Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 340533 |
|---|---|
| ensemblid | ENSG00000050030.16 |
| hgncid | 29433 |
| symbol | NEXMIF |
| name | neurite extension and migration factor |
| refseq_nuc | NM_001008537.3 |
| refseq_prot | NP_001008537.1 |
| ensembl_nuc | ENST00000055682.12 |
| ensembl_prot | ENSP00000055682.5 |
| mane_status | MANE Select |
| chr | chrX |
| start | 74732856 |
| end | 74925452 |
| strand | - |
| ver | v1.2 |
| region | chrX:74732856-74925452 |
| region5000 | chrX:74727856-74930452 |
| regionname0 | NEXMIF_chrX_74732856_74925452 |
| regionname5000 | NEXMIF_chrX_74727856_74930452 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1516 | 215 | 60 | 43 | 76 | 7 | 27 | 52 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0002 | 0/0 | 1516 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0003 | 0/0 | 1516 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0004 | 0/0 | 1516 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0005 | 0/0 | 1159 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0006 | 0/0 | 1516 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0007 | 0/0 | 1516 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0008 | 0/0 | 1516 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0009 | 0/0 | 1516 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 4551 | 200 | 59 | 39 | 69 | 6 | 25 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| c0002 | 0/0 | 4551 | 6 | 0 | 3 | 0 | 1 | 2 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| c0003 | 0/0 | 4551 | 3 | 0 | 0 | 3 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| c0004 | 0/0 | 4551 | 2 | 2 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| c0005 | 0/0 | 4551 | 2 | 0 | 1 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| c0006 | 0/0 | 4551 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| c0007 | 0/0 | 4552 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| c0008 | 0/0 | 4551 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| c0009 | 0/0 | 4551 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| c0010 | 0/0 | 4551 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| c0011 | 0/0 | 4551 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| c0012 | 0/0 | 4551 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| c0013 | 0/0 | 4551 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| c0014 | 0/0 | 4551 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| c0015 | 0/0 | 4551 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| c0016 | 0/0 | 4551 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 7167 | 119 | 33 | 15 | 55 | 2 | 13 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| t0002 | 0/1 | 7167 | 48 | 7 | 24 | 1 | 4 | 11 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| t0003 | 0/0 | 7167 | 11 | 0 | 0 | 11 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| t0004 | 0/0 | 7165 | 6 | 3 | 1 | 0 | 0 | 2 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| t0005 | 0/0 | 7167 | 5 | 5 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| t0006 | 0/0 | 7167 | 3 | 3 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| t0007 | 0/0 | 7166 | 2 | 2 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| t0008 | 0/0 | 7167 | 2 | 2 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| t0009 | 0/0 | 7164 | 2 | 0 | 0 | 0 | 0 | 2 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| t0010 | 0/0 | 7169 | 2 | 1 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| t0011 | 0/0 | 7167 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| t0012 | 0/0 | 7167 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| t0013 | 0/0 | 7167 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| t0014 | 0/0 | 7167 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| t0015 | 0/0 | 7169 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| t0016 | 0/0 | 7167 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| t0017 | 0/0 | 7167 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| t0018 | 0/0 | 7167 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| t0019 | 0/0 | 7173 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| t0020 | 0/0 | 7167 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| t0021 | 0/0 | 7167 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| t0022 | 0/0 | 7167 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| t0023 | 0/0 | 7167 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| t0024 | 0/0 | 7168 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| t0025 | 0/0 | 7167 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| t0026 | 0/0 | 7167 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| t0027 | 0/0 | 7168 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| t0028 | 0/0 | 7166 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| t0029 | 0/0 | 7167 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| t0030 | 0/0 | 7167 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| t0031 | 0/0 | 7167 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| t0032 | 0/0 | 7166 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| t0033 | 0/0 | 7167 | 1 | 0 | 0 | 0 | 1 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| t0034 | 0/0 | 7173 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0131 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0154 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 4551 | 200 | 59 | 39 | 69 | 6 | 25 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0002 | 0/0 | 4551 | 6 | 0 | 3 | 0 | 1 | 2 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0003 | 0/0 | 4551 | 3 | 0 | 0 | 3 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0005 | 0/0 | 4551 | 2 | 0 | 1 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0008 | 0/0 | 4551 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0011 | 0/0 | 4551 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0013 | 0/0 | 4551 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0016 | 0/0 | 4551 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0002c0004 | 0/0 | 4551 | 2 | 2 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0003c0015 | 0/0 | 4551 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0004c0014 | 0/0 | 4551 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0005c0007 | 0/0 | 4552 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0006c0006 | 0/0 | 4551 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0007c0010 | 0/0 | 4551 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0008c0009 | 0/0 | 4551 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0009c0012 | 0/0 | 4551 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 11717 | 101 | 31 | 11 | 48 | 1 | 9 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0001t0002 | 0/1 | 11717 | 46 | 7 | 23 | 1 | 4 | 10 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0001t0003 | 0/0 | 11717 | 10 | 0 | 0 | 10 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0001t0004 | 0/0 | 11715 | 6 | 3 | 1 | 0 | 0 | 2 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0001t0005 | 0/0 | 11717 | 5 | 5 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0001t0006 | 0/0 | 11717 | 3 | 3 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0001t0007 | 0/0 | 11716 | 2 | 2 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0001t0008 | 0/0 | 11717 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0001t0009 | 0/0 | 11714 | 2 | 0 | 0 | 0 | 0 | 2 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0001t0010 | 0/0 | 11719 | 2 | 1 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0001t0012 | 0/0 | 11717 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0001t0013 | 0/0 | 11717 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0001t0014 | 0/0 | 11717 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0001t0015 | 0/0 | 11719 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0001t0016 | 0/0 | 11717 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0001t0017 | 0/0 | 11717 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0001t0018 | 0/0 | 11717 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0001t0019 | 0/0 | 11723 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0001t0020 | 0/0 | 11717 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0001t0021 | 0/0 | 11717 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0001t0022 | 0/0 | 11717 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0001t0023 | 0/0 | 11717 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0001t0024 | 0/0 | 11718 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0001t0025 | 0/0 | 11717 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0001t0026 | 0/0 | 11717 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0001t0027 | 0/0 | 11718 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0001t0028 | 0/0 | 11716 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0001t0029 | 0/0 | 11717 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0001t0030 | 0/0 | 11717 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0001t0031 | 0/0 | 11717 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0001t0032 | 0/0 | 11716 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0001t0033 | 0/0 | 11717 | 1 | 0 | 0 | 0 | 1 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0002t0001 | 0/0 | 11717 | 6 | 0 | 3 | 0 | 1 | 2 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0003t0001 | 0/0 | 11717 | 3 | 0 | 0 | 3 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0005t0001 | 0/0 | 11717 | 2 | 0 | 1 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0008t0001 | 0/0 | 11717 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0011t0001 | 0/0 | 11717 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0013t0001 | 0/0 | 11717 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0001c0016t0001 | 0/0 | 11717 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0002c0004t0001 | 0/0 | 11717 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0002c0004t0011 | 0/0 | 11717 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0003c0015t0008 | 0/0 | 11717 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0004c0014t0001 | 0/0 | 11717 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0005c0007t0003 | 0/0 | 11718 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0006c0006t0034 | 0/0 | 11723 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0007c0010t0001 | 0/0 | 11717 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0008c0009t0002 | 0/0 | 11717 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| a0009c0012t0002 | 0/0 | 11717 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | copy fasta | chrX | 74727856 | 74930452 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0131 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0154 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0004g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0005g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0005g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0006g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0006g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0006g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0007g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0007g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0008g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0009g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0009g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0010g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0010g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0012g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0013g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0014g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0015g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0016g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0017g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0018g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0019g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0020g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0021g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0022g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0023g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0024g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0025g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0026g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0027g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0028g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0029g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0030g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0031g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0032g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0001t0033g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0005t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0005t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0008t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0011t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0013t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0001c0016t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0002c0004t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0002c0004t0011g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0003c0015t0008g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0004c0014t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0005c0007t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0006c0006t0034g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0007c0010t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0008c0009t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| a0009c0012t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0171 | EUR | GBR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0030 | EUR | FIN | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | FIN | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG00323 | hp2 | a0001 | c0001 | t0033 | g0130 | EUR | FIN | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG00408 | hp1 | a0001 | c0001 | t0021 | g0185 | EAS | CHS | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | CHS | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0081 | EAS | CHS | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | CHS | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0161 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG00735 | hp2 | a0001 | c0001 | t0015 | g0207 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG00738 | hp1 | a0001 | c0001 | t0014 | g0213 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0176 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0071 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0072 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0183 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0151 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0031 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0157 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0182 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0149 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01168 | hp1 | a0001 | c0001 | t0030 | g0004 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0148 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0189 | AMR | PUR | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | CLM | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0144 | AMR | CLM | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01261 | hp1 | a0001 | c0001 | t0012 | g0002 | AMR | CLM | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0163 | AMR | CLM | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0166 | EUR | IBS | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0119 | AFR | ACB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0160 | AMR | PEL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PEL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | PEL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01975 | hp1 | a0001 | c0005 | t0001 | g0011 | AMR | PEL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0142 | AMR | PEL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | PEL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0156 | AMR | PEL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0223 | AMR | PEL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02040 | hp1 | a0001 | c0003 | t0001 | g0041 | EAS | KHV | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0187 | AFR | ACB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02056 | hp1 | a0005 | c0007 | t0003 | g0016 | EAS | KHV | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02071 | hp1 | a0001 | c0003 | t0001 | g0050 | EAS | KHV | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | KHV | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0097 | EAS | KHV | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | KHV | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02135 | hp1 | a0001 | c0001 | t0022 | g0017 | EAS | KHV | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | ACB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CDX | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CDX | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02273 | hp1 | a0009 | c0012 | t0002 | g0141 | AMR | PEL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0146 | AFR | ACB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02523 | hp2 | a0001 | c0003 | t0001 | g0051 | EAS | KHV | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0123 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0158 | SAS | PJL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0098 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0121 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0153 | SAS | PJL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0120 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0067 | SAS | PJL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02738 | hp1 | a0001 | c0001 | t0031 | g0126 | SAS | PJL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0219 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0197 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0167 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02886 | hp2 | a0006 | c0006 | t0034 | g0118 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02896 | hp1 | a0002 | c0004 | t0011 | g0001 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0177 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02922 | hp1 | a0001 | c0001 | t0008 | g0105 | AFR | ESN | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0122 | AFR | ESN | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ESN | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ESN | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0150 | AFR | ESN | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0129 | SAS | PJL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0220 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | MSL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03130 | hp1 | a0001 | c0001 | t0013 | g0003 | AFR | ESN | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ESN | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ESN | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0139 | AFR | ESN | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03239 | hp1 | a0007 | c0010 | t0001 | g0180 | SAS | PJL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03490 | hp1 | a0001 | c0001 | t0029 | g0172 | SAS | PJL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03491 | hp1 | a0001 | c0001 | t0009 | g0135 | SAS | PJL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03492 | hp1 | a0001 | c0001 | t0009 | g0136 | SAS | PJL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03516 | hp2 | a0003 | c0015 | t0008 | g0104 | AFR | ESN | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03540 | hp1 | a0002 | c0004 | t0001 | g0202 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03540 | hp2 | a0001 | c0001 | t0020 | g0217 | AFR | GWD | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03579 | hp1 | a0001 | c0001 | t0032 | g0145 | AFR | MSL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0181 | SAS | PJL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0175 | SAS | PJL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0049 | SAS | PJL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0191 | SAS | STU | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0178 | SAS | PJL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03831 | hp2 | a0008 | c0009 | t0002 | g0132 | SAS | BEB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0192 | SAS | BEB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0062 | SAS | BEB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | BEB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | STU | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0179 | SAS | BEB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0133 | SAS | STU | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0169 | SAS | STU | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | STU | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18522 | hp1 | a0001 | c0001 | t0025 | g0212 | AFR | YRI | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0088 | EAS | CHB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18747 | hp1 | a0001 | c0001 | t0018 | g0090 | EAS | CHB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | YRI | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | YRI | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18944 | hp1 | a0001 | c0008 | t0001 | g0029 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18961 | hp1 | a0001 | c0001 | t0024 | g0095 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18962 | hp1 | a0001 | c0001 | t0026 | g0037 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18965 | hp1 | a0001 | c0001 | t0023 | g0027 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18971 | hp1 | a0001 | c0016 | t0001 | g0008 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18977 | hp1 | a0001 | c0001 | t0019 | g0094 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19011 | hp2 | a0001 | c0013 | t0001 | g0143 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19030 | hp1 | a0001 | c0001 | t0017 | g0208 | AFR | LWK | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0188 | AFR | LWK | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19043 | hp1 | a0001 | c0001 | t0010 | g0190 | AFR | LWK | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19056 | hp1 | a0001 | c0005 | t0001 | g0012 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19086 | hp1 | a0001 | c0001 | t0010 | g0025 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19089 | hp1 | a0001 | c0001 | t0028 | g0006 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0147 | AFR | ASW | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ASW | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0170 | EUR | TSI | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0152 | EUR | TSI | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA20905 | hp1 | a0004 | c0014 | t0001 | g0076 | SAS | GIH | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02109 | hp1 | a0001 | c0001 | t0007 | g0224 | AFR | ACB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02559 | hp1 | a0001 | c0001 | t0016 | g0114 | AFR | ACB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| HG03471 | hp1 | a0001 | c0011 | t0001 | g0209 | AFR | MSL | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA18955 | hp1 | a0001 | c0001 | t0027 | g0023 | EAS | JPT | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA20300 | hp1 | a0001 | c0001 | t0007 | g0005 | AFR | USA | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | USA | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0154 | REF | REF | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0131 | REF | REF | NEXMIF_chrX_74727856_74930452 | NEXMIF | chrX | 74727856 | 74930452 |
| 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:74740311
|
G | A | 1 | a0008 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.4246C>T | p.Pro1416Ser | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 3/4 | 4863/11717 | 4246/4551 | 1416/1516 | chrX | 74740311 | ||
| chrX:74740734
|
T | C | 1 | a0007 | 1 | HG03239.hp1 | missense_variant | MODERATE | c.3823A>G | p.Ser1275Gly | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 3/4 | 4440/11717 | 3823/4551 | 1275/1516 | chrX | 74740734 | ||
| chrX:74740848
|
T | A | 1 | a0006 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.3709A>T | p.Met1237Leu | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 3/4 | 4326/11717 | 3709/4551 | 1237/1516 | chrX | 74740848 | ||
| chrX:74741098
|
G | GT | 1 | a0005 | 1 | HG02056.hp1 | frameshift_variant | HIGH | c.3458dupA | p.Asn1153fs | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 3/4 | 4075/11717 | 3458/4551 | 1153/1516 | chrX | 74741098 | ||
| chrX:74741756
|
T | C | 1 | a0009 | 1 | HG02273.hp1 | missense_variant | MODERATE | c.2801A>G | p.Asn934Ser | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 3/4 | 3418/11717 | 2801/4551 | 934/1516 | chrX | 74741756 | ||
| chrX:74742020
|
G | A | 1 | a0004 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.2537C>T | p.Thr846Ile | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 3/4 | 3154/11717 | 2537/4551 | 846/1516 | chrX | 74742020 | ||
| chrX:74742711
|
T | C | 1 | a0003 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.1846A>G | p.Ser616Gly | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 3/4 | 2463/11717 | 1846/4551 | 616/1516 | chrX | 74742711 | ||
| chrX:74744406
|
G | T | 1 | a0002 | 2 | HG02896.hp1 HG03540.hp1 |
missense_variant | MODERATE | c.151C>A | p.Pro51Thr | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 3/4 | 768/11717 | 151/4551 | 51/1516 | chrX | 74744406 |
| 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:74739492
|
G | T | 1 | a0001c0008 | 1 | NA18944.hp1 | synonymous_variant | LOW | c.4464C>A | p.Ser1488Ser | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 5081/11717 | 4464/4551 | 1488/1516 | chrX | 74739492 | ||
| chrX:74741002
|
C | A | 1 | a0001c0003 | 3 | HG02040.hp1 HG02071.hp1 HG02523.hp2 |
synonymous_variant | LOW | c.3555G>T | p.Gly1185Gly | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 3/4 | 4172/11717 | 3555/4551 | 1185/1516 | chrX | 74741002 | ||
| chrX:74741383
|
G | A | 1 | a0001c0011 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.3174C>T | p.Phe1058Phe | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 3/4 | 3791/11717 | 3174/4551 | 1058/1516 | chrX | 74741383 | ||
| chrX:74741821
|
T | C | 1 | a0001c0013 | 1 | NA19011.hp2 | synonymous_variant | LOW | c.2736A>G | p.Gln912Gln | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 3/4 | 3353/11717 | 2736/4551 | 912/1516 | chrX | 74741821 | ||
| chrX:74741959
|
G | T | 1 | a0001c0002 | 6 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
synonymous_variant | LOW | c.2598C>A | p.Ser866Ser | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 3/4 | 3215/11717 | 2598/4551 | 866/1516 | chrX | 74741959 | ||
| chrX:74742184
|
T | G | 1 | a0006c0006 | 1 | HG02886.hp2 | synonymous_variant | LOW | c.2373A>C | p.Thr791Thr | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 3/4 | 2990/11717 | 2373/4551 | 791/1516 | chrX | 74742184 | ||
| chrX:74742403
|
A | G | 1 | a0006c0006 | 1 | HG02886.hp2 | synonymous_variant | LOW | c.2154T>C | p.Asn718Asn | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 3/4 | 2771/11717 | 2154/4551 | 718/1516 | chrX | 74742403 | ||
| chrX:74743483
|
G | A | 1 | a0001c0016 | 1 | NA18971.hp1 | synonymous_variant | LOW | c.1074C>T | p.Ser358Ser | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 3/4 | 1691/11717 | 1074/4551 | 358/1516 | chrX | 74743483 | ||
| chrX:74743702
|
T | C | 1 | a0001c0005 | 2 | HG01975.hp1 NA19056.hp1 |
synonymous_variant | LOW | c.855A>G | p.Leu285Leu | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 3/4 | 1472/11717 | 855/4551 | 285/1516 | chrX | 74743702 |
| 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:74733005
|
CA | C | 1 | a0001c0001t0019 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6399delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 6399 | chrX | 74733005 | |||||
| chrX:74733025
|
T | C | 1 | a0001c0001t0005 | 5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6380A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 6380 | chrX | 74733025 | |||||
| chrX:74733094
|
G | GT | 1 | a0001c0001t0019 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6310dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 6310 | chrX | 74733094 | |||||
| chrX:74733245
|
A | AG | 1 | a0001c0001t0019 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6159dupC | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 6159 | chrX | 74733245 | |||||
| chrX:74733441
|
T | G | 1 | a0001c0001t0025 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5964A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 5964 | chrX | 74733441 | |||||
| chrX:74733472
|
GT | G | 1 | a0001c0001t0019 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5932delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 5932 | chrX | 74733472 | |||||
| chrX:74733679
|
C | CA | 1 | a0001c0001t0019 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5725dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 5725 | chrX | 74733679 | |||||
| chrX:74733761
|
A | AT | 1 | a0001c0001t0024 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5643dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 5643 | chrX | 74733761 | |||||
| chrX:74734190
|
C | T | 1 | a0001c0001t0005 | 5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5215G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 5215 | chrX | 74734190 | |||||
| chrX:74734238
|
GA | G | 1 | a0001c0001t0031 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5166delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 5166 | chrX | 74734238 | |||||
| chrX:74734432
|
G | GC | 1 | a0001c0001t0019 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4972dupG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 4972 | chrX | 74734432 | |||||
| chrX:74734588
|
T | C | 1 | a0001c0001t0026 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4817A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 4817 | chrX | 74734588 | |||||
| chrX:74734608
|
T | TGA | 1 | a0001c0001t0019 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4795_*4796dupTC | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 4796 | chrX | 74734608 | |||||
| chrX:74734889
|
A | AC | 1 | a0001c0001t0019 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4515dupG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 4515 | chrX | 74734889 | |||||
| chrX:74734912
|
T | TC | 1 | a0001c0001t0019 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4492dupG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 4492 | chrX | 74734912 | |||||
| chrX:74734946
|
TC | T | 1 | a0001c0001t0019 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4458delG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 4458 | chrX | 74734946 | |||||
| chrX:74735032
|
AT | A | 1 | a0001c0001t0019 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4372delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 4372 | chrX | 74735032 | |||||
| chrX:74735097
|
C | CA | 1 | a0001c0001t0027 | 1 | NA18955.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4307dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 4307 | chrX | 74735097 | |||||
| chrX:74735278
|
C | CT | 1 | a0001c0001t0019 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4126dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 4126 | chrX | 74735278 | |||||
| chrX:74735289
|
A | C | 1 | a0001c0001t0023 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4116T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 4116 | chrX | 74735289 | |||||
| chrX:74735330
|
T | A | 1 | a0001c0001t0029 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4075A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 4075 | chrX | 74735330 | |||||
| chrX:74735710
|
G | A | 2 | a0001c0001t0018a0001c0001t0019 | 2 | NA18747.hp1 NA18977.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3695C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 3695 | chrX | 74735710 | |||||
| chrX:74736024
|
G | GA | 1 | a0001c0001t0019 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3380dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 3380 | chrX | 74736024 | |||||
| chrX:74736060
|
A | AC | 1 | a0001c0001t0019 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3344dupG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 3344 | chrX | 74736060 | |||||
| chrX:74736139
|
C | T | 1 | a0001c0001t0022 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3266G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 3266 | chrX | 74736139 | |||||
| chrX:74736387
|
A | AC | 1 | a0001c0001t0019 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3017dupG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 3017 | chrX | 74736387 | |||||
| chrX:74736457
|
AG | A | 1 | a0001c0001t0019 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2947delC | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 2947 | chrX | 74736457 | |||||
| chrX:74736562
|
C | G | 1 | a0001c0001t0021 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2843G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 2843 | chrX | 74736562 | |||||
| chrX:74736630
|
C | T | 1 | a0001c0001t0020 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2775G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 2775 | chrX | 74736630 | |||||
| chrX:74736739
|
CT | C | 1 | a0001c0001t0019 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2665delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 2665 | chrX | 74736739 | |||||
| chrX:74736853
|
G | A | 1 | a0001c0001t0030 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2552C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 2552 | chrX | 74736853 | |||||
| chrX:74737029
|
G | GA | 1 | a0001c0001t0031 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2375dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 2375 | chrX | 74737029 | |||||
| chrX:74737338
|
TAGA | T | 1 | a0001c0001t0009 | 2 | HG03491.hp1 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2064_*2066delTCT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 2064 | chrX | 74737338 | |||||
| chrX:74737341
|
A | G | 1 | a0001c0001t0006 | 3 | HG02615.hp2 HG02809.hp1 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2064T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 2064 | chrX | 74737341 | |||||
| chrX:74737705
|
G | T | 1 | a0006c0006t0034 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1700C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 1700 | chrX | 74737705 | |||||
| chrX:74737833
|
A | G | 4 | a0001c0001t0003a0001c0001t0018a0001c0001t0019others(1): Show | 13 | HG00558.hp2 HG00621.hp1 HG00673.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1572T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 1572 | chrX | 74737833 | |||||
| chrX:74737895
|
C | T | 1 | a0001c0001t0017 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1510G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 1510 | chrX | 74737895 | |||||
| chrX:74737903
|
A | T | 2 | a0001c0001t0008a0003c0015t0008 | 2 | HG02922.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1502T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 1502 | chrX | 74737903 | |||||
| chrX:74738117
|
AT | A | 1 | a0001c0001t0028 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1287delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 1287 | chrX | 74738117 | |||||
| chrX:74738131
|
GT | G | 1 | a0001c0001t0032 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1273delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 1273 | chrX | 74738131 | |||||
| chrX:74738764
|
G | T | 1 | a0001c0001t0016 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*641C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 641 | chrX | 74738764 | |||||
| chrX:74738794
|
G | A | 8 | a0001c0001t0002a0001c0001t0029a0001c0001t0030others(5): Show | 53 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*611C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 611 | chrX | 74738794 | |||||
| chrX:74738823
|
C | CGT | 1 | a0001c0001t0015 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*580_*581dupAC | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 581 | chrX | 74738823 | |||||
| chrX:74738857
|
T | C | 2 | a0001c0001t0006a0001c0001t0033 | 4 | HG00323.hp2 HG02615.hp2 HG02809.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*548A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 548 | chrX | 74738857 | |||||
| chrX:74738857
|
T | TAC | 1 | a0001c0001t0010 | 2 | NA19043.hp1 NA19086.hp1 |
3_prime_UTR_variant | MODIFIER | c.*546_*547dupGT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 547 | chrX | 74738857 | |||||
| chrX:74738857
|
T | TACACAC | 1 | a0006c0006t0034 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*542_*547dupGTGTGT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 547 | chrX | 74738857 | |||||
| chrX:74738857
|
TAC | T | 1 | a0001c0001t0004 | 6 | HG01243.hp1 HG02055.hp1 HG02735.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*546_*547delGT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 546 | chrX | 74738857 | |||||
| chrX:74738859
|
C | T | 2 | a0001c0001t0012a0001c0001t0014 | 2 | HG00738.hp1 HG01261.hp1 |
3_prime_UTR_variant | MODIFIER | c.*546G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 546 | chrX | 74738859 | |||||
| chrX:74738877
|
CA | C | 1 | a0001c0001t0007 | 2 | HG02109.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*527delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 527 | chrX | 74738877 | |||||
| chrX:74739271
|
G | C | 1 | a0001c0001t0006 | 3 | HG02615.hp2 HG02809.hp1 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*134C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 4/4 | 134 | chrX | 74739271 | |||||
| chrX:74924904
|
C | T | 1 | a0001c0001t0013 | 1 | HG03130.hp1 | 5_prime_UTR_variant | MODIFIER | c.-69G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/4 | 179254 | chrX | 74924904 | |||||
| chrX:74925213
|
C | T | 1 | a0001c0001t0012 | 1 | HG01261.hp1 | 5_prime_UTR_variant | MODIFIER | c.-378G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/4 | 179563 | chrX | 74925213 | |||||
| chrX:74925232
|
C | T | 1 | a0002c0004t0011 | 1 | HG02896.hp1 | 5_prime_UTR_variant | MODIFIER | c.-397G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/4 | 179582 | chrX | 74925232 |
| 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:74739692
|
T | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4458-194A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 3/3 | chrX | 74739692 | ||||||
| chrX:74744736
|
A | G | 1 | a0001c0001t0001g0106 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.80-259T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74744736 | ||||||
| chrX:74744897
|
T | TCTC | 1 | a0001c0001t0028g0006 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.80-421_80-420insGA others(1): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74744897 | ||||||
| chrX:74744897
|
T | TTC | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.80-422_80-421dupGA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74744897 | ||||||
| chrX:74744909
|
C | CTCTCT | 1 | a0001c0001t0010g0025 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.80-437_80-433dupAG others(3): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74744909 | ||||||
| chrX:74744911
|
C | CT | 1 | a0001c0001t0028g0006 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.80-435dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74744911 | ||||||
| chrX:74744911
|
C | CTCT | 7 | a0001c0001t0001g0026a0001c0001t0001g0032a0001c0001t0001g0033others(4): Show | 7 | NA18945.hp1 NA18953.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-437_80-435dupAG others(1): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74744911 | ||||||
| chrX:74744915
|
C | CT | 6 | a0001c0001t0001g0204a0001c0001t0005g0119a0001c0001t0005g0120others(3): Show | 6 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-439dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74744915 | ||||||
| chrX:74744920
|
T | C | 1 | a0001c0001t0010g0025 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.80-443A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74744920 | ||||||
| chrX:74744920
|
T | TC | 5 | a0001c0001t0005g0119a0001c0001t0005g0120a0001c0001t0005g0121others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-444_80-443insG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74744920 | ||||||
| chrX:74744921
|
T | C | 8 | a0001c0001t0001g0026a0001c0001t0001g0032a0001c0001t0001g0033others(5): Show | 8 | NA18945.hp1 NA18953.hp1 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.80-444A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74744921 | ||||||
| chrX:74744923
|
T | TC | 4 | a0001c0001t0005g0119a0001c0001t0005g0120a0001c0001t0005g0121others(1): Show | 4 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-447dupG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74744923 | ||||||
| chrX:74744929
|
TC | T | 4 | a0001c0001t0005g0119a0001c0001t0005g0120a0001c0001t0005g0121others(1): Show | 4 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-453delG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74744929 | ||||||
| chrX:74744930
|
C | CCT | 5 | a0001c0001t0001g0070a0001c0001t0001g0194a0001c0001t0001g0199others(2): Show | 5 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-455_80-454dupAG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74744930 | ||||||
| chrX:74744930
|
C | CCTCT | 3 | a0001c0001t0001g0138a0001c0001t0001g0214a0001c0001t0001g0215 | 3 | HG02717.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.80-457_80-454dupAG others(2): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74744930 | ||||||
| chrX:74744930
|
C | CCTCTCT | 17 | a0001c0001t0001g0099a0001c0001t0001g0102a0001c0001t0001g0103others(14): Show | 17 | HG00323.hp1 HG02015.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.80-459_80-454dupAG others(4): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74744930 | ||||||
| chrX:74744930
|
C | CCTCTCTC others(1): Show |
66 | a0001c0001t0001g0080a0001c0001t0001g0115a0001c0001t0001g0134others(63): Show | 66 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.80-461_80-454dupAG others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74744930 | ||||||
| chrX:74744930
|
C | CCTCTCTC others(3): Show |
87 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(84): Show | 87 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.80-463_80-454dupAG others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74744930 | ||||||
| chrX:74744930
|
C | CCTCTCTC others(5): Show |
13 | a0001c0001t0001g0014a0001c0001t0001g0064a0001c0001t0001g0074others(10): Show | 13 | HG00673.hp1 HG02523.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.80-465_80-454dupAG others(10): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74744930 | ||||||
| chrX:74744930
|
C | CCTCTCTC others(7): Show |
4 | a0001c0001t0001g0019a0001c0001t0022g0017a0001c0003t0001g0041others(1): Show | 4 | HG02040.hp1 HG02071.hp1 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-467_80-454dupAG others(12): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74744930 | ||||||
| chrX:74744930
|
C | CT | 10 | a0001c0001t0001g0026a0001c0001t0001g0032a0001c0001t0001g0033others(7): Show | 10 | HG02970.hp1 NA18945.hp1 NA18953.hp1 others(7): Show |
intron_variant | MODIFIER | c.80-454_80-453insA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74744930 | ||||||
| chrX:74744930
|
C | CTCTCTCT others(2): Show |
1 | a0001c0001t0002g0186 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.80-454_80-453insAG others(7): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74744930 | ||||||
| chrX:74744930
|
C | CTCTCTCT others(4): Show |
1 | a0001c0001t0001g0101 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.80-454_80-453insAG others(9): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74744930 | ||||||
| chrX:74744962
|
C | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.80-485G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74744962 | ||||||
| chrX:74745111
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.79+461T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74745111 | ||||||
| chrX:74745278
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.79+294G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74745278 | ||||||
| chrX:74745394
|
C | T | 2 | a0002c0004t0001g0202a0002c0004t0011g0001 | 2 | HG02896.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.79+178G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2/3 | chrX | 74745394 | ||||||
| chrX:74746462
|
TAGG | T | 2 | a0001c0001t0002g0162a0009c0012t0002g0141 | 2 | HG01978.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.-47-768_-47-766del others(3): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74746462 | ||||||
| chrX:74747161
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-47-1464G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74747161 | ||||||
| chrX:74747642
|
C | CT | 150 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(147): Show | 150 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.-47-1946dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74747642 | ||||||
| chrX:74747642
|
C | CTT | 1 | a0001c0001t0001g0221 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-47-1947_-47-1946d others(4): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74747642 | ||||||
| chrX:74747642
|
CT | C | 4 | a0001c0001t0002g0144a0001c0001t0002g0148a0001c0001t0002g0153others(1): Show | 4 | HG01069.hp1 HG01169.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-1946delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74747642 | ||||||
| chrX:74747835
|
T | C | 1 | a0001c0001t0001g0010 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-47-2138A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74747835 | ||||||
| chrX:74747869
|
G | A | 3 | a0001c0001t0006g0098a0001c0001t0006g0219a0001c0001t0006g0220 | 3 | HG02615.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-47-2172C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74747869 | ||||||
| chrX:74748406
|
G | A | 6 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0148others(3): Show | 6 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.-47-2709C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74748406 | ||||||
| chrX:74748759
|
A | G | 4 | a0001c0001t0001g0194a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 4 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-3062T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74748759 | ||||||
| chrX:74748838
|
T | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-3141A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74748838 | ||||||
| chrX:74749194
|
G | A | 2 | a0001c0001t0008g0105a0003c0015t0008g0104 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-47-3497C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74749194 | ||||||
| chrX:74749215
|
C | T | 2 | a0001c0001t0002g0175a0001c0001t0002g0178 | 2 | HG03669.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.-47-3518G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74749215 | ||||||
| chrX:74749494
|
G | A | 2 | a0001c0001t0009g0135a0001c0001t0009g0136 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-47-3797C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74749494 | ||||||
| chrX:74749525
|
T | C | 1 | a0001c0001t0001g0216 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-47-3828A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74749525 | ||||||
| chrX:74749739
|
G | T | 1 | a0001c0001t0001g0061 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-47-4042C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74749739 | ||||||
| chrX:74749891
|
A | G | 2 | a0001c0001t0001g0103a0001c0001t0001g0115 | 2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-47-4194T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74749891 | ||||||
| chrX:74750094
|
G | C | 1 | a0001c0001t0001g0024 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-47-4397C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74750094 | ||||||
| chrX:74750096
|
G | A | 21 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(18): Show | 21 | HG00408.hp1 HG01243.hp1 HG02015.hp1 others(18): Show |
intron_variant | MODIFIER | c.-47-4399C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74750096 | ||||||
| chrX:74750326
|
T | C | 1 | a0001c0001t0010g0190 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-47-4629A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74750326 | ||||||
| chrX:74750606
|
G | C | 1 | a0001c0001t0002g0169 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-47-4909C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74750606 | ||||||
| chrX:74750865
|
G | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-5168C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74750865 | ||||||
| chrX:74751031
|
C | T | 1 | a0001c0001t0001g0014 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-47-5334G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751031 | ||||||
| chrX:74751057
|
G | A | 4 | a0001c0001t0001g0194a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 4 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-5360C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751057 | ||||||
| chrX:74751185
|
G | A | 151 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(148): Show | 151 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.-47-5488C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751185 | ||||||
| chrX:74751229
|
C | CA | 1 | a0001c0001t0001g0083 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-47-5533dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751229 | ||||||
| chrX:74751309
|
C | T | 1 | a0001c0001t0003g0091 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-47-5612G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751309 | ||||||
| chrX:74751492
|
C | CT | 1 | a0001c0001t0001g0115 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-47-5796dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751492 | ||||||
| chrX:74751492
|
CT | C | 2 | a0001c0001t0001g0026a0001c0001t0002g0176 | 2 | HG01070.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.-47-5796delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751492 | ||||||
| chrX:74751494
|
T | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-5797A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751494 | ||||||
| chrX:74751505
|
T | G | 1 | a0001c0001t0001g0107 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-47-5808A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751505 | ||||||
| chrX:74751592
|
C | T | 2 | a0001c0001t0004g0187a0001c0001t0007g0005 | 2 | HG02055.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-47-5895G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751592 | ||||||
| chrX:74751623
|
C | CCCTT | 25 | a0001c0001t0001g0103a0001c0001t0001g0115a0001c0001t0001g0134others(22): Show | 25 | HG00408.hp1 HG01243.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.-47-5930_-47-5927d others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751623 | ||||||
| chrX:74751623
|
C | CCCTTCCT others(1): Show |
12 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0194others(9): Show | 12 | HG02015.hp1 HG02559.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-47-5934_-47-5927d others(10): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751623 | ||||||
| chrX:74751623
|
C | CCCTTCCT others(5): Show |
3 | a0001c0001t0006g0098a0001c0001t0006g0219a0001c0001t0007g0224 | 3 | HG02109.hp1 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-47-5938_-47-5927d others(14): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751623 | ||||||
| chrX:74751623
|
C | CCCTTCCT others(9): Show |
1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-5942_-47-5927d others(18): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751623 | ||||||
| chrX:74751623
|
CCCTT | C | 4 | a0001c0001t0002g0169a0001c0001t0002g0171a0001c0001t0002g0181others(1): Show | 4 | HG00140.hp1 HG03654.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-5930_-47-5927d others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751623 | ||||||
| chrX:74751658
|
T | TTCC | 17 | a0001c0001t0001g0019a0001c0001t0001g0054a0001c0001t0001g0055others(14): Show | 17 | HG01978.hp1 HG01993.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.-47-5962_-47-5961i others(5): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751658 | ||||||
| chrX:74751658
|
T | TTCCTTCC | 68 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0014others(65): Show | 68 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.-47-5962_-47-5961i others(9): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751658 | ||||||
| chrX:74751658
|
T | TTCCTTCC others(4): Show |
27 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0026others(24): Show | 27 | HG00609.hp1 HG01070.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.-47-5962_-47-5961i others(13): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751658 | ||||||
| chrX:74751658
|
T | TTCCTTCC others(8): Show |
3 | a0001c0001t0001g0007a0001c0001t0001g0096a0001c0001t0001g0099 | 3 | HG00323.hp1 NA18984.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-47-5962_-47-5961i others(17): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751658 | ||||||
| chrX:74751660
|
T | C | 1 | a0001c0001t0001g0047 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-47-5963A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751660 | ||||||
| chrX:74751662
|
C | CT | 113 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(110): Show | 113 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.-47-5966dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751662 | ||||||
| chrX:74751662
|
C | T | 1 | a0001c0001t0001g0047 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-47-5965G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751662 | ||||||
| chrX:74751666
|
C | CT | 2 | a0001c0001t0001g0055a0001c0001t0001g0101 | 2 | HG04184.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.-47-5970dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751666 | ||||||
| chrX:74751675
|
C | T | 116 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(113): Show | 116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-47-5978G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751675 | ||||||
| chrX:74751679
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-47-5982G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751679 | ||||||
| chrX:74751688
|
T | TC | 116 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(113): Show | 116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-47-5992dupG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751688 | ||||||
| chrX:74751693
|
TCTTC | T | 1 | a0001c0001t0002g0192 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-47-6000_-47-5997d others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751693 | ||||||
| chrX:74751742
|
T | TCTTC | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-6049_-47-6046d others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74751742 | ||||||
| chrX:74752048
|
C | G | 1 | a0001c0001t0033g0130 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-47-6351G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74752048 | ||||||
| chrX:74752064
|
C | T | 1 | a0001c0001t0002g0177 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-47-6367G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74752064 | ||||||
| chrX:74752491
|
T | C | 5 | a0001c0001t0005g0119a0001c0001t0005g0120a0001c0001t0005g0121others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47-6794A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74752491 | ||||||
| chrX:74752535
|
CAAG | C | 4 | a0001c0001t0001g0194a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 4 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-6841_-47-6839d others(5): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74752535 | ||||||
| chrX:74753500
|
TACTA | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-7807_-47-7804d others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74753500 | ||||||
| chrX:74753534
|
G | C | 2 | a0001c0001t0002g0161a0001c0001t0033g0130 | 2 | HG00323.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.-47-7837C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74753534 | ||||||
| chrX:74753598
|
G | A | 1 | a0009c0012t0002g0141 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-47-7901C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74753598 | ||||||
| chrX:74753715
|
G | GCA | 138 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(135): Show | 138 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.-47-8020_-47-8019d others(4): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74753715 | ||||||
| chrX:74753715
|
GCA | G | 8 | a0001c0001t0001g0103a0001c0001t0001g0115a0001c0001t0005g0119others(5): Show | 8 | HG01884.hp1 HG02572.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-47-8020_-47-8019d others(4): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74753715 | ||||||
| chrX:74753715
|
GCACA | G | 1 | a0001c0001t0002g0174 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-47-8022_-47-8019d others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74753715 | ||||||
| chrX:74753950
|
G | A | 1 | a0001c0001t0002g0157 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-47-8253C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74753950 | ||||||
| chrX:74754312
|
A | AT | 1 | a0001c0001t0027g0023 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-47-8616dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74754312 | ||||||
| chrX:74754312
|
AT | A | 5 | a0001c0001t0002g0162a0001c0001t0002g0183a0001c0001t0002g0184others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-8616delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74754312 | ||||||
| chrX:74754317
|
T | A | 3 | a0001c0001t0006g0098a0001c0001t0006g0219a0001c0001t0006g0220 | 3 | HG02615.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-47-8620A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74754317 | ||||||
| chrX:74754318
|
T | A | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-8621A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74754318 | ||||||
| chrX:74754410
|
G | A | 7 | a0001c0001t0001g0026a0001c0001t0001g0032a0001c0001t0001g0033others(4): Show | 7 | NA18945.hp1 NA18953.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.-47-8713C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74754410 | ||||||
| chrX:74754512
|
T | G | 1 | a0001c0001t0007g0224 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-47-8815A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74754512 | ||||||
| chrX:74754596
|
C | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-8899G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74754596 | ||||||
| chrX:74754812
|
C | G | 1 | a0001c0001t0031g0126 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-47-9115G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74754812 | ||||||
| chrX:74755187
|
A | G | 1 | a0001c0001t0001g0222 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-47-9490T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74755187 | ||||||
| chrX:74755218
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-47-9521C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74755218 | ||||||
| chrX:74755240
|
G | A | 1 | a0001c0001t0001g0007 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-47-9543C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74755240 | ||||||
| chrX:74755560
|
C | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-9863G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74755560 | ||||||
| chrX:74755892
|
A | T | 1 | a0001c0001t0001g0082 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-47-10195T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74755892 | ||||||
| chrX:74755892
|
AT | A | 1 | a0001c0001t0003g0088 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-47-10196delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74755892 | ||||||
| chrX:74756025
|
GCCACCAT others(81): Show |
G | 2 | a0001c0001t0002g0168a0001c0001t0002g0182 | 2 | HG01106.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.-47-10416_-47-1032 others(92): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74756025 | ||||||
| chrX:74756048
|
G | T | 1 | a0001c0001t0001g0070 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-47-10351C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74756048 | ||||||
| chrX:74756803
|
C | T | 5 | a0001c0001t0009g0135a0001c0001t0009g0136a0001c0003t0001g0041others(2): Show | 5 | HG02040.hp1 HG02071.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-11106G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74756803 | ||||||
| chrX:74756860
|
C | CA | 3 | a0001c0001t0013g0003a0001c0001t0014g0213a0001c0011t0001g0209 | 3 | HG00738.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-47-11164dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74756860 | ||||||
| chrX:74757031
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-47-11334G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74757031 | ||||||
| chrX:74757282
|
C | T | 2 | a0001c0001t0002g0183a0001c0001t0002g0184 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-47-11585G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74757282 | ||||||
| chrX:74757798
|
T | C | 1 | a0007c0010t0001g0180 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-47-12101A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74757798 | ||||||
| chrX:74757820
|
G | A | 11 | a0001c0001t0001g0103a0001c0001t0001g0115a0001c0001t0001g0194others(8): Show | 11 | HG01884.hp1 HG02559.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-47-12123C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74757820 | ||||||
| chrX:74758149
|
C | T | 2 | a0002c0004t0001g0202a0002c0004t0011g0001 | 2 | HG02896.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-47-12452G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74758149 | ||||||
| chrX:74758156
|
T | C | 3 | a0001c0003t0001g0041a0001c0003t0001g0050a0001c0003t0001g0051 | 3 | HG02040.hp1 HG02071.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.-47-12459A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74758156 | ||||||
| chrX:74758193
|
A | G | 221 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(218): Show | 221 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.-47-12496T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74758193 | ||||||
| chrX:74758199
|
T | C | 2 | a0001c0001t0001g0020a0001c0001t0001g0075 | 2 | HG00558.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.-47-12502A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74758199 | ||||||
| chrX:74758235
|
A | T | 1 | a0001c0001t0020g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-47-12538T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74758235 | ||||||
| chrX:74758267
|
A | AC | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-12571_-47-1257 others(5): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74758267 | ||||||
| chrX:74758367
|
C | G | 1 | a0001c0001t0001g0044 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-47-12670G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74758367 | ||||||
| chrX:74758410
|
T | TA | 1 | a0008c0009t0002g0132 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-47-12714dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74758410 | ||||||
| chrX:74758410
|
TA | T | 1 | a0001c0001t0004g0188 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-47-12714delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74758410 | ||||||
| chrX:74758420
|
CTTTTA | C | 1 | a0001c0001t0001g0099 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-47-12728_-47-1272 others(9): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74758420 | ||||||
| chrX:74758430
|
A | G | 53 | a0001c0001t0002g0127a0001c0001t0002g0128a0001c0001t0002g0129others(50): Show | 53 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.-47-12733T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74758430 | ||||||
| chrX:74758475
|
G | C | 2 | a0001c0001t0003g0085a0001c0001t0003g0086 | 2 | HG00673.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-47-12778C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74758475 | ||||||
| chrX:74758694
|
A | G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-12997T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74758694 | ||||||
| chrX:74759053
|
C | T | 1 | a0007c0010t0001g0180 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-47-13356G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74759053 | ||||||
| chrX:74759157
|
C | T | 2 | a0001c0001t0001g0021a0001c0001t0027g0023 | 2 | NA18955.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.-47-13460G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74759157 | ||||||
| chrX:74759297
|
G | A | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-13600C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74759297 | ||||||
| chrX:74759653
|
C | T | 1 | a0001c0001t0004g0188 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-47-13956G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74759653 | ||||||
| chrX:74759842
|
C | T | 1 | a0001c0001t0002g0129 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-47-14145G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74759842 | ||||||
| chrX:74760461
|
G | A | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-14764C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74760461 | ||||||
| chrX:74760551
|
A | T | 7 | a0001c0001t0001g0103a0001c0001t0001g0115a0001c0001t0005g0119others(4): Show | 7 | HG01884.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-47-14854T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74760551 | ||||||
| chrX:74760671
|
T | C | 1 | a0001c0001t0002g0193 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-47-14974A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74760671 | ||||||
| chrX:74760713
|
T | C | 6 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0148others(3): Show | 6 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.-47-15016A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74760713 | ||||||
| chrX:74760722
|
TC | T | 1 | a0001c0001t0001g0046 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-47-15026delG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74760722 | ||||||
| chrX:74760841
|
G | GATTT | 4 | a0001c0001t0001g0102a0001c0001t0001g0214a0001c0001t0003g0097others(1): Show | 4 | HG02080.hp2 HG03139.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-15148_-47-1514 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74760841 | ||||||
| chrX:74760841
|
G | GATTTATT others(1): Show |
2 | a0001c0001t0001g0215a0001c0001t0014g0213 | 2 | HG00738.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-47-15152_-47-1514 others(12): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74760841 | ||||||
| chrX:74760841
|
GATTT | G | 137 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0013others(134): Show | 137 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.-47-15148_-47-1514 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74760841 | ||||||
| chrX:74760841
|
GATTTATT others(1): Show |
G | 46 | a0001c0001t0002g0127a0001c0001t0002g0128a0001c0001t0002g0129others(43): Show | 46 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.-47-15152_-47-1514 others(12): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74760841 | ||||||
| chrX:74760841
|
GATTTATT others(5): Show |
G | 2 | a0001c0001t0006g0098a0001c0001t0006g0219 | 2 | HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-47-15156_-47-1514 others(16): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74760841 | ||||||
| chrX:74760841
|
GATTTATT others(9): Show |
G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-15160_-47-1514 others(20): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74760841 | ||||||
| chrX:74760845
|
T | G | 1 | a0001c0001t0001g0099 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-47-15148A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74760845 | ||||||
| chrX:74760906
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-47-15209A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74760906 | ||||||
| chrX:74760925
|
C | T | 1 | a0001c0001t0021g0185 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-47-15228G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74760925 | ||||||
| chrX:74760977
|
CT | C | 1 | a0001c0001t0001g0046 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-47-15281delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74760977 | ||||||
| chrX:74761022
|
C | A | 1 | a0001c0001t0003g0088 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-47-15325G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74761022 | ||||||
| chrX:74761034
|
A | AT | 1 | a0001c0001t0001g0109 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-47-15338dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74761034 | ||||||
| chrX:74761092
|
G | A | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-15395C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74761092 | ||||||
| chrX:74761112
|
C | A | 2 | a0001c0001t0002g0169a0001c0001t0002g0181 | 2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-47-15415G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74761112 | ||||||
| chrX:74761157
|
C | A | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-15460G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74761157 | ||||||
| chrX:74761343
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-47-15646C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74761343 | ||||||
| chrX:74761431
|
C | T | 1 | a0001c0001t0033g0130 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-47-15734G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74761431 | ||||||
| chrX:74761449
|
G | T | 1 | a0001c0001t0033g0130 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-47-15752C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74761449 | ||||||
| chrX:74761654
|
A | AT | 1 | a0001c0001t0001g0024 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-47-15958dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74761654 | ||||||
| chrX:74761737
|
A | G | 1 | a0001c0001t0001g0063 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-47-16040T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74761737 | ||||||
| chrX:74761881
|
C | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-16184G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74761881 | ||||||
| chrX:74761952
|
ATTTCTTT others(1): Show |
A | 1 | a0001c0001t0001g0059 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-47-16263_-47-1625 others(12): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74761952 | ||||||
| chrX:74761997
|
G | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-16300C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74761997 | ||||||
| chrX:74762014
|
G | A | 3 | a0001c0001t0006g0098a0001c0001t0006g0219a0001c0001t0006g0220 | 3 | HG02615.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-47-16317C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74762014 | ||||||
| chrX:74762065
|
T | TA | 1 | a0001c0001t0001g0046 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-47-16369dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74762065 | ||||||
| chrX:74762180
|
T | C | 5 | a0001c0001t0005g0119a0001c0001t0005g0120a0001c0001t0005g0121others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47-16483A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74762180 | ||||||
| chrX:74762221
|
GT | G | 1 | a0001c0001t0001g0046 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-47-16525delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74762221 | ||||||
| chrX:74762235
|
T | C | 155 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(152): Show | 155 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.-47-16538A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74762235 | ||||||
| chrX:74762484
|
TG | T | 1 | a0001c0001t0001g0046 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-47-16788delC | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74762484 | ||||||
| chrX:74762490
|
C | G | 3 | a0001c0001t0006g0098a0001c0001t0006g0219a0001c0001t0006g0220 | 3 | HG02615.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-47-16793G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74762490 | ||||||
| chrX:74762506
|
AT | A | 1 | a0001c0001t0001g0046 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-47-16810delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74762506 | ||||||
| chrX:74762581
|
C | T | 6 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0148others(3): Show | 6 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.-47-16884G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74762581 | ||||||
| chrX:74762622
|
C | G | 1 | a0001c0001t0007g0224 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-47-16925G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74762622 | ||||||
| chrX:74762707
|
C | A | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-17010G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74762707 | ||||||
| chrX:74762810
|
T | G | 1 | a0001c0001t0001g0020 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-47-17113A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74762810 | ||||||
| chrX:74762889
|
GC | G | 1 | a0001c0001t0001g0138 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-47-17193delG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74762889 | ||||||
| chrX:74762891
|
A | G | 1 | a0001c0001t0001g0215 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-47-17194T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74762891 | ||||||
| chrX:74763250
|
C | G | 1 | a0001c0001t0001g0079 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-47-17553G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74763250 | ||||||
| chrX:74763301
|
C | G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-17604G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74763301 | ||||||
| chrX:74763301
|
CCT | C | 1 | a0001c0001t0033g0130 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-47-17606_-47-1760 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74763301 | ||||||
| chrX:74763320
|
G | A | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-17623C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74763320 | ||||||
| chrX:74763320
|
G | T | 1 | a0001c0001t0001g0115 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-47-17623C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74763320 | ||||||
| chrX:74763342
|
C | A | 1 | a0001c0005t0001g0011 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-47-17645G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74763342 | ||||||
| chrX:74763447
|
C | T | 2 | a0001c0001t0008g0105a0003c0015t0008g0104 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-47-17750G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74763447 | ||||||
| chrX:74763526
|
T | G | 1 | a0001c0001t0002g0167 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-47-17829A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74763526 | ||||||
| chrX:74763550
|
C | T | 130 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(127): Show | 130 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.-47-17853G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74763550 | ||||||
| chrX:74763557
|
C | A | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-17860G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74763557 | ||||||
| chrX:74763557
|
C | T | 1 | a0001c0001t0002g0176 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-47-17860G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74763557 | ||||||
| chrX:74763596
|
T | A | 1 | a0001c0001t0001g0078 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-47-17899A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74763596 | ||||||
| chrX:74763650
|
T | C | 1 | a0001c0001t0021g0185 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-47-17953A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74763650 | ||||||
| chrX:74763726
|
GC | G | 208 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(205): Show | 208 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.-47-18030delG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74763726 | ||||||
| chrX:74763944
|
T | C | 8 | a0001c0001t0001g0103a0001c0001t0001g0115a0001c0001t0005g0119others(5): Show | 8 | HG01884.hp1 HG02572.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-47-18247A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74763944 | ||||||
| chrX:74764068
|
C | A | 117 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(114): Show | 117 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.-47-18371G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74764068 | ||||||
| chrX:74764154
|
T | A | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-18457A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74764154 | ||||||
| chrX:74764299
|
T | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-18602A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74764299 | ||||||
| chrX:74764515
|
G | A | 1 | a0001c0001t0004g0188 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-47-18818C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74764515 | ||||||
| chrX:74764558
|
T | A | 1 | a0001c0001t0010g0190 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-47-18861A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74764558 | ||||||
| chrX:74764596
|
C | T | 1 | a0001c0001t0001g0013 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-47-18899G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74764596 | ||||||
| chrX:74764670
|
A | T | 2 | a0001c0002t0001g0071a0001c0002t0001g0072 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-47-18973T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74764670 | ||||||
| chrX:74765812
|
G | A | 1 | a0001c0001t0004g0133 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-47-20115C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74765812 | ||||||
| chrX:74765871
|
C | CA | 25 | a0001c0001t0001g0007a0001c0001t0001g0046a0001c0001t0001g0058others(22): Show | 25 | HG00408.hp1 HG00408.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.-47-20175dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74765871 | ||||||
| chrX:74765871
|
C | CAA | 2 | a0001c0001t0005g0120a0001c0001t0005g0121 | 2 | HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-47-20176_-47-2017 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74765871 | ||||||
| chrX:74765871
|
CA | C | 10 | a0001c0001t0001g0107a0001c0001t0001g0218a0001c0001t0004g0187others(7): Show | 10 | HG01243.hp1 HG02055.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.-47-20175delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74765871 | ||||||
| chrX:74765871
|
CAAAA | C | 3 | a0001c0001t0001g0009a0001c0001t0028g0006a0001c0016t0001g0008 | 3 | NA18971.hp1 NA19005.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.-47-20178_-47-2017 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74765871 | ||||||
| chrX:74766012
|
G | A | 2 | a0001c0001t0008g0105a0003c0015t0008g0104 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-47-20315C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74766012 | ||||||
| chrX:74766041
|
C | CA | 14 | a0001c0001t0001g0024a0001c0001t0001g0042a0001c0001t0001g0100others(11): Show | 14 | HG02135.hp1 HG02165.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.-47-20345dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74766041 | ||||||
| chrX:74766041
|
CA | C | 4 | a0001c0001t0001g0020a0001c0001t0002g0127a0006c0006t0034g0118others(1): Show | 4 | HG00558.hp1 HG00642.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-20345delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74766041 | ||||||
| chrX:74766041
|
CAA | C | 51 | a0001c0001t0002g0128a0001c0001t0002g0129a0001c0001t0002g0139others(48): Show | 51 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.-47-20346_-47-2034 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74766041 | ||||||
| chrX:74766177
|
C | T | 1 | a0001c0001t0016g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-47-20480G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74766177 | ||||||
| chrX:74766326
|
AT | A | 1 | a0001c0001t0001g0046 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-47-20630delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74766326 | ||||||
| chrX:74766872
|
C | G | 2 | a0001c0001t0008g0105a0003c0015t0008g0104 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-47-21175G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74766872 | ||||||
| chrX:74766968
|
G | A | 1 | a0001c0001t0001g0138 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-47-21271C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74766968 | ||||||
| chrX:74766999
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-47-21302C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74766999 | ||||||
| chrX:74767108
|
C | G | 42 | a0001c0001t0002g0127a0001c0001t0002g0128a0001c0001t0002g0129others(39): Show | 42 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.-47-21411G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74767108 | ||||||
| chrX:74767321
|
A | G | 1 | a0001c0008t0001g0029 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-47-21624T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74767321 | ||||||
| chrX:74767373
|
G | A | 117 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(114): Show | 117 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.-47-21676C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74767373 | ||||||
| chrX:74767429
|
C | A | 1 | a0001c0001t0001g0010 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-47-21732G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74767429 | ||||||
| chrX:74767697
|
C | A | 11 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0164others(8): Show | 11 | HG00408.hp1 HG02015.hp1 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.-47-22000G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74767697 | ||||||
| chrX:74767971
|
A | AG | 1 | a0001c0001t0002g0223 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-47-22275dupC | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74767971 | ||||||
| chrX:74768054
|
C | T | 1 | a0001c0001t0025g0212 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-47-22357G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74768054 | ||||||
| chrX:74768250
|
A | G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-22553T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74768250 | ||||||
| chrX:74768487
|
C | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-22790G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74768487 | ||||||
| chrX:74768503
|
C | A | 98 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0013others(95): Show | 98 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.-47-22806G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74768503 | ||||||
| chrX:74768833
|
C | A | 1 | a0001c0001t0002g0186 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-47-23136G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74768833 | ||||||
| chrX:74768878
|
C | T | 1 | a0001c0005t0001g0012 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-47-23181G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74768878 | ||||||
| chrX:74769093
|
G | GT | 2 | a0001c0001t0001g0079a0001c0001t0001g0137 | 2 | HG02015.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-47-23397dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74769093 | ||||||
| chrX:74769093
|
GTT | G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-23398_-47-2339 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74769093 | ||||||
| chrX:74769210
|
C | A | 1 | a0001c0001t0001g0210 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-47-23513G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74769210 | ||||||
| chrX:74769605
|
A | G | 4 | a0001c0001t0001g0194a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 4 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-23908T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74769605 | ||||||
| chrX:74770121
|
T | C | 1 | a0001c0001t0004g0188 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-47-24424A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74770121 | ||||||
| chrX:74770331
|
T | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-24634A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74770331 | ||||||
| chrX:74770448
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-47-24751C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74770448 | ||||||
| chrX:74770679
|
G | A | 12 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0110others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.-47-24982C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74770679 | ||||||
| chrX:74771119
|
T | C | 1 | a0001c0001t0002g0162 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-47-25422A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74771119 | ||||||
| chrX:74771304
|
A | T | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-47-25607T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74771304 | ||||||
| chrX:74771381
|
A | AT | 1 | a0001c0001t0005g0123 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-47-25685dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74771381 | ||||||
| chrX:74771550
|
T | C | 130 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(127): Show | 130 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.-47-25853A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74771550 | ||||||
| chrX:74771821
|
C | CTG | 3 | a0001c0001t0001g0103a0001c0001t0001g0115a0001c0001t0001g0138 | 3 | HG02630.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-47-26126_-47-2612 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74771821 | ||||||
| chrX:74771821
|
CTG | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-26126_-47-2612 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74771821 | ||||||
| chrX:74771829
|
G | C | 5 | a0001c0001t0002g0162a0001c0001t0002g0183a0001c0001t0002g0184others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-26132C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74771829 | ||||||
| chrX:74771865
|
G | A | 3 | a0001c0001t0006g0098a0001c0001t0006g0219a0001c0001t0006g0220 | 3 | HG02615.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-47-26168C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74771865 | ||||||
| chrX:74772039
|
C | A | 1 | a0001c0005t0001g0012 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-47-26342G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74772039 | ||||||
| chrX:74772091
|
T | A | 1 | a0001c0005t0001g0012 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-47-26394A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74772091 | ||||||
| chrX:74772685
|
A | T | 1 | a0001c0001t0010g0190 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-47-26988T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74772685 | ||||||
| chrX:74773097
|
A | T | 21 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(18): Show | 21 | HG00408.hp1 HG01243.hp1 HG02015.hp1 others(18): Show |
intron_variant | MODIFIER | c.-47-27400T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74773097 | ||||||
| chrX:74773106
|
AT | A | 2 | a0001c0001t0002g0148a0001c0001t0002g0149 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-47-27410delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74773106 | ||||||
| chrX:74773220
|
G | A | 2 | a0001c0001t0002g0166a0001c0001t0029g0172 | 2 | HG01515.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.-47-27523C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74773220 | ||||||
| chrX:74773476
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-47-27779G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74773476 | ||||||
| chrX:74773543
|
G | GCAA | 1 | a0001c0001t0002g0163 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-47-27849_-47-2784 others(7): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74773543 | ||||||
| chrX:74773547
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-47-27850G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74773547 | ||||||
| chrX:74773775
|
G | T | 117 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(114): Show | 117 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.-47-28078C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74773775 | ||||||
| chrX:74773801
|
C | T | 1 | a0001c0001t0007g0224 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-47-28104G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74773801 | ||||||
| chrX:74773887
|
C | T | 1 | a0001c0001t0001g0013 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-47-28190G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74773887 | ||||||
| chrX:74773888
|
G | A | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-28191C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74773888 | ||||||
| chrX:74773908
|
C | CA | 1 | a0001c0001t0002g0155 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-47-28212dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74773908 | ||||||
| chrX:74773908
|
CA | C | 49 | a0001c0001t0001g0103a0001c0001t0001g0115a0001c0001t0001g0138others(46): Show | 49 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.-47-28212delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74773908 | ||||||
| chrX:74773908
|
CAA | C | 36 | a0001c0001t0001g0033a0001c0001t0001g0134a0001c0001t0001g0137others(33): Show | 36 | HG00408.hp1 HG00735.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.-47-28213_-47-2821 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74773908 | ||||||
| chrX:74773908
|
CAAA | C | 28 | a0001c0001t0001g0010a0001c0001t0001g0026a0001c0001t0001g0032others(25): Show | 28 | HG01109.hp1 HG01243.hp1 HG02040.hp1 others(25): Show |
intron_variant | MODIFIER | c.-47-28214_-47-2821 others(7): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74773908 | ||||||
| chrX:74773908
|
CAAAA | C | 95 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0013others(92): Show | 95 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.-47-28215_-47-2821 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74773908 | ||||||
| chrX:74773908
|
CAAAAA | C | 8 | a0001c0001t0001g0068a0001c0001t0001g0074a0001c0001t0001g0218others(5): Show | 8 | HG01070.hp2 HG02615.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-47-28216_-47-2821 others(9): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74773908 | ||||||
| chrX:74773925
|
A | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-28228T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74773925 | ||||||
| chrX:74774330
|
T | A | 36 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0021others(33): Show | 36 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.-47-28633A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74774330 | ||||||
| chrX:74774813
|
A | C | 1 | a0001c0001t0002g0223 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-47-29116T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74774813 | ||||||
| chrX:74775390
|
T | A | 1 | a0001c0001t0001g0010 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-47-29693A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74775390 | ||||||
| chrX:74775794
|
T | C | 1 | a0001c0001t0004g0133 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-47-30097A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74775794 | ||||||
| chrX:74776056
|
G | T | 1 | a0001c0005t0001g0011 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-47-30359C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74776056 | ||||||
| chrX:74776596
|
G | A | 117 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(114): Show | 117 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.-47-30899C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74776596 | ||||||
| chrX:74776724
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-47-31027A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74776724 | ||||||
| chrX:74776727
|
C | CA | 47 | a0001c0001t0001g0203a0001c0001t0002g0127a0001c0001t0002g0128others(44): Show | 47 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.-47-31031dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74776727 | ||||||
| chrX:74776727
|
C | CAA | 2 | a0001c0001t0002g0160a0001c0001t0002g0177 | 2 | HG01928.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-47-31032_-47-3103 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74776727 | ||||||
| chrX:74776727
|
C | CAAA | 5 | a0001c0001t0002g0162a0001c0001t0002g0183a0001c0001t0002g0184others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-31033_-47-3103 others(7): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74776727 | ||||||
| chrX:74776727
|
CA | C | 5 | a0001c0001t0001g0014a0001c0001t0001g0102a0001c0001t0016g0114others(2): Show | 5 | HG02559.hp1 HG02896.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-31031delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74776727 | ||||||
| chrX:74776727
|
CAA | C | 143 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(140): Show | 143 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.-47-31032_-47-3103 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74776727 | ||||||
| chrX:74776727
|
CAAA | C | 1 | a0001c0016t0001g0008 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-47-31033_-47-3103 others(7): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74776727 | ||||||
| chrX:74777275
|
G | A | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-31578C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74777275 | ||||||
| chrX:74777481
|
A | G | 2 | a0001c0001t0001g0111a0001c0001t0001g0116 | 2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-47-31784T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74777481 | ||||||
| chrX:74777681
|
T | C | 2 | a0001c0001t0002g0161a0001c0001t0033g0130 | 2 | HG00323.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.-47-31984A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74777681 | ||||||
| chrX:74777756
|
A | C | 3 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201 | 3 | HG02818.hp2 HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-47-32059T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74777756 | ||||||
| chrX:74778117
|
T | A | 1 | a0001c0001t0002g0192 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-47-32420A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74778117 | ||||||
| chrX:74778425
|
C | T | 12 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0110others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.-47-32728G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74778425 | ||||||
| chrX:74778804
|
C | T | 1 | a0001c0001t0002g0174 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-47-33107G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74778804 | ||||||
| chrX:74779729
|
G | A | 4 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(1): Show | 4 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-34032C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74779729 | ||||||
| chrX:74779869
|
T | C | 1 | a0001c0001t0002g0186 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-47-34172A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74779869 | ||||||
| chrX:74779986
|
A | G | 208 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(205): Show | 208 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.-47-34289T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74779986 | ||||||
| chrX:74780375
|
G | GT | 8 | a0001c0001t0001g0083a0001c0001t0001g0100a0001c0001t0002g0158others(5): Show | 8 | HG01074.hp1 HG02080.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.-47-34679dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74780375 | ||||||
| chrX:74780375
|
GT | G | 7 | a0001c0001t0002g0159a0001c0001t0005g0119a0001c0001t0005g0120others(4): Show | 7 | HG01884.hp1 HG01943.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-47-34679delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74780375 | ||||||
| chrX:74780383
|
T | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-34686A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74780383 | ||||||
| chrX:74780535
|
A | AT | 3 | a0001c0001t0001g0045a0001c0001t0001g0100a0006c0006t0034g0118 | 3 | HG02886.hp2 NA18967.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.-47-34839dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74780535 | ||||||
| chrX:74780535
|
AT | A | 5 | a0001c0001t0005g0119a0001c0001t0005g0120a0001c0001t0005g0121others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47-34839delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74780535 | ||||||
| chrX:74780558
|
C | G | 7 | a0001c0001t0002g0142a0001c0001t0002g0144a0001c0001t0002g0155others(4): Show | 7 | HG01256.hp1 HG01928.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.-47-34861G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74780558 | ||||||
| chrX:74780575
|
C | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0073 | 2 | NA18970.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-47-34878G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74780575 | ||||||
| chrX:74780582
|
G | T | 1 | a0001c0001t0004g0197 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-47-34885C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74780582 | ||||||
| chrX:74780588
|
A | T | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-47-34891T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74780588 | ||||||
| chrX:74780618
|
C | T | 3 | a0001c0001t0001g0210a0001c0001t0002g0166a0001c0001t0029g0172 | 3 | HG01515.hp1 HG02257.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.-47-34921G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74780618 | ||||||
| chrX:74781150
|
C | T | 1 | a0001c0001t0001g0022 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-47-35453G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74781150 | ||||||
| chrX:74781312
|
T | A | 1 | a0001c0001t0001g0036 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-47-35615A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74781312 | ||||||
| chrX:74781708
|
T | TGTGTATG others(12): Show |
53 | a0001c0001t0002g0127a0001c0001t0002g0128a0001c0001t0002g0129others(50): Show | 53 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.-47-36030_-47-3601 others(23): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74781708 | ||||||
| chrX:74781901
|
T | G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-36204A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74781901 | ||||||
| chrX:74782005
|
C | G | 2 | a0001c0001t0001g0103a0001c0001t0001g0115 | 2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-47-36308G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74782005 | ||||||
| chrX:74782072
|
C | T | 208 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(205): Show | 208 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.-47-36375G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74782072 | ||||||
| chrX:74782495
|
C | A | 2 | a0001c0001t0008g0105a0003c0015t0008g0104 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-47-36798G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74782495 | ||||||
| chrX:74782509
|
T | C | 208 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(205): Show | 208 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.-47-36812A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74782509 | ||||||
| chrX:74782512
|
A | T | 1 | a0001c0001t0003g0081 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-47-36815T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74782512 | ||||||
| chrX:74782515
|
TA | T | 1 | a0004c0014t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-47-36819delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74782515 | ||||||
| chrX:74782674
|
C | T | 5 | a0001c0001t0002g0146a0001c0001t0002g0148a0001c0001t0002g0149others(2): Show | 5 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-36977G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74782674 | ||||||
| chrX:74782862
|
T | C | 1 | a0001c0001t0001g0014 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-47-37165A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74782862 | ||||||
| chrX:74783374
|
C | A | 1 | a0001c0001t0010g0190 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-47-37677G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74783374 | ||||||
| chrX:74783462
|
T | G | 2 | a0001c0001t0002g0158a0001c0001t0002g0179 | 2 | HG02602.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-47-37765A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74783462 | ||||||
| chrX:74783893
|
C | T | 5 | a0001c0001t0005g0119a0001c0001t0005g0120a0001c0001t0005g0121others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47-38196G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74783893 | ||||||
| chrX:74783936
|
T | C | 208 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(205): Show | 208 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.-47-38239A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74783936 | ||||||
| chrX:74784178
|
C | A | 1 | a0001c0001t0001g0103 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-47-38481G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74784178 | ||||||
| chrX:74784587
|
A | G | 5 | a0001c0001t0002g0162a0001c0001t0002g0183a0001c0001t0002g0184others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-38890T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74784587 | ||||||
| chrX:74784612
|
T | TTA | 3 | a0001c0001t0002g0176a0001c0001t0005g0123a0006c0006t0034g0118 | 3 | HG01070.hp1 HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-47-38917_-47-3891 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74784612 | ||||||
| chrX:74784802
|
A | G | 1 | a0001c0001t0001g0087 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-47-39105T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74784802 | ||||||
| chrX:74785111
|
T | C | 223 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(220): Show | 223 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.-47-39414A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74785111 | ||||||
| chrX:74785522
|
T | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-39825A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74785522 | ||||||
| chrX:74785809
|
C | T | 1 | a0001c0002t0001g0062 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-47-40112G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74785809 | ||||||
| chrX:74785947
|
T | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-40250A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74785947 | ||||||
| chrX:74786032
|
C | A | 130 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(127): Show | 130 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.-47-40335G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74786032 | ||||||
| chrX:74786094
|
A | AT | 1 | a0001c0001t0001g0083 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-47-40398dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74786094 | ||||||
| chrX:74786139
|
G | A | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-47-40442C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74786139 | ||||||
| chrX:74786342
|
G | A | 1 | a0001c0001t0020g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-47-40645C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74786342 | ||||||
| chrX:74786557
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-47-40860C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74786557 | ||||||
| chrX:74786621
|
A | G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-40924T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74786621 | ||||||
| chrX:74786816
|
T | TAC | 9 | a0001c0001t0001g0047a0001c0001t0001g0060a0001c0001t0001g0078others(6): Show | 9 | HG01261.hp1 HG02602.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-47-41121_-47-4112 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74786816 | ||||||
| chrX:74786823
|
ACACACAC others(35): Show |
A | 2 | a0001c0001t0001g0034a0001c0001t0022g0017 | 2 | HG02074.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.-47-41168_-47-4112 others(46): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74786823 | ||||||
| chrX:74786827
|
ACACACAC others(31): Show |
A | 1 | a0001c0001t0001g0020 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-47-41168_-47-4113 others(42): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74786827 | ||||||
| chrX:74786848
|
T | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-41151A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74786848 | ||||||
| chrX:74786864
|
T | C | 16 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(13): Show | 16 | HG01243.hp1 HG02015.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47-41167A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74786864 | ||||||
| chrX:74786865
|
G | A | 16 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(13): Show | 16 | HG01243.hp1 HG02015.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47-41168C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74786865 | ||||||
| chrX:74786865
|
G | GCACA | 1 | a0001c0001t0001g0106 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-47-41172_-47-4116 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74786865 | ||||||
| chrX:74787093
|
T | C | 116 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(113): Show | 116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-47-41396A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74787093 | ||||||
| chrX:74787104
|
C | CA | 116 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(113): Show | 116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-47-41408dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74787104 | ||||||
| chrX:74787104
|
C | CAA | 6 | a0001c0001t0001g0069a0001c0001t0001g0080a0001c0001t0001g0083others(3): Show | 6 | HG02559.hp1 NA18906.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47-41409_-47-4140 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74787104 | ||||||
| chrX:74787104
|
CA | C | 5 | a0001c0001t0002g0179a0001c0001t0004g0187a0001c0001t0007g0005others(2): Show | 5 | HG02055.hp1 HG02886.hp2 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-41408delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74787104 | ||||||
| chrX:74787104
|
CAA | C | 1 | a0001c0001t0020g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-47-41409_-47-4140 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74787104 | ||||||
| chrX:74787269
|
C | A | 1 | a0001c0001t0001g0173 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-41572G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74787269 | ||||||
| chrX:74787294
|
G | GA | 58 | a0001c0001t0001g0100a0001c0001t0001g0164a0001c0001t0001g0173others(55): Show | 58 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.-47-41598dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74787294 | ||||||
| chrX:74787294
|
GA | G | 6 | a0001c0001t0001g0052a0001c0001t0005g0119a0001c0001t0005g0120others(3): Show | 6 | HG01884.hp1 HG01981.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47-41598delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74787294 | ||||||
| chrX:74787386
|
G | A | 16 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(13): Show | 16 | HG01243.hp1 HG02015.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47-41689C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74787386 | ||||||
| chrX:74787470
|
T | C | 1 | a0001c0001t0001g0134 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-47-41773A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74787470 | ||||||
| chrX:74787769
|
G | T | 1 | a0001c0001t0004g0133 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-47-42072C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74787769 | ||||||
| chrX:74787999
|
C | T | 6 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0148others(3): Show | 6 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.-47-42302G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74787999 | ||||||
| chrX:74788169
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-47-42472T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74788169 | ||||||
| chrX:74788371
|
T | C | 116 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(113): Show | 116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-47-42674A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74788371 | ||||||
| chrX:74788390
|
T | G | 1 | a0001c0001t0002g0175 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-47-42693A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74788390 | ||||||
| chrX:74788420
|
A | G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-42723T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74788420 | ||||||
| chrX:74788484
|
A | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-42787T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74788484 | ||||||
| chrX:74788520
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-47-42823A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74788520 | ||||||
| chrX:74788714
|
T | G | 3 | a0001c0001t0001g0216a0002c0004t0001g0202a0002c0004t0011g0001 | 3 | HG02109.hp2 HG02896.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-47-43017A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74788714 | ||||||
| chrX:74788809
|
A | AG | 2 | a0001c0001t0001g0083a0001c0001t0001g0100 | 2 | NA18967.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.-47-43113dupC | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74788809 | ||||||
| chrX:74788952
|
T | TTTTA | 1 | a0001c0001t0015g0207 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-47-43259_-47-4325 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74788952 | ||||||
| chrX:74789105
|
C | T | 1 | a0001c0001t0002g0161 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-47-43408G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74789105 | ||||||
| chrX:74789127
|
T | TC | 34 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0060others(31): Show | 34 | HG00408.hp1 HG00609.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.-47-43431dupG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74789127 | ||||||
| chrX:74789169
|
C | T | 58 | a0001c0001t0001g0164a0001c0001t0001g0173a0001c0001t0002g0127others(55): Show | 58 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.-47-43472G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74789169 | ||||||
| chrX:74789216
|
T | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-43519A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74789216 | ||||||
| chrX:74789404
|
T | C | 3 | a0001c0001t0006g0098a0001c0001t0006g0219a0001c0001t0006g0220 | 3 | HG02615.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-47-43707A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74789404 | ||||||
| chrX:74789479
|
G | C | 1 | a0001c0001t0001g0077 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-47-43782C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74789479 | ||||||
| chrX:74789505
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47-43808C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74789505 | ||||||
| chrX:74789544
|
T | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-43847A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74789544 | ||||||
| chrX:74789572
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-47-43875G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74789572 | ||||||
| chrX:74789660
|
T | C | 5 | a0001c0001t0002g0162a0001c0001t0002g0183a0001c0001t0002g0184others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-43963A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74789660 | ||||||
| chrX:74789671
|
C | A | 116 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(113): Show | 116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-47-43974G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74789671 | ||||||
| chrX:74789697
|
G | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-44000C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74789697 | ||||||
| chrX:74789801
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-47-44104G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74789801 | ||||||
| chrX:74789921
|
G | C | 1 | a0001c0001t0001g0137 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-47-44224C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74789921 | ||||||
| chrX:74790057
|
G | A | 208 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(205): Show | 208 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.-47-44360C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74790057 | ||||||
| chrX:74790099
|
A | T | 1 | a0001c0001t0002g0169 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-47-44402T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74790099 | ||||||
| chrX:74790279
|
T | A | 1 | a0001c0001t0001g0198 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-47-44582A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74790279 | ||||||
| chrX:74790311
|
C | G | 3 | a0001c0001t0001g0216a0002c0004t0001g0202a0002c0004t0011g0001 | 3 | HG02109.hp2 HG02896.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-47-44614G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74790311 | ||||||
| chrX:74790350
|
A | C | 2 | a0001c0001t0009g0135a0001c0001t0009g0136 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-47-44653T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74790350 | ||||||
| chrX:74790361
|
A | C | 3 | a0001c0001t0002g0129a0001c0001t0009g0135a0001c0001t0009g0136 | 3 | HG03017.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-47-44664T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74790361 | ||||||
| chrX:74790374
|
T | C | 2 | a0001c0001t0009g0135a0001c0001t0009g0136 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-47-44677A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74790374 | ||||||
| chrX:74790456
|
C | T | 1 | a0001c0001t0001g0092 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-47-44759G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74790456 | ||||||
| chrX:74790495
|
T | G | 1 | a0001c0001t0016g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-47-44798A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74790495 | ||||||
| chrX:74790586
|
T | G | 7 | a0001c0001t0001g0103a0001c0001t0001g0115a0001c0001t0005g0119others(4): Show | 7 | HG01884.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-47-44889A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74790586 | ||||||
| chrX:74790588
|
C | T | 7 | a0001c0001t0001g0103a0001c0001t0001g0115a0001c0001t0005g0119others(4): Show | 7 | HG01884.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-47-44891G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74790588 | ||||||
| chrX:74790638
|
C | G | 1 | a0001c0001t0016g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-47-44941G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74790638 | ||||||
| chrX:74790742
|
C | G | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-47-45045G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74790742 | ||||||
| chrX:74790903
|
A | G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-45206T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74790903 | ||||||
| chrX:74790937
|
G | C | 1 | a0001c0001t0001g0007 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-47-45240C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74790937 | ||||||
| chrX:74791145
|
C | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-45448G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74791145 | ||||||
| chrX:74791205
|
A | C | 1 | a0001c0001t0001g0010 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-47-45508T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74791205 | ||||||
| chrX:74791237
|
T | C | 116 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(113): Show | 116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-47-45540A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74791237 | ||||||
| chrX:74791340
|
C | G | 2 | a0001c0001t0009g0135a0001c0001t0009g0136 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-47-45643G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74791340 | ||||||
| chrX:74791417
|
A | G | 1 | a0001c0001t0016g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-47-45720T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74791417 | ||||||
| chrX:74791447
|
T | C | 6 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0148others(3): Show | 6 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.-47-45750A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74791447 | ||||||
| chrX:74791574
|
C | A | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-45877G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74791574 | ||||||
| chrX:74791711
|
T | A | 1 | a0001c0001t0002g0193 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-47-46014A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74791711 | ||||||
| chrX:74791763
|
A | G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-46066T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74791763 | ||||||
| chrX:74791775
|
T | G | 208 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(205): Show | 208 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.-47-46078A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74791775 | ||||||
| chrX:74791846
|
C | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-46149G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74791846 | ||||||
| chrX:74791907
|
A | G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-46210T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74791907 | ||||||
| chrX:74792073
|
T | C | 4 | a0001c0001t0001g0194a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 4 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-46376A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74792073 | ||||||
| chrX:74792104
|
G | A | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-46407C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74792104 | ||||||
| chrX:74792281
|
G | A | 1 | a0001c0001t0001g0046 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-47-46584C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74792281 | ||||||
| chrX:74792342
|
G | T | 2 | a0001c0001t0009g0135a0001c0001t0009g0136 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-47-46645C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74792342 | ||||||
| chrX:74792430
|
G | A | 1 | a0001c0013t0001g0143 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-47-46733C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74792430 | ||||||
| chrX:74792568
|
AGTGG | A | 1 | a0001c0001t0001g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-47-46875_-47-4687 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74792568 | ||||||
| chrX:74792601
|
T | TG | 1 | a0001c0001t0001g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-47-46905dupC | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74792601 | ||||||
| chrX:74792693
|
C | CT | 1 | a0001c0001t0001g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-47-46997dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74792693 | ||||||
| chrX:74792785
|
C | A | 1 | a0001c0001t0004g0188 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-47-47088G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74792785 | ||||||
| chrX:74792812
|
G | GT | 1 | a0001c0001t0001g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-47-47116dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74792812 | ||||||
| chrX:74792901
|
T | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-47204A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74792901 | ||||||
| chrX:74792984
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-47-47287A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74792984 | ||||||
| chrX:74792989
|
T | G | 2 | a0001c0001t0004g0187a0001c0001t0007g0005 | 2 | HG02055.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-47-47292A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74792989 | ||||||
| chrX:74793210
|
T | G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-47513A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74793210 | ||||||
| chrX:74793215
|
A | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-47518T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74793215 | ||||||
| chrX:74793345
|
G | A | 2 | a0001c0001t0002g0163a0001c0001t0002g0177 | 2 | HG01433.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-47-47648C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74793345 | ||||||
| chrX:74793379
|
C | T | 3 | a0001c0001t0001g0216a0002c0004t0001g0202a0002c0004t0011g0001 | 3 | HG02109.hp2 HG02896.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-47-47682G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74793379 | ||||||
| chrX:74793586
|
C | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-47889G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74793586 | ||||||
| chrX:74793691
|
C | G | 1 | a0001c0002t0001g0031 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-47-47994G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74793691 | ||||||
| chrX:74793709
|
G | A | 3 | a0001c0001t0006g0098a0001c0001t0006g0219a0001c0001t0006g0220 | 3 | HG02615.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-47-48012C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74793709 | ||||||
| chrX:74793722
|
C | A | 10 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0110others(7): Show | 10 | HG02257.hp1 HG02451.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-47-48025G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74793722 | ||||||
| chrX:74793737
|
T | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-48040A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74793737 | ||||||
| chrX:74793952
|
G | A | 1 | a0001c0001t0005g0122 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-47-48255C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74793952 | ||||||
| chrX:74794006
|
T | C | 208 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(205): Show | 208 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.-47-48309A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74794006 | ||||||
| chrX:74794015
|
G | A | 1 | a0001c0005t0001g0012 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-47-48318C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74794015 | ||||||
| chrX:74794235
|
G | A | 1 | a0008c0009t0002g0132 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-47-48538C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74794235 | ||||||
| chrX:74794299
|
G | C | 1 | a0001c0001t0001g0082 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-47-48602C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74794299 | ||||||
| chrX:74794322
|
A | G | 1 | a0001c0001t0003g0124 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-47-48625T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74794322 | ||||||
| chrX:74794519
|
C | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-48822G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74794519 | ||||||
| chrX:74794602
|
G | A | 5 | a0001c0001t0001g0194a0001c0001t0001g0199a0001c0001t0001g0200others(2): Show | 5 | HG02559.hp2 HG02698.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-48905C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74794602 | ||||||
| chrX:74794625
|
G | A | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-48928C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74794625 | ||||||
| chrX:74794674
|
C | T | 1 | a0001c0001t0007g0005 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-47-48977G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74794674 | ||||||
| chrX:74794698
|
G | A | 130 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(127): Show | 130 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.-47-49001C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74794698 | ||||||
| chrX:74794700
|
C | T | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-47-49003G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74794700 | ||||||
| chrX:74794708
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-47-49011G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74794708 | ||||||
| chrX:74794712
|
A | G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-49015T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74794712 | ||||||
| chrX:74794834
|
C | G | 3 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201 | 3 | HG02818.hp2 HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-47-49137G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74794834 | ||||||
| chrX:74794865
|
C | G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-49168G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74794865 | ||||||
| chrX:74794900
|
T | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-49203A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74794900 | ||||||
| chrX:74794948
|
C | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-49251G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74794948 | ||||||
| chrX:74794962
|
G | C | 2 | a0001c0001t0004g0187a0001c0001t0007g0005 | 2 | HG02055.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-47-49265C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74794962 | ||||||
| chrX:74795026
|
C | T | 1 | a0001c0001t0002g0161 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-47-49329G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74795026 | ||||||
| chrX:74795198
|
T | C | 4 | a0001c0001t0001g0111a0001c0001t0001g0116a0001c0001t0001g0218others(1): Show | 4 | HG02257.hp1 HG02615.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-49501A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74795198 | ||||||
| chrX:74795423
|
A | G | 1 | a0001c0001t0020g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-47-49726T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74795423 | ||||||
| chrX:74795523
|
A | G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-49826T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74795523 | ||||||
| chrX:74795800
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-47-50103C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74795800 | ||||||
| chrX:74795954
|
T | C | 1 | a0001c0001t0001g0083 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-47-50257A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74795954 | ||||||
| chrX:74796104
|
T | TTATATAT others(23): Show |
4 | a0001c0001t0001g0216a0001c0001t0010g0190a0002c0004t0001g0202others(1): Show | 4 | HG02109.hp2 HG02896.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-50437_-47-5040 others(34): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796104 | ||||||
| chrX:74796126
|
T | A | 5 | a0001c0001t0005g0119a0001c0001t0005g0120a0001c0001t0005g0121others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47-50429A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796126 | ||||||
| chrX:74796126
|
T | TATATATA others(21): Show |
1 | a0001c0001t0003g0086 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-47-50457_-47-5043 others(32): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796126 | ||||||
| chrX:74796133
|
AAT | A | 2 | a0001c0001t0002g0154a0001c0001t0002g0182 | 2 | HG01106.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-47-50438_-47-5043 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796133 | ||||||
| chrX:74796134
|
A | ATATATAT others(21): Show |
1 | a0001c0001t0001g0115 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-47-50465_-47-5043 others(32): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796134 | ||||||
| chrX:74796135
|
T | TATATATA others(12): Show |
1 | a0001c0001t0001g0164 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-47-50457_-47-5043 others(23): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796135 | ||||||
| chrX:74796138
|
ATATAT | A | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-50446_-47-5044 others(9): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796138 | ||||||
| chrX:74796144
|
T | A | 1 | a0001c0001t0001g0084 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-47-50447A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796144 | ||||||
| chrX:74796151
|
A | G | 1 | a0001c0001t0032g0145 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-47-50454T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796151 | ||||||
| chrX:74796153
|
A | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-50456T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796153 | ||||||
| chrX:74796154
|
C | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-50457G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796154 | ||||||
| chrX:74796154
|
CATATATA others(2): Show |
C | 1 | a0001c0001t0003g0086 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-47-50466_-47-5045 others(13): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796154 | ||||||
| chrX:74796159
|
ATAT | A | 2 | a0001c0001t0002g0175a0001c0001t0002g0178 | 2 | HG03669.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.-47-50465_-47-5046 others(7): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796159 | ||||||
| chrX:74796162
|
T | A | 116 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(113): Show | 116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-47-50465A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796162 | ||||||
| chrX:74796181
|
A | ATTTATAT others(90): Show |
3 | a0001c0001t0006g0098a0001c0001t0006g0219a0001c0001t0006g0220 | 3 | HG02615.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-47-50485_-47-5048 others(101): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796181 | ||||||
| chrX:74796181
|
AC | A | 3 | a0001c0001t0001g0216a0002c0004t0001g0202a0002c0004t0011g0001 | 3 | HG02109.hp2 HG02896.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-47-50485delG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796181 | ||||||
| chrX:74796182
|
C | CATATATA others(2): Show |
1 | a0001c0001t0001g0074 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-47-50486_-47-5048 others(13): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796182 | ||||||
| chrX:74796182
|
C | T | 3 | a0001c0001t0006g0098a0001c0001t0006g0219a0001c0001t0006g0220 | 3 | HG02615.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-47-50485G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796182 | ||||||
| chrX:74796182
|
CAT | C | 1 | a0001c0001t0001g0173 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-50487_-47-5048 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796182 | ||||||
| chrX:74796190
|
T | TTA | 1 | a0001c0001t0001g0164 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-47-50495_-47-5049 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796190 | ||||||
| chrX:74796200
|
A | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-50503T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796200 | ||||||
| chrX:74796201
|
C | CT | 2 | a0001c0001t0002g0169a0001c0001t0002g0181 | 2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-47-50505_-47-5050 others(5): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796201 | ||||||
| chrX:74796201
|
C | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-50504G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796201 | ||||||
| chrX:74796203
|
T | TATATATT others(10): Show |
1 | a0008c0009t0002g0132 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-47-50507_-47-5050 others(21): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796203 | ||||||
| chrX:74796209
|
T | A | 1 | a0001c0001t0001g0164 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-47-50512A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796209 | ||||||
| chrX:74796209
|
T | TTATATAT others(14): Show |
1 | a0001c0001t0002g0176 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-47-50533_-47-5051 others(25): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796209 | ||||||
| chrX:74796209
|
T | TTATATAT others(16): Show |
42 | a0001c0001t0002g0127a0001c0001t0002g0128a0001c0001t0002g0129others(39): Show | 42 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.-47-50535_-47-5051 others(27): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796209 | ||||||
| chrX:74796209
|
T | TTATATAT others(18): Show |
1 | a0001c0001t0001g0173 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-50537_-47-5051 others(29): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796209 | ||||||
| chrX:74796209
|
TTA | T | 11 | a0001c0001t0001g0026a0001c0001t0001g0032a0001c0001t0001g0033others(8): Show | 11 | HG01884.hp1 NA18945.hp1 NA18953.hp1 others(8): Show |
intron_variant | MODIFIER | c.-47-50514_-47-5051 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796209 | ||||||
| chrX:74796210
|
T | A | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-50513A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796210 | ||||||
| chrX:74796220
|
T | C | 3 | a0001c0001t0006g0098a0001c0001t0006g0219a0001c0001t0006g0220 | 3 | HG02615.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-47-50523A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796220 | ||||||
| chrX:74796220
|
T | TACATATA others(16): Show |
1 | a0001c0001t0002g0166 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-47-50524_-47-5052 others(27): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796220 | ||||||
| chrX:74796220
|
TACA | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-50526_-47-5052 others(7): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796220 | ||||||
| chrX:74796222
|
C | T | 3 | a0001c0001t0006g0098a0001c0001t0006g0219a0001c0001t0006g0220 | 3 | HG02615.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-47-50525G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796222 | ||||||
| chrX:74796228
|
TA | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-50532delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796228 | ||||||
| chrX:74796229
|
A | AAT | 1 | a0001c0001t0001g0079 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-47-50534_-47-5053 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796229 | ||||||
| chrX:74796229
|
A | T | 7 | a0001c0001t0002g0162a0001c0001t0002g0183a0001c0001t0002g0184others(4): Show | 7 | HG01069.hp1 HG01071.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.-47-50532T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796229 | ||||||
| chrX:74796229
|
AAT | A | 14 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0048others(11): Show | 14 | HG00323.hp1 HG00558.hp1 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.-47-50534_-47-5053 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796229 | ||||||
| chrX:74796231
|
T | TATATATA others(10): Show |
4 | a0001c0001t0002g0162a0001c0001t0002g0183a0001c0001t0002g0184others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-50535_-47-5053 others(21): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796231 | ||||||
| chrX:74796231
|
T | TATATATA others(14): Show |
4 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0182others(1): Show | 4 | HG00408.hp1 HG01106.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-50535_-47-5053 others(25): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796231 | ||||||
| chrX:74796233
|
TA | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-50537delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796233 | ||||||
| chrX:74796235
|
T | TATACATA others(4): Show |
3 | a0001c0001t0006g0098a0001c0001t0006g0219a0001c0001t0006g0220 | 3 | HG02615.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-47-50539_-47-5053 others(15): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796235 | ||||||
| chrX:74796236
|
A | ATATATAC others(19): Show |
2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-47-50540_-47-5053 others(30): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796236 | ||||||
| chrX:74796243
|
T | TACATATA others(16): Show |
3 | a0001c0001t0002g0163a0001c0001t0002g0175a0001c0001t0002g0178 | 3 | HG01433.hp1 HG03669.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.-47-50547_-47-5054 others(27): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796243 | ||||||
| chrX:74796245
|
C | CACATATA others(21): Show |
1 | a0001c0001t0025g0212 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-47-50576_-47-5054 others(32): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796245 | ||||||
| chrX:74796245
|
C | T | 5 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0006g0098others(2): Show | 5 | HG02615.hp2 HG02809.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-50548G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796245 | ||||||
| chrX:74796254
|
AT | A | 1 | a0001c0001t0001g0101 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-47-50558delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796254 | ||||||
| chrX:74796266
|
A | C | 1 | a0001c0001t0020g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-47-50569T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796266 | ||||||
| chrX:74796266
|
ATATATAT others(19): Show |
A | 1 | a0001c0001t0004g0187 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-47-50595_-47-5057 others(30): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796266 | ||||||
| chrX:74796268
|
ATATATAC others(17): Show |
A | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-50595_-47-5057 others(28): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796268 | ||||||
| chrX:74796292
|
T | TTATATAT others(32): Show |
2 | a0001c0001t0001g0079a0001c0001t0010g0190 | 2 | HG03239.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-47-50596_-47-5059 others(43): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796292 | ||||||
| chrX:74796301
|
T | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-50604A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796301 | ||||||
| chrX:74796303
|
T | C | 5 | a0001c0001t0001g0079a0001c0001t0004g0133a0001c0001t0004g0187others(2): Show | 5 | HG02055.hp1 HG02886.hp2 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-50606A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796303 | ||||||
| chrX:74796303
|
T | TAC | 202 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(199): Show | 202 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.-47-50608_-47-5060 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796303 | ||||||
| chrX:74796303
|
T | TATAC | 1 | a0001c0001t0022g0017 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-47-50607_-47-5060 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796303 | ||||||
| chrX:74796303
|
TAC | T | 1 | a0001c0001t0020g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-47-50608_-47-5060 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796303 | ||||||
| chrX:74796456
|
T | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-50759A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796456 | ||||||
| chrX:74796626
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-47-50929G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796626 | ||||||
| chrX:74796798
|
T | G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-51101A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74796798 | ||||||
| chrX:74797050
|
T | C | 1 | a0001c0001t0001g0215 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-47-51353A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74797050 | ||||||
| chrX:74797173
|
G | T | 1 | a0001c0001t0002g0181 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-47-51476C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74797173 | ||||||
| chrX:74797613
|
TCTAA | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0115 | 2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-47-51920_-47-5191 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74797613 | ||||||
| chrX:74797744
|
A | G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-52047T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74797744 | ||||||
| chrX:74798102
|
C | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0040 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-47-52405G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74798102 | ||||||
| chrX:74798247
|
CAAACCAA others(6): Show |
C | 1 | a0001c0001t0015g0207 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-47-52563_-47-5255 others(17): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74798247 | ||||||
| chrX:74798400
|
G | A | 2 | a0001c0001t0001g0216a0002c0004t0001g0202 | 2 | HG02109.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-47-52703C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74798400 | ||||||
| chrX:74798439
|
G | C | 2 | a0001c0001t0001g0009a0001c0016t0001g0008 | 2 | NA18971.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-47-52742C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74798439 | ||||||
| chrX:74798466
|
T | G | 1 | a0001c0001t0001g0214 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-47-52769A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74798466 | ||||||
| chrX:74798642
|
TC | T | 1 | a0001c0001t0001g0047 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-47-52946delG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74798642 | ||||||
| chrX:74798798
|
T | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-53101A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74798798 | ||||||
| chrX:74798799
|
C | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-53102G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74798799 | ||||||
| chrX:74798964
|
T | TA | 5 | a0001c0001t0001g0194a0001c0001t0001g0199a0001c0001t0001g0200others(2): Show | 5 | HG02559.hp2 HG02818.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-53268dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74798964 | ||||||
| chrX:74798964
|
TA | T | 2 | a0001c0001t0023g0027a0001c0001t0030g0004 | 2 | HG01168.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.-47-53268delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74798964 | ||||||
| chrX:74799502
|
C | T | 1 | a0001c0001t0002g0174 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-47-53805G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74799502 | ||||||
| chrX:74799588
|
T | A | 2 | a0001c0001t0002g0163a0001c0001t0002g0177 | 2 | HG01433.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-47-53891A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74799588 | ||||||
| chrX:74799699
|
C | T | 208 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(205): Show | 208 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.-47-54002G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74799699 | ||||||
| chrX:74799967
|
C | T | 1 | a0001c0001t0001g0038 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-47-54270G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74799967 | ||||||
| chrX:74800162
|
A | G | 1 | a0001c0008t0001g0029 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-47-54465T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74800162 | ||||||
| chrX:74800166
|
T | C | 1 | a0002c0004t0011g0001 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-47-54469A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74800166 | ||||||
| chrX:74800371
|
T | TG | 1 | a0001c0001t0001g0047 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-47-54675_-47-5467 others(5): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74800371 | ||||||
| chrX:74800374
|
C | CT | 1 | a0001c0001t0005g0119 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-47-54678dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74800374 | ||||||
| chrX:74800398
|
TA | T | 1 | a0001c0001t0001g0047 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-47-54702delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74800398 | ||||||
| chrX:74800435
|
T | G | 1 | a0001c0001t0002g0223 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-47-54738A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74800435 | ||||||
| chrX:74800437
|
C | T | 1 | a0001c0001t0010g0190 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-47-54740G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74800437 | ||||||
| chrX:74800547
|
A | AT | 1 | a0001c0001t0001g0047 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-47-54851dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74800547 | ||||||
| chrX:74800587
|
G | GT | 1 | a0001c0001t0001g0047 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-47-54891dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74800587 | ||||||
| chrX:74800595
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-47-54898C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74800595 | ||||||
| chrX:74800596
|
T | A | 1 | a0001c0001t0001g0134 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-47-54899A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74800596 | ||||||
| chrX:74800623
|
T | TA | 1 | a0001c0001t0001g0047 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-47-54927dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74800623 | ||||||
| chrX:74800666
|
C | CA | 1 | a0001c0001t0001g0047 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-47-54970dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74800666 | ||||||
| chrX:74800712
|
T | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-55015A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74800712 | ||||||
| chrX:74800776
|
C | T | 211 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(208): Show | 211 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.-47-55079G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74800776 | ||||||
| chrX:74800779
|
T | G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-55082A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74800779 | ||||||
| chrX:74800915
|
C | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0075 | 2 | HG00558.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.-47-55218G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74800915 | ||||||
| chrX:74801250
|
T | C | 2 | a0001c0001t0001g0060a0001c0001t0001g0078 | 2 | NA18960.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.-47-55553A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74801250 | ||||||
| chrX:74801407
|
T | C | 1 | a0001c0001t0006g0220 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-47-55710A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74801407 | ||||||
| chrX:74801561
|
AC | A | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-55865delG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74801561 | ||||||
| chrX:74801659
|
C | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-55962G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74801659 | ||||||
| chrX:74801670
|
G | T | 7 | a0001c0001t0001g0103a0001c0001t0001g0115a0001c0001t0005g0119others(4): Show | 7 | HG01884.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-47-55973C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74801670 | ||||||
| chrX:74801936
|
G | A | 1 | a0001c0001t0001g0070 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-47-56239C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74801936 | ||||||
| chrX:74801938
|
C | T | 1 | a0001c0001t0016g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-47-56241G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74801938 | ||||||
| chrX:74802136
|
C | T | 116 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(113): Show | 116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-47-56439G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74802136 | ||||||
| chrX:74802460
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-47-56763G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74802460 | ||||||
| chrX:74802466
|
C | CG | 2 | a0001c0001t0001g0010a0001c0001t0024g0095 | 2 | HG01109.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.-47-56770dupC | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74802466 | ||||||
| chrX:74802467
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0022g0017 | 2 | HG02074.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.-47-56770C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74802467 | ||||||
| chrX:74802607
|
C | A | 5 | a0001c0001t0005g0119a0001c0001t0005g0120a0001c0001t0005g0121others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47-56910G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74802607 | ||||||
| chrX:74802756
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-47-57059G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74802756 | ||||||
| chrX:74802834
|
T | C | 1 | a0001c0001t0015g0207 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-47-57137A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74802834 | ||||||
| chrX:74803194
|
C | T | 1 | a0001c0001t0033g0130 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-47-57497G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74803194 | ||||||
| chrX:74803228
|
G | A | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-57531C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74803228 | ||||||
| chrX:74803246
|
C | G | 16 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(13): Show | 16 | HG01243.hp1 HG02015.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47-57549G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74803246 | ||||||
| chrX:74803346
|
C | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-57649G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74803346 | ||||||
| chrX:74803422
|
G | T | 3 | a0001c0001t0001g0216a0002c0004t0001g0202a0002c0004t0011g0001 | 3 | HG02109.hp2 HG02896.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-47-57725C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74803422 | ||||||
| chrX:74803554
|
C | T | 1 | a0001c0001t0004g0189 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-47-57857G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74803554 | ||||||
| chrX:74803563
|
G | A | 1 | a0001c0001t0002g0179 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-47-57866C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74803563 | ||||||
| chrX:74803567
|
C | CA | 1 | a0001c0001t0001g0194 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-47-57871dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74803567 | ||||||
| chrX:74803571
|
A | AAAAT | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-57878_-47-5787 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74803571 | ||||||
| chrX:74803574
|
AT | A | 2 | a0001c0001t0001g0201a0001c0001t0005g0120 | 2 | HG02723.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-47-57878delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74803574 | ||||||
| chrX:74803575
|
T | A | 10 | a0001c0001t0001g0103a0001c0001t0001g0115a0001c0001t0001g0194others(7): Show | 10 | HG01884.hp1 HG02559.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-47-57878A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74803575 | ||||||
| chrX:74803579
|
T | A | 11 | a0001c0001t0001g0103a0001c0001t0001g0115a0001c0001t0001g0194others(8): Show | 11 | HG01884.hp1 HG02559.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-47-57882A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74803579 | ||||||
| chrX:74803763
|
GA | G | 53 | a0001c0001t0001g0164a0001c0001t0001g0173a0001c0001t0002g0127others(50): Show | 53 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.-47-58067delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74803763 | ||||||
| chrX:74803772
|
A | C | 2 | a0001c0001t0001g0103a0001c0001t0001g0115 | 2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-47-58075T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74803772 | ||||||
| chrX:74803779
|
A | C | 1 | a0001c0001t0002g0168 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-47-58082T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74803779 | ||||||
| chrX:74803827
|
C | T | 2 | a0001c0003t0001g0041a0001c0003t0001g0050 | 2 | HG02040.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.-47-58130G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74803827 | ||||||
| chrX:74803877
|
CA | C | 9 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0048others(6): Show | 9 | HG02027.hp1 HG02074.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.-47-58181delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74803877 | ||||||
| chrX:74803992
|
A | G | 1 | a0001c0001t0001g0007 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-47-58295T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74803992 | ||||||
| chrX:74804081
|
AAAT | A | 1 | a0001c0001t0030g0004 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-47-58387_-47-5838 others(7): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74804081 | ||||||
| chrX:74804344
|
C | T | 1 | a0001c0001t0016g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-47-58647G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74804344 | ||||||
| chrX:74804350
|
G | T | 1 | a0001c0001t0001g0214 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-47-58653C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74804350 | ||||||
| chrX:74804383
|
T | C | 3 | a0001c0001t0001g0216a0002c0004t0001g0202a0002c0004t0011g0001 | 3 | HG02109.hp2 HG02896.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-47-58686A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74804383 | ||||||
| chrX:74804791
|
C | T | 16 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(13): Show | 16 | HG01243.hp1 HG02015.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47-59094G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74804791 | ||||||
| chrX:74804950
|
G | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-59253C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74804950 | ||||||
| chrX:74805219
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-47-59522C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74805219 | ||||||
| chrX:74805343
|
C | A | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-59646G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74805343 | ||||||
| chrX:74805464
|
T | A | 2 | a0001c0001t0001g0021a0001c0001t0027g0023 | 2 | NA18955.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.-47-59767A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74805464 | ||||||
| chrX:74806181
|
G | A | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-60484C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74806181 | ||||||
| chrX:74806273
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0115 | 2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-47-60576G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74806273 | ||||||
| chrX:74806651
|
T | A | 1 | a0001c0001t0016g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-47-60954A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74806651 | ||||||
| chrX:74806887
|
CTATT | C | 4 | a0001c0001t0001g0053a0001c0001t0001g0058a0001c0001t0001g0077others(1): Show | 4 | HG00408.hp2 NA18967.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-61194_-47-6119 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74806887 | ||||||
| chrX:74806899
|
A | C | 2 | a0001c0001t0005g0120a0001c0001t0005g0121 | 2 | HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-47-61202T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74806899 | ||||||
| chrX:74806921
|
A | G | 1 | a0001c0001t0020g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-47-61224T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74806921 | ||||||
| chrX:74806931
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-47-61234C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74806931 | ||||||
| chrX:74807213
|
T | C | 1 | a0001c0001t0005g0119 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-47-61516A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74807213 | ||||||
| chrX:74807468
|
C | A | 1 | a0001c0001t0031g0126 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-47-61771G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74807468 | ||||||
| chrX:74807469
|
C | CT | 2 | a0001c0001t0001g0063a0001c0001t0001g0164 | 2 | HG01952.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.-47-61773dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74807469 | ||||||
| chrX:74807698
|
A | G | 58 | a0001c0001t0001g0164a0001c0001t0001g0173a0001c0001t0002g0127others(55): Show | 58 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.-47-62001T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74807698 | ||||||
| chrX:74807814
|
A | G | 146 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(143): Show | 146 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.-47-62117T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74807814 | ||||||
| chrX:74808036
|
A | G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-62339T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74808036 | ||||||
| chrX:74808143
|
C | T | 4 | a0001c0001t0001g0194a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 4 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-62446G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74808143 | ||||||
| chrX:74808843
|
T | C | 1 | a0001c0001t0002g0157 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-47-63146A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74808843 | ||||||
| chrX:74809520
|
C | G | 1 | a0001c0001t0001g0112 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-47-63823G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74809520 | ||||||
| chrX:74809585
|
T | C | 1 | a0001c0001t0001g0036 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-47-63888A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74809585 | ||||||
| chrX:74809611
|
G | A | 2 | a0001c0001t0001g0103a0001c0001t0001g0115 | 2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-47-63914C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74809611 | ||||||
| chrX:74810249
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-47-64552G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74810249 | ||||||
| chrX:74810562
|
G | A | 116 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(113): Show | 116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-47-64865C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74810562 | ||||||
| chrX:74810635
|
C | CA | 59 | a0001c0001t0001g0164a0001c0001t0001g0173a0001c0001t0001g0221others(56): Show | 59 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.-47-64939dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74810635 | ||||||
| chrX:74810635
|
CA | C | 3 | a0001c0001t0001g0020a0001c0001t0001g0075a0001c0001t0003g0089 | 3 | HG00558.hp1 HG00558.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.-47-64939delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74810635 | ||||||
| chrX:74810723
|
G | C | 3 | a0001c0001t0006g0098a0001c0001t0006g0219a0001c0001t0006g0220 | 3 | HG02615.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-47-65026C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74810723 | ||||||
| chrX:74810795
|
A | T | 3 | a0001c0001t0006g0098a0001c0001t0006g0219a0001c0001t0006g0220 | 3 | HG02615.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-47-65098T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74810795 | ||||||
| chrX:74811285
|
G | A | 2 | a0001c0001t0001g0103a0001c0001t0001g0115 | 2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-47-65588C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74811285 | ||||||
| chrX:74811348
|
TC | T | 5 | a0001c0001t0005g0119a0001c0001t0005g0120a0001c0001t0005g0121others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47-65652delG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74811348 | ||||||
| chrX:74811350
|
C | T | 5 | a0001c0001t0005g0119a0001c0001t0005g0120a0001c0001t0005g0121others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47-65653G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74811350 | ||||||
| chrX:74811351
|
A | T | 5 | a0001c0001t0005g0119a0001c0001t0005g0120a0001c0001t0005g0121others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47-65654T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74811351 | ||||||
| chrX:74811352
|
T | C | 130 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(127): Show | 130 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.-47-65655A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74811352 | ||||||
| chrX:74811435
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47-65738T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74811435 | ||||||
| chrX:74811813
|
T | C | 3 | a0001c0001t0001g0216a0002c0004t0001g0202a0002c0004t0011g0001 | 3 | HG02109.hp2 HG02896.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-47-66116A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74811813 | ||||||
| chrX:74811972
|
A | G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-66275T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74811972 | ||||||
| chrX:74812259
|
A | G | 1 | a0001c0001t0033g0130 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-47-66562T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74812259 | ||||||
| chrX:74812373
|
T | A | 1 | a0001c0001t0025g0212 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-47-66676A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74812373 | ||||||
| chrX:74812434
|
T | A | 6 | a0001c0001t0004g0187a0001c0001t0004g0188a0001c0001t0004g0189others(3): Show | 6 | HG01243.hp1 HG02055.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47-66737A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74812434 | ||||||
| chrX:74812454
|
G | A | 16 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(13): Show | 16 | HG01243.hp1 HG02015.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47-66757C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74812454 | ||||||
| chrX:74812505
|
T | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-66808A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74812505 | ||||||
| chrX:74812762
|
C | G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-67065G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74812762 | ||||||
| chrX:74812819
|
G | T | 6 | a0001c0001t0001g0083a0001c0001t0003g0088a0001c0001t0003g0124others(3): Show | 6 | NA18612.hp1 NA18747.hp1 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47-67122C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74812819 | ||||||
| chrX:74813179
|
CA | C | 1 | a0001c0001t0002g0162 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-47-67483delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74813179 | ||||||
| chrX:74813472
|
C | T | 1 | a0001c0001t0001g0068 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-47-67775G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74813472 | ||||||
| chrX:74813515
|
G | A | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-47-67818C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74813515 | ||||||
| chrX:74813532
|
C | A | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-67835G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74813532 | ||||||
| chrX:74814125
|
C | T | 1 | a0001c0001t0002g0156 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-47-68428G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74814125 | ||||||
| chrX:74814159
|
C | T | 3 | a0001c0001t0006g0098a0001c0001t0006g0219a0001c0001t0006g0220 | 3 | HG02615.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-47-68462G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74814159 | ||||||
| chrX:74814390
|
T | G | 1 | a0001c0001t0004g0133 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-47-68693A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74814390 | ||||||
| chrX:74814723
|
G | T | 1 | a0001c0001t0002g0160 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-47-69026C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74814723 | ||||||
| chrX:74814759
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-47-69062G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74814759 | ||||||
| chrX:74814951
|
G | A | 1 | a0001c0001t0001g0035 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-47-69254C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74814951 | ||||||
| chrX:74815140
|
TTTAGA | T | 1 | a0001c0001t0001g0194 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-47-69448_-47-6944 others(9): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74815140 | ||||||
| chrX:74815635
|
C | CT | 3 | a0001c0001t0001g0042a0004c0014t0001g0076a0005c0007t0003g0016 | 3 | HG02056.hp1 NA19004.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-47-69939dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74815635 | ||||||
| chrX:74815635
|
CT | C | 2 | a0001c0001t0007g0005a0006c0006t0034g0118 | 2 | HG02886.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-47-69939delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74815635 | ||||||
| chrX:74815703
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-47-70006G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74815703 | ||||||
| chrX:74815789
|
C | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-70092G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74815789 | ||||||
| chrX:74815927
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-47-70230G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74815927 | ||||||
| chrX:74816181
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-47-70484G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74816181 | ||||||
| chrX:74816891
|
G | A | 4 | a0001c0001t0001g0111a0001c0001t0001g0116a0001c0001t0001g0218others(1): Show | 4 | HG02257.hp1 HG02615.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-71194C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74816891 | ||||||
| chrX:74816965
|
T | G | 1 | a0001c0001t0001g0103 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-47-71268A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74816965 | ||||||
| chrX:74817043
|
T | C | 1 | a0009c0012t0002g0141 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-47-71346A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74817043 | ||||||
| chrX:74817103
|
A | AT | 1 | a0001c0002t0001g0049 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-47-71407dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74817103 | ||||||
| chrX:74817463
|
G | T | 1 | a0001c0001t0010g0190 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-47-71766C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74817463 | ||||||
| chrX:74817781
|
C | A | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-72084G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74817781 | ||||||
| chrX:74817878
|
A | G | 1 | a0001c0001t0001g0214 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-47-72181T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74817878 | ||||||
| chrX:74818095
|
AAAAAAAA others(5): Show |
A | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-72410_-47-7239 others(16): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74818095 | ||||||
| chrX:74818107
|
T | TA | 3 | a0001c0001t0006g0098a0001c0001t0006g0219a0001c0001t0006g0220 | 3 | HG02615.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-47-72411dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74818107 | ||||||
| chrX:74818107
|
TA | T | 1 | a0001c0001t0001g0059 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-47-72411delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74818107 | ||||||
| chrX:74818253
|
T | A | 2 | a0001c0001t0004g0187a0001c0001t0007g0005 | 2 | HG02055.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-47-72556A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74818253 | ||||||
| chrX:74818258
|
C | T | 15 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(12): Show | 15 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-47-72561G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74818258 | ||||||
| chrX:74818299
|
A | G | 1 | a0009c0012t0002g0141 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-47-72602T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74818299 | ||||||
| chrX:74818340
|
T | C | 1 | a0004c0014t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-47-72643A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74818340 | ||||||
| chrX:74818667
|
A | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-72970T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74818667 | ||||||
| chrX:74819004
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-47-73307C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74819004 | ||||||
| chrX:74819061
|
C | T | 1 | a0001c0001t0016g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-47-73364G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74819061 | ||||||
| chrX:74819459
|
A | T | 1 | a0001c0001t0001g0053 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-47-73762T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74819459 | ||||||
| chrX:74819599
|
C | A | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-47-73902G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74819599 | ||||||
| chrX:74819679
|
A | G | 4 | a0001c0001t0002g0162a0001c0001t0002g0183a0001c0001t0002g0184others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-73982T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74819679 | ||||||
| chrX:74819738
|
G | A | 4 | a0001c0001t0001g0194a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 4 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-74041C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74819738 | ||||||
| chrX:74819986
|
AC | A | 1 | a0001c0001t0001g0053 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-47-74290delG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74819986 | ||||||
| chrX:74819995
|
T | C | 16 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(13): Show | 16 | HG01243.hp1 HG02015.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47-74298A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74819995 | ||||||
| chrX:74820108
|
T | G | 165 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(162): Show | 165 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.-47-74411A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74820108 | ||||||
| chrX:74820122
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-47-74425C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74820122 | ||||||
| chrX:74820175
|
T | C | 209 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(206): Show | 209 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.-47-74478A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74820175 | ||||||
| chrX:74820198
|
T | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-74501A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74820198 | ||||||
| chrX:74820249
|
TG | T | 1 | a0001c0001t0001g0053 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-47-74553delC | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74820249 | ||||||
| chrX:74820304
|
G | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-74607C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74820304 | ||||||
| chrX:74820330
|
T | TATA | 2 | a0001c0001t0001g0078a0002c0004t0011g0001 | 2 | HG02896.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.-47-74636_-47-7463 others(7): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74820330 | ||||||
| chrX:74820330
|
T | TATAATAA others(8): Show |
1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-74648_-47-7463 others(19): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74820330 | ||||||
| chrX:74820506
|
A | G | 1 | a0001c0001t0001g0053 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-47-74809T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74820506 | ||||||
| chrX:74820516
|
AG | A | 1 | a0001c0001t0001g0053 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-47-74820delC | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74820516 | ||||||
| chrX:74820649
|
T | A | 2 | a0001c0001t0001g0064a0001c0001t0001g0073 | 2 | NA18970.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-47-74952A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74820649 | ||||||
| chrX:74820677
|
G | T | 3 | a0001c0001t0006g0098a0001c0001t0006g0219a0001c0001t0006g0220 | 3 | HG02615.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-47-74980C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74820677 | ||||||
| chrX:74820704
|
G | A | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-75007C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74820704 | ||||||
| chrX:74820819
|
C | G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-75122G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74820819 | ||||||
| chrX:74820948
|
G | T | 165 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(162): Show | 165 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.-47-75251C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74820948 | ||||||
| chrX:74820978
|
AC | A | 1 | a0001c0001t0001g0053 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-47-75282delG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74820978 | ||||||
| chrX:74821004
|
T | TC | 1 | a0001c0001t0001g0053 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-47-75308dupG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74821004 | ||||||
| chrX:74821102
|
G | GA | 2 | a0001c0001t0010g0190a0006c0006t0034g0118 | 2 | HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-47-75406dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74821102 | ||||||
| chrX:74821102
|
GA | G | 1 | a0001c0001t0004g0133 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-47-75406delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74821102 | ||||||
| chrX:74821112
|
AT | A | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-47-75416delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74821112 | ||||||
| chrX:74821113
|
T | A | 98 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0013others(95): Show | 98 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.-47-75416A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74821113 | ||||||
| chrX:74821168
|
C | T | 16 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(13): Show | 16 | HG01243.hp1 HG02015.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47-75471G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74821168 | ||||||
| chrX:74821203
|
CA | C | 1 | a0001c0001t0001g0053 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-47-75507delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74821203 | ||||||
| chrX:74821430
|
G | A | 5 | a0001c0001t0005g0119a0001c0001t0005g0120a0001c0001t0005g0121others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47-75733C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74821430 | ||||||
| chrX:74821476
|
G | GT | 1 | a0001c0001t0001g0053 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-47-75780dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74821476 | ||||||
| chrX:74821556
|
T | TG | 1 | a0001c0001t0001g0053 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-47-75860dupC | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74821556 | ||||||
| chrX:74821598
|
CTTAAT | C | 2 | a0001c0001t0001g0218a0001c0001t0001g0222 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-47-75906_-47-7590 others(9): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74821598 | ||||||
| chrX:74821768
|
CA | C | 1 | a0001c0001t0001g0053 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-47-76072delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74821768 | ||||||
| chrX:74821845
|
G | GA | 1 | a0001c0001t0001g0053 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-47-76149dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74821845 | ||||||
| chrX:74822002
|
C | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-76305G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74822002 | ||||||
| chrX:74822300
|
C | A | 1 | a0001c0001t0001g0216 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-47-76603G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74822300 | ||||||
| chrX:74822330
|
T | C | 5 | a0001c0001t0005g0119a0001c0001t0005g0120a0001c0001t0005g0121others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47-76633A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74822330 | ||||||
| chrX:74822466
|
T | C | 3 | a0001c0001t0006g0098a0001c0001t0006g0219a0001c0001t0006g0220 | 3 | HG02615.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-47-76769A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74822466 | ||||||
| chrX:74822751
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-47-77054C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74822751 | ||||||
| chrX:74822970
|
GAATA | G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-77277_-47-7727 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74822970 | ||||||
| chrX:74823031
|
G | A | 15 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(12): Show | 15 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-47-77334C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74823031 | ||||||
| chrX:74823563
|
C | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-77866G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74823563 | ||||||
| chrX:74823687
|
CAGAG | C | 1 | a0001c0008t0001g0029 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-47-77994_-47-7799 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74823687 | ||||||
| chrX:74823697
|
C | CAGAT | 22 | a0001c0001t0001g0138a0001c0001t0001g0203a0001c0001t0001g0206others(19): Show | 22 | HG00408.hp1 HG00735.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.-47-78004_-47-7800 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74823697 | ||||||
| chrX:74823697
|
C | CAGATAGA others(1): Show |
5 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0205others(2): Show | 5 | HG02809.hp2 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47-78008_-47-7800 others(12): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74823697 | ||||||
| chrX:74823697
|
CAGAT | C | 120 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0013others(117): Show | 120 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.-47-78004_-47-7800 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74823697 | ||||||
| chrX:74823697
|
CAGATAGA others(1): Show |
C | 6 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0063others(3): Show | 6 | HG01952.hp1 HG02074.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-47-78008_-47-7800 others(12): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74823697 | ||||||
| chrX:74823697
|
CAGATAGA others(5): Show |
C | 6 | a0001c0001t0001g0010a0001c0001t0001g0214a0001c0001t0001g0215others(3): Show | 6 | HG01109.hp1 HG02615.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47-78012_-47-7800 others(16): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74823697 | ||||||
| chrX:74823782
|
T | TG | 1 | a0001c0001t0001g0083 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-47-78086dupC | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74823782 | ||||||
| chrX:74823824
|
T | C | 1 | a0001c0001t0002g0169 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-47-78127A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74823824 | ||||||
| chrX:74824012
|
C | CA | 1 | a0001c0001t0001g0053 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-47-78316dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74824012 | ||||||
| chrX:74824139
|
A | G | 3 | a0001c0001t0006g0098a0001c0001t0006g0219a0001c0001t0006g0220 | 3 | HG02615.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-47-78442T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74824139 | ||||||
| chrX:74824254
|
G | A | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-78557C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74824254 | ||||||
| chrX:74824284
|
C | A | 1 | a0001c0001t0030g0004 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-47-78587G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74824284 | ||||||
| chrX:74824397
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-47-78700G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74824397 | ||||||
| chrX:74824652
|
G | GT | 18 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(15): Show | 18 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.-47-78956dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74824652 | ||||||
| chrX:74824652
|
G | GTT | 1 | a0001c0001t0001g0206 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-47-78957_-47-7895 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74824652 | ||||||
| chrX:74824797
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-47-79100G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74824797 | ||||||
| chrX:74824884
|
G | A | 2 | a0001c0001t0001g0216a0002c0004t0001g0202 | 2 | HG02109.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-47-79187C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74824884 | ||||||
| chrX:74824891
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0075 | 2 | HG00558.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.-47-79194C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74824891 | ||||||
| chrX:74824912
|
T | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-79215A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74824912 | ||||||
| chrX:74825594
|
G | A | 1 | a0001c0001t0001g0074 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-47-79897C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74825594 | ||||||
| chrX:74825679
|
C | T | 8 | a0001c0001t0001g0026a0001c0001t0001g0032a0001c0001t0001g0033others(5): Show | 8 | NA18945.hp1 NA18953.hp1 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.-47-79982G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74825679 | ||||||
| chrX:74826206
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-47-80509G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74826206 | ||||||
| chrX:74826228
|
G | A | 15 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(12): Show | 15 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-47-80531C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74826228 | ||||||
| chrX:74826764
|
A | G | 1 | a0001c0001t0025g0212 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-47-81067T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74826764 | ||||||
| chrX:74826865
|
A | T | 4 | a0001c0001t0001g0194a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 4 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-81168T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74826865 | ||||||
| chrX:74826932
|
C | T | 2 | a0001c0001t0002g0162a0009c0012t0002g0141 | 2 | HG01978.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.-47-81235G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74826932 | ||||||
| chrX:74827130
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0115 | 2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-47-81433G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74827130 | ||||||
| chrX:74827343
|
C | T | 1 | a0001c0001t0005g0119 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-47-81646G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74827343 | ||||||
| chrX:74827849
|
C | T | 6 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0148others(3): Show | 6 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.-47-82152G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74827849 | ||||||
| chrX:74827886
|
T | G | 1 | a0001c0001t0021g0185 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-47-82189A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74827886 | ||||||
| chrX:74828454
|
A | G | 15 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(12): Show | 15 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-47-82757T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74828454 | ||||||
| chrX:74828720
|
G | A | 1 | a0001c0005t0001g0012 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-47-83023C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74828720 | ||||||
| chrX:74828785
|
C | A | 1 | a0001c0001t0001g0035 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-47-83088G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74828785 | ||||||
| chrX:74828789
|
G | T | 15 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(12): Show | 15 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-47-83092C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74828789 | ||||||
| chrX:74828989
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-47-83292A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74828989 | ||||||
| chrX:74829006
|
C | A | 2 | a0001c0001t0002g0129a0001c0001t0002g0165 | 2 | HG01192.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.-47-83309G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74829006 | ||||||
| chrX:74829712
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-47-84015A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74829712 | ||||||
| chrX:74829756
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-47-84059C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74829756 | ||||||
| chrX:74829834
|
C | T | 16 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(13): Show | 16 | HG01243.hp1 HG02015.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47-84137G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74829834 | ||||||
| chrX:74829903
|
A | AT | 1 | a0001c0001t0002g0174 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-47-84207dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74829903 | ||||||
| chrX:74830158
|
T | A | 1 | a0001c0001t0002g0175 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-47-84461A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74830158 | ||||||
| chrX:74830325
|
G | GT | 1 | a0001c0001t0021g0185 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-47-84629dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74830325 | ||||||
| chrX:74830474
|
A | T | 1 | a0001c0001t0002g0182 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-47-84777T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74830474 | ||||||
| chrX:74830519
|
T | G | 1 | a0001c0001t0027g0023 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-47-84822A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74830519 | ||||||
| chrX:74830543
|
T | C | 1 | a0004c0014t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-47-84846A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74830543 | ||||||
| chrX:74830662
|
T | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-84965A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74830662 | ||||||
| chrX:74830832
|
T | G | 2 | a0001c0001t0001g0099a0001c0001t0001g0102 | 2 | HG00323.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.-47-85135A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74830832 | ||||||
| chrX:74830958
|
CGTT | C | 2 | a0001c0001t0002g0161a0001c0001t0033g0130 | 2 | HG00323.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.-47-85264_-47-8526 others(7): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74830958 | ||||||
| chrX:74831027
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-47-85330A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74831027 | ||||||
| chrX:74831196
|
T | A | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-85499A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74831196 | ||||||
| chrX:74831245
|
A | AG | 1 | a0001c0001t0021g0185 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-47-85549dupC | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74831245 | ||||||
| chrX:74831315
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0075 | 2 | HG00558.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.-47-85618C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74831315 | ||||||
| chrX:74831337
|
G | GC | 2 | a0001c0001t0001g0066a0001c0001t0021g0185 | 2 | HG00408.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.-47-85641dupG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74831337 | ||||||
| chrX:74831350
|
A | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-85653T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74831350 | ||||||
| chrX:74831351
|
A | AC | 1 | a0001c0001t0001g0140 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-47-85655dupG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74831351 | ||||||
| chrX:74831363
|
T | TC | 1 | a0001c0001t0021g0185 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-47-85667dupG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74831363 | ||||||
| chrX:74831379
|
T | TC | 1 | a0001c0001t0021g0185 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-47-85683dupG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74831379 | ||||||
| chrX:74831592
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-47-85895C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74831592 | ||||||
| chrX:74831621
|
C | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-85924G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74831621 | ||||||
| chrX:74831642
|
C | T | 116 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(113): Show | 116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-47-85945G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74831642 | ||||||
| chrX:74831879
|
G | GT | 2 | a0001c0001t0001g0083a0001c0001t0021g0185 | 2 | HG00408.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.-47-86183dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74831879 | ||||||
| chrX:74831903
|
A | G | 1 | a0001c0001t0023g0027 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-47-86206T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74831903 | ||||||
| chrX:74832390
|
T | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-86693A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74832390 | ||||||
| chrX:74832489
|
CT | C | 1 | a0001c0001t0001g0140 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-47-86793delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74832489 | ||||||
| chrX:74832897
|
G | GT | 1 | a0001c0001t0001g0140 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-47-87201dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74832897 | ||||||
| chrX:74833270
|
T | TG | 1 | a0001c0001t0001g0140 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-47-87574_-47-8757 others(5): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74833270 | ||||||
| chrX:74833662
|
C | T | 2 | a0001c0001t0002g0162a0009c0012t0002g0141 | 2 | HG01978.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.-47-87965G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74833662 | ||||||
| chrX:74833857
|
A | AC | 1 | a0001c0001t0001g0140 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-47-88161_-47-8816 others(5): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74833857 | ||||||
| chrX:74833858
|
A | T | 2 | a0001c0001t0005g0122a0001c0001t0005g0123 | 2 | HG02572.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-47-88161T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74833858 | ||||||
| chrX:74833888
|
C | CTG | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-88192_-47-8819 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74833888 | ||||||
| chrX:74834134
|
C | CA | 17 | a0001c0001t0001g0101a0001c0001t0001g0138a0001c0001t0001g0140others(14): Show | 17 | HG01069.hp1 HG01071.hp2 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.-47-88438dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74834134 | ||||||
| chrX:74834134
|
C | CAA | 1 | a0001c0001t0002g0162 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-47-88439_-47-8843 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74834134 | ||||||
| chrX:74834134
|
CA | C | 20 | a0001c0001t0001g0039a0001c0001t0001g0053a0001c0001t0001g0203others(17): Show | 20 | HG00735.hp2 HG00738.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.-47-88438delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74834134 | ||||||
| chrX:74834334
|
T | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-88637A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74834334 | ||||||
| chrX:74834659
|
G | C | 1 | a0001c0001t0003g0086 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-47-88962C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74834659 | ||||||
| chrX:74834689
|
GTATGT | G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-88997_-47-8899 others(9): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74834689 | ||||||
| chrX:74834757
|
TTTGA | T | 1 | a0001c0001t0001g0070 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-47-89064_-47-8906 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74834757 | ||||||
| chrX:74834818
|
C | CCTT | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-89124_-47-8912 others(7): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74834818 | ||||||
| chrX:74834837
|
T | G | 1 | a0001c0001t0001g0101 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-47-89140A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74834837 | ||||||
| chrX:74834858
|
A | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-89161T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74834858 | ||||||
| chrX:74834914
|
C | T | 15 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(12): Show | 15 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-47-89217G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74834914 | ||||||
| chrX:74835174
|
GTTAAGT | G | 1 | a0001c0001t0004g0133 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-47-89483_-47-8947 others(10): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74835174 | ||||||
| chrX:74835208
|
C | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-89511G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74835208 | ||||||
| chrX:74835260
|
C | CTA | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-47-89564_-47-8956 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74835260 | ||||||
| chrX:74835585
|
T | C | 1 | a0001c0001t0001g0092 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-48+89298A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74835585 | ||||||
| chrX:74835589
|
G | GT | 2 | a0001c0001t0002g0174a0001c0001t0004g0133 | 2 | HG01255.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-48+89293dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74835589 | ||||||
| chrX:74835832
|
T | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+89051A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74835832 | ||||||
| chrX:74835907
|
A | G | 1 | a0001c0001t0002g0160 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-48+88976T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74835907 | ||||||
| chrX:74835953
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-48+88930G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74835953 | ||||||
| chrX:74835977
|
G | A | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+88906C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74835977 | ||||||
| chrX:74836706
|
AGAAG | A | 1 | a0001c0001t0016g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-48+88173_-48+8817 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74836706 | ||||||
| chrX:74836753
|
T | TG | 1 | a0005c0007t0003g0016 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-48+88129dupC | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74836753 | ||||||
| chrX:74836946
|
C | T | 15 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(12): Show | 15 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-48+87937G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74836946 | ||||||
| chrX:74837135
|
CACAG | C | 98 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0013others(95): Show | 98 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.-48+87744_-48+8774 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74837135 | ||||||
| chrX:74837203
|
T | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+87680A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74837203 | ||||||
| chrX:74837360
|
A | G | 1 | a0001c0001t0001g0032 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-48+87523T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74837360 | ||||||
| chrX:74837609
|
C | T | 1 | a0001c0001t0002g0176 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-48+87274G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74837609 | ||||||
| chrX:74837856
|
G | GA | 6 | a0001c0001t0001g0038a0001c0001t0001g0194a0001c0001t0001g0199others(3): Show | 6 | HG02559.hp2 HG02818.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-48+87026dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74837856 | ||||||
| chrX:74839684
|
C | T | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-48+85199G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74839684 | ||||||
| chrX:74840148
|
C | A | 2 | a0001c0001t0001g0214a0001c0001t0001g0215 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-48+84735G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74840148 | ||||||
| chrX:74840180
|
T | G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+84703A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74840180 | ||||||
| chrX:74840304
|
AT | A | 1 | a0001c0001t0001g0082 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-48+84578delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74840304 | ||||||
| chrX:74840372
|
CAG | C | 2 | a0001c0001t0001g0103a0001c0001t0001g0115 | 2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-48+84509_-48+8451 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74840372 | ||||||
| chrX:74840651
|
G | GT | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+84231dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74840651 | ||||||
| chrX:74840841
|
G | T | 1 | a0002c0004t0011g0001 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-48+84042C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74840841 | ||||||
| chrX:74841758
|
T | C | 1 | a0001c0001t0004g0188 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-48+83125A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74841758 | ||||||
| chrX:74842065
|
T | C | 2 | a0001c0001t0001g0021a0001c0001t0027g0023 | 2 | NA18955.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.-48+82818A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74842065 | ||||||
| chrX:74842092
|
T | C | 3 | a0001c0001t0001g0216a0002c0004t0001g0202a0002c0004t0011g0001 | 3 | HG02109.hp2 HG02896.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-48+82791A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74842092 | ||||||
| chrX:74842536
|
T | A | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+82347A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74842536 | ||||||
| chrX:74842596
|
A | C | 4 | a0001c0001t0004g0188a0001c0001t0004g0189a0001c0001t0004g0197others(1): Show | 4 | HG01243.hp1 HG02109.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+82287T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74842596 | ||||||
| chrX:74842779
|
T | A | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+82104A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74842779 | ||||||
| chrX:74842907
|
T | A | 1 | a0001c0001t0001g0215 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-48+81976A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74842907 | ||||||
| chrX:74843138
|
T | G | 1 | a0001c0001t0001g0014 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-48+81745A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74843138 | ||||||
| chrX:74843413
|
CT | C | 1 | a0001c0001t0001g0035 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-48+81469delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74843413 | ||||||
| chrX:74843421
|
T | G | 1 | a0009c0012t0002g0141 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-48+81462A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74843421 | ||||||
| chrX:74843555
|
C | T | 1 | a0001c0001t0002g0155 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-48+81328G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74843555 | ||||||
| chrX:74843571
|
C | T | 1 | a0001c0001t0002g0175 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-48+81312G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74843571 | ||||||
| chrX:74843572
|
G | A | 2 | a0001c0001t0001g0087a0001c0001t0024g0095 | 2 | NA18961.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.-48+81311C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74843572 | ||||||
| chrX:74843741
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-48+81142G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74843741 | ||||||
| chrX:74843845
|
T | C | 3 | a0001c0001t0001g0214a0001c0001t0001g0215a0006c0006t0034g0118 | 3 | HG02717.hp1 HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-48+81038A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74843845 | ||||||
| chrX:74844202
|
C | T | 1 | a0001c0001t0032g0145 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-48+80681G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74844202 | ||||||
| chrX:74845060
|
T | C | 1 | a0001c0001t0001g0073 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-48+79823A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74845060 | ||||||
| chrX:74845126
|
A | T | 1 | a0001c0001t0002g0155 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-48+79757T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74845126 | ||||||
| chrX:74845180
|
G | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0115 | 2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-48+79703C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74845180 | ||||||
| chrX:74845508
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-48+79375G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74845508 | ||||||
| chrX:74846020
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-48+78863T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74846020 | ||||||
| chrX:74846094
|
G | T | 1 | a0001c0001t0001g0099 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-48+78789C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74846094 | ||||||
| chrX:74846118
|
C | T | 16 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(13): Show | 16 | HG01243.hp1 HG02015.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-48+78765G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74846118 | ||||||
| chrX:74846252
|
AT | A | 1 | a0001c0001t0002g0161 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-48+78630delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74846252 | ||||||
| chrX:74846769
|
A | G | 165 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(162): Show | 165 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.-48+78114T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74846769 | ||||||
| chrX:74846835
|
T | G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+78048A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74846835 | ||||||
| chrX:74846900
|
C | T | 1 | a0001c0001t0016g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-48+77983G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74846900 | ||||||
| chrX:74847310
|
G | T | 3 | a0001c0001t0001g0218a0001c0001t0006g0219a0001c0001t0006g0220 | 3 | HG02615.hp1 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-48+77573C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74847310 | ||||||
| chrX:74847472
|
C | T | 1 | a0008c0009t0002g0132 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-48+77411G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74847472 | ||||||
| chrX:74847529
|
A | G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+77354T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74847529 | ||||||
| chrX:74847584
|
C | T | 1 | a0001c0001t0002g0144 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-48+77299G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74847584 | ||||||
| chrX:74847758
|
T | C | 1 | a0001c0001t0002g0144 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-48+77125A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74847758 | ||||||
| chrX:74848156
|
C | CA | 1 | a0001c0001t0002g0174 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-48+76726dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74848156 | ||||||
| chrX:74848285
|
G | A | 15 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(12): Show | 15 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-48+76598C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74848285 | ||||||
| chrX:74848413
|
T | G | 1 | a0001c0001t0002g0176 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-48+76470A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74848413 | ||||||
| chrX:74848684
|
T | TA | 1 | a0001c0001t0001g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-48+76198dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74848684 | ||||||
| chrX:74848962
|
G | T | 6 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0148others(3): Show | 6 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.-48+75921C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74848962 | ||||||
| chrX:74849502
|
C | G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+75381G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74849502 | ||||||
| chrX:74849548
|
G | A | 1 | a0001c0001t0001g0036 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-48+75335C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74849548 | ||||||
| chrX:74849707
|
G | A | 2 | a0001c0001t0002g0169a0001c0001t0002g0181 | 2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-48+75176C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74849707 | ||||||
| chrX:74849839
|
C | T | 1 | a0001c0001t0002g0157 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-48+75044G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74849839 | ||||||
| chrX:74849974
|
T | A | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+74909A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74849974 | ||||||
| chrX:74850136
|
C | A | 1 | a0001c0001t0001g0010 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-48+74747G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74850136 | ||||||
| chrX:74850456
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-48+74427G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74850456 | ||||||
| chrX:74850557
|
C | T | 3 | a0001c0001t0001g0164a0001c0001t0001g0173a0001c0001t0021g0185 | 3 | HG00408.hp1 HG02165.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.-48+74326G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74850557 | ||||||
| chrX:74850659
|
C | A | 1 | a0001c0001t0001g0099 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-48+74224G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74850659 | ||||||
| chrX:74850686
|
C | T | 2 | a0001c0001t0002g0129a0001c0001t0002g0165 | 2 | HG01192.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.-48+74197G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74850686 | ||||||
| chrX:74850779
|
C | CCTCA | 1 | a0001c0001t0001g0215 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-48+74103_-48+7410 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74850779 | ||||||
| chrX:74850780
|
A | T | 1 | a0001c0001t0001g0215 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-48+74103T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74850780 | ||||||
| chrX:74850781
|
G | T | 1 | a0001c0001t0001g0215 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-48+74102C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74850781 | ||||||
| chrX:74850782
|
A | G | 1 | a0001c0001t0001g0215 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-48+74101T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74850782 | ||||||
| chrX:74850784
|
A | G | 1 | a0001c0001t0001g0215 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-48+74099T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74850784 | ||||||
| chrX:74851069
|
G | GA | 1 | a0001c0001t0002g0176 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-48+73813dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74851069 | ||||||
| chrX:74851086
|
T | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+73797A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74851086 | ||||||
| chrX:74851161
|
C | A | 14 | a0001c0001t0001g0099a0001c0001t0001g0102a0001c0001t0001g0106others(11): Show | 14 | HG00323.hp1 HG02257.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-48+73722G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74851161 | ||||||
| chrX:74851267
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-48+73616T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74851267 | ||||||
| chrX:74851379
|
T | G | 1 | a0001c0001t0001g0019 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-48+73504A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74851379 | ||||||
| chrX:74851523
|
G | A | 4 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0148others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+73360C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74851523 | ||||||
| chrX:74851581
|
T | C | 222 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(219): Show | 222 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.-48+73302A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74851581 | ||||||
| chrX:74851582
|
G | A | 3 | a0001c0001t0013g0003a0001c0001t0014g0213a0001c0011t0001g0209 | 3 | HG00738.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-48+73301C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74851582 | ||||||
| chrX:74851590
|
G | GA | 9 | a0001c0001t0001g0026a0001c0001t0001g0218a0001c0001t0005g0119others(6): Show | 9 | HG01884.hp1 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-48+73292dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74851590 | ||||||
| chrX:74851590
|
GA | G | 19 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(16): Show | 19 | HG01243.hp1 HG02015.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-48+73292delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74851590 | ||||||
| chrX:74851595
|
A | G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+73288T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74851595 | ||||||
| chrX:74851807
|
A | T | 1 | a0001c0001t0014g0213 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-48+73076T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74851807 | ||||||
| chrX:74851896
|
A | G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+72987T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74851896 | ||||||
| chrX:74852982
|
T | A | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+71901A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74852982 | ||||||
| chrX:74853002
|
T | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+71881A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74853002 | ||||||
| chrX:74853008
|
G | GT | 1 | a0001c0001t0001g0138 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-48+71874dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74853008 | ||||||
| chrX:74853008
|
GT | G | 5 | a0001c0001t0005g0119a0001c0001t0005g0120a0001c0001t0005g0121others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+71874delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74853008 | ||||||
| chrX:74853027
|
T | A | 6 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0148others(3): Show | 6 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.-48+71856A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74853027 | ||||||
| chrX:74853086
|
TTGTCACA others(438): Show |
T | 1 | a0001c0001t0022g0017 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-48+71352_-48+7179 others(4): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74853086 | ||||||
| chrX:74853296
|
G | C | 1 | a0001c0001t0002g0177 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-48+71587C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74853296 | ||||||
| chrX:74853402
|
T | C | 4 | a0001c0001t0001g0194a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 4 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+71481A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74853402 | ||||||
| chrX:74853445
|
C | T | 2 | a0001c0001t0001g0048a0001c0001t0001g0066 | 2 | HG02027.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.-48+71438G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74853445 | ||||||
| chrX:74853785
|
T | C | 1 | a0001c0001t0001g0216 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-48+71098A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74853785 | ||||||
| chrX:74854055
|
G | A | 15 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(12): Show | 15 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-48+70828C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74854055 | ||||||
| chrX:74854265
|
G | A | 1 | a0001c0001t0001g0013 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-48+70618C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74854265 | ||||||
| chrX:74854296
|
C | T | 3 | a0001c0001t0013g0003a0001c0001t0014g0213a0001c0011t0001g0209 | 3 | HG00738.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-48+70587G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74854296 | ||||||
| chrX:74854315
|
C | T | 116 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(113): Show | 116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-48+70568G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74854315 | ||||||
| chrX:74854435
|
A | G | 5 | a0001c0001t0002g0162a0001c0001t0002g0183a0001c0001t0002g0184others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48+70448T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74854435 | ||||||
| chrX:74854442
|
G | A | 116 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(113): Show | 116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-48+70441C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74854442 | ||||||
| chrX:74854734
|
C | A | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+70149G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74854734 | ||||||
| chrX:74854784
|
C | A | 1 | a0005c0007t0003g0016 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-48+70099G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74854784 | ||||||
| chrX:74854816
|
A | G | 5 | a0001c0001t0005g0119a0001c0001t0005g0120a0001c0001t0005g0121others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+70067T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74854816 | ||||||
| chrX:74854861
|
G | A | 5 | a0001c0001t0002g0162a0001c0001t0002g0183a0001c0001t0002g0184others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48+70022C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74854861 | ||||||
| chrX:74855057
|
G | GA | 4 | a0001c0001t0001g0066a0001c0001t0001g0069a0001c0001t0008g0105others(1): Show | 4 | HG02027.hp1 HG02922.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+69825dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74855057 | ||||||
| chrX:74855065
|
A | T | 1 | a0001c0002t0001g0049 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-48+69818T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74855065 | ||||||
| chrX:74855289
|
A | G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+69594T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74855289 | ||||||
| chrX:74855389
|
C | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+69494G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74855389 | ||||||
| chrX:74855599
|
C | A | 1 | a0001c0001t0001g0211 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-48+69284G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74855599 | ||||||
| chrX:74855774
|
T | G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+69109A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74855774 | ||||||
| chrX:74856181
|
T | C | 1 | a0001c0001t0001g0138 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-48+68702A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74856181 | ||||||
| chrX:74856218
|
T | C | 1 | a0001c0001t0024g0095 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-48+68665A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74856218 | ||||||
| chrX:74856245
|
C | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+68638G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74856245 | ||||||
| chrX:74856307
|
T | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+68576A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74856307 | ||||||
| chrX:74856519
|
C | T | 22 | a0001c0001t0001g0014a0001c0001t0001g0036a0001c0001t0001g0083others(19): Show | 22 | HG00558.hp2 HG00621.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.-48+68364G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74856519 | ||||||
| chrX:74856663
|
C | G | 1 | a0001c0001t0015g0207 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-48+68220G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74856663 | ||||||
| chrX:74856862
|
G | A | 3 | a0001c0001t0002g0166a0001c0001t0002g0174a0001c0001t0029g0172 | 3 | HG01255.hp1 HG01515.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.-48+68021C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74856862 | ||||||
| chrX:74856882
|
AC | A | 14 | a0001c0001t0001g0099a0001c0001t0001g0102a0001c0001t0001g0106others(11): Show | 14 | HG00323.hp1 HG02257.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-48+68000delG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74856882 | ||||||
| chrX:74857149
|
G | A | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+67734C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74857149 | ||||||
| chrX:74857158
|
G | A | 1 | a0002c0004t0001g0202 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-48+67725C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74857158 | ||||||
| chrX:74857212
|
C | T | 1 | a0001c0001t0016g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-48+67671G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74857212 | ||||||
| chrX:74857243
|
A | G | 16 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(13): Show | 16 | HG01243.hp1 HG02015.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-48+67640T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74857243 | ||||||
| chrX:74857970
|
G | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+66913C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74857970 | ||||||
| chrX:74858045
|
C | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+66838G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74858045 | ||||||
| chrX:74858145
|
T | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+66738A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74858145 | ||||||
| chrX:74858155
|
C | T | 1 | a0001c0001t0001g0065 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-48+66728G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74858155 | ||||||
| chrX:74858213
|
C | T | 3 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201 | 3 | HG02818.hp2 HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-48+66670G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74858213 | ||||||
| chrX:74858216
|
A | C | 1 | a0001c0001t0001g0137 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-48+66667T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74858216 | ||||||
| chrX:74858312
|
G | A | 2 | a0001c0001t0001g0222a0001c0001t0006g0098 | 2 | HG02615.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-48+66571C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74858312 | ||||||
| chrX:74858359
|
A | G | 1 | a0001c0001t0002g0157 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-48+66524T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74858359 | ||||||
| chrX:74858509
|
T | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+66374A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74858509 | ||||||
| chrX:74858517
|
C | A | 1 | a0001c0001t0001g0111 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-48+66366G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74858517 | ||||||
| chrX:74858594
|
T | A | 1 | a0001c0001t0012g0002 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-48+66289A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74858594 | ||||||
| chrX:74858615
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-48+66268G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74858615 | ||||||
| chrX:74858616
|
G | A | 15 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(12): Show | 15 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-48+66267C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74858616 | ||||||
| chrX:74858689
|
G | T | 1 | a0001c0001t0001g0103 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-48+66194C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74858689 | ||||||
| chrX:74858790
|
C | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+66093G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74858790 | ||||||
| chrX:74858885
|
TCA | T | 2 | a0001c0001t0002g0152a0001c0001t0002g0153 | 2 | HG02698.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-48+65996_-48+6599 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74858885 | ||||||
| chrX:74858971
|
A | G | 1 | a0001c0001t0001g0010 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-48+65912T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74858971 | ||||||
| chrX:74859002
|
C | T | 130 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(127): Show | 130 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.-48+65881G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74859002 | ||||||
| chrX:74859261
|
C | A | 1 | a0001c0001t0010g0190 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-48+65622G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74859261 | ||||||
| chrX:74859369
|
G | T | 1 | a0001c0001t0004g0188 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-48+65514C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74859369 | ||||||
| chrX:74859738
|
C | A | 1 | a0001c0001t0001g0070 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-48+65145G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74859738 | ||||||
| chrX:74859755
|
G | A | 6 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0198others(3): Show | 6 | HG02015.hp1 HG03491.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48+65128C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74859755 | ||||||
| chrX:74859839
|
CA | C | 1 | a0001c0001t0001g0022 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-48+65043delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74859839 | ||||||
| chrX:74859919
|
A | C | 165 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(162): Show | 165 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.-48+64964T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74859919 | ||||||
| chrX:74860201
|
G | A | 146 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(143): Show | 146 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.-48+64682C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74860201 | ||||||
| chrX:74860336
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-48+64547A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74860336 | ||||||
| chrX:74860391
|
C | G | 1 | a0001c0001t0001g0059 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-48+64492G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74860391 | ||||||
| chrX:74860642
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-48+64241G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74860642 | ||||||
| chrX:74860890
|
G | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+63993C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74860890 | ||||||
| chrX:74860989
|
G | C | 1 | a0004c0014t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-48+63894C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74860989 | ||||||
| chrX:74861077
|
C | A | 1 | a0001c0001t0004g0133 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-48+63806G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74861077 | ||||||
| chrX:74861293
|
A | G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+63590T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74861293 | ||||||
| chrX:74861890
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-48+62993G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74861890 | ||||||
| chrX:74861923
|
A | T | 3 | a0001c0001t0001g0083a0001c0001t0003g0124a0001c0001t0003g0125 | 3 | NA18983.hp1 NA18985.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-48+62960T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74861923 | ||||||
| chrX:74861966
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-48+62917A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74861966 | ||||||
| chrX:74862103
|
G | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0096 | 2 | NA18984.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-48+62780C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74862103 | ||||||
| chrX:74862115
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-48+62768T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74862115 | ||||||
| chrX:74862122
|
C | T | 1 | a0001c0001t0002g0157 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-48+62761G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74862122 | ||||||
| chrX:74862894
|
G | A | 1 | a0001c0001t0028g0006 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-48+61989C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74862894 | ||||||
| chrX:74863007
|
C | T | 1 | a0001c0002t0001g0030 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-48+61876G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74863007 | ||||||
| chrX:74863171
|
C | CA | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+61711dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74863171 | ||||||
| chrX:74863171
|
CA | C | 167 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(164): Show | 167 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.-48+61711delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74863171 | ||||||
| chrX:74863195
|
C | A | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+61688G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74863195 | ||||||
| chrX:74863421
|
C | T | 170 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(167): Show | 170 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.-48+61462G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74863421 | ||||||
| chrX:74863781
|
T | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+61102A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74863781 | ||||||
| chrX:74863856
|
T | A | 1 | a0001c0001t0010g0190 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-48+61027A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74863856 | ||||||
| chrX:74864113
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-48+60770G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74864113 | ||||||
| chrX:74864453
|
A | T | 1 | a0001c0001t0001g0013 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-48+60430T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74864453 | ||||||
| chrX:74864473
|
T | C | 1 | a0001c0001t0002g0163 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-48+60410A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74864473 | ||||||
| chrX:74864624
|
A | G | 1 | a0009c0012t0002g0141 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-48+60259T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74864624 | ||||||
| chrX:74864674
|
C | T | 4 | a0001c0001t0004g0188a0001c0001t0004g0189a0001c0001t0004g0197others(1): Show | 4 | HG01243.hp1 HG02109.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+60209G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74864674 | ||||||
| chrX:74864711
|
C | CT | 1 | a0007c0010t0001g0180 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-48+60171dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74864711 | ||||||
| chrX:74864711
|
CT | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+60171delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74864711 | ||||||
| chrX:74865361
|
C | G | 1 | a0001c0001t0004g0133 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-48+59522G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74865361 | ||||||
| chrX:74865541
|
A | G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+59342T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74865541 | ||||||
| chrX:74865604
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-48+59279C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74865604 | ||||||
| chrX:74865772
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-48+59111C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74865772 | ||||||
| chrX:74865892
|
G | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0096 | 2 | NA18984.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-48+58991C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74865892 | ||||||
| chrX:74866137
|
A | AG | 1 | a0001c0001t0001g0083 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-48+58745dupC | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74866137 | ||||||
| chrX:74866430
|
ACTTGT | A | 2 | a0001c0001t0001g0222a0001c0001t0006g0098 | 2 | HG02615.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-48+58448_-48+5845 others(9): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74866430 | ||||||
| chrX:74866452
|
CTT | C | 4 | a0001c0001t0001g0194a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 4 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+58429_-48+5843 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74866452 | ||||||
| chrX:74866463
|
G | T | 1 | a0001c0001t0002g0155 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-48+58420C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74866463 | ||||||
| chrX:74866818
|
C | T | 1 | a0001c0001t0004g0197 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-48+58065G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74866818 | ||||||
| chrX:74866991
|
A | G | 1 | a0001c0001t0001g0013 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-48+57892T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74866991 | ||||||
| chrX:74867248
|
T | C | 1 | a0001c0001t0016g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-48+57635A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74867248 | ||||||
| chrX:74867614
|
C | T | 4 | a0001c0001t0001g0053a0001c0001t0001g0058a0001c0001t0001g0077others(1): Show | 4 | HG00408.hp2 NA18967.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+57269G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74867614 | ||||||
| chrX:74868056
|
A | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+56827T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74868056 | ||||||
| chrX:74868110
|
A | G | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+56773T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74868110 | ||||||
| chrX:74868614
|
T | A | 1 | a0001c0001t0001g0134 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-48+56269A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74868614 | ||||||
| chrX:74868616
|
G | A | 12 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0110others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.-48+56267C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74868616 | ||||||
| chrX:74868686
|
T | A | 1 | a0001c0001t0025g0212 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-48+56197A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74868686 | ||||||
| chrX:74868766
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-48+56117A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74868766 | ||||||
| chrX:74868923
|
T | C | 3 | a0001c0001t0002g0127a0001c0001t0002g0128a0001c0001t0031g0126 | 3 | HG00639.hp1 HG00642.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.-48+55960A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74868923 | ||||||
| chrX:74868965
|
T | C | 2 | a0001c0001t0003g0085a0001c0001t0003g0086 | 2 | HG00673.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-48+55918A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74868965 | ||||||
| chrX:74868980
|
A | G | 1 | a0001c0001t0001g0035 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-48+55903T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74868980 | ||||||
| chrX:74869227
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-48+55656C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74869227 | ||||||
| chrX:74869320
|
T | C | 223 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(220): Show | 223 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.-48+55563A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74869320 | ||||||
| chrX:74869383
|
A | T | 3 | a0001c0001t0001g0055a0001c0001t0001g0068a0001c0001t0023g0027 | 3 | NA18965.hp1 NA19058.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.-48+55500T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74869383 | ||||||
| chrX:74869585
|
C | T | 3 | a0001c0001t0001g0053a0001c0001t0001g0058a0001c0001t0001g0077 | 3 | HG00408.hp2 NA18982.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.-48+55298G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74869585 | ||||||
| chrX:74869629
|
A | G | 148 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(145): Show | 148 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.-48+55254T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74869629 | ||||||
| chrX:74869684
|
G | A | 1 | a0001c0001t0001g0013 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-48+55199C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74869684 | ||||||
| chrX:74869958
|
G | GA | 3 | a0001c0001t0001g0218a0001c0001t0006g0219a0001c0001t0006g0220 | 3 | HG02615.hp1 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-48+54924dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74869958 | ||||||
| chrX:74870249
|
G | T | 165 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(162): Show | 165 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.-48+54634C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74870249 | ||||||
| chrX:74870358
|
C | T | 5 | a0001c0001t0005g0119a0001c0001t0005g0120a0001c0001t0005g0121others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+54525G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74870358 | ||||||
| chrX:74870997
|
A | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+53886T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74870997 | ||||||
| chrX:74871169
|
G | A | 1 | a0001c0001t0006g0220 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-48+53714C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74871169 | ||||||
| chrX:74871749
|
C | G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+53134G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74871749 | ||||||
| chrX:74871807
|
C | A | 1 | a0001c0001t0001g0038 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-48+53076G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74871807 | ||||||
| chrX:74871914
|
G | A | 7 | a0001c0001t0002g0142a0001c0001t0002g0144a0001c0001t0002g0155others(4): Show | 7 | HG01256.hp1 HG01928.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.-48+52969C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74871914 | ||||||
| chrX:74872171
|
T | TC | 1 | a0001c0001t0001g0074 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-48+52711dupG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74872171 | ||||||
| chrX:74872465
|
T | TGAA | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+52417_-48+5241 others(7): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74872465 | ||||||
| chrX:74872552
|
T | G | 12 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(9): Show | 12 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.-48+52331A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74872552 | ||||||
| chrX:74872604
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-48+52279C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74872604 | ||||||
| chrX:74872947
|
G | T | 2 | a0001c0001t0005g0122a0001c0001t0005g0123 | 2 | HG02572.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-48+51936C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74872947 | ||||||
| chrX:74872962
|
A | T | 22 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(19): Show | 22 | HG01243.hp1 HG01884.hp1 HG02015.hp1 others(19): Show |
intron_variant | MODIFIER | c.-48+51921T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74872962 | ||||||
| chrX:74872974
|
G | GT | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+51908dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74872974 | ||||||
| chrX:74872980
|
T | G | 5 | a0001c0001t0002g0162a0001c0001t0002g0183a0001c0001t0002g0184others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48+51903A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74872980 | ||||||
| chrX:74872993
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-48+51890T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74872993 | ||||||
| chrX:74873005
|
T | A | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-48+51878A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74873005 | ||||||
| chrX:74873133
|
C | CT | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+51749dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74873133 | ||||||
| chrX:74873180
|
C | T | 1 | a0001c0001t0001g0035 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-48+51703G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74873180 | ||||||
| chrX:74873398
|
T | C | 5 | a0001c0001t0002g0162a0001c0001t0002g0183a0001c0001t0002g0184others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48+51485A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74873398 | ||||||
| chrX:74873399
|
GT | G | 1 | a0001c0001t0002g0158 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-48+51483delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74873399 | ||||||
| chrX:74873406
|
T | C | 1 | a0001c0001t0002g0161 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-48+51477A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74873406 | ||||||
| chrX:74873440
|
A | G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+51443T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74873440 | ||||||
| chrX:74873452
|
C | A | 3 | a0001c0001t0001g0218a0001c0001t0006g0219a0001c0001t0006g0220 | 3 | HG02615.hp1 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-48+51431G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74873452 | ||||||
| chrX:74873452
|
C | T | 1 | a0001c0001t0001g0013 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-48+51431G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74873452 | ||||||
| chrX:74873453
|
G | A | 2 | a0001c0001t0033g0130a0006c0006t0034g0118 | 2 | HG00323.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-48+51430C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74873453 | ||||||
| chrX:74873631
|
T | G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+51252A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74873631 | ||||||
| chrX:74873772
|
T | C | 1 | a0001c0001t0002g0178 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-48+51111A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74873772 | ||||||
| chrX:74873800
|
A | G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+51083T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74873800 | ||||||
| chrX:74873947
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-48+50936C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74873947 | ||||||
| chrX:74873989
|
TG | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+50893delC | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74873989 | ||||||
| chrX:74874049
|
A | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+50834T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874049 | ||||||
| chrX:74874108
|
G | T | 1 | a0001c0001t0002g0177 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-48+50775C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874108 | ||||||
| chrX:74874110
|
G | GT | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+50772dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874110 | ||||||
| chrX:74874139
|
G | C | 1 | a0001c0001t0002g0161 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-48+50744C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874139 | ||||||
| chrX:74874173
|
G | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+50710C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874173 | ||||||
| chrX:74874209
|
C | A | 7 | a0001c0001t0002g0142a0001c0001t0002g0144a0001c0001t0002g0155others(4): Show | 7 | HG01256.hp1 HG01928.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.-48+50674G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874209 | ||||||
| chrX:74874213
|
C | G | 1 | a0001c0001t0002g0128 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-48+50670G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874213 | ||||||
| chrX:74874258
|
C | T | 1 | a0002c0004t0011g0001 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-48+50625G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874258 | ||||||
| chrX:74874310
|
T | C | 128 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(125): Show | 128 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.-48+50573A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874310 | ||||||
| chrX:74874311
|
G | A | 128 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(125): Show | 128 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.-48+50572C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874311 | ||||||
| chrX:74874414
|
A | G | 6 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0148others(3): Show | 6 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.-48+50469T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874414 | ||||||
| chrX:74874450
|
A | G | 2 | a0001c0001t0001g0059a0006c0006t0034g0118 | 2 | HG02886.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-48+50433T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874450 | ||||||
| chrX:74874473
|
T | C | 1 | a0001c0001t0001g0059 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-48+50410A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874473 | ||||||
| chrX:74874492
|
A | C | 1 | a0001c0001t0001g0059 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-48+50391T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874492 | ||||||
| chrX:74874510
|
C | T | 1 | a0001c0001t0001g0059 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-48+50373G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874510 | ||||||
| chrX:74874549
|
T | TG | 1 | a0008c0009t0002g0132 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-48+50333dupC | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874549 | ||||||
| chrX:74874601
|
G | C | 17 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(14): Show | 17 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-48+50282C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874601 | ||||||
| chrX:74874652
|
G | A | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+50231C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874652 | ||||||
| chrX:74874688
|
C | A | 1 | a0001c0001t0001g0014 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-48+50195G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874688 | ||||||
| chrX:74874688
|
C | G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+50195G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874688 | ||||||
| chrX:74874743
|
C | T | 1 | a0001c0001t0001g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-48+50140G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874743 | ||||||
| chrX:74874776
|
A | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+50107T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874776 | ||||||
| chrX:74874784
|
GCTCT | G | 2 | a0001c0001t0001g0203a0001c0001t0001g0204 | 2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-48+50095_-48+5009 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874784 | ||||||
| chrX:74874794
|
TGTCTGTT others(1): Show |
T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+50081_-48+5008 others(12): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874794 | ||||||
| chrX:74874900
|
C | CGATGGGG others(1): Show |
1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+49975_-48+4998 others(12): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874900 | ||||||
| chrX:74874900
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-48+49983G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874900 | ||||||
| chrX:74874924
|
C | T | 149 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(146): Show | 149 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.-48+49959G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874924 | ||||||
| chrX:74874978
|
A | C | 2 | a0001c0001t0001g0109a0006c0006t0034g0118 | 2 | HG02258.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-48+49905T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874978 | ||||||
| chrX:74874979
|
T | C | 2 | a0001c0001t0001g0109a0006c0006t0034g0118 | 2 | HG02258.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-48+49904A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74874979 | ||||||
| chrX:74875127
|
A | G | 1 | a0001c0005t0001g0012 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-48+49756T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74875127 | ||||||
| chrX:74875160
|
C | T | 170 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(167): Show | 170 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.-48+49723G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74875160 | ||||||
| chrX:74875258
|
GTTT | G | 11 | a0001c0001t0001g0103a0001c0001t0001g0115a0001c0001t0001g0194others(8): Show | 11 | HG01884.hp1 HG02559.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-48+49622_-48+4962 others(7): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74875258 | ||||||
| chrX:74875294
|
A | G | 1 | a0001c0001t0001g0194 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-48+49589T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74875294 | ||||||
| chrX:74875497
|
C | T | 1 | a0001c0001t0004g0133 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-48+49386G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74875497 | ||||||
| chrX:74875563
|
G | T | 2 | a0001c0001t0001g0222a0001c0001t0006g0098 | 2 | HG02615.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-48+49320C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74875563 | ||||||
| chrX:74875585
|
G | C | 5 | a0001c0001t0005g0119a0001c0001t0005g0120a0001c0001t0005g0121others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+49298C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74875585 | ||||||
| chrX:74875602
|
C | A | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+49281G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74875602 | ||||||
| chrX:74875639
|
TG | T | 1 | a0001c0001t0003g0125 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-48+49243delC | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74875639 | ||||||
| chrX:74875767
|
C | G | 1 | a0001c0001t0001g0087 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-48+49116G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74875767 | ||||||
| chrX:74875779
|
T | C | 17 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(14): Show | 17 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-48+49104A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74875779 | ||||||
| chrX:74875780
|
G | A | 17 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(14): Show | 17 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-48+49103C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74875780 | ||||||
| chrX:74875797
|
AT | A | 1 | a0001c0001t0003g0125 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-48+49085delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74875797 | ||||||
| chrX:74875841
|
T | TC | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+49041dupG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74875841 | ||||||
| chrX:74875843
|
C | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+49040G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74875843 | ||||||
| chrX:74875863
|
T | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+49020A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74875863 | ||||||
| chrX:74875863
|
T | TG | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+49019dupC | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74875863 | ||||||
| chrX:74875892
|
C | A | 1 | a0001c0001t0001g0059 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-48+48991G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74875892 | ||||||
| chrX:74875935
|
CA | C | 1 | a0001c0001t0003g0091 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-48+48947delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74875935 | ||||||
| chrX:74875961
|
A | AT | 1 | a0001c0001t0002g0170 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-48+48921dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74875961 | ||||||
| chrX:74875972
|
G | GT | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+48910dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74875972 | ||||||
| chrX:74876007
|
T | C | 1 | a0001c0001t0002g0157 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-48+48876A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876007 | ||||||
| chrX:74876029
|
T | TA | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+48853_-48+4885 others(5): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876029 | ||||||
| chrX:74876070
|
C | T | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+48813G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876070 | ||||||
| chrX:74876072
|
T | C | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+48811A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876072 | ||||||
| chrX:74876072
|
T | TTTAA | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+48810_-48+4881 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876072 | ||||||
| chrX:74876119
|
T | TG | 1 | a0001c0001t0003g0125 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-48+48763dupC | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876119 | ||||||
| chrX:74876144
|
C | A | 1 | a0001c0001t0001g0059 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-48+48739G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876144 | ||||||
| chrX:74876185
|
G | GT | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+48697dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876185 | ||||||
| chrX:74876199
|
C | T | 2 | a0001c0001t0002g0183a0001c0001t0002g0184 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-48+48684G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876199 | ||||||
| chrX:74876228
|
C | A | 2 | a0001c0001t0001g0211a0001c0001t0017g0208 | 2 | HG01884.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-48+48655G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876228 | ||||||
| chrX:74876231
|
C | A | 2 | a0001c0001t0001g0211a0001c0001t0017g0208 | 2 | HG01884.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-48+48652G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876231 | ||||||
| chrX:74876236
|
G | A | 2 | a0001c0001t0001g0211a0001c0001t0017g0208 | 2 | HG01884.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-48+48647C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876236 | ||||||
| chrX:74876241
|
A | G | 2 | a0001c0001t0001g0211a0001c0001t0017g0208 | 2 | HG01884.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-48+48642T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876241 | ||||||
| chrX:74876246
|
G | T | 2 | a0001c0001t0001g0211a0001c0001t0017g0208 | 2 | HG01884.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-48+48637C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876246 | ||||||
| chrX:74876260
|
T | C | 3 | a0001c0001t0001g0218a0001c0001t0006g0219a0001c0001t0006g0220 | 3 | HG02615.hp1 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-48+48623A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876260 | ||||||
| chrX:74876275
|
C | T | 2 | a0001c0001t0001g0211a0001c0001t0017g0208 | 2 | HG01884.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-48+48608G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876275 | ||||||
| chrX:74876284
|
A | C | 2 | a0001c0001t0001g0211a0001c0001t0017g0208 | 2 | HG01884.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-48+48599T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876284 | ||||||
| chrX:74876287
|
G | A | 2 | a0001c0001t0001g0211a0001c0001t0017g0208 | 2 | HG01884.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-48+48596C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876287 | ||||||
| chrX:74876288
|
T | C | 1 | a0007c0010t0001g0180 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-48+48595A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876288 | ||||||
| chrX:74876356
|
C | T | 1 | a0001c0001t0002g0167 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-48+48527G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876356 | ||||||
| chrX:74876405
|
T | C | 4 | a0001c0001t0001g0194a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 4 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+48478A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876405 | ||||||
| chrX:74876449
|
G | GA | 4 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0100others(1): Show | 4 | HG01168.hp2 HG01169.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+48433dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876449 | ||||||
| chrX:74876507
|
T | C | 1 | a0001c0001t0001g0194 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-48+48376A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876507 | ||||||
| chrX:74876508
|
C | T | 2 | a0001c0001t0001g0084a0001c0001t0001g0194 | 2 | HG02165.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-48+48375G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876508 | ||||||
| chrX:74876519
|
G | C | 1 | a0001c0001t0001g0194 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-48+48364C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876519 | ||||||
| chrX:74876536
|
T | TG | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+48346dupC | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876536 | ||||||
| chrX:74876562
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-48+48321G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876562 | ||||||
| chrX:74876567
|
A | G | 1 | a0001c0001t0003g0093 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-48+48316T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876567 | ||||||
| chrX:74876568
|
T | C | 1 | a0001c0001t0001g0215 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-48+48315A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876568 | ||||||
| chrX:74876597
|
A | C | 2 | a0001c0001t0002g0183a0001c0001t0002g0184 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-48+48286T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876597 | ||||||
| chrX:74876604
|
CA | C | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+48278delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876604 | ||||||
| chrX:74876609
|
T | C | 1 | a0001c0001t0001g0020 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-48+48274A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876609 | ||||||
| chrX:74876612
|
A | T | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+48271T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876612 | ||||||
| chrX:74876614
|
G | GT | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+48268dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876614 | ||||||
| chrX:74876643
|
A | G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+48240T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876643 | ||||||
| chrX:74876662
|
A | G | 1 | a0001c0001t0001g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-48+48221T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876662 | ||||||
| chrX:74876727
|
TC | T | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+48155delG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876727 | ||||||
| chrX:74876758
|
T | TC | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+48124dupG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876758 | ||||||
| chrX:74876789
|
T | TG | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+48093_-48+4809 others(5): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876789 | ||||||
| chrX:74876816
|
C | T | 1 | a0001c0001t0004g0188 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-48+48067G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876816 | ||||||
| chrX:74876917
|
CA | C | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+47965delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876917 | ||||||
| chrX:74876991
|
AT | A | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+47891delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74876991 | ||||||
| chrX:74877004
|
AT | A | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+47878delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877004 | ||||||
| chrX:74877093
|
T | TC | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+47789dupG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877093 | ||||||
| chrX:74877153
|
C | T | 2 | a0001c0001t0018g0090a0001c0001t0019g0094 | 2 | NA18747.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.-48+47730G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877153 | ||||||
| chrX:74877175
|
AG | A | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+47707delC | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877175 | ||||||
| chrX:74877208
|
A | AT | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+47674dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877208 | ||||||
| chrX:74877274
|
A | AT | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+47608dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877274 | ||||||
| chrX:74877318
|
C | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+47565G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877318 | ||||||
| chrX:74877325
|
T | A | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+47558A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877325 | ||||||
| chrX:74877335
|
C | T | 1 | a0002c0004t0011g0001 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-48+47548G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877335 | ||||||
| chrX:74877338
|
G | C | 3 | a0001c0001t0001g0218a0001c0001t0006g0219a0001c0001t0006g0220 | 3 | HG02615.hp1 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-48+47545C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877338 | ||||||
| chrX:74877361
|
G | T | 5 | a0001c0001t0001g0034a0001c0001t0001g0065a0001c0001t0001g0069others(2): Show | 5 | HG02074.hp1 HG02135.hp1 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+47522C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877361 | ||||||
| chrX:74877374
|
TG | T | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+47508delC | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877374 | ||||||
| chrX:74877434
|
A | C | 18 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(15): Show | 18 | HG01243.hp1 HG02015.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.-48+47449T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877434 | ||||||
| chrX:74877483
|
C | T | 1 | a0001c0001t0004g0188 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-48+47400G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877483 | ||||||
| chrX:74877485
|
C | A | 1 | a0001c0001t0002g0150 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-48+47398G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877485 | ||||||
| chrX:74877504
|
G | A | 1 | a0001c0001t0001g0138 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-48+47379C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877504 | ||||||
| chrX:74877608
|
C | CGTCA | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+47274_-48+4727 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877608 | ||||||
| chrX:74877611
|
G | C | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+47272C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877611 | ||||||
| chrX:74877613
|
C | T | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+47270G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877613 | ||||||
| chrX:74877614
|
A | C | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+47269T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877614 | ||||||
| chrX:74877779
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-48+47104C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877779 | ||||||
| chrX:74877784
|
G | A | 1 | a0001c0001t0008g0105 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-48+47099C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877784 | ||||||
| chrX:74877801
|
C | A | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+47082G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877801 | ||||||
| chrX:74877810
|
C | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+47073G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877810 | ||||||
| chrX:74877811
|
G | A | 1 | a0002c0004t0011g0001 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-48+47072C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877811 | ||||||
| chrX:74877908
|
G | T | 17 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(14): Show | 17 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-48+46975C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877908 | ||||||
| chrX:74877953
|
G | A | 1 | a0002c0004t0011g0001 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-48+46930C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74877953 | ||||||
| chrX:74878103
|
TC | T | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+46779delG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74878103 | ||||||
| chrX:74878105
|
C | A | 4 | a0001c0001t0001g0194a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 4 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+46778G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74878105 | ||||||
| chrX:74878141
|
T | A | 1 | a0001c0001t0020g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-48+46742A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74878141 | ||||||
| chrX:74878243
|
C | T | 1 | a0001c0001t0010g0190 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-48+46640G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74878243 | ||||||
| chrX:74878248
|
G | GT | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+46634dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74878248 | ||||||
| chrX:74878280
|
T | TG | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+46602dupC | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74878280 | ||||||
| chrX:74878284
|
T | TC | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+46598dupG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74878284 | ||||||
| chrX:74878308
|
A | AG | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+46574dupC | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74878308 | ||||||
| chrX:74878391
|
A | G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+46492T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74878391 | ||||||
| chrX:74878397
|
TCAGA | T | 8 | a0001c0001t0001g0026a0001c0001t0001g0032a0001c0001t0001g0033others(5): Show | 8 | NA18945.hp1 NA18953.hp1 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.-48+46482_-48+4648 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74878397 | ||||||
| chrX:74878418
|
G | T | 3 | a0001c0001t0001g0218a0001c0001t0006g0219a0001c0001t0006g0220 | 3 | HG02615.hp1 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-48+46465C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74878418 | ||||||
| chrX:74878574
|
GC | G | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+46308delG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74878574 | ||||||
| chrX:74878637
|
C | CG | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+46245dupC | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74878637 | ||||||
| chrX:74878638
|
G | A | 1 | a0001c0001t0001g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-48+46245C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74878638 | ||||||
| chrX:74878643
|
TC | T | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+46239delG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74878643 | ||||||
| chrX:74878705
|
A | G | 4 | a0001c0001t0004g0188a0001c0001t0004g0189a0001c0001t0004g0197others(1): Show | 4 | HG01243.hp1 HG02109.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+46178T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74878705 | ||||||
| chrX:74878768
|
A | AC | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+46114dupG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74878768 | ||||||
| chrX:74878835
|
GC | G | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+46047delG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74878835 | ||||||
| chrX:74878862
|
C | CA | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+46020_-48+4602 others(5): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74878862 | ||||||
| chrX:74878863
|
G | A | 1 | a0001c0005t0001g0012 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-48+46020C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74878863 | ||||||
| chrX:74878871
|
T | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+46012A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74878871 | ||||||
| chrX:74878879
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-48+46004C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74878879 | ||||||
| chrX:74878913
|
G | A | 1 | a0001c0001t0001g0022 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-48+45970C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74878913 | ||||||
| chrX:74878929
|
A | AT | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+45953dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74878929 | ||||||
| chrX:74878944
|
G | A | 12 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0110others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.-48+45939C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74878944 | ||||||
| chrX:74878994
|
C | CAG | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+45888_-48+4588 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74878994 | ||||||
| chrX:74878995
|
G | A | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+45888C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74878995 | ||||||
| chrX:74879007
|
T | C | 3 | a0001c0001t0001g0218a0001c0001t0006g0219a0001c0001t0006g0220 | 3 | HG02615.hp1 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-48+45876A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74879007 | ||||||
| chrX:74879023
|
T | A | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+45860A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74879023 | ||||||
| chrX:74879024
|
T | C | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+45859A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74879024 | ||||||
| chrX:74879025
|
T | A | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+45858A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74879025 | ||||||
| chrX:74879026
|
T | C | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+45857A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74879026 | ||||||
| chrX:74879029
|
T | G | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+45854A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74879029 | ||||||
| chrX:74879030
|
C | A | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+45853G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74879030 | ||||||
| chrX:74879031
|
T | TCGCGTG | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+45851_-48+4585 others(10): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74879031 | ||||||
| chrX:74879053
|
C | G | 1 | a0002c0004t0011g0001 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-48+45830G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74879053 | ||||||
| chrX:74879222
|
G | A | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+45661C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74879222 | ||||||
| chrX:74879283
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-48+45600A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74879283 | ||||||
| chrX:74879490
|
A | G | 17 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(14): Show | 17 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-48+45393T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74879490 | ||||||
| chrX:74879493
|
G | A | 4 | a0001c0001t0001g0164a0001c0001t0001g0173a0001c0001t0021g0185others(1): Show | 4 | HG00408.hp1 HG02165.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+45390C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74879493 | ||||||
| chrX:74879494
|
G | A | 4 | a0001c0001t0001g0164a0001c0001t0001g0173a0001c0001t0021g0185others(1): Show | 4 | HG00408.hp1 HG02165.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+45389C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74879494 | ||||||
| chrX:74879628
|
C | G | 1 | a0001c0001t0021g0185 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-48+45255G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74879628 | ||||||
| chrX:74879816
|
T | C | 17 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(14): Show | 17 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-48+45067A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74879816 | ||||||
| chrX:74879912
|
T | C | 2 | a0001c0001t0001g0216a0002c0004t0001g0202 | 2 | HG02109.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-48+44971A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74879912 | ||||||
| chrX:74879932
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-48+44951C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74879932 | ||||||
| chrX:74879960
|
AC | A | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+44922delG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74879960 | ||||||
| chrX:74880001
|
C | T | 1 | a0001c0013t0001g0143 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-48+44882G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74880001 | ||||||
| chrX:74880005
|
T | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+44878A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74880005 | ||||||
| chrX:74880017
|
A | G | 1 | a0007c0010t0001g0180 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-48+44866T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74880017 | ||||||
| chrX:74880220
|
A | AC | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+44662dupG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74880220 | ||||||
| chrX:74880334
|
G | A | 223 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(220): Show | 223 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.-48+44549C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74880334 | ||||||
| chrX:74880397
|
G | A | 1 | a0001c0001t0006g0220 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-48+44486C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74880397 | ||||||
| chrX:74880629
|
T | C | 16 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(13): Show | 16 | HG01243.hp1 HG02015.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-48+44254A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74880629 | ||||||
| chrX:74880754
|
A | G | 148 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(145): Show | 148 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.-48+44129T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74880754 | ||||||
| chrX:74880942
|
A | G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+43941T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74880942 | ||||||
| chrX:74881050
|
G | A | 1 | a0001c0011t0001g0209 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-48+43833C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74881050 | ||||||
| chrX:74881058
|
C | T | 16 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(13): Show | 16 | HG01243.hp1 HG02015.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-48+43825G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74881058 | ||||||
| chrX:74881232
|
C | T | 1 | a0001c0002t0001g0030 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-48+43651G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74881232 | ||||||
| chrX:74881369
|
A | AAC | 1 | a0001c0001t0001g0210 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-48+43512_-48+4351 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74881369 | ||||||
| chrX:74881392
|
G | GCA | 43 | a0001c0001t0001g0164a0001c0001t0001g0173a0001c0001t0001g0199others(40): Show | 43 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(40): Show |
intron_variant | MODIFIER | c.-48+43489_-48+4349 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74881392 | ||||||
| chrX:74881392
|
G | GCACA | 9 | a0001c0001t0001g0200a0001c0001t0001g0211a0001c0001t0002g0128others(6): Show | 9 | HG00639.hp1 HG01884.hp2 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.-48+43487_-48+4349 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74881392 | ||||||
| chrX:74881392
|
G | GCACACA | 7 | a0001c0001t0001g0194a0001c0001t0001g0204a0001c0001t0001g0218others(4): Show | 7 | HG01069.hp1 HG01071.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.-48+43485_-48+4349 others(10): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74881392 | ||||||
| chrX:74881392
|
G | GCACACAC others(1): Show |
5 | a0001c0001t0001g0203a0001c0001t0001g0215a0001c0001t0006g0220others(2): Show | 5 | HG02717.hp1 HG02896.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48+43483_-48+4349 others(12): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74881392 | ||||||
| chrX:74881392
|
G | GCACACAC others(3): Show |
9 | a0001c0001t0001g0138a0001c0001t0001g0195a0001c0001t0001g0196others(6): Show | 9 | HG02109.hp1 HG02273.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-48+43481_-48+4349 others(14): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74881392 | ||||||
| chrX:74881392
|
G | GCACACAC others(5): Show |
28 | a0001c0001t0001g0103a0001c0001t0001g0134a0001c0001t0001g0137others(25): Show | 28 | HG00738.hp1 HG01081.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.-48+43479_-48+4349 others(16): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74881392 | ||||||
| chrX:74881392
|
G | GCACACAC others(7): Show |
3 | a0001c0001t0001g0115a0001c0001t0015g0207a0002c0004t0001g0202 | 3 | HG00735.hp2 HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-48+43477_-48+4349 others(18): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74881392 | ||||||
| chrX:74881419
|
CACACAG | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0092 | 3 | HG01109.hp1 NA18988.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-48+43458_-48+4346 others(10): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74881419 | ||||||
| chrX:74881421
|
CACAG | C | 105 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0014others(102): Show | 105 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.-48+43458_-48+4346 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74881421 | ||||||
| chrX:74881423
|
CAG | C | 8 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0046others(5): Show | 8 | HG01952.hp1 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-48+43458_-48+4345 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74881423 | ||||||
| chrX:74881425
|
G | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+43458C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74881425 | ||||||
| chrX:74881611
|
T | TCCTCTAC others(67): Show |
120 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(117): Show | 120 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.-48+43271_-48+4327 others(78): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74881611 | ||||||
| chrX:74881611
|
T | TCCTCTAC others(67): Show |
1 | a0001c0005t0001g0011 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-48+43271_-48+4327 others(78): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74881611 | ||||||
| chrX:74881676
|
T | C | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-48+43207A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74881676 | ||||||
| chrX:74881872
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-48+43011G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74881872 | ||||||
| chrX:74882134
|
A | G | 116 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(113): Show | 116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-48+42749T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882134 | ||||||
| chrX:74882221
|
G | A | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+42662C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882221 | ||||||
| chrX:74882232
|
T | TG | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+42650dupC | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882232 | ||||||
| chrX:74882244
|
G | A | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+42639C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882244 | ||||||
| chrX:74882247
|
T | C | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+42636A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882247 | ||||||
| chrX:74882249
|
T | A | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+42634A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882249 | ||||||
| chrX:74882250
|
C | G | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+42633G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882250 | ||||||
| chrX:74882251
|
C | A | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+42632G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882251 | ||||||
| chrX:74882252
|
A | T | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+42631T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882252 | ||||||
| chrX:74882253
|
A | C | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+42630T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882253 | ||||||
| chrX:74882254
|
C | G | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+42629G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882254 | ||||||
| chrX:74882255
|
T | C | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+42628A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882255 | ||||||
| chrX:74882257
|
A | T | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+42626T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882257 | ||||||
| chrX:74882259
|
G | T | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+42624C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882259 | ||||||
| chrX:74882331
|
G | A | 6 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0148others(3): Show | 6 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.-48+42552C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882331 | ||||||
| chrX:74882342
|
T | G | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+42541A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882342 | ||||||
| chrX:74882360
|
C | T | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-48+42523G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882360 | ||||||
| chrX:74882405
|
A | AG | 1 | a0001c0001t0002g0175 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-48+42477dupC | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882405 | ||||||
| chrX:74882415
|
G | A | 5 | a0001c0002t0001g0030a0001c0002t0001g0031a0001c0002t0001g0049others(2): Show | 5 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+42468C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882415 | ||||||
| chrX:74882549
|
C | G | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+42334G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882549 | ||||||
| chrX:74882595
|
G | C | 5 | a0001c0002t0001g0030a0001c0002t0001g0031a0001c0002t0001g0049others(2): Show | 5 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+42288C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882595 | ||||||
| chrX:74882636
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-48+42247G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882636 | ||||||
| chrX:74882890
|
G | GC | 1 | a0001c0001t0001g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-48+41992dupG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882890 | ||||||
| chrX:74882996
|
G | A | 116 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(113): Show | 116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-48+41887C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74882996 | ||||||
| chrX:74883109
|
CA | C | 1 | a0001c0001t0001g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-48+41773delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74883109 | ||||||
| chrX:74883142
|
CT | C | 1 | a0001c0001t0033g0130 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-48+41740delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74883142 | ||||||
| chrX:74883194
|
G | GA | 1 | a0001c0001t0001g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-48+41688dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74883194 | ||||||
| chrX:74883215
|
C | G | 5 | a0001c0002t0001g0030a0001c0002t0001g0031a0001c0002t0001g0049others(2): Show | 5 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+41668G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74883215 | ||||||
| chrX:74883216
|
C | T | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+41667G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74883216 | ||||||
| chrX:74883218
|
G | GA | 1 | a0001c0001t0001g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-48+41664dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74883218 | ||||||
| chrX:74883225
|
TA | T | 1 | a0001c0001t0001g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-48+41657delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74883225 | ||||||
| chrX:74883278
|
C | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0040 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-48+41605G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74883278 | ||||||
| chrX:74883309
|
G | T | 1 | a0001c0001t0001g0015 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-48+41574C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74883309 | ||||||
| chrX:74883347
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-48+41536G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74883347 | ||||||
| chrX:74883358
|
A | T | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+41525T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74883358 | ||||||
| chrX:74883363
|
G | C | 1 | a0001c0001t0001g0010 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-48+41520C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74883363 | ||||||
| chrX:74883444
|
A | G | 7 | a0001c0001t0001g0103a0001c0001t0001g0115a0001c0001t0001g0194others(4): Show | 7 | HG02559.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-48+41439T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74883444 | ||||||
| chrX:74883573
|
A | C | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+41310T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74883573 | ||||||
| chrX:74883663
|
C | T | 1 | a0001c0001t0003g0097 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-48+41220G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74883663 | ||||||
| chrX:74883790
|
A | AG | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+41092dupC | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74883790 | ||||||
| chrX:74883868
|
AG | A | 1 | a0001c0001t0001g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-48+41014delC | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74883868 | ||||||
| chrX:74883870
|
G | GA | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+41012dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74883870 | ||||||
| chrX:74883971
|
AAG | A | 1 | a0001c0001t0001g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-48+40910_-48+4091 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74883971 | ||||||
| chrX:74884030
|
C | T | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+40853G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74884030 | ||||||
| chrX:74884109
|
A | C | 1 | a0001c0001t0016g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-48+40774T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74884109 | ||||||
| chrX:74884188
|
C | A | 3 | a0001c0001t0001g0218a0001c0001t0006g0219a0001c0001t0006g0220 | 3 | HG02615.hp1 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-48+40695G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74884188 | ||||||
| chrX:74884305
|
TA | T | 1 | a0001c0001t0001g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-48+40577delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74884305 | ||||||
| chrX:74884347
|
T | C | 3 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0002g0186 | 3 | HG02145.hp1 HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-48+40536A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74884347 | ||||||
| chrX:74884409
|
T | G | 1 | a0001c0001t0001g0009 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-48+40474A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74884409 | ||||||
| chrX:74884540
|
A | AG | 1 | a0001c0001t0001g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-48+40342dupC | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74884540 | ||||||
| chrX:74884658
|
G | C | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+40225C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74884658 | ||||||
| chrX:74884679
|
TC | T | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+40203delG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74884679 | ||||||
| chrX:74884865
|
AC | A | 1 | a0001c0001t0001g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-48+40017delG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74884865 | ||||||
| chrX:74884891
|
TG | T | 1 | a0001c0001t0001g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-48+39991delC | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74884891 | ||||||
| chrX:74884928
|
G | C | 1 | a0001c0001t0001g0013 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-48+39955C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74884928 | ||||||
| chrX:74884976
|
C | G | 6 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0198others(3): Show | 6 | HG02015.hp1 HG03491.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48+39907G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74884976 | ||||||
| chrX:74885152
|
T | TA | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+39730dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74885152 | ||||||
| chrX:74885324
|
C | CA | 1 | a0001c0001t0001g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+39558dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74885324 | ||||||
| chrX:74885375
|
A | T | 1 | a0001c0001t0001g0010 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-48+39508T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74885375 | ||||||
| chrX:74885394
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-48+39489G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74885394 | ||||||
| chrX:74885395
|
G | A | 114 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0013others(111): Show | 114 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.-48+39488C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74885395 | ||||||
| chrX:74885477
|
C | T | 1 | a0001c0001t0002g0161 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-48+39406G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74885477 | ||||||
| chrX:74885495
|
A | G | 1 | a0001c0001t0001g0092 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-48+39388T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74885495 | ||||||
| chrX:74885524
|
C | T | 1 | a0001c0001t0002g0175 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-48+39359G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74885524 | ||||||
| chrX:74885588
|
C | A | 2 | a0001c0001t0002g0163a0001c0001t0002g0177 | 2 | HG01433.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-48+39295G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74885588 | ||||||
| chrX:74885603
|
G | C | 116 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(113): Show | 116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-48+39280C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74885603 | ||||||
| chrX:74885668
|
C | CA | 1 | a0001c0001t0001g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-48+39214dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74885668 | ||||||
| chrX:74885729
|
G | A | 17 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(14): Show | 17 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-48+39154C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74885729 | ||||||
| chrX:74885785
|
C | T | 4 | a0001c0001t0001g0194a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 4 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+39098G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74885785 | ||||||
| chrX:74885808
|
A | G | 149 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(146): Show | 149 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.-48+39075T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74885808 | ||||||
| chrX:74885840
|
A | AC | 1 | a0001c0001t0001g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-48+39042_-48+3904 others(5): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74885840 | ||||||
| chrX:74885925
|
C | CA | 1 | a0001c0001t0001g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-48+38957dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74885925 | ||||||
| chrX:74885972
|
TG | T | 1 | a0001c0001t0001g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-48+38910delC | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74885972 | ||||||
| chrX:74886020
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-48+38863C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74886020 | ||||||
| chrX:74886054
|
G | A | 1 | a0001c0001t0002g0191 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-48+38829C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74886054 | ||||||
| chrX:74886100
|
C | A | 1 | a0002c0004t0001g0202 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-48+38783G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74886100 | ||||||
| chrX:74886101
|
T | C | 1 | a0002c0004t0001g0202 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-48+38782A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74886101 | ||||||
| chrX:74886114
|
A | T | 1 | a0002c0004t0001g0202 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-48+38769T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74886114 | ||||||
| chrX:74886142
|
C | T | 2 | a0001c0001t0002g0191a0001c0001t0002g0192 | 2 | HG03688.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-48+38741G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74886142 | ||||||
| chrX:74886203
|
A | G | 1 | a0001c0001t0002g0179 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-48+38680T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74886203 | ||||||
| chrX:74886204
|
C | CA | 1 | a0001c0001t0001g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-48+38678dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74886204 | ||||||
| chrX:74886208
|
A | G | 1 | a0001c0001t0002g0179 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-48+38675T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74886208 | ||||||
| chrX:74886348
|
G | A | 1 | a0001c0001t0002g0161 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-48+38535C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74886348 | ||||||
| chrX:74886382
|
T | C | 116 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(113): Show | 116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-48+38501A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74886382 | ||||||
| chrX:74886503
|
A | C | 2 | a0001c0001t0001g0221a0001c0008t0001g0029 | 2 | HG01258.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.-48+38380T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74886503 | ||||||
| chrX:74886537
|
A | C | 4 | a0001c0001t0001g0194a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 4 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+38346T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74886537 | ||||||
| chrX:74886566
|
GA | G | 1 | a0001c0001t0001g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-48+38316delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74886566 | ||||||
| chrX:74886813
|
T | G | 115 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(112): Show | 115 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.-48+38070A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74886813 | ||||||
| chrX:74886832
|
A | G | 142 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(139): Show | 142 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.-48+38051T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74886832 | ||||||
| chrX:74886837
|
A | G | 26 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(23): Show | 26 | HG00735.hp2 HG00738.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.-48+38046T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74886837 | ||||||
| chrX:74886881
|
G | A | 17 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(14): Show | 17 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-48+38002C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74886881 | ||||||
| chrX:74886997
|
G | A | 1 | a0001c0001t0002g0178 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-48+37886C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74886997 | ||||||
| chrX:74887001
|
G | C | 1 | a0001c0001t0002g0178 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-48+37882C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887001 | ||||||
| chrX:74887022
|
CA | C | 1 | a0001c0001t0001g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-48+37860delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887022 | ||||||
| chrX:74887026
|
G | C | 4 | a0001c0001t0004g0188a0001c0001t0004g0189a0001c0001t0004g0197others(1): Show | 4 | HG01243.hp1 HG02109.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+37857C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887026 | ||||||
| chrX:74887080
|
A | G | 1 | a0001c0001t0002g0158 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-48+37803T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887080 | ||||||
| chrX:74887096
|
G | T | 1 | a0001c0001t0002g0158 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-48+37787C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887096 | ||||||
| chrX:74887133
|
T | A | 1 | a0001c0001t0002g0193 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-48+37750A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887133 | ||||||
| chrX:74887147
|
A | T | 1 | a0002c0004t0011g0001 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-48+37736T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887147 | ||||||
| chrX:74887187
|
C | G | 17 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(14): Show | 17 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-48+37696G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887187 | ||||||
| chrX:74887205
|
A | C | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+37678T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887205 | ||||||
| chrX:74887255
|
C | CG | 1 | a0001c0001t0001g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-48+37627dupC | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887255 | ||||||
| chrX:74887278
|
G | A | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+37605C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887278 | ||||||
| chrX:74887285
|
C | A | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+37598G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887285 | ||||||
| chrX:74887311
|
A | C | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-48+37572T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887311 | ||||||
| chrX:74887371
|
G | A | 1 | a0001c0001t0003g0093 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-48+37512C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887371 | ||||||
| chrX:74887400
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-48+37483T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887400 | ||||||
| chrX:74887464
|
A | AC | 1 | a0001c0001t0001g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-48+37418dupG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887464 | ||||||
| chrX:74887482
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-48+37401G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887482 | ||||||
| chrX:74887489
|
T | C | 2 | a0001c0001t0003g0085a0001c0001t0003g0086 | 2 | HG00673.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-48+37394A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887489 | ||||||
| chrX:74887492
|
T | G | 3 | a0001c0001t0001g0070a0001c0001t0003g0085a0001c0001t0003g0086 | 3 | HG00673.hp1 NA18943.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-48+37391A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887492 | ||||||
| chrX:74887562
|
G | C | 1 | a0001c0001t0002g0161 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-48+37321C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887562 | ||||||
| chrX:74887582
|
C | G | 12 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0110others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.-48+37301G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887582 | ||||||
| chrX:74887691
|
T | C | 1 | a0001c0001t0001g0045 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-48+37192A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887691 | ||||||
| chrX:74887904
|
C | CAACA | 1 | a0001c0001t0001g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-48+36975_-48+3697 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887904 | ||||||
| chrX:74887929
|
A | C | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+36954T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74887929 | ||||||
| chrX:74888039
|
A | T | 1 | a0001c0001t0007g0005 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-48+36844T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74888039 | ||||||
| chrX:74888144
|
T | TG | 1 | a0001c0001t0001g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-48+36738dupC | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74888144 | ||||||
| chrX:74888254
|
C | T | 2 | a0001c0001t0001g0203a0001c0001t0001g0204 | 2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-48+36629G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74888254 | ||||||
| chrX:74888310
|
CA | C | 2 | a0001c0001t0001g0216a0002c0004t0001g0202 | 2 | HG02109.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-48+36572delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74888310 | ||||||
| chrX:74888314
|
A | C | 125 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(122): Show | 125 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.-48+36569T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74888314 | ||||||
| chrX:74888383
|
TC | T | 1 | a0001c0001t0001g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-48+36499delG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74888383 | ||||||
| chrX:74888410
|
G | GA | 1 | a0001c0001t0001g0046 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-48+36472dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74888410 | ||||||
| chrX:74888522
|
TCA | T | 1 | a0001c0001t0001g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-48+36359_-48+3636 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74888522 | ||||||
| chrX:74888561
|
A | G | 1 | a0001c0001t0001g0092 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-48+36322T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74888561 | ||||||
| chrX:74888647
|
A | C | 2 | a0001c0005t0001g0011a0001c0005t0001g0012 | 2 | HG01975.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.-48+36236T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74888647 | ||||||
| chrX:74888705
|
AAAAC | A | 121 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(118): Show | 121 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.-48+36174_-48+3617 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74888705 | ||||||
| chrX:74888706
|
AAAC | A | 1 | a0001c0001t0001g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-48+36174_-48+3617 others(7): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74888706 | ||||||
| chrX:74888795
|
C | CT | 1 | a0001c0001t0001g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-48+36087dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74888795 | ||||||
| chrX:74888826
|
TC | T | 1 | a0001c0001t0001g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-48+36056delG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74888826 | ||||||
| chrX:74889260
|
G | GA | 1 | a0001c0001t0001g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-48+35622dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74889260 | ||||||
| chrX:74889281
|
GA | G | 1 | a0001c0001t0001g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-48+35601delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74889281 | ||||||
| chrX:74889292
|
A | G | 5 | a0001c0001t0005g0119a0001c0001t0005g0120a0001c0001t0005g0121others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+35591T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74889292 | ||||||
| chrX:74889590
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-48+35293C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74889590 | ||||||
| chrX:74889694
|
A | AAG | 142 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(139): Show | 142 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.-48+35187_-48+3518 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74889694 | ||||||
| chrX:74889767
|
G | GT | 1 | a0001c0001t0001g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-48+35115dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74889767 | ||||||
| chrX:74889895
|
T | TTTC | 1 | a0001c0001t0001g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-48+34985_-48+3498 others(7): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74889895 | ||||||
| chrX:74889895
|
TTTC | T | 4 | a0001c0001t0001g0218a0001c0001t0002g0176a0001c0001t0006g0219others(1): Show | 4 | HG01070.hp1 HG02615.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+34985_-48+3498 others(7): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74889895 | ||||||
| chrX:74889952
|
G | GTC | 1 | a0001c0013t0001g0143 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-48+34929_-48+3493 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74889952 | ||||||
| chrX:74889952
|
G | GTCTC | 1 | a0001c0001t0032g0145 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-48+34927_-48+3493 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74889952 | ||||||
| chrX:74889952
|
GTC | G | 10 | a0001c0001t0001g0047a0001c0001t0001g0060a0001c0001t0001g0078others(7): Show | 10 | HG01884.hp1 HG02145.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-48+34929_-48+3493 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74889952 | ||||||
| chrX:74889952
|
GTCTC | G | 114 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(111): Show | 114 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.-48+34927_-48+3493 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74889952 | ||||||
| chrX:74889952
|
GTCTCTCT others(1): Show |
G | 17 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(14): Show | 17 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-48+34923_-48+3493 others(12): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74889952 | ||||||
| chrX:74890009
|
CCT | C | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+34872_-48+3487 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74890009 | ||||||
| chrX:74890009
|
CCTCTCT | C | 1 | a0001c0001t0020g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-48+34868_-48+3487 others(10): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74890009 | ||||||
| chrX:74890256
|
A | C | 1 | a0001c0001t0001g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-48+34627T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74890256 | ||||||
| chrX:74890264
|
GT | G | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+34618delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74890264 | ||||||
| chrX:74890495
|
T | A | 1 | a0001c0001t0004g0197 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-48+34388A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74890495 | ||||||
| chrX:74890596
|
T | A | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+34287A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74890596 | ||||||
| chrX:74890801
|
T | G | 17 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(14): Show | 17 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-48+34082A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74890801 | ||||||
| chrX:74891074
|
AT | A | 1 | a0001c0001t0001g0069 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-48+33808delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74891074 | ||||||
| chrX:74891170
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-48+33713G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74891170 | ||||||
| chrX:74891193
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-48+33690C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74891193 | ||||||
| chrX:74891316
|
G | GT | 1 | a0001c0001t0002g0175 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-48+33566dupA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74891316 | ||||||
| chrX:74891316
|
GT | G | 125 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(122): Show | 125 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.-48+33566delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74891316 | ||||||
| chrX:74891316
|
GTT | G | 2 | a0001c0001t0001g0101a0001c0001t0001g0205 | 2 | HG02976.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-48+33565_-48+3356 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74891316 | ||||||
| chrX:74891525
|
G | T | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+33358C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74891525 | ||||||
| chrX:74891778
|
A | T | 1 | a0001c0001t0001g0070 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-48+33105T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74891778 | ||||||
| chrX:74892346
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-48+32537G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74892346 | ||||||
| chrX:74892612
|
T | A | 1 | a0001c0001t0001g0080 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-48+32271A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74892612 | ||||||
| chrX:74892816
|
A | G | 2 | a0001c0001t0001g0211a0001c0001t0017g0208 | 2 | HG01884.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-48+32067T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74892816 | ||||||
| chrX:74892940
|
G | GGA | 148 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(145): Show | 148 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.-48+31941_-48+3194 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74892940 | ||||||
| chrX:74892943
|
G | GAC | 1 | a0001c0001t0001g0082 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-48+31939_-48+3194 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74892943 | ||||||
| chrX:74892994
|
T | C | 2 | a0001c0001t0001g0064a0001c0001t0001g0073 | 2 | NA18970.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-48+31889A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74892994 | ||||||
| chrX:74893519
|
G | C | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+31364C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74893519 | ||||||
| chrX:74893947
|
T | G | 1 | a0001c0001t0031g0126 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-48+30936A>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74893947 | ||||||
| chrX:74894084
|
G | C | 17 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(14): Show | 17 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-48+30799C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74894084 | ||||||
| chrX:74894137
|
C | CA | 3 | a0001c0001t0001g0218a0001c0001t0006g0219a0001c0001t0006g0220 | 3 | HG02615.hp1 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-48+30745dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74894137 | ||||||
| chrX:74894137
|
CA | C | 121 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(118): Show | 121 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.-48+30745delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74894137 | ||||||
| chrX:74894147
|
A | T | 5 | a0001c0001t0001g0194a0001c0001t0001g0199a0001c0001t0001g0200others(2): Show | 5 | HG00735.hp2 HG02559.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48+30736T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74894147 | ||||||
| chrX:74894384
|
A | T | 1 | a0001c0001t0001g0066 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-48+30499T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74894384 | ||||||
| chrX:74894558
|
C | G | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+30325G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74894558 | ||||||
| chrX:74894797
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-48+30086T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74894797 | ||||||
| chrX:74895834
|
T | TA | 2 | a0001c0001t0001g0053a0001c0001t0015g0207 | 2 | HG00735.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.-48+29048dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74895834 | ||||||
| chrX:74895834
|
T | TAA | 1 | a0001c0001t0001g0210 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-48+29047_-48+2904 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74895834 | ||||||
| chrX:74895834
|
TA | T | 17 | a0001c0001t0001g0010a0001c0001t0001g0099a0001c0001t0001g0102others(14): Show | 17 | HG00323.hp1 HG01109.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-48+29048delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74895834 | ||||||
| chrX:74895850
|
C | A | 1 | a0001c0001t0026g0037 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-48+29033G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74895850 | ||||||
| chrX:74895946
|
T | A | 2 | a0001c0001t0001g0103a0001c0001t0001g0115 | 2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-48+28937A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74895946 | ||||||
| chrX:74896422
|
A | G | 1 | a0001c0001t0007g0224 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-48+28461T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74896422 | ||||||
| chrX:74896832
|
T | C | 1 | a0001c0001t0001g0138 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-48+28051A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74896832 | ||||||
| chrX:74897324
|
G | A | 1 | a0001c0001t0014g0213 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-48+27559C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74897324 | ||||||
| chrX:74897473
|
T | C | 6 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0198others(3): Show | 6 | HG02015.hp1 HG03491.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48+27410A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74897473 | ||||||
| chrX:74897888
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-48+26995T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74897888 | ||||||
| chrX:74897890
|
A | G | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+26993T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74897890 | ||||||
| chrX:74898111
|
G | A | 1 | a0001c0001t0001g0112 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-48+26772C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74898111 | ||||||
| chrX:74898195
|
T | C | 2 | a0001c0001t0001g0218a0001c0001t0006g0219 | 2 | HG02615.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-48+26688A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74898195 | ||||||
| chrX:74898221
|
A | G | 4 | a0001c0001t0001g0038a0001c0001t0001g0048a0001c0001t0001g0066others(1): Show | 4 | HG02027.hp1 HG02132.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+26662T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74898221 | ||||||
| chrX:74898896
|
A | C | 1 | a0001c0001t0004g0197 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-48+25987T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74898896 | ||||||
| chrX:74899007
|
G | A | 17 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(14): Show | 17 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-48+25876C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74899007 | ||||||
| chrX:74899087
|
A | G | 1 | a0002c0004t0011g0001 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-48+25796T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74899087 | ||||||
| chrX:74899341
|
C | CA | 1 | a0001c0001t0013g0003 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-48+25541dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74899341 | ||||||
| chrX:74899342
|
A | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+25541T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74899342 | ||||||
| chrX:74900006
|
C | T | 1 | a0001c0001t0001g0112 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-48+24877G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74900006 | ||||||
| chrX:74900188
|
G | A | 1 | a0001c0001t0001g0059 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-48+24695C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74900188 | ||||||
| chrX:74900457
|
C | T | 2 | a0001c0001t0002g0139a0001c0001t0002g0186 | 2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-48+24426G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74900457 | ||||||
| chrX:74900462
|
C | CA | 9 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0148others(6): Show | 9 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.-48+24420dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74900462 | ||||||
| chrX:74900474
|
A | AAAAAAAG | 6 | a0001c0001t0001g0080a0001c0001t0001g0110a0001c0001t0001g0112others(3): Show | 6 | HG02080.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48+24408_-48+2440 others(11): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74900474 | ||||||
| chrX:74900474
|
A | AAAAAAG | 103 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(100): Show | 103 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.-48+24403_-48+2440 others(10): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74900474 | ||||||
| chrX:74900474
|
A | AAAAAG | 4 | a0001c0001t0001g0047a0001c0001t0001g0060a0001c0001t0001g0074others(1): Show | 4 | NA18940.hp1 NA18960.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+24408_-48+2440 others(9): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74900474 | ||||||
| chrX:74900474
|
A | AATAAAG | 2 | a0001c0001t0008g0105a0003c0015t0008g0104 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-48+24408_-48+2440 others(10): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74900474 | ||||||
| chrX:74900632
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-48+24251G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74900632 | ||||||
| chrX:74900660
|
G | C | 116 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(113): Show | 116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-48+24223C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74900660 | ||||||
| chrX:74900700
|
G | T | 1 | a0001c0001t0012g0002 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-48+24183C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74900700 | ||||||
| chrX:74900804
|
T | C | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+24079A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74900804 | ||||||
| chrX:74900977
|
T | C | 1 | a0002c0004t0011g0001 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-48+23906A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74900977 | ||||||
| chrX:74901010
|
T | C | 1 | a0001c0001t0001g0010 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-48+23873A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74901010 | ||||||
| chrX:74901026
|
A | T | 116 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(113): Show | 116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-48+23857T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74901026 | ||||||
| chrX:74901031
|
G | A | 116 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(113): Show | 116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-48+23852C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74901031 | ||||||
| chrX:74901094
|
T | C | 5 | a0001c0001t0005g0119a0001c0001t0005g0120a0001c0001t0005g0121others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+23789A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74901094 | ||||||
| chrX:74901120
|
C | T | 1 | a0001c0001t0002g0192 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-48+23763G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74901120 | ||||||
| chrX:74901587
|
T | TCACA | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+23295_-48+2329 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74901587 | ||||||
| chrX:74901777
|
T | C | 1 | a0001c0001t0005g0122 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-48+23106A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74901777 | ||||||
| chrX:74901939
|
T | A | 1 | a0001c0001t0002g0160 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-48+22944A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74901939 | ||||||
| chrX:74902183
|
C | T | 1 | a0001c0001t0010g0190 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-48+22700G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74902183 | ||||||
| chrX:74902427
|
A | G | 1 | a0001c0001t0002g0186 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-48+22456T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74902427 | ||||||
| chrX:74902582
|
T | C | 115 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(112): Show | 115 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.-48+22301A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74902582 | ||||||
| chrX:74902698
|
A | T | 5 | a0001c0001t0005g0119a0001c0001t0005g0120a0001c0001t0005g0121others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+22185T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74902698 | ||||||
| chrX:74902989
|
G | A | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+21894C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74902989 | ||||||
| chrX:74903325
|
T | TAC | 25 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0026others(22): Show | 25 | HG00140.hp1 HG01069.hp1 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.-48+21556_-48+2155 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903325 | ||||||
| chrX:74903325
|
T | TACAC | 28 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0033others(25): Show | 28 | HG00280.hp1 HG01081.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.-48+21554_-48+2155 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903325 | ||||||
| chrX:74903325
|
T | TACACAC | 20 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(17): Show | 20 | HG01168.hp2 HG01169.hp1 HG02040.hp1 others(17): Show |
intron_variant | MODIFIER | c.-48+21552_-48+2155 others(10): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903325 | ||||||
| chrX:74903325
|
T | TACACACA others(1): Show |
17 | a0001c0001t0001g0020a0001c0001t0001g0047a0001c0001t0001g0048others(14): Show | 17 | HG00558.hp1 HG01981.hp1 HG02071.hp1 others(14): Show |
intron_variant | MODIFIER | c.-48+21550_-48+2155 others(12): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903325 | ||||||
| chrX:74903325
|
T | TACACACA others(3): Show |
17 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(14): Show | 17 | HG00408.hp2 HG00558.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.-48+21548_-48+2155 others(14): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903325 | ||||||
| chrX:74903325
|
T | TACACACA others(5): Show |
12 | a0001c0001t0001g0014a0001c0001t0001g0060a0001c0001t0001g0061others(9): Show | 12 | HG00621.hp1 HG01258.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.-48+21546_-48+2155 others(16): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903325 | ||||||
| chrX:74903325
|
T | TACACACA others(7): Show |
11 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0018others(8): Show | 11 | HG00609.hp1 HG01358.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.-48+21544_-48+2155 others(18): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903325 | ||||||
| chrX:74903325
|
T | TACACACA others(9): Show |
7 | a0001c0001t0001g0070a0001c0001t0001g0073a0001c0001t0001g0113others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-48+21542_-48+2155 others(20): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903325 | ||||||
| chrX:74903325
|
T | TACACACA others(11): Show |
5 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0102others(2): Show | 5 | HG01261.hp1 HG02083.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48+21540_-48+2155 others(22): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903325 | ||||||
| chrX:74903325
|
T | TACACACA others(17): Show |
1 | a0001c0001t0001g0077 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-48+21534_-48+2155 others(28): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903325 | ||||||
| chrX:74903325
|
T | TACACACA others(19): Show |
1 | a0001c0001t0001g0078 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-48+21532_-48+2155 others(30): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903325 | ||||||
| chrX:74903325
|
TAC | T | 15 | a0001c0001t0001g0080a0001c0001t0001g0134a0001c0001t0001g0210others(12): Show | 15 | HG00408.hp1 HG00735.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-48+21556_-48+2155 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903325 | ||||||
| chrX:74903325
|
TACAC | T | 20 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0099others(17): Show | 20 | HG00323.hp1 HG00323.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.-48+21554_-48+2155 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903325 | ||||||
| chrX:74903325
|
TACACAC | T | 5 | a0001c0001t0002g0157a0001c0001t0002g0168a0001c0001t0002g0176others(2): Show | 5 | HG01070.hp1 HG01099.hp1 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+21552_-48+2155 others(10): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903325 | ||||||
| chrX:74903325
|
TACACACA others(1): Show |
T | 7 | a0001c0001t0001g0109a0001c0001t0001g0194a0001c0001t0001g0195others(4): Show | 7 | HG00673.hp1 HG02258.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-48+21550_-48+2155 others(12): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903325 | ||||||
| chrX:74903325
|
TACACACA others(3): Show |
T | 4 | a0001c0001t0001g0108a0001c0001t0001g0222a0001c0001t0006g0098others(1): Show | 4 | HG02486.hp1 HG02615.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+21548_-48+2155 others(14): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903325 | ||||||
| chrX:74903325
|
TACACACA others(5): Show |
T | 1 | a0001c0001t0001g0196 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-48+21546_-48+2155 others(16): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903325 | ||||||
| chrX:74903325
|
TACACACA others(9): Show |
T | 2 | a0001c0001t0001g0115a0001c0001t0004g0189 | 2 | HG01243.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-48+21542_-48+2155 others(20): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903325 | ||||||
| chrX:74903325
|
TACACACA others(21): Show |
T | 1 | a0001c0001t0001g0214 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-48+21530_-48+2155 others(32): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903325 | ||||||
| chrX:74903703
|
T | C | 3 | a0001c0001t0002g0139a0001c0001t0002g0167a0001c0001t0002g0186 | 3 | HG02145.hp1 HG02818.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-48+21180A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903703 | ||||||
| chrX:74903782
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-48+21101C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903782 | ||||||
| chrX:74903790
|
CCT | C | 1 | a0001c0001t0004g0189 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-48+21091_-48+2109 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903790 | ||||||
| chrX:74903880
|
C | CGT | 5 | a0001c0001t0001g0103a0001c0001t0001g0138a0001c0001t0001g0199others(2): Show | 5 | HG01515.hp1 HG02818.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+21001_-48+2100 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903880 | ||||||
| chrX:74903880
|
CGT | C | 39 | a0001c0001t0001g0115a0001c0001t0001g0137a0001c0001t0001g0164others(36): Show | 39 | HG00408.hp1 HG00639.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.-48+21001_-48+2100 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903880 | ||||||
| chrX:74903880
|
CGTGT | C | 18 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(15): Show | 18 | HG00735.hp2 HG01192.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.-48+20999_-48+2100 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903880 | ||||||
| chrX:74903880
|
CGTGTGT | C | 2 | a0001c0001t0006g0219a0006c0006t0034g0118 | 2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-48+20997_-48+2100 others(10): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903880 | ||||||
| chrX:74903880
|
CGTGTGTG others(1): Show |
C | 4 | a0001c0001t0001g0218a0001c0001t0002g0183a0001c0001t0002g0184others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+20995_-48+2100 others(12): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903880 | ||||||
| chrX:74903880
|
CGTGTGTG others(3): Show |
C | 6 | a0001c0001t0001g0107a0001c0001t0005g0119a0001c0001t0005g0120others(3): Show | 6 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48+20993_-48+2100 others(14): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903880 | ||||||
| chrX:74903880
|
CGTGTGTG others(5): Show |
C | 113 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(110): Show | 113 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.-48+20991_-48+2100 others(16): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903880 | ||||||
| chrX:74903880
|
CGTGTGTG others(7): Show |
C | 1 | a0001c0001t0016g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-48+20989_-48+2100 others(18): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903880 | ||||||
| chrX:74903880
|
CGTGTGTG others(9): Show |
C | 1 | a0001c0001t0028g0006 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-48+20987_-48+2100 others(20): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74903880 | ||||||
| chrX:74904222
|
T | C | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+20661A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74904222 | ||||||
| chrX:74905048
|
G | C | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+19835C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74905048 | ||||||
| chrX:74905093
|
T | C | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-48+19790A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74905093 | ||||||
| chrX:74905456
|
A | G | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+19427T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74905456 | ||||||
| chrX:74905468
|
A | G | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+19415T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74905468 | ||||||
| chrX:74905639
|
G | A | 1 | a0001c0001t0004g0197 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-48+19244C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74905639 | ||||||
| chrX:74905678
|
C | T | 4 | a0001c0001t0001g0194a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 4 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+19205G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74905678 | ||||||
| chrX:74905744
|
A | T | 1 | a0001c0001t0001g0214 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-48+19139T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74905744 | ||||||
| chrX:74905828
|
AC | A | 2 | a0001c0001t0008g0105a0003c0015t0008g0104 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-48+19054delG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74905828 | ||||||
| chrX:74905829
|
C | A | 120 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(117): Show | 120 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.-48+19054G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74905829 | ||||||
| chrX:74905897
|
C | T | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+18986G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74905897 | ||||||
| chrX:74905988
|
G | T | 4 | a0001c0001t0001g0194a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 4 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+18895C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74905988 | ||||||
| chrX:74906098
|
T | C | 4 | a0001c0001t0001g0194a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 4 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+18785A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74906098 | ||||||
| chrX:74906110
|
AT | A | 1 | a0001c0001t0002g0154 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-48+18772delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74906110 | ||||||
| chrX:74906120
|
T | A | 8 | a0001c0001t0005g0119a0001c0001t0005g0120a0001c0001t0005g0121others(5): Show | 8 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-48+18763A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74906120 | ||||||
| chrX:74906145
|
C | T | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+18738G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74906145 | ||||||
| chrX:74906154
|
T | C | 3 | a0001c0001t0001g0218a0001c0001t0006g0219a0001c0001t0006g0220 | 3 | HG02615.hp1 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-48+18729A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74906154 | ||||||
| chrX:74906156
|
C | T | 5 | a0001c0001t0005g0119a0001c0001t0005g0120a0001c0001t0005g0121others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+18727G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74906156 | ||||||
| chrX:74906274
|
TA | T | 1 | a0001c0001t0001g0099 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-48+18608delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74906274 | ||||||
| chrX:74906429
|
G | A | 4 | a0001c0001t0001g0194a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 4 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+18454C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74906429 | ||||||
| chrX:74906754
|
A | T | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+18129T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74906754 | ||||||
| chrX:74906789
|
A | C | 13 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(10): Show | 13 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.-48+18094T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74906789 | ||||||
| chrX:74906796
|
T | C | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-48+18087A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74906796 | ||||||
| chrX:74906900
|
T | C | 3 | a0001c0001t0001g0218a0001c0001t0006g0219a0001c0001t0006g0220 | 3 | HG02615.hp1 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-48+17983A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74906900 | ||||||
| chrX:74906996
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-48+17887C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74906996 | ||||||
| chrX:74907007
|
G | T | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+17876C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74907007 | ||||||
| chrX:74907048
|
T | C | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+17835A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74907048 | ||||||
| chrX:74907334
|
A | AC | 34 | a0001c0001t0001g0138a0001c0001t0001g0164a0001c0001t0001g0194others(31): Show | 34 | HG00642.hp1 HG00735.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.-48+17548dupG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74907334 | ||||||
| chrX:74907334
|
A | ACC | 10 | a0001c0001t0001g0195a0001c0001t0001g0199a0001c0001t0001g0203others(7): Show | 10 | HG00735.hp2 HG01934.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.-48+17547_-48+1754 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74907334 | ||||||
| chrX:74907334
|
A | ACCC | 1 | a0008c0009t0002g0132 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-48+17546_-48+1754 others(7): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74907334 | ||||||
| chrX:74907334
|
AC | A | 9 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0148others(6): Show | 9 | HG00408.hp1 HG01081.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.-48+17548delG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74907334 | ||||||
| chrX:74907334
|
ACC | A | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+17547_-48+1754 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74907334 | ||||||
| chrX:74907339
|
C | G | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+17544G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74907339 | ||||||
| chrX:74907701
|
T | C | 2 | a0001c0001t0001g0103a0001c0001t0001g0115 | 2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-48+17182A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74907701 | ||||||
| chrX:74907974
|
C | T | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+16909G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74907974 | ||||||
| chrX:74908187
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-48+16696G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74908187 | ||||||
| chrX:74908225
|
A | C | 3 | a0001c0001t0001g0218a0001c0001t0006g0219a0001c0001t0006g0220 | 3 | HG02615.hp1 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-48+16658T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74908225 | ||||||
| chrX:74908383
|
C | T | 116 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(113): Show | 116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-48+16500G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74908383 | ||||||
| chrX:74908432
|
T | C | 1 | a0001c0001t0004g0189 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-48+16451A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74908432 | ||||||
| chrX:74908495
|
C | T | 1 | a0001c0001t0002g0154 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-48+16388G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74908495 | ||||||
| chrX:74908527
|
C | G | 1 | a0001c0001t0001g0103 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-48+16356G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74908527 | ||||||
| chrX:74909384
|
C | T | 2 | a0001c0001t0002g0152a0001c0001t0002g0153 | 2 | HG02698.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-48+15499G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74909384 | ||||||
| chrX:74909386
|
C | T | 1 | a0001c0013t0001g0143 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-48+15497G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74909386 | ||||||
| chrX:74909459
|
C | T | 4 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(1): Show | 4 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+15424G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74909459 | ||||||
| chrX:74909523
|
A | G | 6 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0148others(3): Show | 6 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.-48+15360T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74909523 | ||||||
| chrX:74909709
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-48+15174G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74909709 | ||||||
| chrX:74909750
|
A | C | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+15133T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74909750 | ||||||
| chrX:74909912
|
G | A | 1 | a0001c0001t0010g0190 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-48+14971C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74909912 | ||||||
| chrX:74909965
|
G | C | 1 | a0001c0001t0005g0123 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-48+14918C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74909965 | ||||||
| chrX:74910032
|
CTGCTAGG others(3): Show |
C | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14841_-48+1485 others(14): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910032 | ||||||
| chrX:74910043
|
G | C | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14840C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910043 | ||||||
| chrX:74910047
|
A | T | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14836T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910047 | ||||||
| chrX:74910049
|
A | C | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14834T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910049 | ||||||
| chrX:74910053
|
A | G | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14830T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910053 | ||||||
| chrX:74910059
|
TG | T | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14823delC | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910059 | ||||||
| chrX:74910064
|
T | C | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14819A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910064 | ||||||
| chrX:74910080
|
G | T | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14803C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910080 | ||||||
| chrX:74910081
|
A | T | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14802T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910081 | ||||||
| chrX:74910082
|
G | T | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14801C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910082 | ||||||
| chrX:74910086
|
CT | C | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14796delA | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910086 | ||||||
| chrX:74910090
|
T | A | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14793A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910090 | ||||||
| chrX:74910092
|
G | C | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14791C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910092 | ||||||
| chrX:74910093
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14790C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910093 | ||||||
| chrX:74910094
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14789C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910094 | ||||||
| chrX:74910095
|
C | T | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14788G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910095 | ||||||
| chrX:74910096
|
A | T | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14787T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910096 | ||||||
| chrX:74910098
|
TG | T | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14784delC | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910098 | ||||||
| chrX:74910104
|
G | C | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14779C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910104 | ||||||
| chrX:74910107
|
G | C | 1 | a0001c0001t0001g0079 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-48+14776C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910107 | ||||||
| chrX:74910107
|
GA | G | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14775delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910107 | ||||||
| chrX:74910111
|
T | TCTG | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14771_-48+1477 others(7): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910111 | ||||||
| chrX:74910112
|
G | C | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14771C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910112 | ||||||
| chrX:74910120
|
A | AC | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14762_-48+1476 others(5): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910120 | ||||||
| chrX:74910126
|
AC | A | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14756delG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910126 | ||||||
| chrX:74910146
|
TGG | T | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14735_-48+1473 others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910146 | ||||||
| chrX:74910151
|
G | T | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14732C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910151 | ||||||
| chrX:74910152
|
A | C | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14731T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910152 | ||||||
| chrX:74910153
|
T | C | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14730A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910153 | ||||||
| chrX:74910154
|
C | T | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14729G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910154 | ||||||
| chrX:74910158
|
T | A | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14725A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910158 | ||||||
| chrX:74910159
|
G | C | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14724C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910159 | ||||||
| chrX:74910160
|
A | T | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14723T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910160 | ||||||
| chrX:74910162
|
A | T | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14721T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910162 | ||||||
| chrX:74910164
|
C | T | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14719G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910164 | ||||||
| chrX:74910165
|
T | A | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14718A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910165 | ||||||
| chrX:74910167
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14716C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910167 | ||||||
| chrX:74910172
|
A | C | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14711T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910172 | ||||||
| chrX:74910173
|
T | TATC | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14709_-48+1471 others(7): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910173 | ||||||
| chrX:74910176
|
G | GC | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-48+14706dupG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910176 | ||||||
| chrX:74910294
|
G | A | 17 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(14): Show | 17 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-48+14589C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910294 | ||||||
| chrX:74910475
|
C | T | 6 | a0001c0001t0005g0119a0001c0001t0005g0120a0001c0001t0005g0121others(3): Show | 6 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48+14408G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910475 | ||||||
| chrX:74910502
|
A | G | 2 | a0001c0001t0001g0103a0001c0001t0001g0115 | 2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-48+14381T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910502 | ||||||
| chrX:74910758
|
G | A | 2 | a0001c0001t0002g0139a0001c0001t0002g0186 | 2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-48+14125C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910758 | ||||||
| chrX:74910816
|
G | A | 2 | a0001c0001t0001g0137a0001c0001t0003g0097 | 2 | HG02015.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.-48+14067C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74910816 | ||||||
| chrX:74911223
|
C | T | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+13660G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74911223 | ||||||
| chrX:74911288
|
C | T | 123 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(120): Show | 123 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.-48+13595G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74911288 | ||||||
| chrX:74911629
|
T | A | 1 | a0001c0001t0001g0080 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-48+13254A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74911629 | ||||||
| chrX:74911738
|
C | T | 1 | a0001c0001t0002g0144 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-48+13145G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74911738 | ||||||
| chrX:74912705
|
G | A | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+12178C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74912705 | ||||||
| chrX:74913240
|
C | T | 1 | a0001c0013t0001g0143 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-48+11643G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74913240 | ||||||
| chrX:74913377
|
C | T | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+11506G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74913377 | ||||||
| chrX:74913413
|
T | C | 1 | a0001c0001t0016g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-48+11470A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74913413 | ||||||
| chrX:74913531
|
T | C | 1 | a0001c0001t0013g0003 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-48+11352A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74913531 | ||||||
| chrX:74913628
|
G | GA | 2 | a0001c0001t0003g0081a0008c0009t0002g0132 | 2 | HG00621.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.-48+11254dupT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74913628 | ||||||
| chrX:74913628
|
GA | G | 10 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0004g0187others(7): Show | 10 | HG01243.hp1 HG02055.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.-48+11254delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74913628 | ||||||
| chrX:74914389
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-48+10494G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74914389 | ||||||
| chrX:74914554
|
G | A | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+10329C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74914554 | ||||||
| chrX:74914683
|
TCAAA | T | 1 | a0001c0001t0002g0142 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-48+10196_-48+1019 others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74914683 | ||||||
| chrX:74914713
|
C | A | 1 | a0006c0006t0034g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48+10170G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74914713 | ||||||
| chrX:74914739
|
T | C | 2 | a0001c0001t0004g0187a0001c0001t0007g0005 | 2 | HG02055.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-48+10144A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74914739 | ||||||
| chrX:74915001
|
G | T | 1 | a0009c0012t0002g0141 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-48+9882C>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74915001 | ||||||
| chrX:74915034
|
C | A | 3 | a0001c0001t0001g0218a0001c0001t0006g0219a0001c0001t0006g0220 | 3 | HG02615.hp1 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-48+9849G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74915034 | ||||||
| chrX:74915307
|
A | C | 116 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(113): Show | 116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-48+9576T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74915307 | ||||||
| chrX:74915337
|
G | C | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+9546C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74915337 | ||||||
| chrX:74915431
|
C | T | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+9452G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74915431 | ||||||
| chrX:74915465
|
C | G | 1 | a0002c0004t0001g0202 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-48+9418G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74915465 | ||||||
| chrX:74915508
|
A | G | 1 | a0001c0001t0001g0018 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-48+9375T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74915508 | ||||||
| chrX:74915602
|
G | A | 7 | a0001c0001t0001g0103a0001c0001t0001g0115a0001c0001t0001g0194others(4): Show | 7 | HG02559.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-48+9281C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74915602 | ||||||
| chrX:74915612
|
TC | T | 1 | a0001c0001t0001g0083 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-48+9270delG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74915612 | ||||||
| chrX:74915713
|
T | C | 116 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(113): Show | 116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-48+9170A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74915713 | ||||||
| chrX:74915899
|
T | C | 165 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(162): Show | 165 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.-48+8984A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74915899 | ||||||
| chrX:74915917
|
A | C | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+8966T>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74915917 | ||||||
| chrX:74916649
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-48+8234G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74916649 | ||||||
| chrX:74917010
|
C | G | 2 | a0001c0001t0004g0187a0001c0001t0007g0005 | 2 | HG02055.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-48+7873G>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74917010 | ||||||
| chrX:74917057
|
AC | A | 4 | a0001c0001t0001g0194a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 4 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+7825delG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74917057 | ||||||
| chrX:74917286
|
C | T | 116 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(113): Show | 116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-48+7597G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74917286 | ||||||
| chrX:74917421
|
T | C | 16 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(13): Show | 16 | HG01243.hp1 HG02015.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-48+7462A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74917421 | ||||||
| chrX:74917840
|
G | A | 2 | a0001c0001t0002g0191a0001c0001t0002g0192 | 2 | HG03688.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-48+7043C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74917840 | ||||||
| chrX:74917841
|
T | C | 1 | a0001c0001t0002g0128 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-48+7042A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74917841 | ||||||
| chrX:74918029
|
G | A | 1 | a0002c0004t0011g0001 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-48+6854C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74918029 | ||||||
| chrX:74918062
|
G | A | 1 | a0001c0001t0016g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-48+6821C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74918062 | ||||||
| chrX:74918396
|
A | G | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+6487T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74918396 | ||||||
| chrX:74918854
|
T | C | 4 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0028g0006others(1): Show | 4 | NA18971.hp1 NA19005.hp1 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+6029A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74918854 | ||||||
| chrX:74918892
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-48+5991C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74918892 | ||||||
| chrX:74919426
|
G | A | 18 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0087others(15): Show | 18 | HG00558.hp2 HG00673.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.-48+5457C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74919426 | ||||||
| chrX:74919429
|
T | C | 1 | a0001c0001t0002g0193 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-48+5454A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74919429 | ||||||
| chrX:74919629
|
T | A | 17 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(14): Show | 17 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-48+5254A>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74919629 | ||||||
| chrX:74919633
|
T | C | 5 | a0001c0001t0005g0119a0001c0001t0005g0120a0001c0001t0005g0121others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+5250A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74919633 | ||||||
| chrX:74919691
|
C | T | 1 | a0001c0001t0022g0017 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-48+5192G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74919691 | ||||||
| chrX:74919773
|
C | T | 1 | a0001c0001t0002g0139 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-48+5110G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74919773 | ||||||
| chrX:74919815
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-48+5068G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74919815 | ||||||
| chrX:74919867
|
C | T | 116 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0013others(113): Show | 116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-48+5016G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74919867 | ||||||
| chrX:74919869
|
C | T | 119 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0013others(116): Show | 119 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.-48+5014G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74919869 | ||||||
| chrX:74919871
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-48+5012G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74919871 | ||||||
| chrX:74920196
|
G | A | 4 | a0001c0001t0001g0194a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 4 | HG02559.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+4687C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74920196 | ||||||
| chrX:74920208
|
T | C | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-48+4675A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74920208 | ||||||
| chrX:74920239
|
G | C | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0013others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+4644C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74920239 | ||||||
| chrX:74920248
|
T | C | 1 | a0001c0001t0001g0014 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-48+4635A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74920248 | ||||||
| chrX:74920541
|
A | G | 1 | a0005c0007t0003g0016 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-48+4342T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74920541 | ||||||
| chrX:74920549
|
G | A | 3 | a0001c0001t0001g0218a0001c0001t0006g0219a0001c0001t0006g0220 | 3 | HG02615.hp1 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-48+4334C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74920549 | ||||||
| chrX:74920775
|
C | A | 1 | a0001c0001t0001g0116 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-48+4108G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74920775 | ||||||
| chrX:74921356
|
C | T | 17 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(14): Show | 17 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-48+3527G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74921356 | ||||||
| chrX:74921512
|
C | CTTTGTT | 2 | a0001c0001t0008g0105a0003c0015t0008g0104 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-48+3365_-48+3370d others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74921512 | ||||||
| chrX:74921663
|
C | T | 2 | a0001c0001t0001g0222a0001c0001t0006g0098 | 2 | HG02615.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-48+3220G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74921663 | ||||||
| chrX:74921722
|
GA | G | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0013others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+3160delT | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74921722 | ||||||
| chrX:74921985
|
A | G | 1 | a0001c0001t0001g0015 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-48+2898T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74921985 | ||||||
| chrX:74922113
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-48+2770A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74922113 | ||||||
| chrX:74922337
|
GGT | G | 159 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(156): Show | 159 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.-48+2544_-48+2545d others(4): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74922337 | ||||||
| chrX:74922337
|
GGTGT | G | 11 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(8): Show | 11 | HG00323.hp1 HG02615.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.-48+2542_-48+2545d others(6): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74922337 | ||||||
| chrX:74922337
|
GGTGTGT | G | 32 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(29): Show | 32 | HG00735.hp2 HG00738.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.-48+2540_-48+2545d others(8): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74922337 | ||||||
| chrX:74922337
|
GGTGTGTG others(1): Show |
G | 6 | a0001c0001t0005g0119a0001c0001t0005g0120a0001c0001t0005g0121others(3): Show | 6 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48+2538_-48+2545d others(10): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74922337 | ||||||
| chrX:74922584
|
T | C | 2 | a0001c0001t0003g0124a0001c0001t0003g0125 | 2 | NA18983.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-48+2299A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74922584 | ||||||
| chrX:74922642
|
A | G | 3 | a0001c0001t0002g0127a0001c0001t0002g0128a0001c0001t0031g0126 | 3 | HG00639.hp1 HG00642.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.-48+2241T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74922642 | ||||||
| chrX:74922734
|
T | C | 3 | a0001c0001t0001g0218a0001c0001t0006g0219a0001c0001t0006g0220 | 3 | HG02615.hp1 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-48+2149A>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74922734 | ||||||
| chrX:74922888
|
C | T | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0013others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-48+1995G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74922888 | ||||||
| chrX:74922899
|
A | T | 1 | a0001c0001t0001g0010 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-48+1984T>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74922899 | ||||||
| chrX:74923102
|
A | AG | 4 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0028g0006others(1): Show | 4 | NA18971.hp1 NA19005.hp1 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+1780dupC | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74923102 | ||||||
| chrX:74923447
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-48+1436C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74923447 | ||||||
| chrX:74923924
|
A | G | 1 | a0001c0001t0028g0006 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-48+959T>C | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74923924 | ||||||
| chrX:74924073
|
C | A | 1 | a0001c0001t0001g0222 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-48+810G>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74924073 | ||||||
| chrX:74924159
|
C | T | 1 | a0001c0001t0007g0005 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-48+724G>A | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74924159 | ||||||
| chrX:74924162
|
G | C | 1 | a0001c0001t0002g0223 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-48+721C>G | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74924162 | ||||||
| chrX:74924803
|
A | AC | 1 | a0001c0001t0030g0004 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-48+79dupG | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74924803 | ||||||
| chrX:74924838
|
G | A | 1 | a0001c0001t0007g0224 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-48+45C>T | NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | 74924838 |