Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| 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 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1454 | 244 | 62 | 40 | 114 | 7 | 19 | 89 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0002 | 0/0 | 45 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0003 | 0/0 | 1454 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0004 | 0/0 | 1454 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0005 | 0/0 | 1454 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0006 | 0/0 | 1454 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0007 | 0/0 | 1454 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0008 | 0/0 | 470 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 4365 | 174 | 28 | 37 | 89 | 7 | 11 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| c0002 | 0/0 | 4365 | 59 | 26 | 3 | 23 | 0 | 7 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| c0003 | 0/0 | 4365 | 4 | 4 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| c0004 | 0/0 | 4365 | 3 | 3 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| c0005 | 0/0 | 4365 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| c0006 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| c0007 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| c0008 | 0/0 | 4365 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| c0009 | 0/0 | 4365 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| c0010 | 0/0 | 4365 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| c0011 | 0/0 | 4357 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| c0012 | 0/0 | 4365 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| c0013 | 0/0 | 4365 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| c0014 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| c0015 | 0/0 | 4366 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 3632 | 209 | 49 | 26 | 111 | 4 | 18 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| t0002 | 0/1 | 3632 | 26 | 9 | 13 | 0 | 2 | 1 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| t0003 | 0/0 | 3632 | 3 | 3 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| t0004 | 0/0 | 3632 | 3 | 3 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| t0005 | 0/0 | 3632 | 2 | 0 | 0 | 2 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| t0006 | 0/0 | 3632 | 1 | 0 | 0 | 0 | 1 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| t0007 | 0/0 | 3630 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| t0008 | 0/0 | 3632 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| t0009 | 0/0 | 3632 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| t0010 | 0/0 | 3632 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| t0011 | 0/0 | 3632 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| t0012 | 0/0 | 3632 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| t0013 | 0/0 | 3633 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0003 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0065 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0141 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 4365 | 174 | 28 | 37 | 89 | 7 | 11 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0001c0002 | 0/0 | 4365 | 59 | 26 | 3 | 23 | 0 | 7 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0001c0003 | 0/0 | 4365 | 4 | 4 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0001c0004 | 0/0 | 4365 | 3 | 3 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0001c0008 | 0/0 | 4365 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0001c0009 | 0/0 | 4365 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0001c0013 | 0/0 | 4365 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0001c0014 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0002c0015 | 0/0 | 4366 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0003c0012 | 0/0 | 4365 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0004c0010 | 0/0 | 4365 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0005c0005 | 0/0 | 4365 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0006c0007 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0007c0006 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0008c0011 | 0/0 | 4357 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | 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 | copy fasta | chrX | 40643305 | 40740542 |
| a0001c0001t0002 | 0/1 | 7996 | 24 | 8 | 13 | 0 | 2 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0001c0001t0003 | 0/0 | 7996 | 3 | 3 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0001c0001t0005 | 0/0 | 7996 | 2 | 0 | 0 | 2 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0001c0001t0006 | 0/0 | 7996 | 1 | 0 | 0 | 0 | 1 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0001c0001t0009 | 0/0 | 7996 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0001c0001t0011 | 0/0 | 7996 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0001c0001t0012 | 0/0 | 7996 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0001c0002t0001 | 0/0 | 7996 | 53 | 23 | 2 | 21 | 0 | 7 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0001c0002t0004 | 0/0 | 7996 | 3 | 3 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0001c0002t0007 | 0/0 | 7994 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0001c0002t0008 | 0/0 | 7996 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0001c0002t0010 | 0/0 | 7996 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0001c0003t0001 | 0/0 | 7996 | 4 | 4 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0001c0004t0001 | 0/0 | 7996 | 3 | 3 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0001c0008t0001 | 0/0 | 7996 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0001c0009t0001 | 0/0 | 7996 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0001c0013t0001 | 0/0 | 7996 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0001c0014t0001 | 0/0 | 7996 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0002c0015t0013 | 0/0 | 7998 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0003c0012t0001 | 0/0 | 7996 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0004c0010t0002 | 0/0 | 7996 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0005c0005t0001 | 0/0 | 7996 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0006c0007t0002 | 0/0 | 7996 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0007c0006t0001 | 0/0 | 7996 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| a0008c0011t0001 | 0/0 | 7988 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | copy fasta | chrX | 40643305 | 40740542 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0065 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0078 | 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 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | 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 | 0 | 1 | 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 | 0 | 1 | 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 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0133 | 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 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0183 | 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 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 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 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0002g0126 | 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 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0002g0139 | 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 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0005g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0005g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0006g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0009g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0011g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0001t0012g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0002t0001g0221 | 0/0 | 1 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0226 | 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 |
| a0001c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0007g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0008g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0002t0010g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0003t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0003t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0003t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0003t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0004t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0008t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0009t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0013t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0001c0014t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0002c0015t0013g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0003c0012t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0004c0010t0002g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0005c0005t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0006c0007t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0007c0006t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| a0008c0011t0001g0077 | 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 | g0112 | EUR | GBR | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0100 | EUR | FIN | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0034 | 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 | g0131 | EAS | CHS | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0144 | AMR | PUR | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG00673 | hp1 | a0001 | c0001 | t0005 | g0164 | EAS | CHS | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG00733 | hp1 | a0001 | c0002 | t0010 | g0237 | AMR | PUR | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | PUR | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0138 | AMR | PUR | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0025 | AMR | PUR | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0233 | AMR | CLM | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0172 | 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 | g0174 | AMR | CLM | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0134 | AMR | CLM | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | CLM | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | CLM | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0128 | EUR | IBS | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0067 | EUR | IBS | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01516 | hp2 | a0001 | c0001 | t0006 | g0137 | EUR | IBS | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | ACB | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | ACB | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | ACB | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | PEL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0162 | AMR | PEL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0130 | AMR | PEL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02027 | hp1 | a0001 | c0001 | t0012 | g0111 | EAS | KHV | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02055 | hp1 | a0001 | c0014 | t0001 | g0169 | AFR | ACB | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | KHV | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02080 | hp1 | a0001 | c0001 | t0005 | g0163 | EAS | KHV | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0041 | EAS | KHV | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02135 | hp1 | a0001 | c0001 | t0011 | g0191 | EAS | KHV | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0109 | AMR | PEL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CDX | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CDX | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0016 | AFR | ACB | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0086 | AMR | PEL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0029 | AFR | ACB | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02280 | hp2 | a0001 | c0004 | t0001 | g0002 | AFR | ACB | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0081 | AFR | ACB | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0040 | 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 | g0188 | AFR | GWD | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02615 | hp1 | a0001 | c0003 | t0001 | g0211 | AFR | GWD | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0015 | AFR | GWD | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0223 | AFR | GWD | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | GWD | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0217 | AFR | GWD | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0022 | SAS | PJL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02738 | hp1 | a0004 | c0010 | t0002 | g0006 | SAS | PJL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0240 | AFR | GWD | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02809 | hp2 | a0001 | c0002 | t0004 | g0218 | AFR | GWD | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0239 | AFR | GWD | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0225 | AFR | GWD | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0181 | AFR | GWD | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0039 | AFR | GWD | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0228 | AFR | GWD | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0013 | AFR | GWD | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0229 | AFR | ESN | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02965 | hp1 | a0006 | c0007 | t0002 | g0049 | AFR | ESN | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ESN | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02976 | hp1 | a0001 | c0002 | t0004 | g0219 | AFR | ESN | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02976 | hp2 | a0001 | c0003 | t0001 | g0212 | AFR | ESN | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0230 | AFR | MSL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03130 | hp1 | a0001 | c0003 | t0001 | g0213 | AFR | ESN | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03139 | hp1 | a0001 | c0002 | t0004 | g0220 | AFR | ESN | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0221 | AFR | ESN | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03195 | hp2 | a0001 | c0003 | t0001 | g0214 | AFR | ESN | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | MSL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0227 | AFR | MSL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | MSL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | MSL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | MSL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0231 | AFR | MSL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0024 | SAS | PJL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0167 | AFR | ESN | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0224 | AFR | ESN | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03540 | hp1 | a0007 | c0006 | t0001 | g0210 | AFR | GWD | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03540 | hp2 | a0001 | c0004 | t0001 | g0002 | AFR | GWD | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | MSL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0008 | SAS | PJL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0235 | 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 | g0083 | SAS | PJL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03831 | hp1 | a0001 | c0013 | t0001 | g0236 | SAS | BEB | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | BEB | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0045 | SAS | BEB | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG04115 | hp1 | a0001 | c0001 | t0009 | g0156 | SAS | STU | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0226 | SAS | STU | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0007 | SAS | STU | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | STU | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | YRI | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CHB | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHB | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0052 | AFR | YRI | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0232 | AFR | YRI | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18946 | hp2 | a0001 | c0002 | t0008 | g0026 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0010 | 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 | g0030 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18950 | hp2 | a0003 | c0012 | t0001 | g0043 | 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 | g0058 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0056 | 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 | g0104 | 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 | t0007 | g0019 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0021 | 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 | g0133 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18992 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0168 | 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 | g0142 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0190 | AFR | LWK | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0238 | AFR | LWK | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19043 | hp1 | a0001 | c0004 | t0001 | g0002 | AFR | LWK | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0127 | 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 | g0207 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19072 | hp1 | a0008 | c0011 | t0001 | g0077 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19075 | hp1 | a0002 | c0015 | t0013 | g0242 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19078 | hp1 | a0001 | c0009 | t0001 | g0088 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19078 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19082 | hp1 | a0001 | c0008 | t0001 | g0129 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0158 | 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 | g0193 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19087 | hp1 | a0005 | c0005 | t0001 | g0093 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0155 | 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 | g0079 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0139 | EUR | TSI | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | TSI | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | GIH | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0234 | AFR | ACB | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | ACB | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0023 | AFR | USA | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | USA | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0141 | REF | REF | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0065 | REF | REF | MED14_chrX_40643305_40740542 | MED14 | chrX | 40643305 | 40740542 |
| 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 | a0006 | 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 | a0007 | 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 | a0005 | 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 | a0004 | 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:40692798
|
T | TG | 1 | a0008 | 1 | NA19072.hp1 | frameshift_variant | HIGH | c.1754dupC | p.Leu586fs | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 14/31 | 1884/7996 | 1754/4365 | 585/1454 | chrX | 40692798 | ||
| chrX:40692878
|
TGGGAACC others(3): Show |
T | 1 | a0008 | 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 | a0003 | 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 | ||
| chrX:40703465
|
G | GA | 1 | a0008 | 1 | NA19072.hp1 | frameshift_variant | HIGH | c.1389dupT | p.Gln464fs | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 11/31 | 1519/7996 | 1389/4365 | 463/1454 | chrX | 40703465 | ||
| chrX:40735353
|
G | GC | 1 | a0002 | 1 | NA19075.hp1 | frameshift_variant | HIGH | c.59dupG | p.Ser21fs | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/31 | 189/7996 | 59/4365 | 20/1454 | chrX | 40735353 |
| 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 | a0001c0008 | 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 | a0001c0009 | 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 | a0001c0003a0001c0013 | 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 | 6 | a0001c0002a0001c0003a0001c0004others(3): 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 |
| 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 | a0001c0001t0009 | 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 | a0001c0002t0008 | 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 | a0001c0002t0010 | 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 | a0001c0001t0011 | 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:40651216
|
AG | A | 1 | a0001c0002t0007 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*589delC | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 31/31 | 589 | chrX | 40651216 | |||||
| chrX:40651313
|
TG | T | 1 | a0001c0002t0007 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*492delC | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 31/31 | 492 | chrX | 40651313 | |||||
| chrX:40651521
|
A | G | 4 | a0001c0001t0002a0001c0001t0006a0004c0010t0002others(1): Show | 27 | HG00642.hp1 HG01069.hp1 HG01099.hp1 others(24): 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 | a0001c0001t0012 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*206A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 31/31 | 206 | chrX | 40651600 | |||||
| chrX:40735537
|
G | GA | 1 | a0002c0015t0013 | 1 | NA19075.hp1 | 5_prime_UTR_variant | MODIFIER | c.-126dupT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/31 | 126 | chrX | 40735537 |
| 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 | a0001c0001t0002g0048a0001c0001t0002g0081a0001c0001t0002g0181 | 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 | a0001c0002t0001g0015 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4292-405G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 30/30 | chrX | 40652284 | ||||||
| chrX:40652309
|
T | TGTTTAGG | 2 | a0001c0002t0001g0238a0001c0002t0010g0237 | 2 | HG00733.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4292-437_4292-431d others(9): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 30/30 | chrX | 40652309 | ||||||
| chrX:40652882
|
C | T | 123 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(120): Show | 129 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.4292-1003G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 30/30 | chrX | 40652882 | ||||||
| chrX:40652982
|
GA | G | 20 | a0001c0001t0001g0005a0001c0001t0001g0166a0001c0001t0001g0168others(17): 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 | a0001c0002t0001g0013 | 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 | a0001c0001t0002g0048a0001c0001t0002g0081 | 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 | 20 | a0001c0001t0001g0005a0001c0001t0001g0166a0001c0001t0001g0168others(17): 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 | a0001c0002t0001g0221 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4291+738T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 30/30 | chrX | 40653626 | ||||||
| chrX:40653752
|
TC | T | 1 | a0001c0002t0007g0019 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.4291+611delG | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 30/30 | chrX | 40653752 | ||||||
| chrX:40653845
|
T | C | 1 | a0004c0010t0002g0006 | 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 | 18 | a0001c0001t0001g0005a0001c0001t0001g0168a0001c0001t0001g0171others(15): 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 | a0001c0002t0001g0239a0001c0002t0001g0240 | 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 | a0001c0001t0001g0073 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.4099-150T>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 29/30 | chrX | 40654706 | ||||||
| chrX:40654745
|
TG | T | 1 | a0001c0001t0001g0102 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.4098+189delC | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 29/30 | chrX | 40654745 | ||||||
| chrX:40655070
|
G | A | 124 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(121): Show | 130 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(127): 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 | a0001c0001t0001g0076 | 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 | 3 | a0001c0002t0004g0218a0001c0002t0004g0219a0001c0002t0004g0220 | 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 | a0001c0002t0001g0234 | 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 | a0001c0001t0001g0140 | 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 | a0001c0002t0001g0018a0001c0002t0001g0021 | 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 | a0001c0001t0006g0137 | 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 | a0001c0001t0001g0116 | 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 | a0001c0001t0001g0101 | 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 | 137 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 143 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(140): 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 | a0001c0001t0001g0056 | 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 | a0001c0002t0001g0239a0001c0002t0001g0240 | 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 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0003t0001g0211 | 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 | 6 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0003t0001g0211others(3): 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 | 164 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(161): Show | 171 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(168): 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 | a0001c0013t0001g0236 | 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 | a0001c0001t0001g0104a0001c0001t0001g0105 | 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 | a0001c0002t0001g0239a0001c0002t0001g0240 | 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 | 20 | a0001c0001t0001g0005a0001c0001t0001g0166a0001c0001t0001g0168others(17): 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 | a0001c0002t0008g0026 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.3972+740G>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 28/30 | chrX | 40658487 | ||||||
| chrX:40658688
|
C | CA | 2 | a0001c0002t0001g0014a0001c0002t0001g0230 | 2 | HG03098.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.3972+538dupT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 28/30 | chrX | 40658688 | ||||||
| chrX:40658688
|
CA | C | 38 | a0001c0001t0001g0012a0001c0001t0001g0160a0001c0001t0001g0196others(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 | 28 | a0001c0001t0001g0003a0001c0001t0001g0055a0001c0001t0001g0056others(25): 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 | 105 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0053others(102): Show | 112 | HG00280.hp1 HG00408.hp2 HG00609.hp1 others(109): 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 | 16 | a0001c0001t0001g0161a0001c0001t0001g0173a0001c0001t0001g0175others(13): 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 | 20 | a0001c0001t0001g0005a0001c0001t0001g0165a0001c0001t0001g0166others(17): 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 | a0001c0002t0001g0013a0001c0002t0001g0017a0001c0002t0001g0023others(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 | 178 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(175): Show | 187 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.3685-457G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 26/30 | chrX | 40660064 | ||||||
| chrX:40660088
|
TA | T | 6 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0050others(3): 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:40660124
|
TTTTTG | T | 2 | a0001c0001t0001g0165a0001c0002t0001g0223 | 2 | HG02622.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.3685-522_3685-518d others(7): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 26/30 | chrX | 40660124 | ||||||
| chrX:40660252
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3685-645T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 26/30 | chrX | 40660252 | ||||||
| chrX:40660624
|
CA | C | 1 | a0001c0001t0001g0070 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.3685-1018delT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 26/30 | chrX | 40660624 | ||||||
| chrX:40660770
|
G | C | 1 | a0001c0001t0002g0130 | 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 | a0001c0001t0001g0085 | 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 | a0001c0002t0010g0237 | 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 | 129 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(126): Show | 135 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(132): 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 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(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 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(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 | a0001c0004t0001g0002 | 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 | a0001c0001t0005g0163a0001c0001t0005g0164 | 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 | a0001c0001t0001g0241 | 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 | a0001c0001t0003g0167a0001c0001t0003g0188a0001c0001t0003g0190 | 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 | a0001c0001t0001g0108 | 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 | 160 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(157): Show | 167 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(164): 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 | a0001c0002t0001g0007 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3684+829G>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 26/30 | chrX | 40662096 | ||||||
| chrX:40662412
|
AG | A | 1 | a0001c0001t0001g0192 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3684+512delC | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 26/30 | chrX | 40662412 | ||||||
| chrX:40662567
|
C | T | 123 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(120): Show | 129 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.3684+358G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 26/30 | chrX | 40662567 | ||||||
| chrX:40662574
|
G | T | 158 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(155): Show | 165 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(162): 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 | a0001c0001t0001g0194 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3684+13A>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 26/30 | chrX | 40662912 | ||||||
| chrX:40663432
|
T | TG | 241 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(238): Show | 250 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.3449-273_3449-272i others(3): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 25/30 | chrX | 40663432 | ||||||
| chrX:40663974
|
C | T | 1 | a0001c0001t0001g0114 | 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 | a0002c0015t0013g0242 | 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 | a0001c0001t0001g0153 | 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 | 177 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 186 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(183): 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 | a0001c0002t0001g0238a0001c0002t0010g0237 | 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 | a0001c0002t0001g0238a0001c0002t0010g0237 | 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 | a0001c0001t0001g0222 | 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 | 124 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(121): Show | 130 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(127): 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 | a0001c0001t0001g0084 | 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 | 3 | a0001c0002t0004g0218a0001c0002t0004g0219a0001c0002t0004g0220 | 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 | 5 | a0001c0002t0001g0223a0001c0003t0001g0211a0001c0003t0001g0212others(2): 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:40665532
|
C | CA | 1 | a0001c0002t0001g0035 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.3266-1044dupT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 24/30 | chrX | 40665532 | ||||||
| chrX:40665536
|
A | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 142 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(139): 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 | a0001c0001t0001g0196 | 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 | a0003c0012t0001g0043 | 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 | a0001c0002t0001g0239a0001c0002t0001g0240 | 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 | a0001c0002t0010g0237 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3265+75A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 24/30 | chrX | 40666645 | ||||||
| chrX:40666916
|
C | CAAG | 1 | a0001c0001t0001g0061 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.3134-68_3134-66dup others(3): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40666916 | ||||||
| chrX:40667060
|
T | TA | 3 | a0001c0001t0001g0004a0001c0001t0001g0057a0001c0001t0001g0095 | 4 | HG00639.hp1 HG01074.hp1 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.3134-210dupT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40667060 | ||||||
| chrX:40667060
|
TA | T | 2 | a0001c0001t0001g0087a0001c0002t0001g0021 | 2 | NA18982.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.3134-210delT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40667060 | ||||||
| chrX:40667144
|
T | C | 1 | a0001c0002t0001g0221 | 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 | a0001c0003t0001g0211 | 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 | a0001c0001t0001g0189 | 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 | a0001c0001t0001g0194 | 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 | a0001c0001t0001g0165 | 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 | a0001c0001t0003g0167a0001c0001t0003g0188a0001c0001t0003g0190 | 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 | 118 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(115): 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 | 37 | a0001c0001t0001g0069a0001c0001t0001g0075a0001c0001t0001g0078others(34): Show | 39 | HG00642.hp1 HG01069.hp1 HG01099.hp1 others(36): 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:40668383
|
C | CAAA | 3 | a0001c0001t0001g0199a0001c0001t0002g0047a0001c0001t0002g0126 | 3 | HG01928.hp1 HG03209.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.3134-1535_3134-153 others(7): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40668383 | ||||||
| chrX:40668383
|
CA | C | 3 | a0001c0002t0001g0010a0001c0002t0004g0219a0001c0003t0001g0211 | 3 | HG02615.hp1 HG02976.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.3134-1533delT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40668383 | ||||||
| chrX:40668414
|
A | G | 6 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(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 | a0001c0001t0001g0185 | 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 | a0001c0002t0001g0031 | 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 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(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 | a0001c0002t0010g0237 | 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 | a0001c0013t0001g0236 | 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 | 8 | a0001c0001t0001g0058a0001c0001t0001g0084a0001c0001t0001g0091others(5): 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 | a0001c0001t0001g0182 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3134-2288T>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40669139 | ||||||
| chrX:40669250
|
TC | T | 1 | a0001c0001t0001g0061 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.3134-2400delG | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40669250 | ||||||
| chrX:40669355
|
G | A | 1 | a0001c0001t0001g0116 | 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 | a0001c0001t0001g0165 | 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 | a0001c0002t0010g0237 | 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 | a0001c0001t0001g0194 | 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 | a0001c0001t0001g0096 | 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 | a0001c0002t0001g0028 | 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 | a0001c0013t0001g0236 | 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 | a0001c0001t0003g0188 | 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 | 14 | a0001c0001t0001g0005a0001c0001t0001g0168a0001c0001t0001g0171others(11): 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 | a0001c0001t0001g0165 | 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 | a0001c0001t0001g0089a0001c0009t0001g0088 | 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 | a0001c0002t0001g0223 | 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 | a0001c0002t0001g0223 | 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 | 15 | a0001c0001t0001g0194a0001c0001t0001g0215a0001c0001t0001g0216others(12): 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
|
C | CAA | 1 | a0001c0003t0001g0211 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3133+1092_3133+109 others(6): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40670767 | ||||||
| chrX:40670767
|
CA | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(117): Show | 126 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.3133+1093delT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40670767 | ||||||
| chrX:40670767
|
CAA | C | 1 | a0001c0001t0001g0153 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.3133+1092_3133+109 others(6): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 23/30 | chrX | 40670767 | ||||||
| chrX:40670777
|
A | T | 2 | a0001c0001t0002g0109a0001c0002t0001g0238 | 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 | a0001c0002t0001g0033a0001c0002t0001g0036 | 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 | 153 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(150): Show | 160 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(157): 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 | a0001c0001t0002g0144 | 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 | 8 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0002g0181others(5): 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:40672116
|
AAAAT | A | 1 | a0001c0001t0001g0159 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.3022-148_3022-145d others(6): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 22/30 | chrX | 40672116 | ||||||
| chrX:40672138
|
A | G | 1 | a0001c0001t0001g0194 | 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 | 2 | a0001c0001t0001g0058a0001c0001t0001g0091 | 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 | 21 | a0001c0001t0001g0005a0001c0001t0001g0166a0001c0001t0001g0168others(18): 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 | a0001c0001t0001g0105 | 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 | 3 | a0001c0002t0004g0218a0001c0002t0004g0219a0001c0002t0004g0220 | 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 | 9 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0002g0181others(6): 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 | a0001c0001t0001g0054a0001c0001t0001g0071a0001c0001t0001g0074others(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 | a0001c0001t0001g0197a0001c0001t0001g0198 | 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 | a0001c0001t0001g0153 | 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 | a0001c0002t0001g0239a0001c0002t0001g0240 | 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 | 96 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(93): 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 | 16 | a0001c0001t0001g0060a0001c0001t0001g0085a0001c0001t0001g0215others(13): 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 | 149 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(146): Show | 156 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(153): 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:40673936
|
TC | T | 1 | a0001c0001t0001g0054 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.3021+1284delG | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 22/30 | chrX | 40673936 | ||||||
| chrX:40674138
|
C | A | 2 | a0001c0001t0001g0117a0001c0001t0001g0118 | 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 | CT | 1 | a0001c0001t0001g0054 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.3021+1079dupA | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 22/30 | chrX | 40674141 | ||||||
| chrX:40674141
|
C | T | 1 | a0001c0002t0001g0233 | 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 | a0001c0001t0001g0096 | 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 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206 | 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 | a0001c0001t0003g0167a0001c0001t0003g0188a0001c0001t0003g0190 | 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 | 10 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0002g0181others(7): 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 | a0001c0002t0001g0007a0001c0002t0001g0008a0001c0002t0001g0009others(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 | a0001c0002t0001g0041 | 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 | 3 | a0001c0002t0004g0218a0001c0002t0004g0219a0001c0002t0004g0220 | 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 | a0001c0001t0001g0061a0001c0001t0001g0076 | 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 | a0001c0004t0001g0002 | 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 | a0001c0001t0001g0069a0001c0001t0001g0070 | 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 | 69 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0002t0001g0007others(66): 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 | a0001c0001t0001g0165 | 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 | a0001c0001t0001g0172a0001c0001t0001g0174a0001c0001t0001g0178 | 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:40677453
|
A | AC | 1 | a0001c0001t0001g0054 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2881-2093dupG | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 21/30 | chrX | 40677453 | ||||||
| chrX:40677539
|
T | TAA | 1 | a0001c0001t0002g0067 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2881-2179_2881-217 others(6): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 21/30 | chrX | 40677539 | ||||||
| chrX:40677540
|
T | A | 1 | a0001c0001t0002g0067 | 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 | a0001c0001t0002g0067 | 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 | a0001c0001t0002g0067 | 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 | a0001c0001t0002g0067 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2881-2192A>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 21/30 | chrX | 40677553 | ||||||
| chrX:40677559
|
C | CA | 4 | a0001c0001t0001g0073a0001c0001t0001g0177a0001c0002t0001g0035others(1): Show | 4 | HG02738.hp1 NA18961.hp1 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.2881-2199dupT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 21/30 | chrX | 40677559 | ||||||
| chrX:40677796
|
G | A | 1 | a0001c0013t0001g0236 | 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 | a0001c0001t0001g0208a0001c0001t0001g0209a0007c0006t0001g0210 | 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 | 6 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0003t0001g0211others(3): 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 | a0001c0001t0001g0110 | 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 | 104 | a0001c0001t0001g0005a0001c0001t0001g0165a0001c0001t0001g0166others(101): 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 | 32 | a0001c0001t0001g0005a0001c0001t0001g0165a0001c0001t0001g0166others(29): 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 | a0001c0003t0001g0211 | 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 | a0001c0002t0001g0223 | 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 | 29 | a0001c0001t0001g0005a0001c0001t0001g0166a0001c0001t0001g0168others(26): 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 | a0001c0001t0001g0186 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2880+991G>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 21/30 | chrX | 40678873 | ||||||
| chrX:40679234
|
G | GATTA | 1 | a0001c0001t0001g0194 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2880+626_2880+629d others(6): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 21/30 | chrX | 40679234 | ||||||
| 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 | a0001c0013t0001g0236 | 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 | a0001c0001t0001g0147a0001c0001t0001g0148 | 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 | a0001c0002t0010g0237 | 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 | a0001c0004t0001g0002 | 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 | a0001c0001t0001g0114 | 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 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0002t0001g0223others(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 | a0001c0002t0010g0237 | 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 | a0001c0002t0001g0238 | 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 | a0001c0001t0001g0185 | 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 | a0001c0002t0001g0238 | 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 | a0001c0013t0001g0236 | 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 | 4 | a0001c0003t0001g0211a0001c0003t0001g0212a0001c0003t0001g0213others(1): Show | 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 | 105 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0165others(102): 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 | a0001c0002t0001g0041 | 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 | 2 | a0001c0001t0001g0097a0001c0001t0001g0102 | 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 | a0001c0001t0001g0194 | 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 | a0001c0001t0001g0098a0001c0002t0001g0013a0001c0002t0001g0017others(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 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(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 | a0001c0002t0001g0217 | 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 | a0001c0001t0001g0075 | 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 | a0001c0004t0001g0002 | 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 | a0001c0004t0001g0002 | 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:40683836
|
CACAT | C | 2 | a0001c0002t0001g0017a0001c0002t0001g0023 | 2 | HG02622.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2058-844_2058-841d others(6): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 16/30 | chrX | 40683836 | ||||||
| chrX:40684346
|
G | A | 1 | a0001c0013t0001g0236 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2058-1350C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 16/30 | chrX | 40684346 | ||||||
| chrX:40684386
|
CA | C | 1 | a0001c0001t0001g0071 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.2058-1391delT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 16/30 | chrX | 40684386 | ||||||
| chrX:40684590
|
G | A | 29 | a0001c0001t0001g0005a0001c0001t0001g0165a0001c0001t0001g0166others(26): 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 | a0001c0001t0001g0085 | 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 | a0001c0002t0001g0045a0001c0002t0001g0235 | 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 | a0001c0002t0001g0238 | 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 | a0001c0001t0001g0165a0001c0001t0001g0208a0001c0001t0001g0209others(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 | 60 | a0001c0001t0001g0012a0001c0001t0001g0208a0001c0001t0001g0209others(57): 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 | a0001c0001t0001g0083 | 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 | a0001c0001t0001g0207 | 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 | a0001c0002t0001g0232a0001c0002t0001g0233a0001c0002t0001g0234 | 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 | a0001c0002t0001g0039 | 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 | a0001c0002t0001g0224a0001c0002t0001g0225a0001c0002t0001g0227others(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 | a0001c0002t0001g0226 | 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 | a0001c0001t0001g0132 | 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 | 105 | a0001c0001t0001g0005a0001c0001t0001g0160a0001c0001t0001g0165others(102): 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 | a0001c0001t0001g0150 | 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 | a0001c0001t0001g0074 | 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 | 103 | a0001c0001t0001g0005a0001c0001t0001g0165a0001c0001t0001g0166others(100): 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 | 57 | a0001c0002t0001g0007a0001c0002t0001g0008a0001c0002t0001g0009others(54): 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 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0187others(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 | 62 | a0001c0001t0001g0012a0001c0001t0001g0208a0001c0001t0001g0209others(59): 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 | a0001c0001t0001g0170 | 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 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(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:40688806
|
AG | A | 1 | a0008c0011t0001g0077 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1981-277delC | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40688806 | ||||||
| chrX:40688832
|
AT | A | 1 | a0008c0011t0001g0077 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1981-303delA | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40688832 | ||||||
| chrX:40688868
|
C | T | 4 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0187others(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 | a0001c0001t0001g0199 | 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 | a0001c0001t0001g0122 | 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 | a0001c0002t0001g0240 | 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 | a0001c0001t0001g0222a0001c0002t0001g0010a0001c0002t0001g0014others(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:40689104
|
AC | A | 1 | a0008c0011t0001g0077 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1981-575delG | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40689104 | ||||||
| chrX:40689126
|
TA | T | 1 | a0008c0011t0001g0077 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1981-597delT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40689126 | ||||||
| chrX:40689226
|
C | G | 1 | a0001c0008t0001g0129 | 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 | a0001c0001t0001g0197 | 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 | a0001c0002t0001g0224a0001c0002t0001g0225a0001c0002t0001g0227others(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:40689328
|
AG | A | 1 | a0008c0011t0001g0077 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1981-799delC | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40689328 | ||||||
| chrX:40689352
|
GA | G | 1 | a0008c0011t0001g0077 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1981-823delT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40689352 | ||||||
| chrX:40689354
|
A | G | 3 | a0001c0001t0001g0208a0001c0001t0001g0209a0007c0006t0001g0210 | 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:40689368
|
CA | C | 1 | a0008c0011t0001g0077 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1981-839delT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40689368 | ||||||
| chrX:40689691
|
C | CA | 1 | a0001c0009t0001g0088 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1981-1162dupT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40689691 | ||||||
| chrX:40689869
|
G | C | 1 | a0001c0004t0001g0002 | 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:40690031
|
TA | T | 1 | a0008c0011t0001g0077 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1981-1502delT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40690031 | ||||||
| chrX:40690185
|
G | A | 1 | a0001c0001t0001g0152 | 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 | a0001c0002t0001g0223 | 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 | 76 | a0001c0001t0001g0012a0001c0001t0001g0160a0001c0001t0001g0208others(73): 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 | 64 | a0001c0001t0001g0012a0001c0001t0001g0160a0001c0001t0001g0208others(61): 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:40691018
|
AG | A | 1 | a0008c0011t0001g0077 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1980+1164delC | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40691018 | ||||||
| chrX:40691069
|
T | A | 1 | a0001c0001t0012g0111 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1980+1114A>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40691069 | ||||||
| chrX:40691122
|
GA | G | 1 | a0008c0011t0001g0077 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1980+1060delT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40691122 | ||||||
| chrX:40691405
|
G | C | 2 | a0001c0002t0001g0239a0001c0002t0001g0240 | 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:40691406
|
AG | A | 1 | a0008c0011t0001g0077 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1980+776delC | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40691406 | ||||||
| chrX:40691417
|
TA | T | 1 | a0008c0011t0001g0077 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1980+765delT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40691417 | ||||||
| chrX:40691466
|
TA | T | 1 | a0008c0011t0001g0077 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1980+716delT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40691466 | ||||||
| chrX:40691572
|
T | C | 3 | a0001c0002t0001g0232a0001c0002t0001g0233a0001c0002t0001g0234 | 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 | a0001c0001t0001g0153 | 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 | a0001c0001t0001g0153 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1980+582A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40691601 | ||||||
| chrX:40691603
|
TA | T | 1 | a0001c0001t0001g0153 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1980+579delT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40691603 | ||||||
| chrX:40691604
|
A | AT | 72 | a0001c0001t0001g0172a0001c0001t0001g0184a0001c0001t0001g0185others(69): 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 | a0001c0001t0001g0183a0001c0001t0002g0081a0001c0002t0001g0017others(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 | 22 | a0001c0001t0001g0071a0001c0001t0001g0117a0001c0001t0002g0046others(19): Show | 22 | HG01069.hp1 HG01106.hp1 HG01167.hp1 others(19): 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 | 96 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(93): 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 | a0001c0001t0001g0057a0001c0001t0001g0060a0001c0001t0001g0061others(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 | 72 | a0001c0001t0001g0172a0001c0001t0001g0184a0001c0001t0001g0185others(69): 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:40691605
|
A | T | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(166): Show | 176 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.1980+578T>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40691605 | ||||||
| chrX:40691606
|
T | C | 28 | a0001c0001t0001g0005a0001c0001t0001g0165a0001c0001t0001g0166others(25): 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:40691607
|
C | T | 241 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(238): Show | 250 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.1980+576G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40691607 | ||||||
| chrX:40691773
|
G | A | 1 | a0001c0013t0001g0236 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1980+410C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40691773 | ||||||
| chrX:40691868
|
TC | T | 1 | a0008c0011t0001g0077 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1980+314delG | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40691868 | ||||||
| chrX:40691901
|
C | T | 1 | a0001c0001t0001g0113 | 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 | 6 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0003t0001g0211others(3): 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 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(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:40692151
|
TG | T | 1 | a0008c0011t0001g0077 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1980+31delC | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 15/30 | chrX | 40692151 | ||||||
| chrX:40692347
|
TA | T | 87 | a0001c0001t0001g0005a0001c0001t0001g0165a0001c0001t0001g0166others(84): Show | 90 | HG00438.hp2 HG00639.hp2 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.1846-31delT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 14/30 | chrX | 40692347 | ||||||
| chrX:40692347
|
TAA | T | 17 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0002t0001g0010others(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:40692540
|
T | TA | 1 | a0008c0011t0001g0077 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1845+167dupT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 14/30 | chrX | 40692540 | ||||||
| chrX:40692991
|
T | C | 62 | a0001c0001t0001g0160a0001c0001t0001g0208a0001c0001t0001g0209others(59): 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:40693011
|
T | TA | 4 | a0001c0001t0001g0107a0001c0001t0001g0175a0001c0001t0001g0241others(1): Show | 4 | HG01256.hp1 HG01993.hp2 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.1651-110dupT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 13/30 | chrX | 40693011 | ||||||
| chrX:40693011
|
TA | T | 5 | a0001c0003t0001g0211a0001c0003t0001g0212a0001c0003t0001g0213others(2): Show | 5 | HG02615.hp1 HG02976.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1651-110delT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 13/30 | chrX | 40693011 | ||||||
| chrX:40693294
|
G | A | 1 | a0001c0001t0001g0112 | 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 | 4 | a0001c0003t0001g0211a0001c0003t0001g0212a0001c0003t0001g0213others(1): Show | 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 | a0001c0002t0001g0217a0001c0002t0001g0226a0001c0002t0001g0229 | 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 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(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 | a0001c0002t0001g0238 | 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 | a0001c0013t0001g0236 | 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 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(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 | 103 | a0001c0001t0001g0005a0001c0001t0001g0165a0001c0001t0001g0166others(100): 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 | 3 | a0001c0003t0001g0212a0001c0003t0001g0213a0001c0003t0001g0214 | 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 | a0001c0013t0001g0236 | 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 | a0001c0001t0001g0012a0001c0001t0001g0075a0001c0001t0001g0082others(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 | a0001c0001t0001g0099a0001c0001t0001g0122a0001c0001t0001g0123others(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 | a0001c0002t0001g0239 | 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 | a0001c0013t0001g0236 | 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 | 231 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(228): 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 | 27 | a0001c0001t0001g0005a0001c0001t0001g0166a0001c0001t0001g0168others(24): 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:40696894
|
AC | A | 1 | a0001c0001t0001g0071 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1650+129delG | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 13/30 | chrX | 40696894 | ||||||
| chrX:40696999
|
C | A | 4 | a0001c0003t0001g0211a0001c0003t0001g0212a0001c0003t0001g0213others(1): Show | 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 | 226 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(223): 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:40697716
|
T | TA | 2 | a0001c0002t0001g0238a0001c0002t0010g0237 | 2 | HG00733.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1491-534dupT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 12/30 | chrX | 40697716 | ||||||
| chrX:40697831
|
C | A | 4 | a0001c0003t0001g0211a0001c0003t0001g0212a0001c0003t0001g0213others(1): Show | 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 | a0001c0002t0001g0238a0001c0002t0010g0237 | 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 | a0001c0001t0001g0085 | 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 | a0001c0001t0001g0194 | 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 | a0001c0001t0001g0194 | 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 | a0001c0001t0001g0175a0001c0001t0001g0241 | 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 | a0001c0004t0001g0002 | 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 | a0001c0002t0001g0039 | 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 | a0001c0001t0002g0067 | 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 | a0001c0002t0001g0016 | 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 | a0001c0001t0001g0143 | 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 | 3 | a0001c0003t0001g0212a0001c0003t0001g0213a0001c0003t0001g0214 | 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 | a0001c0001t0001g0208a0001c0001t0001g0209a0007c0006t0001g0210 | 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 | a0001c0001t0001g0100 | 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 | a0001c0004t0001g0002 | 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 | a0001c0002t0001g0238a0001c0002t0010g0237 | 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 | a0001c0003t0001g0211 | 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 | 23 | a0001c0001t0001g0005a0001c0001t0001g0166a0001c0001t0001g0168others(20): 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 | a0001c0001t0001g0012a0001c0001t0001g0196a0001c0001t0001g0197others(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 | 6 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0003t0001g0211others(3): 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 | a0001c0001t0001g0012a0001c0001t0001g0160a0001c0001t0001g0208others(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 | a0001c0002t0001g0238 | 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 | a0001c0002t0001g0239a0001c0002t0001g0240 | 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 | 28 | a0001c0001t0001g0196a0001c0001t0001g0201a0001c0001t0001g0208others(25): 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 | a0001c0001t0001g0207a0001c0001t0002g0052a0001c0002t0001g0009others(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:40700363
|
C | CAAAAA | 1 | a0001c0001t0001g0177 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1490+797_1490+801d others(7): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 12/30 | chrX | 40700363 | ||||||
| chrX:40700381
|
AAAAAAAA others(5): Show |
A | 1 | a0001c0002t0001g0225 | 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:40700384
|
AAAAAAAA others(2): Show |
A | 1 | a0001c0004t0001g0002 | 3 | HG02280.hp2 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1490+772_1490+780d others(11): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 12/30 | chrX | 40700384 | ||||||
| chrX:40700390
|
AAAT | A | 7 | a0001c0001t0001g0071a0001c0001t0001g0183a0001c0001t0001g0184others(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 | 28 | a0001c0001t0001g0005a0001c0001t0001g0064a0001c0001t0001g0074others(25): 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 | 79 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(76): 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 | 125 | a0001c0001t0001g0012a0001c0001t0001g0053a0001c0001t0001g0056others(122): Show | 125 | HG00280.hp1 HG00408.hp1 HG00642.hp1 others(122): Show |
intron_variant | MODIFIER | c.1490+772A>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 12/30 | chrX | 40700393 | ||||||
| chrX:40700522
|
G | GC | 1 | a0001c0001t0001g0054 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1490+642dupG | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 12/30 | chrX | 40700522 | ||||||
| chrX:40700690
|
T | C | 1 | a0001c0002t0001g0042 | 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 | a0001c0002t0001g0028 | 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 | 3 | a0001c0002t0004g0218a0001c0002t0004g0219a0001c0002t0004g0220 | 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 | a0001c0001t0001g0132 | 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 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105 | 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 | a0001c0001t0001g0104a0001c0001t0001g0105 | 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 | a0001c0002t0001g0239a0001c0002t0001g0240 | 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:40701773
|
CA | C | 1 | a0001c0002t0001g0035 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1412-531delT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 11/30 | chrX | 40701773 | ||||||
| chrX:40701835
|
A | G | 1 | a0001c0002t0010g0237 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1412-592T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 11/30 | chrX | 40701835 | ||||||
| chrX:40701892
|
TC | T | 1 | a0001c0002t0001g0035 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1412-650delG | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 11/30 | chrX | 40701892 | ||||||
| chrX:40701904
|
TG | T | 1 | a0001c0002t0001g0029 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1412-662delC | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 11/30 | chrX | 40701904 | ||||||
| chrX:40702043
|
G | A | 1 | a0001c0002t0001g0229 | 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 | a0001c0001t0003g0167a0001c0001t0003g0188a0001c0001t0003g0190 | 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 | a0001c0001t0001g0012a0001c0001t0001g0160a0001c0001t0001g0208others(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 | 41 | a0001c0001t0001g0005a0001c0001t0001g0071a0001c0001t0001g0076others(38): Show | 44 | HG00438.hp2 HG00639.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.1411+1097dupA | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 11/30 | chrX | 40702346 | ||||||
| chrX:40702346
|
G | GTT | 57 | a0001c0001t0001g0012a0001c0001t0001g0160a0001c0001t0001g0166others(54): 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 | a0001c0001t0001g0168a0001c0001t0001g0177a0001c0002t0001g0014others(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:40702346
|
G | GTTTT | 1 | a0001c0002t0001g0232 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1411+1094_1411+109 others(8): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 11/30 | chrX | 40702346 | ||||||
| chrX:40702346
|
GT | G | 1 | a0001c0001t0001g0113 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1411+1097delA | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 11/30 | chrX | 40702346 | ||||||
| chrX:40702349
|
T | TTG | 3 | a0001c0001t0001g0208a0001c0001t0001g0209a0007c0006t0001g0210 | 3 | HG02145.hp1 HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1411+1094_1411+109 others(6): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 11/30 | chrX | 40702349 | ||||||
| chrX:40702415
|
C | T | 6 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0003t0001g0211others(3): 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 | a0001c0001t0001g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1411+1021A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 11/30 | chrX | 40702423 | ||||||
| chrX:40702439
|
C | CA | 1 | a0001c0001t0001g0194 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1411+1004dupT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 11/30 | chrX | 40702439 | ||||||
| chrX:40702513
|
A | AT | 1 | a0008c0011t0001g0077 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1411+930dupA | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 11/30 | chrX | 40702513 | ||||||
| chrX:40702756
|
T | C | 1 | a0001c0002t0001g0038 | 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 | a0001c0001t0003g0167a0001c0001t0003g0188a0001c0001t0003g0190 | 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 | a0001c0001t0001g0153 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1411+222C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 11/30 | chrX | 40703222 | ||||||
| chrX:40703683
|
G | GA | 1 | a0008c0011t0001g0077 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1286-115dupT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40703683 | ||||||
| chrX:40703722
|
T | TG | 2 | a0001c0002t0001g0239a0001c0002t0001g0240 | 2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1286-154dupC | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40703722 | ||||||
| chrX:40703874
|
T | C | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 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 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(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 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(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 | a0001c0001t0001g0215a0001c0001t0001g0216 | 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 | a0001c0001t0001g0182 | 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 | a0001c0002t0001g0007a0001c0002t0001g0008a0001c0002t0001g0009others(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 | a0001c0002t0001g0007a0001c0002t0001g0008a0001c0002t0001g0020others(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 | a0001c0001t0001g0108 | 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 | a0001c0001t0001g0194 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1286-1505A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40705074 | ||||||
| chrX:40705153
|
G | GT | 1 | a0008c0011t0001g0077 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1286-1585dupA | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40705153 | ||||||
| chrX:40705337
|
T | TG | 11 | a0001c0001t0001g0063a0001c0001t0001g0115a0001c0001t0001g0157others(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:40705465
|
A | AT | 1 | a0008c0011t0001g0077 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1286-1897dupA | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40705465 | ||||||
| chrX:40705487
|
T | C | 1 | a0001c0001t0001g0125 | 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 | a0001c0001t0001g0165a0001c0002t0001g0239a0001c0002t0001g0240 | 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:40705662
|
C | CT | 1 | a0008c0011t0001g0077 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1286-2094dupA | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40705662 | ||||||
| chrX:40705778
|
T | C | 35 | a0001c0001t0001g0005a0001c0001t0001g0165a0001c0001t0001g0166others(32): 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:40705903
|
CT | C | 1 | a0008c0011t0001g0077 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1286-2335delA | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40705903 | ||||||
| chrX:40705945
|
T | TC | 1 | a0008c0011t0001g0077 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1286-2377dupG | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40705945 | ||||||
| chrX:40705962
|
T | TA | 1 | a0008c0011t0001g0077 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1286-2394dupT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40705962 | ||||||
| chrX:40706067
|
C | CA | 1 | a0008c0011t0001g0077 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1286-2499dupT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40706067 | ||||||
| chrX:40706129
|
C | T | 1 | a0001c0003t0001g0211 | 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 | 69 | a0001c0001t0001g0160a0001c0001t0001g0196a0001c0001t0001g0197others(66): 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 | 224 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(221): 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:40706407
|
T | TC | 1 | a0008c0011t0001g0077 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1286-2839dupG | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40706407 | ||||||
| chrX:40706556
|
C | T | 1 | a0001c0002t0001g0217 | 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 | 27 | a0001c0001t0001g0005a0001c0001t0001g0166a0001c0001t0001g0168others(24): 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 | a0001c0001t0003g0167a0001c0001t0003g0188a0001c0001t0003g0190 | 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 | a0001c0002t0001g0017a0001c0002t0001g0023 | 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:40706922
|
G | GA | 1 | a0008c0011t0001g0077 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1285+2425dupT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40706922 | ||||||
| chrX:40707051
|
A | C | 83 | a0001c0001t0001g0012a0001c0001t0001g0160a0001c0001t0001g0196others(80): 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 | 45 | a0001c0001t0001g0056a0001c0001t0001g0061a0001c0001t0001g0070others(42): 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 | a0001c0001t0001g0113a0001c0002t0001g0020a0001c0002t0001g0038 | 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 | a0001c0002t0001g0037 | 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 | 36 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(33): 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:40707107
|
GGATAGAT others(1): Show |
G | 1 | a0001c0003t0001g0211 | 1 | HG02615.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:40707138
|
T | C | 1 | a0001c0001t0001g0168 | 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 | 35 | a0001c0001t0001g0005a0001c0001t0001g0165a0001c0001t0001g0166others(32): 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:40707520
|
G | GA | 1 | a0008c0011t0001g0077 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1285+1827dupT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40707520 | ||||||
| chrX:40707684
|
C | T | 2 | a0001c0002t0001g0239a0001c0002t0001g0240 | 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:40707800
|
C | CA | 1 | a0001c0001t0001g0061 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1285+1547dupT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40707800 | ||||||
| chrX:40707802
|
C | T | 3 | a0001c0001t0001g0082a0001c0001t0001g0127a0001c0001t0001g0140 | 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:40707853
|
G | GT | 1 | a0008c0011t0001g0077 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1285+1494dupA | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40707853 | ||||||
| chrX:40707857
|
C | G | 1 | a0001c0002t0001g0007 | 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 | a0001c0001t0001g0201 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1285+1411G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40707937 | ||||||
| chrX:40707981
|
G | GT | 1 | a0008c0011t0001g0077 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1285+1366dupA | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40707981 | ||||||
| chrX:40708052
|
AG | A | 1 | a0008c0011t0001g0077 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1285+1295delC | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40708052 | ||||||
| chrX:40708343
|
C | T | 1 | a0001c0002t0001g0238 | 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 | a0001c0002t0001g0239a0001c0002t0001g0240 | 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:40709006
|
A | AT | 1 | a0008c0011t0001g0077 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1285+341dupA | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 10/30 | chrX | 40709006 | ||||||
| chrX:40709030
|
G | A | 78 | a0001c0001t0001g0160a0001c0001t0001g0196a0001c0001t0001g0197others(75): 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 | a0001c0013t0001g0236 | 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 | a0001c0001t0001g0208a0001c0001t0001g0209a0007c0006t0001g0210 | 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 | a0001c0013t0001g0236 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1023-333C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 8/30 | chrX | 40710462 | ||||||
| chrX:40710472
|
G | GA | 1 | a0001c0001t0001g0061 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1023-344dupT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 8/30 | chrX | 40710472 | ||||||
| chrX:40710641
|
T | C | 2 | a0001c0002t0001g0238a0001c0002t0010g0237 | 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 | 67 | a0001c0002t0001g0007a0001c0002t0001g0008a0001c0002t0001g0009others(64): 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 | a0001c0001t0001g0202a0001c0001t0001g0203 | 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 | a0001c0001t0001g0114 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.890-264C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 7/30 | chrX | 40711565 | ||||||
| chrX:40711789
|
CT | C | 1 | a0001c0001t0001g0115 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.889+396delA | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 7/30 | chrX | 40711789 | ||||||
| chrX:40712073
|
G | A | 2 | a0001c0002t0001g0239a0001c0002t0001g0240 | 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 | a0001c0002t0001g0014a0001c0002t0001g0034 | 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 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0002t0001g0217others(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 | a0001c0001t0001g0133 | 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 | 106 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0165others(103): 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 | a0001c0001t0001g0170 | 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 | 105 | a0001c0001t0001g0005a0001c0001t0001g0165a0001c0001t0001g0166others(102): 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:40712857
|
T | TA | 2 | a0001c0002t0001g0238a0001c0002t0010g0237 | 2 | HG00733.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.781+56dupT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 6/30 | chrX | 40712857 | ||||||
| chrX:40713598
|
G | A | 2 | a0001c0002t0001g0239a0001c0002t0001g0240 | 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:40713952
|
AT | A | 1 | a0001c0002t0001g0035 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.523-46delA | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 4/30 | chrX | 40713952 | ||||||
| chrX:40714051
|
G | A | 4 | a0001c0001t0001g0165a0001c0001t0001g0208a0001c0001t0001g0209others(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 | a0001c0002t0001g0007a0001c0002t0001g0008a0001c0002t0001g0009others(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:40714230
|
TA | T | 1 | a0001c0002t0001g0035 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.522+306delT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 4/30 | chrX | 40714230 | ||||||
| chrX:40714310
|
C | T | 2 | a0001c0001t0002g0080a0001c0001t0002g0081 | 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:40714449
|
G | GT | 1 | a0002c0015t0013g0242 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.522+87dupA | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 4/30 | chrX | 40714449 | ||||||
| chrX:40714462
|
C | T | 2 | a0001c0001t0001g0166a0001c0001t0001g0170 | 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 | 7 | a0001c0002t0001g0223a0001c0002t0001g0238a0001c0002t0010g0237others(4): 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 | 19 | a0001c0001t0001g0005a0001c0001t0001g0168a0001c0001t0001g0171others(16): 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 | a0001c0001t0001g0116 | 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 | 77 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0198others(74): 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 | a0001c0002t0001g0018a0001c0002t0001g0021 | 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 | a0001c0001t0001g0200a0001c0001t0001g0207 | 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 | a0001c0002t0001g0221 | 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 | a0001c0013t0001g0236 | 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 | a0001c0001t0001g0117a0001c0001t0001g0118 | 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 | 37 | a0001c0001t0001g0005a0001c0001t0001g0165a0001c0001t0001g0166others(34): 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 | 34 | a0001c0001t0001g0054a0001c0001t0001g0056a0001c0001t0001g0060others(31): Show | 34 | HG00438.hp1 HG00738.hp1 HG01175.hp1 others(31): Show |
intron_variant | MODIFIER | c.349-1076dupT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40715785 | ||||||
| chrX:40715785
|
C | CAA | 1 | a0001c0001t0001g0127 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.349-1077_349-1076d others(4): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40715785 | ||||||
| chrX:40715810
|
AAAG | A | 3 | a0001c0002t0004g0218a0001c0002t0004g0219a0001c0002t0004g0220 | 3 | HG02809.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.349-1103_349-1101d others(5): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40715810 | ||||||
| chrX:40715811
|
AAG | A | 60 | a0001c0001t0001g0012a0001c0001t0001g0196a0001c0001t0001g0197others(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 | a0001c0001t0001g0079a0001c0001t0001g0165a0001c0001t0002g0066others(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 | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 172 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(169): 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 | a0001c0001t0001g0128 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.349-1143A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40715853 | ||||||
| chrX:40716019
|
TA | T | 1 | a0002c0015t0013g0242 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.349-1310delT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40716019 | ||||||
| chrX:40716040
|
G | A | 1 | a0001c0002t0001g0238 | 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 | a0001c0002t0001g0239a0001c0002t0001g0240 | 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 | 73 | a0001c0001t0001g0012a0001c0001t0001g0160a0001c0001t0001g0196others(70): 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 | a0001c0002t0001g0229 | 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 | 39 | a0001c0001t0001g0005a0001c0001t0001g0143a0001c0001t0001g0165others(36): 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 | a0001c0002t0001g0238 | 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 | a0001c0002t0001g0239a0001c0002t0001g0240 | 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 | 3 | a0001c0002t0004g0218a0001c0002t0004g0219a0001c0002t0004g0220 | 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 | 5 | a0001c0002t0001g0223a0001c0003t0001g0211a0001c0003t0001g0212others(2): 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 | 5 | a0001c0002t0001g0223a0001c0003t0001g0211a0001c0003t0001g0212others(2): 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 | a0001c0002t0001g0239a0001c0002t0001g0240 | 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:40717276
|
G | GA | 2 | a0001c0001t0002g0130a0001c0003t0001g0214 | 2 | HG01993.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.349-2567dupT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40717276 | ||||||
| chrX:40717503
|
G | GT | 1 | a0001c0002t0001g0011 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.349-2794dupA | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40717503 | ||||||
| chrX:40717524
|
CATTTT | C | 53 | a0001c0002t0001g0007a0001c0002t0001g0008a0001c0002t0001g0009others(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:40717908
|
AG | A | 1 | a0001c0001t0001g0194 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.349-3199delC | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40717908 | ||||||
| chrX:40718149
|
A | G | 2 | a0001c0001t0001g0166a0001c0001t0001g0170 | 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 | a0001c0001t0001g0060a0001c0001t0001g0072a0001c0001t0001g0073others(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 | a0001c0001t0001g0078 | 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 | a0001c0001t0003g0167a0001c0001t0003g0188a0001c0001t0003g0190 | 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 | a0001c0002t0001g0238 | 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 | a0001c0001t0001g0215a0001c0001t0001g0216 | 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:40719519
|
TA | T | 1 | a0001c0013t0001g0236 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.349-4810delT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40719519 | ||||||
| chrX:40719535
|
A | G | 1 | a0001c0001t0001g0222 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.349-4825T>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40719535 | ||||||
| chrX:40719593
|
GA | G | 1 | a0008c0011t0001g0077 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.349-4884delT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40719593 | ||||||
| chrX:40719764
|
G | A | 1 | a0001c0001t0001g0194 | 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 | 14 | a0001c0001t0001g0005a0001c0001t0001g0168a0001c0001t0001g0171others(11): 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 | 4 | a0001c0002t0001g0223a0001c0003t0001g0212a0001c0003t0001g0213others(1): Show | 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 | a0001c0003t0001g0211 | 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 | a0001c0001t0001g0132 | 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 | a0001c0002t0001g0038 | 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 | a0001c0002t0001g0039 | 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 | a0001c0002t0001g0239a0001c0002t0001g0240 | 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 | 67 | a0001c0002t0001g0007a0001c0002t0001g0008a0001c0002t0001g0009others(64): 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 | a0001c0002t0001g0232a0001c0002t0001g0233a0001c0002t0001g0234 | 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 | a0001c0001t0001g0165 | 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 | a0001c0001t0001g0206 | 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 | a0001c0002t0010g0237 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.348+5355C>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40721391 | ||||||
| chrX:40721853
|
G | GC | 1 | a0001c0001t0001g0062 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.348+4892dupG | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40721853 | ||||||
| chrX:40721914
|
C | T | 1 | a0001c0013t0001g0236 | 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 | a0001c0001t0001g0166a0001c0001t0001g0170 | 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:40721982
|
G | GCCCCCCC others(2): Show |
1 | a0001c0001t0001g0062 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.348+4763_348+4764i others(11): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40721982 | ||||||
| chrX:40721985
|
T | C | 1 | a0001c0001t0001g0062 | 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 | a0001c0001t0001g0069a0001c0001t0001g0070 | 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:40722525
|
GAA | G | 2 | a0001c0001t0001g0166a0001c0001t0001g0170 | 2 | HG03486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.348+4219_348+4220d others(4): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40722525 | ||||||
| chrX:40723092
|
G | A | 1 | a0001c0002t0001g0013 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.348+3654C>T | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40723092 | ||||||
| chrX:40723153
|
G | GT | 1 | a0001c0002t0001g0020 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.348+3592dupA | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40723153 | ||||||
| chrX:40723271
|
T | C | 1 | a0001c0013t0001g0236 | 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 | a0001c0001t0001g0076 | 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 | a0001c0001t0001g0133 | 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 | a0001c0001t0001g0194 | 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 | 119 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0160others(116): 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 | 3 | a0001c0002t0004g0218a0001c0002t0004g0219a0001c0002t0004g0220 | 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 | a0001c0001t0001g0054a0001c0001t0001g0071a0001c0001t0001g0074others(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 | 87 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0160others(84): 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 | a0001c0001t0001g0192a0001c0001t0001g0203a0001c0001t0001g0208others(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
|
G | GAAA | 2 | a0001c0002t0001g0234a0001c0002t0001g0238 | 2 | HG02109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.348+3076_348+3078d others(5): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40723667 | ||||||
| chrX:40723667
|
GA | G | 96 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(93): 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 | a0001c0001t0001g0060a0001c0001t0001g0071a0001c0001t0001g0072others(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(2): Show |
G | 1 | a0001c0001t0001g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.348+3070_348+3078d others(11): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40723667 | ||||||
| chrX:40723667
|
GAAAAAAA others(3): Show |
G | 2 | a0001c0001t0001g0215a0001c0001t0001g0216 | 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 | a0001c0001t0001g0069a0001c0001t0001g0070 | 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 | 238 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(235): Show | 247 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(244): 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 | a0001c0001t0001g0145a0001c0001t0001g0146 | 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 | a0001c0002t0001g0238 | 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 | 5 | a0001c0002t0001g0223a0001c0003t0001g0211a0001c0003t0001g0212others(2): 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 | a0001c0002t0001g0017 | 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 | a0001c0001t0001g0064 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.348+2051T>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40724695 | ||||||
| chrX:40724709
|
CA | C | 1 | a0001c0001t0001g0062 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.348+2036delT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40724709 | ||||||
| chrX:40724808
|
T | C | 4 | a0001c0001t0001g0165a0001c0001t0001g0208a0001c0001t0001g0209others(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:40725004
|
C | CAA | 2 | a0001c0001t0001g0147a0001c0001t0001g0148 | 2 | HG01192.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.348+1740_348+1741d others(4): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40725004 | ||||||
| chrX:40725008
|
G | A | 2 | a0001c0001t0001g0147a0001c0001t0001g0148 | 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 | 3 | a0001c0002t0004g0218a0001c0002t0004g0219a0001c0002t0004g0220 | 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:40725442
|
GCAAAC | G | 2 | a0001c0002t0001g0015a0001c0002t0001g0016 | 2 | HG02258.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.348+1299_348+1303d others(7): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40725442 | ||||||
| chrX:40725541
|
A | G | 1 | a0001c0002t0001g0226 | 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 | a0001c0001t0001g0189 | 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 | 65 | a0001c0001t0001g0012a0001c0001t0001g0160a0001c0001t0001g0208others(62): 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 | 4 | a0001c0003t0001g0211a0001c0003t0001g0212a0001c0003t0001g0213others(1): Show | 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 | a0001c0001t0001g0149 | 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 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0003g0190others(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:40726374
|
GA | G | 4 | a0001c0001t0001g0053a0001c0001t0001g0062a0001c0001t0001g0063others(1): Show | 4 | HG00733.hp2 HG01358.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+371delT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 3/30 | chrX | 40726374 | ||||||
| chrX:40726532
|
T | A | 1 | a0001c0001t0001g0192 | 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 | a0001c0002t0001g0232a0001c0002t0001g0233a0001c0002t0001g0234 | 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 | 34 | a0001c0001t0001g0005a0001c0001t0001g0165a0001c0001t0001g0166others(31): 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 | a0001c0001t0001g0165 | 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 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206 | 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:40728234
|
T | TC | 1 | a0002c0015t0013g0242 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.242+1084dupG | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 2/30 | chrX | 40728234 | ||||||
| chrX:40728442
|
C | T | 104 | a0001c0001t0001g0005a0001c0001t0001g0165a0001c0001t0001g0166others(101): 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 | a0001c0002t0001g0238 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.242+845C>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 2/30 | chrX | 40728474 | ||||||
| chrX:40728534
|
T | TA | 2 | a0001c0001t0001g0152a0001c0002t0001g0044 | 2 | HG03831.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.242+784dupT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 2/30 | chrX | 40728534 | ||||||
| chrX:40728580
|
C | T | 1 | a0001c0002t0001g0014 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.242+739G>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 2/30 | chrX | 40728580 | ||||||
| chrX:40728580
|
CG | C | 1 | a0001c0001t0001g0153 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.242+738delC | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 2/30 | chrX | 40728580 | ||||||
| chrX:40728629
|
T | G | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 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 | a0001c0001t0001g0197a0001c0001t0001g0198 | 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 | 38 | a0001c0001t0001g0005a0001c0001t0001g0165a0001c0001t0001g0166others(35): 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 | a0001c0002t0001g0238 | 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 | a0001c0003t0001g0211 | 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 | 58 | a0001c0001t0001g0222a0001c0002t0001g0007a0001c0002t0001g0008others(55): 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 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0196others(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:40729353
|
G | GA | 3 | a0001c0001t0001g0193a0001c0002t0001g0007a0002c0015t0013g0242 | 3 | HG04204.hp1 NA19075.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.216-9dupT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40729353 | ||||||
| chrX:40729353
|
GA | G | 3 | a0001c0001t0002g0046a0001c0002t0004g0218a0001c0004t0001g0002 | 5 | HG01243.hp1 HG02280.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.216-9delT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40729353 | ||||||
| chrX:40729738
|
G | GT | 1 | a0002c0015t0013g0242 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.216-394dupA | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40729738 | ||||||
| chrX:40729927
|
T | C | 2 | a0001c0002t0001g0239a0001c0002t0001g0240 | 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 | a0001c0001t0001g0165 | 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 | a0001c0004t0001g0002 | 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 | a0001c0013t0001g0236 | 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 | a0001c0001t0001g0012a0001c0002t0001g0011 | 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:40730651
|
T | TC | 1 | a0001c0001t0001g0195 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.216-1307dupG | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40730651 | ||||||
| chrX:40730850
|
C | CG | 7 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(4): Show | 7 | HG01109.hp1 HG02055.hp1 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.216-1506dupC | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40730850 | ||||||
| chrX:40730851
|
G | A | 1 | a0001c0004t0001g0002 | 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:40730910
|
C | CG | 4 | a0001c0001t0001g0056a0001c0001t0001g0208a0001c0002t0001g0010others(1): Show | 4 | HG02145.hp1 HG02818.hp1 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.216-1566dupC | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40730910 | ||||||
| chrX:40730958
|
C | G | 81 | a0001c0001t0001g0012a0001c0001t0001g0196a0001c0001t0001g0197others(78): 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 | 4 | a0001c0003t0001g0211a0001c0003t0001g0212a0001c0003t0001g0213others(1): Show | 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:40731066
|
TG | T | 1 | a0001c0013t0001g0236 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.216-1722delC | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40731066 | ||||||
| chrX:40731071
|
G | A | 12 | a0001c0002t0001g0217a0001c0002t0001g0224a0001c0002t0001g0225others(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 | a0001c0001t0009g0156 | 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 | 117 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0157others(114): 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:40731140
|
C | CAA | 1 | a0001c0001t0001g0194 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.216-1797_216-1796d others(4): Show |
MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40731140 | ||||||
| chrX:40731225
|
G | A | 1 | a0001c0001t0001g0207 | 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 | a0001c0002t0001g0238a0001c0002t0010g0237 | 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 | a0001c0002t0001g0045a0001c0002t0001g0235 | 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 | a0001c0004t0001g0002 | 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 | a0001c0002t0001g0009 | 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 | a0001c0013t0001g0236 | 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 | a0001c0013t0001g0236 | 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 | 7 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(4): 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 | a0001c0001t0001g0194 | 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 | a0001c0002t0001g0238 | 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 | a0001c0002t0001g0217 | 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 | 77 | a0001c0001t0001g0012a0001c0001t0001g0158a0001c0001t0001g0159others(74): 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 | a0001c0002t0001g0238a0001c0002t0001g0239a0001c0002t0001g0240others(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 | a0001c0004t0001g0002 | 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 | a0001c0001t0001g0055 | 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 | a0001c0003t0001g0211 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.215+2404T>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40732794 | ||||||
| chrX:40732901
|
G | GA | 1 | a0002c0015t0013g0242 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.215+2296dupT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40732901 | ||||||
| chrX:40733081
|
TGGTCACT others(5): Show |
T | 1 | a0002c0015t0013g0242 | 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 | AT | 4 | a0001c0001t0001g0054a0001c0001t0001g0166a0001c0001t0003g0167others(1): Show | 4 | HG03486.hp1 HG03516.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.215+2090dupA | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40733107 | ||||||
| chrX:40733107
|
A | T | 4 | a0001c0001t0001g0165a0001c0001t0001g0208a0001c0001t0001g0209others(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:40733107
|
AT | A | 2 | a0001c0001t0001g0161a0001c0001t0002g0162 | 2 | HG01943.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.215+2090delA | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40733107 | ||||||
| chrX:40733109
|
T | A | 2 | a0001c0001t0005g0163a0001c0001t0005g0164 | 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:40733188
|
C | CA | 1 | a0002c0015t0013g0242 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.215+2009dupT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40733188 | ||||||
| chrX:40733588
|
G | A | 106 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0165others(103): 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 | a0001c0001t0001g0053 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.215+1576G>C | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40733622 | ||||||
| chrX:40733687
|
AT | A | 1 | a0001c0001t0001g0195 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.215+1510delA | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40733687 | ||||||
| chrX:40734098
|
T | C | 2 | a0001c0002t0001g0239a0001c0002t0001g0240 | 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 | 7 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(4): 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:40734370
|
T | TA | 1 | a0002c0015t0013g0242 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.215+827dupT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40734370 | ||||||
| chrX:40734401
|
T | C | 86 | a0001c0001t0001g0012a0001c0001t0001g0196a0001c0001t0001g0197others(83): 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 | a0001c0001t0001g0012a0001c0002t0001g0007a0001c0002t0001g0008others(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 | a0004c0010t0002g0006 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.215+694T>A | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40734504 | ||||||
| chrX:40734738
|
G | GA | 1 | a0002c0015t0013g0242 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.215+459dupT | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40734738 | ||||||
| chrX:40735004
|
T | C | 1 | a0001c0001t0001g0241 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.215+194A>G | MED14 | ENSG00000180182.11 | transcript | ENST00000324817.6 | protein_coding | 1/30 | chrX | 40735004 |