Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9282 |
| ensemblid | ENSG00000180182.11 |
| hgncid | 2370 |
| symbol | MED14 |
| name | mediator complex subunit 14 |
| refseq_nuc | NM_004229.4 |
| refseq_prot | NP_004220.2 |
| ensembl_nuc | ENST00000324817.6 |
| ensembl_prot | ENSP00000323720.1 |
| mane_status | MANE Select |
| chr | chrX |
| start | 40648305 |
| end | 40735542 |
| strand | - |
| ver | v1.2 |
| region | chrX:40648305-40735542 |
| region5000 | chrX:40643305-40740542 |
| regionname0 | MED14_chrX_40648305_40735542 |
| regionname5000 | MED14_chrX_40643305_40740542 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1454 | 245 | 62 | 40 | 115 | 7 | 19 | 90 | MED14_chrX_40643305_40740542 | MED14 | MAPVQ others(1449): Show |
chrX | 40643305 | 40740542 |
| a0002 | 0/0 | 1454 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MED14_chrX_40643305_40740542 | MED14 | MAPVQ others(1449): Show |
chrX | 40643305 | 40740542 |
| a0003 | 0/0 | 1454 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | MAPVQ others(1449): Show |
chrX | 40643305 | 40740542 |
| a0004 | 0/0 | 1454 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | MAPVQ others(1449): Show |
chrX | 40643305 | 40740542 |
| a0005 | 0/0 | 1454 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | MAPVQ others(1449): Show |
chrX | 40643305 | 40740542 |
| a0006 | 0/0 | 569 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | MAPVQ others(564): Show |
chrX | 40643305 | 40740542 |
| a0007 | 0/0 | 1454 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | MAPVQ others(1449): Show |
chrX | 40643305 | 40740542 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 4362 | 174 | 28 | 37 | 89 | 7 | 11 | MED14_chrX_40643305_40740542 | MED14 | ATGGC others(4357): Show |
chrX | 40643305 | 40740542 | ||
| a0001c0002 | 0/0 | 4362 | 60 | 26 | 3 | 24 | 0 | 7 | MED14_chrX_40643305_40740542 | MED14 | ATGGC others(4357): Show |
chrX | 40643305 | 40740542 | ||
| a0001c0003 | 0/0 | 4362 | 4 | 4 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | ATGGC others(4357): Show |
chrX | 40643305 | 40740542 | ||
| a0001c0004 | 0/0 | 4362 | 3 | 3 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | ATGGC others(4357): Show |
chrX | 40643305 | 40740542 | ||
| a0001c0009 | 0/0 | 4362 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | ATGGC others(4357): Show |
chrX | 40643305 | 40740542 | ||
| a0001c0010 | 0/0 | 4362 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | ATGGC others(4357): Show |
chrX | 40643305 | 40740542 | ||
| a0001c0013 | 0/0 | 4362 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | ATGGC others(4357): Show |
chrX | 40643305 | 40740542 | ||
| a0001c0014 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | ATGGC others(4357): Show |
chrX | 40643305 | 40740542 | ||
| a0002c0011 | 0/0 | 4362 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | ATGGC others(4357): Show |
chrX | 40643305 | 40740542 | ||
| a0003c0008 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | ATGGC others(4357): Show |
chrX | 40643305 | 40740542 | ||
| a0004c0007 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | ATGGC others(4357): Show |
chrX | 40643305 | 40740542 | ||
| a0005c0012 | 0/0 | 4362 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | ATGGC others(4357): Show |
chrX | 40643305 | 40740542 | ||
| a0006c0005 | 0/0 | 4352 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | ATGGC others(4347): Show |
chrX | 40643305 | 40740542 | ||
| a0007c0006 | 0/0 | 4362 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | ATGGC others(4357): Show |
chrX | 40643305 | 40740542 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 7996 | 141 | 17 | 24 | 85 | 4 | 10 | MED14_chrX_40643305_40740542 | MED14 | CTGTT others(7991): Show |
chrX | 40643305 | 40740542 |
| a0001c0001t0002 | 0/1 | 7996 | 24 | 8 | 13 | 0 | 2 | 0 | MED14_chrX_40643305_40740542 | MED14 | CTGTT others(7991): Show |
chrX | 40643305 | 40740542 |
| a0001c0001t0003 | 0/0 | 7996 | 3 | 3 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | CTGTT others(7991): Show |
chrX | 40643305 | 40740542 |
| a0001c0001t0005 | 0/0 | 7996 | 2 | 0 | 0 | 2 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | CTGTT others(7991): Show |
chrX | 40643305 | 40740542 |
| a0001c0001t0006 | 0/0 | 7996 | 1 | 0 | 0 | 0 | 1 | 0 | MED14_chrX_40643305_40740542 | MED14 | CTGTT others(7991): Show |
chrX | 40643305 | 40740542 |
| a0001c0001t0008 | 0/0 | 7996 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | CTGTT others(7991): Show |
chrX | 40643305 | 40740542 |
| a0001c0001t0010 | 0/0 | 7996 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | CTGTT others(7991): Show |
chrX | 40643305 | 40740542 |
| a0001c0001t0011 | 0/0 | 7996 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | CTGTT others(7991): Show |
chrX | 40643305 | 40740542 |
| a0001c0002t0001 | 0/0 | 7996 | 55 | 23 | 2 | 23 | 0 | 7 | MED14_chrX_40643305_40740542 | MED14 | CTGTT others(7991): Show |
chrX | 40643305 | 40740542 |
| a0001c0002t0004 | 0/0 | 7996 | 3 | 3 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | CTGTT others(7991): Show |
chrX | 40643305 | 40740542 |
| a0001c0002t0007 | 0/0 | 7996 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | CTGTT others(7991): Show |
chrX | 40643305 | 40740542 |
| a0001c0002t0009 | 0/0 | 7996 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | CTGTT others(7991): Show |
chrX | 40643305 | 40740542 |
| a0001c0003t0001 | 0/0 | 7996 | 4 | 4 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | CTGTT others(7991): Show |
chrX | 40643305 | 40740542 |
| a0001c0004t0001 | 0/0 | 7996 | 3 | 3 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | CTGTT others(7991): Show |
chrX | 40643305 | 40740542 |
| a0001c0009t0001 | 0/0 | 7996 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | CTGTT others(7991): Show |
chrX | 40643305 | 40740542 |
| a0001c0010t0001 | 0/0 | 7996 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | CTGTT others(7991): Show |
chrX | 40643305 | 40740542 |
| a0001c0013t0001 | 0/0 | 7996 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | CTGTT others(7991): Show |
chrX | 40643305 | 40740542 |
| a0001c0014t0001 | 0/0 | 7996 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | CTGTT others(7991): Show |
chrX | 40643305 | 40740542 |
| a0002c0011t0002 | 0/0 | 7996 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | CTGTT others(7991): Show |
chrX | 40643305 | 40740542 |
| a0003c0008t0002 | 0/0 | 7996 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | CTGTT others(7991): Show |
chrX | 40643305 | 40740542 |
| a0004c0007t0001 | 0/0 | 7996 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | CTGTT others(7991): Show |
chrX | 40643305 | 40740542 |
| a0005c0012t0001 | 0/0 | 7996 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | CTGTT others(7991): Show |
chrX | 40643305 | 40740542 |
| a0006c0005t0001 | 0/0 | 7986 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | CTGTT others(7981): Show |
chrX | 40643305 | 40740542 |
| a0007c0006t0001 | 0/0 | 7996 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | CTGTT others(7991): Show |
chrX | 40643305 | 40740542 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 9 | 0 | 3 | 6 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0064 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0002g0141 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0005g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0005g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0006g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0008g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0010g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0011g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0004g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0007g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0009g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0003t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0003t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0003t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0004t0001g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0009t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0010t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0013t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0014t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0002c0011t0002g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0003c0008t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0004c0007t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0005c0012t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0006c0005t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0007c0006t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0111 | EUR | GBR | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0089 | EUR | FIN | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0044 | EAS | CHS | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0143 | AMR | PUR | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG00673 | hp1 | a0001 | c0001 | t0005 | g0159 | EAS | CHS | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG00733 | hp1 | a0001 | c0002 | t0009 | g0226 | AMR | PUR | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0133 | AMR | PUR | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0131 | AMR | PUR | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0134 | AMR | PUR | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0027 | AMR | PUR | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0056 | AMR | PUR | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0222 | AMR | CLM | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0130 | AMR | CLM | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | CLM | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | CLM | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0123 | EUR | IBS | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0065 | EUR | IBS | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01516 | hp2 | a0001 | c0001 | t0006 | g0132 | EUR | IBS | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | ACB | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | ACB | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0122 | AMR | PEL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0106 | AMR | PEL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0107 | AMR | PEL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02027 | hp1 | a0001 | c0001 | t0011 | g0110 | EAS | KHV | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02055 | hp1 | a0001 | c0014 | t0001 | g0180 | AFR | ACB | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | KHV | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02080 | hp1 | a0001 | c0001 | t0005 | g0158 | EAS | KHV | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | KHV | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02135 | hp1 | a0001 | c0001 | t0010 | g0186 | EAS | KHV | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0108 | AMR | PEL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CDX | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CDX | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0037 | AFR | ACB | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | PEL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0035 | AFR | ACB | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02280 | hp2 | a0001 | c0004 | t0001 | g0004 | AFR | ACB | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0077 | AFR | ACB | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0048 | EAS | KHV | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0183 | AFR | GWD | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02615 | hp1 | a0001 | c0003 | t0001 | g0204 | AFR | GWD | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0034 | AFR | GWD | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0212 | AFR | GWD | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0020 | AFR | GWD | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0208 | AFR | GWD | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0024 | SAS | PJL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02738 | hp1 | a0002 | c0011 | t0002 | g0012 | SAS | PJL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0229 | AFR | GWD | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02809 | hp2 | a0001 | c0002 | t0004 | g0209 | AFR | GWD | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0228 | AFR | GWD | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0214 | AFR | GWD | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0173 | AFR | GWD | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0046 | AFR | GWD | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0217 | AFR | GWD | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0018 | AFR | GWD | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0218 | AFR | ESN | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02965 | hp1 | a0003 | c0008 | t0002 | g0054 | AFR | ESN | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02976 | hp1 | a0001 | c0002 | t0004 | g0011 | AFR | ESN | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02976 | hp2 | a0001 | c0003 | t0001 | g0010 | AFR | ESN | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0219 | AFR | MSL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03130 | hp1 | a0001 | c0003 | t0001 | g0205 | AFR | ESN | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03139 | hp1 | a0001 | c0002 | t0004 | g0011 | AFR | ESN | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0210 | AFR | ESN | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03195 | hp2 | a0001 | c0003 | t0001 | g0010 | AFR | ESN | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | MSL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0216 | AFR | MSL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0030 | AFR | MSL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | MSL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0220 | AFR | MSL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0026 | SAS | PJL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0182 | AFR | ESN | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0213 | AFR | ESN | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03540 | hp1 | a0004 | c0007 | t0001 | g0202 | AFR | GWD | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03540 | hp2 | a0001 | c0004 | t0001 | g0004 | AFR | GWD | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | MSL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0014 | SAS | PJL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0224 | SAS | PJL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | STU | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03831 | hp1 | a0001 | c0013 | t0001 | g0225 | SAS | BEB | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | BEB | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0052 | SAS | BEB | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG04115 | hp1 | a0001 | c0001 | t0008 | g0153 | SAS | STU | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0215 | SAS | STU | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0047 | SAS | STU | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | STU | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | YRI | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CHB | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CHB | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | YRI | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0223 | AFR | YRI | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18946 | hp2 | a0001 | c0002 | t0007 | g0028 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18950 | hp2 | a0005 | c0012 | t0001 | g0051 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18992 | hp1 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0185 | AFR | LWK | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0227 | AFR | LWK | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19043 | hp1 | a0001 | c0004 | t0001 | g0004 | AFR | LWK | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19072 | hp1 | a0006 | c0005 | t0001 | g0085 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19075 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19078 | hp1 | a0001 | c0010 | t0001 | g0087 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19078 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19082 | hp1 | a0001 | c0009 | t0001 | g0124 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19087 | hp1 | a0007 | c0006 | t0001 | g0093 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0135 | EUR | TSI | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0114 | EUR | TSI | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | GIH | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0221 | AFR | ACB | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | USA | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | USA | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0141 | REF | REF | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0064 | REF | REF | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| 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:40659464 | A | T | 1 | a0003 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.3828T>A | p.Asp1276Glu | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 27/31 | 3958/7996 | 3828/4365 | 1276/1454 | chrX | 40659464 | |||
| chrX:40659484 | C | T | 1 | a0004 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.3808G>A | p.Ala1270Thr | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 27/31 | 3938/7996 | 3808/4365 | 1270/1454 | chrX | 40659484 | |||
| chrX:40664409 | A | C | 1 | a0007 | 1 | NA19087.hp1 | missense_variant | MODERATE | c.3346T>G | p.Ser1116Ala | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 25/31 | 3476/7996 | 3346/4365 | 1116/1454 | chrX | 40664409 | |||
| chrX:40692752 | G | A | 1 | a0002 | 1 | HG02738.hp1 | missense_variant | MODERATE | c.1801C>T | p.Arg601Cys | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 14/31 | 1931/7996 | 1801/4365 | 601/1454 | chrX | 40692752 | |||
| chrX:40692878 | TGGGAACC others(3): Show |
T | 1 | a0006 | 1 | NA19072.hp1 | frameshift_variant | HIGH | c.1665_1674delGGAGGT others(4): Show |
p.Glu556fs | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 14/31 | 1804/7996 | 1665/4365 | 555/1454 | chrX | 40692878 | |||
| chrX:40692894 | C | G | 1 | a0005 | 1 | NA18950.hp2 | missense_variant | MODERATE | c.1659G>C | p.Glu553Asp | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 14/31 | 1789/7996 | 1659/4365 | 553/1454 | chrX | 40692894 |
| 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:40659263 | G | A | 1 | a0001c0009 | 1 | NA19082.hp1 | synonymous_variant | LOW | c.3936C>T | p.Ile1312Ile | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 28/31 | 4066/7996 | 3936/4365 | 1312/1454 | chrX | 40659263 | |||
| chrX:40679900 | T | C | 1 | a0001c0010 | 1 | NA19078.hp1 | synonymous_variant | LOW | c.2844A>G | p.Lys948Lys | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 21/31 | 2974/7996 | 2844/4365 | 948/1454 | chrX | 40679900 | |||
| chrX:40682891 | T | C | 1 | a0001c0013 | 1 | HG03831.hp1 | synonymous_variant | LOW | c.2163A>G | p.Val721Val | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 17/31 | 2293/7996 | 2163/4365 | 721/1454 | chrX | 40682891 | |||
| chrX:40692741 | G | A | 2 | a0001c0003 a0001c0013 |
5 | HG02615.hp1 HG02976.hp2 HG03130.hp1 others(2): Show |
synonymous_variant | LOW | c.1812C>T | p.Thr604Thr | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 14/31 | 1942/7996 | 1812/4365 | 604/1454 | chrX | 40692741 | |||
| chrX:40713905 | G | A | 5 | a0001c0002 a0001c0003 a0001c0004 others(2): Show |
69 | HG00408.hp1 HG00733.hp1 HG01169.hp1 others(66): Show |
splice_region_variant&synonymous_variant | LOW | c.525C>T | p.Asp175Asp | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 5/31 | 655/7996 | 525/4365 | 175/1454 | chrX | 40713905 | |||
| chrX:40714672 | A | G | 1 | a0001c0004 | 3 | HG02280.hp2 HG03540.hp2 NA19043.hp1 |
synonymous_variant | LOW | c.387T>C | p.Phe129Phe | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 4/31 | 517/7996 | 387/4365 | 129/1454 | chrX | 40714672 | |||
| chrX:40714702 | T | C | 1 | a0001c0014 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.357A>G | p.Ser119Ser | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 4/31 | 487/7996 | 357/4365 | 119/1454 | chrX | 40714702 |
| 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:40648367 | T | C | 1 | a0001c0001t0006 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3439A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 31/31 | 3439 | chrX | 40648367 | ||||||
| chrX:40649709 | T | C | 1 | a0001c0001t0005 | 2 | HG00673.hp1 HG02080.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2097A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 31/31 | 2097 | chrX | 40649709 | ||||||
| chrX:40649800 | C | T | 1 | a0001c0001t0008 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2006G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 31/31 | 2006 | chrX | 40649800 | ||||||
| chrX:40649928 | T | A | 1 | a0001c0002t0004 | 3 | HG02809.hp2 HG02976.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1878A>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 31/31 | 1878 | chrX | 40649928 | ||||||
| chrX:40649946 | A | G | 1 | a0001c0002t0007 | 1 | NA18946.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1860T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 31/31 | 1860 | chrX | 40649946 | ||||||
| chrX:40649990 | C | T | 1 | a0001c0001t0003 | 3 | HG02572.hp1 HG03516.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1816G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 31/31 | 1816 | chrX | 40649990 | ||||||
| chrX:40650141 | G | A | 1 | a0001c0002t0009 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1665C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 31/31 | 1665 | chrX | 40650141 | ||||||
| chrX:40650594 | T | C | 1 | a0001c0001t0010 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1212A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 31/31 | 1212 | chrX | 40650594 | ||||||
| chrX:40651521 | A | G | 4 | a0001c0001t0002 a0001c0001t0006 a0002c0011t0002 others(1): Show |
26 | HG00642.hp1 HG01069.hp1 HG01099.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*285T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 31/31 | 285 | chrX | 40651521 | ||||||
| chrX:40651600 | T | C | 1 | a0001c0001t0011 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*206A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 31/31 | 206 | chrX | 40651600 |
| 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:40652122 | G | T | 3 | a0001c0001t0002g0055 a0001c0001t0002g0077 a0001c0001t0002g0173 |
3 | HG01884.hp1 HG02451.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.4292-243C>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 30/30 | chrX | 40652122 | |||||||
| chrX:40652284 | C | T | 1 | a0001c0002t0001g0034 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4292-405G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 30/30 | chrX | 40652284 | |||||||
| chrX:40652882 | C | T | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(110): Show |
128 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.4292-1003G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 30/30 | chrX | 40652882 | |||||||
| chrX:40652982 | GA | G | 19 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0162 others(16): Show |
21 | HG00438.hp2 HG00639.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.4292-1104delT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 30/30 | chrX | 40652982 | |||||||
| chrX:40653016 | A | G | 1 | a0001c0002t0001g0018 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.4292-1137T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 30/30 | chrX | 40653016 | |||||||
| chrX:40653338 | C | T | 2 | a0001c0001t0002g0055 a0001c0001t0002g0077 |
2 | HG01884.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.4291+1026G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 30/30 | chrX | 40653338 | |||||||
| chrX:40653558 | CAGAG | C | 19 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0162 others(16): Show |
21 | HG00438.hp2 HG00639.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.4291+802_4291+805d others(6): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 30/30 | chrX | 40653558 | |||||||
| chrX:40653626 | A | G | 1 | a0001c0002t0001g0210 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4291+738T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 30/30 | chrX | 40653626 | |||||||
| chrX:40653845 | T | C | 1 | a0002c0011t0002g0012 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.4291+519A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 30/30 | chrX | 40653845 | |||||||
| chrX:40654223 | G | T | 17 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0163 others(14): Show |
19 | HG00438.hp2 HG00639.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.4291+141C>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 30/30 | chrX | 40654223 | |||||||
| chrX:40654593 | A | T | 1 | a0001c0001t0001g0094 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.4099-37T>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 29/30 | chrX | 40654593 | |||||||
| chrX:40654704 | T | G | 2 | a0001c0002t0001g0228 a0001c0002t0001g0229 |
2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.4099-148A>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 29/30 | chrX | 40654704 | |||||||
| chrX:40654706 | A | T | 1 | a0001c0001t0001g0070 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.4099-150T>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 29/30 | chrX | 40654706 | |||||||
| chrX:40655070 | G | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(111): Show |
129 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.3973-10C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 28/30 | chrX | 40655070 | |||||||
| chrX:40655215 | T | C | 1 | a0001c0001t0001g0075 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.3973-155A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 28/30 | chrX | 40655215 | |||||||
| chrX:40655383 | C | A | 2 | a0001c0002t0004g0011 a0001c0002t0004g0209 |
3 | HG02809.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3973-323G>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 28/30 | chrX | 40655383 | |||||||
| chrX:40655513 | C | T | 1 | a0001c0002t0001g0221 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3973-453G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 28/30 | chrX | 40655513 | |||||||
| chrX:40655553 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3973-493G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 28/30 | chrX | 40655553 | |||||||
| chrX:40655970 | T | G | 2 | a0001c0002t0001g0021 a0001c0002t0001g0023 |
2 | NA18982.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3973-910A>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 28/30 | chrX | 40655970 | |||||||
| chrX:40656284 | C | G | 1 | a0001c0001t0006g0132 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.3973-1224G>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 28/30 | chrX | 40656284 | |||||||
| chrX:40656364 | C | T | 1 | a0001c0001t0001g0114 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3973-1304G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 28/30 | chrX | 40656364 | |||||||
| chrX:40656366 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3973-1306G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 28/30 | chrX | 40656366 | |||||||
| chrX:40656671 | A | C | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(124): Show |
142 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.3973-1611T>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 28/30 | chrX | 40656671 | |||||||
| chrX:40656818 | T | C | 1 | a0001c0001t0001g0140 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.3973-1758A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 28/30 | chrX | 40656818 | |||||||
| chrX:40656854 | A | G | 2 | a0001c0002t0001g0228 a0001c0002t0001g0229 |
2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.3973-1794T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 28/30 | chrX | 40656854 | |||||||
| chrX:40656953 | T | A | 3 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0003t0001g0204 |
3 | HG02615.hp1 HG02723.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.3973-1893A>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 28/30 | chrX | 40656953 | |||||||
| chrX:40657728 | C | T | 5 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0003t0001g0010 others(2): Show |
6 | HG02615.hp1 HG02723.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.3972+1499G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 28/30 | chrX | 40657728 | |||||||
| chrX:40657794 | C | T | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(149): Show |
170 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.3972+1433G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 28/30 | chrX | 40657794 | |||||||
| chrX:40657842 | A | G | 1 | a0001c0013t0001g0225 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3972+1385T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 28/30 | chrX | 40657842 | |||||||
| chrX:40657867 | C | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG00609.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.3972+1360G>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 28/30 | chrX | 40657867 | |||||||
| chrX:40657976 | T | C | 2 | a0001c0002t0001g0228 a0001c0002t0001g0229 |
2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.3972+1251A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 28/30 | chrX | 40657976 | |||||||
| chrX:40658059 | G | T | 19 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0162 others(16): Show |
21 | HG00438.hp2 HG00639.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.3972+1168C>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 28/30 | chrX | 40658059 | |||||||
| chrX:40658487 | C | A | 1 | a0001c0002t0007g0028 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.3972+740G>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 28/30 | chrX | 40658487 | |||||||
| chrX:40658688 | CA | C | 38 | a0001c0001t0001g0017 a0001c0001t0001g0157 a0001c0001t0001g0189 others(35): Show |
38 | HG00408.hp1 HG02015.hp1 HG02071.hp1 others(35): Show |
intron_variant | MODIFIER | c.3972+538delT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 28/30 | chrX | 40658688 | |||||||
| chrX:40658688 | CAA | C | 27 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0067 others(24): Show |
29 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.3972+537_3972+538d others(4): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 28/30 | chrX | 40658688 | |||||||
| chrX:40658688 | CAAA | C | 95 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(92): Show |
111 | HG00280.hp1 HG00408.hp2 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.3972+536_3972+538d others(5): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 28/30 | chrX | 40658688 | |||||||
| chrX:40658688 | CAAAA | C | 15 | a0001c0001t0001g0095 a0001c0001t0001g0166 a0001c0001t0001g0168 others(12): Show |
16 | HG01496.hp1 HG01891.hp2 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.3972+535_3972+538d others(6): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 28/30 | chrX | 40658688 | |||||||
| chrX:40658688 | CAAAAA | C | 19 | a0001c0001t0001g0003 a0001c0001t0001g0160 a0001c0001t0001g0161 others(16): Show |
21 | HG00438.hp2 HG00639.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.3972+534_3972+538d others(7): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 28/30 | chrX | 40658688 | |||||||
| chrX:40659124 | T | C | 4 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0025 others(1): Show |
4 | HG02280.hp1 HG02622.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.3972+103A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 28/30 | chrX | 40659124 | |||||||
| chrX:40660064 | C | T | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
186 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.3685-457G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 26/30 | chrX | 40660064 | |||||||
| chrX:40660088 | TA | T | 5 | a0001c0001t0002g0005 a0001c0001t0002g0053 a0001c0001t0002g0056 others(2): Show |
6 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.3685-482delT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 26/30 | chrX | 40660088 | |||||||
| chrX:40660252 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3685-645T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 26/30 | chrX | 40660252 | |||||||
| chrX:40660770 | G | C | 1 | a0001c0001t0002g0107 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.3685-1163C>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 26/30 | chrX | 40660770 | |||||||
| chrX:40660937 | C | T | 1 | a0001c0001t0001g0083 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3685-1330G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 26/30 | chrX | 40660937 | |||||||
| chrX:40660980 | T | C | 1 | a0001c0002t0009g0226 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3685-1373A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 26/30 | chrX | 40660980 | |||||||
| chrX:40661175 | G | A | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(116): Show |
134 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.3685-1568C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 26/30 | chrX | 40661175 | |||||||
| chrX:40661214 | T | C | 6 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(3): Show |
6 | HG01891.hp2 HG02055.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.3685-1607A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 26/30 | chrX | 40661214 | |||||||
| chrX:40661279 | ACCATGTT others(123): Show |
A | 6 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(3): Show |
6 | HG01891.hp2 HG02055.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.3684+1516_3684+164 others(4): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 26/30 | chrX | 40661279 | |||||||
| chrX:40661281 | C | T | 1 | a0001c0004t0001g0004 | 3 | HG02280.hp2 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3684+1644G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 26/30 | chrX | 40661281 | |||||||
| chrX:40661373 | C | T | 2 | a0001c0001t0005g0158 a0001c0001t0005g0159 |
2 | HG00673.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.3684+1552G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 26/30 | chrX | 40661373 | |||||||
| chrX:40661400 | T | C | 1 | a0001c0001t0001g0230 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.3684+1525A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 26/30 | chrX | 40661400 | |||||||
| chrX:40661418 | G | C | 3 | a0001c0001t0003g0182 a0001c0001t0003g0183 a0001c0001t0003g0185 |
3 | HG02572.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3684+1507C>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 26/30 | chrX | 40661418 | |||||||
| chrX:40661624 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.3684+1301G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 26/30 | chrX | 40661624 | |||||||
| chrX:40661783 | T | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
166 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.3684+1142A>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 26/30 | chrX | 40661783 | |||||||
| chrX:40662096 | C | G | 1 | a0001c0002t0001g0047 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3684+829G>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 26/30 | chrX | 40662096 | |||||||
| chrX:40662567 | C | T | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(110): Show |
128 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.3684+358G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 26/30 | chrX | 40662567 | |||||||
| chrX:40662574 | G | T | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(144): Show |
164 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.3684+351C>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 26/30 | chrX | 40662574 | |||||||
| chrX:40662912 | T | G | 1 | a0001c0001t0001g0188 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3684+13A>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 26/30 | chrX | 40662912 | |||||||
| chrX:40663974 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3448+333G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 25/30 | chrX | 40663974 | |||||||
| chrX:40664018 | T | C | 1 | a0001c0002t0001g0013 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.3448+289A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 25/30 | chrX | 40664018 | |||||||
| chrX:40664043 | T | C | 1 | a0001c0001t0001g0139 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.3448+264A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 25/30 | chrX | 40664043 | |||||||
| chrX:40664113 | G | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
185 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.3448+194C>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 25/30 | chrX | 40664113 | |||||||
| chrX:40664281 | A | C | 2 | a0001c0002t0001g0227 a0001c0002t0009g0226 |
2 | HG00733.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3448+26T>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 25/30 | chrX | 40664281 | |||||||
| chrX:40664631 | C | G | 2 | a0001c0002t0001g0227 a0001c0002t0009g0226 |
2 | HG00733.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3266-142G>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 24/30 | chrX | 40664631 | |||||||
| chrX:40664708 | G | C | 1 | a0001c0001t0001g0211 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.3266-219C>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 24/30 | chrX | 40664708 | |||||||
| chrX:40664921 | C | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(111): Show |
129 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.3266-432G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 24/30 | chrX | 40664921 | |||||||
| chrX:40665111 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3266-622T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 24/30 | chrX | 40665111 | |||||||
| chrX:40665311 | T | C | 2 | a0001c0002t0004g0011 a0001c0002t0004g0209 |
3 | HG02809.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3266-822A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 24/30 | chrX | 40665311 | |||||||
| chrX:40665449 | C | G | 4 | a0001c0002t0001g0212 a0001c0003t0001g0010 a0001c0003t0001g0204 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.3266-960G>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 24/30 | chrX | 40665449 | |||||||
| chrX:40665536 | A | C | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(123): Show |
141 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.3266-1047T>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 24/30 | chrX | 40665536 | |||||||
| chrX:40665580 | T | C | 1 | a0001c0001t0001g0189 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.3266-1091A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 24/30 | chrX | 40665580 | |||||||
| chrX:40666079 | C | T | 1 | a0005c0012t0001g0051 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.3265+641G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 24/30 | chrX | 40666079 | |||||||
| chrX:40666446 | A | G | 2 | a0001c0002t0001g0228 a0001c0002t0001g0229 |
2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.3265+274T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 24/30 | chrX | 40666446 | |||||||
| chrX:40666645 | T | C | 1 | a0001c0002t0009g0226 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3265+75A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 24/30 | chrX | 40666645 | |||||||
| chrX:40667144 | T | C | 1 | a0001c0002t0001g0210 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3134-293A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40667144 | |||||||
| chrX:40667224 | G | A | 1 | a0001c0003t0001g0204 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3134-373C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40667224 | |||||||
| chrX:40667405 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3134-554A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40667405 | |||||||
| chrX:40667487 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3134-636G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40667487 | |||||||
| chrX:40667952 | C | G | 1 | a0001c0001t0001g0160 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3134-1101G>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40667952 | |||||||
| chrX:40668361 | C | G | 3 | a0001c0001t0003g0182 a0001c0001t0003g0183 a0001c0001t0003g0185 |
3 | HG02572.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3134-1510G>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40668361 | |||||||
| chrX:40668383 | C | CA | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(107): Show |
124 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.3134-1533dupT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40668383 | |||||||
| chrX:40668383 | C | CAA | 35 | a0001c0001t0001g0067 a0001c0001t0001g0072 a0001c0001t0001g0076 others(32): Show |
38 | HG00642.hp1 HG01069.hp1 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.3134-1534_3134-153 others(6): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40668383 | |||||||
| chrX:40668414 | A | G | 6 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(3): Show |
6 | HG01891.hp2 HG02055.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.3134-1563T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40668414 | |||||||
| chrX:40668552 | T | C | 1 | a0001c0001t0001g0177 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3134-1701A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40668552 | |||||||
| chrX:40668585 | T | C | 1 | a0001c0002t0001g0033 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.3134-1734A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40668585 | |||||||
| chrX:40668731 | T | C | 6 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(3): Show |
6 | HG01891.hp2 HG02055.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.3134-1880A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40668731 | |||||||
| chrX:40668819 | A | G | 1 | a0001c0002t0009g0226 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3134-1968T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40668819 | |||||||
| chrX:40668895 | G | C | 1 | a0001c0013t0001g0225 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3134-2044C>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40668895 | |||||||
| chrX:40668961 | A | G | 7 | a0001c0001t0001g0006 a0001c0001t0001g0082 a0001c0001t0001g0092 others(4): Show |
8 | HG02165.hp1 HG03017.hp1 HG03688.hp1 others(5): Show |
intron_variant | MODIFIER | c.3134-2110T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40668961 | |||||||
| chrX:40669139 | A | C | 1 | a0001c0001t0001g0174 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3134-2288T>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40669139 | |||||||
| chrX:40669355 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3134-2504C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40669355 | |||||||
| chrX:40669525 | A | T | 1 | a0001c0001t0001g0160 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3133+2336T>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40669525 | |||||||
| chrX:40669574 | C | A | 1 | a0001c0002t0009g0226 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3133+2287G>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40669574 | |||||||
| chrX:40669775 | C | G | 1 | a0001c0001t0001g0188 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3133+2086G>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40669775 | |||||||
| chrX:40669868 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3133+1993T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40669868 | |||||||
| chrX:40669901 | C | T | 1 | a0001c0002t0001g0031 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.3133+1960G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40669901 | |||||||
| chrX:40669934 | C | T | 1 | a0001c0013t0001g0225 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3133+1927G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40669934 | |||||||
| chrX:40670200 | G | C | 1 | a0001c0001t0003g0183 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3133+1661C>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40670200 | |||||||
| chrX:40670623 | C | T | 13 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0163 others(10): Show |
15 | HG00438.hp2 HG00639.hp2 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.3133+1238G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40670623 | |||||||
| chrX:40670661 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3133+1200A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40670661 | |||||||
| chrX:40670677 | C | T | 2 | a0001c0001t0001g0091 a0001c0010t0001g0087 |
2 | NA19077.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.3133+1184G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40670677 | |||||||
| chrX:40670692 | C | T | 1 | a0001c0002t0001g0212 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3133+1169G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40670692 | |||||||
| chrX:40670697 | C | A | 1 | a0001c0002t0001g0212 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3133+1164G>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40670697 | |||||||
| chrX:40670767 | C | CA | 13 | a0001c0001t0001g0188 a0001c0001t0001g0206 a0001c0001t0001g0207 others(10): Show |
15 | HG01255.hp1 HG02109.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.3133+1093dupT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40670767 | |||||||
| chrX:40670767 | CA | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(107): Show |
125 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.3133+1093delT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40670767 | |||||||
| chrX:40670777 | A | T | 2 | a0001c0001t0002g0108 a0001c0002t0001g0227 |
2 | HG02148.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3133+1084T>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40670777 | |||||||
| chrX:40671085 | T | G | 2 | a0001c0002t0001g0036 a0001c0002t0001g0041 |
2 | NA18960.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.3133+776A>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40671085 | |||||||
| chrX:40671212 | G | A | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(139): Show |
159 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.3133+649C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40671212 | |||||||
| chrX:40671516 | A | G | 1 | a0001c0001t0002g0143 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3133+345T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40671516 | |||||||
| chrX:40671727 | T | C | 7 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0002g0173 others(4): Show |
8 | HG02615.hp1 HG02622.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.3133+134A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40671727 | |||||||
| chrX:40672138 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3022-166T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 22/30 | chrX | 40672138 | |||||||
| chrX:40672259 | C | T | 1 | a0001c0001t0001g0006 | 2 | NA18953.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.3022-287G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 22/30 | chrX | 40672259 | |||||||
| chrX:40672271 | A | G | 20 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0162 others(17): Show |
22 | HG00438.hp2 HG00639.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.3022-299T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 22/30 | chrX | 40672271 | |||||||
| chrX:40672376 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3022-404C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 22/30 | chrX | 40672376 | |||||||
| chrX:40672519 | T | A | 2 | a0001c0002t0004g0011 a0001c0002t0004g0209 |
3 | HG02809.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3022-547A>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 22/30 | chrX | 40672519 | |||||||
| chrX:40672643 | A | G | 8 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0002g0173 others(5): Show |
9 | HG02615.hp1 HG02622.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.3022-671T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 22/30 | chrX | 40672643 | |||||||
| chrX:40672680 | G | A | 4 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0073 others(1): Show |
4 | NA18987.hp2 NA19006.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.3022-708C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 22/30 | chrX | 40672680 | |||||||
| chrX:40672739 | T | A | 2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | NA19062.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.3022-767A>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 22/30 | chrX | 40672739 | |||||||
| chrX:40673148 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.3022-1176G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 22/30 | chrX | 40673148 | |||||||
| chrX:40673640 | A | G | 2 | a0001c0002t0001g0228 a0001c0002t0001g0229 |
2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.3021+1581T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 22/30 | chrX | 40673640 | |||||||
| chrX:40673834 | GA | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(85): Show |
102 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.3021+1386delT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 22/30 | chrX | 40673834 | |||||||
| chrX:40673846 | CA | C | 14 | a0001c0001t0001g0060 a0001c0001t0001g0083 a0001c0001t0001g0206 others(11): Show |
18 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.3021+1374delT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 22/30 | chrX | 40673846 | |||||||
| chrX:40673846 | CAA | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(136): Show |
155 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.3021+1373_3021+137 others(6): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 22/30 | chrX | 40673846 | |||||||
| chrX:40674138 | C | A | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.3021+1083G>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 22/30 | chrX | 40674138 | |||||||
| chrX:40674141 | C | T | 1 | a0001c0002t0001g0222 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3021+1080G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 22/30 | chrX | 40674141 | |||||||
| chrX:40674568 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3021+653A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 22/30 | chrX | 40674568 | |||||||
| chrX:40674580 | C | A | 3 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 |
3 | NA18954.hp1 NA18957.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.3021+641G>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 22/30 | chrX | 40674580 | |||||||
| chrX:40675118 | G | A | 3 | a0001c0001t0003g0182 a0001c0001t0003g0183 a0001c0001t0003g0185 |
3 | HG02572.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3021+103C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 22/30 | chrX | 40675118 | |||||||
| chrX:40676009 | A | G | 9 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0002g0173 others(6): Show |
10 | HG00733.hp1 HG02615.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.2881-648T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 21/30 | chrX | 40676009 | |||||||
| chrX:40676085 | C | A | 53 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(50): Show |
53 | HG00408.hp1 HG01169.hp1 HG01255.hp1 others(50): Show |
intron_variant | MODIFIER | c.2881-724G>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 21/30 | chrX | 40676085 | |||||||
| chrX:40676275 | C | G | 1 | a0001c0002t0001g0049 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2881-914G>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 21/30 | chrX | 40676275 | |||||||
| chrX:40676354 | A | C | 2 | a0001c0002t0004g0011 a0001c0002t0004g0209 |
3 | HG02809.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2881-993T>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 21/30 | chrX | 40676354 | |||||||
| chrX:40676698 | C | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0075 |
2 | NA18943.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.2881-1337G>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 21/30 | chrX | 40676698 | |||||||
| chrX:40676782 | G | T | 1 | a0001c0004t0001g0004 | 3 | HG02280.hp2 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2881-1421C>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 21/30 | chrX | 40676782 | |||||||
| chrX:40676845 | C | T | 2 | a0001c0001t0001g0067 a0001c0001t0001g0068 |
2 | HG00738.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.2881-1484G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 21/30 | chrX | 40676845 | |||||||
| chrX:40676869 | C | T | 67 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0002t0001g0013 others(64): Show |
71 | HG00408.hp1 HG00733.hp1 HG01169.hp1 others(68): Show |
intron_variant | MODIFIER | c.2881-1508G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 21/30 | chrX | 40676869 | |||||||
| chrX:40677068 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2881-1707G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 21/30 | chrX | 40677068 | |||||||
| chrX:40677135 | G | A | 3 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0171 |
3 | HG01257.hp1 HG01258.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.2881-1774C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 21/30 | chrX | 40677135 | |||||||
| chrX:40677540 | T | A | 1 | a0001c0001t0002g0065 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2881-2179A>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 21/30 | chrX | 40677540 | |||||||
| chrX:40677545 | T | A | 1 | a0001c0001t0002g0065 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2881-2184A>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 21/30 | chrX | 40677545 | |||||||
| chrX:40677549 | C | A | 1 | a0001c0001t0002g0065 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2881-2188G>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 21/30 | chrX | 40677549 | |||||||
| chrX:40677553 | T | A | 1 | a0001c0001t0002g0065 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2881-2192A>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 21/30 | chrX | 40677553 | |||||||
| chrX:40677796 | G | A | 1 | a0001c0013t0001g0225 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2880+2068C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 21/30 | chrX | 40677796 | |||||||
| chrX:40678075 | A | C | 3 | a0001c0001t0001g0201 a0001c0001t0001g0203 a0004c0007t0001g0202 |
3 | HG02145.hp1 HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2880+1789T>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 21/30 | chrX | 40678075 | |||||||
| chrX:40678135 | C | T | 5 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0003t0001g0010 others(2): Show |
6 | HG02615.hp1 HG02723.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.2880+1729G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 21/30 | chrX | 40678135 | |||||||
| chrX:40678248 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2880+1616G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 21/30 | chrX | 40678248 | |||||||
| chrX:40678332 | GA | G | 101 | a0001c0001t0001g0003 a0001c0001t0001g0160 a0001c0001t0001g0161 others(98): Show |
107 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.2880+1531delT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 21/30 | chrX | 40678332 | |||||||
| chrX:40678486 | C | T | 31 | a0001c0001t0001g0003 a0001c0001t0001g0160 a0001c0001t0001g0161 others(28): Show |
33 | HG00438.hp2 HG00639.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.2880+1378G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 21/30 | chrX | 40678486 | |||||||
| chrX:40678521 | A | G | 1 | a0001c0003t0001g0204 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2880+1343T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 21/30 | chrX | 40678521 | |||||||
| chrX:40678651 | A | G | 1 | a0001c0002t0001g0212 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2880+1213T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 21/30 | chrX | 40678651 | |||||||
| chrX:40678827 | G | GA | 28 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0162 others(25): Show |
30 | HG00438.hp2 HG00639.hp2 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.2880+1036dupT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 21/30 | chrX | 40678827 | |||||||
| chrX:40678873 | C | G | 1 | a0001c0001t0001g0178 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2880+991G>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 21/30 | chrX | 40678873 | |||||||
| chrX:40679273 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2880+591C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 21/30 | chrX | 40679273 | |||||||
| chrX:40679294 | G | A | 1 | a0001c0013t0001g0225 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2880+570C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 21/30 | chrX | 40679294 | |||||||
| chrX:40679299 | G | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG01192.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.2880+565C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 21/30 | chrX | 40679299 | |||||||
| chrX:40679396 | A | T | 1 | a0001c0002t0009g0226 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2880+468T>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 21/30 | chrX | 40679396 | |||||||
| chrX:40679446 | G | A | 1 | a0001c0004t0001g0004 | 3 | HG02280.hp2 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2880+418C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 21/30 | chrX | 40679446 | |||||||
| chrX:40679488 | C | G | 1 | a0001c0001t0001g0090 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2880+376G>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 21/30 | chrX | 40679488 | |||||||
| chrX:40680303 | G | T | 1 | a0001c0001t0001g0113 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2611-170C>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 20/30 | chrX | 40680303 | |||||||
| chrX:40680366 | C | G | 4 | a0001c0001t0001g0201 a0001c0001t0001g0203 a0001c0002t0001g0212 others(1): Show |
4 | HG02145.hp1 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2611-233G>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 20/30 | chrX | 40680366 | |||||||
| chrX:40680487 | C | T | 1 | a0001c0002t0009g0226 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2610+271G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 20/30 | chrX | 40680487 | |||||||
| chrX:40680511 | C | G | 1 | a0001c0002t0001g0227 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2610+247G>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 20/30 | chrX | 40680511 | |||||||
| chrX:40680657 | A | C | 1 | a0001c0001t0001g0177 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2610+101T>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 20/30 | chrX | 40680657 | |||||||
| chrX:40680664 | C | T | 1 | a0001c0002t0001g0227 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2610+94G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 20/30 | chrX | 40680664 | |||||||
| chrX:40681140 | C | T | 1 | a0001c0013t0001g0225 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2458-230G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 19/30 | chrX | 40681140 | |||||||
| chrX:40681411 | GA | G | 3 | a0001c0003t0001g0010 a0001c0003t0001g0204 a0001c0003t0001g0205 |
4 | HG02615.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2457+440delT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 19/30 | chrX | 40681411 | |||||||
| chrX:40681568 | C | T | 102 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0160 others(99): Show |
108 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(105): Show |
intron_variant | MODIFIER | c.2457+284G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 19/30 | chrX | 40681568 | |||||||
| chrX:40681994 | A | C | 1 | a0001c0002t0001g0049 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2366-51T>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 18/30 | chrX | 40681994 | |||||||
| chrX:40682110 | G | A | 1 | a0001c0001t0001g0007 | 2 | NA18962.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.2366-167C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 18/30 | chrX | 40682110 | |||||||
| chrX:40682290 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2365+313A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 18/30 | chrX | 40682290 | |||||||
| chrX:40682567 | T | A | 4 | a0001c0001t0001g0098 a0001c0002t0001g0018 a0001c0002t0001g0020 others(1): Show |
4 | HG01257.hp2 HG02622.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.2365+36A>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 18/30 | chrX | 40682567 | |||||||
| chrX:40683264 | A | C | 6 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(3): Show |
6 | HG01891.hp2 HG02055.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2058-268T>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 16/30 | chrX | 40683264 | |||||||
| chrX:40683401 | C | T | 1 | a0001c0002t0001g0208 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2058-405G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 16/30 | chrX | 40683401 | |||||||
| chrX:40683403 | A | G | 1 | a0001c0001t0001g0072 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2058-407T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 16/30 | chrX | 40683403 | |||||||
| chrX:40683502 | A | G | 1 | a0001c0004t0001g0004 | 3 | HG02280.hp2 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2058-506T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 16/30 | chrX | 40683502 | |||||||
| chrX:40683774 | G | GA | 1 | a0001c0004t0001g0004 | 3 | HG02280.hp2 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2058-779dupT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 16/30 | chrX | 40683774 | |||||||
| chrX:40684346 | G | A | 1 | a0001c0013t0001g0225 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2058-1350C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 16/30 | chrX | 40684346 | |||||||
| chrX:40684590 | G | A | 28 | a0001c0001t0001g0003 a0001c0001t0001g0160 a0001c0001t0001g0161 others(25): Show |
30 | HG00438.hp2 HG00639.hp2 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.2058-1594C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 16/30 | chrX | 40684590 | |||||||
| chrX:40684636 | G | A | 1 | a0001c0001t0001g0083 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2058-1640C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 16/30 | chrX | 40684636 | |||||||
| chrX:40684702 | T | C | 2 | a0001c0002t0001g0052 a0001c0002t0001g0224 |
2 | HG03669.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.2058-1706A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 16/30 | chrX | 40684702 | |||||||
| chrX:40684912 | G | A | 1 | a0001c0002t0001g0227 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2058-1916C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 16/30 | chrX | 40684912 | |||||||
| chrX:40684931 | T | C | 4 | a0001c0001t0001g0160 a0001c0001t0001g0201 a0001c0001t0001g0203 others(1): Show |
4 | HG02145.hp1 HG02723.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2058-1935A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 16/30 | chrX | 40684931 | |||||||
| chrX:40685573 | C | G | 59 | a0001c0001t0001g0017 a0001c0001t0001g0201 a0001c0001t0001g0203 others(56): Show |
60 | HG00408.hp1 HG01169.hp1 HG01255.hp1 others(57): Show |
intron_variant | MODIFIER | c.2058-2577G>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 16/30 | chrX | 40685573 | |||||||
| chrX:40685617 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2058-2621T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 16/30 | chrX | 40685617 | |||||||
| chrX:40686071 | C | G | 1 | a0001c0001t0001g0200 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2057+2383G>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 16/30 | chrX | 40686071 | |||||||
| chrX:40686154 | A | C | 3 | a0001c0002t0001g0221 a0001c0002t0001g0222 a0001c0002t0001g0223 |
3 | HG01255.hp1 HG02109.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2057+2300T>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 16/30 | chrX | 40686154 | |||||||
| chrX:40686252 | C | T | 1 | a0001c0002t0001g0046 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2057+2202G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 16/30 | chrX | 40686252 | |||||||
| chrX:40686320 | T | G | 6 | a0001c0002t0001g0213 a0001c0002t0001g0214 a0001c0002t0001g0216 others(3): Show |
6 | HG02818.hp2 HG02895.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2057+2134A>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 16/30 | chrX | 40686320 | |||||||
| chrX:40686429 | C | A | 1 | a0001c0002t0001g0215 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2057+2025G>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 16/30 | chrX | 40686429 | |||||||
| chrX:40686529 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2057+1925G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 16/30 | chrX | 40686529 | |||||||
| chrX:40686545 | T | G | 102 | a0001c0001t0001g0003 a0001c0001t0001g0157 a0001c0001t0001g0160 others(99): Show |
108 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(105): Show |
intron_variant | MODIFIER | c.2057+1909A>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 16/30 | chrX | 40686545 | |||||||
| chrX:40686620 | G | C | 1 | a0001c0001t0001g0149 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2057+1834C>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 16/30 | chrX | 40686620 | |||||||
| chrX:40686654 | T | C | 1 | a0001c0001t0001g0073 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2057+1800A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 16/30 | chrX | 40686654 | |||||||
| chrX:40686968 | CT | C | 100 | a0001c0001t0001g0003 a0001c0001t0001g0160 a0001c0001t0001g0161 others(97): Show |
106 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.2057+1485delA | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 16/30 | chrX | 40686968 | |||||||
| chrX:40687130 | G | A | 56 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(53): Show |
59 | HG00408.hp1 HG01169.hp1 HG01255.hp1 others(56): Show |
intron_variant | MODIFIER | c.2057+1324C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 16/30 | chrX | 40687130 | |||||||
| chrX:40687159 | A | C | 4 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0179 others(1): Show |
4 | HG01891.hp2 HG02055.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2057+1295T>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 16/30 | chrX | 40687159 | |||||||
| chrX:40687429 | G | C | 61 | a0001c0001t0001g0017 a0001c0001t0001g0201 a0001c0001t0001g0203 others(58): Show |
64 | HG00408.hp1 HG01169.hp1 HG01255.hp1 others(61): Show |
intron_variant | MODIFIER | c.2057+1025C>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 16/30 | chrX | 40687429 | |||||||
| chrX:40688094 | G | A | 1 | a0001c0001t0001g0181 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2057+360C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 16/30 | chrX | 40688094 | |||||||
| chrX:40688762 | A | G | 6 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(3): Show |
6 | HG01891.hp2 HG02055.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1981-232T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40688762 | |||||||
| chrX:40688868 | C | T | 4 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0179 others(1): Show |
4 | HG01891.hp2 HG02055.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1981-338G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40688868 | |||||||
| chrX:40688938 | T | G | 1 | a0001c0001t0001g0192 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1981-408A>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40688938 | |||||||
| chrX:40688949 | A | G | 1 | a0001c0001t0001g0119 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1981-419T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40688949 | |||||||
| chrX:40689029 | C | A | 1 | a0001c0002t0001g0229 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1981-499G>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40689029 | |||||||
| chrX:40689030 | C | G | 15 | a0001c0001t0001g0211 a0001c0002t0001g0013 a0001c0002t0001g0019 others(12): Show |
15 | HG00408.hp1 HG02523.hp1 NA18946.hp2 others(12): Show |
intron_variant | MODIFIER | c.1981-500G>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40689030 | |||||||
| chrX:40689226 | C | G | 1 | a0001c0009t0001g0124 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1981-696G>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40689226 | |||||||
| chrX:40689259 | A | G | 1 | a0001c0001t0001g0190 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1981-729T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40689259 | |||||||
| chrX:40689269 | G | A | 6 | a0001c0002t0001g0213 a0001c0002t0001g0214 a0001c0002t0001g0216 others(3): Show |
6 | HG02818.hp2 HG02895.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1981-739C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40689269 | |||||||
| chrX:40689354 | A | G | 3 | a0001c0001t0001g0201 a0001c0001t0001g0203 a0004c0007t0001g0202 |
3 | HG02145.hp1 HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1981-824T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40689354 | |||||||
| chrX:40689869 | G | C | 1 | a0001c0004t0001g0004 | 3 | HG02280.hp2 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1981-1339C>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40689869 | |||||||
| chrX:40690185 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1981-1655C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40690185 | |||||||
| chrX:40690559 | C | T | 1 | a0001c0002t0001g0212 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1980+1624G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40690559 | |||||||
| chrX:40690706 | T | C | 74 | a0001c0001t0001g0017 a0001c0001t0001g0157 a0001c0001t0001g0201 others(71): Show |
78 | HG00408.hp1 HG00733.hp1 HG01169.hp1 others(75): Show |
intron_variant | MODIFIER | c.1980+1477A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40690706 | |||||||
| chrX:40690716 | A | C | 63 | a0001c0001t0001g0017 a0001c0001t0001g0157 a0001c0001t0001g0201 others(60): Show |
64 | HG00408.hp1 HG00733.hp1 HG01169.hp1 others(61): Show |
intron_variant | MODIFIER | c.1980+1467T>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40690716 | |||||||
| chrX:40691069 | T | A | 1 | a0001c0001t0011g0110 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1980+1114A>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40691069 | |||||||
| chrX:40691405 | G | C | 2 | a0001c0002t0001g0228 a0001c0002t0001g0229 |
2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1980+778C>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40691405 | |||||||
| chrX:40691572 | T | C | 3 | a0001c0002t0001g0221 a0001c0002t0001g0222 a0001c0002t0001g0223 |
3 | HG01255.hp1 HG02109.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1980+611A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40691572 | |||||||
| chrX:40691599 | C | A | 1 | a0001c0001t0001g0139 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1980+584G>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40691599 | |||||||
| chrX:40691601 | T | C | 1 | a0001c0001t0001g0139 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1980+582A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40691601 | |||||||
| chrX:40691604 | A | AT | 71 | a0001c0001t0001g0165 a0001c0001t0001g0175 a0001c0001t0001g0176 others(68): Show |
74 | HG00408.hp1 HG00733.hp1 HG01169.hp1 others(71): Show |
intron_variant | MODIFIER | c.1980+578_1980+579i others(3): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40691604 | |||||||
| chrX:40691604 | A | ATC | 7 | a0001c0001t0001g0179 a0001c0001t0002g0077 a0001c0002t0001g0020 others(4): Show |
7 | HG02451.hp2 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1980+578_1980+579i others(4): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40691604 | |||||||
| chrX:40691604 | A | ATCT | 21 | a0001c0001t0001g0069 a0001c0001t0001g0116 a0001c0001t0002g0005 others(18): Show |
21 | HG01069.hp1 HG01106.hp1 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.1980+578_1980+579i others(5): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40691604 | |||||||
| chrX:40691604 | A | ATCTT | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(86): Show |
102 | HG00280.hp1 HG00408.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.1980+578_1980+579i others(6): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40691604 | |||||||
| chrX:40691604 | A | ATCTTT | 15 | a0001c0001t0001g0001 a0001c0001t0001g0060 a0001c0001t0001g0061 others(12): Show |
15 | HG00140.hp1 HG00438.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.1980+578_1980+579i others(7): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40691604 | |||||||
| chrX:40691605 | A | C | 71 | a0001c0001t0001g0165 a0001c0001t0001g0175 a0001c0001t0001g0176 others(68): Show |
74 | HG00408.hp1 HG00733.hp1 HG01169.hp1 others(71): Show |
intron_variant | MODIFIER | c.1980+578T>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40691605 | |||||||
| chrX:40691606 | T | C | 26 | a0001c0001t0001g0003 a0001c0001t0001g0160 a0001c0001t0001g0161 others(23): Show |
29 | HG00438.hp2 HG00639.hp2 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.1980+577A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40691606 | |||||||
| chrX:40691773 | G | A | 1 | a0001c0013t0001g0225 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1980+410C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40691773 | |||||||
| chrX:40691901 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1980+282G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40691901 | |||||||
| chrX:40691919 | C | CT | 5 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0003t0001g0010 others(2): Show |
6 | HG02615.hp1 HG02723.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1980+263dupA | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40691919 | |||||||
| chrX:40692119 | C | G | 6 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(3): Show |
6 | HG01891.hp2 HG02055.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1980+64G>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40692119 | |||||||
| chrX:40692347 | TA | T | 83 | a0001c0001t0001g0003 a0001c0001t0001g0160 a0001c0001t0001g0161 others(80): Show |
89 | HG00438.hp2 HG00639.hp2 HG00733.hp1 others(86): Show |
intron_variant | MODIFIER | c.1846-31delT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 14/30 | chrX | 40692347 | |||||||
| chrX:40692347 | TAA | T | 17 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0002t0001g0013 others(14): Show |
17 | HG00408.hp1 HG02523.hp1 HG02698.hp1 others(14): Show |
intron_variant | MODIFIER | c.1846-32_1846-31del others(2): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 14/30 | chrX | 40692347 | |||||||
| chrX:40692991 | T | C | 61 | a0001c0001t0001g0157 a0001c0001t0001g0201 a0001c0001t0001g0203 others(58): Show |
62 | HG00408.hp1 HG00733.hp1 HG01169.hp1 others(59): Show |
intron_variant | MODIFIER | c.1651-89A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 13/30 | chrX | 40692991 | |||||||
| chrX:40693294 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1651-392C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 13/30 | chrX | 40693294 | |||||||
| chrX:40693317 | G | A | 3 | a0001c0003t0001g0010 a0001c0003t0001g0204 a0001c0003t0001g0205 |
4 | HG02615.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1651-415C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 13/30 | chrX | 40693317 | |||||||
| chrX:40693322 | T | C | 3 | a0001c0002t0001g0208 a0001c0002t0001g0215 a0001c0002t0001g0218 |
3 | HG02647.hp1 HG02922.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1651-420A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 13/30 | chrX | 40693322 | |||||||
| chrX:40693383 | T | C | 6 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(3): Show |
6 | HG01891.hp2 HG02055.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1651-481A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 13/30 | chrX | 40693383 | |||||||
| chrX:40694002 | A | T | 1 | a0001c0002t0001g0227 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1651-1100T>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 13/30 | chrX | 40694002 | |||||||
| chrX:40694188 | C | T | 1 | a0001c0013t0001g0225 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1651-1286G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 13/30 | chrX | 40694188 | |||||||
| chrX:40694420 | A | G | 6 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(3): Show |
6 | HG01891.hp2 HG02055.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1651-1518T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 13/30 | chrX | 40694420 | |||||||
| chrX:40694589 | C | T | 100 | a0001c0001t0001g0003 a0001c0001t0001g0160 a0001c0001t0001g0161 others(97): Show |
106 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.1651-1687G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 13/30 | chrX | 40694589 | |||||||
| chrX:40696026 | G | A | 2 | a0001c0003t0001g0010 a0001c0003t0001g0205 |
3 | HG02976.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1650+998C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 13/30 | chrX | 40696026 | |||||||
| chrX:40696066 | C | T | 1 | a0001c0013t0001g0225 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1650+958G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 13/30 | chrX | 40696066 | |||||||
| chrX:40696133 | A | AT | 8 | a0001c0001t0001g0017 a0001c0001t0001g0072 a0001c0001t0001g0079 others(5): Show |
8 | HG02015.hp1 HG03654.hp1 HG03831.hp1 others(5): Show |
intron_variant | MODIFIER | c.1650+890dupA | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 13/30 | chrX | 40696133 | |||||||
| chrX:40696133 | AT | A | 7 | a0001c0001t0001g0099 a0001c0001t0001g0119 a0001c0001t0001g0120 others(4): Show |
7 | HG02056.hp1 HG02523.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.1650+890delA | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 13/30 | chrX | 40696133 | |||||||
| chrX:40696189 | C | T | 1 | a0001c0002t0001g0228 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1650+835G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 13/30 | chrX | 40696189 | |||||||
| chrX:40696344 | G | A | 1 | a0001c0013t0001g0225 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1650+680C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 13/30 | chrX | 40696344 | |||||||
| chrX:40696475 | G | A | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(216): Show |
240 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1650+549C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 13/30 | chrX | 40696475 | |||||||
| chrX:40696481 | T | C | 26 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0162 others(23): Show |
28 | HG00438.hp2 HG00639.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.1650+543A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 13/30 | chrX | 40696481 | |||||||
| chrX:40696999 | C | A | 3 | a0001c0003t0001g0010 a0001c0003t0001g0204 a0001c0003t0001g0205 |
4 | HG02615.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1650+25G>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 13/30 | chrX | 40696999 | |||||||
| chrX:40697240 | C | G | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
235 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.1491-57G>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 12/30 | chrX | 40697240 | |||||||
| chrX:40697831 | C | A | 3 | a0001c0003t0001g0010 a0001c0003t0001g0204 a0001c0003t0001g0205 |
4 | HG02615.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1491-648G>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 12/30 | chrX | 40697831 | |||||||
| chrX:40697871 | G | A | 2 | a0001c0002t0001g0227 a0001c0002t0009g0226 |
2 | HG00733.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1491-688C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 12/30 | chrX | 40697871 | |||||||
| chrX:40698033 | G | A | 1 | a0001c0001t0001g0083 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1491-850C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 12/30 | chrX | 40698033 | |||||||
| chrX:40698389 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1491-1206G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 12/30 | chrX | 40698389 | |||||||
| chrX:40698423 | T | G | 1 | a0001c0001t0001g0188 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1491-1240A>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 12/30 | chrX | 40698423 | |||||||
| chrX:40698577 | T | C | 2 | a0001c0001t0001g0168 a0001c0001t0001g0230 |
2 | HG01256.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.1491-1394A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 12/30 | chrX | 40698577 | |||||||
| chrX:40698680 | T | A | 1 | a0001c0004t0001g0004 | 3 | HG02280.hp2 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1491-1497A>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 12/30 | chrX | 40698680 | |||||||
| chrX:40698805 | A | G | 1 | a0001c0002t0001g0046 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1491-1622T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 12/30 | chrX | 40698805 | |||||||
| chrX:40698828 | G | A | 1 | a0001c0001t0002g0065 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1491-1645C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 12/30 | chrX | 40698828 | |||||||
| chrX:40698889 | G | A | 1 | a0001c0002t0001g0037 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1491-1706C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 12/30 | chrX | 40698889 | |||||||
| chrX:40699030 | G | C | 1 | a0001c0001t0001g0142 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1491-1847C>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 12/30 | chrX | 40699030 | |||||||
| chrX:40699065 | G | A | 2 | a0001c0003t0001g0010 a0001c0003t0001g0205 |
3 | HG02976.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1491-1882C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 12/30 | chrX | 40699065 | |||||||
| chrX:40699205 | G | A | 3 | a0001c0001t0001g0201 a0001c0001t0001g0203 a0004c0007t0001g0202 |
3 | HG02145.hp1 HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1490+1960C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 12/30 | chrX | 40699205 | |||||||
| chrX:40699206 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1490+1959T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 12/30 | chrX | 40699206 | |||||||
| chrX:40699272 | C | T | 1 | a0001c0004t0001g0004 | 3 | HG02280.hp2 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1490+1893G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 12/30 | chrX | 40699272 | |||||||
| chrX:40699426 | T | C | 2 | a0001c0002t0001g0227 a0001c0002t0009g0226 |
2 | HG00733.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1490+1739A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 12/30 | chrX | 40699426 | |||||||
| chrX:40699544 | G | A | 1 | a0001c0003t0001g0204 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1490+1621C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 12/30 | chrX | 40699544 | |||||||
| chrX:40699873 | C | T | 22 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0162 others(19): Show |
24 | HG00438.hp2 HG00639.hp2 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.1490+1292G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 12/30 | chrX | 40699873 | |||||||
| chrX:40699980 | T | C | 72 | a0001c0001t0001g0017 a0001c0001t0001g0189 a0001c0001t0001g0190 others(69): Show |
72 | HG00408.hp1 HG00733.hp1 HG01169.hp1 others(69): Show |
intron_variant | MODIFIER | c.1490+1185A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 12/30 | chrX | 40699980 | |||||||
| chrX:40700016 | GCA | G | 5 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0003t0001g0010 others(2): Show |
6 | HG02615.hp1 HG02723.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1490+1147_1490+114 others(6): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 12/30 | chrX | 40700016 | |||||||
| chrX:40700046 | G | C | 61 | a0001c0001t0001g0017 a0001c0001t0001g0157 a0001c0001t0001g0201 others(58): Show |
61 | HG00408.hp1 HG00733.hp1 HG01169.hp1 others(58): Show |
intron_variant | MODIFIER | c.1490+1119C>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 12/30 | chrX | 40700046 | |||||||
| chrX:40700225 | A | G | 1 | a0001c0002t0001g0227 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1490+940T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 12/30 | chrX | 40700225 | |||||||
| chrX:40700282 | G | C | 2 | a0001c0002t0001g0228 a0001c0002t0001g0229 |
2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1490+883C>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 12/30 | chrX | 40700282 | |||||||
| chrX:40700363 | C | CA | 25 | a0001c0001t0001g0189 a0001c0001t0001g0194 a0001c0001t0001g0203 others(22): Show |
28 | HG01169.hp1 HG01243.hp1 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.1490+801dupT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 12/30 | chrX | 40700363 | |||||||
| chrX:40700363 | C | CAA | 6 | a0001c0001t0001g0200 a0001c0001t0002g0057 a0001c0002t0001g0015 others(3): Show |
6 | NA18906.hp1 NA18950.hp2 NA19058.hp1 others(3): Show |
intron_variant | MODIFIER | c.1490+800_1490+801d others(4): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 12/30 | chrX | 40700363 | |||||||
| chrX:40700381 | AAAAAAAA others(5): Show |
A | 1 | a0001c0002t0001g0214 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1490+772_1490+783d others(14): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 12/30 | chrX | 40700381 | |||||||
| chrX:40700390 | AAAT | A | 7 | a0001c0001t0001g0069 a0001c0001t0001g0175 a0001c0001t0001g0177 others(4): Show |
7 | HG01891.hp2 HG02572.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1490+772_1490+774d others(5): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 12/30 | chrX | 40700390 | |||||||
| chrX:40700391 | AAT | A | 27 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(24): Show |
29 | HG00621.hp1 HG00639.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.1490+772_1490+773d others(4): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 12/30 | chrX | 40700391 | |||||||
| chrX:40700392 | AT | A | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(71): Show |
85 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1490+772delA | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 12/30 | chrX | 40700392 | |||||||
| chrX:40700393 | T | A | 121 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0017 others(118): Show |
124 | HG00280.hp1 HG00408.hp1 HG00642.hp1 others(121): Show |
intron_variant | MODIFIER | c.1490+772A>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 12/30 | chrX | 40700393 | |||||||
| chrX:40700690 | T | C | 1 | a0001c0002t0001g0050 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1490+475A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 12/30 | chrX | 40700690 | |||||||
| chrX:40700796 | G | A | 1 | a0001c0002t0001g0031 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1490+369C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 12/30 | chrX | 40700796 | |||||||
| chrX:40700871 | T | G | 2 | a0001c0002t0004g0011 a0001c0002t0004g0209 |
3 | HG02809.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1490+294A>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 12/30 | chrX | 40700871 | |||||||
| chrX:40700914 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1490+251A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 12/30 | chrX | 40700914 | |||||||
| chrX:40701156 | T | C | 3 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 |
3 | HG00609.hp1 NA18939.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1490+9A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 12/30 | chrX | 40701156 | |||||||
| chrX:40701597 | G | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG00609.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1412-354C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 11/30 | chrX | 40701597 | |||||||
| chrX:40701601 | T | C | 2 | a0001c0002t0001g0228 a0001c0002t0001g0229 |
2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1412-358A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 11/30 | chrX | 40701601 | |||||||
| chrX:40701835 | A | G | 1 | a0001c0002t0009g0226 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1412-592T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 11/30 | chrX | 40701835 | |||||||
| chrX:40702043 | G | A | 1 | a0001c0002t0001g0218 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1412-800C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 11/30 | chrX | 40702043 | |||||||
| chrX:40702110 | C | T | 3 | a0001c0001t0003g0182 a0001c0001t0003g0183 a0001c0001t0003g0185 |
3 | HG02572.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1412-867G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 11/30 | chrX | 40702110 | |||||||
| chrX:40702311 | G | C | 60 | a0001c0001t0001g0017 a0001c0001t0001g0157 a0001c0001t0001g0201 others(57): Show |
60 | HG00408.hp1 HG01169.hp1 HG01255.hp1 others(57): Show |
intron_variant | MODIFIER | c.1412-1068C>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 11/30 | chrX | 40702311 | |||||||
| chrX:40702346 | G | GT | 38 | a0001c0001t0001g0003 a0001c0001t0001g0069 a0001c0001t0001g0075 others(35): Show |
43 | HG00438.hp2 HG00639.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.1411+1097dupA | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 11/30 | chrX | 40702346 | |||||||
| chrX:40702346 | G | GTT | 56 | a0001c0001t0001g0017 a0001c0001t0001g0157 a0001c0001t0001g0162 others(53): Show |
57 | HG00408.hp1 HG01169.hp1 HG02015.hp1 others(54): Show |
intron_variant | MODIFIER | c.1411+1096_1411+109 others(6): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 11/30 | chrX | 40702346 | |||||||
| chrX:40702346 | G | GTTT | 11 | a0001c0001t0001g0161 a0001c0001t0001g0169 a0001c0002t0001g0019 others(8): Show |
11 | HG01255.hp1 HG02109.hp1 HG03225.hp1 others(8): Show |
intron_variant | MODIFIER | c.1411+1095_1411+109 others(7): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 11/30 | chrX | 40702346 | |||||||
| chrX:40702415 | C | T | 5 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0003t0001g0010 others(2): Show |
6 | HG02615.hp1 HG02723.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1411+1029G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 11/30 | chrX | 40702415 | |||||||
| chrX:40702423 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1411+1021A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 11/30 | chrX | 40702423 | |||||||
| chrX:40702756 | T | C | 1 | a0001c0002t0001g0045 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1411+688A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 11/30 | chrX | 40702756 | |||||||
| chrX:40703210 | A | G | 3 | a0001c0001t0003g0182 a0001c0001t0003g0183 a0001c0001t0003g0185 |
3 | HG02572.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1411+234T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 11/30 | chrX | 40703210 | |||||||
| chrX:40703222 | G | A | 1 | a0001c0001t0001g0139 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1411+222C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 11/30 | chrX | 40703222 | |||||||
| chrX:40703874 | T | C | 1 | a0001c0001t0001g0008 | 2 | NA18945.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1286-305A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40703874 | |||||||
| chrX:40704047 | C | T | 6 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(3): Show |
6 | HG01891.hp2 HG02055.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1286-478G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40704047 | |||||||
| chrX:40704433 | C | CG | 6 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(3): Show |
6 | HG01891.hp2 HG02055.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1286-865dupC | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40704433 | |||||||
| chrX:40704671 | A | T | 2 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
2 | HG02723.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1286-1102T>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40704671 | |||||||
| chrX:40704752 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1286-1183A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40704752 | |||||||
| chrX:40704878 | G | A | 53 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(50): Show |
53 | HG00408.hp1 HG01169.hp1 HG01255.hp1 others(50): Show |
intron_variant | MODIFIER | c.1286-1309C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40704878 | |||||||
| chrX:40704920 | C | T | 8 | a0001c0002t0001g0014 a0001c0002t0001g0026 a0001c0002t0001g0027 others(5): Show |
8 | HG01169.hp1 HG02080.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.1286-1351G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40704920 | |||||||
| chrX:40704928 | T | C | 1 | a0001c0001t0001g0103 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1286-1359A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40704928 | |||||||
| chrX:40705074 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1286-1505A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40705074 | |||||||
| chrX:40705337 | T | TG | 11 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0154 others(8): Show |
11 | HG00733.hp2 HG01358.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1286-1769dupC | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40705337 | |||||||
| chrX:40705487 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1286-1918A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40705487 | |||||||
| chrX:40705648 | C | CAT | 3 | a0001c0001t0001g0160 a0001c0002t0001g0228 a0001c0002t0001g0229 |
3 | HG02809.hp1 HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1286-2081_1286-208 others(6): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40705648 | |||||||
| chrX:40705778 | T | C | 34 | a0001c0001t0001g0003 a0001c0001t0001g0160 a0001c0001t0001g0161 others(31): Show |
36 | HG00438.hp2 HG00639.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.1286-2209A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40705778 | |||||||
| chrX:40706129 | C | T | 1 | a0001c0003t0001g0204 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1286-2560G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40706129 | |||||||
| chrX:40706197 | G | A | 68 | a0001c0001t0001g0157 a0001c0001t0001g0189 a0001c0001t0001g0190 others(65): Show |
69 | HG00408.hp1 HG01169.hp1 HG01255.hp1 others(66): Show |
intron_variant | MODIFIER | c.1286-2628C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40706197 | |||||||
| chrX:40706263 | G | A | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(209): Show |
233 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.1286-2694C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40706263 | |||||||
| chrX:40706556 | C | T | 1 | a0001c0002t0001g0208 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1285+2792G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40706556 | |||||||
| chrX:40706592 | C | T | 26 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0162 others(23): Show |
28 | HG00438.hp2 HG00639.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.1285+2756G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40706592 | |||||||
| chrX:40706768 | AT | A | 3 | a0001c0001t0003g0182 a0001c0001t0003g0183 a0001c0001t0003g0185 |
3 | HG02572.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1285+2579delA | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40706768 | |||||||
| chrX:40706782 | TTTCTGTT others(21): Show |
T | 2 | a0001c0002t0001g0020 a0001c0002t0001g0025 |
2 | HG02622.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1285+2538_1285+256 others(32): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40706782 | |||||||
| chrX:40707051 | A | C | 81 | a0001c0001t0001g0017 a0001c0001t0001g0157 a0001c0001t0001g0189 others(78): Show |
85 | HG00408.hp1 HG00733.hp1 HG01169.hp1 others(82): Show |
intron_variant | MODIFIER | c.1285+2297T>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40707051 | |||||||
| chrX:40707107 | G | GGATA | 44 | a0001c0001t0001g0061 a0001c0001t0001g0068 a0001c0001t0001g0109 others(41): Show |
45 | HG00140.hp1 HG00621.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.1285+2237_1285+224 others(8): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40707107 | |||||||
| chrX:40707107 | G | GGATAGAT others(1): Show |
3 | a0001c0001t0001g0112 a0001c0002t0001g0042 a0001c0002t0001g0045 |
3 | NA18939.hp1 NA18957.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1285+2233_1285+224 others(12): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40707107 | |||||||
| chrX:40707107 | G | GGATAGAT others(5): Show |
1 | a0001c0002t0001g0043 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1285+2229_1285+224 others(16): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40707107 | |||||||
| chrX:40707107 | GGATA | G | 35 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(32): Show |
38 | HG00733.hp1 HG01167.hp1 HG01169.hp2 others(35): Show |
intron_variant | MODIFIER | c.1285+2237_1285+224 others(8): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40707107 | |||||||
| chrX:40707138 | T | C | 1 | a0001c0001t0001g0161 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1285+2210A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40707138 | |||||||
| chrX:40707142 | T | C | 34 | a0001c0001t0001g0003 a0001c0001t0001g0160 a0001c0001t0001g0161 others(31): Show |
36 | HG00438.hp2 HG00639.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.1285+2206A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40707142 | |||||||
| chrX:40707684 | C | T | 2 | a0001c0002t0001g0228 a0001c0002t0001g0229 |
2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1285+1664G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40707684 | |||||||
| chrX:40707802 | C | T | 3 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0137 |
3 | NA18940.hp1 NA18979.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1285+1546G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40707802 | |||||||
| chrX:40707857 | C | G | 1 | a0001c0002t0001g0047 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1285+1491G>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40707857 | |||||||
| chrX:40707937 | C | T | 1 | a0001c0001t0001g0194 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1285+1411G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40707937 | |||||||
| chrX:40708343 | C | T | 1 | a0001c0002t0001g0227 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1285+1005G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40708343 | |||||||
| chrX:40708561 | G | A | 2 | a0001c0002t0001g0228 a0001c0002t0001g0229 |
2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1285+787C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40708561 | |||||||
| chrX:40709030 | G | A | 76 | a0001c0001t0001g0157 a0001c0001t0001g0189 a0001c0001t0001g0190 others(73): Show |
80 | HG00408.hp1 HG00733.hp1 HG01169.hp1 others(77): Show |
intron_variant | MODIFIER | c.1285+318C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40709030 | |||||||
| chrX:40709650 | T | C | 1 | a0001c0013t0001g0225 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1174-191A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 9/30 | chrX | 40709650 | |||||||
| chrX:40710139 | AAAATG | A | 3 | a0001c0001t0001g0201 a0001c0001t0001g0203 a0004c0007t0001g0202 |
3 | HG02145.hp1 HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1023-15_1023-11del others(5): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 8/30 | chrX | 40710139 | |||||||
| chrX:40710462 | G | A | 1 | a0001c0013t0001g0225 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1023-333C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 8/30 | chrX | 40710462 | |||||||
| chrX:40710641 | T | C | 2 | a0001c0002t0001g0227 a0001c0002t0009g0226 |
2 | HG00733.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1023-512A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 8/30 | chrX | 40710641 | |||||||
| chrX:40710700 | CTT | C | 65 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(62): Show |
69 | HG00408.hp1 HG00733.hp1 HG01169.hp1 others(66): Show |
intron_variant | MODIFIER | c.1022+467_1022+468d others(4): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 8/30 | chrX | 40710700 | |||||||
| chrX:40711538 | T | C | 2 | a0001c0001t0001g0195 a0001c0001t0001g0196 |
2 | HG02148.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.890-237A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 7/30 | chrX | 40711538 | |||||||
| chrX:40711565 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.890-264C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 7/30 | chrX | 40711565 | |||||||
| chrX:40712073 | G | A | 2 | a0001c0002t0001g0228 a0001c0002t0001g0229 |
2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.889+113C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 7/30 | chrX | 40712073 | |||||||
| chrX:40712137 | G | C | 2 | a0001c0002t0001g0019 a0001c0002t0001g0044 |
2 | HG00408.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.889+49C>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 7/30 | chrX | 40712137 | |||||||
| chrX:40712139 | T | C | 16 | a0001c0001t0001g0201 a0001c0001t0001g0203 a0001c0002t0001g0208 others(13): Show |
16 | HG01255.hp1 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.889+47A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 7/30 | chrX | 40712139 | |||||||
| chrX:40712144 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.889+42G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 7/30 | chrX | 40712144 | |||||||
| chrX:40712161 | T | C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0160 others(100): Show |
109 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(106): Show |
intron_variant | MODIFIER | c.889+25A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 7/30 | chrX | 40712161 | |||||||
| chrX:40712455 | C | T | 1 | a0001c0001t0001g0181 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.782-162G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 6/30 | chrX | 40712455 | |||||||
| chrX:40712699 | C | T | 102 | a0001c0001t0001g0003 a0001c0001t0001g0160 a0001c0001t0001g0161 others(99): Show |
108 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(105): Show |
intron_variant | MODIFIER | c.781+215G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 6/30 | chrX | 40712699 | |||||||
| chrX:40713598 | G | A | 2 | a0001c0002t0001g0228 a0001c0002t0001g0229 |
2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.652+180C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 5/30 | chrX | 40713598 | |||||||
| chrX:40714051 | G | A | 4 | a0001c0001t0001g0160 a0001c0001t0001g0201 a0001c0001t0001g0203 others(1): Show |
4 | HG02145.hp1 HG02723.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.523-144C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 4/30 | chrX | 40714051 | |||||||
| chrX:40714073 | G | A | 53 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(50): Show |
53 | HG00408.hp1 HG01169.hp1 HG01255.hp1 others(50): Show |
intron_variant | MODIFIER | c.523-166C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 4/30 | chrX | 40714073 | |||||||
| chrX:40714310 | C | T | 2 | a0001c0001t0002g0077 a0001c0001t0002g0078 |
2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.522+227G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 4/30 | chrX | 40714310 | |||||||
| chrX:40714462 | C | T | 2 | a0001c0001t0001g0162 a0001c0001t0001g0181 |
2 | HG03486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.522+75G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 4/30 | chrX | 40714462 | |||||||
| chrX:40714522 | A | C | 6 | a0001c0002t0001g0212 a0001c0002t0001g0227 a0001c0002t0009g0226 others(3): Show |
7 | HG00733.hp1 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.522+15T>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 4/30 | chrX | 40714522 | |||||||
| chrX:40714882 | A | G | 18 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0163 others(15): Show |
20 | HG00438.hp2 HG00639.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.349-172T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40714882 | |||||||
| chrX:40714995 | T | C | 1 | a0001c0001t0001g0114 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.349-285A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40714995 | |||||||
| chrX:40715045 | G | A | 75 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(72): Show |
79 | HG00408.hp1 HG00733.hp1 HG01169.hp1 others(76): Show |
intron_variant | MODIFIER | c.349-335C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40715045 | |||||||
| chrX:40715358 | A | G | 2 | a0001c0002t0001g0021 a0001c0002t0001g0023 |
2 | NA18982.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.349-648T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40715358 | |||||||
| chrX:40715501 | C | T | 2 | a0001c0001t0001g0193 a0001c0001t0001g0200 |
2 | NA18965.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.349-791G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40715501 | |||||||
| chrX:40715519 | G | A | 1 | a0001c0002t0001g0210 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.349-809C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40715519 | |||||||
| chrX:40715555 | G | C | 1 | a0001c0013t0001g0225 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.349-845C>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40715555 | |||||||
| chrX:40715569 | G | A | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.349-859C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40715569 | |||||||
| chrX:40715607 | A | G | 36 | a0001c0001t0001g0003 a0001c0001t0001g0160 a0001c0001t0001g0161 others(33): Show |
38 | HG00438.hp2 HG00639.hp2 HG01175.hp1 others(35): Show |
intron_variant | MODIFIER | c.349-897T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40715607 | |||||||
| chrX:40715785 | C | CA | 32 | a0001c0001t0001g0009 a0001c0001t0001g0060 a0001c0001t0001g0067 others(29): Show |
33 | HG00438.hp1 HG00738.hp1 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.349-1076dupT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40715785 | |||||||
| chrX:40715811 | AAG | A | 60 | a0001c0001t0001g0017 a0001c0001t0001g0189 a0001c0001t0001g0190 others(57): Show |
60 | HG00408.hp1 HG01169.hp1 HG01255.hp1 others(57): Show |
intron_variant | MODIFIER | c.349-1103_349-1102d others(4): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40715811 | |||||||
| chrX:40715812 | AG | A | 13 | a0001c0001t0001g0001 a0001c0001t0001g0160 a0001c0001t0002g0063 others(10): Show |
15 | HG01496.hp2 HG02280.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.349-1103delC | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40715812 | |||||||
| chrX:40715813 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
171 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.349-1103C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40715813 | |||||||
| chrX:40715853 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.349-1143A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40715853 | |||||||
| chrX:40716040 | G | A | 1 | a0001c0002t0001g0227 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.349-1330C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40716040 | |||||||
| chrX:40716073 | G | A | 2 | a0001c0002t0001g0228 a0001c0002t0001g0229 |
2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.349-1363C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40716073 | |||||||
| chrX:40716171 | T | C | 72 | a0001c0001t0001g0017 a0001c0001t0001g0157 a0001c0001t0001g0189 others(69): Show |
73 | HG00408.hp1 HG00733.hp1 HG01169.hp1 others(70): Show |
intron_variant | MODIFIER | c.349-1461A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40716171 | |||||||
| chrX:40716218 | G | A | 1 | a0001c0002t0001g0218 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.349-1508C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40716218 | |||||||
| chrX:40716589 | C | CA | 38 | a0001c0001t0001g0003 a0001c0001t0001g0142 a0001c0001t0001g0160 others(35): Show |
40 | HG00438.hp2 HG00639.hp2 HG01175.hp1 others(37): Show |
intron_variant | MODIFIER | c.349-1880dupT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40716589 | |||||||
| chrX:40716651 | C | G | 1 | a0001c0002t0001g0227 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.349-1941G>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40716651 | |||||||
| chrX:40716700 | G | A | 2 | a0001c0002t0001g0228 a0001c0002t0001g0229 |
2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.349-1990C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40716700 | |||||||
| chrX:40716804 | T | C | 2 | a0001c0002t0004g0011 a0001c0002t0004g0209 |
3 | HG02809.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.349-2094A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40716804 | |||||||
| chrX:40717027 | G | A | 4 | a0001c0002t0001g0212 a0001c0003t0001g0010 a0001c0003t0001g0204 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.349-2317C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40717027 | |||||||
| chrX:40717050 | T | A | 4 | a0001c0002t0001g0212 a0001c0003t0001g0010 a0001c0003t0001g0204 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.349-2340A>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40717050 | |||||||
| chrX:40717158 | A | G | 2 | a0001c0002t0001g0228 a0001c0002t0001g0229 |
2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.349-2448T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40717158 | |||||||
| chrX:40717524 | CATTTT | C | 53 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(50): Show |
53 | HG00408.hp1 HG01169.hp1 HG01255.hp1 others(50): Show |
intron_variant | MODIFIER | c.349-2819_349-2815d others(7): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40717524 | |||||||
| chrX:40718149 | A | G | 2 | a0001c0001t0001g0162 a0001c0001t0001g0181 |
2 | HG03486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.349-3439T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40718149 | |||||||
| chrX:40718191 | T | G | 5 | a0001c0001t0001g0060 a0001c0001t0001g0070 a0001c0001t0001g0071 others(2): Show |
5 | HG00438.hp1 NA18612.hp1 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.349-3481A>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40718191 | |||||||
| chrX:40718423 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.349-3713G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40718423 | |||||||
| chrX:40718681 | T | A | 3 | a0001c0001t0003g0182 a0001c0001t0003g0183 a0001c0001t0003g0185 |
3 | HG02572.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.349-3971A>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40718681 | |||||||
| chrX:40718967 | T | C | 1 | a0001c0002t0001g0227 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.349-4257A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40718967 | |||||||
| chrX:40719251 | T | A | 2 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
2 | HG02723.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.349-4541A>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40719251 | |||||||
| chrX:40719535 | A | G | 1 | a0001c0001t0001g0211 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.349-4825T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40719535 | |||||||
| chrX:40719764 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.349-5054C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40719764 | |||||||
| chrX:40719786 | G | T | 13 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0163 others(10): Show |
15 | HG00438.hp2 HG00639.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.349-5076C>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40719786 | |||||||
| chrX:40720019 | A | G | 3 | a0001c0002t0001g0212 a0001c0003t0001g0010 a0001c0003t0001g0205 |
4 | HG02622.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.349-5309T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40720019 | |||||||
| chrX:40720158 | C | G | 1 | a0001c0003t0001g0204 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.349-5448G>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40720158 | |||||||
| chrX:40720164 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.349-5454C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40720164 | |||||||
| chrX:40720275 | G | A | 1 | a0001c0002t0001g0045 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.349-5565C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40720275 | |||||||
| chrX:40720483 | C | T | 1 | a0001c0002t0001g0046 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.349-5773G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40720483 | |||||||
| chrX:40720493 | T | C | 2 | a0001c0002t0001g0228 a0001c0002t0001g0229 |
2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.349-5783A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40720493 | |||||||
| chrX:40720843 | G | A | 65 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(62): Show |
69 | HG00408.hp1 HG00733.hp1 HG01169.hp1 others(66): Show |
intron_variant | MODIFIER | c.348+5903C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40720843 | |||||||
| chrX:40720989 | C | T | 3 | a0001c0002t0001g0221 a0001c0002t0001g0222 a0001c0002t0001g0223 |
3 | HG01255.hp1 HG02109.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.348+5757G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40720989 | |||||||
| chrX:40721106 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.348+5640T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40721106 | |||||||
| chrX:40721167 | T | C | 1 | a0001c0001t0001g0199 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.348+5579A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40721167 | |||||||
| chrX:40721391 | G | T | 1 | a0001c0002t0009g0226 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.348+5355C>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40721391 | |||||||
| chrX:40721914 | C | T | 1 | a0001c0013t0001g0225 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.348+4832G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40721914 | |||||||
| chrX:40721920 | G | A | 2 | a0001c0001t0001g0162 a0001c0001t0001g0181 |
2 | HG03486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.348+4826C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40721920 | |||||||
| chrX:40721985 | T | C | 1 | a0001c0001t0001g0128 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.348+4761A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40721985 | |||||||
| chrX:40722104 | C | T | 2 | a0001c0001t0001g0067 a0001c0001t0001g0068 |
2 | HG00738.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.348+4642G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40722104 | |||||||
| chrX:40723092 | G | A | 1 | a0001c0002t0001g0018 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.348+3654C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40723092 | |||||||
| chrX:40723271 | T | C | 1 | a0001c0013t0001g0225 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.348+3475A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40723271 | |||||||
| chrX:40723317 | A | T | 1 | a0001c0001t0001g0075 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.348+3429T>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40723317 | |||||||
| chrX:40723377 | T | C | 1 | a0001c0001t0001g0129 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.348+3369A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40723377 | |||||||
| chrX:40723476 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.348+3270C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40723476 | |||||||
| chrX:40723619 | C | T | 116 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0157 others(113): Show |
122 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(119): Show |
intron_variant | MODIFIER | c.348+3127G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40723619 | |||||||
| chrX:40723622 | C | T | 2 | a0001c0002t0004g0011 a0001c0002t0004g0209 |
3 | HG02809.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.348+3124G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40723622 | |||||||
| chrX:40723650 | A | T | 4 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0073 others(1): Show |
4 | NA18987.hp2 NA19006.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+3096T>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40723650 | |||||||
| chrX:40723667 | G | GA | 85 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0157 others(82): Show |
90 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.348+3078dupT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40723667 | |||||||
| chrX:40723667 | G | GAA | 18 | a0001c0001t0001g0187 a0001c0001t0001g0196 a0001c0001t0001g0203 others(15): Show |
18 | HG01175.hp1 HG01255.hp1 HG02135.hp1 others(15): Show |
intron_variant | MODIFIER | c.348+3077_348+3078d others(4): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40723667 | |||||||
| chrX:40723667 | GA | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(84): Show |
102 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.348+3078delT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40723667 | |||||||
| chrX:40723667 | GAA | G | 6 | a0001c0001t0001g0060 a0001c0001t0001g0069 a0001c0001t0001g0070 others(3): Show |
6 | HG02970.hp1 HG03209.hp1 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.348+3077_348+3078d others(4): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40723667 | |||||||
| chrX:40723667 | GAAAAAAA others(3): Show |
G | 2 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
2 | HG02723.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.348+3069_348+3078d others(12): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40723667 | |||||||
| chrX:40723697 | C | T | 2 | a0001c0001t0001g0067 a0001c0001t0001g0068 |
2 | HG00738.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.348+3049G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40723697 | |||||||
| chrX:40723759 | T | C | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(222): Show |
246 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.348+2987A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40723759 | |||||||
| chrX:40723807 | G | C | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | NA18964.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.348+2939C>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40723807 | |||||||
| chrX:40723981 | T | C | 1 | a0001c0002t0001g0227 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.348+2765A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40723981 | |||||||
| chrX:40724132 | A | G | 4 | a0001c0002t0001g0212 a0001c0003t0001g0010 a0001c0003t0001g0204 others(1): Show |
5 | HG02615.hp1 HG02622.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.348+2614T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40724132 | |||||||
| chrX:40724138 | A | G | 1 | a0001c0002t0001g0020 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.348+2608T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40724138 | |||||||
| chrX:40724695 | A | C | 1 | a0001c0001t0001g0062 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.348+2051T>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40724695 | |||||||
| chrX:40724808 | T | C | 4 | a0001c0001t0001g0160 a0001c0001t0001g0201 a0001c0001t0001g0203 others(1): Show |
4 | HG02145.hp1 HG02723.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+1938A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40724808 | |||||||
| chrX:40725008 | G | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG01192.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.348+1738C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40725008 | |||||||
| chrX:40725267 | C | G | 2 | a0001c0002t0004g0011 a0001c0002t0004g0209 |
3 | HG02809.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.348+1479G>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40725267 | |||||||
| chrX:40725541 | A | G | 1 | a0001c0002t0001g0215 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.348+1205T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40725541 | |||||||
| chrX:40725561 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.348+1185A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40725561 | |||||||
| chrX:40725980 | T | C | 64 | a0001c0001t0001g0017 a0001c0001t0001g0157 a0001c0001t0001g0201 others(61): Show |
67 | HG00408.hp1 HG00733.hp1 HG01169.hp1 others(64): Show |
intron_variant | MODIFIER | c.348+766A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40725980 | |||||||
| chrX:40726044 | C | A | 3 | a0001c0003t0001g0010 a0001c0003t0001g0204 a0001c0003t0001g0205 |
4 | HG02615.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+702G>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40726044 | |||||||
| chrX:40726340 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.348+406A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40726340 | |||||||
| chrX:40726374 | G | GA | 9 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0003g0185 others(6): Show |
9 | HG02080.hp2 HG02135.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.348+371dupT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40726374 | |||||||
| chrX:40726532 | T | A | 1 | a0001c0001t0001g0187 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.348+214A>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40726532 | |||||||
| chrX:40727308 | CTG | C | 3 | a0001c0002t0001g0221 a0001c0002t0001g0222 a0001c0002t0001g0223 |
3 | HG01255.hp1 HG02109.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.243-459_243-458del others(2): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 2/30 | chrX | 40727308 | |||||||
| chrX:40727598 | G | A | 33 | a0001c0001t0001g0003 a0001c0001t0001g0160 a0001c0001t0001g0161 others(30): Show |
35 | HG00438.hp2 HG00639.hp2 HG01175.hp1 others(32): Show |
intron_variant | MODIFIER | c.243-747C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 2/30 | chrX | 40727598 | |||||||
| chrX:40727831 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.243-980C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 2/30 | chrX | 40727831 | |||||||
| chrX:40728234 | T | C | 3 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 |
3 | NA18954.hp1 NA18957.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.242+1085A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 2/30 | chrX | 40728234 | |||||||
| chrX:40728442 | C | T | 101 | a0001c0001t0001g0003 a0001c0001t0001g0160 a0001c0001t0001g0161 others(98): Show |
107 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.242+877G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 2/30 | chrX | 40728442 | |||||||
| chrX:40728474 | G | C | 1 | a0001c0002t0001g0227 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.242+845C>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 2/30 | chrX | 40728474 | |||||||
| chrX:40728580 | C | T | 1 | a0001c0002t0001g0019 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.242+739G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 2/30 | chrX | 40728580 | |||||||
| chrX:40728629 | T | G | 2 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
2 | NA19009.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.242+690A>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 2/30 | chrX | 40728629 | |||||||
| chrX:40728726 | G | T | 2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | NA19062.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.242+593C>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 2/30 | chrX | 40728726 | |||||||
| chrX:40728823 | C | CT | 37 | a0001c0001t0001g0003 a0001c0001t0001g0160 a0001c0001t0001g0161 others(34): Show |
39 | HG00438.hp2 HG00639.hp2 HG01175.hp1 others(36): Show |
intron_variant | MODIFIER | c.242+495dupA | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 2/30 | chrX | 40728823 | |||||||
| chrX:40728905 | C | A | 1 | a0001c0002t0001g0227 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.242+414G>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 2/30 | chrX | 40728905 | |||||||
| chrX:40728910 | T | C | 1 | a0001c0003t0001g0204 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.242+409A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 2/30 | chrX | 40728910 | |||||||
| chrX:40728966 | C | T | 57 | a0001c0001t0001g0211 a0001c0002t0001g0013 a0001c0002t0001g0014 others(54): Show |
58 | HG00408.hp1 HG00733.hp1 HG01169.hp1 others(55): Show |
intron_variant | MODIFIER | c.242+353G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 2/30 | chrX | 40728966 | |||||||
| chrX:40729298 | G | GT | 6 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0189 others(3): Show |
6 | HG02896.hp1 HG03516.hp2 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.242+20dupA | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 2/30 | chrX | 40729298 | |||||||
| chrX:40729927 | T | C | 2 | a0001c0002t0001g0228 a0001c0002t0001g0229 |
2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.216-582A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40729927 | |||||||
| chrX:40730123 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.216-778G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40730123 | |||||||
| chrX:40730133 | T | C | 1 | a0001c0004t0001g0004 | 3 | HG02280.hp2 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.216-788A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40730133 | |||||||
| chrX:40730292 | A | G | 1 | a0001c0013t0001g0225 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.216-947T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40730292 | |||||||
| chrX:40730518 | A | C | 2 | a0001c0001t0001g0017 a0001c0002t0001g0016 |
2 | HG02015.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.216-1173T>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40730518 | |||||||
| chrX:40730851 | G | A | 1 | a0001c0004t0001g0004 | 3 | HG02280.hp2 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.216-1506C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40730851 | |||||||
| chrX:40730958 | C | G | 79 | a0001c0001t0001g0017 a0001c0001t0001g0189 a0001c0001t0001g0190 others(76): Show |
83 | HG00408.hp1 HG00733.hp1 HG01169.hp1 others(80): Show |
intron_variant | MODIFIER | c.216-1613G>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40730958 | |||||||
| chrX:40730963 | C | T | 3 | a0001c0003t0001g0010 a0001c0003t0001g0204 a0001c0003t0001g0205 |
4 | HG02615.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.216-1618G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40730963 | |||||||
| chrX:40731071 | G | A | 12 | a0001c0002t0001g0208 a0001c0002t0001g0213 a0001c0002t0001g0214 others(9): Show |
12 | HG01255.hp1 HG02109.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.216-1726C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40731071 | |||||||
| chrX:40731120 | G | A | 1 | a0001c0001t0008g0153 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.216-1775C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40731120 | |||||||
| chrX:40731140 | C | CA | 114 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0154 others(111): Show |
120 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(117): Show |
intron_variant | MODIFIER | c.216-1796dupT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40731140 | |||||||
| chrX:40731225 | G | A | 1 | a0001c0001t0001g0200 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.216-1880C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40731225 | |||||||
| chrX:40731226 | G | C | 2 | a0001c0002t0001g0227 a0001c0002t0009g0226 |
2 | HG00733.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.216-1881C>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40731226 | |||||||
| chrX:40731440 | T | C | 2 | a0001c0002t0001g0052 a0001c0002t0001g0224 |
2 | HG03669.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.216-2095A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40731440 | |||||||
| chrX:40731914 | C | T | 1 | a0001c0004t0001g0004 | 3 | HG02280.hp2 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.216-2569G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40731914 | |||||||
| chrX:40731963 | C | T | 1 | a0001c0002t0001g0015 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.216-2618G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40731963 | |||||||
| chrX:40732050 | A | C | 1 | a0001c0013t0001g0225 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.216-2705T>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40732050 | |||||||
| chrX:40732328 | G | A | 1 | a0001c0013t0001g0225 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.215+2870C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40732328 | |||||||
| chrX:40732355 | C | A | 6 | a0001c0001t0002g0005 a0001c0001t0002g0053 a0001c0001t0002g0055 others(3): Show |
7 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.215+2843G>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40732355 | |||||||
| chrX:40732388 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.215+2810C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40732388 | |||||||
| chrX:40732417 | G | A | 1 | a0001c0002t0001g0227 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.215+2781C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40732417 | |||||||
| chrX:40732476 | A | G | 1 | a0001c0002t0001g0208 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.215+2722T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40732476 | |||||||
| chrX:40732518 | C | CA | 76 | a0001c0001t0001g0017 a0001c0001t0001g0155 a0001c0001t0001g0156 others(73): Show |
79 | HG00408.hp1 HG01169.hp1 HG01255.hp1 others(76): Show |
intron_variant | MODIFIER | c.215+2679dupT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40732518 | |||||||
| chrX:40732518 | C | CAA | 5 | a0001c0002t0001g0013 a0001c0002t0001g0227 a0001c0002t0001g0228 others(2): Show |
5 | HG00733.hp1 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.215+2678_215+2679d others(4): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40732518 | |||||||
| chrX:40732634 | G | T | 1 | a0001c0004t0001g0004 | 3 | HG02280.hp2 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.215+2564C>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40732634 | |||||||
| chrX:40732709 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.215+2489G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40732709 | |||||||
| chrX:40732794 | A | T | 1 | a0001c0003t0001g0204 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.215+2404T>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40732794 | |||||||
| chrX:40733081 | TGGTCACT others(5): Show |
T | 1 | a0001c0002t0001g0013 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.215+2105_215+2116d others(14): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40733081 | |||||||
| chrX:40733107 | A | T | 4 | a0001c0001t0001g0160 a0001c0001t0001g0201 a0001c0001t0001g0203 others(1): Show |
4 | HG02145.hp1 HG02723.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.215+2091T>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40733107 | |||||||
| chrX:40733109 | T | A | 2 | a0001c0001t0005g0158 a0001c0001t0005g0159 |
2 | HG00673.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.215+2089A>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40733109 | |||||||
| chrX:40733588 | G | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0160 others(100): Show |
109 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(106): Show |
intron_variant | MODIFIER | c.215+1610C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40733588 | |||||||
| chrX:40733622 | C | G | 1 | a0001c0001t0001g0058 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.215+1576G>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40733622 | |||||||
| chrX:40734098 | T | C | 2 | a0001c0002t0001g0228 a0001c0002t0001g0229 |
2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.215+1100A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40734098 | |||||||
| chrX:40734325 | C | T | 6 | a0001c0001t0002g0005 a0001c0001t0002g0053 a0001c0001t0002g0055 others(3): Show |
7 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.215+873G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40734325 | |||||||
| chrX:40734401 | T | C | 84 | a0001c0001t0001g0017 a0001c0001t0001g0189 a0001c0001t0001g0190 others(81): Show |
88 | HG00408.hp1 HG00733.hp1 HG01169.hp1 others(85): Show |
intron_variant | MODIFIER | c.215+797A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40734401 | |||||||
| chrX:40734423 | C | T | 40 | a0001c0001t0001g0017 a0001c0002t0001g0013 a0001c0002t0001g0014 others(37): Show |
40 | HG00408.hp1 HG01169.hp1 HG02015.hp1 others(37): Show |
intron_variant | MODIFIER | c.215+775G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40734423 | |||||||
| chrX:40734504 | A | T | 1 | a0002c0011t0002g0012 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.215+694T>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40734504 | |||||||
| chrX:40735004 | T | C | 1 | a0001c0001t0001g0230 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.215+194A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40735004 |