Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 367 |
| ensemblid | ENSG00000169083.18 |
| hgncid | 644 |
| symbol | AR |
| name | androgen receptor |
| refseq_nuc | NM_000044.6 |
| refseq_prot | NP_000035.2 |
| ensembl_nuc | ENST00000374690.9 |
| ensembl_prot | ENSP00000363822.3 |
| mane_status | MANE Select |
| chr | chrX |
| start | 67544021 |
| end | 67730619 |
| strand | + |
| ver | v1.2 |
| region | chrX:67544021-67730619 |
| region5000 | chrX:67539021-67735619 |
| regionname0 | AR_chrX_67544021_67730619 |
| regionname5000 | AR_chrX_67539021_67735619 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 919 | 34 | 10 | 5 | 13 | 1 | 5 | 10 | AR_chrX_67539021_67735619 | AR | MEVQL others(914): Show |
chrX | 67539021 | 67735619 |
| a0002 | 1/0 | 920 | 25 | 10 | 2 | 10 | 0 | 2 | 8 | AR_chrX_67539021_67735619 | AR | MEVQL others(915): Show |
chrX | 67539021 | 67735619 |
| a0003 | 0/0 | 923 | 21 | 3 | 4 | 9 | 1 | 4 | 5 | AR_chrX_67539021_67735619 | AR | MEVQL others(918): Show |
chrX | 67539021 | 67735619 |
| a0004 | 0/0 | 922 | 19 | 5 | 2 | 10 | 1 | 1 | 8 | AR_chrX_67539021_67735619 | AR | MEVQL others(917): Show |
chrX | 67539021 | 67735619 |
| a0005 | 0/0 | 918 | 18 | 7 | 2 | 2 | 1 | 6 | 2 | AR_chrX_67539021_67735619 | AR | MEVQL others(913): Show |
chrX | 67539021 | 67735619 |
| a0006 | 0/0 | 921 | 18 | 3 | 6 | 7 | 1 | 1 | 6 | AR_chrX_67539021_67735619 | AR | MEVQL others(916): Show |
chrX | 67539021 | 67735619 |
| a0007 | 0/0 | 917 | 13 | 7 | 3 | 2 | 0 | 1 | 1 | AR_chrX_67539021_67735619 | AR | MEVQL others(912): Show |
chrX | 67539021 | 67735619 |
| a0008 | 0/0 | 916 | 11 | 7 | 1 | 1 | 2 | 0 | 1 | AR_chrX_67539021_67735619 | AR | MEVQL others(911): Show |
chrX | 67539021 | 67735619 |
| a0009 | 0/0 | 915 | 10 | 7 | 0 | 2 | 0 | 1 | 2 | AR_chrX_67539021_67735619 | AR | MEVQL others(910): Show |
chrX | 67539021 | 67735619 |
| a0010 | 0/0 | 925 | 6 | 1 | 1 | 3 | 0 | 1 | 3 | AR_chrX_67539021_67735619 | AR | MEVQL others(920): Show |
chrX | 67539021 | 67735619 |
| a0011 | 0/0 | 924 | 5 | 0 | 1 | 4 | 0 | 0 | 3 | AR_chrX_67539021_67735619 | AR | MEVQL others(919): Show |
chrX | 67539021 | 67735619 |
| a0012 | 0/0 | 911 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | MEVQL others(906): Show |
chrX | 67539021 | 67735619 |
| a0013 | 0/0 | 912 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | MEVQL others(907): Show |
chrX | 67539021 | 67735619 |
| a0014 | 0/0 | 913 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | AR_chrX_67539021_67735619 | AR | MEVQL others(908): Show |
chrX | 67539021 | 67735619 |
| a0015 | 0/0 | 914 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | MEVQL others(909): Show |
chrX | 67539021 | 67735619 |
| a0016 | 0/0 | 495 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | MEVQL others(490): Show |
chrX | 67539021 | 67735619 |
| a0017 | 0/0 | 915 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | MEVQL others(910): Show |
chrX | 67539021 | 67735619 |
| a0018 | 0/0 | 926 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AR_chrX_67539021_67735619 | AR | MEVQL others(921): Show |
chrX | 67539021 | 67735619 |
| a0019 | 0/0 | 927 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AR_chrX_67539021_67735619 | AR | MEVQL others(922): Show |
chrX | 67539021 | 67735619 |
| a0020 | 0/1 | 921 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | MEVQL others(916): Show |
chrX | 67539021 | 67735619 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2757 | 24 | 4 | 2 | 13 | 1 | 4 | AR_chrX_67539021_67735619 | AR | ATGGA others(2752): Show |
chrX | 67539021 | 67735619 | ||
| a0001c0009 | 0/0 | 2757 | 8 | 5 | 3 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | ATGGA others(2752): Show |
chrX | 67539021 | 67735619 | ||
| a0001c0026 | 0/0 | 2757 | 1 | 0 | 0 | 0 | 0 | 1 | AR_chrX_67539021_67735619 | AR | ATGGA others(2752): Show |
chrX | 67539021 | 67735619 | ||
| a0001c0028 | 0/0 | 2757 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | ATGGA others(2752): Show |
chrX | 67539021 | 67735619 | ||
| a0002c0005 | 1/0 | 2760 | 16 | 3 | 1 | 10 | 0 | 1 | AR_chrX_67539021_67735619 | AR | ATGGA others(2755): Show |
chrX | 67539021 | 67735619 | ||
| a0002c0010 | 0/0 | 2760 | 8 | 7 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | ATGGA others(2755): Show |
chrX | 67539021 | 67735619 | ||
| a0002c0030 | 0/0 | 2760 | 1 | 0 | 0 | 0 | 0 | 1 | AR_chrX_67539021_67735619 | AR | ATGGA others(2755): Show |
chrX | 67539021 | 67735619 | ||
| a0003c0002 | 0/0 | 2769 | 18 | 0 | 4 | 9 | 1 | 4 | AR_chrX_67539021_67735619 | AR | ATGGA others(2764): Show |
chrX | 67539021 | 67735619 | ||
| a0003c0021 | 0/0 | 2769 | 2 | 2 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | ATGGA others(2764): Show |
chrX | 67539021 | 67735619 | ||
| a0003c0034 | 0/0 | 2769 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | ATGGA others(2764): Show |
chrX | 67539021 | 67735619 | ||
| a0004c0004 | 0/0 | 2766 | 17 | 3 | 2 | 10 | 1 | 1 | AR_chrX_67539021_67735619 | AR | ATGGA others(2761): Show |
chrX | 67539021 | 67735619 | ||
| a0004c0032 | 0/0 | 2766 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | ATGGA others(2761): Show |
chrX | 67539021 | 67735619 | ||
| a0004c0033 | 0/0 | 2766 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | ATGGA others(2761): Show |
chrX | 67539021 | 67735619 | ||
| a0005c0006 | 0/0 | 2754 | 11 | 7 | 0 | 0 | 1 | 3 | AR_chrX_67539021_67735619 | AR | ATGGA others(2749): Show |
chrX | 67539021 | 67735619 | ||
| a0005c0011 | 0/0 | 2754 | 7 | 0 | 2 | 2 | 0 | 3 | AR_chrX_67539021_67735619 | AR | ATGGA others(2749): Show |
chrX | 67539021 | 67735619 | ||
| a0006c0003 | 0/0 | 2763 | 17 | 2 | 6 | 7 | 1 | 1 | AR_chrX_67539021_67735619 | AR | ATGGA others(2758): Show |
chrX | 67539021 | 67735619 | ||
| a0006c0031 | 0/0 | 2763 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | ATGGA others(2758): Show |
chrX | 67539021 | 67735619 | ||
| a0007c0008 | 0/0 | 2751 | 8 | 6 | 2 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | ATGGA others(2746): Show |
chrX | 67539021 | 67735619 | ||
| a0007c0016 | 0/0 | 2751 | 4 | 0 | 1 | 2 | 0 | 1 | AR_chrX_67539021_67735619 | AR | ATGGA others(2746): Show |
chrX | 67539021 | 67735619 | ||
| a0007c0025 | 0/0 | 2751 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | ATGGA others(2746): Show |
chrX | 67539021 | 67735619 | ||
| a0008c0007 | 0/0 | 2748 | 8 | 6 | 1 | 0 | 1 | 0 | AR_chrX_67539021_67735619 | AR | ATGGA others(2743): Show |
chrX | 67539021 | 67735619 | ||
| a0008c0017 | 0/0 | 2748 | 3 | 1 | 0 | 1 | 1 | 0 | AR_chrX_67539021_67735619 | AR | ATGGA others(2743): Show |
chrX | 67539021 | 67735619 | ||
| a0009c0012 | 0/0 | 2745 | 6 | 6 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | ATGGA others(2740): Show |
chrX | 67539021 | 67735619 | ||
| a0009c0015 | 0/0 | 2745 | 4 | 1 | 0 | 2 | 0 | 1 | AR_chrX_67539021_67735619 | AR | ATGGA others(2740): Show |
chrX | 67539021 | 67735619 | ||
| a0010c0014 | 0/0 | 2775 | 5 | 0 | 1 | 3 | 0 | 1 | AR_chrX_67539021_67735619 | AR | ATGGA others(2770): Show |
chrX | 67539021 | 67735619 | ||
| a0010c0035 | 0/0 | 2775 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | ATGGA others(2770): Show |
chrX | 67539021 | 67735619 | ||
| a0011c0013 | 0/0 | 2772 | 5 | 0 | 1 | 4 | 0 | 0 | AR_chrX_67539021_67735619 | AR | ATGGA others(2767): Show |
chrX | 67539021 | 67735619 | ||
| a0012c0018 | 0/0 | 2733 | 2 | 0 | 2 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | ATGGA others(2728): Show |
chrX | 67539021 | 67735619 | ||
| a0013c0019 | 0/0 | 2736 | 2 | 2 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | ATGGA others(2731): Show |
chrX | 67539021 | 67735619 | ||
| a0014c0020 | 0/0 | 2739 | 2 | 0 | 0 | 2 | 0 | 0 | AR_chrX_67539021_67735619 | AR | ATGGA others(2734): Show |
chrX | 67539021 | 67735619 | ||
| a0015c0022 | 0/0 | 2742 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | ATGGA others(2737): Show |
chrX | 67539021 | 67735619 | ||
| a0015c0023 | 0/0 | 2742 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | ATGGA others(2737): Show |
chrX | 67539021 | 67735619 | ||
| a0016c0027 | 0/0 | 2746 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | ATGGA others(2741): Show |
chrX | 67539021 | 67735619 | ||
| a0017c0024 | 0/0 | 2745 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | ATGGA others(2740): Show |
chrX | 67539021 | 67735619 | ||
| a0018c0036 | 0/0 | 2778 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | ATGGA others(2773): Show |
chrX | 67539021 | 67735619 | ||
| a0019c0037 | 0/0 | 2781 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | ATGGA others(2776): Show |
chrX | 67539021 | 67735619 | ||
| a0020c0029 | 0/1 | 2763 | 1 | 0 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | ATGGA others(2758): Show |
chrX | 67539021 | 67735619 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 10665 | 5 | 0 | 1 | 2 | 0 | 2 | AR_chrX_67539021_67735619 | AR | AGCGC others(10660): Show |
chrX | 67539021 | 67735619 |
| a0001c0001t0002 | 0/0 | 10663 | 7 | 0 | 0 | 5 | 1 | 1 | AR_chrX_67539021_67735619 | AR | AGCGC others(10658): Show |
chrX | 67539021 | 67735619 |
| a0001c0001t0003 | 0/0 | 10667 | 2 | 0 | 0 | 2 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10662): Show |
chrX | 67539021 | 67735619 |
| a0001c0001t0004 | 0/0 | 10664 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10659): Show |
chrX | 67539021 | 67735619 |
| a0001c0001t0007 | 0/0 | 10661 | 4 | 0 | 0 | 4 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10656): Show |
chrX | 67539021 | 67735619 |
| a0001c0001t0010 | 0/0 | 10668 | 1 | 0 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10663): Show |
chrX | 67539021 | 67735619 |
| a0001c0001t0014 | 0/0 | 10662 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10657): Show |
chrX | 67539021 | 67735619 |
| a0001c0001t0019 | 0/0 | 10667 | 2 | 2 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10662): Show |
chrX | 67539021 | 67735619 |
| a0001c0001t0050 | 0/0 | 10651 | 1 | 0 | 0 | 0 | 0 | 1 | AR_chrX_67539021_67735619 | AR | AGCGC others(10646): Show |
chrX | 67539021 | 67735619 |
| a0001c0009t0004 | 0/0 | 10664 | 2 | 2 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10659): Show |
chrX | 67539021 | 67735619 |
| a0001c0009t0006 | 0/0 | 10666 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10661): Show |
chrX | 67539021 | 67735619 |
| a0001c0009t0008 | 0/0 | 10666 | 2 | 0 | 2 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10661): Show |
chrX | 67539021 | 67735619 |
| a0001c0009t0010 | 0/0 | 10668 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10663): Show |
chrX | 67539021 | 67735619 |
| a0001c0009t0033 | 0/0 | 10680 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10675): Show |
chrX | 67539021 | 67735619 |
| a0001c0009t0042 | 0/0 | 10678 | 1 | 0 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10673): Show |
chrX | 67539021 | 67735619 |
| a0001c0026t0025 | 0/0 | 10676 | 1 | 0 | 0 | 0 | 0 | 1 | AR_chrX_67539021_67735619 | AR | AGCGC others(10671): Show |
chrX | 67539021 | 67735619 |
| a0001c0028t0004 | 0/0 | 10664 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10659): Show |
chrX | 67539021 | 67735619 |
| a0002c0005t0001 | 0/0 | 10668 | 5 | 0 | 0 | 4 | 0 | 1 | AR_chrX_67539021_67735619 | AR | AGCGC others(10663): Show |
chrX | 67539021 | 67735619 |
| a0002c0005t0002 | 0/0 | 10666 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10661): Show |
chrX | 67539021 | 67735619 |
| a0002c0005t0004 | 0/0 | 10667 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10662): Show |
chrX | 67539021 | 67735619 |
| a0002c0005t0005 | 1/0 | 10667 | 1 | 0 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10662): Show |
chrX | 67539021 | 67735619 |
| a0002c0005t0007 | 0/0 | 10664 | 3 | 0 | 0 | 3 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10659): Show |
chrX | 67539021 | 67735619 |
| a0002c0005t0009 | 0/0 | 10676 | 1 | 0 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10671): Show |
chrX | 67539021 | 67735619 |
| a0002c0005t0015 | 0/0 | 10662 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10657): Show |
chrX | 67539021 | 67735619 |
| a0002c0005t0016 | 0/0 | 10674 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10669): Show |
chrX | 67539021 | 67735619 |
| a0002c0005t0044 | 0/0 | 10665 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10660): Show |
chrX | 67539021 | 67735619 |
| a0002c0005t0056 | 0/0 | 10665 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10660): Show |
chrX | 67539021 | 67735619 |
| a0002c0010t0004 | 0/0 | 10667 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10662): Show |
chrX | 67539021 | 67735619 |
| a0002c0010t0008 | 0/0 | 10669 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10664): Show |
chrX | 67539021 | 67735619 |
| a0002c0010t0014 | 0/0 | 10665 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10660): Show |
chrX | 67539021 | 67735619 |
| a0002c0010t0018 | 0/0 | 10677 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10672): Show |
chrX | 67539021 | 67735619 |
| a0002c0010t0020 | 0/0 | 10672 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10667): Show |
chrX | 67539021 | 67735619 |
| a0002c0010t0030 | 0/0 | 10663 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10658): Show |
chrX | 67539021 | 67735619 |
| a0002c0010t0035 | 0/0 | 10669 | 1 | 0 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10664): Show |
chrX | 67539021 | 67735619 |
| a0002c0010t0036 | 0/0 | 10673 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10668): Show |
chrX | 67539021 | 67735619 |
| a0002c0030t0016 | 0/0 | 10674 | 1 | 0 | 0 | 0 | 0 | 1 | AR_chrX_67539021_67735619 | AR | AGCGC others(10669): Show |
chrX | 67539021 | 67735619 |
| a0003c0002t0001 | 0/0 | 10677 | 5 | 0 | 2 | 3 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10672): Show |
chrX | 67539021 | 67735619 |
| a0003c0002t0002 | 0/0 | 10675 | 1 | 0 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10670): Show |
chrX | 67539021 | 67735619 |
| a0003c0002t0003 | 0/0 | 10679 | 3 | 0 | 1 | 2 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10674): Show |
chrX | 67539021 | 67735619 |
| a0003c0002t0009 | 0/0 | 10685 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10680): Show |
chrX | 67539021 | 67735619 |
| a0003c0002t0012 | 0/0 | 10667 | 3 | 0 | 0 | 0 | 0 | 3 | AR_chrX_67539021_67735619 | AR | AGCGC others(10662): Show |
chrX | 67539021 | 67735619 |
| a0003c0002t0013 | 0/0 | 10659 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10654): Show |
chrX | 67539021 | 67735619 |
| a0003c0002t0015 | 0/0 | 10671 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10666): Show |
chrX | 67539021 | 67735619 |
| a0003c0002t0017 | 0/0 | 10687 | 2 | 0 | 0 | 0 | 1 | 1 | AR_chrX_67539021_67735619 | AR | AGCGC others(10682): Show |
chrX | 67539021 | 67735619 |
| a0003c0002t0055 | 0/0 | 10659 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10654): Show |
chrX | 67539021 | 67735619 |
| a0003c0021t0006 | 0/0 | 10678 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10673): Show |
chrX | 67539021 | 67735619 |
| a0003c0021t0008 | 0/0 | 10678 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10673): Show |
chrX | 67539021 | 67735619 |
| a0003c0034t0008 | 0/0 | 10678 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10673): Show |
chrX | 67539021 | 67735619 |
| a0004c0004t0001 | 0/0 | 10674 | 6 | 0 | 0 | 4 | 1 | 1 | AR_chrX_67539021_67735619 | AR | AGCGC others(10669): Show |
chrX | 67539021 | 67735619 |
| a0004c0004t0003 | 0/0 | 10676 | 2 | 0 | 0 | 2 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10671): Show |
chrX | 67539021 | 67735619 |
| a0004c0004t0007 | 0/0 | 10670 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10665): Show |
chrX | 67539021 | 67735619 |
| a0004c0004t0012 | 0/0 | 10664 | 1 | 0 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10659): Show |
chrX | 67539021 | 67735619 |
| a0004c0004t0021 | 0/0 | 10678 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10673): Show |
chrX | 67539021 | 67735619 |
| a0004c0004t0027 | 0/0 | 10673 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10668): Show |
chrX | 67539021 | 67735619 |
| a0004c0004t0031 | 0/0 | 10685 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10680): Show |
chrX | 67539021 | 67735619 |
| a0004c0004t0046 | 0/0 | 10674 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10669): Show |
chrX | 67539021 | 67735619 |
| a0004c0004t0047 | 0/0 | 10672 | 1 | 0 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10667): Show |
chrX | 67539021 | 67735619 |
| a0004c0004t0048 | 0/0 | 10668 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10663): Show |
chrX | 67539021 | 67735619 |
| a0004c0004t0051 | 0/0 | 10670 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10665): Show |
chrX | 67539021 | 67735619 |
| a0004c0032t0058 | 0/0 | 10677 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10672): Show |
chrX | 67539021 | 67735619 |
| a0004c0033t0054 | 0/0 | 10690 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10685): Show |
chrX | 67539021 | 67735619 |
| a0005c0006t0001 | 0/0 | 10662 | 1 | 0 | 0 | 0 | 1 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10657): Show |
chrX | 67539021 | 67735619 |
| a0005c0006t0003 | 0/0 | 10664 | 1 | 0 | 0 | 0 | 0 | 1 | AR_chrX_67539021_67735619 | AR | AGCGC others(10659): Show |
chrX | 67539021 | 67735619 |
| a0005c0006t0008 | 0/0 | 10663 | 1 | 0 | 0 | 0 | 0 | 1 | AR_chrX_67539021_67735619 | AR | AGCGC others(10658): Show |
chrX | 67539021 | 67735619 |
| a0005c0006t0010 | 0/0 | 10665 | 2 | 1 | 0 | 0 | 0 | 1 | AR_chrX_67539021_67735619 | AR | AGCGC others(10660): Show |
chrX | 67539021 | 67735619 |
| a0005c0006t0011 | 0/0 | 10665 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10660): Show |
chrX | 67539021 | 67735619 |
| a0005c0006t0020 | 0/0 | 10666 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10661): Show |
chrX | 67539021 | 67735619 |
| a0005c0006t0028 | 0/0 | 10659 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10654): Show |
chrX | 67539021 | 67735619 |
| a0005c0006t0032 | 0/0 | 10662 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10657): Show |
chrX | 67539021 | 67735619 |
| a0005c0006t0038 | 0/0 | 10661 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10656): Show |
chrX | 67539021 | 67735619 |
| a0005c0006t0040 | 0/0 | 10667 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10662): Show |
chrX | 67539021 | 67735619 |
| a0005c0011t0001 | 0/0 | 10662 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10657): Show |
chrX | 67539021 | 67735619 |
| a0005c0011t0003 | 0/0 | 10664 | 1 | 0 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10659): Show |
chrX | 67539021 | 67735619 |
| a0005c0011t0009 | 0/0 | 10670 | 2 | 0 | 0 | 1 | 0 | 1 | AR_chrX_67539021_67735619 | AR | AGCGC others(10665): Show |
chrX | 67539021 | 67735619 |
| a0005c0011t0012 | 0/0 | 10652 | 1 | 0 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10647): Show |
chrX | 67539021 | 67735619 |
| a0005c0011t0052 | 0/0 | 10672 | 1 | 0 | 0 | 0 | 0 | 1 | AR_chrX_67539021_67735619 | AR | AGCGC others(10667): Show |
chrX | 67539021 | 67735619 |
| a0005c0011t0053 | 0/0 | 10674 | 1 | 0 | 0 | 0 | 0 | 1 | AR_chrX_67539021_67735619 | AR | AGCGC others(10669): Show |
chrX | 67539021 | 67735619 |
| a0006c0003t0001 | 0/0 | 10671 | 5 | 0 | 2 | 3 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10666): Show |
chrX | 67539021 | 67735619 |
| a0006c0003t0002 | 0/0 | 10669 | 5 | 0 | 2 | 3 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10664): Show |
chrX | 67539021 | 67735619 |
| a0006c0003t0004 | 0/0 | 10670 | 2 | 2 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10665): Show |
chrX | 67539021 | 67735619 |
| a0006c0003t0007 | 0/0 | 10667 | 1 | 0 | 0 | 0 | 1 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10662): Show |
chrX | 67539021 | 67735619 |
| a0006c0003t0009 | 0/0 | 10679 | 1 | 0 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10674): Show |
chrX | 67539021 | 67735619 |
| a0006c0003t0015 | 0/0 | 10665 | 1 | 0 | 0 | 0 | 0 | 1 | AR_chrX_67539021_67735619 | AR | AGCGC others(10660): Show |
chrX | 67539021 | 67735619 |
| a0006c0003t0017 | 0/0 | 10681 | 1 | 0 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10676): Show |
chrX | 67539021 | 67735619 |
| a0006c0003t0026 | 0/0 | 10671 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10666): Show |
chrX | 67539021 | 67735619 |
| a0006c0031t0043 | 0/0 | 10672 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10667): Show |
chrX | 67539021 | 67735619 |
| a0007c0008t0005 | 0/0 | 10658 | 2 | 1 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10653): Show |
chrX | 67539021 | 67735619 |
| a0007c0008t0006 | 0/0 | 10660 | 3 | 3 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10655): Show |
chrX | 67539021 | 67735619 |
| a0007c0008t0018 | 0/0 | 10668 | 1 | 0 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10663): Show |
chrX | 67539021 | 67735619 |
| a0007c0008t0023 | 0/0 | 10658 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10653): Show |
chrX | 67539021 | 67735619 |
| a0007c0008t0057 | 0/0 | 10657 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10652): Show |
chrX | 67539021 | 67735619 |
| a0007c0016t0001 | 0/0 | 10659 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10654): Show |
chrX | 67539021 | 67735619 |
| a0007c0016t0003 | 0/0 | 10661 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10656): Show |
chrX | 67539021 | 67735619 |
| a0007c0016t0005 | 0/0 | 10658 | 1 | 0 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10653): Show |
chrX | 67539021 | 67735619 |
| a0007c0016t0022 | 0/0 | 10659 | 1 | 0 | 0 | 0 | 0 | 1 | AR_chrX_67539021_67735619 | AR | AGCGC others(10654): Show |
chrX | 67539021 | 67735619 |
| a0007c0025t0045 | 0/0 | 10648 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10643): Show |
chrX | 67539021 | 67735619 |
| a0008c0007t0006 | 0/0 | 10657 | 4 | 3 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10652): Show |
chrX | 67539021 | 67735619 |
| a0008c0007t0010 | 0/0 | 10659 | 1 | 0 | 0 | 0 | 1 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10654): Show |
chrX | 67539021 | 67735619 |
| a0008c0007t0011 | 0/0 | 10659 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10654): Show |
chrX | 67539021 | 67735619 |
| a0008c0007t0034 | 0/0 | 10655 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10650): Show |
chrX | 67539021 | 67735619 |
| a0008c0007t0039 | 0/0 | 10657 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10652): Show |
chrX | 67539021 | 67735619 |
| a0008c0017t0001 | 0/0 | 10656 | 2 | 0 | 0 | 1 | 1 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10651): Show |
chrX | 67539021 | 67735619 |
| a0008c0017t0005 | 0/0 | 10655 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10650): Show |
chrX | 67539021 | 67735619 |
| a0009c0012t0005 | 0/0 | 10652 | 3 | 3 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10647): Show |
chrX | 67539021 | 67735619 |
| a0009c0012t0024 | 0/0 | 10654 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10649): Show |
chrX | 67539021 | 67735619 |
| a0009c0012t0037 | 0/0 | 10650 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10645): Show |
chrX | 67539021 | 67735619 |
| a0009c0012t0041 | 0/0 | 10664 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10659): Show |
chrX | 67539021 | 67735619 |
| a0009c0015t0001 | 0/0 | 10653 | 1 | 0 | 0 | 0 | 0 | 1 | AR_chrX_67539021_67735619 | AR | AGCGC others(10648): Show |
chrX | 67539021 | 67735619 |
| a0009c0015t0002 | 0/0 | 10651 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10646): Show |
chrX | 67539021 | 67735619 |
| a0009c0015t0003 | 0/0 | 10655 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10650): Show |
chrX | 67539021 | 67735619 |
| a0009c0015t0005 | 0/0 | 10652 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10647): Show |
chrX | 67539021 | 67735619 |
| a0010c0014t0001 | 0/0 | 10683 | 2 | 0 | 1 | 0 | 0 | 1 | AR_chrX_67539021_67735619 | AR | AGCGC others(10678): Show |
chrX | 67539021 | 67735619 |
| a0010c0014t0003 | 0/0 | 10685 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10680): Show |
chrX | 67539021 | 67735619 |
| a0010c0014t0013 | 0/0 | 10665 | 2 | 0 | 0 | 2 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10660): Show |
chrX | 67539021 | 67735619 |
| a0010c0035t0014 | 0/0 | 10680 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10675): Show |
chrX | 67539021 | 67735619 |
| a0011c0013t0001 | 0/0 | 10680 | 2 | 0 | 1 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10675): Show |
chrX | 67539021 | 67735619 |
| a0011c0013t0003 | 0/0 | 10682 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10677): Show |
chrX | 67539021 | 67735619 |
| a0011c0013t0009 | 0/0 | 10688 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10683): Show |
chrX | 67539021 | 67735619 |
| a0011c0013t0013 | 0/0 | 10662 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10657): Show |
chrX | 67539021 | 67735619 |
| a0012c0018t0011 | 0/0 | 10644 | 2 | 0 | 2 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10639): Show |
chrX | 67539021 | 67735619 |
| a0013c0019t0016 | 0/0 | 10650 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10645): Show |
chrX | 67539021 | 67735619 |
| a0013c0019t0029 | 0/0 | 10643 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10638): Show |
chrX | 67539021 | 67735619 |
| a0014c0020t0001 | 0/0 | 10647 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10642): Show |
chrX | 67539021 | 67735619 |
| a0014c0020t0003 | 0/0 | 10649 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10644): Show |
chrX | 67539021 | 67735619 |
| a0015c0022t0004 | 0/0 | 10649 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10644): Show |
chrX | 67539021 | 67735619 |
| a0015c0023t0008 | 0/0 | 10651 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10646): Show |
chrX | 67539021 | 67735619 |
| a0016c0027t0010 | 0/0 | 10657 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10652): Show |
chrX | 67539021 | 67735619 |
| a0017c0024t0011 | 0/0 | 10656 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10651): Show |
chrX | 67539021 | 67735619 |
| a0018c0036t0021 | 0/0 | 10690 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10685): Show |
chrX | 67539021 | 67735619 |
| a0019c0037t0049 | 0/0 | 10673 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10668): Show |
chrX | 67539021 | 67735619 |
| a0020c0029t0009 | 0/1 | 10679 | 1 | 0 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | AGCGC others(10674): Show |
chrX | 67539021 | 67735619 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0001c0001t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0001c0001t0007g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0001c0001t0007g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0001c0001t0007g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0001c0001t0010g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0001c0001t0014g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0001c0001t0019g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0001c0001t0019g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0001c0001t0050g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0001c0009t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0001c0009t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0001c0009t0006g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0001c0009t0008g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0001c0009t0008g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0001c0009t0010g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0001c0009t0033g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0001c0009t0042g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0001c0026t0025g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0001c0028t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0002c0005t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0002c0005t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0002c0005t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0002c0005t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0002c0005t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0002c0005t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0002c0005t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0002c0005t0005g0188 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0002c0005t0007g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0002c0005t0007g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0002c0005t0007g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0002c0005t0009g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0002c0005t0015g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0002c0005t0016g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0002c0005t0044g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0002c0005t0056g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0002c0010t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0002c0010t0008g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0002c0010t0014g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0002c0010t0018g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0002c0010t0020g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0002c0010t0030g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0002c0010t0035g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0002c0010t0036g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0002c0030t0016g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0003c0002t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0003c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0003c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0003c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0003c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0003c0002t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0003c0002t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0003c0002t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0003c0002t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0003c0002t0009g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0003c0002t0012g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0003c0002t0012g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0003c0002t0012g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0003c0002t0013g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0003c0002t0015g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0003c0002t0017g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0003c0002t0017g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0003c0002t0055g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0003c0021t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0003c0021t0008g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0003c0034t0008g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0004c0004t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0004c0004t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0004c0004t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0004c0004t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0004c0004t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0004c0004t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0004c0004t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0004c0004t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0004c0004t0007g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0004c0004t0012g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0004c0004t0021g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0004c0004t0027g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0004c0004t0031g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0004c0004t0046g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0004c0004t0047g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0004c0004t0048g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0004c0004t0051g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0004c0032t0058g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0004c0033t0054g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0005c0006t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0005c0006t0003g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0005c0006t0008g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0005c0006t0010g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0005c0006t0010g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0005c0006t0011g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0005c0006t0020g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0005c0006t0028g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0005c0006t0032g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0005c0006t0038g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0005c0006t0040g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0005c0011t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0005c0011t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0005c0011t0009g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0005c0011t0009g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0005c0011t0012g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0005c0011t0052g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0005c0011t0053g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0006c0003t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0006c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0006c0003t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0006c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0006c0003t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0006c0003t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0006c0003t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0006c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0006c0003t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0006c0003t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0006c0003t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0006c0003t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0006c0003t0007g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0006c0003t0009g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0006c0003t0015g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0006c0003t0017g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0006c0003t0026g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0006c0031t0043g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0007c0008t0005g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0007c0008t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0007c0008t0006g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0007c0008t0006g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0007c0008t0006g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0007c0008t0018g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0007c0008t0023g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0007c0008t0057g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0007c0016t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0007c0016t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0007c0016t0005g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0007c0016t0022g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0007c0025t0045g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0008c0007t0006g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0008c0007t0006g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0008c0007t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0008c0007t0006g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0008c0007t0010g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0008c0007t0011g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0008c0007t0034g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0008c0007t0039g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0008c0017t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0008c0017t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0008c0017t0005g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0009c0012t0005g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0009c0012t0005g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0009c0012t0005g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0009c0012t0024g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0009c0012t0037g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0009c0012t0041g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0009c0015t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0009c0015t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0009c0015t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0009c0015t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0010c0014t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0010c0014t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0010c0014t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0010c0014t0013g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0010c0014t0013g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0010c0035t0014g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0011c0013t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0011c0013t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0011c0013t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0011c0013t0009g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0011c0013t0013g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0012c0018t0011g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0012c0018t0011g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0013c0019t0016g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0013c0019t0029g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0014c0020t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0014c0020t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0015c0022t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0015c0023t0008g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0016c0027t0010g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0017c0024t0011g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0018c0036t0021g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0019c0037t0049g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| a0020c0029t0009g0024 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0008 | c0007 | t0010 | g0124 | EUR | GBR | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG00099 | hp2 | a0008 | c0017 | t0001 | g0187 | EUR | GBR | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG00140 | hp1 | a0004 | c0004 | t0001 | g0051 | EUR | GBR | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG00280 | hp1 | a0005 | c0006 | t0001 | g0129 | EUR | FIN | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG00609 | hp1 | a0003 | c0002 | t0001 | g0027 | EAS | CHS | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG00621 | hp1 | a0004 | c0004 | t0001 | g0076 | EAS | CHS | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG00642 | hp1 | a0001 | c0009 | t0008 | g0132 | AMR | PUR | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG00673 | hp1 | a0003 | c0002 | t0001 | g0069 | EAS | CHS | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG00735 | hp1 | a0004 | c0004 | t0012 | g0103 | AMR | PUR | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG00735 | hp2 | a0008 | c0007 | t0006 | g0133 | AMR | PUR | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG00738 | hp1 | a0001 | c0009 | t0042 | g0135 | AMR | PUR | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG00741 | hp1 | a0007 | c0008 | t0018 | g0130 | AMR | PUR | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG00741 | hp2 | a0006 | c0003 | t0002 | g0097 | AMR | PUR | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG01069 | hp1 | a0003 | c0002 | t0001 | g0093 | AMR | PUR | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG01074 | hp1 | a0005 | c0011 | t0003 | g0066 | AMR | PUR | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG01081 | hp1 | a0003 | c0002 | t0002 | g0040 | AMR | PUR | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG01081 | hp2 | a0007 | c0016 | t0005 | g0173 | AMR | PUR | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG01099 | hp1 | a0002 | c0005 | t0009 | g0035 | AMR | PUR | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG01106 | hp1 | a0005 | c0011 | t0012 | g0108 | AMR | PUR | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG01109 | hp1 | a0001 | c0001 | t0010 | g0166 | AMR | PUR | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG01167 | hp1 | a0012 | c0018 | t0011 | g0134 | AMR | PUR | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG01169 | hp1 | a0006 | c0003 | t0009 | g0084 | AMR | PUR | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG01169 | hp2 | a0012 | c0018 | t0011 | g0019 | AMR | PUR | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG01192 | hp1 | a0001 | c0009 | t0008 | g0128 | AMR | PUR | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG01243 | hp1 | a0002 | c0010 | t0035 | g0151 | AMR | PUR | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG01255 | hp1 | a0007 | c0008 | t0005 | g0142 | AMR | CLM | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG01258 | hp1 | a0003 | c0002 | t0003 | g0057 | AMR | CLM | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG01261 | hp1 | a0011 | c0013 | t0001 | g0052 | AMR | CLM | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG01358 | hp1 | a0003 | c0002 | t0001 | g0023 | AMR | CLM | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG01433 | hp1 | a0004 | c0004 | t0047 | g0053 | AMR | CLM | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG01515 | hp1 | a0006 | c0003 | t0007 | g0058 | EUR | IBS | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG01891 | hp1 | a0013 | c0019 | t0016 | g0125 | AFR | ACB | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG01891 | hp2 | a0001 | c0001 | t0019 | g0176 | AFR | ACB | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG01928 | hp1 | a0006 | c0003 | t0017 | g0060 | AMR | PEL | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG01934 | hp1 | a0010 | c0014 | t0001 | g0099 | AMR | PEL | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG01943 | hp1 | a0006 | c0003 | t0002 | g0036 | AMR | PEL | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG01952 | hp1 | a0006 | c0003 | t0001 | g0110 | AMR | PEL | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02015 | hp1 | a0002 | c0005 | t0007 | g0045 | EAS | KHV | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02027 | hp1 | a0011 | c0013 | t0001 | g0015 | EAS | KHV | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02040 | hp1 | a0003 | c0002 | t0003 | g0017 | EAS | KHV | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02055 | hp1 | a0008 | c0017 | t0005 | g0174 | AFR | ACB | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | KHV | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02071 | hp1 | a0006 | c0003 | t0002 | g0009 | EAS | KHV | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02074 | hp1 | a0002 | c0005 | t0001 | g0044 | EAS | KHV | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02083 | hp1 | a0003 | c0002 | t0001 | g0055 | EAS | KHV | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | KHV | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02132 | hp1 | a0001 | c0001 | t0007 | g0032 | EAS | KHV | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02135 | hp1 | a0014 | c0020 | t0003 | g0073 | EAS | KHV | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02145 | hp1 | a0008 | c0007 | t0006 | g0150 | AFR | ACB | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02257 | hp1 | a0001 | c0009 | t0010 | g0113 | AFR | ACB | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02257 | hp2 | a0007 | c0008 | t0023 | g0127 | AFR | ACB | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02258 | hp1 | a0003 | c0034 | t0008 | g0185 | AFR | ACB | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02300 | hp1 | a0006 | c0003 | t0001 | g0098 | AMR | PEL | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02451 | hp1 | a0002 | c0010 | t0036 | g0119 | AFR | ACB | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02451 | hp2 | a0001 | c0009 | t0033 | g0138 | AFR | ACB | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02572 | hp1 | a0001 | c0009 | t0004 | g0118 | AFR | GWD | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02615 | hp1 | a0004 | c0032 | t0058 | g0169 | AFR | GWD | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02615 | hp2 | a0005 | c0006 | t0010 | g0120 | AFR | GWD | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02630 | hp1 | a0008 | c0007 | t0034 | g0159 | AFR | GWD | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02630 | hp2 | a0002 | c0010 | t0014 | g0158 | AFR | GWD | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02647 | hp1 | a0009 | c0015 | t0005 | g0007 | AFR | GWD | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02698 | hp1 | a0003 | c0002 | t0012 | g0189 | SAS | PJL | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02717 | hp1 | a0006 | c0003 | t0004 | g0178 | AFR | GWD | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02723 | hp1 | a0002 | c0010 | t0030 | g0164 | AFR | GWD | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02723 | hp2 | a0010 | c0035 | t0014 | g0157 | AFR | GWD | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02735 | hp1 | a0005 | c0011 | t0009 | g0094 | SAS | PJL | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02738 | hp1 | a0010 | c0014 | t0001 | g0077 | SAS | PJL | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02809 | hp1 | a0007 | c0025 | t0045 | g0008 | AFR | GWD | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02809 | hp2 | a0001 | c0001 | t0019 | g0175 | AFR | GWD | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02818 | hp1 | a0005 | c0006 | t0028 | g0153 | AFR | GWD | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02818 | hp2 | a0016 | c0027 | t0010 | g0171 | AFR | GWD | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02886 | hp1 | a0013 | c0019 | t0029 | g0152 | AFR | GWD | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0186 | AFR | GWD | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02895 | hp1 | a0015 | c0023 | t0008 | g0180 | AFR | GWD | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02896 | hp1 | a0009 | c0012 | t0041 | g0114 | AFR | GWD | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02896 | hp2 | a0002 | c0005 | t0004 | g0184 | AFR | GWD | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02922 | hp1 | a0002 | c0010 | t0008 | g0156 | AFR | ESN | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02922 | hp2 | a0008 | c0007 | t0011 | g0148 | AFR | ESN | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02965 | hp1 | a0009 | c0012 | t0005 | g0144 | AFR | ESN | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02976 | hp1 | a0006 | c0003 | t0004 | g0177 | AFR | ESN | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02976 | hp2 | a0001 | c0009 | t0004 | g0155 | AFR | ESN | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG03017 | hp1 | a0002 | c0030 | t0016 | g0013 | SAS | PJL | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG03041 | hp1 | a0003 | c0021 | t0008 | g0123 | AFR | GWD | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG03041 | hp2 | a0007 | c0008 | t0006 | g0137 | AFR | GWD | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG03098 | hp1 | a0009 | c0012 | t0037 | g0143 | AFR | MSL | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG03130 | hp1 | a0004 | c0004 | t0031 | g0170 | AFR | ESN | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG03139 | hp1 | a0009 | c0012 | t0005 | g0147 | AFR | ESN | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG03195 | hp1 | a0009 | c0012 | t0005 | g0145 | AFR | ESN | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG03195 | hp2 | a0006 | c0031 | t0043 | g0167 | AFR | ESN | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG03209 | hp1 | a0005 | c0006 | t0020 | g0115 | AFR | MSL | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG03225 | hp1 | a0017 | c0024 | t0011 | g0162 | AFR | MSL | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG03453 | hp1 | a0009 | c0012 | t0024 | g0146 | AFR | MSL | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG03453 | hp2 | a0007 | c0008 | t0006 | g0136 | AFR | MSL | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG03486 | hp1 | a0002 | c0010 | t0020 | g0116 | AFR | MSL | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG03486 | hp2 | a0008 | c0007 | t0006 | g0163 | AFR | MSL | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG03490 | hp1 | a0004 | c0004 | t0001 | g0091 | SAS | PJL | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG03491 | hp1 | a0005 | c0006 | t0003 | g0003 | SAS | PJL | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG03491 | hp2 | a0003 | c0002 | t0012 | g0190 | SAS | PJL | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG03492 | hp1 | a0005 | c0006 | t0010 | g0003 | SAS | PJL | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG03516 | hp1 | a0007 | c0008 | t0005 | g0160 | AFR | ESN | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG03516 | hp2 | a0005 | c0006 | t0032 | g0117 | AFR | ESN | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG03540 | hp1 | a0003 | c0021 | t0006 | g0161 | AFR | GWD | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG03540 | hp2 | a0001 | c0028 | t0004 | g0183 | AFR | GWD | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG03579 | hp1 | a0007 | c0008 | t0006 | g0149 | AFR | MSL | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG03654 | hp1 | a0005 | c0011 | t0052 | g0068 | SAS | PJL | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG03688 | hp1 | a0005 | c0011 | t0053 | g0095 | SAS | STU | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG03704 | hp1 | a0003 | c0002 | t0012 | g0020 | SAS | PJL | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG03704 | hp2 | a0007 | c0016 | t0022 | g0043 | SAS | PJL | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG03710 | hp1 | a0006 | c0003 | t0015 | g0006 | SAS | PJL | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG03834 | hp1 | a0003 | c0002 | t0017 | g0005 | SAS | BEB | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG03834 | hp2 | a0005 | c0006 | t0008 | g0122 | SAS | BEB | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG03942 | hp1 | a0009 | c0015 | t0001 | g0059 | SAS | BEB | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG04115 | hp1 | a0002 | c0005 | t0001 | g0018 | SAS | STU | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG04199 | hp1 | a0001 | c0026 | t0025 | g0139 | SAS | STU | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0100 | SAS | STU | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | STU | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA18522 | hp1 | a0002 | c0010 | t0004 | g0154 | AFR | YRI | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA18612 | hp1 | a0004 | c0004 | t0003 | g0037 | EAS | CHB | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA18747 | hp1 | a0007 | c0016 | t0001 | g0030 | EAS | CHB | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA18906 | hp1 | a0005 | c0006 | t0040 | g0141 | AFR | YRI | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA18906 | hp2 | a0005 | c0006 | t0011 | g0004 | AFR | YRI | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA18940 | hp1 | a0003 | c0002 | t0013 | g0086 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA18943 | hp1 | a0002 | c0005 | t0016 | g0111 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA18944 | hp1 | a0004 | c0004 | t0007 | g0038 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA18945 | hp1 | a0003 | c0002 | t0015 | g0026 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA18952 | hp1 | a0006 | c0003 | t0001 | g0033 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA18953 | hp1 | a0002 | c0005 | t0007 | g0011 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA18960 | hp1 | a0014 | c0020 | t0001 | g0002 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA18962 | hp1 | a0010 | c0014 | t0003 | g0064 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA18965 | hp1 | a0006 | c0003 | t0026 | g0061 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA18966 | hp1 | a0002 | c0005 | t0001 | g0046 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA18967 | hp1 | a0004 | c0004 | t0051 | g0078 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA18971 | hp1 | a0010 | c0014 | t0013 | g0090 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA18974 | hp1 | a0011 | c0013 | t0003 | g0107 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA18977 | hp1 | a0005 | c0011 | t0001 | g0105 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA18982 | hp1 | a0003 | c0002 | t0055 | g0056 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA18983 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA18984 | hp1 | a0005 | c0011 | t0009 | g0074 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA18985 | hp1 | a0001 | c0001 | t0007 | g0012 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA18986 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA18988 | hp1 | a0006 | c0003 | t0002 | g0089 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA18989 | hp1 | a0007 | c0016 | t0003 | g0071 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA18994 | hp1 | a0002 | c0005 | t0001 | g0109 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA18995 | hp1 | a0018 | c0036 | t0021 | g0063 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA19000 | hp1 | a0006 | c0003 | t0001 | g0104 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA19004 | hp1 | a0008 | c0017 | t0001 | g0072 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA19005 | hp1 | a0011 | c0013 | t0009 | g0047 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA19006 | hp1 | a0011 | c0013 | t0013 | g0106 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA19007 | hp1 | a0006 | c0003 | t0001 | g0002 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA19009 | hp1 | a0003 | c0002 | t0009 | g0028 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA19012 | hp1 | a0002 | c0005 | t0007 | g0010 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA19043 | hp1 | a0004 | c0004 | t0027 | g0182 | AFR | LWK | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA19056 | hp1 | a0010 | c0014 | t0013 | g0031 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA19060 | hp1 | a0019 | c0037 | t0049 | g0082 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA19063 | hp1 | a0002 | c0005 | t0001 | g0041 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA19066 | hp1 | a0004 | c0004 | t0003 | g0081 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA19067 | hp1 | a0004 | c0004 | t0001 | g0102 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA19068 | hp1 | a0003 | c0002 | t0003 | g0034 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA19072 | hp1 | a0004 | c0004 | t0021 | g0021 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA19079 | hp1 | a0004 | c0004 | t0001 | g0042 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA19082 | hp1 | a0009 | c0015 | t0003 | g0048 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA19083 | hp1 | a0006 | c0003 | t0002 | g0067 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA19085 | hp1 | a0002 | c0005 | t0015 | g0088 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA19086 | hp1 | a0002 | c0005 | t0002 | g0096 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA19088 | hp1 | a0004 | c0004 | t0048 | g0087 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA19091 | hp1 | a0009 | c0015 | t0002 | g0022 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA20129 | hp1 | a0002 | c0005 | t0044 | g0181 | AFR | ASW | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA20129 | hp2 | a0005 | c0006 | t0038 | g0126 | AFR | ASW | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA20752 | hp1 | a0003 | c0002 | t0017 | g0014 | EUR | TSI | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0049 | EUR | TSI | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA20905 | hp1 | a0001 | c0001 | t0050 | g0050 | SAS | GIH | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02109 | hp1 | a0008 | c0007 | t0006 | g0140 | AFR | ACB | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02109 | hp2 | a0002 | c0005 | t0056 | g0172 | AFR | ACB | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG02486 | hp1 | a0008 | c0007 | t0039 | g0131 | AFR | ACB | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG03471 | hp1 | a0001 | c0009 | t0006 | g0168 | AFR | MSL | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG06807 | hp1 | a0002 | c0010 | t0018 | g0165 | AFR | USA | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| HG06807 | hp2 | a0001 | c0001 | t0014 | g0179 | AFR | USA | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA18955 | hp1 | a0004 | c0004 | t0001 | g0054 | EAS | JPT | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA20300 | hp1 | a0004 | c0033 | t0054 | g0101 | AFR | USA | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA20300 | hp2 | a0015 | c0022 | t0004 | g0112 | AFR | USA | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA21309 | hp1 | a0004 | c0004 | t0046 | g0016 | AFR | LWK | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| NA21309 | hp2 | a0007 | c0008 | t0057 | g0121 | AFR | LWK | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| homoSapiens | chm13v2 | a0020 | c0029 | t0009 | g0024 | REF | REF | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| homoSapiens | grch38p0 | a0002 | c0005 | t0005 | g0188 | REF | REF | AR_chrX_67539021_67735619 | AR | chrX | 67539021 | 67735619 |
| 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:67545316 | T | TGCA | 1 | a0006 | 18 | HG00741.hp2 HG01169.hp1 HG01515.hp1 others(15): Show |
disruptive_inframe_insertion | MODERATE | c.237_239dupGCA | p.Gln80dup | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/8 | 1366/10667 | 240/2763 | 80/920 | INFO_REALIGN_3_PRIME | chrX | 67545316 | ||
| chrX:67545316 | T | TGCAGCA | 1 | a0004 | 19 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(16): Show |
disruptive_inframe_insertion | MODERATE | c.234_239dupGCAGCA | p.Gln79_Gln80dup | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/8 | 1366/10667 | 240/2763 | 80/920 | INFO_REALIGN_3_PRIME | chrX | 67545316 | ||
| chrX:67545316 | T | TGCAGCAG others(2): Show |
1 | a0003 | 21 | HG00609.hp1 HG00673.hp1 HG01069.hp1 others(18): Show |
disruptive_inframe_insertion | MODERATE | c.231_239dupGCAGCAGC others(1): Show |
p.Gln78_Gln80dup | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/8 | 1366/10667 | 240/2763 | 80/920 | INFO_REALIGN_3_PRIME | chrX | 67545316 | ||
| chrX:67545316 | T | TGCAGCAG others(5): Show |
1 | a0011 | 5 | HG01261.hp1 HG02027.hp1 NA18974.hp1 others(2): Show |
disruptive_inframe_insertion | MODERATE | c.228_239dupGCAGCAGC others(4): Show |
p.Gln77_Gln80dup | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/8 | 1366/10667 | 240/2763 | 80/920 | INFO_REALIGN_3_PRIME | chrX | 67545316 | ||
| chrX:67545316 | T | TGCAGCAG others(8): Show |
1 | a0010 | 6 | HG01934.hp1 HG02723.hp2 HG02738.hp1 others(3): Show |
disruptive_inframe_insertion | MODERATE | c.225_239dupGCAGCAGC others(7): Show |
p.Gln76_Gln80dup | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/8 | 1366/10667 | 240/2763 | 80/920 | INFO_REALIGN_3_PRIME | chrX | 67545316 | ||
| chrX:67545316 | T | TGCAGCAG others(11): Show |
1 | a0018 | 1 | NA18995.hp1 | disruptive_inframe_insertion | MODERATE | c.222_239dupGCAGCAGC others(10): Show |
p.Gln75_Gln80dup | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/8 | 1366/10667 | 240/2763 | 80/920 | INFO_REALIGN_3_PRIME | chrX | 67545316 | ||
| chrX:67545316 | T | TGCAGCAG others(14): Show |
1 | a0019 | 1 | NA19060.hp1 | disruptive_inframe_insertion | MODERATE | c.219_239dupGCAGCAGC others(13): Show |
p.Gln74_Gln80dup | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/8 | 1366/10667 | 240/2763 | 80/920 | INFO_REALIGN_3_PRIME | chrX | 67545316 | ||
| chrX:67545316 | TGCA | T | 2 | a0001 a0016 |
35 | HG00642.hp1 HG00738.hp1 HG01109.hp1 others(32): Show |
disruptive_inframe_deletion | MODERATE | c.237_239delGCA | p.Gln80del | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/8 | 1363/10667 | 237/2763 | 79/920 | INFO_REALIGN_3_PRIME | chrX | 67545316 | ||
| chrX:67545316 | TGCAGCA | T | 1 | a0005 | 18 | HG00280.hp1 HG01074.hp1 HG01106.hp1 others(15): Show |
disruptive_inframe_deletion | MODERATE | c.234_239delGCAGCA | p.Gln79_Gln80del | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/8 | 1360/10667 | 234/2763 | 78/920 | INFO_REALIGN_3_PRIME | chrX | 67545316 | ||
| chrX:67545316 | TGCAGCAG others(2): Show |
T | 1 | a0007 | 13 | HG00741.hp1 HG01081.hp2 HG01255.hp1 others(10): Show |
disruptive_inframe_deletion | MODERATE | c.231_239delGCAGCAGC others(1): Show |
p.Gln78_Gln80del | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/8 | 1357/10667 | 231/2763 | 77/920 | INFO_REALIGN_3_PRIME | chrX | 67545316 | ||
| chrX:67545316 | TGCAGCAG others(5): Show |
T | 1 | a0008 | 11 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(8): Show |
disruptive_inframe_deletion | MODERATE | c.228_239delGCAGCAGC others(4): Show |
p.Gln77_Gln80del | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/8 | 1354/10667 | 228/2763 | 76/920 | INFO_REALIGN_3_PRIME | chrX | 67545316 | ||
| chrX:67545316 | TGCAGCAG others(8): Show |
T | 2 | a0009 a0017 |
11 | HG02647.hp1 HG02896.hp1 HG02965.hp1 others(8): Show |
disruptive_inframe_deletion | MODERATE | c.225_239delGCAGCAGC others(7): Show |
p.Gln76_Gln80del | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/8 | 1351/10667 | 225/2763 | 75/920 | INFO_REALIGN_3_PRIME | chrX | 67545316 | ||
| chrX:67545316 | TGCAGCAG others(11): Show |
T | 1 | a0015 | 2 | HG02895.hp1 NA20300.hp2 |
disruptive_inframe_deletion | MODERATE | c.222_239delGCAGCAGC others(10): Show |
p.Gln75_Gln80del | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/8 | 1348/10667 | 222/2763 | 74/920 | INFO_REALIGN_3_PRIME | chrX | 67545316 | ||
| chrX:67545316 | TGCAGCAG others(14): Show |
T | 1 | a0014 | 2 | HG02135.hp1 NA18960.hp1 |
disruptive_inframe_deletion | MODERATE | c.219_239delGCAGCAGC others(13): Show |
p.Gln74_Gln80del | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/8 | 1345/10667 | 219/2763 | 73/920 | INFO_REALIGN_3_PRIME | chrX | 67545316 | ||
| chrX:67545316 | TGCAGCAG others(17): Show |
T | 1 | a0013 | 2 | HG01891.hp1 HG02886.hp1 |
disruptive_inframe_deletion | MODERATE | c.216_239delGCAGCAGC others(16): Show |
p.Gln73_Gln80del | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/8 | 1342/10667 | 216/2763 | 72/920 | INFO_REALIGN_3_PRIME | chrX | 67545316 | ||
| chrX:67545316 | TGCAGCAG others(20): Show |
T | 1 | a0012 | 2 | HG01167.hp1 HG01169.hp2 |
disruptive_inframe_deletion | MODERATE | c.213_239delGCAGCAGC others(19): Show |
p.Gln72_Gln80del | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/8 | 1339/10667 | 213/2763 | 71/920 | INFO_REALIGN_3_PRIME | chrX | 67545316 | ||
| chrX:67546285 | C | G | 1 | a0017 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.1139C>G | p.Pro380Arg | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/8 | 2265/10667 | 1139/2763 | 380/920 | chrX | 67546285 | |||
| chrX:67546303 | G | A | 1 | a0001 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.1157G>A | p.Arg386His | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/8 | 2283/10667 | 1157/2763 | 386/920 | chrX | 67546303 | |||
| chrX:67546509 | GGTGGTGG others(4): Show |
G | 1 | a0016 | 1 | HG02818.hp2 | frameshift_variant | HIGH | c.1365_1375delTGGTGG others(5): Show |
p.Gly456fs | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/8 | 2491/10667 | 1365/2763 | 455/920 | INFO_REALIGN_3_PRIME | chrX | 67546509 | ||
| chrX:67546514 | T | TGGC | 10 | a0001 a0002 a0003 others(7): Show |
32 | HG00099.hp1 HG00642.hp1 HG00738.hp1 others(29): Show |
disruptive_inframe_insertion | MODERATE | c.1418_1420dupGCG | p.Gly473dup | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/8 | 2547/10667 | 1421/2763 | 474/920 | INFO_REALIGN_3_PRIME | chrX | 67546514 | ||
| chrX:67546514 | T | TGGCGGC | 7 | a0001 a0005 a0006 others(4): Show |
10 | HG01106.hp1 HG01891.hp1 HG02257.hp2 others(7): Show |
disruptive_inframe_insertion | MODERATE | c.1415_1420dupGCGGCG | p.Gly472_Gly473dup | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/8 | 2547/10667 | 1421/2763 | 474/920 | INFO_REALIGN_3_PRIME | chrX | 67546514 | ||
| chrX:67546514 | T | TGGCGGCG others(5): Show |
3 | a0001 a0007 a0008 |
3 | HG01081.hp2 HG02055.hp1 HG02257.hp1 |
disruptive_inframe_insertion | MODERATE | c.1409_1420dupGCGGCG others(6): Show |
p.Gly470_Gly473dup | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/8 | 2547/10667 | 1421/2763 | 474/920 | INFO_REALIGN_3_PRIME | chrX | 67546514 | ||
| chrX:67546514 | T | TGGCGGCG others(11): Show |
1 | a0012 | 2 | HG01167.hp1 HG01169.hp2 |
disruptive_inframe_insertion | MODERATE | c.1403_1420dupGCGGCG others(12): Show |
p.Gly468_Gly473dup | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/8 | 2547/10667 | 1421/2763 | 474/920 | INFO_REALIGN_3_PRIME | chrX | 67546514 | ||
| chrX:67546514 | TGGC | T | 12 | a0001 a0002 a0003 others(9): Show |
33 | HG00673.hp1 HG01891.hp2 HG02040.hp1 others(30): Show |
disruptive_inframe_deletion | MODERATE | c.1418_1420delGCG | p.Gly473del | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/8 | 2544/10667 | 1418/2763 | 473/920 | INFO_REALIGN_3_PRIME | chrX | 67546514 | ||
| chrX:67546514 | TGGCGGC | T | 8 | a0001 a0002 a0004 others(5): Show |
11 | HG00735.hp2 HG02451.hp2 HG02615.hp1 others(8): Show |
disruptive_inframe_deletion | MODERATE | c.1415_1420delGCGGCG | p.Gly472_Gly473del | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/8 | 2541/10667 | 1415/2763 | 472/920 | INFO_REALIGN_3_PRIME | chrX | 67546514 | ||
| chrX:67546514 | TGGCGGCG others(2): Show |
T | 5 | a0002 a0004 a0007 others(2): Show |
8 | HG01243.hp1 HG02451.hp1 HG02486.hp1 others(5): Show |
disruptive_inframe_deletion | MODERATE | c.1412_1420delGCGGCG others(3): Show |
p.Gly471_Gly473del | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/8 | 2538/10667 | 1412/2763 | 471/920 | INFO_REALIGN_3_PRIME | chrX | 67546514 | ||
| chrX:67546514 | TGGCGGCG others(5): Show |
T | 4 | a0002 a0003 a0004 others(1): Show |
5 | HG01358.hp1 HG01433.hp1 NA18953.hp1 others(2): Show |
disruptive_inframe_deletion | MODERATE | c.1409_1420delGCGGCG others(6): Show |
p.Gly470_Gly473del | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/8 | 2535/10667 | 1409/2763 | 470/920 | INFO_REALIGN_3_PRIME | chrX | 67546514 | ||
| chrX:67546514 | TGGCGGCG others(8): Show |
T | 3 | a0002 a0004 a0005 |
4 | HG00280.hp1 NA19085.hp1 NA19088.hp1 others(1): Show |
disruptive_inframe_deletion | MODERATE | c.1406_1420delGCGGCG others(9): Show |
p.Gly469_Gly473del | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/8 | 2532/10667 | 1406/2763 | 469/920 | INFO_REALIGN_3_PRIME | chrX | 67546514 | ||
| chrX:67546514 | TGGCGGCG others(11): Show |
T | 1 | a0007 | 1 | HG03704.hp2 | disruptive_inframe_deletion | MODERATE | c.1403_1420delGCGGCG others(12): Show |
p.Gly468_Gly473del | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/8 | 2529/10667 | 1403/2763 | 468/920 | INFO_REALIGN_3_PRIME | chrX | 67546514 | ||
| chrX:67546514 | TGGCGGCG others(23): Show |
T | 1 | a0007 | 1 | HG01255.hp1 | disruptive_inframe_deletion | MODERATE | c.1391_1420delGCGGCG others(24): Show |
p.Gly464_Gly473del | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/8 | 2517/10667 | 1391/2763 | 464/920 | INFO_REALIGN_3_PRIME | chrX | 67546514 | ||
| chrX:67546722 | C | A | 1 | a0001 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.1576C>A | p.Pro526Thr | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/8 | 2702/10667 | 1576/2763 | 526/920 | chrX | 67546722 |
| 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:67545470 | G | C | 1 | a0003c0034 | 1 | HG02258.hp1 | synonymous_variant | LOW | c.324G>C | p.Leu108Leu | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/8 | 1450/10667 | 324/2763 | 108/920 | chrX | 67545470 | |||
| chrX:67545785 | G | A | 14 | a0001c0009 a0001c0026 a0002c0010 others(11): Show |
60 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(57): Show |
synonymous_variant | LOW | c.639G>A | p.Glu213Glu | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/8 | 1765/10667 | 639/2763 | 213/920 | chrX | 67545785 | |||
| chrX:67545800 | C | T | 1 | a0002c0030 | 1 | HG03017.hp1 | synonymous_variant | LOW | c.654C>T | p.Pro218Pro | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/8 | 1780/10667 | 654/2763 | 218/920 | chrX | 67545800 | |||
| chrX:67546175 | T | C | 1 | a0007c0025 | 1 | HG02809.hp1 | synonymous_variant | LOW | c.1029T>C | p.Ser343Ser | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/8 | 2155/10667 | 1029/2763 | 343/920 | chrX | 67546175 | |||
| chrX:67546433 | C | T | 1 | a0004c0033 | 1 | NA20300.hp1 | synonymous_variant | LOW | c.1287C>T | p.Ala429Ala | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/8 | 2413/10667 | 1287/2763 | 429/920 | chrX | 67546433 | |||
| chrX:67546523 | C | T | 1 | a0016c0027 | 1 | HG02818.hp2 | synonymous_variant | LOW | c.1377C>T | p.Gly459Gly | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/8 | 2503/10667 | 1377/2763 | 459/920 | chrX | 67546523 | |||
| chrX:67546526 | C | T | 1 | a0016c0027 | 1 | HG02818.hp2 | synonymous_variant | LOW | c.1380C>T | p.Gly460Gly | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/8 | 2506/10667 | 1380/2763 | 460/920 | chrX | 67546526 | |||
| chrX:67643382 | G | A | 1 | a0004c0032 | 1 | HG02615.hp1 | synonymous_variant | LOW | c.1743G>A | p.Lys581Lys | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/8 | 2869/10667 | 1743/2763 | 581/920 | chrX | 67643382 |
| 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:67544059 | G | C | 1 | a0007c0016t0022 | 1 | HG03704.hp2 | 5_prime_UTR_variant | MODIFIER | c.-1088G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/8 | 1088 | chrX | 67544059 | ||||||
| chrX:67544661 | C | T | 1 | a0004c0032t0058 | 1 | HG02615.hp1 | 5_prime_UTR_variant | MODIFIER | c.-486C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/8 | 486 | chrX | 67544661 | ||||||
| chrX:67544960 | G | C | 1 | a0007c0008t0023 | 1 | HG02257.hp2 | 5_prime_UTR_variant | MODIFIER | c.-187G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/8 | 187 | chrX | 67544960 | ||||||
| chrX:67544991 | G | C | 1 | a0009c0012t0024 | 1 | HG03453.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-156G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/8 | chrX | 67544991 | |||||||
| chrX:67723957 | T | C | 1 | a0001c0026t0025 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*116T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 116 | chrX | 67723957 | ||||||
| chrX:67723996 | G | A | 1 | a0006c0003t0026 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*155G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 155 | chrX | 67723996 | ||||||
| chrX:67724049 | A | G | 1 | a0007c0008t0057 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*208A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 208 | chrX | 67724049 | ||||||
| chrX:67724136 | G | T | 1 | a0002c0005t0056 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*295G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 295 | chrX | 67724136 | ||||||
| chrX:67724277 | CA | C | 65 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(62): Show |
113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*447delA | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 447 | INFO_REALIGN_3_PRIME | chrX | 67724277 | |||||
| chrX:67724373 | A | G | 1 | a0007c0025t0045 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*532A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 532 | chrX | 67724373 | ||||||
| chrX:67724501 | T | C | 1 | a0004c0004t0046 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*660T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 660 | chrX | 67724501 | ||||||
| chrX:67724583 | C | A | 1 | a0004c0004t0047 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*742C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 742 | chrX | 67724583 | ||||||
| chrX:67725344 | G | T | 1 | a0002c0005t0044 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1503G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 1503 | chrX | 67725344 | ||||||
| chrX:67725898 | T | C | 102 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(99): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*2057T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 2057 | chrX | 67725898 | ||||||
| chrX:67726016 | C | T | 1 | a0003c0002t0055 | 1 | NA18982.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2175C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 2175 | chrX | 67726016 | ||||||
| chrX:67726139 | G | A | 3 | a0002c0010t0035 a0002c0010t0036 a0008c0007t0034 |
3 | HG01243.hp1 HG02451.hp1 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2298G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 2298 | chrX | 67726139 | ||||||
| chrX:67726515 | T | A | 1 | a0004c0004t0027 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2674T>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 2674 | chrX | 67726515 | ||||||
| chrX:67727009 | T | C | 102 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(99): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*3168T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 3168 | chrX | 67727009 | ||||||
| chrX:67727072 | C | T | 1 | a0001c0009t0033 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3231C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 3231 | chrX | 67727072 | ||||||
| chrX:67727310 | C | T | 1 | a0006c0031t0043 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3469C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 3469 | chrX | 67727310 | ||||||
| chrX:67727594 | C | A | 1 | a0004c0004t0048 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3753C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 3753 | chrX | 67727594 | ||||||
| chrX:67728091 | G | A | 2 | a0005c0006t0028 a0013c0019t0029 |
2 | HG02818.hp1 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4250G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 4250 | chrX | 67728091 | ||||||
| chrX:67728177 | G | GT | 101 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(98): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*4345dupT | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 4346 | INFO_REALIGN_3_PRIME | chrX | 67728177 | |||||
| chrX:67728238 | G | T | 4 | a0001c0001t0019 a0002c0010t0020 a0005c0006t0020 others(1): Show |
5 | HG01891.hp2 HG02809.hp2 HG03209.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4397G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 4397 | chrX | 67728238 | ||||||
| chrX:67728574 | A | AAT | 25 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0019 others(22): Show |
43 | HG00735.hp2 HG00741.hp2 HG01081.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*4773_*4774dupTA | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 4775 | INFO_REALIGN_3_PRIME | chrX | 67728574 | |||||
| chrX:67728574 | A | AATAT | 29 | a0001c0001t0001 a0001c0009t0008 a0002c0005t0001 others(26): Show |
55 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*4771_*4774dupTATA | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 4775 | INFO_REALIGN_3_PRIME | chrX | 67728574 | |||||
| chrX:67728574 | A | AATATAT | 17 | a0001c0001t0003 a0001c0001t0010 a0001c0009t0010 others(14): Show |
22 | HG00099.hp1 HG01074.hp1 HG01109.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*4769_*4774dupTATA others(2): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 4775 | INFO_REALIGN_3_PRIME | chrX | 67728574 | |||||
| chrX:67728574 | A | AATATATA others(1): Show |
2 | a0004c0004t0021 a0018c0036t0021 |
2 | NA18995.hp1 NA19072.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4767_*4774dupTATA others(4): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 4775 | INFO_REALIGN_3_PRIME | chrX | 67728574 | |||||
| chrX:67728574 | A | AATATATA others(3): Show |
3 | a0002c0005t0016 a0002c0030t0016 a0013c0019t0016 |
3 | HG01891.hp1 HG03017.hp1 NA18943.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4765_*4774dupTATA others(6): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 4775 | INFO_REALIGN_3_PRIME | chrX | 67728574 | |||||
| chrX:67728574 | A | AATATATA others(5): Show |
8 | a0002c0005t0009 a0002c0010t0018 a0003c0002t0009 others(5): Show |
9 | HG00741.hp1 HG01099.hp1 HG01169.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4763_*4774dupTATA others(8): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 4775 | INFO_REALIGN_3_PRIME | chrX | 67728574 | |||||
| chrX:67728574 | A | AATATATA others(7): Show |
6 | a0001c0009t0042 a0001c0026t0025 a0003c0002t0017 others(3): Show |
7 | HG00738.hp1 HG01928.hp1 HG03130.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4761_*4774dupTATA others(10): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 4775 | INFO_REALIGN_3_PRIME | chrX | 67728574 | |||||
| chrX:67728574 | A | AATATATA others(9): Show |
1 | a0005c0011t0053 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4759_*4774dupTATA others(12): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 4775 | INFO_REALIGN_3_PRIME | chrX | 67728574 | |||||
| chrX:67728574 | A | AATATATA others(11): Show |
1 | a0001c0009t0033 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4757_*4774dupTATA others(14): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 4775 | INFO_REALIGN_3_PRIME | chrX | 67728574 | |||||
| chrX:67728574 | A | AATATATA others(13): Show |
1 | a0004c0033t0054 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4755_*4774dupTATA others(16): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 4775 | INFO_REALIGN_3_PRIME | chrX | 67728574 | |||||
| chrX:67728574 | AAT | A | 6 | a0002c0005t0015 a0002c0010t0030 a0003c0002t0015 others(3): Show |
6 | HG02723.hp1 HG03098.hp1 HG03710.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4773_*4774delTA | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 4773 | INFO_REALIGN_3_PRIME | chrX | 67728574 | |||||
| chrX:67728574 | AATATAT | A | 3 | a0003c0002t0012 a0004c0004t0012 a0005c0011t0012 |
5 | HG00735.hp1 HG01106.hp1 HG02698.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4769_*4774delTATA others(2): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 4769 | INFO_REALIGN_3_PRIME | chrX | 67728574 | |||||
| chrX:67728574 | AATATATA others(3): Show |
A | 2 | a0001c0001t0050 a0007c0025t0045 |
2 | HG02809.hp1 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4765_*4774delTATA others(6): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 4765 | INFO_REALIGN_3_PRIME | chrX | 67728574 | |||||
| chrX:67728574 | AATATATA others(5): Show |
A | 1 | a0019c0037t0049 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4763_*4774delTATA others(8): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 4763 | INFO_REALIGN_3_PRIME | chrX | 67728574 | |||||
| chrX:67728574 | AATATATA others(7): Show |
A | 4 | a0003c0002t0013 a0003c0002t0055 a0010c0014t0013 others(1): Show |
5 | NA18940.hp1 NA18971.hp1 NA18982.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4761_*4774delTATA others(10): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 4761 | INFO_REALIGN_3_PRIME | chrX | 67728574 | |||||
| chrX:67728616 | G | T | 1 | a0004c0004t0051 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4775G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 4775 | chrX | 67728616 | ||||||
| chrX:67728617 | T | A | 1 | a0004c0004t0051 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4776T>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 4776 | chrX | 67728617 | ||||||
| chrX:67729079 | G | A | 1 | a0008c0007t0039 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5238G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 5238 | chrX | 67729079 | ||||||
| chrX:67729102 | C | T | 1 | a0004c0032t0058 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5261C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 5261 | chrX | 67729102 | ||||||
| chrX:67729827 | C | T | 2 | a0002c0010t0035 a0002c0010t0036 |
2 | HG01243.hp1 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5986C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 5986 | chrX | 67729827 | ||||||
| chrX:67729880 | C | T | 102 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(99): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*6039C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 6039 | chrX | 67729880 | ||||||
| chrX:67730180 | TAAG | T | 98 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(95): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*6344_*6346delAGA | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 6344 | INFO_REALIGN_3_PRIME | chrX | 67730180 | |||||
| chrX:67730181 | AAGAAGAG | A | 4 | a0001c0001t0019 a0002c0010t0020 a0005c0006t0020 others(1): Show |
5 | HG01891.hp2 HG02809.hp2 HG03209.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6344_*6350delAGAG others(3): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 6344 | INFO_REALIGN_3_PRIME | chrX | 67730181 | |||||
| chrX:67730263 | C | T | 102 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(99): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*6422C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 6422 | chrX | 67730263 | ||||||
| chrX:67730305 | C | T | 1 | a0005c0006t0038 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6464C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 6464 | chrX | 67730305 | ||||||
| chrX:67730527 | A | G | 3 | a0002c0010t0035 a0002c0010t0036 a0008c0007t0034 |
3 | HG01243.hp1 HG02451.hp1 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6686A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 6686 | chrX | 67730527 | ||||||
| chrX:67730597 | A | T | 1 | a0005c0011t0052 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6756A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 8/8 | 6756 | chrX | 67730597 |
| 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:67547814 | T | C | 1 | a0005c0006t0011g0004 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1616+1052T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67547814 | |||||||
| chrX:67547830 | G | A | 1 | a0003c0002t0017g0005 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1616+1068G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67547830 | |||||||
| chrX:67548107 | G | A | 187 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(184): Show |
188 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.1616+1345G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67548107 | |||||||
| chrX:67548513 | T | C | 1 | a0006c0003t0015g0006 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1616+1751T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67548513 | |||||||
| chrX:67548780 | T | C | 1 | a0009c0015t0005g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1616+2018T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67548780 | |||||||
| chrX:67548878 | A | G | 19 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(16): Show |
19 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1616+2116A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67548878 | |||||||
| chrX:67549404 | C | T | 2 | a0001c0009t0006g0168 a0006c0031t0043g0167 |
2 | HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1616+2642C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67549404 | |||||||
| chrX:67550275 | A | G | 1 | a0001c0001t0010g0166 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1616+3513A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67550275 | |||||||
| chrX:67550434 | T | C | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1616+3672T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67550434 | |||||||
| chrX:67550442 | T | G | 1 | a0006c0003t0002g0009 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1616+3680T>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67550442 | |||||||
| chrX:67550456 | T | C | 2 | a0002c0005t0007g0010 a0002c0005t0007g0011 |
2 | NA18953.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1616+3694T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67550456 | |||||||
| chrX:67550461 | G | A | 2 | a0001c0001t0007g0001 a0001c0001t0007g0012 |
3 | NA18983.hp1 NA18985.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.1616+3699G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67550461 | |||||||
| chrX:67550656 | TA | T | 77 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(74): Show |
77 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.1616+3908delA | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67550656 | ||||||
| chrX:67550735 | C | A | 1 | a0002c0030t0016g0013 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1616+3973C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67550735 | |||||||
| chrX:67550902 | C | A | 1 | a0004c0004t0031g0170 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1616+4140C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67550902 | |||||||
| chrX:67550977 | G | C | 1 | a0008c0017t0001g0187 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1616+4215G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67550977 | |||||||
| chrX:67551001 | G | GT | 34 | a0001c0001t0002g0100 a0001c0001t0004g0186 a0001c0001t0010g0166 others(31): Show |
34 | HG00735.hp1 HG00741.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.1616+4262dupT | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67551001 | ||||||
| chrX:67551001 | G | GTTTT | 37 | a0001c0009t0006g0168 a0001c0009t0008g0128 a0001c0009t0008g0132 others(34): Show |
37 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1616+4259_1616+426 others(8): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67551001 | ||||||
| chrX:67551001 | G | GTTTTT | 16 | a0001c0009t0004g0155 a0002c0010t0004g0154 a0002c0010t0008g0156 others(13): Show |
16 | HG01243.hp1 HG02630.hp1 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1616+4258_1616+426 others(9): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67551001 | ||||||
| chrX:67551311 | T | C | 2 | a0002c0010t0035g0151 a0002c0010t0036g0119 |
2 | HG01243.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1616+4549T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67551311 | |||||||
| chrX:67551508 | C | G | 2 | a0002c0010t0018g0165 a0002c0010t0030g0164 |
2 | HG02723.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1616+4746C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67551508 | |||||||
| chrX:67551519 | C | T | 1 | a0001c0001t0004g0186 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1616+4757C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67551519 | |||||||
| chrX:67551835 | A | G | 2 | a0005c0011t0009g0094 a0005c0011t0053g0095 |
2 | HG02735.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1616+5073A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67551835 | |||||||
| chrX:67552436 | C | T | 1 | a0003c0002t0001g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1616+5674C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67552436 | |||||||
| chrX:67552668 | G | A | 1 | a0005c0006t0010g0120 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1616+5906G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67552668 | |||||||
| chrX:67552851 | T | G | 10 | a0003c0021t0008g0123 a0005c0006t0003g0003 a0005c0006t0008g0122 others(7): Show |
10 | HG00099.hp1 HG01891.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1616+6089T>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67552851 | |||||||
| chrX:67552866 | T | C | 1 | a0003c0002t0017g0014 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1616+6104T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67552866 | |||||||
| chrX:67553117 | G | A | 1 | a0005c0006t0011g0004 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1616+6355G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67553117 | |||||||
| chrX:67553179 | G | T | 1 | a0006c0003t0002g0009 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1616+6417G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67553179 | |||||||
| chrX:67553437 | G | A | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1616+6675G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67553437 | |||||||
| chrX:67553598 | G | A | 1 | a0001c0009t0010g0113 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1616+6836G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67553598 | |||||||
| chrX:67553726 | A | C | 1 | a0003c0034t0008g0185 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1616+6964A>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67553726 | |||||||
| chrX:67553765 | T | A | 1 | a0011c0013t0001g0015 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1616+7003T>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67553765 | |||||||
| chrX:67554074 | C | T | 1 | a0002c0005t0016g0111 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1616+7312C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67554074 | |||||||
| chrX:67554075 | G | A | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1616+7313G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67554075 | |||||||
| chrX:67554165 | T | C | 1 | a0009c0012t0041g0114 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1616+7403T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67554165 | |||||||
| chrX:67554469 | T | C | 17 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(14): Show |
17 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1616+7707T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67554469 | |||||||
| chrX:67554553 | A | G | 16 | a0003c0021t0006g0161 a0005c0006t0040g0141 a0007c0008t0005g0142 others(13): Show |
16 | HG01255.hp1 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1616+7791A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67554553 | |||||||
| chrX:67554633 | G | A | 1 | a0005c0006t0038g0126 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1616+7871G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67554633 | |||||||
| chrX:67554915 | CA | C | 5 | a0001c0001t0001g0092 a0001c0026t0025g0139 a0002c0030t0016g0013 others(2): Show |
5 | HG01256.hp1 HG02896.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.1616+8171delA | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67554915 | ||||||
| chrX:67555002 | G | A | 1 | a0007c0008t0057g0121 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1616+8240G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67555002 | |||||||
| chrX:67555145 | A | G | 1 | a0002c0005t0016g0111 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1616+8383A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67555145 | |||||||
| chrX:67555194 | A | T | 1 | a0010c0014t0013g0090 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1616+8432A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67555194 | |||||||
| chrX:67555304 | A | G | 1 | a0001c0001t0010g0166 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1616+8542A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67555304 | |||||||
| chrX:67555404 | A | T | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1616+8642A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67555404 | |||||||
| chrX:67555704 | C | G | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1616+8942C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67555704 | |||||||
| chrX:67555922 | A | G | 1 | a0008c0007t0034g0159 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1616+9160A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67555922 | |||||||
| chrX:67556088 | A | G | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1616+9326A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67556088 | |||||||
| chrX:67556190 | A | G | 1 | a0002c0005t0056g0172 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1616+9428A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67556190 | |||||||
| chrX:67556384 | A | T | 3 | a0002c0005t0015g0088 a0004c0004t0048g0087 a0006c0003t0002g0089 |
3 | NA18988.hp1 NA19085.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1616+9622A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67556384 | |||||||
| chrX:67556404 | C | T | 1 | a0006c0003t0001g0110 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1616+9642C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67556404 | |||||||
| chrX:67556842 | CGCAAAGG others(7): Show |
C | 17 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(14): Show |
17 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1616+10084_1616+10 others(20): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67556842 | ||||||
| chrX:67556861 | G | A | 1 | a0004c0004t0046g0016 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1616+10099G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67556861 | |||||||
| chrX:67557103 | T | G | 2 | a0007c0016t0005g0173 a0008c0017t0005g0174 |
2 | HG01081.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1616+10341T>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67557103 | |||||||
| chrX:67557224 | G | A | 34 | a0001c0009t0008g0128 a0001c0009t0008g0132 a0001c0026t0025g0139 others(31): Show |
34 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.1616+10462G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67557224 | |||||||
| chrX:67557388 | T | C | 1 | a0003c0002t0003g0017 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1616+10626T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67557388 | |||||||
| chrX:67558763 | G | C | 1 | a0006c0031t0043g0167 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1616+12001G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67558763 | |||||||
| chrX:67559190 | G | A | 1 | a0002c0005t0001g0018 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1616+12428G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67559190 | |||||||
| chrX:67559349 | G | A | 1 | a0007c0008t0023g0127 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1616+12587G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67559349 | |||||||
| chrX:67559412 | A | T | 1 | a0008c0007t0006g0133 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1616+12650A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67559412 | |||||||
| chrX:67559839 | C | T | 1 | a0002c0005t0001g0109 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1616+13077C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67559839 | |||||||
| chrX:67560168 | C | A | 6 | a0001c0009t0006g0168 a0001c0009t0042g0135 a0005c0006t0038g0126 others(3): Show |
6 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.1616+13406C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67560168 | |||||||
| chrX:67560375 | T | C | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1616+13613T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67560375 | |||||||
| chrX:67560481 | A | T | 3 | a0002c0010t0014g0158 a0002c0010t0035g0151 a0002c0010t0036g0119 |
3 | HG01243.hp1 HG02451.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1616+13719A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67560481 | |||||||
| chrX:67560694 | G | A | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1616+13932G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67560694 | |||||||
| chrX:67560899 | G | A | 1 | a0003c0002t0012g0020 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1616+14137G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67560899 | |||||||
| chrX:67561017 | A | G | 1 | a0005c0011t0012g0108 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1616+14255A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67561017 | |||||||
| chrX:67561136 | G | A | 2 | a0002c0010t0018g0165 a0002c0010t0030g0164 |
2 | HG02723.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1616+14374G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67561136 | |||||||
| chrX:67561748 | A | G | 1 | a0009c0015t0005g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1616+14986A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67561748 | |||||||
| chrX:67561835 | G | T | 1 | a0008c0007t0034g0159 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1616+15073G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67561835 | |||||||
| chrX:67561928 | G | GT | 40 | a0001c0001t0001g0079 a0001c0001t0001g0085 a0001c0001t0002g0075 others(37): Show |
40 | HG00621.hp1 HG00642.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.1616+15193dupT | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67561928 | ||||||
| chrX:67561928 | GT | G | 17 | a0001c0001t0014g0179 a0001c0001t0019g0175 a0001c0001t0019g0176 others(14): Show |
17 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1616+15193delT | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67561928 | ||||||
| chrX:67562033 | G | A | 6 | a0001c0009t0006g0168 a0001c0009t0042g0135 a0005c0006t0038g0126 others(3): Show |
6 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.1616+15271G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67562033 | |||||||
| chrX:67562356 | A | ATG | 13 | a0001c0001t0001g0070 a0001c0001t0002g0100 a0001c0001t0007g0012 others(10): Show |
13 | HG02135.hp1 HG02451.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1616+15632_1616+15 others(8): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67562356 | ||||||
| chrX:67562356 | A | ATGTG | 8 | a0001c0009t0004g0118 a0001c0009t0004g0155 a0002c0010t0004g0154 others(5): Show |
8 | HG02572.hp1 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1616+15630_1616+15 others(10): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67562356 | ||||||
| chrX:67562356 | ATG | A | 30 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(27): Show |
30 | HG00099.hp1 HG01081.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.1616+15632_1616+15 others(8): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67562356 | ||||||
| chrX:67562356 | ATGTG | A | 4 | a0004c0004t0001g0091 a0005c0006t0003g0003 a0005c0006t0010g0003 others(1): Show |
4 | HG03490.hp1 HG03491.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.1616+15630_1616+15 others(10): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67562356 | ||||||
| chrX:67562356 | ATGTGTG | A | 3 | a0002c0010t0020g0116 a0005c0006t0020g0115 a0005c0006t0032g0117 |
3 | HG03209.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1616+15628_1616+15 others(12): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67562356 | ||||||
| chrX:67562376 | G | GTGTGTGT others(7): Show |
1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1616+15627_1616+15 others(20): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67562376 | ||||||
| chrX:67562580 | T | C | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1616+15818T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67562580 | |||||||
| chrX:67562881 | G | T | 1 | a0001c0009t0008g0132 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1616+16119G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67562881 | |||||||
| chrX:67562957 | C | T | 1 | a0005c0006t0011g0004 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1616+16195C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67562957 | |||||||
| chrX:67563124 | A | G | 1 | a0006c0003t0002g0009 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1616+16362A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67563124 | |||||||
| chrX:67563498 | T | G | 1 | a0004c0004t0048g0087 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1616+16736T>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67563498 | |||||||
| chrX:67563501 | G | T | 10 | a0001c0001t0004g0186 a0002c0005t0044g0181 a0002c0010t0020g0116 others(7): Show |
10 | HG00673.hp1 HG02258.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.1616+16739G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67563501 | |||||||
| chrX:67564651 | G | C | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1616+17889G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67564651 | |||||||
| chrX:67564748 | T | A | 13 | a0001c0001t0001g0070 a0001c0001t0002g0025 a0001c0001t0002g0075 others(10): Show |
13 | HG00609.hp1 HG00621.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.1616+17986T>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67564748 | |||||||
| chrX:67565181 | G | A | 1 | a0004c0004t0051g0078 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1616+18419G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67565181 | |||||||
| chrX:67565182 | G | C | 1 | a0004c0004t0051g0078 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1616+18420G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67565182 | |||||||
| chrX:67565183 | G | T | 1 | a0004c0004t0051g0078 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1616+18421G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67565183 | |||||||
| chrX:67565185 | A | G | 1 | a0004c0004t0051g0078 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1616+18423A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67565185 | |||||||
| chrX:67565189 | A | G | 1 | a0004c0004t0051g0078 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1616+18427A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67565189 | |||||||
| chrX:67565193 | T | G | 1 | a0004c0004t0051g0078 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1616+18431T>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67565193 | |||||||
| chrX:67565194 | G | T | 1 | a0004c0004t0051g0078 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1616+18432G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67565194 | |||||||
| chrX:67565196 | A | T | 1 | a0004c0004t0051g0078 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1616+18434A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67565196 | |||||||
| chrX:67565232 | T | G | 3 | a0002c0010t0020g0116 a0005c0006t0020g0115 a0005c0006t0032g0117 |
3 | HG03209.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1616+18470T>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67565232 | |||||||
| chrX:67565709 | G | A | 2 | a0008c0007t0006g0133 a0009c0012t0041g0114 |
2 | HG00735.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1616+18947G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67565709 | |||||||
| chrX:67565758 | T | C | 1 | a0005c0006t0011g0004 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1616+18996T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67565758 | |||||||
| chrX:67565846 | C | T | 34 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(31): Show |
34 | HG01081.hp2 HG01255.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.1616+19084C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67565846 | |||||||
| chrX:67565906 | C | A | 57 | a0001c0009t0004g0118 a0001c0009t0004g0155 a0001c0009t0006g0168 others(54): Show |
57 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.1616+19144C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67565906 | |||||||
| chrX:67566174 | G | A | 80 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(77): Show |
80 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.1616+19412G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67566174 | |||||||
| chrX:67566347 | T | C | 1 | a0001c0001t0002g0029 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1616+19585T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67566347 | |||||||
| chrX:67566366 | C | T | 4 | a0002c0010t0020g0116 a0005c0006t0020g0115 a0005c0006t0032g0117 others(1): Show |
4 | HG02809.hp1 HG03209.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1616+19604C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67566366 | |||||||
| chrX:67566773 | G | C | 1 | a0015c0022t0004g0112 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1616+20011G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67566773 | |||||||
| chrX:67566773 | G | T | 1 | a0001c0009t0006g0168 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1616+20011G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67566773 | |||||||
| chrX:67567167 | C | G | 1 | a0008c0007t0011g0148 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1616+20405C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67567167 | |||||||
| chrX:67567781 | A | T | 1 | a0001c0009t0010g0113 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1616+21019A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67567781 | |||||||
| chrX:67567839 | G | A | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1616+21077G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67567839 | |||||||
| chrX:67568144 | G | T | 1 | a0001c0009t0010g0113 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1616+21382G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67568144 | |||||||
| chrX:67568204 | G | A | 1 | a0005c0006t0011g0004 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1616+21442G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67568204 | |||||||
| chrX:67568311 | A | C | 1 | a0005c0011t0052g0068 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1616+21549A>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67568311 | |||||||
| chrX:67568383 | G | A | 80 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(77): Show |
80 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.1616+21621G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67568383 | |||||||
| chrX:67569146 | G | T | 1 | a0007c0008t0006g0137 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1616+22384G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67569146 | |||||||
| chrX:67569169 | C | T | 1 | a0004c0033t0054g0101 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1616+22407C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67569169 | |||||||
| chrX:67569214 | G | T | 1 | a0011c0013t0003g0107 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1616+22452G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67569214 | |||||||
| chrX:67569516 | G | A | 1 | a0004c0032t0058g0169 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1616+22754G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67569516 | |||||||
| chrX:67570038 | T | G | 2 | a0001c0001t0019g0175 a0001c0001t0019g0176 |
2 | HG01891.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1616+23276T>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67570038 | |||||||
| chrX:67570125 | G | A | 1 | a0002c0005t0001g0018 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1616+23363G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67570125 | |||||||
| chrX:67570281 | G | C | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1616+23519G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67570281 | |||||||
| chrX:67570684 | A | G | 1 | a0006c0003t0002g0067 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1616+23922A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67570684 | |||||||
| chrX:67571168 | A | G | 1 | a0002c0005t0056g0172 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1616+24406A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67571168 | |||||||
| chrX:67571747 | C | T | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1616+24985C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67571747 | |||||||
| chrX:67571994 | G | C | 13 | a0001c0001t0001g0070 a0001c0001t0002g0025 a0001c0001t0002g0075 others(10): Show |
13 | HG00609.hp1 HG00621.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.1616+25232G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67571994 | |||||||
| chrX:67572130 | G | C | 1 | a0009c0012t0041g0114 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1616+25368G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67572130 | |||||||
| chrX:67572198 | T | A | 1 | a0001c0009t0006g0168 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1616+25436T>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67572198 | |||||||
| chrX:67572272 | G | A | 3 | a0002c0010t0020g0116 a0005c0006t0020g0115 a0005c0006t0032g0117 |
3 | HG03209.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1616+25510G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67572272 | |||||||
| chrX:67572647 | A | G | 1 | a0004c0032t0058g0169 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1616+25885A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67572647 | |||||||
| chrX:67572773 | G | A | 3 | a0002c0010t0014g0158 a0002c0010t0035g0151 a0002c0010t0036g0119 |
3 | HG01243.hp1 HG02451.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1616+26011G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67572773 | |||||||
| chrX:67573903 | A | C | 1 | a0008c0007t0010g0124 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1616+27141A>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67573903 | |||||||
| chrX:67574022 | C | T | 1 | a0004c0004t0046g0016 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1616+27260C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67574022 | |||||||
| chrX:67574602 | C | T | 1 | a0010c0014t0001g0099 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1616+27840C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67574602 | |||||||
| chrX:67575696 | T | A | 4 | a0002c0010t0020g0116 a0005c0006t0020g0115 a0005c0006t0032g0117 others(1): Show |
4 | HG02809.hp1 HG03209.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1616+28934T>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67575696 | |||||||
| chrX:67576245 | A | G | 80 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(77): Show |
80 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.1616+29483A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67576245 | |||||||
| chrX:67576347 | C | T | 3 | a0005c0006t0011g0004 a0007c0008t0006g0136 a0007c0008t0006g0137 |
3 | HG03041.hp2 HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1616+29585C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67576347 | |||||||
| chrX:67576877 | A | T | 1 | a0005c0011t0053g0095 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1616+30115A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67576877 | |||||||
| chrX:67577004 | C | CT | 10 | a0001c0009t0004g0118 a0001c0009t0004g0155 a0002c0010t0004g0154 others(7): Show |
10 | HG01074.hp1 HG02572.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1616+30259dupT | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67577004 | ||||||
| chrX:67577004 | CT | C | 6 | a0003c0002t0012g0020 a0003c0034t0008g0185 a0004c0004t0021g0021 others(3): Show |
6 | HG02258.hp1 HG02895.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1616+30259delT | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67577004 | ||||||
| chrX:67577095 | T | C | 1 | a0003c0002t0001g0069 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1616+30333T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67577095 | |||||||
| chrX:67577127 | C | G | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1616+30365C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67577127 | |||||||
| chrX:67577134 | A | C | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1616+30372A>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67577134 | |||||||
| chrX:67577776 | T | C | 2 | a0002c0005t0001g0109 a0007c0016t0001g0030 |
2 | NA18747.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1616+31014T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67577776 | |||||||
| chrX:67577780 | A | T | 1 | a0002c0005t0016g0111 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1616+31018A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67577780 | |||||||
| chrX:67577829 | A | G | 2 | a0002c0010t0018g0165 a0002c0010t0030g0164 |
2 | HG02723.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1616+31067A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67577829 | |||||||
| chrX:67577925 | G | A | 1 | a0008c0007t0034g0159 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1616+31163G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67577925 | |||||||
| chrX:67578269 | C | T | 80 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(77): Show |
80 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.1616+31507C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67578269 | |||||||
| chrX:67578273 | C | G | 1 | a0001c0001t0002g0065 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1616+31511C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67578273 | |||||||
| chrX:67578825 | T | C | 1 | a0004c0004t0031g0170 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1616+32063T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67578825 | |||||||
| chrX:67579179 | G | A | 1 | a0001c0009t0004g0118 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1616+32417G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67579179 | |||||||
| chrX:67579752 | C | T | 6 | a0001c0001t0002g0065 a0006c0003t0002g0009 a0006c0003t0002g0067 others(3): Show |
6 | HG02071.hp1 NA18962.hp1 NA18995.hp1 others(3): Show |
intron_variant | MODIFIER | c.1616+32990C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67579752 | |||||||
| chrX:67579756 | G | T | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1616+32994G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67579756 | |||||||
| chrX:67580261 | A | T | 2 | a0003c0002t0009g0028 a0005c0011t0009g0074 |
2 | NA18984.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1616+33499A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67580261 | |||||||
| chrX:67580882 | A | G | 2 | a0003c0021t0008g0123 a0005c0006t0010g0120 |
2 | HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1616+34120A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67580882 | |||||||
| chrX:67581463 | C | T | 2 | a0001c0001t0001g0062 a0001c0001t0001g0085 |
2 | HG02602.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1616+34701C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67581463 | |||||||
| chrX:67581467 | C | T | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1616+34705C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67581467 | |||||||
| chrX:67581646 | A | G | 1 | a0001c0001t0002g0065 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1616+34884A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67581646 | |||||||
| chrX:67581688 | C | T | 1 | a0006c0003t0026g0061 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1616+34926C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67581688 | |||||||
| chrX:67581900 | C | T | 3 | a0002c0010t0020g0116 a0005c0006t0020g0115 a0005c0006t0032g0117 |
3 | HG03209.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1616+35138C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67581900 | |||||||
| chrX:67582441 | C | G | 1 | a0002c0005t0056g0172 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1616+35679C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67582441 | |||||||
| chrX:67582744 | T | C | 1 | a0001c0009t0008g0132 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1616+35982T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67582744 | |||||||
| chrX:67583121 | C | G | 1 | a0001c0001t0002g0065 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1616+36359C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67583121 | |||||||
| chrX:67583626 | G | C | 1 | a0001c0009t0008g0128 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1616+36864G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67583626 | |||||||
| chrX:67583728 | A | G | 8 | a0001c0001t0014g0179 a0001c0001t0019g0175 a0001c0001t0019g0176 others(5): Show |
8 | HG01891.hp2 HG02717.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1616+36966A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67583728 | |||||||
| chrX:67583791 | A | C | 1 | a0005c0006t0028g0153 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1616+37029A>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67583791 | |||||||
| chrX:67583864 | G | A | 1 | a0004c0004t0031g0170 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1616+37102G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67583864 | |||||||
| chrX:67584544 | T | A | 2 | a0007c0016t0005g0173 a0008c0017t0005g0174 |
2 | HG01081.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1616+37782T>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67584544 | |||||||
| chrX:67584850 | G | A | 1 | a0001c0009t0010g0113 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1616+38088G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67584850 | |||||||
| chrX:67584974 | G | A | 8 | a0001c0001t0014g0179 a0001c0001t0019g0175 a0001c0001t0019g0176 others(5): Show |
8 | HG01891.hp2 HG02717.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1616+38212G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67584974 | |||||||
| chrX:67585127 | A | G | 134 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(131): Show |
135 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.1616+38365A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67585127 | |||||||
| chrX:67585258 | C | CA | 5 | a0001c0001t0004g0186 a0002c0005t0044g0181 a0003c0034t0008g0185 others(2): Show |
5 | HG02258.hp1 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1616+38514dupA | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67585258 | ||||||
| chrX:67585258 | CA | C | 113 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(110): Show |
114 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.1616+38514delA | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67585258 | ||||||
| chrX:67585370 | A | G | 1 | a0006c0003t0001g0098 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1616+38608A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67585370 | |||||||
| chrX:67585390 | A | T | 8 | a0001c0001t0014g0179 a0001c0001t0019g0175 a0001c0001t0019g0176 others(5): Show |
8 | HG01891.hp2 HG02717.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1616+38628A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67585390 | |||||||
| chrX:67585401 | G | A | 3 | a0001c0001t0007g0001 a0001c0001t0007g0012 a0004c0004t0001g0102 |
4 | NA18983.hp1 NA18985.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.1616+38639G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67585401 | |||||||
| chrX:67586188 | G | A | 133 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(130): Show |
134 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.1616+39426G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67586188 | |||||||
| chrX:67586465 | C | T | 2 | a0002c0005t0007g0010 a0002c0005t0007g0011 |
2 | NA18953.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1616+39703C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67586465 | |||||||
| chrX:67586631 | T | A | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1616+39869T>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67586631 | |||||||
| chrX:67586730 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1616+39968T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67586730 | |||||||
| chrX:67586738 | G | A | 1 | a0001c0009t0042g0135 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1616+39976G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67586738 | |||||||
| chrX:67587076 | G | A | 1 | a0001c0001t0004g0186 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1616+40314G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67587076 | |||||||
| chrX:67587238 | G | C | 1 | a0004c0032t0058g0169 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1616+40476G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67587238 | |||||||
| chrX:67587317 | G | A | 1 | a0001c0009t0033g0138 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1616+40555G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67587317 | |||||||
| chrX:67587476 | G | T | 2 | a0008c0007t0006g0133 a0009c0012t0041g0114 |
2 | HG00735.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1616+40714G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67587476 | |||||||
| chrX:67588028 | C | A | 1 | a0013c0019t0016g0125 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1616+41266C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67588028 | |||||||
| chrX:67588202 | A | G | 2 | a0002c0005t0007g0010 a0002c0005t0007g0011 |
2 | NA18953.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1616+41440A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67588202 | |||||||
| chrX:67588203 | C | T | 2 | a0002c0005t0007g0010 a0002c0005t0007g0011 |
2 | NA18953.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1616+41441C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67588203 | |||||||
| chrX:67588284 | C | G | 1 | a0003c0002t0012g0020 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1616+41522C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67588284 | |||||||
| chrX:67588771 | A | G | 1 | a0006c0031t0043g0167 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1616+42009A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67588771 | |||||||
| chrX:67589046 | C | T | 1 | a0004c0032t0058g0169 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1616+42284C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67589046 | |||||||
| chrX:67589443 | C | T | 1 | a0003c0002t0001g0023 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1616+42681C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67589443 | |||||||
| chrX:67589494 | T | C | 1 | a0006c0003t0001g0033 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1616+42732T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67589494 | |||||||
| chrX:67590192 | G | A | 1 | a0003c0002t0017g0005 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1616+43430G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67590192 | |||||||
| chrX:67590222 | G | A | 3 | a0002c0010t0020g0116 a0005c0006t0020g0115 a0005c0006t0032g0117 |
3 | HG03209.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1616+43460G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67590222 | |||||||
| chrX:67590323 | C | T | 1 | a0001c0009t0006g0168 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1616+43561C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67590323 | |||||||
| chrX:67590438 | C | A | 3 | a0005c0006t0011g0004 a0007c0008t0006g0136 a0007c0008t0006g0137 |
3 | HG03041.hp2 HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1616+43676C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67590438 | |||||||
| chrX:67590501 | A | G | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1616+43739A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67590501 | |||||||
| chrX:67590801 | A | G | 1 | a0001c0001t0019g0176 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1616+44039A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67590801 | |||||||
| chrX:67590955 | T | C | 5 | a0001c0001t0002g0025 a0001c0001t0002g0075 a0002c0005t0016g0111 others(2): Show |
5 | NA18943.hp1 NA18961.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.1616+44193T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67590955 | |||||||
| chrX:67591161 | G | T | 19 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(16): Show |
19 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1616+44399G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67591161 | |||||||
| chrX:67591796 | G | C | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1616+45034G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67591796 | |||||||
| chrX:67592617 | T | C | 133 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(130): Show |
134 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.1616+45855T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67592617 | |||||||
| chrX:67592636 | G | GA | 104 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(101): Show |
105 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.1616+45886dupA | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67592636 | ||||||
| chrX:67592649 | C | A | 2 | a0003c0002t0003g0034 a0004c0004t0012g0103 |
2 | HG00735.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1616+45887C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67592649 | |||||||
| chrX:67592650 | T | C | 2 | a0003c0002t0003g0034 a0004c0004t0012g0103 |
2 | HG00735.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1616+45888T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67592650 | |||||||
| chrX:67592662 | A | T | 184 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(181): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.1616+45900A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67592662 | |||||||
| chrX:67592787 | G | A | 11 | a0001c0001t0014g0179 a0001c0001t0019g0175 a0001c0001t0019g0176 others(8): Show |
11 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1616+46025G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67592787 | |||||||
| chrX:67593196 | T | A | 1 | a0002c0005t0015g0088 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1616+46434T>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67593196 | |||||||
| chrX:67593232 | C | T | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1616+46470C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67593232 | |||||||
| chrX:67593443 | C | A | 1 | a0002c0005t0056g0172 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1616+46681C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67593443 | |||||||
| chrX:67593597 | G | A | 4 | a0001c0009t0006g0168 a0002c0010t0020g0116 a0005c0006t0020g0115 others(1): Show |
4 | HG03209.hp1 HG03471.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1616+46835G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67593597 | |||||||
| chrX:67593601 | T | C | 161 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(158): Show |
162 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.1616+46839T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67593601 | |||||||
| chrX:67593984 | A | G | 1 | a0002c0005t0056g0172 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1616+47222A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67593984 | |||||||
| chrX:67594006 | T | C | 1 | a0001c0009t0033g0138 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1616+47244T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67594006 | |||||||
| chrX:67594025 | T | C | 1 | a0004c0004t0001g0091 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1616+47263T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67594025 | |||||||
| chrX:67594194 | A | G | 1 | a0002c0005t0044g0181 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1616+47432A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67594194 | |||||||
| chrX:67595016 | C | T | 1 | a0005c0006t0038g0126 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1617-48240C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67595016 | |||||||
| chrX:67595645 | A | C | 6 | a0001c0009t0004g0118 a0001c0009t0004g0155 a0002c0010t0004g0154 others(3): Show |
6 | HG02572.hp1 HG02630.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1617-47611A>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67595645 | |||||||
| chrX:67595651 | CA | C | 172 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(169): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.1617-47591delA | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67595651 | ||||||
| chrX:67595670 | C | T | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1617-47586C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67595670 | |||||||
| chrX:67597047 | G | A | 1 | a0007c0008t0023g0127 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1617-46209G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67597047 | |||||||
| chrX:67597089 | G | GTTTC | 3 | a0003c0002t0013g0086 a0010c0014t0013g0031 a0011c0013t0013g0106 |
3 | NA18940.hp1 NA19006.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1617-46165_1617-46 others(10): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67597089 | ||||||
| chrX:67597238 | A | T | 2 | a0007c0008t0006g0136 a0007c0008t0006g0137 |
2 | HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1617-46018A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67597238 | |||||||
| chrX:67597334 | G | A | 2 | a0005c0011t0009g0094 a0005c0011t0053g0095 |
2 | HG02735.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1617-45922G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67597334 | |||||||
| chrX:67597505 | G | A | 1 | a0013c0019t0029g0152 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1617-45751G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67597505 | |||||||
| chrX:67597677 | C | G | 1 | a0009c0015t0001g0059 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1617-45579C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67597677 | |||||||
| chrX:67597801 | G | A | 2 | a0003c0002t0015g0026 a0011c0013t0001g0015 |
2 | HG02027.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.1617-45455G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67597801 | |||||||
| chrX:67597816 | G | A | 2 | a0001c0001t0001g0079 a0001c0001t0003g0080 |
2 | NA19062.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1617-45440G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67597816 | |||||||
| chrX:67598012 | G | A | 1 | a0015c0022t0004g0112 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1617-45244G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67598012 | |||||||
| chrX:67598162 | C | T | 22 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(19): Show |
22 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.1617-45094C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67598162 | |||||||
| chrX:67598252 | T | G | 1 | a0006c0003t0015g0006 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1617-45004T>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67598252 | |||||||
| chrX:67598283 | G | GT | 9 | a0001c0001t0007g0012 a0001c0009t0008g0132 a0002c0005t0016g0111 others(6): Show |
9 | HG00642.hp1 HG00741.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1617-44956dupT | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67598283 | ||||||
| chrX:67598437 | C | T | 1 | a0003c0002t0001g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1617-44819C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67598437 | |||||||
| chrX:67598657 | G | C | 1 | a0008c0017t0001g0072 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1617-44599G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67598657 | |||||||
| chrX:67598768 | T | C | 19 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(16): Show |
19 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1617-44488T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67598768 | |||||||
| chrX:67598771 | A | AT | 16 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(13): Show |
16 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1617-44474dupT | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67598771 | ||||||
| chrX:67599060 | C | A | 1 | a0002c0005t0009g0035 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1617-44196C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67599060 | |||||||
| chrX:67599338 | G | A | 19 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(16): Show |
19 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1617-43918G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67599338 | |||||||
| chrX:67599499 | G | A | 1 | a0006c0003t0002g0036 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1617-43757G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67599499 | |||||||
| chrX:67599562 | C | T | 20 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(17): Show |
20 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1617-43694C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67599562 | |||||||
| chrX:67599733 | C | T | 1 | a0002c0005t0056g0172 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1617-43523C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67599733 | |||||||
| chrX:67599935 | A | G | 1 | a0003c0002t0015g0026 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1617-43321A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67599935 | |||||||
| chrX:67600256 | A | T | 1 | a0001c0001t0007g0012 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1617-43000A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67600256 | |||||||
| chrX:67600257 | T | A | 1 | a0001c0001t0007g0012 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1617-42999T>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67600257 | |||||||
| chrX:67600258 | A | T | 1 | a0001c0001t0007g0012 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1617-42998A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67600258 | |||||||
| chrX:67600282 | A | G | 1 | a0008c0007t0006g0150 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1617-42974A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67600282 | |||||||
| chrX:67600297 | C | T | 1 | a0003c0002t0017g0005 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1617-42959C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67600297 | |||||||
| chrX:67600520 | T | C | 1 | a0004c0004t0003g0037 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1617-42736T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67600520 | |||||||
| chrX:67600563 | C | G | 1 | a0001c0009t0042g0135 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1617-42693C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67600563 | |||||||
| chrX:67601555 | A | C | 3 | a0002c0010t0014g0158 a0002c0010t0035g0151 a0002c0010t0036g0119 |
3 | HG01243.hp1 HG02451.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1617-41701A>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67601555 | |||||||
| chrX:67601833 | G | A | 12 | a0001c0001t0014g0179 a0001c0001t0019g0175 a0001c0001t0019g0176 others(9): Show |
12 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1617-41423G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67601833 | |||||||
| chrX:67601861 | T | A | 1 | a0018c0036t0021g0063 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1617-41395T>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67601861 | |||||||
| chrX:67602206 | C | G | 3 | a0002c0010t0020g0116 a0005c0006t0020g0115 a0005c0006t0032g0117 |
3 | HG03209.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1617-41050C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67602206 | |||||||
| chrX:67602212 | A | C | 1 | a0013c0019t0029g0152 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1617-41044A>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67602212 | |||||||
| chrX:67602321 | G | A | 134 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(131): Show |
135 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.1617-40935G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67602321 | |||||||
| chrX:67602659 | C | G | 1 | a0004c0004t0027g0182 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1617-40597C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67602659 | |||||||
| chrX:67602683 | G | C | 1 | a0001c0001t0001g0092 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1617-40573G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67602683 | |||||||
| chrX:67602994 | T | C | 20 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(17): Show |
20 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1617-40262T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67602994 | |||||||
| chrX:67603162 | G | A | 1 | a0004c0004t0027g0182 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1617-40094G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67603162 | |||||||
| chrX:67603264 | A | G | 9 | a0003c0021t0008g0123 a0005c0006t0003g0003 a0005c0006t0008g0122 others(6): Show |
9 | HG00099.hp1 HG02615.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1617-39992A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67603264 | |||||||
| chrX:67604080 | G | A | 1 | a0001c0001t0010g0166 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1617-39176G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67604080 | |||||||
| chrX:67604198 | A | ATG | 69 | a0001c0001t0001g0079 a0001c0001t0001g0085 a0001c0001t0002g0025 others(66): Show |
70 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.1617-39012_1617-39 others(8): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67604198 | ||||||
| chrX:67604198 | A | ATGTG | 15 | a0002c0005t0007g0010 a0002c0005t0007g0011 a0002c0005t0044g0181 others(12): Show |
15 | HG01074.hp1 HG01258.hp1 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.1617-39014_1617-39 others(10): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67604198 | ||||||
| chrX:67604198 | A | ATGTGTG | 13 | a0001c0001t0001g0092 a0002c0005t0001g0018 a0003c0002t0009g0028 others(10): Show |
13 | HG00741.hp2 HG01256.hp1 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.1617-39016_1617-39 others(12): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67604198 | ||||||
| chrX:67604198 | A | ATGTGTGT others(1): Show |
2 | a0001c0001t0004g0186 a0009c0015t0005g0007 |
2 | HG02647.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1617-39018_1617-39 others(14): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67604198 | ||||||
| chrX:67604198 | A | ATGTGTGT others(3): Show |
3 | a0004c0004t0027g0182 a0007c0016t0005g0173 a0008c0017t0001g0072 |
3 | HG01081.hp2 NA19004.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1617-39020_1617-39 others(16): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67604198 | ||||||
| chrX:67604198 | A | ATGTGTGT others(5): Show |
1 | a0008c0017t0005g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1617-39022_1617-39 others(18): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67604198 | ||||||
| chrX:67604198 | A | ATGTGTGT others(7): Show |
4 | a0001c0001t0019g0175 a0001c0001t0019g0176 a0006c0003t0004g0177 others(1): Show |
4 | HG01891.hp2 HG02809.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1617-39024_1617-39 others(20): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67604198 | ||||||
| chrX:67604198 | A | ATGTGTGT others(9): Show |
3 | a0001c0028t0004g0183 a0002c0005t0004g0184 a0006c0003t0004g0178 |
3 | HG02717.hp1 HG02896.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1617-39026_1617-39 others(22): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67604198 | ||||||
| chrX:67604198 | A | ATGTGTGT others(11): Show |
1 | a0001c0001t0014g0179 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1617-39028_1617-39 others(24): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67604198 | ||||||
| chrX:67604198 | ATG | A | 27 | a0001c0001t0002g0029 a0002c0005t0002g0096 a0002c0010t0008g0156 others(24): Show |
27 | HG00099.hp1 HG00673.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.1617-39012_1617-39 others(8): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67604198 | ||||||
| chrX:67604198 | ATGTG | A | 25 | a0001c0001t0001g0070 a0001c0009t0004g0155 a0001c0009t0006g0168 others(22): Show |
25 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.1617-39014_1617-39 others(10): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67604198 | ||||||
| chrX:67604198 | ATGTGTG | A | 4 | a0002c0010t0020g0116 a0005c0006t0028g0153 a0008c0007t0034g0159 others(1): Show |
4 | HG02630.hp1 HG02818.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1617-39016_1617-39 others(12): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67604198 | ||||||
| chrX:67604198 | ATGTGTGT others(1): Show |
A | 2 | a0008c0007t0011g0148 a0009c0012t0037g0143 |
2 | HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1617-39018_1617-39 others(14): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67604198 | ||||||
| chrX:67604198 | ATGTGTGT others(3): Show |
A | 1 | a0007c0008t0018g0130 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1617-39020_1617-39 others(16): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67604198 | ||||||
| chrX:67605441 | G | T | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1617-37815G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67605441 | |||||||
| chrX:67605515 | C | T | 111 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(108): Show |
112 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.1617-37741C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67605515 | |||||||
| chrX:67605725 | C | G | 1 | a0004c0004t0027g0182 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1617-37531C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67605725 | |||||||
| chrX:67606063 | A | T | 1 | a0002c0005t0056g0172 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1617-37193A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67606063 | |||||||
| chrX:67606700 | T | C | 1 | a0001c0001t0002g0039 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1617-36556T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67606700 | |||||||
| chrX:67606726 | A | T | 19 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(16): Show |
19 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1617-36530A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67606726 | |||||||
| chrX:67607042 | T | A | 1 | a0009c0015t0005g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1617-36214T>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67607042 | |||||||
| chrX:67607215 | A | G | 8 | a0001c0001t0014g0179 a0001c0001t0019g0175 a0001c0001t0019g0176 others(5): Show |
8 | HG01891.hp2 HG02717.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1617-36041A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67607215 | |||||||
| chrX:67607731 | C | T | 20 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(17): Show |
20 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1617-35525C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67607731 | |||||||
| chrX:67607793 | A | G | 20 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(17): Show |
20 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1617-35463A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67607793 | |||||||
| chrX:67608273 | C | T | 2 | a0001c0009t0033g0138 a0002c0010t0008g0156 |
2 | HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1617-34983C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67608273 | |||||||
| chrX:67608543 | A | G | 134 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(131): Show |
135 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.1617-34713A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67608543 | |||||||
| chrX:67608811 | A | G | 47 | a0001c0001t0001g0070 a0001c0001t0002g0025 a0001c0001t0002g0049 others(44): Show |
47 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.1617-34445A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67608811 | |||||||
| chrX:67608902 | C | T | 1 | a0004c0032t0058g0169 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1617-34354C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67608902 | |||||||
| chrX:67608924 | C | A | 20 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(17): Show |
20 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1617-34332C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67608924 | |||||||
| chrX:67609195 | C | T | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1617-34061C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67609195 | |||||||
| chrX:67609218 | G | A | 111 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(108): Show |
112 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.1617-34038G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67609218 | |||||||
| chrX:67609759 | T | G | 175 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(172): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.1617-33497T>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67609759 | |||||||
| chrX:67609772 | A | G | 10 | a0001c0009t0004g0118 a0001c0009t0004g0155 a0001c0009t0033g0138 others(7): Show |
10 | HG02451.hp2 HG02572.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1617-33484A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67609772 | |||||||
| chrX:67610667 | C | T | 111 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(108): Show |
112 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.1617-32589C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67610667 | |||||||
| chrX:67610727 | G | A | 3 | a0003c0002t0001g0093 a0004c0033t0054g0101 a0010c0014t0001g0099 |
3 | HG01069.hp1 HG01934.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1617-32529G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67610727 | |||||||
| chrX:67610765 | A | G | 2 | a0005c0011t0009g0094 a0005c0011t0053g0095 |
2 | HG02735.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1617-32491A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67610765 | |||||||
| chrX:67611381 | C | T | 134 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(131): Show |
135 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.1617-31875C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67611381 | |||||||
| chrX:67611387 | A | G | 20 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(17): Show |
20 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1617-31869A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67611387 | |||||||
| chrX:67611681 | C | T | 20 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(17): Show |
20 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1617-31575C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67611681 | |||||||
| chrX:67612376 | G | T | 1 | a0004c0004t0021g0021 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1617-30880G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67612376 | |||||||
| chrX:67612596 | C | T | 1 | a0009c0012t0005g0147 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1617-30660C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67612596 | |||||||
| chrX:67612871 | G | A | 1 | a0009c0015t0005g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1617-30385G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67612871 | |||||||
| chrX:67613151 | A | G | 19 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(16): Show |
19 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1617-30105A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67613151 | |||||||
| chrX:67613252 | A | T | 2 | a0002c0005t0007g0010 a0002c0005t0007g0011 |
2 | NA18953.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1617-30004A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67613252 | |||||||
| chrX:67613966 | G | T | 1 | a0002c0010t0030g0164 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1617-29290G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67613966 | |||||||
| chrX:67614169 | A | C | 1 | a0005c0006t0032g0117 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1617-29087A>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67614169 | |||||||
| chrX:67615310 | A | G | 1 | a0001c0009t0010g0113 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1617-27946A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67615310 | |||||||
| chrX:67615428 | G | A | 1 | a0002c0030t0016g0013 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1617-27828G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67615428 | |||||||
| chrX:67615587 | G | C | 20 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(17): Show |
20 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1617-27669G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67615587 | |||||||
| chrX:67615731 | A | G | 1 | a0005c0006t0011g0004 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1617-27525A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67615731 | |||||||
| chrX:67616127 | G | A | 1 | a0004c0004t0031g0170 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1617-27129G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67616127 | |||||||
| chrX:67616207 | T | C | 5 | a0002c0005t0001g0109 a0006c0003t0001g0002 a0006c0003t0001g0104 others(2): Show |
5 | NA18747.hp1 NA18960.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.1617-27049T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67616207 | |||||||
| chrX:67616429 | A | T | 1 | a0004c0004t0012g0103 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1617-26827A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67616429 | |||||||
| chrX:67616538 | T | C | 1 | a0001c0001t0002g0100 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1617-26718T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67616538 | |||||||
| chrX:67616682 | G | T | 2 | a0004c0032t0058g0169 a0009c0015t0005g0007 |
2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1617-26574G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67616682 | |||||||
| chrX:67616840 | C | A | 6 | a0001c0009t0006g0168 a0001c0009t0042g0135 a0005c0006t0038g0126 others(3): Show |
6 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.1617-26416C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67616840 | |||||||
| chrX:67616858 | C | T | 111 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(108): Show |
112 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.1617-26398C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67616858 | |||||||
| chrX:67616907 | G | A | 1 | a0005c0011t0003g0066 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1617-26349G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67616907 | |||||||
| chrX:67617024 | C | T | 1 | a0015c0023t0008g0180 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1617-26232C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67617024 | |||||||
| chrX:67617148 | G | C | 19 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(16): Show |
19 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1617-26108G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67617148 | |||||||
| chrX:67617476 | T | C | 1 | a0006c0003t0026g0061 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1617-25780T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67617476 | |||||||
| chrX:67618238 | G | T | 134 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(131): Show |
135 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.1617-25018G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67618238 | |||||||
| chrX:67618656 | A | G | 1 | a0005c0006t0028g0153 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1617-24600A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67618656 | |||||||
| chrX:67618749 | T | G | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1617-24507T>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67618749 | |||||||
| chrX:67618837 | G | C | 1 | a0013c0019t0016g0125 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1617-24419G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67618837 | |||||||
| chrX:67618865 | G | A | 1 | a0006c0003t0002g0067 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1617-24391G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67618865 | |||||||
| chrX:67618909 | T | C | 111 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(108): Show |
112 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.1617-24347T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67618909 | |||||||
| chrX:67619254 | G | A | 1 | a0009c0015t0005g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1617-24002G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67619254 | |||||||
| chrX:67619315 | TTC | T | 4 | a0005c0006t0003g0003 a0005c0006t0008g0122 a0005c0006t0010g0003 others(1): Show |
4 | HG00099.hp1 HG03491.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.1617-23925_1617-23 others(8): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67619315 | ||||||
| chrX:67619329 | C | G | 1 | a0010c0014t0013g0090 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1617-23927C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67619329 | |||||||
| chrX:67619331 | C | CTG | 6 | a0001c0001t0004g0186 a0001c0009t0004g0155 a0003c0034t0008g0185 others(3): Show |
6 | HG01433.hp1 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1617-23905_1617-23 others(8): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67619331 | ||||||
| chrX:67619331 | C | G | 20 | a0001c0001t0001g0092 a0001c0001t0003g0080 a0001c0001t0003g0083 others(17): Show |
20 | HG00099.hp2 HG00673.hp1 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.1617-23925C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67619331 | |||||||
| chrX:67619333 | G | C | 3 | a0003c0002t0017g0014 a0004c0032t0058g0169 a0007c0008t0006g0137 |
3 | HG02615.hp1 HG03041.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1617-23923G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67619333 | |||||||
| chrX:67619692 | T | C | 11 | a0001c0001t0014g0179 a0001c0001t0019g0175 a0001c0001t0019g0176 others(8): Show |
11 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1617-23564T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67619692 | |||||||
| chrX:67620085 | C | T | 2 | a0003c0002t0001g0055 a0003c0002t0055g0056 |
2 | HG02083.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1617-23171C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67620085 | |||||||
| chrX:67620162 | C | G | 1 | a0003c0002t0012g0020 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1617-23094C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67620162 | |||||||
| chrX:67620335 | C | A | 1 | a0013c0019t0016g0125 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1617-22921C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67620335 | |||||||
| chrX:67620384 | G | T | 19 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(16): Show |
19 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1617-22872G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67620384 | |||||||
| chrX:67620397 | A | T | 2 | a0003c0002t0003g0057 a0011c0013t0001g0052 |
2 | HG01258.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1617-22859A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67620397 | |||||||
| chrX:67620439 | G | C | 1 | a0009c0015t0005g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1617-22817G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67620439 | |||||||
| chrX:67621171 | C | T | 1 | a0006c0003t0017g0060 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1617-22085C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67621171 | |||||||
| chrX:67621204 | T | C | 2 | a0004c0004t0012g0103 a0004c0004t0047g0053 |
2 | HG00735.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1617-22052T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67621204 | |||||||
| chrX:67621540 | G | C | 111 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(108): Show |
112 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.1617-21716G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67621540 | |||||||
| chrX:67621767 | T | C | 17 | a0001c0001t0001g0079 a0001c0001t0001g0092 a0001c0001t0003g0080 others(14): Show |
17 | HG00673.hp1 HG01256.hp1 HG02040.hp1 others(14): Show |
intron_variant | MODIFIER | c.1617-21489T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67621767 | |||||||
| chrX:67622320 | G | GA | 21 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(18): Show |
21 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.1617-20926dupA | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67622320 | ||||||
| chrX:67622720 | T | C | 1 | a0008c0017t0001g0187 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1617-20536T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67622720 | |||||||
| chrX:67623103 | G | A | 3 | a0002c0010t0020g0116 a0005c0006t0020g0115 a0005c0006t0032g0117 |
3 | HG03209.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1617-20153G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67623103 | |||||||
| chrX:67623345 | A | G | 1 | a0007c0008t0018g0130 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1617-19911A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67623345 | |||||||
| chrX:67623499 | T | C | 1 | a0008c0007t0006g0140 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1617-19757T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67623499 | |||||||
| chrX:67623717 | C | T | 2 | a0004c0032t0058g0169 a0009c0015t0005g0007 |
2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1617-19539C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67623717 | |||||||
| chrX:67623775 | A | G | 11 | a0001c0001t0014g0179 a0001c0001t0019g0175 a0001c0001t0019g0176 others(8): Show |
11 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1617-19481A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67623775 | |||||||
| chrX:67624004 | G | A | 2 | a0008c0007t0006g0133 a0009c0012t0041g0114 |
2 | HG00735.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1617-19252G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67624004 | |||||||
| chrX:67624797 | G | A | 1 | a0006c0003t0002g0089 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1617-18459G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67624797 | |||||||
| chrX:67624904 | C | CA | 32 | a0001c0001t0001g0070 a0001c0001t0014g0179 a0001c0009t0006g0168 others(29): Show |
32 | HG00099.hp1 HG00642.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.1617-18322dupA | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67624904 | ||||||
| chrX:67624904 | C | CAA | 11 | a0002c0010t0020g0116 a0005c0006t0032g0117 a0007c0008t0006g0149 others(8): Show |
11 | HG02055.hp1 HG02965.hp1 HG03139.hp1 others(8): Show |
intron_variant | MODIFIER | c.1617-18323_1617-18 others(8): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67624904 | ||||||
| chrX:67624904 | CA | C | 74 | a0001c0001t0001g0062 a0001c0001t0001g0085 a0001c0001t0002g0025 others(71): Show |
74 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.1617-18322delA | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67624904 | ||||||
| chrX:67624904 | CAAAAAAA others(5): Show |
C | 1 | a0013c0019t0029g0152 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1617-18333_1617-18 others(18): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67624904 | ||||||
| chrX:67624948 | G | C | 1 | a0002c0005t0004g0184 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1617-18308G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67624948 | |||||||
| chrX:67625241 | C | T | 2 | a0004c0032t0058g0169 a0009c0015t0005g0007 |
2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1617-18015C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67625241 | |||||||
| chrX:67625439 | A | G | 17 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(14): Show |
17 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1617-17817A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67625439 | |||||||
| chrX:67625847 | G | A | 1 | a0011c0013t0009g0047 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1617-17409G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67625847 | |||||||
| chrX:67625899 | A | T | 2 | a0005c0006t0020g0115 a0005c0006t0032g0117 |
2 | HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1617-17357A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67625899 | |||||||
| chrX:67625907 | A | T | 131 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(128): Show |
132 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(129): Show |
intron_variant | MODIFIER | c.1617-17349A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67625907 | |||||||
| chrX:67625908 | A | T | 1 | a0006c0003t0002g0067 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1617-17348A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67625908 | |||||||
| chrX:67625921 | T | C | 2 | a0004c0032t0058g0169 a0009c0015t0005g0007 |
2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1617-17335T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67625921 | |||||||
| chrX:67625969 | A | G | 1 | a0005c0006t0011g0004 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1617-17287A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67625969 | |||||||
| chrX:67626436 | C | CT | 105 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(102): Show |
106 | HG00099.hp2 HG00609.hp1 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.1617-16796dupT | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67626436 | ||||||
| chrX:67626436 | C | CTT | 11 | a0001c0001t0001g0085 a0002c0005t0001g0041 a0003c0002t0009g0028 others(8): Show |
11 | HG00140.hp1 HG00741.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.1617-16797_1617-16 others(8): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67626436 | ||||||
| chrX:67626540 | A | C | 111 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(108): Show |
112 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.1617-16716A>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67626540 | |||||||
| chrX:67626610 | T | TTA | 13 | a0001c0001t0004g0186 a0001c0009t0006g0168 a0001c0009t0042g0135 others(10): Show |
13 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.1617-16622_1617-16 others(8): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67626610 | ||||||
| chrX:67626610 | T | TTATA | 15 | a0001c0001t0014g0179 a0001c0001t0019g0175 a0001c0001t0019g0176 others(12): Show |
15 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1617-16624_1617-16 others(10): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67626610 | ||||||
| chrX:67626610 | TTA | T | 92 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(89): Show |
92 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.1617-16622_1617-16 others(8): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67626610 | ||||||
| chrX:67626618 | A | G | 1 | a0009c0012t0005g0145 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1617-16638A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67626618 | |||||||
| chrX:67626626 | A | G | 1 | a0007c0008t0023g0127 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1617-16630A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67626626 | |||||||
| chrX:67626729 | C | A | 17 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(14): Show |
17 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1617-16527C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67626729 | |||||||
| chrX:67626797 | C | T | 2 | a0003c0021t0008g0123 a0005c0006t0010g0120 |
2 | HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1617-16459C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67626797 | |||||||
| chrX:67626833 | A | G | 2 | a0004c0032t0058g0169 a0009c0015t0005g0007 |
2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1617-16423A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67626833 | |||||||
| chrX:67626876 | C | T | 8 | a0001c0001t0014g0179 a0001c0001t0019g0175 a0001c0001t0019g0176 others(5): Show |
8 | HG01891.hp2 HG02717.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1617-16380C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67626876 | |||||||
| chrX:67626900 | G | A | 1 | a0005c0006t0028g0153 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1617-16356G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67626900 | |||||||
| chrX:67627130 | C | G | 1 | a0003c0002t0003g0017 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1617-16126C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67627130 | |||||||
| chrX:67627175 | T | A | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1617-16081T>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67627175 | |||||||
| chrX:67627254 | C | A | 19 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(16): Show |
19 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1617-16002C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67627254 | |||||||
| chrX:67627424 | G | T | 9 | a0007c0008t0005g0160 a0008c0007t0006g0163 a0008c0007t0011g0148 others(6): Show |
9 | HG02922.hp2 HG02965.hp1 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.1617-15832G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67627424 | |||||||
| chrX:67627548 | T | G | 5 | a0001c0009t0008g0128 a0001c0009t0008g0132 a0001c0026t0025g0139 others(2): Show |
5 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.1617-15708T>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67627548 | |||||||
| chrX:67627709 | C | T | 17 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(14): Show |
17 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1617-15547C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67627709 | |||||||
| chrX:67627777 | G | A | 3 | a0004c0004t0027g0182 a0007c0016t0005g0173 a0008c0017t0005g0174 |
3 | HG01081.hp2 HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1617-15479G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67627777 | |||||||
| chrX:67627815 | A | G | 1 | a0005c0006t0028g0153 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1617-15441A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67627815 | |||||||
| chrX:67627955 | G | A | 3 | a0004c0004t0031g0170 a0004c0032t0058g0169 a0009c0015t0005g0007 |
3 | HG02615.hp1 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1617-15301G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67627955 | |||||||
| chrX:67628002 | C | G | 3 | a0005c0006t0011g0004 a0007c0008t0006g0136 a0007c0008t0006g0137 |
3 | HG03041.hp2 HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1617-15254C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67628002 | |||||||
| chrX:67628065 | G | T | 1 | a0001c0001t0002g0039 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1617-15191G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67628065 | |||||||
| chrX:67628253 | T | G | 19 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(16): Show |
19 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1617-15003T>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67628253 | |||||||
| chrX:67628356 | C | G | 2 | a0003c0021t0008g0123 a0005c0006t0010g0120 |
2 | HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1617-14900C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67628356 | |||||||
| chrX:67628361 | A | T | 111 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(108): Show |
112 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.1617-14895A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67628361 | |||||||
| chrX:67628372 | C | G | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1617-14884C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67628372 | |||||||
| chrX:67628433 | CTGTT | C | 2 | a0004c0032t0058g0169 a0009c0015t0005g0007 |
2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1617-14819_1617-14 others(10): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67628433 | ||||||
| chrX:67628574 | A | G | 2 | a0002c0010t0014g0158 a0002c0010t0030g0164 |
2 | HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1617-14682A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67628574 | |||||||
| chrX:67628695 | G | C | 10 | a0001c0009t0004g0118 a0001c0009t0004g0155 a0001c0009t0033g0138 others(7): Show |
10 | HG02451.hp2 HG02572.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1617-14561G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67628695 | |||||||
| chrX:67628756 | T | A | 1 | a0001c0001t0002g0029 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1617-14500T>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67628756 | |||||||
| chrX:67628827 | T | A | 2 | a0004c0032t0058g0169 a0009c0015t0005g0007 |
2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1617-14429T>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67628827 | |||||||
| chrX:67628993 | G | C | 1 | a0005c0006t0020g0115 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1617-14263G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67628993 | |||||||
| chrX:67629066 | A | G | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1617-14190A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67629066 | |||||||
| chrX:67629246 | G | A | 134 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(131): Show |
135 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.1617-14010G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67629246 | |||||||
| chrX:67629315 | T | G | 3 | a0002c0010t0035g0151 a0002c0010t0036g0119 a0008c0007t0034g0159 |
3 | HG01243.hp1 HG02451.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1617-13941T>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67629315 | |||||||
| chrX:67629333 | C | G | 1 | a0001c0001t0004g0186 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1617-13923C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67629333 | |||||||
| chrX:67629385 | A | G | 1 | a0004c0004t0001g0076 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1617-13871A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67629385 | |||||||
| chrX:67629422 | C | A | 2 | a0001c0009t0033g0138 a0002c0010t0008g0156 |
2 | HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1617-13834C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67629422 | |||||||
| chrX:67629423 | G | A | 1 | a0003c0002t0017g0005 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1617-13833G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67629423 | |||||||
| chrX:67629766 | C | T | 1 | a0001c0001t0050g0050 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1617-13490C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67629766 | |||||||
| chrX:67629869 | T | G | 3 | a0001c0001t0004g0186 a0002c0005t0044g0181 a0003c0034t0008g0185 |
3 | HG02258.hp1 HG02886.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1617-13387T>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67629869 | |||||||
| chrX:67629921 | G | T | 3 | a0005c0006t0011g0004 a0007c0008t0006g0136 a0007c0008t0006g0137 |
3 | HG03041.hp2 HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1617-13335G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67629921 | |||||||
| chrX:67629989 | G | T | 8 | a0001c0001t0002g0029 a0002c0005t0001g0109 a0002c0005t0002g0096 others(5): Show |
8 | HG02056.hp1 NA18747.hp1 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.1617-13267G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67629989 | |||||||
| chrX:67629995 | C | T | 2 | a0005c0011t0009g0094 a0005c0011t0053g0095 |
2 | HG02735.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1617-13261C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67629995 | |||||||
| chrX:67630106 | T | C | 1 | a0013c0019t0016g0125 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1617-13150T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67630106 | |||||||
| chrX:67630351 | C | G | 2 | a0002c0010t0035g0151 a0002c0010t0036g0119 |
2 | HG01243.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1617-12905C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67630351 | |||||||
| chrX:67630486 | T | G | 2 | a0004c0032t0058g0169 a0009c0015t0005g0007 |
2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1617-12770T>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67630486 | |||||||
| chrX:67630594 | A | G | 1 | a0005c0011t0052g0068 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1617-12662A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67630594 | |||||||
| chrX:67630783 | G | A | 1 | a0004c0004t0007g0038 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1617-12473G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67630783 | |||||||
| chrX:67630852 | C | T | 17 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(14): Show |
17 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1617-12404C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67630852 | |||||||
| chrX:67630913 | G | A | 1 | a0006c0003t0002g0036 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1617-12343G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67630913 | |||||||
| chrX:67630949 | T | C | 19 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(16): Show |
19 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1617-12307T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67630949 | |||||||
| chrX:67631322 | G | A | 2 | a0007c0008t0006g0136 a0007c0008t0006g0137 |
2 | HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1617-11934G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67631322 | |||||||
| chrX:67631347 | TC | T | 3 | a0002c0010t0020g0116 a0005c0006t0020g0115 a0005c0006t0032g0117 |
3 | HG03209.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1617-11908delC | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67631347 | |||||||
| chrX:67631459 | C | T | 3 | a0006c0003t0002g0009 a0006c0003t0002g0067 a0009c0015t0002g0022 |
3 | HG02071.hp1 NA19083.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1617-11797C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67631459 | |||||||
| chrX:67631460 | G | A | 1 | a0002c0005t0007g0010 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1617-11796G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67631460 | |||||||
| chrX:67631656 | T | C | 1 | a0001c0026t0025g0139 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1617-11600T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67631656 | |||||||
| chrX:67631657 | G | A | 1 | a0001c0026t0025g0139 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1617-11599G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67631657 | |||||||
| chrX:67631894 | G | A | 1 | a0001c0009t0010g0113 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1617-11362G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67631894 | |||||||
| chrX:67632082 | C | T | 2 | a0002c0005t0001g0041 a0002c0005t0001g0046 |
2 | NA18966.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1617-11174C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67632082 | |||||||
| chrX:67632197 | C | T | 19 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(16): Show |
19 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1617-11059C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67632197 | |||||||
| chrX:67632324 | C | T | 17 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(14): Show |
17 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1617-10932C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67632324 | |||||||
| chrX:67632325 | G | A | 2 | a0001c0001t0001g0079 a0001c0001t0003g0080 |
2 | NA19062.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1617-10931G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67632325 | |||||||
| chrX:67632338 | C | A | 1 | a0004c0004t0001g0102 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1617-10918C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67632338 | |||||||
| chrX:67632380 | T | C | 157 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(154): Show |
158 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(155): Show |
intron_variant | MODIFIER | c.1617-10876T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67632380 | |||||||
| chrX:67632506 | G | C | 17 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(14): Show |
17 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1617-10750G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67632506 | |||||||
| chrX:67632510 | C | T | 1 | a0009c0015t0005g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1617-10746C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67632510 | |||||||
| chrX:67632515 | C | T | 2 | a0004c0032t0058g0169 a0009c0015t0005g0007 |
2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1617-10741C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67632515 | |||||||
| chrX:67632561 | G | A | 19 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(16): Show |
19 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1617-10695G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67632561 | |||||||
| chrX:67632607 | C | T | 1 | a0007c0008t0006g0136 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1617-10649C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67632607 | |||||||
| chrX:67632833 | A | G | 11 | a0001c0001t0014g0179 a0001c0001t0019g0175 a0001c0001t0019g0176 others(8): Show |
11 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1617-10423A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67632833 | |||||||
| chrX:67632849 | A | G | 2 | a0004c0032t0058g0169 a0009c0015t0005g0007 |
2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1617-10407A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67632849 | |||||||
| chrX:67632995 | A | G | 17 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(14): Show |
17 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1617-10261A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67632995 | |||||||
| chrX:67633711 | G | A | 2 | a0003c0002t0003g0034 a0004c0004t0003g0081 |
2 | NA19066.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1617-9545G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67633711 | |||||||
| chrX:67633749 | C | A | 1 | a0002c0005t0001g0041 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1617-9507C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67633749 | |||||||
| chrX:67633768 | A | G | 3 | a0002c0010t0020g0116 a0005c0006t0020g0115 a0005c0006t0032g0117 |
3 | HG03209.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1617-9488A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67633768 | |||||||
| chrX:67633802 | G | A | 3 | a0003c0021t0006g0161 a0005c0006t0040g0141 a0007c0008t0006g0149 |
3 | HG03540.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1617-9454G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67633802 | |||||||
| chrX:67633934 | G | A | 4 | a0001c0009t0008g0128 a0001c0009t0008g0132 a0005c0006t0001g0129 others(1): Show |
4 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(1): Show |
intron_variant | MODIFIER | c.1617-9322G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67633934 | |||||||
| chrX:67633970 | C | T | 17 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(14): Show |
17 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1617-9286C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67633970 | |||||||
| chrX:67633990 | T | TA | 17 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(14): Show |
17 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1617-9265dupA | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67633990 | ||||||
| chrX:67634049 | C | G | 1 | a0002c0005t0001g0041 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1617-9207C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67634049 | |||||||
| chrX:67634050 | C | T | 2 | a0004c0032t0058g0169 a0009c0015t0005g0007 |
2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1617-9206C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67634050 | |||||||
| chrX:67634063 | C | T | 2 | a0004c0032t0058g0169 a0009c0015t0005g0007 |
2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1617-9193C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67634063 | |||||||
| chrX:67634164 | T | G | 3 | a0002c0010t0020g0116 a0005c0006t0020g0115 a0005c0006t0032g0117 |
3 | HG03209.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1617-9092T>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67634164 | |||||||
| chrX:67634480 | G | A | 5 | a0001c0001t0004g0186 a0002c0005t0044g0181 a0003c0034t0008g0185 others(2): Show |
5 | HG02258.hp1 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1617-8776G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67634480 | |||||||
| chrX:67635008 | CT | C | 19 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(16): Show |
19 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1617-8247delT | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67635008 | |||||||
| chrX:67635050 | G | C | 19 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(16): Show |
19 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1617-8206G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67635050 | |||||||
| chrX:67635089 | C | A | 4 | a0005c0006t0003g0003 a0005c0006t0008g0122 a0005c0006t0010g0003 others(1): Show |
4 | HG00099.hp1 HG03491.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.1617-8167C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67635089 | |||||||
| chrX:67635147 | T | C | 2 | a0005c0006t0028g0153 a0013c0019t0029g0152 |
2 | HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1617-8109T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67635147 | |||||||
| chrX:67635244 | T | C | 1 | a0007c0008t0005g0142 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1617-8012T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67635244 | |||||||
| chrX:67635369 | T | A | 1 | a0005c0011t0052g0068 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1617-7887T>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67635369 | |||||||
| chrX:67635399 | A | G | 1 | a0001c0009t0010g0113 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1617-7857A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67635399 | |||||||
| chrX:67635535 | G | A | 1 | a0016c0027t0010g0171 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1617-7721G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67635535 | |||||||
| chrX:67635583 | G | A | 1 | a0009c0015t0005g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1617-7673G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67635583 | |||||||
| chrX:67636017 | G | A | 1 | a0002c0005t0007g0011 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1617-7239G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67636017 | |||||||
| chrX:67636629 | T | C | 1 | a0002c0005t0044g0181 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1617-6627T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67636629 | |||||||
| chrX:67636686 | A | T | 19 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(16): Show |
19 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1617-6570A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67636686 | |||||||
| chrX:67636798 | G | C | 1 | a0005c0006t0011g0004 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1617-6458G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67636798 | |||||||
| chrX:67637304 | T | C | 1 | a0011c0013t0001g0015 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1617-5952T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67637304 | |||||||
| chrX:67637327 | C | T | 1 | a0003c0002t0002g0040 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1617-5929C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67637327 | |||||||
| chrX:67637328 | T | C | 1 | a0006c0003t0002g0067 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1617-5928T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67637328 | |||||||
| chrX:67637518 | T | C | 1 | a0002c0005t0056g0172 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1617-5738T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67637518 | |||||||
| chrX:67637694 | G | A | 1 | a0001c0026t0025g0139 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1617-5562G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67637694 | |||||||
| chrX:67638057 | G | A | 1 | a0008c0007t0039g0131 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1617-5199G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67638057 | |||||||
| chrX:67638105 | G | C | 1 | a0008c0017t0001g0187 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1617-5151G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67638105 | |||||||
| chrX:67638169 | G | A | 1 | a0006c0003t0004g0178 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1617-5087G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67638169 | |||||||
| chrX:67638364 | G | T | 1 | a0005c0006t0011g0004 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1617-4892G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67638364 | |||||||
| chrX:67638479 | G | A | 110 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(107): Show |
111 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.1617-4777G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67638479 | |||||||
| chrX:67638607 | G | A | 17 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(14): Show |
17 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1617-4649G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67638607 | |||||||
| chrX:67638613 | A | T | 1 | a0006c0003t0015g0006 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1617-4643A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67638613 | |||||||
| chrX:67638790 | G | T | 1 | a0015c0022t0004g0112 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1617-4466G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67638790 | |||||||
| chrX:67639307 | A | C | 1 | a0007c0008t0018g0130 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1617-3949A>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67639307 | |||||||
| chrX:67639383 | T | C | 150 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(147): Show |
151 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.1617-3873T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67639383 | |||||||
| chrX:67639561 | T | G | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1617-3695T>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67639561 | |||||||
| chrX:67639579 | A | T | 2 | a0004c0032t0058g0169 a0009c0015t0005g0007 |
2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1617-3677A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67639579 | |||||||
| chrX:67639656 | G | A | 3 | a0002c0010t0035g0151 a0002c0010t0036g0119 a0008c0007t0034g0159 |
3 | HG01243.hp1 HG02451.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1617-3600G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67639656 | |||||||
| chrX:67639877 | C | T | 1 | a0005c0006t0028g0153 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1617-3379C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67639877 | |||||||
| chrX:67640577 | C | A | 1 | a0006c0003t0015g0006 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1617-2679C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67640577 | |||||||
| chrX:67640821 | C | A | 1 | a0007c0016t0022g0043 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1617-2435C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67640821 | |||||||
| chrX:67640850 | T | A | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1617-2406T>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67640850 | |||||||
| chrX:67640885 | C | G | 3 | a0002c0010t0035g0151 a0002c0010t0036g0119 a0008c0007t0034g0159 |
3 | HG01243.hp1 HG02451.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1617-2371C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67640885 | |||||||
| chrX:67641120 | G | A | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1617-2136G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67641120 | |||||||
| chrX:67641326 | C | T | 3 | a0002c0010t0035g0151 a0002c0010t0036g0119 a0008c0007t0034g0159 |
3 | HG01243.hp1 HG02451.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1617-1930C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67641326 | |||||||
| chrX:67641492 | C | G | 17 | a0001c0001t0010g0166 a0001c0009t0004g0118 a0001c0009t0004g0155 others(14): Show |
17 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.1617-1764C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67641492 | |||||||
| chrX:67641542 | A | G | 3 | a0002c0010t0035g0151 a0002c0010t0036g0119 a0008c0007t0034g0159 |
3 | HG01243.hp1 HG02451.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1617-1714A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67641542 | |||||||
| chrX:67641817 | A | T | 2 | a0004c0032t0058g0169 a0009c0015t0005g0007 |
2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1617-1439A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67641817 | |||||||
| chrX:67641841 | G | C | 1 | a0018c0036t0021g0063 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1617-1415G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67641841 | |||||||
| chrX:67641860 | G | GT | 123 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(120): Show |
124 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(121): Show |
intron_variant | MODIFIER | c.1617-1384dupT | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67641860 | ||||||
| chrX:67641873 | C | T | 174 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(171): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.1617-1383C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67641873 | |||||||
| chrX:67641930 | A | G | 2 | a0001c0009t0033g0138 a0002c0010t0008g0156 |
2 | HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1617-1326A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67641930 | |||||||
| chrX:67642097 | C | A | 1 | a0004c0004t0031g0170 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1617-1159C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67642097 | |||||||
| chrX:67642201 | G | T | 1 | a0006c0003t0001g0110 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1617-1055G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67642201 | |||||||
| chrX:67642393 | G | T | 1 | a0008c0007t0039g0131 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1617-863G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67642393 | |||||||
| chrX:67642396 | C | T | 1 | a0005c0006t0010g0120 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1617-860C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67642396 | |||||||
| chrX:67642467 | C | T | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1617-789C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67642467 | |||||||
| chrX:67642562 | G | T | 17 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(14): Show |
17 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1617-694G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67642562 | |||||||
| chrX:67643001 | A | G | 2 | a0003c0002t0012g0189 a0003c0002t0012g0190 |
2 | HG02698.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1617-255A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | chrX | 67643001 | |||||||
| chrX:67643069 | GCT | G | 2 | a0004c0032t0058g0169 a0009c0015t0005g0007 |
2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1617-185_1617-184d others(4): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 67643069 | ||||||
| chrX:67643633 | G | T | 1 | a0011c0013t0003g0107 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1768+226G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67643633 | |||||||
| chrX:67643988 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1768+581T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67643988 | |||||||
| chrX:67644150 | G | A | 3 | a0006c0003t0001g0002 a0006c0003t0001g0104 a0014c0020t0001g0002 |
3 | NA18960.hp1 NA19000.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1768+743G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67644150 | |||||||
| chrX:67644387 | T | C | 1 | a0005c0011t0009g0094 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1768+980T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67644387 | |||||||
| chrX:67644707 | G | A | 7 | a0001c0001t0010g0166 a0001c0009t0008g0128 a0001c0009t0008g0132 others(4): Show |
7 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.1768+1300G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67644707 | |||||||
| chrX:67644825 | T | C | 2 | a0003c0002t0015g0026 a0011c0013t0001g0015 |
2 | HG02027.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.1768+1418T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67644825 | |||||||
| chrX:67645503 | C | T | 2 | a0001c0009t0033g0138 a0002c0010t0008g0156 |
2 | HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1768+2096C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67645503 | |||||||
| chrX:67645654 | C | T | 110 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(107): Show |
111 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.1768+2247C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67645654 | |||||||
| chrX:67645742 | G | A | 17 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(14): Show |
17 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1768+2335G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67645742 | |||||||
| chrX:67646283 | A | C | 1 | a0003c0002t0012g0189 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1768+2876A>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67646283 | |||||||
| chrX:67647071 | C | T | 17 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(14): Show |
17 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1768+3664C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67647071 | |||||||
| chrX:67647121 | A | C | 1 | a0006c0003t0004g0178 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1768+3714A>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67647121 | |||||||
| chrX:67647173 | T | C | 2 | a0001c0001t0003g0083 a0009c0015t0003g0048 |
2 | NA18970.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1768+3766T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67647173 | |||||||
| chrX:67647448 | G | C | 1 | a0005c0011t0012g0108 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1768+4041G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67647448 | |||||||
| chrX:67647463 | T | C | 1 | a0006c0003t0015g0006 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1768+4056T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67647463 | |||||||
| chrX:67647559 | C | T | 2 | a0004c0032t0058g0169 a0009c0015t0005g0007 |
2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1768+4152C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67647559 | |||||||
| chrX:67647738 | G | T | 1 | a0003c0021t0008g0123 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1768+4331G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67647738 | |||||||
| chrX:67648523 | C | G | 1 | a0008c0007t0006g0133 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1768+5116C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67648523 | |||||||
| chrX:67648614 | A | C | 1 | a0010c0014t0001g0077 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1768+5207A>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67648614 | |||||||
| chrX:67650050 | C | A | 1 | a0001c0001t0002g0100 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1768+6643C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67650050 | |||||||
| chrX:67650101 | G | A | 1 | a0008c0007t0034g0159 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1768+6694G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67650101 | |||||||
| chrX:67650112 | A | T | 1 | a0011c0013t0003g0107 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1768+6705A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67650112 | |||||||
| chrX:67650228 | C | T | 1 | a0007c0008t0006g0136 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1768+6821C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67650228 | |||||||
| chrX:67650257 | T | G | 1 | a0001c0009t0033g0138 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1768+6850T>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67650257 | |||||||
| chrX:67650344 | A | G | 1 | a0007c0008t0006g0137 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1768+6937A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67650344 | |||||||
| chrX:67650514 | C | A | 1 | a0001c0009t0006g0168 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1768+7107C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67650514 | |||||||
| chrX:67650811 | A | G | 2 | a0004c0032t0058g0169 a0009c0015t0005g0007 |
2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1768+7404A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67650811 | |||||||
| chrX:67651204 | C | CT | 108 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(105): Show |
109 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.1768+7811dupT | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 67651204 | ||||||
| chrX:67651204 | CT | C | 6 | a0001c0028t0004g0183 a0004c0032t0058g0169 a0005c0006t0038g0126 others(3): Show |
6 | HG02615.hp1 HG02647.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1768+7811delT | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 67651204 | ||||||
| chrX:67651668 | A | G | 1 | a0001c0026t0025g0139 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1768+8261A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67651668 | |||||||
| chrX:67651708 | A | G | 1 | a0006c0003t0004g0178 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1768+8301A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67651708 | |||||||
| chrX:67651744 | A | C | 1 | a0002c0010t0008g0156 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1768+8337A>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67651744 | |||||||
| chrX:67652770 | T | C | 19 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(16): Show |
19 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1768+9363T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67652770 | |||||||
| chrX:67652771 | G | A | 17 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(14): Show |
17 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1768+9364G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67652771 | |||||||
| chrX:67653098 | G | A | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1768+9691G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67653098 | |||||||
| chrX:67653556 | G | A | 1 | a0003c0002t0001g0023 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1768+10149G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67653556 | |||||||
| chrX:67653598 | G | C | 1 | a0003c0002t0002g0040 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1768+10191G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67653598 | |||||||
| chrX:67653668 | G | A | 1 | a0007c0008t0023g0127 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1768+10261G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67653668 | |||||||
| chrX:67654278 | C | T | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1768+10871C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67654278 | |||||||
| chrX:67654287 | T | C | 2 | a0001c0009t0010g0113 a0009c0012t0041g0114 |
2 | HG02257.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1768+10880T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67654287 | |||||||
| chrX:67654348 | A | G | 1 | a0009c0015t0005g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1768+10941A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67654348 | |||||||
| chrX:67654626 | C | G | 17 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(14): Show |
17 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1768+11219C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67654626 | |||||||
| chrX:67654662 | T | C | 1 | a0011c0013t0001g0015 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1768+11255T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67654662 | |||||||
| chrX:67654834 | G | A | 19 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(16): Show |
19 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1768+11427G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67654834 | |||||||
| chrX:67654916 | T | G | 2 | a0001c0009t0010g0113 a0009c0012t0041g0114 |
2 | HG02257.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1768+11509T>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67654916 | |||||||
| chrX:67655199 | A | G | 19 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(16): Show |
19 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1768+11792A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67655199 | |||||||
| chrX:67655611 | C | G | 1 | a0006c0003t0001g0110 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1768+12204C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67655611 | |||||||
| chrX:67655735 | C | A | 3 | a0001c0001t0001g0070 a0003c0002t0001g0027 a0010c0014t0001g0077 |
3 | HG00609.hp1 HG02738.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1768+12328C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67655735 | |||||||
| chrX:67655914 | T | C | 110 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(107): Show |
111 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.1768+12507T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67655914 | |||||||
| chrX:67656780 | T | C | 1 | a0008c0007t0039g0131 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1768+13373T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67656780 | |||||||
| chrX:67657475 | T | G | 17 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(14): Show |
17 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1768+14068T>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67657475 | |||||||
| chrX:67657611 | G | A | 1 | a0007c0008t0023g0127 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1768+14204G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67657611 | |||||||
| chrX:67657643 | C | G | 2 | a0003c0021t0008g0123 a0005c0006t0010g0120 |
2 | HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1768+14236C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67657643 | |||||||
| chrX:67658171 | G | A | 2 | a0004c0032t0058g0169 a0009c0015t0005g0007 |
2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1768+14764G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67658171 | |||||||
| chrX:67658250 | A | G | 1 | a0007c0016t0003g0071 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1768+14843A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67658250 | |||||||
| chrX:67658626 | G | C | 1 | a0006c0003t0002g0089 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1768+15219G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67658626 | |||||||
| chrX:67658756 | C | T | 1 | a0004c0004t0003g0081 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1768+15349C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67658756 | |||||||
| chrX:67658779 | C | T | 1 | a0001c0009t0010g0113 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1768+15372C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67658779 | |||||||
| chrX:67658830 | A | G | 19 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(16): Show |
19 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1768+15423A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67658830 | |||||||
| chrX:67658930 | G | T | 1 | a0002c0010t0030g0164 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1768+15523G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67658930 | |||||||
| chrX:67659059 | C | T | 1 | a0003c0002t0003g0017 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1768+15652C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67659059 | |||||||
| chrX:67659077 | G | A | 162 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(159): Show |
163 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.1768+15670G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67659077 | |||||||
| chrX:67659095 | C | T | 1 | a0004c0004t0031g0170 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1768+15688C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67659095 | |||||||
| chrX:67659212 | A | G | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1768+15805A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67659212 | |||||||
| chrX:67659232 | TA | T | 2 | a0004c0032t0058g0169 a0009c0015t0005g0007 |
2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1768+15826delA | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67659232 | |||||||
| chrX:67659558 | T | C | 8 | a0001c0001t0014g0179 a0001c0001t0019g0175 a0001c0001t0019g0176 others(5): Show |
8 | HG01891.hp2 HG02717.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1768+16151T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67659558 | |||||||
| chrX:67659611 | T | C | 19 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(16): Show |
19 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1768+16204T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67659611 | |||||||
| chrX:67659750 | G | A | 17 | a0001c0001t0010g0166 a0001c0009t0004g0118 a0001c0009t0004g0155 others(14): Show |
17 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.1768+16343G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67659750 | |||||||
| chrX:67659891 | C | A | 1 | a0001c0026t0025g0139 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1768+16484C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67659891 | |||||||
| chrX:67660021 | C | T | 3 | a0001c0001t0002g0049 a0002c0010t0014g0158 a0004c0004t0051g0078 |
3 | HG02630.hp2 NA18967.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1768+16614C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67660021 | |||||||
| chrX:67660361 | T | C | 1 | a0004c0032t0058g0169 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1768+16954T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67660361 | |||||||
| chrX:67660390 | A | T | 2 | a0001c0009t0006g0168 a0006c0031t0043g0167 |
2 | HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1768+16983A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67660390 | |||||||
| chrX:67660450 | A | G | 159 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(156): Show |
160 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1768+17043A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67660450 | |||||||
| chrX:67660453 | C | T | 1 | a0004c0004t0031g0170 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1768+17046C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67660453 | |||||||
| chrX:67660717 | G | A | 1 | a0002c0005t0056g0172 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1768+17310G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67660717 | |||||||
| chrX:67660762 | T | A | 2 | a0001c0009t0033g0138 a0002c0010t0008g0156 |
2 | HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1768+17355T>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67660762 | |||||||
| chrX:67660938 | T | G | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1768+17531T>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67660938 | |||||||
| chrX:67660980 | C | T | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1768+17573C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67660980 | |||||||
| chrX:67661120 | C | T | 2 | a0004c0032t0058g0169 a0009c0015t0005g0007 |
2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1768+17713C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67661120 | |||||||
| chrX:67661124 | G | A | 1 | a0001c0009t0004g0118 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1768+17717G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67661124 | |||||||
| chrX:67661246 | G | A | 1 | a0004c0004t0021g0021 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1768+17839G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67661246 | |||||||
| chrX:67661298 | C | A | 188 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(185): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.1768+17891C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67661298 | |||||||
| chrX:67661425 | C | T | 1 | a0004c0004t0027g0182 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1768+18018C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67661425 | |||||||
| chrX:67661457 | A | C | 1 | a0001c0009t0008g0128 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1768+18050A>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67661457 | |||||||
| chrX:67661655 | T | G | 17 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(14): Show |
17 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1768+18248T>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67661655 | |||||||
| chrX:67661741 | T | G | 110 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(107): Show |
111 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.1768+18334T>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67661741 | |||||||
| chrX:67662028 | G | A | 1 | a0013c0019t0029g0152 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1768+18621G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67662028 | |||||||
| chrX:67662041 | C | A | 1 | a0003c0002t0012g0020 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1768+18634C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67662041 | |||||||
| chrX:67662326 | T | C | 1 | a0004c0032t0058g0169 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1768+18919T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67662326 | |||||||
| chrX:67662349 | C | A | 19 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(16): Show |
19 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1768+18942C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67662349 | |||||||
| chrX:67662403 | A | G | 151 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(148): Show |
152 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.1768+18996A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67662403 | |||||||
| chrX:67662773 | G | T | 1 | a0005c0011t0003g0066 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1768+19366G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67662773 | |||||||
| chrX:67662812 | A | T | 8 | a0001c0001t0014g0179 a0001c0001t0019g0175 a0001c0001t0019g0176 others(5): Show |
8 | HG01891.hp2 HG02717.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1768+19405A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67662812 | |||||||
| chrX:67662977 | A | G | 19 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(16): Show |
19 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1768+19570A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67662977 | |||||||
| chrX:67663024 | A | T | 2 | a0007c0016t0005g0173 a0008c0017t0005g0174 |
2 | HG01081.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1768+19617A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67663024 | |||||||
| chrX:67663145 | G | A | 3 | a0002c0005t0001g0041 a0002c0005t0001g0046 a0004c0004t0001g0054 |
3 | NA18955.hp1 NA18966.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1768+19738G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67663145 | |||||||
| chrX:67663159 | C | T | 17 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(14): Show |
17 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1768+19752C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67663159 | |||||||
| chrX:67663192 | G | C | 1 | a0003c0002t0001g0093 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1768+19785G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67663192 | |||||||
| chrX:67663239 | G | A | 3 | a0002c0010t0020g0116 a0005c0006t0020g0115 a0005c0006t0032g0117 |
3 | HG03209.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1768+19832G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67663239 | |||||||
| chrX:67663704 | A | G | 2 | a0001c0009t0010g0113 a0009c0012t0041g0114 |
2 | HG02257.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1768+20297A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67663704 | |||||||
| chrX:67663707 | T | A | 1 | a0002c0005t0001g0018 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1768+20300T>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67663707 | |||||||
| chrX:67663766 | C | G | 2 | a0010c0014t0013g0090 a0019c0037t0049g0082 |
2 | NA18971.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1768+20359C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67663766 | |||||||
| chrX:67663948 | C | T | 1 | a0001c0001t0050g0050 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1768+20541C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67663948 | |||||||
| chrX:67663949 | G | A | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1768+20542G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67663949 | |||||||
| chrX:67663957 | T | G | 19 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(16): Show |
19 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1768+20550T>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67663957 | |||||||
| chrX:67664063 | G | A | 5 | a0007c0008t0005g0160 a0009c0012t0005g0144 a0009c0012t0005g0145 others(2): Show |
5 | HG02965.hp1 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1768+20656G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67664063 | |||||||
| chrX:67664389 | C | G | 1 | a0002c0010t0008g0156 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1768+20982C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67664389 | |||||||
| chrX:67664428 | G | C | 3 | a0002c0010t0020g0116 a0005c0006t0020g0115 a0005c0006t0032g0117 |
3 | HG03209.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1768+21021G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67664428 | |||||||
| chrX:67664520 | G | T | 6 | a0001c0001t0010g0166 a0001c0009t0008g0128 a0001c0009t0008g0132 others(3): Show |
6 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.1768+21113G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67664520 | |||||||
| chrX:67664529 | T | C | 19 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(16): Show |
19 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1768+21122T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67664529 | |||||||
| chrX:67664555 | C | T | 2 | a0003c0002t0012g0189 a0003c0002t0012g0190 |
2 | HG02698.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1768+21148C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67664555 | |||||||
| chrX:67664804 | C | A | 5 | a0001c0001t0002g0025 a0001c0001t0002g0075 a0002c0005t0016g0111 others(2): Show |
5 | NA18943.hp1 NA18961.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.1769-21206C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67664804 | |||||||
| chrX:67664974 | A | G | 3 | a0002c0010t0035g0151 a0002c0010t0036g0119 a0008c0007t0034g0159 |
3 | HG01243.hp1 HG02451.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1769-21036A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67664974 | |||||||
| chrX:67665064 | T | C | 19 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(16): Show |
19 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1769-20946T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67665064 | |||||||
| chrX:67665076 | T | C | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1769-20934T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67665076 | |||||||
| chrX:67665162 | G | A | 1 | a0002c0010t0004g0154 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1769-20848G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67665162 | |||||||
| chrX:67665865 | G | A | 2 | a0005c0006t0040g0141 a0007c0008t0006g0149 |
2 | HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1769-20145G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67665865 | |||||||
| chrX:67666300 | G | A | 17 | a0001c0001t0010g0166 a0001c0009t0004g0118 a0001c0009t0004g0155 others(14): Show |
17 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.1769-19710G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67666300 | |||||||
| chrX:67667034 | G | A | 6 | a0001c0009t0006g0168 a0001c0009t0042g0135 a0005c0006t0038g0126 others(3): Show |
6 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.1769-18976G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67667034 | |||||||
| chrX:67667315 | T | C | 151 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(148): Show |
152 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.1769-18695T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67667315 | |||||||
| chrX:67667372 | A | G | 2 | a0001c0028t0004g0183 a0006c0003t0004g0177 |
2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1769-18638A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67667372 | |||||||
| chrX:67667550 | T | C | 4 | a0003c0034t0008g0185 a0004c0004t0027g0182 a0007c0016t0005g0173 others(1): Show |
4 | HG01081.hp2 HG02055.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1769-18460T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67667550 | |||||||
| chrX:67667626 | C | T | 1 | a0002c0010t0035g0151 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1769-18384C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67667626 | |||||||
| chrX:67667640 | A | G | 1 | a0013c0019t0029g0152 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1769-18370A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67667640 | |||||||
| chrX:67668390 | T | A | 5 | a0007c0008t0005g0160 a0009c0012t0005g0144 a0009c0012t0005g0145 others(2): Show |
5 | HG02965.hp1 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1769-17620T>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67668390 | |||||||
| chrX:67668486 | G | A | 1 | a0008c0007t0006g0133 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1769-17524G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67668486 | |||||||
| chrX:67668516 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1769-17494T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67668516 | |||||||
| chrX:67668532 | T | TA | 17 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(14): Show |
17 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1769-17477dupA | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 67668532 | ||||||
| chrX:67668677 | T | C | 1 | a0004c0032t0058g0169 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1769-17333T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67668677 | |||||||
| chrX:67668697 | T | C | 1 | a0002c0005t0004g0184 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1769-17313T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67668697 | |||||||
| chrX:67669333 | T | A | 1 | a0002c0005t0044g0181 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1769-16677T>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67669333 | |||||||
| chrX:67669625 | G | A | 19 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(16): Show |
19 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1769-16385G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67669625 | |||||||
| chrX:67670033 | A | T | 5 | a0008c0007t0006g0140 a0008c0007t0006g0150 a0008c0007t0011g0148 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1769-15977A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67670033 | |||||||
| chrX:67670416 | A | T | 1 | a0009c0015t0005g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1769-15594A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67670416 | |||||||
| chrX:67670499 | A | C | 2 | a0004c0032t0058g0169 a0009c0015t0005g0007 |
2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1769-15511A>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67670499 | |||||||
| chrX:67670518 | T | C | 17 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(14): Show |
17 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1769-15492T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67670518 | |||||||
| chrX:67670526 | A | G | 1 | a0004c0004t0001g0102 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1769-15484A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67670526 | |||||||
| chrX:67670593 | A | G | 110 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(107): Show |
111 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.1769-15417A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67670593 | |||||||
| chrX:67670652 | G | A | 1 | a0001c0001t0002g0065 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1769-15358G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67670652 | |||||||
| chrX:67670712 | A | G | 1 | a0008c0007t0039g0131 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1769-15298A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67670712 | |||||||
| chrX:67670982 | T | G | 1 | a0004c0004t0007g0038 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1769-15028T>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67670982 | |||||||
| chrX:67671589 | G | C | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1769-14421G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67671589 | |||||||
| chrX:67671645 | C | T | 151 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(148): Show |
152 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.1769-14365C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67671645 | |||||||
| chrX:67671649 | T | A | 1 | a0001c0001t0004g0186 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1769-14361T>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67671649 | |||||||
| chrX:67671822 | C | T | 9 | a0001c0001t0002g0029 a0002c0005t0001g0109 a0002c0005t0002g0096 others(6): Show |
9 | HG02056.hp1 NA18747.hp1 NA18952.hp1 others(6): Show |
intron_variant | MODIFIER | c.1769-14188C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67671822 | |||||||
| chrX:67671834 | A | G | 2 | a0002c0010t0018g0165 a0010c0035t0014g0157 |
2 | HG02723.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1769-14176A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67671834 | |||||||
| chrX:67671856 | T | C | 1 | a0004c0032t0058g0169 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1769-14154T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67671856 | |||||||
| chrX:67671923 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1769-14087T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67671923 | |||||||
| chrX:67671992 | G | A | 1 | a0005c0006t0011g0004 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1769-14018G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67671992 | |||||||
| chrX:67672020 | G | T | 1 | a0010c0014t0013g0090 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1769-13990G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67672020 | |||||||
| chrX:67672249 | T | A | 186 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(183): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.1769-13761T>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67672249 | |||||||
| chrX:67672308 | A | T | 19 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(16): Show |
19 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1769-13702A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67672308 | |||||||
| chrX:67672314 | G | T | 2 | a0004c0032t0058g0169 a0009c0015t0005g0007 |
2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1769-13696G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67672314 | |||||||
| chrX:67672377 | C | T | 16 | a0001c0001t0002g0029 a0002c0005t0001g0041 a0002c0005t0001g0046 others(13): Show |
16 | HG01069.hp1 HG01934.hp1 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.1769-13633C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67672377 | |||||||
| chrX:67672502 | G | A | 3 | a0001c0001t0001g0070 a0003c0002t0001g0027 a0010c0014t0001g0077 |
3 | HG00609.hp1 HG02738.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1769-13508G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67672502 | |||||||
| chrX:67672728 | G | A | 2 | a0001c0001t0001g0070 a0003c0002t0001g0027 |
2 | HG00609.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1769-13282G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67672728 | |||||||
| chrX:67672824 | C | T | 1 | a0003c0002t0001g0069 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1769-13186C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67672824 | |||||||
| chrX:67672872 | T | A | 2 | a0004c0032t0058g0169 a0009c0015t0005g0007 |
2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1769-13138T>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67672872 | |||||||
| chrX:67673043 | GT | G | 24 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(21): Show |
24 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1769-12951delT | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 67673043 | ||||||
| chrX:67673266 | G | A | 1 | a0007c0016t0022g0043 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1769-12744G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67673266 | |||||||
| chrX:67673369 | G | GTC | 110 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(107): Show |
111 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.1769-12620_1769-12 others(8): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 67673369 | ||||||
| chrX:67673371 | C | G | 2 | a0004c0032t0058g0169 a0009c0015t0005g0007 |
2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1769-12639C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67673371 | |||||||
| chrX:67673471 | A | AT | 7 | a0002c0010t0035g0151 a0002c0010t0036g0119 a0003c0002t0001g0069 others(4): Show |
7 | HG00673.hp1 HG01243.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.1769-12523dupT | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 67673471 | ||||||
| chrX:67673471 | AT | A | 22 | a0001c0001t0002g0025 a0001c0001t0004g0186 a0001c0009t0008g0132 others(19): Show |
22 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.1769-12523delT | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 67673471 | ||||||
| chrX:67673471 | ATT | A | 20 | a0001c0001t0010g0166 a0001c0001t0014g0179 a0001c0001t0019g0175 others(17): Show |
20 | HG00280.hp1 HG00741.hp1 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1769-12524_1769-12 others(8): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 67673471 | ||||||
| chrX:67673747 | G | A | 1 | a0005c0011t0052g0068 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1769-12263G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67673747 | |||||||
| chrX:67673930 | C | T | 1 | a0002c0010t0014g0158 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1769-12080C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67673930 | |||||||
| chrX:67674401 | G | A | 1 | a0011c0013t0001g0052 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1769-11609G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67674401 | |||||||
| chrX:67674443 | G | A | 2 | a0004c0032t0058g0169 a0009c0015t0005g0007 |
2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1769-11567G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67674443 | |||||||
| chrX:67674635 | C | T | 1 | a0009c0012t0024g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1769-11375C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67674635 | |||||||
| chrX:67674956 | G | A | 1 | a0001c0001t0002g0100 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1769-11054G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67674956 | |||||||
| chrX:67675225 | G | A | 1 | a0001c0009t0042g0135 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1769-10785G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67675225 | |||||||
| chrX:67675279 | A | T | 1 | a0002c0005t0056g0172 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1769-10731A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67675279 | |||||||
| chrX:67675586 | T | C | 19 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(16): Show |
19 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1769-10424T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67675586 | |||||||
| chrX:67675712 | C | T | 1 | a0004c0033t0054g0101 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1769-10298C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67675712 | |||||||
| chrX:67675758 | G | T | 18 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(15): Show |
18 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1769-10252G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67675758 | |||||||
| chrX:67675842 | A | G | 1 | a0011c0013t0009g0047 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1769-10168A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67675842 | |||||||
| chrX:67675855 | T | C | 18 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(15): Show |
18 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1769-10155T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67675855 | |||||||
| chrX:67675940 | G | A | 1 | a0002c0010t0030g0164 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1769-10070G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67675940 | |||||||
| chrX:67675957 | G | A | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1769-10053G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67675957 | |||||||
| chrX:67676069 | GA | G | 3 | a0002c0010t0035g0151 a0002c0010t0036g0119 a0008c0007t0034g0159 |
3 | HG01243.hp1 HG02451.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1769-9937delA | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 67676069 | ||||||
| chrX:67676352 | G | T | 2 | a0001c0001t0002g0049 a0004c0004t0051g0078 |
2 | NA18967.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1769-9658G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67676352 | |||||||
| chrX:67676602 | G | T | 2 | a0004c0032t0058g0169 a0009c0015t0005g0007 |
2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1769-9408G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67676602 | |||||||
| chrX:67676854 | G | A | 2 | a0006c0003t0009g0084 a0006c0003t0017g0060 |
2 | HG01169.hp1 HG01928.hp1 |
intron_variant | MODIFIER | c.1769-9156G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67676854 | |||||||
| chrX:67676939 | C | T | 1 | a0003c0002t0017g0005 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1769-9071C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67676939 | |||||||
| chrX:67677010 | G | A | 4 | a0005c0006t0003g0003 a0005c0006t0008g0122 a0005c0006t0010g0003 others(1): Show |
4 | HG00099.hp1 HG03491.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.1769-9000G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67677010 | |||||||
| chrX:67677168 | C | T | 3 | a0004c0004t0027g0182 a0007c0016t0005g0173 a0008c0017t0005g0174 |
3 | HG01081.hp2 HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1769-8842C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67677168 | |||||||
| chrX:67677202 | C | A | 2 | a0004c0032t0058g0169 a0009c0015t0005g0007 |
2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1769-8808C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67677202 | |||||||
| chrX:67677253 | A | G | 3 | a0001c0001t0007g0001 a0001c0001t0007g0012 a0003c0034t0008g0185 |
4 | HG02258.hp1 NA18983.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.1769-8757A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67677253 | |||||||
| chrX:67677274 | T | C | 1 | a0011c0013t0009g0047 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1769-8736T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67677274 | |||||||
| chrX:67677645 | A | G | 1 | a0003c0034t0008g0185 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1769-8365A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67677645 | |||||||
| chrX:67677951 | C | T | 1 | a0001c0009t0042g0135 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1769-8059C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67677951 | |||||||
| chrX:67678106 | T | C | 1 | a0004c0004t0048g0087 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1769-7904T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67678106 | |||||||
| chrX:67678218 | C | T | 2 | a0002c0005t0015g0088 a0004c0004t0048g0087 |
2 | NA19085.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1769-7792C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67678218 | |||||||
| chrX:67678279 | T | G | 1 | a0003c0002t0017g0005 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1769-7731T>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67678279 | |||||||
| chrX:67678332 | A | G | 1 | a0007c0008t0023g0127 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1769-7678A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67678332 | |||||||
| chrX:67678353 | A | T | 16 | a0001c0001t0010g0166 a0001c0009t0004g0118 a0001c0009t0004g0155 others(13): Show |
16 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.1769-7657A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67678353 | |||||||
| chrX:67678440 | C | T | 1 | a0001c0001t0007g0032 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1769-7570C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67678440 | |||||||
| chrX:67678677 | C | T | 1 | a0009c0015t0005g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1769-7333C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67678677 | |||||||
| chrX:67678710 | G | A | 3 | a0003c0021t0006g0161 a0005c0006t0040g0141 a0007c0008t0006g0149 |
3 | HG03540.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1769-7300G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67678710 | |||||||
| chrX:67678952 | T | C | 6 | a0001c0001t0002g0049 a0003c0002t0003g0034 a0004c0004t0003g0081 others(3): Show |
6 | HG02135.hp1 NA18944.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.1769-7058T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67678952 | |||||||
| chrX:67678998 | A | G | 2 | a0004c0032t0058g0169 a0009c0015t0005g0007 |
2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1769-7012A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67678998 | |||||||
| chrX:67680277 | T | G | 1 | a0004c0004t0021g0021 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1769-5733T>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67680277 | |||||||
| chrX:67680370 | G | C | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1769-5640G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67680370 | |||||||
| chrX:67680510 | C | A | 1 | a0001c0026t0025g0139 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1769-5500C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67680510 | |||||||
| chrX:67680974 | C | A | 2 | a0002c0005t0001g0041 a0002c0005t0001g0046 |
2 | NA18966.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1769-5036C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67680974 | |||||||
| chrX:67681065 | C | A | 1 | a0004c0004t0051g0078 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1769-4945C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67681065 | |||||||
| chrX:67681465 | C | T | 1 | a0003c0002t0001g0069 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1769-4545C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67681465 | |||||||
| chrX:67681563 | T | C | 1 | a0008c0007t0034g0159 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1769-4447T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67681563 | |||||||
| chrX:67682019 | C | A | 1 | a0001c0001t0002g0029 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1769-3991C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67682019 | |||||||
| chrX:67682382 | A | G | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1769-3628A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67682382 | |||||||
| chrX:67682667 | C | A | 1 | a0006c0003t0002g0036 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1769-3343C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67682667 | |||||||
| chrX:67682703 | A | G | 1 | a0003c0002t0012g0020 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1769-3307A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67682703 | |||||||
| chrX:67682950 | A | T | 6 | a0001c0001t0010g0166 a0001c0009t0008g0128 a0001c0009t0008g0132 others(3): Show |
6 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.1769-3060A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67682950 | |||||||
| chrX:67683518 | C | A | 1 | a0008c0007t0010g0124 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1769-2492C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67683518 | |||||||
| chrX:67683533 | G | T | 2 | a0004c0032t0058g0169 a0009c0015t0005g0007 |
2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1769-2477G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67683533 | |||||||
| chrX:67683537 | T | C | 2 | a0004c0032t0058g0169 a0009c0015t0005g0007 |
2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1769-2473T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67683537 | |||||||
| chrX:67683901 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1769-2109C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67683901 | |||||||
| chrX:67683902 | G | T | 1 | a0002c0005t0044g0181 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1769-2108G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67683902 | |||||||
| chrX:67683905 | A | G | 1 | a0006c0003t0015g0006 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1769-2105A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67683905 | |||||||
| chrX:67684271 | G | T | 19 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(16): Show |
19 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1769-1739G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67684271 | |||||||
| chrX:67685091 | A | C | 1 | a0003c0002t0013g0086 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1769-919A>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67685091 | |||||||
| chrX:67685092 | A | T | 1 | a0003c0002t0013g0086 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1769-918A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67685092 | |||||||
| chrX:67685093 | G | A | 1 | a0003c0002t0013g0086 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1769-917G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67685093 | |||||||
| chrX:67685095 | T | A | 1 | a0003c0002t0013g0086 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1769-915T>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67685095 | |||||||
| chrX:67685097 | T | A | 1 | a0003c0002t0013g0086 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1769-913T>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67685097 | |||||||
| chrX:67685098 | G | T | 1 | a0003c0002t0013g0086 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1769-912G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67685098 | |||||||
| chrX:67685099 | C | A | 1 | a0003c0002t0013g0086 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1769-911C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67685099 | |||||||
| chrX:67685103 | T | A | 1 | a0003c0002t0013g0086 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1769-907T>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67685103 | |||||||
| chrX:67685105 | T | G | 1 | a0003c0002t0013g0086 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1769-905T>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67685105 | |||||||
| chrX:67685106 | C | T | 1 | a0003c0002t0013g0086 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1769-904C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67685106 | |||||||
| chrX:67685107 | A | T | 1 | a0003c0002t0013g0086 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1769-903A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67685107 | |||||||
| chrX:67685160 | A | T | 18 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(15): Show |
18 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1769-850A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67685160 | |||||||
| chrX:67685243 | G | A | 2 | a0003c0002t0012g0189 a0003c0002t0012g0190 |
2 | HG02698.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1769-767G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67685243 | |||||||
| chrX:67685415 | G | T | 1 | a0001c0001t0002g0065 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1769-595G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67685415 | |||||||
| chrX:67685493 | A | G | 1 | a0002c0005t0044g0181 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1769-517A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67685493 | |||||||
| chrX:67685741 | A | C | 1 | a0003c0002t0013g0086 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1769-269A>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67685741 | |||||||
| chrX:67685744 | G | A | 1 | a0003c0002t0013g0086 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1769-266G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67685744 | |||||||
| chrX:67685745 | A | C | 1 | a0003c0002t0013g0086 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1769-265A>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67685745 | |||||||
| chrX:67685746 | G | A | 1 | a0003c0002t0013g0086 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1769-264G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67685746 | |||||||
| chrX:67685751 | C | G | 1 | a0003c0002t0013g0086 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1769-259C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67685751 | |||||||
| chrX:67685752 | C | A | 1 | a0003c0002t0013g0086 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1769-258C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67685752 | |||||||
| chrX:67685754 | A | G | 1 | a0003c0002t0013g0086 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1769-256A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67685754 | |||||||
| chrX:67685755 | A | T | 1 | a0003c0002t0013g0086 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1769-255A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 2/7 | chrX | 67685755 | |||||||
| chrX:67686427 | G | T | 1 | a0001c0001t0010g0166 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1885+301G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67686427 | |||||||
| chrX:67686694 | G | A | 1 | a0002c0010t0014g0158 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1885+568G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67686694 | |||||||
| chrX:67686896 | G | A | 1 | a0003c0034t0008g0185 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1885+770G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67686896 | |||||||
| chrX:67687086 | T | A | 1 | a0008c0007t0006g0140 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1885+960T>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67687086 | |||||||
| chrX:67687471 | C | T | 1 | a0001c0026t0025g0139 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1885+1345C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67687471 | |||||||
| chrX:67687617 | A | T | 110 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(107): Show |
111 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.1885+1491A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67687617 | |||||||
| chrX:67687832 | C | T | 1 | a0006c0003t0004g0178 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1885+1706C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67687832 | |||||||
| chrX:67687874 | T | C | 1 | a0005c0011t0012g0108 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1885+1748T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67687874 | |||||||
| chrX:67687981 | A | G | 1 | a0001c0009t0008g0128 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1885+1855A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67687981 | |||||||
| chrX:67688117 | TGACTGGC | T | 2 | a0007c0016t0005g0173 a0008c0017t0005g0174 |
2 | HG01081.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1885+1992_1885+199 others(11): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67688117 | |||||||
| chrX:67688435 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1885+2309C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67688435 | |||||||
| chrX:67688512 | C | T | 1 | a0010c0035t0014g0157 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1885+2386C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67688512 | |||||||
| chrX:67689329 | C | G | 163 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(160): Show |
164 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.1885+3203C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67689329 | |||||||
| chrX:67689442 | T | C | 1 | a0002c0005t0056g0172 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1885+3316T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67689442 | |||||||
| chrX:67689559 | C | T | 1 | a0011c0013t0001g0015 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1885+3433C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67689559 | |||||||
| chrX:67689581 | C | T | 18 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(15): Show |
18 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1885+3455C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67689581 | |||||||
| chrX:67689849 | A | C | 3 | a0002c0010t0020g0116 a0005c0006t0020g0115 a0005c0006t0032g0117 |
3 | HG03209.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1885+3723A>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67689849 | |||||||
| chrX:67689861 | A | T | 2 | a0004c0004t0031g0170 a0015c0023t0008g0180 |
2 | HG02895.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1885+3735A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67689861 | |||||||
| chrX:67689874 | C | G | 1 | a0003c0002t0015g0026 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1885+3748C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67689874 | |||||||
| chrX:67690487 | G | A | 2 | a0002c0005t0001g0018 a0004c0004t0001g0091 |
2 | HG03490.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1885+4361G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67690487 | |||||||
| chrX:67690557 | A | G | 1 | a0006c0003t0015g0006 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1885+4431A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67690557 | |||||||
| chrX:67690693 | A | G | 2 | a0012c0018t0011g0019 a0012c0018t0011g0134 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1885+4567A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67690693 | |||||||
| chrX:67690762 | T | A | 150 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(147): Show |
151 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.1885+4636T>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67690762 | |||||||
| chrX:67690814 | T | C | 1 | a0009c0015t0005g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1885+4688T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67690814 | |||||||
| chrX:67691002 | A | G | 1 | a0002c0005t0056g0172 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1885+4876A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67691002 | |||||||
| chrX:67691140 | A | C | 1 | a0007c0008t0057g0121 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1885+5014A>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67691140 | |||||||
| chrX:67691162 | T | C | 1 | a0009c0012t0037g0143 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1885+5036T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67691162 | |||||||
| chrX:67691655 | T | C | 1 | a0002c0005t0007g0010 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1885+5529T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67691655 | |||||||
| chrX:67691661 | T | C | 1 | a0002c0005t0007g0010 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1885+5535T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67691661 | |||||||
| chrX:67691912 | A | G | 19 | a0001c0001t0010g0166 a0001c0009t0004g0118 a0001c0009t0004g0155 others(16): Show |
19 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.1885+5786A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67691912 | |||||||
| chrX:67691934 | G | T | 2 | a0002c0010t0018g0165 a0010c0035t0014g0157 |
2 | HG02723.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1885+5808G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67691934 | |||||||
| chrX:67692052 | C | T | 1 | a0007c0016t0005g0173 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1885+5926C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67692052 | |||||||
| chrX:67692549 | G | A | 1 | a0007c0008t0005g0160 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1885+6423G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67692549 | |||||||
| chrX:67692623 | G | A | 1 | a0007c0008t0006g0137 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1885+6497G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67692623 | |||||||
| chrX:67692662 | C | A | 1 | a0006c0003t0015g0006 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1885+6536C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67692662 | |||||||
| chrX:67693072 | G | A | 2 | a0004c0032t0058g0169 a0009c0015t0005g0007 |
2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1885+6946G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67693072 | |||||||
| chrX:67693583 | G | A | 1 | a0004c0004t0021g0021 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1885+7457G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67693583 | |||||||
| chrX:67693630 | T | G | 1 | a0003c0002t0017g0014 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1885+7504T>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67693630 | |||||||
| chrX:67694362 | A | G | 1 | a0002c0010t0030g0164 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1885+8236A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67694362 | |||||||
| chrX:67694794 | C | T | 2 | a0002c0005t0007g0010 a0002c0005t0007g0011 |
2 | NA18953.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1885+8668C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67694794 | |||||||
| chrX:67694795 | G | A | 2 | a0002c0005t0001g0018 a0004c0004t0001g0091 |
2 | HG03490.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1885+8669G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67694795 | |||||||
| chrX:67694851 | T | C | 6 | a0001c0009t0006g0168 a0001c0009t0042g0135 a0005c0006t0038g0126 others(3): Show |
6 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.1885+8725T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67694851 | |||||||
| chrX:67694890 | G | A | 2 | a0001c0009t0033g0138 a0002c0010t0008g0156 |
2 | HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1885+8764G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67694890 | |||||||
| chrX:67694959 | T | C | 110 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(107): Show |
111 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.1885+8833T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67694959 | |||||||
| chrX:67695251 | C | T | 1 | a0008c0007t0006g0163 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1885+9125C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67695251 | |||||||
| chrX:67695729 | G | C | 2 | a0003c0002t0001g0069 a0003c0002t0003g0017 |
2 | HG00673.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.1885+9603G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67695729 | |||||||
| chrX:67695738 | A | AAC | 96 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(93): Show |
97 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(94): Show |
intron_variant | MODIFIER | c.1885+9645_1885+964 others(6): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 67695738 | ||||||
| chrX:67695738 | A | AACAC | 9 | a0001c0001t0002g0100 a0001c0001t0007g0012 a0002c0005t0015g0088 others(6): Show |
9 | HG03491.hp2 HG03710.hp1 HG04204.hp1 others(6): Show |
intron_variant | MODIFIER | c.1885+9643_1885+964 others(8): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 67695738 | ||||||
| chrX:67695738 | A | AACACAC | 2 | a0003c0002t0012g0189 a0004c0004t0047g0053 |
2 | HG01433.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.1885+9641_1885+964 others(10): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 67695738 | ||||||
| chrX:67695765 | A | T | 36 | a0001c0001t0004g0186 a0001c0001t0010g0166 a0001c0001t0014g0179 others(33): Show |
36 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.1885+9639A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67695765 | |||||||
| chrX:67695773 | G | A | 4 | a0003c0002t0003g0034 a0004c0004t0003g0081 a0006c0003t0009g0084 others(1): Show |
4 | HG01169.hp1 NA18974.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.1885+9647G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67695773 | |||||||
| chrX:67695775 | T | G | 4 | a0003c0002t0003g0034 a0004c0004t0003g0081 a0006c0003t0009g0084 others(1): Show |
4 | HG01169.hp1 NA18974.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.1885+9649T>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67695775 | |||||||
| chrX:67695777 | T | C | 1 | a0002c0010t0004g0154 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1885+9651T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67695777 | |||||||
| chrX:67695788 | C | CT | 2 | a0006c0003t0009g0084 a0011c0013t0003g0107 |
2 | HG01169.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.1885+9662_1885+966 others(5): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67695788 | |||||||
| chrX:67695814 | C | G | 16 | a0001c0001t0010g0166 a0001c0009t0004g0118 a0001c0009t0004g0155 others(13): Show |
16 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.1885+9688C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67695814 | |||||||
| chrX:67695821 | T | A | 3 | a0004c0004t0001g0054 a0006c0003t0009g0084 a0006c0003t0017g0060 |
3 | HG01169.hp1 HG01928.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.1885+9695T>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67695821 | |||||||
| chrX:67695823 | A | T | 3 | a0002c0010t0035g0151 a0002c0010t0036g0119 a0008c0007t0034g0159 |
3 | HG01243.hp1 HG02451.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1885+9697A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67695823 | |||||||
| chrX:67695982 | G | T | 1 | a0002c0030t0016g0013 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1885+9856G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67695982 | |||||||
| chrX:67695996 | T | C | 2 | a0003c0002t0003g0034 a0004c0004t0003g0081 |
2 | NA19066.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1885+9870T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67695996 | |||||||
| chrX:67696139 | C | CT | 118 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(115): Show |
119 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(116): Show |
intron_variant | MODIFIER | c.1885+10025dupT | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 67696139 | ||||||
| chrX:67696309 | G | A | 9 | a0003c0021t0008g0123 a0005c0006t0003g0003 a0005c0006t0008g0122 others(6): Show |
9 | HG00099.hp1 HG02615.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1885+10183G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67696309 | |||||||
| chrX:67696416 | G | A | 1 | a0004c0004t0001g0102 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1885+10290G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67696416 | |||||||
| chrX:67696793 | A | G | 1 | a0001c0028t0004g0183 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1885+10667A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67696793 | |||||||
| chrX:67696795 | C | G | 1 | a0002c0005t0056g0172 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1885+10669C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67696795 | |||||||
| chrX:67696812 | T | C | 36 | a0001c0001t0004g0186 a0001c0001t0010g0166 a0001c0001t0014g0179 others(33): Show |
36 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.1885+10686T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67696812 | |||||||
| chrX:67697129 | A | G | 1 | a0009c0015t0005g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1885+11003A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67697129 | |||||||
| chrX:67697136 | T | C | 1 | a0003c0002t0001g0055 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1885+11010T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67697136 | |||||||
| chrX:67697152 | C | T | 2 | a0001c0001t0007g0001 a0001c0001t0007g0012 |
3 | NA18983.hp1 NA18985.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.1885+11026C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67697152 | |||||||
| chrX:67697340 | G | A | 1 | a0007c0008t0023g0127 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1885+11214G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67697340 | |||||||
| chrX:67697425 | C | T | 186 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(183): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.1885+11299C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67697425 | |||||||
| chrX:67697456 | CT | C | 3 | a0006c0003t0002g0009 a0006c0003t0002g0067 a0009c0015t0002g0022 |
3 | HG02071.hp1 NA19083.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1885+11331delT | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67697456 | |||||||
| chrX:67697559 | C | T | 1 | a0011c0013t0001g0015 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1885+11433C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67697559 | |||||||
| chrX:67697745 | G | A | 1 | a0004c0004t0048g0087 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1885+11619G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67697745 | |||||||
| chrX:67697777 | G | C | 16 | a0001c0001t0010g0166 a0001c0009t0004g0118 a0001c0009t0004g0155 others(13): Show |
16 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.1885+11651G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67697777 | |||||||
| chrX:67698005 | T | C | 1 | a0003c0002t0017g0005 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1885+11879T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67698005 | |||||||
| chrX:67698154 | A | G | 1 | a0004c0032t0058g0169 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1885+12028A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67698154 | |||||||
| chrX:67698249 | T | C | 34 | a0001c0001t0004g0186 a0001c0001t0010g0166 a0001c0001t0014g0179 others(31): Show |
34 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.1885+12123T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67698249 | |||||||
| chrX:67698444 | G | T | 1 | a0011c0013t0009g0047 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1885+12318G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67698444 | |||||||
| chrX:67698611 | C | T | 36 | a0001c0001t0004g0186 a0001c0001t0010g0166 a0001c0001t0014g0179 others(33): Show |
36 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.1885+12485C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67698611 | |||||||
| chrX:67698713 | AG | A | 2 | a0003c0021t0008g0123 a0005c0006t0010g0120 |
2 | HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1885+12588delG | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67698713 | |||||||
| chrX:67698871 | A | G | 150 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(147): Show |
151 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.1886-12531A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67698871 | |||||||
| chrX:67699019 | G | A | 19 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(16): Show |
19 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1886-12383G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67699019 | |||||||
| chrX:67699048 | G | A | 1 | a0002c0005t0044g0181 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1886-12354G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67699048 | |||||||
| chrX:67699154 | A | G | 3 | a0005c0006t0011g0004 a0007c0008t0006g0136 a0007c0008t0006g0137 |
3 | HG03041.hp2 HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1886-12248A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67699154 | |||||||
| chrX:67699345 | A | T | 2 | a0005c0006t0028g0153 a0013c0019t0029g0152 |
2 | HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1886-12057A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67699345 | |||||||
| chrX:67699502 | C | T | 1 | a0009c0012t0037g0143 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1886-11900C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67699502 | |||||||
| chrX:67699678 | A | G | 36 | a0001c0001t0004g0186 a0001c0001t0010g0166 a0001c0001t0014g0179 others(33): Show |
36 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.1886-11724A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67699678 | |||||||
| chrX:67699757 | A | G | 2 | a0002c0005t0007g0010 a0002c0005t0007g0011 |
2 | NA18953.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1886-11645A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67699757 | |||||||
| chrX:67700445 | G | A | 3 | a0003c0002t0001g0093 a0004c0033t0054g0101 a0010c0014t0001g0099 |
3 | HG01069.hp1 HG01934.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1886-10957G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67700445 | |||||||
| chrX:67700597 | G | A | 20 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(17): Show |
20 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1886-10805G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67700597 | |||||||
| chrX:67700846 | G | C | 1 | a0018c0036t0021g0063 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1886-10556G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67700846 | |||||||
| chrX:67701030 | C | G | 16 | a0001c0001t0010g0166 a0001c0009t0004g0118 a0001c0009t0004g0155 others(13): Show |
16 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.1886-10372C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67701030 | |||||||
| chrX:67701103 | A | G | 1 | a0002c0010t0014g0158 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1886-10299A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67701103 | |||||||
| chrX:67701113 | A | G | 1 | a0016c0027t0010g0171 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1886-10289A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67701113 | |||||||
| chrX:67701148 | G | A | 1 | a0004c0032t0058g0169 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1886-10254G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67701148 | |||||||
| chrX:67701320 | C | T | 2 | a0001c0001t0007g0032 a0004c0004t0003g0037 |
2 | HG02132.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1886-10082C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67701320 | |||||||
| chrX:67701597 | G | A | 1 | a0011c0013t0001g0052 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1886-9805G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67701597 | |||||||
| chrX:67701641 | G | A | 1 | a0002c0005t0016g0111 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1886-9761G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67701641 | |||||||
| chrX:67701674 | T | TCA | 7 | a0004c0004t0001g0076 a0004c0004t0001g0102 a0005c0006t0011g0004 others(4): Show |
7 | HG00621.hp1 HG03041.hp2 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.1886-9693_1886-969 others(6): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 67701674 | ||||||
| chrX:67701674 | T | TCACA | 2 | a0005c0006t0028g0153 a0008c0017t0001g0187 |
2 | HG00099.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1886-9695_1886-969 others(8): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 67701674 | ||||||
| chrX:67701674 | TCA | T | 6 | a0001c0001t0050g0050 a0005c0011t0009g0094 a0005c0011t0053g0095 others(3): Show |
6 | HG02647.hp1 HG02735.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1886-9693_1886-969 others(6): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 67701674 | ||||||
| chrX:67701674 | TCACA | T | 22 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(19): Show |
22 | HG00735.hp2 HG00738.hp1 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.1886-9695_1886-969 others(8): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 67701674 | ||||||
| chrX:67701674 | TCACACA | T | 16 | a0001c0001t0010g0166 a0001c0009t0004g0118 a0001c0009t0004g0155 others(13): Show |
16 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.1886-9697_1886-969 others(10): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 67701674 | ||||||
| chrX:67701674 | TCACACAC others(7): Show |
T | 3 | a0002c0010t0020g0116 a0005c0006t0020g0115 a0005c0006t0032g0117 |
3 | HG03209.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1886-9705_1886-969 others(18): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 67701674 | ||||||
| chrX:67701723 | C | G | 6 | a0002c0005t0001g0041 a0002c0005t0001g0046 a0003c0002t0001g0093 others(3): Show |
6 | HG01069.hp1 HG01934.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.1886-9679C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67701723 | |||||||
| chrX:67701833 | A | G | 1 | a0005c0011t0001g0105 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1886-9569A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67701833 | |||||||
| chrX:67701890 | C | T | 2 | a0002c0010t0018g0165 a0010c0035t0014g0157 |
2 | HG02723.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1886-9512C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67701890 | |||||||
| chrX:67702098 | A | T | 20 | a0001c0001t0004g0186 a0001c0001t0014g0179 a0001c0001t0019g0175 others(17): Show |
20 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1886-9304A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67702098 | |||||||
| chrX:67702293 | A | G | 1 | a0008c0017t0001g0187 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1886-9109A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67702293 | |||||||
| chrX:67702579 | A | C | 1 | a0009c0015t0001g0059 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1886-8823A>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67702579 | |||||||
| chrX:67702952 | A | C | 36 | a0001c0001t0004g0186 a0001c0001t0010g0166 a0001c0001t0014g0179 others(33): Show |
36 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.1886-8450A>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67702952 | |||||||
| chrX:67703096 | A | C | 1 | a0011c0013t0001g0015 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1886-8306A>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67703096 | |||||||
| chrX:67703486 | A | G | 1 | a0001c0009t0008g0132 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1886-7916A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67703486 | |||||||
| chrX:67703583 | C | G | 1 | a0005c0011t0009g0094 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1886-7819C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67703583 | |||||||
| chrX:67703647 | T | A | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1886-7755T>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67703647 | |||||||
| chrX:67704073 | C | T | 1 | a0002c0010t0030g0164 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1886-7329C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67704073 | |||||||
| chrX:67704674 | G | C | 3 | a0001c0009t0004g0118 a0001c0009t0004g0155 a0002c0010t0004g0154 |
3 | HG02572.hp1 HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1886-6728G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67704674 | |||||||
| chrX:67705254 | G | A | 3 | a0001c0001t0001g0070 a0003c0002t0001g0027 a0010c0014t0001g0077 |
3 | HG00609.hp1 HG02738.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1886-6148G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67705254 | |||||||
| chrX:67705341 | C | A | 1 | a0001c0026t0025g0139 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1886-6061C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67705341 | |||||||
| chrX:67705362 | G | A | 1 | a0006c0003t0002g0067 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1886-6040G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67705362 | |||||||
| chrX:67705425 | A | G | 5 | a0008c0007t0006g0140 a0008c0007t0006g0150 a0008c0007t0011g0148 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1886-5977A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67705425 | |||||||
| chrX:67705449 | G | C | 1 | a0002c0010t0004g0154 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1886-5953G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67705449 | |||||||
| chrX:67705587 | G | A | 1 | a0004c0004t0001g0091 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1886-5815G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67705587 | |||||||
| chrX:67705896 | G | A | 1 | a0005c0006t0010g0120 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1886-5506G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67705896 | |||||||
| chrX:67706035 | G | C | 110 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(107): Show |
111 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.1886-5367G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67706035 | |||||||
| chrX:67706078 | A | G | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1886-5324A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67706078 | |||||||
| chrX:67706433 | A | G | 1 | a0015c0022t0004g0112 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1886-4969A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67706433 | |||||||
| chrX:67706492 | T | A | 1 | a0011c0013t0003g0107 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1886-4910T>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67706492 | |||||||
| chrX:67707057 | T | C | 1 | a0002c0010t0030g0164 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1886-4345T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67707057 | |||||||
| chrX:67707323 | C | T | 1 | a0002c0005t0009g0035 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1886-4079C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67707323 | |||||||
| chrX:67707326 | G | A | 36 | a0001c0001t0004g0186 a0001c0001t0010g0166 a0001c0001t0014g0179 others(33): Show |
36 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.1886-4076G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67707326 | |||||||
| chrX:67707333 | T | C | 1 | a0005c0011t0012g0108 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1886-4069T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67707333 | |||||||
| chrX:67707500 | T | C | 16 | a0001c0001t0010g0166 a0001c0009t0004g0118 a0001c0009t0004g0155 others(13): Show |
16 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.1886-3902T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67707500 | |||||||
| chrX:67707576 | G | T | 110 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(107): Show |
111 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.1886-3826G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67707576 | |||||||
| chrX:67707738 | C | T | 3 | a0004c0004t0027g0182 a0007c0016t0005g0173 a0008c0017t0005g0174 |
3 | HG01081.hp2 HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1886-3664C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67707738 | |||||||
| chrX:67707936 | A | C | 1 | a0015c0022t0004g0112 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1886-3466A>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67707936 | |||||||
| chrX:67708109 | A | C | 1 | a0002c0010t0030g0164 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1886-3293A>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67708109 | |||||||
| chrX:67708360 | CTAA | C | 6 | a0001c0001t0002g0065 a0006c0003t0002g0009 a0006c0003t0002g0067 others(3): Show |
6 | HG02071.hp1 NA18962.hp1 NA18995.hp1 others(3): Show |
intron_variant | MODIFIER | c.1886-3041_1886-303 others(7): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67708360 | |||||||
| chrX:67708364 | A | G | 6 | a0001c0001t0002g0065 a0006c0003t0002g0009 a0006c0003t0002g0067 others(3): Show |
6 | HG02071.hp1 NA18962.hp1 NA18995.hp1 others(3): Show |
intron_variant | MODIFIER | c.1886-3038A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67708364 | |||||||
| chrX:67708366 | TTC | T | 6 | a0001c0001t0002g0065 a0006c0003t0002g0009 a0006c0003t0002g0067 others(3): Show |
6 | HG02071.hp1 NA18962.hp1 NA18995.hp1 others(3): Show |
intron_variant | MODIFIER | c.1886-3032_1886-303 others(6): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 67708366 | ||||||
| chrX:67708410 | T | C | 3 | a0004c0004t0027g0182 a0007c0016t0005g0173 a0008c0017t0005g0174 |
3 | HG01081.hp2 HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1886-2992T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67708410 | |||||||
| chrX:67708412 | C | A | 2 | a0007c0008t0006g0136 a0007c0008t0006g0137 |
2 | HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1886-2990C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67708412 | |||||||
| chrX:67708657 | G | A | 16 | a0001c0001t0010g0166 a0001c0009t0004g0118 a0001c0009t0004g0155 others(13): Show |
16 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.1886-2745G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67708657 | |||||||
| chrX:67708744 | G | T | 16 | a0001c0001t0010g0166 a0001c0009t0004g0118 a0001c0009t0004g0155 others(13): Show |
16 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.1886-2658G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67708744 | |||||||
| chrX:67708854 | C | G | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1886-2548C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67708854 | |||||||
| chrX:67708914 | C | T | 6 | a0002c0005t0001g0041 a0002c0005t0001g0046 a0003c0002t0001g0093 others(3): Show |
6 | HG01069.hp1 HG01934.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.1886-2488C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67708914 | |||||||
| chrX:67709073 | G | T | 1 | a0007c0008t0057g0121 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1886-2329G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67709073 | |||||||
| chrX:67709109 | T | C | 1 | a0015c0023t0008g0180 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1886-2293T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67709109 | |||||||
| chrX:67709149 | C | T | 1 | a0001c0026t0025g0139 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1886-2253C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67709149 | |||||||
| chrX:67709340 | C | T | 1 | a0005c0011t0012g0108 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1886-2062C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67709340 | |||||||
| chrX:67709435 | G | A | 3 | a0002c0010t0020g0116 a0005c0006t0020g0115 a0005c0006t0032g0117 |
3 | HG03209.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1886-1967G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67709435 | |||||||
| chrX:67709507 | G | A | 2 | a0001c0009t0006g0168 a0006c0031t0043g0167 |
2 | HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1886-1895G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67709507 | |||||||
| chrX:67709686 | G | A | 2 | a0002c0005t0001g0044 a0002c0005t0007g0045 |
2 | HG02015.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.1886-1716G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67709686 | |||||||
| chrX:67709844 | G | A | 175 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(172): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.1886-1558G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67709844 | |||||||
| chrX:67709934 | A | G | 1 | a0004c0004t0031g0170 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1886-1468A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67709934 | |||||||
| chrX:67710227 | G | C | 1 | a0003c0002t0017g0005 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1886-1175G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67710227 | |||||||
| chrX:67710502 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1886-900A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67710502 | |||||||
| chrX:67710611 | G | T | 1 | a0001c0001t0001g0085 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1886-791G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67710611 | |||||||
| chrX:67710879 | C | T | 3 | a0002c0010t0020g0116 a0005c0006t0020g0115 a0005c0006t0032g0117 |
3 | HG03209.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1886-523C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67710879 | |||||||
| chrX:67710935 | C | T | 1 | a0005c0011t0052g0068 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1886-467C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67710935 | |||||||
| chrX:67710964 | G | A | 2 | a0001c0001t0007g0032 a0004c0004t0003g0037 |
2 | HG02132.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1886-438G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67710964 | |||||||
| chrX:67711195 | A | T | 16 | a0001c0001t0010g0166 a0001c0009t0004g0118 a0001c0009t0004g0155 others(13): Show |
16 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.1886-207A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67711195 | |||||||
| chrX:67711230 | T | G | 1 | a0004c0032t0058g0169 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1886-172T>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67711230 | |||||||
| chrX:67711342 | G | A | 2 | a0004c0004t0031g0170 a0015c0023t0008g0180 |
2 | HG02895.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1886-60G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 3/7 | chrX | 67711342 | |||||||
| chrX:67711789 | C | T | 1 | a0001c0009t0010g0113 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2173+100C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 4/7 | chrX | 67711789 | |||||||
| chrX:67712067 | T | C | 1 | a0001c0001t0002g0075 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2173+378T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 4/7 | chrX | 67712067 | |||||||
| chrX:67712999 | A | G | 3 | a0002c0010t0035g0151 a0002c0010t0036g0119 a0008c0007t0034g0159 |
3 | HG01243.hp1 HG02451.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.2173+1310A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 4/7 | chrX | 67712999 | |||||||
| chrX:67713131 | G | T | 1 | a0003c0002t0012g0020 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2173+1442G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 4/7 | chrX | 67713131 | |||||||
| chrX:67713194 | G | T | 15 | a0001c0001t0010g0166 a0001c0009t0004g0118 a0001c0009t0004g0155 others(12): Show |
15 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.2173+1505G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 4/7 | chrX | 67713194 | |||||||
| chrX:67713195 | G | T | 15 | a0001c0001t0010g0166 a0001c0009t0004g0118 a0001c0009t0004g0155 others(12): Show |
15 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.2173+1506G>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 4/7 | chrX | 67713195 | |||||||
| chrX:67713308 | G | C | 3 | a0002c0010t0020g0116 a0005c0006t0020g0115 a0005c0006t0032g0117 |
3 | HG03209.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2173+1619G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 4/7 | chrX | 67713308 | |||||||
| chrX:67713324 | G | A | 1 | a0001c0001t0010g0166 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2173+1635G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 4/7 | chrX | 67713324 | |||||||
| chrX:67713847 | C | A | 2 | a0001c0001t0007g0032 a0004c0004t0003g0037 |
2 | HG02132.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.2173+2158C>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 4/7 | chrX | 67713847 | |||||||
| chrX:67714409 | C | T | 1 | a0006c0003t0015g0006 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2173+2720C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 4/7 | chrX | 67714409 | |||||||
| chrX:67715201 | C | T | 1 | a0005c0006t0011g0004 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2174-2277C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 4/7 | chrX | 67715201 | |||||||
| chrX:67715308 | C | CA | 36 | a0001c0001t0004g0186 a0001c0001t0010g0166 a0001c0001t0014g0179 others(33): Show |
36 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.2174-2168dupA | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 67715308 | ||||||
| chrX:67715450 | C | G | 1 | a0005c0006t0020g0115 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2174-2028C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 4/7 | chrX | 67715450 | |||||||
| chrX:67715548 | A | T | 1 | a0002c0010t0008g0156 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2174-1930A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 4/7 | chrX | 67715548 | |||||||
| chrX:67715818 | T | G | 1 | a0011c0013t0003g0107 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2174-1660T>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 4/7 | chrX | 67715818 | |||||||
| chrX:67716502 | C | G | 162 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(159): Show |
163 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.2174-976C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 4/7 | chrX | 67716502 | |||||||
| chrX:67716577 | A | G | 36 | a0001c0001t0004g0186 a0001c0001t0010g0166 a0001c0001t0014g0179 others(33): Show |
36 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.2174-901A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 4/7 | chrX | 67716577 | |||||||
| chrX:67716807 | T | C | 1 | a0007c0008t0006g0149 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2174-671T>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 4/7 | chrX | 67716807 | |||||||
| chrX:67716868 | G | A | 9 | a0001c0001t0014g0179 a0001c0001t0019g0175 a0001c0001t0019g0176 others(6): Show |
9 | HG01891.hp2 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.2174-610G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 4/7 | chrX | 67716868 | |||||||
| chrX:67717102 | A | G | 2 | a0003c0002t0012g0189 a0003c0002t0012g0190 |
2 | HG02698.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.2174-376A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 4/7 | chrX | 67717102 | |||||||
| chrX:67717167 | G | GA | 6 | a0001c0001t0002g0049 a0003c0002t0003g0034 a0004c0004t0003g0081 others(3): Show |
6 | HG02135.hp1 NA18944.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.2174-304dupA | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 67717167 | ||||||
| chrX:67717754 | C | T | 2 | a0002c0005t0001g0044 a0002c0005t0007g0045 |
2 | HG02015.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.2318+132C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 5/7 | chrX | 67717754 | |||||||
| chrX:67717773 | C | T | 1 | a0008c0007t0006g0150 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2318+151C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 5/7 | chrX | 67717773 | |||||||
| chrX:67717865 | A | G | 149 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(146): Show |
150 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.2318+243A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 5/7 | chrX | 67717865 | |||||||
| chrX:67717907 | A | G | 36 | a0001c0001t0004g0186 a0001c0001t0010g0166 a0001c0001t0014g0179 others(33): Show |
36 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.2318+285A>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 5/7 | chrX | 67717907 | |||||||
| chrX:67718015 | C | T | 1 | a0009c0015t0005g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2318+393C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 5/7 | chrX | 67718015 | |||||||
| chrX:67718624 | T | G | 36 | a0001c0001t0004g0186 a0001c0001t0010g0166 a0001c0001t0014g0179 others(33): Show |
36 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.2318+1002T>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 5/7 | chrX | 67718624 | |||||||
| chrX:67718692 | G | A | 1 | a0002c0010t0014g0158 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2318+1070G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 5/7 | chrX | 67718692 | |||||||
| chrX:67718709 | G | C | 36 | a0001c0001t0004g0186 a0001c0001t0010g0166 a0001c0001t0014g0179 others(33): Show |
36 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.2318+1087G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 5/7 | chrX | 67718709 | |||||||
| chrX:67718991 | C | T | 1 | a0001c0009t0006g0168 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2318+1369C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 5/7 | chrX | 67718991 | |||||||
| chrX:67719247 | C | T | 1 | a0003c0002t0055g0056 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2318+1625C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 5/7 | chrX | 67719247 | |||||||
| chrX:67719300 | T | G | 1 | a0007c0008t0057g0121 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2318+1678T>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 5/7 | chrX | 67719300 | |||||||
| chrX:67719321 | C | T | 1 | a0004c0032t0058g0169 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2318+1699C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 5/7 | chrX | 67719321 | |||||||
| chrX:67719671 | G | A | 1 | a0004c0004t0031g0170 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2318+2049G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 5/7 | chrX | 67719671 | |||||||
| chrX:67719851 | C | T | 1 | a0002c0005t0007g0045 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2319-1982C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 5/7 | chrX | 67719851 | |||||||
| chrX:67719915 | A | T | 1 | a0001c0001t0003g0080 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2319-1918A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 5/7 | chrX | 67719915 | |||||||
| chrX:67720175 | C | T | 1 | a0004c0004t0051g0078 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2319-1658C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 5/7 | chrX | 67720175 | |||||||
| chrX:67720805 | CTTTG | C | 9 | a0001c0009t0006g0168 a0001c0009t0042g0135 a0004c0032t0058g0169 others(6): Show |
9 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.2319-1026_2319-102 others(8): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 67720805 | ||||||
| chrX:67720879 | T | TAC | 11 | a0001c0009t0004g0118 a0002c0005t0044g0181 a0003c0002t0001g0027 others(8): Show |
11 | HG00099.hp2 HG00609.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.2319-925_2319-924d others(4): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 67720879 | ||||||
| chrX:67720879 | T | TACAC | 2 | a0001c0001t0004g0186 a0004c0004t0031g0170 |
2 | HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2319-927_2319-924d others(6): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 67720879 | ||||||
| chrX:67720879 | TAC | T | 19 | a0001c0009t0006g0168 a0001c0009t0008g0128 a0001c0009t0042g0135 others(16): Show |
19 | HG00735.hp2 HG00738.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.2319-925_2319-924d others(4): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 67720879 | ||||||
| chrX:67720920 | G | A | 1 | a0001c0009t0042g0135 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2319-913G>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 5/7 | chrX | 67720920 | |||||||
| chrX:67721348 | C | T | 2 | a0002c0010t0018g0165 a0010c0035t0014g0157 |
2 | HG02723.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2319-485C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 5/7 | chrX | 67721348 | |||||||
| chrX:67721755 | T | G | 168 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0079 others(165): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.2319-78T>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 5/7 | chrX | 67721755 | |||||||
| chrX:67722076 | C | T | 1 | a0007c0016t0001g0030 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2449+113C>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 6/7 | chrX | 67722076 | |||||||
| chrX:67723310 | G | GTC | 57 | a0001c0001t0001g0062 a0001c0001t0002g0029 a0001c0001t0002g0039 others(54): Show |
58 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.2607+328_2607+329d others(4): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 67723310 | ||||||
| chrX:67723312 | C | CTCTG | 14 | a0001c0001t0002g0100 a0001c0001t0003g0083 a0002c0005t0007g0010 others(11): Show |
14 | HG01099.hp1 HG01106.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.2607+329_2607+330i others(6): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 67723312 | ||||||
| chrX:67723312 | C | CTCTGTG | 11 | a0001c0001t0001g0079 a0001c0001t0003g0080 a0001c0001t0019g0175 others(8): Show |
11 | HG00741.hp1 HG01074.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.2607+329_2607+330i others(8): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 67723312 | ||||||
| chrX:67723312 | C | CTCTGTGT others(1): Show |
6 | a0001c0001t0001g0092 a0001c0001t0004g0186 a0002c0005t0056g0172 others(3): Show |
6 | HG01256.hp1 HG02109.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2607+329_2607+330i others(10): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 67723312 | ||||||
| chrX:67723312 | C | CTCTGTGT others(3): Show |
7 | a0001c0001t0014g0179 a0001c0028t0004g0183 a0002c0005t0004g0184 others(4): Show |
7 | HG02258.hp1 HG02818.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.2607+329_2607+330i others(12): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 67723312 | ||||||
| chrX:67723312 | C | CTCTGTGT others(5): Show |
4 | a0001c0009t0033g0138 a0002c0010t0008g0156 a0004c0004t0031g0170 others(1): Show |
4 | HG02451.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2607+329_2607+330i others(14): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 67723312 | ||||||
| chrX:67723312 | C | CTCTGTGT others(7): Show |
9 | a0001c0001t0010g0166 a0001c0009t0008g0132 a0002c0010t0014g0158 others(6): Show |
9 | HG00099.hp1 HG00642.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.2607+329_2607+330i others(16): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 67723312 | ||||||
| chrX:67723312 | C | CTCTGTGT others(9): Show |
6 | a0001c0009t0004g0118 a0001c0009t0004g0155 a0001c0026t0025g0139 others(3): Show |
6 | HG02572.hp1 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2607+329_2607+330i others(18): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 67723312 | ||||||
| chrX:67723312 | C | CTCTGTGT others(11): Show |
2 | a0005c0006t0003g0003 a0005c0006t0010g0003 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2607+329_2607+330i others(20): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 67723312 | ||||||
| chrX:67723312 | C | CTCTGTGT others(15): Show |
1 | a0001c0009t0010g0113 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2607+329_2607+330i others(24): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 67723312 | ||||||
| chrX:67723312 | C | CTG | 17 | a0001c0001t0001g0070 a0001c0001t0002g0049 a0001c0001t0002g0075 others(14): Show |
17 | HG00609.hp1 HG00621.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.2608-334_2608-333d others(4): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 67723312 | ||||||
| chrX:67723312 | C | CTGTG | 9 | a0001c0001t0002g0025 a0001c0009t0042g0135 a0002c0010t0035g0151 others(6): Show |
9 | HG00738.hp1 HG01243.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2608-336_2608-333d others(6): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 67723312 | ||||||
| chrX:67723312 | C | CTGTGTG | 2 | a0007c0008t0023g0127 a0008c0007t0039g0131 |
2 | HG02257.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.2608-338_2608-333d others(8): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 67723312 | ||||||
| chrX:67723312 | C | CTGTGTGT others(5): Show |
1 | a0008c0017t0005g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2608-344_2608-333d others(14): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 67723312 | ||||||
| chrX:67723312 | CTG | C | 8 | a0001c0001t0002g0065 a0006c0003t0002g0009 a0006c0003t0002g0067 others(5): Show |
8 | HG00741.hp2 HG01515.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.2608-334_2608-333d others(4): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 67723312 | ||||||
| chrX:67723314 | G | C | 10 | a0001c0001t0001g0085 a0001c0001t0007g0032 a0002c0005t0001g0041 others(7): Show |
10 | HG01069.hp1 HG01934.hp1 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.2607+330G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 7/7 | chrX | 67723314 | |||||||
| chrX:67723316 | G | C | 7 | a0001c0001t0002g0065 a0006c0003t0002g0009 a0006c0003t0002g0067 others(4): Show |
7 | HG00741.hp2 HG01515.hp1 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.2607+332G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 7/7 | chrX | 67723316 | |||||||
| chrX:67723344 | G | C | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2608-342G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 7/7 | chrX | 67723344 | |||||||
| chrX:67723345 | T | A | 1 | a0007c0025t0045g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2608-341T>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 7/7 | chrX | 67723345 | |||||||
| chrX:67723352 | G | C | 2 | a0007c0008t0006g0136 a0007c0008t0006g0137 |
2 | HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2608-334G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 7/7 | chrX | 67723352 | |||||||
| chrX:67723353 | T | A | 2 | a0007c0008t0006g0136 a0007c0008t0006g0137 |
2 | HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2608-333T>A | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 7/7 | chrX | 67723353 | |||||||
| chrX:67723353 | T | TGTGTGTC others(1): Show |
2 | a0004c0032t0058g0169 a0005c0006t0011g0004 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2608-333_2608-332i others(10): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 7/7 | chrX | 67723353 | |||||||
| chrX:67723353 | TCA | T | 2 | a0001c0001t0001g0085 a0002c0005t0002g0096 |
2 | HG02602.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.2608-332_2608-331d others(4): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 7/7 | chrX | 67723353 | |||||||
| chrX:67723354 | C | CAG | 4 | a0003c0002t0012g0189 a0003c0002t0012g0190 a0004c0004t0012g0103 others(1): Show |
4 | HG00099.hp2 HG00735.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.2608-308_2608-307d others(4): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 67723354 | ||||||
| chrX:67723354 | C | G | 14 | a0001c0001t0004g0186 a0001c0001t0019g0175 a0001c0001t0019g0176 others(11): Show |
14 | HG01891.hp2 HG02615.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.2608-332C>G | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 7/7 | chrX | 67723354 | |||||||
| chrX:67723355 | A | T | 9 | a0001c0001t0004g0186 a0001c0001t0019g0175 a0001c0001t0019g0176 others(6): Show |
9 | HG01891.hp2 HG02809.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.2608-331A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 7/7 | chrX | 67723355 | |||||||
| chrX:67723356 | G | C | 1 | a0004c0004t0051g0078 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2608-330G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 7/7 | chrX | 67723356 | |||||||
| chrX:67723357 | A | T | 10 | a0001c0001t0001g0085 a0001c0001t0004g0186 a0001c0001t0019g0175 others(7): Show |
10 | HG01891.hp2 HG02602.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.2608-329A>T | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 7/7 | chrX | 67723357 | |||||||
| chrX:67723358 | G | C | 10 | a0001c0001t0001g0085 a0001c0001t0004g0186 a0001c0001t0019g0175 others(7): Show |
10 | HG01891.hp2 HG02602.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.2608-328G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 7/7 | chrX | 67723358 | |||||||
| chrX:67723494 | T | TTC | 2 | a0004c0004t0031g0170 a0015c0023t0008g0180 |
2 | HG02895.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2608-181_2608-180d others(4): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 67723494 | ||||||
| chrX:67723520 | A | AAC | 5 | a0001c0009t0006g0168 a0001c0009t0042g0135 a0005c0006t0038g0126 others(2): Show |
5 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.2608-147_2608-146d others(4): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 67723520 | ||||||
| chrX:67723520 | A | AACACACA others(1): Show |
129 | a0001c0001t0001g0062 a0001c0001t0001g0070 a0001c0001t0001g0085 others(126): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.2608-153_2608-146d others(10): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 67723520 | ||||||
| chrX:67723520 | A | AACACACA others(3): Show |
25 | a0001c0001t0001g0079 a0001c0001t0003g0080 a0001c0001t0003g0083 others(22): Show |
25 | HG01891.hp2 HG01952.hp1 HG02630.hp2 others(22): Show |
intron_variant | MODIFIER | c.2608-155_2608-146d others(12): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 67723520 | ||||||
| chrX:67723520 | A | AACACACA others(5): Show |
1 | a0001c0001t0001g0092 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2608-157_2608-146d others(14): Show |
AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 67723520 | ||||||
| chrX:67723553 | G | C | 2 | a0002c0005t0001g0041 a0002c0005t0001g0046 |
2 | NA18966.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.2608-133G>C | AR | ENSG00000169083.18 | transcript | ENST00000374690.9 | protein_coding | 7/7 | chrX | 67723553 |