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17428908 | |||||||
| chrX:17428996 | C | T | 5 | a0006c0007t0002g0115 a0006c0007t0002g0118 a0006c0008t0001g0114 others(2): Show |
5 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.565+52674C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17428996 | |||||||
| chrX:17429224 | A | ATG | 4 | a0001c0001t0001g0041 a0001c0001t0001g0137 a0002c0002t0001g0016 others(1): Show |
4 | HG02257.hp1 HG02451.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.565+52935_565+5293 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17429224 | ||||||
| chrX:17429224 | ATG | A | 42 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(39): Show |
42 | HG00609.hp1 HG01358.hp1 HG02015.hp1 others(39): Show |
intron_variant | MODIFIER | c.565+52935_565+5293 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17429224 | ||||||
| chrX:17429224 | ATGTG | A | 7 | a0002c0002t0001g0031 a0002c0002t0001g0069 a0002c0002t0001g0072 others(4): Show |
7 | HG01099.hp1 HG02129.hp1 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.565+52933_565+5293 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17429224 | ||||||
| chrX:17429239 | T | TGTGTGTG others(3): Show |
3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+52926_565+5292 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17429239 | ||||||
| chrX:17429257 | T | C | 3 | a0001c0001t0001g0140 a0001c0001t0001g0145 a0002c0002t0001g0123 |
3 | HG00639.hp1 HG00639.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.565+52935T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17429257 | |||||||
| chrX:17429257 | T | TGC | 2 | a0001c0001t0002g0116 a0001c0001t0002g0120 |
2 | HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.565+52936_565+5293 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17429257 | ||||||
| chrX:17429257 | T | TGTGC | 7 | a0001c0001t0001g0112 a0001c0001t0002g0121 a0005c0005t0003g0117 others(4): Show |
7 | HG02280.hp1 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.565+52936_565+5293 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17429257 | ||||||
| chrX:17429257 | T | TGTGTGTG others(1): Show |
3 | a0001c0001t0005g0111 a0001c0003t0002g0102 a0003c0006t0002g0161 |
3 | HG02922.hp2 HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.565+52936_565+5293 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17429257 | ||||||
| chrX:17429257 | T | TGTGTGTG others(3): Show |
6 | a0001c0003t0002g0128 a0003c0006t0001g0157 a0003c0006t0001g0162 others(3): Show |
6 | HG01106.hp1 HG02280.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.565+52936_565+5293 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17429257 | ||||||
| chrX:17429265 | T | C | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+52943T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17429265 | |||||||
| chrX:17429608 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.565+53286C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17429608 | |||||||
| chrX:17429855 | G | A | 1 | a0002c0002t0001g0007 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.565+53533G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17429855 | |||||||
| chrX:17430005 | C | G | 127 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0041 others(124): Show |
127 | HG00140.hp1 HG00408.hp1 HG00609.hp1 others(124): Show |
intron_variant | MODIFIER | c.565+53683C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17430005 | |||||||
| chrX:17430075 | T | TTTCC | 28 | a0001c0001t0001g0073 a0001c0001t0001g0112 a0001c0001t0001g0127 others(25): Show |
28 | HG01071.hp1 HG01928.hp1 HG01975.hp1 others(25): Show |
intron_variant | MODIFIER | c.565+53792_565+5379 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430075 | ||||||
| chrX:17430075 | T | TTTCCTTC others(9): Show |
1 | a0008c0011t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.565+53780_565+5379 others(20): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430075 | ||||||
| chrX:17430075 | TTTCC | T | 10 | a0001c0001t0001g0083 a0001c0001t0001g0151 a0001c0001t0005g0111 others(7): Show |
10 | HG00408.hp1 HG01106.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.565+53792_565+5379 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430075 | ||||||
| chrX:17430075 | TTTCCTTC others(5): Show |
T | 1 | a0002c0002t0001g0108 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.565+53784_565+5379 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430075 | ||||||
| chrX:17430075 | TTTCCTTC others(9): Show |
T | 1 | a0001c0003t0002g0014 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.565+53780_565+5379 others(20): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430075 | ||||||
| chrX:17430151 | C | CCTT | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+53833_565+5383 others(7): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430151 | ||||||
| chrX:17430230 | TTCCCTCC others(1): Show |
T | 3 | a0001c0001t0001g0061 a0001c0001t0001g0098 a0001c0001t0001g0099 |
3 | NA18967.hp1 NA18983.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.565+53921_565+5392 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430230 | ||||||
| chrX:17430259 | T | TTTTC | 21 | a0001c0001t0001g0029 a0001c0001t0001g0041 a0001c0001t0001g0137 others(18): Show |
21 | HG00642.hp1 HG01099.hp1 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.565+53990_565+5399 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430259 | ||||||
| chrX:17430259 | T | TTTTCTTT others(1): Show |
10 | a0001c0001t0001g0083 a0001c0001t0001g0094 a0001c0001t0001g0124 others(7): Show |
10 | HG00280.hp1 HG01069.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.565+53986_565+5399 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430259 | ||||||
| chrX:17430259 | T | TTTTCTTT others(5): Show |
9 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0021 others(6): Show |
9 | HG01258.hp1 HG01433.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.565+53982_565+5399 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430259 | ||||||
| chrX:17430259 | T | TTTTCTTT others(9): Show |
1 | a0002c0002t0001g0030 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.565+53978_565+5399 others(20): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430259 | ||||||
| chrX:17430259 | TTTTC | T | 42 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0001t0001g0051 others(39): Show |
42 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.565+53990_565+5399 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430259 | ||||||
| chrX:17430259 | TTTTCTTT others(1): Show |
T | 33 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0049 others(30): Show |
33 | HG00408.hp1 HG01106.hp1 HG01934.hp1 others(30): Show |
intron_variant | MODIFIER | c.565+53986_565+5399 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430259 | ||||||
| chrX:17430259 | TTTTCTTT others(5): Show |
T | 10 | a0001c0001t0001g0073 a0001c0001t0001g0085 a0001c0001t0002g0121 others(7): Show |
10 | HG00621.hp1 HG02040.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.565+53982_565+5399 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430259 | ||||||
| chrX:17430259 | TTTTCTTT others(9): Show |
T | 4 | a0002c0002t0001g0084 a0002c0002t0001g0109 a0002c0002t0001g0138 others(1): Show |
4 | HG00673.hp1 HG02074.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+53978_565+5399 others(20): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430259 | ||||||
| chrX:17430259 | TTTTCTTT others(17): Show |
T | 1 | a0001c0001t0002g0003 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.565+53970_565+5399 others(28): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430259 | ||||||
| chrX:17430269 | T | C | 1 | a0002c0002t0001g0076 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.565+53947T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17430269 | |||||||
| chrX:17430283 | C | T | 1 | a0001c0001t0001g0035 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.565+53961C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17430283 | |||||||
| chrX:17430316 | C | T | 1 | a0008c0011t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.565+53994C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17430316 | |||||||
| chrX:17430319 | T | C | 1 | a0008c0011t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.565+53997T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17430319 | |||||||
| chrX:17430337 | CTCTT | C | 3 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0005g0104 |
3 | HG03139.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.565+54029_565+5403 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430337 | ||||||
| chrX:17430355 | T | C | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+54033T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17430355 | |||||||
| chrX:17430357 | C | T | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+54035C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17430357 | |||||||
| chrX:17430360 | C | T | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+54038C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17430360 | |||||||
| chrX:17430361 | T | C | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+54039T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17430361 | |||||||
| chrX:17430410 | C | CTCCT | 4 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0001c0001t0007g0125 others(1): Show |
4 | HG01243.hp1 HG02257.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+54106_565+5410 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17430410 | ||||||
| chrX:17430870 | T | A | 1 | a0001c0001t0001g0083 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.565+54548T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17430870 | |||||||
| chrX:17431023 | T | A | 3 | a0001c0001t0001g0140 a0001c0001t0001g0145 a0002c0002t0001g0123 |
3 | HG00639.hp1 HG00639.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.565+54701T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17431023 | |||||||
| chrX:17431888 | T | C | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+55566T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17431888 | |||||||
| chrX:17432152 | C | G | 1 | a0001c0001t0001g0029 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.565+55830C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17432152 | |||||||
| chrX:17432219 | A | AG | 4 | a0001c0001t0001g0061 a0001c0001t0001g0098 a0001c0001t0001g0099 others(1): Show |
4 | NA18967.hp1 NA18983.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+55899dupG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17432219 | ||||||
| chrX:17432444 | A | G | 2 | a0001c0001t0005g0111 a0001c0003t0002g0102 |
2 | HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.565+56122A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17432444 | |||||||
| chrX:17432848 | A | T | 9 | a0001c0001t0005g0111 a0001c0003t0002g0102 a0001c0003t0002g0128 others(6): Show |
9 | HG01106.hp1 HG02280.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.565+56526A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17432848 | |||||||
| chrX:17432885 | G | A | 19 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(16): Show |
19 | HG01106.hp1 HG02145.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.565+56563G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17432885 | |||||||
| chrX:17432901 | G | A | 1 | a0002c0002t0001g0017 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.565+56579G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17432901 | |||||||
| chrX:17432930 | G | A | 1 | a0002c0002t0001g0040 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.565+56608G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17432930 | |||||||
| chrX:17433036 | C | T | 38 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(35): Show |
38 | HG00609.hp1 HG01358.hp1 HG02015.hp1 others(35): Show |
intron_variant | MODIFIER | c.565+56714C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17433036 | |||||||
| chrX:17433105 | C | T | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+56783C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17433105 | |||||||
| chrX:17433115 | T | C | 1 | a0002c0002t0001g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.565+56793T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17433115 | |||||||
| chrX:17433116 | C | G | 1 | a0002c0002t0001g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.565+56794C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17433116 | |||||||
| chrX:17433123 | A | G | 1 | a0002c0002t0001g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.565+56801A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17433123 | |||||||
| chrX:17433130 | C | T | 1 | a0002c0002t0001g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.565+56808C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17433130 | |||||||
| chrX:17433142 | G | A | 1 | a0002c0002t0001g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.565+56820G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17433142 | |||||||
| chrX:17433184 | C | G | 1 | a0002c0002t0001g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.565+56862C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17433184 | |||||||
| chrX:17433196 | C | CT | 30 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0056 others(27): Show |
30 | HG00609.hp1 HG00621.hp1 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.565+56900dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17433196 | ||||||
| chrX:17433196 | CTTTTT | C | 17 | a0001c0001t0001g0112 a0001c0001t0002g0120 a0001c0001t0002g0121 others(14): Show |
17 | HG01106.hp1 HG02280.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.565+56896_565+5690 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17433196 | ||||||
| chrX:17433196 | CTTTTTTT others(3): Show |
C | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+56891_565+5690 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17433196 | ||||||
| chrX:17433196 | CTTTTTTT others(6): Show |
C | 1 | a0004c0004t0001g0065 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.565+56888_565+5690 others(17): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17433196 | ||||||
| chrX:17433282 | A | C | 1 | a0002c0002t0001g0130 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.565+56960A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17433282 | |||||||
| chrX:17433284 | T | C | 1 | a0002c0002t0001g0130 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.565+56962T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17433284 | |||||||
| chrX:17433291 | T | C | 160 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0021 others(157): Show |
160 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.565+56969T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17433291 | |||||||
| chrX:17433552 | C | T | 1 | a0002c0002t0001g0062 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.565+57230C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17433552 | |||||||
| chrX:17433891 | A | T | 9 | a0001c0001t0005g0111 a0001c0003t0002g0102 a0001c0003t0002g0128 others(6): Show |
9 | HG01106.hp1 HG02280.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.565+57569A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17433891 | |||||||
| chrX:17433928 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.565+57606T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17433928 | |||||||
| chrX:17434169 | T | C | 1 | a0001c0001t0002g0143 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.565+57847T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17434169 | |||||||
| chrX:17434313 | A | C | 1 | a0001c0001t0002g0100 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.565+57991A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17434313 | |||||||
| chrX:17434441 | A | AT | 22 | a0001c0001t0001g0029 a0001c0001t0001g0099 a0001c0001t0001g0112 others(19): Show |
22 | HG01109.hp1 HG01243.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.565+58140dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17434441 | ||||||
| chrX:17434441 | AT | A | 28 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0129 others(25): Show |
28 | HG00408.hp1 HG00621.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.565+58140delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17434441 | ||||||
| chrX:17434515 | T | C | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+58193T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17434515 | |||||||
| chrX:17434594 | C | T | 9 | a0001c0001t0005g0111 a0001c0003t0002g0102 a0001c0003t0002g0128 others(6): Show |
9 | HG01106.hp1 HG02280.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.565+58272C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17434594 | |||||||
| chrX:17436132 | T | G | 1 | a0002c0002t0001g0013 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.565+59810T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17436132 | |||||||
| chrX:17436612 | T | TA | 9 | a0001c0001t0005g0111 a0001c0003t0002g0102 a0001c0003t0002g0128 others(6): Show |
9 | HG01106.hp1 HG02280.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.565+60306dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17436612 | ||||||
| chrX:17436612 | TA | T | 8 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0002g0100 others(5): Show |
8 | HG01243.hp1 HG02257.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.565+60306delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17436612 | ||||||
| chrX:17436624 | A | G | 1 | a0002c0002t0001g0022 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.565+60302A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17436624 | |||||||
| chrX:17436907 | A | G | 1 | a0001c0001t0001g0029 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.565+60585A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17436907 | |||||||
| chrX:17437156 | G | A | 1 | a0001c0003t0002g0014 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.565+60834G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17437156 | |||||||
| chrX:17437248 | C | G | 13 | a0001c0001t0001g0112 a0001c0001t0002g0100 a0001c0001t0002g0116 others(10): Show |
13 | HG01243.hp1 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.565+60926C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17437248 | |||||||
| chrX:17437673 | T | C | 1 | a0003c0006t0002g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.565+61351T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17437673 | |||||||
| chrX:17439178 | A | T | 163 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0021 others(160): Show |
163 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.565+62856A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17439178 | |||||||
| chrX:17439578 | A | G | 1 | a0003c0006t0002g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.565+63256A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17439578 | |||||||
| chrX:17439767 | A | T | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+63445A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17439767 | |||||||
| chrX:17440258 | T | TA | 25 | a0001c0001t0001g0070 a0001c0001t0001g0083 a0001c0001t0001g0112 others(22): Show |
25 | HG01358.hp1 HG01928.hp1 HG02056.hp1 others(22): Show |
intron_variant | MODIFIER | c.565+63963dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17440258 | ||||||
| chrX:17440258 | TA | T | 8 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0085 others(5): Show |
8 | HG01167.hp1 HG02040.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.565+63963delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17440258 | ||||||
| chrX:17440396 | G | C | 1 | a0003c0006t0002g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.565+64074G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17440396 | |||||||
| chrX:17440618 | A | G | 5 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0096 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+64296A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17440618 | |||||||
| chrX:17440733 | G | A | 1 | a0002c0002t0001g0005 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.565+64411G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17440733 | |||||||
| chrX:17441153 | G | A | 1 | a0005c0005t0003g0101 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.565+64831G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17441153 | |||||||
| chrX:17441666 | CTTCCTTC others(5): Show |
C | 3 | a0003c0006t0001g0157 a0003c0006t0005g0159 a0010c0010t0003g0158 |
3 | HG01106.hp1 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.565+65356_565+6536 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17441666 | ||||||
| chrX:17441673 | C | T | 2 | a0002c0002t0001g0020 a0002c0015t0001g0039 |
2 | HG00280.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.565+65351C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17441673 | |||||||
| chrX:17441958 | A | G | 1 | a0002c0002t0001g0020 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.565+65636A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17441958 | |||||||
| chrX:17442339 | A | G | 1 | a0001c0001t0002g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.565+66017A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17442339 | |||||||
| chrX:17442703 | G | A | 1 | a0001c0001t0002g0044 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.565+66381G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17442703 | |||||||
| chrX:17443230 | C | T | 1 | a0003c0006t0002g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.565+66908C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17443230 | |||||||
| chrX:17443255 | G | A | 1 | a0002c0002t0001g0131 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.565+66933G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17443255 | |||||||
| chrX:17443453 | G | A | 13 | a0001c0001t0001g0112 a0001c0001t0002g0100 a0001c0001t0002g0116 others(10): Show |
13 | HG01243.hp1 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.565+67131G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17443453 | |||||||
| chrX:17443614 | G | T | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+67292G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17443614 | |||||||
| chrX:17443722 | G | A | 2 | a0001c0001t0005g0111 a0001c0003t0002g0102 |
2 | HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.565+67400G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17443722 | |||||||
| chrX:17444253 | G | T | 1 | a0002c0002t0001g0063 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.565+67931G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17444253 | |||||||
| chrX:17444311 | G | C | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+67989G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17444311 | |||||||
| chrX:17444634 | A | G | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+68312A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17444634 | |||||||
| chrX:17444704 | C | T | 1 | a0002c0002t0001g0013 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.565+68382C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17444704 | |||||||
| chrX:17445069 | C | T | 1 | a0004c0004t0001g0055 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.565+68747C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17445069 | |||||||
| chrX:17445756 | A | AG | 13 | a0001c0001t0001g0098 a0001c0001t0001g0112 a0001c0001t0002g0120 others(10): Show |
13 | HG00621.hp1 HG01099.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.565+69444dupG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17445756 | ||||||
| chrX:17445756 | A | G | 1 | a0001c0001t0004g0058 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.565+69434A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17445756 | |||||||
| chrX:17445758 | G | C | 1 | a0002c0002t0001g0033 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.565+69436G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17445758 | |||||||
| chrX:17445837 | TA | T | 5 | a0001c0001t0001g0124 a0001c0001t0002g0100 a0001c0001t0002g0146 others(2): Show |
5 | HG01243.hp1 HG01943.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.565+69531delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17445837 | ||||||
| chrX:17445851 | A | C | 1 | a0001c0001t0001g0021 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.565+69529A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17445851 | |||||||
| chrX:17445890 | C | G | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+69568C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17445890 | |||||||
| chrX:17445963 | A | T | 1 | a0001c0001t0004g0071 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.565+69641A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17445963 | |||||||
| chrX:17445991 | C | G | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+69669C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17445991 | |||||||
| chrX:17446169 | G | A | 1 | a0002c0002t0001g0109 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.565+69847G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17446169 | |||||||
| chrX:17446552 | C | T | 4 | a0001c0001t0001g0127 a0001c0001t0002g0126 a0001c0001t0007g0125 others(1): Show |
4 | HG01071.hp1 HG02647.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+70230C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17446552 | |||||||
| chrX:17446656 | C | CA | 8 | a0001c0001t0001g0061 a0001c0001t0001g0098 a0001c0001t0001g0099 others(5): Show |
8 | HG00140.hp1 HG01934.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.565+70349dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17446656 | ||||||
| chrX:17446656 | CA | C | 14 | a0001c0001t0001g0151 a0001c0001t0002g0100 a0001c0001t0002g0116 others(11): Show |
14 | HG00408.hp1 HG01243.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.565+70349delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17446656 | ||||||
| chrX:17447114 | T | G | 1 | a0012c0013t0001g0038 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.565+70792T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17447114 | |||||||
| chrX:17447165 | T | C | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+70843T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17447165 | |||||||
| chrX:17447396 | A | AT | 7 | a0001c0001t0001g0098 a0001c0001t0001g0127 a0001c0001t0002g0126 others(4): Show |
7 | HG01071.hp1 HG02257.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.565+71084dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17447396 | ||||||
| chrX:17447773 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.565+71451G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17447773 | |||||||
| chrX:17447773 | GCACACAC others(19): Show |
G | 1 | a0002c0002t0001g0022 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.565+71463_565+7148 others(30): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17447773 | ||||||
| chrX:17447775 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.565+71453A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17447775 | |||||||
| chrX:17447785 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.565+71463G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17447785 | |||||||
| chrX:17447785 | G | GCA | 13 | a0001c0001t0001g0041 a0001c0001t0002g0002 a0001c0001t0002g0086 others(10): Show |
13 | HG00140.hp1 HG01071.hp1 HG02293.hp2 others(10): Show |
intron_variant | MODIFIER | c.565+71496_565+7149 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17447785 | ||||||
| chrX:17447785 | G | GCACA | 6 | a0001c0001t0001g0070 a0001c0001t0002g0044 a0005c0005t0003g0101 others(3): Show |
6 | HG01109.hp1 HG02055.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.565+71494_565+7149 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17447785 | ||||||
| chrX:17447785 | G | GCACACA | 6 | a0001c0001t0002g0116 a0001c0001t0002g0120 a0001c0001t0002g0121 others(3): Show |
6 | HG02145.hp1 HG02280.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.565+71492_565+7149 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17447785 | ||||||
| chrX:17447785 | G | GCACACAC others(3): Show |
1 | a0001c0001t0001g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.565+71488_565+7149 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17447785 | ||||||
| chrX:17447785 | GCA | G | 43 | a0001c0001t0001g0029 a0001c0001t0001g0048 a0001c0001t0001g0049 others(40): Show |
43 | HG00280.hp1 HG00609.hp1 HG01106.hp1 others(40): Show |
intron_variant | MODIFIER | c.565+71496_565+7149 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17447785 | ||||||
| chrX:17447785 | GCACA | G | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+71494_565+7149 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17447785 | ||||||
| chrX:17447785 | GCACACA | G | 2 | a0002c0002t0001g0067 a0002c0002t0001g0069 |
2 | HG02015.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.565+71492_565+7149 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17447785 | ||||||
| chrX:17447787 | A | G | 3 | a0001c0001t0001g0068 a0001c0001t0012g0154 a0002c0002t0001g0006 |
3 | HG01975.hp1 HG03130.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.565+71465A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17447787 | |||||||
| chrX:17447820 | G | C | 2 | a0002c0002t0001g0138 a0002c0002t0001g0139 |
2 | HG00673.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.565+71498G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17447820 | |||||||
| chrX:17447935 | A | G | 1 | a0002c0002t0001g0079 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.565+71613A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17447935 | |||||||
| chrX:17447977 | C | G | 1 | a0002c0002t0001g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.565+71655C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17447977 | |||||||
| chrX:17448138 | G | T | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+71816G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17448138 | |||||||
| chrX:17449252 | G | A | 1 | a0010c0010t0003g0158 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.565+72930G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17449252 | |||||||
| chrX:17449585 | G | T | 1 | a0001c0003t0002g0128 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.565+73263G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17449585 | |||||||
| chrX:17449797 | C | T | 9 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(6): Show |
9 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.565+73475C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17449797 | |||||||
| chrX:17450509 | GT | G | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+74189delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17450509 | ||||||
| chrX:17450642 | G | A | 10 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(7): Show |
10 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.565+74320G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17450642 | |||||||
| chrX:17451058 | A | ATACT | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+74738_565+7473 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17451058 | ||||||
| chrX:17451157 | T | C | 1 | a0001c0001t0001g0029 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.565+74835T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17451157 | |||||||
| chrX:17451252 | T | C | 4 | a0001c0001t0001g0068 a0001c0001t0002g0106 a0001c0001t0002g0107 others(1): Show |
4 | HG02258.hp1 HG03130.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+74930T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17451252 | |||||||
| chrX:17451621 | G | A | 14 | a0001c0001t0001g0112 a0001c0001t0002g0100 a0001c0001t0002g0116 others(11): Show |
14 | HG01243.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.565+75299G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17451621 | |||||||
| chrX:17452131 | C | T | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+75809C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17452131 | |||||||
| chrX:17452278 | G | A | 1 | a0001c0001t0002g0044 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.565+75956G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17452278 | |||||||
| chrX:17452418 | C | T | 1 | a0003c0006t0001g0162 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.565+76096C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17452418 | |||||||
| chrX:17452440 | A | G | 1 | a0002c0002t0001g0025 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.565+76118A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17452440 | |||||||
| chrX:17452484 | T | C | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+76162T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17452484 | |||||||
| chrX:17452498 | T | G | 3 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0005g0104 |
3 | HG03139.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.565+76176T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17452498 | |||||||
| chrX:17452665 | A | T | 7 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0096 others(4): Show |
7 | HG01069.hp1 HG01071.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.565+76343A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17452665 | |||||||
| chrX:17453074 | A | G | 5 | a0006c0007t0002g0115 a0006c0007t0002g0118 a0006c0008t0001g0114 others(2): Show |
5 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.565+76752A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17453074 | |||||||
| chrX:17453185 | T | C | 1 | a0003c0006t0001g0162 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.565+76863T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17453185 | |||||||
| chrX:17453546 | A | G | 14 | a0001c0001t0001g0112 a0001c0001t0002g0100 a0001c0001t0002g0116 others(11): Show |
14 | HG01243.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.565+77224A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17453546 | |||||||
| chrX:17453753 | A | T | 4 | a0003c0006t0001g0157 a0003c0006t0005g0159 a0003c0009t0002g0160 others(1): Show |
4 | HG01106.hp1 HG02622.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.565+77431A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17453753 | |||||||
| chrX:17453781 | A | G | 53 | a0001c0001t0001g0029 a0001c0001t0001g0048 a0001c0001t0001g0049 others(50): Show |
53 | HG00609.hp1 HG01358.hp1 HG02015.hp1 others(50): Show |
intron_variant | MODIFIER | c.565+77459A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17453781 | |||||||
| chrX:17453815 | G | T | 1 | a0002c0002t0001g0069 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.565+77493G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17453815 | |||||||
| chrX:17454663 | C | A | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+78341C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17454663 | |||||||
| chrX:17454787 | C | T | 1 | a0002c0002t0001g0063 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.565+78465C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17454787 | |||||||
| chrX:17455212 | T | A | 1 | a0004c0004t0001g0132 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.565+78890T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17455212 | |||||||
| chrX:17455377 | A | T | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+79055A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17455377 | |||||||
| chrX:17455453 | A | T | 2 | a0001c0001t0005g0111 a0001c0003t0002g0102 |
2 | HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.565+79131A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17455453 | |||||||
| chrX:17455553 | TAGA | T | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+79233_565+7923 others(7): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17455553 | ||||||
| chrX:17455714 | C | T | 10 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0001c0003t0002g0128 others(7): Show |
10 | HG01106.hp1 HG01243.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.565+79392C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17455714 | |||||||
| chrX:17456155 | G | T | 6 | a0001c0001t0001g0056 a0001c0001t0001g0066 a0001c0001t0001g0070 others(3): Show |
6 | HG02132.hp1 HG02698.hp1 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.565+79833G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17456155 | |||||||
| chrX:17456248 | A | G | 1 | a0001c0001t0002g0100 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.565+79926A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17456248 | |||||||
| chrX:17456480 | A | G | 1 | a0002c0002t0001g0108 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.565+80158A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17456480 | |||||||
| chrX:17456861 | T | C | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+80539T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17456861 | |||||||
| chrX:17457218 | G | A | 1 | a0001c0001t0002g0121 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.565+80896G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17457218 | |||||||
| chrX:17457539 | C | A | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+81217C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17457539 | |||||||
| chrX:17457912 | A | G | 2 | a0001c0001t0005g0111 a0001c0003t0002g0102 |
2 | HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.565+81590A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17457912 | |||||||
| chrX:17458221 | CTTTG | C | 4 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0110 others(1): Show |
4 | HG02258.hp1 HG03041.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+81919_565+8192 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17458221 | ||||||
| chrX:17458452 | C | G | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+82130C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17458452 | |||||||
| chrX:17458467 | C | T | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+82145C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17458467 | |||||||
| chrX:17458481 | G | A | 1 | a0001c0001t0001g0029 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.565+82159G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17458481 | |||||||
| chrX:17458586 | G | A | 1 | a0001c0001t0002g0116 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.565+82264G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17458586 | |||||||
| chrX:17458674 | T | G | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+82352T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17458674 | |||||||
| chrX:17458736 | G | C | 4 | a0001c0001t0001g0026 a0002c0002t0001g0023 a0002c0002t0001g0053 others(1): Show |
4 | HG02083.hp1 NA18747.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+82414G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17458736 | |||||||
| chrX:17459148 | T | G | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+82826T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17459148 | |||||||
| chrX:17459346 | C | A | 1 | a0002c0002t0001g0043 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.565+83024C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17459346 | |||||||
| chrX:17459941 | A | G | 10 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(7): Show |
10 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.565+83619A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17459941 | |||||||
| chrX:17460057 | G | C | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+83735G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17460057 | |||||||
| chrX:17460192 | A | G | 1 | a0001c0003t0002g0128 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.565+83870A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17460192 | |||||||
| chrX:17460370 | A | C | 14 | a0001c0001t0001g0112 a0001c0001t0002g0100 a0001c0001t0002g0116 others(11): Show |
14 | HG01243.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.565+84048A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17460370 | |||||||
| chrX:17460614 | C | T | 1 | a0009c0016t0002g0119 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.565+84292C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17460614 | |||||||
| chrX:17460628 | A | C | 7 | a0001c0003t0002g0128 a0003c0006t0001g0157 a0003c0006t0001g0162 others(4): Show |
7 | HG01106.hp1 HG02280.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.565+84306A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17460628 | |||||||
| chrX:17460712 | G | A | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+84390G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17460712 | |||||||
| chrX:17461020 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.565+84698A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17461020 | |||||||
| chrX:17461035 | AT | A | 10 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(7): Show |
10 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.565+84715delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17461035 | ||||||
| chrX:17461131 | A | C | 1 | a0002c0002t0001g0040 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.565+84809A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17461131 | |||||||
| chrX:17461148 | G | A | 20 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0129 others(17): Show |
20 | HG00408.hp1 HG00621.hp1 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.565+84826G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17461148 | |||||||
| chrX:17461308 | C | G | 1 | a0001c0001t0001g0008 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.565+84986C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17461308 | |||||||
| chrX:17462035 | A | G | 1 | a0001c0001t0004g0071 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.565+85713A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17462035 | |||||||
| chrX:17462072 | T | C | 2 | a0001c0001t0005g0111 a0001c0003t0002g0102 |
2 | HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.565+85750T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17462072 | |||||||
| chrX:17462083 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.565+85761A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17462083 | |||||||
| chrX:17462806 | T | C | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+86484T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17462806 | |||||||
| chrX:17462863 | C | G | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+86541C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17462863 | |||||||
| chrX:17463262 | G | A | 10 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(7): Show |
10 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.565+86940G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17463262 | |||||||
| chrX:17463515 | A | G | 14 | a0001c0001t0001g0112 a0001c0001t0002g0100 a0001c0001t0002g0116 others(11): Show |
14 | HG01243.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.565+87193A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17463515 | |||||||
| chrX:17463713 | C | G | 1 | a0009c0016t0002g0119 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.565+87391C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17463713 | |||||||
| chrX:17463725 | C | T | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+87403C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17463725 | |||||||
| chrX:17463946 | G | T | 1 | a0002c0002t0001g0084 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.565+87624G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17463946 | |||||||
| chrX:17464095 | G | GT | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+87777dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17464095 | ||||||
| chrX:17464156 | A | G | 1 | a0002c0002t0001g0043 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.565+87834A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17464156 | |||||||
| chrX:17464787 | A | G | 3 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0005g0104 |
3 | HG03139.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.565+88465A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17464787 | |||||||
| chrX:17465038 | G | A | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+88716G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17465038 | |||||||
| chrX:17465122 | C | A | 1 | a0001c0001t0002g0100 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.565+88800C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17465122 | |||||||
| chrX:17465616 | C | CA | 10 | a0001c0001t0001g0112 a0001c0001t0002g0120 a0001c0001t0002g0121 others(7): Show |
10 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.565+89311dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17465616 | ||||||
| chrX:17465616 | CA | C | 145 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0026 others(142): Show |
145 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.565+89311delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17465616 | ||||||
| chrX:17466117 | A | G | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+89795A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17466117 | |||||||
| chrX:17466134 | C | T | 1 | a0001c0003t0002g0142 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.565+89812C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17466134 | |||||||
| chrX:17466516 | C | T | 2 | a0001c0003t0002g0128 a0003c0006t0001g0162 |
2 | HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.565+90194C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17466516 | |||||||
| chrX:17466623 | G | A | 1 | a0002c0002t0001g0009 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.565+90301G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17466623 | |||||||
| chrX:17466759 | A | G | 45 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0041 others(42): Show |
45 | HG00140.hp1 HG00408.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.565+90437A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17466759 | |||||||
| chrX:17466854 | A | G | 1 | a0001c0003t0002g0142 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.565+90532A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17466854 | |||||||
| chrX:17466857 | C | G | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+90535C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17466857 | |||||||
| chrX:17466864 | C | A | 1 | a0004c0004t0001g0055 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.565+90542C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17466864 | |||||||
| chrX:17467085 | G | A | 40 | a0001c0001t0001g0029 a0001c0001t0001g0048 a0001c0001t0001g0049 others(37): Show |
40 | HG00609.hp1 HG01358.hp1 HG02015.hp1 others(37): Show |
intron_variant | MODIFIER | c.565+90763G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17467085 | |||||||
| chrX:17467319 | G | T | 1 | a0002c0002t0001g0025 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.565+90997G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17467319 | |||||||
| chrX:17467651 | G | A | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+91329G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17467651 | |||||||
| chrX:17468044 | CTGCT | C | 3 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0110 |
3 | HG02258.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.565+91724_565+9172 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17468044 | ||||||
| chrX:17468435 | C | CT | 18 | a0001c0001t0001g0029 a0001c0001t0001g0048 a0001c0001t0001g0049 others(15): Show |
18 | HG00609.hp1 HG02056.hp1 HG02129.hp1 others(15): Show |
intron_variant | MODIFIER | c.565+92126dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17468435 | ||||||
| chrX:17468447 | T | A | 1 | a0008c0011t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.565+92125T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17468447 | |||||||
| chrX:17468544 | G | T | 1 | a0002c0002t0001g0131 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.565+92222G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17468544 | |||||||
| chrX:17468877 | G | A | 2 | a0001c0001t0001g0048 a0002c0002t0001g0052 |
2 | NA18612.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.565+92555G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17468877 | |||||||
| chrX:17468934 | A | G | 2 | a0001c0003t0002g0142 a0001c0003t0002g0155 |
2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.565+92612A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17468934 | |||||||
| chrX:17468947 | A | C | 1 | a0002c0002t0001g0046 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.565+92625A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17468947 | |||||||
| chrX:17469071 | C | T | 1 | a0006c0007t0002g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.565+92749C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17469071 | |||||||
| chrX:17469397 | C | T | 1 | a0001c0001t0002g0143 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.565+93075C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17469397 | |||||||
| chrX:17470269 | A | T | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+93947A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17470269 | |||||||
| chrX:17470789 | C | G | 1 | a0003c0009t0002g0160 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.565+94467C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17470789 | |||||||
| chrX:17470892 | G | A | 20 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(17): Show |
20 | HG01106.hp1 HG02145.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.565+94570G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17470892 | |||||||
| chrX:17470964 | G | A | 1 | a0004c0004t0001g0012 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.565+94642G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17470964 | |||||||
| chrX:17471000 | A | T | 23 | a0001c0001t0001g0112 a0001c0001t0002g0100 a0001c0001t0002g0116 others(20): Show |
23 | HG01106.hp1 HG01243.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.565+94678A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17471000 | |||||||
| chrX:17471428 | C | A | 4 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0144 others(1): Show |
4 | NA18994.hp1 NA18995.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+95106C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17471428 | |||||||
| chrX:17472311 | A | AAG | 5 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(2): Show |
5 | HG02280.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+96005_565+9600 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17472311 | ||||||
| chrX:17472349 | G | A | 1 | a0002c0002t0001g0046 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.565+96027G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17472349 | |||||||
| chrX:17472353 | G | A | 1 | a0002c0002t0001g0084 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.565+96031G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17472353 | |||||||
| chrX:17472563 | A | G | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+96241A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17472563 | |||||||
| chrX:17472833 | G | A | 1 | a0001c0001t0005g0104 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.565+96511G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17472833 | |||||||
| chrX:17473322 | A | C | 1 | a0002c0002t0001g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.565+97000A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17473322 | |||||||
| chrX:17473483 | C | T | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+97161C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17473483 | |||||||
| chrX:17473698 | C | A | 1 | a0002c0002t0001g0108 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.565+97376C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17473698 | |||||||
| chrX:17473902 | A | ATATT | 3 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0110 |
3 | HG02258.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.565+97602_565+9760 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17473902 | ||||||
| chrX:17474041 | C | T | 1 | a0005c0005t0008g0097 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.565+97719C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17474041 | |||||||
| chrX:17474045 | A | G | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+97723A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17474045 | |||||||
| chrX:17474097 | G | A | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+97775G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17474097 | |||||||
| chrX:17474100 | T | C | 3 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565+97778T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17474100 | |||||||
| chrX:17474141 | C | T | 12 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(9): Show |
12 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.565+97819C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17474141 | |||||||
| chrX:17474158 | A | G | 2 | a0001c0001t0002g0100 a0008c0011t0002g0147 |
2 | HG01243.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.565+97836A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17474158 | |||||||
| chrX:17474627 | G | A | 1 | a0001c0001t0001g0083 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.565+98305G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17474627 | |||||||
| chrX:17474850 | T | C | 7 | a0001c0001t0005g0111 a0001c0003t0002g0102 a0006c0007t0002g0115 others(4): Show |
7 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.565+98528T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17474850 | |||||||
| chrX:17474852 | T | G | 7 | a0001c0001t0005g0111 a0001c0003t0002g0102 a0006c0007t0002g0115 others(4): Show |
7 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.565+98530T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17474852 | |||||||
| chrX:17474915 | A | G | 8 | a0001c0001t0002g0100 a0001c0001t0005g0111 a0001c0003t0002g0102 others(5): Show |
8 | HG01243.hp1 HG02145.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.565+98593A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17474915 | |||||||
| chrX:17475535 | C | A | 1 | a0001c0001t0006g0103 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.565+99213C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17475535 | |||||||
| chrX:17475649 | A | G | 12 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0001c0001t0002g0164 others(9): Show |
12 | HG01243.hp1 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.565+99327A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17475649 | |||||||
| chrX:17475831 | C | G | 10 | a0001c0001t0002g0100 a0001c0001t0005g0111 a0001c0003t0002g0102 others(7): Show |
10 | HG01243.hp1 HG02145.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.565+99509C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17475831 | |||||||
| chrX:17475835 | G | A | 2 | a0002c0002t0001g0138 a0002c0002t0001g0139 |
2 | HG00673.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.565+99513G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17475835 | |||||||
| chrX:17476013 | G | A | 1 | a0001c0001t0002g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.565+99691G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17476013 | |||||||
| chrX:17476020 | GA | G | 4 | a0001c0001t0001g0026 a0002c0002t0001g0023 a0002c0002t0001g0053 others(1): Show |
4 | HG02083.hp1 NA18747.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+99700delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17476020 | ||||||
| chrX:17476176 | A | G | 5 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(2): Show |
5 | HG02280.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+99854A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17476176 | |||||||
| chrX:17476347 | G | A | 2 | a0001c0001t0002g0100 a0008c0011t0002g0147 |
2 | HG01243.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.565+100025G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17476347 | |||||||
| chrX:17476478 | T | C | 41 | a0001c0001t0001g0029 a0001c0001t0001g0048 a0001c0001t0001g0049 others(38): Show |
41 | HG00609.hp1 HG00639.hp2 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.565+100156T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17476478 | |||||||
| chrX:17476489 | T | C | 2 | a0001c0003t0002g0142 a0001c0003t0002g0155 |
2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.565+100167T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17476489 | |||||||
| chrX:17476599 | T | G | 1 | a0002c0002t0001g0023 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.565+100277T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17476599 | |||||||
| chrX:17476850 | A | T | 5 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(2): Show |
5 | HG02280.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+100528A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17476850 | |||||||
| chrX:17477291 | T | C | 5 | a0002c0002t0001g0033 a0002c0002t0001g0040 a0002c0002t0001g0042 others(2): Show |
5 | HG01167.hp1 HG02735.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+100969T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17477291 | |||||||
| chrX:17477305 | C | T | 1 | a0002c0002t0001g0043 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.565+100983C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17477305 | |||||||
| chrX:17477384 | C | T | 1 | a0005c0005t0003g0101 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.565+101062C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17477384 | |||||||
| chrX:17477434 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.565+101112C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17477434 | |||||||
| chrX:17477471 | T | A | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.565+101149T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17477471 | |||||||
| chrX:17478019 | G | T | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+101697G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17478019 | |||||||
| chrX:17478077 | G | A | 16 | a0001c0001t0001g0112 a0001c0001t0002g0100 a0001c0001t0002g0116 others(13): Show |
16 | HG01243.hp1 HG02145.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.565+101755G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17478077 | |||||||
| chrX:17478209 | C | T | 108 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0029 others(105): Show |
108 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.565+101887C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17478209 | |||||||
| chrX:17478598 | A | C | 1 | a0001c0001t0004g0071 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.565+102276A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17478598 | |||||||
| chrX:17478916 | T | A | 143 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0029 others(140): Show |
143 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.565+102594T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17478916 | |||||||
| chrX:17479677 | G | A | 2 | a0001c0001t0001g0049 a0001c0001t0011g0081 |
2 | NA18952.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.565+103355G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17479677 | |||||||
| chrX:17479979 | C | G | 108 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0029 others(105): Show |
108 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.565+103657C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17479979 | |||||||
| chrX:17481320 | G | A | 37 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0061 others(34): Show |
37 | HG00280.hp1 HG00639.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.565+104998G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17481320 | |||||||
| chrX:17481610 | GA | G | 37 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0061 others(34): Show |
37 | HG00280.hp1 HG00639.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.565+105294delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17481610 | ||||||
| chrX:17482011 | C | T | 2 | a0002c0002t0001g0148 a0002c0002t0001g0152 |
2 | HG00642.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.565+105689C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17482011 | |||||||
| chrX:17482094 | A | G | 3 | a0001c0001t0012g0154 a0002c0002t0009g0015 a0005c0005t0008g0097 |
3 | HG01975.hp1 HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.565+105772A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17482094 | |||||||
| chrX:17482275 | A | C | 1 | a0005c0005t0003g0101 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.565+105953A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17482275 | |||||||
| chrX:17482539 | A | G | 1 | a0002c0002t0001g0046 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.565+106217A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17482539 | |||||||
| chrX:17482605 | T | C | 1 | a0001c0001t0002g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.565+106283T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17482605 | |||||||
| chrX:17482659 | A | G | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+106337A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17482659 | |||||||
| chrX:17482913 | G | T | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+106591G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17482913 | |||||||
| chrX:17482919 | G | A | 5 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(2): Show |
5 | HG02280.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+106597G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17482919 | |||||||
| chrX:17482978 | C | T | 1 | a0001c0001t0002g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.565+106656C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17482978 | |||||||
| chrX:17483007 | G | C | 1 | a0001c0001t0002g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.565+106685G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17483007 | |||||||
| chrX:17483041 | G | GC | 110 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0029 others(107): Show |
110 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.565+106723dupC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17483041 | ||||||
| chrX:17483550 | A | C | 2 | a0004c0004t0001g0149 a0011c0012t0001g0150 |
2 | NA18948.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.565+107228A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17483550 | |||||||
| chrX:17484472 | A | G | 1 | a0005c0005t0008g0097 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.565+108150A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17484472 | |||||||
| chrX:17484630 | GGGCTCTG others(62): Show |
G | 110 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0029 others(107): Show |
110 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.565+108312_565+108 others(75): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17484630 | ||||||
| chrX:17484890 | A | G | 1 | a0002c0002t0001g0006 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.565+108568A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17484890 | |||||||
| chrX:17484952 | T | G | 3 | a0002c0002t0001g0018 a0002c0002t0001g0028 a0002c0002t0001g0123 |
3 | HG00639.hp1 HG01074.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.565+108630T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17484952 | |||||||
| chrX:17484959 | A | C | 109 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0029 others(106): Show |
109 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(106): Show |
intron_variant | MODIFIER | c.565+108637A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17484959 | |||||||
| chrX:17484966 | G | C | 3 | a0002c0002t0001g0018 a0002c0002t0001g0028 a0002c0002t0001g0123 |
3 | HG00639.hp1 HG01074.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.565+108644G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17484966 | |||||||
| chrX:17485193 | T | C | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+108871T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17485193 | |||||||
| chrX:17485251 | G | A | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.565+108929G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17485251 | |||||||
| chrX:17485768 | G | C | 111 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0029 others(108): Show |
111 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.565+109446G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17485768 | |||||||
| chrX:17486061 | C | T | 111 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0029 others(108): Show |
111 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.565+109739C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17486061 | |||||||
| chrX:17486239 | T | C | 110 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0029 others(107): Show |
110 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.565+109917T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17486239 | |||||||
| chrX:17486452 | A | C | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+110130A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17486452 | |||||||
| chrX:17486712 | A | C | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+110390A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17486712 | |||||||
| chrX:17486794 | T | C | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+110472T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17486794 | |||||||
| chrX:17486937 | G | A | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+110615G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17486937 | |||||||
| chrX:17487129 | T | G | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+110807T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17487129 | |||||||
| chrX:17487289 | G | C | 4 | a0001c0001t0002g0143 a0001c0003t0002g0128 a0003c0006t0001g0162 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.565+110967G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17487289 | |||||||
| chrX:17487363 | G | C | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+111041G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17487363 | |||||||
| chrX:17487890 | G | C | 1 | a0002c0002t0001g0130 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.565+111568G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17487890 | |||||||
| chrX:17488305 | A | C | 110 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0029 others(107): Show |
110 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.565+111983A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17488305 | |||||||
| chrX:17488495 | C | T | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.565+112173C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17488495 | |||||||
| chrX:17488573 | C | T | 8 | a0001c0001t0005g0111 a0001c0003t0002g0102 a0006c0007t0002g0115 others(5): Show |
8 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.565+112251C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17488573 | |||||||
| chrX:17488658 | T | C | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+112336T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17488658 | |||||||
| chrX:17488904 | C | CTACATTA others(2893): Show |
1 | a0002c0002t0001g0152 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.565+112598_565+112 others(2906): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17488904 | ||||||
| chrX:17488904 | C | CTACATTA others(2894): Show |
1 | a0002c0002t0001g0148 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.565+112598_565+112 others(2907): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17488904 | ||||||
| chrX:17489079 | A | G | 1 | a0009c0016t0002g0119 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.565+112757A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17489079 | |||||||
| chrX:17489143 | A | G | 1 | a0005c0005t0003g0117 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.565+112821A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17489143 | |||||||
| chrX:17489332 | A | G | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+113010A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17489332 | |||||||
| chrX:17489420 | T | C | 110 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0029 others(107): Show |
110 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.565+113098T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17489420 | |||||||
| chrX:17489463 | G | A | 110 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0029 others(107): Show |
110 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.565+113141G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17489463 | |||||||
| chrX:17489502 | G | T | 110 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0029 others(107): Show |
110 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.565+113180G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17489502 | |||||||
| chrX:17489527 | A | C | 1 | a0002c0002t0001g0010 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.565+113205A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17489527 | |||||||
| chrX:17489527 | A | G | 105 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0029 others(102): Show |
105 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.565+113205A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17489527 | |||||||
| chrX:17489582 | G | A | 2 | a0006c0007t0002g0115 a0006c0007t0002g0118 |
2 | HG02615.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.565+113260G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17489582 | |||||||
| chrX:17489739 | G | A | 3 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0005g0104 |
3 | HG03139.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.565+113417G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17489739 | |||||||
| chrX:17489793 | T | C | 1 | a0002c0002t0001g0033 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.565+113471T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17489793 | |||||||
| chrX:17489801 | C | T | 109 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0029 others(106): Show |
109 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(106): Show |
intron_variant | MODIFIER | c.565+113479C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17489801 | |||||||
| chrX:17489817 | A | G | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+113495A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17489817 | |||||||
| chrX:17489913 | G | T | 1 | a0002c0002t0001g0005 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.565+113591G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17489913 | |||||||
| chrX:17490235 | T | G | 3 | a0002c0002t0001g0013 a0002c0002t0001g0019 a0002c0002t0001g0022 |
3 | HG00408.hp2 HG01975.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.565+113913T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17490235 | |||||||
| chrX:17490246 | T | G | 110 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0029 others(107): Show |
110 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.565+113924T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17490246 | |||||||
| chrX:17490256 | A | C | 3 | a0002c0002t0001g0013 a0002c0002t0001g0019 a0002c0002t0001g0022 |
3 | HG00408.hp2 HG01975.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.565+113934A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17490256 | |||||||
| chrX:17490505 | G | T | 1 | a0001c0003t0002g0142 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.565+114183G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17490505 | |||||||
| chrX:17490536 | T | G | 1 | a0008c0011t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.565+114214T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17490536 | |||||||
| chrX:17490839 | A | G | 8 | a0001c0001t0005g0111 a0001c0003t0002g0102 a0006c0007t0002g0115 others(5): Show |
8 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.565+114517A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17490839 | |||||||
| chrX:17491081 | T | C | 5 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(2): Show |
5 | HG02280.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+114759T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17491081 | |||||||
| chrX:17491205 | C | G | 114 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0029 others(111): Show |
114 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(111): Show |
intron_variant | MODIFIER | c.565+114883C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17491205 | |||||||
| chrX:17491277 | C | T | 3 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0110 |
3 | HG02258.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.565+114955C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17491277 | |||||||
| chrX:17491397 | G | T | 3 | a0002c0002t0001g0013 a0002c0002t0001g0019 a0002c0002t0001g0022 |
3 | HG00408.hp2 HG01975.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.565+115075G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17491397 | |||||||
| chrX:17491434 | G | A | 1 | a0001c0001t0006g0103 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.565+115112G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17491434 | |||||||
| chrX:17491701 | G | A | 1 | a0002c0002t0001g0010 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.565+115379G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17491701 | |||||||
| chrX:17491723 | G | A | 8 | a0001c0001t0005g0111 a0001c0003t0002g0102 a0006c0007t0002g0115 others(5): Show |
8 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.565+115401G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17491723 | |||||||
| chrX:17491754 | C | CT | 10 | a0001c0001t0001g0029 a0001c0001t0001g0112 a0001c0001t0002g0116 others(7): Show |
10 | HG01928.hp1 HG02257.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.565+115450dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17491754 | ||||||
| chrX:17491836 | G | A | 1 | a0002c0002t0001g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.565+115514G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17491836 | |||||||
| chrX:17491861 | A | T | 1 | a0002c0002t0001g0062 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.565+115539A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17491861 | |||||||
| chrX:17491940 | T | C | 109 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0029 others(106): Show |
109 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(106): Show |
intron_variant | MODIFIER | c.565+115618T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17491940 | |||||||
| chrX:17492247 | T | C | 3 | a0001c0001t0001g0112 a0001c0001t0002g0121 a0005c0005t0003g0117 |
3 | HG02280.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.565+115925T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17492247 | |||||||
| chrX:17492260 | T | C | 5 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(2): Show |
5 | HG02280.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+115938T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17492260 | |||||||
| chrX:17492455 | T | C | 5 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(2): Show |
5 | HG02280.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+116133T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17492455 | |||||||
| chrX:17492705 | C | T | 2 | a0001c0001t0002g0143 a0003c0009t0002g0160 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.565+116383C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17492705 | |||||||
| chrX:17492748 | A | C | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+116426A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17492748 | |||||||
| chrX:17492765 | G | A | 41 | a0001c0001t0001g0029 a0001c0001t0001g0048 a0001c0001t0001g0049 others(38): Show |
41 | HG00609.hp1 HG00639.hp2 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.565+116443G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17492765 | |||||||
| chrX:17493329 | T | G | 1 | a0006c0007t0002g0118 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.565+117007T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17493329 | |||||||
| chrX:17493427 | T | G | 1 | a0001c0001t0001g0145 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.565+117105T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17493427 | |||||||
| chrX:17493612 | G | A | 3 | a0001c0001t0001g0073 a0001c0001t0006g0074 a0001c0001t0006g0103 |
3 | NA18955.hp1 NA18962.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.565+117290G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17493612 | |||||||
| chrX:17493730 | G | T | 109 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0029 others(106): Show |
109 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(106): Show |
intron_variant | MODIFIER | c.565+117408G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17493730 | |||||||
| chrX:17493734 | G | T | 1 | a0001c0001t0001g0057 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.565+117412G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17493734 | |||||||
| chrX:17493924 | T | G | 111 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0029 others(108): Show |
111 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.565+117602T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17493924 | |||||||
| chrX:17494076 | C | CT | 53 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0056 others(50): Show |
53 | HG00639.hp1 HG01074.hp1 HG01106.hp1 others(50): Show |
intron_variant | MODIFIER | c.565+117776dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17494076 | ||||||
| chrX:17494076 | C | CTT | 40 | a0001c0001t0001g0029 a0001c0001t0001g0048 a0001c0001t0001g0049 others(37): Show |
40 | HG00609.hp1 HG00639.hp2 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.565+117775_565+117 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17494076 | ||||||
| chrX:17494286 | C | G | 110 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0029 others(107): Show |
110 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.565+117964C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17494286 | |||||||
| chrX:17494579 | C | T | 1 | a0010c0010t0003g0158 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.565+118257C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17494579 | |||||||
| chrX:17495151 | C | T | 1 | a0005c0005t0008g0087 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.565+118829C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17495151 | |||||||
| chrX:17495956 | G | T | 3 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0005g0104 |
3 | HG03139.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.565+119634G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17495956 | |||||||
| chrX:17496094 | C | G | 1 | a0003c0006t0002g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.565+119772C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17496094 | |||||||
| chrX:17496477 | C | A | 3 | a0001c0001t0001g0073 a0001c0001t0006g0074 a0001c0001t0006g0103 |
3 | NA18955.hp1 NA18962.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.565+120155C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17496477 | |||||||
| chrX:17496640 | A | C | 4 | a0001c0001t0002g0143 a0001c0003t0002g0128 a0003c0006t0001g0162 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.565+120318A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17496640 | |||||||
| chrX:17496695 | C | T | 3 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0005g0104 |
3 | HG03139.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.565+120373C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17496695 | |||||||
| chrX:17497077 | C | T | 1 | a0002c0002t0001g0033 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.565+120755C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17497077 | |||||||
| chrX:17497377 | C | T | 1 | a0002c0002t0001g0072 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.565+121055C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17497377 | |||||||
| chrX:17497819 | A | G | 106 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0029 others(103): Show |
106 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.565+121497A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17497819 | |||||||
| chrX:17498171 | T | A | 1 | a0001c0001t0002g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.565+121849T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17498171 | |||||||
| chrX:17498232 | G | A | 1 | a0006c0007t0002g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.565+121910G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17498232 | |||||||
| chrX:17498411 | T | C | 1 | a0005c0005t0008g0097 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.565+122089T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17498411 | |||||||
| chrX:17498748 | A | T | 113 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0029 others(110): Show |
113 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(110): Show |
intron_variant | MODIFIER | c.565+122426A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17498748 | |||||||
| chrX:17499044 | T | C | 6 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(3): Show |
6 | HG02280.hp1 HG02717.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.565+122722T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17499044 | |||||||
| chrX:17499602 | C | CA | 5 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(2): Show |
5 | HG02280.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+123280_565+123 others(7): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17499602 | |||||||
| chrX:17500037 | G | A | 6 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(3): Show |
6 | HG02280.hp1 HG03098.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.565+123715G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17500037 | |||||||
| chrX:17500115 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.565+123793G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17500115 | |||||||
| chrX:17500191 | G | A | 1 | a0002c0002t0001g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.565+123869G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17500191 | |||||||
| chrX:17500457 | T | C | 6 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(3): Show |
6 | HG02280.hp1 HG02717.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.565+124135T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17500457 | |||||||
| chrX:17500668 | T | C | 1 | a0001c0001t0002g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.565+124346T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17500668 | |||||||
| chrX:17500825 | C | T | 5 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(2): Show |
5 | HG02280.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+124503C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17500825 | |||||||
| chrX:17500956 | A | ATTG | 117 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0029 others(114): Show |
117 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(114): Show |
intron_variant | MODIFIER | c.565+124636_565+124 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17500956 | ||||||
| chrX:17501134 | T | A | 1 | a0002c0002t0001g0006 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.565+124812T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17501134 | |||||||
| chrX:17501197 | C | T | 2 | a0001c0003t0002g0128 a0003c0006t0001g0162 |
2 | HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.565+124875C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17501197 | |||||||
| chrX:17501355 | G | GA | 54 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0035 others(51): Show |
54 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.565+125044dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17501355 | ||||||
| chrX:17502493 | TAAGAAGT others(308): Show |
T | 112 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0029 others(109): Show |
112 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(109): Show |
intron_variant | MODIFIER | c.565+126186_565+126 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17502493 | ||||||
| chrX:17503306 | T | C | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+126984T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17503306 | |||||||
| chrX:17503379 | T | G | 8 | a0001c0001t0005g0111 a0001c0003t0002g0102 a0006c0007t0002g0115 others(5): Show |
8 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.565+127057T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17503379 | |||||||
| chrX:17503691 | A | G | 5 | a0001c0001t0001g0127 a0001c0001t0007g0125 a0003c0006t0002g0161 others(2): Show |
5 | HG01071.hp2 HG02647.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+127369A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17503691 | |||||||
| chrX:17503911 | C | G | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+127589C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17503911 | |||||||
| chrX:17504360 | T | C | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+128038T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17504360 | |||||||
| chrX:17505627 | G | GT | 13 | a0001c0001t0001g0011 a0001c0001t0005g0111 a0001c0001t0012g0154 others(10): Show |
13 | HG00642.hp1 HG01975.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.565+129319dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17505627 | ||||||
| chrX:17505875 | A | G | 151 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0029 others(148): Show |
151 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.565+129553A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17505875 | |||||||
| chrX:17506423 | A | G | 1 | a0001c0001t0002g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.565+130101A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17506423 | |||||||
| chrX:17506461 | G | A | 27 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0061 others(24): Show |
27 | HG00280.hp1 HG00639.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.565+130139G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17506461 | |||||||
| chrX:17506527 | T | TAATA | 9 | a0001c0001t0001g0112 a0001c0001t0002g0003 a0001c0001t0002g0093 others(6): Show |
9 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.565+130243_565+130 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17506527 | ||||||
| chrX:17506527 | TAATA | T | 15 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0124 others(12): Show |
15 | HG00408.hp1 HG00408.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.565+130243_565+130 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17506527 | ||||||
| chrX:17506527 | TAATAAAT others(1): Show |
T | 6 | a0001c0001t0001g0068 a0001c0001t0002g0106 a0001c0001t0002g0107 others(3): Show |
6 | HG01106.hp1 HG02258.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.565+130239_565+130 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17506527 | ||||||
| chrX:17506527 | TAATAAAT others(5): Show |
T | 1 | a0002c0002t0001g0078 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.565+130235_565+130 others(18): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17506527 | ||||||
| chrX:17506565 | A | ATAAATAA others(1): Show |
3 | a0001c0001t0001g0073 a0001c0001t0007g0122 a0010c0010t0003g0158 |
3 | HG02615.hp2 HG02723.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.565+130246_565+130 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17506565 | ||||||
| chrX:17506565 | A | ATAAG | 22 | a0001c0001t0001g0049 a0001c0001t0002g0100 a0001c0001t0005g0104 others(19): Show |
22 | HG00639.hp1 HG01074.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.565+130247_565+130 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17506565 | ||||||
| chrX:17506565 | A | G | 85 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0029 others(82): Show |
85 | HG00280.hp1 HG00609.hp1 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.565+130243A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17506565 | |||||||
| chrX:17507106 | A | G | 1 | a0001c0001t0002g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.565+130784A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17507106 | |||||||
| chrX:17507109 | C | T | 2 | a0006c0008t0001g0114 a0006c0008t0002g0113 |
2 | HG02145.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.565+130787C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17507109 | |||||||
| chrX:17507294 | T | C | 1 | a0002c0002t0001g0009 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.565+130972T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17507294 | |||||||
| chrX:17507376 | C | T | 1 | a0002c0002t0001g0077 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.565+131054C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17507376 | |||||||
| chrX:17507672 | G | A | 1 | a0002c0002t0001g0069 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.565+131350G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17507672 | |||||||
| chrX:17507728 | G | C | 1 | a0001c0001t0002g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.565+131406G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17507728 | |||||||
| chrX:17507751 | A | G | 116 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0029 others(113): Show |
116 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(113): Show |
intron_variant | MODIFIER | c.565+131429A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17507751 | |||||||
| chrX:17508116 | AATGGTAC others(17): Show |
A | 1 | a0001c0001t0002g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.565+131808_565+131 others(30): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17508116 | ||||||
| chrX:17508242 | C | T | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.565+131920C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17508242 | |||||||
| chrX:17508257 | A | G | 114 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0029 others(111): Show |
114 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(111): Show |
intron_variant | MODIFIER | c.565+131935A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17508257 | |||||||
| chrX:17508270 | C | T | 1 | a0002c0002t0001g0022 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.565+131948C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17508270 | |||||||
| chrX:17508292 | G | T | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+131970G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17508292 | |||||||
| chrX:17508371 | T | G | 5 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(2): Show |
5 | HG02280.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+132049T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17508371 | |||||||
| chrX:17508470 | GTTGT | G | 8 | a0001c0001t0001g0137 a0001c0001t0002g0044 a0001c0001t0013g0045 others(5): Show |
8 | HG01109.hp1 HG01167.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.565+132163_565+132 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17508470 | ||||||
| chrX:17508655 | A | G | 1 | a0005c0005t0003g0117 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.565+132333A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17508655 | |||||||
| chrX:17508841 | G | T | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+132519G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17508841 | |||||||
| chrX:17509201 | C | G | 112 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0029 others(109): Show |
112 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(109): Show |
intron_variant | MODIFIER | c.565+132879C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17509201 | |||||||
| chrX:17509206 | A | AATTT | 20 | a0001c0001t0001g0029 a0001c0001t0001g0112 a0001c0001t0002g0002 others(17): Show |
20 | HG01069.hp1 HG01071.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.565+132919_565+132 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17509206 | ||||||
| chrX:17509206 | A | AATTTATT others(1): Show |
5 | a0001c0001t0001g0041 a0001c0001t0001g0048 a0001c0001t0002g0003 others(2): Show |
5 | HG02451.hp1 HG02809.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.565+132915_565+132 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17509206 | ||||||
| chrX:17509206 | AATTT | A | 82 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0049 others(79): Show |
82 | HG00280.hp1 HG00609.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.565+132919_565+132 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17509206 | ||||||
| chrX:17509678 | GA | G | 3 | a0001c0001t0002g0100 a0001c0001t0007g0122 a0008c0011t0002g0147 |
3 | HG01243.hp1 HG02257.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.565+133357delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17509678 | |||||||
| chrX:17509698 | C | G | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+133376C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17509698 | |||||||
| chrX:17509750 | A | G | 2 | a0001c0003t0002g0142 a0001c0003t0002g0155 |
2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.565+133428A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17509750 | |||||||
| chrX:17509779 | A | C | 115 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0029 others(112): Show |
115 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(112): Show |
intron_variant | MODIFIER | c.565+133457A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17509779 | |||||||
| chrX:17509936 | G | T | 1 | a0001c0001t0002g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.565+133614G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17509936 | |||||||
| chrX:17510481 | G | C | 1 | a0001c0001t0002g0100 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.565+134159G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17510481 | |||||||
| chrX:17510493 | G | A | 110 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0029 others(107): Show |
110 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.565+134171G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17510493 | |||||||
| chrX:17510721 | A | C | 5 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(2): Show |
5 | HG02280.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+134399A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17510721 | |||||||
| chrX:17511078 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.565+134756A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17511078 | |||||||
| chrX:17511209 | A | G | 116 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0029 others(113): Show |
116 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(113): Show |
intron_variant | MODIFIER | c.565+134887A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17511209 | |||||||
| chrX:17511860 | CCTT | C | 48 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0035 others(45): Show |
48 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.565+135542_565+135 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17511860 | ||||||
| chrX:17512201 | C | T | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.565+135879C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17512201 | |||||||
| chrX:17512457 | G | C | 17 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0134 others(14): Show |
17 | HG00140.hp1 HG00408.hp1 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.565+136135G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17512457 | |||||||
| chrX:17512638 | A | C | 54 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0035 others(51): Show |
54 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.565+136316A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17512638 | |||||||
| chrX:17512792 | C | T | 1 | a0001c0001t0002g0120 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.565+136470C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17512792 | |||||||
| chrX:17512794 | T | TA | 59 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0035 others(56): Show |
59 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.565+136473dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17512794 | ||||||
| chrX:17514158 | C | A | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+137836C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17514158 | |||||||
| chrX:17514165 | G | T | 13 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0124 others(10): Show |
13 | HG00408.hp2 HG01258.hp1 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.565+137843G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17514165 | |||||||
| chrX:17514325 | A | C | 1 | a0002c0015t0001g0039 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.565+138003A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17514325 | |||||||
| chrX:17515061 | T | A | 6 | a0001c0001t0005g0111 a0001c0003t0002g0102 a0006c0007t0002g0115 others(3): Show |
6 | HG02615.hp1 HG02630.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.565+138739T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17515061 | |||||||
| chrX:17515370 | AG | A | 16 | a0001c0001t0001g0112 a0001c0001t0002g0106 a0001c0001t0002g0107 others(13): Show |
16 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.565+139050delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17515370 | ||||||
| chrX:17516044 | T | TA | 18 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0110 others(15): Show |
18 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.565+139737dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17516044 | ||||||
| chrX:17516246 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.565+139924C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17516246 | |||||||
| chrX:17516267 | G | A | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.565+139945G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17516267 | |||||||
| chrX:17516314 | C | G | 2 | a0002c0002t0009g0015 a0005c0005t0008g0097 |
2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.565+139992C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17516314 | |||||||
| chrX:17516417 | T | C | 16 | a0001c0001t0001g0112 a0001c0001t0002g0106 a0001c0001t0002g0107 others(13): Show |
16 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.565+140095T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17516417 | |||||||
| chrX:17516565 | ACACGCG | A | 3 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0110 |
3 | HG02258.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.565+140247_565+140 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17516565 | ||||||
| chrX:17516567 | ACG | A | 6 | a0001c0001t0001g0070 a0001c0001t0001g0127 a0001c0001t0007g0125 others(3): Show |
6 | HG01071.hp2 HG02647.hp1 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.565+140249_565+140 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17516567 | ||||||
| chrX:17516569 | G | A | 15 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(12): Show |
15 | HG02145.hp1 HG02280.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.565+140247G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17516569 | |||||||
| chrX:17516569 | GCGCA | G | 5 | a0001c0001t0001g0056 a0001c0001t0001g0066 a0001c0001t0004g0071 others(2): Show |
5 | HG02132.hp1 NA18989.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+140249_565+140 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17516569 | ||||||
| chrX:17516571 | G | GCA | 37 | a0001c0001t0001g0026 a0001c0001t0001g0049 a0001c0001t0001g0051 others(34): Show |
37 | HG00621.hp1 HG00639.hp2 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.565+140283_565+140 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17516571 | ||||||
| chrX:17516571 | G | GCACA | 4 | a0001c0001t0001g0050 a0002c0002t0001g0054 a0002c0002t0001g0108 others(1): Show |
4 | HG02056.hp1 NA18974.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+140281_565+140 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17516571 | ||||||
| chrX:17516571 | GCA | G | 31 | a0001c0001t0001g0008 a0001c0001t0001g0029 a0001c0001t0001g0061 others(28): Show |
31 | HG00140.hp1 HG00673.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.565+140283_565+140 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17516571 | ||||||
| chrX:17516571 | GCACA | G | 8 | a0001c0001t0001g0048 a0001c0001t0002g0002 a0001c0001t0002g0164 others(5): Show |
8 | HG02055.hp1 HG02293.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.565+140281_565+140 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17516571 | ||||||
| chrX:17516571 | GCACACAC others(5): Show |
G | 1 | a0002c0002t0001g0020 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.565+140273_565+140 others(18): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17516571 | ||||||
| chrX:17516573 | A | G | 2 | a0001c0003t0002g0142 a0001c0003t0002g0155 |
2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.565+140251A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17516573 | |||||||
| chrX:17516577 | A | G | 3 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0110 |
3 | HG02258.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.565+140255A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17516577 | |||||||
| chrX:17516773 | GCACACA | G | 3 | a0001c0001t0001g0021 a0001c0001t0004g0163 a0002c0002t0001g0001 |
3 | HG01261.hp1 HG02135.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.565+140465_565+140 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17516773 | ||||||
| chrX:17516791 | A | G | 1 | a0002c0002t0001g0022 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.565+140469A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17516791 | |||||||
| chrX:17516863 | C | T | 1 | a0001c0001t0002g0107 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.565+140541C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17516863 | |||||||
| chrX:17516898 | T | C | 1 | a0002c0002t0001g0108 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.565+140576T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17516898 | |||||||
| chrX:17516987 | C | A | 6 | a0001c0001t0001g0041 a0001c0001t0002g0003 a0001c0001t0002g0093 others(3): Show |
6 | HG01069.hp1 HG01071.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.565+140665C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17516987 | |||||||
| chrX:17517015 | G | A | 1 | a0009c0016t0002g0119 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.565+140693G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17517015 | |||||||
| chrX:17517290 | C | T | 16 | a0001c0001t0001g0112 a0001c0001t0002g0106 a0001c0001t0002g0107 others(13): Show |
16 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.565+140968C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17517290 | |||||||
| chrX:17517414 | G | T | 2 | a0002c0002t0001g0138 a0002c0002t0001g0139 |
2 | HG00673.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.565+141092G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17517414 | |||||||
| chrX:17517753 | T | C | 1 | a0002c0002t0001g0131 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.565+141431T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17517753 | |||||||
| chrX:17517794 | T | A | 16 | a0001c0001t0001g0112 a0001c0001t0002g0106 a0001c0001t0002g0107 others(13): Show |
16 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.565+141472T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17517794 | |||||||
| chrX:17518084 | C | G | 16 | a0001c0001t0001g0112 a0001c0001t0002g0106 a0001c0001t0002g0107 others(13): Show |
16 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.565+141762C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17518084 | |||||||
| chrX:17518219 | C | T | 1 | a0003c0006t0002g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.565+141897C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17518219 | |||||||
| chrX:17518346 | A | G | 3 | a0002c0002t0001g0013 a0002c0002t0001g0019 a0002c0002t0001g0022 |
3 | HG00408.hp2 HG01975.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.565+142024A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17518346 | |||||||
| chrX:17519127 | C | T | 1 | a0001c0001t0010g0059 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.565+142805C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17519127 | |||||||
| chrX:17519185 | TA | T | 16 | a0001c0001t0001g0112 a0001c0001t0002g0106 a0001c0001t0002g0107 others(13): Show |
16 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.565+142867delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17519185 | ||||||
| chrX:17519448 | C | G | 3 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0110 |
3 | HG02258.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.565+143126C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17519448 | |||||||
| chrX:17519829 | G | A | 2 | a0001c0001t0002g0164 a0005c0005t0003g0101 |
2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.565+143507G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17519829 | |||||||
| chrX:17520131 | G | T | 5 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0110 others(2): Show |
5 | HG02055.hp1 HG02258.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+143809G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17520131 | |||||||
| chrX:17520662 | G | A | 18 | a0001c0001t0001g0112 a0001c0001t0002g0086 a0001c0001t0002g0106 others(15): Show |
18 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.565+144340G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17520662 | |||||||
| chrX:17520720 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.565+144398G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17520720 | |||||||
| chrX:17521366 | C | CTTTTTTT others(11): Show |
3 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0110 |
3 | HG02258.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.565+145057_565+145 others(24): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17521366 | ||||||
| chrX:17521366 | C | CTTTTTTT others(15): Show |
1 | a0005c0005t0003g0101 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.565+145057_565+145 others(28): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17521366 | ||||||
| chrX:17521366 | C | CTTTTTTT others(16): Show |
2 | a0001c0001t0002g0164 a0001c0003t0002g0102 |
2 | HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.565+145057_565+145 others(29): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17521366 | ||||||
| chrX:17521366 | C | CTTTTTTT others(18): Show |
1 | a0001c0001t0005g0111 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.565+145057_565+145 others(31): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17521366 | ||||||
| chrX:17521366 | C | CTTTTTTT others(24): Show |
1 | a0006c0007t0002g0118 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.565+145057_565+145 others(37): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17521366 | ||||||
| chrX:17521366 | C | CTTTTTTT others(26): Show |
1 | a0006c0007t0002g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.565+145057_565+145 others(39): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17521366 | ||||||
| chrX:17521366 | C | CTTTTTTT others(27): Show |
1 | a0001c0001t0002g0086 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.565+145057_565+145 others(40): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17521366 | ||||||
| chrX:17521366 | C | CTTTTTTT others(28): Show |
1 | a0010c0010t0003g0158 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.565+145057_565+145 others(41): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17521366 | ||||||
| chrX:17521366 | C | CTTTTTTT others(32): Show |
1 | a0006c0008t0001g0114 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.565+145057_565+145 others(45): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17521366 | ||||||
| chrX:17521366 | C | CTTTTTTT others(34): Show |
1 | a0006c0008t0002g0113 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.565+145057_565+145 others(47): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17521366 | ||||||
| chrX:17521366 | C | CTTTTTTT others(40): Show |
1 | a0009c0016t0002g0119 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.565+145057_565+145 others(53): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17521366 | ||||||
| chrX:17521433 | G | A | 1 | a0001c0001t0002g0044 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.565+145111G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17521433 | |||||||
| chrX:17521449 | C | T | 9 | a0001c0001t0002g0086 a0001c0001t0005g0111 a0001c0003t0002g0102 others(6): Show |
9 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.565+145127C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17521449 | |||||||
| chrX:17521472 | C | T | 9 | a0001c0001t0002g0086 a0001c0001t0005g0111 a0001c0003t0002g0102 others(6): Show |
9 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.565+145150C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17521472 | |||||||
| chrX:17521475 | A | G | 4 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(1): Show |
4 | HG03098.hp1 HG03209.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+145153A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17521475 | |||||||
| chrX:17522059 | T | C | 1 | a0001c0001t0001g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.565+145737T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17522059 | |||||||
| chrX:17522318 | G | A | 1 | a0002c0002t0001g0156 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.565+145996G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17522318 | |||||||
| chrX:17522493 | G | GC | 38 | a0001c0001t0001g0035 a0001c0001t0001g0094 a0001c0001t0001g0134 others(35): Show |
38 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(35): Show |
intron_variant | MODIFIER | c.565+146184dupC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17522493 | ||||||
| chrX:17522493 | G | GCC | 31 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0061 others(28): Show |
31 | HG01074.hp1 HG01433.hp1 HG01515.hp1 others(28): Show |
intron_variant | MODIFIER | c.565+146183_565+146 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17522493 | ||||||
| chrX:17522493 | G | GCCC | 15 | a0001c0001t0001g0083 a0001c0001t0001g0140 a0001c0001t0006g0103 others(12): Show |
15 | HG00639.hp1 HG01192.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.565+146182_565+146 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17522493 | ||||||
| chrX:17522493 | G | GCCCC | 10 | a0001c0001t0001g0073 a0001c0001t0001g0129 a0001c0001t0001g0145 others(7): Show |
10 | HG00639.hp2 HG01099.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.565+146181_565+146 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17522493 | ||||||
| chrX:17522493 | G | GCCCCC | 10 | a0001c0001t0001g0029 a0001c0001t0001g0049 a0001c0001t0001g0057 others(7): Show |
10 | HG00609.hp1 HG02698.hp1 HG03471.hp1 others(7): Show |
intron_variant | MODIFIER | c.565+146180_565+146 others(11): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17522493 | ||||||
| chrX:17522493 | GC | G | 16 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0041 others(13): Show |
16 | HG00408.hp2 HG01069.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.565+146184delC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17522493 | ||||||
| chrX:17522501 | C | A | 5 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0096 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+146179C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17522501 | |||||||
| chrX:17522502 | C | A | 5 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0096 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+146180C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17522502 | |||||||
| chrX:17522502 | C | G | 1 | a0008c0011t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.565+146180C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17522502 | |||||||
| chrX:17522623 | G | C | 18 | a0001c0001t0001g0112 a0001c0001t0002g0086 a0001c0001t0002g0106 others(15): Show |
18 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.565+146301G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17522623 | |||||||
| chrX:17522744 | TGGCCTGT others(3): Show |
T | 1 | a0001c0001t0001g0098 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.565+146424_565+146 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17522744 | ||||||
| chrX:17523116 | A | T | 1 | a0001c0001t0002g0044 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.565+146794A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17523116 | |||||||
| chrX:17523251 | G | A | 1 | a0002c0002t0001g0072 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.565+146929G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17523251 | |||||||
| chrX:17523359 | G | T | 5 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0110 others(2): Show |
5 | HG02055.hp1 HG02258.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+147037G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17523359 | |||||||
| chrX:17523510 | G | A | 5 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0110 others(2): Show |
5 | HG02055.hp1 HG02258.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+147188G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17523510 | |||||||
| chrX:17523716 | T | TCCCCTCA others(45): Show |
1 | a0002c0002t0001g0024 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.565+147397_565+147 others(58): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17523716 | ||||||
| chrX:17523914 | A | G | 1 | a0003c0006t0002g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.565+147592A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17523914 | |||||||
| chrX:17523943 | G | A | 5 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0110 others(2): Show |
5 | HG02055.hp1 HG02258.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+147621G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17523943 | |||||||
| chrX:17524061 | A | ATTTGTCT others(17): Show |
1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+147739_565+147 others(30): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17524061 | |||||||
| chrX:17524062 | C | A | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+147740C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17524062 | |||||||
| chrX:17524077 | G | A | 18 | a0001c0001t0001g0112 a0001c0001t0002g0086 a0001c0001t0002g0106 others(15): Show |
18 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.565+147755G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17524077 | |||||||
| chrX:17524424 | A | G | 9 | a0001c0001t0002g0086 a0001c0001t0005g0111 a0001c0003t0002g0102 others(6): Show |
9 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.565+148102A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17524424 | |||||||
| chrX:17524481 | T | C | 9 | a0001c0001t0001g0112 a0001c0001t0002g0106 a0001c0001t0002g0107 others(6): Show |
9 | HG02055.hp1 HG02258.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.565+148159T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17524481 | |||||||
| chrX:17524514 | G | A | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+148192G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17524514 | |||||||
| chrX:17524515 | T | G | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+148193T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17524515 | |||||||
| chrX:17524925 | T | A | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+148603T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17524925 | |||||||
| chrX:17525019 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.565+148697G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17525019 | |||||||
| chrX:17525026 | G | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0099 |
2 | NA18967.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.565+148704G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17525026 | |||||||
| chrX:17525106 | T | C | 1 | a0001c0001t0002g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.565+148784T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17525106 | |||||||
| chrX:17525135 | T | G | 19 | a0001c0001t0001g0112 a0001c0001t0002g0086 a0001c0001t0002g0106 others(16): Show |
19 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.565+148813T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17525135 | |||||||
| chrX:17525357 | T | C | 1 | a0006c0007t0002g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.565+149035T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17525357 | |||||||
| chrX:17525450 | T | G | 1 | a0001c0001t0001g0137 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.565+149128T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17525450 | |||||||
| chrX:17525624 | T | C | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+149302T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17525624 | |||||||
| chrX:17525630 | TTTC | T | 3 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0110 |
3 | HG02258.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.565+149311_565+149 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17525630 | ||||||
| chrX:17525638 | C | CT | 26 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0098 others(23): Show |
26 | HG00140.hp1 HG00408.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.565+149337dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17525638 | ||||||
| chrX:17525638 | C | CTT | 10 | a0001c0001t0002g0086 a0001c0001t0002g0120 a0001c0003t0002g0102 others(7): Show |
10 | HG00642.hp1 HG02145.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.565+149336_565+149 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17525638 | ||||||
| chrX:17525638 | CT | C | 7 | a0001c0001t0001g0073 a0001c0001t0002g0093 a0001c0001t0002g0106 others(4): Show |
7 | HG01069.hp1 HG02258.hp1 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.565+149337delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17525638 | ||||||
| chrX:17525668 | G | A | 1 | a0002c0002t0001g0080 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.565+149346G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17525668 | |||||||
| chrX:17525759 | G | C | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+149437G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17525759 | |||||||
| chrX:17525760 | C | G | 2 | a0001c0001t0002g0093 a0001c0001t0002g0143 |
2 | HG01069.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.565+149438C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17525760 | |||||||
| chrX:17525787 | G | C | 2 | a0001c0001t0002g0164 a0005c0005t0003g0101 |
2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.565+149465G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17525787 | |||||||
| chrX:17525843 | G | T | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+149521G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17525843 | |||||||
| chrX:17525845 | T | G | 1 | a0001c0001t0002g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.565+149523T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17525845 | |||||||
| chrX:17526156 | C | T | 5 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0110 others(2): Show |
5 | HG02055.hp1 HG02258.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+149834C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17526156 | |||||||
| chrX:17526239 | G | T | 13 | a0001c0001t0001g0112 a0001c0001t0002g0086 a0001c0001t0002g0116 others(10): Show |
13 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.565+149917G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17526239 | |||||||
| chrX:17526311 | T | C | 28 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0061 others(25): Show |
28 | HG00280.hp1 HG00639.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.565+149989T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17526311 | |||||||
| chrX:17526377 | C | G | 1 | a0002c0002t0001g0130 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.565+150055C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17526377 | |||||||
| chrX:17526381 | T | C | 1 | a0008c0011t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.565+150059T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17526381 | |||||||
| chrX:17526414 | G | T | 1 | a0002c0002t0001g0130 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.565+150092G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17526414 | |||||||
| chrX:17526658 | A | G | 1 | a0001c0001t0001g0135 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.565+150336A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17526658 | |||||||
| chrX:17527225 | T | C | 1 | a0001c0001t0012g0154 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.565+150903T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17527225 | |||||||
| chrX:17527249 | T | C | 29 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0061 others(26): Show |
29 | HG00280.hp1 HG00639.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.565+150927T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17527249 | |||||||
| chrX:17527413 | A | G | 2 | a0001c0001t0002g0164 a0005c0005t0003g0101 |
2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.565+151091A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17527413 | |||||||
| chrX:17527776 | T | C | 1 | a0001c0001t0002g0121 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.565+151454T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17527776 | |||||||
| chrX:17528367 | A | G | 9 | a0001c0001t0001g0112 a0001c0001t0002g0106 a0001c0001t0002g0107 others(6): Show |
9 | HG02055.hp1 HG02258.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.565+152045A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17528367 | |||||||
| chrX:17528503 | G | A | 1 | a0002c0002t0001g0109 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.565+152181G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17528503 | |||||||
| chrX:17528673 | C | T | 4 | a0001c0001t0002g0093 a0001c0001t0002g0096 a0001c0001t0002g0126 others(1): Show |
4 | HG01069.hp1 HG01071.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+152351C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17528673 | |||||||
| chrX:17528675 | CGCTGTGT others(9): Show |
C | 2 | a0001c0003t0002g0142 a0001c0003t0002g0155 |
2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.565+152354_565+152 others(22): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17528675 | |||||||
| chrX:17528880 | C | T | 1 | a0002c0002t0001g0024 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.565+152558C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17528880 | |||||||
| chrX:17528881 | G | A | 19 | a0001c0001t0001g0112 a0001c0001t0002g0086 a0001c0001t0002g0106 others(16): Show |
19 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.565+152559G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17528881 | |||||||
| chrX:17529262 | C | T | 29 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0061 others(26): Show |
29 | HG00280.hp1 HG00639.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.565+152940C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17529262 | |||||||
| chrX:17529527 | G | A | 1 | a0001c0001t0002g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.565+153205G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17529527 | |||||||
| chrX:17529621 | A | G | 13 | a0001c0001t0001g0112 a0001c0001t0002g0086 a0001c0001t0002g0116 others(10): Show |
13 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.565+153299A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17529621 | |||||||
| chrX:17529974 | T | G | 1 | a0001c0001t0002g0107 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.565+153652T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17529974 | |||||||
| chrX:17530192 | A | G | 1 | a0002c0002t0001g0040 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.565+153870A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17530192 | |||||||
| chrX:17530709 | T | C | 7 | a0001c0001t0001g0112 a0001c0001t0002g0106 a0001c0001t0002g0107 others(4): Show |
7 | HG02258.hp1 HG03098.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.565+154387T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17530709 | |||||||
| chrX:17530856 | G | A | 13 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0057 others(10): Show |
13 | HG00408.hp2 HG00609.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.565+154534G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17530856 | |||||||
| chrX:17530942 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.565+154620C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17530942 | |||||||
| chrX:17531112 | A | G | 4 | a0001c0001t0001g0112 a0001c0001t0002g0116 a0001c0001t0002g0120 others(1): Show |
4 | HG03098.hp1 HG03209.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+154790A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17531112 | |||||||
| chrX:17531144 | C | G | 9 | a0001c0001t0002g0086 a0001c0001t0005g0111 a0001c0003t0002g0102 others(6): Show |
9 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.565+154822C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17531144 | |||||||
| chrX:17531323 | G | C | 71 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0035 others(68): Show |
71 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.565+155001G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17531323 | |||||||
| chrX:17531817 | A | G | 7 | a0001c0001t0001g0112 a0001c0001t0002g0106 a0001c0001t0002g0107 others(4): Show |
7 | HG02258.hp1 HG03098.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.565+155495A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17531817 | |||||||
| chrX:17532031 | C | T | 16 | a0001c0001t0001g0112 a0001c0001t0002g0086 a0001c0001t0002g0106 others(13): Show |
16 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.565+155709C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17532031 | |||||||
| chrX:17532343 | C | T | 1 | a0005c0005t0003g0101 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.566-155399C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17532343 | |||||||
| chrX:17532853 | T | G | 54 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0035 others(51): Show |
54 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.566-154889T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17532853 | |||||||
| chrX:17533006 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.566-154736G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17533006 | |||||||
| chrX:17533069 | A | G | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.566-154673A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17533069 | |||||||
| chrX:17533210 | G | A | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.566-154532G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17533210 | |||||||
| chrX:17533443 | C | T | 1 | a0001c0001t0004g0163 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.566-154299C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17533443 | |||||||
| chrX:17533445 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.566-154297C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17533445 | |||||||
| chrX:17533649 | AC | A | 12 | a0001c0001t0002g0086 a0001c0001t0002g0106 a0001c0001t0002g0107 others(9): Show |
12 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.566-154092delC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17533649 | |||||||
| chrX:17533883 | A | G | 16 | a0001c0001t0001g0112 a0001c0001t0002g0086 a0001c0001t0002g0106 others(13): Show |
16 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.566-153859A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17533883 | |||||||
| chrX:17534096 | T | TTG | 6 | a0001c0001t0002g0096 a0002c0002t0001g0022 a0002c0002t0001g0024 others(3): Show |
6 | HG02015.hp1 HG02027.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-153621_566-153 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17534096 | ||||||
| chrX:17534096 | T | TTGTG | 25 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0057 others(22): Show |
25 | HG00408.hp2 HG00609.hp1 HG01258.hp1 others(22): Show |
intron_variant | MODIFIER | c.566-153623_566-153 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17534096 | ||||||
| chrX:17534096 | T | TTGTGTG | 83 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0037 others(80): Show |
83 | HG00140.hp1 HG00408.hp1 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.566-153625_566-153 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17534096 | ||||||
| chrX:17534096 | T | TTGTGTGT others(1): Show |
9 | a0001c0001t0002g0100 a0001c0001t0002g0143 a0001c0001t0002g0146 others(6): Show |
9 | HG01243.hp1 HG02257.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.566-153627_566-153 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17534096 | ||||||
| chrX:17534096 | T | TTGTGTGT others(3): Show |
1 | a0008c0011t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.566-153629_566-153 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17534096 | ||||||
| chrX:17534527 | G | A | 67 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0035 others(64): Show |
67 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.566-153215G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17534527 | |||||||
| chrX:17534595 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.566-153147G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17534595 | |||||||
| chrX:17534845 | T | A | 1 | a0001c0001t0007g0122 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.566-152897T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17534845 | |||||||
| chrX:17534983 | C | A | 1 | a0001c0001t0004g0058 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.566-152759C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17534983 | |||||||
| chrX:17535283 | G | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0099 |
2 | NA18967.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.566-152459G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17535283 | |||||||
| chrX:17535659 | A | G | 19 | a0001c0001t0001g0112 a0001c0001t0002g0086 a0001c0001t0002g0106 others(16): Show |
19 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.566-152083A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17535659 | |||||||
| chrX:17535792 | G | C | 1 | a0001c0001t0001g0137 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.566-151950G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17535792 | |||||||
| chrX:17536179 | C | T | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.566-151563C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17536179 | |||||||
| chrX:17536215 | C | T | 2 | a0002c0002t0001g0033 a0002c0002t0001g0075 |
2 | HG01358.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.566-151527C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17536215 | |||||||
| chrX:17536256 | G | A | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.566-151486G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17536256 | |||||||
| chrX:17536260 | C | A | 12 | a0001c0001t0002g0086 a0001c0001t0002g0106 a0001c0001t0002g0107 others(9): Show |
12 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.566-151482C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17536260 | |||||||
| chrX:17536310 | G | A | 9 | a0001c0001t0002g0086 a0001c0001t0005g0111 a0001c0003t0002g0102 others(6): Show |
9 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.566-151432G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17536310 | |||||||
| chrX:17536354 | C | CA | 6 | a0001c0001t0001g0026 a0002c0002t0001g0001 a0002c0002t0001g0023 others(3): Show |
6 | HG02083.hp1 NA18747.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-151381dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17536354 | ||||||
| chrX:17536474 | C | T | 13 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0057 others(10): Show |
13 | HG00408.hp2 HG00609.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.566-151268C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17536474 | |||||||
| chrX:17536481 | C | G | 1 | a0002c0002t0001g0109 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.566-151261C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17536481 | |||||||
| chrX:17536502 | T | C | 1 | a0005c0005t0003g0101 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.566-151240T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17536502 | |||||||
| chrX:17536521 | A | G | 3 | a0002c0002t0001g0025 a0004c0004t0001g0149 a0011c0012t0001g0150 |
3 | NA18948.hp1 NA18990.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.566-151221A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17536521 | |||||||
| chrX:17536564 | G | T | 1 | a0002c0002t0001g0031 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.566-151178G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17536564 | |||||||
| chrX:17536746 | C | G | 3 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0110 |
3 | HG02258.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.566-150996C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17536746 | |||||||
| chrX:17536749 | C | T | 3 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0110 |
3 | HG02258.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.566-150993C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17536749 | |||||||
| chrX:17536799 | C | A | 1 | a0001c0001t0001g0135 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.566-150943C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17536799 | |||||||
| chrX:17537036 | C | G | 1 | a0004c0004t0001g0012 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.566-150706C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17537036 | |||||||
| chrX:17537109 | A | G | 2 | a0001c0001t0001g0137 a0001c0001t0013g0045 |
2 | HG02451.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.566-150633A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17537109 | |||||||
| chrX:17537167 | C | T | 16 | a0001c0001t0001g0068 a0001c0001t0001g0112 a0001c0001t0002g0086 others(13): Show |
16 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.566-150575C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17537167 | |||||||
| chrX:17537249 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.566-150493G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17537249 | |||||||
| chrX:17537869 | C | T | 1 | a0002c0002t0001g0007 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.566-149873C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17537869 | |||||||
| chrX:17537966 | A | G | 2 | a0001c0001t0001g0112 a0008c0011t0002g0147 |
2 | HG02257.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.566-149776A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17537966 | |||||||
| chrX:17538176 | G | C | 1 | a0001c0001t0005g0104 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.566-149566G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17538176 | |||||||
| chrX:17538492 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.566-149250T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17538492 | |||||||
| chrX:17538751 | C | T | 1 | a0002c0002t0001g0131 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.566-148991C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17538751 | |||||||
| chrX:17538851 | G | A | 11 | a0001c0001t0002g0100 a0001c0001t0002g0116 a0001c0001t0002g0120 others(8): Show |
11 | HG01243.hp1 HG02257.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.566-148891G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17538851 | |||||||
| chrX:17538906 | T | C | 2 | a0002c0002t0001g0036 a0002c0002t0001g0076 |
2 | HG04228.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.566-148836T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17538906 | |||||||
| chrX:17539017 | G | A | 1 | a0009c0016t0002g0119 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.566-148725G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17539017 | |||||||
| chrX:17539315 | T | G | 1 | a0002c0002t0001g0006 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.566-148427T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17539315 | |||||||
| chrX:17539964 | G | C | 2 | a0001c0001t0002g0002 a0001c0001t0002g0164 |
2 | HG02293.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.566-147778G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17539964 | |||||||
| chrX:17540601 | G | A | 2 | a0001c0001t0002g0002 a0001c0001t0002g0164 |
2 | HG02293.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.566-147141G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17540601 | |||||||
| chrX:17540778 | G | A | 2 | a0003c0006t0001g0162 a0003c0006t0002g0161 |
2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.566-146964G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17540778 | |||||||
| chrX:17540850 | C | T | 1 | a0009c0016t0002g0119 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.566-146892C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17540850 | |||||||
| chrX:17540889 | G | A | 3 | a0001c0001t0001g0048 a0002c0002t0001g0005 a0002c0002t0001g0052 |
3 | HG00621.hp1 NA18612.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.566-146853G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17540889 | |||||||
| chrX:17541082 | TA | T | 5 | a0001c0003t0002g0128 a0001c0003t0002g0142 a0001c0003t0002g0155 others(2): Show |
5 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-146650delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17541082 | ||||||
| chrX:17541093 | T | A | 3 | a0003c0006t0001g0157 a0006c0008t0001g0114 a0009c0016t0002g0119 |
3 | HG01106.hp1 HG02630.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.566-146649T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17541093 | |||||||
| chrX:17541187 | T | C | 115 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0029 others(112): Show |
115 | HG00280.hp1 HG00408.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.566-146555T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17541187 | |||||||
| chrX:17541462 | G | T | 5 | a0001c0001t0002g0116 a0001c0001t0002g0120 a0001c0001t0007g0122 others(2): Show |
5 | HG02257.hp2 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.566-146280G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17541462 | |||||||
| chrX:17541561 | A | G | 1 | a0001c0003t0002g0014 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.566-146181A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17541561 | |||||||
| chrX:17541767 | A | AAC | 11 | a0001c0001t0001g0050 a0001c0001t0001g0085 a0001c0001t0001g0129 others(8): Show |
11 | HG01099.hp1 HG01255.hp1 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.566-145928_566-145 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17541767 | ||||||
| chrX:17541767 | A | AACAC | 12 | a0001c0001t0001g0026 a0001c0001t0002g0116 a0001c0001t0004g0058 others(9): Show |
12 | HG00140.hp1 HG02027.hp1 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.566-145930_566-145 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17541767 | ||||||
| chrX:17541767 | A | AACACAC | 3 | a0001c0001t0001g0068 a0002c0002t0001g0032 a0010c0010t0003g0158 |
3 | HG01192.hp1 HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.566-145932_566-145 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17541767 | ||||||
| chrX:17541767 | A | AACACACA others(1): Show |
8 | a0001c0001t0002g0110 a0001c0001t0002g0120 a0001c0001t0002g0146 others(5): Show |
8 | HG02630.hp1 HG02922.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.566-145934_566-145 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17541767 | ||||||
| chrX:17541767 | A | AACACACA others(3): Show |
8 | a0001c0001t0001g0021 a0001c0001t0002g0106 a0001c0001t0002g0107 others(5): Show |
8 | HG02135.hp1 HG02258.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.566-145936_566-145 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17541767 | ||||||
| chrX:17541767 | A | AACACACA others(5): Show |
13 | a0001c0001t0001g0049 a0001c0001t0001g0057 a0001c0001t0001g0112 others(10): Show |
13 | HG00280.hp1 HG00609.hp1 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.566-145938_566-145 others(18): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17541767 | ||||||
| chrX:17541767 | A | AACACACA others(7): Show |
20 | a0001c0001t0001g0127 a0001c0001t0001g0135 a0001c0001t0002g0121 others(17): Show |
20 | HG00673.hp1 HG01167.hp1 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.566-145940_566-145 others(20): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17541767 | ||||||
| chrX:17541767 | A | AACACACA others(9): Show |
18 | a0001c0001t0002g0003 a0001c0001t0002g0096 a0001c0001t0004g0163 others(15): Show |
18 | HG01261.hp1 HG01515.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.566-145942_566-145 others(22): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17541767 | ||||||
| chrX:17541767 | A | AACACACA others(11): Show |
15 | a0001c0001t0001g0048 a0001c0001t0001g0070 a0001c0001t0001g0073 others(12): Show |
15 | HG01258.hp1 HG02015.hp1 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.566-145944_566-145 others(24): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17541767 | ||||||
| chrX:17541767 | A | AACACACA others(13): Show |
11 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0001c0001t0001g0144 others(8): Show |
11 | HG01069.hp1 HG01071.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.566-145946_566-145 others(26): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17541767 | ||||||
| chrX:17541767 | A | AACACACA others(15): Show |
3 | a0001c0001t0001g0095 a0002c0015t0001g0039 a0003c0006t0001g0157 |
3 | HG01106.hp1 NA18522.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.566-145948_566-145 others(28): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17541767 | ||||||
| chrX:17541767 | A | AACACACA others(17): Show |
1 | a0001c0001t0006g0103 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.566-145950_566-145 others(30): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17541767 | ||||||
| chrX:17541767 | AAC | A | 4 | a0001c0001t0001g0035 a0001c0001t0001g0056 a0001c0001t0002g0044 others(1): Show |
4 | HG01074.hp1 HG01109.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-145928_566-145 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17541767 | ||||||
| chrX:17541767 | AACAC | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0051 others(1): Show |
4 | HG02071.hp1 NA18961.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-145930_566-145 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17541767 | ||||||
| chrX:17541814 | A | ACACACAC others(4): Show |
1 | a0001c0001t0002g0100 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.566-145927_566-145 others(17): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17541814 | ||||||
| chrX:17541847 | A | G | 7 | a0001c0001t0002g0002 a0001c0001t0002g0164 a0001c0003t0002g0128 others(4): Show |
7 | HG02280.hp2 HG02293.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.566-145895A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17541847 | |||||||
| chrX:17541930 | T | C | 105 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0029 others(102): Show |
105 | HG00280.hp1 HG00408.hp2 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.566-145812T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17541930 | |||||||
| chrX:17542246 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.566-145496C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17542246 | |||||||
| chrX:17542276 | T | C | 10 | a0001c0001t0002g0002 a0001c0001t0002g0164 a0001c0003t0002g0128 others(7): Show |
10 | HG01106.hp1 HG02280.hp2 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.566-145466T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17542276 | |||||||
| chrX:17542278 | C | T | 2 | a0001c0001t0013g0045 a0005c0005t0008g0087 |
2 | HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.566-145464C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17542278 | |||||||
| chrX:17542329 | G | A | 2 | a0003c0006t0001g0157 a0006c0008t0001g0114 |
2 | HG01106.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.566-145413G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17542329 | |||||||
| chrX:17542689 | C | CAG | 14 | a0001c0001t0002g0002 a0001c0001t0002g0086 a0001c0001t0002g0164 others(11): Show |
14 | HG01106.hp1 HG02293.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.566-145029_566-145 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17542689 | ||||||
| chrX:17542689 | C | CAGAG | 2 | a0001c0001t0001g0041 a0001c0003t0002g0128 |
2 | HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.566-145031_566-145 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17542689 | ||||||
| chrX:17542719 | G | A | 1 | a0005c0005t0008g0097 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.566-145023G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17542719 | |||||||
| chrX:17542854 | C | T | 100 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0029 others(97): Show |
100 | HG00280.hp1 HG00408.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.566-144888C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17542854 | |||||||
| chrX:17543182 | C | T | 8 | a0001c0003t0002g0128 a0001c0003t0002g0142 a0001c0003t0002g0155 others(5): Show |
8 | HG01106.hp1 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.566-144560C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17543182 | |||||||
| chrX:17543238 | C | G | 2 | a0003c0006t0001g0157 a0009c0016t0002g0119 |
2 | HG01106.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.566-144504C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17543238 | |||||||
| chrX:17543279 | A | G | 10 | a0001c0001t0002g0002 a0001c0001t0002g0164 a0001c0003t0002g0128 others(7): Show |
10 | HG01106.hp1 HG02280.hp2 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.566-144463A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17543279 | |||||||
| chrX:17543356 | A | G | 2 | a0002c0002t0001g0020 a0002c0002t0001g0033 |
2 | HG00280.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.566-144386A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17543356 | |||||||
| chrX:17543791 | G | A | 1 | a0001c0001t0010g0059 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.566-143951G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17543791 | |||||||
| chrX:17543832 | C | T | 1 | a0002c0002t0001g0033 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.566-143910C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17543832 | |||||||
| chrX:17543877 | G | T | 2 | a0003c0006t0001g0157 a0009c0016t0002g0119 |
2 | HG01106.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.566-143865G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17543877 | |||||||
| chrX:17544634 | T | C | 2 | a0001c0001t0002g0002 a0001c0001t0002g0164 |
2 | HG02293.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.566-143108T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17544634 | |||||||
| chrX:17545297 | T | C | 6 | a0001c0003t0002g0128 a0001c0003t0002g0142 a0001c0003t0002g0155 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-142445T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17545297 | |||||||
| chrX:17545311 | G | A | 8 | a0001c0001t0001g0127 a0001c0001t0002g0106 a0001c0001t0002g0107 others(5): Show |
8 | HG01071.hp2 HG02055.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.566-142431G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17545311 | |||||||
| chrX:17545374 | G | A | 10 | a0001c0001t0002g0002 a0001c0001t0002g0164 a0001c0003t0002g0128 others(7): Show |
10 | HG01106.hp1 HG02280.hp2 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.566-142368G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17545374 | |||||||
| chrX:17545453 | G | A | 2 | a0001c0001t0001g0050 a0002c0002t0001g0156 |
2 | NA18974.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.566-142289G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17545453 | |||||||
| chrX:17545496 | A | G | 8 | a0001c0001t0002g0002 a0001c0001t0002g0164 a0001c0003t0002g0128 others(5): Show |
8 | HG02280.hp2 HG02293.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.566-142246A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17545496 | |||||||
| chrX:17545513 | T | A | 2 | a0003c0006t0001g0157 a0009c0016t0002g0119 |
2 | HG01106.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.566-142229T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17545513 | |||||||
| chrX:17545627 | T | C | 2 | a0001c0001t0002g0002 a0001c0001t0002g0164 |
2 | HG02293.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.566-142115T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17545627 | |||||||
| chrX:17545646 | G | A | 2 | a0003c0006t0001g0157 a0009c0016t0002g0119 |
2 | HG01106.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.566-142096G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17545646 | |||||||
| chrX:17545881 | A | G | 1 | a0001c0001t0001g0050 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.566-141861A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17545881 | |||||||
| chrX:17545915 | C | A | 1 | a0001c0001t0001g0145 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.566-141827C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17545915 | |||||||
| chrX:17546126 | G | C | 6 | a0001c0003t0002g0128 a0001c0003t0002g0142 a0001c0003t0002g0155 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-141616G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17546126 | |||||||
| chrX:17546207 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.566-141535C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17546207 | |||||||
| chrX:17546308 | G | A | 2 | a0002c0002t0001g0016 a0002c0002t0001g0063 |
2 | HG03492.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.566-141434G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17546308 | |||||||
| chrX:17546346 | G | A | 1 | a0002c0002t0001g0006 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.566-141396G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17546346 | |||||||
| chrX:17546382 | A | T | 2 | a0002c0002t0001g0077 a0002c0002t0001g0079 |
2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.566-141360A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17546382 | |||||||
| chrX:17546594 | A | T | 8 | a0001c0001t0002g0002 a0001c0001t0002g0164 a0001c0003t0002g0128 others(5): Show |
8 | HG02280.hp2 HG02293.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.566-141148A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17546594 | |||||||
| chrX:17546690 | G | A | 1 | a0001c0001t0012g0154 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.566-141052G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17546690 | |||||||
| chrX:17546787 | G | A | 1 | a0001c0001t0001g0029 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.566-140955G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17546787 | |||||||
| chrX:17546985 | T | G | 1 | a0001c0001t0001g0029 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.566-140757T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17546985 | |||||||
| chrX:17547119 | A | G | 8 | a0001c0001t0002g0002 a0001c0001t0002g0164 a0001c0003t0002g0128 others(5): Show |
8 | HG02280.hp2 HG02293.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.566-140623A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17547119 | |||||||
| chrX:17547276 | A | G | 1 | a0002c0015t0001g0039 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.566-140466A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17547276 | |||||||
| chrX:17547821 | C | T | 2 | a0001c0001t0001g0137 a0005c0005t0003g0117 |
2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.566-139921C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17547821 | |||||||
| chrX:17547856 | T | C | 3 | a0003c0006t0001g0157 a0006c0008t0001g0114 a0009c0016t0002g0119 |
3 | HG01106.hp1 HG02630.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.566-139886T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17547856 | |||||||
| chrX:17547878 | C | T | 2 | a0001c0001t0002g0002 a0001c0001t0002g0164 |
2 | HG02293.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.566-139864C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17547878 | |||||||
| chrX:17548055 | A | G | 1 | a0002c0002t0001g0030 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.566-139687A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17548055 | |||||||
| chrX:17548160 | C | T | 7 | a0001c0001t0002g0002 a0001c0001t0002g0164 a0001c0003t0002g0128 others(4): Show |
7 | HG02280.hp2 HG02293.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.566-139582C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17548160 | |||||||
| chrX:17548586 | G | A | 5 | a0001c0003t0002g0128 a0001c0003t0002g0142 a0001c0003t0002g0155 others(2): Show |
5 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-139156G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17548586 | |||||||
| chrX:17548837 | G | A | 1 | a0002c0015t0001g0039 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.566-138905G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17548837 | |||||||
| chrX:17548859 | C | A | 17 | a0001c0001t0001g0021 a0001c0001t0001g0048 a0001c0001t0001g0057 others(14): Show |
17 | HG00408.hp1 HG00609.hp1 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.566-138883C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17548859 | |||||||
| chrX:17549134 | T | TA | 33 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0001c0001t0001g0070 others(30): Show |
33 | HG01071.hp2 HG01074.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.566-138592dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17549134 | ||||||
| chrX:17549134 | TA | T | 6 | a0001c0001t0001g0151 a0001c0001t0002g0002 a0001c0001t0004g0071 others(3): Show |
6 | HG00408.hp1 HG01515.hp1 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.566-138592delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17549134 | ||||||
| chrX:17549210 | TGCCAGGC others(3): Show |
T | 44 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0049 others(41): Show |
44 | HG00280.hp1 HG00639.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.566-138525_566-138 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17549210 | ||||||
| chrX:17549214 | A | AG | 119 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0021 others(116): Show |
119 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.566-138526dupG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17549214 | ||||||
| chrX:17549219 | A | AG | 120 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0021 others(117): Show |
120 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.566-138521dupG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17549219 | ||||||
| chrX:17549484 | T | C | 28 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0137 others(25): Show |
28 | HG00408.hp2 HG01109.hp1 HG01258.hp1 others(25): Show |
intron_variant | MODIFIER | c.566-138258T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17549484 | |||||||
| chrX:17549515 | G | A | 3 | a0001c0001t0001g0137 a0001c0001t0002g0002 a0005c0005t0003g0117 |
3 | HG02293.hp2 HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.566-138227G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17549515 | |||||||
| chrX:17549577 | G | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0051 others(1): Show |
4 | HG02071.hp1 NA18961.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-138165G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17549577 | |||||||
| chrX:17549609 | G | A | 2 | a0001c0001t0002g0100 a0001c0001t0002g0143 |
2 | HG01243.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.566-138133G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17549609 | |||||||
| chrX:17549936 | C | T | 85 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0029 others(82): Show |
85 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.566-137806C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17549936 | |||||||
| chrX:17550177 | G | A | 12 | a0001c0001t0001g0127 a0001c0001t0001g0137 a0001c0001t0002g0002 others(9): Show |
12 | HG01071.hp2 HG02055.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.566-137565G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17550177 | |||||||
| chrX:17550288 | A | G | 16 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0001c0001t0001g0094 others(13): Show |
16 | HG01106.hp1 HG01109.hp1 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.566-137454A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17550288 | |||||||
| chrX:17550395 | A | T | 85 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0029 others(82): Show |
85 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.566-137347A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17550395 | |||||||
| chrX:17550531 | G | C | 3 | a0002c0002t0001g0062 a0002c0002t0001g0077 a0002c0002t0001g0131 |
3 | HG02602.hp1 HG03654.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.566-137211G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17550531 | |||||||
| chrX:17550897 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.566-136845C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17550897 | |||||||
| chrX:17551378 | T | G | 5 | a0001c0001t0002g0086 a0001c0001t0005g0104 a0001c0001t0005g0111 others(2): Show |
5 | HG02622.hp2 HG02922.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-136364T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17551378 | |||||||
| chrX:17551763 | C | T | 1 | a0010c0010t0003g0158 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.566-135979C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17551763 | |||||||
| chrX:17551821 | C | G | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.566-135921C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17551821 | |||||||
| chrX:17552008 | G | A | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.566-135734G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17552008 | |||||||
| chrX:17552031 | GA | G | 46 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0049 others(43): Show |
46 | HG00280.hp1 HG00639.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.566-135710delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17552031 | |||||||
| chrX:17552032 | A | G | 44 | a0001c0001t0001g0021 a0001c0001t0001g0048 a0001c0001t0001g0057 others(41): Show |
44 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.566-135710A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17552032 | |||||||
| chrX:17552035 | A | G | 46 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0049 others(43): Show |
46 | HG00280.hp1 HG00639.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.566-135707A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17552035 | |||||||
| chrX:17552063 | G | C | 6 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0003c0006t0001g0157 others(3): Show |
6 | HG01106.hp1 HG02145.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-135679G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17552063 | |||||||
| chrX:17552079 | G | C | 1 | a0002c0002t0001g0028 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.566-135663G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17552079 | |||||||
| chrX:17552261 | G | A | 73 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0029 others(70): Show |
73 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.566-135481G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17552261 | |||||||
| chrX:17552710 | G | A | 24 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0001c0001t0001g0094 others(21): Show |
24 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.566-135032G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17552710 | |||||||
| chrX:17552722 | G | A | 14 | a0001c0001t0001g0137 a0001c0001t0002g0002 a0001c0001t0002g0100 others(11): Show |
14 | HG01243.hp1 HG01975.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.566-135020G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17552722 | |||||||
| chrX:17552769 | A | G | 1 | a0001c0001t0001g0049 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.566-134973A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17552769 | |||||||
| chrX:17552795 | G | A | 86 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0029 others(83): Show |
86 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.566-134947G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17552795 | |||||||
| chrX:17552864 | T | G | 80 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0029 others(77): Show |
80 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.566-134878T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17552864 | |||||||
| chrX:17553002 | C | A | 1 | a0002c0002t0001g0013 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.566-134740C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17553002 | |||||||
| chrX:17553036 | T | A | 90 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0029 others(87): Show |
90 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.566-134706T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17553036 | |||||||
| chrX:17553072 | G | A | 1 | a0006c0007t0002g0118 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.566-134670G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17553072 | |||||||
| chrX:17553118 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.566-134624C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17553118 | |||||||
| chrX:17553174 | C | T | 2 | a0001c0003t0002g0142 a0006c0007t0002g0115 |
2 | HG02572.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.566-134568C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17553174 | |||||||
| chrX:17553259 | AAG | A | 7 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0001c0001t0002g0044 others(4): Show |
7 | HG01106.hp1 HG01109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.566-134481_566-134 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17553259 | ||||||
| chrX:17553320 | T | C | 1 | a0002c0002t0009g0015 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.566-134422T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17553320 | |||||||
| chrX:17553759 | C | T | 6 | a0001c0001t0002g0086 a0001c0001t0005g0104 a0001c0001t0005g0111 others(3): Show |
6 | HG02622.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.566-133983C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17553759 | |||||||
| chrX:17553795 | C | G | 25 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0001c0001t0001g0094 others(22): Show |
25 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.566-133947C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17553795 | |||||||
| chrX:17553957 | G | C | 91 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0029 others(88): Show |
91 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.566-133785G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17553957 | |||||||
| chrX:17554269 | G | A | 6 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0003c0006t0001g0157 others(3): Show |
6 | HG01106.hp1 HG02145.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-133473G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17554269 | |||||||
| chrX:17554405 | G | A | 11 | a0001c0001t0001g0127 a0001c0001t0001g0137 a0001c0001t0002g0002 others(8): Show |
11 | HG01928.hp1 HG01952.hp1 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.566-133337G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17554405 | |||||||
| chrX:17554407 | AG | A | 11 | a0001c0001t0001g0127 a0001c0001t0001g0137 a0001c0001t0002g0002 others(8): Show |
11 | HG01928.hp1 HG01952.hp1 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.566-133329delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17554407 | ||||||
| chrX:17554843 | C | CT | 25 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0001c0001t0001g0094 others(22): Show |
25 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.566-132890dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17554843 | ||||||
| chrX:17555118 | C | T | 2 | a0002c0002t0001g0007 a0002c0002t0001g0040 |
2 | HG01167.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.566-132624C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17555118 | |||||||
| chrX:17555228 | AT | A | 12 | a0001c0001t0001g0083 a0001c0001t0002g0096 a0001c0001t0002g0106 others(9): Show |
12 | HG01071.hp2 HG02055.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.566-132498delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17555228 | ||||||
| chrX:17555306 | G | A | 25 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0001c0001t0001g0094 others(22): Show |
25 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.566-132436G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17555306 | |||||||
| chrX:17555308 | G | A | 4 | a0001c0001t0012g0154 a0001c0001t0013g0045 a0005c0005t0008g0087 others(1): Show |
4 | HG01975.hp1 HG02257.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-132434G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17555308 | |||||||
| chrX:17555328 | T | C | 116 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0029 others(113): Show |
116 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.566-132414T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17555328 | |||||||
| chrX:17555638 | T | C | 1 | a0009c0016t0002g0119 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.566-132104T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17555638 | |||||||
| chrX:17555782 | C | T | 80 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0029 others(77): Show |
80 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.566-131960C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17555782 | |||||||
| chrX:17555961 | A | G | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.566-131781A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17555961 | |||||||
| chrX:17556162 | C | T | 18 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0001c0001t0001g0094 others(15): Show |
18 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.566-131580C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17556162 | |||||||
| chrX:17556470 | TA | T | 34 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0001c0001t0001g0094 others(31): Show |
34 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.566-131269delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17556470 | ||||||
| chrX:17556650 | G | C | 35 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0001c0001t0001g0094 others(32): Show |
35 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.566-131092G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17556650 | |||||||
| chrX:17556740 | A | G | 5 | a0001c0001t0002g0086 a0001c0001t0005g0104 a0001c0001t0005g0111 others(2): Show |
5 | HG02622.hp2 HG02922.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-131002A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17556740 | |||||||
| chrX:17556772 | G | A | 163 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0021 others(160): Show |
163 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.566-130970G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17556772 | |||||||
| chrX:17556973 | G | GAT | 37 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0001c0001t0001g0094 others(34): Show |
37 | HG00408.hp2 HG01071.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.566-130756_566-130 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17556973 | ||||||
| chrX:17557109 | T | TTG | 21 | a0001c0001t0001g0026 a0001c0001t0001g0035 a0001c0001t0002g0121 others(18): Show |
21 | HG00280.hp1 HG00408.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.566-130591_566-130 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17557109 | ||||||
| chrX:17557109 | T | TTGTG | 3 | a0001c0001t0004g0163 a0002c0002t0001g0018 a0002c0002t0001g0082 |
3 | HG01074.hp1 HG01261.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.566-130593_566-130 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17557109 | ||||||
| chrX:17557109 | T | TTGTGTG | 6 | a0001c0001t0002g0044 a0002c0002t0001g0024 a0002c0002t0001g0088 others(3): Show |
6 | HG01109.hp1 HG02922.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-130595_566-130 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17557109 | ||||||
| chrX:17557109 | TTG | T | 10 | a0001c0001t0001g0008 a0001c0001t0001g0041 a0001c0001t0001g0068 others(7): Show |
10 | HG01358.hp1 HG01515.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.566-130591_566-130 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17557109 | ||||||
| chrX:17557109 | TTGTG | T | 6 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0003t0002g0128 others(3): Show |
6 | HG01106.hp1 HG01256.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.566-130593_566-130 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17557109 | ||||||
| chrX:17557109 | TTGTGTG | T | 20 | a0001c0001t0002g0086 a0001c0001t0002g0096 a0001c0001t0002g0106 others(17): Show |
20 | HG01071.hp2 HG01258.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.566-130595_566-130 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17557109 | ||||||
| chrX:17557109 | TTGTGTGT others(1): Show |
T | 4 | a0001c0001t0002g0116 a0001c0001t0002g0120 a0001c0001t0007g0122 others(1): Show |
4 | HG02615.hp2 HG02723.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-130597_566-130 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17557109 | ||||||
| chrX:17557109 | TTGTGTGT others(3): Show |
T | 6 | a0001c0001t0002g0100 a0001c0001t0002g0146 a0001c0001t0012g0154 others(3): Show |
6 | HG01243.hp1 HG01975.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.566-130599_566-130 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17557109 | ||||||
| chrX:17557109 | TTGTGTGT others(7): Show |
T | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.566-130603_566-130 others(20): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17557109 | ||||||
| chrX:17557109 | TTGTGTGT others(13): Show |
T | 1 | a0001c0001t0001g0137 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.566-130609_566-130 others(26): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17557109 | ||||||
| chrX:17557196 | A | C | 108 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0041 others(105): Show |
108 | HG00280.hp1 HG00408.hp2 HG00639.hp2 others(105): Show |
intron_variant | MODIFIER | c.566-130546A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17557196 | |||||||
| chrX:17557326 | G | GAT | 11 | a0001c0001t0002g0086 a0001c0001t0002g0121 a0001c0001t0005g0104 others(8): Show |
11 | HG00738.hp1 HG02280.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.566-130395_566-130 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17557326 | ||||||
| chrX:17557326 | G | GATAT | 9 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0001c0001t0001g0094 others(6): Show |
9 | HG00639.hp1 HG01106.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.566-130397_566-130 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17557326 | ||||||
| chrX:17557326 | G | GATATAT | 14 | a0001c0001t0002g0096 a0001c0001t0002g0106 a0001c0001t0002g0107 others(11): Show |
14 | HG00408.hp2 HG01071.hp2 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.566-130399_566-130 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17557326 | ||||||
| chrX:17557326 | G | GATATATA others(1): Show |
5 | a0001c0001t0007g0125 a0002c0002t0001g0072 a0003c0006t0002g0161 others(2): Show |
5 | HG01952.hp1 HG02055.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-130401_566-130 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17557326 | ||||||
| chrX:17557326 | G | GATATATA others(3): Show |
2 | a0001c0001t0001g0127 a0003c0006t0001g0162 |
2 | HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.566-130403_566-130 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17557326 | ||||||
| chrX:17557326 | GAT | G | 5 | a0001c0001t0001g0137 a0001c0001t0002g0002 a0001c0001t0002g0100 others(2): Show |
5 | HG01243.hp1 HG02293.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.566-130395_566-130 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17557326 | ||||||
| chrX:17557349 | C | G | 35 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0001c0001t0001g0094 others(32): Show |
35 | HG00408.hp2 HG01071.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.566-130393C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17557349 | |||||||
| chrX:17557711 | T | TG | 49 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0001c0001t0001g0094 others(46): Show |
49 | HG00408.hp2 HG01071.hp2 HG01106.hp1 others(46): Show |
intron_variant | MODIFIER | c.566-130027dupG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17557711 | ||||||
| chrX:17557774 | G | C | 12 | a0001c0001t0001g0127 a0001c0001t0002g0003 a0002c0002t0001g0013 others(9): Show |
12 | HG00408.hp2 HG01928.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.566-129968G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17557774 | |||||||
| chrX:17558106 | T | C | 12 | a0001c0001t0001g0127 a0001c0001t0002g0003 a0002c0002t0001g0013 others(9): Show |
12 | HG00408.hp2 HG01928.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.566-129636T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17558106 | |||||||
| chrX:17558469 | C | T | 25 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0001c0001t0001g0094 others(22): Show |
25 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.566-129273C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17558469 | |||||||
| chrX:17558619 | G | C | 56 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0001c0001t0001g0094 others(53): Show |
56 | HG00408.hp2 HG01071.hp2 HG01106.hp1 others(53): Show |
intron_variant | MODIFIER | c.566-129123G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17558619 | |||||||
| chrX:17558730 | A | G | 29 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0001c0001t0001g0094 others(26): Show |
29 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.566-129012A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17558730 | |||||||
| chrX:17558780 | T | C | 3 | a0002c0002t0001g0004 a0002c0002t0001g0053 a0002c0002t0001g0080 |
3 | NA18953.hp1 NA18966.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.566-128962T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17558780 | |||||||
| chrX:17559799 | C | T | 1 | a0001c0001t0002g0107 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.566-127943C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17559799 | |||||||
| chrX:17559800 | C | A | 73 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0029 others(70): Show |
73 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.566-127942C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17559800 | |||||||
| chrX:17559845 | T | C | 6 | a0001c0001t0002g0086 a0001c0001t0005g0104 a0001c0001t0005g0111 others(3): Show |
6 | HG02622.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.566-127897T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17559845 | |||||||
| chrX:17559926 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.566-127816C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17559926 | |||||||
| chrX:17559937 | G | A | 1 | a0001c0001t0002g0044 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.566-127805G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17559937 | |||||||
| chrX:17560716 | T | C | 6 | a0001c0001t0002g0086 a0001c0001t0005g0104 a0001c0001t0005g0111 others(3): Show |
6 | HG02622.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.566-127026T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17560716 | |||||||
| chrX:17561003 | A | C | 2 | a0001c0001t0001g0026 a0012c0013t0001g0038 |
2 | NA18747.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.566-126739A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17561003 | |||||||
| chrX:17561189 | C | T | 9 | a0001c0001t0002g0096 a0001c0001t0002g0106 a0001c0001t0002g0107 others(6): Show |
9 | HG01071.hp2 HG02055.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.566-126553C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17561189 | |||||||
| chrX:17561381 | A | G | 11 | a0001c0001t0001g0127 a0001c0001t0002g0003 a0002c0002t0001g0013 others(8): Show |
11 | HG00408.hp2 HG01928.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.566-126361A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17561381 | |||||||
| chrX:17561395 | G | A | 1 | a0002c0002t0001g0084 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.566-126347G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17561395 | |||||||
| chrX:17561450 | G | C | 49 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0001c0001t0001g0094 others(46): Show |
49 | HG00408.hp2 HG01071.hp2 HG01106.hp1 others(46): Show |
intron_variant | MODIFIER | c.566-126292G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17561450 | |||||||
| chrX:17561468 | G | T | 15 | a0001c0001t0002g0096 a0001c0001t0002g0106 a0001c0001t0002g0107 others(12): Show |
15 | HG01071.hp2 HG01258.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.566-126274G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17561468 | |||||||
| chrX:17561557 | T | TGC | 3 | a0002c0002t0001g0046 a0002c0002t0001g0054 a0002c0002t0001g0130 |
3 | HG00140.hp1 HG00738.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.566-126168_566-126 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561557 | ||||||
| chrX:17561557 | TGC | T | 5 | a0001c0001t0001g0041 a0001c0001t0002g0044 a0003c0006t0002g0161 others(2): Show |
5 | HG01109.hp1 HG02451.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-126168_566-126 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561557 | ||||||
| chrX:17561557 | TGCGC | T | 4 | a0001c0001t0002g0003 a0001c0001t0002g0107 a0001c0001t0002g0110 others(1): Show |
4 | HG02055.hp1 HG02809.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-126170_566-126 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561557 | ||||||
| chrX:17561557 | TGCGCGC | T | 5 | a0001c0001t0002g0106 a0001c0001t0007g0125 a0005c0005t0003g0136 others(2): Show |
5 | HG01071.hp2 HG02258.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-126172_566-126 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561557 | ||||||
| chrX:17561564 | GCGCGCGC others(5): Show |
G | 2 | a0001c0003t0002g0142 a0006c0007t0002g0115 |
2 | HG02572.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.566-126176_566-126 others(18): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561564 | ||||||
| chrX:17561564 | GCGCGCGC others(7): Show |
G | 4 | a0001c0003t0002g0014 a0001c0003t0002g0128 a0001c0003t0002g0155 others(1): Show |
4 | HG01258.hp1 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-126176_566-126 others(20): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561564 | ||||||
| chrX:17561564 | GCGCGCGC others(9): Show |
G | 2 | a0001c0001t0001g0151 a0002c0002t0001g0060 |
2 | HG00408.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.566-126176_566-126 others(22): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561564 | ||||||
| chrX:17561568 | G | A | 1 | a0001c0001t0002g0096 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.566-126174G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17561568 | |||||||
| chrX:17561568 | G | GCACA | 3 | a0001c0001t0002g0086 a0001c0001t0005g0104 a0001c0003t0002g0102 |
3 | HG02922.hp2 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.566-126173_566-126 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561568 | ||||||
| chrX:17561568 | G | GCACACAC others(1): Show |
2 | a0001c0001t0005g0111 a0003c0006t0005g0159 |
2 | HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.566-126173_566-126 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561568 | ||||||
| chrX:17561568 | GCGCGCGC others(5): Show |
G | 1 | a0003c0006t0001g0162 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.566-126172_566-126 others(18): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561568 | ||||||
| chrX:17561570 | G | A | 11 | a0001c0001t0001g0127 a0001c0001t0002g0086 a0001c0001t0002g0096 others(8): Show |
11 | HG01928.hp1 HG01952.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.566-126172G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17561570 | |||||||
| chrX:17561570 | G | GCA | 2 | a0001c0001t0012g0154 a0005c0005t0008g0087 |
2 | HG01975.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.566-126171_566-126 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561570 | ||||||
| chrX:17561570 | G | GCACACA | 3 | a0003c0009t0002g0160 a0005c0005t0003g0117 a0006c0008t0002g0113 |
3 | HG02145.hp1 HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.566-126171_566-126 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561570 | ||||||
| chrX:17561570 | G | GCACACAC others(1): Show |
2 | a0001c0001t0013g0045 a0008c0011t0002g0147 |
2 | HG02257.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.566-126171_566-126 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561570 | ||||||
| chrX:17561570 | G | GCACACAC others(3): Show |
3 | a0001c0001t0002g0143 a0001c0001t0002g0146 a0003c0006t0001g0157 |
3 | HG01106.hp1 HG02630.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.566-126171_566-126 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561570 | ||||||
| chrX:17561570 | G | GCACACAC others(5): Show |
1 | a0001c0001t0002g0100 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.566-126171_566-126 others(18): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561570 | ||||||
| chrX:17561572 | G | A | 28 | a0001c0001t0001g0127 a0001c0001t0002g0086 a0001c0001t0002g0096 others(25): Show |
28 | HG01106.hp1 HG01243.hp1 HG01928.hp1 others(25): Show |
intron_variant | MODIFIER | c.566-126170G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17561572 | |||||||
| chrX:17561572 | G | GCACA | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0002g0120 others(1): Show |
4 | HG03041.hp1 HG03098.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-126169_566-126 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561572 | ||||||
| chrX:17561572 | G | GCACACA | 2 | a0001c0001t0001g0068 a0001c0001t0002g0116 |
2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.566-126169_566-126 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561572 | ||||||
| chrX:17561572 | G | GCACACAC others(3): Show |
1 | a0010c0010t0003g0158 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.566-126169_566-126 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561572 | ||||||
| chrX:17561574 | G | A | 46 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0001c0001t0001g0094 others(43): Show |
46 | HG00280.hp1 HG01071.hp2 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.566-126168G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17561574 | |||||||
| chrX:17561574 | G | GCA | 8 | a0001c0001t0001g0011 a0001c0001t0001g0051 a0001c0001t0001g0061 others(5): Show |
8 | HG02071.hp1 HG02293.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.566-126123_566-126 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | ||||||
| chrX:17561574 | G | GCACA | 4 | a0001c0001t0002g0002 a0002c0002t0001g0022 a0002c0002t0001g0052 others(1): Show |
4 | HG02027.hp1 HG02293.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-126125_566-126 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | ||||||
| chrX:17561574 | G | GCACACA | 8 | a0001c0001t0001g0070 a0002c0002t0001g0010 a0002c0002t0001g0013 others(5): Show |
8 | HG00408.hp2 HG02698.hp1 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.566-126127_566-126 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | ||||||
| chrX:17561574 | G | GCACACAC others(1): Show |
6 | a0002c0002t0001g0019 a0002c0002t0001g0024 a0002c0002t0001g0025 others(3): Show |
6 | HG01975.hp2 HG02735.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-126129_566-126 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | ||||||
| chrX:17561574 | G | GCACACAC others(3): Show |
5 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0002c0002t0001g0016 others(2): Show |
5 | HG02129.hp1 NA18747.hp1 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-126131_566-126 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | ||||||
| chrX:17561574 | G | GCACACAC others(5): Show |
3 | a0001c0001t0002g0093 a0001c0001t0002g0126 a0002c0002t0001g0108 |
3 | HG01069.hp1 HG01071.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.566-126133_566-126 others(18): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | ||||||
| chrX:17561574 | G | GCACACAC others(7): Show |
1 | a0002c0002t0001g0064 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.566-126135_566-126 others(20): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | ||||||
| chrX:17561574 | G | GCACACAC others(11): Show |
1 | a0002c0002t0001g0148 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.566-126139_566-126 others(24): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | ||||||
| chrX:17561574 | G | GCGCACAC others(1): Show |
3 | a0001c0001t0001g0145 a0001c0001t0002g0121 a0002c0002t0001g0091 |
3 | HG00639.hp2 HG02280.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.566-126167_566-126 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | ||||||
| chrX:17561574 | G | GCGCACAC others(3): Show |
2 | a0002c0002t0001g0023 a0002c0002t0001g0141 |
2 | HG02083.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.566-126167_566-126 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | ||||||
| chrX:17561574 | G | GCGCACAC others(5): Show |
1 | a0002c0002t0001g0079 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.566-126167_566-126 others(18): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | ||||||
| chrX:17561574 | G | GCGCACAC others(7): Show |
1 | a0002c0002t0001g0080 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.566-126167_566-126 others(20): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | ||||||
| chrX:17561574 | G | GCGCGCAC others(3): Show |
2 | a0002c0002t0001g0053 a0002c0002t0001g0067 |
2 | HG02015.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.566-126167_566-126 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | ||||||
| chrX:17561574 | G | GCGCGCAC others(5): Show |
2 | a0002c0002t0001g0004 a0002c0002t0001g0034 |
2 | HG04115.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.566-126167_566-126 others(18): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | ||||||
| chrX:17561574 | G | GCGCGCAC others(7): Show |
1 | a0001c0001t0001g0049 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.566-126167_566-126 others(20): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | ||||||
| chrX:17561574 | GCA | G | 15 | a0001c0001t0001g0035 a0001c0001t0001g0050 a0001c0001t0001g0056 others(12): Show |
15 | HG00639.hp1 HG01074.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.566-126123_566-126 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | ||||||
| chrX:17561574 | GCACA | G | 10 | a0001c0001t0001g0021 a0001c0001t0001g0129 a0001c0001t0001g0140 others(7): Show |
10 | HG00642.hp1 HG00673.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.566-126125_566-126 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | ||||||
| chrX:17561574 | GCACACA | G | 10 | a0001c0001t0001g0057 a0001c0001t0001g0066 a0001c0001t0001g0124 others(7): Show |
10 | HG00609.hp1 HG01167.hp1 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.566-126127_566-126 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | ||||||
| chrX:17561574 | GCACACAC others(1): Show |
G | 2 | a0001c0001t0001g0048 a0001c0001t0010g0059 |
2 | NA18965.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.566-126129_566-126 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | ||||||
| chrX:17561574 | GCACACAC others(3): Show |
G | 2 | a0001c0001t0011g0081 a0002c0002t0001g0005 |
2 | HG00621.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.566-126131_566-126 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | ||||||
| chrX:17561574 | GCACACAC others(9): Show |
G | 2 | a0001c0001t0006g0074 a0001c0001t0006g0103 |
2 | NA18955.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.566-126137_566-126 others(22): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17561574 | ||||||
| chrX:17561576 | A | G | 6 | a0001c0001t0001g0083 a0002c0002t0001g0009 a0002c0002t0001g0027 others(3): Show |
6 | HG00140.hp1 HG01192.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-126166A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17561576 | |||||||
| chrX:17561578 | A | G | 6 | a0001c0001t0004g0163 a0002c0002t0001g0018 a0002c0002t0001g0027 others(3): Show |
6 | HG00140.hp1 HG01074.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-126164A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17561578 | |||||||
| chrX:17561580 | A | G | 6 | a0001c0001t0001g0129 a0001c0001t0001g0140 a0001c0001t0004g0058 others(3): Show |
6 | HG00642.hp1 HG01099.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-126162A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17561580 | |||||||
| chrX:17561582 | A | G | 1 | a0002c0015t0001g0039 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.566-126160A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17561582 | |||||||
| chrX:17561584 | A | G | 1 | a0001c0001t0001g0048 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.566-126158A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17561584 | |||||||
| chrX:17561801 | A | C | 1 | a0002c0002t0001g0018 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.566-125941A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17561801 | |||||||
| chrX:17562070 | T | C | 12 | a0001c0001t0001g0127 a0001c0001t0002g0003 a0002c0002t0001g0013 others(9): Show |
12 | HG00408.hp2 HG01928.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.566-125672T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17562070 | |||||||
| chrX:17562530 | T | C | 1 | a0005c0005t0008g0087 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.566-125212T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17562530 | |||||||
| chrX:17562559 | C | A | 1 | a0001c0001t0001g0050 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.566-125183C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17562559 | |||||||
| chrX:17562880 | A | AT | 157 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0021 others(154): Show |
157 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.566-124860dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17562880 | ||||||
| chrX:17562914 | G | A | 6 | a0001c0001t0002g0086 a0001c0001t0005g0104 a0001c0001t0005g0111 others(3): Show |
6 | HG02622.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.566-124828G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17562914 | |||||||
| chrX:17563124 | A | G | 12 | a0001c0001t0001g0127 a0001c0001t0002g0003 a0002c0002t0001g0013 others(9): Show |
12 | HG00408.hp2 HG01928.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.566-124618A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17563124 | |||||||
| chrX:17563143 | C | T | 1 | a0002c0002t0001g0023 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.566-124599C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17563143 | |||||||
| chrX:17563682 | C | T | 73 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0029 others(70): Show |
73 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.566-124060C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17563682 | |||||||
| chrX:17563683 | G | C | 15 | a0001c0001t0002g0096 a0001c0001t0002g0106 a0001c0001t0002g0107 others(12): Show |
15 | HG01071.hp2 HG01258.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.566-124059G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17563683 | |||||||
| chrX:17563782 | C | T | 10 | a0001c0001t0001g0127 a0001c0001t0002g0003 a0002c0002t0001g0013 others(7): Show |
10 | HG00408.hp2 HG01952.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.566-123960C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17563782 | |||||||
| chrX:17564331 | A | G | 1 | a0002c0002t0001g0078 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.566-123411A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17564331 | |||||||
| chrX:17564577 | A | G | 21 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0127 others(18): Show |
21 | HG01071.hp2 HG01258.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.566-123165A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17564577 | |||||||
| chrX:17564622 | C | G | 1 | a0002c0002t0001g0156 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.566-123120C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17564622 | |||||||
| chrX:17564969 | A | AT | 5 | a0001c0001t0001g0127 a0002c0002t0001g0072 a0002c0002t0001g0082 others(2): Show |
5 | HG01952.hp1 HG02922.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-122764dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17564969 | ||||||
| chrX:17564975 | TTTTA | T | 5 | a0001c0003t0002g0014 a0001c0003t0002g0128 a0001c0003t0002g0142 others(2): Show |
5 | HG01258.hp1 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-122759_566-122 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17564975 | ||||||
| chrX:17564976 | TTTA | T | 13 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0001c0001t0002g0096 others(10): Show |
13 | HG01106.hp1 HG02055.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.566-122763_566-122 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17564976 | ||||||
| chrX:17564977 | TTA | T | 5 | a0001c0001t0002g0044 a0001c0001t0007g0125 a0005c0005t0003g0136 others(2): Show |
5 | HG01071.hp2 HG01109.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-122763_566-122 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17564977 | ||||||
| chrX:17564978 | TA | T | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.566-122763delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17564978 | |||||||
| chrX:17564979 | A | T | 9 | a0001c0001t0001g0127 a0001c0001t0002g0003 a0002c0002t0001g0072 others(6): Show |
9 | HG01952.hp1 HG02809.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.566-122763A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17564979 | |||||||
| chrX:17564983 | A | T | 34 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0001c0001t0001g0094 others(31): Show |
34 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.566-122759A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17564983 | |||||||
| chrX:17565051 | CTGACTTT others(1): Show |
C | 9 | a0001c0001t0001g0127 a0001c0001t0002g0003 a0002c0002t0001g0072 others(6): Show |
9 | HG01952.hp1 HG02809.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.566-122684_566-122 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17565051 | ||||||
| chrX:17565139 | G | A | 1 | a0002c0002t0001g0033 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.566-122603G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17565139 | |||||||
| chrX:17565320 | C | T | 2 | a0001c0001t0001g0083 a0001c0001t0001g0144 |
2 | NA18943.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.566-122422C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17565320 | |||||||
| chrX:17565399 | A | C | 1 | a0002c0002t0001g0075 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.566-122343A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17565399 | |||||||
| chrX:17565983 | C | CT | 6 | a0001c0001t0001g0035 a0001c0001t0002g0044 a0001c0001t0002g0100 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-121743dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17565983 | ||||||
| chrX:17565983 | CT | C | 19 | a0001c0001t0001g0011 a0001c0001t0001g0051 a0001c0001t0001g0127 others(16): Show |
19 | HG01952.hp1 HG02071.hp1 HG02622.hp2 others(16): Show |
intron_variant | MODIFIER | c.566-121743delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17565983 | ||||||
| chrX:17566068 | A | C | 9 | a0001c0001t0001g0127 a0001c0001t0002g0003 a0002c0002t0001g0072 others(6): Show |
9 | HG01952.hp1 HG02809.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.566-121674A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17566068 | |||||||
| chrX:17566241 | C | T | 1 | a0002c0002t0001g0130 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.566-121501C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17566241 | |||||||
| chrX:17566258 | C | T | 9 | a0001c0001t0001g0127 a0001c0001t0002g0003 a0002c0002t0001g0072 others(6): Show |
9 | HG01952.hp1 HG02809.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.566-121484C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17566258 | |||||||
| chrX:17566286 | G | C | 9 | a0001c0001t0001g0127 a0001c0001t0002g0003 a0002c0002t0001g0072 others(6): Show |
9 | HG01952.hp1 HG02809.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.566-121456G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17566286 | |||||||
| chrX:17566459 | G | A | 5 | a0002c0002t0001g0072 a0002c0002t0001g0082 a0004c0004t0001g0132 others(2): Show |
5 | HG01952.hp1 HG03017.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-121283G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17566459 | |||||||
| chrX:17566537 | C | T | 1 | a0002c0002t0001g0033 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.566-121205C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17566537 | |||||||
| chrX:17566544 | A | G | 9 | a0001c0001t0001g0127 a0001c0001t0002g0003 a0002c0002t0001g0072 others(6): Show |
9 | HG01952.hp1 HG02809.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.566-121198A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17566544 | |||||||
| chrX:17566600 | G | A | 81 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0029 others(78): Show |
81 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.566-121142G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17566600 | |||||||
| chrX:17566612 | G | A | 117 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0029 others(114): Show |
117 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.566-121130G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17566612 | |||||||
| chrX:17566693 | T | G | 115 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0029 others(112): Show |
115 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.566-121049T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17566693 | |||||||
| chrX:17566697 | T | G | 81 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0029 others(78): Show |
81 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.566-121045T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17566697 | |||||||
| chrX:17566754 | T | C | 1 | a0001c0001t0004g0071 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.566-120988T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17566754 | |||||||
| chrX:17566755 | G | T | 1 | a0001c0001t0004g0071 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.566-120987G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17566755 | |||||||
| chrX:17567020 | G | A | 10 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0050 others(7): Show |
10 | HG02040.hp1 NA18960.hp1 NA18962.hp1 others(7): Show |
intron_variant | MODIFIER | c.566-120722G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17567020 | |||||||
| chrX:17567782 | G | A | 6 | a0001c0003t0002g0014 a0001c0003t0002g0128 a0001c0003t0002g0142 others(3): Show |
6 | HG01258.hp1 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-119960G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17567782 | |||||||
| chrX:17567814 | G | A | 31 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0001c0001t0001g0094 others(28): Show |
31 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.566-119928G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17567814 | |||||||
| chrX:17567874 | A | G | 3 | a0001c0001t0002g0116 a0001c0001t0002g0120 a0001c0001t0007g0122 |
3 | HG02615.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.566-119868A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17567874 | |||||||
| chrX:17568227 | C | A | 115 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0029 others(112): Show |
115 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.566-119515C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17568227 | |||||||
| chrX:17568520 | C | CTT | 10 | a0001c0001t0001g0127 a0002c0002t0001g0013 a0002c0002t0001g0072 others(7): Show |
10 | HG00408.hp2 HG01952.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.566-119209_566-119 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17568520 | ||||||
| chrX:17568647 | G | GTTA | 111 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0029 others(108): Show |
111 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.566-119060_566-119 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17568647 | ||||||
| chrX:17568647 | G | GTTATTA | 24 | a0001c0001t0001g0026 a0001c0001t0001g0049 a0001c0001t0001g0124 others(21): Show |
24 | HG01943.hp1 HG01952.hp1 HG01975.hp1 others(21): Show |
intron_variant | MODIFIER | c.566-119063_566-119 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17568647 | ||||||
| chrX:17568647 | G | GTTATTAT others(2): Show |
2 | a0004c0004t0001g0149 a0011c0012t0001g0150 |
2 | NA18948.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.566-119066_566-119 others(15): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17568647 | ||||||
| chrX:17568647 | G | GTTGTTAT others(5): Show |
1 | a0001c0001t0001g0021 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.566-119093_566-119 others(18): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17568647 | ||||||
| chrX:17568647 | GTTA | G | 6 | a0001c0001t0001g0068 a0001c0001t0001g0083 a0001c0001t0002g0044 others(3): Show |
6 | HG01106.hp1 HG01109.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-119060_566-119 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17568647 | ||||||
| chrX:17568647 | GTTATTA | G | 2 | a0001c0001t0001g0041 a0005c0005t0003g0117 |
2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.566-119063_566-119 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17568647 | ||||||
| chrX:17568647 | GTTATTAT others(5): Show |
G | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.566-119069_566-119 others(18): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17568647 | ||||||
| chrX:17568973 | T | C | 1 | a0002c0002t0001g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.566-118769T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17568973 | |||||||
| chrX:17569113 | C | T | 1 | a0005c0005t0008g0097 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.566-118629C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17569113 | |||||||
| chrX:17569178 | C | A | 6 | a0001c0001t0002g0086 a0001c0001t0005g0104 a0001c0001t0005g0111 others(3): Show |
6 | HG02622.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.566-118564C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17569178 | |||||||
| chrX:17569192 | T | G | 13 | a0001c0001t0001g0137 a0001c0001t0002g0002 a0001c0001t0002g0100 others(10): Show |
13 | HG01243.hp1 HG01975.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.566-118550T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17569192 | |||||||
| chrX:17569351 | C | T | 46 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0001c0001t0001g0094 others(43): Show |
46 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.566-118391C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17569351 | |||||||
| chrX:17569359 | TAA | T | 46 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0001c0001t0001g0094 others(43): Show |
46 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.566-118380_566-118 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17569359 | ||||||
| chrX:17569386 | T | A | 13 | a0001c0001t0001g0137 a0001c0001t0002g0002 a0001c0001t0002g0100 others(10): Show |
13 | HG01243.hp1 HG01975.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.566-118356T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17569386 | |||||||
| chrX:17569521 | T | G | 1 | a0001c0001t0002g0121 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.566-118221T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17569521 | |||||||
| chrX:17569638 | A | C | 13 | a0001c0001t0001g0137 a0001c0001t0002g0002 a0001c0001t0002g0100 others(10): Show |
13 | HG01243.hp1 HG01975.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.566-118104A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17569638 | |||||||
| chrX:17569639 | G | A | 13 | a0001c0001t0001g0137 a0001c0001t0002g0002 a0001c0001t0002g0100 others(10): Show |
13 | HG01243.hp1 HG01975.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.566-118103G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17569639 | |||||||
| chrX:17569652 | G | T | 21 | a0001c0001t0001g0127 a0001c0001t0001g0137 a0001c0001t0002g0002 others(18): Show |
21 | HG01243.hp1 HG01952.hp1 HG01975.hp1 others(18): Show |
intron_variant | MODIFIER | c.566-118090G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17569652 | |||||||
| chrX:17569672 | A | C | 1 | a0005c0005t0003g0136 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.566-118070A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17569672 | |||||||
| chrX:17569730 | T | C | 13 | a0001c0001t0001g0137 a0001c0001t0002g0002 a0001c0001t0002g0100 others(10): Show |
13 | HG01243.hp1 HG01975.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.566-118012T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17569730 | |||||||
| chrX:17569939 | T | G | 9 | a0001c0001t0001g0127 a0002c0002t0001g0013 a0002c0002t0001g0072 others(6): Show |
9 | HG00408.hp2 HG01952.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.566-117803T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17569939 | |||||||
| chrX:17570148 | G | A | 1 | a0001c0003t0002g0142 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.566-117594G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17570148 | |||||||
| chrX:17570481 | G | T | 8 | a0001c0001t0001g0127 a0002c0002t0001g0072 a0002c0002t0001g0082 others(5): Show |
8 | HG01952.hp1 HG02922.hp1 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.566-117261G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17570481 | |||||||
| chrX:17570718 | C | T | 29 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0001c0001t0001g0094 others(26): Show |
29 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.566-117024C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17570718 | |||||||
| chrX:17570864 | G | A | 15 | a0001c0001t0002g0096 a0001c0001t0002g0106 a0001c0001t0002g0107 others(12): Show |
15 | HG01071.hp2 HG01258.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.566-116878G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17570864 | |||||||
| chrX:17570963 | G | A | 1 | a0002c0002t0001g0152 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.566-116779G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17570963 | |||||||
| chrX:17571052 | C | T | 116 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0029 others(113): Show |
116 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.566-116690C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17571052 | |||||||
| chrX:17571109 | G | A | 115 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0029 others(112): Show |
115 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.566-116633G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17571109 | |||||||
| chrX:17571255 | T | G | 1 | a0002c0002t0001g0017 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.566-116487T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17571255 | |||||||
| chrX:17571303 | T | C | 116 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0029 others(113): Show |
116 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.566-116439T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17571303 | |||||||
| chrX:17571397 | A | G | 125 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0029 others(122): Show |
125 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.566-116345A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17571397 | |||||||
| chrX:17571539 | A | G | 116 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0029 others(113): Show |
116 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.566-116203A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17571539 | |||||||
| chrX:17571572 | T | C | 9 | a0001c0001t0001g0127 a0002c0002t0001g0013 a0002c0002t0001g0072 others(6): Show |
9 | HG00408.hp2 HG01952.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.566-116170T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17571572 | |||||||
| chrX:17571609 | A | G | 1 | a0002c0002t0009g0015 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.566-116133A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17571609 | |||||||
| chrX:17571756 | G | A | 1 | a0002c0002t0001g0013 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.566-115986G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17571756 | |||||||
| chrX:17571778 | A | T | 116 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0029 others(113): Show |
116 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.566-115964A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17571778 | |||||||
| chrX:17572135 | G | A | 47 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0001c0001t0001g0094 others(44): Show |
47 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.566-115607G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17572135 | |||||||
| chrX:17572181 | T | C | 1 | a0001c0001t0001g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.566-115561T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17572181 | |||||||
| chrX:17572446 | T | C | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.566-115296T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17572446 | |||||||
| chrX:17572491 | C | CCTT | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.566-115251_566-115 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17572491 | |||||||
| chrX:17572491 | C | CT | 56 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0029 others(53): Show |
56 | HG00280.hp1 HG00639.hp2 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.566-115229dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17572491 | ||||||
| chrX:17572491 | C | CTT | 24 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0001c0001t0001g0144 others(21): Show |
24 | HG01071.hp2 HG01258.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.566-115230_566-115 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17572491 | ||||||
| chrX:17572491 | C | CTTTT | 6 | a0001c0001t0001g0137 a0001c0001t0002g0086 a0001c0001t0005g0104 others(3): Show |
6 | HG02451.hp2 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.566-115232_566-115 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17572491 | ||||||
| chrX:17572491 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0002g0143 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.566-115242_566-115 others(20): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17572491 | ||||||
| chrX:17572491 | C | CTTTTTTT others(8): Show |
2 | a0001c0001t0002g0100 a0001c0001t0002g0146 |
2 | HG01243.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.566-115243_566-115 others(21): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17572491 | ||||||
| chrX:17572491 | C | CTTTTTTT others(9): Show |
2 | a0001c0001t0002g0116 a0001c0001t0012g0154 |
2 | HG01975.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.566-115244_566-115 others(22): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17572491 | ||||||
| chrX:17572491 | C | CTTTTTTT others(10): Show |
3 | a0001c0001t0002g0002 a0001c0001t0007g0122 a0010c0010t0003g0158 |
3 | HG02293.hp2 HG02615.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.566-115245_566-115 others(23): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17572491 | ||||||
| chrX:17572491 | C | CTTTTTTT others(11): Show |
2 | a0001c0001t0013g0045 a0005c0005t0008g0087 |
2 | HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.566-115246_566-115 others(24): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17572491 | ||||||
| chrX:17572491 | C | CTTTTTTT others(12): Show |
1 | a0008c0011t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.566-115247_566-115 others(25): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17572491 | ||||||
| chrX:17572491 | C | CTTTTTTT others(15): Show |
1 | a0001c0001t0002g0120 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.566-115250_566-115 others(28): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17572491 | ||||||
| chrX:17572491 | CTTTTTTT others(2): Show |
C | 9 | a0001c0001t0001g0127 a0001c0001t0002g0003 a0002c0002t0001g0072 others(6): Show |
9 | HG01952.hp1 HG02809.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.566-115237_566-115 others(15): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17572491 | ||||||
| chrX:17572576 | C | A | 15 | a0001c0001t0002g0096 a0001c0001t0002g0106 a0001c0001t0002g0107 others(12): Show |
15 | HG01071.hp2 HG01258.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.566-115166C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17572576 | |||||||
| chrX:17572719 | C | T | 1 | a0002c0002t0001g0079 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.566-115023C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17572719 | |||||||
| chrX:17572927 | G | T | 22 | a0001c0001t0001g0127 a0001c0001t0001g0137 a0001c0001t0002g0002 others(19): Show |
22 | HG01243.hp1 HG01952.hp1 HG01975.hp1 others(19): Show |
intron_variant | MODIFIER | c.566-114815G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17572927 | |||||||
| chrX:17572935 | T | A | 9 | a0001c0001t0001g0127 a0001c0001t0002g0003 a0002c0002t0001g0072 others(6): Show |
9 | HG01952.hp1 HG02809.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.566-114807T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17572935 | |||||||
| chrX:17572958 | G | T | 116 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0029 others(113): Show |
116 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.566-114784G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17572958 | |||||||
| chrX:17573188 | G | A | 2 | a0001c0001t0001g0137 a0001c0001t0002g0002 |
2 | HG02293.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.566-114554G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17573188 | |||||||
| chrX:17573518 | T | G | 6 | a0001c0001t0002g0086 a0001c0001t0005g0104 a0001c0001t0005g0111 others(3): Show |
6 | HG02622.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.566-114224T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17573518 | |||||||
| chrX:17573525 | C | T | 6 | a0001c0001t0002g0086 a0001c0001t0005g0104 a0001c0001t0005g0111 others(3): Show |
6 | HG02622.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.566-114217C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17573525 | |||||||
| chrX:17573669 | C | T | 2 | a0002c0002t0001g0018 a0002c0002t0001g0123 |
2 | HG00639.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.566-114073C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17573669 | |||||||
| chrX:17573725 | G | A | 2 | a0002c0002t0001g0032 a0004c0004t0001g0012 |
2 | HG01192.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.566-114017G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17573725 | |||||||
| chrX:17574503 | G | A | 79 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0029 others(76): Show |
79 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.566-113239G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17574503 | |||||||
| chrX:17574591 | A | G | 1 | a0001c0001t0002g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.566-113151A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17574591 | |||||||
| chrX:17574639 | G | A | 2 | a0002c0002t0001g0088 a0002c0002t0001g0089 |
2 | NA18945.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.566-113103G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17574639 | |||||||
| chrX:17574643 | C | T | 1 | a0001c0001t0001g0008 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.566-113099C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17574643 | |||||||
| chrX:17574718 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.566-113024C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17574718 | |||||||
| chrX:17574918 | G | A | 1 | a0001c0001t0002g0044 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.566-112824G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17574918 | |||||||
| chrX:17575124 | G | A | 1 | a0001c0001t0002g0120 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.566-112618G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17575124 | |||||||
| chrX:17575219 | C | T | 115 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0029 others(112): Show |
115 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.566-112523C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17575219 | |||||||
| chrX:17575351 | C | CCATCACC others(13): Show |
1 | a0006c0008t0002g0113 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.566-112347_566-112 others(26): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17575351 | ||||||
| chrX:17575351 | CCATCACC others(13): Show |
C | 1 | a0002c0002t0001g0108 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.566-112347_566-112 others(26): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17575351 | ||||||
| chrX:17575457 | C | T | 80 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0029 others(77): Show |
80 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.566-112285C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17575457 | |||||||
| chrX:17575582 | A | G | 1 | a0001c0003t0002g0155 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.566-112160A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17575582 | |||||||
| chrX:17575783 | A | G | 127 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0029 others(124): Show |
127 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.566-111959A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17575783 | |||||||
| chrX:17575937 | A | G | 1 | a0002c0002t0001g0108 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.566-111805A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17575937 | |||||||
| chrX:17576160 | C | T | 104 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0029 others(101): Show |
104 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.566-111582C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17576160 | |||||||
| chrX:17576347 | T | C | 10 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0001c0001t0001g0094 others(7): Show |
10 | HG01106.hp1 HG01109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.566-111395T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17576347 | |||||||
| chrX:17576691 | G | A | 1 | a0002c0002t0001g0076 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.566-111051G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17576691 | |||||||
| chrX:17577107 | C | T | 1 | a0002c0002t0001g0023 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.566-110635C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17577107 | |||||||
| chrX:17577201 | G | A | 115 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0029 others(112): Show |
115 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.566-110541G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17577201 | |||||||
| chrX:17577826 | T | G | 9 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0003t0002g0014 others(6): Show |
9 | HG01258.hp1 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.566-109916T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17577826 | |||||||
| chrX:17578097 | A | G | 12 | a0001c0001t0001g0137 a0001c0001t0002g0002 a0001c0001t0002g0100 others(9): Show |
12 | HG01243.hp1 HG02257.hp2 HG02293.hp2 others(9): Show |
intron_variant | MODIFIER | c.566-109645A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17578097 | |||||||
| chrX:17578156 | G | C | 12 | a0001c0001t0001g0137 a0001c0001t0002g0002 a0001c0001t0002g0100 others(9): Show |
12 | HG01243.hp1 HG02257.hp2 HG02293.hp2 others(9): Show |
intron_variant | MODIFIER | c.566-109586G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17578156 | |||||||
| chrX:17578417 | C | T | 1 | a0001c0001t0002g0086 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.566-109325C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17578417 | |||||||
| chrX:17578590 | C | T | 1 | a0002c0002t0001g0123 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.566-109152C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17578590 | |||||||
| chrX:17578644 | A | C | 1 | a0001c0001t0002g0044 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.566-109098A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17578644 | |||||||
| chrX:17578848 | G | T | 51 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0001c0001t0001g0094 others(48): Show |
51 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.566-108894G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17578848 | |||||||
| chrX:17579154 | T | A | 13 | a0001c0001t0001g0137 a0001c0001t0002g0002 a0001c0001t0002g0100 others(10): Show |
13 | HG01243.hp1 HG01975.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.566-108588T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17579154 | |||||||
| chrX:17579165 | G | A | 2 | a0002c0002t0001g0138 a0002c0002t0001g0139 |
2 | HG00673.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.566-108577G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17579165 | |||||||
| chrX:17579469 | T | C | 13 | a0001c0001t0001g0137 a0001c0001t0002g0002 a0001c0001t0002g0100 others(10): Show |
13 | HG01243.hp1 HG01975.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.566-108273T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17579469 | |||||||
| chrX:17579688 | G | A | 50 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0001c0001t0001g0094 others(47): Show |
50 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.566-108054G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17579688 | |||||||
| chrX:17579760 | C | T | 1 | a0001c0001t0007g0122 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.566-107982C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17579760 | |||||||
| chrX:17579876 | A | G | 12 | a0001c0001t0001g0137 a0001c0001t0002g0002 a0001c0001t0002g0100 others(9): Show |
12 | HG01243.hp1 HG02257.hp2 HG02293.hp2 others(9): Show |
intron_variant | MODIFIER | c.566-107866A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17579876 | |||||||
| chrX:17580181 | GA | G | 24 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0001c0001t0001g0094 others(21): Show |
24 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.566-107549delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17580181 | ||||||
| chrX:17580181 | GAA | G | 12 | a0001c0001t0001g0137 a0001c0001t0002g0002 a0001c0001t0002g0100 others(9): Show |
12 | HG01243.hp1 HG02257.hp2 HG02293.hp2 others(9): Show |
intron_variant | MODIFIER | c.566-107550_566-107 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17580181 | ||||||
| chrX:17580810 | C | T | 8 | a0001c0001t0001g0127 a0002c0002t0001g0072 a0002c0002t0001g0082 others(5): Show |
8 | HG01952.hp1 HG02922.hp1 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.566-106932C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17580810 | |||||||
| chrX:17581021 | A | G | 1 | a0001c0001t0001g0021 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.566-106721A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17581021 | |||||||
| chrX:17581054 | G | A | 24 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0001c0001t0001g0094 others(21): Show |
24 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.566-106688G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17581054 | |||||||
| chrX:17581402 | G | T | 8 | a0001c0001t0001g0127 a0002c0002t0001g0072 a0002c0002t0001g0082 others(5): Show |
8 | HG01952.hp1 HG02922.hp1 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.566-106340G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17581402 | |||||||
| chrX:17581796 | C | T | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.566-105946C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17581796 | |||||||
| chrX:17582740 | C | T | 48 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0049 others(45): Show |
48 | HG00280.hp1 HG00639.hp2 HG01261.hp1 others(45): Show |
intron_variant | MODIFIER | c.566-105002C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17582740 | |||||||
| chrX:17583407 | C | T | 6 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0001c0001t0002g0044 others(3): Show |
6 | HG01106.hp1 HG01109.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-104335C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17583407 | |||||||
| chrX:17583535 | G | C | 9 | a0001c0001t0001g0127 a0001c0001t0002g0003 a0002c0002t0001g0072 others(6): Show |
9 | HG01952.hp1 HG02809.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.566-104207G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17583535 | |||||||
| chrX:17583887 | C | A | 1 | a0001c0001t0004g0163 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.566-103855C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17583887 | |||||||
| chrX:17584195 | T | C | 6 | a0001c0003t0002g0014 a0001c0003t0002g0128 a0001c0003t0002g0142 others(3): Show |
6 | HG01258.hp1 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-103547T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17584195 | |||||||
| chrX:17584334 | A | C | 116 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0029 others(113): Show |
116 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.566-103408A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17584334 | |||||||
| chrX:17584340 | C | T | 4 | a0001c0001t0002g0116 a0001c0001t0002g0120 a0001c0001t0007g0122 others(1): Show |
4 | HG02615.hp2 HG02723.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-103402C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17584340 | |||||||
| chrX:17584408 | T | C | 1 | a0001c0001t0002g0002 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.566-103334T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17584408 | |||||||
| chrX:17584434 | A | G | 1 | a0002c0002t0001g0020 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.566-103308A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17584434 | |||||||
| chrX:17584461 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.566-103281C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17584461 | |||||||
| chrX:17584734 | T | C | 16 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0002g0106 others(13): Show |
16 | HG01071.hp2 HG01258.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.566-103008T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17584734 | |||||||
| chrX:17584847 | T | C | 128 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0029 others(125): Show |
128 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.566-102895T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17584847 | |||||||
| chrX:17584913 | C | G | 1 | a0001c0003t0002g0014 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.566-102829C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17584913 | |||||||
| chrX:17584997 | C | T | 106 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0029 others(103): Show |
106 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(103): Show |
intron_variant | MODIFIER | c.566-102745C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17584997 | |||||||
| chrX:17585418 | G | A | 12 | a0001c0001t0001g0137 a0001c0001t0002g0002 a0001c0001t0002g0100 others(9): Show |
12 | HG01243.hp1 HG02257.hp2 HG02293.hp2 others(9): Show |
intron_variant | MODIFIER | c.566-102324G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17585418 | |||||||
| chrX:17585555 | A | G | 12 | a0001c0001t0001g0137 a0001c0001t0002g0002 a0001c0001t0002g0100 others(9): Show |
12 | HG01243.hp1 HG02257.hp2 HG02293.hp2 others(9): Show |
intron_variant | MODIFIER | c.566-102187A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17585555 | |||||||
| chrX:17585658 | A | G | 28 | a0001c0001t0001g0127 a0001c0001t0001g0137 a0001c0001t0002g0002 others(25): Show |
28 | HG00408.hp2 HG01071.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.566-102084A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17585658 | |||||||
| chrX:17585738 | G | GTAA | 9 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0051 others(6): Show |
9 | HG00673.hp1 HG01109.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.566-101976_566-101 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17585738 | ||||||
| chrX:17585738 | G | GTAATAAT others(2): Show |
5 | a0002c0002t0001g0013 a0002c0002t0001g0072 a0002c0002t0001g0076 others(2): Show |
5 | HG00408.hp2 HG01952.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-101982_566-101 others(15): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17585738 | ||||||
| chrX:17585738 | G | GTAATAAT others(5): Show |
4 | a0003c0006t0001g0162 a0003c0006t0002g0161 a0004c0004t0001g0149 others(1): Show |
4 | HG02922.hp1 HG03471.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-101985_566-101 others(18): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17585738 | ||||||
| chrX:17585738 | G | GTAATAAT others(8): Show |
1 | a0001c0001t0001g0127 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.566-101988_566-101 others(21): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17585738 | ||||||
| chrX:17585738 | GTAA | G | 11 | a0001c0001t0001g0137 a0001c0001t0002g0002 a0001c0001t0002g0116 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.566-101976_566-101 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17585738 | ||||||
| chrX:17585753 | A | T | 3 | a0001c0001t0013g0045 a0005c0005t0008g0087 a0008c0011t0002g0147 |
3 | HG02257.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.566-101989A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17585753 | |||||||
| chrX:17585836 | G | GT | 23 | a0001c0001t0001g0041 a0001c0001t0001g0094 a0001c0001t0001g0095 others(20): Show |
23 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.566-101898dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17585836 | ||||||
| chrX:17585837 | T | G | 22 | a0001c0001t0001g0127 a0001c0001t0001g0137 a0001c0001t0002g0002 others(19): Show |
22 | HG00408.hp2 HG01243.hp1 HG01952.hp1 others(19): Show |
intron_variant | MODIFIER | c.566-101905T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17585837 | |||||||
| chrX:17585977 | G | A | 1 | a0002c0002t0001g0109 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.566-101765G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17585977 | |||||||
| chrX:17586107 | C | T | 5 | a0001c0001t0001g0041 a0001c0001t0002g0121 a0003c0006t0001g0157 others(2): Show |
5 | HG01106.hp1 HG02280.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-101635C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17586107 | |||||||
| chrX:17586676 | C | T | 12 | a0001c0001t0001g0137 a0001c0001t0002g0002 a0001c0001t0002g0100 others(9): Show |
12 | HG01243.hp1 HG02257.hp2 HG02293.hp2 others(9): Show |
intron_variant | MODIFIER | c.566-101066C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17586676 | |||||||
| chrX:17587208 | G | A | 1 | a0001c0001t0001g0049 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.566-100534G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17587208 | |||||||
| chrX:17587419 | T | C | 4 | a0001c0001t0007g0125 a0005c0005t0003g0101 a0005c0005t0003g0136 others(1): Show |
4 | HG01071.hp2 HG02055.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-100323T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17587419 | |||||||
| chrX:17587688 | G | A | 6 | a0001c0003t0002g0014 a0001c0003t0002g0128 a0001c0003t0002g0142 others(3): Show |
6 | HG01258.hp1 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-100054G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17587688 | |||||||
| chrX:17588256 | A | G | 101 | a0001c0001t0001g0021 a0001c0001t0001g0029 a0001c0001t0001g0041 others(98): Show |
101 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.566-99486A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17588256 | |||||||
| chrX:17588590 | G | A | 1 | a0007c0014t0003g0092 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.566-99152G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17588590 | |||||||
| chrX:17588591 | AT | A | 89 | a0001c0001t0001g0021 a0001c0001t0001g0029 a0001c0001t0001g0048 others(86): Show |
89 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.566-99139delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17588591 | ||||||
| chrX:17588703 | C | G | 75 | a0001c0001t0001g0021 a0001c0001t0001g0029 a0001c0001t0001g0048 others(72): Show |
75 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.566-99039C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17588703 | |||||||
| chrX:17588970 | C | T | 10 | a0001c0001t0001g0041 a0001c0001t0001g0094 a0001c0001t0001g0095 others(7): Show |
10 | HG01106.hp1 HG01109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.566-98772C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17588970 | |||||||
| chrX:17589023 | C | T | 10 | a0001c0001t0007g0125 a0001c0003t0002g0014 a0001c0003t0002g0128 others(7): Show |
10 | HG01071.hp2 HG01258.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.566-98719C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17589023 | |||||||
| chrX:17589156 | TATTTTTT others(1): Show |
T | 4 | a0001c0001t0001g0068 a0001c0001t0001g0112 a0001c0001t0002g0096 others(1): Show |
4 | HG02486.hp1 HG02723.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-98577_566-9857 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17589156 | ||||||
| chrX:17589201 | C | T | 89 | a0001c0001t0001g0021 a0001c0001t0001g0029 a0001c0001t0001g0048 others(86): Show |
89 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.566-98541C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17589201 | |||||||
| chrX:17589319 | T | C | 109 | a0001c0001t0001g0021 a0001c0001t0001g0029 a0001c0001t0001g0041 others(106): Show |
109 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.566-98423T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17589319 | |||||||
| chrX:17589571 | C | A | 89 | a0001c0001t0001g0021 a0001c0001t0001g0029 a0001c0001t0001g0048 others(86): Show |
89 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.566-98171C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17589571 | |||||||
| chrX:17589650 | A | AGTGAGTA others(213): Show |
1 | a0004c0004t0001g0132 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.566-98077_566-9807 others(224): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17589650 | ||||||
| chrX:17589650 | A | AGTGAGTA others(212): Show |
1 | a0003c0006t0001g0162 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.566-98077_566-9807 others(223): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17589650 | ||||||
| chrX:17589650 | A | AGTGAGTA others(213): Show |
5 | a0001c0001t0001g0127 a0002c0002t0001g0072 a0002c0002t0001g0082 others(2): Show |
5 | HG03017.hp1 HG03453.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-98077_566-9807 others(224): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17589650 | ||||||
| chrX:17589650 | A | AGTGAGTA others(214): Show |
2 | a0002c0002t0001g0076 a0011c0012t0001g0150 |
2 | HG04228.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.566-98077_566-9807 others(225): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17589650 | ||||||
| chrX:17589677 | T | C | 2 | a0001c0001t0004g0071 a0001c0001t0004g0163 |
2 | HG01261.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.566-98065T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17589677 | |||||||
| chrX:17589934 | G | C | 6 | a0001c0001t0002g0086 a0001c0001t0005g0104 a0001c0001t0005g0111 others(3): Show |
6 | HG02622.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.566-97808G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17589934 | |||||||
| chrX:17589958 | T | C | 1 | a0001c0003t0002g0102 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.566-97784T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17589958 | |||||||
| chrX:17589988 | G | A | 1 | a0004c0004t0001g0012 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.566-97754G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17589988 | |||||||
| chrX:17590235 | C | T | 9 | a0001c0001t0001g0127 a0002c0002t0001g0072 a0002c0002t0001g0076 others(6): Show |
9 | HG01952.hp1 HG02922.hp1 HG03017.hp1 others(6): Show |
intron_variant | MODIFIER | c.566-97507C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17590235 | |||||||
| chrX:17590814 | C | T | 1 | a0001c0001t0002g0086 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.566-96928C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17590814 | |||||||
| chrX:17590818 | C | A | 5 | a0002c0002t0001g0022 a0002c0002t0001g0023 a0002c0002t0001g0088 others(2): Show |
5 | HG02027.hp1 HG02083.hp1 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-96924C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17590818 | |||||||
| chrX:17590837 | A | G | 1 | a0002c0002t0001g0063 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.566-96905A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17590837 | |||||||
| chrX:17590855 | A | G | 32 | a0001c0001t0001g0041 a0001c0001t0001g0094 a0001c0001t0001g0095 others(29): Show |
32 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.566-96887A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17590855 | |||||||
| chrX:17591075 | C | T | 1 | a0001c0001t0002g0044 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.566-96667C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17591075 | |||||||
| chrX:17591284 | T | G | 7 | a0002c0002t0001g0022 a0002c0002t0001g0023 a0002c0002t0001g0024 others(4): Show |
7 | HG02027.hp1 HG02083.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.566-96458T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17591284 | |||||||
| chrX:17591303 | C | T | 7 | a0002c0002t0001g0022 a0002c0002t0001g0023 a0002c0002t0001g0024 others(4): Show |
7 | HG02027.hp1 HG02083.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.566-96439C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17591303 | |||||||
| chrX:17591659 | C | T | 1 | a0002c0002t0001g0067 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.566-96083C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17591659 | |||||||
| chrX:17591677 | A | T | 20 | a0001c0001t0001g0041 a0001c0001t0001g0094 a0001c0001t0001g0095 others(17): Show |
20 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.566-96065A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17591677 | |||||||
| chrX:17591815 | G | A | 4 | a0001c0001t0007g0125 a0005c0005t0003g0101 a0005c0005t0003g0136 others(1): Show |
4 | HG01071.hp2 HG02055.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-95927G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17591815 | |||||||
| chrX:17592010 | A | ATG | 14 | a0001c0001t0001g0041 a0001c0001t0001g0145 a0001c0001t0002g0121 others(11): Show |
14 | HG00280.hp1 HG00639.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.566-95706_566-9570 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17592010 | ||||||
| chrX:17592010 | A | ATGTG | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.566-95708_566-9570 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17592010 | ||||||
| chrX:17592010 | ATG | A | 12 | a0001c0001t0001g0137 a0001c0001t0002g0002 a0001c0001t0002g0100 others(9): Show |
12 | HG01243.hp1 HG02257.hp2 HG02293.hp2 others(9): Show |
intron_variant | MODIFIER | c.566-95706_566-9570 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17592010 | ||||||
| chrX:17592010 | ATGTG | A | 11 | a0001c0001t0002g0044 a0001c0001t0002g0086 a0001c0001t0005g0104 others(8): Show |
11 | HG01071.hp2 HG01109.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.566-95708_566-9570 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17592010 | ||||||
| chrX:17592119 | T | G | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.566-95623T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17592119 | |||||||
| chrX:17592176 | C | T | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.566-95566C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17592176 | |||||||
| chrX:17592178 | G | A | 41 | a0001c0001t0001g0041 a0001c0001t0001g0094 a0001c0001t0001g0095 others(38): Show |
41 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.566-95564G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17592178 | |||||||
| chrX:17592411 | C | T | 32 | a0001c0001t0001g0041 a0001c0001t0001g0094 a0001c0001t0001g0095 others(29): Show |
32 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.566-95331C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17592411 | |||||||
| chrX:17592979 | G | A | 109 | a0001c0001t0001g0021 a0001c0001t0001g0029 a0001c0001t0001g0041 others(106): Show |
109 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.566-94763G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17592979 | |||||||
| chrX:17593263 | C | G | 89 | a0001c0001t0001g0021 a0001c0001t0001g0029 a0001c0001t0001g0048 others(86): Show |
89 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.566-94479C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17593263 | |||||||
| chrX:17593556 | T | C | 89 | a0001c0001t0001g0021 a0001c0001t0001g0029 a0001c0001t0001g0048 others(86): Show |
89 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.566-94186T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17593556 | |||||||
| chrX:17594076 | T | C | 1 | a0002c0002t0001g0019 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.566-93666T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17594076 | |||||||
| chrX:17594183 | G | A | 41 | a0001c0001t0001g0041 a0001c0001t0001g0094 a0001c0001t0001g0095 others(38): Show |
41 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.566-93559G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17594183 | |||||||
| chrX:17594376 | G | A | 80 | a0001c0001t0001g0021 a0001c0001t0001g0029 a0001c0001t0001g0048 others(77): Show |
80 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.566-93366G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17594376 | |||||||
| chrX:17594732 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0056 |
2 | NA18988.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.566-93010C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17594732 | |||||||
| chrX:17595340 | C | T | 118 | a0001c0001t0001g0021 a0001c0001t0001g0029 a0001c0001t0001g0041 others(115): Show |
118 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.566-92402C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17595340 | |||||||
| chrX:17595354 | G | A | 1 | a0001c0001t0011g0081 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.566-92388G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17595354 | |||||||
| chrX:17595560 | G | T | 2 | a0001c0001t0006g0074 a0001c0001t0006g0103 |
2 | NA18955.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.566-92182G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17595560 | |||||||
| chrX:17596041 | CA | C | 89 | a0001c0001t0001g0021 a0001c0001t0001g0029 a0001c0001t0001g0048 others(86): Show |
89 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.566-91690delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17596041 | ||||||
| chrX:17596196 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.566-91546A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17596196 | |||||||
| chrX:17596348 | G | C | 6 | a0001c0001t0002g0086 a0001c0001t0005g0104 a0001c0001t0005g0111 others(3): Show |
6 | HG02622.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.566-91394G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17596348 | |||||||
| chrX:17596399 | C | T | 80 | a0001c0001t0001g0021 a0001c0001t0001g0029 a0001c0001t0001g0048 others(77): Show |
80 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.566-91343C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17596399 | |||||||
| chrX:17596697 | A | G | 6 | a0001c0001t0002g0086 a0001c0001t0005g0104 a0001c0001t0005g0111 others(3): Show |
6 | HG02622.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.566-91045A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17596697 | |||||||
| chrX:17597116 | G | GT | 23 | a0001c0001t0001g0029 a0001c0001t0001g0099 a0001c0001t0001g0127 others(20): Show |
23 | HG00639.hp2 HG01952.hp1 HG02027.hp1 others(20): Show |
intron_variant | MODIFIER | c.566-90605dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17597116 | ||||||
| chrX:17597116 | GTT | G | 5 | a0001c0001t0002g0086 a0001c0001t0005g0104 a0001c0001t0005g0111 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-90606_566-9060 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17597116 | ||||||
| chrX:17597116 | GTTTTT | G | 32 | a0001c0001t0001g0041 a0001c0001t0001g0094 a0001c0001t0001g0095 others(29): Show |
32 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.566-90609_566-9060 others(9): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17597116 | ||||||
| chrX:17597215 | G | A | 32 | a0001c0001t0001g0041 a0001c0001t0001g0094 a0001c0001t0001g0095 others(29): Show |
32 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.566-90527G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17597215 | |||||||
| chrX:17597245 | A | G | 32 | a0001c0001t0001g0041 a0001c0001t0001g0094 a0001c0001t0001g0095 others(29): Show |
32 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.566-90497A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17597245 | |||||||
| chrX:17597247 | A | G | 32 | a0001c0001t0001g0041 a0001c0001t0001g0094 a0001c0001t0001g0095 others(29): Show |
32 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.566-90495A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17597247 | |||||||
| chrX:17597372 | A | G | 47 | a0001c0001t0001g0041 a0001c0001t0001g0094 a0001c0001t0001g0095 others(44): Show |
47 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.566-90370A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17597372 | |||||||
| chrX:17597426 | T | TTC | 3 | a0004c0004t0001g0132 a0004c0004t0001g0149 a0011c0012t0001g0150 |
3 | HG01952.hp1 NA18948.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.566-90312_566-9031 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17597426 | ||||||
| chrX:17597430 | C | CT | 11 | a0001c0001t0002g0086 a0001c0001t0002g0106 a0001c0001t0002g0107 others(8): Show |
11 | HG02258.hp1 HG02280.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.566-90296dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17597430 | ||||||
| chrX:17597430 | C | CTT | 6 | a0001c0001t0001g0127 a0002c0002t0001g0072 a0002c0002t0001g0076 others(3): Show |
6 | HG02922.hp1 HG03017.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-90297_566-9029 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17597430 | ||||||
| chrX:17597430 | CT | C | 5 | a0001c0001t0004g0071 a0002c0002t0001g0016 a0002c0002t0001g0042 others(2): Show |
5 | HG00639.hp1 NA19043.hp1 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-90296delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17597430 | ||||||
| chrX:17597638 | G | C | 6 | a0001c0001t0002g0086 a0001c0001t0005g0104 a0001c0001t0005g0111 others(3): Show |
6 | HG02622.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.566-90104G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17597638 | |||||||
| chrX:17597735 | A | C | 1 | a0002c0002t0001g0019 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.566-90007A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17597735 | |||||||
| chrX:17598201 | T | C | 20 | a0001c0001t0001g0041 a0001c0001t0001g0094 a0001c0001t0001g0095 others(17): Show |
20 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.566-89541T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17598201 | |||||||
| chrX:17598599 | G | A | 1 | a0002c0002t0001g0054 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.566-89143G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17598599 | |||||||
| chrX:17598604 | C | G | 15 | a0001c0001t0001g0127 a0001c0001t0002g0086 a0001c0001t0005g0104 others(12): Show |
15 | HG01952.hp1 HG02622.hp2 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.566-89138C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17598604 | |||||||
| chrX:17598822 | T | C | 109 | a0001c0001t0001g0021 a0001c0001t0001g0029 a0001c0001t0001g0041 others(106): Show |
109 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.566-88920T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17598822 | |||||||
| chrX:17598959 | G | T | 2 | a0001c0001t0001g0124 a0001c0001t0010g0059 |
2 | HG01943.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.566-88783G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17598959 | |||||||
| chrX:17598986 | G | A | 9 | a0001c0001t0001g0127 a0002c0002t0001g0072 a0002c0002t0001g0076 others(6): Show |
9 | HG01952.hp1 HG02922.hp1 HG03017.hp1 others(6): Show |
intron_variant | MODIFIER | c.566-88756G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17598986 | |||||||
| chrX:17599712 | G | A | 1 | a0002c0002t0001g0080 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.566-88030G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17599712 | |||||||
| chrX:17600150 | G | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0112 |
2 | HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.566-87592G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17600150 | |||||||
| chrX:17600286 | C | CAG | 22 | a0001c0001t0001g0029 a0001c0001t0001g0127 a0001c0001t0002g0086 others(19): Show |
22 | HG00280.hp1 HG01952.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.566-87429_566-8742 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17600286 | ||||||
| chrX:17600296 | G | C | 11 | a0001c0001t0007g0125 a0001c0003t0002g0014 a0001c0003t0002g0128 others(8): Show |
11 | HG01071.hp2 HG01258.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.566-87446G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17600296 | |||||||
| chrX:17600311 | A | T | 1 | a0001c0001t0002g0044 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.566-87431A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17600311 | |||||||
| chrX:17600509 | A | G | 13 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0007g0125 others(10): Show |
13 | HG01071.hp2 HG01258.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.566-87233A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17600509 | |||||||
| chrX:17600770 | C | T | 90 | a0001c0001t0001g0021 a0001c0001t0001g0029 a0001c0001t0001g0048 others(87): Show |
90 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.566-86972C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17600770 | |||||||
| chrX:17600965 | A | G | 1 | a0002c0002t0001g0005 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.566-86777A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17600965 | |||||||
| chrX:17601008 | G | A | 1 | a0002c0002t0001g0010 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.566-86734G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17601008 | |||||||
| chrX:17601049 | C | G | 1 | a0001c0001t0002g0121 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.566-86693C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17601049 | |||||||
| chrX:17601257 | A | G | 12 | a0001c0001t0002g0086 a0001c0001t0005g0104 a0001c0001t0005g0111 others(9): Show |
12 | HG01952.hp1 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.566-86485A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17601257 | |||||||
| chrX:17601390 | T | C | 1 | a0001c0001t0002g0116 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.566-86352T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17601390 | |||||||
| chrX:17601437 | A | G | 1 | a0001c0003t0002g0128 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.566-86305A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17601437 | |||||||
| chrX:17601508 | C | T | 6 | a0002c0002t0001g0072 a0002c0002t0001g0076 a0002c0002t0001g0082 others(3): Show |
6 | HG01952.hp1 HG03017.hp1 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-86234C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17601508 | |||||||
| chrX:17601691 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.566-86051T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17601691 | |||||||
| chrX:17602182 | CACA | C | 10 | a0001c0001t0002g0116 a0001c0001t0002g0120 a0001c0001t0007g0122 others(7): Show |
10 | HG01952.hp1 HG02615.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.566-85543_566-8554 others(7): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17602182 | ||||||
| chrX:17602196 | CAACA | C | 2 | a0001c0003t0002g0142 a0006c0007t0002g0115 |
2 | HG02572.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.566-85527_566-8552 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17602196 | ||||||
| chrX:17602315 | A | C | 12 | a0001c0001t0002g0086 a0001c0001t0005g0104 a0001c0001t0005g0111 others(9): Show |
12 | HG01952.hp1 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.566-85427A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17602315 | |||||||
| chrX:17602684 | C | CT | 6 | a0002c0002t0001g0072 a0002c0002t0001g0076 a0002c0002t0001g0082 others(3): Show |
6 | HG01952.hp1 HG03017.hp1 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-85047dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17602684 | ||||||
| chrX:17602749 | G | A | 122 | a0001c0001t0001g0021 a0001c0001t0001g0029 a0001c0001t0001g0041 others(119): Show |
122 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.566-84993G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17602749 | |||||||
| chrX:17602809 | T | C | 13 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0007g0125 others(10): Show |
13 | HG01071.hp2 HG01258.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.566-84933T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17602809 | |||||||
| chrX:17602834 | A | AT | 12 | a0001c0001t0002g0121 a0001c0001t0002g0126 a0001c0001t0004g0058 others(9): Show |
12 | HG01071.hp1 HG01071.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.566-84885dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17602834 | ||||||
| chrX:17602834 | A | ATT | 8 | a0001c0001t0001g0041 a0001c0001t0002g0044 a0001c0001t0002g0146 others(5): Show |
8 | HG01109.hp1 HG02055.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.566-84886_566-8488 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17602834 | ||||||
| chrX:17602834 | A | ATTT | 5 | a0001c0003t0002g0014 a0001c0003t0002g0128 a0001c0003t0002g0155 others(2): Show |
5 | HG01258.hp1 HG02280.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-84887_566-8488 others(7): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17602834 | ||||||
| chrX:17602834 | AT | A | 18 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0029 others(15): Show |
18 | HG01074.hp1 HG02040.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.566-84885delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17602834 | ||||||
| chrX:17602939 | C | G | 4 | a0001c0001t0001g0135 a0001c0001t0001g0151 a0002c0002t0001g0060 others(1): Show |
4 | HG00408.hp1 HG02074.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-84803C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17602939 | |||||||
| chrX:17603221 | G | A | 39 | a0001c0001t0001g0041 a0001c0001t0001g0094 a0001c0001t0001g0095 others(36): Show |
39 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.566-84521G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17603221 | |||||||
| chrX:17603295 | G | A | 6 | a0001c0001t0002g0086 a0001c0001t0005g0104 a0001c0001t0005g0111 others(3): Show |
6 | HG02622.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.566-84447G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17603295 | |||||||
| chrX:17603557 | A | G | 12 | a0001c0001t0001g0137 a0001c0001t0002g0002 a0001c0001t0002g0100 others(9): Show |
12 | HG01243.hp1 HG01975.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.566-84185A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17603557 | |||||||
| chrX:17603699 | C | T | 12 | a0001c0001t0002g0086 a0001c0001t0005g0104 a0001c0001t0005g0111 others(9): Show |
12 | HG01952.hp1 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.566-84043C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17603699 | |||||||
| chrX:17603882 | A | G | 12 | a0001c0001t0002g0086 a0001c0001t0005g0104 a0001c0001t0005g0111 others(9): Show |
12 | HG01952.hp1 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.566-83860A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17603882 | |||||||
| chrX:17603949 | C | T | 6 | a0002c0002t0001g0072 a0002c0002t0001g0076 a0002c0002t0001g0082 others(3): Show |
6 | HG01952.hp1 HG03017.hp1 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-83793C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17603949 | |||||||
| chrX:17604134 | A | T | 12 | a0001c0001t0002g0086 a0001c0001t0005g0104 a0001c0001t0005g0111 others(9): Show |
12 | HG01952.hp1 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.566-83608A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17604134 | |||||||
| chrX:17604228 | T | TCA | 15 | a0001c0001t0001g0137 a0001c0001t0002g0002 a0001c0001t0002g0100 others(12): Show |
15 | HG01106.hp1 HG01243.hp1 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.566-83475_566-8347 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17604228 | ||||||
| chrX:17604228 | T | TCACA | 7 | a0001c0001t0002g0116 a0001c0001t0002g0121 a0001c0001t0002g0143 others(4): Show |
7 | HG02074.hp1 HG02280.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.566-83477_566-8347 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17604228 | ||||||
| chrX:17604228 | T | TCACACA | 12 | a0001c0001t0001g0041 a0001c0001t0002g0120 a0001c0001t0007g0125 others(9): Show |
12 | HG01071.hp2 HG01258.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.566-83479_566-8347 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17604228 | ||||||
| chrX:17604228 | T | TCACACAC others(3): Show |
1 | a0001c0001t0002g0044 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.566-83483_566-8347 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17604228 | ||||||
| chrX:17604228 | T | TCACACAC others(5): Show |
2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.566-83485_566-8347 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17604228 | ||||||
| chrX:17604228 | T | TCACACAC others(7): Show |
1 | a0001c0001t0002g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.566-83487_566-8347 others(18): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17604228 | ||||||
| chrX:17604228 | TCA | T | 47 | a0001c0001t0001g0049 a0001c0001t0001g0066 a0001c0001t0001g0068 others(44): Show |
47 | HG00280.hp1 HG00639.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.566-83475_566-8347 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17604228 | ||||||
| chrX:17604228 | TCACA | T | 2 | a0001c0001t0001g0026 a0012c0013t0001g0038 |
2 | NA18747.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.566-83477_566-8347 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17604228 | ||||||
| chrX:17604228 | TCACACA | T | 11 | a0001c0001t0005g0111 a0001c0003t0002g0102 a0002c0002t0001g0033 others(8): Show |
11 | HG01952.hp1 HG02622.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.566-83479_566-8347 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17604228 | ||||||
| chrX:17604228 | TCACACAC others(7): Show |
T | 1 | a0001c0001t0005g0104 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.566-83487_566-8347 others(18): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17604228 | ||||||
| chrX:17605093 | T | C | 1 | a0002c0002t0001g0130 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.566-82649T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17605093 | |||||||
| chrX:17605417 | A | G | 6 | a0001c0001t0002g0086 a0001c0001t0005g0104 a0001c0001t0005g0111 others(3): Show |
6 | HG02622.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.566-82325A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17605417 | |||||||
| chrX:17606098 | C | T | 2 | a0001c0001t0002g0003 a0001c0001t0006g0074 |
2 | HG02809.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.566-81644C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17606098 | |||||||
| chrX:17606421 | C | T | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.566-81321C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17606421 | |||||||
| chrX:17606751 | G | A | 18 | a0001c0001t0001g0137 a0001c0001t0002g0002 a0001c0001t0002g0044 others(15): Show |
18 | HG01109.hp1 HG01243.hp1 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.566-80991G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17606751 | |||||||
| chrX:17606840 | G | A | 6 | a0001c0001t0002g0086 a0001c0001t0005g0104 a0001c0001t0005g0111 others(3): Show |
6 | HG02622.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.566-80902G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17606840 | |||||||
| chrX:17606870 | G | C | 2 | a0001c0001t0012g0154 a0001c0001t0013g0045 |
2 | HG01975.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.566-80872G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17606870 | |||||||
| chrX:17607022 | G | A | 2 | a0002c0002t0001g0034 a0002c0002t0001g0141 |
2 | HG03942.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.566-80720G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17607022 | |||||||
| chrX:17607495 | G | A | 1 | a0005c0005t0008g0087 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.566-80247G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17607495 | |||||||
| chrX:17607511 | G | T | 1 | a0001c0001t0011g0081 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.566-80231G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17607511 | |||||||
| chrX:17607905 | T | C | 3 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0110 |
3 | HG02258.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.566-79837T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17607905 | |||||||
| chrX:17607919 | CT | C | 14 | a0001c0001t0001g0035 a0001c0001t0002g0086 a0001c0001t0005g0104 others(11): Show |
14 | HG01258.hp1 HG01975.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.566-79806delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17607919 | ||||||
| chrX:17607980 | A | C | 7 | a0001c0001t0001g0041 a0001c0001t0002g0121 a0003c0006t0001g0157 others(4): Show |
7 | HG01106.hp1 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.566-79762A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17607980 | |||||||
| chrX:17608071 | T | C | 1 | a0001c0001t0002g0143 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.566-79671T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17608071 | |||||||
| chrX:17608167 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0056 |
2 | NA18988.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.566-79575C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17608167 | |||||||
| chrX:17608401 | A | G | 1 | a0001c0001t0002g0121 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.566-79341A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17608401 | |||||||
| chrX:17608669 | G | T | 1 | a0001c0001t0013g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.566-79073G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17608669 | |||||||
| chrX:17608685 | T | G | 26 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0137 others(23): Show |
26 | HG01071.hp2 HG01109.hp1 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.566-79057T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17608685 | |||||||
| chrX:17608685 | TG | T | 8 | a0001c0001t0002g0100 a0001c0001t0002g0116 a0001c0001t0002g0120 others(5): Show |
8 | HG01243.hp1 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.566-79051delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17608685 | ||||||
| chrX:17608687 | G | T | 8 | a0001c0001t0002g0100 a0001c0001t0002g0116 a0001c0001t0002g0120 others(5): Show |
8 | HG01243.hp1 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.566-79055G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17608687 | |||||||
| chrX:17608688 | G | T | 8 | a0001c0001t0002g0100 a0001c0001t0002g0116 a0001c0001t0002g0120 others(5): Show |
8 | HG01243.hp1 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.566-79054G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17608688 | |||||||
| chrX:17608702 | A | G | 8 | a0001c0001t0002g0100 a0001c0001t0002g0116 a0001c0001t0002g0120 others(5): Show |
8 | HG01243.hp1 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.566-79040A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17608702 | |||||||
| chrX:17608818 | A | G | 4 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0110 others(1): Show |
4 | HG02258.hp1 HG03516.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-78924A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17608818 | |||||||
| chrX:17609658 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0056 |
2 | NA18988.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.566-78084G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17609658 | |||||||
| chrX:17609753 | A | T | 15 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0096 others(12): Show |
15 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.566-77989A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17609753 | |||||||
| chrX:17609983 | C | T | 1 | a0002c0002t0001g0018 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.566-77759C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17609983 | |||||||
| chrX:17610277 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.566-77465G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17610277 | |||||||
| chrX:17610499 | T | C | 11 | a0001c0001t0001g0137 a0001c0001t0002g0100 a0001c0001t0002g0143 others(8): Show |
11 | HG01243.hp1 HG01258.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.566-77243T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17610499 | |||||||
| chrX:17610581 | T | G | 2 | a0001c0001t0001g0124 a0001c0001t0010g0059 |
2 | HG01943.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.566-77161T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17610581 | |||||||
| chrX:17611300 | C | T | 1 | a0004c0004t0001g0132 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.566-76442C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17611300 | |||||||
| chrX:17611308 | G | A | 16 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0093 others(13): Show |
16 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.566-76434G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17611308 | |||||||
| chrX:17611459 | C | T | 1 | a0002c0002t0001g0034 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.566-76283C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17611459 | |||||||
| chrX:17611628 | C | T | 2 | a0001c0001t0012g0154 a0005c0005t0008g0087 |
2 | HG01975.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.566-76114C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17611628 | |||||||
| chrX:17611919 | T | C | 1 | a0002c0002t0001g0005 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.566-75823T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17611919 | |||||||
| chrX:17612047 | T | C | 66 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0041 others(63): Show |
66 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(63): Show |
intron_variant | MODIFIER | c.566-75695T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17612047 | |||||||
| chrX:17612205 | TG | T | 17 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0093 others(14): Show |
17 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.566-75534delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17612205 | ||||||
| chrX:17612206 | G | T | 49 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0041 others(46): Show |
49 | HG00639.hp2 HG01071.hp2 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.566-75536G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17612206 | |||||||
| chrX:17612938 | T | G | 27 | a0001c0001t0001g0112 a0001c0001t0001g0137 a0001c0001t0002g0002 others(24): Show |
27 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.566-74804T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17612938 | |||||||
| chrX:17613017 | CTTT | C | 41 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0041 others(38): Show |
41 | HG00639.hp2 HG01071.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.566-74712_566-7471 others(7): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17613017 | ||||||
| chrX:17613417 | C | A | 37 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0041 others(34): Show |
37 | HG00639.hp2 HG01071.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.566-74325C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17613417 | |||||||
| chrX:17613761 | T | A | 1 | a0002c0002t0001g0077 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.566-73981T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17613761 | |||||||
| chrX:17613961 | G | A | 18 | a0001c0001t0001g0112 a0001c0001t0002g0002 a0001c0001t0002g0003 others(15): Show |
18 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.566-73781G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17613961 | |||||||
| chrX:17614109 | G | A | 1 | a0001c0001t0007g0122 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.566-73633G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17614109 | |||||||
| chrX:17614124 | GTC | G | 4 | a0001c0001t0002g0116 a0001c0001t0007g0122 a0001c0001t0013g0045 others(1): Show |
4 | HG02615.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-73616_566-7361 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17614124 | ||||||
| chrX:17614622 | G | C | 8 | a0001c0001t0001g0137 a0001c0003t0002g0014 a0001c0003t0002g0128 others(5): Show |
8 | HG01258.hp1 HG02280.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.566-73120G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17614622 | |||||||
| chrX:17614640 | C | T | 1 | a0002c0002t0001g0019 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.566-73102C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17614640 | |||||||
| chrX:17614724 | C | G | 2 | a0003c0009t0002g0160 a0006c0008t0002g0113 |
2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.566-73018C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17614724 | |||||||
| chrX:17614862 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.566-72880G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17614862 | |||||||
| chrX:17615073 | CAT | C | 17 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0093 others(14): Show |
17 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.566-72656_566-7265 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17615073 | ||||||
| chrX:17615086 | A | G | 4 | a0001c0001t0002g0116 a0001c0001t0007g0122 a0001c0001t0013g0045 others(1): Show |
4 | HG02615.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-72656A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17615086 | |||||||
| chrX:17615117 | T | C | 1 | a0002c0002t0001g0105 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.566-72625T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17615117 | |||||||
| chrX:17615137 | T | TGTATATA others(28): Show |
1 | a0003c0006t0002g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.566-72593_566-7255 others(39): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17615137 | ||||||
| chrX:17615149 | C | T | 1 | a0001c0001t0004g0058 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.566-72593C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17615149 | |||||||
| chrX:17615152 | G | A | 9 | a0001c0001t0002g0086 a0001c0001t0002g0116 a0001c0001t0005g0104 others(6): Show |
9 | HG02615.hp2 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.566-72590G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17615152 | |||||||
| chrX:17615154 | A | G | 1 | a0001c0001t0004g0058 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.566-72588A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17615154 | |||||||
| chrX:17615170 | T | C | 17 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0093 others(14): Show |
17 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.566-72572T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17615170 | |||||||
| chrX:17615181 | AT | A | 17 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0093 others(14): Show |
17 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.566-72560delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17615181 | |||||||
| chrX:17615183 | A | AC | 115 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0021 others(112): Show |
115 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.566-72559_566-7255 others(5): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17615183 | |||||||
| chrX:17615183 | A | ACGTATAT others(26): Show |
3 | a0002c0002t0001g0053 a0004c0004t0001g0055 a0004c0004t0001g0065 |
3 | NA18966.hp1 NA19007.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.566-72559_566-7255 others(37): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17615183 | |||||||
| chrX:17615183 | A | C | 17 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0093 others(14): Show |
17 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.566-72559A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17615183 | |||||||
| chrX:17615187 | TATATACA others(1): Show |
T | 17 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0093 others(14): Show |
17 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.566-72549_566-7254 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17615187 | ||||||
| chrX:17615195 | C | CATATATA others(27): Show |
23 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0026 others(20): Show |
23 | HG00408.hp2 HG00609.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.566-72526_566-7249 others(38): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17615195 | ||||||
| chrX:17615203 | C | CGTATATA others(25): Show |
1 | a0001c0001t0001g0095 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.566-72527_566-7252 others(36): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17615203 | ||||||
| chrX:17615204 | G | GTA | 13 | a0001c0001t0001g0008 a0001c0001t0001g0050 a0001c0001t0001g0061 others(10): Show |
13 | HG00408.hp1 HG02040.hp1 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.566-72529_566-7252 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17615204 | ||||||
| chrX:17615216 | G | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.566-72526G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17615216 | |||||||
| chrX:17615227 | CAT | C | 17 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0093 others(14): Show |
17 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.566-72507_566-7250 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17615227 | ||||||
| chrX:17615229 | T | TATATATA others(13): Show |
11 | a0001c0001t0002g0086 a0001c0001t0002g0116 a0001c0001t0005g0104 others(8): Show |
11 | HG01975.hp1 HG02615.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.566-72496_566-7249 others(24): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17615229 | ||||||
| chrX:17615261 | C | CATATAT | 13 | a0001c0001t0002g0002 a0001c0001t0002g0096 a0001c0001t0002g0106 others(10): Show |
13 | HG01106.hp1 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.566-72470_566-7246 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17615261 | ||||||
| chrX:17615261 | C | CATATATA others(5): Show |
4 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0126 others(1): Show |
4 | HG01069.hp1 HG01071.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-72476_566-7246 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17615261 | ||||||
| chrX:17615263 | T | C | 5 | a0001c0001t0002g0086 a0001c0001t0005g0104 a0001c0001t0005g0111 others(2): Show |
5 | HG02622.hp2 HG02922.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-72479T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17615263 | |||||||
| chrX:17615779 | A | AC | 9 | a0001c0001t0001g0011 a0001c0001t0001g0029 a0001c0001t0001g0048 others(6): Show |
9 | HG02145.hp1 HG03688.hp1 NA18994.hp1 others(6): Show |
intron_variant | MODIFIER | c.566-71956dupC | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17615779 | ||||||
| chrX:17616087 | AT | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0051 others(1): Show |
4 | HG02071.hp1 NA18961.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-71654delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17616087 | |||||||
| chrX:17616143 | G | A | 1 | a0005c0005t0008g0087 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.566-71599G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17616143 | |||||||
| chrX:17616143 | G | T | 1 | a0001c0001t0001g0070 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.566-71599G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17616143 | |||||||
| chrX:17616144 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.566-71598C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17616144 | |||||||
| chrX:17616703 | A | G | 25 | a0001c0001t0001g0112 a0001c0001t0001g0137 a0001c0001t0002g0002 others(22): Show |
25 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.566-71039A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17616703 | |||||||
| chrX:17616753 | A | C | 1 | a0003c0009t0002g0160 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.566-70989A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17616753 | |||||||
| chrX:17616901 | C | T | 1 | a0002c0002t0009g0015 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.566-70841C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17616901 | |||||||
| chrX:17617209 | G | A | 1 | a0002c0015t0001g0039 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.566-70533G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17617209 | |||||||
| chrX:17617485 | G | A | 5 | a0001c0001t0002g0086 a0001c0001t0005g0104 a0001c0001t0005g0111 others(2): Show |
5 | HG02622.hp2 HG02922.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-70257G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17617485 | |||||||
| chrX:17617757 | A | C | 1 | a0005c0005t0008g0097 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.566-69985A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17617757 | |||||||
| chrX:17618166 | T | C | 7 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0002g0086 others(4): Show |
7 | HG02622.hp2 HG02922.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.566-69576T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17618166 | |||||||
| chrX:17618757 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.566-68985A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17618757 | |||||||
| chrX:17618884 | T | C | 11 | a0001c0001t0001g0137 a0001c0001t0002g0100 a0001c0001t0002g0143 others(8): Show |
11 | HG01243.hp1 HG01258.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.566-68858T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17618884 | |||||||
| chrX:17618885 | C | T | 4 | a0001c0001t0007g0125 a0005c0005t0003g0101 a0005c0005t0003g0136 others(1): Show |
4 | HG01071.hp2 HG02055.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-68857C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17618885 | |||||||
| chrX:17619311 | ATCTCAGC others(725): Show |
A | 3 | a0001c0001t0002g0100 a0001c0001t0002g0143 a0010c0010t0003g0158 |
3 | HG01243.hp1 HG02723.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.566-68430_566-6769 others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17619311 | |||||||
| chrX:17619621 | T | C | 24 | a0001c0001t0001g0137 a0001c0001t0002g0002 a0001c0001t0002g0003 others(21): Show |
24 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.566-68121T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17619621 | |||||||
| chrX:17619661 | A | G | 1 | a0001c0003t0002g0155 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.566-68081A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17619661 | |||||||
| chrX:17619805 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.566-67937C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17619805 | |||||||
| chrX:17619959 | G | A | 4 | a0001c0001t0005g0104 a0001c0001t0005g0111 a0001c0003t0002g0102 others(1): Show |
4 | HG02622.hp2 HG02922.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-67783G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17619959 | |||||||
| chrX:17620033 | A | G | 2 | a0002c0002t0001g0018 a0002c0002t0001g0123 |
2 | HG00639.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.566-67709A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17620033 | |||||||
| chrX:17620044 | A | C | 3 | a0001c0001t0002g0100 a0001c0001t0002g0143 a0010c0010t0003g0158 |
3 | HG01243.hp1 HG02723.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.566-67698A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17620044 | |||||||
| chrX:17620596 | GA | G | 25 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0086 others(22): Show |
25 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.566-67133delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17620596 | ||||||
| chrX:17620750 | G | A | 1 | a0001c0001t0001g0008 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.566-66992G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17620750 | |||||||
| chrX:17620786 | G | C | 38 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0137 others(35): Show |
38 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.566-66956G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17620786 | |||||||
| chrX:17621619 | G | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.566-66123G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17621619 | |||||||
| chrX:17621788 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.566-65954G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17621788 | |||||||
| chrX:17622114 | C | T | 1 | a0001c0003t0002g0102 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.566-65628C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17622114 | |||||||
| chrX:17622130 | C | G | 6 | a0001c0003t0002g0014 a0001c0003t0002g0128 a0001c0003t0002g0142 others(3): Show |
6 | HG01258.hp1 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-65612C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17622130 | |||||||
| chrX:17622372 | G | A | 1 | a0002c0002t0001g0084 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.566-65370G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17622372 | |||||||
| chrX:17622937 | T | A | 2 | a0001c0001t0002g0093 a0001c0001t0002g0126 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.566-64805T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17622937 | |||||||
| chrX:17623019 | C | T | 1 | a0001c0001t0002g0096 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.566-64723C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17623019 | |||||||
| chrX:17623425 | C | T | 75 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0026 others(72): Show |
75 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.566-64317C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17623425 | |||||||
| chrX:17623910 | T | C | 1 | a0002c0002t0001g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.566-63832T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17623910 | |||||||
| chrX:17624370 | A | C | 4 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0051 others(1): Show |
4 | HG02071.hp1 NA18961.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-63372A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17624370 | |||||||
| chrX:17626249 | C | T | 1 | a0001c0001t0002g0096 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.566-61493C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17626249 | |||||||
| chrX:17626823 | C | T | 73 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0026 others(70): Show |
73 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.566-60919C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17626823 | |||||||
| chrX:17627175 | G | A | 1 | a0001c0001t0002g0120 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.566-60567G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17627175 | |||||||
| chrX:17627573 | C | T | 80 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0026 others(77): Show |
80 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.566-60169C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17627573 | |||||||
| chrX:17627635 | A | C | 1 | a0002c0002t0001g0091 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.566-60107A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17627635 | |||||||
| chrX:17627860 | C | T | 1 | a0002c0015t0001g0039 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.566-59882C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17627860 | |||||||
| chrX:17628066 | G | A | 2 | a0002c0002t0001g0034 a0002c0002t0001g0141 |
2 | HG03942.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.566-59676G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17628066 | |||||||
| chrX:17628314 | T | A | 1 | a0002c0002t0001g0076 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.566-59428T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17628314 | |||||||
| chrX:17628736 | C | A | 73 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0026 others(70): Show |
73 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.566-59006C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17628736 | |||||||
| chrX:17629922 | G | A | 20 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0086 others(17): Show |
20 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.566-57820G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17629922 | |||||||
| chrX:17630011 | C | T | 83 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0026 others(80): Show |
83 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.566-57731C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17630011 | |||||||
| chrX:17630045 | C | T | 25 | a0001c0001t0001g0066 a0001c0001t0001g0145 a0001c0001t0002g0002 others(22): Show |
25 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.566-57697C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17630045 | |||||||
| chrX:17630182 | G | T | 1 | a0001c0001t0006g0103 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.566-57560G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17630182 | |||||||
| chrX:17630481 | G | A | 78 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0026 others(75): Show |
78 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.566-57261G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17630481 | |||||||
| chrX:17630575 | C | G | 81 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0026 others(78): Show |
81 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.566-57167C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17630575 | |||||||
| chrX:17630638 | C | A | 1 | a0001c0001t0001g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.566-57104C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17630638 | |||||||
| chrX:17630946 | G | A | 2 | a0002c0002t0001g0077 a0002c0002t0001g0131 |
2 | HG02602.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.566-56796G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17630946 | |||||||
| chrX:17632082 | G | T | 15 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0093 others(12): Show |
15 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.566-55660G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17632082 | |||||||
| chrX:17632191 | T | C | 1 | a0002c0002t0001g0022 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.566-55551T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17632191 | |||||||
| chrX:17632263 | T | C | 62 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0026 others(59): Show |
62 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.566-55479T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17632263 | |||||||
| chrX:17632608 | CA | C | 76 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0026 others(73): Show |
76 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.566-55125delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17632608 | ||||||
| chrX:17633080 | G | GT | 10 | a0001c0001t0001g0041 a0001c0001t0001g0137 a0001c0001t0002g0086 others(7): Show |
10 | HG01258.hp1 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.566-54651dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17633080 | ||||||
| chrX:17633163 | A | G | 1 | a0008c0011t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.566-54579A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17633163 | |||||||
| chrX:17633233 | T | C | 1 | a0002c0002t0001g0109 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.566-54509T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17633233 | |||||||
| chrX:17633718 | G | C | 1 | a0006c0008t0001g0114 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.566-54024G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17633718 | |||||||
| chrX:17634658 | C | T | 1 | a0002c0002t0001g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.566-53084C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17634658 | |||||||
| chrX:17634771 | G | A | 3 | a0001c0001t0002g0116 a0001c0001t0007g0122 a0009c0016t0002g0119 |
3 | HG02615.hp2 HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.566-52971G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17634771 | |||||||
| chrX:17634826 | C | T | 73 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0026 others(70): Show |
73 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.566-52916C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17634826 | |||||||
| chrX:17634854 | C | T | 5 | a0001c0001t0001g0029 a0002c0002t0001g0022 a0002c0002t0001g0023 others(2): Show |
5 | HG02027.hp1 HG02083.hp1 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-52888C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17634854 | |||||||
| chrX:17635360 | C | A | 20 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0086 others(17): Show |
20 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.566-52382C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17635360 | |||||||
| chrX:17635422 | T | G | 1 | a0001c0001t0001g0068 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.566-52320T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17635422 | |||||||
| chrX:17635479 | C | G | 20 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0086 others(17): Show |
20 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.566-52263C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17635479 | |||||||
| chrX:17635660 | C | T | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.566-52082C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17635660 | |||||||
| chrX:17635668 | G | T | 3 | a0001c0001t0002g0116 a0001c0001t0007g0122 a0009c0016t0002g0119 |
3 | HG02615.hp2 HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.566-52074G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17635668 | |||||||
| chrX:17635940 | G | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.566-51802G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17635940 | |||||||
| chrX:17635943 | C | T | 1 | a0002c0002t0001g0047 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.566-51799C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17635943 | |||||||
| chrX:17635949 | T | C | 1 | a0001c0001t0002g0116 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.566-51793T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17635949 | |||||||
| chrX:17636169 | A | G | 1 | a0001c0001t0013g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.566-51573A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17636169 | |||||||
| chrX:17636511 | G | A | 1 | a0001c0003t0002g0155 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.566-51231G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17636511 | |||||||
| chrX:17636781 | G | A | 1 | a0001c0001t0013g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.566-50961G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17636781 | |||||||
| chrX:17636826 | A | G | 1 | a0005c0005t0008g0087 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.566-50916A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17636826 | |||||||
| chrX:17636855 | T | C | 1 | a0002c0002t0001g0046 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.566-50887T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17636855 | |||||||
| chrX:17636941 | C | A | 73 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0026 others(70): Show |
73 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.566-50801C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17636941 | |||||||
| chrX:17637070 | C | T | 1 | a0002c0002t0001g0032 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.566-50672C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17637070 | |||||||
| chrX:17637342 | G | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0051 others(1): Show |
4 | HG02071.hp1 NA18961.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-50400G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17637342 | |||||||
| chrX:17637660 | G | T | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.566-50082G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17637660 | |||||||
| chrX:17637680 | C | G | 8 | a0001c0001t0002g0086 a0001c0001t0002g0116 a0001c0001t0005g0104 others(5): Show |
8 | HG02615.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.566-50062C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17637680 | |||||||
| chrX:17638000 | A | G | 1 | a0002c0002t0001g0130 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.566-49742A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17638000 | |||||||
| chrX:17638289 | G | A | 1 | a0001c0003t0002g0155 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.566-49453G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17638289 | |||||||
| chrX:17638965 | G | A | 2 | a0002c0002t0001g0034 a0002c0002t0001g0141 |
2 | HG03942.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.566-48777G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17638965 | |||||||
| chrX:17639273 | T | G | 2 | a0001c0001t0002g0096 a0005c0005t0003g0117 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.566-48469T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17639273 | |||||||
| chrX:17639318 | C | A | 3 | a0001c0001t0002g0116 a0001c0001t0007g0122 a0009c0016t0002g0119 |
3 | HG02615.hp2 HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.566-48424C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17639318 | |||||||
| chrX:17639325 | A | G | 2 | a0001c0001t0001g0135 a0002c0002t0001g0010 |
2 | NA19067.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.566-48417A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17639325 | |||||||
| chrX:17640178 | G | A | 1 | a0005c0005t0003g0101 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.566-47564G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17640178 | |||||||
| chrX:17640263 | A | G | 2 | a0001c0001t0002g0044 a0001c0001t0002g0146 |
2 | HG01109.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.566-47479A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17640263 | |||||||
| chrX:17640823 | C | T | 1 | a0002c0002t0001g0040 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.566-46919C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17640823 | |||||||
| chrX:17641321 | C | T | 15 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0093 others(12): Show |
15 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.566-46421C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17641321 | |||||||
| chrX:17641370 | T | A | 1 | a0001c0001t0013g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.566-46372T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17641370 | |||||||
| chrX:17641702 | C | A | 1 | a0001c0001t0001g0144 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.566-46040C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17641702 | |||||||
| chrX:17641762 | TA | T | 25 | a0001c0001t0001g0029 a0001c0001t0001g0041 a0001c0001t0001g0095 others(22): Show |
25 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.566-45967delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17641762 | ||||||
| chrX:17641848 | G | C | 3 | a0001c0001t0002g0116 a0001c0001t0007g0122 a0009c0016t0002g0119 |
3 | HG02615.hp2 HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.566-45894G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17641848 | |||||||
| chrX:17642497 | A | G | 26 | a0001c0001t0001g0112 a0001c0001t0001g0137 a0001c0001t0002g0002 others(23): Show |
26 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.566-45245A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17642497 | |||||||
| chrX:17642655 | C | A | 1 | a0002c0002t0001g0130 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.566-45087C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17642655 | |||||||
| chrX:17643258 | C | T | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.566-44484C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17643258 | |||||||
| chrX:17643264 | T | A | 2 | a0002c0002t0001g0007 a0002c0002t0001g0040 |
2 | HG01167.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.566-44478T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17643264 | |||||||
| chrX:17643322 | G | A | 5 | a0001c0001t0002g0086 a0001c0001t0005g0104 a0001c0001t0005g0111 others(2): Show |
5 | HG02622.hp2 HG02922.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-44420G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17643322 | |||||||
| chrX:17643596 | C | G | 1 | a0002c0002t0001g0020 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.566-44146C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17643596 | |||||||
| chrX:17644517 | C | T | 1 | a0002c0002t0001g0033 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.566-43225C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17644517 | |||||||
| chrX:17645633 | A | G | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.566-42109A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17645633 | |||||||
| chrX:17646663 | T | C | 1 | a0002c0002t0001g0053 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.566-41079T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17646663 | |||||||
| chrX:17646918 | G | A | 1 | a0002c0002t0001g0091 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.566-40824G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17646918 | |||||||
| chrX:17647047 | A | AT | 5 | a0001c0001t0002g0086 a0001c0001t0005g0104 a0001c0001t0005g0111 others(2): Show |
5 | HG02622.hp2 HG02922.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-40688dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17647047 | ||||||
| chrX:17647649 | C | T | 2 | a0001c0001t0002g0044 a0001c0001t0002g0146 |
2 | HG01109.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.566-40093C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17647649 | |||||||
| chrX:17647947 | C | T | 5 | a0001c0001t0002g0086 a0001c0001t0005g0104 a0001c0001t0005g0111 others(2): Show |
5 | HG02622.hp2 HG02922.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-39795C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17647947 | |||||||
| chrX:17647948 | G | A | 5 | a0002c0002t0001g0019 a0002c0002t0001g0025 a0002c0002t0001g0030 others(2): Show |
5 | HG00642.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.566-39794G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17647948 | |||||||
| chrX:17647980 | CT | C | 73 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0026 others(70): Show |
73 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.566-39750delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17647980 | ||||||
| chrX:17648432 | C | A | 1 | a0002c0002t0001g0139 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.566-39310C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17648432 | |||||||
| chrX:17649637 | G | A | 15 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0093 others(12): Show |
15 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.566-38105G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17649637 | |||||||
| chrX:17650046 | C | A | 1 | a0001c0001t0001g0041 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.566-37696C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17650046 | |||||||
| chrX:17650512 | T | C | 1 | a0002c0002t0001g0032 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.566-37230T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17650512 | |||||||
| chrX:17650922 | T | A | 61 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0026 others(58): Show |
61 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.566-36820T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17650922 | |||||||
| chrX:17651232 | G | A | 8 | a0001c0001t0002g0086 a0001c0001t0002g0116 a0001c0001t0005g0104 others(5): Show |
8 | HG02615.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.566-36510G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17651232 | |||||||
| chrX:17651243 | TAGA | T | 15 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0093 others(12): Show |
15 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.566-36493_566-3649 others(7): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17651243 | ||||||
| chrX:17651394 | T | G | 1 | a0012c0013t0001g0038 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.566-36348T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17651394 | |||||||
| chrX:17651589 | G | A | 2 | a0002c0002t0001g0031 a0002c0002t0001g0078 |
2 | HG01099.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.566-36153G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17651589 | |||||||
| chrX:17651660 | C | G | 1 | a0001c0001t0002g0121 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.566-36082C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17651660 | |||||||
| chrX:17651918 | T | G | 1 | a0005c0005t0008g0087 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.566-35824T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17651918 | |||||||
| chrX:17652078 | C | G | 1 | a0001c0001t0002g0121 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.566-35664C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17652078 | |||||||
| chrX:17652273 | G | A | 1 | a0001c0001t0004g0058 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.566-35469G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17652273 | |||||||
| chrX:17652401 | T | A | 16 | a0001c0001t0001g0112 a0001c0001t0002g0002 a0001c0001t0002g0003 others(13): Show |
16 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.566-35341T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17652401 | |||||||
| chrX:17652417 | G | T | 1 | a0002c0002t0001g0072 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.566-35325G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17652417 | |||||||
| chrX:17653576 | T | C | 1 | a0002c0002t0001g0043 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.566-34166T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17653576 | |||||||
| chrX:17653918 | C | T | 2 | a0002c0002t0001g0017 a0002c0002t0001g0075 |
2 | HG01358.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.566-33824C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17653918 | |||||||
| chrX:17654486 | A | G | 1 | a0002c0002t0001g0018 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.566-33256A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17654486 | |||||||
| chrX:17655116 | C | T | 3 | a0001c0001t0002g0116 a0001c0001t0007g0122 a0009c0016t0002g0119 |
3 | HG02615.hp2 HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.566-32626C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17655116 | |||||||
| chrX:17655379 | A | G | 1 | a0002c0002t0001g0123 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.566-32363A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17655379 | |||||||
| chrX:17655390 | A | G | 1 | a0002c0002t0001g0033 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.566-32352A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17655390 | |||||||
| chrX:17655570 | G | T | 10 | a0001c0001t0001g0066 a0001c0001t0001g0145 a0001c0001t0006g0074 others(7): Show |
10 | HG00639.hp2 HG01952.hp1 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.566-32172G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17655570 | |||||||
| chrX:17655703 | A | G | 10 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0002g0086 others(7): Show |
10 | HG02615.hp2 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.566-32039A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17655703 | |||||||
| chrX:17655872 | A | C | 2 | a0001c0001t0001g0026 a0002c0002t0001g0013 |
2 | HG00408.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.566-31870A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17655872 | |||||||
| chrX:17655993 | A | AG | 162 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0021 others(159): Show |
162 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.566-31747dupG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17655993 | ||||||
| chrX:17655994 | G | GA | 2 | a0002c0002t0001g0088 a0002c0002t0001g0089 |
2 | NA18945.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.566-31748_566-3174 others(5): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17655994 | |||||||
| chrX:17656482 | C | T | 1 | a0002c0002t0001g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.566-31260C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17656482 | |||||||
| chrX:17656728 | C | T | 73 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0026 others(70): Show |
73 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.566-31014C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17656728 | |||||||
| chrX:17659229 | G | T | 1 | a0002c0002t0001g0009 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.566-28513G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17659229 | |||||||
| chrX:17659683 | A | T | 83 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0026 others(80): Show |
83 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.566-28059A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17659683 | |||||||
| chrX:17659759 | C | T | 2 | a0003c0009t0002g0160 a0006c0008t0002g0113 |
2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.566-27983C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17659759 | |||||||
| chrX:17659909 | C | T | 1 | a0001c0001t0010g0059 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.566-27833C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17659909 | |||||||
| chrX:17660000 | T | C | 1 | a0002c0002t0001g0067 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.566-27742T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17660000 | |||||||
| chrX:17660147 | G | A | 75 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0026 others(72): Show |
75 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.566-27595G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17660147 | |||||||
| chrX:17660168 | C | T | 1 | a0002c0002t0001g0079 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.566-27574C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17660168 | |||||||
| chrX:17660346 | C | T | 15 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0035 others(12): Show |
15 | HG00408.hp2 HG00609.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.566-27396C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17660346 | |||||||
| chrX:17660374 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.566-27368C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17660374 | |||||||
| chrX:17660660 | A | G | 1 | a0001c0001t0011g0081 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.566-27082A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17660660 | |||||||
| chrX:17660995 | A | G | 2 | a0003c0009t0002g0160 a0006c0008t0002g0113 |
2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.566-26747A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17660995 | |||||||
| chrX:17661229 | A | G | 5 | a0001c0001t0002g0086 a0001c0001t0005g0104 a0001c0001t0005g0111 others(2): Show |
5 | HG02622.hp2 HG02922.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-26513A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17661229 | |||||||
| chrX:17661448 | C | T | 3 | a0001c0001t0002g0116 a0001c0001t0007g0122 a0009c0016t0002g0119 |
3 | HG02615.hp2 HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.566-26294C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17661448 | |||||||
| chrX:17661761 | C | T | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.566-25981C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17661761 | |||||||
| chrX:17661883 | G | A | 25 | a0001c0001t0001g0137 a0001c0001t0002g0002 a0001c0001t0002g0003 others(22): Show |
25 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.566-25859G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17661883 | |||||||
| chrX:17662034 | C | T | 1 | a0002c0002t0001g0046 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.566-25708C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17662034 | |||||||
| chrX:17662331 | T | C | 1 | a0002c0002t0001g0072 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.566-25411T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17662331 | |||||||
| chrX:17663168 | A | G | 2 | a0001c0001t0012g0154 a0005c0005t0008g0087 |
2 | HG01975.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.566-24574A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17663168 | |||||||
| chrX:17663492 | A | T | 4 | a0001c0001t0007g0125 a0005c0005t0003g0117 a0005c0005t0003g0136 others(1): Show |
4 | HG01071.hp2 HG02647.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-24250A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17663492 | |||||||
| chrX:17664246 | A | T | 1 | a0002c0002t0001g0082 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.566-23496A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17664246 | |||||||
| chrX:17664341 | A | G | 2 | a0001c0001t0002g0093 a0001c0001t0002g0126 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.566-23401A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17664341 | |||||||
| chrX:17664701 | C | G | 57 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0026 others(54): Show |
57 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.566-23041C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17664701 | |||||||
| chrX:17665042 | A | G | 1 | a0004c0004t0001g0132 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.566-22700A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17665042 | |||||||
| chrX:17665093 | A | T | 5 | a0001c0001t0002g0086 a0001c0001t0005g0104 a0001c0001t0005g0111 others(2): Show |
5 | HG02622.hp2 HG02922.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-22649A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17665093 | |||||||
| chrX:17665304 | T | C | 1 | a0002c0002t0001g0067 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.566-22438T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17665304 | |||||||
| chrX:17665318 | A | AT | 38 | a0001c0001t0001g0029 a0001c0001t0001g0048 a0001c0001t0001g0098 others(35): Show |
38 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.566-22396dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17665318 | ||||||
| chrX:17665318 | A | ATT | 7 | a0001c0001t0001g0112 a0001c0001t0002g0086 a0001c0001t0002g0121 others(4): Show |
7 | HG00642.hp1 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.566-22397_566-2239 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17665318 | ||||||
| chrX:17665318 | A | ATTT | 5 | a0001c0001t0002g0002 a0001c0001t0002g0107 a0001c0001t0002g0110 others(2): Show |
5 | HG01358.hp1 HG02293.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-22398_566-2239 others(7): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17665318 | ||||||
| chrX:17665318 | AT | A | 49 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0026 others(46): Show |
49 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.566-22396delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17665318 | ||||||
| chrX:17665536 | C | T | 21 | a0001c0001t0001g0112 a0001c0001t0002g0002 a0001c0001t0002g0003 others(18): Show |
21 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.566-22206C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17665536 | |||||||
| chrX:17665801 | T | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0051 |
2 | NA18961.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.566-21941T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17665801 | |||||||
| chrX:17666420 | G | GTATT | 24 | a0001c0001t0001g0112 a0001c0001t0002g0002 a0001c0001t0002g0003 others(21): Show |
24 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.566-21320_566-2131 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17666420 | ||||||
| chrX:17666654 | GTGAA | G | 23 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0086 others(20): Show |
23 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.566-21068_566-2106 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17666654 | ||||||
| chrX:17666703 | A | G | 24 | a0001c0001t0001g0112 a0001c0001t0002g0002 a0001c0001t0002g0003 others(21): Show |
24 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.566-21039A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17666703 | |||||||
| chrX:17666751 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.566-20991T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17666751 | |||||||
| chrX:17666774 | T | G | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.566-20968T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17666774 | |||||||
| chrX:17666830 | G | A | 15 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0093 others(12): Show |
15 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.566-20912G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17666830 | |||||||
| chrX:17667578 | C | A | 1 | a0003c0006t0001g0157 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.566-20164C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17667578 | |||||||
| chrX:17667678 | T | C | 2 | a0001c0001t0012g0154 a0005c0005t0008g0087 |
2 | HG01975.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.566-20064T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17667678 | |||||||
| chrX:17667731 | G | T | 10 | a0001c0001t0002g0096 a0001c0001t0002g0100 a0001c0001t0002g0143 others(7): Show |
10 | HG01243.hp1 HG01258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.566-20011G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17667731 | |||||||
| chrX:17667939 | A | AT | 22 | a0001c0001t0001g0137 a0001c0001t0002g0002 a0001c0001t0002g0003 others(19): Show |
22 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.566-19794dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17667939 | ||||||
| chrX:17668088 | T | TA | 6 | a0001c0001t0001g0153 a0002c0002t0001g0009 a0002c0002t0001g0030 others(3): Show |
6 | HG01433.hp1 HG01928.hp1 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-19631dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17668088 | ||||||
| chrX:17668088 | TA | T | 18 | a0001c0001t0001g0135 a0001c0001t0002g0086 a0001c0001t0002g0096 others(15): Show |
18 | HG00639.hp1 HG01074.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.566-19631delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17668088 | ||||||
| chrX:17668088 | TAA | T | 23 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0137 others(20): Show |
23 | HG01071.hp1 HG01106.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.566-19632_566-1963 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17668088 | ||||||
| chrX:17668089 | A | T | 1 | a0001c0001t0001g0083 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.566-19653A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17668089 | |||||||
| chrX:17668313 | C | CA | 8 | a0001c0001t0002g0086 a0001c0001t0005g0104 a0001c0001t0005g0111 others(5): Show |
8 | HG02602.hp1 HG02622.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.566-19420dupA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17668313 | ||||||
| chrX:17668724 | T | A | 16 | a0001c0001t0001g0112 a0001c0001t0002g0002 a0001c0001t0002g0003 others(13): Show |
16 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.566-19018T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17668724 | |||||||
| chrX:17668810 | G | A | 3 | a0002c0002t0001g0088 a0002c0002t0001g0089 a0002c0002t0001g0090 |
3 | HG02129.hp1 NA18945.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.566-18932G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17668810 | |||||||
| chrX:17668919 | G | A | 1 | a0002c0002t0001g0032 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.566-18823G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17668919 | |||||||
| chrX:17669180 | A | G | 5 | a0001c0001t0002g0086 a0001c0001t0005g0104 a0001c0001t0005g0111 others(2): Show |
5 | HG02622.hp2 HG02922.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-18562A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17669180 | |||||||
| chrX:17669466 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.566-18276T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17669466 | |||||||
| chrX:17669647 | G | A | 1 | a0002c0002t0001g0032 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.566-18095G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17669647 | |||||||
| chrX:17670910 | C | A | 1 | a0001c0001t0013g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.566-16832C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17670910 | |||||||
| chrX:17671302 | C | A | 3 | a0002c0002t0001g0019 a0002c0002t0001g0030 a0002c0002t0001g0152 |
3 | HG00642.hp1 HG01928.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.566-16440C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17671302 | |||||||
| chrX:17671394 | C | T | 1 | a0002c0002t0001g0030 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.566-16348C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17671394 | |||||||
| chrX:17671958 | G | A | 3 | a0001c0001t0002g0116 a0001c0001t0007g0122 a0009c0016t0002g0119 |
3 | HG02615.hp2 HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.566-15784G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17671958 | |||||||
| chrX:17672680 | C | G | 3 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0126 |
3 | HG01069.hp1 HG01071.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.566-15062C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17672680 | |||||||
| chrX:17673145 | G | GT | 4 | a0002c0002t0001g0006 a0002c0002t0001g0031 a0002c0002t0001g0042 others(1): Show |
4 | HG01099.hp1 HG02293.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-14596dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17673145 | ||||||
| chrX:17673175 | GA | G | 3 | a0001c0001t0001g0048 a0002c0002t0001g0023 a0002c0002t0001g0152 |
3 | HG00642.hp1 HG02083.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.566-14564delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17673175 | ||||||
| chrX:17673177 | A | AAC | 13 | a0001c0001t0001g0061 a0001c0001t0001g0073 a0001c0001t0001g0083 others(10): Show |
13 | HG00639.hp2 HG01071.hp2 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.566-14505_566-1450 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17673177 | ||||||
| chrX:17673177 | A | AACACACA others(1): Show |
3 | a0001c0001t0007g0122 a0002c0002t0001g0025 a0002c0002t0001g0076 |
3 | HG02615.hp2 HG04228.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.566-14511_566-1450 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17673177 | ||||||
| chrX:17673177 | A | AACACACA others(9): Show |
1 | a0001c0001t0002g0116 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.566-14519_566-1450 others(20): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17673177 | ||||||
| chrX:17673177 | AAC | A | 33 | a0001c0001t0001g0008 a0001c0001t0001g0094 a0001c0001t0001g0095 others(30): Show |
33 | HG01099.hp1 HG01192.hp1 HG01256.hp1 others(30): Show |
intron_variant | MODIFIER | c.566-14505_566-1450 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17673177 | ||||||
| chrX:17673177 | AACAC | A | 16 | a0001c0001t0001g0066 a0001c0001t0001g0068 a0001c0001t0001g0137 others(13): Show |
16 | HG00639.hp1 HG01074.hp1 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.566-14507_566-1450 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17673177 | ||||||
| chrX:17673177 | AACACAC | A | 13 | a0001c0001t0001g0050 a0001c0001t0002g0093 a0001c0001t0002g0120 others(10): Show |
13 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.566-14509_566-1450 others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17673177 | ||||||
| chrX:17673177 | AACACACA others(1): Show |
A | 14 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0096 others(11): Show |
14 | HG01243.hp1 HG01258.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.566-14511_566-1450 others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17673177 | ||||||
| chrX:17673177 | AACACACA others(3): Show |
A | 2 | a0001c0001t0002g0107 a0005c0005t0008g0087 |
2 | HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.566-14513_566-1450 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17673177 | ||||||
| chrX:17673177 | AACACACA others(5): Show |
A | 4 | a0002c0002t0001g0007 a0002c0002t0001g0034 a0002c0002t0001g0141 others(1): Show |
4 | HG01515.hp1 HG02257.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-14515_566-1450 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17673177 | ||||||
| chrX:17673177 | AACACACA others(7): Show |
A | 1 | a0001c0001t0013g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.566-14517_566-1450 others(18): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17673177 | ||||||
| chrX:17673177 | AACACACA others(9): Show |
A | 1 | a0001c0001t0001g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.566-14519_566-1450 others(20): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17673177 | ||||||
| chrX:17673177 | AACACACA others(11): Show |
A | 2 | a0001c0001t0001g0144 a0002c0002t0001g0019 |
2 | HG01975.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.566-14521_566-1450 others(22): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17673177 | ||||||
| chrX:17673177 | AACACACA others(15): Show |
A | 1 | a0001c0001t0001g0037 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.566-14525_566-1450 others(26): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17673177 | ||||||
| chrX:17673177 | AACACACA others(17): Show |
A | 30 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0026 others(27): Show |
30 | HG00280.hp1 HG00408.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.566-14527_566-1450 others(28): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17673177 | ||||||
| chrX:17673237 | C | A | 1 | a0001c0001t0006g0103 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.566-14505C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17673237 | |||||||
| chrX:17673237 | C | CACACACA others(3): Show |
1 | a0002c0002t0001g0130 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.566-14504_566-1450 others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17673237 | ||||||
| chrX:17673237 | C | CACAG | 2 | a0002c0002t0001g0046 a0002c0002t0001g0054 |
2 | HG00140.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.566-14504_566-1450 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17673237 | ||||||
| chrX:17673237 | C | G | 23 | a0001c0001t0001g0050 a0001c0001t0012g0154 a0002c0002t0001g0006 others(20): Show |
23 | HG00639.hp1 HG01074.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.566-14505C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17673237 | |||||||
| chrX:17673429 | C | T | 3 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0126 |
3 | HG01069.hp1 HG01071.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.566-14313C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17673429 | |||||||
| chrX:17673476 | G | A | 5 | a0004c0004t0001g0055 a0004c0004t0001g0065 a0004c0004t0001g0132 others(2): Show |
5 | HG01952.hp1 NA18948.hp1 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-14266G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17673476 | |||||||
| chrX:17674031 | C | T | 85 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0026 others(82): Show |
85 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.566-13711C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17674031 | |||||||
| chrX:17674142 | C | G | 1 | a0008c0011t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.566-13600C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17674142 | |||||||
| chrX:17674784 | G | C | 1 | a0001c0001t0002g0003 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.566-12958G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17674784 | |||||||
| chrX:17675626 | C | T | 75 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0026 others(72): Show |
75 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.566-12116C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17675626 | |||||||
| chrX:17675929 | A | G | 3 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0126 |
3 | HG01069.hp1 HG01071.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.566-11813A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17675929 | |||||||
| chrX:17676009 | A | G | 10 | a0001c0001t0002g0096 a0001c0001t0002g0100 a0001c0001t0002g0143 others(7): Show |
10 | HG01243.hp1 HG01258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.566-11733A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17676009 | |||||||
| chrX:17676293 | T | C | 1 | a0002c0002t0001g0013 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.566-11449T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17676293 | |||||||
| chrX:17676788 | C | T | 2 | a0002c0002t0001g0064 a0002c0002t0001g0148 |
2 | NA19012.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.566-10954C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17676788 | |||||||
| chrX:17677043 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.566-10699C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17677043 | |||||||
| chrX:17677070 | C | A | 58 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0026 others(55): Show |
58 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.566-10672C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17677070 | |||||||
| chrX:17677621 | C | G | 1 | a0005c0005t0008g0087 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.566-10121C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17677621 | |||||||
| chrX:17677978 | T | TTTGTTG | 5 | a0001c0001t0001g0112 a0001c0001t0002g0003 a0001c0001t0002g0093 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-9743_566-9738d others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17677978 | ||||||
| chrX:17678293 | T | A | 3 | a0001c0001t0001g0041 a0001c0001t0012g0154 a0002c0002t0009g0015 |
3 | HG01975.hp1 HG02257.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.566-9449T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17678293 | |||||||
| chrX:17678293 | T | TGA | 12 | a0001c0001t0001g0051 a0001c0001t0001g0112 a0001c0001t0001g0137 others(9): Show |
12 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.566-9426_566-9425d others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17678293 | ||||||
| chrX:17678293 | T | TGAGA | 7 | a0001c0001t0002g0002 a0001c0001t0002g0106 a0001c0001t0002g0107 others(4): Show |
7 | HG02145.hp1 HG02258.hp1 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.566-9428_566-9425d others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17678293 | ||||||
| chrX:17678293 | T | TGTGA | 6 | a0001c0001t0002g0086 a0001c0001t0005g0104 a0001c0001t0005g0111 others(3): Show |
6 | HG02622.hp2 HG02922.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-9448_566-9447i others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17678293 | ||||||
| chrX:17678440 | T | G | 1 | a0001c0001t0013g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.566-9302T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17678440 | |||||||
| chrX:17678888 | CT | C | 17 | a0001c0001t0001g0112 a0001c0001t0002g0002 a0001c0001t0002g0003 others(14): Show |
17 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.566-8853delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17678888 | |||||||
| chrX:17679228 | A | T | 1 | a0001c0001t0001g0066 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.566-8514A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17679228 | |||||||
| chrX:17679359 | A | G | 2 | a0001c0001t0002g0093 a0001c0001t0002g0126 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.566-8383A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17679359 | |||||||
| chrX:17679399 | A | G | 1 | a0002c0002t0001g0007 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.566-8343A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17679399 | |||||||
| chrX:17679859 | A | AG | 18 | a0001c0001t0001g0137 a0001c0001t0001g0144 a0001c0001t0013g0045 others(15): Show |
18 | HG00140.hp1 HG01928.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.566-7872dupG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17679859 | ||||||
| chrX:17679859 | AG | A | 51 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0035 others(48): Show |
51 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.566-7872delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17679859 | ||||||
| chrX:17679863 | G | C | 2 | a0001c0001t0001g0127 a0003c0006t0001g0162 |
2 | HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.566-7879G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17679863 | |||||||
| chrX:17680277 | A | G | 62 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0026 others(59): Show |
62 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.566-7465A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17680277 | |||||||
| chrX:17680693 | C | T | 1 | a0001c0003t0002g0014 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.566-7049C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17680693 | |||||||
| chrX:17680896 | G | A | 1 | a0002c0002t0001g0131 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.566-6846G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17680896 | |||||||
| chrX:17681040 | TG | T | 2 | a0005c0005t0003g0136 a0007c0014t0003g0092 |
2 | HG01071.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.566-6700delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17681040 | ||||||
| chrX:17681385 | C | A | 55 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0026 others(52): Show |
55 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.566-6357C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17681385 | |||||||
| chrX:17681396 | A | G | 1 | a0002c0002t0001g0077 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.566-6346A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17681396 | |||||||
| chrX:17681714 | C | A | 75 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0026 others(72): Show |
75 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.566-6028C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17681714 | |||||||
| chrX:17681789 | C | G | 5 | a0002c0002t0001g0019 a0002c0002t0001g0025 a0002c0002t0001g0030 others(2): Show |
5 | HG00642.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.566-5953C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17681789 | |||||||
| chrX:17682137 | C | T | 16 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0093 others(13): Show |
16 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.566-5605C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17682137 | |||||||
| chrX:17682266 | A | C | 22 | a0001c0001t0001g0112 a0001c0001t0002g0002 a0001c0001t0002g0003 others(19): Show |
22 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.566-5476A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17682266 | |||||||
| chrX:17682406 | G | T | 1 | a0002c0002t0001g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.566-5336G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17682406 | |||||||
| chrX:17682695 | A | G | 4 | a0001c0001t0004g0163 a0002c0002t0001g0004 a0002c0002t0001g0053 others(1): Show |
4 | HG01261.hp1 NA18953.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-5047A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17682695 | |||||||
| chrX:17682912 | C | G | 85 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0026 others(82): Show |
85 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.566-4830C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17682912 | |||||||
| chrX:17682938 | C | G | 5 | a0001c0001t0002g0002 a0001c0001t0002g0106 a0001c0001t0002g0107 others(2): Show |
5 | HG02258.hp1 HG02293.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-4804C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17682938 | |||||||
| chrX:17683001 | T | C | 22 | a0001c0001t0001g0112 a0001c0001t0001g0137 a0001c0001t0002g0002 others(19): Show |
22 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.566-4741T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17683001 | |||||||
| chrX:17683229 | G | C | 1 | a0002c0002t0001g0138 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.566-4513G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17683229 | |||||||
| chrX:17683552 | G | C | 1 | a0002c0002t0001g0009 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.566-4190G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17683552 | |||||||
| chrX:17683797 | C | T | 1 | a0001c0001t0004g0163 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.566-3945C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17683797 | |||||||
| chrX:17684245 | A | C | 3 | a0002c0002t0001g0088 a0002c0002t0001g0089 a0002c0002t0001g0156 |
3 | NA18945.hp1 NA19009.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.566-3497A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17684245 | |||||||
| chrX:17684886 | T | C | 2 | a0001c0001t0001g0029 a0002c0002t0001g0036 |
2 | NA18940.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.566-2856T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17684886 | |||||||
| chrX:17685166 | C | T | 7 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0002g0086 others(4): Show |
7 | HG02622.hp2 HG02717.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.566-2576C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17685166 | |||||||
| chrX:17685486 | C | T | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.566-2256C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17685486 | |||||||
| chrX:17685599 | CT | C | 13 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0044 others(10): Show |
13 | HG01069.hp1 HG01071.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.566-2134delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 17685599 | ||||||
| chrX:17686309 | C | G | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.566-1433C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17686309 | |||||||
| chrX:17686519 | A | G | 1 | a0002c0002t0001g0046 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.566-1223A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17686519 | |||||||
| chrX:17687592 | T | C | 3 | a0001c0001t0002g0116 a0001c0001t0007g0122 a0009c0016t0002g0119 |
3 | HG02615.hp2 HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.566-150T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | chrX | 17687592 | |||||||
| chrX:17687925 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0056 |
2 | NA18988.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.718+31G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | chrX | 17687925 | |||||||
| chrX:17688057 | A | C | 1 | a0001c0001t0001g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.718+163A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | chrX | 17688057 | |||||||
| chrX:17688882 | T | A | 32 | a0001c0001t0001g0066 a0001c0001t0001g0112 a0001c0001t0001g0137 others(29): Show |
32 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.718+988T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | chrX | 17688882 | |||||||
| chrX:17689034 | C | A | 1 | a0002c0002t0001g0108 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.718+1140C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | chrX | 17689034 | |||||||
| chrX:17689309 | A | G | 2 | a0002c0002t0001g0042 a0002c0002t0001g0139 |
2 | HG00673.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.718+1415A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | chrX | 17689309 | |||||||
| chrX:17689329 | T | A | 1 | a0008c0011t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.718+1435T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | chrX | 17689329 | |||||||
| chrX:17689761 | C | T | 28 | a0001c0001t0001g0066 a0001c0001t0001g0145 a0001c0001t0002g0002 others(25): Show |
28 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.718+1867C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | chrX | 17689761 | |||||||
| chrX:17690643 | A | T | 1 | a0001c0001t0006g0103 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.719-1692A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | chrX | 17690643 | |||||||
| chrX:17690682 | A | T | 1 | a0001c0001t0006g0103 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.719-1653A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | chrX | 17690682 | |||||||
| chrX:17690765 | A | T | 1 | a0008c0011t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.719-1570A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | chrX | 17690765 | |||||||
| chrX:17691125 | T | C | 1 | a0002c0002t0001g0043 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.719-1210T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | chrX | 17691125 | |||||||
| chrX:17691246 | C | A | 1 | a0002c0002t0001g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.719-1089C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | chrX | 17691246 | |||||||
| chrX:17691258 | T | G | 1 | a0001c0001t0012g0154 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.719-1077T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | chrX | 17691258 | |||||||
| chrX:17691419 | A | G | 1 | a0001c0001t0001g0037 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.719-916A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | chrX | 17691419 | |||||||
| chrX:17691706 | A | G | 85 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0026 others(82): Show |
85 | HG00609.hp1 HG00639.hp2 HG01069.hp1 others(82): Show |
intron_variant | MODIFIER | c.719-629A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | chrX | 17691706 | |||||||
| chrX:17691743 | A | G | 1 | a0002c0002t0001g0040 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.719-592A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | chrX | 17691743 | |||||||
| chrX:17691842 | G | C | 1 | a0001c0003t0002g0014 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.719-493G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | chrX | 17691842 | |||||||
| chrX:17691936 | G | A | 1 | a0001c0001t0002g0121 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.719-399G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | chrX | 17691936 | |||||||
| chrX:17692027 | A | G | 1 | a0002c0002t0001g0009 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.719-308A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | chrX | 17692027 | |||||||
| chrX:17692233 | CT | C | 54 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0026 others(51): Show |
54 | HG00609.hp1 HG01071.hp2 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.719-88delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 17692233 | ||||||
| chrX:17692233 | CTT | C | 24 | a0001c0001t0001g0066 a0001c0001t0001g0145 a0001c0001t0002g0002 others(21): Show |
24 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.719-89_719-88delTT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 17692233 | ||||||
| chrX:17692899 | A | G | 85 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0026 others(82): Show |
85 | HG00609.hp1 HG00639.hp2 HG01069.hp1 others(82): Show |
intron_variant | MODIFIER | c.852+431A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17692899 | |||||||
| chrX:17693406 | G | A | 1 | a0001c0001t0002g0100 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.852+938G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17693406 | |||||||
| chrX:17693596 | C | T | 3 | a0001c0001t0013g0045 a0005c0005t0008g0087 a0010c0010t0003g0158 |
3 | HG02723.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.852+1128C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17693596 | |||||||
| chrX:17693736 | G | A | 3 | a0001c0001t0002g0116 a0001c0001t0007g0122 a0009c0016t0002g0119 |
3 | HG02615.hp2 HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.852+1268G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17693736 | |||||||
| chrX:17694125 | C | T | 3 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0008c0011t0002g0147 |
3 | HG02257.hp2 HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.852+1657C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17694125 | |||||||
| chrX:17694481 | G | C | 51 | a0001c0001t0001g0066 a0001c0001t0001g0094 a0001c0001t0001g0095 others(48): Show |
51 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.852+2013G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17694481 | |||||||
| chrX:17694931 | T | C | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.852+2463T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17694931 | |||||||
| chrX:17695079 | T | A | 2 | a0001c0001t0006g0074 a0001c0001t0006g0103 |
2 | NA18955.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.852+2611T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17695079 | |||||||
| chrX:17695100 | C | G | 1 | a0001c0001t0013g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.852+2632C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17695100 | |||||||
| chrX:17695474 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.852+3006G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17695474 | |||||||
| chrX:17695942 | A | G | 3 | a0002c0002t0001g0018 a0002c0002t0001g0123 a0002c0015t0001g0039 |
3 | HG00639.hp1 HG01074.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.852+3474A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17695942 | |||||||
| chrX:17695942 | AG | A | 34 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0044 others(31): Show |
34 | HG01069.hp1 HG01071.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.852+3483delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17695942 | ||||||
| chrX:17695949 | G | A | 1 | a0002c0002t0001g0077 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.852+3481G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17695949 | |||||||
| chrX:17695951 | G | T | 1 | a0002c0002t0001g0046 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.852+3483G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17695951 | |||||||
| chrX:17695983 | C | G | 1 | a0001c0003t0002g0128 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.852+3515C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17695983 | |||||||
| chrX:17696221 | C | T | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.852+3753C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17696221 | |||||||
| chrX:17696344 | G | A | 1 | a0001c0001t0004g0071 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.852+3876G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17696344 | |||||||
| chrX:17696417 | T | G | 161 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0021 others(158): Show |
161 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.852+3949T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17696417 | |||||||
| chrX:17696491 | G | C | 1 | a0001c0001t0013g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.852+4023G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17696491 | |||||||
| chrX:17697106 | C | G | 3 | a0001c0001t0001g0021 a0001c0001t0001g0124 a0001c0001t0010g0059 |
3 | HG01943.hp1 HG02135.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.852+4638C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17697106 | |||||||
| chrX:17697444 | G | A | 30 | a0001c0001t0001g0112 a0001c0001t0002g0002 a0001c0001t0002g0003 others(27): Show |
30 | HG01069.hp1 HG01071.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.852+4976G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17697444 | |||||||
| chrX:17697771 | A | C | 2 | a0001c0001t0007g0122 a0001c0001t0007g0125 |
2 | HG02615.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.852+5303A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17697771 | |||||||
| chrX:17697844 | T | C | 1 | a0008c0011t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.852+5376T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17697844 | |||||||
| chrX:17698059 | G | C | 1 | a0010c0010t0003g0158 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.852+5591G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17698059 | |||||||
| chrX:17698071 | A | G | 3 | a0001c0001t0005g0104 a0001c0001t0005g0111 a0003c0006t0005g0159 |
3 | HG02622.hp2 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.852+5603A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17698071 | |||||||
| chrX:17698374 | G | A | 31 | a0001c0001t0001g0112 a0001c0001t0002g0002 a0001c0001t0002g0003 others(28): Show |
31 | HG01069.hp1 HG01071.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.852+5906G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17698374 | |||||||
| chrX:17698584 | T | C | 27 | a0001c0001t0001g0112 a0001c0001t0001g0137 a0001c0001t0002g0002 others(24): Show |
27 | HG01069.hp1 HG01071.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.852+6116T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17698584 | |||||||
| chrX:17699010 | A | G | 2 | a0001c0001t0007g0122 a0001c0001t0007g0125 |
2 | HG02615.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.852+6542A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17699010 | |||||||
| chrX:17699265 | A | G | 1 | a0001c0003t0002g0102 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.852+6797A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17699265 | |||||||
| chrX:17699539 | T | A | 1 | a0001c0001t0001g0050 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.852+7071T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17699539 | |||||||
| chrX:17699607 | A | C | 1 | a0008c0011t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.852+7139A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17699607 | |||||||
| chrX:17700272 | G | A | 1 | a0002c0002t0001g0079 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.852+7804G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17700272 | |||||||
| chrX:17700507 | G | T | 28 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0044 others(25): Show |
28 | HG01069.hp1 HG01071.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.852+8039G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17700507 | |||||||
| chrX:17700746 | T | C | 61 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0026 others(58): Show |
61 | HG00408.hp1 HG00609.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.852+8278T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17700746 | |||||||
| chrX:17701516 | TA | T | 86 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0026 others(83): Show |
86 | HG00408.hp1 HG00609.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.852+9054delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17701516 | ||||||
| chrX:17702277 | G | A | 1 | a0002c0002t0001g0138 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.852+9809G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17702277 | |||||||
| chrX:17702996 | C | T | 1 | a0002c0002t0001g0033 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.852+10528C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17702996 | |||||||
| chrX:17703082 | A | AATGT | 3 | a0001c0001t0005g0104 a0001c0001t0005g0111 a0003c0006t0005g0159 |
3 | HG02622.hp2 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.852+10615_852+1061 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17703082 | ||||||
| chrX:17703721 | T | G | 5 | a0001c0001t0002g0002 a0001c0001t0002g0106 a0001c0001t0002g0107 others(2): Show |
5 | HG02258.hp1 HG02293.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.852+11253T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17703721 | |||||||
| chrX:17704376 | C | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.852+11908C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17704376 | |||||||
| chrX:17704540 | C | T | 42 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0026 others(39): Show |
42 | HG00408.hp1 HG00609.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.852+12072C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17704540 | |||||||
| chrX:17705440 | T | C | 1 | a0001c0001t0001g0153 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.852+12972T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17705440 | |||||||
| chrX:17705794 | C | A | 1 | a0001c0001t0002g0110 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.852+13326C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17705794 | |||||||
| chrX:17706133 | A | G | 5 | a0001c0001t0002g0002 a0001c0001t0002g0106 a0001c0001t0002g0107 others(2): Show |
5 | HG02258.hp1 HG02293.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.853-13211A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17706133 | |||||||
| chrX:17706208 | A | G | 3 | a0001c0001t0001g0021 a0001c0001t0001g0124 a0001c0001t0010g0059 |
3 | HG01943.hp1 HG02135.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.853-13136A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17706208 | |||||||
| chrX:17706417 | A | C | 3 | a0001c0001t0005g0104 a0001c0001t0005g0111 a0003c0006t0005g0159 |
3 | HG02622.hp2 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.853-12927A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17706417 | |||||||
| chrX:17706490 | A | AAC | 12 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0016 others(9): Show |
12 | HG00408.hp2 HG00673.hp1 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.853-12820_853-1281 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17706490 | ||||||
| chrX:17706490 | AAC | A | 32 | a0001c0001t0001g0011 a0001c0001t0001g0051 a0001c0001t0001g0068 others(29): Show |
32 | HG01069.hp1 HG01071.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.853-12820_853-1281 others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17706490 | ||||||
| chrX:17706490 | AACAC | A | 51 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0035 others(48): Show |
51 | HG00408.hp1 HG00609.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.853-12822_853-1281 others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17706490 | ||||||
| chrX:17706532 | G | A | 1 | a0002c0002t0001g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.853-12812G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17706532 | |||||||
| chrX:17706711 | C | T | 86 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0026 others(83): Show |
86 | HG00408.hp1 HG00609.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.853-12633C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17706711 | |||||||
| chrX:17707759 | GTACAAGA others(5): Show |
G | 87 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0026 others(84): Show |
87 | HG00408.hp1 HG00609.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.853-11584_853-1157 others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17707759 | |||||||
| chrX:17707903 | G | A | 1 | a0001c0001t0002g0044 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.853-11441G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17707903 | |||||||
| chrX:17708023 | C | T | 39 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0026 others(36): Show |
39 | HG00408.hp1 HG00609.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.853-11321C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17708023 | |||||||
| chrX:17708029 | G | A | 27 | a0001c0001t0001g0112 a0001c0001t0002g0002 a0001c0001t0002g0003 others(24): Show |
27 | HG01069.hp1 HG01071.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.853-11315G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17708029 | |||||||
| chrX:17708418 | C | A | 4 | a0005c0005t0003g0101 a0005c0005t0003g0117 a0005c0005t0003g0136 others(1): Show |
4 | HG01071.hp2 HG02055.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-10926C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17708418 | |||||||
| chrX:17708985 | T | C | 1 | a0005c0005t0003g0101 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.853-10359T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17708985 | |||||||
| chrX:17709288 | T | G | 5 | a0001c0001t0002g0002 a0001c0001t0002g0106 a0001c0001t0002g0107 others(2): Show |
5 | HG02258.hp1 HG02293.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.853-10056T>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17709288 | |||||||
| chrX:17709290 | T | C | 3 | a0001c0001t0001g0137 a0001c0001t0002g0086 a0006c0008t0001g0114 |
3 | HG02451.hp2 HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.853-10054T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17709290 | |||||||
| chrX:17709500 | TCAGTCAG others(4): Show |
T | 13 | a0001c0001t0001g0137 a0001c0001t0002g0086 a0001c0001t0002g0096 others(10): Show |
13 | HG01243.hp1 HG01258.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.853-9835_853-9825d others(13): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17709500 | ||||||
| chrX:17709637 | A | G | 57 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0021 others(54): Show |
57 | HG00408.hp1 HG00609.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.853-9707A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17709637 | |||||||
| chrX:17709751 | G | A | 1 | a0002c0002t0001g0031 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.853-9593G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17709751 | |||||||
| chrX:17709927 | G | A | 1 | a0002c0002t0001g0007 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.853-9417G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17709927 | |||||||
| chrX:17710263 | T | C | 1 | a0001c0001t0005g0111 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.853-9081T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17710263 | |||||||
| chrX:17710520 | G | C | 3 | a0001c0001t0005g0104 a0001c0001t0005g0111 a0003c0006t0005g0159 |
3 | HG02622.hp2 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.853-8824G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17710520 | |||||||
| chrX:17710773 | AG | A | 44 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0026 others(41): Show |
44 | HG00408.hp1 HG00609.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.853-8567delG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17710773 | ||||||
| chrX:17710902 | A | G | 65 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0021 others(62): Show |
65 | HG00408.hp1 HG00609.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.853-8442A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17710902 | |||||||
| chrX:17710980 | C | A | 1 | a0005c0005t0003g0101 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.853-8364C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17710980 | |||||||
| chrX:17711012 | C | T | 1 | a0002c0002t0001g0030 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.853-8332C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17711012 | |||||||
| chrX:17711096 | T | C | 5 | a0001c0001t0002g0002 a0001c0001t0002g0106 a0001c0001t0002g0107 others(2): Show |
5 | HG02258.hp1 HG02293.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.853-8248T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17711096 | |||||||
| chrX:17711621 | C | T | 1 | a0001c0001t0013g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.853-7723C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17711621 | |||||||
| chrX:17711689 | C | A | 1 | a0002c0002t0001g0001 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.853-7655C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17711689 | |||||||
| chrX:17711851 | G | A | 2 | a0002c0002t0001g0064 a0002c0002t0001g0148 |
2 | NA19012.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.853-7493G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17711851 | |||||||
| chrX:17712253 | G | GTA | 11 | a0001c0001t0001g0026 a0001c0001t0001g0066 a0001c0001t0001g0144 others(8): Show |
11 | HG00621.hp1 HG00673.hp1 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.853-7054_853-7053d others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712253 | ||||||
| chrX:17712253 | G | GTATA | 8 | a0001c0001t0006g0074 a0001c0001t0006g0103 a0001c0001t0007g0122 others(5): Show |
8 | HG01074.hp1 HG02027.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.853-7056_853-7053d others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712253 | ||||||
| chrX:17712253 | G | GTATATA | 11 | a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0061 others(8): Show |
11 | HG00609.hp1 HG00639.hp1 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.853-7058_853-7053d others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712253 | ||||||
| chrX:17712253 | G | GTATATAT others(1): Show |
4 | a0001c0001t0001g0049 a0001c0001t0002g0116 a0001c0001t0007g0125 others(1): Show |
4 | HG03209.hp1 HG03516.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-7060_853-7053d others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712253 | ||||||
| chrX:17712253 | G | GTATATAT others(3): Show |
3 | a0001c0001t0001g0050 a0001c0001t0002g0096 a0009c0016t0002g0119 |
3 | HG02630.hp2 HG02723.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.853-7062_853-7053d others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712253 | ||||||
| chrX:17712253 | G | GTATATAT others(5): Show |
1 | a0001c0001t0004g0163 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.853-7064_853-7053d others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712253 | ||||||
| chrX:17712253 | G | GTATATAT others(7): Show |
3 | a0001c0001t0001g0070 a0001c0001t0004g0071 a0001c0001t0010g0059 |
3 | HG02698.hp1 NA18965.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.853-7066_853-7053d others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712253 | ||||||
| chrX:17712253 | G | GTATATAT others(9): Show |
3 | a0001c0001t0001g0021 a0001c0001t0001g0124 a0001c0001t0004g0058 |
3 | HG01943.hp1 HG02135.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.853-7068_853-7053d others(18): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712253 | ||||||
| chrX:17712253 | G | GTATATAT others(11): Show |
1 | a0001c0001t0001g0085 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.853-7070_853-7053d others(20): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712253 | ||||||
| chrX:17712253 | G | GTGTATA | 2 | a0001c0001t0002g0100 a0001c0001t0002g0143 |
2 | HG01243.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.853-7090_853-7089i others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712253 | ||||||
| chrX:17712253 | GTA | G | 14 | a0001c0001t0001g0127 a0001c0001t0001g0151 a0001c0001t0002g0086 others(11): Show |
14 | HG00140.hp1 HG00408.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.853-7054_853-7053d others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712253 | ||||||
| chrX:17712253 | GTATA | G | 5 | a0001c0001t0001g0008 a0001c0001t0012g0154 a0005c0005t0003g0101 others(2): Show |
5 | HG01975.hp1 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.853-7056_853-7053d others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712253 | ||||||
| chrX:17712253 | GTATATA | G | 2 | a0002c0002t0001g0032 a0002c0002t0001g0076 |
2 | HG01192.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.853-7058_853-7053d others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712253 | ||||||
| chrX:17712253 | GTATATAT others(3): Show |
G | 22 | a0001c0001t0001g0112 a0001c0001t0001g0137 a0001c0001t0002g0002 others(19): Show |
22 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.853-7062_853-7053d others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712253 | ||||||
| chrX:17712255 | A | G | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0135 others(1): Show |
4 | HG01952.hp1 HG03139.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-7089A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17712255 | |||||||
| chrX:17712257 | A | G | 3 | a0005c0005t0003g0117 a0005c0005t0003g0136 a0007c0014t0003g0092 |
3 | HG01071.hp2 HG02647.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.853-7087A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17712257 | |||||||
| chrX:17712259 | A | G | 4 | a0001c0001t0012g0154 a0005c0005t0003g0101 a0005c0005t0008g0087 others(1): Show |
4 | HG01975.hp1 HG02055.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-7085A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17712259 | |||||||
| chrX:17712265 | A | G | 22 | a0001c0001t0001g0112 a0001c0001t0001g0137 a0001c0001t0002g0002 others(19): Show |
22 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.853-7079A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17712265 | |||||||
| chrX:17712267 | A | G | 1 | a0003c0006t0001g0157 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.853-7077A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17712267 | |||||||
| chrX:17712268 | TATATATA others(19): Show |
T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0056 |
2 | NA18988.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.853-7074_853-7049d others(28): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712268 | ||||||
| chrX:17712278 | TATATATA others(7): Show |
T | 1 | a0008c0011t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.853-7064_853-7051d others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712278 | ||||||
| chrX:17712288 | T | C | 3 | a0001c0001t0012g0154 a0005c0005t0008g0087 a0005c0005t0008g0097 |
3 | HG01975.hp1 HG02486.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.853-7056T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17712288 | |||||||
| chrX:17712290 | T | C | 19 | a0001c0001t0001g0127 a0001c0001t0001g0135 a0002c0002t0001g0004 others(16): Show |
19 | HG00280.hp1 HG00408.hp2 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.853-7054T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17712290 | |||||||
| chrX:17712290 | T | TAC | 14 | a0001c0001t0001g0011 a0001c0001t0001g0048 a0001c0001t0001g0051 others(11): Show |
14 | HG00642.hp1 HG01928.hp1 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.853-7034_853-7033d others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712290 | ||||||
| chrX:17712290 | T | TATAC | 5 | a0001c0001t0001g0068 a0002c0002t0001g0047 a0002c0002t0001g0053 others(2): Show |
5 | HG03130.hp1 HG04199.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.853-7053_853-7052i others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712290 | ||||||
| chrX:17712290 | T | TATATAC | 2 | a0002c0002t0001g0090 a0002c0002t0001g0105 |
2 | HG02129.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.853-7053_853-7052i others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712290 | ||||||
| chrX:17712290 | T | TATATATA others(7): Show |
1 | a0002c0002t0001g0017 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.853-7053_853-7052i others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712290 | ||||||
| chrX:17712292 | C | T | 3 | a0001c0001t0002g0116 a0002c0002t0001g0072 a0009c0016t0002g0119 |
3 | HG02630.hp2 HG03017.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.853-7052C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17712292 | |||||||
| chrX:17712312 | T | C | 1 | a0004c0004t0001g0132 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.853-7032T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17712312 | |||||||
| chrX:17712361 | T | TAC | 10 | a0001c0001t0001g0008 a0001c0001t0001g0061 a0001c0001t0001g0073 others(7): Show |
10 | HG02040.hp1 HG03942.hp1 HG04115.hp1 others(7): Show |
intron_variant | MODIFIER | c.853-6951_853-6950d others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712361 | ||||||
| chrX:17712361 | T | TACAC | 8 | a0001c0001t0001g0050 a0001c0001t0001g0099 a0001c0003t0002g0014 others(5): Show |
8 | HG01258.hp1 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.853-6953_853-6950d others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712361 | ||||||
| chrX:17712361 | TAC | T | 2 | a0002c0002t0001g0040 a0008c0011t0002g0147 |
2 | HG01167.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.853-6951_853-6950d others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712361 | ||||||
| chrX:17712361 | TACAC | T | 2 | a0002c0002t0001g0017 a0002c0002t0001g0078 |
2 | HG02293.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.853-6953_853-6950d others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712361 | ||||||
| chrX:17712371 | C | G | 2 | a0001c0001t0002g0093 a0001c0001t0002g0126 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.853-6973C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17712371 | |||||||
| chrX:17712391 | C | CAT | 18 | a0001c0001t0001g0112 a0001c0001t0001g0137 a0001c0001t0002g0002 others(15): Show |
18 | HG01106.hp1 HG01109.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.853-6952_853-6951i others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712391 | ||||||
| chrX:17712393 | C | CACACAT | 2 | a0001c0001t0002g0164 a0005c0005t0003g0101 |
2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.853-6950_853-6949i others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712393 | ||||||
| chrX:17712393 | C | CACAT | 6 | a0001c0001t0012g0154 a0005c0005t0003g0117 a0005c0005t0003g0136 others(3): Show |
6 | HG01071.hp2 HG01975.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.853-6950_853-6949i others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712393 | ||||||
| chrX:17712393 | C | CAT | 5 | a0001c0001t0006g0074 a0001c0001t0006g0103 a0002c0002t0001g0025 others(2): Show |
5 | HG02056.hp1 HG04199.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.853-6932_853-6931d others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712393 | ||||||
| chrX:17712393 | C | CATAT | 4 | a0001c0001t0002g0003 a0001c0001t0002g0093 a0001c0001t0002g0126 others(1): Show |
4 | HG01069.hp1 HG01071.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-6934_853-6931d others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17712393 | ||||||
| chrX:17712393 | C | T | 22 | a0001c0001t0001g0112 a0001c0001t0001g0137 a0001c0001t0002g0002 others(19): Show |
22 | HG01106.hp1 HG01109.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.853-6951C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17712393 | |||||||
| chrX:17712395 | T | C | 2 | a0001c0001t0001g0068 a0012c0013t0001g0038 |
2 | HG03130.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.853-6949T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17712395 | |||||||
| chrX:17712550 | G | T | 30 | a0001c0001t0001g0112 a0001c0001t0001g0137 a0001c0001t0002g0002 others(27): Show |
30 | HG01069.hp1 HG01071.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.853-6794G>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17712550 | |||||||
| chrX:17713052 | A | G | 2 | a0001c0001t0013g0045 a0008c0011t0002g0147 |
2 | HG02257.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.853-6292A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17713052 | |||||||
| chrX:17713091 | ATTTTGAG others(13): Show |
A | 1 | a0002c0002t0001g0028 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.853-6252_853-6233d others(22): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17713091 | |||||||
| chrX:17713263 | T | C | 1 | a0002c0002t0001g0032 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.853-6081T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17713263 | |||||||
| chrX:17713840 | C | T | 1 | a0001c0001t0007g0125 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.853-5504C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17713840 | |||||||
| chrX:17714280 | G | A | 2 | a0002c0002t0001g0007 a0002c0002t0001g0040 |
2 | HG01167.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.853-5064G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17714280 | |||||||
| chrX:17714576 | T | C | 4 | a0004c0004t0001g0012 a0004c0004t0001g0132 a0004c0004t0001g0149 others(1): Show |
4 | HG01952.hp1 HG02300.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-4768T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17714576 | |||||||
| chrX:17715226 | G | C | 8 | a0001c0001t0012g0154 a0005c0005t0003g0101 a0005c0005t0003g0117 others(5): Show |
8 | HG01071.hp2 HG01975.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.853-4118G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17715226 | |||||||
| chrX:17715321 | T | C | 3 | a0001c0001t0002g0093 a0001c0001t0002g0126 a0001c0001t0002g0146 |
3 | HG01069.hp1 HG01071.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.853-4023T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17715321 | |||||||
| chrX:17716785 | A | G | 3 | a0001c0001t0005g0104 a0001c0001t0005g0111 a0003c0006t0005g0159 |
3 | HG02622.hp2 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.853-2559A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17716785 | |||||||
| chrX:17716962 | C | CT | 11 | a0001c0001t0001g0099 a0001c0001t0001g0144 a0001c0001t0006g0074 others(8): Show |
11 | HG00642.hp1 HG02074.hp1 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.853-2365dupT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17716962 | ||||||
| chrX:17716962 | C | T | 26 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0044 others(23): Show |
26 | HG01069.hp1 HG01071.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.853-2382C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17716962 | |||||||
| chrX:17717074 | TCTC | T | 6 | a0002c0002t0001g0024 a0004c0004t0001g0055 a0004c0004t0001g0065 others(3): Show |
6 | HG01952.hp1 NA18948.hp1 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.853-2267_853-2265d others(5): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17717074 | ||||||
| chrX:17717282 | T | C | 1 | a0010c0010t0003g0158 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.853-2062T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17717282 | |||||||
| chrX:17717465 | T | C | 4 | a0001c0001t0002g0116 a0001c0001t0013g0045 a0008c0011t0002g0147 others(1): Show |
4 | HG02257.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-1879T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17717465 | |||||||
| chrX:17718068 | T | C | 3 | a0001c0001t0005g0104 a0001c0001t0005g0111 a0003c0006t0005g0159 |
3 | HG02622.hp2 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.853-1276T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17718068 | |||||||
| chrX:17718106 | T | C | 1 | a0002c0002t0001g0109 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.853-1238T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17718106 | |||||||
| chrX:17718319 | G | A | 1 | a0001c0003t0002g0102 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.853-1025G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17718319 | |||||||
| chrX:17718346 | A | AG | 4 | a0001c0001t0001g0050 a0002c0002t0001g0032 a0002c0002t0001g0141 others(1): Show |
4 | HG00642.hp1 HG01192.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-995dupG | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17718346 | ||||||
| chrX:17718427 | GAAGA | G | 25 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0044 others(22): Show |
25 | HG01069.hp1 HG01071.hp1 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.853-913_853-910del others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17718427 | ||||||
| chrX:17718736 | G | A | 1 | a0002c0002t0001g0131 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.853-608G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | chrX | 17718736 | |||||||
| chrX:17719136 | A | AAAGG | 3 | a0001c0001t0005g0104 a0001c0001t0005g0111 a0003c0006t0005g0159 |
3 | HG02622.hp2 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.853-201_853-198dup others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 17719136 | ||||||
| chrX:17719648 | C | G | 1 | a0001c0001t0001g0145 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.915+242C>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 4/8 | chrX | 17719648 | |||||||
| chrX:17719978 | T | TTC | 2 | a0001c0001t0002g0116 a0009c0016t0002g0119 |
2 | HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.915+590_915+591dup others(2): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 17719978 | ||||||
| chrX:17720425 | C | A | 3 | a0001c0001t0001g0137 a0001c0001t0002g0086 a0006c0008t0001g0114 |
3 | HG02451.hp2 HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.916-1016C>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 4/8 | chrX | 17720425 | |||||||
| chrX:17720437 | A | G | 2 | a0002c0002t0001g0022 a0002c0002t0001g0054 |
2 | HG02027.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.916-1004A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 4/8 | chrX | 17720437 | |||||||
| chrX:17720662 | A | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0056 |
2 | NA18988.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.916-779A>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 4/8 | chrX | 17720662 | |||||||
| chrX:17722243 | C | T | 1 | a0002c0002t0001g0025 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1108+610C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | chrX | 17722243 | |||||||
| chrX:17723028 | G | A | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1109-1271G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | chrX | 17723028 | |||||||
| chrX:17723203 | C | T | 2 | a0001c0001t0002g0116 a0009c0016t0002g0119 |
2 | HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1109-1096C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | chrX | 17723203 | |||||||
| chrX:17723572 | T | C | 3 | a0001c0001t0005g0104 a0001c0001t0005g0111 a0003c0006t0005g0159 |
3 | HG02622.hp2 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1109-727T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | chrX | 17723572 | |||||||
| chrX:17723726 | G | GGT | 10 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0051 others(7): Show |
10 | HG01243.hp1 HG01975.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.1109-529_1109-528d others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723726 | ||||||
| chrX:17723726 | G | GGTGT | 9 | a0001c0001t0001g0133 a0001c0001t0002g0143 a0002c0002t0001g0016 others(6): Show |
9 | HG00280.hp1 HG01975.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1109-531_1109-528d others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723726 | ||||||
| chrX:17723726 | G | GGTGTGT | 12 | a0001c0001t0001g0151 a0001c0003t0002g0128 a0002c0002t0001g0009 others(9): Show |
12 | HG00408.hp1 HG01256.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.1109-533_1109-528d others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723726 | ||||||
| chrX:17723726 | G | GGTGTGTG others(1): Show |
20 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0094 others(17): Show |
20 | HG00642.hp1 HG01099.hp1 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.1109-535_1109-528d others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723726 | ||||||
| chrX:17723726 | G | GGTGTGTG others(3): Show |
20 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0041 others(17): Show |
20 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.1109-537_1109-528d others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723726 | ||||||
| chrX:17723726 | G | GGTGTGTG others(5): Show |
11 | a0001c0001t0001g0021 a0001c0001t0001g0061 a0001c0001t0001g0085 others(8): Show |
11 | HG02040.hp1 HG02135.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1109-539_1109-528d others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723726 | ||||||
| chrX:17723726 | G | GGTGTGTG others(7): Show |
7 | a0001c0001t0001g0037 a0001c0001t0001g0049 a0001c0001t0001g0050 others(4): Show |
7 | HG00639.hp2 HG01515.hp1 HG04199.hp1 others(4): Show |
intron_variant | MODIFIER | c.1109-541_1109-528d others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723726 | ||||||
| chrX:17723726 | G | GGTGTGTG others(9): Show |
8 | a0001c0001t0001g0057 a0001c0001t0001g0083 a0001c0001t0001g0153 others(5): Show |
8 | HG00609.hp1 HG00673.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1109-543_1109-528d others(18): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723726 | ||||||
| chrX:17723726 | G | GGTGTGTG others(11): Show |
4 | a0001c0001t0001g0070 a0001c0003t0002g0014 a0002c0002t0001g0064 others(1): Show |
4 | HG01258.hp1 HG02698.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.1109-545_1109-528d others(20): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723726 | ||||||
| chrX:17723726 | G | GGTGTGTG others(13): Show |
1 | a0002c0002t0001g0060 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1109-547_1109-528d others(22): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723726 | ||||||
| chrX:17723726 | G | GTGTGTGT others(8): Show |
1 | a0001c0001t0001g0134 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1109-573_1109-572i others(17): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | chrX | 17723726 | |||||||
| chrX:17723726 | GGT | G | 4 | a0001c0001t0001g0135 a0002c0002t0001g0054 a0010c0010t0003g0158 others(1): Show |
4 | HG02056.hp1 HG02723.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.1109-529_1109-528d others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723726 | ||||||
| chrX:17723741 | G | GTGTGTGT others(6): Show |
1 | a0004c0004t0001g0065 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1109-557_1109-545d others(15): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723741 | ||||||
| chrX:17723741 | G | GTGTGTGT others(11): Show |
1 | a0001c0001t0005g0111 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1109-541_1109-540i others(20): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723741 | ||||||
| chrX:17723762 | TGTGTGTG others(7): Show |
T | 1 | a0001c0001t0002g0116 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1109-535_1109-522d others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723762 | ||||||
| chrX:17723763 | G | A | 2 | a0001c0001t0005g0104 a0003c0006t0005g0159 |
2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1109-536G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | chrX | 17723763 | |||||||
| chrX:17723764 | TGTGTGTG others(5): Show |
T | 1 | a0009c0016t0002g0119 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1109-533_1109-522d others(14): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723764 | ||||||
| chrX:17723770 | T | C | 3 | a0002c0002t0001g0010 a0005c0005t0008g0087 a0010c0010t0003g0158 |
3 | HG02723.hp2 HG02965.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1109-529T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | chrX | 17723770 | |||||||
| chrX:17723770 | T | TGC | 3 | a0001c0001t0002g0121 a0005c0005t0003g0101 a0005c0005t0008g0097 |
3 | HG02055.hp1 HG02280.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1109-521_1109-520d others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | ||||||
| chrX:17723770 | T | TGCGCGC | 2 | a0001c0001t0001g0112 a0001c0001t0002g0120 |
2 | HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1109-525_1109-520d others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | ||||||
| chrX:17723770 | T | TGTGC | 5 | a0001c0001t0002g0164 a0002c0002t0001g0001 a0002c0002t0001g0005 others(2): Show |
5 | HG00621.hp1 HG01106.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1109-528_1109-527i others(6): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | ||||||
| chrX:17723770 | T | TGTGCGC | 5 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0110 others(2): Show |
5 | HG02145.hp1 HG02258.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1109-528_1109-527i others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | ||||||
| chrX:17723770 | T | TGTGCGCG others(3): Show |
1 | a0001c0001t0001g0137 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1109-528_1109-527i others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | ||||||
| chrX:17723770 | T | TGTGTGC | 5 | a0001c0001t0002g0093 a0001c0001t0002g0126 a0001c0001t0002g0146 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1109-528_1109-527i others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | ||||||
| chrX:17723770 | T | TGTGTGCG others(1): Show |
2 | a0006c0008t0001g0114 a0008c0011t0002g0147 |
2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1109-528_1109-527i others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | ||||||
| chrX:17723770 | T | TGTGTGCG others(3): Show |
1 | a0002c0002t0001g0032 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1109-528_1109-527i others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | ||||||
| chrX:17723770 | T | TGTGTGTG others(1): Show |
4 | a0001c0001t0013g0045 a0001c0003t0002g0102 a0002c0002t0001g0076 others(1): Show |
4 | HG02922.hp2 HG03453.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.1109-528_1109-527i others(10): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | ||||||
| chrX:17723770 | T | TGTGTGTG others(3): Show |
1 | a0002c0002t0001g0077 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1109-528_1109-527i others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | ||||||
| chrX:17723770 | T | TGTGTGTG others(3): Show |
1 | a0006c0007t0002g0118 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1109-528_1109-527i others(12): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | ||||||
| chrX:17723770 | T | TGTGTGTG others(7): Show |
1 | a0002c0002t0001g0082 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1109-528_1109-527i others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | ||||||
| chrX:17723770 | T | TGTGTGTG others(7): Show |
1 | a0001c0001t0002g0003 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1109-528_1109-527i others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | ||||||
| chrX:17723770 | T | TGTGTGTG others(9): Show |
1 | a0001c0001t0004g0163 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1109-528_1109-527i others(18): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | ||||||
| chrX:17723770 | T | TGTGTGTG others(7): Show |
1 | a0002c0002t0001g0034 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1109-528_1109-527i others(16): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | ||||||
| chrX:17723770 | T | TGTGTGTG others(9): Show |
1 | a0001c0001t0007g0122 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1109-528_1109-527i others(18): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | ||||||
| chrX:17723770 | T | TGTGTGTG others(9): Show |
2 | a0001c0001t0001g0140 a0001c0001t0007g0125 |
2 | HG01934.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1109-528_1109-527i others(18): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | ||||||
| chrX:17723770 | T | TGTGTGTG others(11): Show |
2 | a0001c0001t0001g0144 a0006c0007t0002g0115 |
2 | HG02809.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1109-528_1109-527i others(20): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | ||||||
| chrX:17723770 | T | TGTGTGTG others(13): Show |
1 | a0001c0001t0001g0129 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1109-528_1109-527i others(22): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | ||||||
| chrX:17723770 | T | TGTGTGTG others(19): Show |
1 | a0003c0006t0005g0159 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1109-528_1109-527i others(28): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | ||||||
| chrX:17723770 | T | TGTGTGTG others(19): Show |
1 | a0001c0001t0005g0104 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1109-528_1109-527i others(28): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 17723770 | ||||||
| chrX:17723772 | C | T | 15 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0048 others(12): Show |
15 | HG01243.hp1 HG02071.hp1 HG02293.hp2 others(12): Show |
intron_variant | MODIFIER | c.1109-527C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | chrX | 17723772 | |||||||
| chrX:17723773 | G | A | 2 | a0001c0001t0005g0104 a0003c0006t0005g0159 |
2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1109-526G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | chrX | 17723773 | |||||||
| chrX:17723780 | T | A | 2 | a0001c0001t0002g0002 a0002c0002t0001g0010 |
2 | HG02293.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.1109-519T>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | chrX | 17723780 | |||||||
| chrX:17723798 | A | G | 33 | a0001c0001t0001g0112 a0001c0001t0001g0137 a0001c0001t0002g0002 others(30): Show |
33 | HG01069.hp1 HG01071.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.1109-501A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | chrX | 17723798 | |||||||
| chrX:17724211 | C | T | 1 | a0002c0002t0001g0090 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1109-88C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 5/8 | chrX | 17724211 | |||||||
| chrX:17724709 | A | C | 1 | a0008c0011t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1240+279A>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 6/8 | chrX | 17724709 | |||||||
| chrX:17724776 | T | C | 1 | a0001c0001t0001g0026 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1240+346T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 6/8 | chrX | 17724776 | |||||||
| chrX:17725234 | GA | G | 12 | a0001c0001t0001g0037 a0001c0001t0001g0066 a0001c0001t0001g0083 others(9): Show |
12 | HG00639.hp2 HG02132.hp1 HG03579.hp1 others(9): Show |
intron_variant | MODIFIER | c.1241-102delA | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 17725234 | ||||||
| chrX:17728549 | C | CTGTT | 37 | a0001c0001t0001g0112 a0001c0001t0001g0137 a0001c0001t0002g0002 others(34): Show |
37 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.4223-75_4223-72dup others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 17728549 | ||||||
| chrX:17728549 | C | CTGTTTGT others(1): Show |
3 | a0003c0006t0002g0161 a0003c0009t0002g0160 a0006c0008t0002g0113 |
3 | HG02145.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.4223-79_4223-72dup others(8): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 17728549 | ||||||
| chrX:17728549 | CTGTT | C | 2 | a0001c0003t0002g0128 a0005c0005t0003g0101 |
2 | HG02055.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.4223-75_4223-72del others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 17728549 | ||||||
| chrX:17729431 | G | A | 2 | a0001c0001t0007g0122 a0001c0001t0007g0125 |
2 | HG02615.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.4349+656G>A | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 8/8 | chrX | 17729431 | |||||||
| chrX:17729925 | C | T | 1 | a0002c0002t0001g0033 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.4349+1150C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 8/8 | chrX | 17729925 | |||||||
| chrX:17730091 | T | C | 3 | a0001c0001t0005g0104 a0001c0001t0005g0111 a0003c0006t0005g0159 |
3 | HG02622.hp2 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4349+1316T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 8/8 | chrX | 17730091 | |||||||
| chrX:17730551 | A | G | 3 | a0001c0001t0005g0104 a0001c0001t0005g0111 a0003c0006t0005g0159 |
3 | HG02622.hp2 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4350-1307A>G | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 8/8 | chrX | 17730551 | |||||||
| chrX:17730732 | C | T | 1 | a0002c0002t0001g0109 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.4350-1126C>T | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 8/8 | chrX | 17730732 | |||||||
| chrX:17731020 | T | C | 3 | a0001c0001t0005g0104 a0001c0001t0005g0111 a0003c0006t0005g0159 |
3 | HG02622.hp2 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4350-838T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 8/8 | chrX | 17731020 | |||||||
| chrX:17731224 | CT | C | 114 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0021 others(111): Show |
114 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.4350-606delT | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 17731224 | ||||||
| chrX:17731224 | CTT | C | 18 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0002g0086 others(15): Show |
18 | HG01243.hp1 HG01258.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.4350-607_4350-606d others(4): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 17731224 | ||||||
| chrX:17731287 | G | C | 4 | a0002c0002t0001g0088 a0002c0002t0001g0089 a0002c0002t0001g0090 others(1): Show |
4 | HG02074.hp1 HG02129.hp1 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.4350-571G>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 8/8 | chrX | 17731287 | |||||||
| chrX:17731510 | T | C | 17 | a0001c0001t0001g0112 a0001c0001t0001g0137 a0001c0001t0002g0003 others(14): Show |
17 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.4350-348T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 8/8 | chrX | 17731510 | |||||||
| chrX:17731783 | T | C | 3 | a0001c0001t0005g0104 a0001c0001t0005g0111 a0003c0006t0005g0159 |
3 | HG02622.hp2 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4350-75T>C | NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 8/8 | chrX | 17731783 |