Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 203447 |
| ensemblid | ENSG00000123572.17 |
| hgncid | 25391 |
| symbol | NRK |
| name | Nik related kinase |
| refseq_nuc | NM_198465.4 |
| refseq_prot | NP_940867.2 |
| ensembl_nuc | ENST00000243300.14 |
| ensembl_prot | ENSP00000434830.1 |
| mane_status | MANE Select |
| chr | chrX |
| start | 105822539 |
| end | 105958610 |
| strand | + |
| ver | v1.2 |
| region | chrX:105822539-105958610 |
| region5000 | chrX:105817539-105963610 |
| regionname0 | NRK_chrX_105822539_105958610 |
| regionname5000 | NRK_chrX_105817539_105963610 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1582 | 126 | 17 | 23 | 63 | 4 | 17 | 52 | NRK_chrX_105817539_105963610 | NRK | MAGPG others(1577): Show |
chrX | 105817539 | 105963610 |
| a0002 | 0/0 | 1582 | 52 | 17 | 12 | 14 | 0 | 9 | 6 | NRK_chrX_105817539_105963610 | NRK | MAGPG others(1577): Show |
chrX | 105817539 | 105963610 |
| a0003 | 0/0 | 1582 | 29 | 28 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | MAGPG others(1577): Show |
chrX | 105817539 | 105963610 |
| a0004 | 0/0 | 1582 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | MAGPG others(1577): Show |
chrX | 105817539 | 105963610 |
| a0005 | 0/0 | 1582 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | MAGPG others(1577): Show |
chrX | 105817539 | 105963610 |
| a0006 | 0/0 | 1582 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | MAGPG others(1577): Show |
chrX | 105817539 | 105963610 |
| a0007 | 0/0 | 1582 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | MAGPG others(1577): Show |
chrX | 105817539 | 105963610 |
| a0008 | 0/0 | 1540 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | MAGPG others(1535): Show |
chrX | 105817539 | 105963610 |
| a0009 | 0/0 | 1582 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | MAGPG others(1577): Show |
chrX | 105817539 | 105963610 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 4746 | 123 | 15 | 23 | 62 | 4 | 17 | NRK_chrX_105817539_105963610 | NRK | ATGGC others(4741): Show |
chrX | 105817539 | 105963610 | ||
| a0001c0005 | 0/0 | 4746 | 2 | 2 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | ATGGC others(4741): Show |
chrX | 105817539 | 105963610 | ||
| a0001c0012 | 0/0 | 4746 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | ATGGC others(4741): Show |
chrX | 105817539 | 105963610 | ||
| a0002c0002 | 0/0 | 4746 | 51 | 16 | 12 | 14 | 0 | 9 | NRK_chrX_105817539_105963610 | NRK | ATGGC others(4741): Show |
chrX | 105817539 | 105963610 | ||
| a0002c0009 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | ATGGC others(4741): Show |
chrX | 105817539 | 105963610 | ||
| a0003c0003 | 0/0 | 4746 | 28 | 27 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | ATGGC others(4741): Show |
chrX | 105817539 | 105963610 | ||
| a0003c0011 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | ATGGC others(4741): Show |
chrX | 105817539 | 105963610 | ||
| a0004c0004 | 0/0 | 4746 | 7 | 7 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | ATGGC others(4741): Show |
chrX | 105817539 | 105963610 | ||
| a0005c0013 | 0/0 | 4746 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | ATGGC others(4741): Show |
chrX | 105817539 | 105963610 | ||
| a0006c0007 | 0/0 | 4746 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | ATGGC others(4741): Show |
chrX | 105817539 | 105963610 | ||
| a0007c0008 | 0/0 | 4746 | 1 | 0 | 0 | 0 | 1 | 0 | NRK_chrX_105817539_105963610 | NRK | ATGGC others(4741): Show |
chrX | 105817539 | 105963610 | ||
| a0008c0006 | 0/0 | 4620 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | ATGGC others(4615): Show |
chrX | 105817539 | 105963610 | ||
| a0009c0010 | 0/0 | 4746 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | ATGGC others(4741): Show |
chrX | 105817539 | 105963610 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 8066 | 102 | 3 | 18 | 61 | 2 | 17 | NRK_chrX_105817539_105963610 | NRK | AGACA others(8061): Show |
chrX | 105817539 | 105963610 |
| a0001c0001t0004 | 0/1 | 8066 | 19 | 12 | 4 | 0 | 2 | 0 | NRK_chrX_105817539_105963610 | NRK | AGACA others(8061): Show |
chrX | 105817539 | 105963610 |
| a0001c0001t0006 | 0/0 | 8066 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | AGACA others(8061): Show |
chrX | 105817539 | 105963610 |
| a0001c0001t0007 | 0/0 | 8066 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | AGACA others(8061): Show |
chrX | 105817539 | 105963610 |
| a0001c0005t0001 | 0/0 | 8066 | 2 | 2 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | AGACA others(8061): Show |
chrX | 105817539 | 105963610 |
| a0001c0012t0001 | 0/0 | 8066 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | AGACA others(8061): Show |
chrX | 105817539 | 105963610 |
| a0002c0002t0002 | 0/0 | 8066 | 41 | 8 | 12 | 12 | 0 | 9 | NRK_chrX_105817539_105963610 | NRK | AGACA others(8061): Show |
chrX | 105817539 | 105963610 |
| a0002c0002t0005 | 0/0 | 8066 | 7 | 5 | 0 | 2 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | AGACA others(8061): Show |
chrX | 105817539 | 105963610 |
| a0002c0002t0008 | 0/0 | 8066 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | AGACA others(8061): Show |
chrX | 105817539 | 105963610 |
| a0002c0002t0009 | 0/0 | 8066 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | AGACA others(8061): Show |
chrX | 105817539 | 105963610 |
| a0002c0002t0010 | 0/0 | 8066 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | AGACA others(8061): Show |
chrX | 105817539 | 105963610 |
| a0002c0009t0005 | 0/0 | 8066 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | AGACA others(8061): Show |
chrX | 105817539 | 105963610 |
| a0003c0003t0003 | 0/0 | 8066 | 28 | 27 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | AGACA others(8061): Show |
chrX | 105817539 | 105963610 |
| a0003c0011t0003 | 0/0 | 8066 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | AGACA others(8061): Show |
chrX | 105817539 | 105963610 |
| a0004c0004t0003 | 0/0 | 8066 | 7 | 7 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | AGACA others(8061): Show |
chrX | 105817539 | 105963610 |
| a0005c0013t0001 | 0/0 | 8066 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | AGACA others(8061): Show |
chrX | 105817539 | 105963610 |
| a0006c0007t0003 | 0/0 | 8066 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | AGACA others(8061): Show |
chrX | 105817539 | 105963610 |
| a0007c0008t0002 | 0/0 | 8066 | 1 | 0 | 0 | 0 | 1 | 0 | NRK_chrX_105817539_105963610 | NRK | AGACA others(8061): Show |
chrX | 105817539 | 105963610 |
| a0008c0006t0001 | 0/0 | 7940 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | AGACA others(7935): Show |
chrX | 105817539 | 105963610 |
| a0009c0010t0005 | 0/0 | 8066 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | AGACA others(8061): Show |
chrX | 105817539 | 105963610 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0194 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0004g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0004g0198 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0006g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0001t0007g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0005t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0001c0012t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0005g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0005g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0008g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0009g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0002t0010g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0002c0009t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0003t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0003c0011t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0004c0004t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0004c0004t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0004c0004t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0004c0004t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0004c0004t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0004c0004t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0004c0004t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0005c0013t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0006c0007t0003g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0007c0008t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0008c0006t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| a0009c0010t0005g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0004 | g0193 | EUR | GBR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0196 | EUR | FIN | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG00673 | hp1 | a0002 | c0002 | t0002 | g0044 | EAS | CHS | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG00733 | hp1 | a0002 | c0002 | t0002 | g0058 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG00735 | hp1 | a0002 | c0002 | t0002 | g0050 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0079 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG00741 | hp1 | a0002 | c0002 | t0002 | g0078 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0049 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01074 | hp1 | a0005 | c0013 | t0001 | g0147 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01109 | hp1 | a0003 | c0003 | t0003 | g0020 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0087 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01168 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0195 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0086 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01169 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01192 | hp1 | a0002 | c0002 | t0002 | g0060 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01243 | hp1 | a0006 | c0007 | t0003 | g0014 | AMR | PUR | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01255 | hp1 | a0002 | c0002 | t0002 | g0053 | AMR | CLM | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01258 | hp1 | a0001 | c0001 | t0006 | g0176 | AMR | CLM | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0192 | AMR | CLM | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0043 | AMR | CLM | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01433 | hp1 | a0002 | c0002 | t0002 | g0056 | AMR | CLM | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01515 | hp1 | a0007 | c0008 | t0002 | g0042 | EUR | IBS | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01884 | hp1 | a0002 | c0002 | t0002 | g0046 | AFR | ACB | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01884 | hp2 | a0003 | c0003 | t0003 | g0038 | AFR | ACB | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0199 | AFR | ACB | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01891 | hp2 | a0004 | c0004 | t0003 | g0011 | AFR | ACB | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01981 | hp1 | a0008 | c0006 | t0001 | g0114 | AMR | PEL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0048 | AMR | PEL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0070 | EAS | KHV | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0066 | EAS | KHV | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0118 | AFR | ACB | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02071 | hp1 | a0002 | c0002 | t0002 | g0069 | EAS | KHV | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02074 | hp1 | a0002 | c0002 | t0002 | g0076 | EAS | KHV | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02080 | hp1 | a0002 | c0002 | t0002 | g0067 | EAS | KHV | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02145 | hp1 | a0004 | c0004 | t0003 | g0015 | AFR | ACB | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02258 | hp1 | a0003 | c0003 | t0003 | g0033 | AFR | ACB | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02451 | hp1 | a0003 | c0003 | t0003 | g0213 | AFR | ACB | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02451 | hp2 | a0002 | c0002 | t0009 | g0204 | AFR | ACB | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02523 | hp1 | a0002 | c0002 | t0002 | g0073 | EAS | KHV | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02572 | hp1 | a0003 | c0003 | t0003 | g0029 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0130 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02622 | hp2 | a0003 | c0011 | t0003 | g0037 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02630 | hp1 | a0003 | c0003 | t0003 | g0006 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02630 | hp2 | a0003 | c0003 | t0003 | g0027 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02647 | hp1 | a0001 | c0005 | t0001 | g0004 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02683 | hp1 | a0002 | c0002 | t0002 | g0054 | SAS | PJL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02717 | hp1 | a0002 | c0002 | t0010 | g0119 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0189 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02723 | hp2 | a0003 | c0003 | t0003 | g0031 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02735 | hp1 | a0002 | c0002 | t0002 | g0055 | SAS | PJL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02809 | hp1 | a0003 | c0003 | t0003 | g0028 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02809 | hp2 | a0002 | c0009 | t0005 | g0210 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0091 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02818 | hp2 | a0003 | c0003 | t0003 | g0035 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02886 | hp1 | a0003 | c0003 | t0003 | g0009 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02886 | hp2 | a0002 | c0002 | t0002 | g0063 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02895 | hp1 | a0003 | c0003 | t0003 | g0040 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02897 | hp1 | a0003 | c0003 | t0003 | g0039 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02897 | hp2 | a0002 | c0002 | t0008 | g0179 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02922 | hp1 | a0004 | c0004 | t0003 | g0018 | AFR | ESN | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02922 | hp2 | a0003 | c0003 | t0003 | g0010 | AFR | ESN | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02965 | hp1 | a0003 | c0003 | t0003 | g0026 | AFR | ESN | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02970 | hp1 | a0002 | c0002 | t0005 | g0208 | AFR | ESN | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02970 | hp2 | a0004 | c0004 | t0003 | g0019 | AFR | ESN | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02976 | hp1 | a0003 | c0003 | t0003 | g0024 | AFR | ESN | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02976 | hp2 | a0009 | c0010 | t0005 | g0090 | AFR | ESN | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0200 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03041 | hp2 | a0002 | c0002 | t0002 | g0051 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03098 | hp1 | a0003 | c0003 | t0003 | g0023 | AFR | MSL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03130 | hp1 | a0002 | c0002 | t0005 | g0120 | AFR | ESN | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0095 | AFR | ESN | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03209 | hp1 | a0003 | c0003 | t0003 | g0016 | AFR | MSL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03225 | hp1 | a0001 | c0005 | t0001 | g0004 | AFR | MSL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0059 | SAS | PJL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0168 | AFR | MSL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03453 | hp2 | a0003 | c0003 | t0003 | g0008 | AFR | MSL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03486 | hp1 | a0004 | c0004 | t0003 | g0013 | AFR | MSL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03486 | hp2 | a0002 | c0002 | t0005 | g0211 | AFR | MSL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03540 | hp1 | a0004 | c0004 | t0003 | g0012 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03540 | hp2 | a0002 | c0002 | t0002 | g0064 | AFR | GWD | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03579 | hp1 | a0003 | c0003 | t0003 | g0212 | AFR | MSL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03669 | hp1 | a0002 | c0002 | t0002 | g0045 | SAS | PJL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | STU | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03710 | hp1 | a0002 | c0002 | t0002 | g0047 | SAS | PJL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0074 | SAS | BEB | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | BEB | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0065 | SAS | BEB | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | STU | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG04184 | hp1 | a0002 | c0002 | t0002 | g0075 | SAS | BEB | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | BEB | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | STU | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | STU | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | STU | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18522 | hp1 | a0003 | c0003 | t0003 | g0025 | AFR | YRI | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18612 | hp1 | a0002 | c0002 | t0005 | g0203 | EAS | CHB | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHB | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0096 | AFR | YRI | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18906 | hp2 | a0003 | c0003 | t0003 | g0021 | AFR | YRI | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18939 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18961 | hp1 | a0002 | c0002 | t0005 | g0201 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18975 | hp2 | a0002 | c0002 | t0002 | g0071 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19004 | hp1 | a0002 | c0002 | t0002 | g0068 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | LWK | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19030 | hp2 | a0002 | c0002 | t0002 | g0062 | AFR | LWK | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19043 | hp1 | a0002 | c0002 | t0005 | g0205 | AFR | LWK | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19058 | hp1 | a0001 | c0001 | t0007 | g0116 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19062 | hp1 | a0001 | c0012 | t0001 | g0089 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19070 | hp1 | a0002 | c0002 | t0002 | g0072 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19081 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19240 | hp1 | a0002 | c0002 | t0002 | g0052 | AFR | YRI | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA19240 | hp2 | a0004 | c0004 | t0003 | g0017 | AFR | YRI | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0197 | AFR | ASW | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA20129 | hp2 | a0003 | c0003 | t0003 | g0036 | AFR | ASW | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0140 | EUR | TSI | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | TSI | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA20905 | hp1 | a0002 | c0002 | t0002 | g0077 | SAS | GIH | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02109 | hp1 | a0002 | c0002 | t0005 | g0209 | AFR | ACB | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02109 | hp2 | a0003 | c0003 | t0003 | g0032 | AFR | ACB | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02486 | hp1 | a0002 | c0002 | t0002 | g0061 | AFR | ACB | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0092 | AFR | ACB | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG02559 | hp2 | a0003 | c0003 | t0003 | g0007 | AFR | ACB | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0167 | AFR | MSL | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG06807 | hp1 | a0003 | c0003 | t0003 | g0030 | AFR | USA | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0057 | AFR | USA | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | USA | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA20300 | hp2 | a0003 | c0003 | t0003 | g0022 | AFR | USA | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA21309 | hp1 | a0003 | c0003 | t0003 | g0034 | AFR | LWK | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | LWK | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0198 | REF | REF | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0194 | REF | REF | NRK_chrX_105817539_105963610 | NRK | chrX | 105817539 | 105963610 |
| 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:105887094 | ATTAAAAT others(1388): Show |
A | 1 | a0008 | 1 | HG01981.hp1 | exon_loss_variant&splice_acceptor_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.253-1196_378+73del | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chrX | 105887094 | ||||||
| chrX:105888396 | C | T | 1 | a0002 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.355C>T | p.Pro119Ser | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/29 | 662/8066 | 355/4749 | 119/1582 | chrX | 105888396 | |||
| chrX:105908290 | G | A | 6 | a0002 a0003 a0004 others(3): Show |
91 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(88): Show |
missense_variant | MODERATE | c.1072G>A | p.Val358Met | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 12/29 | 1379/8066 | 1072/4749 | 358/1582 | chrX | 105908290 | |||
| chrX:105909821 | G | A | 2 | a0004 a0006 |
8 | HG01243.hp1 HG01891.hp2 HG02145.hp1 others(5): Show |
missense_variant | MODERATE | c.2180G>A | p.Arg727His | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 13/29 | 2487/8066 | 2180/4749 | 727/1582 | chrX | 105909821 | |||
| chrX:105915745 | C | T | 1 | a0005 | 1 | HG01074.hp1 | missense_variant | MODERATE | c.2365C>T | p.Pro789Ser | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 15/29 | 2672/8066 | 2365/4749 | 789/1582 | chrX | 105915745 | |||
| chrX:105923287 | G | A | 1 | a0007 | 1 | HG01515.hp1 | missense_variant | MODERATE | c.2780G>A | p.Ser927Asn | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/29 | 3087/8066 | 2780/4749 | 927/1582 | chrX | 105923287 | |||
| chrX:105924697 | C | A | 3 | a0003 a0004 a0006 |
37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
missense_variant&splice_region_variant | MODERATE | c.2978C>A | p.Ala993Glu | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/29 | 3285/8066 | 2978/4749 | 993/1582 | chrX | 105924697 | |||
| chrX:105924827 | C | A | 1 | a0009 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.3108C>A | p.Asp1036Glu | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/29 | 3415/8066 | 3108/4749 | 1036/1582 | chrX | 105924827 | |||
| chrX:105924862 | C | G | 1 | a0006 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.3143C>G | p.Ala1048Gly | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/29 | 3450/8066 | 3143/4749 | 1048/1582 | chrX | 105924862 | |||
| chrX:105958608 | A | T | 7 | a0001 a0002 a0003 others(4): Show |
109 | HG00140.hp1 HG00280.hp1 HG00673.hp1 others(106): Show |
splice_region_variant | LOW | c.*3008A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | chrX | 105958608 |
| 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:105900620 | T | C | 1 | a0001c0005 | 2 | HG02647.hp1 HG03225.hp1 |
splice_region_variant&synonymous_variant | LOW | c.714T>C | p.Ser238Ser | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 9/29 | 1021/8066 | 714/4749 | 238/1582 | chrX | 105900620 | |||
| chrX:105909048 | A | G | 1 | a0003c0011 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.1407A>G | p.Pro469Pro | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 13/29 | 1714/8066 | 1407/4749 | 469/1582 | chrX | 105909048 | |||
| chrX:105923468 | G | A | 1 | a0002c0009 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.2961G>A | p.Ala987Ala | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/29 | 3268/8066 | 2961/4749 | 987/1582 | chrX | 105923468 | |||
| chrX:105939912 | T | C | 1 | a0001c0012 | 1 | NA19062.hp1 | synonymous_variant | LOW | c.3838T>C | p.Leu1280Leu | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/29 | 4145/8066 | 3838/4749 | 1280/1582 | chrX | 105939912 |
| 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:105822592 | T | G | 4 | a0003c0003t0003 a0003c0011t0003 a0004c0004t0003 others(1): Show |
37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
5_prime_UTR_variant | MODIFIER | c.-254T>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/29 | 254 | chrX | 105822592 | ||||||
| chrX:105955712 | C | A | 1 | a0001c0001t0006 | 1 | HG01258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*112C>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 112 | chrX | 105955712 | ||||||
| chrX:105956698 | G | T | 2 | a0002c0002t0002 a0007c0008t0002 |
42 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1098G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1098 | chrX | 105956698 | ||||||
| chrX:105956919 | A | G | 1 | a0002c0002t0010 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1319A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1319 | chrX | 105956919 | ||||||
| chrX:105956920 | A | C | 1 | a0002c0002t0010 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1320A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1320 | chrX | 105956920 | ||||||
| chrX:105956934 | A | G | 1 | a0002c0002t0010 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1334A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1334 | chrX | 105956934 | ||||||
| chrX:105956936 | A | T | 1 | a0002c0002t0010 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1336A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1336 | chrX | 105956936 | ||||||
| chrX:105956937 | A | G | 1 | a0002c0002t0010 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1337A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1337 | chrX | 105956937 | ||||||
| chrX:105956938 | T | C | 1 | a0002c0002t0010 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1338T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1338 | chrX | 105956938 | ||||||
| chrX:105956940 | C | T | 1 | a0002c0002t0010 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1340C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1340 | chrX | 105956940 | ||||||
| chrX:105956946 | G | T | 1 | a0002c0002t0010 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1346G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1346 | chrX | 105956946 | ||||||
| chrX:105956948 | T | C | 1 | a0002c0002t0010 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1348T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1348 | chrX | 105956948 | ||||||
| chrX:105956950 | T | A | 1 | a0002c0002t0010 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1350T>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1350 | chrX | 105956950 | ||||||
| chrX:105956952 | C | A | 1 | a0002c0002t0010 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1352C>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1352 | chrX | 105956952 | ||||||
| chrX:105956953 | T | A | 1 | a0002c0002t0010 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1353T>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1353 | chrX | 105956953 | ||||||
| chrX:105956955 | C | T | 1 | a0002c0002t0010 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1355C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1355 | chrX | 105956955 | ||||||
| chrX:105956958 | A | C | 1 | a0002c0002t0010 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1358A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1358 | chrX | 105956958 | ||||||
| chrX:105956959 | A | C | 1 | a0002c0002t0010 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1359A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1359 | chrX | 105956959 | ||||||
| chrX:105956962 | C | T | 1 | a0002c0002t0010 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1362C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1362 | chrX | 105956962 | ||||||
| chrX:105956969 | C | T | 1 | a0002c0002t0010 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1369C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1369 | chrX | 105956969 | ||||||
| chrX:105956970 | A | G | 1 | a0002c0002t0010 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1370A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1370 | chrX | 105956970 | ||||||
| chrX:105956980 | G | A | 1 | a0002c0002t0010 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1380G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1380 | chrX | 105956980 | ||||||
| chrX:105956990 | T | C | 1 | a0002c0002t0010 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1390T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1390 | chrX | 105956990 | ||||||
| chrX:105956995 | A | T | 1 | a0002c0002t0010 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1395A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1395 | chrX | 105956995 | ||||||
| chrX:105957286 | T | A | 1 | a0001c0001t0007 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1686T>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1686 | chrX | 105957286 | ||||||
| chrX:105957335 | T | C | 1 | a0002c0002t0008 | 1 | HG02897.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1735T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 1735 | chrX | 105957335 | ||||||
| chrX:105957643 | A | G | 12 | a0002c0002t0002 a0002c0002t0005 a0002c0002t0008 others(9): Show |
91 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*2043A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 2043 | chrX | 105957643 | ||||||
| chrX:105957979 | G | A | 1 | a0002c0002t0009 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2379G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 29/29 | 2379 | chrX | 105957979 |
| 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:105823105 | A | G | 2 | a0003c0003t0003g0212 a0003c0003t0003g0213 |
2 | HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.57+203A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105823105 | |||||||
| chrX:105823265 | C | T | 4 | a0002c0002t0005g0208 a0002c0002t0005g0209 a0002c0002t0005g0211 others(1): Show |
4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+363C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105823265 | |||||||
| chrX:105823296 | T | C | 37 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(34): Show |
37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.57+394T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105823296 | |||||||
| chrX:105823337 | C | T | 1 | a0001c0001t0001g0207 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.57+435C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105823337 | |||||||
| chrX:105823459 | G | A | 1 | a0001c0001t0001g0041 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.57+557G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105823459 | |||||||
| chrX:105824202 | G | A | 40 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(37): Show |
42 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.57+1300G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105824202 | |||||||
| chrX:105824255 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.57+1353C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105824255 | |||||||
| chrX:105824372 | C | T | 1 | a0002c0002t0002g0079 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.57+1470C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105824372 | |||||||
| chrX:105824553 | A | G | 1 | a0002c0002t0005g0205 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.57+1651A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105824553 | |||||||
| chrX:105824565 | G | A | 1 | a0007c0008t0002g0042 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.57+1663G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105824565 | |||||||
| chrX:105824617 | C | CA | 8 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(5): Show |
8 | HG00621.hp1 HG02109.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.57+1732dupA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105824617 | ||||||
| chrX:105824617 | CA | C | 37 | a0001c0001t0001g0202 a0001c0001t0004g0199 a0001c0001t0004g0200 others(34): Show |
37 | HG00673.hp1 HG01109.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.57+1732delA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105824617 | ||||||
| chrX:105824617 | CAA | C | 46 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0046 others(43): Show |
48 | HG00733.hp1 HG00735.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.57+1731_57+1732del others(2): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105824617 | ||||||
| chrX:105824634 | AT | A | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.57+1733delT | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105824634 | |||||||
| chrX:105824792 | G | A | 2 | a0001c0001t0004g0086 a0001c0001t0004g0087 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.57+1890G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105824792 | |||||||
| chrX:105825846 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.57+2944T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105825846 | |||||||
| chrX:105825884 | G | A | 204 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0041 others(201): Show |
210 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(207): Show |
intron_variant | MODIFIER | c.57+2982G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105825884 | |||||||
| chrX:105825968 | A | G | 2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | HG00735.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.57+3066A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105825968 | |||||||
| chrX:105826001 | A | G | 1 | a0002c0002t0002g0045 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.57+3099A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105826001 | |||||||
| chrX:105826038 | G | GTC | 3 | a0002c0002t0002g0003 a0002c0002t0002g0078 a0002c0002t0008g0179 |
4 | HG00741.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.57+3154_57+3155dup others(2): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105826038 | ||||||
| chrX:105826056 | C | A | 16 | a0001c0001t0004g0192 a0002c0002t0002g0043 a0002c0002t0002g0046 others(13): Show |
16 | HG01358.hp1 HG01361.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.57+3154C>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105826056 | |||||||
| chrX:105826056 | C | CTA | 3 | a0002c0002t0002g0059 a0002c0002t0002g0060 a0003c0003t0003g0030 |
3 | HG01192.hp1 HG03239.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.57+3169_57+3170dup others(2): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105826056 | ||||||
| chrX:105826058 | A | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0041 others(134): Show |
143 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(140): Show |
intron_variant | MODIFIER | c.57+3156A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105826058 | |||||||
| chrX:105826060 | A | C | 12 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0180 others(9): Show |
12 | HG00621.hp1 HG00741.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.57+3158A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105826060 | |||||||
| chrX:105826062 | A | C | 1 | a0001c0001t0004g0189 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.57+3160A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105826062 | |||||||
| chrX:105826204 | T | C | 16 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(13): Show |
16 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.57+3302T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105826204 | |||||||
| chrX:105826208 | TATA | T | 4 | a0002c0002t0005g0208 a0002c0002t0005g0209 a0002c0002t0005g0211 others(1): Show |
4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+3313_57+3315del others(3): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105826208 | ||||||
| chrX:105826222 | A | G | 1 | a0002c0002t0002g0058 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.57+3320A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105826222 | |||||||
| chrX:105826232 | A | ATCATATA others(23): Show |
1 | a0001c0001t0001g0178 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.57+3350_57+3379dup others(30): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105826232 | ||||||
| chrX:105826249 | T | TGATAATA others(50): Show |
3 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 |
3 | NA18962.hp1 NA18977.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.57+3370_57+3426dup others(57): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105826249 | ||||||
| chrX:105826291 | TA | T | 85 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(82): Show |
87 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.57+3390delA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105826291 | |||||||
| chrX:105826354 | T | C | 1 | a0002c0002t0005g0201 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.57+3452T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105826354 | |||||||
| chrX:105826368 | T | TTATATAT others(43): Show |
1 | a0001c0001t0004g0096 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.57+3499_57+3500ins others(50): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105826368 | ||||||
| chrX:105826391 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.57+3489A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105826391 | |||||||
| chrX:105826392 | TATATATA others(2): Show |
T | 20 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0044 others(17): Show |
22 | HG00673.hp1 HG00738.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.57+3500_57+3508del others(9): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105826392 | ||||||
| chrX:105826400 | T | TTATATA | 2 | a0002c0002t0005g0208 a0002c0002t0005g0209 |
2 | HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.57+3498_57+3499ins others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105826400 | |||||||
| chrX:105826401 | A | AAT | 58 | a0002c0002t0002g0043 a0002c0002t0002g0046 a0002c0002t0002g0047 others(55): Show |
58 | HG00733.hp1 HG00735.hp1 HG01071.hp2 others(55): Show |
intron_variant | MODIFIER | c.57+3510_57+3511dup others(2): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105826401 | ||||||
| chrX:105826401 | A | AATAT | 2 | a0002c0002t0005g0211 a0002c0009t0005g0210 |
2 | HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.57+3508_57+3511dup others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105826401 | ||||||
| chrX:105826401 | A | AATATATT others(23): Show |
1 | a0002c0002t0005g0203 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.57+3505_57+3506ins others(30): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105826401 | ||||||
| chrX:105826401 | A | AATATATT others(34): Show |
2 | a0002c0002t0005g0201 a0002c0002t0009g0204 |
2 | HG02451.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.57+3505_57+3506ins others(41): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105826401 | ||||||
| chrX:105826401 | A | T | 2 | a0002c0002t0005g0208 a0002c0002t0005g0209 |
2 | HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.57+3499A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105826401 | |||||||
| chrX:105826827 | A | G | 1 | a0001c0001t0001g0177 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.57+3925A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105826827 | |||||||
| chrX:105826856 | G | A | 1 | a0002c0002t0002g0048 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.57+3954G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105826856 | |||||||
| chrX:105827068 | C | T | 1 | a0002c0002t0008g0179 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.58-3986C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105827068 | |||||||
| chrX:105827676 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.58-3378G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105827676 | |||||||
| chrX:105828486 | C | T | 4 | a0002c0002t0005g0208 a0002c0002t0005g0209 a0002c0002t0005g0211 others(1): Show |
4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-2568C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105828486 | |||||||
| chrX:105828764 | A | G | 1 | a0002c0002t0002g0064 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.58-2290A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105828764 | |||||||
| chrX:105829097 | T | C | 1 | a0002c0002t0008g0179 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.58-1957T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105829097 | |||||||
| chrX:105829243 | C | G | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0006g0176 |
3 | HG01069.hp1 HG01071.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.58-1811C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105829243 | |||||||
| chrX:105829451 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.58-1603T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105829451 | |||||||
| chrX:105829718 | G | T | 2 | a0001c0001t0001g0005 a0001c0001t0001g0175 |
3 | HG00609.hp1 NA18944.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.58-1336G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105829718 | |||||||
| chrX:105829828 | C | G | 1 | a0001c0001t0004g0095 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.58-1226C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105829828 | |||||||
| chrX:105829840 | T | G | 40 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(37): Show |
42 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.58-1214T>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105829840 | |||||||
| chrX:105830224 | C | G | 16 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(13): Show |
16 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.58-830C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105830224 | |||||||
| chrX:105830314 | CA | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0041 others(102): Show |
110 | HG00280.hp1 HG00609.hp1 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.58-709delA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105830314 | ||||||
| chrX:105830314 | CAA | C | 40 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(37): Show |
41 | HG00673.hp1 HG00733.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.58-710_58-709delAA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105830314 | ||||||
| chrX:105830314 | CAAA | C | 22 | a0002c0002t0008g0179 a0003c0003t0003g0006 a0003c0003t0003g0009 others(19): Show |
22 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.58-711_58-709delAA others(1): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105830314 | ||||||
| chrX:105830314 | CAAAA | C | 10 | a0003c0003t0003g0007 a0003c0003t0003g0008 a0003c0003t0003g0016 others(7): Show |
10 | HG02109.hp2 HG02258.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.58-712_58-709delAA others(2): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chrX | 105830314 | ||||||
| chrX:105830785 | G | A | 1 | a0002c0002t0002g0051 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.58-269G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105830785 | |||||||
| chrX:105830847 | G | A | 1 | a0004c0004t0003g0011 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.58-207G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 1/28 | chrX | 105830847 | |||||||
| chrX:105831740 | T | G | 37 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(34): Show |
37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.123+621T>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105831740 | |||||||
| chrX:105831805 | C | T | 2 | a0002c0002t0002g0059 a0002c0002t0002g0060 |
2 | HG01192.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.123+686C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105831805 | |||||||
| chrX:105832065 | G | A | 1 | a0002c0002t0002g0048 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.123+946G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105832065 | |||||||
| chrX:105832080 | C | G | 1 | a0001c0001t0001g0171 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.123+961C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105832080 | |||||||
| chrX:105832491 | C | T | 1 | a0002c0002t0002g0064 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.123+1372C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105832491 | |||||||
| chrX:105832655 | A | G | 3 | a0002c0002t0005g0120 a0002c0002t0010g0119 a0009c0010t0005g0090 |
3 | HG02717.hp1 HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.123+1536A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105832655 | |||||||
| chrX:105832759 | C | G | 3 | a0001c0001t0001g0080 a0001c0001t0001g0169 a0001c0001t0001g0170 |
3 | HG02683.hp2 HG03669.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.123+1640C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105832759 | |||||||
| chrX:105833058 | C | G | 4 | a0001c0001t0004g0118 a0001c0001t0004g0167 a0001c0001t0004g0168 others(1): Show |
4 | HG02055.hp1 HG02723.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.123+1939C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105833058 | |||||||
| chrX:105833313 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.123+2194C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105833313 | |||||||
| chrX:105833811 | A | G | 2 | a0001c0001t0001g0117 a0001c0001t0001g0165 |
2 | NA18982.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.123+2692A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105833811 | |||||||
| chrX:105834090 | G | A | 1 | a0002c0002t0008g0179 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.123+2971G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105834090 | |||||||
| chrX:105834330 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.123+3211C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105834330 | |||||||
| chrX:105834442 | G | GGT | 5 | a0002c0002t0005g0208 a0003c0003t0003g0020 a0003c0003t0003g0032 others(2): Show |
5 | HG01109.hp1 HG02109.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+3329_123+3330d others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105834442 | ||||||
| chrX:105834450 | C | T | 89 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(86): Show |
91 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.123+3331C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105834450 | |||||||
| chrX:105834463 | G | A | 1 | a0002c0002t0002g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.123+3344G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105834463 | |||||||
| chrX:105834539 | G | T | 2 | a0002c0002t0005g0201 a0002c0002t0005g0203 |
2 | NA18612.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.123+3420G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105834539 | |||||||
| chrX:105834546 | C | T | 1 | a0001c0001t0001g0081 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.123+3427C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105834546 | |||||||
| chrX:105834718 | C | A | 1 | a0001c0001t0001g0097 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.123+3599C>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105834718 | |||||||
| chrX:105835146 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.123+4027G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105835146 | |||||||
| chrX:105835241 | T | G | 38 | a0002c0002t0009g0204 a0003c0003t0003g0006 a0003c0003t0003g0007 others(35): Show |
38 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.123+4122T>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105835241 | |||||||
| chrX:105835549 | T | C | 1 | a0002c0002t0002g0068 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.123+4430T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105835549 | |||||||
| chrX:105835628 | CT | C | 37 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(34): Show |
37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.123+4524delT | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105835628 | ||||||
| chrX:105835944 | C | T | 16 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(13): Show |
16 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.123+4825C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105835944 | |||||||
| chrX:105835953 | A | G | 1 | a0001c0001t0004g0192 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.123+4834A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105835953 | |||||||
| chrX:105836040 | C | A | 1 | a0001c0001t0001g0122 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.123+4921C>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105836040 | |||||||
| chrX:105836148 | A | G | 1 | a0001c0001t0004g0096 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.123+5029A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105836148 | |||||||
| chrX:105836455 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.123+5336A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105836455 | |||||||
| chrX:105836481 | C | T | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0006g0176 |
3 | HG01069.hp1 HG01071.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.123+5362C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105836481 | |||||||
| chrX:105836520 | A | C | 1 | a0002c0002t0005g0211 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.123+5401A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105836520 | |||||||
| chrX:105836589 | A | C | 3 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 |
3 | NA18986.hp1 NA18989.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.123+5470A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105836589 | |||||||
| chrX:105836682 | T | A | 1 | a0002c0002t0002g0069 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.123+5563T>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105836682 | |||||||
| chrX:105836919 | C | T | 1 | a0002c0002t0008g0179 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.123+5800C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105836919 | |||||||
| chrX:105837466 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.123+6347T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105837466 | |||||||
| chrX:105837964 | G | C | 1 | a0001c0001t0001g0123 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.123+6845G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105837964 | |||||||
| chrX:105838727 | C | T | 1 | a0001c0001t0004g0095 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.123+7608C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105838727 | |||||||
| chrX:105838827 | A | C | 3 | a0002c0002t0005g0201 a0002c0002t0005g0203 a0002c0002t0009g0204 |
3 | HG02451.hp2 NA18612.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.123+7708A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105838827 | |||||||
| chrX:105839252 | A | C | 1 | a0001c0001t0001g0175 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.123+8133A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105839252 | |||||||
| chrX:105839296 | G | C | 1 | a0001c0001t0004g0091 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.123+8177G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105839296 | |||||||
| chrX:105839379 | T | G | 43 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(40): Show |
45 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.123+8260T>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105839379 | |||||||
| chrX:105839632 | A | T | 35 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(32): Show |
37 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.123+8513A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105839632 | |||||||
| chrX:105839765 | G | A | 4 | a0002c0002t0005g0208 a0002c0002t0005g0209 a0002c0002t0005g0211 others(1): Show |
4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.123+8646G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105839765 | |||||||
| chrX:105839790 | C | T | 3 | a0001c0001t0004g0168 a0001c0001t0004g0189 a0001c0001t0007g0116 |
3 | HG02723.hp1 HG03453.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.123+8671C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105839790 | |||||||
| chrX:105839821 | G | A | 2 | a0001c0001t0004g0086 a0001c0001t0004g0087 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.123+8702G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105839821 | |||||||
| chrX:105839950 | T | C | 1 | a0002c0002t0002g0065 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.123+8831T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105839950 | |||||||
| chrX:105840002 | G | A | 1 | a0003c0003t0003g0007 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.123+8883G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105840002 | |||||||
| chrX:105840454 | A | C | 1 | a0002c0002t0002g0064 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.123+9335A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105840454 | |||||||
| chrX:105840463 | A | C | 1 | a0002c0002t0002g0064 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.123+9344A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105840463 | |||||||
| chrX:105840638 | C | T | 3 | a0001c0001t0001g0080 a0001c0001t0001g0169 a0001c0001t0001g0170 |
3 | HG02683.hp2 HG03669.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.123+9519C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105840638 | |||||||
| chrX:105840646 | C | A | 2 | a0004c0004t0003g0012 a0004c0004t0003g0013 |
2 | HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.123+9527C>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105840646 | |||||||
| chrX:105840659 | A | G | 1 | a0002c0002t0008g0179 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.123+9540A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105840659 | |||||||
| chrX:105840794 | G | C | 5 | a0002c0002t0002g0002 a0002c0002t0002g0066 a0002c0002t0002g0070 others(2): Show |
6 | HG02015.hp1 HG02027.hp1 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.123+9675G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105840794 | |||||||
| chrX:105840821 | G | A | 11 | a0003c0003t0003g0009 a0003c0003t0003g0021 a0003c0003t0003g0022 others(8): Show |
11 | HG02451.hp1 HG02630.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.123+9702G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105840821 | |||||||
| chrX:105840855 | G | A | 2 | a0002c0002t0002g0059 a0002c0002t0002g0060 |
2 | HG01192.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.123+9736G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105840855 | |||||||
| chrX:105840855 | G | GTA | 6 | a0001c0001t0001g0160 a0002c0002t0002g0002 a0002c0002t0002g0071 others(3): Show |
7 | HG03098.hp1 HG03486.hp2 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.123+9751_123+9752d others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105840855 | ||||||
| chrX:105840874 | T | TAGAG | 37 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(34): Show |
37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.123+9762_123+9765d others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105840874 | ||||||
| chrX:105840874 | TAGAG | T | 3 | a0002c0002t0005g0120 a0002c0002t0010g0119 a0009c0010t0005g0090 |
3 | HG02717.hp1 HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.123+9762_123+9765d others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105840874 | ||||||
| chrX:105841879 | A | T | 1 | a0001c0001t0001g0100 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.123+10760A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105841879 | |||||||
| chrX:105841923 | C | T | 1 | a0001c0001t0001g0174 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.123+10804C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105841923 | |||||||
| chrX:105842803 | A | G | 3 | a0002c0002t0005g0201 a0002c0002t0005g0203 a0002c0002t0009g0204 |
3 | HG02451.hp2 NA18612.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.123+11684A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105842803 | |||||||
| chrX:105843223 | T | G | 16 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(13): Show |
16 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.123+12104T>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105843223 | |||||||
| chrX:105843767 | G | A | 1 | a0002c0002t0002g0003 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.123+12648G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105843767 | |||||||
| chrX:105843977 | C | CTG | 11 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(8): Show |
11 | HG01258.hp1 HG03453.hp2 HG03490.hp1 others(8): Show |
intron_variant | MODIFIER | c.123+12898_123+1289 others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105843977 | ||||||
| chrX:105843977 | C | CTGTG | 18 | a0001c0001t0004g0095 a0001c0001t0004g0118 a0001c0001t0004g0167 others(15): Show |
18 | HG01891.hp2 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.123+12896_123+1289 others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105843977 | ||||||
| chrX:105843977 | CTG | C | 11 | a0001c0001t0001g0005 a0001c0001t0001g0101 a0001c0001t0001g0102 others(8): Show |
12 | HG00609.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.123+12898_123+1289 others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105843977 | ||||||
| chrX:105843977 | CTGTGTGT others(3): Show |
C | 1 | a0001c0001t0001g0124 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.123+12890_123+1289 others(14): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105843977 | ||||||
| chrX:105844011 | G | C | 19 | a0003c0003t0003g0009 a0003c0003t0003g0010 a0003c0003t0003g0020 others(16): Show |
19 | HG01109.hp1 HG01884.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.123+12892G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105844011 | |||||||
| chrX:105844011 | G | GTGTGTGT others(9): Show |
1 | a0002c0002t0008g0179 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.123+12899_123+1290 others(20): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105844011 | ||||||
| chrX:105844013 | G | C | 4 | a0002c0002t0005g0208 a0002c0002t0005g0209 a0003c0003t0003g0027 others(1): Show |
4 | HG02109.hp1 HG02630.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.123+12894G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105844013 | |||||||
| chrX:105844015 | G | C | 32 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0044 others(29): Show |
34 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.123+12896G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105844015 | |||||||
| chrX:105844015 | G | GTC | 10 | a0002c0002t0002g0043 a0002c0002t0002g0046 a0002c0002t0002g0047 others(7): Show |
10 | HG01192.hp1 HG01361.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.123+12897_123+1289 others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105844015 | ||||||
| chrX:105844017 | G | C | 1 | a0001c0001t0001g0202 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.123+12898G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105844017 | |||||||
| chrX:105844017 | GTC | G | 5 | a0002c0002t0005g0208 a0002c0002t0005g0209 a0003c0003t0003g0016 others(2): Show |
5 | HG02109.hp1 HG02630.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+12900_123+1290 others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105844017 | ||||||
| chrX:105844019 | C | G | 46 | a0001c0001t0001g0183 a0001c0001t0001g0202 a0002c0002t0002g0002 others(43): Show |
48 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.123+12900C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105844019 | |||||||
| chrX:105844019 | CTGTG | C | 19 | a0003c0003t0003g0009 a0003c0003t0003g0010 a0003c0003t0003g0020 others(16): Show |
19 | HG01109.hp1 HG01884.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.123+12920_123+1292 others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105844019 | ||||||
| chrX:105844021 | G | C | 2 | a0001c0001t0001g0183 a0002c0002t0005g0205 |
2 | NA18939.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.123+12902G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105844021 | |||||||
| chrX:105844021 | G | GTCTGTGT others(3): Show |
1 | a0006c0007t0003g0014 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.123+12903_123+1290 others(14): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105844021 | ||||||
| chrX:105844023 | G | C | 47 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(44): Show |
49 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.123+12904G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105844023 | |||||||
| chrX:105844023 | G | GTGTC | 17 | a0002c0002t0002g0064 a0002c0002t0005g0201 a0002c0002t0005g0203 others(14): Show |
17 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.123+12907_123+1290 others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105844023 | ||||||
| chrX:105844035 | G | C | 1 | a0006c0007t0003g0014 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.123+12916G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105844035 | |||||||
| chrX:105844464 | C | T | 2 | a0003c0003t0003g0008 a0003c0003t0003g0016 |
2 | HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.123+13345C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105844464 | |||||||
| chrX:105844707 | G | A | 1 | a0001c0001t0004g0095 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.123+13588G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105844707 | |||||||
| chrX:105844949 | G | C | 37 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(34): Show |
37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.123+13830G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105844949 | |||||||
| chrX:105845123 | G | A | 44 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(41): Show |
46 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.123+14004G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105845123 | |||||||
| chrX:105845193 | C | T | 37 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(34): Show |
37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.123+14074C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105845193 | |||||||
| chrX:105845454 | G | A | 4 | a0002c0002t0005g0208 a0002c0002t0005g0209 a0002c0002t0005g0211 others(1): Show |
4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.123+14335G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105845454 | |||||||
| chrX:105845659 | G | A | 1 | a0002c0002t0010g0119 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.123+14540G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105845659 | |||||||
| chrX:105845946 | T | A | 4 | a0002c0002t0005g0208 a0002c0002t0005g0209 a0002c0002t0005g0211 others(1): Show |
4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.123+14827T>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105845946 | |||||||
| chrX:105846034 | A | G | 1 | a0002c0002t0009g0204 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.123+14915A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105846034 | |||||||
| chrX:105846116 | C | T | 37 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(34): Show |
37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.123+14997C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105846116 | |||||||
| chrX:105846662 | G | C | 3 | a0001c0001t0001g0080 a0001c0001t0001g0169 a0001c0001t0001g0170 |
3 | HG02683.hp2 HG03669.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.123+15543G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105846662 | |||||||
| chrX:105846936 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.123+15817G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105846936 | |||||||
| chrX:105847135 | A | G | 37 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(34): Show |
37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.123+16016A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105847135 | |||||||
| chrX:105847140 | A | G | 1 | a0003c0003t0003g0030 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.123+16021A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105847140 | |||||||
| chrX:105847403 | C | T | 1 | a0001c0001t0001g0160 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.123+16284C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105847403 | |||||||
| chrX:105848159 | G | A | 44 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(41): Show |
46 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.123+17040G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105848159 | |||||||
| chrX:105848286 | G | T | 85 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(82): Show |
87 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.123+17167G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105848286 | |||||||
| chrX:105848446 | G | T | 1 | a0003c0003t0003g0212 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.123+17327G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105848446 | |||||||
| chrX:105848659 | A | G | 1 | a0001c0001t0001g0187 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.123+17540A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105848659 | |||||||
| chrX:105848895 | A | T | 1 | a0001c0001t0001g0182 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.123+17776A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105848895 | |||||||
| chrX:105849068 | A | G | 1 | a0004c0004t0003g0019 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.123+17949A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105849068 | |||||||
| chrX:105849780 | C | T | 42 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(39): Show |
44 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.123+18661C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105849780 | |||||||
| chrX:105850261 | C | T | 1 | a0002c0002t0002g0068 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.123+19142C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105850261 | |||||||
| chrX:105850534 | A | G | 1 | a0002c0002t0005g0120 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.123+19415A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105850534 | |||||||
| chrX:105851265 | T | C | 1 | a0002c0002t0005g0120 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.123+20146T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105851265 | |||||||
| chrX:105851297 | C | T | 3 | a0002c0002t0005g0201 a0002c0002t0005g0203 a0002c0002t0009g0204 |
3 | HG02451.hp2 NA18612.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.123+20178C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105851297 | |||||||
| chrX:105851300 | T | C | 10 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0125 others(7): Show |
12 | HG00642.hp1 HG01256.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.123+20181T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105851300 | |||||||
| chrX:105851359 | C | T | 37 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(34): Show |
37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.123+20240C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105851359 | |||||||
| chrX:105851718 | C | A | 37 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(34): Show |
37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.123+20599C>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105851718 | |||||||
| chrX:105851866 | G | A | 7 | a0001c0001t0004g0091 a0001c0001t0004g0092 a0001c0001t0004g0095 others(4): Show |
7 | HG01891.hp1 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.123+20747G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105851866 | |||||||
| chrX:105852109 | T | C | 1 | a0003c0003t0003g0035 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.123+20990T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105852109 | |||||||
| chrX:105852383 | C | T | 4 | a0002c0002t0005g0208 a0002c0002t0005g0209 a0002c0002t0005g0211 others(1): Show |
4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.123+21264C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105852383 | |||||||
| chrX:105852676 | C | G | 1 | a0002c0002t0002g0063 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.123+21557C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105852676 | |||||||
| chrX:105852829 | G | A | 16 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(13): Show |
16 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.123+21710G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105852829 | |||||||
| chrX:105853515 | G | A | 43 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(40): Show |
45 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.123+22396G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105853515 | |||||||
| chrX:105853928 | A | G | 1 | a0003c0003t0003g0027 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.123+22809A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105853928 | |||||||
| chrX:105854310 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.123+23191A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105854310 | |||||||
| chrX:105854723 | G | A | 2 | a0002c0002t0002g0003 a0002c0002t0002g0078 |
3 | HG00741.hp1 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.123+23604G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105854723 | |||||||
| chrX:105855212 | A | C | 1 | a0001c0001t0001g0182 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.123+24093A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105855212 | |||||||
| chrX:105855338 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.123+24219G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105855338 | |||||||
| chrX:105855721 | C | T | 1 | a0001c0005t0001g0004 | 2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.124-24478C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105855721 | |||||||
| chrX:105856036 | T | G | 4 | a0002c0002t0005g0208 a0002c0002t0005g0209 a0002c0002t0005g0211 others(1): Show |
4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-24163T>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105856036 | |||||||
| chrX:105856163 | A | C | 1 | a0002c0002t0002g0061 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.124-24036A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105856163 | |||||||
| chrX:105856287 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.124-23912A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105856287 | |||||||
| chrX:105856308 | A | G | 1 | a0001c0001t0004g0200 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.124-23891A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105856308 | |||||||
| chrX:105856480 | A | G | 1 | a0002c0002t0008g0179 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.124-23719A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105856480 | |||||||
| chrX:105856677 | A | G | 1 | a0001c0001t0001g0154 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.124-23522A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105856677 | |||||||
| chrX:105856935 | G | T | 40 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(37): Show |
42 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.124-23264G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105856935 | |||||||
| chrX:105856948 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.124-23251C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105856948 | |||||||
| chrX:105857002 | A | T | 1 | a0003c0003t0003g0006 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.124-23197A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105857002 | |||||||
| chrX:105857071 | A | G | 1 | a0002c0002t0008g0179 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.124-23128A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105857071 | |||||||
| chrX:105857114 | T | C | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | NA19006.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.124-23085T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105857114 | |||||||
| chrX:105857116 | T | C | 43 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(40): Show |
45 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.124-23083T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105857116 | |||||||
| chrX:105857587 | A | T | 40 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(37): Show |
42 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.124-22612A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105857587 | |||||||
| chrX:105857689 | T | C | 1 | a0002c0002t0002g0073 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.124-22510T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105857689 | |||||||
| chrX:105858382 | G | GT | 54 | a0001c0001t0001g0083 a0001c0001t0004g0118 a0002c0002t0002g0002 others(51): Show |
56 | HG00621.hp1 HG00673.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.124-21802dupT | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105858382 | ||||||
| chrX:105858382 | G | GTT | 31 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(28): Show |
31 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.124-21803_124-2180 others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105858382 | ||||||
| chrX:105858492 | A | G | 1 | a0004c0004t0003g0019 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.124-21707A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105858492 | |||||||
| chrX:105858749 | T | C | 1 | a0007c0008t0002g0042 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.124-21450T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105858749 | |||||||
| chrX:105859323 | T | C | 1 | a0001c0001t0001g0206 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.124-20876T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105859323 | |||||||
| chrX:105860009 | G | T | 1 | a0003c0003t0003g0027 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.124-20190G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105860009 | |||||||
| chrX:105860014 | A | G | 1 | a0001c0001t0001g0153 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.124-20185A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105860014 | |||||||
| chrX:105860057 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.124-20142G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105860057 | |||||||
| chrX:105860091 | G | C | 85 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(82): Show |
87 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.124-20108G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105860091 | |||||||
| chrX:105860647 | A | G | 2 | a0003c0003t0003g0039 a0003c0003t0003g0040 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.124-19552A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105860647 | |||||||
| chrX:105860797 | A | T | 1 | a0009c0010t0005g0090 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.124-19402A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105860797 | |||||||
| chrX:105861085 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.124-19114A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105861085 | |||||||
| chrX:105861308 | A | G | 37 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(34): Show |
37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.124-18891A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105861308 | |||||||
| chrX:105861531 | A | G | 1 | a0008c0006t0001g0114 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.124-18668A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105861531 | |||||||
| chrX:105861839 | A | C | 37 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(34): Show |
37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.124-18360A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105861839 | |||||||
| chrX:105861902 | CA | C | 85 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(82): Show |
87 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.124-18286delA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105861902 | ||||||
| chrX:105861916 | AGCCGGGC others(2): Show |
A | 7 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(4): Show |
7 | HG01934.hp1 HG02300.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.124-18281_124-1827 others(13): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105861916 | ||||||
| chrX:105862041 | C | T | 1 | a0002c0002t0005g0120 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.124-18158C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105862041 | |||||||
| chrX:105862074 | G | GATCT | 5 | a0001c0001t0001g0093 a0001c0001t0001g0121 a0001c0001t0001g0134 others(2): Show |
5 | HG02080.hp2 HG02083.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-18098_124-1809 others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105862074 | ||||||
| chrX:105862074 | GATCT | G | 85 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(82): Show |
87 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.124-18098_124-1809 others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105862074 | ||||||
| chrX:105862684 | T | G | 1 | a0002c0002t0005g0203 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.124-17515T>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105862684 | |||||||
| chrX:105863190 | T | A | 1 | a0002c0002t0008g0179 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.124-17009T>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105863190 | |||||||
| chrX:105863227 | T | C | 1 | a0002c0002t0008g0179 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.124-16972T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105863227 | |||||||
| chrX:105863321 | G | GAC | 12 | a0001c0001t0004g0193 a0002c0002t0002g0044 a0002c0002t0002g0064 others(9): Show |
12 | HG00140.hp1 HG00673.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.124-16842_124-1684 others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105863321 | ||||||
| chrX:105863321 | G | GACAC | 4 | a0002c0002t0002g0002 a0002c0002t0002g0047 a0002c0002t0002g0071 others(1): Show |
5 | HG03710.hp1 NA18939.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.124-16844_124-1684 others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105863321 | ||||||
| chrX:105863321 | G | GACACAC | 21 | a0002c0002t0002g0003 a0002c0002t0002g0043 a0002c0002t0002g0045 others(18): Show |
22 | HG00733.hp1 HG00735.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.124-16846_124-1684 others(10): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105863321 | ||||||
| chrX:105863321 | G | GACACACA others(1): Show |
6 | a0002c0002t0002g0052 a0002c0002t0002g0057 a0002c0002t0002g0061 others(3): Show |
6 | HG01515.hp1 HG02486.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.124-16848_124-1684 others(12): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105863321 | ||||||
| chrX:105863321 | G | GACACACA others(3): Show |
1 | a0002c0002t0002g0063 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.124-16850_124-1684 others(14): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105863321 | ||||||
| chrX:105863321 | GAC | G | 3 | a0002c0002t0005g0208 a0002c0002t0005g0211 a0002c0009t0005g0210 |
3 | HG02809.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.124-16842_124-1684 others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105863321 | ||||||
| chrX:105863357 | C | CACACACA others(7): Show |
2 | a0003c0003t0003g0027 a0003c0003t0003g0212 |
2 | HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.124-16841_124-1684 others(18): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105863357 | ||||||
| chrX:105863357 | C | CACACACA others(5): Show |
13 | a0003c0003t0003g0009 a0003c0003t0003g0021 a0003c0003t0003g0022 others(10): Show |
13 | HG01884.hp2 HG02451.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.124-16841_124-1684 others(16): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105863357 | ||||||
| chrX:105863357 | C | CACACACA others(3): Show |
2 | a0002c0002t0008g0179 a0006c0007t0003g0014 |
2 | HG01243.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.124-16841_124-1684 others(14): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105863357 | ||||||
| chrX:105863357 | C | CACACACA others(1): Show |
10 | a0001c0001t0001g0083 a0001c0001t0001g0184 a0003c0003t0003g0010 others(7): Show |
10 | HG00621.hp1 HG01109.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.124-16841_124-1684 others(12): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105863357 | ||||||
| chrX:105863357 | C | CACACAT | 14 | a0001c0001t0001g0103 a0001c0001t0001g0127 a0001c0001t0001g0132 others(11): Show |
14 | HG01891.hp2 HG01978.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.124-16841_124-1684 others(10): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105863357 | ||||||
| chrX:105863357 | C | CACAT | 35 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0082 others(32): Show |
37 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.124-16841_124-1684 others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105863357 | ||||||
| chrX:105863357 | C | CAT | 87 | a0001c0001t0001g0005 a0001c0001t0001g0041 a0001c0001t0001g0081 others(84): Show |
89 | HG00280.hp1 HG00609.hp1 HG00733.hp2 others(86): Show |
intron_variant | MODIFIER | c.124-16840_124-1683 others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105863357 | ||||||
| chrX:105863357 | C | T | 4 | a0002c0002t0005g0205 a0002c0002t0005g0208 a0002c0002t0005g0211 others(1): Show |
4 | HG02809.hp2 HG02970.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-16842C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105863357 | |||||||
| chrX:105864157 | G | A | 1 | a0001c0001t0004g0092 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.124-16042G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105864157 | |||||||
| chrX:105864598 | A | G | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | NA18955.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.124-15601A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105864598 | |||||||
| chrX:105864693 | C | G | 1 | a0007c0008t0002g0042 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.124-15506C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105864693 | |||||||
| chrX:105864908 | GGGCTGGA others(27): Show |
G | 1 | a0003c0003t0003g0031 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.124-15289_124-1525 others(38): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105864908 | ||||||
| chrX:105865110 | C | T | 35 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(32): Show |
37 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.124-15089C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105865110 | |||||||
| chrX:105865223 | G | C | 6 | a0001c0001t0004g0167 a0001c0001t0004g0168 a0001c0001t0004g0189 others(3): Show |
6 | HG02486.hp1 HG02723.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.124-14976G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105865223 | |||||||
| chrX:105865511 | G | A | 85 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(82): Show |
87 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.124-14688G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105865511 | |||||||
| chrX:105865968 | T | C | 1 | a0001c0001t0001g0133 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.124-14231T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105865968 | |||||||
| chrX:105865969 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.124-14230C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105865969 | |||||||
| chrX:105865970 | A | C | 1 | a0001c0001t0001g0133 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.124-14229A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105865970 | |||||||
| chrX:105866014 | C | CA | 47 | a0001c0001t0001g0041 a0001c0001t0001g0113 a0001c0001t0001g0132 others(44): Show |
48 | HG00673.hp1 HG00733.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.124-14171dupA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105866014 | ||||||
| chrX:105866014 | C | CAAA | 21 | a0003c0003t0003g0009 a0003c0003t0003g0010 a0003c0003t0003g0020 others(18): Show |
21 | HG01109.hp1 HG01884.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.124-14173_124-1417 others(7): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105866014 | ||||||
| chrX:105866014 | C | CAAAA | 16 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(13): Show |
16 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.124-14174_124-1417 others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105866014 | ||||||
| chrX:105866045 | C | CT | 7 | a0001c0001t0001g0101 a0001c0001t0001g0126 a0001c0001t0001g0149 others(4): Show |
7 | HG01978.hp2 NA18939.hp2 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.124-14148dupT | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105866045 | ||||||
| chrX:105866261 | CCATAATC others(203): Show |
C | 7 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(4): Show |
7 | HG01934.hp1 HG02300.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.124-13934_124-1372 others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105866261 | ||||||
| chrX:105866457 | C | A | 2 | a0002c0002t0002g0068 a0002c0002t0002g0076 |
2 | HG02074.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.124-13742C>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105866457 | |||||||
| chrX:105866559 | A | G | 21 | a0003c0003t0003g0009 a0003c0003t0003g0010 a0003c0003t0003g0020 others(18): Show |
21 | HG01109.hp1 HG01884.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.124-13640A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105866559 | |||||||
| chrX:105866843 | G | T | 1 | a0001c0001t0001g0127 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.124-13356G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105866843 | |||||||
| chrX:105866940 | A | G | 40 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(37): Show |
42 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.124-13259A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105866940 | |||||||
| chrX:105866950 | TC | T | 4 | a0001c0001t0001g0093 a0001c0001t0001g0134 a0001c0001t0001g0173 others(1): Show |
4 | HG02080.hp2 HG02083.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-13247delC | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105866950 | ||||||
| chrX:105866972 | C | T | 1 | a0002c0002t0002g0067 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.124-13227C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105866972 | |||||||
| chrX:105867036 | T | C | 1 | a0002c0002t0002g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.124-13163T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105867036 | |||||||
| chrX:105867278 | G | A | 2 | a0001c0001t0001g0080 a0001c0001t0001g0169 |
2 | HG02683.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.124-12921G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105867278 | |||||||
| chrX:105867323 | A | G | 1 | a0002c0002t0010g0119 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.124-12876A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105867323 | |||||||
| chrX:105867369 | G | A | 1 | a0003c0003t0003g0036 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.124-12830G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105867369 | |||||||
| chrX:105867713 | T | A | 1 | a0001c0001t0001g0123 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.124-12486T>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105867713 | |||||||
| chrX:105867714 | G | T | 1 | a0001c0001t0001g0123 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.124-12485G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105867714 | |||||||
| chrX:105867904 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.124-12295C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105867904 | |||||||
| chrX:105868027 | T | C | 6 | a0001c0001t0004g0091 a0001c0001t0004g0092 a0001c0001t0004g0095 others(3): Show |
6 | HG01891.hp1 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.124-12172T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105868027 | |||||||
| chrX:105868220 | A | T | 1 | a0001c0001t0001g0133 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.124-11979A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105868220 | |||||||
| chrX:105868318 | T | C | 85 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(82): Show |
87 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.124-11881T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105868318 | |||||||
| chrX:105868630 | G | C | 8 | a0004c0004t0003g0011 a0004c0004t0003g0012 a0004c0004t0003g0013 others(5): Show |
8 | HG01243.hp1 HG01891.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.124-11569G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105868630 | |||||||
| chrX:105868680 | G | T | 21 | a0003c0003t0003g0009 a0003c0003t0003g0010 a0003c0003t0003g0020 others(18): Show |
21 | HG01109.hp1 HG01884.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.124-11519G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105868680 | |||||||
| chrX:105868720 | C | T | 16 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(13): Show |
16 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.124-11479C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105868720 | |||||||
| chrX:105868974 | A | G | 1 | a0003c0003t0003g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.124-11225A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105868974 | |||||||
| chrX:105868975 | C | A | 3 | a0001c0001t0004g0091 a0001c0001t0004g0199 a0001c0001t0004g0200 |
3 | HG01891.hp1 HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.124-11224C>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105868975 | |||||||
| chrX:105869028 | A | T | 37 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(34): Show |
37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.124-11171A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105869028 | |||||||
| chrX:105869065 | T | C | 37 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(34): Show |
37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.124-11134T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105869065 | |||||||
| chrX:105869068 | G | A | 1 | a0001c0001t0004g0096 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.124-11131G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105869068 | |||||||
| chrX:105869268 | G | A | 4 | a0002c0002t0005g0208 a0002c0002t0005g0209 a0002c0002t0005g0211 others(1): Show |
4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-10931G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105869268 | |||||||
| chrX:105869549 | C | T | 37 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(34): Show |
37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.124-10650C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105869549 | |||||||
| chrX:105869639 | C | T | 210 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0041 others(207): Show |
216 | HG00280.hp1 HG00609.hp1 HG00621.hp1 others(213): Show |
intron_variant | MODIFIER | c.124-10560C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105869639 | |||||||
| chrX:105869763 | A | G | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG03492.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.124-10436A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105869763 | |||||||
| chrX:105869811 | T | TTTGATAG others(53): Show |
3 | a0002c0002t0002g0061 a0002c0002t0002g0062 a0002c0002t0002g0063 |
3 | HG02486.hp1 HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.124-10386_124-1032 others(64): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105869811 | ||||||
| chrX:105869893 | A | G | 1 | a0002c0002t0002g0064 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.124-10306A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105869893 | |||||||
| chrX:105869974 | C | T | 1 | a0002c0002t0002g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.124-10225C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105869974 | |||||||
| chrX:105870049 | G | A | 7 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(4): Show |
7 | HG01934.hp1 HG02300.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.124-10150G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105870049 | |||||||
| chrX:105870190 | A | G | 1 | a0002c0002t0005g0208 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.124-10009A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105870190 | |||||||
| chrX:105870636 | T | C | 16 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(13): Show |
16 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.124-9563T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105870636 | |||||||
| chrX:105870843 | G | T | 37 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(34): Show |
37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.124-9356G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105870843 | |||||||
| chrX:105871161 | T | C | 3 | a0002c0002t0002g0061 a0002c0002t0002g0062 a0002c0002t0002g0063 |
3 | HG02486.hp1 HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.124-9038T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105871161 | |||||||
| chrX:105871449 | T | C | 4 | a0002c0002t0005g0208 a0002c0002t0005g0209 a0002c0002t0005g0211 others(1): Show |
4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-8750T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105871449 | |||||||
| chrX:105871485 | A | AAC | 38 | a0001c0001t0001g0106 a0001c0001t0001g0183 a0002c0002t0008g0179 others(35): Show |
38 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.124-8691_124-8690d others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105871485 | ||||||
| chrX:105871485 | A | AACAC | 2 | a0003c0003t0003g0007 a0004c0004t0003g0013 |
2 | HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.124-8693_124-8690d others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105871485 | ||||||
| chrX:105871611 | T | C | 1 | a0002c0002t0008g0179 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.124-8588T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105871611 | |||||||
| chrX:105871633 | G | T | 1 | a0009c0010t0005g0090 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.124-8566G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105871633 | |||||||
| chrX:105871744 | A | T | 1 | a0001c0001t0001g0206 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.124-8455A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105871744 | |||||||
| chrX:105872029 | A | T | 1 | a0007c0008t0002g0042 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.124-8170A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105872029 | |||||||
| chrX:105872564 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.124-7635C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105872564 | |||||||
| chrX:105872701 | C | G | 4 | a0002c0002t0005g0208 a0002c0002t0005g0209 a0002c0002t0005g0211 others(1): Show |
4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-7498C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105872701 | |||||||
| chrX:105872722 | T | C | 1 | a0002c0002t0008g0179 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.124-7477T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105872722 | |||||||
| chrX:105872853 | C | T | 2 | a0003c0003t0003g0008 a0003c0003t0003g0016 |
2 | HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.124-7346C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105872853 | |||||||
| chrX:105872900 | G | A | 1 | a0001c0001t0004g0095 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.124-7299G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105872900 | |||||||
| chrX:105872918 | T | G | 1 | a0001c0001t0001g0166 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.124-7281T>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105872918 | |||||||
| chrX:105873039 | T | C | 3 | a0003c0003t0003g0038 a0003c0003t0003g0039 a0003c0003t0003g0040 |
3 | HG01884.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.124-7160T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105873039 | |||||||
| chrX:105873520 | G | T | 1 | a0002c0009t0005g0210 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.124-6679G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105873520 | |||||||
| chrX:105873539 | A | G | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0006g0176 |
3 | HG01069.hp1 HG01071.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.124-6660A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105873539 | |||||||
| chrX:105873619 | C | T | 6 | a0001c0001t0001g0005 a0001c0001t0001g0081 a0001c0001t0001g0100 others(3): Show |
7 | HG00609.hp1 HG02135.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.124-6580C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105873619 | |||||||
| chrX:105873799 | A | G | 3 | a0002c0002t0002g0061 a0002c0002t0002g0062 a0002c0002t0002g0063 |
3 | HG02486.hp1 HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.124-6400A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105873799 | |||||||
| chrX:105873870 | G | A | 1 | a0002c0002t0002g0065 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.124-6329G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105873870 | |||||||
| chrX:105874291 | A | C | 1 | a0002c0002t0002g0064 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.124-5908A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105874291 | |||||||
| chrX:105874466 | C | G | 37 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(34): Show |
37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.124-5733C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105874466 | |||||||
| chrX:105874478 | A | C | 3 | a0002c0002t0005g0120 a0002c0002t0010g0119 a0009c0010t0005g0090 |
3 | HG02717.hp1 HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.124-5721A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105874478 | |||||||
| chrX:105874690 | A | G | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.124-5509A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105874690 | |||||||
| chrX:105875650 | A | T | 1 | a0002c0002t0005g0120 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.124-4549A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105875650 | |||||||
| chrX:105875816 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.124-4383T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105875816 | |||||||
| chrX:105876225 | TAAC | T | 37 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(34): Show |
37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.124-3971_124-3969d others(5): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105876225 | ||||||
| chrX:105876310 | A | G | 1 | a0002c0002t0002g0047 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.124-3889A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105876310 | |||||||
| chrX:105876746 | T | G | 1 | a0001c0001t0001g0123 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.124-3453T>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105876746 | |||||||
| chrX:105876763 | T | G | 1 | a0001c0001t0004g0095 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.124-3436T>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105876763 | |||||||
| chrX:105876902 | T | C | 1 | a0003c0003t0003g0035 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.124-3297T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105876902 | |||||||
| chrX:105877453 | A | C | 2 | a0001c0001t0001g0101 a0001c0001t0001g0150 |
2 | NA18965.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.124-2746A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105877453 | |||||||
| chrX:105877638 | A | G | 11 | a0003c0003t0003g0009 a0003c0003t0003g0021 a0003c0003t0003g0022 others(8): Show |
11 | HG02451.hp1 HG02630.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.124-2561A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105877638 | |||||||
| chrX:105877833 | AG | A | 40 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(37): Show |
42 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.124-2363delG | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chrX | 105877833 | ||||||
| chrX:105878091 | A | T | 1 | a0002c0002t0002g0074 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.124-2108A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105878091 | |||||||
| chrX:105878329 | G | A | 20 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0044 others(17): Show |
22 | HG00673.hp1 HG00738.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.124-1870G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105878329 | |||||||
| chrX:105878497 | T | A | 1 | a0004c0004t0003g0012 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.124-1702T>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105878497 | |||||||
| chrX:105878550 | G | T | 1 | a0002c0002t0008g0179 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.124-1649G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105878550 | |||||||
| chrX:105878570 | C | G | 3 | a0003c0003t0003g0010 a0003c0003t0003g0020 a0003c0003t0003g0023 |
3 | HG01109.hp1 HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.124-1629C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105878570 | |||||||
| chrX:105878642 | G | A | 2 | a0002c0002t0005g0208 a0002c0002t0005g0209 |
2 | HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.124-1557G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105878642 | |||||||
| chrX:105878677 | A | G | 1 | a0002c0002t0002g0067 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.124-1522A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105878677 | |||||||
| chrX:105878997 | G | A | 8 | a0004c0004t0003g0011 a0004c0004t0003g0012 a0004c0004t0003g0013 others(5): Show |
8 | HG01243.hp1 HG01891.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.124-1202G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105878997 | |||||||
| chrX:105879108 | G | A | 85 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(82): Show |
87 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.124-1091G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105879108 | |||||||
| chrX:105879139 | G | A | 5 | a0001c0001t0001g0175 a0002c0002t0005g0208 a0002c0002t0005g0209 others(2): Show |
5 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-1060G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105879139 | |||||||
| chrX:105879435 | A | G | 3 | a0002c0002t0005g0201 a0002c0002t0005g0203 a0002c0002t0009g0204 |
3 | HG02451.hp2 NA18612.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.124-764A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 2/28 | chrX | 105879435 | |||||||
| chrX:105880283 | T | C | 37 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(34): Show |
37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.180+28T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 3/28 | chrX | 105880283 | |||||||
| chrX:105880304 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.180+49C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 3/28 | chrX | 105880304 | |||||||
| chrX:105880854 | C | T | 1 | a0002c0002t0002g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.180+599C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 3/28 | chrX | 105880854 | |||||||
| chrX:105881919 | A | G | 4 | a0001c0001t0001g0081 a0001c0001t0001g0100 a0001c0001t0001g0102 others(1): Show |
4 | HG02135.hp1 NA18984.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.252+140A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105881919 | |||||||
| chrX:105882519 | T | G | 1 | a0003c0003t0003g0036 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.252+740T>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105882519 | |||||||
| chrX:105882751 | A | G | 1 | a0001c0005t0001g0004 | 2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.252+972A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105882751 | |||||||
| chrX:105883065 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.252+1286A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105883065 | |||||||
| chrX:105883216 | G | A | 6 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0135 others(3): Show |
6 | NA18971.hp1 NA18986.hp1 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.252+1437G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105883216 | |||||||
| chrX:105884042 | C | G | 9 | a0002c0002t0002g0044 a0002c0002t0002g0065 a0002c0002t0002g0067 others(6): Show |
9 | HG00673.hp1 HG02071.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.252+2263C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105884042 | |||||||
| chrX:105884353 | C | T | 1 | a0002c0002t0005g0208 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.252+2574C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105884353 | |||||||
| chrX:105884745 | G | A | 37 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(34): Show |
37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.252+2966G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105884745 | |||||||
| chrX:105884860 | G | A | 1 | a0008c0006t0001g0114 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.252+3081G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105884860 | |||||||
| chrX:105884894 | G | A | 2 | a0003c0003t0003g0021 a0003c0003t0003g0026 |
2 | HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.252+3115G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105884894 | |||||||
| chrX:105884974 | A | G | 37 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(34): Show |
37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.252+3195A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105884974 | |||||||
| chrX:105885470 | TGTC | T | 2 | a0003c0003t0003g0021 a0003c0003t0003g0026 |
2 | HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.253-2823_253-2821d others(5): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105885470 | |||||||
| chrX:105885998 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.253-2296A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105885998 | |||||||
| chrX:105886044 | ACATCACA others(4): Show |
A | 1 | a0008c0006t0001g0114 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.253-2248_253-2238d others(13): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chrX | 105886044 | ||||||
| chrX:105886051 | A | T | 1 | a0001c0001t0001g0128 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.253-2243A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105886051 | |||||||
| chrX:105886489 | TTA | T | 11 | a0003c0003t0003g0009 a0003c0003t0003g0021 a0003c0003t0003g0022 others(8): Show |
11 | HG02451.hp1 HG02630.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.253-1797_253-1796d others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chrX | 105886489 | ||||||
| chrX:105886526 | G | A | 5 | a0001c0001t0001g0093 a0001c0001t0001g0121 a0001c0001t0001g0134 others(2): Show |
5 | HG02080.hp2 HG02083.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.253-1768G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105886526 | |||||||
| chrX:105886683 | A | G | 1 | a0002c0002t0008g0179 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.253-1611A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105886683 | |||||||
| chrX:105886832 | A | G | 1 | a0001c0001t0001g0207 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.253-1462A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105886832 | |||||||
| chrX:105886940 | A | G | 3 | a0002c0002t0005g0201 a0002c0002t0005g0203 a0002c0002t0009g0204 |
3 | HG02451.hp2 NA18612.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.253-1354A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105886940 | |||||||
| chrX:105887178 | G | C | 1 | a0002c0002t0002g0002 | 2 | NA18939.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.253-1116G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105887178 | |||||||
| chrX:105887955 | T | C | 2 | a0002c0002t0002g0054 a0002c0002t0002g0055 |
2 | HG02683.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.253-339T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105887955 | |||||||
| chrX:105888083 | C | T | 2 | a0001c0001t0001g0123 a0001c0001t0004g0096 |
2 | HG02040.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.253-211C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105888083 | |||||||
| chrX:105888149 | C | A | 81 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(78): Show |
83 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.253-145C>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105888149 | |||||||
| chrX:105888232 | T | C | 3 | a0001c0001t0004g0192 a0001c0001t0004g0196 a0001c0001t0004g0197 |
3 | HG00280.hp1 HG01358.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.253-62T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 4/28 | chrX | 105888232 | |||||||
| chrX:105888694 | C | T | 1 | a0002c0002t0005g0205 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.378+275C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105888694 | |||||||
| chrX:105888695 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.378+276G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105888695 | |||||||
| chrX:105888724 | G | A | 21 | a0003c0003t0003g0009 a0003c0003t0003g0010 a0003c0003t0003g0020 others(18): Show |
21 | HG01109.hp1 HG01884.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.378+305G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105888724 | |||||||
| chrX:105888831 | C | T | 4 | a0002c0002t0005g0208 a0002c0002t0005g0209 a0002c0002t0005g0211 others(1): Show |
4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.378+412C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105888831 | |||||||
| chrX:105888832 | G | A | 3 | a0003c0003t0003g0032 a0003c0003t0003g0033 a0003c0003t0003g0035 |
3 | HG02109.hp2 HG02258.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.378+413G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105888832 | |||||||
| chrX:105888835 | C | T | 1 | a0003c0003t0003g0006 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.378+416C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105888835 | |||||||
| chrX:105889115 | G | A | 3 | a0001c0001t0001g0103 a0001c0001t0001g0138 a0001c0001t0001g0139 |
3 | HG03492.hp1 HG03927.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.378+696G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105889115 | |||||||
| chrX:105889345 | C | G | 81 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(78): Show |
83 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.378+926C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105889345 | |||||||
| chrX:105889570 | T | C | 85 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(82): Show |
87 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.378+1151T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105889570 | |||||||
| chrX:105889594 | T | C | 3 | a0003c0003t0003g0032 a0003c0003t0003g0033 a0003c0003t0003g0035 |
3 | HG02109.hp2 HG02258.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.378+1175T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105889594 | |||||||
| chrX:105889611 | C | G | 1 | a0001c0001t0001g0103 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.378+1192C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105889611 | |||||||
| chrX:105890323 | A | C | 2 | a0002c0002t0005g0208 a0002c0002t0005g0209 |
2 | HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.378+1904A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105890323 | |||||||
| chrX:105890913 | G | T | 1 | a0003c0003t0003g0006 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.378+2494G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105890913 | |||||||
| chrX:105891085 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.378+2666G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105891085 | |||||||
| chrX:105891086 | C | A | 1 | a0001c0001t0001g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.378+2667C>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105891086 | |||||||
| chrX:105891904 | G | A | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0006g0176 |
3 | HG01069.hp1 HG01071.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.379-1928G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105891904 | |||||||
| chrX:105892195 | A | C | 1 | a0008c0006t0001g0114 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.379-1637A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105892195 | |||||||
| chrX:105892551 | A | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0081 a0001c0001t0001g0100 others(3): Show |
7 | HG00609.hp1 HG02135.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.379-1281A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105892551 | |||||||
| chrX:105892732 | T | C | 4 | a0002c0002t0002g0049 a0002c0002t0002g0050 a0002c0002t0002g0051 others(1): Show |
4 | HG00735.hp1 HG01071.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.379-1100T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105892732 | |||||||
| chrX:105892745 | G | A | 2 | a0002c0002t0005g0211 a0002c0009t0005g0210 |
2 | HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.379-1087G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105892745 | |||||||
| chrX:105892797 | C | T | 1 | a0002c0002t0008g0179 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.379-1035C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105892797 | |||||||
| chrX:105893221 | A | G | 1 | a0001c0001t0001g0177 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.379-611A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105893221 | |||||||
| chrX:105893246 | C | G | 1 | a0002c0002t0005g0203 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.379-586C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105893246 | |||||||
| chrX:105893261 | C | A | 1 | a0001c0001t0001g0202 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.379-571C>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105893261 | |||||||
| chrX:105893693 | A | C | 1 | a0002c0002t0008g0179 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.379-139A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 5/28 | chrX | 105893693 | |||||||
| chrX:105894114 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.489+172C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 6/28 | chrX | 105894114 | |||||||
| chrX:105894228 | T | C | 2 | a0004c0004t0003g0017 a0004c0004t0003g0018 |
2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.489+286T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 6/28 | chrX | 105894228 | |||||||
| chrX:105894314 | G | A | 3 | a0001c0001t0001g0101 a0001c0001t0001g0126 a0001c0001t0001g0150 |
3 | NA18965.hp1 NA19063.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.489+372G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 6/28 | chrX | 105894314 | |||||||
| chrX:105894502 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.489+560A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 6/28 | chrX | 105894502 | |||||||
| chrX:105894579 | G | A | 3 | a0002c0002t0005g0201 a0002c0002t0005g0203 a0002c0002t0009g0204 |
3 | HG02451.hp2 NA18612.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.489+637G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 6/28 | chrX | 105894579 | |||||||
| chrX:105894835 | G | C | 1 | a0001c0001t0001g0206 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.490-598G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 6/28 | chrX | 105894835 | |||||||
| chrX:105894946 | G | A | 1 | a0002c0002t0008g0179 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.490-487G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 6/28 | chrX | 105894946 | |||||||
| chrX:105894960 | C | A | 3 | a0003c0003t0003g0032 a0003c0003t0003g0033 a0003c0003t0003g0035 |
3 | HG02109.hp2 HG02258.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.490-473C>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 6/28 | chrX | 105894960 | |||||||
| chrX:105895363 | C | CAGAA | 12 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0104 others(9): Show |
12 | HG01069.hp1 HG01071.hp1 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.490-40_490-37dupGA others(2): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chrX | 105895363 | ||||||
| chrX:105895363 | C | CAGAAAGA others(1): Show |
2 | a0001c0001t0001g0177 a0002c0002t0009g0204 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.490-44_490-37dupGA others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chrX | 105895363 | ||||||
| chrX:105895363 | CAGAA | C | 37 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(34): Show |
37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.490-40_490-37delGA others(2): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chrX | 105895363 | ||||||
| chrX:105895363 | CAGAAAGA others(5): Show |
C | 4 | a0002c0002t0005g0208 a0002c0002t0005g0209 a0002c0002t0005g0211 others(1): Show |
4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-48_490-37delGA others(10): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chrX | 105895363 | ||||||
| chrX:105896248 | A | C | 1 | a0006c0007t0003g0014 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.580+725A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 7/28 | chrX | 105896248 | |||||||
| chrX:105896434 | G | A | 1 | a0002c0002t0008g0179 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.580+911G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 7/28 | chrX | 105896434 | |||||||
| chrX:105896447 | A | G | 1 | a0001c0001t0004g0189 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.580+924A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 7/28 | chrX | 105896447 | |||||||
| chrX:105896924 | ATAGT | A | 4 | a0002c0002t0005g0208 a0002c0002t0005g0209 a0002c0002t0005g0211 others(1): Show |
4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.580+1404_580+1407d others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chrX | 105896924 | ||||||
| chrX:105897068 | A | C | 3 | a0002c0002t0005g0201 a0002c0002t0005g0203 a0002c0002t0009g0204 |
3 | HG02451.hp2 NA18612.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.581-1516A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 7/28 | chrX | 105897068 | |||||||
| chrX:105897243 | C | A | 1 | a0001c0001t0001g0155 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.581-1341C>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 7/28 | chrX | 105897243 | |||||||
| chrX:105897410 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.581-1174C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 7/28 | chrX | 105897410 | |||||||
| chrX:105897518 | T | G | 3 | a0002c0002t0005g0201 a0002c0002t0005g0203 a0002c0002t0009g0204 |
3 | HG02451.hp2 NA18612.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.581-1066T>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 7/28 | chrX | 105897518 | |||||||
| chrX:105897755 | G | A | 3 | a0002c0002t0005g0201 a0002c0002t0005g0203 a0002c0002t0009g0204 |
3 | HG02451.hp2 NA18612.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.581-829G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 7/28 | chrX | 105897755 | |||||||
| chrX:105898024 | G | T | 2 | a0002c0002t0005g0208 a0002c0002t0005g0209 |
2 | HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.581-560G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 7/28 | chrX | 105898024 | |||||||
| chrX:105898500 | G | T | 1 | a0002c0002t0002g0068 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.581-84G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 7/28 | chrX | 105898500 | |||||||
| chrX:105898521 | G | A | 2 | a0002c0002t0005g0208 a0002c0002t0005g0209 |
2 | HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.581-63G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 7/28 | chrX | 105898521 | |||||||
| chrX:105898915 | G | A | 43 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(40): Show |
45 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.711+201G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 8/28 | chrX | 105898915 | |||||||
| chrX:105899005 | A | C | 4 | a0001c0001t0001g0093 a0001c0001t0001g0134 a0001c0001t0001g0173 others(1): Show |
4 | HG02080.hp2 HG02083.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.711+291A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 8/28 | chrX | 105899005 | |||||||
| chrX:105899038 | G | A | 2 | a0001c0001t0001g0080 a0001c0001t0001g0169 |
2 | HG02683.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.711+324G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 8/28 | chrX | 105899038 | |||||||
| chrX:105899646 | T | C | 1 | a0001c0001t0004g0096 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.711+932T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 8/28 | chrX | 105899646 | |||||||
| chrX:105899827 | G | T | 3 | a0002c0002t0005g0120 a0002c0002t0010g0119 a0009c0010t0005g0090 |
3 | HG02717.hp1 HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.712-791G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 8/28 | chrX | 105899827 | |||||||
| chrX:105899832 | G | C | 1 | a0001c0001t0001g0148 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.712-786G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 8/28 | chrX | 105899832 | |||||||
| chrX:105899957 | G | A | 1 | a0003c0003t0003g0006 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.712-661G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 8/28 | chrX | 105899957 | |||||||
| chrX:105900151 | T | TAC | 32 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0100 others(29): Show |
34 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.712-425_712-424dup others(2): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chrX | 105900151 | ||||||
| chrX:105900151 | T | TACAC | 7 | a0001c0001t0001g0080 a0002c0002t0002g0044 a0002c0002t0002g0046 others(4): Show |
7 | HG00673.hp1 HG00733.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.712-427_712-424dup others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chrX | 105900151 | ||||||
| chrX:105900151 | T | TACACAC | 4 | a0001c0001t0001g0188 a0002c0002t0002g0075 a0002c0002t0005g0120 others(1): Show |
4 | HG02976.hp2 HG03130.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.712-429_712-424dup others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chrX | 105900151 | ||||||
| chrX:105900151 | TAC | T | 17 | a0001c0001t0001g0093 a0001c0001t0001g0105 a0001c0001t0001g0117 others(14): Show |
17 | HG01071.hp2 HG02080.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.712-425_712-424del others(2): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chrX | 105900151 | ||||||
| chrX:105900151 | TACAC | T | 10 | a0001c0001t0001g0101 a0001c0001t0001g0152 a0001c0001t0001g0165 others(7): Show |
10 | HG01074.hp1 HG02451.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.712-427_712-424del others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chrX | 105900151 | ||||||
| chrX:105900151 | TACACAC | T | 3 | a0001c0001t0001g0157 a0001c0001t0001g0163 a0002c0009t0005g0210 |
3 | HG02809.hp2 HG04204.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.712-429_712-424del others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chrX | 105900151 | ||||||
| chrX:105900151 | TACACACA others(3): Show |
T | 15 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(12): Show |
15 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.712-433_712-424del others(10): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chrX | 105900151 | ||||||
| chrX:105900151 | TACACACA others(5): Show |
T | 21 | a0003c0003t0003g0009 a0003c0003t0003g0010 a0003c0003t0003g0020 others(18): Show |
21 | HG01109.hp1 HG01884.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.712-435_712-424del others(12): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chrX | 105900151 | ||||||
| chrX:105900747 | C | T | 8 | a0004c0004t0003g0011 a0004c0004t0003g0012 a0004c0004t0003g0013 others(5): Show |
8 | HG01243.hp1 HG01891.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.766+75C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 9/28 | chrX | 105900747 | |||||||
| chrX:105900823 | G | A | 4 | a0002c0002t0005g0208 a0002c0002t0005g0209 a0002c0002t0005g0211 others(1): Show |
4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.766+151G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 9/28 | chrX | 105900823 | |||||||
| chrX:105900913 | A | G | 3 | a0002c0002t0005g0201 a0002c0002t0005g0203 a0002c0002t0009g0204 |
3 | HG02451.hp2 NA18612.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.766+241A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 9/28 | chrX | 105900913 | |||||||
| chrX:105901011 | G | A | 85 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(82): Show |
87 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.766+339G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 9/28 | chrX | 105901011 | |||||||
| chrX:105901795 | A | C | 1 | a0001c0001t0001g0169 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.766+1123A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 9/28 | chrX | 105901795 | |||||||
| chrX:105901966 | T | C | 2 | a0002c0002t0005g0208 a0002c0002t0005g0209 |
2 | HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.766+1294T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 9/28 | chrX | 105901966 | |||||||
| chrX:105902355 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.766+1683C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 9/28 | chrX | 105902355 | |||||||
| chrX:105902444 | G | A | 1 | a0002c0002t0002g0064 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.766+1772G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 9/28 | chrX | 105902444 | |||||||
| chrX:105902559 | C | A | 1 | a0009c0010t0005g0090 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.766+1887C>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 9/28 | chrX | 105902559 | |||||||
| chrX:105903073 | A | G | 1 | a0002c0002t0005g0120 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.767-2192A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 9/28 | chrX | 105903073 | |||||||
| chrX:105903562 | C | G | 1 | a0002c0002t0008g0179 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.767-1703C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 9/28 | chrX | 105903562 | |||||||
| chrX:105903700 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.767-1565T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 9/28 | chrX | 105903700 | |||||||
| chrX:105903841 | C | T | 4 | a0002c0002t0005g0208 a0002c0002t0005g0209 a0002c0002t0005g0211 others(1): Show |
4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.767-1424C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 9/28 | chrX | 105903841 | |||||||
| chrX:105903880 | G | T | 37 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(34): Show |
37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.767-1385G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 9/28 | chrX | 105903880 | |||||||
| chrX:105904766 | G | T | 1 | a0002c0002t0002g0044 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.767-499G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 9/28 | chrX | 105904766 | |||||||
| chrX:105904823 | G | C | 40 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(37): Show |
42 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.767-442G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 9/28 | chrX | 105904823 | |||||||
| chrX:105905247 | A | G | 1 | a0001c0001t0001g0146 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.767-18A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 9/28 | chrX | 105905247 | |||||||
| chrX:105905755 | T | A | 4 | a0002c0002t0005g0208 a0002c0002t0005g0209 a0002c0002t0005g0211 others(1): Show |
4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.845+412T>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 10/28 | chrX | 105905755 | |||||||
| chrX:105906764 | C | CGT | 19 | a0001c0001t0001g0041 a0001c0001t0001g0081 a0001c0001t0001g0100 others(16): Show |
19 | HG00735.hp2 HG01981.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.1021+218_1021+219d others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chrX | 105906764 | ||||||
| chrX:105906764 | C | CGTGT | 14 | a0002c0002t0002g0002 a0002c0002t0002g0045 a0002c0002t0002g0049 others(11): Show |
15 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1021+216_1021+219d others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chrX | 105906764 | ||||||
| chrX:105906764 | C | CGTGTGT | 14 | a0001c0001t0001g0102 a0001c0001t0001g0191 a0002c0002t0002g0003 others(11): Show |
15 | HG01099.hp1 HG01168.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1021+214_1021+219d others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chrX | 105906764 | ||||||
| chrX:105906764 | C | CGTGTGTG others(1): Show |
8 | a0001c0001t0001g0152 a0002c0002t0002g0043 a0002c0002t0002g0046 others(5): Show |
8 | HG00733.hp1 HG01361.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1021+212_1021+219d others(10): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chrX | 105906764 | ||||||
| chrX:105906764 | C | CGTGTGTG others(3): Show |
1 | a0002c0002t0002g0056 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1021+210_1021+219d others(12): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chrX | 105906764 | ||||||
| chrX:105906764 | C | CGTGTGTG others(5): Show |
1 | a0002c0002t0002g0060 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1021+208_1021+219d others(14): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chrX | 105906764 | ||||||
| chrX:105906764 | CGT | C | 25 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0124 others(22): Show |
25 | HG00280.hp1 HG01358.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.1021+218_1021+219d others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chrX | 105906764 | ||||||
| chrX:105906764 | CGTGT | C | 17 | a0001c0001t0001g0140 a0001c0001t0001g0184 a0002c0002t0002g0044 others(14): Show |
17 | HG00673.hp1 HG01243.hp1 HG02071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1021+216_1021+219d others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chrX | 105906764 | ||||||
| chrX:105906764 | CGTGTGT | C | 30 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0082 others(27): Show |
33 | HG00621.hp1 HG00642.hp1 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.1021+214_1021+219d others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chrX | 105906764 | ||||||
| chrX:105906764 | CGTGTGTG others(1): Show |
C | 23 | a0001c0001t0001g0133 a0001c0001t0001g0158 a0001c0001t0001g0160 others(20): Show |
23 | HG01109.hp1 HG01884.hp2 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.1021+212_1021+219d others(10): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chrX | 105906764 | ||||||
| chrX:105907040 | G | A | 1 | a0002c0002t0008g0179 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1021+451G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 11/28 | chrX | 105907040 | |||||||
| chrX:105907109 | A | G | 1 | a0002c0002t0002g0061 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1021+520A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 11/28 | chrX | 105907109 | |||||||
| chrX:105907352 | G | A | 1 | a0003c0003t0003g0027 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1021+763G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 11/28 | chrX | 105907352 | |||||||
| chrX:105907672 | C | T | 24 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0044 others(21): Show |
26 | HG00673.hp1 HG00735.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.1022-568C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 11/28 | chrX | 105907672 | |||||||
| chrX:105907942 | T | TCATTCTC others(9): Show |
1 | a0001c0001t0001g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1022-290_1022-275d others(18): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chrX | 105907942 | ||||||
| chrX:105908114 | G | A | 1 | a0002c0002t0002g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1022-126G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 11/28 | chrX | 105908114 | |||||||
| chrX:105908369 | C | T | 2 | a0002c0002t0005g0201 a0002c0002t0005g0203 |
2 | NA18612.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.1085+66C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 12/28 | chrX | 105908369 | |||||||
| chrX:105910171 | A | G | 16 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(13): Show |
16 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.2241+289A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 13/28 | chrX | 105910171 | |||||||
| chrX:105910516 | C | T | 81 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(78): Show |
83 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.2241+634C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 13/28 | chrX | 105910516 | |||||||
| chrX:105910529 | C | T | 1 | a0005c0013t0001g0147 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2241+647C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 13/28 | chrX | 105910529 | |||||||
| chrX:105910782 | T | G | 1 | a0001c0001t0001g0082 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2241+900T>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 13/28 | chrX | 105910782 | |||||||
| chrX:105911288 | C | A | 1 | a0003c0003t0003g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2242-1360C>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 13/28 | chrX | 105911288 | |||||||
| chrX:105911407 | T | A | 1 | a0002c0002t0002g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2242-1241T>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 13/28 | chrX | 105911407 | |||||||
| chrX:105911796 | A | G | 1 | a0001c0001t0001g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2242-852A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 13/28 | chrX | 105911796 | |||||||
| chrX:105911836 | G | A | 1 | a0001c0001t0004g0096 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2242-812G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 13/28 | chrX | 105911836 | |||||||
| chrX:105911849 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2242-799G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 13/28 | chrX | 105911849 | |||||||
| chrX:105911882 | C | T | 37 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(34): Show |
37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.2242-766C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 13/28 | chrX | 105911882 | |||||||
| chrX:105911884 | A | G | 3 | a0003c0003t0003g0032 a0003c0003t0003g0033 a0003c0003t0003g0035 |
3 | HG02109.hp2 HG02258.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.2242-764A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 13/28 | chrX | 105911884 | |||||||
| chrX:105912506 | A | G | 7 | a0003c0003t0003g0028 a0003c0003t0003g0029 a0003c0003t0003g0036 others(4): Show |
7 | HG01884.hp2 HG02572.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2242-142A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 13/28 | chrX | 105912506 | |||||||
| chrX:105912539 | A | G | 1 | a0002c0002t0005g0201 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2242-109A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 13/28 | chrX | 105912539 | |||||||
| chrX:105912976 | A | C | 4 | a0002c0002t0005g0208 a0002c0002t0005g0209 a0002c0002t0005g0211 others(1): Show |
4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2349+221A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 14/28 | chrX | 105912976 | |||||||
| chrX:105913171 | A | T | 1 | a0001c0001t0001g0134 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2349+416A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 14/28 | chrX | 105913171 | |||||||
| chrX:105913328 | T | C | 2 | a0001c0001t0001g0106 a0001c0001t0001g0124 |
2 | HG01952.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.2349+573T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 14/28 | chrX | 105913328 | |||||||
| chrX:105913663 | G | A | 11 | a0002c0002t0002g0043 a0002c0002t0002g0046 a0002c0002t0002g0047 others(8): Show |
11 | HG00733.hp1 HG01192.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.2349+908G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 14/28 | chrX | 105913663 | |||||||
| chrX:105913731 | A | G | 43 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(40): Show |
45 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.2349+976A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 14/28 | chrX | 105913731 | |||||||
| chrX:105913937 | T | G | 1 | a0002c0002t0002g0063 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2349+1182T>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 14/28 | chrX | 105913937 | |||||||
| chrX:105914292 | T | A | 85 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(82): Show |
87 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.2350-1438T>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 14/28 | chrX | 105914292 | |||||||
| chrX:105914377 | G | T | 1 | a0001c0001t0001g0132 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2350-1353G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 14/28 | chrX | 105914377 | |||||||
| chrX:105914510 | A | G | 21 | a0003c0003t0003g0009 a0003c0003t0003g0010 a0003c0003t0003g0020 others(18): Show |
21 | HG01109.hp1 HG01884.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.2350-1220A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 14/28 | chrX | 105914510 | |||||||
| chrX:105914714 | G | A | 2 | a0001c0001t0001g0123 a0002c0002t0009g0204 |
2 | HG02040.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2350-1016G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 14/28 | chrX | 105914714 | |||||||
| chrX:105914726 | G | A | 1 | a0001c0001t0004g0118 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2350-1004G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 14/28 | chrX | 105914726 | |||||||
| chrX:105914751 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2350-979G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 14/28 | chrX | 105914751 | |||||||
| chrX:105915544 | A | G | 1 | a0001c0001t0001g0122 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2350-186A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 14/28 | chrX | 105915544 | |||||||
| chrX:105916328 | A | G | 1 | a0001c0001t0004g0200 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2417+531A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 15/28 | chrX | 105916328 | |||||||
| chrX:105916381 | A | G | 1 | a0002c0002t0008g0179 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2417+584A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 15/28 | chrX | 105916381 | |||||||
| chrX:105916423 | T | A | 107 | a0001c0001t0004g0086 a0001c0001t0004g0087 a0001c0001t0004g0091 others(104): Show |
109 | HG00140.hp1 HG00280.hp1 HG00673.hp1 others(106): Show |
intron_variant | MODIFIER | c.2417+626T>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 15/28 | chrX | 105916423 | |||||||
| chrX:105916589 | A | G | 1 | a0003c0003t0003g0025 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2417+792A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 15/28 | chrX | 105916589 | |||||||
| chrX:105916662 | C | T | 37 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(34): Show |
37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.2417+865C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 15/28 | chrX | 105916662 | |||||||
| chrX:105916702 | T | C | 43 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(40): Show |
45 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.2418-876T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 15/28 | chrX | 105916702 | |||||||
| chrX:105916879 | T | A | 4 | a0001c0001t0001g0081 a0001c0001t0001g0100 a0001c0001t0001g0102 others(1): Show |
4 | HG02135.hp1 NA18984.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.2418-699T>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 15/28 | chrX | 105916879 | |||||||
| chrX:105916930 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2418-648C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 15/28 | chrX | 105916930 | |||||||
| chrX:105917042 | C | T | 2 | a0001c0001t0004g0199 a0001c0001t0004g0200 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2418-536C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 15/28 | chrX | 105917042 | |||||||
| chrX:105917145 | C | T | 21 | a0003c0003t0003g0009 a0003c0003t0003g0010 a0003c0003t0003g0020 others(18): Show |
21 | HG01109.hp1 HG01884.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.2418-433C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 15/28 | chrX | 105917145 | |||||||
| chrX:105917181 | A | G | 3 | a0001c0001t0001g0101 a0001c0001t0001g0126 a0001c0001t0001g0150 |
3 | NA18965.hp1 NA19063.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.2418-397A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 15/28 | chrX | 105917181 | |||||||
| chrX:105917188 | A | T | 43 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(40): Show |
45 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.2418-390A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 15/28 | chrX | 105917188 | |||||||
| chrX:105917986 | T | C | 1 | a0002c0002t0002g0064 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2512+314T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105917986 | |||||||
| chrX:105918780 | C | G | 2 | a0001c0001t0001g0107 a0001c0001t0001g0110 |
2 | HG02129.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.2512+1108C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105918780 | |||||||
| chrX:105918889 | TG | T | 3 | a0002c0002t0005g0201 a0002c0002t0005g0203 a0002c0002t0009g0204 |
3 | HG02451.hp2 NA18612.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.2512+1219delG | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | INFO_REALIGN_3_PRIME | chrX | 105918889 | ||||||
| chrX:105919002 | G | GA | 10 | a0001c0001t0001g0041 a0001c0001t0001g0082 a0001c0001t0001g0132 others(7): Show |
10 | HG01978.hp2 HG01981.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2512+1352dupA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | INFO_REALIGN_3_PRIME | chrX | 105919002 | ||||||
| chrX:105919002 | GA | G | 75 | a0001c0001t0001g0104 a0001c0001t0001g0165 a0001c0001t0001g0183 others(72): Show |
76 | HG00673.hp1 HG00733.hp1 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.2512+1352delA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | INFO_REALIGN_3_PRIME | chrX | 105919002 | ||||||
| chrX:105919002 | GAA | G | 7 | a0002c0002t0002g0002 a0002c0002t0002g0061 a0002c0002t0002g0062 others(4): Show |
8 | HG01515.hp1 HG02486.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2512+1351_2512+135 others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | INFO_REALIGN_3_PRIME | chrX | 105919002 | ||||||
| chrX:105919055 | A | G | 16 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(13): Show |
16 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.2512+1383A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105919055 | |||||||
| chrX:105919385 | A | G | 43 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(40): Show |
45 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.2512+1713A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105919385 | |||||||
| chrX:105919392 | A | G | 4 | a0002c0002t0005g0208 a0002c0002t0005g0209 a0002c0002t0005g0211 others(1): Show |
4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2512+1720A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105919392 | |||||||
| chrX:105919446 | C | T | 1 | a0002c0002t0005g0120 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2512+1774C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105919446 | |||||||
| chrX:105919458 | A | C | 1 | a0002c0002t0002g0043 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2512+1786A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105919458 | |||||||
| chrX:105919536 | A | G | 32 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0082 others(29): Show |
34 | HG00621.hp1 HG00642.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.2512+1864A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105919536 | |||||||
| chrX:105920231 | C | G | 4 | a0002c0002t0005g0208 a0002c0002t0005g0209 a0002c0002t0005g0211 others(1): Show |
4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2513-1733C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105920231 | |||||||
| chrX:105920260 | T | C | 37 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(34): Show |
37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.2513-1704T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105920260 | |||||||
| chrX:105920272 | T | C | 1 | a0001c0005t0001g0004 | 2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2513-1692T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105920272 | |||||||
| chrX:105920318 | G | C | 37 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(34): Show |
37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.2513-1646G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105920318 | |||||||
| chrX:105920589 | C | A | 2 | a0003c0003t0003g0039 a0003c0003t0003g0040 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2513-1375C>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105920589 | |||||||
| chrX:105920666 | C | T | 4 | a0002c0002t0005g0208 a0002c0002t0005g0209 a0002c0002t0005g0211 others(1): Show |
4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2513-1298C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105920666 | |||||||
| chrX:105920786 | A | G | 1 | a0001c0001t0001g0165 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2513-1178A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105920786 | |||||||
| chrX:105920875 | T | C | 16 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(13): Show |
16 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.2513-1089T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105920875 | |||||||
| chrX:105920924 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2513-1040G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105920924 | |||||||
| chrX:105920981 | G | C | 1 | a0001c0001t0001g0153 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2513-983G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105920981 | |||||||
| chrX:105921095 | T | C | 1 | a0002c0002t0002g0067 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2513-869T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105921095 | |||||||
| chrX:105921098 | T | C | 1 | a0002c0002t0002g0079 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2513-866T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105921098 | |||||||
| chrX:105921105 | G | C | 1 | a0002c0002t0008g0179 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2513-859G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105921105 | |||||||
| chrX:105921398 | G | C | 21 | a0003c0003t0003g0009 a0003c0003t0003g0010 a0003c0003t0003g0020 others(18): Show |
21 | HG01109.hp1 HG01884.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.2513-566G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105921398 | |||||||
| chrX:105921404 | T | C | 37 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(34): Show |
37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.2513-560T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105921404 | |||||||
| chrX:105921405 | G | A | 37 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(34): Show |
37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.2513-559G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105921405 | |||||||
| chrX:105921520 | A | G | 4 | a0002c0002t0002g0049 a0002c0002t0002g0050 a0002c0002t0002g0051 others(1): Show |
4 | HG00735.hp1 HG01071.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.2513-444A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105921520 | |||||||
| chrX:105921564 | G | A | 1 | a0003c0003t0003g0213 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2513-400G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105921564 | |||||||
| chrX:105921855 | C | CA | 36 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(33): Show |
36 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.2513-107dupA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | INFO_REALIGN_3_PRIME | chrX | 105921855 | ||||||
| chrX:105921858 | G | A | 81 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(78): Show |
83 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.2513-106G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 16/28 | chrX | 105921858 | |||||||
| chrX:105922147 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2610+86G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 17/28 | chrX | 105922147 | |||||||
| chrX:105922150 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2610+89A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 17/28 | chrX | 105922150 | |||||||
| chrX:105922152 | G | T | 1 | a0001c0001t0001g0104 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2610+91G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 17/28 | chrX | 105922152 | |||||||
| chrX:105922560 | A | C | 1 | a0001c0001t0001g0150 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2610+499A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 17/28 | chrX | 105922560 | |||||||
| chrX:105922803 | C | G | 2 | a0002c0002t0002g0044 a0002c0002t0002g0069 |
2 | HG00673.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.2611-315C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 17/28 | chrX | 105922803 | |||||||
| chrX:105923574 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2975+92G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | chrX | 105923574 | |||||||
| chrX:105923591 | T | A | 21 | a0003c0003t0003g0009 a0003c0003t0003g0010 a0003c0003t0003g0020 others(18): Show |
21 | HG01109.hp1 HG01884.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.2975+109T>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | chrX | 105923591 | |||||||
| chrX:105923634 | A | G | 1 | a0002c0002t0009g0204 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2975+152A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | chrX | 105923634 | |||||||
| chrX:105923891 | C | CTA | 15 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0088 others(12): Show |
15 | HG01168.hp2 HG02056.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.2975+443_2975+444d others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chrX | 105923891 | ||||||
| chrX:105923891 | C | CTATA | 12 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0140 others(9): Show |
12 | HG00741.hp1 HG01071.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.2975+441_2975+444d others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chrX | 105923891 | ||||||
| chrX:105923891 | C | CTATATA | 16 | a0001c0001t0001g0123 a0001c0001t0001g0170 a0001c0001t0001g0186 others(13): Show |
18 | HG00140.hp1 HG00280.hp1 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.2975+439_2975+444d others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chrX | 105923891 | ||||||
| chrX:105923891 | C | CTATATAT others(1): Show |
19 | a0002c0002t0002g0043 a0002c0002t0002g0045 a0002c0002t0002g0047 others(16): Show |
19 | HG00735.hp1 HG00738.hp1 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.2975+437_2975+444d others(10): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chrX | 105923891 | ||||||
| chrX:105923891 | C | CTATATAT others(3): Show |
4 | a0002c0002t0002g0046 a0002c0002t0002g0068 a0002c0002t0002g0077 others(1): Show |
4 | HG01884.hp1 HG02809.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.2975+435_2975+444d others(12): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chrX | 105923891 | ||||||
| chrX:105923891 | C | CTATATAT others(5): Show |
4 | a0002c0002t0002g0051 a0002c0002t0002g0059 a0002c0002t0002g0071 others(1): Show |
4 | HG03041.hp2 HG03239.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.2975+433_2975+444d others(14): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chrX | 105923891 | ||||||
| chrX:105923891 | C | CTATATAT others(9): Show |
1 | a0001c0001t0001g0153 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2975+429_2975+444d others(18): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chrX | 105923891 | ||||||
| chrX:105923891 | C | CTATATAT others(11): Show |
1 | a0002c0002t0002g0060 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2975+427_2975+444d others(20): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chrX | 105923891 | ||||||
| chrX:105923891 | CTA | C | 60 | a0001c0001t0001g0005 a0001c0001t0001g0041 a0001c0001t0001g0093 others(57): Show |
62 | HG00609.hp1 HG00735.hp2 HG01074.hp1 others(59): Show |
intron_variant | MODIFIER | c.2975+443_2975+444d others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chrX | 105923891 | ||||||
| chrX:105923891 | CTATA | C | 6 | a0001c0001t0001g0113 a0001c0001t0001g0151 a0001c0001t0001g0152 others(3): Show |
6 | HG01934.hp1 HG02300.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2975+441_2975+444d others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chrX | 105923891 | ||||||
| chrX:105923891 | CTATATA | C | 2 | a0002c0002t0005g0120 a0009c0010t0005g0090 |
2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2975+439_2975+444d others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chrX | 105923891 | ||||||
| chrX:105923907 | ATATATAT others(13): Show |
A | 1 | a0002c0002t0008g0179 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2975+427_2975+446d others(22): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chrX | 105923907 | ||||||
| chrX:105923921 | ATATATG | A | 11 | a0003c0003t0003g0006 a0003c0003t0003g0008 a0003c0003t0003g0016 others(8): Show |
11 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.2975+441_2975+446d others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chrX | 105923921 | ||||||
| chrX:105923923 | ATATG | A | 11 | a0002c0002t0002g0052 a0003c0003t0003g0010 a0003c0003t0003g0020 others(8): Show |
11 | HG01109.hp1 HG01884.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.2975+443_2975+446d others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chrX | 105923923 | ||||||
| chrX:105923925 | ATG | A | 13 | a0003c0003t0003g0007 a0003c0003t0003g0009 a0003c0003t0003g0021 others(10): Show |
13 | HG02451.hp1 HG02559.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.2975+446_2975+447d others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chrX | 105923925 | ||||||
| chrX:105923926 | T | C | 2 | a0001c0001t0001g0117 a0001c0001t0001g0165 |
2 | NA18982.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.2975+444T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | chrX | 105923926 | |||||||
| chrX:105923927 | G | A | 45 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(42): Show |
47 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.2975+445G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | chrX | 105923927 | |||||||
| chrX:105924485 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2976-210G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | chrX | 105924485 | |||||||
| chrX:105924541 | G | T | 85 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(82): Show |
87 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.2976-154G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | chrX | 105924541 | |||||||
| chrX:105924602 | G | T | 37 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(34): Show |
37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.2976-93G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 18/28 | chrX | 105924602 | |||||||
| chrX:105925566 | G | T | 1 | a0002c0002t0005g0205 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3312+535G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105925566 | |||||||
| chrX:105926068 | C | T | 2 | a0001c0001t0001g0005 a0001c0001t0001g0175 |
3 | HG00609.hp1 NA18944.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.3312+1037C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105926068 | |||||||
| chrX:105926069 | G | A | 1 | a0001c0001t0001g0145 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.3312+1038G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105926069 | |||||||
| chrX:105926202 | G | A | 44 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(41): Show |
46 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.3312+1171G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105926202 | |||||||
| chrX:105926378 | T | C | 2 | a0002c0002t0005g0208 a0002c0002t0005g0209 |
2 | HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.3312+1347T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105926378 | |||||||
| chrX:105926418 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3312+1387C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105926418 | |||||||
| chrX:105927398 | A | G | 1 | a0001c0001t0001g0121 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3312+2367A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105927398 | |||||||
| chrX:105927674 | T | C | 1 | a0002c0002t0002g0064 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3312+2643T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105927674 | |||||||
| chrX:105927786 | A | T | 43 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(40): Show |
45 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.3312+2755A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105927786 | |||||||
| chrX:105928532 | G | T | 1 | a0001c0001t0007g0116 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.3312+3501G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105928532 | |||||||
| chrX:105928852 | T | C | 1 | a0002c0002t0008g0179 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.3312+3821T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105928852 | |||||||
| chrX:105928858 | T | A | 1 | a0003c0003t0003g0034 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3312+3827T>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105928858 | |||||||
| chrX:105929394 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3312+4363A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105929394 | |||||||
| chrX:105929542 | CTG | C | 21 | a0003c0003t0003g0009 a0003c0003t0003g0010 a0003c0003t0003g0020 others(18): Show |
21 | HG01109.hp1 HG01884.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.3312+4513_3312+451 others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chrX | 105929542 | ||||||
| chrX:105929552 | G | A | 1 | a0006c0007t0003g0014 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3312+4521G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105929552 | |||||||
| chrX:105929764 | G | C | 1 | a0002c0002t0002g0045 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3313-4494G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105929764 | |||||||
| chrX:105929850 | G | A | 1 | a0001c0001t0001g0144 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.3313-4408G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105929850 | |||||||
| chrX:105930041 | G | A | 85 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(82): Show |
87 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.3313-4217G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105930041 | |||||||
| chrX:105930105 | A | G | 1 | a0005c0013t0001g0147 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.3313-4153A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105930105 | |||||||
| chrX:105930117 | C | T | 37 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(34): Show |
37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.3313-4141C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105930117 | |||||||
| chrX:105930447 | G | T | 4 | a0002c0002t0005g0208 a0002c0002t0005g0209 a0002c0002t0005g0211 others(1): Show |
4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.3313-3811G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105930447 | |||||||
| chrX:105930896 | C | T | 1 | a0003c0003t0003g0025 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3313-3362C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105930896 | |||||||
| chrX:105930900 | G | T | 1 | a0002c0009t0005g0210 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3313-3358G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105930900 | |||||||
| chrX:105930985 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3313-3273C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105930985 | |||||||
| chrX:105931076 | T | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0041 others(207): Show |
216 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(213): Show |
intron_variant | MODIFIER | c.3313-3182T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105931076 | |||||||
| chrX:105931404 | A | G | 5 | a0003c0003t0003g0036 a0003c0003t0003g0038 a0003c0003t0003g0039 others(2): Show |
5 | HG01884.hp2 HG02622.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.3313-2854A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105931404 | |||||||
| chrX:105931425 | G | A | 1 | a0004c0004t0003g0011 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3313-2833G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105931425 | |||||||
| chrX:105931562 | G | A | 37 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(34): Show |
37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.3313-2696G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105931562 | |||||||
| chrX:105931721 | G | T | 1 | a0001c0001t0001g0177 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3313-2537G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105931721 | |||||||
| chrX:105933166 | G | GTCTA | 37 | a0001c0001t0001g0041 a0001c0001t0001g0102 a0001c0001t0001g0153 others(34): Show |
37 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.3313-1044_3313-104 others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chrX | 105933166 | ||||||
| chrX:105933166 | G | GTCTATCT others(1): Show |
3 | a0001c0001t0004g0096 a0002c0002t0002g0060 a0002c0002t0005g0201 |
3 | HG01192.hp1 NA18906.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.3313-1048_3313-104 others(12): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chrX | 105933166 | ||||||
| chrX:105933166 | GTCTA | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0082 a0001c0001t0001g0093 others(84): Show |
89 | HG00642.hp1 HG00673.hp1 HG00733.hp2 others(86): Show |
intron_variant | MODIFIER | c.3313-1044_3313-104 others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chrX | 105933166 | ||||||
| chrX:105933166 | GTCTATCT others(1): Show |
G | 5 | a0001c0001t0001g0088 a0001c0001t0001g0117 a0001c0001t0001g0137 others(2): Show |
5 | HG02056.hp1 NA18982.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.3313-1048_3313-104 others(12): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chrX | 105933166 | ||||||
| chrX:105933166 | GTCTATCT others(5): Show |
G | 2 | a0001c0001t0001g0105 a0001c0001t0001g0136 |
2 | HG02523.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.3313-1052_3313-104 others(16): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chrX | 105933166 | ||||||
| chrX:105933166 | GTCTATCT others(13): Show |
G | 1 | a0001c0005t0001g0004 | 2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3313-1060_3313-104 others(24): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chrX | 105933166 | ||||||
| chrX:105933486 | A | G | 1 | a0002c0002t0005g0120 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3313-772A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105933486 | |||||||
| chrX:105933824 | T | C | 81 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(78): Show |
83 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.3313-434T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 19/28 | chrX | 105933824 | |||||||
| chrX:105934729 | C | T | 7 | a0001c0001t0004g0086 a0001c0001t0004g0087 a0001c0001t0004g0192 others(4): Show |
7 | HG00140.hp1 HG00280.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.3499+285C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 20/28 | chrX | 105934729 | |||||||
| chrX:105934841 | C | T | 3 | a0002c0002t0002g0061 a0002c0002t0002g0062 a0002c0002t0002g0063 |
3 | HG02486.hp1 HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3500-329C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 20/28 | chrX | 105934841 | |||||||
| chrX:105934865 | C | T | 1 | a0001c0001t0004g0197 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3500-305C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 20/28 | chrX | 105934865 | |||||||
| chrX:105934997 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.3500-173C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 20/28 | chrX | 105934997 | |||||||
| chrX:105935140 | C | T | 107 | a0001c0001t0004g0086 a0001c0001t0004g0087 a0001c0001t0004g0091 others(104): Show |
109 | HG00140.hp1 HG00280.hp1 HG00673.hp1 others(106): Show |
intron_variant | MODIFIER | c.3500-30C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 20/28 | chrX | 105935140 | |||||||
| chrX:105935418 | C | A | 37 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(34): Show |
37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.3655+93C>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 21/28 | chrX | 105935418 | |||||||
| chrX:105935513 | C | T | 1 | a0003c0003t0003g0006 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3655+188C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 21/28 | chrX | 105935513 | |||||||
| chrX:105935567 | G | A | 40 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(37): Show |
42 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.3655+242G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 21/28 | chrX | 105935567 | |||||||
| chrX:105935770 | G | A | 1 | a0002c0002t0002g0048 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3655+445G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 21/28 | chrX | 105935770 | |||||||
| chrX:105935790 | A | C | 1 | a0009c0010t0005g0090 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3655+465A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 21/28 | chrX | 105935790 | |||||||
| chrX:105935813 | T | TTA | 3 | a0001c0001t0001g0131 a0001c0001t0004g0091 a0002c0002t0005g0205 |
3 | HG00733.hp2 HG02818.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3655+505_3655+506d others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 21/28 | INFO_REALIGN_3_PRIME | chrX | 105935813 | ||||||
| chrX:105935813 | TTA | T | 37 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(34): Show |
37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.3655+505_3655+506d others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 21/28 | INFO_REALIGN_3_PRIME | chrX | 105935813 | ||||||
| chrX:105935831 | A | G | 1 | a0003c0003t0003g0030 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3655+506A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 21/28 | chrX | 105935831 | |||||||
| chrX:105936179 | T | C | 1 | a0002c0002t0002g0049 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.3655+854T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 21/28 | chrX | 105936179 | |||||||
| chrX:105936386 | C | A | 1 | a0001c0001t0004g0195 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.3656-1053C>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 21/28 | chrX | 105936386 | |||||||
| chrX:105936435 | A | G | 4 | a0001c0001t0001g0093 a0001c0001t0001g0134 a0001c0001t0001g0173 others(1): Show |
4 | HG02080.hp2 HG02083.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.3656-1004A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 21/28 | chrX | 105936435 | |||||||
| chrX:105936509 | A | G | 44 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(41): Show |
46 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.3656-930A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 21/28 | chrX | 105936509 | |||||||
| chrX:105936711 | C | A | 1 | a0001c0001t0001g0191 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3656-728C>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 21/28 | chrX | 105936711 | |||||||
| chrX:105936719 | T | G | 1 | a0001c0001t0001g0169 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3656-720T>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 21/28 | chrX | 105936719 | |||||||
| chrX:105936976 | C | T | 37 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(34): Show |
37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.3656-463C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 21/28 | chrX | 105936976 | |||||||
| chrX:105937306 | T | A | 4 | a0002c0002t0005g0208 a0002c0002t0005g0209 a0002c0002t0005g0211 others(1): Show |
4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.3656-133T>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 21/28 | chrX | 105937306 | |||||||
| chrX:105937915 | G | A | 1 | a0002c0002t0008g0179 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.3799+333G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 22/28 | chrX | 105937915 | |||||||
| chrX:105938154 | G | A | 1 | a0002c0002t0009g0204 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3799+572G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 22/28 | chrX | 105938154 | |||||||
| chrX:105938207 | A | G | 9 | a0001c0001t0001g0101 a0001c0001t0001g0117 a0001c0001t0001g0126 others(6): Show |
9 | HG01978.hp2 NA18939.hp2 NA18955.hp1 others(6): Show |
intron_variant | MODIFIER | c.3799+625A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 22/28 | chrX | 105938207 | |||||||
| chrX:105938236 | A | G | 210 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0041 others(207): Show |
216 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(213): Show |
intron_variant | MODIFIER | c.3799+654A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 22/28 | chrX | 105938236 | |||||||
| chrX:105938515 | A | C | 1 | a0001c0001t0001g0188 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3799+933A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 22/28 | chrX | 105938515 | |||||||
| chrX:105938608 | C | G | 1 | a0003c0003t0003g0213 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3799+1026C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 22/28 | chrX | 105938608 | |||||||
| chrX:105938668 | C | T | 21 | a0003c0003t0003g0009 a0003c0003t0003g0010 a0003c0003t0003g0020 others(18): Show |
21 | HG01109.hp1 HG01884.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.3799+1086C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 22/28 | chrX | 105938668 | |||||||
| chrX:105939005 | TG | T | 4 | a0003c0003t0003g0009 a0003c0003t0003g0022 a0003c0003t0003g0212 others(1): Show |
4 | HG02451.hp1 HG02886.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.3800-868delG | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 22/28 | chrX | 105939005 | |||||||
| chrX:105939007 | A | T | 4 | a0003c0003t0003g0009 a0003c0003t0003g0022 a0003c0003t0003g0212 others(1): Show |
4 | HG02451.hp1 HG02886.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.3800-867A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 22/28 | chrX | 105939007 | |||||||
| chrX:105939008 | A | T | 4 | a0003c0003t0003g0009 a0003c0003t0003g0022 a0003c0003t0003g0212 others(1): Show |
4 | HG02451.hp1 HG02886.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.3800-866A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 22/28 | chrX | 105939008 | |||||||
| chrX:105939009 | A | T | 4 | a0003c0003t0003g0009 a0003c0003t0003g0022 a0003c0003t0003g0212 others(1): Show |
4 | HG02451.hp1 HG02886.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.3800-865A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 22/28 | chrX | 105939009 | |||||||
| chrX:105939010 | G | T | 4 | a0003c0003t0003g0009 a0003c0003t0003g0022 a0003c0003t0003g0212 others(1): Show |
4 | HG02451.hp1 HG02886.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.3800-864G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 22/28 | chrX | 105939010 | |||||||
| chrX:105939012 | A | T | 4 | a0003c0003t0003g0009 a0003c0003t0003g0022 a0003c0003t0003g0212 others(1): Show |
4 | HG02451.hp1 HG02886.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.3800-862A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 22/28 | chrX | 105939012 | |||||||
| chrX:105939621 | A | C | 1 | a0001c0001t0001g0110 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.3800-253A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 22/28 | chrX | 105939621 | |||||||
| chrX:105939685 | G | A | 1 | a0003c0003t0003g0007 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3800-189G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 22/28 | chrX | 105939685 | |||||||
| chrX:105939769 | G | A | 17 | a0002c0002t0008g0179 a0003c0003t0003g0006 a0003c0003t0003g0007 others(14): Show |
17 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.3800-105G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 22/28 | chrX | 105939769 | |||||||
| chrX:105940477 | T | A | 43 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(40): Show |
45 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.3958+445T>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | chrX | 105940477 | |||||||
| chrX:105940519 | T | C | 1 | a0002c0002t0009g0204 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3958+487T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | chrX | 105940519 | |||||||
| chrX:105940764 | A | G | 81 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(78): Show |
83 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.3958+732A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | chrX | 105940764 | |||||||
| chrX:105940862 | A | G | 1 | a0002c0002t0002g0067 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3958+830A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | chrX | 105940862 | |||||||
| chrX:105941551 | C | CAG | 4 | a0002c0002t0005g0208 a0002c0002t0005g0209 a0002c0002t0005g0211 others(1): Show |
4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.3958+1521_3958+152 others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chrX | 105941551 | ||||||
| chrX:105941555 | A | AAG | 18 | a0001c0001t0001g0106 a0001c0001t0001g0153 a0001c0001t0001g0183 others(15): Show |
18 | HG00140.hp1 HG00673.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.3958+1559_3958+156 others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chrX | 105941555 | ||||||
| chrX:105941555 | A | AAGAG | 39 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0082 others(36): Show |
41 | HG00642.hp1 HG01106.hp1 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.3958+1557_3958+156 others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chrX | 105941555 | ||||||
| chrX:105941555 | A | AAGAGAG | 23 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0098 others(20): Show |
23 | HG01069.hp1 HG01071.hp1 HG01258.hp1 others(20): Show |
intron_variant | MODIFIER | c.3958+1555_3958+156 others(10): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chrX | 105941555 | ||||||
| chrX:105941555 | A | AAGAGAGA others(1): Show |
7 | a0001c0001t0001g0083 a0001c0001t0001g0160 a0002c0002t0002g0057 others(4): Show |
7 | HG00621.hp1 HG01884.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.3958+1553_3958+156 others(12): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chrX | 105941555 | ||||||
| chrX:105941555 | A | AAGAGAGA others(3): Show |
3 | a0003c0003t0003g0020 a0003c0003t0003g0025 a0003c0003t0003g0031 |
3 | HG01109.hp1 HG02723.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3958+1551_3958+156 others(14): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chrX | 105941555 | ||||||
| chrX:105941555 | A | AAGAGAGA others(5): Show |
3 | a0003c0003t0003g0010 a0003c0003t0003g0021 a0003c0003t0003g0026 |
3 | HG02922.hp2 HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3958+1549_3958+156 others(16): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chrX | 105941555 | ||||||
| chrX:105941555 | A | AAGAGAGA others(7): Show |
3 | a0003c0003t0003g0023 a0003c0003t0003g0039 a0003c0003t0003g0040 |
3 | HG02895.hp1 HG02897.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3958+1547_3958+156 others(18): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chrX | 105941555 | ||||||
| chrX:105941555 | A | AGAGAG | 3 | a0001c0001t0001g0099 a0001c0001t0001g0104 a0004c0004t0003g0015 |
3 | HG02145.hp1 NA18977.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.3958+1523_3958+152 others(9): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | chrX | 105941555 | |||||||
| chrX:105941555 | A | AGAGAGAG others(8): Show |
1 | a0003c0011t0003g0037 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3958+1523_3958+152 others(19): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | chrX | 105941555 | |||||||
| chrX:105941555 | A | G | 4 | a0002c0002t0005g0208 a0002c0002t0005g0209 a0002c0002t0005g0211 others(1): Show |
4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.3958+1523A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | chrX | 105941555 | |||||||
| chrX:105941555 | AAG | A | 4 | a0001c0001t0004g0199 a0001c0001t0004g0200 a0001c0001t0007g0116 others(1): Show |
4 | HG01891.hp1 HG02630.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.3958+1559_3958+156 others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chrX | 105941555 | ||||||
| chrX:105941555 | AAGAG | A | 3 | a0001c0001t0001g0088 a0002c0002t0002g0003 a0002c0002t0002g0078 |
4 | HG00741.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.3958+1557_3958+156 others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chrX | 105941555 | ||||||
| chrX:105941555 | AAGAGAGA others(1): Show |
A | 3 | a0002c0002t0005g0201 a0002c0002t0005g0203 a0002c0002t0009g0204 |
3 | HG02451.hp2 NA18612.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.3958+1553_3958+156 others(12): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chrX | 105941555 | ||||||
| chrX:105942258 | A | G | 2 | a0002c0002t0005g0208 a0002c0002t0005g0209 |
2 | HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.3959-1683A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | chrX | 105942258 | |||||||
| chrX:105942278 | A | G | 1 | a0002c0002t0002g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3959-1663A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | chrX | 105942278 | |||||||
| chrX:105942824 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3959-1117C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | chrX | 105942824 | |||||||
| chrX:105942888 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3959-1053G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | chrX | 105942888 | |||||||
| chrX:105943070 | T | C | 1 | a0003c0003t0003g0007 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3959-871T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | chrX | 105943070 | |||||||
| chrX:105943097 | G | A | 1 | a0002c0002t0005g0205 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3959-844G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | chrX | 105943097 | |||||||
| chrX:105943165 | T | C | 37 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(34): Show |
37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.3959-776T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | chrX | 105943165 | |||||||
| chrX:105943260 | C | T | 1 | a0002c0002t0005g0120 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3959-681C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | chrX | 105943260 | |||||||
| chrX:105943316 | A | G | 1 | a0002c0002t0002g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3959-625A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | chrX | 105943316 | |||||||
| chrX:105943913 | G | A | 1 | a0002c0002t0002g0058 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3959-28G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 23/28 | chrX | 105943913 | |||||||
| chrX:105944251 | T | C | 1 | a0001c0001t0001g0041 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.4059+210T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 24/28 | chrX | 105944251 | |||||||
| chrX:105944456 | T | C | 89 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(86): Show |
91 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.4059+415T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 24/28 | chrX | 105944456 | |||||||
| chrX:105944474 | C | T | 3 | a0001c0001t0001g0088 a0001c0001t0001g0136 a0001c0001t0001g0137 |
3 | HG02056.hp1 HG02523.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.4059+433C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 24/28 | chrX | 105944474 | |||||||
| chrX:105944554 | C | T | 1 | a0002c0002t0002g0057 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4059+513C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 24/28 | chrX | 105944554 | |||||||
| chrX:105944704 | G | A | 40 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(37): Show |
42 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.4059+663G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 24/28 | chrX | 105944704 | |||||||
| chrX:105944801 | G | A | 4 | a0002c0002t0005g0208 a0002c0002t0005g0209 a0002c0002t0005g0211 others(1): Show |
4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.4059+760G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 24/28 | chrX | 105944801 | |||||||
| chrX:105944832 | T | A | 37 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(34): Show |
37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.4059+791T>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 24/28 | chrX | 105944832 | |||||||
| chrX:105945149 | C | G | 1 | a0002c0002t0005g0120 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4060-723C>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 24/28 | chrX | 105945149 | |||||||
| chrX:105945223 | G | T | 1 | a0001c0001t0001g0162 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.4060-649G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 24/28 | chrX | 105945223 | |||||||
| chrX:105945241 | A | G | 1 | a0001c0001t0001g0112 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.4060-631A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 24/28 | chrX | 105945241 | |||||||
| chrX:105945332 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.4060-540G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 24/28 | chrX | 105945332 | |||||||
| chrX:105945584 | G | A | 1 | a0002c0002t0002g0064 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4060-288G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 24/28 | chrX | 105945584 | |||||||
| chrX:105946208 | A | G | 3 | a0002c0002t0002g0061 a0002c0002t0002g0062 a0002c0002t0002g0063 |
3 | HG02486.hp1 HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.4204-107A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 25/28 | chrX | 105946208 | |||||||
| chrX:105946816 | A | C | 1 | a0002c0002t0009g0204 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4353+352A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 26/28 | chrX | 105946816 | |||||||
| chrX:105946864 | T | C | 1 | a0002c0002t0009g0204 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4353+400T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 26/28 | chrX | 105946864 | |||||||
| chrX:105947061 | A | G | 3 | a0002c0002t0005g0120 a0002c0002t0010g0119 a0009c0010t0005g0090 |
3 | HG02717.hp1 HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.4353+597A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 26/28 | chrX | 105947061 | |||||||
| chrX:105947093 | T | C | 2 | a0001c0001t0004g0092 a0001c0001t0004g0130 |
2 | HG02559.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.4353+629T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 26/28 | chrX | 105947093 | |||||||
| chrX:105947164 | TGAAATAC others(296): Show |
T | 85 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(82): Show |
87 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.4353+717_4353+1019 others(3): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chrX | 105947164 | ||||||
| chrX:105947442 | C | CA | 5 | a0001c0001t0001g0103 a0001c0001t0001g0111 a0001c0001t0001g0138 others(2): Show |
5 | HG03492.hp1 HG03927.hp2 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.4353+999dupA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chrX | 105947442 | ||||||
| chrX:105947442 | CA | C | 6 | a0001c0001t0001g0084 a0001c0001t0001g0132 a0001c0001t0001g0158 others(3): Show |
6 | HG01069.hp1 HG01168.hp2 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.4353+999delA | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chrX | 105947442 | ||||||
| chrX:105947642 | A | T | 7 | a0001c0001t0004g0086 a0001c0001t0004g0087 a0001c0001t0004g0192 others(4): Show |
7 | HG00140.hp1 HG00280.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.4353+1178A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 26/28 | chrX | 105947642 | |||||||
| chrX:105947911 | TACTC | T | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0006g0176 |
3 | HG01069.hp1 HG01071.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.4353+1449_4353+145 others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chrX | 105947911 | ||||||
| chrX:105948364 | G | A | 1 | a0002c0002t0002g0054 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.4354-1211G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 26/28 | chrX | 105948364 | |||||||
| chrX:105948617 | T | A | 1 | a0001c0001t0001g0105 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.4354-958T>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 26/28 | chrX | 105948617 | |||||||
| chrX:105948748 | A | G | 4 | a0003c0003t0003g0021 a0003c0003t0003g0025 a0003c0003t0003g0026 others(1): Show |
4 | HG02723.hp2 HG02965.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.4354-827A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 26/28 | chrX | 105948748 | |||||||
| chrX:105948777 | CT | C | 41 | a0001c0001t0001g0084 a0001c0001t0001g0158 a0001c0001t0004g0086 others(38): Show |
41 | HG01069.hp1 HG01109.hp1 HG01169.hp1 others(38): Show |
intron_variant | MODIFIER | c.4354-784delT | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chrX | 105948777 | ||||||
| chrX:105948840 | A | T | 1 | a0001c0001t0001g0122 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.4354-735A>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 26/28 | chrX | 105948840 | |||||||
| chrX:105948985 | G | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0081 a0001c0001t0001g0100 others(3): Show |
7 | HG00609.hp1 HG02135.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.4354-590G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 26/28 | chrX | 105948985 | |||||||
| chrX:105949246 | A | G | 40 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(37): Show |
42 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.4354-329A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 26/28 | chrX | 105949246 | |||||||
| chrX:105949919 | G | A | 1 | a0002c0002t0008g0179 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.4513+185G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | chrX | 105949919 | |||||||
| chrX:105950191 | G | C | 37 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(34): Show |
37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.4513+457G>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | chrX | 105950191 | |||||||
| chrX:105950244 | G | A | 1 | a0006c0007t0003g0014 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4513+510G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | chrX | 105950244 | |||||||
| chrX:105950527 | A | AGT | 17 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0085 others(14): Show |
17 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.4513+843_4513+844d others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chrX | 105950527 | ||||||
| chrX:105950527 | A | AGTGT | 8 | a0001c0001t0001g0001 a0001c0001t0001g0104 a0001c0001t0001g0125 others(5): Show |
10 | HG00642.hp1 HG01256.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.4513+841_4513+844d others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chrX | 105950527 | ||||||
| chrX:105950527 | A | AGTGTGT | 3 | a0001c0001t0001g0129 a0001c0001t0001g0169 a0002c0002t0002g0045 |
3 | HG01928.hp1 HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.4513+839_4513+844d others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chrX | 105950527 | ||||||
| chrX:105950527 | AGT | A | 21 | a0001c0001t0001g0099 a0001c0001t0001g0106 a0001c0001t0001g0115 others(18): Show |
21 | HG00735.hp1 HG01071.hp2 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.4513+843_4513+844d others(4): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chrX | 105950527 | ||||||
| chrX:105950527 | AGTGT | A | 74 | a0001c0001t0001g0005 a0001c0001t0001g0041 a0001c0001t0001g0081 others(71): Show |
75 | HG00140.hp1 HG00609.hp1 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.4513+841_4513+844d others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chrX | 105950527 | ||||||
| chrX:105950527 | AGTGTGT | A | 22 | a0001c0001t0001g0093 a0001c0001t0001g0103 a0001c0001t0001g0121 others(19): Show |
23 | HG00280.hp1 HG01167.hp1 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.4513+839_4513+844d others(8): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chrX | 105950527 | ||||||
| chrX:105950527 | AGTGTGTG others(1): Show |
A | 8 | a0001c0001t0001g0101 a0001c0001t0001g0126 a0001c0001t0001g0152 others(5): Show |
8 | HG03209.hp1 HG03453.hp1 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.4513+837_4513+844d others(10): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chrX | 105950527 | ||||||
| chrX:105950527 | AGTGTGTG others(3): Show |
A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0188 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.4513+835_4513+844d others(12): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chrX | 105950527 | ||||||
| chrX:105950527 | AGTGTGTG others(11): Show |
A | 1 | a0003c0003t0003g0027 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4513+827_4513+844d others(20): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chrX | 105950527 | ||||||
| chrX:105950527 | AGTGTGTG others(13): Show |
A | 21 | a0003c0003t0003g0007 a0003c0003t0003g0009 a0003c0003t0003g0010 others(18): Show |
21 | HG01109.hp1 HG01884.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.4513+825_4513+844d others(22): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chrX | 105950527 | ||||||
| chrX:105950614 | A | G | 85 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0043 others(82): Show |
87 | HG00673.hp1 HG00733.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.4513+880A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | chrX | 105950614 | |||||||
| chrX:105950823 | C | CAG | 19 | a0002c0002t0005g0201 a0002c0002t0005g0203 a0002c0002t0009g0204 others(16): Show |
19 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.4513+1113_4513+111 others(6): Show |
NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chrX | 105950823 | ||||||
| chrX:105951281 | T | C | 1 | a0002c0002t0002g0077 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.4513+1547T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | chrX | 105951281 | |||||||
| chrX:105951477 | G | A | 21 | a0003c0003t0003g0009 a0003c0003t0003g0010 a0003c0003t0003g0020 others(18): Show |
21 | HG01109.hp1 HG01884.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.4514-1557G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | chrX | 105951477 | |||||||
| chrX:105951508 | A | G | 1 | a0002c0002t0002g0055 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.4514-1526A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | chrX | 105951508 | |||||||
| chrX:105952057 | C | T | 1 | a0002c0002t0008g0179 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.4514-977C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | chrX | 105952057 | |||||||
| chrX:105952115 | G | T | 3 | a0002c0002t0005g0201 a0002c0002t0005g0203 a0002c0002t0009g0204 |
3 | HG02451.hp2 NA18612.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.4514-919G>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | chrX | 105952115 | |||||||
| chrX:105952451 | A | C | 1 | a0002c0002t0005g0120 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4514-583A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | chrX | 105952451 | |||||||
| chrX:105952755 | C | T | 3 | a0002c0002t0005g0201 a0002c0002t0005g0203 a0002c0002t0009g0204 |
3 | HG02451.hp2 NA18612.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.4514-279C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | chrX | 105952755 | |||||||
| chrX:105952763 | A | G | 3 | a0002c0002t0002g0061 a0002c0002t0002g0062 a0002c0002t0002g0063 |
3 | HG02486.hp1 HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.4514-271A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 27/28 | chrX | 105952763 | |||||||
| chrX:105953262 | C | T | 1 | a0002c0009t0005g0210 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4653+89C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 28/28 | chrX | 105953262 | |||||||
| chrX:105953549 | C | T | 1 | a0002c0002t0008g0179 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.4653+376C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 28/28 | chrX | 105953549 | |||||||
| chrX:105953755 | C | T | 3 | a0002c0002t0005g0201 a0002c0002t0005g0203 a0002c0002t0009g0204 |
3 | HG02451.hp2 NA18612.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.4653+582C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 28/28 | chrX | 105953755 | |||||||
| chrX:105953993 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.4653+820G>A | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 28/28 | chrX | 105953993 | |||||||
| chrX:105954007 | A | C | 37 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(34): Show |
37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.4653+834A>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 28/28 | chrX | 105954007 | |||||||
| chrX:105954086 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.4653+913T>C | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 28/28 | chrX | 105954086 | |||||||
| chrX:105954203 | A | G | 5 | a0001c0001t0001g0083 a0001c0001t0001g0132 a0001c0001t0001g0133 others(2): Show |
5 | HG00621.hp1 NA18966.hp1 NA19006.hp1 others(2): Show |
intron_variant | MODIFIER | c.4653+1030A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 28/28 | chrX | 105954203 | |||||||
| chrX:105954388 | C | T | 2 | a0003c0003t0003g0008 a0003c0003t0003g0016 |
2 | HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4654-1117C>T | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 28/28 | chrX | 105954388 | |||||||
| chrX:105954530 | A | G | 37 | a0003c0003t0003g0006 a0003c0003t0003g0007 a0003c0003t0003g0008 others(34): Show |
37 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.4654-975A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 28/28 | chrX | 105954530 | |||||||
| chrX:105955435 | A | G | 4 | a0002c0002t0005g0208 a0002c0002t0005g0209 a0002c0002t0005g0211 others(1): Show |
4 | HG02109.hp1 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.4654-70A>G | NRK | ENSG00000123572.17 | transcript | ENST00000243300.14 | protein_coding | 28/28 | chrX | 105955435 |